The Most Important Thing You May Not Know about Hypothyroidism | Chris Kresser

The Most Important Thing You May Not Know about Hypothyroidism

by Chris Kresser

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This article is part of a special report on Thyroid Disorders. To see the other articles in this series, click here.

An estimated 20 million Americans have some form of thyroid disease. Up to 60 percent of these people are unaware of their condition. One in eight women will develop a thyroid disorder during her lifetime. Levothyroxine, a synthetic form of thyroid hormone, is the 4th highest selling drug in the U.S. 13 of the top 50 selling drugs are either directly or indirectly related to hypothyroidism. The number of people suffering from thyroid disorders continues to rise each year.

Hypothyroidism is one of the most common thyroid disorders. One recent analysis suggested up to 10% of women over 60 have clinical or subclinical hypothyroidism. It is characterized by mental slowing, depression, dementia, weight gain, constipation, dry skin, hair loss, cold intolerance, hoarse voice, irregular menstruation, infertility, muscle stiffness and pain, and a wide range of other not-so-fun symptoms.

Every cell in the body has receptors for thyroid hormone. These hormones are responsible for the most basic aspects of body function, impacting all major systems of the body.

Thyroid hormone directly acts on the brain, the G.I. tract, the cardiovascular system, bone metabolism, red blood cell metabolism, gall bladder and liver function, steroid hormone production, glucose metabolism, lipid and cholesterol metabolism, protein metabolism and body temperature regulation. For starters.

You can think of the thyroid as the central gear in a sophisticated engine. If that gear breaks, the entire engine goes down with it.

That’s why people with hypothyroidism experience everything from weight gain and depression to infertility, bone fractures and hair loss.

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One of the biggest challenges facing those with hypothyroidism is that the standard of care for thyroid disorders in both conventional and alternative medicine is hopelessly inadequate.

The dream of patients with thyroid disorders and the practitioners who treat them is to find that single substance that will magically reverse the course of the disease. For doctors, this is either synthetic or bio-identical thyroid hormone. For the alternative types, this is iodine.

Unfortunately, in the vast majority of cases neither approach is effective. Patients may get relief for a short period of time, but inevitably symptoms return or the disease progresses.

So what’s the problem? Why have replacement hormones and supplemental iodine been such dismal failures?

Because Hypothyroidism Is Caused by an Autoimmune Disease

Studies show that 90% of people with hypothyroidism are producing antibodies to thyroid tissue. This causes the immune system to attack and destroy the thyroid, which over time causes a decline in thyroid hormone levels.

This autoimmune form of hypothyroidism is called Hashimoto’s disease. Hashimoto’s is the most common autoimmune disorder in the U.S., affecting between 7-8% of the population. While not all people with Hashimoto’s have hypothyroid symptoms, thyroid antibodies have been found to be a marker for future thyroid disease.

Most doctors know hypothyroidism is an autoimmune disease. But most patients don’t. The reason doctors don’t tell their patients is simple: it doesn’t affect their treatment plan.

Conventional medicine doesn’t have effective treatments for autoimmunity. They use steroids and other medications to suppress the immune system in certain conditions with more potentially damaging effects, such as multiple sclerosis, rheumatoid arthritis and Crohn’s disease.

But in the case of Hashimoto’s, the consequences – i.e. side effects and complications – of using immunosuppressive drugs are believed to outweigh the potential benefits. (Thanks to conventional medicine for a relative moment of sanity here.)

So the standard of care for a Hashimoto’s patient is to simply wait until the immune system has destroyed enough thyroid tissue to classify them as hypothyroid, and then give them thyroid hormone replacement. If they start to exhibit other symptoms commonly associated with their condition, like depression or insulin resistance, they’ll get additional drugs for those problems.

The obvious shortcoming of this approach is that it doesn’t address the underlying cause of the problem, which is the immune system attacking the thyroid gland. And if the underlying cause isn’t addressed, the treatment isn’t going to work very well – or for very long.

If you’re in a leaky rowboat, bailing water will only get you so far. If you want to stop the boat from sinking, you’ve got to plug the leaks.

Extending this metaphor to Hashimoto’s disease, thyroid hormones are like bailing water. They may be a necessary part of the treatment. But unless the immune dysregulation is addressed (plugging the leaks), whoever is in that boat will be fighting a losing battle to keep it from sinking.

What the vast majority of hypothyroidism patients need to understand is that they don’t have a problem with their thyroid, they have a problem with their immune system attacking the thyroid. This is crucial to understand, because when the immune system is out of control, it’s not only the thyroid that will be affected.

Hashimoto’s often manifests as a “polyendocrine autoimmune pattern”. This means that in addition to having antibodies to thyroid tissue, it’s not uncommon for Hashimoto’s patients to have antibodies to other tissues or enzymes as well. The most common are transglutaminase (Celiac disease), the cerebellum (neurological disorders), intrinsic factor (pernicious anemia), glutamic acid decarboxylase (anxiety/panic attacks and late onset type 1 diabetes).

In the next post we’ll look more closely at why Hashimoto’s can’t be treated successfully without addressing the autoimmune component, and why both the conventional and alternative approaches to treating hypothyroidism are destined to fail from the start.


Join the conversation

  1. Hello,

    I had TSH 0.102 low and TSH receptor antibody 3.89 High.
    Anti thyrogobulin was 39.84
    anti microsomal was 13.10

    I am living in vietnam and one doctor said it was hyperhtyroidism graves and another said could be hashimotos.
    I had an ultrasound, nothing abnormal seen.
    i was given was thyrozon 10 mg
    and the other was dorocardyl 40 mg.

    There is so much information online, and it seems a lot of contradictory information by experts and I dont know if doctors know the underlying causes of these problems and are just treating symptoms without knowing the causes.

    I would like to know whats the best thing to do to know exactly if i have graves, hashimotos?

    And i heard they not curable, but merely can get them under control. I have felt very tired over 10 months.

    Thank you.

    • Hi James, try to go the natural route. See a naturopathic/functional medical practitioner if you can, they are much more experienced in this field and will recommend/provide natural products. Also google Medical Medium and Dr Jess.
      Best wishes

  2. Hi everyone. I have suffered for years. I was diagnosed 2 years ago with hashimotos autoimmune disease. I could have been diagnosed 5 years ago if my previous Dr. Had read the test results properly. Instead she kept try to tell me I was depressed and in denial. Thank goodness I eventually got my file and found a new Dr.. The biggest problem with this disease is the Dr.s.. At least my new Dr. Admits he does’nt know how to help me and he’s trying to get me to someone who can, so far that has been a bit of a nightmare to. They tell you what you’ve got, give you a pill that barely works and send you on your way. These are my symtoms. No menstration since 30 (I’m 47 now) sweats, chills, fever like body aches but no fever, Arthritis, lots of mucus in my throat, very low blood pressure, feels like I’m going to pass out often. B 12 deficiency, heart palpitations. Horrible pain and major bloating when I eat. Extremely dry skin, some skin pigmentation loss. Very dry hair. Joint and body pain, and now I have a cataract in my right eye. This isn’t all of it but the majority. I also work a full time job. My Dr. Says that I am a highly functional very very sick person. Yay me, seriously. Sorry I’m trying to keep this short. 20 years of suffering has not been fun. Here’s the thing, I realized two weeks ago after a bad specialists appointment, that I wasn’t going to get the help I needed to maybe have a bit of a normal life. Doctors do not have it all going on the way we all think. Infact this disease is way to time consuming for them so what do we do! Take your own life back. I finally realize that I actually can have some impact here. I have been reaserching like crazy to figure this out. So far I have started to journal everything I do, feel, and eat. I definitely have a big digestion problem I lost 40 lbs because I can’t eat do to pain and swelling. So I’m working on healing my gut. It’s definitely helping, my pain is much more tolerable. Still tired all the time but more energy. I watch what I eat. I’m taking a prebiotic and a probiotic as well as a vitamin D. I have a few other thing I’m going to try but I’m introducing things one at a time to see what the reaction is. I’ve read a lot of things about heal your gut heal most of your symptoms. So far so good. Food elimination diet. I highly recommend this for anyone with autoimmune and Hashimotos. Get rid of all gluten, watch foods high in lectin. I’ts not easy ( lots of salads and lean chicken breasts) but it’s necessary if I want to try and live a bit of a normal life. I’m finally listening to what my body is saying. I hope this might help some of you out there. Thanks for reading. I’ll keep you posted.

    • Gina, have a read through the comments on here they can be helpful, if you want to get better it’s best to gain as much knowledge as possible. See a functional/nutritional practitioner if you can, also look into the medical medium and Dr Stephen Cabral. Best

    • Colostrum will heal your gut immune tree 6 powder. I know God sent this as a tool for my child with many gut issues from Autism and it works! God Bless

  3. Am 60 yr old lady. Had thyroidectomy 10 yrs ago cos of v large goitre. Previously on 200mg thyroxine for 20 yrs and still on same dosage. Havent felt “right ” for many yrs. Deeloped weight probs so now got bad arthritis but also now seem to catch one cold after another. Obviously comprimised immune system. Can anyone suggest something to help?

    • I’m a male 34 and feel the same way for the past 7 years. Watch the program Fat,Sick, and Nearly dead. I’m on my 5th day and I’m going the whole 60. I’ve already lost 18lbs and I’m more social. My depression is almost nonexistent and my energy is crazy high! I had tried everything but nutrition and this is nooo joke. Please check it out. Let me know if you have any questions. I do the mean green juice. Anything that’s green I juice. Good luck Tracie

  4. I’m actually quite young to have this disease/condition (i’m 16 years old) and all I want is for my teachers and administration to understand that when i’m sick, i’m actually sick, i’m not pretending because I don’t want to be there. I tend to become sick more than other kids, I have told them multiple times that i’ve got Hypothyroidism and that it affects my immune system, and they don’t seem to believe me.
    What should I do?

    • Hi Sydnee, firstly read through the comments on here you may find them to be helpful. Secondly it may help you to cut out or at least reduce dairy and gluten for 2 weeks and see how you feel (both of these foods are inflammatory). Lastly, if you are able to get a juicer and have a glass of straight celery juice every morning on an empty stomach; celery juice is one of the most powerful and healing juices you can drink and can transform your health in as little as a week. Best wishes

    • Vitamin D deficiency is common with hypothyroidism. Vit D will effect your immune system, as well as your thyroid function. I recommend finding a naturopath and ask to switch to Armour Thyroid, or another form on Natural Desciated Thyroid

      • Yes. The natural thyroid replacements work much better for many people. Vitamin B,C,D Calcium, Magnesium and Selenium are important. I also take a baby aspirin, Turmeric and low dose Naltrexone to lower the inflammation levels.

    • We’re also same Sydnee..

      I’m not that prepared and having enough knowledge about this diseases until i’m already experiencing these symptoms this time so I’ve made my efforts to do researches.Thank you for this article by the way.I’m only 17 years old..and I can’t remove my fears for this..I have my dreams needed to fulfill to..but then joint pains and other symptoms hinder me..I’m having my medication for almost one’s really not easy to deal with.

      But don’t feel alone’re and we’re not alone for this fight..We have look for strengths in times when this disease really causing pains for us. He’ll never fail us.

      To your condition Sydney, it’s better to have time for them to explain your condition..or just your medical certificate speaks for you to really have an excuse..and to let them believe..I’ve aslo through with that neck seems larger than the normal size and even my teachers noticed it. My confidence to talk in front slowly ate (or eaten?, sorry for some wrong grammars if there’s any.) up by it..and as of these days, i’m also feeling the same way..I have to give an excuse letters for my check ups and blood tests..My teachers keep asking, are you ok?how could I tell them seriously,it’s not at all. They feel that pityness for me..and that’s not really nice to know when they’ll do your favor just because they considering your condition..How I view myself is really in low state..

      It maybe hard for others to understand our condition but the again, you’re not alone..

      Since now, i’m also searching for a relief for my joint pains and for the other symptoms..Can somebody help me?or any suggestions what to do to help me ease the pain?Your replies are much appreciated for me.Thank you.

    • Hello, Sydnee! Please check out Hypothyroidism Revolution, It’s has done amazing things for me, and I am hypothyroid.

  5. First of all, my heart goes out to those who – like me – are dealing with a multitude of symptoms. I’d like some advice on what I should do next. I apologize now as I’m going to be wordy! 🙂

    * I’ve been overweight my entire life. At my highest, I was 403.

    * Had a Gastric Bypass in 2001. Lost 171 lbs. Gained 68 lbs of that back by 2015.

    * Between a 2015 revisional to my GBP and taking 37.5 mg of Phentermine, I’ve lost 56 lbs and kept it off.

    * Diagnosed with Hashimoto’s in 2014. I take 50 mcg of Levothyroxine and my TSH/T4 comes back in the “normal” range per my endocrinologist

    * Tested for low Cortisol in 2014 by my endo – told it was fine. I started the test with a level of 1.3 (low “norm” is 3.7!) but did raise up to normal after the two injections.

    * Since 2014 I’ve been battling with low ferritin, and some times anemia. Told by my PCP, GBP doc, and endocrinologist this is because of the GBP. The thing is, I recall in the mid 80’s feeling much like I do now, BEFORE my bypass!

    * Been on iron supplements several times. They would help – but only temporarily.

    * Just saw a hematologist – who again says my current low
    ferritin is because of the GBP. She says the supplements won’t help though and ordered 2 Feraheme Infusions for me. Had the first on 3/15 – with another 3/21. Don’t feel anything yet, but that’s common I know.

    * As of 2/20 my ferritin was 8 (scale of 12-260), my Iron is 66 (scale of 25-170), my TIBC is 402 (scale of 250-450) and my Iron % Saturation is 16% (scale of 20 – 50%)

    * I’ve been tested for RA, and Lupus. Been told I don’t have either.

    * List of current issues I’ve been dealing with for nearly a month now:
    – extreme, extreme fatigue (sleep just fine, no sleep apnea as I’ve been tested)
    – always cold
    – craving sugar like mad
    – very depressed (I was diagnosed with Anxiety/Depression back in 1994 – take 30 mgs of Paxil for this)
    – Itchy skin
    – mild edema in left leg (sometimes in right leg as well as fingers)
    – achy joints
    – sore muscles
    – cramping muscles
    – unexplained weight gain/weight loss (though I’m still trying to stick to my diet – I want to lose another 44 lbs at least!)
    – slightly elevated bun/creat (31.3 with the “norm high” being 25) – told I was “slightly dehydrated” by my endocrinologist.
    – drink at least 60oz of liquid a day (if not more). Also eat a lot of “wet” foods – watermelon, broccoli, brussel sprouts. I can’t imagine why I’m dehydrated!

    One thought from all this: Going to my PCP on the 22nd – hoping she’ll refer me to a nephrologist. I want to revisit the cortisol issue again.

    Another thought: I’m wondering if I don’t possibly have Autoimmune Hemolytic Anemia – but the hematologist completely disagrees. My PCP and endocrinologist have no idea.

    WHEW! Wordy, I know!

    Does anyone have any advice for me? Should I just chalk it up with low iron and be done? Or should I pursue the nephrologist? The hematologist thinks most of my symptoms are from the “slightly low” iron levels. She feels given a few weeks with the 2 infusions, I should be fine.


    Thanks everyone!

    • Capodo – sounds like you have an autoimmune issue. Heal your gut. 3 days of bone broth fast and/or juice celery (celery: 16oz/2 glasses); drink both broth and celery on empty stomach (you should notice a difference in a week, if not two). Also look into Colostrum by Immune Tree. Best wishes.

    • Sounds like hypothyroidism to me. I am hypothyroid as well, and I have been following a program by Tom Brimeyer called Hypothyroidism Revolution, look him up. I have had AMAZING results from it! Good luck!

    • A friend of mine normalized her very low iron when she switched from levothyroxine, a T4 medication to NatureThroid, a T4-T3 combination medication. She was not expecting that to happen and her nurse practitioner was amazed! After years of infusions for low iron, the right thyroid medication made a surprising difference for my friend. I’m not qualified to give medical advice, however, I thought you might like to hear what happened.

    • It sounds like you might have candida yeast overgrowth, especially with the sugar cravings, or parasites or even adrenal fatigue. Conventional doctors won’t help you with that. FInd a GI specialist and ask for a comprehensive stool test and other testing. Good book to check out is Digestive Wellness 4the edition. You can buy it on hope this helps you. I also have hashimotos but can’t take my armour thyroid Med 1/4 grain because it makes me have side effects of turning bitchy and irritable and it makes me look so wired I could get arrested for looking like I am high on drugs. W t f. My body is also out of progesterone (0.5) and I am trying to get my insurance company to pay for a script of the biodentical version. I don’t know if you all know this but if yout have any hormonal imbalance at all (estrogen, progesterone) adrenal hormone imbalance etc, it will screw with your thyroid gland and make you get hashimtos or worse. It will also cause your thyroid meds not to work right no matter what. Also since hashomtos is an autoimmune disease the problem is not with your thyroid its with your immune system and that is what needs to be addressed first in order to heal your thyroid. I just love falling apart as I get older. I can relate to what some other person was saying aboyt their dictor thinking they are crazy because i told mine that i have IBS C( used to be d before menopause) and the quack told me it was all in my head and she even had the gall and audacity to put in the notes in my medical record that all of my symptoms are probably “psychologically” related. I was so insulted and pissed when i read that i called the clinic and told off the doctor and told her i dont know where you get off but if you EVER contact me again for anytjhing I swear to god i am going to call an attorney
      and file a lawsuit against you, the clinic and 4 other doctors for medical malpractice and negligence. She even refused to give me a script for progrsterone when i showed her the results of my last blood tests and told me i didnt need prigesterone because i am getting old and it didnt matter if i got fat and my breasts go flat etc. i am so sick of stupid conventional doctors who dont teally give a s….. lol

      • I have found this for more than 20 years. Wellness clinics, nutritionists, or alternative medicine doctors are more accepting of these types of symptoms and methods to heal them. I am no asymptomatic but I have made a 75% improvement, mostly through glutamine powder for leaky gut and food sensitivity testing and elimination. I believe probiotics are an absolute must. I really trust a company called optibac in the UK. They have done extensive studies on strains. I use them exclusively. Progesterone has been a huge help for me for any number of symptoms. You can buy progesterone cream over the counter. The skin absorbs most of the medicine unlike digestion killing 80-90% of what is taken orally. You can even get progesterone cream from cow or pig thyroid that has been dessicated. Lastly, take a look at CBD oil. It is derived legally from hemp and it is exploding right now. It is the only thing that helps my pain. I was convinced I had rheumatoid arthritis. I take 25 mg CBD oil under my tongue 3 times a day. There are numerous ways to take it. You should see whats out there and the results that they are getting. Emergency Rooms are going to start using it. I wish you well in this quest. I have not found everything I need yet but I don’t give up and neither should you (I have wanted to give up at least 3 times but dissability income is really low).

        • Hi Rena, may I ask how much glutamine powder you took and how long it took from starting it when you seem to notice a difference? Also which CDB oil have you been using? Unfortunately there are a lot out there which are no good. Thank you

  6. Why are the number of people suffering from thyroid disorder continuing to rise each year as you stated in the beginning of your artical?
    I have had conversations with GP and endocrinologist about wheat, glyren etc. they tell me I’m nuts no connection ?

    • Environment+genetic predisposition+stressful trigger. Leaky gut= gluten and lactose intolerance over time. Thyroid+leaky gut=autoimmune diseases. Body mistaking and attacking healthy cells. Some say it might be cause by bacteria, viruses, or dependence on antibiotics that kill off healthy instestinal flora. I went to school with your brother, Mark!

    • Milk,eggs, soy etc.. The food served in this country is the issue. It causes the DNA damage, attacks the gluten particles on your thyroid, then life as you know it is over!!! I’ve suffered my whole adult life (30 +yrs). No doctor will help you, its simply not in the medical protocol. Medical biz will only give you more chemicals to throw you into a deeper tailspin. There is no answers. I found that measles,mono have a lot to do with your future health.. They’re killing us all slowly…

  7. I suffer from fatigue where I just want to stare at the walls and get nothing accomplished. My feet are cold and tingly, suffer weight gain, dry skin, hair loss and all the rest of the hypothyroid symptoms. I experience low blood sugar and all my blood work for diabetes comes back normal. My A1C is at 56. I check my glucose at home and my blood sugar has been low as 35 or 37. All other blood work came back normal last week. I was tested for Hashimoto in 2009 and it to came back normal. I feel achy all the time. I feel as if all I want to do is sleep and do nothing. I have been getting headaches also.

    • Hi Becky – I am familiar with the symptoms. I am trying lugols iodine as suggested by Bonnie (see comments in this post) also I have been trying different natural herbal supplements including Gaia herbs adrenal health. Read about VeganSafe B-12 one of the best B12 supplements which can work wonders for energy. Also read about celery juice and how this can heal. Hope this somewhat helps.

      • Elizabeth, Thank you for responding.

        Could this be my adrenal gland? I never had any tests done for my adrenal glands at all. should I get them tested?

        As I said in my previous comment, I was tested for Hashimoto in 2009 and it came back normal. I started taking Levothyroxin 25mcg since 2010. Now I am at 50 mcg. Does Hashimoto develop later?

        • Hi Becky, the thyroid has a number of functions, the most important of which, is that it is responsible for regulating metabolism and energy levels in the body. Low thyroid function is known as hypothyroidism. Many thyroid deficiency symptoms are also typical candida overgrowth symptoms, so there is also a connection between candida and thyroid problems. It can be a little overwhelming and no doubt leaves you thinking so where do I start. If you are happy to have your adrenals tested I would do it with a certified functional medicine practitioner. Hypothyroid is known to be difficult to test for, so it’s very unlikely it will be picked up on through a regular test with your GP (hence it’s best to get it done with someone who runs these tests all the time and are familiar with the results). For the meantime I suggested the Gaia herbs, B-12 and celery juice as these are all natural supplements which should help you on your way to feeling better. It also helps to do a lot of research. I follow a few other naturopathic doctors and do a lot of research myself so hopefully these things may be of some help. Best wishes

    • You may want to be retested for Hashimoto again. I only say this because last year my cycle became really out of wack and my OB performed a thyroid test on me. They told me that my results were normal and that sometimes these things happen. Well come December I go to my primary care clinic with symptoms of numbness/tingling, foggy headiness, extreme tiredness, achey joints, and dry itchy skin. At first I see the nurse practicener ask if I’ve had a thyroid test and I tell her my OB did it last year. After a month and half run around that included a cancer scare she finally diagnoses me with a B12 deficiency because my B12 was 230. So they give me a shot of B12. Within the hour my symptoms get worse. It takes me two weeks to get back in to see the real doctor. He looks at my chart and states that he doesn’t see that a Thyroid test has been performed. I decided to keep my mouth shut this time and let him test it. Thus this week I was diagnosed with Hashimoto with a B12 deficiency and put on the proper medication.

    • An auto-immune response can progress for a couple of years before any data shows up on a test. You know your body, if things feel out of whack, you’d know better than anyone. If you have a low basal body temp 97.8 or lower (check for 3-5 days in a row), feel “wired” inside even when you’re relatively calm, you feel tired even after getting 7-8 hours of sleep and have difficulty doing the normal everyday things you used to do, like simply washing the dishes, then there is something wrong, no matter what the tests are showing.

      All organs work together, so it isn’t isolated to your thyroid; your adrenals, gut, pituitary, kidney’s, liver, etc need to be healed. You start with the gut – get your digestive system in order, which will lead to balancing your hormones, which will balance your immune system…..

      Emerita progesterone cream, vitamins D3, k2, vit c, b12 (Methylcobalamin form & sublingual only) hcl, trace minerals. If you’re taking antacids including prescription antacids, ditch ’em, the problem isn’t too much stomach acid – it’s almost ALWAYS too little stomach acid. Too little stomach acid will reek havoc, like a domino effect, with your health.

      Get rid of the packaged foods, no fast food, no soda-none, (not even diet(it’s actually worse), only whole, un-processed, non-GMO foods. Do not eat any factory farmed meats, dairy, or eggs -which are full of growth hormones, toxins, GMO-feed, and antibiotics. Eat only pastured raised, grass-fed. Period. It will take some time, but you will start to heal.


  8. Hi!
    I would love some feedback from you guys as I am not sure what to do.

    Over the past 3 months I’ve experienced alot of anxiety, sleeping issues, fatigue and bloating. My lab results found that I have low progesterone, making me estrogen dominant which could explain many of my symptoms. But I have also tested my thyroid for anti bodies 3 times. First time it was 50 IU/ml, second time 72 IU/ml, and third time 101 IU/ml. So I have an antibody present. My TGAb was always 0. All the doctors I’ve seen all say my thyroid is fine. But if there is an antibody present doesn’t that indicate an autoimmune disease?
    I don’t eat gluten, dairy, soy, sugar or nuts so my diet can not be the cause of any inflammation.

    I’m not sure what to do now. Should I just accept what the doctors are saying that my thuroid is fine or does this seem strange to anyone else as well?

    Many Thanks!

    • Hi Linda, it can be immensely frustrating I know. If you are convinced you have a thyroid issue presumably you have seen a certified practioner or someone very experienced in that field. If you want to try an alternative method look into celery juice (simply juicing celery), apparently it has amazing healing effects (I am yet to try) also if you haven’t yet read the comments on here, try iodine. Wish you well.

    • A leaky gut is most likely your issue. This means you have a pourus gut. A condition in which bacteria, food particles etc., fall into the bloodstream. Your immune system responds by becoming hyper vigilant and attacking the foreign invador. This increases/ worsens allergies and causes major inflammation.

  9. Hi There,

    I just got these labs from my endocrinologist and I wanted a different perspective on them.

    Can you tell me your thoughts?

    I am a 47 year old Lebanese female who is “5” ‘4 3/4″ and weighs 169 lbs. I have lost 46 lbs since last December 19, 2015.

    I have PCOS and genetically inherited high cholesterol and high blood sugar. Besides genetics I am a sugar addict and have binge eating disorder.

    I have been pre diabetic off and on for at least 5 years. I have never been diagnosed with diabetes as I have never reached diabetic numbers through a self induced OGTT, A1c tests, fructosamine and fasting blood sugars.

    I am working on my diet and exercise to reduce certain blood markers.

    My blood sugar has come down and I am still working on my cholesterol. The cholesterol was measured by my primary care doctor and cardiologist.

    The blood work below was from last week at my Endocrinologists office.

    My last total cholesterol was 360 but my hdl and triglycerides were in normal range. Taken about a couple months ago.

    Last spring my total cholesterol was 259 coming down from 312. Prior to 312 it was 344.

    When it was 259 my hdl and trigs had also improved.

    I think it went high again because I started eating sugar again. I was still losing weight and monitoring my caloric intake but I went Paleo almost sugar free from December 2015 to April 2016 and that’s when my cholesterol came down from 312 to 259.

    I am back to minimizing sugar intake.

    I also suffer from depression, anxiety and ocd.

    I started gaining weight when I hit puberty and developed PCOS. I have lost and gained weight many times since then.

    I carry most of my weight in my belly.

    I am having a hyperoscopy done on Dec 15. Some hyperplasia was found in my uterus.

    I have never had kids. My period has been regular since my early thirties.

    Please let me know if you need any more information.

    I appreciate your insight!!

    Thank you very much.




    T3, Free: 2.6

    TSH: 2.33



    Fructosamine: 243

    A1C: 5.4



    Insulin: 3.8


    C-PEPTIDE: 1.31

    Vitamin D: 25

    SODIUM 137


    CHLORIDE 103


    GLUCOSE 92



    Bun/Creatinine ratio is not reported when the BUN
    and creatinine values are within normal limits.

    CALCIUM 9.9


    ALBUMIN 4.2


    A/G RATIO 1.4


    AST 12

    ALT 13


    Fasting reference interval


    • Your lab looks pretty good. You mentioned total cholesterol. But LDL and HDL value is more important so we can assess the potential risks. PCOS is making it difficult for you to keep your ideal weight. But it’s very important to keep physically active. Regarding your diet, low carb, high protein is good. Don’t stress yourself too much, try to be more relaxed in general, try yoga or other forms of meditation.

  10. My doc wants me to go off of naturethyroid (which seems to be working) except for my TSH is very low (0.05). My doc wants me to switch to Synthroid as she says it will work better. I’d rather not but my TSH is very low… Any thoughts or advice?

      • I’d ask her reasoning why taking synthroid with only one, omitting 3 other thyroid hormones in Nature-thyroid would be better for you. Some drs. have the misconception that natural is inconsistent. Also research comparisons and consider getting a second opinion from a doctor who routinely prescribes natural thyroid and can manage your condition. After years unregulated by a traditional Dr., I changed drs. and merely needed precise adjustment of the dose.

          • NatureThroid and other natural medicines contain T1, T2, T3, T4 and Calcitonin.
            Conventional, synthetic, thyroid medications, like Synthroid and Levoxyl and Levothyroxine contain T4… and that’s it! T4 is your storage hormone and your body has to be able to convert the T4 from the meds to T3, which is the active hormone. If you are not able to convert the T4 to the active T3 you will remain “sick” and hypo on the T4 meds.

      • Low TSH isn’t really a good thing, it’s hypothyroidism.. I’m pretty sure that 0.5 is the lowest “normal” TSH level that most endocrinologists are comfortable with. Even with that, your body is constantly trying to produce & convert thyroid stimulating hormone, T3 & T4. That’s part of why so many of us are sooo exhausted when our doses aren’t right.
        BTW, I have Hashimoto’s, am on Levothyroxine (same as synthroid), was diagnosed in my mid20’s (after what everyone thought was a seizure while I was bartending), & my levels, which were done as a last resort effort before they released me by the supervisory Dr, since they couldn’t figure out what was wrong, were so unbelievable that they called me at home to come back. They re-did them, confirmed that it was a HUGE, VERRYYY LONG TIME thyroid problem & sent me on to endocrinology.. And there was “no way” it could be my thyroid bc I was “just too young.” Always get a second opinion if the first one feels wrong.. Good Luck!

  11. I am intolerant to gluten including corn dairy and other foods.I have tried to heal leaky gut but had very severe reaction to l glutamine and am now super sensitive to even very small amounts of intolerant foods i.e. Found in vitamins.
    I have been diagnosed with Graves’ disease and coeliac disease is in the family.My son is a type 1 diabetic.
    I want to take priobotics was thinking of taking bio kult.
    I live in England so cannot get hold of a lot of things sold in America. Please could you give me some advice Many Thanks

  12. I have been diagnosed with hypothyroidism post delivery. But I don’t have auto immune thyroid disorder. My anti microsomal antibodies are negative. But still Doctor put me on thyroid medication. I’m almost taking the medication for 5 years.if not auto immune what might be the reason for hypothyroidism.i want to quit medication slowly.
    I have corrected all other related deficiencies like vitamin D B 12 etc
    Please help

  13. My girlfriend has been diagnosed with Hypothyroidism for several years and has been taking 25mb of
    Eutirox (Levothyroxine). She has also been told it is an Auto Immune Disease. She also has some gut sensitivities and with no proper diagnosis I believe she may have leaky gut. Typical story that she ‘grew up’ on antibiotics.

    Basically I have been reading Chris’s articles and listening to podcasts for a few weeks so am only a BEGINNER in all of this. Focus of my reading has been on auto immune disease, leaky gut and thyroid issues. Forgive me if I have this all wrong.

    My girlfriend also has other issues such as breast and ovarian cysts, Hair Loss, Tiredness in afternoon, puffy eyes (if she is off Levothyroxine).

    So my first comment is that Hypothyroidism is not listed as an Auto Immune Disease. I found the list here:

    So my assumption is that Hypothyroidism is a symptom of something else. Of course Hypothyroidism is a symptom of Hashimotos, listed as an auto immune disease, as well as a symptom of Iodine deficiency. All covered by Chris in his articles.

    Chris mentions that some cases of Hypothyroidism have shown improvements with supplementing on Iodine and he references Dr. David Brownstein as an expert on Iodine.

    Listening to Dr. Brownstein speaking about Iodine supplementation (referenced below) he gives higher dosages in his recommendations for daily Iodine supplementation.

    All recommend supplementing Iodine along with Selenium.

    Chris also states the following:

    “Iodine deficiency is the most common cause of hypothyroidism worldwide. Once
    researchers realized this, health authorities around the world began adding iodine to
    table salt.

    This strategy was effective in correcting iodine deficiency. But it had an unanticipated—and undesired—effect. In countries where iodine has been added to table salt, the rates of autoimmune thyroid disease have risen.

    Why does this happen? Because increased iodine intake, especially in supplement form, can increase the autoimmune attack on the thyroid. Iodine reduces the activity of an
    enzyme called thyroid peroxidase (TPO). TPO is required for proper thyroid hormone production.
    On the other hand, restricting intake of iodine can reverse hypothyroidism. In one study, 78% of patients with Hashimoto’s regained normal thyroid function with iodine restriction alone.”

    So some conflicting information about Iodine but is Chris actually referring to Hypothyroidism when it is caused by Hashimotos? Rather than Hypothyroidism caused by Iodine deficiency?

    According to Dr Group (referenced below) Iodized Salt is not a good source of dietary iodine but note Dr Group does sell an Iodine supplement.

    Dr Brownstein

    Video of Dr. Brownstein interviewed by Dr Joseph Mercola has some interesting info on Iodine. Dr Mercola has been interviewed by Chris himself on one of his podcasts.

    Generic Information on Iodine:

    RDA for Iodine is 150 mcg which is said to be insufficient by Dr Group and Dr Brownstein. Also Chris recommends a higher dose as does Dave Asprey on (supplements) Dr. Group explains the RDA of 150 mcg was set by FDA to be enough to combat Goiters.

    FAO.ORG above lists the upper limit of Iodine intake per day is 30 mcg per kg of body weight.

    Another reference I found about Iodine deficiency is

    Dr Edward Group
    15 Must Know Facts About Iodine

    On this page is a 1 hr video where Dr. Group discusses Iodine and Iodine deficiency.

    Dr. Group lists all the other symptoms that my girlfriend has as being caused by Iodine deficiency.

    Note: Global Healing Centre sell various products one of which Detoxadine is a high dose Iodine supplement.

    Both Dr Brownstein and Dr Edward recommend a much higher dose of Iodine and also mention that 19 out of 20 people in USA are deficient in Iodine.

    Summary: So in summary I believe that my girlfriends doctors have confused us with their diagnosis of Hypothyroidism as an Auto Immune Disease and have not included her other symptoms namely breast and ovarian cysts, Hair Loss, tiredness in afternoon, puffy eyes, which they knew about, as possibly caused by Iodine deficiency alone. Or they have not found the true cause of the Hypothyroidism which could be Hashimotos.

    We will need to find a Dr or FMP to help here further investigate her hypothyroidism cause and subsequent healing plan.

    I hope this information is accurate and if it is that it helps someone in their own investigation

    • Please say where you live, so that the community can help. I know of great Drs. in St. Paul, MN and San Diego. It took me years to find them. Thanks for the info on Iodine. I have Hashimotos, and am on Nature-Throid. Good luck to your girlfriend and I hope she appreciates such a thoughtful boyfriend.

      • I need help..please…I have hypothyroidism, I hurt all over, just walking to the bathroom from my living room is so painful that I have to hold on to things…I am starting to have stomach problems, like an achey feeling…I feel like my body is falling apart one limb at a time.

      • Hi, Carey. I was just diagnosed with non-autoimmune hypothyroidism. My doctor, a functional medicine doc, prescribed natural thyroid. I’ll pick it up tomorrow. I’m not a fan of medication and would love to hear of someone else’s experience on this medication. My TSH is 4.5 and my vit D is 17. I started Vit D/K2 this week. My concern with the medication is that it will inhibit my body’s ability to produce it’s own hormones. I’m also not excited at the prospect of being on a medication for life, although my doctor says I don’t have to be on it for life. I’m reading conflicting info on that. Any info would help. Thanks!

      • St. Paul, you say? I am certain I have hypothyroidism after yet another blood test indicated a change in my thyroid level, but I know I’ve never been tested for an autoimmune disease as the potential cause. My first endocrinologist wrecked absolute havoc on my hormones, and I lost a job and a marriage thanks to the spiralling depression, fatigue, and nearly all of the other known positive symptoms. I’ll take any good local suggestion versus any unknown clinic.

  14. hi everyone i am a bit more unlucky than u as i have swelling in my legs and forearms due to my thyroids problems very uncomfortable ???mixedema ?will i ever get rid of these edemas?anyone there suffering from the swelling related to hypothyroid ?thanks and all the best

    • Darling this was one of the first signs I had of this disease. You need high levels of Levothyroxin. You also need to be monitored by testing of your T4 and T5 levels. I am taking 250 mg of Levothyroxin and am just now feeling some relief and have lost 20lbs in a year. This is significant for me as I have weighed over 200lbs for some time now. I now can see my bones in my ankles. No more Kankles. lol

  15. Hello,
    I recently went to the Endocrinologist and he ordered blood work and I received a phone call 2 days ago from the nurse telling me that it I have Central hypothyroid but it is not caused by an autoimmune disease. If it is not an autoimmune disease then what could it possibly be? I can not find anything on the internet regarding Central Hypothyroidism without cause of an autoimmune disease. Hope someone can shed some light onto what maybe going on.
    Thank you in advance

    • I have hypothyroidism…on synthroid 75 MG. I go back and forth trying to figure out a better schedule in taking meds. I usually take them at night…but I am in pain all the time…muscle and joint/bone pain. I am not one for taking meds…not even Advil…but its getting ridiculous. I am also taking D vitamins/Calcium… what gived…any suggestions… I’m thinking rheumatoid arthritis but test came bag neg..and TSH levels etc. What do u guys think? Cleared for lupus, cleared for MS… this sucks.

      • Do you smoke? My test results always said I was fine too, I stopped smoking and had my thyroid checked a month after quitting and I had TSH levels all out of whack! I had been telling the Dr over and over that I think I have something wrong with my thyroid and they would do the test and always came back within range. I do believe smoking causes a false reading.

        • Hi Charlie, your situation sounds so much like mine did yrs ago. I had been getting joint pain for yrs and thought I was just pushing myself too much. When I turned 35 I found out I had hypothyroidism and only a year and a half ago which was 6 yrs later I was diagnosed with rheumatoid arthritis. My synthroid dosage is 125 mcg.

      • When you take D-3, you also need to supplement with Magnesium. Unless you supplement with magnesium, the D-3 will consume all of the magnesium in your body and make your joints ache. Also take probiotics to heal your gut.

      • Do you drink things with aspartame in them? Diet sodas? That was major for my joint pain. Kicked all artificial sweeteners to the curb and relief from joint pain. Never knew it to be related to my hypothyroidism.

      • I was diagnosed with hypothyroidism about about 5 months ago at the ER. I’m 30, felt 70, and it got to a point that I couldn’t cut my own meat my hands hurt so bad. It felt like my hips were going out of place. My lower back felt like it was punched and beaten, I would hunch over for relief. All my joints seemed audible. I had to bend and crack my toes every morning so I could walk without pain.

        I did a little research and tried out potassium gluconate suppliments I came across at Walmart. It’s absolutely like night and day. I can stand tall, use my body again, especially my hands without that grinding piercing ache.

        I’m also now taking B12 suppliments, magnesium citrate, and flaxseed oil due to hypo research. It feels like two years ago when nothing felt wrong. You may want to have a vitamin deficiency panel done by your doc to make sure you take the right amount of vitamins. Good luck!

      • You may need a higher dose of levo. I have hypothyroidism diagnosed by symptoms rather than thyroid blood tests. The test results were always normal. Fortunately my sinus doctor suggested to my primary physician that I be started on medication because of years of sinus 6-7 infections a year. And it worked!!!!!
        Gradually over the years the dosage has been increased. I am now on Synthroid 250mcg a day. My thyroid levels except for the TSH remain in normal range. My TSH is way low which freaks my doctors out. But I continue on because I have no symptoms of hyperthyroidism. My temperature which is my guideline remains below 98F. Although it is creeping up. Thank Good for my sinus doctor who encouraged my primary care physician to step out of the box.
        An excellent resource for on hypothyroidism is “Thyroid Power” by Dr Richard L. Shames and KarileeH. Shames. Good Luck!

  16. Hi! Does anyone know if hypothyroidism would effect wbc? I doing great other than that my EBV is low, at 2.9. Vit D is a little low as is iron, but everything else is good and I feel better than I have in a long time. I’m on 2grains armour thyroid, and although my bloodwork indicates hyperthyroidism, I’m not experiencing any hyperthyroid symptoms at all. I’m most concerned with my wbc and am praying its thyroid related. Help! Thanks!

    • What is your white blood cell count? If your neutrophils are low, it could be a B12, folate or copper deficiency. B12 and folate are the most common deficiencies and especially common for folks with thyroid issues. Copper deficiency can happen to anyone taking high iron supplements or taking too much zinc. Zinc is common in thyroid supplements. More than 50mg a day for even a week or two can lead to a copper deficiency, which can be very dangerous. It can cause permanent nerve damage by the time it’s diagnosed.

      The EBV is for the Epstein-Barr virus, right? Isn’t it generally looked at as a positive or negative test? If it’s not zero, it means you had Mononucleosis at some point in the past. I don’t know what it has to do with the white blood count.

      • There is such a huge misunderstanding about EBV. Many times EBV resides in places or lies dormant and does not show up on tests. EBV and heavy metals is the root cause of most all auto immune diseases and can be eliminated! Check out the book Medical Medium a must read if you want to cure the root cause.

  17. Hi! I was diagnosed with hypothyroidism at age 11. The only symptom was very irregular periods. I was prescribed 25mcg of levothyroxine. At 15, the doctor changed the dose to 50, at 19 to 88 and at 21 to 100. I’m now 26. Have been sluggish and overweight for at least 3 years… Nothing really seems to help much. My numbers- from what I could tell have been normal. Now, my TSH is a little low .31 and my antibidies are high (ATA- 8 and TPO 198). I don’t know if the antibodies were checked before. I have been experiencing sweeling of my hands and feet and very dry skin and hair. My question is, should I be more worried about the antibidies- does that mean I have Hashimoto’s and should I seek a second opinion because my doctor does not seem worried about it at all?

    • The symptoms you describe suggest hypothyroid. There could also be some other issues. Antibodies are produced by the immune system. I recommend that you do some reading yourself and find an Integrative Dr. who understands the entire endocrine and immune systems. Synthroid doesn’t work for everyone, take me with Hashimotos. You may want to consider natural thyroid.

    • Hi P, I don’t think majority of general doctors care much at all about these cases or at least don’t have the knowledge about it to help. The best bet is to see an integrative doctor. They have a much better understanding and are much more able to help in this area. Also do some good research on the web, there are also a lot of herbal supplements which may be of help to you.

    • There are a few things that can lower thyroid function without raising TSH. Zinc deficiency and too much fluoride are two examples. Zinc deficiency affects the pituitary’s ability to make TSH, as well as other things. Fluoride lowers the function of several glands, including the pituitary and the thyroid. Fluoride is found in very high amounts in tea (both organic and conventional), and in conventionally grown grapes and wine made in the US.

      Tea is actually how I ended up with a thyroid issue. It’s probably the biggest health misconception out there right now. Especially green tea – supposed to be so healthy – it’s NOT. I used to drink Chai every morning. I liked it strong and that was part of the issue – more fluoride. Over about two years, it made me seriously hypothyroid, but with a normal TSH. I was so cold I wore socks to bed in the summer. Once I stopped the tea, my TSH rocketed in a matter of weeks, and I started feeling better.

    • Your TSH at 0.31 is so low that it’s basically turned off. Normally the thyroid would make a little bit of T3 and a lot of T4. Levothyroxine is only T4, which is fine for some people, but maybe not for you.

      Selenium is important for making deiodinases which convert T4 to T3. Vitamin A is also important for converting T4 to T3, although the mechanism is not well understood. Supplementing with retinal palmitate or acetate has been shown to increase conversion of T4 to T3. It’s also not uncommon to be deficient in Vit A when hypothyroid, unless you eat a lot of egg yolks or organ meat like beef liver. A one time dose of 25,000 IU retinal palmitate should answer the question for you. If you feel a big boost of energy from it, you may want to follow the study, and take it every day for four months. And make sure you’re getting about 100mcg of selenium.

    • First of all, you may well need T3. Levothyroxin and other synthetic big pharma drugs only have T4. About half of patients with low thyroid need T3 as well, their bodies don’t make it. So get your T3 nd T4 tested.
      You have symptoms of low thyroid with swelling feet, hands and dry skin. Most docs know just about zero about the thyroid and never prescribe natural dessicated thyroid, which WORKS FAR BETTER FOR MOST HYPOTHYROID SUFFERERS. I struggled for 15 yrs with low thyroid and then was put on synthroid, which did almost nothing for me. Only when I went on NDT did I get better. I use Naturethroid but there are other brands and it is prescription.
      LOTS more info here:
      A great website with LOTS of info. You may also have adrenal fatigue, so read about that on the site. Good luck!

  18. My 17 year old daughter was recently diagnosed with Hashimoto’s Disease, but because it has not affected her thyroid, they tell me that there is no treatment at this time. They suggested that we have her thyroid checked in a year. So, what do we do in the meantime? She is tired all of the time, which for an active junior in high school it is just not convenient. She is taking vitamin supplements (including one for Adrenal Function, thinking she may also be suffering from Adrenal Fatigue), and we are hoping these will help soon. Am I supposed to just take this one doctors results and just “wait and see”? Or is there something I’m missing? It just isn’t in my heart to tell my daughter that there is no treatment for her and she is just going to have to learn to live with it. This tiredness is causing depression, and she is feeling like she will never get better. Any advice?

    • Hi Toni, it’s hard enough for an adult let alone someone so young. As much as I see little value in doctors it always helps to get a second opinion. More often than not it depends on the person you speak to. If it is adrenal fatigue (the two are closely linked) it’s best to put that right first. The web is full of info and Google is your friend so do some good reading. Majority if not all problems stem from the gut. Without a properly functioning immune system we become vulnerable to disease. Strengthening the immune system is the best thing. Probiotics are key for that (good ones from experience tend to be primal defense ultra, prescript assist and VSL3) again can all be found online. I am currently taking Ashwagandha and there are other natural herbs that can be beneficial. Hope this somewhat helps.

    • Toni, p.s. try to get your daughter to cut out gluten (and ideally sugar) for 2 weeks. See if there are any changes.

      • I know you are trying to be helpful and that is admirable, but from someone who has celiac disease and leads a support group, please know that advising someone to eliminate gluten from their diet before being tested is not a good idea (unless one does not have insurance or the means to pay for testing). One must be consuming gluten in order to get accurate test results for celiac disease. If gluten is the problem and you eliminate it from your diet, the only way you can get an official diagnosis is go back on a “gluten challenge” (eat gluten for at least a month). Unfortunately, once you eliminate gluten and reintroduce it, you will become even more ill than you were before. Some people ask why it’s so important to have an official diagnosis. It is important to know because it is hereditary and other family members may also be at risk. Research shows that individuals who are diagnosed are much more likely to strictly adhere to a GF diet, which is important in preventing other serious associated autoimmune diseases/complications. Early diagnosis is crucial to avoiding additional serious health complications.

        • ALB – Obviously it’s always down to the individual themselves what they wish to do. Generally I believe it’s good for anyone to reduce gluten (there is too much in the western diet, possibly contributing to health problems in this generation) however cutting it out entirely is a personal option of course. Agree, you do need to be consuming gluten before doing a test otherwise it won’t be accurate. It’s whether one wishes to do the test or not. I personally feel you can tell a lot more about your body from making slight changes but that doesn’t mean I am against testing I just think there are many out there that are expensive and not necessarily accurate. In regards to research showing someone is much more likely to strictly adhere to a GF diet once diagnosed, I guess that all depends how good you feel after cutting gluten out (tested or not).

    • Has your daughter’s Cortisol and DHEA levels been checked, along with an ACTH test? That would tell you if there’s “Adrenal Insufficiency”, which could be treated with those hormones.

    • im 27 years old i had graves and i was in a coma for 4 mouths get her checked its some thing to worry about it really is i had my removed when i was 21 and know i am still fighting for the medd to work for me im on 150 m and im allways my doctor dont take me serious i am 100 pounds know i use to 150 i have lost so much waight it crazy please take care i never post on these thing but my mom worries about loosing me every day she only 17 please take care of it its no joke have a blessed day

      • Chrystal I can totally relate to you , I feel weak all the time & I’m losing weight . I just don’t feel well at all & feel my dr does not take me serious I’m very worried something bad is going to happen . How did you fall into a coma & how are you feeling now ?

    • I started looking into adrenal supplements after going off flonase, a glucorticosteroid which I’d been taking for ten years, and from what I saw, adrenal supplements are all over the map in terms of their content. I read the most important things for the adrenals are B2, B5 and vitamin C. But B1 is probably also very important because you need B1, or thiamine, for glucose metabolism and energy production.

      Another reason to take B1,…. there is a study out there about taking high dose B1 for the fatigue associated with Hashimoto’s. I found an extended release version of B1 and it has really helped.

      I’m guessing your daughter has already been tested for anemia? It can go hand-in-hand with hypothyroidism, and isn’t always only due to iron levels, but also vitamin A, B2, B12, folate, and B6. You said your daughter is already taking vitamins. Not all of them are created equal. I found much better results taking B-vitamins separately from a multi, and in the coenzymated form.

      Regarding iron, some research has shown the range for ferritin (storage iron) levels are not appropriate for everyone. Some people can have symptoms of fatigue with a ferritin that is considered normal, but in the low end of the range. Athletes in particular feel better when their ferritin levels are in the middle of the range. The thyroid needs iron too, in order to make TPO for thyroid hormone synthesis. So iron is really key when the symptom is fatigue. Vitamin A and copper are important for iron metabolism and many multivitamins do not have enough, especially of vitamin A in retinyl form.

    • Hi Tony I have had hypothyroidism since I was in my teens and I am 60 now. I was so tired and depressed that my mom took me to the ER because she thought I was going to hurt myself. I was admitted and they put me on drugs for anti depression these helped a little but did not fix the problem. My mom asked a friend of hers who was a nurse about my condition and she asked if I had ever had my thyroid checked and suggested I see an Endocrinologist, they specialize in diseases such as thyroid. I went and they put me on thyroid meds and took me off the depression drugs. I turned into a different person within a month I felt fantastic the depression was gone and my energy level was back. I know its not exactly what your daughter has but it sure would not hurt. You can ask her doctor to refer you to one or depending on your insurance check out some reviews on doctors in your area. I am still taking the meds today and doing well. I would highly suggest you check this out and I wish your daughter the best.

    • Go to a naturopathic doctor. Most likely she does have adrenal fatigue. She may also have a leaky gut and loosing vital nutrients like iron which will make you very tired.

      • Hi, what are her T3, T4 and Tsh levels? Not likely normal. If not, she should be taking thyroid hormone, preferably natural, I.e. Armour, WestThroid or Nature-Thyroid brands vs common synthetics like Levothyroxine/Synthroid; which did nothing with my Hashimotos. Find a good Integrative Medicine MD or endocrinologist. And get her checked for adrenal insufficiency: Cortisone, DHEA and pregnenolone levels. I need those also. Good luck 2u.

    • Go to another doctor, talk about the symptoms your daughter has and ask if they would put her on low dose thyroxine (usually 25). That would make her feel better. If that doesnt, maybe she needs a but higher dosage. She is subclinical based on her lab, but obviously has increased antibodies, since she has been diagnosed with Hashimoto. Healthy lifestyle and self-awareness of any new/unusual symptoms with regular thyroid lab tests.

    • Hey, Toni! Please google, Hypothyroidism Revolution by Tom Brimeyer. I am on this program and it has really been helping me. It explains and guides how you can reverse hypo/ hyper thyroidism, and Hashimoto’s, mainly by changing your diet. I am so sorry to hear this about your daughter.

  19. I was diagnosed with Graves in March 2009, radioactive iodine treated the Graves, however now hypothyroid taken levothyroxin ever since with dosage unchanged at 125mcg (overweight for height at 76kg, 171cm). Recently I keep getting colds, and feel fatigued more often than not and also cannot lose weight, even though I’ve been carefully counting the calories. Awaiting blood test results but would,like to know if constantly getting colds is something others suffer with – and what have you managed to find out about this to help you. Thanks

    • Hi Julie, I would say yes, on the basis that there is a huge connection between hypothyroid and the immune system. Generally speaking any health concern originates/stems from the gut. If your gut is out of balance you will eventually notice other areas of the body will start to slow down / have problems. Usually with hypothyroid the immune system is weak and out of whack. A week immune system is obviously susceptible to colds / getting sick. Particularly if you are intolerant to feeling cold which tends to be a trigger with hypothyroid. What can you do? Try to rebuild your immune system, make it stronger, help it fight for your body and help it to help your body. Prebiotic and probiotics are majorly important for that. A diet high in veg, garlic, ginger, turmeric and multivitamins. Try avoid / cut out gluten. Fresh lemon in warm water or apple cider vinegar every morning will help alkaline the body. Have a search online for anything else that may help, Google is your friend! Your best bet is to strengthen your gut / immune system. Hope you get some answers from the test.

  20. I have a 12 year old son who was diagnosed with Hashimoto’s about 6 months ago, though I think he has had it for at least 3-4 years. I really don’t what set it off yet. We are seeing a ND who has been very helpful with bloodwork, and general diet guidelines (gluten free) but follow the Type O blood diet. Unfortunately, trying to convince a 12 year old to go gluten free is not an easy thing to do, especially when he doesn’t really understand how or why he is sick. (He has a goiter and he has been extremely tired and grumpy or bouncy and goofy for years – both extremes). Has anybody else had this kind of situation? I’ve been trying to get the whole family gluten free – I think it’s the only way it will work, but I can’t monitor every little thing that goes into his mouth! Does anybody know of any good resources for teaching a 12 year old what is wrong with him??

    • I agree with the correlation between healthy gut and immune system. However Gluten Free isn’t always the solution.

      • Gluten is known to cause issues for the thyroid, see “gluten-thyroid connection”. Gluten is one of the main culprits for attacking the thyroid. If you have hypothyroidism it is advised to cut it out or least reduce it as much as possible. Gluten intolerance is not just a celiac problem.

        • Either you’re 100% gf or you shouldn’t be at all. If you say “at least cut the gluten down”, you don’t really understand what is the theory about gliadin (and other proteins) and Hashimoto, or other autoimmune diseases, besides Celiac sprue.

          • Natasa – Gluten is very difficult for one to just cut out cold turkey, hence reduce as much as possible (at least for the first couple of weeks) it’s called easing off, letting the body adapt.

    • Maybe ask your ND about a digestive enzyme your son can take. There are some designed to specifically help with gluten.

      I’m probably a broken record about now on this page, but try an extended release version of B1, it will really help with the mood swings. It has been studied with relationship to Hashi’s.

      Also, vitamin A deficiency is associated with goiter when iodine is sufficient. The World Health Organization has a lot of information about the interaction between iodine and vitamin A in thyroid disorder.

      A deficiency can develop unless the diet includes a lot of egg yolks or beef liver. Plant sources contain only beta-carotene which is not converted to vitamin A during hypothyroidism. I tried beef liver myself, and felt like the energizer bunny for the next three days – it has about 40,000 IU of vitamin A. My kids wouldn’t touch beef liver, and so supplementing may be required for your son. There was a recent study on hypothyroid women and 25,000IU a day reduced their TSH over four months. You may want to discuss with your ND.

  21. I’m 51 and was just diagnosed with hyprthroidism. I don’t know my levels or what strength meds I’m taking. Only been at this for a month. I’m so tired all of the time. I’ve gained so much weight over the last year. Foggy doesn’t even begin to describe how my brain feels. I’ve been reading everything I can find on this illness and I’ve managed to scare myself half to death. Will this lead to cancer? Other illnesses? Sounds like it.

    • Don’t be afraid. There is a lot of material out there to educate yourself. You must be your own advocate and not depend on doctors though. We fight for the quality of life by understanding our condition. I have a pinterest board with articles collected to help others. Hypothyroidism is complicated. You need to replace the thyroid hormones. It is best to go with a T3/T4 combination. I take Synthroid and Cytomel. It took two years to find the right place for my body to function at it’s best. Be patient. With hypothyroidism we are deficient in Vitamin D, D3, B, and B12. You want your level for D to be around 50-75, Iron to be 100 to work best with your thyroid meds and for foggy brain cut the gluten and sugar. Drink a ton of water. Great Facebook pages are Thyroid Sexy and Hypothyroid Mom. Here is more info:

    • Dont be afraid just listen to your gut and keep check ups very regular.i was “watched” for years, by many doctors, with nodules on both sides that continued to get larger. I was told by all endo’s “don’t worry, its common. I finally went with my gut and demanded a biopsy. It was cancer, and I had to have a total thyroidectomy. If ever it does turn cancerous it is the best cancer to have, if caught early no chemo like normal cancers. The only thing I wish I had done was listen more to my gut and my body. Also I wish I had done a lot more in the way of nutrition. I am learning so much maybe a little too late as the loss of a throud changes so much in your body. Good luck and listen to your body!

      • I am facing thyroid surgery next week. I am 62 and female. 30 yrs ago I had left lobe removed and it was benign. So getting the right one removed it will put me hypothyroidism the rest of my life as I will not have a thyroid and will have to depend on meds to regulate all the many functions ur thyroid controls. How did u do with ur weight and other issues not having a thyroid can change to ur body? So frightened of what changes I’m going to have to endure. Please share how u made out after living without ur thyroid. Vicki 3-24-16

    • Meichell P, Please check out Hypothyroidism Revolution by Tom Brimeyer. This is a great program that reverses hypo/hyperthyroidism,and Hashimoto’s, and has really been helping me with my hypothyroidism.

  22. Hi, I’m 16 and I have Hashimoto’s disease. I was diagnosed at the age of 2 & I’ve had it for basically my whole life (14 years), but I was wondering if since I was diagnosed at such a young age if it could raise the risk of me having problems in the future.
    Right now i have the symptoms of unexpected weight gain all the time, dry skin, tiredness, etc.
    I would also like to ask if theres different ways that I could try to lose weight because everytime I try it seems like i just gain more weight. Then I’ll exercise with friends for awhile and they’ll be making progress and nothing will happen to me.
    So does anybody know a different path i could take at attacking my weight problem?

    • Hi Rhiannon, you seem very mature for your age so I am sure you’re being smart about it. The weight gain can be a symptom and the best thing to do is try to get to the root of the cause/the problem. An out of whack immune system is one of the main causes of Hashimoto’s and hypothyroidism. Do your best to support your immune system and get it healthy. Probiotics will help. Lemon / apple cider vinegar in warm water in the morning will help. Cutting out gluten and sugar will help (the hard part is the first 2 wks but after that your body will have adjusted and gotten used to being without it). Don’t stress over it, stress can cause more weight gain. Take time and listen to your body.

    • Rhiannon, google Hypothyroidism Revolution by Tom Brimeyer. I am on this program, and it has been really helping in healing and reversing my hypothyroidism, and it works for Hashimoto’s as well. I wish you well.

  23. Hi I’ve suffer with under active thyroid I’m on levothyroxine for over 10 years but I keep coming down with flu, tonsillitis, colds and depression is this all down to my thyroid my doctors are not helpful at all I’m so tired of it all I just want to be normal and have a normal life

    • I was diagnosed with hypothyroidism 15 years ago, and suffer the same. I was also diagnosed with Crohns in 2015, both autoimmune problems.

      • Steve I also have Crohns can U tell me your symptoms of hypothyroidism , I’ve had some T4 tests that were on the low normal side, one t3 came back high ? Then normal , I’ve had really dry skin , psoriasis , dry eyes, exhausted a lot of the time , Vitamix d is low, depression , no appetite , weight gain , I Dont sleep well, shortness of breath on occasion a rapid heartbeat that comes n goes over 100 beats per minute , muscle cramps, I feel cold a lot,

  24. polyendocrine autoimmune pattern?
    I have congenital Hashimoto’s. I was also born with Pernicious Anemia that went away as I got older. I’ve had MANY health issues with the Hashimoto’s til the finally diagnosed me at 33. I am male.

    I am now 50 and am experiencing some “new” more serious symptoms:
    My levothyroxine seems to have quit working. [email protected] 39 WITH MEDS
    Testing high on sugar, 179 with no warning.
    Blood in stool, not visually noticeable.
    Becoming lactose intolerant.
    Moderate to severe abdominal blaoting.
    Blood pressure going high when not previously a problem…

    My Dr is checking me for the ussual:
    Colon cancer
    Prostate cancer…
    I believe she is taking the wrong path.
    How do I have this “talk” with my Dr without compromising Dr/patient relationship?

      • Yes, it is quite common to develop more than one autoimmune disease and have a whole collection of specialists to treat you. Definitely get checked for celiac disease if you have abdominal pain and bloating. Celiac disease and lactose intolerance frequently go hand-in-hand. Sometimes the lactose intolerance resolves if you strictly adhere to a gluten-free diet after being diagnosed (do not start eating GF before testing is completed!), especially after your leaky gut heals.

    • Have you tried probiotics? The ones with 30-50 billion live cultures You could have an over groth of candidia (yeast) if so cut all the extra sugar out of your diet

    • You can get thyroid problems at any age. I’m 19 and have Hashimotos and I was diagnosed at age 16. Some people begin to have thyroid problems during pregnancy, & some in adulthood. There’s no “most common age” but usually thyroid problems are diagnosed in people ages 16 and up.

    • it can happen at any age. I was told with Hashimotos it is caused by a virus that attacked the thyroid. I’m not sure what it was for me…I started having symptoms after having my 3rd baby and didn’t get diagnosed until 10 plus years later. Now for my middle daughter, she had mono and soon was losing lots of hair that the hair stylist suggested she get her thyroid checked. But you have to make sure they order TSH, T3, T4 and antibody tests.

  25. This is my first time on any site asking questions regarding my thyroid. I’m 36 and 8 years ago I was diagnosed with autoimmune thyroiditis. I was a-symptomatical until about 3-4 years ago. My only symptom at first was hairloss, and not so much on my scalp but my eyelashes. Then I started feeling tired and foggy. Then my eyelashes started falling out in clumps. I finally went in and through some testing I was then diagnosed with Graves disease 2 years ago and was told I only had 2 options, 1 was to remove the thyroid and 2 was to take a radioactive iodine pill to kill my thyroid. I chose the pill. I have regretted this decision ever since. I took the pill 2 years ago and have since lost over half of my hair on my scalp. My eyelashes are very very thin now. I ‘ve been told by one doctor that these are symptoms I have to deal with. My labs are finally within the “normal” range, 2.9 tsh. A different dr then told me he can’t fix normal labs. I am still having bouts of fogginess, my hair loss has slowed down, very little though. My eyelashes don’t seem to be growing back. I am currently taking 100mcg of levoxyl and 2.5 mcg of liothyronine. I am eating, for the most part, as organically as I can, and also take iron, omega 3 fish oil, and evening primrose daily. I guess my question is, is there any hope? Or am I going to be bald with no eyelashes by the time I’m 45? I’m at a loss right now and any advice would be greatly appreciated. I feel like I’m fighting this on my own. Thank you for taking the time to read this.

    • I recommend you take the natural Armour, Nature-throid or Westhroid, which have 4 thyroid hormones, instead of only two of the synthetics you’re taking. If your Vitamin D3 level and/or Tyrosine levels are low, your thyroid can’t function. Also a Biotin (B vitamin) deficiency can cause hair loss. Foltene scalp treatment, purchased from a beauty supply really helps. I had “widow’s peak” balding until I supplemented nutrients I am deficient in. It all grew back!

      • You’re lucky to have found a doctor who prescribed T3, I really don’t advise switching to Armour or the like if you are a Graves’ patient. The T3:T4 ratio is too high in Armour, and without tests showing you are very low in T3, it can cause more problems that can ramp up your antibodies and make all Graves’ complications worse.

        Best of luck, Melissa!

        There’s a great Graves discussion group on Face book run by expert Val Collins. It’s called Graves Disease Research News.

        A Graves’ patient without a thyroid is NOT the same as a Hashimoto’s patient, or a patient with both Hashi’s and Graves,’ which you may be (and I am, as well).

        Do you know whether you had both sets of antibodies?

        To quell your immune response, you may be better off with a slightly lower TSH, but also keep an eye on T4 and T3 numbers and figure out where you feel your best.

        As far as alopecia goes, it may or may not be related to thyroid. You could try a low-inflammation diet (I do paleo), and see if you have good results. At least you’d likely feel better.

        • Thank you! Sorry it has taken so long to reply. No, I don’t know if both antibodies have been tested. I know I had a thyroid uptake scan which showed I had graves. I know a couple of weeks ago my tsh was at 2.9. In July it was at 1.9 and I felt better. The doctor increased my levoxyl to 112mcg. I start that on Tuesday. ..back in April my free t4 was at 148 and in April my total t4 was at 7.5. I have an appointment with a nature path doctor in a couple of weeks. Thank you for the advice. My eyelashes are falling out at a much higher rate this week and am feeling pretty defeted. Like I said though, I sure appreciate the advice and will look at the site on Facebook.

          • My hair was falling out profusely and my eyebrows were only half full (none on the ends). When my doctor added Cytomel (a T3 synthetic medication) I slowly started getting better. You have to be careful and go slow with T3 and increase every 6 weeks in small increments. I was extremely nauseated the first month, but then it went away. With each increase by 2mg, I got better and better, but it was a process you have to be patient with. I now take 15mg of Cytomel with 75mg of Synthroid each morning. My hair has stopped falling out and is growing back in. I have energy (since T3 is what makes your ATP and mitochondria work on the cellular level). My doctor first argued with me I didn’t need it because I was in the “normal range”, I argued back and asked what did he care as long as I didn’t get OUT of the “normal range”. Ends up that I was right. I do better on the higher end and am sick as a dog on the lower end. Even my reflexes went from Hypo to NORMAL. My Dr. is now a believer and listens when we talk.

        • Thanks, I didn’t know someone can have both! That could be why I have so much inflammation on Nature-throid. I was diagnosed with Hashimotos.

          Ref: One or more of the following tests may be performed to help establish a diagnosis of and/or monitor an autoimmune thyroid disorder:

          Thyroid peroxidase antibody (TPO)—the most common test for autoimmune thyroid disease; it can be detected in Graves disease or Hashimoto thyroiditis.
          Thyroglobulin antibody (TGAb)— this antibody targets thyroglobulin, the storage form of thyroid hormones.
          Thyroid stimulating hormone receptor antibodies (TSHRAb)—includes two types of autoantibodies that attach to proteins in the thyroid to which TSH normally binds (TSH receptors):
          Thyroid stimulating immunoglobulin (TSI) binds to receptors and promotes the production of thyroid hormones, leading to hyperthyroidism.
          Thyroid binding inhibitory immunoglobulin (TBII) blocks TSH from binding to receptors, blocking production of thyroid hormones and resulting in hypothyroidism.

          TBII is not routinely tested, but TSI is often used to help diagnose Graves disease.

    • So sorry about your eyelashes and hair:( hope it gets better for you! I am losing hair from my scalp and eyebrows. Ugh thyroid

    • Hi I would really recommend looking up or researching Isabelle Wentz and Suzie Cohen. Isabelle has a book called the Root Cause. Suzie Cohen has books out too but u can find her on you tube too. They both have given me a lot of hope. I’m am now seeing a Naturopath. And she has given me a lot of hope. I prayed about who to see and her name popped up. You can go on Isabelle website and she will daily send you emails with loads of info. You are not alone. Will keep you in my prayers. That you may find the answer you need. Blessings.

    • Here’s some of what Isabelle Sent a has to say,

      Hair loss is a distressing symptom experienced by women with Hashimoto’s. For women, our hair represents our femininity, and losing our hair is a constant reminder that something is off and that we are not well.

      I hope that some of these strategies can help you get your hair back! If you have tried all of the strategies mentioned below.

      Here are some tips that may put hair loss at bay…

      1. Be sure to check you TSH, Free T3, Free T4.
      Sometimes, when your TSH is on the outskirts of the normal range, you can continue to lose hair, and your hair may lack luster and shine. If you hair tangles easily, this is a sign that you may not be getting enough thyroid hormone. Talk to your doctor. You should see a change within 4-6 weeks.

      2. Consider the type of thyroid medication you are taking.
      T3, the more active thyroid hormone, is actually your “beautiful hair” hormone that helps you grow your hair and prevents it from falling out. Synthroid, Levoxyl and Tirosint only contain T4, the less active hormone. T4 should be converted to T3 in the body…except this doesn’t always happen. Sometimes an addition of Cytomel (a T3 medication) or a switch to a medication that contains a combination of T3/T4 such as Armour, Nature-Throid or compounded T4/T3 may result in a return of your hair’s luster and shine.

      3. Iron deficiency
      Iron deficiency is one of the most common reasons for hair loss in pre-menopausal women. People with Hashimoto’s often have poor levels of stomach acid, which is required to extract Iron from foods. Be sure to check your Ferritin levels. Ferritin is the Iron storage protein and is an early indicator of Iron deficiency. When we have a lack or Iron, our body pulls it from hair, and conserves it for more vital processes.

      4. Balance your blood sugar!
      Blood sugar swings brought on by eating too many carbohydrates and not enough quality proteins and fats can wreak havoc on your health and hair! Blood sugar swings encourage the conversion of T4 to reverse T3. Reverse T3 is a inactive hormone that blocks the body’s utilization of T3, resulting in increased hair shedding.

      5. Consider a Biotin supplement.
      Hashimoto’s always co-occurs with inflammation in the body. The inflammation puts the adrenals on overdrive, depleting our Biotin stores. Biotin is an important vitamin and deficiencies have been found to cause hair loss.

      6. Be sure to get enough essential fatty acids; “good fats”.
      Fatty acid deficiencies result in dry, dull, lifeless hair. Eating Omega-3 containing fish, taking an Omega-6 supplement like Evening Primrose Oil and even doing an Olive oil hair mask at home can help bring back the shine to your hair.

      7. Ditch those processed hair products
      Opt for an organic shampoo and conditioner. Although I believe that healthy hair comes from within, shampoos that contain toxic chemicals and gluten can be detrimental to your scalp resulting in inflamed hair follicles.


      Dr. Izabella Wentz, PharmD
      [email protected]

      Join me on Facebook

      Wentz LLC PO BOX 1471 Des Plaines, Illinois 60017 United States 844-Dr-Wentz

      Click here to update your email preferences

    • Melissa,

      You’re the only other person I’ve ever heard who has lost eyelashes! Years ago they said it was alopecia. I knew that wasn’t the case. Recently, I’ve been researching pyroluria and I think I’ve finally stumbled upon something. I’ve got a test coming my way. You can test without a doctor’s order. It’s inexpensive. Though labs for zinc, copper, ceruloplasmin, B6, etc. might be helpful especially if the pyrrole test is positive. Then you know where to start with supplementation (pyrrole is due to a zinc and B6 deficiency) as well as gauge progress with followup labwork. Maybe it’s something for you to investigate too.

    • you need to go to a natural path doctor. Primary care physicians only treat if your labs are abnormal. The natural paths will treat if you have symptoms. That’s what I’ve experienced and I feel so much better…

    • Find an Integrative Medicine Doctor who treats the entire body. You could be “Subclinical”, having symptoms but within normal range. I was diagnosed with Hashimotos when I was 30, now 60. Initially hyper thyroid, now hypo with weight gain, fogginess and hair loss. Synthroid didn’t assimilate in my system. Switched to Nature-Throid aka natural thyroid (I was allergic to the binder in Armour) which has both T3 and T4. My thyroid has totally atrophied to not seen on an ultrasound. Since menopause, med. has to be adjusted 1 -2x yr., spring and fall is recommended.

    • Hi I just found this site and I am feeling like if I have ant chance of feeling normal again it is going to be by my own hand in research. I have been to so many doctors of many specialties and to no avail. I have had so many side effects from throid cancer that resulted in a thyroidectomy. I have severe burning nerve damaged peripheral neuropathy that has really affected my quality of life. It started within 2 months of thyroidectomy. As well as blood sugar going into duabetic range, cholesterol etc.After 5 years of research I have determined that gluten is a no no, exercise is a must, a contnual watch of vitamin absorption. But above all there is definitely a direct relationship
      between what is happening in my gut. The only doctor that I have received some confirmation from was a neurologist on tv, Dr. Daniel Aman. Next step I think is holistic nutritionist. Any comments would be greatly appreciated. My feet hurt within 15 minutes of eating and I cannot sleep without a pain pill. 6 years is enough! Help please!

  26. i am hypothyroid patient , i am taking 75mg tablet now , iam giveing blood each 6 month once , few days ago i told i have a such type of issue , blood bank refuse to take blood , they told u haave tyroid patient so not possible to take ur blood , so i am asking u to is it not possible to give a blood as thyroid patient , is that any problem if i give blood ?

  27. Hey I just wanted to leave a comment here on “steroids used for autoimmune disease” which can have heavier consequences than the initial problem. IF any one here is considering taking humira/already is taking humira. I IMPLORE YOU to do a search on “humira, cancer” on google. You had better be sure beyond a shadow of a doubt that your particular issue is BAD ENOUGH to put yourself at VERY HIGH RISK of cancer. I am not saying that every one who takes humira gets cancer. But it is not an arguable case to say that humira doesn’t increase your risk of cancer. My doctor didn’t explain this to me, but it SHUTS OFF YOUR IMMUNE SYSTEM. Not just thee part that’s attacking your body but also your defenses. People are getting sick from simple celled cancers that would have been killed off by the body’s natural immune system, or not being able to fight off a basic cold. Please just be wary.

    • Hey it’s John updating my status. I’m sorry for speaking from my angry emotions from the CDC and just have to move on.
      First I like to thank you for the reply and recommendation.
      Its hard trying to live on my own with numerous disabilities.
      My Thyroid level is coming close to the limit. (I have no Thyroid) I’m getting my blood work done every 2 months unless something comes up to do it weekly. So my cholesterol is still high, and I just got a frantic call from the Dr. Office that I need to increase my Vitamin D. The gallon of milk, cheese, sun and daily Vitamin D just haven’t been working. Now this is my thyroid doctor and I’m not sure he took blood samples for my Liver. Can the illness confirmed on this blood work test, (and I know all doctors do not like to here the word LYMES) and have an excuse for something else. But I was in perfect health until I contracted Lyme Disease twice. But read the LRN article on line where we had 13 people die from LYME including children. I believe they are now considering it’s a chronic disease and what damage it does to your body after having it very bad your entire life. Not everyone gets it bad if its caught right away but some do and it just stays with them.
      As of today, I am numb from my waste down and have taken several falls, still having my seizures, also the arms and the typical joint pain enhanced from all my accidents with broken back, arms, legs, ribs, 10 concussions i received from 11 car accidents. ( I was the passenger) 1400 hundred pounds slammed to the ground which took 15 min to get off. 7 of the accidents I shouldn’t have lived. so with that being said I have a lot of factors which could have caused these diseases and illness’s I have today.
      All I can say is smile if you wake up, if its a bed day or week whatever. God Bless and keep the faith

      • Hi John, thanks for the reminder about enjoying one day at a time. I was wondering if you ever contacted Dr. Foley(?) I saw a Lyme specialist article by Dr. Paul G. Auwaerter who seems to understand the disease. Good Luck to you.

      • I sent a relative info from somewhere on the internet a few months back regarding hyperthermal treatments for her lyme disease. One site directed basically home hot bath type treatments. You will have to google this as I don’t recall much.There are some centers that use such therapy but apparently the cyst form is resistant so it has to go on regularly to catch the spirochetes out of that form.

  28. Hello everyone, I really don’t read many sites with blogs etc.
    I guess I just very angry with the CDC, Ins companies Board of doctors etc. I’v have Lyme since 1997, Now im 54 and received other tick bites with the bullseye and tested positive several times. Anyway my story is in 97 I developed the wonderful cyst you can get from LD. Had 8 surgically removed and actually was able to remove them myself thats how bad and disgusting it was. But after numerous diasese treatments, (Lupus, as, ms, and several others. After insisting treatment for LD after 9 months of the disease and medication games, i began to feel better) Long story short, after the 4th massive bulls eye, it attacked my thyroid which had to be removed last year, we cannot get it under control going from hypo to hyper and visa versa. Im on total disability because of passing out driving, seizures,and 63 more out of the 85 symptoms of LTL, and other autoimmune diseases.
    Im poked like a pin cushion every 2-3 weeks.My question is when it ends up attacking the Liver is that basically it for people whom died from this disease? and is this what I should be expecting. I would like to hear from people who’s brother, friend mother, child etc who actually died from this disease and let them be heard. Maybe it will help people what to expect. And please this is no disrespect to anyone, and I apologize if I offended anyone.

    • I take Nature Throid by Western Laboratories – no additives. Because I am also allergic/get a rash from the preservative in Armour Thyroid. Best price at Costco, not kept in pharmacy inventory though, has to be ordered. Most pharmacies will get it for you as well. Western Laboratories also mfrs an alternate less expensive formula with less additives than Armour.

      For best results, take the tablets sublingually, dissolved under your tongue, to bypass stomach maldigestion issues.

    • i too would like to know the answer to your question, because my liver has been affected by my throid condition,or the lack there of. I had mine out in 09

      • All tests are a good recommendation to others.
        I’ve had them. I would add Amino Acid assay. Tyrosine is necessary for thyroid function. Thyroid affects lipids like Cholesterol, therefore the liver.

  29. I never thought to look for support online for hypothyroid. It took over 30 years to finally get diagnosed. For decades I was told I was borrderline and my symptoms were ignored.

    I have several autoimmune issues which began with endomitriosis. Later I was just diagnosed with IBS, Fibromyalgia, high blood pressure, borderline cholesterol problem, Reynauds Syndrome and much more. Finally, I was diagnosed with hypothyroid.

    I have major intolerances to medication. I am allergic to Armour Thyroid and have had doctors tell me I cannot be. Once they see my hives everywhere they finally see I can’t take it. Synthroid/Levothyroxin seems to do nothing for me. Out of 5 doctors, not one has ever said to not take it 12 hours prior to having blood testing done.

    I had lost weight but now no matter what it is coming back with a vengeance. I have major spinal issues and exercise is beyond painful.

    Wow….finally sharing this. I have not had anyone to talk to but i cope. Where do we go for true help with hypothyroid? My daughters dog has hypothyroid and the medicine she is taking seems to be working great for her. How us it her dog gets better help than we do?

    • You just asked the question of the century that no one seems to have an answer for. I dropped from 2.5 to .65 in 2 weeks. Still in considered okay range but that’s a big drop. And I get the everything is okay blah blah blah. Here, do some more blood work and we’ll call you next month. I wish the best of luck.

      Here’s mine

      anti dna antibodies 9
      anca asculitides myeloperoxidase ab 20.8
      thyroid peroxidase ab >900
      histamine release 94
      c reactive protein 1.6
      tsh .65
      cortisol 7.3 am highest
      rheumatoid factor 17
      3 thryroid masses and giant goiter
      more than 20 fatty tissue benign tumors
      severe back pain
      cancelled my gallbladder surgery till JULY!
      gained 48 pounds since fall
      and last but not least Alapesha

      I honestly believe no one cares or will care until I become comatose.

    • I bet you the dog gets better because his medicine is something nutritional. I came across the cause and cure for those hives recently but I just cant remember what it was. 2 things everybody should do is cut out all the genetically engineered wheat because of the gluten as stop with all the polyunsaturated oils.. All the supposedly healthy oils like canola, safflower, vegetable, soybean,, etc.. That means no salad dressing or mayo because these are all made with soybean. these polyunsaturated oils destroy your ability to produce and absorb thyroid hormone. Switch to butter, REAL olive oil (Put it in your fridge overnight.. if it isnt solidifying by morning then its not olive oil and throw it out) coconut oil and red palm oil

      • Mike, you’re spot on! I’ve been sick due to low thyroid over 10 years. Traditional western medicine hasn’t helped me. Since I’ve married an Aussie, I’ve been seeing a naturopath in Oz. She has totally changed my nutritional lifestyle – gluten free, soy free, refined sugar free, cow’s milk free. Butter, coconut oil, gluten-free grains, nut milk, & lots of veggies are my new life-long friends. Eating a clean diet with appropriate supplements help decrease the inflammatory response that many low thyroid patients experience. Although we’re still searching for other triggers &/or conditions that continue to plague me, I have seen some improvements. And knowing that what I’m putting in my body is good for it brings peace of mind. Good luck & prayers to everyone on the road to better health!

        • Hello,
          I have a 1.1 papillary nodule plus hoshimotos. The doctors I have seen recommend I remove my entire thyroid mainly because they say the hoshimotos will evently burn it completly out anyway. From what I read I could get the hoshi under control by diet. I feel like I would have less trouble taking medication if half thyroid= half dose?!?! Does anyone have any experiece/advice for me? I have also read a lot linking leaky gut with Hoshimotos. Does anyone know anything about that either?

          • I was diagnosed with Hashimotos and a cyst at age 31. I take Nature Throid at the average daily dose, because it has all 4 thyroid hormones and no additives, unlike Synthroid/Levothyroxine, and Armour Thyroid. I’m nearly 60 now. My thyroid hormone levels (T3, T4, TSH) have fluctuated but I get it checked annually and dosage adjusted accordingly. My thyroid has shrunk, but remains noncancerous. Fortunately I had a conservative Endocrinologist who believed the thyroid shouldn’t be radiated or removed unless it is cancer. I’m glad I didn’t do surgery. I know several people who had the complication of damaged vocal chords after surgery, and it affected their voice for life. They have a large obvious scar, besides. Take Thyroid sublingually, without caffeine. Good luck on your decision.

              • All tests are a good recommendation to others.
                I’ve had them. I would add Amino Acid assay. Tyrosine is necessary for thyroid function.

              • Hi Missy, Would you please advise what specific tests your Dr. routinely does, and if he’s nearby S. CA. I’ve noted a link to an excellent explanation of how the Thyroid hormones function.

        • Try “the plan ” by lyn genet
          Its a life style change that helps you pin point your trigger foods, that cause you, hives, bloating, migraines everything that you put in your body. There is a 20 meal plan to go by and it helped me alot? Found a ton of triggers for me

      • I don’t mean to fight with you. But from what I can tell, and research on tip toeing around inflammation from food, here’s a much better explanation for oils for people.

        Regardless of what any one has every told you, OLIVE OIL is made to be kept at very low temperatures and is NOT meant to be cooked with. Coconut oil, on the other hand can remain fairly well intact at high temperatures and is perfectly safe, and healthy to cook with, unless of course you have a coconut allergy.

        So, I suggest using Extra-virgin, First Cold pressed Olive oil for anything that is NEVER going to be heated, so dressings and such

        Coconut oil for the things that you heat. Perhaps I just don’t cook as often as you guys, but you can buy GIANT containers of coconut oil for reasonable prices at sams club and costco around here, and I don’t know why I’d ever need any other oil.

    • I have been on thyroid meds for almost 50 years.I wish they gave me my energy back,I wish they would control my weight gain,my hair loss my dry skin,my fog and yes my vitiligo “loss of pigment “that makes me look like I’ve been burned.It is an autoimmune disease. Which makes sense now that I read that thyroid problems are that.I had gastric bypass surgery thinking that would take care of the weight problem,but that lasted a whole 6 months.My metabolism is so slow.My 96.8.Dr. are so dumb on this subject. Now there is a ciest on my thyroid and I’m thinking hey maybe it will grow and some how speed up metabolism. Wishful thinking.

      • Candy, this is John. I had a cyst on my thyroid, Mine began to grow because of my LYME Disease. I started to having a hard time swallowing then I started to choke and almost died a few times. Anyway it had nothing to do with cancer the cyst turned into this goiter which grew around my esophagus and trachea. The ins didn’t approve and the CDC to have it removed because it wasnt big enough to remove. Now thanks to them the entire thyroid had to be removed and cannot get it under control. Seizure after seizure, almost into a coma. And now I can’t take the pain day after day, treatment after treatment. It feels like Chinese torchur. I just want it to end. So If I were you, I would have paid a doctor to remove it now.

        • Wow i am so glad I stumble onto this article. First I have seen quite a few doctors in the last year in a half. Feel like I’m dying trying to get my social security. I was rushed into surgery without much information or testing be,side of a 50 gram growth on my thyroid so they took half of my parathyroid as well with no voice at all for 4 1/2 months A.D. the Igor was not the same A.D. barely any sound to my laugh. Eight months after my surgery and almost died of a bacterial infection I had to look it up on the internet and with the bulleted well I have lyme disease and cannot get it to clear up. Doctors talking to me and testing me like I am crazy be,side I have been saying it is an auto immune disease if would of knowthis I would t n

        • Wow i am so glad I stumble onto this article. First I have seen quite a few doctors in the last year in a half. Feel like I’m dying trying to get my social security. I was rushed into surgery without much information or testing be,side of a 50 gram growth on my thyroid so they took half of my parathyroid as well with no voice at all for 4 1/2 months A.D. the Igor was not the same A.D. barely any sound to my laugh. Eight months after my surgery and almost died of a bacterial infection I had to look it up on the internet and with the bulleted well I have lyme disease and cannot get it to clear up. Doctors talking to me and testing me like I am crazy be,side I have been saying it is an auto immune diseaseif would of knowthis I would of known this I would of let nature take it course. People think I am on method and want nothing to do with me. And the pain is unbearable.

      • An Immunologist told me that if your average morning temp. before rising is less than 98, you have a thyroid problem, despite “normal” lab results.

      • Did you try Natural Dessicated Thyroid. Also Selenium helps perk you up. I also do Adrenal Complex and Dhea 10mg compounded time release Vitamins Fish Oil Vit C Vit D3 Turmeric I take Armour Thyroid. Magnesium if I feel jittery. Low carb diet to lose weight.

    • Hi Judy…your journey sounds identical to mine. Feel free to add me on facebook-
      Jill Calderone – maybe we can help each other. Things we have or haven’t tried, what works and doesn’t work for us.

    • BEWARE: ANYONE WHO IS ALLERGIC TO PORK SHOULD NOT TAKE ARMOUR THYROID! Doctors and pharmacists are clueless about patients with pork allergies and their need to avoid Armour Thyroid. I made my all my physicians aware of my pork allergy and NONE of them were aware that the symptoms I experienced were related. I figured it out myself after first not realizing that Armour Thyroid comes from pigs. DUH. I called the pharmaceutical company that makes Armour Thyroid and was told by a nurse that NO ONE with a pork allergy should be taking Armour Thyroid. I encouraged them to be more assertive in informing physicians and pharmacists of the need for those with pork allergies to avoid Armour thyroid. My symptoms were: abnormally high thyroid levels, intolerance to a heat and a fever everyday for 7 months. When I brought this to my doctor’s attention, he said he didn’t go by the thyroid blood test results, but by how I felt. I told him I felt AWFUL, but he wouldn’t believe me. BTW, the reason I was put on Armour back in 2009, was because I was also diagnosed with celiac disease and at that time I was told my synthetic thyroid med could not be guaranteed to be gluten-free. That has changed since then. I eventually went back on a synthetic thyroid med.

  30. im 38 i just opened a booming bussiness and 3 months in i might have to close ,im in extreme pain all the time burning pain through my wrist up my arms into my shoulders i now have carpel tunnel and im so hypo and have hashimoto. i am really thinking of driving my car off a bridge. wont be able to see the specialist for 3 weeks

    • I have had two carpal tunnel surgeries and know that pain well. I have had 29 surgeries in my adulthood for varying medical issues, and those two surgeries were so worth it!!! It made a huge difference.

      Researching is important so you can find the right doctor/surgeon. You can make it through….honest!!

    • Becca your too young to feel sorry for yourself… I’m 11 yrs. older then you I to have Hashimoto’s, but was and you to can reverse it to just a thyroid disfunction. It first starts with a vela very organic diet. Al-cat test to see what your body can’t tolerate. I was only diagnosed 3 yrs ago. Decided myself it’s up to me to fix it. After cleaning my diet going organic cooking mostly my own food I’m now in a very normal range under 1. You have to decide to make a commitment because with that disease comes lots of other organs to go under attack. Al-cat testing and hormone testing I suggest to do it to get yourself better to heal your cells. Sorry but you can blame the company Monsanto for all the crap in our soil today and foods you think are healthy from your local grocery are just killing your system. Educate yourself clean your diet and taking vitamin D3 is a must. It took me about 3 yrs to really get better. Start by detoxifying your body. Go on a colon and liver cleanse. I promise there’s hope when you feel line it’s a dead end. Drugs levothyroxin or nature thyroid is a must. You will probably never get off hormones either natural or synthetic, but rest assure Hashi disease can be reversed. Christina k.

      • Christina.. She is not feeling sorry for herself..she is sick.

        What is Al-Cat?

        what do you mean by you are normal at 1?

        There is no proof Hashimoto’s can be reversed. There is no proof these “cleanses” do anything and many say they are not safe or necessary. Vitamion D3 has really not been carefully/fully studied. I got mine to optimal and i felt no better.

    • hi all, this is the first time I’m joining an online conversation referring my complicated history of thyroid tryst since 11 years old. especially to Becca, I can say that pure colloidal silver saved my wrists and a lot of pain gone. I moved to France 2 years ago from Melbourne, Australia. I can say due to the autoimmune nature of my body, I find colloidal silver indispensible in my life. in Australia it’s perfectly legal and safe and you can purchase it in natural health food stores. or, you can enquire direct at the source I had autoimmune graves disease first diagnosed at age 11. following I burnt out at 24 and had to have emergency radioactive iodine which destroyed my thyroid gland. following that episode my body was so weak and for months I wasn’t sure if I’d ever recover. I now just turned 36 and my battle with thyroid issues has plagued me much of my life. however I was perhaps born naturally otimistic. I was my own guinea pig out of lack of choice and lack of adequate medical help. doctor after doctor I sought and all of them told me a “sorry”, that’s the “best” they could do… so, I found alternative GPs who prescribed me what I asked for- natural dessicated thyroid which is not on the subsidised list of medication in Australia (originally I was living in New Zealand). I had lupus-like symptoms prior to going on NDT. my fingers went bent, I was told I had all kinds of illnesses under the sun. but I sought my own answers online while still in NZ. colloidal silver was and still is my answer for the past 10 years to a compormised immune system since young. it took the pains away and helps my body to cope. I haven’t gone blue yet! lol. by all means I’m an attractive Asian woman still not by my own account, but others ;). I can only recount my own trials and errors. everyone is different. now that I’m in France, I found out that NDT (natural dessicated thyroid) is illegal and not available in this country! this really goes to show just how convoluted and tiresome the entire matter is concerning our addressing our health. I feel strongly that we should have the right to chose our own course of treatment, especially given the blatant discrepancies. yesterday I prepared myself for going into the French endocrinologist’s office and triumphed against the man in prescribing me for the first time the best that France can offer me: combination treatment of T4/T3 called Euthyral here. apparently, just across the border I can get NDT from Holland… yes. this makes me mad. but you have to work the system and not let them, a stupid endocrinologist defeat you. he even said something as dumb as that L-thyroxine is “natural”… can you believe that? anyhow, this is the first time I’m trialling synthetic T4/T3 combination, having had to forego all hormone replacement to find my true thyroid levels. sadly, after 25 years, there’s definitely no hope of my thyroid returning and my tests came back whopping terrible. but becuase I eat a very healthy diet, take a lot of supplements to support my body and recently making effort to get back to freshest food possible, I gained a few kgs and feel a bit more tired but nothing too terrible physically. on the morbid upside, I should do quite well should there be a nuclear disaster given my thyroid was already taken? lol… I hope this gives others hope and encourage all to seek own answers. get educated. no doctor can fix you. my holy grail on top of the colloidal silver recently has been the rediscovery of larger doses of vitamin C and Taurine together. both very helpful in fast acting detoxification. this is from a girl who’s literally tried everything under the sun… made my own strangest vegetable juices and all!

    • Becca…Perhaps you should also test for Lyme Disease. I have been reading many of these comments, and so many of us with Hashimoto’s Thyroiditis have Lyme Disease, which can cause Hashimoto’s. The problem is getting accurate results from the blood tests, so I would recommend testing through IgeneX Laboratories in Palo Alto, CA. It is a Specialty Lab for vector-borne diseases that utilizes much more sensitive criteria to screen the blood. Treatment for LD is usually an antibiotic protocol or an herbal protocol. You also need to get inflammation under control with diet; including gluten-free, dairy-free, non-processed organic food. You also need to strengthen your immune system. This can also be achieved with healthy food and lifestyle choices, but there are supplements for this too, such as “Russian Choice Immune”, “Cat’s Claw”, “Astralagus” and others. Best of luck to you!

      • RE: Vector Diseases (Lyme) Labss is one of the best. Fry Labs is one of the most advanced. Also for parasites: Genova Diagnostics and Institute of Parasitology in Scottsdale, AZ

    • Please don’t do that. There is hope. You can feel better. I am 41 and have been in your shoes. You are strong and you will get through this.

      Have a great day!

  31. I have had hyperthyroidism for 7 years after taking radioactive iodine because I suffered from hyperthyroidism. I was on Levothyroxine for a long time, and often never felt better. I now take a natural NDT medication and feel so much better, although I am still struggling to lose weight. I keep reading that gluten is bad for you if you are hypo, but mine was not caused by an autoimmune, should I cut it out too? Or would I just benefit from cutting gluten because I am now hypo? Thank You!

    • Christina.. She is not feeling sorry for herself..she is sick.

      What is Al-Cat?

      what do you mean by you are normal at 1?

      There is no proof Hashimoto’s can be reversed. There is no proof these “cleanses” do anything and many say they are not safe or necessary. Vitamion D3 has really not been carefully/fully studied. I got mine to optimal and i felt no better.

      • In The Thyroid Cure, Ms. Coley has had no anti-body response for 5 years after having anti-thyroid antibodies previously. She does take a small dose of T3 still.

  32. So I am scheduled to take out my gallbladder on Wed. Good riddance! Hashimoto’s and Graves, IBS or IBD , severe hives, joint pain, muscle weakness, sweat like a pig in the sun but freeze to death too. I can’t sleep at times and others I sleep all the time. I have dry skin and oily hair, bumps all in my scalp and my hair is falling out, terrible ear aches that last months and tinnitus. I’ve gaining so much weight. I’m steady gaining a couple pounds every couple of weeks. My pulse is high even at rest and my blood pressure goes up but then comes back down. I have a bi polar body it seems. My rheumatoid factor is now up and about to start that route. I have 3 nodules and an appointment for that in another month and getting a biopsy. I’m vitamin D deficient and B12 is steady going down. Oh and some COPD thrown in there for good measure. I did that one to myself.

    I’ve give up cigarettes, eat healthy now and exercise when there isn’t a foot of snow on the ground and above 40 degrees. I am not giving up coffee. That’s all I have left and about the only thing that gets me out of bed now days. I’m just now finding most of this out and have a long way to go. I am no spring chicken at 46 but I hope that there is some hope for us. I am really hoping someone on here is going to say “yeah, I was all screwed up but things are looking up”? I’d love to hear someone say their hair started growing back in and they lost all kinds of weights. It bad enough to feel like death but do we have to look like it too?

    • I need help if anyone has any ideas I’m hypo thyroid I’m on 75mg synthroid a keep gaining weight but they tell me my number are good now I have been diagnosed with crohns except for the fact I have constipation and weight gain any ideas any one need help please

  33. I have been on 50 mcg and 75 mcg of Levothoxine, i,e Eurothox. Intially, I was happy to recognize that my problem is not mental as I had problems concentrating, depressions and lethargy, later I realized that it was my hashimatos – was happy to see the cause of my problem. After , i started the medication for a few days I was happy and everything was fine, and alter I started gaining weight and a hugs covering over my belly sack, made me a little depressing. I planning to stop the medicine, and counter it by healthy food and habits. Any suggestions?

  34. The Dr. told me yesterday I had hypothyroid, wanted me taking levothyroxione25mcg for the rest of my life. Also said something going on with my liver, no alcohol, no tylenol, herbs, or juices from other countries. Also, blood pressure 130/90, too high, no caffeine or sodium and will test thyroid after pill taking and liver in two weeks, blood test. I am unsure of the pills and her summary. My cholesterol very good, H and L. everything else great. I did have lyme disease twice since 2006 and was not treated very long. Should I have a blood test again for lyme before starting this thyroid treatment and questionable liver? I am 61, weigh 170 and have been more tired and cannot lose weight in past year. I question the cholesterol being so good in comparison to liver and also, gall bladder out since 1986. Thank you.

    • Linda, yes, I agree with you, that you might benefit from being screened for Lyme Disease, as, if you have read so many of these comments, they are from people with Hashimoto’s Thyroiditis, and they also have Lyme Disease. Lyme Disease causes a number of autoimmune conditions, and Hashimoto’s seems to be common in LD patients. I would recommend blood testing through IgeneX Laboratories in Palo Alto, CA. This would give you the best chance for an accurate diagnosis, as they specialize in vector-borne diseases and utilize much more sensitive testing methods, and analyse more blood bands to detect the Lyme bacteria (Bb).

  35. Hi I’m a 42 woman that began with a horrible itch and rash through out my body (July 2014) At first I was told I had fatty liver and I needed to lose weight. After about 2 months I had lost a total of 5 pounds WOW!!. Later(October 2014) I began to have blurry vision, I was very tired, I had severe joint pain in wrists and knees, my face looked like I aged about 10 years from rash and wrinkles, my skin felt like leather, I would scratch until i made my skin bleed i would wake up at all hours of the night from itchy skin…. I became very irritable and not to mention ugly and mean( can you blame me)…. I saw a skin specialist, a joint specialist and they could not figure out what my body was doing, BUT that it was an Auto Immune disease!! I finally got a thyroid test done(November 2014) and it was so out of wack… my TSH was 22.4 ,my antibodies were over 1,000, and had signs of different
    disorders(Lupus, graves diseases, etc) but tested negative. so I had an Iodine test done that showed several nodules (hot and cold). They weren’t sure if I had cancer or not. So I started to see a nutritionist to help me stay on the right track and it seems to help my energy bit. I also MAKE myself get up and walk around the block,and or run if i feel good… I was sent to a wonderful Clinic in Santa Barbra(Feb 2015) were they diagnosed me with Hashimoto’s Disease. The doctors were awesome and had results for me the same day. When they did an ultrasound to see exactly where the nodules were to do a biopsy, they were nowhere to be found. Miracle!!!
    I know this disease can take what little sanity you have left, but please don’t give up. I am very spiritual and know my heavenly father listens to me. I have awesome support from my husband, kids, family and friends… Dont get me wrong I still scratch and have sores that bleed, still losing my hair, and good and bad days… But I know somewhere else someone is worse then me and I pray that everyone gets well. I know changing your diet, some exercise, and prayer helps…love Elizabeth

  36. Hello All,
    I could really use some guidance. I am a 50 year old male. I had a substantial growth on my thyroid with abnormal biopsy results about 10 years ago. Diagnosed with Hashimoto at the same time, it was recommended by my GP and the endo that the thyroid be removed. Foolishly perhaps, I went in that direction. I have been on synthroid and levoxyl and never quite felt right. I recently started going to an alternative guy/acupuncturist. He has weaned me down to ¼ of my dosage and I am much worse. My temp bounces between 95.3 and 97.4, checking 4 times a day. I am dismayed that the Alternative doc did not suggest taking my temps at all. Seems to me, the general consensus is that low temps are a excellent indicator. He has run a thorough panel of blood before I started the wean and I hope to go again soon before I freeze to death. My general questions are as follows:
    1) Is moving to Armour or a similar NDT a good idea?
    2) Is my low temp a good indicator of too low dose of medications?
    3) Should I be trying to fix Hashimoto and if so how?
    4) Is abdominal cramping an indicator of an issue…

    Thanks for anyone who might respond!

    • Joe –

      Yes, switching to an NDT is a great idea. It makes sense that our thyroids need T3 and T4 which you are not getting in your current synthetic meds. People stay on Synthroid way too many years – not feeling well.

      Yes low temps are a very good indicator that your thyroids are not healthy. When people begin to be optimal they do see their temps rise back to normal!

      Yes you should try to help fix your Hashimotos. The only other choice is to be satisfied with how you’re feeling now and I’m gathering that you don’t feel that great!.

      It would be a good idea to seek out another medical professional – one that truly understands the thyroids and Hashimotos. This is not an easy task but don’t give up until you find one that helps you feel better. A functional medicine doctor is a good place to start or there are some MD’s who actually practice holistically. Those are usually the ones that are open to prescribing NDTs.

      There is an excellent website and or facebook forum that will be of interest to you. It’s called Stop the thyroid madness. Check it out.

      Best wishes to you.

      • Thanks Val,
        All makes sense. Saw the Doc today, he “does not think” my symptoms are from the lack of thyroid hormone but he did order the blood work anyhow. I think I will see low levels of T3 and T4 which would explain my low temps.

        • Hi again Joe – remember to NOT take your thyroid medicine 12 hours prior to your blood draw! This way you’ll get a true reading of your thyroids working on their own, not what the medicine is doing to your thyroids. Many doctors forget to remind their patients of this. : )

          • Too late……he told me to take as normal. I have been down to 1/4 dose for over a week so I think we will find out some stuff anyhow. Whereas I have at most, 10% of my thyroid intact, I think blood test will show that most if not all of the hormone is from the levoxl.

    • Joe–

      Look into low dose naltroxene (Aka LDN). It has taken away the doom & gloom, fatigue, & brain fog & hashi symptoms. I too have hashi. It has been a miracle drug & definite game changer. It has given me my life back. Good luck in your journey to good health.

    • Sure you should be trying to fix your hashimotos because thats the cure. Cut out grains and polyunsaturated oils and any garbage food that would deplete your vitamin/mineral stores like white sugar.. Eat nutritionally dense foods from the cruciferous family and make sure you get iodine from some dried seaweed or kelp capsules… Its also very important to get Vitamin D, Iodine, and selenium in your diet. I dont recommend vitamin capsules but you can walk in the sun, or take cod liver oil (walmart sells a good tasting type),..

      If you buy selenium tables make sure the source is from l-selenomethionine.. It will say on the back of the bottle. Other sources are unreliable.

      For heavy duty iodine you can get lugols solution of iodine but i wouldnt recommend starting off on that until youve taken 200mcg of selenium a day for a month.

      Bottom line is you have to change your nutrition. You have to increase your intake of minerals and trace minerals and stop eating foods that deplete those nutrients..And in order to do that you are going to have to eat things from the ocean .. I like Sardines and, herring.. Seaweed is probably the best thing you can do. you can buy a package of dulse from whole foods and sprinkle it on anything.. Vitamin D and selenium should immediately give you improvements to your thyroid.. They will lessen oxidative damage

      • As far as I’ve read, Cruciferous veggies are goiter forming foods & unless cooked/steamed can cause more problems for Hashi/thyroid problems than might be imagined.

        If I eat them, I do so very infrequently & w/caution. But I usually avoid.

      • I also tried NDT (Armour) and it didn’t work for me. I actually felt worse. Like Emily said it is all trial & error, one med can work for one person & make someone else feel horrible. I believe the first thing anyone diagnosed with Hashi’s should do is go gluten free and eliminate processed foods. I believe there is definitely a correlation between Hashi’s & digestive health.

    • Hi I suggest you test for gluten intolerance if you are sensitive to it will be a must to get it out of your diet. I’m completely gluten free. Al cat testing also to see what your body can’t tolerate. I suggest a organic diet. Also taking a supplement to clean your blood. Digestive enzymes after each meal. Good luck.

    • yes going to a natural thyroid medication is most helpful,and a more healthy choice. i was on synthroid.levothyroixine for many years. i have been on armour and now my dr. added a t3 called cytomel. taking a ndt med is not equivalent to the synthetics. alot of people ask about the conversion. truth is ,its a learning game. finding the right dose for your body will take some time. but you will start to realize when your starting to feel better that your getting close. ndt is a t4 and t3 thyroid medication. the t3 gets used up pretty quickly and the t4 build in time in your body. for me i needed a lower dose of t4 and a higher t3 because i wasnt converting my t4 into my t3. so my reverse t3 was too high and its called pooling. so thats why im on armour and cytomel.

      • Missy, That’s very interesting, could be my problem. Who is your Dr., or does anyone know of a good thyroid doctor in S. CA?

    • I don’t mean to be negative but I had multiple nodules for years that kept multiplying and growing. 5 endos kept ordering ultra sounds, blood work, took temp. Etc, and all were normal. I finally insisted on a biopsy and was diagnosed with stage 4 cancer. So go with you gut and keep a close check on nodules, size and if they begin to multiply. Good luck.

  37. I find this article a little… negative…

    Unfortunately, if you have Hashimotos Disease, there is indeed no cure for it and most people are likely to have their thyroid slowly get more scarred. What this article seems to dismiss if fortunately, it is easily treatable for most people. Although i do acknowledge there are complications and uncertainties with the disease, such as people commenting on this site who complain they still have symptoms despite normal TSH. (this is a small percentage compared with all the people who have thyroid disease, though, it must be acknowledged).

    For example, i am a more typical case. I had hypothyroidism, to the point my TSH level was somewhere around 19. I felt terrible, with many of the typical symptoms. I was given Levothyroxine and then had blood tests for Thyroid Antibodies. They were present and it was confirmed that i had Hashimotos Disease. Within a few weeks i started feeling better… gradually… and within a few months i was completely healthy again.

    I have indeed had to raise my dose over time, due to my immune system still attacking more of my thyroid, which isn’t ideal, but at the same time it isn’t really a concern when your tablets are doing the job your thyroid is failing to do. I feel completely healthy again due to being in a normal TSH range.

    Therefore, the analogy that you are on a sinking boat to doom is completely uncalled for. Once treated for, most people feel much better again. It isn’t ideal that your thyroid is still being damaged, but can you really say it is a big deal even if your thyroid completely packs up, if your tablets do the function your thyroid was supposed to do and makes you feel better again? I can’t say it is in my scenario. Ideally, i would look to the future for Stem cell treatment or Lab grown thyroid organs to replace my own damaged thyroid, but until then i am perfectly fine on my tablets.

    I do sympathise for those who have had complications but it seems no way representative of most people with Hashimotos. Yet i do agree T3 and T4 need to be considered in the blood samples when treating the disease, and general blood tests should be done for some select hormones and vitamins / minerals which can be affected from thyroid disease. Lifestyle factors such as stress and diet also need to be considered and maintained as they do cause inflammation / immune hyperactivity, and so would make the onset of the disease worse.

    • I’d say your situation is a little unique and you’re one of the lucky ones.
      – Also, TSH is a rather useless lab nowadays when determining full thyroid function. I wouldn’t rely so heavily on that….

  38. Hi Chris,
    I am doing a research project for school. I am in a CAM program at American College of Healthcare Sciences. I was wondering when this article was originally published as I have not been able to find that info here. Thanks so much! Your research is so great!!


  39. My daughter is 17 and has no thyroid. It was removed with radiation (not sure the correct medical term) She is on levothyroxine now. I am trying to figure out what she should not be eating. Her skin is so messed up and she eats nothing but JUNK. Starbucks mocha frappacinno’s, chips, cookies, etc. I try to explain to her but I am wondering if she should eliminate gluten and what other foods she needs to eliminate

  40. There’s a huge option for treatment that you completely left out and the only one that has a good proven track record that it works. Natural Desiccated Thyroid (NDTs) It’s FDA approved and has been well before synthetic Synthroid came out. Even though Synthroid is among the most prescribed it does not mean it has good results. It only gives back to the patient T4. Our a normal healthy thyroid produces and requires T3 and T4. Natural Desiccated Thyroid contains both and is effective. There’s no explanation why so many Doctors want to argue this or continue to keep their patients sick. Patients need to do the research and advocate for themselves.

    • This has helped me understand what is happening with me and as you said the doctors just want to argue with what is going on. They act as if you don’t know your own body. I have been suffering with that condition for some time now. I’m just looking for some relief from these symptoms and get back to life as best I can. Looking forward to going back to the doctor to discuss this article and to compare it to what is happening with me. Thank you and God bless !

  41. Hello, my name is Marissa i am 18. I was diagnosed with hypothyroidism at age 11. My last dosage of levothyroxin was .175 and was still not high enough. I am now on .75 because my current doc. lowerd it due to me not being able to take it for over a month. I am now not on any because i can’t make it into the doc. atm due to lack of transportation. My doc refuses to refil my script, and i am feeling awfull. I am honestly worried for my life. I am cold even when sweating, i get shakes, my s and feet go numb, i get sharp side pains on both left and right, i cant sleep throught the night but when i do sleep i get lethargic and almost comotosed. I have moments when i get dizzy and light headed, almost to the pint of passing out, im nauses almost constantly, and constatly in pain all over. I supose my questions are
    Is this all due to thyroids?
    Can my doc refuse refils?
    Why havnt i been tested for other disorders like hoshimotos
    Is there a way to convince my doc. Im not crazy and there is something not right

    • Hi! You need to find another doctor. I had a doctor who basically told me just do what I say & be quiet. I got rid of her fast. You will need blood tests to check your TSH levels for the doctor to prescribe the correct dose of meds. You also need to check for Hashimotos. Your health is important so find a way to get to the doctor or hospital asap.

    • You need to ask for several things to chech, not just the TSH. Free T3 & T4, Iron levels, glucose levels, Total T3 & T4, antibodies, Vit D & Bs, progesterone and testosterone, magnesium, selenium, and probably zinc too. Find someone who can tell you what your test results are saying. If it says you’re in the “normal range”, you need to find out what the Optimal range is for you to start feeling better. Find a DO, Not an MD. Maybe a female one. I’ve also been this way since 05 and I’m just Now learning what I need to know.

    • Find another doctor. Consider switching to a Natural Dessicated Thyroid medicine instead of the synthetic one you’re on which is only giving your body T4.
      The website Stop The Thyroid Madness has a ton of great info – there is also an online facebook group.

      FYI, learn about which lab work is the necessary lab work – FreeT3, FreeT4, Reverse T3 and Thyroid antibodies. TSH is pretty useless. Be your own advocate!

    • Your doctor cannot refill your prescription unless you get tested so that he knows he has the right dose. You need to be responsible for yourself and stop blaming others – I can say this because I have been in your shoes. Do whatever it takes to get to your doctors and pay for your appt. It is more important that food. Walk to your doctor if you need to -even if it takes you 3 or 4 hours. Then once he/she writes that prescription, take it to Walmart – they only charge $4 for it! Take your pill every morning on an empty stomach and wait an hour before eating anything. This will be your new lifestyle and you will feel much better. I do and I made this change 20 years ago. Since you haven’t taken it in a while, you will not notice a change immediately because it is something that has to build in your system over time. Give it at least a week.
      Good luck

      • I have been taking my pills for over a month and I still don’t feel any better fatigue nausea sweats/cold tingling in my feet and hands chronic pain in neck and shoulders. Most days I can’t function properly. Tired constantly taking 100mg of my pill a day

    • Marissa,
      Everything you have mentioned sounds like you are going into a myxedema coma; this can be DEADLY, and you must seek emergency care. This happened to me, I am very lucky to be alive and blessed beyond words to be functioning mentally. I lost 90% of my neurological functioning for about 3 months and I had to do my own physical therapy to get them back, my short-term memory is still lagging. Doctors do not know diddly squat! I finally had to find out what happened to me through extensive research. Good luck to everyone who is in need of a neurologist! I went to ER at least 4 times and NOTHING, they were more concerned with me seeing a psychologist and my every month mouth sore (blister on roof of mouth) for two years, “was an abscessed tooth.” Yeah, right; the tooth has never hurt! This happened in August of 2013 and finally sent on a voyage of 18 months to 8 different “Specialists” for ALL the symptoms to be treated. I have been through Hell and back and still not being properly treated and misdiagnosed with other issues instead of focusing on the damage caused by the disease itself. Trying to get my Endo to medicate me correctly is like pulling teeth! What’s the problem? They act as if Levothyroxin and Lionthyronine are controlled substances and I’m an addict. It’s not her that is losing her hair and skin by the handfuls, freezing to death, tired, brain fogged, and dizzy every time I get up to the point of falling hard. There is no excuse for you not to get into your doctor! Especially, knowing you have Hasimoto’s Hypothyroidism, I didn’t! GO to ER!!! You need urgent treatment for myxedema and you are more likely to be deficient in vitamin’s B12 and D. I realize you posted awhile ago, I truly hope you are still around to read this!

      • I am 49 and peridot have always needed B12 shots. Medical record gone (made the mistake of telling my Dr a yr ago I was going for my ssi) he stopped seeing me and now I cannot get another primary to treat me. Thank God my encronologist didn’t call him. He put me on D3 which seems to be helping some if I could get a Dr to properly treat the lyme disease almost a year later and still picking out ticks. I would rather be dead than exist like this with no income no car and not even a friend to help me with anything.

  42. I was FINALLY diagnosed with Hashimoto’s 2 years ago after having blood tests every 4 months for 10 years. After 10 years of blood tests and changing medications by a supposed Thyroid Specialist and continuously telling him my symptoms, I changed Dr.’s and went to Massachusetts General Hospital, where I was diagnosed with Hashimoto’s and she told me I probably have had it all my life. I also have IBS and Ringing in my ears.

    Previous Doctors had explained to me that as soon as I’m on the right Thyroid medication and dosage, I will be myself again. And that’s how it worked…no big deal.right? But it was a big deal to me because I didn’t feel better and the more I told them the more they looked at me like I was Crazy. So I stopped telling them and just took the medication and had my blood tests, which consistently came back abnormal.

    I’m very happy that I finally found the time and strength to change to Mass General Hospital, and do feel better. Changing my diet completely definitely was a huge positive factor in my feeling better. Kale and coconut milk/oil I add to almost every meal. BUT, I wish I could find an Autoimmune Specialist. Is there such a Dr.? My Thyroid Specialist doesn’t know of one either. I feel like I still need a Dr. who will treat my immune system…if that makes sense?

    In the Summer, I still get a fever for about a week or so and ache all over and in the night, my asthma is horrible. My Dr. says it because I’m putting too much stress on my body and I need to relax more. I have 2 very active teenage boys 1 of which has Aspergers, so my Anxiety (worry level) is pretty high.

    My questions are:

    1. Is there such a Dr. as an Autoimmune Specialist?
    2. Does anyone else get Fevers for over a week?
    3. Does anyone else lose track thoughts in the middle of conversations?
    4. Does anyone elses family treat them as if they wish they were never born?

    • Hi Kathryn,

      I’ve been diagnosed with Hashimotos and have had a long stint of illnesses due to a damaged immune system. From what I have been discovering, I am trying to improve the immune system through vitamin supplements and cutting back on gluten. I am in Melbourne Australia and have discovered medical doctors who also integrate ‘alternative’ medicine (the supplements, diet, etc) to help their patients. These doctors are called Integrative doctors and you might have some close to where you live. I have found since taking the supplements, my health is feeling improved. Vitamin B multi, Vitamin B12 and Vitamin K all work as a team. People with weakened immune systems often have deficiencies in these vitamins. I also take vitamin C powder. Hope this helps

    • Oh also Vitamin D3. That one is very important and is often very low in people with hypothyroid. My sister and I both have been diagnosed with Hashimotos and we both had extremely low readings for vitamin D

    • Kathryn, for concerns about autoimmune diseases, I recommend seeing a rheumatologist. Your symptoms you described overlap with mine caused by my lupus, fibromyalgia, hashi’s and other illnesses. I hope you get the help you need. Definitely do some research. Good luck!

  43. I sent this letter to two Endocrinologist clinics I recently had appointments at.
    I have had symptoms of low thyroid for about twenty years and had every primary care doctor
    say, “Your TSH is normal, you do not have a thyroid problem”
    I recently had below normal temps each am that never even reached 98.0
    but three times from mid October 2013 until late April when I spent
    hours and days online with Naturepathic doctors, a DO, Nurse
    Practitioner reading their research and
    researching myself the thyroid gland and how it works, and the whole
    thyroid hormone process.

    Dr. Manoff looked at me as I described all of those in my Mom’s family
    with thyroid disorders, my own sister having half her thyroid removed, and he said “I don’t think you have hypothyroidism” and did another TSH which my primary doc had just done and nothing else.

    Dr. Purnell at OSHU did a thyroid panel as I requested, never called me and I requested a copy and his nurse mailed me one. He looked at the TSH as normal and completely ignored the free T4 at the highest level and the free T3 at the bottom of the level. From my studies and advice I knew plenty of T4 was being made by my Thyroid but it was not
    being converted to T3. A normal level of free T3 for an elderly person would be halfway or better in the range
    consistently. He ingnored all that because TSH was normal!!

    Seven weeks after that thyroid panel Dr Purnell called me and said he could not tell me why I had low temperatures. By that time I had been taking a Dessicated Bovine supplement and my temps were back to normal 24 hours a day. Now
    they are many day back to under 97.6 most of the 24 hours and the symptoms are much worse and I am very sick from a very slow metabolism that just is not working.

    Endocrinologists are no longer Endocrinologists, they are Defenders of TSH, that does not work and 20-30 million (estimated ) Americans have hypo or hyperthyroidism and cannot get a diagnosis and suffer year after year with no help.

    I will not go to another Endocrinologist that charges Medicare but does NOTHING! I will use a Naturopathic doctor who is doing what Endocrinologists use to do
    before TSH and doing great things for patients, even though I have to save up and pay for it myself.

    Elena Parton

    • I had to go to a surgeon with all of my blood work, US, etc to be treated for low free T4 and low T3 levels. She said just because my TSH is normal that doesn’t mean my thyroid is working just fine. What she said is that because my TSH is normal that tells her that the T4 and T4 is able to travel to the pituitary. I had other problems besides low levels–which is why my GP referred me to her–but she started me on synthroid and within 5 days or so I’d noticed a huge difference! I no longer had that extreme exhaustion mid-afternoon. I’ve come to realize that specialist don’t necessarily know anymore than regular GP’s or only look at numbers from blood work. There is more going on than numbers. The endocrinologist that I was seeing refused to listen to me and how I was feeling. He only said “Your TSH is normal so there’s nothing wrong.” You know your body best. Don’t give up. I know it’s frustrating but you deserve to feel good! BTW–I’m 10 days post-surgery for a total thyroidectomy due to large nodules that were affecting my breathing and swallowing. I see my surgeon on Thursday and am feeling so-so. She already told me before I left the hospital that she will be doing regular blood work to make sure my levels are consistent and where they need to be. I’m expecting my synthroid to be raised. Hang in there everyone!

  44. Hi !
    I contracted Hashimoto’s at the age of 39 and was diagnosed with type one diabetes. (C petide and all blood tests confirmed) at the age of 54. I seem to follow your theory. I’d like to hear more of your ideas.

  45. Hi Chris,
    I am writing to you out of total frustration.. since it appears that my beloved GP feels it best to just send me by referral to an endocrinologist, and since I am permanently disabled, and do not have the greatest insurance in the world, it is becoming apparent that there are few endocrinologists that are willing to take me on.
    I was fortunate to find one however, and had my levels tested. of course she said that there was nothing she could do for me, and I would just need to “deal with it”… lol.
    I cannot tell you what they were, but I can tell you this much.
    At this time I suffer from many of the same things that I see everyone else suffers from on your site. Brain fog(which is significant, I am 52yrs old), I have had hypothyroidism for approx. 19yrs. , not too bad with the weight gain, although whether it be fortunate or unfortunate, I suffer from seizures and need to take medicine that not only causes memory loss(plus major brain fog), it also causes weight loss. So I am actually on the thin side. And I believe I fluctuate between the hypo and hyperthyroidism..having days of incredible fatigue..exhaustion, you name it. Then other days I feel like I’m on uppers, as we would have said in my younger days, running around like someone has lit a fire under my nether regions, lol.
    I have extreme issues with fatigue. But then I am a single mother of 3 children, the youngest being 9. So that is probably part of the problem for the fatigue…lol.
    But my major concern at the moment, and I know this may seem vain, but it the substantial hair loss!
    It doesn’t look significant when I brush it and doesn’t look as if its coming out in handfuls. And I need to say, I have NEVER been one to have this huge luscious head of hair to begin with. I guess this is the reason for my panic. I am down to this teeny tiny little wisp of a pony tail and I am not exaggerating one bit. It’s scary to think where this may go if it continues.. The other day when brushing my hair and looking at it from the back in the mirror to make sure that I had all of it combed, i could see, I mean actually SEE how thin it was at the crown of my hair!!! I almost wanted to cry!!
    I mean I am only 52 years old, I look like I’m 42 ( or so I am told). And I feel like I am starting to look like those older women that I use to pity that you could see their scalps through their hair!!!
    What can I do? I have tried supplements that I have read about that are suppose to be good for hair growth. products that have been recommended for me, but well, as I am sure you are aware. Not much is working.
    I am right now taking 137mcg. of synthroid. and i pretty much have been taking this dosage for years.
    If you or ANYONE has any thoughts or help/advise to offer, I would be greatly appreciative!!
    Thank you!!

    • I am currently 30 years old and was diagnosed with Hashimotos at 4 years old. Almost completely unheard of. I have been on Levo ever since but my levels are constantly up and down and have been my whole life. People who don’t live with it, including my husband, do not understand and often times think it isn’t real. Growing up it didn’t seem to phase me or my body. However, now that I am an adult it takes a huge toll on my life. I can’t remember a time in my adult life when I haven’t been overly fatigued. I wake up every morning from 8-10 hours of sleep ready to go back to bed. On the weekends I generally sleep 8-10 hours at night, wake up for 3-4 hours, then take a 3-4 hour nap. Due to the fact that I don’t have time to take naps on weekdays, Monday through Friday tend to be somewhat of a blur. Living with this disease is terrible. It isn’t a visible disease worn on the outside and, is thus, misunderstood by many people. Unfortunately for me, this includes my spouse who many times says I use it as an excuse (completely untrue). As a result of Hashimotos I am constantly fatigued, suffer from depression and anxiety, have shooting electric type pains in my extremities almost daily (although this has seemed to have gotten better recently), thin hair, extremely dry hands, and the list goes on. I would love to know what normal people feel like. I can only hope that one day they will find a better, more effective treatment.

        • It does make me feel better to hear that I am not alone in my misery! I Was diagnosed with Hashimotos 2 years ago by my endocrinologist but it did not really register with me because I was not very symptomatic. Then it hit me! I had an emergency radical hysterectomy last december. About 2 weeks following I fell into a deep depression, lethargy, puffy eyes and face, memory loss…..the list goes on. I changed my diet and was put on levothyroxine as well as estrodial. Things seemed to improve. Then I caught the flu a few weeks ago and all of a sudden the hashi symptoms are back and worse than ever. I am so depressed. I feel like I would rather not live than go on the rest of my life feeling and acting like I do…this is not me!!! Someone please give me a magic trick to make it all better.

      • 2 years ago I found the best endocrinologist Ever. After the initial 1st meeting and blood brawling with in 48 hours she called me and said “yes you do have Hashimoto thyroid disease but your D level is so low it barely registered.” She put me on Ergocalciferol(vitamin d2) 50,000 units. 1 per week. Yes 50,000 not a type o.
        This got rid of the phantom pain pulsing through my arms, legs anywhere else it hurt. It also put my sleeping pattern back on track. I was sleeping 8 hours at night and waking up like I actually got 8 hours of sleep. Now I’m on over the counter vitamin d3 but she still keeps an eye on all my levels. I feel like a human again.

      • Oh my gosh Jen!! You are the first person I have come across that has the same story!! I was diag when I was 5, I am now 38… the hardest part is knowing ‘what is normal’. All the research i have been doing all assumes you know what normal energy levels are… it is sooo frustrating. Thank you for sharing. You are not alone in suffering.

    • Have you googled lyme disease symptoms…..I was bit years ago by a tick and had begun getting very sick ( slowly) because I was so active and fit.My thyroid was so out of control that they removed it when I was 20…I noticed my hair go first. Skip ahead many years …when I went to my physician of 14 years with my thyroid results…My T3 wasn’t being absorbed either, he just didn’t tell me ..he said ..because he doesn’t know why. But: I was the one that had to ask him about it.
      What I’m trying to get at is..alot of the symptoms you’re talking about may well be lyme disease.Thyroid disease symptoms are caused by what. I bet you’re exhausted and need to check your adrenals , as well.
      Just something to consider.
      Wish you the best

    • Hi Darla, I am going through the same issues with hair loss. I am 37 years old and I have always had a thick head of hair but recently my hypo symptoms became much worse. The doctor had to up my levo to 175 mcg. I have read that at higher doses levo can actually lead to increased hair loss. Three weeks ago I started taking evening prlmrose oil, I have not seen any new hair growth yet but I have noticed my hairbrush is not filling up with my hair anymore. From what I have read and what my hairdresser actually told me it will take up to three months on two capsules of evening primrose a day to see new hair growth. I am waiting patiently and hopefully.

      • Hi Darla and Kara…I came across an article written by “Hypothyroid Mom” (she has a facebook page), and her recommendations for the hair loss reversal aspect of Hashimoto’s/hypothyroidism are to also check Ferritin (iron) levels (make sure it is Ferritin), and you may need to supplement to correct your iron levels if too low. Low iron and low Vit. D can result in hair loss, and it seems common to be low in those with low thyroid conditions. She recommends a supplement called Carlson Labs Buffalo Liver. She also suggested making sure you are getting an adequate supply of protein, so eat alot of chicken and other high protein foods. She also wrote that low stomach acid is often a factor, and recommends ingesting a couple of tsp daily of apple cider vinegar. Also, drinking lemon in water. Another recommendation was to iincrease alpha omega 3 fatty acids with using at least 2 tsp daily of fresh ground flaxseeds; as well as a GLA supplement (Black current oil or evening primrose oil 500 mg 2xdaily), a Biotin supplement, and a supplement she called Biosil Silicon (ch-OSA). Test for adrenal fatigue as well (saliva test for Cortisol levels)..If adrenal fatigue is an issue, she recommends the supplements: ashwaghanda, rhodiola, Holy Basil. I just found this article, so I haven’t implemented these suggestions as yet. I have Hashimoto’s Thyroiditis as a result of chronic Lyme Disease.

  46. Has anyone tried meditation as a way to help heal the autoimmune system? When I left the drs office today after being diagnosed with Hashimotos I listened to a teaching from Jai Dev at the Life Force Academy and ironically he talked about the Digestive and Autoimmune systems being KEY to our health. He went on to promote how meditation can help to heal these systems and bring about balance. I then went on to research a little more and found this article
    It’s free and it’s worth a try! No negative side effects! Would love to find out if anyone has tried this or is willing to try.
    The video I talked about is here:
    You should watch them all so it’s easier to understand.
    Please note I am not here to promote anyone or anything. Just thought id share what I came across today. Freaky how I just so happen to play this video today after being diagnosed….
    Let me known if anyone has any luck with this type of treatment. I’ll be giving it a try!

  47. I was taking 6.25 mg per day (1/2 of an Iodoral tablet) for about 2 1/2 years. After reading that it may not be safe to take so much, I reduced my dosage to 225 mcg per day. Now I have become hyperthyroid. TSH extremely low or zero, Free T3 & Free T4 both high & outside the normal range. I’ve lost about 20 lbs on my already slim frame. Dr thinks I may have Grave’s but I haven’t had the antibody test yet. What on earth did I do to myself? How do I fix it? Why would I feel ok all the time on 6.25 mg’s, then fall apart when I reduced my dosage to 225 mcg’s? Should I go back to the large dosage, or should I never take iodine again. As of now I’ve completely stopped both iodine & selenium. Thanks.

    • Hello, Steve.

      I did the exact same thing except that I took a full Iodoral tablet every day and for a longer time period than you did. I reduced the amount also about six months ago (although I did this because my new multi vitamin had iodine in it). I have also lost 20 pounds on a slender frame. I have an appointment with an endocrinologist on January 7 and will be tested for antibodies before then. They found this after a bone scan showed significant deterioration in bone mineral density. I have cut out all iodine and am eating lots of cruciferous vegetables (raw, in salads). I have also ordered some tea that is apparently good for hyperthyroidism. Good luck to you and please let us know if there are any updates. Best wishes

    • I went to an endocrinologist and he did not tell me I had Hashimoto. I got my lab results and diagnosed myself. I asked the endocrinologist if I had Hashimoto. His comment was good investgation work. I was disappointed he did not tell after 4 visits. I had to find it myself. So, I ordered the book hashimoto’s thyroiditis lifestyle interventions for finding and treating the root cause by Izabella Wentz. So far following her book my antibodies have dropped to half of what they were and I found a new MD that is working with me and following the book to find the root cause. This can be cured in 3 months to 3 years with the right MD and your own research. Do not depend on doctors to find the cure. You need a doctor that is willing to look for the root cause and stop it there.

  48. I just read Ann Stones post. I was confirmed with Hashimotos disease 3 years ago. I had all of the same symptoms migraine headaches, extreme fatigue, 30 lb. weight gain, depression. My regular medical doctor put me on Levothyroxine and that was it. It helped momentarily and then I swung back unto the myriad of symptoms. I prayed I would get to the bottom of why I felt so badly still! I could relate to Ms. Stone’s feelings. I seriously did not feel the need to live as my quality of life had deteriorated so fast. I could barely get up with my kids in the morning- I would go back to bed after I got them off to school and get up when they came home. I’m able to keep up with the day now. A girl at my church suggested a Doctor who has helped me feel normal again. The doctor’s name is Hilda Maldinado in Westlake, California. After a series of blood tests I have been put on Naturethyroid and about 30 vitamins a day which include adrenals, magnesium, fish oil, etc.. I am able to function as a normal person now. I still have fatigue but I can manage it. This program saved my life. The vitamins are a must! Especially my latest edition to the lineup a vegetable based Vitamin B. When I went off the magnesium for a month the headaches came back. See the best doctors! It’s well worth it for a better quality of life!

    • Hi,

      I am 29 now and was diagnosed with Hashimoto’s thyroiditis 3 years ago after being 6 months post-partem. I feel as you described yourself feeling, tired all the time, and have been taking Synthroid 118mcg daily.

      I live in NY and Dr. Maldinodo is in California. Can you please list all the supplements you take, how many milligrams per day, and which name brand you use. I would really appreciate it.

      Thank You!
      – tired in NY

  49. You are the first sane person I’ve come across in the medical field, which is driven (owned) by pharmaceutical companies. I told my doctor I was not myself regardless of the levothyroxin keeping my levels in an acceptable range. She refused to do anything further. I went to Mayo for my huge list of additional symptoms. After spending $60,000 of my own money in the past five years on medical bills, I was diagnosed as having fibromyalgia. I have IBS, overactive bladder, mental fogginess, extreme fatigue, headaches, muscle pain, hoarseness, depression and anxiety, which they say are part of that. But couldn’t they be part of the thyroid issue? I was diagnosed 8 years ago after I had my first son. I would honestly rather die than live like this. I am not myself, and I wonder if I could donate my body to a research organization that studies hypothyroidism. Please let me know so I can put it in my will.

    • Hi,just read your comment and i sympathise with you.I was diagnosed with Hypothyroidism 7 years ago,never been the same since.Ive had a myriad of complaints from migraines to weight gain(a lot)mood(angry)swings.A permanent sore throat,tiredness and the list goes on and on and on.I have had 16 cysts removed from my chest, been diagnosed with a 6cmx8cm fibroid,been through the disgusting menopause and now im waiting to see a specialist for RA.Ive been in agony for 7 weeks now, taken 2 trips to A and E,and they just send you home again.I was going to ask if they wanted my body for research, but to be fair, i dont think there will be much left that hasnt been chewed up and spat out by the autoimmune friend in my system!

    • I can completely relate to this. The suffering, the endless misdiagnosis over 20 years from a young age, unable to function anymore, losing a job and ability to work at age 35, useless useless useless doctors, wasted money I did not have as a single parent with no financial help from anyone. I have zero income. Zero. This disease is horribly painful, frustrating, mind altering, depressing, hopeless. Each symptom requires a different treatment. Exhausting and bitter. I say the same thing every day, “how can I end this life and allow others to research what lies beneath because I literally do not have the resources, support, money or energy to live one more day like this”. And the worst part is, no one around me, and there are not many, understand this disease and the suffering. Hashimotos is the worst kind of heartache I have ever tried to endure. It is the pure essence of loneliness. Chronic invisible duress. Just so we are clear, I had to diagnose myself. Twenty years of self analysis, journalling and research gave me the answer. Now I am too far gone and my neural networks no longer function. Earlier genetic testing and unconventional aware eager to listen and affordable to treat health care providers are needed. In all countries. There are zero in person support groups in Ontario Canada for people with Hashimotos disease. Zero support. Zero recognition. Unfortunately, if one ends their life here, one cannot donate their body to science….only ” natural cause deaths” are accepted. How many more ways are we going to be denied?

      • Bella –

        I sincerely hope that you are at least still alive. I just saw this post as I was searching for more Hashimoto’s info. Sounds like you were thinking of taking things into your own hands, which I understand, since I have had Hashimoto’s for at least 15 years. I can relate to everyone’s symptoms and feelings. I’m so sorry you have no support for this. I hope that you have at least found some support online. Please update us. I wish I (or someone) could help.

      • Bella, don’t give up! As Chris Kresser mentions in another article, there is another option that is meeting with success for a number of auto-immune diseases, including Hashimotos. It’s called LDN (low-dose naltrexone). Please do a youtube video search on it’s efficacy. Here is a good website:
        You can read up about it here too. Also, they recommend purchase of the capsules at The first doctor (Bernard Bihari) who did research on it in the 80s said that 3mg amounts per day worked excellent for many conditions. It’s about $40 for 3mg caps/30 day supply. Not bad really. It may be worth checking out. Good luck!

    • Dear Ann Stone, I have all of the symptoms that you do, and I have Lyme Disease and the co-infection, Bartonella. Bartonella has caused alot of the neurological things, such as panic, vision changes, memory loss, and Interstitial Cystitis (overactive bladder due to inflammation) I have had extreme chronic pain in muscles and joints and mostly musculoskelatal issues and skin changes from Lyme Disease. Your symptoms are also so suggestive. If you research the symptoms of Lyme Disease and Bartonella, and think you may want to be tested, I would recommend IgeneX Laboratories in Palo Alto, CA. It is a lab which specializes in vector-borne diseases and utilizes much more sensitive testing methods to find the Lyme bacteria (Bb). I have Hashimoto’s Thyroiditis as a result of LD, and have just started treatment at a very low dose of 15mg Armour. Antibiotic and herbals have improved many of the symptoms I had, that you are experiencing.

  50. Thank you for a brilliant article on Autoimmune Thyroiditis.
    Happy I found this article.

    I’d like to know what is the correct age for menopause? I’ve been told the NEW findings is from 31, I am 43 and was diagnosed as menopausal at 42. My gynae informed me that I would experience earlier aging despite the fact that I feel 27, he also mentioned earlier death etc. I’m saddened as I’ve taken great care of myself and feel life is such a waste of time. I’ve also been diagnosed with hashimotos thyroiditis and on the Paleo diet, bio-identical hormones, selenium, moducare and a whole lot of supplements to reverse the condition, excluding iodine. Should I be taking this? What are the symptoms that one experiences at a later stage of autoimmune thyroiditis?

  51. I was taking anatabine and metformin. my thyroid harmone TSH is now very low and the T3 is very high. Either could have caused it. Does anyone know of any information about anatabine affects on normal thyroid.

  52. Hello, I am 25 and have been diagnosed with Hashis a couple years ago. I have most of the symptoms there is with it which can be a hard thing to live around. Not that I am surrounded around my looks or anything but we all know that women with hair loss get looked at in a totally different way than men do.. My hormone levels are under control and normal right now with my hormone replacement therapy but I still suffer from some pretty crappy symptoms of brain foggyness, fatigue and hair loss. I have been on spirlactalone for about a year and with that not working, my Endocrinologist wants to put me on finasteride, a pharm made for men. My pharmacist strongly urges that I do not take it, and so far I haven’t. What else can I do for hair loss? How to I treat the underlying problem for it? Can that even be done? Or should I start shopping for wigs and head wraps?

    • Lily…There are some great suggestions to reverse hair loss from low thyroid conditions…I wrote about it on this forum already, but if you can, go to “Hypothyroid Mom” on facebook. If you don’t find her article there, I did post her suggestions on an earlier post!

  53. I have hypothyrodism and have all the symptons you have indicated when a lower dosage is prescribed for me.. Unfortunateley for me, I have a gland that functions partially. My current doctor relys soley on the lab report and not on symptoms I report. I have tried to explain that I can tell when the gland begins to work and many times when my levels are checked it is on one of those days. Medication is then prescribed based on those labs. After the doctor reduces the dosages, I start having the symptons. Do you have any suggestions. My wieght has increased by 50 lbs over the past 6 months.

  54. I like your article except for the point where you say alternative doctors will inadequately address autoimmune hypothyroidism. I am a naturopathic doctor and 90% of naturopathic doctors I know would treat the underlying cause of autoimmune thyroiditis from stress, to nutrient deficiencies, sleep disturbance, other related hormone imbalances, high toxin burden, dysbiosis, and food intolerances to start.

  55. Hi there, I just wanted to give some of you hope out there if you have Hypothyroidism. I had a partial thyroidectomy and was diagnosed two years later with severe hypothyroidism. I am the 10% that is not autoimmune, but caused by surgical removal; however, have experienced the same hurdles and inadequate medical assistance. I have fought for year to educate myself. The long and short of it is, after one year of treatment I am better. I take started out taking Synthroid T4 and still had a miserable quality of life, even after entering the “normal range”. I requested that my doctor add a T3 medication. He recommended Cytomel. Cytomel has changed my life. I reasoned with him why should he care as long as I stayed within the “normal ranges” on T3, T4 and TSH. He could not argue, and hesitantly gave the medication. I was extremely nauseated the first month, but then my body adapted. With each increase the quality of life improved. I take 75mg of Synthroid and 10mg of Cytomel at 5am on an empty stomach. It jump starts my body with the T3 (energy to the cells) and I wake around 7am. I take 5mg at noon. This last visit my reflexes went from reacting hypo to normal. That is a huge deal. I am at the TOP range of the “normal range” now. I was diagnosed with a second chronic illness six months ago (three years after surgery) called arthritis. I fight it every day with 2 hours of stretching/ walking. I am getting healthier, better, and stronger every day. With the proper thyroid levels I am no longer lethargic, my cells are receiving T3 (energy) and ABLE to exercise, focus, and work. I also eat well in order to reduce the inflammation in the body by eating gluten free, sugar free, and dairy free. I have discovered that Cytomel treats Myxedema (all that swelling you get in your face, arms and all over). People thought I was loosing weight when I started the Cytomel, but really I was loosing all that swelling. The tops of my arms have definition again. After my reflexes changed and my body was getting proper levels of thyroid hormone for me, then I started loosing weight effortlessly (remember I also started walking daily for the arthritis and eating right). From what I understand with arthritis is the rest of my life and I will have to fight it daily as it battles me daily to lock up. I went through the five stages of learning to deal with chronic illness and now I am at acceptance. Grieving was the worst part. The loss of who you were and used to be is a hard one. But, it is easier to talk about and share with others now, I accept that I have a different level of abilities and learning to live this new life. I refuse to be miserable. I look for the good in each day and how I can have the best quality of life possible. I am constantly learning more and more about this disease and how to manage it. Vitamin deficiencies are important such as D3, B12, Selenium, and Iron (100-130). We must be proactive, persevere, and live life the fullest of our ability. Where we fall short we have to learn to accept and love ourselves completely regardless of circumstances. When you have a bad day you have the small quiet voice inside that is called courage and say “tomorrow I will try again”. On the really bad days I think about those who have kids with cancer, incurable cancer themselves and dying, and I count my blessings. Fight for you health and don’t ever give up.

    • I’ve been on synthroid for 20 years and armour. They chemically removed my thyroid
      I’m so confused. How do I know if I have hashimoto or just no thyroid. I’ve been on 50 synthroid and 30 armour My latest blood test said I went from hypo to hyper so dr decreased synthroid to 25. My tsh is now 2.3. Feeling better
      Eating well. Does it sound like I have Hashemite. I was never told that??

    • WOW….. I didn’t know how much I NEEDED to find this website.
      I was diagnosed with hypothyroidism last week and am an absolute mess :'(
      But I guess my feelings ARE normal…. I’ve started the regiment of meds (75mcg of Synthroid each morning) and of course LOTS of vitamins because I am very deficient in Vit. C, D and Iron.

      BUT my question is… do I have “Hashi”. Is it all the same …. ????” “hypothyroidism” and “hashi”?
      Please help someone.

      I am feeling so confused and alone. I just want to feel happy again… lose weight… and not gain…. ahhhh. HELP!

      Thanks in advance. I really hope someone can answer my question.

    • I don’t know what kind of arthritis you have but taking Nettle, Boswella and Chinese Skullcap quickly eliminated all the pain and stiffness all over in all affected joints and in a few months even the lumps on finger joints except a slight bit in three spots. I could actually “unstick” my fingers from their curved positions and flatten my hands except for a slight curving left in my right hand. This was self researched to address some common cytokines involved in inflammation.

  56. I have Hashimotos as a hereditary condition as do 3 of my 5 siblings. Shows up at age 45. Controlled fine with Armour. Can I expect other symptoms/issues? I am 65 and have been primal diet for 2 years.

  57. Suffering from Hypothyroidism for about 2 years now, I have been taking Moringa enhanced products for about two months and I have seen increasing levels in vitamin d(30 points) and good cholesterol(20 points).
    (Moringa is packed with all sorts of vitamins, minerals, antioxidants and inflammatories).

    I have also lost 15 pounds in that same time frame. This is a major accomplishment with all of the problems that hypothyroidism brings to the table.

    Now in order for this to happen, I had to stop taking my prescribed Synthroid because I felt the Synthroid was causing more issues than exactly helping.

    My thyroid is inactive due to taking the RAI twice and this is the part, I would like to receive some advice on. My TSH levels are off and my bad cholesterol is still high which was pretty much expected.

    My main goal is to find a good alternative thyroid medication to resolve this issue. I think once I find a thyroid medication that works better than the synthroid, hopefully that would be the key.


  58. I’ve had Hashimoto’s for about 7 or 8 years. Synthroid has been what my Doctor has been treating me with. Recently my symptoms were bad enough that I went to the Dr, and pushed for testing (normal) and then requested a T3 med (Cytomel) which she gave me.
    I then requested an ultrasound for a feeling of pressure in my throat, this revealed multi-nodules, the largest one over 2 cm.
    So I am getting referred to a ENT Dr. What should I be aware of before this new Dr. starts treating me? Thank you

  59. Hi Chris
    What about non auto immune? I have been tested and found to not have Hashimotos. There seems to be no explanation for my thyroid failure?

  60. Chris, thank you for your good work. One thing I seem to find unclear is how to know when your thyroid is completely destroyed from Hashis and how to proceed if it is beyond repair. It may be a simple answer but in my research I don’t seem to find anything explicitly stated. This would be a much appreciated post. Thanks again!

    • I was under the impression that if yo are taking maximum dose of Levothyroxine (I think this is 200mcg?) to balance your TSH levels within 0.5 – 3, then it would mean your Thyroid is releasing absolutely no T3 and T4 hormone any longer and you are supplementing these hormones solely from your tablets. This would mean your Thyroid would be as good as gone, unless future Stem Cell treatment can fix a scarred Thyroid.

  61. Thrnks for all this info. I have just been diagnosed with the hashimoto today after two pregnancies having post partum thyroiditis after delivery & now two years of being on levothyroxin. Im at my breaking point with this. Im stuck with no good doctors or treatments… For the last week ive been waking after just falling asleep shaking, anxiety, blurry vision, naseauted, so scared & unable to sleep. Insomnia for days. Im not sure what to do next. Any advice?nks fo

    • Amy D. I too have had the insomnia as you describe it and after 2 years of misdiagnosis and sleeping pills/anti depressants, I found out myself that it is caused through blood sugar issues. Mine is adrenaline compensating for low blood sugar. Some organic orange juice with salt helps. Sugar for blood and salt to decrease adrenaline. All the best.

  62. My neurologist at UT Southwestern-Dallas/
    MS Clinic will not entertain the idea of using LDN. Instead, they only encouraged and explained the three new oral drugs. Sigh….. all while going through the worst exacerbation ever in my 24 year history with MS.

    By the way, I am seeking a new appointment with another neurologist who is open to other therapies–such as LDN. I am also hypothyroid and using Armour and a small amount of liothyronine. I suspect that my recent MS flare is due to thyroid (mis)treatment when other doctors (including UTSW) insisted that I get off all thyroid meds, so I did that for about 6 months. New labs after that showed me hypo again so back on the thyroid meds. My symptoms have improved however I suspect this current horrible MS flare is partially due to improperly treated hypothyroidism, and stress of course. (I survived 3 layoffs in 6 months time!)

  63. I was put on medication with a TSH of 5.8 10 years ago
    Now I take Armour
    My antibodies are high just have been told I have hashimoto’s
    3 small nodules on thyroid lobes. No symptoms.
    FNA inconclusive .
    now what?

  64. If your going to continue to post old postings I wish you would update them!!! I’ve come to the point that since they are not dated at the top I zip down to the comments to see when people have first commented. This is now 4 years old…

  65. I’m looking for a good endocrinologist for my hypothyroid in the Bradenton/Sarasota area. Anyone live here that can make a recommendation?

  66. Is it possible for diagnosed hashimoto’s to continue many years later and develop fast growing lesion near trigeminal nerve area? As of yet negative testing, did not resond to IV steroids, infact grew. R Facial numbness and R sided arm and leg weakness, balance issues. Trying to decide if bx is right thing to do?

  67. After seven years of having very abnormally low temps and symptoms of Hypothyroidism and doctors would just say you have no thyroid problem because your TSH is normal. The symptoms which only happened for a few days, maybe only every couple of months were happening everyday and I was so sick and exhausted I had to do something.

    With referrals I saw two Endocrinologists, the first only did TSH & T4, like had just been done. The second said I would be happy to do a thyroid panel, and did. TSH was normal, free T4 high end of range and free T3 at bottom of range. But he said you do not have hypothyroidism!

    They only know how to test for primary hypothyroidism and will not go any further. WHY? I see my tests showing my T4 is not converting to T3 properly.

    I had cancer 12 years ago and went through a year of weekly chemo and Have many on my Mom’s side with Hypothyroism. I could have pituitary or hypothalamus damage. How would I find out if a doctor will not go further?

    Plus, I told my new primary care doctor about trying to get diagnosed and of course do not expect her to take that on, but in talking about tests, she said T3 converts to T4, but I am not going to argue about it with you, go back to your Endocrinologist! Elaina Parton

  68. Hi Chris, thank you so much for this post. I was diagnosed with Grave’s Disease a few years back and ended up undergoing Radioactive Iodine treatment because at the time I had no idea that there might be better alternatives. I would love to see an article from you regarding people like me who have Hypothyroidism as a result of RAI, and not because of Hashimoto’s. I would imagine there are many parallels to Hashimoto’s in the sense that Grave’s is also autoimmune, and that as such is not actually “cured” with RAI. But I would love to hear any specific insights or advice you have regarding this particular scenario.

  69. thanks chris – interesting – I have under active thyroid plus pernicious anaemia – and the both of them together try to ruin my health most days and succeed most of the time – am on b12 injections every three months (not enough) and levothyroxine (75mg/day) probably not enough – am knackered all the time – but docs here in Scotland wont budge an inch

  70. Thanks for all your information! I am interested in how Hashimoto’s (and hypothyroidism in general) relates to menopause and the changing hormone levels. I have Hashimoto’s, I’m 48 and finding that my mood swings and energy levels seems to be connected to the hormones and the Hashimoto’s. I’m trying to switch to NDT from Synthroid to see if that will help.

  71. I went to a alternative doctor and she told me to stop eating gluten for Hashimotos. I had searched the internet for answers and was surprised that this information wasn’t more available. Gluten causes your intestines to become come permeable, aka leaky gut. Gluten and thyroid tissue are very similar so when your immune system attacks the gluten that leaks out of your intestines and into your body it also attacks your thyroid. My antibodies were very high and after sticking to a strict gluten free diet they were almost normal and all my symptoms went away! One of the keys is healing your gut which means you need to take probiotics and stay away from foods with pesticides which kill the healthy bacteria in your gut. I have cheated on my gluten free diet and felt the effects. I also think avoiding sugar and keeping my life as low stress as possible makes a huge difference in how I feel.

  72. Thanks for this post. Looking forward to part 2…
    I have a question about iodine for hypothyroidism with an autoimmune component (not full Hashimotos) Recommended or not? Thanks!

  73. I was diagnosed with hypothyroidism 8 years ago and I take levothyroxine sodium 1 tablet .125mg per day but my question is I still feel like Im going crazy I cry all the time always depressed and cant hold a steady job because I feel ppl are out to get me so paranoid. what can I do I need to work. HELP HELP

  74. I was diagnosed with Hashimoto’s 10 years ago when they removed half of my thyroid. I have a new doctor who tested my antibodies just to make sure I really have Hashimoto’s and she said it was negative. Is it possible for the antibodies to go away or is one wrong. Also my TSH numbers went from 1. something to .0001. But free t4 and free t3 are both 1.27. HELP She lowered my medication from 125mg to 75. I’ve been here before and not looking forward to gaining 30 pounds in a couple of months again and sleeping 12 hours a day. Again HELP

  75. Hi Everyone,

    7 years ago, when I was 16, I was diagnosed as hypothyroid (VERY high TSH) and was told that it was probably Hashimoto’s (my thyroid glands are a bit swollen).

    But I just got lab work done today and my Thyroid Peroxidase Antibodies (TPO Ab) were only 4 IU/ML (within the normal range of <9). I don't think my TPO Ab had ever been tested before, it was only done this time per my request. Does this mean I don't have Hashimoto's!? Any answer would be helpful 🙂

    PS. In case it matters, my other results were:
    TSH 0.411 (slightly low?)
    T3 2.9
    T4 1.40

    I have been on synthroid (88 ug) for the last 7 years…hadn't really had a problem with anything till about a year ago, when I started feeling exhausted all the time…

  76. I have been researching as of lately alot about proper diet for hypothyroid disorder. I have been diagnosed with it for about 8 years now and have been on medication. My biggest problem is the fact that I cannot burn fat not matter how much I workout or eat well. I workout 5 to 6 times a week and love to be active which has been helpful because I don’t see the benefits in my size, it would be easy to just stop but I actually enjoy it. I experience brain fog, extreme fatigue, heart palpitations, you name it I experience it. I have recently done a 30 day vegan diet and it has actually made my symptoms worse so I decided to stop that. I just want to be the healthiest I can be and to feel good for once. I will try ANYTHING to help correct my thyroid symptoms. I am big on being natural so I really hate taking medication, I would love suggestions on a new way of eating to help me look and feel my best. Any suggestions would be great!

    • Hi Kendall,

      The biggest three dietary recommendations I have read are (in order of importance, I think):
      1. Gluten free
      2. Soy free
      3. Dairy free

      I would try one or all of these…good luck!

      PS. I don’t think that going vegan is especially good for thyroid disease…there are essential amino acids/proteins we can only get from animal products. I personally do not usually eat meat, for ethical reasons, or dairy, because it doesn’t agree with me…but I do eat eggs and fish, and I have found those two things to be an important part of my diet.

    • I am feeling better since I dropped grains. I used to eat lots of soy and grains including gluten products some of which made me really tired and bothered my vision.

  77. I have been dealing with Thyroid issues since I did research on my symtoms and let the physician know to check my thyroid. Amazingly it was out of whack so they put me on levothyroxine. Now I’m having heart palpatations! I keep telling them that I want to know what is causing the thyroid issue and they tell me it just sometimes happens. I will NOT accept that because it just does not happen without a cause. I want to get to the bottom of the autoimmune issue so that I can get better. I’m tired of being sick! I have low vitamin D & Potassium and positive ANA along with Shrunken Thyroid elevated cholesterol. Any suggestions???

    • Deb,
      I also had very low vitamin D, so I now take D-3 2000, at night.
      I also atke Triple Magnesium w/ coconut oil. Coconut oil helps so much with constipation from low thyroid.

      During the day, I started taking CO-Q-10, Green tea complex, and resveratrol. The resveratrol gave me much needed energy, but suddenly, when I went to re-order, the price nearly doubled.

      My TSH levels change every time I get tested, and I am back to being exhausted once again. I get up at 8am, and usually by either 11AM or 1PM, I HAVE to take a nap for like 3 hours! This cannot be normal.

      I am not feeling as good as I should be, and I have notes from an online seminar (it was free) I attended for an hour, through another endocrinologist. I need to get my cortisol levels tested, and also my hormone levels. All these come into play, and need to be addressed.

      This is the most annoying disease, and it took 11 years for me to be diagnosed. Every doctor I have, blamed me for the weight gain.

      I hope you find someone to help you, so you feel better.

  78. It took 11 years to find out I had Hashimotos, and it was myself, that figured it out.
    All my doctors kept telling me to stop eating Burger King.
    I do not eat burgers at all. What a bunch of idiots out there.

    I have been on synthroid, different doses, as my TSH levels go up and down like the stock market.

    I am exhausted again, and I sleep most of the day, after sleeping 9 hours every night. I cannot get anything done, and even cooking dinner, is a burden.

    Who wants to go on like this? Not me. There has to be a better way to deal with this chronic disease. I am so fed up, I do not know what else to do, or what they are missing.

    Anyone else, lose weight, then go back to being tired full time?

  79. My 5 year old daughter has just been diagnosed by her pediatrician that her auto immune system has killed off her thyroid. She is now taking medication daily and I am looking to gain a better understanding of what is going on. I have asked the doctors hundreds of questions and the only responses that I seem to get are that now she is taking the meds, she will be fine.

    I was quite satisfied with these answers but after looking online, I am now quite scared (infertility, anxiety, depression etc).

    What should I be doing to help her other than the medication her specialists have prescribed? She is a very intelligent girl but since her diagnosis, I have noticed a very distinct change in behavior. Being so young, I definitely do not want to see her spiral out of control before she even reaches puberty!

    Is it a good or a bad thing that we have diagnosed her so young? The reports I have been reading have really got me scared for her, but I am not really sure what I should be doing from here?

    Any advice would be helpful. Thanks..

  80. I just switched from Armour to Naturthroid when I found out that Armour has gluten in it. The pharmacist said they cannnot keep track of these companies since they change the formula at random. Is this true and if so, how can we be safe?

  81. Hi all. I am a newcomer to this site and will give you a bit of my history. Diagnosed with UCTD 5 years ago. Hypothyroid 6months ago and just diagnosed with Hashimotos. Have the usual symptoms …. tired, alopecia, raynauds, high cholesterol, blood pressure, weight gain etc. Have just commenced on Armour (having taken Eltroxin for 6months with no improvement in energy levels). My question is… Does Hashimotos come before Hypothyroidism???

  82. When does Chris Kresser ever answer any of these questions. I wrote over a year answer…any place we can go to find some help from Chris Kresser? Thank yo!

  83. Hi!
    Blood type A says do not eat meat especially red meat then vegetarian diet is also not good for hypothyroid disorders. I eat fish but eating fish almost for everyday makes me wonder about mercury issue. I actually don’t know what to eat exactly:(. but I love coconut oil.

  84. Good luck bc it’s a long road….Definitely find you an ENT or GP that believes you. I got my ENT to believe that I was having almost all the symptoms(which I was) and it ran in my family distantly which I didn’t even know st the time. I told him my lab work over 10 years had always looked normal, and asked if there is a chance that it could be wrong?! He said an ultrasound of my thyroid would show him definitive answers and if that came up positive then a antibodies test for Hashimoto’s disease would be the next step. I had the symptoms for 10 years and endured horrible symptoms and it made me miserable. I felt bi-polar (extremely moody), lost tons of hair, had dry skin, my thought would swell up & hurt occasionally, etc… I had nodgules on my thyroid, am extremely big thyroid, etc… from the disease. I now see an Endocrynologist and have been finally been properly diagnosed after 10 years of hell. The doctors started thinking I was crazy, but I stuck to my guns and went with my gut. Eventually it paid off lol. I went so long in diagnosed though after a year of treatment I still have many problems and permanent/irreversible damage… Is what I believe. It affected my back and lead to many other problems like Fibromyalgia that I have severe pain all over my body all the time. And have had rods and screws put in my back also bc of these doctors not believing me.

  85. Im 24 yrs old and was diagnosed with hypothyroidism one year ago but never took the medicine for the thyroid. Until one month ago I started taking armor thyroid 30mg.
    But came a cross a big problem Im having sexual problems and can seem to get an erection or think about sex i dont know what to do or what test should I get done to help this problem im having?? Any help is highly appreciate thanks in advance.

  86. I have been diagnosed with Hashimotos disease & am currently seeing a endocrinologist. She has done ever test imaginable & have been on meds. Levels for thyroid are in range but I am still extremely fatigued, bowl problems, & all the other symptoms that are associated with this autoimmune disease. My life has dramatically been affected by this disease. I had to quit my job as an aerobics teacher for 15 yrs. now I don’t even have the energy to exercise. Weight gain is off the charts. Depression is another big issue & life just sucks! I have been doing more research on this disease & have seen a lot of information on changing eating habits. Yesterday I started eating an autoimmune diet, but still trying to educate myself. I ran across your site & am asking for any advise you can give me. Thank you.

    • Hi,
      I was diagnosed with Hashimotos in 2009 and
      I was getting the same symptoms as you and started a gluten-free diet and since then most of these problems have disappeared and I have much more energy. It doesn’t work for everyone but you could try it alongside your present diet to see, though maybe your autoimmune diet already restricts gluten?

  87. Can you please help me understand why, after removing half my thyroid 14 years ago and being diagnosed with Hashimoto, that I now also have Graves disease. I was told back then, I would be on thyroid hormone for the rest of my life, and now, my dose is so small, that the next step is to just go off of it. I’m very confused as to how I can have antibodies for both diseases. My levels have been pretty steady up until this last year, and they started lowering the dose. I’m getting worried that its not heading in a good direction,

    • I was diagnosed with Hashi hypothyroid in 2009 and also Graves disease because I have what they called ‘hot nodules’, areas that are hyperthyroid, mostly I am hypo but sometimes the hyper has the upper hand so I get hot flushes and other hyper symptoms.Normally I take thyroxin but if I get the hyper symptoms I reduce the dose or stop it altogether for a few days till I feel better. The specialist explained that the two coditions are fighting each other so we don’t know which will win out in the end, every so often I have tests to check how things are going, really I’m hopeful that maybe the two will settle down and my thyroid will return to normal eventually but maybe I will just have to put up with this forever.

  88. Hi,

    My son is 11 years old but look like 8 years old as he diagnosed hypothyroid (primary level) 2 years back. He is taking thyroxin 100mcg at this stage. Most of the time he doesn’t feel well. i am worried about his poor growth.. Please suggest me what another tests i have to go for him to improve his health and growth..also recommend me diets as well.. Should i send him to the gym or let him participate in regular physical activities (football, tennis, ice-hockey, swimming etc).

    • Surprise from Celiac Disease

      Study of a potentially fatal food-triggered disease has uncovered a process that may contribute to many autoimmune disorders.

      Scientific American
      August 2009
      By Allesio Fasano professor of pediatrics, medicine and physiology and director of the Mucosal Biology Research Center and Center for Celiac Research at the University of Maryland School of Medicine

      “For years CD (celiac disease) was considered a rare disease outside of Europe. In North America, for example, classic symptoms were recognized in fewer than one in 10,000 people. In 2003, we published the results of our study – the largest hunt for people with CD ever conducted in a North America, involving more than 13,000 people. Astoundingly, we found that one in 133 apparently healthy subjects was affected, meaning the disease was nearly 100 times more common than had been thought. Work by others researchers has confirmed similar levels in many countries, with no continent spared.

      How did 99 percent of cases escape detection for so long? The classical outward signs – persistent indigestion and chronic diarrhea – appear only when large and crucial sections of the intestine are damaged. If a small segment of the intestine is dysfunctional or if inflammation is fairly mild, symptoms may be less dramatic or atypical.

      It is also now clear that CD often manifests in a previously unappreciated spectrum of symptoms driven by local disruptions of nutrient absorption from the intestine. Disruption of iron absorption, for example, can cause anemia, and poor folate uptake can lead to a variety of neurological problems. By robbing the body of particular nutrients, CD can thus produce such symptoms as osteoporosis, joint pain, chronic fatigue, SHORT STATURE, epilepsy, dementia, schizophrenia and seizure.

      Because CD often presents in an atypical fashion, many cases still go undianosed. This new ability to recognize the disease in all its forms at an early stage allows gluten to be removed from the diet before more serious complications develop.”

      I was just recently diagnosed with gluten sensitivity (blood test) and autoimmune thyroid disease (Hashimotos). So far other book resources I’ve found informative are Dangerous Grains (authors?) and Grain Brain by Dr. David Perlmutter (neurologist).

      I’m currently working with a functional medicine practitioner to help identify other autoimmune triggers. Gluten sensitivity or celiac disease most often coexists with other food sensitivities. This involves an elimination diet and then adding foods back in one at a time. No easy task. Plus all the blood, saliva (hormone) and stool sample testing in beginning then in 3 months all over again to monitor progression.

      I feel positive for your son as he has a great advocate in you. Plus he has many years before he gets to my age 47 to get to the root cause of his issues. I played sports in middle school, but unfortunately not in high school cause I slept through most of it. Surprise surprise. My cousin (47 male) had same issue as your son and took growth hormone. Doubt he was ever tested for gluten sensitivity/celiac. To this day he suffers from IBS as does his other 3 siblings. I believe it’s all connected (families). He did participate in sports and does to this day and is very athletic.

      Good luck in your journey. I believe your son has a bright future.

  89. Hi Chris, I have a question. Your link in the sentence starting with “Studies show that 90% of people with hypothyroidism are producing antibodies to thyroid tissue” does not actually take me to any studies but to an article stub of which I can’t read the rest due to a paywall. The article does not actually cite any studies either. It doesn’t even say that 90 % of hypothyroid patients have antibodies to thyroid tissue, it says that “An autoimmune cause accounts for approximately 90% of adult hypothyroidism”, which is not the same thing. I for one have Ulcerative Colitis and I do have hypothyroidism, but no antibodies to thyroid tissue have ever been detected. Now, I know that you think this doesn’t prove that I don’t have Hashimoto’s and maybe it doesn’t, but the thing is that my main problem seems to be in the conversion of T4 to T3. The one sort-of capable endocrinologist I ended up finding after scouring the internet (and after lots of arguing with my former doctor) seems to think that the body intentionally cuts down on the conversion of T4 to T3 (leading to increased production of rT3) when there are certain systemic problems present such as inflammation in the gut. He said it was sort of like taking the foot off the gas pedal to prevent the engine from overheating while you’re going uphill. I think there is merit to that idea. I’m now on naturally desiccated thyroid (50µg T4 and 14µg T3) and while my TSH has plummeted and the fT3 has gone up, the fT4 has actually gone down. It seems like my brain is telling the thyroid to do anything to *prevent* the level of hormones in my blood to rise above a certain level. So basically what I’m saying is that while my hypothyroidism might be caused by my autoimmune disease, I don’t actually think it is Hashimoto’s and I don’t think the article says that either. I would still like to see those studies though.

  90. Hi, I started reading your book yesterday, and am wanting to start my 30day reset. The problem is, I can’t figure out if my hypothyroidism (not hashimotos) is an autoimmune form, as stated in the book. I have plain old hypothyroidism.

  91. After being diagnosed with hypothyroidism 17 years ago I was sent to endocrinologist who tested me for hashimoto’s and test said I had it. However was recently tested and doctor says I don’t have it. Is it possible for this to happen? I have been treated with synthroid then changed to armour then back to t4 and t3 combo.

    • Unless the first diagnosis was misdiagnosed, then i can’t see how this is possible.

      Either you have the Genetic Mutation which causes your Immune System / Antibodies to attack your Thyroid and slowly destroy it, or you don’t.

      Various lifestyle factors can make this worse, but i would say it is unlikely that the disease would just disappear if you have it. It will likely continue to slowly scar your thyroid again. Thyroid destroying Antibodies should be present in your blood samples.

  92. Hi, I have hypothyroidism, osteoporosis, sponyliolesthesis (decompression and fusion on L5) spinal stenosis, bowel prolapse (bowel resection), bladder prolapse (2 bladder repairs) silent sinus syndrome, depression, memory loss, early menopause (38). Could all of this be related to my immune system? I’m just wondering why all the health problems. I’m 52. I’m. On Synthroid, Fosovance, Wellbutrin. Thanks.


  93. Dr. Chris,

    What are your thoughts on human trial results recently released re
    ‘Anatabine supplementation decreases thyroglobulin antibodies in patients with chronic lymphocytic autoimmune (Hashimoto’s) thyroiditis: A randomized controlled clinical trial’

    Objective: The effects of anatabine in patients with Hashimoto’s thyroiditis.

    Results: Anatabine treated patients had a significant reduction in absolute serum TgAb levels from baseline by study end relative to those on placebo (p=0.027); however, there were no significant changes or differences in treatment group means for TPOAb or TgAb. Mean (±SD) TgAb values decreased by 46.2 (±101.1) and 3.9 (±83.9) WHO units for the anatabine and placebo groups, respectively. Significantly more patients had a >20% drop in TgAb in the anatabine than placebo group (p=0.023). Overall the anatabine supplement was safe and well tolerated, although significantly (p<0.05) more patients in the anatabine group reported AEs.

    Conclusions: These results demonstrate an immunological effect of anatabine on TgAb levels. Further studies are warranted to dissect longer-term effects and possible actions of anatabine on the course of Hashimoto’s thyroiditis.

  94. Dr. Chris,

    The condition of my sister with a toxic thyroid goiter really bothered me so much.

    Please educate me her sickness so that I know where to start.

    Thank you!

  95. Loving this site. Very informative. Does anyone have info on being thyroid hormone replacement resistant. I had the iodin ablation done 15 years ago been to the highest dose of of meds three diffrent times three different doctors. All three say I’m replacement resistant. Im 36 and feel and act like I’m in my 80s. I do have a vitamin b12 shot once a month and take iron and vitimin left feeling hopeless. That I’ll ever feel good. And afraid of loseing my mind.

  96. If hypothyroid condition caused by an autoimmune reaction , is it possible to test the person for the specific cause of the autoimmune disease, perhaps specific antibodies present, in order to avoid something in future ? Also if it’s been an autoimmune response does it become permanent with a gradual worsening as the response antibody continues to attack affected area, or other areas, or can you minimise or reverse condition by omitting cause, if it was identified. Finally can stress cause an autoimmune response severe enough to trigger hypothyroidism ?? Lots of questions but I would appreciate a medical response, can you tell I’m newly diagnosed and desperate to minimise condition ???

  97. My husband is 77, still working full time and has had Parkinson’s symptoms for over 10 years. He isn’t on any Parkinson’s meds yet. He is on a lot of nutritional supplements and has had a favorable response to the Coconut Oil Diet. He is on 4.5 mg of LDN for about 1 year. Everything helps a little but then the disease continues to progress. He was recently started on 25 mcg of Synthroid for elevated TSH and low normal T4 and free T4. (One study showed Parkinson’s patients with untreated Hypothyroidism seem to have exacerbation of symptoms which get better when properly medicated. We are hoping that his increased tremor, fatigue and brachycardia will improve once his thyroid is better regulated.) He had been experiencing “flushing” the month before and this disappeared the first month (but no effect on tremor). Starting this second month he is flushing and feels hot from lunch to about 4 PM and getting up more often at night (usually 2, sometimes 3 times). I read recent research that suggested people have less symptoms taking Synthroid before bed rather than first things in the morning. Since he takes LDN before bed, do you know if the two could interact? Also, any known interaction with Melatonin which he also takes in the evening?

  98. I had PIP implants and following removal and new implants 1 1/2 yrs ago I haven’t been feeling well physically I’ve been affected in my lymph glands and can feel the lumps of silicone in my neck and armpits, also been diagnosed with depressionrecently had my TSH levels amongst tests for my thyroid these were high, my doctor wants them repeated in a month then ? start treatment for hypothyroidism. Does anyone know if there could be a connection between my lymph glands being affectected and the risk of autoimmune disease therefore leading to hypothyroidism (complicated I know, my brains trying to work out things)

  99. i had cancer and had a complete thyroidectomy and I am hypothyroid and I take 300 synthroid and I feel horrible I have severe sleep apnea I have edema in my legs real bad my body hurts I lose hair and so many other problems I have been to several doctors and no one seems to help me I cant lose weight and my thyroid changes all the time and low on vit d I have no energy and mental fog please help any suggestions

    • I haven’t had a thyroidectomy but am hypothyroid and I still felt like this even after taking synthroid. My doctor said it was just my age (65) and there was nothing more he could do!!! So, after investigating a bit online, I started a gluten-free diet and take vitamin D3 and I am now feeling so much better, I have much more energy, my legs no longer swell up as before and my arms have stopped hurting, maybe it could help you.

  100. i have a question hashimotos autoimmune my ths is 150.00 and thyroid peroxidase is 1000 if it does not go down am on synthnoid 175 already ?

  101. Hello,
    Am I understanding correctly your expertise is Licensed Acupuncturist? Or did I miss something in your base information?
    Thank you

  102. Greetings,

    I usually just read peoples suggestions on things to try. But I find I’ve exhausted almost every avenue with no luck.

    Everyone is so desperate for help, me included. We would just like one pill, we take it, and everything is cured, and OK. If only that existed…

    Well anyway, my biggest problem is that I’ve always felt “not fully conscious”. It is like I am going through life without living it. Its difficult to explain.

    I have all the other associated symptoms also… Fatigue, droopy eyes, sun hurts my eyes etc etc…..

    My TSH is 1.50 and free T4 is 14.7

    I’m 22 and have been on the doctor rollercoaster since 13.

    I’ve had these symptoms since childhood.

    I decided to see a private endocrinologist 2 days ago, and his suggestion was that I exercise more!!!

    Anyway, if you have some suggestions for me Chris, would be much appreciated.

    Also if anyone relates to what I’m saying I’d be happy to hear from you also.

  103. Hi,
    I really hope that somebody fromthis web site will take few moments to read and to answer to my questions.

    First of all, I am 27, I have TSH, T3 and T4 in the normal range (TSH is near the superior level, but still normal) and Anti-TPO level around 100 (max should be 34). Some doctors told me that I should already start taking diferent synthetic hormones and some that I should still wait until the hormones will not be any more in the range..when I was asking for causes, for diff thinks that I can do for decreasing AntiTPO, everybody was saying the well-known slogan: ‘ This is for live, you cannot do anything against it!’..

    Reading more via Internet, since April I started a gluten free diet, but I would like more guidence here where I am leaving, in Austria.
    If by any chance you can recomand me a doctor in Austria or if you can recomand me anything else (blood tests, books,etc.), please let me know here or via [email protected].

    Thank you and kind regards,

  104. Hi I have hypothyroid as well as pcos and almost 50% of my hair are gone,I hv put on 20kg. In last five years now I hv decided to go to gym n work hard , I am taking eltroxcin125mcg and now I hv started taking thyro max support +cla+l-carnitine daily twice 2 tab each of I doing right please help me I just want to reduce some weight and want my hair back as I am 25 yrs old female, not married and I have been suffering with this please guide what should I do. Pls help

    • Somewhere, I think on this site it indicated that T3 help prevent (restore?) hair loss. I had no hair on my body except head and eyebrows/eyelashes before T3. Noe a new endo M.D. stopped access even with normal blood levels so we’ll see what happens.

  105. I was just told I have high thyroid antibodies and am guessing that I have Hashimoto’s. I have been 3 years off of a cold turkey from a 17 year stint with a benzodiazepine Klonopin. I have been through Hell with this drug withdrawal and recovery. I am slowly tapering Prozac. What I want to know is could the Benzo cold turkey and the Prozac taper be causing this raised antibody test and will my thyroid/body ever return to normal again…I did not have a thyroid problem before I went on either drug…or is this permanent damage…hoping you can help me figure this out. Thank you!

  106. I’m only a senior in highschool, and I recently had been losing my hair, getting sick and gaining weight gradually even though my diet and exercise was the same. I also started to get tired during volleyball games and classes for no reason though I had a great nights sleep the night before. Then I suffered from severe constipation and had blood and urine samples taken to see what was wrong. My doctor told me I had hypothyroidism and prescribed medication, but I have yet to fill the prescription because I dont know what I should and shouldnt take. I decided to go home and research everything I could to figure out how to fix what was wrong with me. I started to double my exercise and decrease my food intake and still my metabolism seems to be slow. My hair is still falling out and my sleep schedule seems to be getting worse. I would like to know what medications I am supposed to take for my hypothyroidism so I can get back to feeling better and get back to playing volleyball.

  107. How do I find a doctor that will do the correct testing? My daughter has hashimoto and I have all the symptoms…loss of hair, dry skin, tiredness, weight gain and depression. My family dr did the normal blood test that came back negative and an endocrinologist won’t see me without a diagnosis. I know I have a thyroid problem. I am in Tampa,Fl. Can anyone recommend someone?

  108. This is an excellent series on hypothyroidism. I’d like to add a possible cause of hypothyroidism to your list. I was born with a “lingual thyroid” and the gland is only partially developed. Tis was revealed in scans and tests when I was 14 but my thyroid levels were normal at the time. I am 36 now. About 7 years ago I was finally diagnosed with hypothyroidism (my TSH was measured at 12 a I was barely functioning!) and given synthroid which has been extremely successful in boosting my thyroid t3 and helping me live normally. I think this possibility should be examined especially for prematurely born people, as I understand that thyroid formation is one of the last functions during pregnancy.

  109. Dear Dr Kresser

    You have an amazingly informative website – Thank you.
    I’m 29 years old, otherwise fit and healthy individual.
    I have recently had blood tests from my GP revealing very high thyroid antibodies but euthyroid (my symptoms were that I felt my neck was swollen in the thyroid region). I would like some direction on what I should do next. I have been to see an endocrinologist who just said I have Hashimoto’s and to come back and see him when I am hypothyroid.
    I am extremely health conscious and just feel helpless that I’m just supposed to wait until I have more symptoms as a result of my thyroid gland being completely destroyed!

    Thank you in advance for any advice!

    • Firstly I would recommend that you go gluten free as this is recommended for Hashimoto, which is an auto-immune condition, where your immune system has gone crazy and is attacking your thyroid. Whether this will help your thyroid much I don’t know but it may stop you getting more complications. Depends really how much damage your immune system has already done to your thyroid.
      When I was diagnosed with Hashi in 2009 my endocrinologist did not mention a GFdiet to me and even after medication I still had many problems which I was told were my age, I was then 62, In 2012 I had a bout of what I thought was IBS and also eczema and while looking for a solution I came across the GF recommendation. All I can say is it worked like magic for me and I haven’t felt so well for years, I am still on medication but I have been a year on 100mg and sometimes even only 75mg so it doesn’t seem to be advancing. I can’t help thinking that if I had known about gluten in 2009 maybe going GF then I could have avoided all the other problems, maybe my immune system could have righted itself at least partially, or maybe it still can whos to know but GF seems to me to be the right path. Maybe you should also change your endocrinologist if you can but I’ve found that it’s difficult to find one that has any interest in his/her patients welfare!

  110. Hi Chris,

    My thyroid antibodies have twice come back <1. So does that mean I'm positive for antibodies, even though they're low (maybe because I'm gluten free)? Does this mean Hashimoto's? My TSH is slightly elevated and I'm getting on Armour.

  111. I have always had many alergies, sinus, skin, etc. Could this be a sign of autoimmune disease? In 2008, my hypothyroid was discovered. I went on synthroid 50, and it seemed to work (goiters run in my family). In 2009, my high parathyroid numbers were found to be very high (due to what I called bone pain). I had not had menepause but was already showing early osteroperosis. In 2011, My endocrinologist told me I had a vitamin D deficiency, and hashimoto in 2011. He told me to keep taking Vit D in high dose, and not to increase synthroid, and take randidine for gerd, but not to worry, my blood calcium was OK. I always thought I was cooking, and eating healthy, whole grains, rice, lots of milk, yogurt, olive oil, low fat, etc, but now I think that may have triggered my autoimmune disease, and it may be attacking my whole body. Vitamin D helps with bone pain, but my biggest concern is that I use to be a great multi tasker, and now my short term memory, and word recall is really affecting all of my skills, and I sleep very lightly.

  112. Hi chris. Found your articles afew days ago. I hope you answer. My tsh was 2.5 and i have all the clinical signs of hypo. The past three yeats have been aweful. I often get headaches at the back of my head and they feel like my brain glitches like a messed up computer or like i go in and out of reality for split seconds when i feel swelling back there. Can hypothyroidism cause this? I wont be tested for antibodies until next week. But thr pain at the base of my head makes me wonder if its related. Thanks!!

  113. Hi Chris,

    Thank you so much for providing all the information!!!

    I’d be very happy if you (or some of your readers) find some time to reply to my message.
    I am 35 years old and am taking levothyroxine 75mcg for about ten years now, but I haven’t really felt a difference when taking it.
    My TSH tests showed 0.68 (in 2010), 0.21 (in 2011) and 0.38 (in 2012) from a morning blood test without taking the medication. Free T4 was 0.9 (in 2012, not taken before).
    Since 2009 I am experiencing fatigue, feeling exhausted, foggy brain, lethargy, depression, cold hands and feet & easily feeling cold in general, menstruational problems, back pain.
    A saliva test showed very low progesterone which I treated with progesterone cream.
    Parts of the menstruational and depression problems improved a lot.

    Can you give me advice how to proceed from here?

    Thanks again!!!

    • Helen,
      This might be of interest;
      Star Scientific Thyroiditis Data Published

      First, preliminary results of the study, yet to be peer-reviewed and published, provide the most compelling evidence yet that Anatabloc is what I’ve said it is — the first effective therapy for endemic autoimmune disorders. While this study demonstrated the first-ever ability to reverse the course of thyroiditis, its importance is in its ability to treat or prevent autoimmune disorder, which plays a role in virtually all age-related diseases, including thyroiditis.

      Second, the famously cautious Dr. Paul Ladenson, one of the top endocrinologists in the world, has gone on record saying, “Data from this rigorously conducted, placebo-controlled, double-blind trial show that anatabine-treated subjects had progressive decreases in circulating thyroglobulin antibody levels, which became significant by the end of the trial.”

      Dr. Curtis Wright, Medical Director for Ross Creek Pharmaceuticals, said:

      “It is remarkable that dietary supplementation is able to help lower the thyroid antibody activity. To see antibodies that may have been elevated for years beginning to come down in a significant way after three months of supplementation is exciting. Given the rate of decline over three months, it is quite reasonable to expect that the effect may continue with longer use, which has already been observed in individual cases. I look forward to following subjects over a longer period in order to establish how profound and clinically meaningful the effect is going to be. The thyroglobulin levels in some patients returned entirely to normal in this three-month study.”
      They are talking about Anatabloc. I take it with good results.

    • You may benefit from changing your levothyroxine to natural dessicated thyroid. Also, for myself while the Progesterone cream did raise my levels in bloodwork, they didn’t make me feel any better. Once I switched to Oral Progesterone (Prometrium) I started feeling way better. Seems that even though you waste a lot of it as it goes through your liver to be metabolized, it seems to act more “slow release” that way and really improved my condition. that, plus natural dessicated thyroid, and now added some bi est estrogen, going gluten/grain free, and I’m way better than before. no more cold hands and feet. even my eyeballs and mouth were cold. not anymore!

  114. I have hasimoto hypothyroidism and eventhough I am only in middle school I found it very informative… but I am wondering if this could cause anemia, and is it very rare in children under 14 years old. Thanks, UNICORN LOVER!!!

    • Erin,
      Have your parents and your physician look into Anatabloc. A human study completed in January this year showed ‘significant’ results in ‘halting’ the progression of this disease.

  115. Hi Dr Kesser,
    I have been treated for Hashi since mid 1980s. I also had a pit tumor resected in 1985 (prolactinoma) and I wonder if that precipitated the Hashi. Have been on Synthroid since 1980s in gradually increasing doses. A couple of years my GP added Cytomel to my regimen. My doc doesn’t understand that I feel really bad when my TSH is super low…I think his feeling is the lower the better. I now take 200 mcg levothryoxine 1/2 tab M-F and 1 tab Sat & Sun. TSH stays between 1 and 3 which is okay. But I have lots of other auto immune symptoms that I never related to the thyroid issues….bloating, gas, fatigue, mental fog, sluggish, joint aching.

    Thinking I need to look at the gluten issue. I am a South Beach diet person with limited carbs anyway, but have not restricted gluten per se. Feel better with less joint inflammation etc on SB phase 1, but again that is not necessarily gluten free.

    What are you thoughts on this?
    Thank you,

    • From my own experience with Hashi, diagnosed in 2009, and on synthetic thyroid meds, I had all the symptoms you have. After a bout of IBS symptoms last year I decided to try gluten free for this and, like magic, the IBS and all the other symptoms dissappeared, including severe migraines that I had had since I was 11 years old.
      GF may be tiresome, all the checking food packet info and being careful when eating out, but it’s worth it, I feel so much better, now I feel human again, I hadn’t felt really well since the Hashi decended on me so obviosly going to stick with GF forever, I feel 50 again (I’m now 65) ! Not been diagnosed as I’m not willing to eat gluten again even to do the tests!

  116. I have been diagnosed with Hoshimotos disease and about 6 months ago had 5 nodules that were growing from six months before. My doctor never advised me on anything I could do to decrease or treat in any way the inflammation. I was introduced to a product that lowers inflammation in the body and other health improving things that is all natural. I had been taking it for TWO weeks and I now have only three nodules and they have shrunk. Is this normal?

  117. Hi Chris,
    I was diagnosed as hyperthyroid after I gave birth in 2000, took the iodine treatment and have been hypothyroid ever since. The amount of weight I have gained is astonishing. I am on levothyroxine 175 MCG
    daily and I feel terrible all the time..tired, hair is brittle and falling out, heels are rough, can’t remember alot and my doctor just tells me my levels are fine and I must be eating too much, but I don’t eat alot at all. Now I have been diagnosed with sleep life just sucks right now! My question is since I started with hyperthyroid could Hashimoto’s Disease still apply to me? Thanks for any help you can give..

    • I had my thyroid out at 20 years old,now 59, I tend to think they may have been in a bit of a hurry to do the surgery. Nonetheless, this is some of what I have done personally to help myself.
      I just started on apple cider vinegar( has to have mothers’) on the bottle. The brand I use is Omega Nutrition organic. Anyway, my hair was falling out, dry, brittle, skin was dry and loosing collagen. I started taking this, about a tblsp. before I ate a meal and one before bed. My hair is growing like a weed and is coming in dark, at 59!, I was always plagued with yeast infections, they seem to have disappeared, back to the hair, IT HAS BOUNCE BACK, I remember the day when I realized something was really wrong with my hair before they took my thyroid out. Now, it’s just startling how healthy it has become. I also added liquid minerals daily. Just thought this might help.

      Take care , Lorraine

      • About Apple Cider Vinegar internally….
        It is high in Vitamin B’s
        It absolutely normalized my ph levels within a week, which were non existant on the litmus tests.
        My digestion and elimination has improved dramatically
        No more bloating when I eat
        It kills yeast, bacteria and parasites ( note: probiotics seem to work properly now)

        Apple Cider Vinegar is different than wine or beer in that it undergo’s a different fermentation; giving a different reaction to the body.

  118. Hi Chris,

    I have hypothyroidism due to my pituitary gland being completely damaged by a brain tumor. I was 9 year old at the time and am now in my 40’s. Up until about 7 years ago I didn’t have much of a problem losing weight when / if I needed to. But now I’m finding it so incredibly hard to lose weight. I’ve been on synthroid or the generic form of it all my life. As I’m sure you know, I have to take many other medications like prednisone to make my body function “normally”. Do you have any suggestions for someone in my case??

    Cathy P

  119. I am taking carbimazole, for hyperthyroid, and also ferrograd for low in iron, can i possible to drink Barly grass powder.

    my question is will it have bad side effect knowing i got this hyperthyroidism and low iron. if i drink Barly grass.

    Please help, if any one can give me information about this.

    appreciate for any info..


  120. I have ab negative blood type, severe scolisis, compression of L4-L5, l am also a Gemini, which may affect something, I continually gain weight, I cannot lose no matter what, please can anyone give me some advice.

  121. A retrospective conducted in Germany following 36 women and 2 men showed that treatment with levothyroxine (synthroid) reduced thyroid antibodies by 70% after 5 years of treatment for 92% of these patients. From these results it appears that treatment with thyroid hormone replacement alone does indeed treat the underlying autoimmune dysfunction. There may be more studies out there on this subject specifically but I cannot devote more time at present to research the issue, nevertheless I wonder if any large scale studies have been conducted with this in mind.

    Here is a link to the article

  122. Can anyone help. Hypo and hashi for many years. Been on synthroid 100 for long time. Taking cytomel for almost a year. I have never ever felt good as a matter of fact I feel worse every day. I’m severely lethargic. I am not able to think anything over like my brain is broken I’m depressed I can’t seem to gain weight I actually get thinner. I have crazy periods I have no sex drive I have no tolerance for for loud noises I’m always cold even in summer. My anti thyroid whatever it’s called is in the 500s I have a large goiter where I feel constriction. I need help the drs say I’m fine but I’m so not fine I feel terrible. Help!

    • Sissy,
      Have you heard of Anatabloc? Many are reporting significant positive benefits even before this study result was released last month.
      Rock Creek Pharmaceuticals Report Positive Initial Results Of ASAP Human Thyroid Health Study Showing Benefits In Immune System Support
      The study is a three-month, five-visit, double-blind, placebo-controlled study of the impact of anatabine dietary supplementation in humans with autoimmune disease of the thyroid. The study was conducted at nine sites and builds upon previous epidemiological and animal experimental studies. Initial results for all study subjects suggest that dietary supplementation with anatabine ameliorates the immune system’s targeting of the thyroid gland in autoimmune thyroiditis.

      • I finally found references to abstracts dealing with the subject of molecular mimicry and explaining the mechanism. A lot of research was done on this in the late 1990’s. It’s worth a read. The link is on a multiple sclerosis site:

        It looks as though certain viruses cause the body to release antibodies that in turn target specific tissues e.g. thyroid, that have similar amino acid sequences. This is exacerbated by also consuming foods that have similar amino acid sequences to both the virus and the target organ affected e.g. anti-gliadin antibodies against wheat agglutinin. For the MS people it can be dairy, grains and beans and the viruses from memory were quite a few such as rotavirus and Epstein-Barr (glandular fever). But it’s better that it is read rather than what I’ve written here as it’s only recall.

    • I have Hashimoto and am on synthetic thyroid replacement too, and the best thing that has worked for me is going on a gluten-free diet, I had a lot of your symptoms but after only a few days without gluten I started to feel human again. Its been almost a year now and I feel like my old self like before Hashi struck, It may take longer than a few days for you, and it may not help all your symptoms, but going gluten free for a week or a month can’t do you any harm, so I advize you to at least try it and see as it may help you.

  123. @Carol:

    My whole life I was unable to tolerate alcohol, and would become flushed and tipsy after only a couple of sips. Fast-forward many years, and I discovered I had severe adrenal fatigue (cortisol levels undetectable most of the day, then higher at night, when it shouldn’t be). A 24-hour saliva panel revealed this, plus secondary hypothyroidism — years of blood testing yielded nothing but frustration and “your thyroid is perfectly normal,” even though I was a poster child for its symptoms.

    Addressing the adrenal deficiency with natural methods (healthy, undamaged forms of dietary cholesterol, plus high-quality, non-synthetic vitamin B and C supplements and physiologic, not pharmacologic, doses of sheep-sourced adrenal cortex at the beginning), helped to bring my cortisol back without the use of synthetic drugs, plus it brought my thyroid numbers up to normal levels. Undiagnosed adrenal deficiencies are behind a lot of thyroid issues. Addressing the thyroid without taking the adrenals into account can be dangerous — if the adrenals are exhausted and slowed way down, they cannot accommodate a higher-functioning thyroid.

    Most of the thyroid’s T4 hormone is converted to active T3 through an enzyme in the liver. If the liver isn’t functioning optimally for any reason, this will be compromised. A chance meeting with a TCM practitioner revealed a sluggish liver that was affecting my thyroid as well as my ability to metabolize alcohol. I ended up moving out of a big, polluted city and doing a total 180 with my lifestyle, drinking clean well water, producing our own food and not eating anything processed. I can now drink wine with meals (not a big drinker, but once in a while I enjoy it) and don’t get flushed anymore. I was surprised at the time, to learn that my liver was overloaded, as I never drank, did drugs (prescription or otherwise), smoked, or ate a lot of junk. I was told that a polluted environment, tainted city water, and stress were enough of a burden on the liver to cause problems.

    I don’t know if such a drastic lifestyle change is feasible or even necessary for you, but wanted to share my experience, whatever it’s worth.

  124. Is there any connection between Hypothyroidism and alcohol intolerance? I am unable to drink even small amounts of alcohol without becoming sick. I have just started seeing a homeopath and have started a gluten-free/dairy-free diet to deal with healing the gut, inflammation, etc. My endocrinologist dismissed any connection to my thyroid. I would like to be able to enjoy a nice glass of wine now and then!

  125. GLEN ALLEN, Va., Jan. 7, 2013 /PRNewswire/ — Star Scientific, Inc. announced today the preliminary results of the Company’s ASAP (Anatabloc Supplementation Autoimmune Prevention) Human Thyroid Study that analyzes the impact of anatabine dietary supplementation on thyroid health.
    The title of the study is, “A Multi-Site, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Trial to Evaluate the Safety and Potential Effects of the Dietary Supplement Anatabine on Antithyroid Autoantibodies and Thyroid Function in Subjects with Autoimmune Thyroiditis”.
    ‘Dr. Paul Ladenson, senior endocrinological consultant for the study, stated, “Data from this rigorously conducted, placebo-controlled, double blind trial show that anatabine-treated subjects had progressive decreases in circulating thyroglobulin antibody levels, which became significant by the end of the trial. Current treatment for autoimmune thyroiditis is limited to end-stage disease when irreversible gland damage necessitates lifelong thyroid hormone replacement. The prospect of a novel nutritional or pharmaceutical intervention that could preserve thyroid health represents an encouraging advance.’

  126. hello Jeff s
    It appears you have hashimotos which is an autoimmune disease. Usually a gluten free diet is recommended. Test should be run for a celiac panel as well to rule out celiac disease. Usually with a thyroid panel you want to test FREE t3 , FREE t4, TSH as well as both anitbodies. Reverse T3 can also be tested if one suspects that might be an issue. This happens when body converts the active T3 into the inactive reverse T3 so the body can not use it . Usually the reason why some people develop reverse t3 issues is due to low iron and cortisol. Free t3 and reverse T3 should be done from the same blood sample when testing for reverse t3 issues. The treatment from my understanding for hashis is thyroid meds to suppress your TSH so your own thryroid gland is not under attack. In Hashis, the body starts to attack its own thyroid gland. I hope that helps answer your questions a bit. I have read quite a bit on thyroid issues but I am no expert. Chris might want to comment on this as well.
    Take care and wish you all the best.

    • Hi Toni
      I have been gluten free for more than 2 years–I’m fairly strict Paleo (very strict on the grains/gluten side). The tests that were done were ordered by my regular doctor. He has told me I should now see a Thyroid Dr. The two he has recommended don’t have any openings until March, unfortunately. Will try to insure they do the tests you suggest.

  127. Hi Chris and Others:

    I’m a 59 yr old male who has been Paleo for more than 2 years and for the most part have been doing fine. However, over the last couple of months, I started having a feeling like food was stuck in my throat and some tenderness near my Adam’s apple. Went in for a Dr’s visit and my thyroid was definitely tender, so the Dr. ordered a Thyroid panel. Got a call today saying that my thyroid is inflamed (their words) and that I should go see a thyroid Dr. I have a copy of my report, but am not sure how to read it. So any insights appreciated.

    The report has TSH+Free T4; CBC with Differential/Platelet; Comp. Metabolic Panel; Thyroid Antibodies; Thyroxine; T3 Uptake; Triiodothyronine; and Sedimentation Rate-Westergren. I have posted some of the results below (mostly those that I think pertain to the Thyroid and a couple of items that showed up high.) If I should list anything else, let me know.

    Test 1: TSH+Free T4

    TSH: 2.200 uIU/ml (range: .450-4.500) T4, Free (Direct): 1.38 ng/dL (range: .82-1.77)

    Test 2: CBC (Too many items to list, but everything seems to be within range)

    Test 3: Comp. Metabolic Panel (mot things in range, but listed a couple that were high)

    Glucose, Serum: 90 mg/dL (range: 65-99) BUN: 27 mg/dL (this was flagged as high. Range: 6-24) Creatine, Serum: 1.15 mg/dL (range:.76-1.27) BUN/Creatine Ratio: 23 (flagged as high. Range: 9-20) Calcium, Serum: 10.3 mg/dL (flagged as high. Range: 8.7-10.2)

    Test 4: Thyroid Antibodies

    Thyroid Peroxidase (TPO) Ab: 60 IU/mL (flagged as high. Range: 0-34) Antithyroglobulin Ab: <20 IU/ml (range: 0-40)

    Test 5: Thyroxine (T4)

    Thyroxine (T4): 9.3 ug/dL (range: 4.5-12.0)

    Test 6: T3 Uptake

    T3 Uptake: 30% (range: 24-39)

    Test 7: Triiodothyronine (T3)

    Triiodothyronine: 90 ng/dL (range: 71-180)

    Test 8: Sedimentation Rate

    Sedimentation Rate-Westergren 6mm/hr (range: 0-30)

    Am setting up an appointment with a Thyroid Dr. that my Dr. recommended. But in the meantime, does anyone have any comments/insights. Is the TPO high enough to worry about?

    • Autoimmune thyroiditis is inflammation driven. I think you will find treatment method beyond hormonal supplementation will be to suppress the inflammation process with only marginally effective drugs until the gland is totally fried.
      But there’s hope!. It’s 2013 after all and science continues to progress. See the latest human trial results on using a small molecule alkaloid anatabine citrate. ‘Rock Creek Pharmaceuticals Report Positive Initial Results of ASAP Human Thyroid Health Study Showing Benefits in Immune System Support’

      Anatabine supplementation suppresses several pro-inflammatory molecules (cytokines) in the blood. And suppresses NFKB and STAT3 activation.

  128. Hello Chris

    I am a 50 yr old white female. I was diagnosed with Cutaneous Limited Scleroderma with secondary Raynaulds Phenomenon. Since there is no cure for my Scleroderma or Raynaulds my doctors can only manage my symptoms with a variety of medications. I was just recently diagnosed with Hypothyroidism. They haven’t told me that it is Hashimoto disease as of yet but they have put me on Levonthroxine 0.05 mg per day. I also have Gastro problems associated with my Scleroderma. I have extremely dry skin, and hair loss that we associated with Scleroderma and a consistent chill throughout my body along with 2nd stage Raynaulds. I’m on 100mg Viagra daily to help the hands and feet. I also take a 400/500 Calcium & Vitamin D supplement twice daily without it I cannot keep my Vitamin D level above 18. I have difficulties swallowing which they associated with my Scleroderma and have had my first esophagus stretching. It helped some but not as much as it should have.

    My question is how to control the Hypothyroidism along with fights the affect of my other two major illnesses? Is it going to possible to have all of or some of these illnesses under some type of management since there are no cures for them? While fighting to control one or two am I damaging the other? Is there a proper diet to help maintain a happy medium between them all?

  129. I have been dealing with hypothyroidism for 5 years. I have been tested for Hashimotos at least twice and have been told I do not have it. I did test for an autoimmune disease at 1:164 titer homogenous. However, further tests for autoimmune were negative. I have been told it is my normal to test positive and to not have the test run again unless I have worsening symptoms. I have 2 siblings and a nephew who have been diagnosed with celiac disease (blood and biopsy). I have tested negative with blood tests for celiac but an IgG ELISA came back as positive, IgA negative. I take vit. D for a deficient (16) level and take Tirosint for thyroid. I have 2 siblings with psoriasis and numerous other relatives with hypothyroid and psoriasis. I have what I think is extreme fatigue, bowel issues (I would say it is IBS), achy joints and very dry eyes- I started restasis this summer. The rheumatologist suggested that the dry eye is my thyroid, the medication for my depression (zoloft for 18 years) causes my dry eye and I am one in 20 percent who test positive for autoimmune but don’t have any autoimmune!!
    I am very confused. I am 51 and menopause has begun. I feel like most dr. would like for me to ride out my menopause and then I will miraculously feel better. Why are the dr’s giving me no definitive answers? or are there none? Do I have food allergies? I did a skin test and a blood test which I have read are not good indicators of food allergies. FRUSTRATED.
    Thank you for your articles they are giving me the insight and courage to continue to find an answer. Insurance and money are major obstacles for a lot of us in this situation.

  130. If i took RAI to switch from HYPER to HYPO, does it follow that i may not have the AUTOIMMUNE issue because its not my body that killed my thyroid but rather the RAI?

    • The primary cause of hyperthyroidism is autoimmune (Graves’), and RAI doesn’t address the autoimmunity — it just kills the thyroid.

  131. Hi Chris, I was diagnosed with Hashimoto’s about 5 yrs ago. I also have a multi nodule thyroid with nodules on both sides. I have annual FNA’s and they have come back non cancerous. My endocinologist wanted to remove my thyroid last year due to the nodules causing me discomfort (the only reason for the surgery). I decided not to have the removal as I did not want to go hypo and be on medication when my thyroid levels were more on the hyper side. I just wasn’t ready to have my thyroid removed and felt there should be something else I can do besides surgery. I have not been prescribed any medication but all my symptoms are hypo – hair loss, fatigue, weight gain, dry skin, constipation, I could go on and on. My endo had the wait and see attitude or else just whip my thyroid out and medicate me. I have since moved and I’m in the process of looking for a new doctor. Should I go with an endocrinologist, I didn’t have any luck with my last one, or search for a different doctor? I do think that Hashimoto’s is genetic as my Mother had thyroid problems but was never diagnosed properly (long story, health system in Ireland), my sister had most of her thyroid removed about 20 yrs ago due to nodules and she now suffers from Chron’s disease. She has never been tested for Hashimoto’s, but is showing symptoms of other autoimmune disease including Celiac disease and rheumatoid arthritis. Is it better to go ahead and have my thyroid removed as due to the Hashimoto’s my immune system will end up destroying it anyway? I realllllly don’t want surgery and would like to keep my thyroid in place in the hopes that there will be some kind of break through in the future for Hashimoto’s. Yes, the nodules are bothersome but I can put up with them for now as they aren’t growing.

  132. Chris

    I have had multiple miscarriages before having my healthy baby in 2012. I am on 25 mcg levothyroxin even after the baby and before the baby + during pregnancy -the dose remained same. I feel sluggish, I have knee/joint pains, muscle stiffness, lazy, memory loss. I got my detailed thyroid bloddwork done which came normal just a week ago. I need to know, why I feel this way, shall I get myself checked for Hashimoto’s? Or shall I get thyroid scan,ct scan or any xray done since i feel phlegm in my throat mostly and a little pain in the throat area. I do not have difficulty swallowing at all.

  133. I would like to know if it is even possible to have Hashimoto’s disease or a thyroid autoimmune disease with out a thyroid. I had a thyroidectomy 10 years ago, but fit the symptoms of these autoimmune diseases. One ENT tells me I can and do have Hashimoto’s, another has told me no and that it is impossible to have an autoimmune disease without a thyroid. Please give me info on this, so that I can understand and know what I should do.
    Thank you

    • Hello Christopher,

      Read some of the earlier comments 🙂 Dulce Leon asked a similar question. The answer as Chris put it is that having a thyroidectomy is a lot like scrapping gum off the shoe – its almost impossible to remove all traces of the thyroid tissue, therefore you can still produce antibodies that could attack what is left of the thyroid. If you run a test for antibodies and are still producing them, its a problem. I suggest finding a naturopath or someone into integrative medicine that will run multiple tests and help you manage your thyroid condition.

      Diane Sanfillipo has a great book called practical paleo that has an autoimmune protocol which is great to follow if you have autoimmune disease.

    • Yes, it is absolutely possible to have autoimmune thyroid disease without a thyroid. Megan did a good job of answering your question; the autoimmune process underlies the thyroid condition and doesn’t stop when you take the thyroid out.

  134. I have been dealing w/ Hashimoto’s or over 4 years now. I have been dealing with very bad health the whole time. I have severe leg pain & weakness, also am very fatigued all the time, I have had many episodes where i can barely walk due to the pain. I am on 137mcg levothyroxine. I have had numerous tests, a mri showed that i had just 1 lesion on brain also. My neuro doctor doesn’t seem very concerned about this and my last visit to him he pretty much said he is giving up and doesn’t know why i am having all this pain. I am @ my wits end with feeling this way & no doctors can figure out or even care what i am going through. Is this all caused by my hashi’s or should i be concerned about other things? I am a 40 year old male and before this I had perfect health.

  135. Hello,I’m a pro athlete 37 yrs old,out of the blue I was diagnosed the graves disease,I believe it was because I was taking T3 CYTOMEL which is greatly used in sports and Hollywood for weight loss about (125-150MCG’S a day as high as 200 at times,and liquid version) am I correct that this caused this ? so I was on Tapazol for about 1 1/2 yrs,but never felt good I always felt I had a slow thyroid,so now Im on Synthroid 50 mcg for 6 weeks,Felt better for the 1st 4,now feel terrible again and gaining about 8-10lbs a month with out vigorous exercise..I want and need to feel better I have found the huge debate of T3 and Armour some say T3 is needed some so are my latest labs
    T4 12.3 (4.5-12.0)
    T3 UPTAKE 31.4 ( 22-36%)
    T7 3.9 (1.08-4.08)
    TSH 1.59 (0.35-5.5)
    Any help would be great ,and the proper tests to get,full panel ? should I get antibodies tested ?
    thank you very much

    • Hey Ken – you need more tests. Cytomel wouldnt cause graves disease as graves disease is an autoimmune thyroid disease that is diagnosed usually through antibody tests. You could most definitely give yourself hyperthyroidism though. Chris has other great thyroid articles you should check out. One in particular addresses the T3/T4 “natural” versus “synthetic” debate.

      • I for sure had graves always had symptoms of hypo…I can not find that article ?? and thank you for the if anyone could answer..if your on T4 but feel better is it because its not converting to T3? only thing I seem to get from T4 is faster heart rate..but ALL other symptoms of SLOW THYROID..

  136. Hello Mr.Kessler,

    first – thank you for all this great information!
    At the moment I am suffering from a acute or subacute thyroid inflammation. The blood-test is still in work. My doctor says the inflammation has to be treated with strong anti-inflammatory medication for the next 6 month in order not to come back. Is there any alternative way to reduce the acute inflammation?

    Best regards from Germany,
    Melanie Bong

  137. can TSH levels just decrease from one month to the next significantly? for instance my TSH last month was 3.1 and in a trip to the ER for racing pounding heart rate recently, a TSH was drawn and is now 4.7 and dr. is trying to put me on levothyroxine without doing any extensive testing to find the cause. my symptoms of fatigue, tiredness, bruising and wounds that dont heal , anxiety , depression and all have been the issue for some time now. I have recently been told that I have tested positive for ANA.. is there a possible reason besides hypothyroid for such symptoms?

    • Hey Christy,

      If you want to find out whether your hypothyroidism is due to Hashimoto’s disease (the great majority is), you could ask for an anti-TPO test that will measure the antibodies in your blood. Your positive ANA could well be because you have autoimmune thyroid disease but it usually just points to autoimmune issues in general; it will be raised in any number of diseases. Unfortunately, those with autoimmune thyroid disease (or any other autoimmune disease) are much more likely to come down with another autoimmune disease of some kind.

      If your doctor refuses to order the test, you can visit a naturopath, they are usually quite up to date on these things. Or you can order and pay for the test yourself, it’s not that expensive, about $49:

      It is very likely that low thyroid is caused by Hashimoto’s disease (an autoimmune disease), that is, by far, the most common cause of it, especially for someone like you who has had symptoms for such a long time. All low-thyroid patients are treated with thyroid medication, and levothyroxine is the go-to. Most patients to fine on it, although some benefit from the addition of a T3 only drug (Cytomel) or from natural desiccated thyroid which contains all the thyroid hormones. I suspect that the different treatment plan that Dr. Kresser is referring to is the addition of an autoimmune protocol diet and supplements, like antioxidants and fish oil that decrease inflammation. I have found the paleo diet a godsend for reducing my inflammatory response, but there are other good ones such as the GAPS diet, This page offers an overview that looks pretty right-on to me, except for recommending fruit juices…that’s probably way too much sugar, and sugar, even natural sugar, can promote inflammation:

      Actually, you might consider yourself fairly lucky that your doctor is willing to treat you even though your TSH is under 5.0. Although some people in the AACE tried to get the normal TSH lab range narrowed from (.5 – 5.0) to (.3 – 3.0), it was voted down by less progressive members.

  138. Please correct me if I’ve read this incorrectly, but basically you are saying there is no hope for those of us with hashimotos and hypothyroidism. Did I read that right? I’m 26 and was diagnosed at the age of 24. My mom was diagnosed at 40. If this fatigue and brittle hair continues, I’m not quite sure what to look forward to in the future – that is, unless stem cell treatment truly finds its way to the public. Otherwise, your article is perhaps the most depressing news I’ve heard in a while.

    • That’s absolutely the opposite of what I’m saying. My point is that determining the cause of the problem (in this case Hashimoto’s as the cause of hypothyroidism) is the most important step in successfully treating it. Conventional medicine does not treat people with Hashimoto’s any differently than they treat people with hypothyroidism from other causes. But in functional medicine, discovering a patient has Hashimoto’s completely alters the course of the treatment plan. We then focus on regulating and balancing the immune system above all else, because that is what’s causing the decline in thyroid function.

      • Hi , love these posts. I’m a 39 year old, who at 19 discovered large goiter, and had Right side thyroid removed. Never given any medicine for thyroid. Later after having kids, hit a very bad patch . Hair loss , felt like crap, no labido. Doctor ran thyroid said levels normal, he was perplexed since to him my symptoms were hypothyroid, decided to have thyroid sonogrammed found two small nodules on left side. At that time too small to operate, he ordered a dye test to see if nodules might look suspicious(cancerous) and he said they looked low risk advised me to have follow up sonograms every year to check for growth. Since then my youngest daughter was diagnosed for severe autism, you can imagine my health problems took a back burner for some time. I believe it has been 8 years since last sonogram. Meanwhile I’ve had numerous female problems all my life cysts on ovaries fibroid tumors in uterus menstual periods that have always been irregular and extremely heavy, my monthly llasts 7 to 9 days. And 4 years ago I went to a new doctor told him of my history and also my moms hypothyroid issues, told him I had gained forty pounds in 2 years and felt so tired all the time that I thought my thyroid function needed to be tested, he tested said normal, arrrg! Honestly I wanted to choke him. He believed my symptoms are due to stress. Also had strange sores like rash have had for 4 years now and doesn’t go away. Then ran across an article for hashimotos and eureka I think this might be what’s wrong with me. So off to another doctor to have all thyroid panel and antibody test done. Which I can assure you the other doctors didn’t run on me. So my question is this does anyone think NOT being on thyroid mess after the first goiter found at 19 could be why I grew nodules on left side and feel so terrible now?

      • What is your recommendation for treating Hashimoto’s? How do you get your body to stop attacking the thyroid hormone?
        I was just diagnosed as “sub-clinical” Hashimoto’s in October 2013. I am new to researching and learning a lot, but it is terribly confusing. I realize I have had several symptoms for years but it was not until I gained 15 pounds in 3 weeks that I knew something was wrong. Then when I strictly followed a diet and increased exercise for 2 weeks following the weight gain and did not lose a pound, I made an appointment with a dr.

        I was on 30 mg Armour, Vitamin D, DHEA, B12, testosterone, progesterone, and pregnenalone. All of these were extremely low or not even registering on the blood tests.
        It has now been 8 weeks and I have noticed NO changes in how I feel. I went back to dr yesterday and levels had increased but were still low. She said she did not need to test the antibodies again or the reverse T3, etc. She only tested TSH, T3 and T4.

        I am reading everything I can find, but there is a lot of conflicting information and what works for one person does not necessarily work for another. I just want to know how to get the immune part healed so I can lose this weight (now up to 20 pounds). It is causing major depression and almost become an obsession.

  139. I had my thyroid ablated nearly 30 years ago with radioactive iodine due to Graves disease. For nearly 25 years, my PCP had my medication dialed in with a combo of Synthroid and Cytomel. He then retired and I had to find another doctor who was clueless and decided to reduce my Synthroid because of the test numbers. After about 1 month, I began to experience typical hypo symptoms, but she wouldn’t change my RX because of the numbers, regardless of my symptoms, but I don’t have a thyroid to be “acting up”. I have “fired” her and will be looking for another PCP ,. I am transitioning to a Paleo lifestyle and don’t consume much gluten anyway. I have read your articles on thyroid, but they all seem to point to someone who has a thyroid. ANysuggestions for someone without a thyroid??? thanks

    • Removing the thyroid is like removing gum from a shoe. In most cases, some tissue remains even after the surgery. As long as there’s tissue there, and as long as the body is producing antibodies (which it is in Graves’), you are still subject to an autoimmune response. I’d suggest investigating low-dose naltrexone and finding a practitioner to work with on autoimmune issues.

      • Regarding the analogy of removing gum from a shoe, most thyroid cancer patients undergo ablation (RAI), so can Hashimoto’s linger even after a successful ablation?

  140. Hey Chris,

    Thanks for this wonderful post about hypothyroidism. Your U.K. adversary reminds me of why women in London protested outside the NHS for better testing and more medication options. Here is a post by U.S. thyroid guru Mary Shomon on the subject of the terrible care that U.K. thyroid sufferers get:

    One thing you might revise, though, is the free T3/ free T4 subject. The new doctors are now being educated that total T3/T4 uptake tests are obsolete. Only the older, less informed doctors use the uptake tests. An entire panel including TSH, free t3 and free t4 can now be had for $79 without a prescription from places like “Any Lab Test Now,” a national lab-testing franchise. My internist is a Washington University trained doctor, she is totally hip to T3 augmentation (Cytomel) and reverse T3 testing…in no way is she a maverick (she won’t prescribe Armour or ERFA, etc.).

  141. Wow! what a great post! Thank you for making it so easy to understand. It’s amazing how many people have the disease without them knowing what causes it. I got diagnosed with Hashimoto’s 8 years ago and no doctor ever told me that it’s an autoimmune disease. Now I am taking matters into my own hands and try to get to the root of the problem.

  142. I am a 27 y/o female – 3 weeks ago I was told I had a TSH of 100. Starting with no knowledge of hypothyroidism, I’ve been continuing to educate myself and have found this site very helpful – so thank you.

    Background: I was prescribed 50mcg of Levothyroxine. I was told only about my TSH level. I now understand why testing T3, T4, and antibodies are also important. I also understand that the “best medication” depends on the individual, and the cause of the hypo.

    Questions: Since starting medication, I’ve felt an energy increase, which was positive. Now I’ve noticed my hair shedding like crazy (not a symptom previously). When this is a symptom of hypo and also a side effect of the drug, how do I tell which one is the main cause? My other question is knowing my next step: when TSH was the only testing done, do I push for finding the root of my hypo? Thus hopefully leading to finding the correct medication for myself? Personally interested in health/wellness myself, I feel inclined to learn more before settling on a generic drug. Thank you so very much for your time!

  143. Hi Chris,
    I have read your information on Heartburn and how low stomach acid is associated with Graves disease. I was diagnosed with Graves disease 12 months ago, along with high cholesterol and a 15% blocked artery, which was picked up while investigating symptoms of aterial fibrilation and irregular heart beat. I am taking 5mg Carbimazole daily and my TSH receptor antibodies have come down to 3.0 U/L.
    I was hoping to find more information on Graves disease on your website with possible ideas of treatment. I will embark on a low carb diet and will be taking apple cider vinegar and milk thistle to help restore my stomach acid levels. I can’t take HCL as I am on 100mg Aspirin daily for the AF (only read this on your website after I had already ordered HCL online).
    Is there anything else I can try to help me restore my thyroid levels back to normal.
    Also suffering from weight problems (100kg), but am hopeful that this all has to do with low stomach acid/high carb diet and will start loosing some weight soon.
    Thanks for your wonderful website and information.

  144. Hi Chris,

    I have Hashimotos since 2007 and am 6 weeks pregnant. Why is it bad to leave the thyroid in a euthyroid state i.e. mine is 0.015. Are there any repercussions to me and more importantly my baby?

    • I wish I knew more about it. I did research way back when and couldn’t find anything. All I know is that the cramps were horrible at first but as the years went by, they got a lot less. I guess that could mean my parathyroids could have been stressed and then as I worked on my health and got stronger, they healed (does that happen?).

      I didn’t take any calcium, I had already tried every form and they all hurt my stomach badly. Now I take cod liver oil (for the V.D that makes calcium in food more accessible?) but only for about a year, so that’s not why they got better. They’re not totally gone. I often feel certain muscles in my thighs, calves and ankles start to pull if I turn or twist a certain way and I know I better straighten out fast or I’m gonna get a burner.

      Conscious relaxing helps a lot. Sometimes I think mine are mostly from muscle clenching, at least now. I never had a single cramp until after the thyroid surgery, tho I had been on synthroid for a month and that’s one of the side effects, I believe. It could have been that kicking in, and maybe that’s why they’re still around. I was on a higher dose then, 125 as compared to 75mcg now.

  145. Hi, Chris, this is going to sound like the alltime dumb question, but I can tell from reading your site that you’re going to know the answer and I need to know this. In 2003 my windpipe collapsed from a lump on my throat which was thyroid lymphoma. After emergency surgery that removed half of the thyroid, then chemo and radiation, the lymphoma went away & after 8yrs, the doctor stated that the clinic felt that this particular cancer would probably not return. At that time, I asked my doctor if I had Hashimotos but his response was vague. I figured it didn’t make any difference because I see him every year and feel pretty good. But lately I’ve felt my energy is down and now, after reading your site, I see that it does matter a great deal whether I have/had (does it go away after the lymphoma goes away?) Hashimotos. So my question to you is, does my having had thyroid lymphoma mean that I have/had Hashimotos? Does it go away if my system is balanced or is it a permanent diagnosis? (I take 60mcg levoxyl & 4mcg liothyronine daily) Thanks so much. I am really getting a lot out of your site, it is so clearly written. I’ve been studing hypothyroidism since ’03 and I still have tons of questions.

    • You can’t know from that information alone, but when there’s cancer it’s more likely an autoimmune mechanism was involved. The way to find out is to get your thyroid antibodies tested – TPO and thyroglobulin.

  146. Please ignore previous comment it did not contain all my paragraphs, as i see. I have had hypothyroidism since age five. I have seen a specialist since my pediatrician suspected that something was up. Hypothyroidism for me is mainly a genetic issue; seeing as it runs in my family. I am now sixteen and have had no side affects or anything up until this past year and a half. I take Levothroxine 200mcg tab. I am starting to have more and more frequent leg cramps (Normally waking me up early in the morning like clock work. Bringing me to tears because of the pain. And then I can’t walk for the next two days.) I am trying Bananas, but nothing seems to work…any advise? Also, my blood pressure has been out of the roof averaging at 170/90 (One time it was 190/100.) Luckily it hasn’t gotten quite that high again. My Dr. has told me to cut down on carbohydrates, to continue my exercising, and to avoid salt. I have been doing this but my BP is still elevated about the same. Hypothyroidism is from my mothers side. High blood pressure is from my fathers side. My dad has been on BP medicine since he was 20. His Dr. told him to lay off the same thing and his BP levels did not change either. My Dr. has told me to monitor it. I have and I’m seeing no changes. My check up is next month. I already know shes going to send my to a cardiologist and to see what they say. Any ideas on how to lower my BP? I can’t be mad all of the time it stresses my body out. Also, I have a biopsy done on my thyroid nodules. Happily they all came back benign. 🙂 And my thyroid is starting to effect my swallowing and stuff so my specialist says it might need to be taken out. She said it was my call. It needs to be done because of me, well, not being able to swallow very well, but also because it could be cancerous later on. And if its taken out that risk will leave. I am deciding whether or not to have it by the end of this year. If I understand correctly, but if I don’t someone please let me know. Also, I don’t know what to expect I’ve never had a surgery like this before. Can anybody tell me what to expect? Here are some of my questions: Will I have a scar? How long will I be bed ridden, if at all? How long will I have a bandage? Will they put me in a neck brace to help keep me from tearing it open? When I wake up from the surgery will I feel anything?

    • Dear Robin, I am so sorry you have to pass through all of this…. I have hashimoto and since I cut almost all carbs like sugar, grains, reduce fruits, milk I got much much well. First it was hard because I loved pasta, rice and etc…. hardly ate eggs, red meat and so on…. since I changed my intake everything got better. For an idea I eat in the morning 2 scrabled eggs, some fruit; lunch salmon /hering or chicken or beef (some 140g) and a lot of veggies like green beans, broccoli, carrots, kale, red onion, red bell pepper and so on…. I eat 300g veggies for 100g meat so I have a good amount of food for lunch and dinner and I am not running after sweets anymore. I steam everything and do not heat any oil. I cook with clarified butter or just butter. OK I used fresh cream…so I make my own ice…. blueberry eis; mango ice and so on…. I hope you try this kind of “diet” for one month and see if things change for you-…. for me it is wonderful! Even hot flashed got away…..!!!! See for paleo diet…. avoinding grains, milk, legumes like (pinto-kidney-black beans, lentils)… after a while you can introduce them again…but sporadicaly…. your doc was probably right: reduce carbs!!!!! Wish you all the best and if you ttry it…let me know…. Regards Ingrid

    • Hi, Robin,
      I too am sorry that you have to go through this, it’s not fun but it does seem to be treatable. I had surgery in ’03. You can’t see the scar at all. I was up pretty fast after the surgery, a couple days, and that may only have been because I still had the lymphoma and so the cancer was making me weak. I was 53 and you’re young so you’re probably going to be even stronger and heal faster than I did. No neck brace or anything like that, don’t remember how long the bandage was on, it didn’t seem to matter.
      I also had severe leg cramps similar to yours for years after the surgery but as I got healthier they went away. I still get one every once in awhile but there’s usually a cause – too much exercise or not enough is the major cause for me. If you’re not getting any exercise now and can begin, work into it slowly so as not to aggravate the cramps. I also use a hotpad on the cramps and that helps tremendously. I make them but you can just put uncooked rice in a big sock and tie the end, about 2/3 full of rice. Microwave till it’s hot but not so hot it burns your skin.
      I agree with Lingrid that diet also has a huge affect. I too cut out most carbs (in the form of grains), alcohol, and all dairy except butter and it has helped a lot. That change also helped me get my weight down to where I wanted it. This is just my experience, perhaps yours will be different. Good luck to you.

    • It was the easiest surgery I’ve ever had. You really won’t feel too badly. There will be a scar for several months. I’m much older and mine lasted less than a year, you should heal sooner. I wore a scarf until it wasn’t noticeable. You can’t see it today.

  147. I have had hypothyroidism since age five. I have seen a specialist since my pediatrician suspected that something was up. Hypothyroidism for me is mainly a genetic issue; seeing as it runs in my family. I am now sixteen and have had no side affects or anything up until this past year and a half. I take Levothroxine 200mcg tab. I am starting to have more and more frequent leg cramps (Normally waking me up early in the morning like clock work. Bringing me to tears because of the pain. And then I can’t walk for the next two days.) I am trying Bananas, but nothing seems to work…any advise? Also, my blood pressure has been out of the roof averaging at 170/90 (One time it was 190/100.) Luckily it hasn’t gotten quite that high again. My Dr. has told me to cut down on carbohydrates, to continue my exercising, and to avoid salt. I have been doing this but my BP is still elevated about the same. Hypothyroidism is from my mothers side. High blood pressure is from my fathers side. My dad has been on BP medicine since he was 20. His Dr. told him to lay off the same thing and his BP levels did not change either. My Dr. has told me to monitor it. I have and I’m seeing no changes. My check up is next month. I already know shes going to send my to a cardiologist and to see what they say. Any ideas on how to lower my BP? I can’t be mad all of the time it stresses my body out. Also, I have a biopsy done on my thyroid nodules. Happily they all came back benign. 🙂 And my thyroid is starting to effect my swallowing and stuff so my specialist says it might need to be taken out. She said it was my call. It needs to be done because of me, well, not being able to swallow very well, but also because it could be cancerous later on. And if its taken out that risk will leave. I am deciding whether or not to have it by the end of this year. If I understand correctly, but if I don’t someone please let me know. Also, I don’t know what to expect I’ve never had a surgery like this before. Can anybody tell me what to expect? Here are some of my questions: Will I have a scar? How long will I be bed ridden, if at all? How long will I have a bandage? Will they put me in a neck brace to help keep me from tearing it open? When I wake up from the surgery will I feel anything? What risks are there concerning infection etc…?

  148. I have had hypothyroidism since age five. I have seen a specialist since my pediatrician suspected something was up. Hypothyroidism for me is mainly a genetic issue; seeing as it runs in my family. I am now sixteen and have had no side affects or anything up until this past year and a half. I take Levothroxine 200mcg tab. I am starting to have more and more frequent leg cramps (Normally waking me up early in the morning like clock work. Bringing me to tears because of the pain. And then I can’t walk for the next two days.) Also, my blood pressure has been out of the roof averaging at 170/90 (One time it was 190/100.) Luckily it hasn’t gotten quite that high again. My Dr. has told me to cut down on carbohydrates, to continue my exercising, and to avoid salt. I have been doing this but my BP is still elevated about the same. Hypothyroidism is from my mother side. High blood pressure is from my fathers side. My dad has been on since he was 20.


    • Dr. Deo,
      It takes a while for symptoms to catch up to blood levels. Best to be patient and don’t overdose yourself on thyroid hormone, that can be very dangerous.

      What is your pulse rate?

  150. I have Hashimoto’s but it’s not following the typical path. I have never taken thyroid meds yet I keep having bouts of hyperthyroidism and then go back to euthryoid. I’ve only ever been slightly hypo….then back to major hyper periods that only last about a month. Now I think I’ve figured out the underlying cause. I was recently diagnosed with hemochromatosis but that’s also not following the typical path. My iron and iron staturation are high yet my ferritin is normal so again, no one will treat me. I didn’t have a period for a year and a half from lactation induced amenorrhea. I can only imagine what my iron levels were like during that time, yikes! But after a year of extremely heavy periods that often came every 3 weeks, my iron saturation was 102%. My dr thinks it’s unrelated but I’m thinking having all that iron in my thyroid may be what is causing my body to attack it. And my periods may be what are causing me to feel like I’m constantly going back and forth. I really don’t know what to do about it though.

    • Erin,

      Why don’t you get your thyroid antibodies checked? You could be like me and have both Hashimoto’s disease and Graves’ disease. One causes hypothyroidism, one causes hyperthyroidism. I bounced back and forth for seven years until I finally got my thyroid removed to save my sanity.

      How hyper did you get? Did you have rapid heart beat? Be careful, that can be really serious.

      Here’s a pretty good post on ferritin as it affect thyroid levels if you haven’t seen it yet:

  151. Thank you for all your information on this site and in your podcast. I just deleted a looong comment to you and instead post the question below:

    Do you have a link to a list of definitive tests to ask our health care providers? I want to figure out if my Hypothyroidism is Hashi’s and if that and my Crohn’s, very early menopause, Asthma, Fungal and Yeast issues all could be pieces of one autoimmune puzzle.

    I see you recommended to someone else the test for antibodies (TPO, TG and TSI) but anything else I should be asking for? Reverse T3? Anything? I will be seeing an endocrinologist for the first time in 2 weeks. FYI, primal for a couple months now and asthma and allergies are noticeably better!

    Thanks in advance.

  152. Are there functional lab ranges for all the thyroid test online somewhere? I have only been able to find the TSH functional range of 1.8-3.0. Would the functional range for antibodies be different for someone on a gluten free, sugar free diet since gluten and sugar can cause increases in autoimmune activity?

  153. Thank you again for mentioning the transdermal LDN (above) – I am pleased to say that it’s now available in the UK too via Dicksons pharmacy. I started using it on Saturday, and so far, so good! Also my recent annual thyroid results are already moving in the right direction, so maybe a year’s acupuncture has helped too, along with the better diet.

  154. Hi,

    I’ve read your posts on iodine and selenium. I have come across this research (see link below) that suggests that iodine and selenium have no combined effect (although I may have grossly misinterpreted this). Would you care to comment?

    My interest in iodine is not in using it for thyroid problems (although from what you and others say I will have problems if I take it with too high a dose). I have a few cherry angiomas, I’ve seen that this may be caused by bromine poisoning which iodine supplementation can help:

    However, I suspect that we may be getting into the realms of snake oil here…

    Thanks in advance for any reply.

  155. Hi. I posted a couple months ago up there and was things are only getting worse. I’ve been getting more and more fatigued, and my memory seems to be going. More of an absent-mindedness, but I feel like I can’t remember anything unless I write it down, and even then, sometimes I forget to look at the paper I wrote it down on to remember what was written.

    Please, if you could offer some advice to me. As I said in my last post, because everything started to go wrong when I had an enlarged thyroid and my doctors decided to remove half of it instead of find the cause of they hyperthyroidism, I really wonder if this is now one of two things. 1) whatever was wrong in the first place finding a new way out since the thyroid was partially removed or 2) negative/downfalls or continuing problems related to hypothyroidism caused by the thyroid removal.

  156. Thank you Chris – I really appreciate your response. I did not know of the transdermal LDN and I am now looking into that possibility.

    I wish I had known what I know now (I am almost 60) when I was your age, but I probably wouldn’t have listened then! I suspect that my autoimmune issues were triggered by my last pregnancy when I had Immune Thrombocytopenic Purpura, though luckily not until the last few weeks. My Hashimotos didn’t appear until around 10 yrs later. I also have had issues with Lichen Planus since then, also thought to be autoimmune.

    Looking back I can track the medical history now, (also have had gastritis now healed by the diet), but at least I can do my best for my old age. I was into healthy eating too, and thought I was doing the right thing, but the gluten was probably the worst thing I was eating then without knowing it.

  157. I have just found this wonderful website. I have ME/CFS as well as hypothyroidism (Hashimotos I assume though I am in the UK and it’s never been called that to me).

    I have taken synthetic Thyroxine for nearly 20 years so is it too late for any improvement now? I have changed my diet in the last 2 yrs (to try and improve the ME/CFS), and on reading the articles it seems I am doing it almost as well as I can already as I am on a Paleo(ish) diet, and gave up gluten a year ago, which has ended my horrible stomach pain, and have solved my acid issues with kefir. I have even been to acupuncture weekly for a year.

    I have just started on LDN ….. more to help with the ME/CFS than the thyroid though it seems it could help with that too. Sadly, I have sensitivity issues and get terrible stomach pain on it, so can only tolerate a tiny dose every other night at present.

    Would be grateful for your view if it’s all too late for me having been on the synthetic Thyroxine for 20 yrs, and if my ME/CFS and thyroid is likely to be improved too with what I am doing?

    There is no advice via my GP in the UK – they have no understanding of these things at all. I am getting a little help with a private GP who specialises in ME/CFS and who has prescribed the LDN for me.

    • Elaine: there’s another way of administering LDN that you might want to look into. You can take it in transdermal form as a cream. Skip’s Pharmacy in Florida can prepare it that way. I’m not sure if you can get order it from Florida since you’re in the UK, but you may want to consider that. I don’t think it’s too late for improvement, and I think LDN will probably be helpful for both your thyroid and ME/CFS if you can get on a solid dose.

  158. I wish I’d known all this a long time ago. I was diagnosed with hypothyroidism at age 4 with a bone age of 9 months. My TSH test came back borderline, and apparently a low-grade deficiency was enough to retard my growth that much. My doctor pretty much guessed that maybe a low dose of Synthroid would help, and with that I grew twelve inches in twelve months. Throughout the years afterward, though, as long as my TSH test came back “normal” I was told I was fine, any residual fatigue, depression, malaise, whatever was in my head or would pass soon enough. Or maybe, it was suggested, I should be on an antidepressant. I was on Lexapro for two and a half years, beginning with my third pregnancy. It didn’t help, and it took a long time to break free of it (several months to find a slow-enough tapering-off schedule and six months on that schedule). I don’t want to take another anti-depressant, but if it would help to take a supplemental dose of T3 (like Cytomel or its generic form) or a different thyroid medicine with T4 & T3 combined, I’m all for trying that.

  159. Hi. I had some questions and was wondering if you had any insight as to what might be going on or some other things that I should be checking for. A few years ago, I had an enlarged thyroid. The doctors drained the fluid out, tested it, and when it filled back up decided that the best course of action was to send me straight to the surgeon. I didnt know any better so I had half my thyroid removed, and now have hypothroidism as a result. No doctor seemed to think it was important to find out why my thyroid was acting up in the first place. A little over a year later (had a child in that time) i started having a multitude of symptoms: fainting, dizziness/lightheadedness, chest pains, extreme fatigue, hard time loosing weight, tingling/numbing in hands/feet. for about the last 2.5 years now I have had all of these symptoms and have had just about every medical test known to man done, everything comes back normal. I have been a guinea pig for so many medicines because the doctors don’t know what else to do so they just throw medicines at me to try. Because my thryroid was the first thing to go wrong, i’ve begun to look into that more on my own and have really been wondering if that’s where everything went wrong, and because the doctors I had at the time decided to just cut out what was causing a problem instead of trying to fix the problem, it really didnt solve anything. Any help or tips or advice you can offer to me would be greatly appreciated. I am so tired figuratively and literally from doctors trying to tell me everything is fine because the tests come back ‘normal’. Thank you.

    • Dear Melissa, I really hope you find soon out what is wrong with you and your Tyroid. I can only write about myself and I still do not know if all what I have done was/is the right for me…. but since I am feeling well I do believe I did it right:

      – cut off all grains and dairy;
      – use only olive oil extra virgen over cooked veggies (I dio not heat oils)
      – use ghee (Butterschmalz) as fat for almost everything;
      – Eat eggs and meat (chicken, beef, duck, fish) in every meal
      – Eat at least 200g veggies….better 300g for each meal (even mornings)
      – avoid any industrialized product
      – Eat fruits but not too many (2 a day)

      One year has passed…. I can walk without problems again…. I could not so tired I was…. Now once in a while I use some butter, heavy cream and eat some rice (very seldom). I lost weight (10 kg) and feel great. I do hope that was the right thing I did…I am still a little afraid that the missing grains / dairy can harm my health…. but up to now…. it only made me feel better and better!

      I wish you all the best! (I did not mentioned: I do have Hashi…. but even that is changing for better)

  160. Hi Chris,

    First off, thank you so much for your skeptical health blog. You are a rare voice in a field filled with superstition, miracle cures, and snake oil salesmen looking to make a quick buck on the vulnerable.

    About me: I am 24 years old, just got diagnosed with hypothyroid after around 3-4 years of being “borderline.” I’ve had conflicted feelings about this diagnosis because in one way, it ties together all these other health problems that I have been having (and that I feel like I am too young to have 🙁 ), namely: polycystic ovaries/irregular menstruation, constant low energy and fatigue, serious anxiety/panic disorder, and what I recently found out was mild scoliosis (causing constant pain in the joints on my right side). Honestly, reading all this on your blog has made me feel rather hopeless…autoimmune diseases are so serious and I was unprepared for the thought that I will be dealing with a lifetime of serious problems.

    I just wanted to find out from you if there is any hope in handling this disease. I haven’t yet found out if I have Hashimoto’s or not, but of course chances are that I do. I am at the point in my life where I am preparing for graduate school. Do you think that I need to take some time off to address these health problems before I get lost in the world of grad school (high stress, overwhelming responsibilities, little free time, etc)? I know this is a strange question, but this all really worries me. I’d appreciate your perspective on what it takes to begin managing it.

    • Eva: hypothyroidism (and Hashimoto’s) are treatable, and it’s entirely possible to live a full and happy live with the proper care. Identifying whether you have Hashimoto’s, or iodine deficiency, or both, or perhaps another cause of thyroid hypofunction is the most important step. From there, the next steps become more clear. Best of luck.

  161. I have a question. I am currently waiting on another endo visit; but I have a month to wait. I have Hashimotos. I also developed a toxic adenoma (approx 3″ in diameter. I had both the adenoma and total Thyroid removed 1 year ago (I am 38). I actually tested negative for both hashi’s and Graves antibodies the day before my surgery (it was believed I had both? My mother has graves). I recently tested my antibodies and they were 2,300+. I feel horrible, and I feel like there is a new lump in my throat forming. Anyone ever experience a Hashi’s tumor post Thyroidectomy??? It feels very much the same; the weird pain at times in the mass. *sigh* Ideas? Tips? My doc tested many other antibodies and they were all negative. My insulin production is slightly elevated and I’m experiencing bouts of Hypoglycemia (my daughter is Type 1 Diabetic so we have meters everywhere).

    • **** Also autoimmune disorders are rampant in my family. Besides the diabetes with my child, and Hashi’s for me so far- my mother has Lupus, antiphospholipid syndrome, short bowl syndrome, Graves, and something with her bone marrow as well (not sure what, that’s a new development theory)

  162. Meg you sent me a message about the LGS diet. I don’t see your comment here. If you are still interested I can email it to you. There is a PDF file that is too large to post here.

  163. Bejeesus! A TSH of 47.60…I hope the decimal point’s in the wrong place. Everyone seems to be using the same unit of measure (mU/L) so I guess it’s has high as it sounds.

  164. Jennifer your doctor should be testing more than your TSH level. What meds are you taking? If you are on Synthroid, that is synthetic and is only T4. If you are hypo, you aren’t converting T4 to T3 so you need a med that will provide you w/ T3 as well. I am talking out of experience as Synthroid was NOT the drug for me. I did my research and insisted that my doc write me a script for Nature Throid which has T4 and T3. I feel like my old self again! Also, watch what you eat as you could be insulin resistant. Cut out any refined sugar which is in just about everything, eat low glycemic fruit if you have a sweet tooth and stay away from rice, pasta, bread and potato’s. An organic diet consiting of veggies, lean meat or beans [for protein] is a good way to help you feel better too. Also, have your Vit. D level checked as it is a hormone not a vitamin. I hope that helps. I went thru hell before I started my research. Good luck and if I can help…………

  165. Hi Iam 29 yrs old in 2009 had thyroid cancer followed by radioactive iodine and total thyroidectomy . Tsh has been normal last 2 months have felt awful have no energy and excessive sleepiness. Tsh was just checked last week now is 47.60 Have been on same doage for a year. What could be the problem

  166. Hi Chris –

    I am getting a prescription for LDN thanks to your informative podcasts. In researching LDN in various user groups, some people talk about LDN not being as effective if you have candida overgrowth. Have you found this to be the case with your patients? Have you seen anything about it in your research?

    Thanks! Pam

  167. Hi
    Just discovered your forum. Great info! I was diagnosed with celiac 2 yrs ago and have been on a strict gluten free diet. I had adrenal fatigue (low cortisol levels about 7 for 8 am) and fluctuating high TSH levels. My free t3 and free t 4 have always been in upper 1/3 and 1/2 of range respectively. Antibodies have always been negative. Recently again my TSH is 4.53 free t4 1.1 (range .74-1.83) and free t3 3.74 (range 2.28 -4.81). SO since free t3 and free 4 seems to be ok but TSH is high, should I try .5 grain armour to see if I feel better? The thyroid is working hard to keep levels normal but why is this happening?
    On a side note my liver enzymes have been in upper limit AST is 41 (range 8-39)ALT 48 (range 9-52).
    I have been struggling with low motivation and energy for 3 years now..any feedback would be greatly appreciated!

  168. Hi Chris –

    I have Hashimoto’s and have had it most of my life. I was always told that my enlarged red blood cells were due to my thyroid problems and that there was nothing I could do about it. Is that true? Is this a type of anemia? I am curious if this is a common symptom you have seen in your research and if there is anything I can do about it.

    Thanks, Pam

    PS I also posted this on your podcast questions

    • Macrocytosis is a common complication of Hashimoto’s. To treat it, you need to treat the Hashimoto’s itself, which means addressing the immune dysregulation. Thyroid medication only replaces the thyroid hormone. It doesn’t address the immune issues.

  169. I had a total thyroidectomy due to hyperthyroidsm and graves disease in August 2010. I take 150mg Eltroxin daily. I am tired 24-7 my arms ache and I generally feel bad. Are there any energy supplements I should be taking?

    • Try going Gluten-Free. I have Hashimotos and Graves disease, take thyroxin and had these same symptoms among others, since going GF the pains in my arms have dissappeared (after only a few days), I have much more energy and generally feel very much better. Other symptoms, (IBS type) have also gone, going GF was meant to be only a trial, its not been 6 weeks yet since I started, but I will definately be keeping it up, even though its a nuisance having to read all the food packets and trying to find a decent bread I can eat, i’m going to stick with it. I hope it helps you too.

      • Hi Geliza,
        I do have the same and I am going on GF almost one year so I found out how to make my own bread…. of course it is not the same… but it works very well:
        – 500g Linseed (grinded)
        – 5 eggs beaten
        – 1 tsp. salt
        – 1 tsp. baking powder or soda bicarbonate
        – aprox. 300ml water

        mix all and baked 375 F/180C for aprox. 30-45 minutes. Make the toothpick procedure to see if it is done.

        Hope you enjoy like I do when I’m craving for a “bread”


        • Thanks very much for the recipe, I shall certainly try it, I am in the process of trying out different ones.

          I found one that looked really good, on the net, but when I tried it out it didn’t quite work out, from the fotos its the nearest I have seen to real bread. I could give you the link but it is in spanish, suffice to say it’s bread made with mandioca, (yuca, tapioca) starch, and the process is much more complicated than your recipe.

          • Thank you Geliza – but I am so tired of trying recipes….. he he he…. now I found this and I think for me the Linseed is just perfect (until someone find out it is not good for your health…he he he) Thank you again! (PS no problems with spanish – I speak a little). Ingrid

  170. Yeah the thyroid blinks in and out while in the process of completely not working so that is what you are feeling with the ups and downs. Believe it or not, eating oranges at my lows helped me a lot. Like I said you MUST find a good ENDO and what makes a good endo is one that listens and takes into account your input. Drinking cinnamon or coffee will help with the low blood pressure. Make cinnamon tea (use real cinnamon) 1 cup and see if that doesn’t help with the blood pressure. You need to leave the naturalpathic doc and find an endochrinologidt not just a reg. doc because they know nothing about thyroid. after my thyroid was taken out I had a lot of problems but ONLY because I couldnot tolerate synthroid and had to go to a natural thyroid hormone called Armour. Bother your doctors and don’t let them bully you. THIS IS YOUR LIFE AND YOUR BODY and they are there to help, so be strong even to the point of being obnoxious. ONce your thyroid is taken out and your hormones are level you will no longer have diareah since it is cause by your hyperthyroid state. YOU MUST drink a lot of water until this resolves so that you do not become dehydrated. Also, many of us are lactose intolerant to some degree or another. My GI issues went away somewhat when I started doing the towel thing that I mentioned earlier and they completely went away when I had to have my gallbladder removed aabout 6 yrs after my thyroid was removed. Once you are stable, many of the symptoms will just disappear and you will be healthy again. You need to keep a diary right now of what you are eating and pay attention to how your stomach and blood pressure reacts to them and eliminate them from your diet. I do not consume anything with milk. I do not eat beans. My diet right now is mostly protiens with a little carbs but since you are hyper right now it should be the other way around. More carbs than protien so you don’t lose an enormous amount of weight until you become healthy again. Don’t worry. This does not last forever even though it feels like an eternity for you right now. Everything will fall into place once you have the correct amount of thyroid hormone in your body. Don’t give up and don’t think that this is how you will feel forever because this is not true. You will be OK just pay attention even to the littlest symptom like your legs cramping or feeling like there are spiders crawling on your cheek. All of this, although little symptoms can drive you crazy. Write them down so you don’t forget to tell the doc. When you go see the ENDO, make sure you have a list written down of all your symptoms and when your feel them or what makes it worse or better. Just remember that you have to fight for your well being even if you have to change ENDO’s 3 times till you find one that will listen. Like I said before the best way to find an ENDO is by patient referral so use the website of Mary Shoman to help you in your search. my email is [email protected] and you can email me anytime for support. I will be happy to help in anyway I can.

  171. Sisi, Thanks for the tip, I will definately take my temp everyday now. I have been questioning whether my thyroid was going back and forth everyday, I actually wonder if it does that throughout the day actually, because some days I’ll wake up feeling great but then by lunch or after feel like crap, and then other days it’s the opposite, i’ll wake up feeling like crap and then have a burst of energy for several hours and then feel like crap, but I always feel better everyday at about 9pm at night. It’s the weirdest thing. I did take my blood pressure this morning and it was 98 over 68, That is really low, and I don’t know what I should be doing. But I agree with you about how eventually it needs to just come out. I just hope my doctors listen to me, I get the worst luck with doctors. I have been seeing a natural path and she even has been a pain to deal with at times. So I might be switching general doctors again, we’ll see. Did your stomach issues go away after you had it taken out? I can handle everything else that is wrong with me, it’s my constant stomach issues that I am soooo sick of. Thanks

  172. Christina, the title of the book is a bit deceiving. I have been diagnosed w/ full blown Hashimoto’s. And as I stated above, Dr Kharrazian’s book set me on the right path. He explains the many causes of Hashimoto’s. For example here are a few: gluten intolerance, insulin resistance, polycystic ovary syndrome, vit. D deficiency, chronic inflammation/infections/viruses of digestive tract, environmental toxins.

    I’ll say it again, GET THE BOOK 😉 And whoever here told me to not see a regular doctor, well, I don’t 🙂 I see a person who specializes in Hashimoto’s and Fibromyalgia [sp?]. He has been to most of Dr Kharrazians lectures and follows most of the same principles.

    I wish you the best w/ your health!!

    • Renee – this blog is old but if you do see this will you please reply? I am keen to find out about your improvement. I have just began on the fibromyalgia road and anything you can suggest will be much appreciated. I live on an island under Australia (Tasmania) and finding a knowledgeable person here seems impossible. I hope to get a reply form you and to continue some communication, plz.

  173. Chris – my daughter is currently about 13 weeks pregnant. Her thyroid was irradiated years ago & she has taken daily medication since. Her OB-GYN – whom she visited when she was about 6 weeks pregnant, did not seem too concerned about her thyroid – or much of anything else, either. This caused her to switch to a different OB-GYN, who appears to be much more competent & supportive & who performed a battery of tests. Two weeks ago, her test results started to come back in, & her doctor’s office called my daughter & asked her to come back because her thyroid numbers “were so high, they thought it was probably a lab error.” Upon retesting, the numbers came back the same, & her doctor set her up for an emergency meeting with an endocrinologist. Given all I’ve read about the fetus’ dependency on the mother’s thyroid during the first 12 weeks of pregnancy, needless to say I’m concerned – as well as confused. Will this have already had a detrimental impact on her child? What kind of questions should she be asking? What else should she be doing? Thanks so much!

    • Melanie: That is a concern. Autoimmune thyroid disease frequently gets triggered during or right after pregnancy, because of the profound immune shifts that occur. It sounds like she may be experiencing either Hashimoto’s thyrotoxicosis or Graves’. She should have her antibodies (TPO, TG and TSI) tested immediately and take action to bring the hormone levels back into range. This is what her endocrinologist should be suggesting. Feel free to set up a free 15-minute consult at to discuss.

  174. after my second child was born, I began to gain weight eventhough I watched what I ate and walked 7 miles a day. My friend convinced me to go in for a check up. They found a nodule in my thyroid. they did blood tests and a biopsy and they both came back normal. They gave me the option of surgery. Since I was gaining allthis weight and I had noticed things like forgetting things, stomach problems, my hair falling out, arm and leg cramps and many other wierd things and my children were 3 and 5, I decided that I could not live knowing there was something inside my thyroid that wasn’t supposed to be there. I remember that somedays I was exhausted and other days I was going a mile a minute. In hindsight what was happening was that I was hypo one day and hyper the next. My thyroid was malfunctioning and this is what the thyroid does when it is pooping out. It goes back and forth between hypo and hyper until it stayed hypo. So I decided on a thyroidectomy. It turned out to be cancer and Hashimotos which had atrophied my thyroid gland and it was not functioning. In my case (because my body is very sensitive), they had a very hard time after surgery leveling me out. But most people do fine after the surgery. Before any of this thyroid stuff began, I got Vitiligo (loss of pigment) which is an autoimmune disease. (that is why I said that if you have one autoimmune disease you will probaby have a second one as well. All autoimmune diseases do not have cures. They are managed but never cured.) Like you, I had and have GI problems especially horible and painful gas. I know that before surgery I was exhuasted and had diahrea often. When the thyroid is hypo, then everything in your body slows down but when it is hyper, everything speeds up which is the reason you have diareah. Unfortunately, I did not do well on synthroid and I take the natural form of thyroid hormone (armour thyroid). The problem with thyroid is that most doctors focus only on blood tests even though the patient doesn’t feel well. In some people, like you and me, the bloodtests and even a biopsy will come back normal even though your thyroid is blinking out. Hashimotos doesn’t go away until the gland that it is attacking is removed. The surgery is a breeze but the recovery is a little tough and sometimes a little long but once you are level with thyroid hormone, then everything returns to normal. You need to read a book by Dr. Broda (can’t remember the name). This book will educated you on thyroid down to the nitty gritty. There is a way to know if your thyroid is malfunctioning. Take your temperature every morning before you even blink. you must move as little as possible. Do this for one week. you will see that if hypo your temp is below 98.6 and if hyper it will be above 98.6 on average. They used this method in the 50’s and it is still valid. You must remind the docs that your blood tests cannot be relied upon. Tell them often (they tend to not hear you). Only after surgery and thyroid hormone is given that you can rely on the blood tests. Also, thryoid problems are hereditary so start asking mom or dad if anyone else in the family has had problems. Thyroid hormones are found through out the body and even your brain. It controls the speed at which each cell in your body rotates. If hypo your cells are rotating slowly and if hyper they are rotating fast. Why is this important? because thyroid problems manifest themselves in every section of the body from skin to brain. It controls body temperture and metabolism. It is found in abundance not only in the thyroid but in the brain, spinal cord and stomach. It is the only hormone that gives you symptoms that have nothing to do with your thyroid and will mimic many other disordersfor example GI problems, depression, skin moisture, limb pain, foot pain, eyesight, tendons, muscles well you get the idea. It can show up as so many things and can easily be misdiagnosed ESPECIALLY if your blood tests are coming up normal and you feel like crap. The most important decision is to find a GOOD endo. Mary Shoman (google her name) has a website full of info AND how to find a good endo from patient referral. If you decide not to take out your thyroid, eventually you will be permanently hypo since hashi is destroying the gland and then have no other choice but to take it out but like I said by then you have suffered with 15 symptoms that mimic other disorders. This is why I said it is better to take it out and have your thyroid regulated by taking a hormone pill. If you have specific questions you can ask me but if you read Dr. Broda (just google his name and the book will come up) all your questions will be answered.

  175. Oh, sisi, I will try those things and let you know. I’ve wondered about vinegar, since it has healing properties in it. I didn’t know about the body temp thing though, thanks. I will definately try these things.
    Also, renee, this book, I think it was mainly for people with the symptoms and normal test results. All my tests are coming up not normal for Hashi’s so I don’t fit into that catagory.
    Sisi, I would like to know more about your story if you don’t mind, since you said you’ve had similar stuff to me. I’m hoping it will go away if I can get my hashi’s under control or out. I would really like to get it out, since the specialists have such a hard time regulating it for very long and everyone I talk to say it’s easier to regulate it if it’s taken out. My mother in law had hers removed and she felt tons better after, but she had all the classic signs of hypo, not like me who suffers from all hyper but blood comes back hypo.

  176. Thanks for the advice guys. I go in next week. Renee, My doctor who I just found out is more of a natural path than a doctor told me about leaky gut. Ok, here is my take from the research that I did: Do Not play into their hype. Ok, yes changing your diet and getting tested for things you are sensative to is the BEST thing to do for your health, but I actually disagree with you as far as “Autoimmune just don’t happen”, In my case it is hereditary and yes they do develop. They do not start from what you are eating. I have eaten fruits and vegetables my whole life and never had issues until 12 years ago and it has slowly gotten worse. And yes, I did take my natural paths advice, I am off gluten, milk products and everything else that came back as a sensativity including yeast products. I have to live this way for 90 days and then she says we can test them one by one, well here’s the kicker….. I”M STILL SICK. When she told me I would feel better right away. It has been sooo frusterating to have to run to the bathroom every 10 minutes for several hours everyday. I have been on this starvation diet for 2 months now and it’s not working. I am also taking a probiotic and fish oils and peppermint oils. And it’s still not working. I’ve been working with a GI specialist for the last month trying to figure out if it is my intestines or if it’s just related to my thyroid. I’ve done legitimate research and have found that Hashimoto’s when not treated can lead to crohns and other autoimmune diseases because it controls the core of your body. And what an autoimmune disease is… Is where you have normal cells that go haywire and start tagging good cells as bad ones and then starts attacking them, which leads to attacking organs. Now where your food that you eat come into play is that most processed foods are bad for you and feed the bad cells which makes them multiply and spread even farther. So yes, changing your diet will help to make you feel better because it is no longer feeding the bad cells (or malfunctioning cells). But just like what the others are saying though is that once the damage is done, it’s done. Your organs don’t grow back. Just changing your diet doesn’t make the cells go away, I’m proof of that right now! Everything I eat is going straight through me, and I’m eating everything and only the things that this guy talks about in this book your talking about, so there is no link as to the food you eat is creating your illness. Yes it can cause digestive issues if you are allergic to it, but it won’t cause your body to attack itself. If you have a genetic prone or it’s in your blood somewhere then you’re going to get it at some point in your life. You can however put it in remission and have the damage put off for some time and that is probably what your case is, you are just the lucky one that can do it naturally and it worked. But for people like me who need to extra help from medication or doctors, this is what needs to be done. I agree that we do need to take charge and be stern with our doctors to get the right diagnosis and the right treatment though, but I wouldn’t put in too much of myself into this new, “it’s leaky gut syndrome” I think more natural paths are using it as their own way of saying “I don’t know what is wrong with you, but lets try cutting alot out of your diet and see what we can find with that”, it’s the same as the GI’s saying oh it’s just IBS. They don’t know what is wrong. but I have a feeling and a very strong hope that they are connected and that all I need is a beta blocker that will allow me to eat without the urgency to get all foods out of my system right away.
    I just wanted to know if anyone out there has ever had the same problem with hashimoto’s? I keep hearing that with hashi’s you’re supposed to be constipated, you’re supposed to be over weight, ect. Well I’m not and I need to know if it’s normal. I’m tired of living this way.

  177. I know that I didn’t use the word cure 🙂 And I disagree w/ you saying that someone should have their thyroid removed. That should be a last resort. I will say again, when someone has an autoimmune issue there is a cause. The thyroid is one of the least studied parts of the human body. There are only a select few who specialize in it. Maybe you should get the book I suggested. There is alot of information that I think you’ll be surprised about 🙂

  178. I’m sorry to disagree with you renee but hashimoto is an AUTO-IMMUNE DISEASE like diabetes, lupus etc. and IT CANNOT BE CURED. Whoever told you that hashi’s can be cured is lying or misinformed. It will in fact destroy the thyroid gland progressively. No one knows the cause of Hashimoto’s because it is in and of itself an immune conflict with your body. It will continue to destroy your gland and you will feel the symptoms of your thyroid not working and it will progressively get worse. FIND A GOOD ENDOCHRINOLOGIST not a regular doctor since they don’t know anything about the thyroid gland. Once you have 1 auto immune disease it is reasonable to suspect that there maybe another. For me it was Vitiligo but it could be any number of autoimmune disease.


    I will not diagnose (Christina) but I will say that it sounds like you may have Leaky Gut Syndrome (LGS). I was just recently diagnosed w/ it and told that LGS is the cause if my Hashimoto’s, I was put on a strict healing diet and have lost 15 lbs in 2 months!!

    As stated, I am not diagnosing anyone, just talking out of experience. There is an underlying cause to your Hashimoto’s! Your body doesn’t just attack itself for no reason!

    I more than highly recommend getting the book Why Do I Have Thyroid Symptoms When My Lab Tests Are Normal by Dr. Datis Kharrazian. I found mine on Amazon. And it put me on the road to what conventional doctors won’t take – HEALING!!

  180. Hi, I came across your website, and I’m very hopeful in your knowledge. I need help. I have been through the ringer, literally. I was diagnosed with Hashimoto’s in December of 2010, but I didn’t know about it until July of 2011. When I first went to my doctor in november 2010, my blood tests came back showing I was hyperthyroid, which made complete sense, because that’s all the symptoms I have. Then in December it came back hypo and positive for hashimoto’s. This didn’t make sense to me. The only symptoms I have of Hashimoto’s is I am tired all the time, my hair was falling out until I went gluten free, and I have low blood pressure. But I have all the symptoms of hyper still. I have extreme weight loss, I don’t sleep well, and my biggest issue is I have diarrhea (chronic). I went to my doctor who is new in July complaining that it has gotten worse, she tells me that she is also a natural path so I got excited (finally someone to listen to me) well she put me on some herbs that half don’t work, they make me so sick. I am currently on a probiotic 3 times a day and peppermint oil after dinner. She told me that I should not get treated for my Hashi’s because it would make all my hyper symptoms worse. I really need to know if this is true. She then told me that my thyroid and GI issues are seperate, so she sent me to a GI specialist to rule out Crohns, so I’ve had an endoscopy (ruled out celiac, but I’m still gluten free) and a colonoscopy (he says there is no crohns) and he ordered blood work to check for infections. He is also ordering a small bowel series to see if I have any ulcers. I have had sooo many tests, everything comes back normal except for the Hashimoto’s, that has stayed the same. All my symptoms have gone away each time that I am pregnant and yes I have had 3 successful kids without any issues, which I have been told is a miracle because with Hashi’s your not supposed to be able to. I need this chronic diarrhea to go away, I was tested for sensativities and I am trying to stay away from my trigger foods, but it hasn’t helped one bit. I have been at it for 3 months now. I want to know what med would be best for my situation, or what I should be doing. I’m sooo lost. But from what it sounds like on here that synthroid at a low dose might actually help me, is this true.

    • Hashimoto’s is when your body thinks that your thyroid is a foreign body and attacks it continously. As it progressess, you will have hypo/hyper thyroid symptoms until the thyroid gland becomes atrophied or shrunken but by that time you have been through hell and back. There is no cure for hashi”s except to remove the thyroid. It is an auto immune disease. I would go to a good Endochrinlolgist (not all are created equal) and talk about removing the thyroid. Thyroid hormones are throught the body in every cell. Your stomach issues are probably do to a thyroid inbalance. I am not a doctor but just a patient who has been through what you have been through. There is no point is suffering when your thyroid must come out at some point or another. As far as your stomach issues (bloating, pain, burping, gas, nausea) I have two suggestions. Thyroid controls the body’s core temp including thatt of the stomach which must be at a certain temp to do its job. here are two quick fixes that WORK. Have someone get a small towel and wet it in ice cold water and place it on your stomach. You will feel the cold and react to it which is excellent and what is needed. The cold towel will absorb the heat of your stomach and lower it’s temp. Repeat this several times but IT IS IMPORTANT that you do not touch the cold towel because your brain will brace itself and you won’t have that physical reaction of the change in temp that the towel brings to your hot stomach. The second thing is to put 1 tablespoon of vinegar in half a glass and drink it before each meal. It is not that the stomach has too much acid but the opposite, it does not have enough so the vinegar will provide that. You will never have to spend $ on an antacid again. Try this and let me know how it works for you.

  181. It is sad, Mary Ann, to gain that weight and not be able to lose it. Until I found my present endocrinologist, I went through doctors who totally judged my thyroid needs by my TSH number. Every time they lowered my Synthroid, I gained ten pounds. Over a period of ten years, I gained forty pounds. Not one doctor will prescribe Armour for me.I finally just said no, I will not lower my Synthroid further. I have no signs of hyperthyroidism, only hypothroidism, so my endocrinologist is letting me stay on my present prescription.

  182. I understand how the thyroid effects many components of the body – ie the brain. A few years ago my world turned upside down when I took Chantix to stop smoking. My entire hormonal system went wacko, I entered menopause and my thyroid shutdown. Nothing seems to be helping me to lose the weight I gained. I have been on Armour Thyroid, P-Thyroid and now back on Armour Thyroid. I have often wondered if I began to take the nicotine logenzes if this would reverse some of my symptoms. thoughts?

  183. Well, I am reading very interestedall issues about Hashimoto. I was diagnosed many years ago… and I just took my L-Tyroxin 75 mg and took it as natural. So until now…. travelling and experimenting other kind of food like sea weed salads and maki sushis more than 2 times a week, I got pain (join / muscle – I even do not know the difference); area surronding my eyes hurt; when I stand up in the morning I fell like “90 years” old and I am 50!!!! Everything hurts! Nail breaking and hair is falling – first I was looking for high blood pressure problems since I started medication 3 months ago and for the first month I had to change medicantion because I got problem on m throat…… today…. thinking about that, it was not the blood pressure medicine but rather my imune system. I will be off gluten – it is a pitty that it takes 6 months to get rid of all side effects of gluten ingestion – I am so curious what my body / imune system will react. Now I am putting all over my place small notes to remind me not to eat bread – cakes and flour stuff and think Gluten free. Thanks for all information. I do hope I am on the write path! Ingrid

  184. Thank you Renee for the input. I will get serious about the gluten and sugar. I haven’t heard of emulsified vit. D. Will try this also. I did find a doctor in my area that lectures for Dr. K. Hopefully will have enough money soon to be able to afford her. Thanks for the boost. It helps to talk to people who understand how you are feeling.:)

  185. @christine try looking for a practitioner in your area who has studied under Dr. K. try this link: in the comment box tell them what state you are in and they will send you prac. info in and around your area. you may have to travel.
    i have taken myself off gluten and white sugar as much as possible and i have gone mostly organic. i have a grinder/press coming so that i can start juicing. my next step is emulsified vit. D [better absorbed]. just a few ideas for you. i haven’t found the cause of my hashi’s yet but i am saving pennies to see a doc in my area who studied w/ Dr. K. good luck

  186. I had a total thyroidectomy 3 years ago. Felt terrible on Synthoid, now on Armour and starting to feel some results. I have terrible gerd, low iron and very low vitamin D. No improvements with supplements. I had the radiation pill which the doctor says kills all remaining thyroid tissue. Could there be any remaining active thyroid tissue? My funds are limited so I feel overwhelmed with the do list for more labs and more supplements that I read about in Dr. K’s book. Not getting any help from endo or family doctor. Advice is to continue Tagamet and deal with the gerd…. take the iron and get some sun. So confused on what to focus on first. Doctors say I have had the test for gluten and I’m not sensitive. As in one of your posts….should I first focus on removing this completely from my diet?

  187. After I got EBV, my thyroid just dive bombed. I believe now that I had HYPER thyroid… for years before that… but.. after the EBV.. everything just got worse. my last antibody test was 578… range is 0-5. I do my best to just be thankful..but .. i have to admit.. with stress… all these symptoms of hashis and hypo.. along with a SLEW of other autoimmune disorders..( UC, psoriasis,shingles, PC) as well as Low iron sats, migraines.. off and on pvc’s.. and being EXTREMELY sensitive to whatever i take for it.. i think i am starting to lose hope. I just had my blood drawn today again.. due to the Westhroid that i take being upped.. well.. somethings just not right now.. the company also started putting a coating on it.. (they stated that people were complaining about the smell and taste)… well. since i started taking the westhroid WITH this new coating.. its not working like it was before.. plus.. i was taking 1/2 grain twice daily.. now.. they put me on 1 whole grain daily. uggh.

  188. The more I read about hypothyroidism, and people’s experiences, plus my own, the more I think there is a huge disconnect between the reality of what people are experiencing and the medical establishment–specifically Endocrinology. It would seem hypothyroidism isn’t an isolated disease, but involves more of the endocrine glands. And doctors practice according to what they are taught to, which is just not helpful enough for far too many sufferers of this disease.

    My subscription for Synthroid is causing my test to show I’m getting too much TSH. My endocrinologist has let me stay on this dosage because it has cleared up so many of my problems, but he is leaving it up to me, largely, to let him know if I start getting heart symptoms such as palpitations. This is a terrible quandry for me, partly because of my age, 80.

    • Elizabeth,

      Your post is interesting. I am 53 years old, have Hashimotos, and heart palpitations and associated insomnia were the reason for visiting my doctor. I haven’t been able to get rid of the palpitations, but have found sugar and salt at bedtime to give me a good night’s sleep, generally, indicating a lowering of blood glucose at night while sleeping (or not).

      I am interested that your dose of thyroid hormone is keeping the palpitations at bay. Is it that a higher dose will put you into a hyperthyroid state and cause palpitations? Or are you taking enough hormone to prevent the palpitations? I believe it is adrenalin/stress hormones causing the palpitations in the hypothyroid/hashimotos condition.

  189. I found this interesting. I had never heard of Hashimoto’s before. I have had my thyroid tested for years, suffering with fagtigue, dry skin, brittle nails, hair loss, allergies, intestinal issues, the list goes on. I have had a goiter since I was 18. My thyroid tests always come back on the ‘low side of normal” so my PCP refuses to treat me for low thyroid because it is technically normal. I have always asked what if normal for me should be higher! About 15 years ago they did a scan which also came back normal. Now, as I learn more I am glad they didn’t medicate me but am looking for nautural remedies to help. Any suggestions?

  190. I am glad to see this blog post is still active. I was diagnosed with hashi’s 10 years ago and went undiagnosed for about 4 years. And only in the last 2 years do I feel like I am on the right track towards better health.

    I have heard all the excuses I can handle from doctors. Things like “This is a lifestyle issue” and “You’re a complicated case” (I have 2 other rare auto-immune diseases, Sarcoidosis and Takayasu’s Arteritis, diagnosed 1.5 years after the hashi’s was diagnosed.) I have a new doctor and during one of my recent visits I told him I don’t want to hear about lifestyle changes and that if I had a nickle for every time I’d be a rich woman. I think he might be working up to a “You are complicated” because of the battery of tests he ordered, the other diseases have resolved themselves, I’m not worried.

    The information that has put me on the right track I’ve been able to find at the following websites:

    The people in some of the posts above are still struggling with inadequate doctors, testing, the interpretation of those tests, and medication.

    The thyroid and all of its complications are a tangled web, but one that I believe can be untangled with the help of posts such as this and the websites mentioned above. This is a great series of articles on the thyroid and I can’t wait to dig into the rest of the blog.

    Thank you!

  191. Yes. A thyroidectomy is like removing gum from your shoe. It’s very difficult to get all of it out without damaging the surrounding structures, so inevitably some of the thyroid gland is left behind – and it can be attacked by the immune system.

  192. OK Now I am confused. If I had a total Thyroidectomy and they found Hashi’s, Can I still have Hashi’s and can it be reaking havoc in my body?

  193. They did. Your TPO antibodies were positive. That’s autoimmune disease.

    The other markers are not specific to Hashimoto’s and may or may not be elevated in people with that condition. For example, I have Crohn’s disease which is an autoimmune disease, but I never test positive for any of the serum autoimmune markers.

  194. Candy: Hashimoto’s is an autoimmune disease, by definition. If you have Hashimoto’s, you have an autoimmune disease. It’s that simple.

    The TPO antibodies that were measured by your doctor indicate that your body is producing antibodies to an enzyme in your thyroid gland. This is autoimmunity, i.e. the body is attacking itself.

  195. I am curious about your article stating that all Hashimoto’s is due to autoimmune disease. I was diagnosed about a year ago after much encouragement from my trainer who saw me doing all the workouts but getting zero results. She too has thyroid issues and she encouraged me to get my results from my general doctor as well as my gyno…both of whom told me “your test results came back normal”.

    On a hunch and and based on my TSH running around a 4 and my symptoms, I made an appointment with an endocrinologist. She did the tsh test as well as tpo…and the tpo antibodies came high… i think 132 out of 0-30 scale. On synthroid I went and a year later… I am starting to feel like a pin cushion experiment, constant retesting of my blood to find the right dose! I went from 25 to 50 to 75 to a combination of 75/50 mg and now I have been switched to armour (1gr). Of course since the switch, some of the terrible symptoms I was having before being on synthroid have returned including my arms falling asleep at night, very itchy skin, edema and headaches.

    A few months ago I suspected the autoimmune relationship, so off to my NEW doctor I went and got the anti-dna, complement C3 and ana blood tests, which all came back normal. So frustrating! My new doctor even checked my pth levels and ordered a scan for my thyroid…which was also “normal”.

    So my question is… If there’s an obvious autoimmune relationship, why isn’t it showing up in my results?

  196. Renee,

    Thanks for sharing your story. I’m so glad this information has helped you to recover your health. That’s my purpose in doing this, so it’s wonderful to hear from folks like you.

    • In our province of Canterbury in New Zealand at a latitude of 43 degrees south, all of the population are deficient in Vitamin D at some time of the year and 50% of the population are deficient all of the time, including me. I’m on the same weekly dose as you but expect that I will need a maintenance dose of a similar level i.e. 50,000 i.u. a week or 7,000 i.u. a day. I’ve discussed with my menopause specialist when we should get my Vitamin D level retested and she and I have agreed that after 6 months on this dose, it will be a realistic time to find out what it has done to my abysmally low Vitamin D level which was around 13ng/ml or whatever unit is used in the USA. It started out at 30mmol/L in our units and I would like it to end up at around 80mmol/L as a minimum and 120mmol/L as an optimum.

      Anyway, my main point is that beyond a certain latitude, Vitamin D deficiency is endemic in a population. Our cousins, the chimps get around their problem by nibbling on skin cells when they’re grooming their buddies/rellies in the troop!

  197. I have to tell you that finding The Healthy Skeptic put me on the right path in finding the cause of my Hashimoto’s! By what you post here, I am sure that you are familiar w/ Dr Datis Kharrazian? You and he have put me on a road to recovery! Once I was diagnosed w/ Hashimoto’s I began my research finding you, then, Dr Kharrazians book. My doctor had no intention of testing me any further once he diagnosed me w/ the immune disease. He simply put me on Synthroid and sent me on my way. As I researched, I discovered that my symptoms [and I had just about every one] subsided during the summer. Mainly my hair loss! In reading Dr Kharrazians book I had the doctor test my vitamin D levels. Well, as I suspected, I AM deficient in the vitamin and now on 50,000 units 1 day a wk for 8 wks, then 1000 units a day after that. Now, the next step is to find out WHAT is causing my deficiency.
    Thank you so much for your website and blog! And a quick note to your readers: TAKE CHARGE OF YOU OWN HEALTH! Listen to your gut! You know your body!! If you suspect something is wrong MAKE your doctor do the tests! Don’t settle for what your doctor “thinks” the problem is! And if your insurance won’t pay for it the testing, YOU PAY FOR IT! Your family and loved ones love you and need you healthy!!
    Again, THANK YOU!!

  198. I just found this article while researching Hashimoto’s. Have you continued on this subject? I am in desperate need of more answers. Thank you.

  199. Patricia,

    The problem isn’t necessarily the tests you’re getting. It’s how they are interpreted. Watch this video to learn more about what I mean.

    Also, remember that Hashimoto’s is an autoimmune disease affecting the thyroid. To treat it properly, the immune system must be addresses since it – not the thyroid gland – is the underlying cause of the problem. Unfortunately, the conventional model doesn’t recognize this even though it’s abundantly clear in the scientific literature that this is what’s happening.

    You’re best bet is to find a functional medicine practitioner that understands these issues.

  200. Could someone please help me by answering one question. I was diagnosed with Hashimotos over 7 years ago and have been taking synthroid since then. The usual thyroid blood test (T3 ) has been performed intermittently since that time (during physicals, or when I had symptoms that I thought might be related to Hashimotos) and it always comes back “normal” according to my PCP. I suffer from depression – am being treated with medication – but have been through an especially difficult 2 years. I have many symptoms right now that are present in both depression and hypothyroid disorders and it’s become necessary for me to figure out what exactly is wrong because I seem to be getting worse rather than better. It’s ression or thyroid related, since so many are identical. My hair is falling out and I’m gaining weight despite not eating. My question is this: is their another blood test that will give an accurate picture of what is going on with the Hashimotos and if it is the cause of my worsening condition? I keep reading that the standard blood tests (T3, T4) do not give the complete picture and that if symptoms are present more examination is needed. My doctor doesn’t seem to give this view any credence and I always feel like a hypochondriac when I bring it up. Should I forget the PCP and see an endocronologist? Is that the only way to get to answers that I need? Any advice that makes sense would be greatly appreciated.

    • an endocrinologist may not be any more enlightened than the jerk you’re currently seeing…. i wish you good luck in finding a better doctor — they’re few, but they’re out there.

  201. The immune attack in Hashimoto’s is focused on the thyroid gland, but many Hashi’s patients also have antibodies to other tissues.  And of course the effects of Hashimoto’s are systemic – the entire body is affected.

  202. ok so the RECEptors  and thyroid hormone are what is throughout the body but not thryoid cells.  Am I correct?  In that case hashi’s would stay within the thryoid gland.  Correct? 

  203. Yes.  Thyroid cells are in the thyroid gland.  Thyroid hormone is present throughout the body. Most cells have receptors for thyroid hormone.  That’s how thyroid hormone regulates metabolism.

  204. but thryoid cells are what allows all cell metaboloism.  which means to me that thryoid cells are located throught the body in order for cell metabolism to take place.  Am I wrong about thryoid cells and cell metabolism?

  205. Thyroid “cells” aren’t located throughout the body.  All cells do have receptor sites for thyroid hormone, though.  That’s not the same thing.

    However, a thyroidectomy is a bit like scraping chewing gum off the bottom of a shoe.  They rarely remove the entire thyroid gland.  It’s very close to other important structures in the throat so they have to be very careful.

    This means that, yes, if you have Hashimoto’s, it’s entirely possible that your immune system will continue to attack what’s left of your thyroid gland.  That’s why it’s so important to address the autoimmune component.

  206. I had hashimotos thyroditis AND papillary thyroid cancer.  I ahs a total thyroidectomy.  My question is this:  Since hashimotos attacks the thyroid cells and gland, is it not possible that even after a thyroidectomy, that the hashimotos could continue to attack thyroid cells in the wholw body since thyroid cells are found in the entire body?  I worry about this because it makes logical sense that hashiotos would attacj thryroid cells where ever they are which is the entire body.  Has anyone done a study of this?  Is this even medically conceivable?  Can you answer my question so  that I can understand this better and not have anxiety over what else is happening in my body?  Thank you for any help or guidance that you can probvide.

  207. I’ve found your series on the thyroid very interesting.  My question is that I was diagnosed with hypothyroidism 7 yrs. ago, but have never tested positive for the antibodies that would indicate it is caused by hashimoto’s.  I’ve researched, but I can’t find a cause for the hypothyroidism.  BTW, I was on Synthroid for a few years, then took myself off of it – never felt any different on or off.  I just had bloodwork done – TSH was high at 8.9, Free T4 on the low end of normal at .98 (range of .82-1.77).  New doctor recommends restarting synthroid, although they aren’t pushing it.  But they did recommend an ultrasound of my thyroid, although she (nor any other past doc.) feels anything unusual upon exam.  Do you have any insight for me as to what could be causing the hypothyroidism?  I hate to treat without a real understanding of the cause.  My symptoms are not severe – some fatigue,but not unusual, don’t like the cold.
    Thank you!

  208. I had a total thyroidectomy and was diagnosed with Hashimotos in june 2010.  Since the thyroid was totally removed how does this affect the hashimotos?  My doctors seem very content ordering Synthroid and testing TSH and T4. Doctor says will take about a year to get on right dose of Synthroid and thinks all symptoms will subside.  Should I be on a gluten free diet?  I am very bloated and cannot lose weight also have bad joint pain and pain in bottoms of feet.  My blood sugar is also high but doctor feels it will go down once meds regulate. I am extremely tired all the time and have temperature fluctations with profuse sweating. 

    • Removing the thyroid gland is somewhat akin to removing chewing gum from a shoe. It’s nearly impossible to remove the whole gland, because it is so close to the trachea / voice box and other important anatomical structures. What this means is that, if you have Hashimoto’s, autoimmune attacks on the thyroid can persist even after thyroidectomy. Therefore all of the information in these articles still applies to you.

      • Hello:

        Thank you very much for your research and insight. I have been told I had a large thyroid since I was a teenager, I’m 35 now. After many, many, many years of frustration and doctors who just kept blaming things on depression–the number go-to diagnosis when doctors can’t figure things out– I was diagnosed with thyroid cancer at age 30. When my thyroid, lymph nodes, and 10 large tumors the size of golf balls were removed, I had to have radiation treatment to kill off my thyroid. It has taken me years to find the right Endocrinologist, just last February 2013, that told me I had Hashimoto’s disease. Let me tell you I fit all of the symptoms of Hashimoto’s disease, down to my feet, hands, joints and unbelievable long menstrual cycles, which began in 2009.

        I was so happy that I had a name for my symptoms, and when my doctor finally gave me a higher Synthroid, something I had been fighting for, for a long time, I thought okay my symptoms will be gone now, right? No, not exactly. Although I do slightly better with the increased Synthroid I am still having problems. Again, I was told it’s depression. Let me just say, I’ve felt depression before, especially on my long menstrual cycles. It’s like everything is bland, or unexciting. There’s always something wrong and dissatisfying–SNL’s Debbie Downer for sure. However, my symptoms and mood were more related to frustration with my health. Anyway, I thought they would go away with the increase in of Synthroid but they haven’t.

        After reading your blog I’m wondering if I still have Hashimoto’s disease even though my thyroid is gone and it was zapped with radiation because I am still feeling most of the symptoms.

  209. As someone who was diag. about 2 years ago with hpothyroidism, I take synthroid daily.  Would I do better on the Armour?  I am a nurse, but never see it ordered, always the synthroid.

    • There are several factors that determine which thyroid hormone is best for each person. I’ll be writing about them in a future article.

  210. I would be curious to know if autoimmune thyroid issues could be a secondary result of other autoimmune conditions. I have had severe rheumatoid arthritis since I was 16 (28 years) and in the last couple of years have had rapid weight gain, extreme menstrual irregularities, and hair loss. According to my doctors, my thyroid is normal. Yet, nothing else seems to account for all of these symptoms.
    I get the brush off when I try to press for more in-depth diagnosis. The GYN blames my medication, the rheumatologist blames my diet (low-carb and < 1000 calories per day), the thyroid specialist found a nodule on the thyroid, but says everything else is normal and since the node has shrunk over the past year, everything is fine.
    Why is it so hard to get anyone to pay attention? I’m hardly a hypochondriac. Having a chronic condition has left me very in tune with my body, so I know when things are minor and can be ignored and also when they’re just not right. It seems like the doctors’ eyes start to glaze over the minute I mention hair loss and weight gain. So frustrating…

    • The short answer is yes. Hashimoto’s is often part of a polyendocrine immune disorder involving multiple tissues. The same is true for other autoimmune conditions. The way to figure it out would be to find a health care practitioner willing to test for antibodies to other tissues commonly attacked by antibodies. Also, as I’ll explain in a future article, many people with autoimmune diseases are gluten intolerant. If you’re not already gluten free, I would highly recommend it.

      • From what I’ve read on some sites, sometimes a low-carb diet mimics starvation and then the body goes into hibernation mode to slow down metabolism. It does that by converting some T4 into Reverse T3 intead of T3. It is possible to have Reverse T3 measured in some laboratories. I think for us here in New Zealand, we have to send our blood samples to Australia. We can do this via the internet, thank goodness.

  211. The idea that bio-identical thyroid products like Armour have unreliable doses is a myth. Armour has a standardized dose of 4.22:1 T4:T3.  It has been tested and confirmed over and over again.

    In fact, as you may be aware, Synthroid was pulled from the market because of unreliable doses and was only re-approved in 2004 I believe.

    • I absolutely agree…..I have taken synthroid for 37 years and I have taken perscriptions back after a week because my body told me that it was inferior. Then the pharmacist told me that I had been given a generic form and that I would have to pay more for the snythroid. Imagine…they made the choice to fill out my prescription with generic without even notifying me……I have heard that this goes on more often than not….

  212. One thing about natural thyroid, according to the doctors, is that the dose is unreliable. Then an odd thing happened. The local pharmacy used to give me enough synthroid  for three months, but then they discovered that it was degrading on the shelf. That is, the old stuff wasn’t as powerful as the new. All of which leads me to think that the synthroid dose is also unreliable.  I really like that thrytrophin. It comes from a company called Standard Process. My dentist gets it for me,

  213. I’ve had hypothyroidism for fifty five years, treated with Synthroid. I’ve never been diagnosed with Hashimotos. I don’t think I’ve ever been tested for antibodies. My lab results over the past three years have been 0.01 TSH, free T4 1.39, free T3 2.1. The T4 and T3 have varied a little, but normal. So my endocrinologist is letting me stay on the Synthroid 137 mcg, until I show signs of hyperthyroidism. I went through four doctors trying to find one that wouldn’t lower my Synthroid dosage. I can’t tolerate a lower dosage, I tried about four years ago. Unfortunately, I haven’t found a doctor in this area who will try natural thyroid.  

    One doctor told me I’ve been on synthetic hormones for so long, that I no longer produce any thyroid hormones at all. About six years ago, I was on 150 mcg, and I felt best on that dosage. Before that, my dosage at one time was as high as 250 mcg. I guess the synthetic dampened down my ability to produce my own hormones. I wish I understood my own situation better.

  214. Fascinating! I am hoping you can help with a question I have that I can’t seem to find an answer too. It seems easy enough for someone with thyroid knowledge though. I am pretty sure I haven’t had an enlarged goiter, and I have high TSH, with low T4 and T3. All of the writings I have read on Hashimoto’s say goiter and low T4, with no mention of T3, nor stating that you can have Hashimoto’s without an enlarged goiter. Would Hashimoto’s be something I may have (I know you aren’t a physician, but I am just curious if an enlarged goiter and only T4 issues are a must for this autoimmune disorder), or is there another type of thyroid disorder that I may be overlooking.

    It just seems like I will have a better chance to naturally treat this issue and get off of medication if I know the cause. I am otherwise of good health and fitness aside from allergies. Thanks!

  215. Chris,
    I know that most recent population-based studies demonstrate that iodinization increased Hashimoto incidence, including here, in Brazil. That’s a fact. But the level of iodine in these populations are very low, compared to what it used to be, and not very long ago. And Hashimoto incidence is higher than it was when iodine level in those populations was higher.
    If iodine was that problematic, Japan would have a much higher incidence of Hashimoto and much worse outcome than they have. Japanese have had allways a very high level of iodine, because of high consumption of algaes, as probably many populations that consumed a diet high in sea food.
    The fact is that bromine, fluorine and chlorine compete with iodine. And we ALL are full of this halides these days. The fact that a little iodine increase in some populations is increasing Hashimoto incidence probably is reflecting this fact with iodine displacing these halides and increasing autoimmune flare.
    Other possibility is that those populations are low in selenium. As you probably know, there are studies that show that populations low in both selenium and iodine, that supplement either one show a high incidence of hypothyroidism.
    Another possibility is that these populations are low in salt. Salt along with iodine is know to increase halide excretion. But, nowadays many people are restricting salt.
    Anyway, what I really know is that Dr. Abraham has been researching this for a long time, Dr. Brownstein has sucessfully treated more than 4.000 people (including him and his father), there are many sucessfully anecdotal testemonies on iodine yahoo group and all these facts made me try iodine, with great success.
    One last thing, if you know a better way of get rid of halides wihout iodine and without moving to live outside of modern civilization, please let me know!

  216. Mario,

    I read the full-text of the China follow-up study Dr. Abraham linked to.  Their conclusion is that excess iodine doesn’t increase the incidence of Graves’ disease.  They didn’t say anything about whether rates of Hashimoto’s increased.

    In any event, there are several other population-based studies that demonstrate this effect, as I’ll share in my next article.

  217. Many years ago, I was diagnosed as hypothroid and prescribed Synthroid. I seemed to have an opposite reaction to the expected one. I gained weight, my hair started to fall out etc. I found a doctor who prescribed something called “thytrophin” .That seemed to work better, so I’ve been taking both for many years. (One to satisfy the doctors and one to feel better.)
    I also had a growth in my thyroid gland and 1/2 of it was removed. The growth was benign and at that point the doctor said that i had Hashimoto’s disease. Now, reading your article I’m wondering how to find out more.
    Are there treatments for autoimmune disease? Are there studies that might clarify some of these things?

    • Stay tuned. I’ll be addressing your questions in the coming articles. Have you read the second one in the series yet?

  218. I had my thyroid removed in 1968 because of thyroid cancer. for years they had me on armor thyroid, 4 mgs, or something. about twenty five years ago they changed me to synthroid. I have never felt great since the change, the doc’s do not seem to want to change me back to armor, they say synthroid is just as good or better. any thoughts about this.

    • The statement “synthroid is as good or better” than Armour reveals a shallow understanding of thyroid physiology and metabolism. For someone who has problems converting T4 to T3, Synthroid is a terrible choice because it only contains T4. For someone without any conversion problems, Armour may cause hyperthyroid symptoms because it has pre-formed T3. There is no single drug that’s right for everyone.

      There are several considerations when choosing a thyroid medication. I will cover these in detail in a future post. Please stay tuned.

      • how do you know if you have problems converting T4 to T3? All I know for sure is that my levels are low and i need the synthroid (I have had a thyroid lobectomy). Even when the tests are normal, they have to be at a certain level within the range for me to feel ok, and I occasionally start feeling the symptoms of mroe hunger/etc and ask for my med to be increased slightly, which the docs are generally willing to do as long as the levels stay within the “normal” range after they adjust the meds.

      • I am very interested in what you will have to say about Armour and Naturthroid. I recently found that Armour has gluten in it and so switched to Naturthroid. I willbe having followup bloodtests in n few weeks. And my hot flashes have not abated.

      • Dear Chris,

        Thank you for your article. I am especially looking forward to your post concerning thyroid meds. I am a 45 year old female who has been on Synthroid 112 mcg for 18 years due to Hashimoto’s. While it was managing my symptoms OK, I still couldn’t exercise without feeling like I had the flu for a week after. Eight months ago, my doctor changed my prescription to Armour Thyroid 45mg plus 25mcg Synthroid. While we had to adjust the dose a few times, my numbers finally read well at T3=3.6, T4=1.21 and TSH=1.3. However, in the last eight weeks, an all over itch has begun (pruritus) and my hair is falling out like crazy. He doesn’t believe I’m hyperthyroid, however, due to my numbers. Therefore, has me slated for allergy testing. I’d really like to know your take on Synthroid vs Armour!

    • Keep trying. Find a Doctor that will switch you back. I went through 2 doctors already and am now with a third. I’ll see what happens. Just remember this…it’s your body!

  219. Just received diagnosis of thyroid auto-immune disease. Longterm stress? Adrenals can no longer react properly? Throat chakra-energy centre-Yes Sara! I am not so into chakra thing but the basic background, premises I find to be good starting points: at some point, some time the person who is dis-eased has had to keep their mouth shut, their spirit shut down.
    The doctor started me on 25 mcg of thyroid. Been taking it for one month. I have found that even that little bit helped me get my energy back and stop thinking that I was losing my mind. But I know this is only a bandage. I have got to work with the stress. Diet. Coffee still tastes good but it doesn’t feel good. Habit makes me want to drink it. So now I just am going to leave it out. Even now I notice that liquorice is a no-no. Going to try it again this weekend to double check reaction.
    Everyone is so different but I think one thing we are all the same on and that is a requirement, a need to have some sort of spiritual life…whatever it is. Diet: elimination diet? I don’t think I am going to get much help from the doctors except for thyroid medicine checks so I go to diet. Leave different foods out of diet for a couple of weeks and reintroduce to see what happens. Any one with experience? advice?
    Anybody have any experience with acupuncture?
    I am glad to find this site. I want to understand better what is going on inside this body that feels like it was falling apart at the seams.

    • I’ll be addressing nutritional strategies for regulating the immune system and reducing inflammation in a future post.

  220. Studies show that 90% of people with hypothyroidism are producing antibodies to thyroid tissue.”

    So that is why in my clinic I treat all thryoid and thyroid like patients with sophisticaltd techniqui of Immunology from the Ling Shu, revealed by Dr Nguyen Van Nghi. (search <>)

  221. This is a great article thank you.  I am hypothyroid and have Rheumatoid Arthritis.  I take LDN (low dose naltrexone) to help with my RA autoimmune disease and am so glad to hear others say it helps with Hashi’s. Chris I look forward to your future articles on thyroid disease.

    • Karen,

      I don’t know whether this is your case or not – but I would like to tell you what helped me. My father had hypothyroidism – and was diagnosed with RA. He was put on steroids and they didn’t help at all. I too am hypothyroid – and about ten years ago my joints started to swell and ache. I could barely stand up straight. I was trying to lose weight and tried the Atkins diet – what surprised me was that the pain in my joints (hips, back, legs, hands…) hurt less. Long story short I finally figured out that I am intolerent to all grains – wheat, rice, corn etc. When I omit them the inflammation in my joints disappears completely. I am pain free. Occasionally, I cheat – and it takes about 3 days and the symptoms return in full force – and it takes about 3 days after stopping for the symptoms to disappear. I am firmly convinced I would be diagnosed with RA if I didn’t know… (Warning – when trying to quit – the cravings – especially to bread – are wicked). Hope this helps…

  222. It is true that the endocrine system is a very complex and if I may say, from my frame for reference, very interesting.  I also find it astounding (and maybe inaccurate) to say 9 out of 10 people with hypothyroid have the autoimmune Hashimoto’s.  This just can’t be!!  But then again, autoimmune dis-ease is so rampant in our society.
    I am an herbalist and cannot disregard that fact the most of these sufferers are women and women have myriad Throat Chakra issues….this should not be excluded.  The emotional variable to any dis-ease should never be left out of the conversation.  With that said, there is also the fact that women are most likely to wear make-up and spray perfumes all over there body, and where else…the neck!!  All these chemicals (endocrine disruptors) in the system are directly correlated to disfunction.  In addition, one cannot ignore the role adrenals play in this situation, with Syndrome X, insulin resistance etc (I know this is another topic altogether).  Diet plays such a huge role, Hashimoto’s or not.  With no antibodies, one MUST look at diet and emotional issues.  And in reading a couple of these posts, it would seem these imbalances are past onto the next generation, which tells me there is not only some learned behavior there, but endocrine system issues from the start. And finally, it’s not only the chemicals we put in and on our bodies that contribute to this, but the deplorable condition of the digestive system and the key role this plays in all our immune functions. I cannot emphasis enough that most every body is deficient in prebiotics AND probiotics and supplementation is crucial. Lastly, mineral deficiencies.  Magnesium, potassium….etc etc.  The SAD diet provides little if any minerals and even if someone eats well (which is relative) assimilation is inefficient due to the digestive flora issues, coated small intestine, and liver/kidney stress do to toxin load.

  223. Given the discussion in the comments on the efficacy of the blood type diet, I thought this recent commentary by Prof Loren Cordain.
    The History And Characterization Of Blood Type Diets

    Blood type diets were first popularized by Peter D’Adamo, a naturopathic physician, in his best selling 1996 book, Eat Right 4 Your Type1. The inspiration for Dr. D’Adamo’s book came from subjective clinical impressions of his father, James D’Adamo; also a naturopathic physician who first proposed this concept in his book, One Man’s Food is Someone Else’s Poison 16 years earlier in 19802. As a member of Bastyr College’s first graduating class of naturopathic physicians in 1982, Peter became interested in attempting to validate his father’s subjective and personal observations from reviews of the scientific and medical literature – thus the fundamental reason for Peter writing his hugely successful diet book.

    The underlying premise for Peter’s dietary ideas is that ABO blood type is the most important issue in determining healthful diets. He advocates separate diets for people with one of the four most common blood types (A, B, O or AB), and has further subdivided his dietary recommendations into three arbitrary ancestral categories: “African, Caucasian and Asian.” Hence 12 subgroups (4 blood types x 3 ancestral categories) exist – each with differing dietary recommendations. Each blood type diet includes 16 food groups which are divided into three categories: 1) highly beneficial, 2) neutral and 3) avoid. For each of the 12 subgroups differing recommendations exist for the three food categories. If these nutritional recommendations sound somewhat complex to you, I had to re-read them about a dozen times to get the drift myself. Although I don’t want to get ahead of the game, for the observant reader, you may be curious to know how Dr. D’Adamo dreamed up this complex dietary system and if a long trail of experimental human clinical trials exist to support Peter’s recommendations? I, too, had to ask myself these same questions.

    Before we get into the science or lack thereof of the blood type diet, I’ve got to flesh out a few more of the underlying concepts. Dr. D’Adamo believes that blood group O (“O for Old”) was the earliest human blood type and that all humans at one time maintained this blood group before the subsequent evolutionary appearance of blood types A, B and AB (reference 1, pp. 6-13). Accordingly, Peter believes that people with the O blood type had ancestors who were skillful hunters and whose diets were high in meat and animal proteins. For modern people with the O blood type he advocates a high meat, low carbohydrate “hunter” diet, with virtually no wheat, few grains or legumes and limited dairy products. Do these dietary recommendations ring a bell for you, or sound vaguely familiar? Keep this thought in mind, as it may well explain the lasting popularity of Peter’s first book.

    Peter now goes on to explain to us that blood group A (“A is for Agrarian”) “appeared somewhere in Asia or the Middle East between 25,000 and 15,000 B.C.” . . . and “allowed them to better tolerate and absorb cultivated grains and other agricultural products” (reference 1, p. 8). For type A’s, Dr. D’Adamo recommends a mainly vegetarian diet – the diet that he personally follows. However, more importantly he recommends that blood type A’s also avoid wheat and dairy (do these recommendations also sound familiar?) and replace meats with some “highly beneficial” fish and seafood – Hmm, lots of fresh fruits and veggies for type A’s, little wheat or dairy and fish instead of meat? Keep these recommendations in mind.

    Peter next tells us that blood type B, “developed sometime between 10,000 and 15,000 B.C. in the area of the Himalayan highlands – now part of present-day Pakistan and India (reference 1, p. 10). Peter suggests that type B’s have evolved the most varied diet and can include both meats and dairy in their daily menu, but again should avoid wheat. Before we move on to the final blood type (AB) it should be noted that Dr. D’Adamo generally eschews highly processed foods (chips, pastries, candy, ice cream, snack food, fast food, etc.) for all blood groups – once again, does this not sound like another familiar dietary suggestion?

    From Peter’s diagram on page 6 of his book, he indicates that blood type AB appeared first in humans sometime between 500 B.C. and 900 A.D. He characterizes “AB is for Modern” and states “Until ten or twelve centuries ago, there was no Type AB blood.” (reference 1, p. 13). Peter indicates that AB’s are a conglomeration of type A and type B blood types, and consequently their diets should reflect a mixture of the recommendations he makes for these blood groups. AB’s are therefore advised to eat meats, seafood and dairy, and to once again avoid wheat.

    The Reality And The Science Of Blood Type Diets

    The reality of Dr. D’Adamo’s book, Eat Right 4 Your Type, is that it has overwhelmingly become one of the sustained, best selling diet books of the past two decades, and continues to sell well on Amazon and other retail outlets – 14 years after its initial release in 1996. Unfortunately, as I will shortly demonstrate, Dr. D’Adamo’s explanations for the health-promoting effects of his diet have little or nothing to do with ABO blood groups. His claims about the origins of human blood types and the dietary selective pressures which elicited the four common blood types are completely incorrect and have no basis in the current scientific literature. By critically examining the faulty concepts and evidence underlying this book, it becomes almost comical how Peter’s series of errors, incorrect assumptions and conclusions actually ended up with dietary recommendations that may have therapeutic value for about 60% or more of the world’s population. The paradoxical nature of this book (bad science, pretty good dietary recommendations) helps to explain its lasting commercial success.

    Actual Origins of Human Blood Types

    Peter’s suggestion that O is the original human blood type is incorrect. Studies in humans, chimpanzees and bonobos (a specific type of chimpanzee) show that alleles (different versions of genes) coding for the A blood type was actually the most ancient version of the ABO blood group, and was shared prior to the evolutionary split between chimpanzees and hominids five to six million years ago3-5. Hence, Peter’s suggestion that blood type A appeared 15,000 to 25,000 years B.C. in response to dietary changes brought about by the new foods (i.e. grains) of the agricultural revolution is not only incorrect, but off base by about five million years. Now, let’s play a little game of logic and apply the correct data to Peter’s reasoning that “the original ancestral human blood type should be eating a high protein meat based diet.” Since type A is the actual ancestral human blood type (rather than O), if we use Peter’s logic then he – himself a type A – should not be following a vegetarian diet, but rather a high protein meat based diet. These kinds of games of logic – although fun to play – more importantly underscore the fundamental and incorrect assumptions upon which Peter’s book is based.

    The next blood type that appeared in the human lineage was B – which split from A – about 3.5 million years ago3-5, not the recent 10,000 to 15,000 years B.C. origin that Peter has proposed. The O blood type split from A about 2.5 million years ago3-5 and consequently does not represent the oldest blood type as claimed by Peter. The only fact that Peter correctly deduced about the origin of human blood types was that AB was the youngest, but once again he completely missed the correct date, as it was actually about 260,000 years ago3 – not the mere 1,500 years ago that he has proposed.

    So Peter has got all of his blood group origins messed up, his dates wrong, and the evolutionary splits incorrect. Why does this matter and how does it affect his dietary theories? To begin with, even if we were to believe in Peter’s underlying assumptions that diets should be prescribed upon blood types, he would have to completely revamp his original recommendations. Type A’s should be eating a high protein, meat-based diet rather than the vegetarian fare he suggests. But what about type O’s? With the correct evolutionary information, should they now be eating a vegetarian menu? And what about type B’s and type AB’s – what should they now be eating? Most telling of the logical failings of Peter’s blood type diet is the observation that all four of the major blood types had evolved almost 250,000 years before the coming of the Agricultural Revolution 10,000 years ago. Yet Peter would have us convinced that three of the four major blood groups only came into existence slightly before or after the Agricultural Revolution, and as a direct result from dietary selective pressures wrought by Neolithic food introductions.

    So, why has Peter’s book become one of the best selling diet books in the past two decades? Because it works – but only for about 44-62% of the people who adopt it. Remember that for blood type O, Peter advocates a high meat, low carbohydrate “hunter” diet; with virtually no wheat, few grains or legumes and limited dairy products. If we look at the frequencies of the four major blood types for the entire world population, blood type O is by far the most frequently occurring version. It is found in 62% of all the world’s people, followed by A (21%), B (16%) and AB (1-3%)6. In the United States, the four blood type frequencies are O (44%), A (42%), B (10%) and AB (4%)7. So you can see that Peter has essentially advocated a diet similar to the Paleo Diet for between 44 and 62% of his readers. Quite simply, Peter’s diet works for about 44 to 62% of the people who adopt it – not because of their blood type, but because it emulates the same diet that natural selection has designed for us all.

    1.D’Adamo, P. with Whitney, C. Eat Right 4 your Type: The Individualized Diet Solution to Staying Healthy, Living Longer & Achieving Your Ideal Weight. Putnam’s Sons, New York, 1996.
    2.D’Adamo, J. One man’s food–is someone else’s poison. R. Marek Publisher, 1980.
    3.Calafell F, Roubinet F, Ramírez-Soriano A, Saitou N, Bertranpetit J, Blancher A. Evolutionary dynamics of the human ABO gene. Hum Genet. 2008 Sep;124(2):123-35.
    4.Saitou N, Yamamoto F. Evolution of primate ABO blood group genes and their homologous genes. Mol Biol Evol. 1997 Apr;14(4):399-411.
    5.Lalueza-Fox C, Gigli E, de la Rasilla M, Fortea J, Rosas A, Bertranpetit J, Krause J. Genetic characterization of the ABO blood group in Neandertals. BMC Evol Biol. 2008 Dec 24;8:342.
    6.Mourant AE, Kopec AC, Domaniewska-Sobczak K. The Distribution of the Human Blood Groups and other Polymorphisms. Oxford University Press, London, 1976, p. 6.
    7.Stanford School of Medicine, Blood Center.


  224. This is great, now hurry up with the follow-up articles, ‘k?  😉  No, really, I am dying to hear what you have to say.  I recently went off synthroid b/c I didn’t want to be on meds.  My TSH went back up but T3 and T4 held steady (I hope i have the right hormone terms there) and my doc said it means my body is fighting hard.  I have been having trouble losing weight, even though I’m exercising regularly and writing down everything I eat and trying to stay away from carbs and sugar.  It’s very frustrating.  I have energy though, so I hate to go back on the meds.  I hope you will have a better solution for me.

  225. If I remember correctly, for the blood type diet, types O, A, and B (which is almost everybody), wheat should be cut out of the diet.  If a lot of people cut out wheat, it would not surprise me if a lot of them felt better.  Most people do better without wheat, regardless of blood type. 

    As a type A blood type, I am supposed to avoid meat and tomatoes because my supposed ‘weak stomach’ can’t handle them, but in reality, I feel weak and suffer from anemia if I don’t eat lots of meat.  In fact, I can eat tons of meat with zero digestion probs. I can also eat hoards of tomatoes all at once with zero ill effects.  The only thing I can’t digest is corn, although it does not make me sick, just simply does not digest at all (comes out in the EXACT same form as came in which is kinda creepy!)   The blood type diet totally does not apply to me.  Ironically, my physiology works well with what they say type Os should eat.  I would not be surprised if many of the type Os who ate the type O diet did well on the diet by avoiding all those grains.  But I suspect that other blood types would also do much better if they ate like a type O.

    • That’s exactly my experience with the blood type diet (both personally and with my patients). It works for Type O’s, but not for the other types. That makes sense, because the Type O plan is closest to our evolutionary diet.

  226. I would also like to know how Acetyl L-Carnitine effects the thyroid hormones, if you know, Chris. I read something about it. I was taking that and started feeling fatigued, so stopped, and not fatigued now. I was using it to improve my aging mental abilities.

  227. I wish I had read through the other comments here because blood type was discussed. I’m type B, so no correlation there.

  228. I’m 80 years old. Unfortunately, I’ve had hypothyroidism since early twenties, so I’ve taken the artificial hormone, Synthroid, for so long that it’s the only thing I can count on. I can’t fight the disease by better health alone, which is where the author of this series is going to take it. But, it is a good thing to know for young people, so they don’t ruin their health with an autoimmune disease. This is especially true if it runs in families, such as mine. It can take different forms.

    My great grandmother was hyperthyroid with a large goiter. I wish I had her energy without the other hyperthyroid symptoms.

    • you really would not want what your grandmother has i wouldnt wish that on anyone as i almost died from hyperthyroid 3 and a half weeks ago ive been over active for 20 years and the probs that come with it is just to much for one person let alone my family as i have 2 young kids 12 yr and 2 yr and im still in shock that my life almost came to an end because the thyroid doctor took me off my meds 3 years ago after telling me the meds im on are not life long and that was that untill the 10th of april 2013 thank god i was staying with my mum when i passed out on her bathroom floor my hole body shut down before i got to A&E and died many times on the way to hospital i was in I.C.U for over a week and when i woke up i didnt no what was going on all i wanted was my kids

      • I shutter to think of how many practicing physicians , not specialist, are reading minimal testing done for suspected thyroid problems and treating or NOT treating because of being ok with the patient living at the LOW end of the scale on the thyroid chart. I wonder , what would they treat themselves with , if the realized they had hypothyroidism or just as bad ,hyper-thyroidism. Hmmm…..makes you wonder a bit.

  229. I was diagnosed with an underperforming thyroid when I was 12 and was never treated. I have now a thyroid that is the size of a 7 year old child. I complained about digestive issues, weak immune system and depression and lethargy. I am taking levothyroxine and have never felt better. Now if this shortens my life so be it but I fell alive .
    I would like to add that I had a grandmother that suffered from hypothyroidism, she had a goiter, she was menopaused before the age of 40 and lived unmedicated a couple month short of 100 years old. She didn’t suffer from dementia and was physically able. I don’t care to live as long and she actually didn’t either.
    So I deducted from that that hypothyroidism doesn’t kill you but makes your life miserable.
    I am skeptical about the thyroxine but I know it made a difference for me.

    • No reason to be skeptical about thyroxine. It can be an essential part of successfully treating hypothyroidism. However, if the underlying immune imbalance isn’t addressed, thyroxine won’t be enough for most people. Or it will be for a short time, but it will stop working and the dose will need to be raised. See the other comments for examples of what I mean.

  230. How long did you try eating for your blood type? Have you really read the specific book I mentioned?
    I am not Peter D’Adamo. I do not pretend to know everything there is about this diet and how or why it works, nor do I agree with absolutely everything he says. But I believe there IS something to his theories. I myself was astounded by the research in this book. The parallels between blood type, food and disease were impossible for me to ignore.
    Thank you very much for your responses and for this wonderful blog.

  231. I have read the books and tried it myself.  It was one of the first “special diets” I tried. The fact that it has helped some people doesn’t mean anything on its own.  If they’re switching to his diet from the SAD, for example, we can’t know whether it was his blood-type diet that helped or whether it was simply eliminating junk foods.

    Please show me the research that supports it.  There is only research that supports his classification of foods into different categories, but nothing that supports the idea that people with different blood types actually require a different diet.

    From an evolutionary perspective, it makes far more sense that humans evolved to eat a particular diet.  This diet is the one humans ate for hundreds of thousands of years prior to the advent of agriculture and modern food processing.

  232. Yes, yes there a lot of d’Adamo haters. I did not believe in it AT ALL at first. However have you actually read his book? Such as “Eat Right For Your Type Complete Blood Type Enclyopedia” ? Have you tried the blood type diet yourself? Do I believe that the blood type diet is the right thing for everyone on the planet? No. But I do believe it would help most people. It is not true that there is ”absolutely no research to support it.” You can read more about how the blood type diet has helped people all over the Internet.

    • There is a lot to the blood type diet – people usually only look scantly at the first) so people reviewing it can’t be bothered or just don’t have time to look into it properly. They just reasearch what others have said on the net (who have vested interests)…

  233. Interesting article. There is so much about the body that we do not fully understand. However, I do know, that iodine HAS and DOES continue to help people who are hypothyroid, and even hyperthyroid. I do not believe it is THE only and final answer. I believe that one form of supplement containing iodine is not one-size-fits-all. For instance, my body does best with a liquid Dulse supplement, and others with Kelp, and others benefit from Black Walnut, or something like Atomidine or Lugol’s solution. My thyroid was hyperactive, and taking liquid iodine along with magnesium brought it back to normal. I know a woman who cured her hypothyroid, that she had for more than decade, with iodine. One cannot simply say “Iodine makes autoimmune thyroid patients worse” because maybe for a few, it would cure them. Probably for some people with thyroid issues, iodine will not help them at all, but removing whatever is in their environment that could be toxic to their thyroid will.  Every person is different. Of course, treating the thyroid must involve treating the whole body and lifestyle because everything in the body is connected. I also believe strongly in the Blood Type Diet now, although I was a skeptic of that at first. Type O blood type are more disposed to having autoimmune thyroid disorders and for being hypothyroid. Things are NOT ONE-SIZE-FITS-ALL.

    • Iodine will help patients with iodine deficiency, but will generally harm those with autoimmune thyroid disease (AITD). I will explain this in further detail in future articles.

      I can’t agree with you on the blood type diet. There’s absolutely no research to support it, and the explanation he offers is based on completely inaccurate information. The most glaring example is that d’Adamo claims type O was the first human blood type, but phylogenetic networks of human and non-human ABO alleles show that the A gene was the first to evolve. You can read more criticism of the blood-type diet all over the Internet.

      • What about someone like me who tested low iodine with antibodies in the thousands?
        My Dr has me on a drop of lugal’s per day. Treating my low progesterone with a compound rx for 2 months along with selenium, Bio D & B12, before starting a compounded thyroid rx.
        She also has me using castor oil on a cloth on my thyroid daily.
        I’d LOVE to hear your thoughts! xx

    • the more I study blood type/genetics the more I see the myriad variations possible for every individual alive. No two people really are the same. Also following blood type diet (and knowing some basic prinicples of what to eat and why behind the diff blood types) really works well for me.

  234. As someone with Hashi’s and excess reverse T3, I’m looking forward to your next article. Good luck with your exams!

  235. Can’t wait until the next post. What is going to be the answer? Maybe thyroid hormone replacement agents such as levothyroxine or desicated thyroid extract? No, surely not. Does it have something to do with soy or grains? Give us the answer soon. VBR Hans

  236. Hi Chris!  I love reading your blog.  I am hoping that in this series you will also address Graves’ Disease.  Good luck on your exam.

    • Some of what I write will be relevant to GD, because it is also an autoimmune thyroid condition. But I’m not planning to address it specifically. Just not enough hours in the day. Check out Elaine Moore’s book and website on Graves.

  237. Regardless of whether you agree or not, there is a large amount of evidence supporting the connection between increasing iodine intake and autoimmune thyroid disease.  I will present it in a future article.

    We cannot draw conclusions based on the experience of one person.  Human physiology is far too complex for that.

  238. Chris,
    I do not agree that there is much evidence of this. Lugol was used in large doses in the past and Hashimotos were not higher prevalent than it is nowadays.
    I do not have a compromised immune system. Other than Hashimoto, I never get sick. I do not even remenber the year I got my last flu.
    And my T-cells are normal. They rised right after I extracted my amalgams, but now are lower than they were when I was diagnosed with subclinical Hashimoto and started with Lugol.
    And, also, I don’t have any Hashi symptoms.

  239. It’s not a myth.  If you understand the physiology of autoimmune thyroiditis, it’s clear why iodine would cause problems.  I will be writing an article on this soon.

    The weight of evidence supports this, Mario.  It’s all over the scientific literature.  I’ll be providing references to these studies in the article.

    Antibody levels are not indicative of the progress of the disease.  For example, low antibody levels may indicate that the immune system is so compromised that it can no longer produce antibodies.  Conversely, there are cases where a patient’s symptoms improve while their antibodies increase (as their immune system gets stronger).

    Basic immunology also tells us that antibodies are not an indicator of tissue destruction. They simply tell the immune system which antigens or tissues to attack.  They don’t do the attacking.  That’s the job of the T-cells.  So high antibody levels don’t necessarily mean more tissue destruction, and low antibody levels don’t necessarily mean less tissue destruction.

    There are so many myths out there about autoimmune thyroid disease.  These are just two of them.

  240. Chris,
    While I would agree that iodine is not a alone solution, it’s far from inefective. Here, in Brazil, all water have chlorine and fluor. Greenpeace have analyzed the dust on houses here and, like USA, there is too much contaminants, bromine among others. A high iodine dose have been proved to help us to excrete this endocrine disruptors.
    But, it’s not a solution per si. I, for one, have been eating a lacto-paleo diet, extracted all my mercury filled amalgams, take 50mg of Lugols, 100ug of selenium, 4000 UI of vitamin D3 when I can’t get it from sun and take 4.5mg of this FANTASTIC medicine: LDN (
    My antibodies are getting lower and lower every time I measure it. The only time it rised was right after I extracted my amalgams. Rised for 3 months and then started again to lower.

    • Mario,

      Iodine may be a solution for people who have hypothyroidism caused by iodine deficiency, but it will make things worse for Hashimoto’s patients. Why? Because iodine upregulates TPO, which is the enzyme that Hashimoto’s patients are producing antibodies to. This means that iodine will increase the autoimmune attack of the thyroid in these people.

      Population-based studies demonstrate that as iodine intake increases, the incidence of autoimmune thyroid disease increases commensurately. This is a little known fact in the alternative medicine community.

      • So good to see you have written this, Chris and explained why. You’re absolutely right that so many of the alternative medicine community haven’t “gotten” this. I’ve copied your explanation and will put a link to this page on the sites I have as Facebook friends.

      • I have always heard to stay away from Iodine for this reason. However, after reading much from Dr. Brownstein, I am learning that yes, iodine uptake alone is like adding gasoline to a fire…but when taken in conjunction with the supplements calcium, magnesium and selenium, it does not increase the autoimmune attack of the thyroid (as iodine alone does). Are you saying this is false? Taking the iodine has helped me with breast cysts and overall breast health. However, I have to be mindful of the Hashimoto’s. Thank you.

      • I have Hashimoto’s and I saw a video that the doctor says we can not supplement with organic iodine but we supplement with Lugol. what do you think?

  241. I have a question. I was diagnosed with Hypothyroidism in 1997 and have been on Synthroid since then.  My doses started at 75mcg then escalated to 100, 125, and here in the last 6 months I have gone from a steady 200mcg  to 212 mcg and just recently 250mcg.  I am concerned as to why the sudden increase in my dosage.  I know that the levels must require this, but why?  Just wondered if you could advise. Thanks,

    • Sherry,

      I’m sorry, I can’t answer specific questions about individual cases. Thyroid physiology is complex. I would have to do a thorough intake and evaluation to know why you are needing that kind of increase. One possibility, as I discussed in this article, is that you have Hashimoto’s and your immune system is increasingly attacking your thyroid. This would cause a worsening of your disease in spite of increased doses of thyroid hormone. I’ll be covering this in the next article.

  242. What a fantastic post!!

    Thyroid is so complex. Adrenal issues, omega-3, omega-6, vitamin D, estrogen, etc appear to all play in as well. I look foward to your thoughts!!  I agree that none of the testing for auto-antibodies nail the problem. We can have auto-antibodies to ANY of the deiodinases, lack a mineral or vitamin B for conversion T4 to T3, or thyroid receptors are can be blocked. Also, I’ve been very curious about the role of rT3. So many things are appear to put humans into ‘hibernation’ where rT3 is formed and all metabolism slows…

    Yes, I have been tested multiple times with no indication of antibodies.
    Further.  I have been on 4.5 mg LDN (low dose naltrexone) since May, 09.  If you are not aware, LDN modulates the immune system and has positive effects on Hashi for the obvious reason that it is autoimmune.  In my case, during this time my Armour 60 was increased to Armour 75 (compounded).  In my opinion, I should move up to Armour 90 as I have almost no eyebrows, eyelashes, body hair, etc.  My doctor disagrees as he thinks my numbers for TSH, T3 & T4 are perfect.  So far, he’s winning.
    Apparently I’m in a small and lonely group but will look forward to your article re non-Hashi hypothyroidism.

    • Apparently in the good old days before all these fancy Thyroid tests you mention above were developed, thyroid specialists used to prescribe Thyroid medication in accordance with the symptoms (fatigue, reflexes etc.). A lot of the facebook groups I peruse e.g. Stop the Thyroid Madness and Thyroid Association of New Zealand think that’s a good idea and it’s a shame that it’s no longer being done. I think those groups recommend your FT3 and FT4 be in the upper third of the normal range.

    This is all well and good for people who have Hashi & antibodies…But you glossed right over those of us who are plain-old, straight-out hypothyroid.  No Hashi, no antibodies.

    • The focus of the article is Hashimoto’s and the 9 out of 10 hypothyroid patients that have it. Have you had multiple antibody tests? A single negative result isn’t sufficient. The immune system can be so depressed that antibodies aren’t being produced. Patients with hypothyroid need to be tested at least twice for antibodies to rule out Hashimoto’s.

      That said, I will be covering some hypothyroid patterns such as under-conversion of T4 to T3 and decreases/increases in thyroid binding proteins that are relevant to people without Hashimoto’s.

      • Hello,
        I have been reading your posts and I haven’t found any dealing with someone who has had their thyroid removed because of Graves and now has a problem with their levithyroxine leveled and staying leveled. The first two years my medicine seemed to stay level then it crashed as if I wasn’t taking my medicine. Then we upped the dose and I was good for about 6months. Then another crash we repeated and again it lasted for about six months then when my thyriod levels crashed so did my B12. My B12 was so low I had to get shots twice a month. This time my thyroid crashed again in 4 months (again like I wasn’t even taking my meds, my doctor asked if I was miss a lot of them. I take them like clock work because if I miss one that same day at about 2pm I am no good. I just want to sleep. Also I take my pill on an empty stomach and I don’t eat till about 2hrs later) and we increased the dose. That increase only lasted about a month. I just got the call that my tests came back low not as low as before but we took the tests faster this time then before. We are going up to 200 now. I’m so tired of this. I’m asking to go to a specialist but I don’t know if it will be approved. Your help would be greatly appreciated. Thank you.

        • Well, I can’t say if my thyroid was removed for the reason you spoke of, but I did have mine remove. My doctor, Dr. Hunter, whom I’m sure has passed on, said the youngest person he had ever did surgery on for removal was 12 yrs. old. I was only 4 yrs. old. I do have the hypothyroid and because of no medical ins. and no $ I have not been able to take my medicine. I have actually lost weight, which was needed, sleep lousy, but tired a lot. I know I should be taking it but until I can afford to get them what are the long term effects (if any) of not. Otherwise, I feel fairly good. I am now 52 yrs. old.

          • I also have no insurance. I am on Natur throid 65 mg and just had my Rx filled at Walmart – 3 mos for $17. They have a discount for no ins. be sure to mention it.

            • Actually, they have the generic version of synthroid called Levothyroxin, if that is something that works for you, it only costs $10 for a 90-day supply. The generic list is available to everyone, even without insurance. You can ask them for the generic prescriptions list.

        • Vanessa – did you ever get this resolved? I am running into the same thing where I feel better initally and then several weeks later crash and feel just as bad as before I was taking it.

          • Hey nuttmegs… I’m searching madly for info on people like myself who do thyroid interventions that work, and then leave them crashed… please let me know if you find anything!

        • just a suggestion: I had my thyroid removed 35 years ago and it seemed that my synthroid 200 just wasn’t working anymore, at least that is what I told the doctors. They tested and said it was OK. I was also having some trouble with my stomach and seeing that it is not working properly , how would my synthroid be able to be absorbed properly.
          I have been on a lot of antibiotics over the years , for numerous problems, chronic sinus infections, yeast constantly…..and even if I ate a properly sized meal, it felt like I was never full and always hungry. Question: What would cause this…..suggestion; Parasites…..they rob you of any nutritional value from your food, so you may eat enough , and the right foods, but if they rob you of your nutrients…vitamins and minerals , how could a person possibly expect their bodies to function properly. If the parasites are quite invasive…they can migrate to other organs as well……Liver cleanse….Parasite Cleanse….garlic….etc. I had horrible stomach pain when eating and instead of taking acid reducers..the next time I started taking Organic Apple Cider Vinegar( with mothers listed on label) just before I ate anything. Amazingly..It wasn’t that I had too much acid in my stomach…but rather..It seems I didn’t have any. Even my hair started growing healthily again. If you start this protocol, buy some ph test strips and check your urine, you will find it will bring your ph levels back up to normal. Strange but true…….Interesting huh. I couldn’t get any answers about why my thyroid pill wasn’t working effectively ….so the next place to look was the area where it was processed in the body…….I’m not a doctor …just another person with a similar problem..iNCIDENTLY, I had been bitten by a tick, infected with Borrelia Burgdorferi …around the time my thyroid started malfunctioning. Maybe , just out of curiosity check out the symptoms list for lyme disease and it’s co-infections.. Then call Dr. Murakami in Hope BC for what to do next,, should you find similar symptoms to yours in the check list. The endoctrine system is complex and connected in some fashion to all functions in the body. There is help ,if this is the case

        • Vanessa,
          I am amazed! Did you say that your thyroid was surgically removed because you had Graves disease?
          Best….I had Graves disease years ago also.

      • re: Hashimoto’s disease / Antibodies / MS

        Dear Dr. Kresser,
        I’m 47 and have been diagnosed with MS since May 10, 2006 and have been taking Tysabri. I just recently tested positive for the JC Virus and going soon to be tested for the Varicella Zoster. They have taken me off the Tysabri. When I was in highschool I was told that I was Hypoglycemic and given Iodine to treat. As I was very young and no real symptoms I discontinued the iodine. You mentioned that Hypothyroid / Autoimmune disease Hashimoto’s can attack the thyroid but other areas. I’m curious if this Hashimoto’s may have been in my system and caused damages to my Mylen sheeth (Brain Lesions) or activated the JC Virus in my system, therefore causing damages and spinal fluids to indicate Multiple Sclerosis. I’m going through tests to determine if PML exists and get a green flag to start a new MS treatment Gilenya. Do you think my neurologist should run the blood test for the Hashimoto antibodies? I do plan on asking him about it, but just wanted to see what your thoughts are on this

        • Hi Cathy

          My husband also has MS and would never use Tysabri (thank goodness youre off it) and Gilenya is also a pretty dangerous drug. To my knowledge 11 people so far have died as a result of taking it. Please consider using LDN. My husband has used nothing but LDN for 7 years and is well and his MS is totally stable. No new lesions and no flares. Non toxic and affordable. There are literally thousands and thousands of people all over the world taking LDN for various autoimmune diseases, MS people making up a huge percent of those. You have nothing to lose and everything to gain.

          • Thanks Bev,

            I do like the reviews I’ve been reading on LDN since Dr. Kresser recommended on May 8th. I never heard of LDN until he mentioned it here. Sounds so much better compared to the side effects and risks I’m reading on Gilenya. I’ll let you know what I decide and follow up here in the next couple months. Thanks again!

          • I have been on nothing but LDN exclusively for many years for my RRMS, following serious side effects from both Copaxone and Tysabri. My MS has remained stable, and there has been no additional development of MS lesions on my brain MRI’s since I started. All previous brain MRI’s have shown new development of MS lesions. Coincidence? Perhaps. But, I don’t think so. I have been following this conversation because I have just had a TSH result of 8.1. I started on supplements today. My FBS was 127 (I’ve never had elevated sugars before.) A1C was 5.5. Triglycerides 225. That’s why I was interested in your topic. Thank you for this wonderful information.

            I must tell you — in the area where I live, it would probably have been easier for me to have procured street drugs. Only one physician in our entire area will give LDN. My uncle had MS — LDN got him on his feet again, after many months of not being able to bear weight. I learned about it by following the course of his disease.

          • My neurologist at UT Southwestern-Dallas/
            MS Clinic will not entertain the idea of using LDN. Instead, they only encouraged and explained the three new oral drugs. Sigh….. all while going through the worst exacerbation ever in my 24 year history with MS.

            • My neurologist at UT Southwestern-Dallas/
              MS Clinic will not entertain the idea of using LDN. Instead, they only encouraged and explained the three new oral drugs. Sigh….. all while going through the worst exacerbation ever in my 24 year history with MS.

            • My neurologist at UT Southwestern-Dallas/
              MS Clinic will not entertain the idea of using LDN. Instead, they only encouraged and explained the three new oral drugs. Sigh….. all while going through the worst exacerbation ever in my 24 year history with MS.

              By the way, I am seeking a new appointment with another neurologist who is open to other therapies–such as LDN. I am also hypothyroid and using Armour and a small amount of liothyronine. I suspect that my recent MS flare is due to thyroid (mis)treatment when other doctors (including UTSW) insisted that I get off all thyroid meds, so I did that for about 6 months. New labs after that showed me hypo again so back on the thyroid meds. My symptoms have improved however I suspect this current horrible MS flare is partially due to improperly treated hypothyroidism, and stress of course. (I survived 3 layoffs in 6 months time!)

        • Did you know that there is a doctor in Hope BC ( Dr. Ernie Murakami ) that has tested MS patients for lyme disease ( also shows lesions in the brain) they tested positive and were treated and left their wheelchairs. True Story. Last April, of 2013 he lectured on this at the Medicine Hat Lodge ( Sammis Room) He has recently advocated for the laws to change in the treatment of lyme disease.There are many co-infections associated with Lyme Disease . I f you check out
          Check out Murakami centre for lyme disease awareness there is a number for you to talk to him directly.. Make sure you check out the sumptoms list for lyme disease . You may be surprised..

      • I am especially interested in the under-conversion of T4 to T3. I was told ,after I asked the physician directly ,if this was happening. He said yes, it seems to be the case, but I don’t know why. So ,I did some researching and am thinking of adding Cytomel to Synthroid 200. What is your take on this. And do you need T4 ( via Synthroid) if you have had your thyroid removed or could you just take T3 ( Cytomel ) ? or do the body functions in other parts of the body need the T4 irreguardless ??
        Thank you

      • Chris
        I love reading your posts. Especially interested in the problem with converting T4 to T3. Any information would be appreciated.

  245. Most goitrogens are reduced quite a lot by cooking. Eating a ton of raw goitrogenic veggies isn’t a good idea, but having some cooked is not so bad, IMHO.

  246. I have been looking forward to your info on hypothyroid and autoimmunity. Great post.
    I am particularly interested in what you have to say on follow-up pertaining to the dessicated porcine replacement therapies (Armour and NatureThroid in the US and THYROID in Canada.)
    I am also interested in having you speak about diet and hypothyroidism. SO much confusing info out there on this. I have read in various places that soy and certain vegetables in their raw form are “goitrogenic” suppressing thyroid function, such as bok choy, broc­coli, brus­sel sprouts, cab­bage, cau­li­flo­wer, gar­den kress, kale, kohl­rabi, mus­tard, mus­tard greens, radishes, ruta­ba­gas, soy, soy milk, soy­bean oil, soy lecithin, soy anything, tem­peh, tofu and turnips. And mildly so, bam­boo shoots, millet, peaches, pea­nuts, pears, pine nuts, radishes, spi­nach, straw­be­rries and sweet potatoes.
    Thanks Chris!

    • Rosemary,

      I will indeed cover those topics. It may take a while to get to them, with my licensing exam coming up, but I will at some point.

      I can tell you this briefly: the effects of dietary goitrogens are negligible. I don’t advise hypothyroid patients to stop eating the foods you listed for that reason.

      • How do I find a doctor that will do the correct testing? My daughter has hashimoto and I have all the symptoms…loss of hair, dry skin, tiredness, weight gain and depression. My family dr did the normal blood test that came back negative and an endocrinologist won’t see me without a diagnosis. I know I have a thyroid problem. I am in Tampa,Fl

        • I had been bitten by an infected tick when I was 24 and within weeks my thyroid went on the blink to the point that they said I had to have it removed. Bummer…..I would tell anyone with this prognosis to have a test done for Lyme Disease . I would bypass the Elisa test and have all the panels done from a test kit , from Igenex , in Paulo California. Then find a Lyme Literate Doctor that has helped many to recover…. It does affect the thyroid. Check it out before any surgery , because surgery means hypo thyroid for the rest of your life. and mine was Lyme afterall. I am now 59 years old and I know there are symptoms of thyroid problems with Lyme…Just saying!!!!

          • I had a similar experience, having first diagnosed with Hashimoto’s then later finding the co infections of Lyme. I’ve gotten fantastic results with essential oils and living the laws of health and have my life back but am still working on the Hoshimotos. I wish any one of my doctors had explained it was an auto immune condition 17 years ago! I would have don’t so many things different. I teach exactly what is written here and am so happy more awareness is occurring.

        • Hi Celeste, I’m in Tampa too and I see Dr Judah, Michelle in Valrico. She’s a great family doctor. I have hypo and she’s the one that diagnosed me with hashimotos. Hope this helps.

          • Hi,
            My lab result say that I have hypothyroiditis in a subclinical setting and that I should be investigated for Hashimoto’s Disease. Some reports say brocolli, bok choy, soy are good while others say they are goitrogenic. I am very confused. A doctor prescribed Synthroid 0.5 mcg – 1 pill daily which I took for 4 days until another doctor told me to stop it. I now hear singing, chanting and wailing and it is causing me so much distress. I understand that hypothyroidits, if untreated, can cause a psychotic reaction. Does anyone out there with hypothyroiditis know the answer? Thanks.

        • Keep fighting, find a new doctor. It took me seven years to find a doctor that sent me to an Endocrinologist. I went in with my own diagnosis. I told them since I am being told I don’t have a thyroid problem (even though it was running through my whole family) then I must have Adrenal Fatigue. Some how that seemed to get the ball rolling….even though first they made me extra ill by giving me all kinds of psychotropic medications. If I were you I would take in lots of articles from the internet. Be sure that you tell them these are your symptoms and that you are not applying the symptoms to yourself after you are finding them but that you were looking up the symptoms you have and everyone’s finger but the doctors is pointing to Thyroid. Then tell him many people are symptomatic before it ever shows up in your blood tests and that you are paying him and want him to refer you to an Endocrinologist and that if he doesn’t you will no longer be his patient.

        • Celeste: I suffered from hypothyroidism for 15 yrs with no diagnosis. I finally discovered that thyroid tests which usually consist of TSH only, don’t give accurate measurements. It’s graded on the curve – IOW, TONS of people have low thyroid that are undiagnosed but they still grade it on the “average” thyroid test of “normal” people – which is why the people who are slightly low don’t get diagnosed. It takes an average of 7 yrs to diagnose simple low thyroid (note: low thyroid is different from Hashimoto’s). Here’s a website that I used to cure myself:

          They help with thyroid-related disorders as well such as adrenal fatigue. I couldn’t heal my thyroid until I dealt with the adrenal fatigue first. I went on natural dessicated thyroid, NDT (Armour, Naturethroid etc.) You have to convince your doctor that you are hypothyroid and then convince him to prescribe NDT. The Synthroid and other synthetics don’t work very well, no matter what your doc says, he doesn’t know because he learns everything from Big Pharma, which doesn’t make NDT. NDT will address T3 and T4 issues, Synthroid onl addresses one of those. I believe there is a list of docs who understand thyroid on the website. Also, there is a terrific book by Dr. Broda Barnes that will tell you most everything you need to know about thyroid issues; it’s called “Hypothyroidism: The Unsuspected Illness also Janie Bowthorpe wrote a book and it’s on the website. You can get both in used books at Amazon. Also Dr. Brownstein has a book “Overcoming Thyroid Issues” and his book on iodine is excellent. I highly recommend all these books. Hope this helps; I’ve been there, I know what it’s like and it’s miserable. Good luck!

          • Emmett: you are right and you need to get gluten and dairy out of your diet as soon as possible as they cause autoimmune disease.

              • It doesn’t. Gluten and wheat can aggravate the immune systems of those with a sensitivity or allergy to it. The same goes for soy and dairy. They have been linked to inflammation, which is an autoimmune response, but they don’t have that effect on everyone. I personally have a mild soy allergy, so when I eat more than a trace of it, I get a lot of immune response (among other unpleasant things). I found out about the allergy the hard way after noshing on edamame (sp?) at a sushi restaurant one night. I also have RA, so my immune system is touchier than most. For the average person, dairy and gluten aren’t a problem. Soy, though, really isn’t a good food for human consumption. It has a lot of not-so-good characteristics.

                • Direct-MS website had some informationon Molecular Mimicry. There was a lot of research done on this in the late 1990’s. The theory goes: the body gets exposed to antigens such as viruses, the body then develops antibodies to these antigens, These antibodies attack the body’s tissues that have similar sequences of amino acids, then when an individual eats a food containing yet again identical sequences of these amino acids, the antibodies formed against the targeted tissues are mobilised to attack the tissue some more. For auto-immune thyroiditis, it’s wheat, for Multiple Sclerosis, it’s wheat (gluten), dairy (casein) and legumes!

        • Definitely find you an ENT or GP that believes you. I got my ENT to believe that I was having almost all the symptoms(which I was) and it ran in my family distantly which I didn’t even know st the time. I told him my lab work over 10 years had always looked normal, and asked if there is a chance that it could be wrong?! He said an ultrasound of my thyroid would show him definitive answers and if that came up positive then a antibodies test for Hashimoto’s disease would be the next step. I had the symptoms for 10 years and endured horrible symptoms and it made me miserable. I felt bi-polar (extremely moody), lost tons of hair, had dry skin, my thought would swell up & hurt occasionally, etc… I had nodgules on my thyroid, am extremely big thyroid, etc… from the disease. I now see an Endocrynologist and have been finally been properly diagnosed after 10 years of hell. The doctors started thinking I was crazy, but I stuck to my guns and went with my gut. Eventually it paid off lol. I went so long in diagnosed though after a year of treatment I still have many problems and permanent/irreversible damage… Is what I believe. It affected my back and lead to many other problems like Fibromyalgia that I have severe pain all over my body all the time. And have had rods and screws put in my back also bc of these doctors not believing me.

          • Lace, I also suffered from fibromyalgia until I saw an item on the internet from a man who said he had cured his by cutting out cows milk entirely. Within one week I was almost completely pain free after thirty years of intense pain. Try this,it may help you.

          • I have suffered severly from this disease.The worstpart ismy family doesn’t believe me.My husband actually said to me,”just get up and go do something ,you will feel better”. At this point ending my life is at the top of my list.

            • it used to be justthe weightngain and No energy, but now its the brain fog, thid deep depression, angry moods swings , no periods, and now these terrible body aches in my legs , feet , neck, the over all no happyness and helplessness.I cant do simple thisngs like I used to, even spell. my husband hates me now and doesn’t think there is anything wrong with me, only that Im a crazy bitch and now so do my kids, honestly I have nothing to live for anymore.My husband said everybody would be happier if I leave, so its probally best!God help me

              • Stefanie,

                Do not give up hope. Contact as many endocrinologists as you can then. Look on Dr. Kharrizian’s website for doctors in your area who specialize in thyroid treatment. Google thyroid doctors and specialists in your area and if there are none, reach out to others in surrounding areas and let them know your symptoms (maybe leave out the family stuff for now so they don’t think it could be other factors). I found even e-mailing doctors out of state helped me. They have networks and can steer you in the right direction. ALSO, if you haven’t already, CHANGE YOUR DIET. No gluten, soy, dairy. I went even further and follow the Paleo Autoimmune Protocol. Google it and follow it immediately. If you are 100% serious about getting better, follow a strict diet and you can get better (I have hashimoto’s and it ruined my life). Maybe sit down with your family and tell them, you are not well and need help but you appreciate their support and one day you will be healthy and happy again.

              • Stephanie – You might consider going to a Naturopathic Doctor (google one near you). Mine ran a full thyroid and autoimmune panel, which is how I found out that I have Hashimoto’s in addition to low thyroid function and low free T3. My pharma doc only ran the basic tsh test yearly and prescribed levothyroxine for 10 years. Once the ND and I found out that my thyroid was also producing antibodies to “something” we ordered the next logical test – a food allergy panel. Here I found out I was allergic to eggs, which may be a cause of my antibody production and attack on my thyroid. I was eating eggs several days a week (or products with egg in it) and since omitting feel so much better. One must be diligent and read labels to avoid those products! I was also deficient in vit D3 which (another cause of tiredness, aches, and pains). The ND has me on D3/Vit K2 drops. Vit D3 and K2 work in tandem, so are good to cover together. I will be testing again after a several months of being egg-free and nourishing my deficiency to check on levels of improvement.

                All is not lost for you! Find a good Naturopathic Doctor (ND). They understand the need to find and treat “root cause”. Pharma docs and specialists only treat our symptoms. Chris Kresser provides a wealth of information on running your own tests too. We don’t need a a doc lab slip to do so:

                Take action for your well-being. Good luck!

              • Stefanie,
                Please don’t give up! I know it is frustrating when your doctor doesn’t listen to you and you feel like you can’t get help. And your family not understanding has to be awful. I have hypothyroidism and before I realized I had it I was so miserable, physically and emotionally. It makes you depressed. I have been having other medical problems lately and can’t seem to get a specialist to take me seriously. I don’t know where you live but if you have access to a larger hospital system, I live an hour from the Cleveland Clinic, maybe you should try a doctor affiliated with them. I know several people who have more success with getting answers by going to the Cleveland Clinic as opposed to the doctors closer to my home. I have an appointment there in early July. So I am praying they can help me. Hang in there. Please don’t take your life it isn’t worth it. Some doctor will help you

              • I felt the same way about 2 weeks ago. I was asked to sign my name and actually had to think for a min. Research adrenal fatigue. I did and got some adrenal support supplements and I feel 100% better and it only took like a week to tell I was feeling better. I even had the allergies. Sneezing all day coughing all day now I don’t even have that anymore. It may be temporary but I’m just thankful to feel good for the moment. I have been diagnosed for a year with hypothyroidism.

              • Stephanie- Please don’t give up! Many of us experience/experienced most of the same feelings you’re experiencing, and we know that it is very difficult to find understanding and compassion at times. Taking one day at a time is extremely important, as well as taking charge of your health- physical, mental, spiritual, and emotional. We sometimes have to be our own cheerleaders and encouragers. I appreciate and applaud your bravery for openly sharing your true thoughts and pain. I have a sneaky suspicion that you articulated what many sufferers feel but feel ashamed or maybe embarrassed say. With heartfelt empathy, this too shall pass!

          • My story sounded like the first half of yours. Did you find out if you had Hashi’s? I don’t, yet still have all the symptoms, even though my tests come back wnl, just not optimal. What finally got you on the right track?

        • Hi Celeste,
          I do not know of a specific doctor I could refer you to in Tampa, but I think you might have better success looking for a chiropractic physician who practices functional medicine rather than limiting yourself to only consulting with medical physician. Most chiropractic physicians trained in functional medicine will know what to do and there are many of them in Florida. Keep in mind too that most conventional doctors not only do not run all the thyroid tests needed, they use the regular laboratory reference ranges to help determine “normal”. These ranges are too broad. Your lab test results could easily run within the regular lab ranges but be significantly outside the optimal function ranges, so your hypothyroidism could still be missed with even running all the right tests. If that happens in your case, most Endocrinologists will conclude you do not have a problem. Also be aware that even if your thyroid antibody tests come out “normal” you could still have an autoimmune problem. I expect Kriss will be getting in to all of this in future posts.
          Hope this helps.
          Vernon Redd, DC, APC

        • There is a great thyroid doctor in Panama City, Florida and you can self refer. He has the diabetes, thyroid and Endocrine Clinic. His name is Dr. Sheriff kamel. I heard about him on a thyroid blog. I live in the upper west most part of Florida and this doc is worth the trip.

      • For someone suffering from hypothyroidism, do you recommend cooking the goitroenic foods a little prior to eating or do you think they’re okay to eat raw?

        • They say to cook Cruciferous vegetables before eating as it reduces the goiter factor in them. I have to say I have been eating most of them raw for my whole life and have not developed any nodules or goiters. I am sure it is like everything else. For some it’s okay and for others they end up with growths and goiters. I say mix it up. That way you are not doing to much raw, but you can still enjoy the flavor of the raw on occasion.

      • Does anyone have a firsthand account of using Anatabloc for treating thyroid symptoms? There’s been at least one apparently successful human trail so far.

        Anatabine supplementation decreases thyroglobulin antibodies in patients with chronic lymphocytic autoimmune (Hashimoto’s) thyroiditis: a randomized controlled clinical trial.

        Results: Anatabine-treated patients had a significant reduction in absolute serum TgAb levels from baseline by study end relative to those receiving placebo (P=.027); however, there were no significant changes or differences in treatment group means for TPOAb or TgAb levels. Mean±SD TgAb values decreased by 46.2±101.1 and 3.9±83.9 World Health Organization units for the anatabine and placebo groups, respectively. Significantly more patients had a >20% drop in TgAb levels in the anatabine than placebo group (P=.023). Overall, the anatabine supplement was safe and well tolerated, although significantly (P<.05) more patients in the anatabine group reported adverse events.

      • Thank you for sharing your knowledge about hypothyrodism. I hope and expect that you will also address hypothyrodism NOT related to auto-immunity, such as stress & adrenal fatigue and how to behave/treat under those circumstances.

      • I like the info but feel it tells people that if you have hypothyroidism you have an autoimmune disease, which isn’t always the case. I have had hypothyroidism for 6yrs now and take a fairly large dose of levo (.225 micrograms) but do not have an autoimmune disease. We definitely need more knowledge on hypothyroidism and better communication. Plus much better medical treatment. I’ve always felt Doctors , pharmacist s and people in general don’t realize the seriousness of our condition, so thanks for writing this.

    • I have Hashimoto’s and have had a full Thyroidectomy at 28 I am now 43 I have a high titer and calcium bone issues. I had to leave OC Cali to live in Canada in which left me with no health care and landed me in a world of trouble even within the US with trying to do this on my own. Remember words like Coma Adrenal Crisis and Death… Yes many of the meds are awful and quality control is not regulated but like me without insurance and without and endocronoligist I am a mess and sick! This is no laughing matter this little thing can turn into your life or there lack of one. Maybe could well land you in a mental institution as it will mimic many other disorders. Today Amor is your best bet but do not deviate from an endo, I am lucky to be alive to today instead of proper care I rec’d parkinsons meds.

        • I am wondering what I can eat since I have IBS? Is there a definative test to say, yes, you definitely have hypothyroidism? Im reading you can have this test or that, but not sure if there is one particular test or if its just a process of elimination?

          • I spent several years with a GP telling me my thyroid was normal. But the range for a standard blood test is huge and therefore not very accurate unless your thyroid disease is raging out of control.
            I was finally seen by an endocrinologist who performed a TRH Sensitivity Test.
            Kind of like the gestational diabetes test they do when your you’re pregnant.
            The TRH test involves drawing blood samples to measure TSH and then giving an intravenous injection of TRH to stimulate the pituitary gland to release TSH. The TSH is measured after the injection at various intervals.
            The standard test says 15, 30, 45 and 60 minutes. By measuring the response of TSH to TRH, one can usually tell whether someone has an overactive or underactive thyroid. When I had that test, the endocrinologist told me I have chronic hypothyroidism. And was able to start medication. Suprisingly, I’ve met several Gp’s who don’t know of this test. But any good endocrinologist will know of and utilize this test.

          • My son wne through a debilitating year with IBS. ER visits, doctors, changing diet, etc.
            We found out that it is widely believed that IBS stems from psychological trauma or stress. A lot of people who suffer from IBS have depression. My son went to a psychologist and they put him on anti anxiety meds. Only helped a little. Then the psychologist suggsted hypnotherapy to address depression, anxiety, etc.
            IT WORKED!!!!!!All of his symptoms have disapeared. He has been symptom free for 2 years now.

          • I started seeing a nutrition specialist with a masters degree. She had me take the TRIAD test. It measures amino acids, gut dysbiosis, all of your good and bad bateria, and also identifies what you have allergies to. I did not realize I was allergic to diary, cheese and eggs. I ate eggs everyday with an avocado, thinking I was eating healthy. I also had to cut gluten and sugar to decrease inflammation and level cortisol levels for fatigue. Good Luck!

    • Hey Chris, and thanks as always for one of the best health blogs out there.
      My peroxidase result was 30, with recommended values of 0-34.

      Should I be worried? I am going for another test to see how it progress in 6 months.

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