3 Steps to Choosing the Right Thyroid Hormone | Chris Kresser
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3 Steps to Choosing the Right Thyroid Hormone

by Chris Kresser

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iStock.com/richcano

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

I often get comments and emails from people asking me which thyroid hormone I think is best. My answer is always the same: “It depends.” As much as some practitioners would like to make us believe, there is simply no “one size fits all” approach to thyroid hormone replacement.

Statements like “Synthroid is best” or “I prefer to use synthetic T4 with my patients” or “I only use bio-identical hormones” demonstrate a lack of understanding of thyroid pathology. Why? Because, as I’ve explained in this series, the underlying causes of thyroid dysfunction are diverse.

Giving all patients the same thyroid medication without understanding the mechanisms involved is analogous to not checking a patient’s blood type before doing a transfusion. Granted, the consequences may not be as severe, but the underlying principle is the same.

Before we continue, let me remind you that I’m not a doctor and I’m not offering you medical advice. My intent is to educate you about the various considerations that should be made when choosing a thyroid medication, so you can discuss them with your doctor. Understood? Great. Let’s move on.

Choosing the right thyroid medication requires answering the following three questions:

  1. What’s the mechanism that led to the need for medication in the first place?
  2. Are there any mechanisms that may interfere with the actions of the medication?
  3. Does the patient have sensitivities to the fillers used in the medications?

Let’s look at each of these in turn.

What’s the Mechanism That Led to the Need for Medication in the First Place?

If you’ve been following this series, you know that there’s no single cause for low thyroid function. Do you have an autoimmune disease (Hashimoto’s) causing destruction of your thyroid gland? Do you have high levels of estrogen causing an increase in thyroid binding proteins and a decrease in free thyroid hormone? Do you have a systemic inflammatory condition affecting your ability to convert T4 to T3, or decreasing the sensitivity of the cells in your body to thyroid hormone?

In order to choose the right hormone, you have to know what the underlying mechanism causing the dysfunction is. Let’s look at an example.

Say you have a problem converting T4 to T3. In this situation, your TSH may or may not be slightly elevated, but let’s say it is, and your doctor prescribes Synthroid. Synthroid is a synthetic T4 hormone. Will this help you?

No. It won’t help because your problem in this example isn’t a lack of T4, it’s an inability to convert T4 to the active T3 form. You could take T4 all day long, and it won’t do a thing unless your body can convert it.

The first step in this case would be to address the causes of the conversion problem (i.e. inflammation), in the hopes that you may not need replacement hormone. If that doesn’t work, though, what you’d need in this situation is either a so-called bio-identical hormone that has a combination of T4 and T3, or a synthetic T3 hormone (like Cytomel). These will deliver the T3 you need directly, bypassing the conversion problem.

Are There Any Mechanisms That May Interfere with the Actions of the Medication?

The vast majority of long-term hypothyroid patients that haven’t been properly managed find that they constantly need to increase the dose of their medication, or switch to new medications, to get the same effect.

There are several reasons for this. First, inflammation (which is characteristic of all autoimmune diseases, and Hashimoto’s is no exception) causes a decrease in thyroid receptor site sensitivity. This means that even though you may be taking a substantial dose of replacement hormone, your cells aren’t able to utilize it properly.

Second, elevations in either testosterone or estrogen (extremely common in hypothyroid patients) affect the levels of circulating free thyroid hormone. For example, high levels of estrogen will increase levels of thyroid binding protein. Thyroid hormone is inactive as long as it’s bound to this protein. If you take thyroid replacement, but you have too much binding protein, there won’t be enough of the active form to produce the desired effect.

Third, there are several medications that alter the absorption or activity of T4. These include commonly prescribed drugs like antibiotics & antifungals (i.e. sulfonamides, rifampin, keoconazole), anti-diabetics (Orinase, Diabinese), diuretics (Lasix), stimulants (amphetamines), cholesterol lowering medications (Colestid, Atromid, LoCholest, Questran, etc.), anti-arrhythmia medications (Cordarone, Inderal, Propanolol, Regitine, etc.), hormone replacement (Premarin, anabolic steroids, growth hormone, etc.), pain medication (morphine, Kadian, MS Contin, etc.), antacids (aluminum hydroxides like Mylanta, etc.) and psychoactive medications (Lithium, Thorazine, etc.).

All of these factors must be considered if a particular medication isn’t having the desired effect.

Does the Patient Have Sensitivities to the Fillers Used in the Medications?

Another important consideration in choosing the right hormone is the fillers contained in each medication. Many popular thyroid medications contain common allergens such as cornstarch, lactose and even gluten. As I explained in a previous post, most hypothyroid patients have sensitivities to gluten, and many of them also react to corn and dairy (which contains lactose).

Synthroid, which is one of the most popular medications prescribed for hypothyroidism, has both cornstarch and lactose as a filler. Cytomel, which is a popular synthetic T3 hormone, has modified food starch – which contains gluten – as a filler.

Even the natural porcine products like Armour suffer from issues with fillers. In 2008, the manufacturers of Armour reformulated the product, reducing the amount of dextrose & increasing the amount of methylcellulose in the filler. This may explain the explosion of reports by patients on internet forums and in doctor’s offices that the new form of Armour was either “miraculous” or “horrible”. Those that had sensitivities to dextrose were reacting less to the new form, and experiencing better results, while those that had sensitivities to methylcellulose were reacting more, and experiencing worse results.

The best choice in these situations is to ask your doctor to have a compounding pharmacy fill the prescription using fillers you aren’t sensitive to. Unfortunately, insurance companies sometimes refuse to cover this.

Other Considerations

Another common question that is hotly debated is whether bio-identical or synthetic hormones are best. Once again, the answer is: “It depends.” In general I think bio-identical hormones are the best choice. A frequently perpetuated myth (in Synthroid marketing, for example) is that the dosages and ratio of T4:T3 in Armour aren’t consistent. Studies have shown this to be false. Armour contains a consistent dose of 38 mcg T4 and 9 mcg T3 in a ratio of 4.22:1.

However, in some cases patients do feel better with synthetic hormones. One reason for this is that a small subset of people with Hashimoto’s produce antibodies not only to their thyroid tissue (TPO and TG), but also to their own thyroid hormones (T4 and T3). These patients do worse with bio-identical sources because they increased the source of the autoimmune attack.

Another issue is the use of T3 hormones. As we’ve discussed, T3 is the active form and has the greatest metabolic effects. The flip side of this, however, is that it’s far easier to “overdose” on T3 than on T4. Patients with trouble converting T4 to T3 do well on synthetic T3 or bio-identical combination T4:T3 products. But for many patients with Hashimoto’s, which is can present with alternating hypo- and hyperthyroid symptoms, T3 can push them over the edge. They are generally better off with T4 based drugs.

As you can see, the best thyroid hormone for each patient can only be determined by a full thyroid work-up and exam, followed by trial and error of different types of replacement medications. Such a work-up would include not just an isolated TSH test, but also a more complete thyroid panel (including antibodies), other important blood markers (glucose, lipids, CBC with diff, urinary DPD, etc.) and possibly a hormone panel.

A history must be taken with particular attention paid to the patient’s subjective response to replacement hormones they may have tried in the past.

Unfortunately, this rarely happens in the conventional model, where the standard of care is to test only for TSH. If it’s elevated, the patient will get whatever hormone that particular practitioner is fond of using without any further investigation. And all too often, as many of you can attest, this simplified and incomplete approach is doomed to failure.

261 Comments

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  1. I have had Hashimoto’s for over 30 years, first diagnosed post partum after my first child. My antibodies have stayed in about the same high range despite the paleo autoimmune protocol. My TSH has been brought to the functionally optimum range of about 1, but I have always had borderline or low normal free T4 and low normal free T3. I struggle with weight despite a carb load usually 50 – 100 grams. I wonder if I may be making antibodies to the T3 and T4, as described by Chris in the article and that is the reason I can’t get my hormones up to an optimal level. Would that be a reason? Are there any tests to determine if this is the case or does one just need to try the synthetic hormones and see how it goes? Any information would be helpful.

  2. One of the greatest moments in this world is when you see your own wife put to bed, this awesome moments makes you a man and not just a man a real man. My wife suffered from Fibroid which made her unable to get pregnant and give us a child for almost 18 years with multiple surgeries done and none seemed to help the situation. I almost gave up but due to the love i had for her because i married her a virgin i had to find a way to help her. I told a member of my church who recommended Dr. martin to me, i contacted him and he sent me a medicine and this medicine shrieked it naturally in weeks it was like magic but it’s science. I am happy writing this because she delivered yesterday a baby girl. Do not loose hope too soon contact him. i am confident he will help you too.

  3. Hi Chris
    Thank you for your info
    I was doing fine on Erfa but with high levels of free T4 and t3, (no hyper symptoms) until my Endo took me off and halved my equivalent dose, putting me on levothyroxine. It’s been horrendous. I now have a diagnosis of fibromyalgia. I recognise I had this before the natural thyroid, so I know the natural stuff would sort me out again.
    SInce all the problems with NDT fillers, I don’t know which one to try. Do you know whether Erfa is now back to normal, DEC 2016, because I used to be ok on that, but I hear it had a formulation blip.
    Does cellulose filler bind to the hormone?
    I am gluten free, plus other insensitivities (many).
    My chiropractor says that non celiac gluten intolerance can be much more difficult than celiac, and that we should avoid even corn and refined rice, all the cereals, except wild black rice. It’s so hard!
    Summary, I want to know which NDT is closest to the old formulations that were soft, i.e. Not so much cellulose. However preferably not using dextrose made from wheat! Thank you

    • Very interesting comment and questions which I hope someone can answer! I’d be interested to find out myself…I have been taking Thai NDT for the past year, after having problems with Erfa back in late 2015, and my latests labs showed midrange FT4 levels and FT3 levels out of range 24 h after taking meds. Yet, no hyper symptoms, I feel good and have much more energy. But I am not sure what ideal FT3 and FT4 levels are supposed to look like when optimally dosed on NDT; if you go to the lab 24 h after taking latest dose, I imagine they would need to be lower than if you take meds the same day you have labs done…? I read somewhere that you can count on your FT3 levels to be +/-20% higher on the previous day if you have not taken your meds before having labs done, and that FT4 levels are basically meaningless once on drugs containing T3, as only FT3 levels count…can anyone corroborate that or does T4 have a role on its own?

    • You said your Dr took you off because you had high T4 and T3. Did you take your thyroid med before your labs? If so then it will cause falsely elevated levels, especially the T3 level. Because T3 is the active hormone it loads to your system right away, do taking your med before the lab draw will show a false high level. Most Drs who understand this have their patients fast from T3 containing meds for at least 12 hrs before labs for accurate results and advise to bring it with and take it after. Dr. Isabella Wentz, Thyroid Pharmacist also has an article about this.

  4. I have been following this blog for a while now and today i felt like i should share my story because i was a victim too. I had endometriosis for 18 years and i never thought i would ever get a cure due to the terrible symptoms i had and this made it impossible for me to get pregnant even after 12 years of marriage and it was a serious issue. I got to know about Dr. Aleta who treated someone and the person shared a story of how she got a cure and let her contact details, i contacted Dr. Aleta and she actually confirmed it and i decided to give a try too and use her herbal medicine that was how my burden ended completely. My son will be 2 this december and i am greatful to God and thankful to her for medicine too. If you have (Endometriosis, PCOS, Fibroid, Ovarian cyst, Ectopic Pregnancy or any infertility issues) just reach her on (aletedwin @ gmail. com) she has professional advise and a cure too.

  5. Thank you for sharing.

    Curious you say:
    “One reason for this is that a small subset of people with Hashimoto’s produce antibodies not only to their thyroid tissue (TPO and TG), but also to their own thyroid hormones (T4 and T3). These patients do worse with bio-identical sources because they increased the source of the autoimmune attack.”

    Is there research to support this?

    My tpo keep going up or staying same on bio-identical and I am gluten free, no old fillings, good nutrient levels, have done many of the things I should do… wondering if I am one of these people and I how to figure that out.

    • I just wanted to add that I fall into this category- I was on synthetic t4/t3 and had much better/stable numbers- when I switched to NDT, no matter how much we tried to increase the dose, my numbers just tanked! I have a large clustering of autoimmune diseases- have to get most medications compounded due to filler issues and my immune system just destroyed the NDT! It is rare, but does happen! I am now taking Tirosint with compounded t3 with better success!

  6. Hi all, 31yo M, 5’9 135lb. I was just diagnosed with hypothyroid by my ND. Low T3 (.6!), high LDL, low alkaline phosphatase, low HCT, low RBC/WBC. What my ND told me is basically border-line anemic (but my iron levels are great) and need to take Cytomel. This is after a 10year battle trying to figure out my IBS, with IBS-A and constipation. The thing is I’ve been losing weight, have enormous stools (lots of undigested food), but otherwise feel fine. Stool tests also reveal complete lack of ANY good bacteria (no SIBO). So I’m wondering if Cytomel to fix thyroid is enough, or if I need to supplement with selenium, iodine, etc. Unlike typical hypothyroidism, I don’t have weight gain (in fact WEIGHT LOSS) but have mild coldness and mild brain fog/tired. This all started with trying to regulate digestion so I wasn’t spending 1.5hr in bathroom daily, and now it’s progressed to thyroid! Thoughts?

    • Yes get a LYME & Babesia panel done at IGENIX or MDlabs.com . Insurance won’t pay so don’t ask. Lyme attacks white cells, Babesia attacks red cells. They usually are in same insect & act synergistically to make you ill. Fibro, cfs, allergies, gastro problems, thyroid etc.

  7. Hi Chris,

    I had a thyroidectomy in April 2015 due to cancer. I was first on Levothyroxine 100 but my menstrual cycles were very heavy and nonstop. I then developed anemia. My tsh was over 50. The doc then put me on Synthroid 125 which was ok, but my tsh was 22. The dr increased the Synthroid to 137mcg but it gave me joint pain and fatigue. I had to quit tennis and hiking. My knee blew out and feet swelled, but tsh was 9. My joints are a mess. I tried switching to NatureThroid 150, but the dose was too hard on my heart and felt like I was having heart attack. Now I am back to Synthroid. Any advise? I feel like these doctors don’t care (I have been to 3 endos). I wish someone would have told me what the aftermath was like because I wouldn’t have had the surgery. Another 10 years of a good life is far better than 20-30 of being miserable.

    The best I felt was on Synthroid 125 but the docs wont let me go back down on dosage. Doesn’t quality of life count for something?

    I keep wondering if there is a good way to convert to Naturethroid that doesn’t hurt your heart such as starting on a low dose and moving upward slowly? I think 150 was way too high. Any thoughts?

      • Tirosint caused me severe problems – I developed Parkinsons type symptoms and severe brain fog within three weeks of Tirosint usage. It made me severely dizzy, off balance, shaky with severe tremors.

        EEI would stay far away from it for me. Each of our bodies are sooooo different and it does not mean that it will work for all of us. Best to allow your body to tell you what it is that works for it.

    • Im sitting here in awwwwe, Ive had my thyroids removed 12/13 and each year feels worse than the first. My hair is so brittle, breaking. My knees started popping and cracking about 7 months or so ago. Im sluggish & depressed. I weigh the most I’ve Ever. The only thing my endocronoligist is doing is “regulating” my medicine. Well after reading and researching im going to see Hormone Dr.

      • Kate,

        You should try Levothyroxine, the generic hormone replacement. It is not comparable in dosage to Synthroid and it may work for you.

        Good luck!

        Vertrell,

        Have you thought about changing your diet and going gluten free? Here are some books that provide lots of information about diet and autoimmune diseases. THE GLUTEN FREE EDGE; IT STARTS WITH FOOD; THE WHOLE 30; just a few. It will help with controlling your cholesterol also.

        • Tirosint is the only thyroid hormone I could take. It is not generic. I too had a thyroidectomy due to a huge goiter. They tried me on Levothyroxide and it was a disaster. So my endo suggested I use Tirosint. It has been a blessing!!! I feel like a normal person now. Ask your doctor about it… Also google it! 🙂 Hope this helps!

    • You were started on too high a dose of ndt. It contains T3 and this can be a shock to the system. You have to work up slowly. Look at the Stop the Thyroid Madness website for advice.

    • You always start low on synthetic or armour thyroid. Read the Book by 14 M.D.s called “Stop the Thyroid Madness” – they are proponents of Armour thyroid. You can check out the website as well.

  8. hi chris, I had complain of fatigue for almost 6 years and tender points all over my body. chronic aches increase after exertion , sometimes rest may help sometime not. I had workup for thyroid,SLE,addiosons,connective tissue disorder. hypothyroid diagnosed 4years back ,m on thyroxin 75mcg since 3 years in past on 50mcg for one year. bt still have all the symptoms.
    recent labs are
    serum tsh= 2.517ulU/ml
    ft3= 2.61 pg/ml
    ft4= 0.97 ng/dl
    cholestrol= 338mg/dl
    uric acid 7.8mg/dl
    anti TPO= 0.65 lU/ml
    TG= (not done yet)
    HBA1c= 6.18 (a/c tp lab 18 is normal.
    u/s shows lipid deposition in right kidney uper pole.
    Also having pcos (hormones derranged LH,insulin,prolactin).
    facing difficulty to conceve (married since 8 months)
    In past= having vitiligo, tonselectomy..
    i thinks its more than enough for disturbing u, feeling sorry for such a long post. please help..! God bless u

  9. I am on Naturethroid. Before that, Synthroid. For years my doctors have been unable to stabilize my thyroid results. I’m either extremely hypo or hyper, never normal. I had RAI in the 80’s. Recent results show a high T3, so doc is having me reduce the dose again. Any thoughts?

    • Hi Nancy. I’m having the same problem as you. I was on Synthroid for hypo and it made me hyper and extremely ill. So, I went off the Synthroid for 2 months and I became super hypothyroid. My TSH shot up to 95. My new doctor put me on WP thyroid and now I am hyperthyroid again. Had blood work done on August 10 and results showed my TSH is 0.13 and my Free T3 is high. My thyroid peroxidase antibodies are also High at 112. I ended up in a cardiologist’s office last week due to heart palpitations and chest and back pain. Had an EKG and I have Premature Ventricular Contractions. I am having chest tightness and fullness, sharp shooting pain behind my eyes, anxiety through the roof, interrupted sleep, my pulse is up to 83 and resting blood pressure has gone up from 112/78 to 142/90. My doctor can’t seem to get my levels to normal range and is going to lower the dose again. I’m either hypo or hyper. I am also looking for answers. I hope we can find one soon. I can’t take this. It’s really taking its toll on my body, not to mention my psyche!

    • I kept looking for answers to WHY my body could not convert T4 to T3? This conversion happens primarily in the liver. I’m still unraveling the puzzle. Getting genetic testing done may help to determine if you have a metabolic issue (like MTHFR – estimated 30-40% of the population has a genetic polymorphism in this area) or you’re missing an essential nutrient causing the metabolic issue. What this means iSync are either not getting a specific nutrient OR somewhere in the body, the intake level of the nutrient can’t be converted into the level your cells need to do their job.

      I strongly believe if anyone with hypothyroidism isn’t on a stable dose of T4, the doctors need to start looking at micronutrient levels.

      There are a lot of documents on the NCBI website related to hypothyroidism.

  10. I am having my thyroid completely removed and will be on medication for the rest of my life. I am definitely swaying towards natural medication. Amour in particular. Do you know if I can get this easily in England. UK

    • Hi Valerie, it’s unlikely you’ll get this through an NHS G.P. because they only prescribe T4 Levothyroxine, unless you’re lucky and they’re willing to prescribe NDT, which is rare as it’s ‘off-licence’ in the UK (frustrating!). The charity Thyroid UK have a private doctors and practitioners list, where you may have more success in finding a medic who will prescribe natural desiccated thyroid hormone in the UK. Armour is the most expensive to buy, there are lots of other brands of NDT that you may get on just as well with e.g. (Erfa, NatureThroid, WP Thyroid, NP Thyroid), that work out a bit cheaper. Information about these other brands can also be found through Thyroid UK. Good luck and hope you find the right thyroid medication for you.

  11. I have Hashi’s and RA. I am in the process of getting the Adrenal/Cortisol and Stool profiles to assess leaky gut. My thyroid values are: T4 direct 1.45, T4 9.1, Free Thyroxine index 28, T3 free serum 2.6, T3 90, T3 uptake 28, Reverse T3 serum 18.6, TSH 1.28, Thyroglobulin Antibody 1363.4 and TPO 63. Any advise on supplementation to calm the thyroid antibodies and immune system would be awesome! I have been Hypo 40 years and never knew about Hashi’s until I was diagnosed with RA!

    • Hi Diana,
      The very fact that you have a complete thyroid panel tells me that perhaps you are seeing a good doctor already?
      Perhaps, Chris Kresser has already responded to you. However, I’m a Clinical Nutritionist and wanted to make one suggestion. Your very high level of Thyroglobulin Antibodies indicates that your thyroid tissue is being destroyed. Go Gluten-free and you will see that number go down quickly! It’s helped many of my patients. Apple Cider Vinegar may help your gut and RA. RA has many factors but usually starts with poor digestion, the Apple Cider Vinegar is a good start. If you get burning in your gut from this vinegar you may have an ulcer. So test it with a small amt. (1-2tsp.)and have a glass of water ready!

      • Thank you Ellen! I am AIP so no gluten, grains or dairy for me since the beginning of April. I cannot seem to drive those antibodies down. I started taking LDN and selenium and still nothing. I just thought I might get an outsider opinion, since I am not having any success, and thought that possibly changing to a natural thyroid might help. I am going to a Naturopath and treating some gut bugs, but nothing that seemed extremely bad. My stool tests did not indicate incomplete digestion, so I stopped the ACV.

        • Hi
          Maybe it’s a late info but it helped me to lower my thyroid antibody level from aug (265), to nov (175)- not significantly I guess it takes time but it’s moving (!). I am gluten, dairy, soy, corn free, no nightshade veggies, detoxed liver with supplements and vitamins, reinforced gut lining, installed water filter, removed silver teeth fillings, take ashwaganda, selenium, vitamins with iron, extra b-vitamins, no thyroid medicine yet still looking for a good match- I’m a borderline Hashimoto. Hope this helps!

      • Stool test reveled (dr data) 3+ for: Citrobacter freundii, Enterobacter cloacae, Enterobacter cloacae isolate 2 and Klibsiella pneumoniae ssp pneumonie. The yeast culture came in with 1+ for Candida orthopsilosis. I have been on Silvercillin and Designs for Health GI Microb-x for the last 3 months. But the labs are not changing much. I am on an AIP diet.

  12. Savvy suggestions – I was enlightened by the information , Does anyone know if my business could possibly find a blank FRB 500 Form URLA PE version to use ?

  13. I was diagnosed with Medullary Thyroid Carcinoma, Multiple Endocrine Neoplasa type IIb in 2007. Two surgeries to remove my thyroid and 3 parathyroids, 152 lymphnodes. I am on Levothyroxine 112 , I feel like crap all the time. I am trying to get into Dr. Kenneth Ain in the University of Kentucky’s Markey Cancer center, (I am having a difficult time getting an appt.) What do I need to be asking him when I get in there? Is Armour the solution? I have read so many articles that it all a blur to me now. Help!!! Please!!!

      • I have been on Tirosent now for 8 weeks. My hair has stopped falling out, some of my brain fog is gone. I have tried every med out there for my thyroid issues, this by far is the best. But my joint pain has gotten much worse. I am going to ask my doctor to try a T3 med along with my current treatment.

      • Greetings
        Tirosint may work for some but I had very bad side effects. Developed severe muscle spasm a month after starting on it and still struggle to get rid of them.
        Each person needs to find what works for their bodies.

        • I’m so sorry it didn’t work for you. 🙁 I hope you can get this ongoing issue resolved soon!!! It is such a bummer! Blessing to you!

  14. I have graves disease with RAI 15 years ago. I have been taking only cytomel for approx 13 years, prior to that time I tried all T-4 synthetics plus armour thyroid but they did not work for me found a new endo who prescribed just cytomel to me. This worked great for me 2014. At that time, I began having strange hyper symptoms. I backed down some on my cytomel which worked for awhile but progressively returned. Approx. 8 weeks ago, I awoke (after feeling quite strange for a few weeks prior) to my face being so swollen I didn’t recognize myself. I had absolutely no idea what what going on at that time. The only other meds I was taken at that time what certain vitamins, D, C, Zinc and calcium plus testosterone/estrogen hormone replacement. Endo was on vacation and internist told me to wean myself off of cytomel some because I was having hyper symptoms till endo returned and I could talk to him. After a few days, my face swelling went down. I have had a past history with other meds becoming toxic in my system due to hereditary fatty liver disease although the test results are only slightly elevated and not really outside the higher range on my test. When endo came back he pulled me COMPLETELY OFF of cytomel and told me to get my numbers down to 0 to start over and quite frankly I though I was dying at this point. BP skyrocketed, anxiety thru the roof and just a mess. I now am on BP meds and anti-anxiety meds to try to alleviate these two issues. He started me back on cytomel at lowest dosage possible 5mcg 3x/day. By 7 day mark having allergic reactions again. Even the 1st day I started it I could feel that something was not right with it. Itching inside, freezing to death all major hypo symptoms possible and just weird feelings I had not ever experienced before.

    So I called him and requested to try Armour…..I was willing to try anything at this point. Began Armour and by second day the old familiar feeling started again with the weird itching feeling, brain fog, insomnia and whole list of bad side effects could only tolerate it for almost 3 weeks till the itch eyes, fuzzy brain, itchy upper body became unbearable. Before Armour, I even went to allergist and had 72 different allergy tests and was negative for all of them. Now endo is trying me once again on Cytomel. Today is 1st day, took 1/2 of a 5 mcg in the am and within minutes the symptoms again started, weird feelings tingling upper body, brain fog and 1 1/2 hours the itching eyes/upper body started. I do not have any test numbers as I am still starting over. Unable to even tell him what I should tell him to test because I have read so much on different sites, I do not know where to being. I am ready to lose it at this point. Could I just be allergic to t-3 period or what??? Any help anyone can give me would be greatly appreciated, I am at my wit’s end.

    • Hi Jannette,

      I too am going through this, can you tell me if your endo has come up with a solution, because life is hell? I have been to every doctor and they tell me this is impossible, I have had shakes and body feels like poison acid is running through it, severly anxious which I have never suffered from in my life!

      • I strongly suggest you go on the thyroid med called Tirosint. I had the very same symptoms you had. I wish I wasn’t taking any thyroid meds but it is what it is. Tirosint helped me feel much more normal and human!!!

    • Donna,
      Please report this adverse reaction. I did when my BP skyrocketed with generic T3. I hope that if more of us do this, we might eventually get an answer.

      Since that reaction, I’m moving forward on two theories – an allergic reaction to microcrystalline cellulose and HPMC (so I take a survival dose of Tirosint) and insufficient cortisol that is not yet Addison’s (IMHO, adrenal fatigue and I’m looking for solutions).

      My TSH is low-normal, so no conventional doc will address obvious hypothyroid symptoms and declining health. I currently supplement with one quarter of a tablet of Nutri-Meds thyroid to protect myself from being hospitalized.

      My serum AM cortisol has always been low, so I asked my conventional doc to test serum ATCH – it flagged Low. Doc claims that the subsequent Stim test is “normal” so I’m stuck without a next step forward.

      Trying not to mess with cortisol until I can find a good doc to help me monitor. I paid cash to see a functional doc, but disagreed with the diagnosis and approach.

      Hoping to find a diagnostician – an endocrinologist/HPA doc who is more interested in “mapping” and testing the related hormones to figure out the disruption.

      • Jane, have you been tested by MRI or CT Scan for an adrenal adenoma? If not, you should. And if you have one get it taken out too. It’s why your ACTH is low and cortisol is low. If not you might have something going on w/pituitary.

    • I feel your pain! I have just recently experienced hormone thyroid toxicity myself with Levothyroxine 125mg. I was experiencing all the symptoms of a heart attack and stroke. The left side of my body went numb, facial numbness, headaches, unbalanced, walking side ways…what a mess! I am now two weeks off the medicine and luckily most of the symptoms have gone away. Currently I am researching new medicines to take myself. I have discovered that the levothyroxine has maize starch in in which I have a reaction to corn and wheat. From what I have read cytomel which is T3 has gluten in it so medications that have that in it will be no good for me. I have recently found a medication called WP thyroid that shows no gluten or corn in it and very few inactivie ingredients. My doctor and I are actually going to look into this after the detox period. Good Luck!

      • I was also poisoned by Synthroid 125mcg. I was super hyperthyroid on it. Thought I was having a heart attack too! Joint pain and stiffness. Scintillating scotomas, migraines, premature ventricular contractions, and full on panic attacks just to name a few. I was so sick. I am 48 and felt like 84. I finally found a functional medicine doctor who prescribed WP thyroid for me. It took a bit for my body to acclimate to it. My body was a wreck. But, after some fussing around with the dosage and going through a 10 day healing crisis where I couldn’t get out of bed, I am actually tolerating WP quite well. I’ve been on it now (1.25 grains) for a little over two months. My only complaint is that my hair is falling out a LOT, but I’ve started taking Biotin 8 by Thorne twice per day. But since getting on WP, I lost 12 pounds in a month and still losing. The joint pain is gone and the massive inflammation in my body is subsiding. I don’t feel poisoned anymore. I hope it works for you too. My best thoughts and hopes for everyone who is suffering with this horrible disease!

  15. Please tell me if ACELLA’S N.P. THYROID would be a good choice for me. I try to stay away from gluten, corn and GMOs.
    After the radioactive treatment for grave’s disease I took 3. mcg Synthroid with good results. Now they have dropped the dose to 1.12 mcg for two years and i’m on the generic. I’ not feeling to well and would like to switch to a natural thyroid replacement. Any advice would be appreciated.
    Thank you, jeannette

    • I was on the 3. Mcg for 20 years. Is it common to reduce the dose to 1.12 after that many years? Can you explain how this works if my thyroid is not active due to the radioactive treatment for Graves disease? Thank you.

  16. My problem is I’m literally allergic to Synthroid and other synthetic thyroid meds. My t4 and tsh are low but my t3 has always been fine. I started taking Naturethoid to bring up my t4 which it did however, now my t3 has gone high making my tsh almost non existant. So I don’t know what to do. The docs want me to take a synthetic but I can’t and don’t know of a med I can take with just t4 that I’m not allergic to. It’s not just the fillers but I’m also allergic to dyes, the gluten, etc. This really is hard, especially when you have a doc that states he doesn’t know what to tell me. And I’m a vet going to the VA hospital, I can’t really go to another doc.

    • Cheryelle,
      Can you talk your doc into trying Tirosint? It’s a gelcap with synthetic T4. I was so desperate I paid for 7 gelcaps at my pharmacy to try it, before i asked my doc’s office to advocate for it to be covered. Still tough to get to the right dose. I’m considering adding a quality NDT supplement after I find a professional to help me understand and monitor test results and symptoms.

    • Are you a 100% disabled veteran or retired? If you are retired or medically retired you can choose to go out in town and terminate in the VA Dr. They do not like to tell you this but that was absolutely the case. Good luck.

    • A low or none existent TSH means your body is satisfied with the level of thyroid hormone, therefore you don’t need to make your own. Patients with a 0 TSH are doing much better than patients with active TSH, the later still having symptoms. I was at 0 TSH and perfectly healthy, now my TSH is 1.5 and I’be gained 25 pounds in one year. I’m an autoimmune patient for two decades including Hashimoto’s. I think I need a gluten free T3.

      Anyone with high thyroid antibodies is autoimmune. Read Datis Kharazzian and Dr Perlmutters books. You shpc gf off gluten immediately.

    • You sound like me – I am the hot potato of all hot potatoes – v stressful actually when you are also dealing with a major problem and coming up with all sorts of allergies and sensitivities making medications very difficult.

    • Hi, Can you tell me how you knew you were allergic to Synthroid? My Dr. has never mentioned this possibility. After 20 years of taking it, I started having tremors, heart palpatations and signs of heart trouble. The zDr. lowered dose ffor six months from 1.38 to .50 wdith no results. Still had tremors etc. I stopped totally and my TSH is34. I am scared to take anything. The Dr. insist it is not the medication and is sending me to a Cardiologist. Thanks for any info.

  17. Hello,
    I just had blood tests done.
    Free T4 within norms but on the high side
    Thyroidperoxidase antibody – within norms
    TSH within norms but on the low side 0.86 (norm 0.2 – 4.00)
    What puzzles me is: thyroglobulin antibodies high at 375.5 (norm 0-115)
    What does it mean. I have to go for a ultrasound and i have palpitations, severe anxiety and some other symptoms consistent with both Hiperthyroism and Grave’s but the doctor does not think it is graves.
    She was vague and i am worried.
    Can somebody tell me these results might mean.
    Thanks!
    Katie

    • LOW thyroid (from a nurse who still has her thyroid):

      We get what appear to be hyPER symptoms when labs prove we are hyPO. What occurs is that when the body senses the metabolism slowing due to low thyroid hormones, in it’s effort to maintain homeostasis, the adrenals are given the signal to increase catecholamine output (adrenalin) which revs up the heart rate and BP, causing anxiety, heart racing and palps.

      NO thyroid (from my experiences):

      We get what appear to be hyPER symptoms AND lab results when we are hyPO. What occurs is that when the body senses the metabolism slowing due to low T3 (the active thyroid hormone), at the CELLULAR level (not in the bloodstream), in it’s effort to maintain homeostasis, the adrenals are given the signal to increase catecholamine output (adrenalin) which revs up the heart rate and BP, causing anxiety, heart racing and palps. Low T3 at the cellular level also stops production of progesterone (elevating estrogen unopposed by progesterone) and increases cortisol. Progesterone is a KNOWN component of converting T4 into FT3, and I notice my T3 works better when I use my OTC progesterone cream.

      • Best answer I’ve read on here, thank you!!!

        Not in menopause, but was going to talk to a Naturopath about Wild Yam cream and progesterone cream to use for depleting hormones. Understanding the connection between progesterone and FT3 is an important point and my endo has never bothered to run a sex hormone panel. Of course I also had to talk him in to prescribing me T3. He thought the answer to all my problems would be to take me off T3 and switch me from Synthroid to Tirosint. I did at his insistence and almost crashed my car I was so tired driving into work. I fell asleep at the office every afternoon- he finally wrote me a script for T3 and I felt better but the few pounds I gained while on Tirosint only, have been practically impossible to lose again despite a rigid diet a exercises daily including HIIT, walking, yoga, pilates and interval trail running.

        Hard to know how much is the thyroid issue and how much is being in perimenopause.

      • Oh my gosh this is exactly what is happening to me. I constantly shake like a leaf but how do I increase my thyroid hormone to prevent the adrenaline surge.

        On 75 mcg Levoxyl and a 1/4 grain of Nature Throid. Nature Throid alone kept my T4 levels way bottom. I now take 50 mcg of Levoxyl at 6am after breakfast the Nature Throid and another 25 mcg of Levoxyl at 3 pm as this is the only way I am able to keep my temperature around 36.4 degrees C. I try to increase my Nature Throid but due to adrenal issues my legs swell when I use more than above. I have low levels of cortisol all the time bar around 3
        1-4 am. Had the Dutch urine test done. Will progesterone help?

        Thanks for any advice as most of all am trying to rid myself of the adrenaline rushes

    • Your dr needs to test ft3 ft4 rt3 and tsh your antibodies r high which means u have hashimotos u need to treat adrenal fatigue and leaky gut.

  18. I have suffered with digestive issues and hormonal issues for as long as I can remember. I was working with a functional dr who helped most of my digestive issues, and SIBO. I was feeling so much better, but still fighting with fatigue. I found out I was hypo and was put on a compounded natural thyroid 30 mg. Since I started taking it in May, my fatigue, anxiety and bloating has been getting worse and worse each day. My drs suspect my sibo came back so I started another round of herbal antibiotics. I was also just put on a compounded progesterone to help with my cycle. My dr has decided to take me off of they thyroid medicine and seems to think that I am sensitive to it. I honestly feel better today not taking it than I have in months. We are retesting next month, but is it possible that I may not need medicine again or possibly need to try another kind? Or is it possible that once my hormones get balanced out, I wont need any medicine? I have been eating a super strict SCD and recently AIP diet

    • I was in your shoes 2 years ago! Found out the doctor didn’t Know how to dose natural desiccated thyroid medication correctly! I found a book called Stop The Thyroid Madness(or STTM).Explains everything you need to know the doctors don’t tell you. I also joined the natural thyroid hormone group in Yahoo groups. They follow a lot of the information in the stop the thyroid madness book. They also periodically print articles from Chris Kesser and Doctor Axe. Being diagnosed properly getting the correct medication for your situation and supplementation can be the key. I have been on WP thyroid for a year and a half and I’m doing really well hope this helps.

  19. Great article Chris thanks. I haven’t gone on medication for this reason. I feel that after 2-3 years on AIP I am still foggy & exhausted so I need medication but am afraid of being given the wrong one by my primary care physician or an end that doesn’t understand what you wrote. I know you aren’t available for patients so who do I see in Los Angeles to be prescribed or advised of the right thyroid hormone replacement for me?

    • Lee, did Chris ever reply to you? Did you find a good doctor in LA? I am in the same boat and I’m also looking for a doctor in LA to work with who has a deep understanding of this stuff. Thanks

  20. My enlarged thyroid was removed three years ago. Levothyoxine did not work for me, so my doctor switched me to Synthroid. Since reading an article that contained numerous photos of deformed piglets from sows fed GMO feed, I’m horrified that all thyroid medication in the U.S. is made with dessicated porcine thyroid. In other words, even if we avoid GMOs in our own food, thyroid extract replacement comes from pigs fed GMOs. Regardless of Monsanto’s lies and even the “approval” of the U.S. corrupt FDA agency, I do not want GMOs in my body. Unfortunately, I must take a thyroid extract. Is there any thyroid replacement medication made from organic porcine thyroid?

    • Synthroid IS levothyroxine (synthetic T4), and is just one of many brand names. You may have been taking a brand name or a generic version of levothyroxine with fillers that you reacted to, but you were and are still taking levothyroxine. Is it better than a hormone from a pig fed GMO’s? I don’t have the answer to that, but I would say your choice should depend on which makes you feel better in the long run. Pick your poison!

    • In my searches for the same, one comment from a man, gave a link to the following product:
      SwansonVitamins.com
      Thyroid Glandular (Thyroxin-Free)
      Look for thyroid glandular (bovine) made from New Zealand cattle. I believe I read, they are 1 in 2 places in the world that have a non-GMO standard for feed for their cattle and pigs.

      Hope this helps. Good luck on your journey to health.

  21. Hi-
    I have celiac, crohns, and will have no thyroid soon due to thyroid cancer. Can anyone suggest a thyroid medication? I’m leaning towards Natural Thyroid, but levothyroxine is also a possibility. Does anyone else with these diseases take a thyroid medication that works for them? I’m very worried about the fillers in thyroid medications (like gluten and dairy) that will trigger autoimmune responses in me and make me very sick. Seems like the perfect storm waiting to happen.

    • I also had Thyroid Cancer in 2010. I have been on Synthroid since then. It never made me feel like myself. I am finally seeing a doc who is willing to see if I have issues converting t4 to t3 or what is going on. I am still exhausted just on t4. It has been this way for the last 5 years. Feel free to contact me if you have any questions.

      • Hello Doris, I also had thyroid cancer in 2010 and have been on synthroid and feel like crap. I’m 55 and don’t expect to be 135 pounds anymore but I’m pushing 200. My current endocrinologist will not try cytomel in addition to synthroid. Apparently, it can cause heart problems…like the 60 extra pounds I’m carrying is healthy for my heart…frustrating!! I know chances are slim that your doctor is in Pittsburgh, but perhaps he/she may be able to recommend someone that will either do further testing, or try a combination of Synthroid and Cytomel. I was on cytomel prior to my radiation and I never felt better!

      • Hi ive been on levothyroxine tirosint, 75mcg for 3 months now! My tsh was 25 while back and now went down to 6.65 which is close to the desire range, but i heard that this gel-medication, its a fast realease and soon while im taking the med, 1 hour after, i have terible palpitations and anxiety, so i have to take propranolol and clonazepam, to lower my heartbeats! After taking these meds, my heart rate its fine and no more anxiety!! Pls help me out, could the thyroid med, has anything to do with my palpitations and anxiety?
        Thanks, Madalina!

        • Wow Madalina!! You are the first person that I’ve read about that is on Tirosint! I too am on Tirosint 88mcg. I couldn’t take the generic thyroid meds. Tirosint seem to be the all and all for me. However I have noticed severe palpitations if I don’t eat in a timely manner. I also have anxiety!! Hmmm….I wonder if this could be due to the Tirosint. Maybe I should go back on the generic??? I just wish I felt NORMAL!!!!!!!!

          • I have had a reasonable amount of success with Tirosint however am bloated and have continued to gain weight…I started Armour two weeks ago.I am less bloated but feel slightly hyperthyroid.I am trying to stick it out at least a month before I give up 🙁

    • Hi. M, sorry to hear you’r having your thyroid removed. I too had mine removed due to cancer about 7 years ago and was on thyroxine until April this year when I switched over to compounded thyroid extract. The best thing I ever did. I had a reverse t3 blood test revealing I wasn’t converting t4 (thyroxine or Levothyroxine) to the active form of t3 which your body must have. Years of that caused many more health conditions for me. I am now getting my life and my body back. Lost 10 kgs. My brain works again, skin clear, eyes sparkle, metabolism works, energy is consistent throughout the day. I eat paleo and very clean, never smoked, don’t take alcohol or drugs, have done for a long time, but not matter what I did I was a mess. Obviously my body needed direct t3 included and I’m finding so far that porcine gland (Armour or thyroid extract as they call it), has been life changing for me and my young family. Getting a good Dr who understands how to dose correctly and transition whilst being able to go by symptoms foremost rather than just blood tests and ranges is probably also the biggest contributing factor to my health. Starting of low and raising your dose around day 7 then around day 10 according to symptoms worked well for me. Holding for 4 weeks from then till blood tests. T3 needs to be high in the range or at the top. T4 needs to be mid range. TSH is to be low. If post Thyca, supressed is great and thyroid extract does a great job at doing this. You do however need to keep an eye on your antibodies. If symptoms are good and your looking after your immune system via all methods (diet and nutrients, selenium, iodine, vitamins etc.) I find my immunity is really good, no lethargy or glandular issues. I’m a sceptic of being on a t4 only medication. A human thyroid gland does not just have t4. It has 5 hormones not just 1, so why would a medication that has only 1 be sufficient for us? Your body must work so hard to convert all the time and not get any direct hormones. This is difficult for someone suffering from cancer, autoimmune diseases etc. I can’t understand why its expected. I’ll never go back to T4 Thyroxine ever again.

      • Melanie,
        You are very smart girl. You have understand perfectly the thyroid philosophy. I’m happy for you doing very well. I have a question. I’m in the same situation like you and I’m still on Synthroid T4 mono therapy. I still have some problems. Did you tried taking selenium, zinc, vitamin D3, B12 and other natural elements in order to help converting T4 to T3?
        Wish you all the best.
        Thank you for posting,
        Sam

        • Hi Sam
          Thank you. Yes I take 200mcg selenium picolinate daily, high zinc picolinate, just finished a few months of boosting my D3 with K2 after winter months it wasnt optimal but still ok & I take Methylcobalamin B12 x 1000mg daily as my B12 was not optimal but in range. I do have problems storing iron (ferritin) & this maybe one contribution to my conversion of t4 to t3 issues. I take an iron supplement at night. I have also worked hard to reduce hormone disruptors in the environment from chlorine, flouride and bromide to also plastics esp. BPA. Since my last post I have made good progress and awaiting latest blood test results to see if my rt3 is still high. I also have mo antibodies and have been taking Lugols iodine about 12mg daily for a few months. I’m also working on my cortisol/adrenals and have made huge progress there. Theres been allot to learn through my health journey this year & I was very scared to change meds however I’m glad I did. I don’t need to have afternoon nanna naps anymore which makes life so much easier especially when caring for young children! Happy to share my experience & answer any questions. Take care. Melanie

      • Hello Melanie. You speak an awful lot of sense! Are you by any chance in the UK? I wondered with you using the name Thyroxine instead of Synthroid. I’m curious to know because I am based in the UK and should like to get Armour but cannot find a source. If you could let me have the name of your supplier I’d be more than grateful. I took Armour many years ago through an enlightened doc but had to stop when I moved from the district. I’m desperate to get back on to it because I felt sooooo much better when I was taking it. Looking forward to your reply.

        • Thank you. Yes I know what you mean as I feel noticabley better since I switched. I live in Australia so we call the synthetic T4 thyroid medication Thyroxine here. Theres a couple of pharmacy brands but they’re all Thyroxine based which is the same as Synthroid in the USA.

          Here in Australia you can only get natural thyroid extract (& natural bio identical hormones) via a prescribing Dr on a script. Then its only supplied by a compounding pharmacist.

          There are a few Drs affiliated with the USA and can order a commercial brand from there but its rare.

          The TGA here only really allow compounded thyroid extract therefore its expensive and leaving many people unable to access it.

          The benefit of compounded for me is that I have my pharmacist make up my medication with vegetable capsules and I can have the filler anything I want. I chose vitamin c and glutamine as the only fillers. This is wonderful as I know I’m not reacting to anything and know what I get.

          I have heard that thyroid extract is difficult in the UK. I believe there are parts of Europe where its been banned so not sure if UK is the same.

          Although I don’t recommend it, there is a company in Thailand where some people here can purchase Thyroid-S which is apparently the similar to Armour. Its cheap and has lots of fillers and colours etc. I wouldn’t take it myself but I hear of others on facebook groups who do and find it ok.

          Can ask what have you done to address underlying issues? How is your Iron, B12, gut, magnesium, other sex hormones, adrenals/cortisol?

          Are you taking selenium, iodine & zinc? How is your liver?

          Have you had a reverse t3 blood test at the same time as a ft3? Have you had your Antibodies tested for Hashimotos or Graves?

    • Hi
      I have celiac and no thyroid. My doc keeps me on synthroid meds which have gluten an lactose in it…the doc has tried cytomel which has no gluten and lactose…which i thought was awesome cuz i had not side affects…but my t4 reading dropped and they put me back on snythroid which i keep telling the doctors I cant take it…makes me sick. But I guess I have no choice as I need something. Let me know what you find out if any

      • Hi Patricia,

        I’m pretty sure Synthroid was cross contaminated with gluten. I switch to levoxyl and have had far fewer digestive issues than I did when taking synthroid. I am also celiac.

  22. Hi I was wondering if any one could help me
    I’m 22 years old and have had hashimoto’s thyroid, type 1 diabetes and aloepecia since I was daignosed in 2002 at the age of 9. I was on synthroid for years but 2 years ago switched to armour because my TSH levels were always high. I have adapted a more lower carb diet to manage my diabetes better, but have lost a significant amount of weight. I’m at 105 pounds for 5’7 height. For the past couple months been having trouble sleeping at more recently severe insomnia. I was originally on 3 grains of armour a year ago, since then I have lowered to 1 & 1/2/2 grains every other day in the past 3-4 months. My last test results were :

    T4,Free(Direct) 1.09
    TSH 0.014 Low uIU/mL 0.450 – 4.500 01
    Antithyroglobulin Ab
    Thyroglobulin, Antibody 113.7 High IU/mL 0.0 – 0.9 01
    Reverse T3, Serum 9.1
    Ferritin, Serum 32 ng/mL 15 – 150 01
    Thyroid Peroxidase (TPO) Ab 770 High IU/mL 0 – 34 01
    Triiodothyronine,Free,Serum 2.0

    I have compounded cytomel, should I add that to the armour or switch back to synthroid and cytomel?

    • Your antibodies are through the roof; antibodies prevent the Free T3 from getting INTO your cells. Antibodies are evidence of autoimmune disease that eats away at your thyroid gland FIRST; then it moves on to other organs/ glands /systems (like your Pancreas and Adrenals–usually other glands that secrete other hormones). 21st Century Medical SCIENCE is slowly proving that ingesting an NDT (your Armour) WHEN you have antibodies is NOT a good idea (because it increases the antibodies, because it’s made from pigs’ thyroids and the pigs are confined to GMO feed, and GMOs are KNOWN endocrine disruptors). Healthy women with healthy thyroids test between 4.25 when blood is drawn in the late afternoon and 6.19 when blood is drawn first thing in the morning, for a Free T3 test; your 2.0 = you are hypOthyroid (INsufficient Free T3 at the CELLULAR level, not in the bloodstream from where they test it). IF I were you, I’d stop ingesting the Armour and ingest ONLY T3. To do that, you need to ingest the T3 you would convert from the T4 in the Armour AND the T3 that’s in the Armour, multiple times per day (for instance, I’m thyroidLESS and ingesting 25 mcg T3 six times a day). If you don’t know how to make these calculations for yourself, to know how much to ingest when (because we are all very individual), then find the help to figure it out elsewhere, because Chris clearly isn’t answering questions unless he gets paid….

    • First of all I cant see all the lab ranges for your results. Secondly, I can’t seem to find your Free T3 result which is essential. You need this done at the same time as your Reverse T3 so you can work out the ratio that you are getting. FT3 measures the active thyroid hormone your body uses. Reverse T3 will show the excess. You need to see how well you are converting your T4 to T3. Many don’t convert well. Your antibodies are high. Are you taking any iodine (Lugols) and selenium? Your Ferritin levels are too low. Did you get a complete iron panel blood test? You need to be at least 70 to be optimum. Have you had a 4 point salivia test done to measure your cortisol and DHEA’s? This will show how well your adrenal glands are functioning. Have you had B12 tested? Optimum is at least 500+. Really need to see your T4 range. T4 should be mid range and T3 top of range.

      • Hi, My 9 year old also has Type 1 Diabetes, he was DX 8/14/13.
        He was recently DX with Hashitomo and his doctor wasnts to take a “wait and see” approach but I am very uncomfortable with that. I cannot seem to fins much information on children with T1D and Hashimotos.
        Can anyone give me advice?
        Here is his lab reports:
        TPO AB: 514 high
        TSH: 6.6 high
        The others were normal range.

    • Do you have lab ranges for these results? Ideally t4 should be mid range, t3 top of range, tsh low <2 & reverse t3 down around 150 or so. Have you had your cortisol/ Adrenals, DHEAs & SHBG checked? Are you taking any thyroid supporting supplements such as selenium and zinc?

  23. I am desperate to find a Dr. in AL or TN that will treat hypothyroidism with Armor or Cytomel. I have made an appointment with Dr. Doekel in Birmingham, AL but he is unable to see me until August. The Dr. I am seeing now is freaking out about my TSH levels and wants me to see someone as fast as possible. Of course she wants me back on Synthroid. Any suggestions?

  24. Hi,

    I just found out that I am low on ft4 which might be the cause for my symptoms like constant nervousness, fatigue and constipation.
    Now if I have to choose between Armour and a T4-only medication, what would it be?

    TSH 2.00 (0.27 – 4.20)
    fT4 0.80 (0.70 – 1.48 ng/dl)
    fT3 2.96 (1.71 – 3.71 ng/l)

    Will Armour work or has it the potential of pushing fT3 over the range?

    Thanks, guys!

    • Are you currently on any medication when you had this test done? If so, how long was it before the test that you took your last tablet? Have you found out the underlying reason for your T4 being so low? Your symptoms sound Hypo though. Did you get a reverse T3 test done at the same time as these? Did you get any other thyroid tests, Iron (ferretin needs to be 70 min), selenium, saliva test for your cortisol (adrenal)? These can all effect your thyroid and conversion. Are you on any selenium or iodine? Your T3 is ok but I suspect you are actually pooling, meaning that you could have a high reverse T3 result. Its an extra blood test that must be done at the same time as your fT3 and TSH. Then you can work out the ratio to see how much you are actually able to use vs. how much is just pooling sitting out in your blood doing nothing but causing horrible symptoms.

  25. Hello all – am seeking informed advice if possible…
    Am currently on Levothyroxine (Synthroid) 75mcg for past 9 months or so. Had been on compounded low dose T3/T4 for about a year. Very bad symptoms started occurring & labs came up clinically hypo so was then put on T3 (in a rising amount to 100 mcg compounded in a private clinic) which caused the horrible symptoms to continue (symptoms that that could only be described as of someone who is HyPER.) A hideous year where that Dr did no investigation of my situation whatsoever. I switched to a Naturopath who tried me on NDT – same thing happened. He then tried me on Synthroid…et voila. Symptoms went away & my labs stabilized. Have recently tested (TSH, T3, T4 all good) but came up slightly anemic. Also have bad tummy. Irritable, gassy, can get very bloaty & continues to grow fat on it like some alien creature as taken up residence. (The rest of me is perfectly normal & responds in a healthy way to my diet & exercise habits the way you might predict. I’m in good shape in other words) Cannot seem to tackle this belly though. Either the discomfort or the alien.

    So my question is; should i be looking at the “Synthroid” as being a culprit here? Am I someone who is permanently “sensitive” to T3 and can never take it – should – never take it? Would I be wise to push on & try to get back to it as it might be a better choice than Synthroid in the long run – & I’ve also heard its sometimes possible to even get off it altogether…Is this anemia thing a red flag that should lead my investigation in a particular direction…

    Ok that was more than one question. But you know it goes…
    I’d appreciate any thoughts from folks who might have them.
    Be Well:)

    • First, my disclaimer: I’m not a doctor or a nurse. I’ve been surviving without a thyroid while ingesting ONLY T3 for the past six years. For the 8 years before that, I was confined to T4-only and mostly-T4 meds and I was barely existing. I’m one of those people who can’t convert T4 into Free T3, who was then repeatedly abused with T4-only and mostly-T4 meds by doctors who didn’t believe I needed T3 at all.

      Ask yourself: Is the compound sustained release? If not, were you ingesting a dose every 3-6 hours when the T3 in it would have worn off? If it is, do you understand now, from your own experiences, that SRT3 doesn’t work?

      T4-only meds cause “early menopause”. Menopause is more about fluctuating hormones than dramatic declines, tho levels decline over time. Testosterone decreases fastest, then progesterone, then estrogens. Adrenals pick up the slack as ovaries shut down. Adrenals, when they notice INsufficient FT3 at the CELLULAR level (not in the bloodstream from where they test it) STOP picking up slack for the ovaries and focus on survival–secreting adrenalin and cortisol to keep the heart pumping, causing symptoms that appear to be hypER, but which are, in reality, hypO. Adrenals also deny women the progesterone they need to oppose their now “excess” estrogens (estrogen dominance). Estrogens store in fat. Get some OTC progesterone cream with USP progesterone in it and apply it where you have “fat”.

      Estrogens unopposed by progesterone make whatever Free T3 you have INactive, it gets bound and processed out as waste. So, just because you have “good numbers” on an FT3 lab test result doesn’t mean that FT3 is getting INto your cells. Progesterone is a KNOWN component of converting T4 into Free T3 (even for men). I’m thyroidlESS and ingest ONLY T3, and my T3 doses work better when I use progesterone cream. Even if you are “post menopausal”, or you’ve had a hysterectomy, you still have a monthly cycle that helps maintain your circadian rhythm; you just don’t have the outward evidence that cycle is happening.

      INsufficient T3 at the cellular level = low body temp, usually. Low body temp = low stomach acids. Food doesn’t get digested enough before leaving the stomach and rips the lining of the duodenum, causing ULCERS. Ingesting acid reducers, protein pump inhibitors, etc. only exaggerate the problems.

      Low stomach acids also cause red blood cell problems, including anemia. Those red blood cell problems also cause air hunger, because red blood cells carry oxygen.

      When food isn’t being digested appropriately, malabsorption can result, depriving your cells of nutrients necessary to use whatever T3 you ingest. Malabsorption also negatively affects your immune system, since your immune system is in your gut.

      Synthroid/Levo are T4-only meds. T4 is a STORAGE hormone; the body and brain can’t use it unless it gets converted into Free T3. Supposedly, 60% is converted in your liver, 20% is converted in your gut, and 20% gets processed out as waste. So, take 80% of the T4 dose you’re ingesting and that’s how much Free T3 you have available for your cells because you’re not ingesting any T3. T3 is the ACTIVE hormone, needed by every individual cell in the body AND the brain. Your Free T3 lab result, currently, reflects what you’re converting from your T4-only med, AND the T3 your thyroid is secreting (if any).

      21st century medical science has proven that the Free T3 converted from T4 (whether secreted by a healthy thyroid or ingested) is NOT enough, so, yes, I’d advise returning to a med that has T3 in it over ingesting a T4-only med by itself. I do NOT recommend ingesting T3 once a day! So, you need to know how much T4 and how much T3 was in the compound, and get it divided up into smaller doses. “Most people” find they need 3-4 doses a day, some more.

      Your reaction to the NDT is common: women need more T3 than men. NDTs were made by men, for men, based on studies of men, by men. The women I know who ingest an NDT at least three times a day (the T3 in an NDT only lasts 3-6 hours as well), AND who feel well, are ALSO ingesting T3 separately, at least three times a day.

      IF you have thyroid antibodies, an NDT is the wrong med. NDTs are made from pigs’ thyroids. The pigs are ingesting, exclusively, GMO feed, and GMOs are known endocrine disruptors. “Thyroid” antibodies are evidence of autoimmune disease, not thyroid disease, which I know because I have NO thyroid gland and yet I have “thyroid” antibodies.

      Get a copy of your actual lab report, and check the reference ranges against those created by testing healthy volunteers with healthy thyroids. My guess is your numbers are not as good as you think, because the labs are using reference ranges based on the sick and suffering people they are testing. Healthy people aren’t being tested. Since you have to ingest more than a healthy thyroid secretes to get the same effect at the cellular level, your FT3, when ingesting enough T3 for YOU, will be lots higher than the lab’s reference range. Ingesting enough T3 for you also suppresses your TSH, indicating your PITUITARY is HEALTHY. Over time, suppressing your TSH teaches your thyroid to shut down, however, and it’s very difficult to “revive” it. I’ve listed reference ranges for various tests in other replies to other comments.

      IF you have antibodies, you can get them “into remission”, but you’ll always have them (they fluctuate). IF the antibodies have already caused damage to your thyroid gland, you’ll probably need to ingest replacements (plural) for “the rest of your life”. IF there’s NO damage, yes, you can, sometimes, heal your thyroid gland and not need to ingest anything from the outside in.

      Hope this helps! Get some progesterone cream, go back to a compound and/OR add T3 separately to any med containing T4, and don’t ingest T3 only once a day. If iron is low, ingest replacements. I drink food-grade aloe vera juice to heal my gut from the inside. I also ingest acidophilus before bed every night (adding the good bacteria my immune system needs to function). Since every individual cell in the body and the brain needs T3, any cell that doesn’t get it will be “impaired”. The longer the impairment continues, the more damage occurs….

      Reverse T3 “occupies” T3 receptors, preventing Free T3 from getting through the receptor and into the cell. Antibodies block the opening to T3 receptors in the bloodstream, preventing the Free T3 in your bloodstream from even getting into the receptors. There is NO test for how much T3 is actually getting into your cells, only RT3 and antibody tests to indicate problems, which we know as SYMPTOMS. In other words, you’re the only one who can know how much T3 you need at any given time on any given day. Lab tests can tell IF you’re converting T4 into Free T3 or Reverse T3, but 21st century medical science has proven that the Free T3 converted from T4 is NOT enough, so I’d encourage you to give T3 another trial, treating symptoms instead of lab tests’ results, whether as contained in a compounded med or ingested separately with your T4-only med (T4-only meds can be ingested just once a day; T3 will need to be ingested every however-many-hours your doses last FOR YOU. Experimentation required! Treat symptoms’ relief (or lack thereof), not lab tests’ results.

      • Thank you so much for your incredible reply.
        So much info to chew on.

        I have been using Progesterone regularly, so thanks for the confirmation.

        When you say “treating symptoms” in instead of labs, in the case of someone who comes up clinically HyPO are those symptoms generally pretty consistent with a lack of thyroid being ingested, produced or converted such as fatigue, weight gain, foggy etc etc or would you consider HyPER symptoms in someone clinically HyPO also a sign of not enough T3 being ingested, produced or converted? Any ideas there?

        When I seek help the general assumption (certainly amongst those I consider enlightened beyond mainstream medicine) is that T3, however often it is ingested is usually the answer & I was convinced of that myself and sought out a Dr who would put me on it rather than jump on the “Standard of Care” bandwagon & throw T4 at me, smack me on the back and send me on my way not minding how I felt…However, when I was switched from a compounded T4/T3 (having experienced an onset of rotten extremely HyPER-ish symptoms on that compound) & put on pure (yes! Sustained Release) T3 for a year, I suffered a continuous stream of the same hideous and alarming symptoms – only worse, much worse. I was taking one SR-T3 pill a day, but it certainly didn’t seem like it wasn’t “enough”. That Dr kept raising it up, till i was on 100mcg. I would call the Dr and inquire as to whether I might just be ingesting too much since as someone clinically HyPO I was feeling symptoms rather more in line with HyPER in my estimation. After a while, I felt like was, trapped in an “alternative” medicine bubble as narrow minded as the mainstream since this Dr seemed not remotely interested in investigating my suffering, but continued to slap me on the back and send me on my way not caring much about my symptoms which I reported to him each and every appt. & beyond.

        These symptoms would often come on violently strongly in the pm (around 11pm), a full 12 hours after ingesting SR-T3 and usually keep me up nightly till very late & often all night wondering if I was having a heart attack/stroke/would I pass out..that sort of thing- palpitations, dry mouth & a head & body feeling like it was experiencing one extremely long adrenaline rush, tingling in hands and arms…and on and on. It wasn’t until I was taken off medication containing any type of T3 & put on T4 that those symptoms abated.

        I had to get away from a “T3 is the only answer for everybody” Doctor in order (in my opinion) to save my life. It was a Naturopath who, at first tested me on NDT (Armour) and then when the HyPER symptoms continued switched me to T4 with finally, some relief. (ie I can sleep, I don’t have palps every night, my brain came back, my daytime energy feels more normal – ie I have enough to do my somewhat demanding job & more, my head & body don’t feel like I am experiencing one long vibrational scream etc etc etc). Real relief.

        Now I know most of you out there are beating your heads against a system that insists that T4-only is the “Standard” and for most of you, it isn’t. But I have found that T3-only has not been my answer. At least not so far & I’m somewhat confused by that. (…antibodies were tested, I never had Hashi’s…)

        But I’d like to know if anyone might have an idea for reasons why or if there’s possibly some reason standing in the way of me being able to successfully use T3 instead. OR does it matter? I feel mostly well on T4. I am though, concerned now about the slight case of anemia (which I had experienced also 15 years ago briefly) & excess belly fat that seems unassailable & quite separate & from the rest of my body which responds well to diet and exercise.

        I agree totally about the digestion issues, low stomach acid & the need to take care of the liver since its working so very hard & I do what I can there. Aloe Vera is wonderful & good probiotics part of my life also.

        • Becca,

          I know it’s been a while since you posted, but for whatever it’s worth, I have had a similar experience with T3. Although I have hypothyroidism, when I take T3 I get many of the same hyper symptoms you described as well as a terrible, itchy rash, usually on my shins.

          I was diagnosed with Hashimoto’s about half a year ago and it’s been a roller coaster getting to the right medication. Two different doctors have tried T3 and both times I tried it, I ended up feeling like I was going to explode. As soon as the T3 starts to leave my system, I feel better. I’m still not on the right dosage yet, but I’m advocating for finding it without added T3.

          I’m no expert, but as I understand it: If you don’t have a conversion problem, you don’t need T3. In fact, if you are successfully converting T4 into T3 and then you add T3, you actually flood your body with too much. This causes your body to down-regulate. Check out this video, he explains it well:
          https://www.youtube.com/watch?v=ODIWvbjK–M

          As for your belly fat, you might talk with your doctor (endo is better than OB/GYN in my opinion, but either will work) about Polycystic Ovarian Syndrome (PCOS). There is a well-documented relationship between Hypothyroidism and PCOS and the symptoms of the two are quite similar. Women with PCOS often hold excess weight in their abdominal region and it makes losing weight extremely difficult, even with proper diet and exercise.

          In the meantime, you might try a super low-carb (50-100g/day) diet and also try going gluten-free, if you haven’t already. Weight-bearing exercise also helps more than cardio. I’m an avid runner, so it was hard for me to adjust to not running every single day–but varying between running and hot power vinyasa, for me, has really helped.

          If none of that makes any sense or seems to matter, then I just want to say I validate your experience on T3. Listen to your body above all others!!

      • Please help me. I feel like I’m slowly being walked off a very long pier. Had a TT 3/15/2013 due to follicular cancer. No RAI. My endo was insistent Synthroid was the only way for me to go. I gained 20 lbs within 10 days (half that time I was hardly able to eat real food). He kept bumping up my dose. Added Cytomel. I continued to say at the 1 yr mark- I feel awful. He kept giving me referrals to primary drs. I refused. Instead I fired him & moved on to a Dr focused on well being & easier approaches. Immediately she offered to put me on Armour. Right before my 1st visit with her I had sent off for hormone saliva testing, full panel, because my prior endo kept saying it wasn’t the Synthroid, I must be in menopause. (I was 40). It did come back that my cortisol was barely registering in the AM & stayed low the entire day. My new Dr explained my adrenals kicked in & were hardly functioning. I was given an adrenal glandular. I kept saying no no no. It’s not working. Now It’s 3/2015. My B12 is under 175. Vit D is 18. Ferritin is 16. And I had the awesome pleasure of wearing a cardiac monitor for 30 days to be told oh, it’s just sinus tachycardia- no big deal. Probably just the medication you’re on.
        Now I beg you. Tell me how to begin dosing with Cytomel only. As I sit here & type this I have a full bottle of 25 mcg & 5 mcg. If you’re saying you have no thyroid (like me) & you’ve managed this barely existing existence on T3 only- I’m desperate to try.
        How much should I take to start. First dose, etc. And how often.
        How bad will the effects be of getting the T4 out of my body.
        How long before I feel any kind of difference.
        I see my endo on the 16th but I want to start now. She needs to follow my lead. I have done it everyone’s way but mine. Tired of being told my TSH is perfect but my Reverse T3 is too high. I’m not converting the T4!
        And on a final note. I was put on 200 mg of oral Progesterone 1 month ago because my estrogen was so high it registered as though I was in 1st stages of pregnancy.
        Maybe based on what I’ve read here, the estrogen dominance is due to the T3 not reaching what it needs to.
        Please help me. I’m done being at the mercy of Drs who are either in big pharma pockets or not inclined to connect the dots.
        Thank you.

        • Your story sounds like mine. I was on T4 only for 7 years after having my first daughter I was diagnosed with Folicular carcinoma thyroid cancer. Had a TT and rai. 7 years of the same rubbish like you have experienced. Fat, fatigued & ugly. I didn’t know who I became. I had enough and fired my Endo. I started reading and learning how to improve my health (already never smoked, alcohol, drugs and ate paleo, so I knew it was my thyroid meds). I started compounded thyroid extract (Armour) in April this year and have lost 10 kgs, feel energetic, happy, stable, enjoying life again. My skin has softened and my eyes are sparkling again. People comment all the time and cant believe the transformation in such a short time. Can I ask did you try Armour? You should check out this website and join their facebook groups for lots of info and support. If you are determined to get well, you can. http://www.stopthethyroidmadness.com/

      • Thank you so much for all this important information! I recently had my thyroid removed and put on levothyroxine. It was like being on methamphetmines for me, bringing back all the hyperthyroid symptoms I thought the surgery would end. It was a terrible 7 weeks until I called my holistic doctor and he suggested Armour. Hearing about the importance of T3 and understanding the effects a deficit can have on the system really explains what I went through. My last blood lab with my holistic doctor showed my T3 at 1.6, no wonder why I felt that way! My endocrinologist who had me on the levothyroxine doesn’t even test for T3! When I told her I had switched to Armour she was very upset and says it doesn’t work. I feel a ton better after only being on it for 5 days and will continue to feel better I hope.Needless to say, I am no longer with that endocrinologist, and sticking with my holistic doc. Since this hypothyroid thing is all new to me I really thank you for your reserach and sharing with us…knowledge is power

      • Hi Barb,
        I know it’s been a year since you posted this comment, but I just had to write to you in the hopes that you get this.
        I just started WP thyroid about 2 weeks ago. I had been on 125mcg Synthroid but not doing well. Dr. started me on 1 1/4 grain of WP. For about 4-5 days I did great, and then after that I noticed that about 6 hours after I took the pill I started having HYPER symptoms. Chest pain, palps, anxiety. Dr. took me down to half a pill once per day in the morning. Same thing. I felt fine for about six hours and then WHAM….anxiety through the roof, chest pain. Dr. took me down to 1/4 pill. Again…same thing. I feel okay for the first six hours and then I start getting anxiety.
        What is wrong with me? Should I be taking the WP in several doses throughout the day? My doctor is lowering the dose while everything I’m reading says the dose should be increased. But, why am I having anxiety and chest pain 6 hours after I take the meds? I hope you see this message. Any advice would be greatly appreciated.

    • You might try Tirosint.
      It doesn’t have conventional fillers.
      Just water, glycerin and gelatin… and the active…. T4(levothyroxine sodium).

      You might also want to start at a lower dosage, being as it tends to be more bio-available due to the lack of fillers.

  26. I have been on thyroid for 20 yrs. I cant take synthroid because real bad gerd and nothing I take helps . I am on armour thyroid and I cant get the numbers right,what do I do? Thank you
    Also my hair is falling out so bad. My TSH is .69 and T4 is low.

    • Women’s bodies change over the course of 20 years! Maybe you need to ingest more than one dose a day of your Armour? Maybe you need more Armour than you’re already ingesting? If T4 is low, my guess is Free T4 is even lower, and your Free T3 will be below the reference range provided by your lab, indicating you’re nearing your deathbed.

      Stopthethyroidmadness.com has multiple pages you’ll find of interest, for free. There’s an answer for almost every question you can think of, for free. Janie is selling her time as well as books, but she knows how to help someone ingest Armour.; it seems pretty clear your doctor(s) hasn’t educated themself(ves) about Armour, even though you’ve been able to get a prescription for it. Getting a prescription for it IS commendable!!!

  27. To thyroidless barb:
    Dec20 13 my general doc found that my right thyroid was enlarged; she ordered an ultrasound. Having over and underactive thyroid since the age of 12( I am 55 now), didn’t scare me. I knew enough to ask if she would run TPO and TgAb along with the TSH she was going to order. My TPO was in the 900 range and my TgAB was also elevated…can’t remember right now, and TSH was low normal. She suggested I see a ENDO. She suspected Hashi. I traveled 100 miles to see a good ENDO. She ordered a FNA biopsy; lymphocytes and normal Hurthle cells; diagnosis Hashis, put on levothyroxine…I felt better within a few weeks. followed up at 3 mos, 6mos, 6mos each repeating Ultrasound…supression therapy not keeping down the main nodule; it is now the size of an egg and has pushed my esophagus over to one side….it is time to come out. I am and have been gluten free since my brother was diagnosed with Celiac’s 3 yrs. ago, even though my testing came back that I don’t have it. I have not had my Antibodies checked again, but I am going to ask my general doc to order them before I have surgery. The 2nd biopsy was similar to the 1st, however they told me there are false negatives. The surgeon also felt another hard nodule on the base of my left lobe, so I am going to have a total thyroidectomy. I know this will not be a picnic. Thank you for posting that you still have Antibodies even though you have no thyroid. My surgeon will do everything he can to save all the parathyroids, which he suspects are fine because my calcium levels are good. My endo wants me to continue on levothyroxine until I see her 6wks post op. Thanks again for the input from everyone.

    • Good luck on your surgery. Suppression therapy never works with a T4-only med like Levo. KNOW that people with healthy thyroids, following any surgery, “normally” convert their own secreted T4 into Reverse T3, which their cells can’t use (this occurs in the liver for seven to ten days after your last INGESTED T4-only dose), so their HEALTHY thyroid STOPS SECRETING T4 and dramatically increases secretion of direct T3 (not the converted kind). Since you’ll have NO thyroid, you’ll need to ingest T3-only (Cytomel), starting the day of your surgery (dissolved in your mouth once you’re awake), because the T4 you’ve been ingesting every day prior to surgery will get converted into Reverse T3, for seven to ten days from your last T4-only ingested dose, which your cells can’t use. You don’t ingest T3 just once a day: It takes 30-45 minutes to get to work after dissolving it in your mouth, then it “wears off” 3-6 hours later. Instructions for starting ingestion of T3, and ONLY T3, are at eaware.org, from Thyroid on the left, from RT3 under Thyroid. Once ingesting T3, you must be treated based on symptom relief or lack thereof, NOT based on ANY lab test result. Your TSH will be suppressed by the T3, and that’s an indication your PITUITARY is HEALTHY, responding EXACTLY as it’s supposed to respond to the T3 you ingest. Most thyroidLESS humans ingesting ONLY T3 need 100-175 mcg per day in multiple doses, once they taper onto the T3 and reach a maintenance dose. Ingesting T3 and ONLY T3 is NOT dangerous! 21st century medical SCIENCE has proven that the Free T3 converted from T4 is NOT enough, precisely because there are times you’ll need an extra dose of T3, and there are times when you’ll need to ingest ONLY T3, like immediately following your surgery. I’m so very sorry your doctors allowed your thyroid’s growth to progress to a point where you have no choice about removing it, but you DO have a choice about which med to ingest and when!!! Get some Cytomel, in your hand, BEFORE you have surgery, and take it with you to the hospital!!! IF they find cancer and try to talk you into swallowing radioactive iodine (RAI or I-131), don’t “assume” you need it–that’s nuclear waste that WILL give you cancer when your thyroid grows back, especially if you’re denied the Cytomel you definitely need. Thyroids grow back, more often than not. When you had cancer or swallowed RAI, they grow back, more often than not, malignant. If your TSH registers when your thyroid grows back malignant, your PITUITARY will be telling your malignant thyroid to secrete malignant T4 to your liver (giving you liver cancer), and malignant T3 to every individual cell in the body and the brain (usually resulting in brain cancer). 21st century medical SCIENCE: EVERY INDIVIDUAL CELL IN THE BODY AND THE BRAIN NEEDS T3 NOT T4. Just because your PITUITARY has enough T3 doesn’t mean every individual cell in the rest of your body and brain has enough T3. ThyroidLESS humans shouldn’t have to pay for Thyroid Stimulating Hormone (TSH) tests!!! Anything else is 20th century medical MYTH…. You’ll be in my prayers, too.

      • Thyroidless Barb
        Thank-you for taking the time to reply. I really appreciate it. I will order some Cytomel. and have it with me when I go to the hospital. Should I expect any side affects from the T3?

      • Thyroidless Barb,
        Funny thing is endo wants me to stay on the same dose of levothyroxine(25ug/day) until I see her 6wks. post op. and surgeon will put me on Synthroid immediately after surgery. Kind of a conflict here. Surgeon specializes in endocrine surgery. From everything that I have read so far in this conversation; Levo(T4 only) sounds like a really bad idea.

        • ok, I am an idiot. I just realized Synthroid and Levo. are both T4 only. Sorry everyone. I also need a reputable Pharmacy that I can order Cytomel. Anyone willing to share that info with me?

          • In my experience, there are no side effects to T3. Whatever your cells can’t use gets processed out just like any other waste. I ingest the brand, which is expensive, so I can’t afford to ingest “too much”. There are, sometimes, allergic reactions to the fillers, but rarely to the T3 itself. Yes, there are contradictions between 20th century medical MYTH and 21st century medical SCIENCE. Your endo surgeon doesn’t have the follow up with patients to understand that there have, in fact, been advances made in his field of specialty since he was taught his medical myth in medical school. That’s why I suggested you read the instructions for tapering onto the T3 at eaware.org, from Thyroid on the left, from RT3 under Thyroid. I increased every third day (because the T3 is completely gone from your body in two days). Start with two doses of 12.5 mcg each. On the third day, add a third dose of 12.5 mcg. You will experience SYMPTOMS of insufficient T3 at the CELLULAR level that doctors interpret as “hyper” symptoms, but they’re NOT “hyper”! They are your adrenals cranking out adrenalin to keep your heart pumping because your adrenals know you’re not yet ingesting enough T3 for every individual cell in your body and your brain. IF, once you get to maintenance doses, each dose lasts six hours for you, then you’ll know you’ll need to ingest a dose at least three times a day while you’re awake.

            The only place I know to get T3 without a prescription right now isn’t responding to the people I know who order it that way. Hopefully this will change soon! In the interim, show your ent/surgeon AND your doc the text at eaware.org, there’s more at recoveringwitht3.com, a list of systemic symptoms is at 21centurymed.com, Hypothyroidism tab and scroll down. It prints on one page.

            • Thank-you so much for your input. I will definitely show these articles to my endo. and surgeon. Hopefully they will be open to treatment with T3.

        • If you’re on Facebook, I’m “Barb Shultz (Barb Boston)” there. I post lots of stuff for Thyroid Awareness Month (January), set for “Public” view so you don’t have to be my friend on Facebook to read them. No “c” in my last name; I’m easy to find. Current profile pic reflects that I’m an Army B.R.A.T. Again, good luck with your surgery, and your (not your doctors’) choices, for YOU, an individual who will be thyroidless. Remember, you’re not “hypothyroid”; you’re thyroidLESS. “Hypothyroid” humans need supplementation; some need replacement and don’t get what they need. ThyroidLESS humans need and deserve 100% replacement, not just supplementation. 25 mcg of a T4-only med when you’re thyroidLESS is NOT replacement. Even if only kept on that dose for six weeks, you will be ingesting supplementation, not replacement, for those six weeks, and you will develop symptoms of INsufficient Free T3 at the CELLULAR level, regardless of your PITUITARY (TSH) lab test result.

  28. I was on Armor thyroid for a year but then switched back to levoxyl because my t3 was high and my t4 was low. TSH was also high.

    Labs were

    TSH 9 (range .27-4.20)
    Total T3 1.60 (range .59-1.63)
    Total T4 4.59 (range 4.20-10.40
    Free Thyroxine Index 4.9 (range 4.2-9.5)
    TPO 6.6 (range 0.0-34.0)
    TG 22.6 (range 0.0-115.0)

    During this time I was experiencing palpitations. etc.

    My doctor switched me back to levoxyl

    First recheck

    TSH .62 (range .27-4.20)
    Total T3 .62 (range .59-1.63)
    Total T4 8.46 (range 4.20-10.40)
    Free Thyroxine Index 8.9 (range 4.2-9.5)

    She wanted to increase the does of levoxyl, but I was having issues with the new formula so I had the new does .88 mcgs compounded.

    Recent labs were

    TSH 16.38 (range .27-4.20)
    Total T3 .57 (range .59-1.63)
    Total T4 7.56 (range 4.20-10.40)
    Free Thyroxine index 8.1 (range 4.2-9.5)

    I don’t know where to go from here. I feel horrible. Plan is to once again increase compounded T4 but I don’t believe this will help.

    Any insight would be greatly appreciated!

      • The T3 in the Armour elevates your Total T3 lab test result, because it is measuring what you last ingested before your blood draw. Total T3 and Total T4 are the wrong tests anyway; you need FREE T3 and FREE T4 tests, which will tell you how much T3 is “free” to be absorbed and used by your cells (probably a very low result , especially if you’re thyroidLESS) and how much T4 is “free” to be converted into Free T3, which every individual cell in the body and the brain NEEDS, and/ how much T4 is “free” to be converted into Reverse T3, which your cells can’t use. Supposedly, 60% of T4 gets converted (into Free T3 and/or Reverse T3) in the liver; 20% gets converted in your gut (where your immune system is located) and the other 20% gets processed out as waste, because it is “bound”. Two issues your doc is ignoring: ingested hormones aren’t as easily absorbed or used by cells, so you need to ingest more than a healthy thyroid would secrete, which will, necessarily, increase your Free Te and Free T4 lab tests’ results. Second, the labs are using reference ranges based on sick and suffering people who have thyroid problems to tell your doc you’re “normal”, just like all the sick and suffering people your lab is testing (healthy people with healthy thyroids aren’t getting tested). Doctors can “control” your TSH and Free T4 lab tests’ results with a T4-only med, but neither lab result tells them or you anything about the T3 you need at the CELLULAR level. Healthy volunteers with healthy thyroids tested .4-2.5 for TSH, .7-1.8 for Free T4, 4.25-6.19 for Free T3 for WOMEN, 2.3-5.0 for Free T3 for MEN. You can “order” your own tests from an online lab, go to an “approved” blood draw station and your results are provided to YOU if your doc won’t order these tests (Free T4, Reverse T3 and Free T3), but it’s out of pocket (not covered by any insurance). I wish you and your doc more education. Read other comments here, because Chris clearly isn’t going to answer any questions unless he can profit financially by providing the answers. We’re all so very individual! We all DESERVE to be treated as individuals, rather than as a set of lab tests’ results compared to other sick and suffering people with thyroid problems….

  29. I am somewhat disappointed. I nearly took this article to my conventional endo as a reference to try NDT. Upon further research I discovered that the starch in Cytomel is not a gluten containing starch — cytomel is gluten free. — Synthroid is gluten free but not made in a gluten free factory therefore legally can not claim the status.———— Had I made this argument against cytomel to my endo I would have been made to look like a fool and loose all credibility as my own health advocate. — please look into it an correct the article.

  30. Hello,
    My endocrine issues started 16 years ago. I had elevated prolactin level >135 ng/dl, but no adenoma detected. Diagnosed Hypo in 2000 and managed on Synthroid 75mg? I never felt well, but normal ranges so diagnosed with depression and adult ADD. In 2008, I had my tubes tied / uteral ablation and with in 6 months bed ridden. Went to wellness dr who switched me to armour. Improvement, however I had several other issues to address; lyme, mold exposure, etc.
    My pcp is an endocrinologist and has me on Armour 1
    gr.
    My labs for the past year are as follows:

    FT4 0.7 (0.7-1.7 ng/dl)
    FT3 2.5-3.6 (2.3-4.2 pg/ml) swings, but mostly low on Armour 1 gr
    TSH 0.3-1.3 (.35-4.5)

    My symptoms are mostly psychiatric in nature. The brain fog is crippling. I have no executive function of my brain. Thoughts do not come automatically to me and I am very easily overwhelmed when I have to make the effort to think something through. I have internal angst that paralyzes me. It is very irrational and because of it I do not leave the house much. I am always irritable and agitated. I have complete apathy and depersonalization that feels like I am always homesick. Around 3pm I can feel the anxiety starting to rise. Most of the time it escalates to a pressure in my brain that feels like it is on fire. I feel like I lose touch with reality. What is odd is that it passes within a few hours. Often I take Ativan to abate the symptoms quicker.

    I decided to get second opinion.

    The new dr. suspected hypo and ordered panel on 11/01/14:
    FT4 0.7
    FT3 2.7
    TSH 0.3
    RT3 21.3 (8-25 ng/dl)

    She suggested that I not take any T4 and use cytomel. She also supported low adrenals with HC.

    The last three weeks have physically been hell. But some of
    the mental symptoms have greatly improved..so we are hitting on something.

    current regimen:
    6am t3 5mcg
    HC 5 mg
    armour .5 grain
    10am HC 5
    12pm T3 5mcg always feel revved
    2pm HC 10 Start to feel fluish, achey, tingly, anxious
    4pm Armour 1/2 gr.

    I’m NOT feeling well on this regimen. The question is if I am on too much or not enough T3. I am hoping to have new labs on Monday.
    Sorry for such long post. Any input would be appreciated. Thanks!

    • YaY! For YOU getting any T3 at all!!! Yes, I’d agree that you’re not getting enough T3. eaware.org describes how to increase T3, and how to ingest it once you’re up to treatment level doses. They suggest starting with 12.5 mcg and increasing by 12.5 mcg every several days. I know one person who increased every eight days; I increased every three days. I’m taking a total of 150 mcg/day in six doses (I’m thyroidless and ingest no T4).

      The Armour is 80% T4, and it’s still converting to RT3 because of everything else going on.

      Rigorously screened, healthy WOMEN test between 4.25-6.19 for FT3. Because you are ingesting instead of secreting, you need more than their healthy thyroid secretes, so your FT3 lab test result “should” be higher than 6.19 (unless you stop ingesting your T3 for 24 hours before your blood draw, in which case it should be really low, like it is now).

      Dissolve the T3 in your mouth; eating immediately before will decrease it’s effectiveness, because a healthy thyroid interprets food as stress and secretes extra T3 to help digest the food. Eating immediately after dissolving in your mouth has no effect, because the T3 doesn’t “kick in” for 30-45 minutes afterward. It WEARS OFF 3-6 hours later, when you need to dissolve another dose in your mouth! “Most people” need 3-4 doses of T3 per day; I ingest six smaller doses, trying to mimic what a healthy thyroid secretes. You need more T3 in colder temps as well. Dose sizes that work in the spring and early summer won’t be enough in the winter, depending on where you live.

      You ARE getting better, but you’re not ingesting enough T3, because the T3 you ARE ingesting is teaching your thyroid to shut down altogether–you need and DESERVE replacement instead of supplemental doses. Your PITUITARY is responding EXACTLY as it’s supposed to respond to ingested T3: it’s getting suppressed, as revealed by your TSH result.

      It’s still a process that takes time, but it takes less time with T3 than it does with T4. Hang in there!!!

      • Thanks TBarb!!
        I will read how to titrate. Since my post, I went up to 10mcg T3 in am and noon. And this morning went up 5mcg more….15mcg total this am and don’t feel so great.
        My dr. called in compounded T3…NOT SR. So I won’t be able to dissolve it.
        My labs came back and levels are the same. RT3 was 12. Can it drop that much in three weeks? However, my FT4 has consistently been low as far back as I can remember. My FT3 levels are never usually at the mid mark.

        I’m just confused why it seems so difficult to titrate dose.
        Thanks so much for your input!!

        • You’re welcome!

          The point in having T3 separately, in known doses, instead of compounded is so YOU can decide how much you need and when you need it. Eventually you learn to anticipate by 30-45 minutes before you need it, so it can “kick in” by the time you need it. Compounded may have different fillers, better for you than the brand or the generic. I’d chew it if it’s not sustained release!!!

          Usually, compounded means sustained release, or a T4/T3 combo, so be clear about what your doc ordered….

          The more T3 you ingest, the quicker you’re clearing the RT3 (so long as you continue to address the causes of your RT3). RT3 can only be converted from T4, so if you’re not ingesting T4, your RT3 will clear.

          If FT4 continues to register after you’re not ingesting any T4, then that FT4 result indicates your thyroid is still working! But, the T3 you’re ingesting will suppress your TSH, which, over time, teaches your thyroid to shut down and stop secreting whatever FT4 shows up in your lab tests.

          Makes sense? Hang in there!!!

  31. HELP!!!! I’m in desperate need of answers. I came upon this site and you all seem to know what you’re talking about, so PLEASE help me.

    In March 2010 (3 months after having a baby) I was diagnosed with hypothyroidism. The doctor said my numbers were significantly low immediately put me on Levo 175. I must’ve taken it only a few weeks then I stopped because I moved away and I lost the medicine (I ended up being homeless and didn’t make trying to replace my Rx a priority….

    Fast forward to March 2014 – I was experiencing the same symptoms which I had back in 2010, so I went to the doctor to get a Rx for Levo, but when my labs returned, the doctor told me she could not put me back on Levo because my numbers were normal and I DON’T have thyroid problem…. I asked for a copy of my labs. I don’t understand the numbers but they were as follows:

    TSH (3rd gener.) 5.359 Ref. Range 0.340-5.600
    FREE T4 1.3

    Now, today 8 months later, I am not feeling any better so I went back to the doctor and I explained to him 1 dr saying I have hypo and the other saying I don’t. You’re probably subclinical. had more blood work a week ago. I got the results for my thyroid and according to this new doctor I do NOT have hypothyroidism. My results are as follows:

    TSH 4.11
    T4, FREE 1.1
    T3, TOTAL 106
    T3, UPTAKE 25

    I left his office feeling relieved that I don’t have a thyroid problem after all……. OR do I ???????

    Because I’m still waiting for the results of the cortisol test (taken on a different day) and I’m looking for answers, I came upon a book, “The Hormone Cure”, and I read it all today- according to this book, it appears that not only do I have Hypothyroidism, but may also have both High AND Low cortisol in the same day….

    If I understand right from what I’ve read, some doctors wont treat subclinical hypothyroidism, and apparently my doctor is one who doesn’t… I have mixed feelings about that!! Part of me is OK with that because I would like to treat it with herbal therapies instead (which I know NOTHING about)…

    I should mention that I’m 47 yrs old. Don’t try to do the math, yep, I was 43 when I had my little girl. So I have a soon to be 4 yr old. I’m perimenopausal. I was just told I have arthritis on both shoulders (losing movility on my left shoulder) and I have a 1 inch fibroid on my uterus….

    I know this is long, but I don’t know where to go from here or where to start because from what I’ve read (so far) if I eat “this” it helps with my thyroid, but screws up my cortisol, and if I eat “that” instead, it wont affect my cortisol, but it’s not good for my fibroid, and eating something else altogether is not good for my arthritis / severe inflammation. It’s all so overwhelming 🙁

    I welcome ANY and ALL responses and/or suggestions. Please if you can recommend any herbs, supplements, vitamins, links, websites, etc….

    Thank you in advance,
    Nena

    • You are PROBABLY “hypothyroid”. Taking the Levo taught your thyroid to shut down; labs indicate you MIGHT be able to “heal” it. See hypothyroidmom.com. She had a guest doc talk about this. You’ll need other tests FIRST, to find out if you have antibodies, and I’d suggest Reverse T3 and Free T3 tests from the same blood draw, with the blood being drawn about 3-4 Pm (not first thing in the am). Levo is a T4-only med; every individual cell in the body and the brain NEEDS T3, not T4. T4 is converted to T3 in the liver, but it also converts to Reverse T3 instead of Free T3, and 21st century medical science has PROVEN that the T3 converted from T4 is NOT enough (you DESERVE to replace your T3 IF you need replacement at all).

      A healthy thyroid makes T4, T3, T2, T1 and Calcitonin. T4 gets converted to Reverse T3 when someone is sick. At that point, a HEALTHY thyroid is exquisitely self-regulating. It stops makes T4, dramatically increases secreting T3 (not the converted kind) and that continues until you are well again. “Most people” who ingest a T4-only med end up with adrenal problems, especially women.

      As our ovaries shut down (perimenopause), our adrenals pick up the slack. Testosterone decreases quickest, then progesterone, then estrogen. Estrogen unopposed by progesterone generates, first, excess stress. Stress depletes the supply of Free T3 quicker than any other drain! Then, estrogen “deactivates” whatever T3 is available. So, I’d suggest some USP progesterone cream. Progesterone is a KNOWN component of converting T4 into Free T3 as well. Remember, menopause is more about fluctuations in hormones’ levels than it is about dramatic drops. Menopause can last up to ten years or more. Most women ovulate for an average of 40 years, so take the age at which you started, add 40 years and know you may have been “pushed into” menopause (as opposed to being perimenopausal).

      Next, know that uterine fibroids go away all by themselves; you don’t HAVE to have surgery; and I don’t suggest ablation. They MAY go away with the use of progesterone cream (balancing out the excess estrogen because your adrenals aren’t working up to par).

      Next, know that adrenal fatigue, or insufficiency, or whatever the doctors call it, generally, doesn’t get treated, just like “subclinical” hypothyroidism. They wait until it’s a disease called Addision’s….

      Rigorously screened, healthy volunteers tested as follows:
      TSH: .4-2.5 (so your 4.whatever IS too high)
      Free T4: .7-1.8
      Free T3 for WOMEN: 4.25-6.19
      Reverse T3: Zero
      “Thyroid” Antibodies (listed elsewhere in other replies here): ZERO, Undetectable!

      TPO is the most common antibody. I have TPO antibodies AND I have NO thyroid, so they are not “thyroid” antibodies. When you have them AND you still have your thyroid, they take “bites” out of your thyroid gland, dump massive amounts of T4 and T3 into your system (causing the T4 to convert to Reverse T3 eventually), and you will fluctuate between hypo and hyper. For a list of systemic symptoms, go to 21centurymed.com, Hypothyroidism tab and scroll down. hypothyroidmom.com also has a list of more specific symptoms–300 of them.

      eaware.org explains a lot, in “lay peoples'” language you can understand.

  32. Hi, I had thyroidectomy in June 2014 due to Graves’ disease. Dr put me on t4 replacement (levo)

    July 16 2014 –
    T4 free results 18.9 (réf range 7.2-21)
    Tsh results <0.03 ( réf range 0.3-5.6)
    Sgpt results 11 (réf range 4-43)

    October 21 2014
    Tsh 0.07 (réf range 0.5- 5)
    Thyroxine free results 19 (réf range 10 – 22)

    I have been trying to conceive with no success…. From blood results any reason I should not be able to conceive? I have conceived twice before being diagnozed and fairly easily. Do you think their would be a benefit in taking t3 replacement as well?

    • Yes! If you don’t have antibodies, you may be better able to conceive with a Natural Desiccated Thyroid (NDT) med. Otherwise, I’d suggest some Cytomel to go with your Levo, because 21st Century medical SCIENCE proves that the T3 converted from T4 is NOT enough. You DESERVE to replace the direct T3 that your otherwise healthy thyroid would have made for you.

  33. Hi All…Recently diagnosed with Hashimoto. Diagnosed 10 years ago with hypo.
    Most current lab results:
    TPO <35 2070
    Thyroglobulin Antibody <40 364
    TSH .350-4.5 13.935 (Down form 52.889)
    FT4 0.80-1.80 1.09
    FT3 2.3-4.2 2.7
    Had 1st appointment with Endo…he changed me from Levo 125 to Synthroid 137 and Vit D and B12. Joint aches are much better but still feeling exhausted and worn out. Irritability is not as bad but not so good either.
    Would I benefit from a T3 or an NDT rather than just Synthroid alone?
    Thanks!!

    • Yes. Hashis CAUSES hypo. Antibodies, literally, “eat” away at your thyroid gland. Four digits of TPO ab is waaaaayyyy too many! My guess, at this point, you may not have any gland left, and yes, you need to replace both T4 (your Levo), assuming you can convert it into Free T3, AND T3 (brand name Cytomel). Lots of references listed in other comments.

      Rigorously screened, healthy volunteers, WITH healthy thyroids, tested as follows:
      TSH: .4-2.5
      Free T4: .7-1.8
      Free T3 for WOMEN: 4.25-6.19
      Free T3 for men: 2.0-5.0
      Reverse T3: Zero
      Antibodies (there are four of them): Zero, UNdetectable.

      A healthy thyroid secretes about 94-110 T4 and 10-22 T3. You must ingest more than a healthy thyroid secretes to get the same effect at the cellular level, so your lab test results will not be within the above ranges (TSH gets suppressed, FT4 and FT3 will be “too high”).

      I have NO thyroid and yet I have TPO ab. Therefore, my conclusion is that ab are evidence of autoimmune disease, not “thyroid” disease. Left unchecked, by YOU (not your doctor), they go on to “attack” other systems/organs (MS, diabetes, etc.). I try to stay away from processed and GMO foods, eat only grass-fed meat and dairy. My ab fluctuate between 0-17, depending on how successful I am at not eating what is, in reality, NOT real food.

      Hang in there, but I’d suggest yes, get some T3 to go with your T4. 🙂

  34. Does an elevated TSH level of 7.2 with normal levels of T4 Free and T3 require thyroid hormone? The doc is suggesting desiccated thyroid at 30mg for a month just to see if it brings the TSH down. The TSH has been slowly rising over the last five years from 3.74 to 7.2 even though the T4 and T3 continue to be normal. The normal TSH range where I live is between 0.35 and 5.00 mIU/L but I know the range is different in other countries. All other lab results are good except for ALT which is slightly elevated at 40 U/L.

    • FT4 and FT3 are “normal”? According to reference ranges generated by testing rigorously screened healthy volunteers (see my response to other comments), or according to the lab where your tests are run, based solely on the sick and suffering people being tested, precisely because their doctors believe they have a thyroid problem!??

      Ingesting any form of T3 will bring your TSH down, because the TSH is a PITUITARY test, not a thyroid test. It’s based on the thyroid hormones IN the pituitary, and thyroid hormones’ concentration is highest IN the pituitary. It tells nothing about thyroid hormone levels in any other part of your body OR your brain. Every individual cell needs T3, not T4.

      If you’re not having any symptoms, why a trial? If you are having symptoms, my guess is you’ll need 30 mg for two weeks, then 60 mg for two weeks (two doses a day), and continue to increase from there. Research shows most people need 3-5 grains to feel well. 60 mg = 1 grain. But you can’t just start taking a grain 3-4 times a day, you have to build up to it. Some people only need 3 grains; others need 5. We’re all very individual.

      Know that just that little amount of medicine will teach your thyroid to shut down, to depend on what you are ingesting instead, because the slightest extra T3 ingested suppresses the TSH. When the TSH is suppressed, the pituitary isn’t telling the thyroid to secrete anything.

      When the TSH is 7.2, it’s screaming at the thyroid to make more T4 and more T3. For you, it appears your pituitary is screaming at your thyroid to make more T4 and more T3, because your pituitary KNOWS whatever T4 and T3 is being secreted is not enough (not “normal”), for YOU, regardless of the lab saying it is “normal” for all the sick and suffering people your lab is testing. In the USA, those healthy volunteers tested between .4-2.5, most of them under 2.0, so even your 3.74 was too high years ago. Ask your doctor to NOT depend upon the lab to tell him what is “normal”; acknowledge he only got one week’s training about dysfunctional thyroids in med school; and then tell him that 21st century medical science trumps 20th century medical myth. There has been progress in the “treatment” of “thyroid problems” since the 1960’s. Today, “treatment” depends on the CAUSE of your thyroid problem, not your TSH lab test result.

      YaY! for desiccated thyroid rather than a T4-only med!!! That’s worthy of paying for that doc’s “care”! From my perspective, you still need to know WHY you need to ingest anything at all. For instance, pituitary tumors are rare, but they do exist=it’s not always a “thyroid” problem, but ingesting supplemental doses of thyroid hormones can cause a thyroid problem if you don’t need them.

      Treat symptoms (or lack thereof), not lab test results (plural).

  35. Hello. I just saw a new doc who gave me Thyroid. He said it was natural, not synthetic. It was given/sold to me by his office staff in a plain medicine bottle with a label printed on the spot. Dosage was 1 grain however the pills were 2 grains so I was told to break them in half. There was no pamphlet or information about the medication, its manufacturer or where it was made. I tried to find information about it online but with such generic name “Thyroid”, I did not have much success. Imprinted on the pill is “TCL 023”. Can someone please help me figure out what I am taking or point me to a manufacturer’s site? My next appointment is not for another month and the office staff doesn’t seem to know much about the medication when I asked beyond the standard “doc always prescribes it for low thyroid and it’s all natural so you’re safe.” Thank you!

    • Natural thyroid usually means thyroid hormones from a cow or a pig (over the counter versions) or from a pig (prescription versions in the USA). IF your doc makes his own concoction, it’s usually made from cows, pigs OR synthetic (chemically equivalent) hormones. I, personally, wouldn’t ingest anything that doesn’t come with a package insert. If his staff doesn’t know what’s in it, or how to ingest it, or how to interpret your lab results differently once you are ingesting it, the doctor may not know either(!), and I’d find another doctor who DOES know.

    • I searched on line for the numbers on your medication and came up with a site “Drugs.com” that says it is 120 mg descicated thyroid. Rugby is the manufacturer.

  36. Chris, I’ve been getting your emails for a while now and really appreciate your work, especially on behalf of hypothyroid patients 🙂

    You made this comment and it caught my eye: …”elevations in either testosterone or estrogen (extremely common in hypothyroid patients) affect the levels of circulating free thyroid hormone. For example, high levels of estrogen will increase levels of thyroid binding protein. Thyroid hormone is inactive as long as it’s bound to this protein. If you take thyroid replacement, but you have too much binding protein, there won’t be enough of the active form to produce the desired effect.”

    As of Feb. 2014 I am under the care of a bioidentical hormone practitioner and she is managing my thyroid. I have Hashi’s, too. My tests showed low everything – flat lined adrenals, low estrogen and low testosterone among other things. My thyroid panel was acceptable but not optimized. Symptoms are somewhat under control and afternoon fatigue and sleeping habits are improving but not great or normal, IMO.

    Now, I’ve suspected for about a year now that the testosterone was making me gain weight in the middle & butt (I’m fighting slow metabolism due to years of low carbing and yo-yo dieting – trying now to heal and following some of Matt Stone’s and Ari Whitten’s guidelines – but the weight gain with refeeding is getting too much, IMO). I’m on 90 mg of Armour thyroid and progesterone compounded cream also. I eat very well with occasional minor slips. Organic whenever possible, green smoothies, raw veggies, salads, mostly fish and chicken and occasional beef.

    Everyone I ask about the possible connection between testosterone replacement and weight think it’s impossible – the general consensus is T makes women and men both tend to lose weight and build muscle. (I can’t really work out much due to some unrepaired orthopedic issues right now).

    Any wisdom would be appreciated. I love the way the T replacement makes me feel, but I HAVE to figure out what all the elements are of my recent huge weight gain (over 20 lbs in 5 months). Doesn’t seem like refeeding could account for it all because of the foods I eat and I know better than to pig out after all those years of paleo and low to zero carbing. Thanks in advance!

    • Testosterone is like most meds: it’s made by men for men, based on studies of men by men. My testosterone is non-existent, but I refuse to ingest any, because doctors don’t really know what it’s doing to men!

      Flat-lined adrenals means you’re probably converting any T4 you’re ingesting into RT3.

      GMO plants and GE animals are not the only source of endocrine disruptors (autoimmune disease). Check all your household cleaners, soaps, shampoos, etc.

      In my experiences since 1998, the weight gain has been 100% related to insufficient FT3 at the cellular level, for which there is no blood test. Estrogens are stored in fat in both men and women; maybe your estrogens’ levels have increased with the 20 pounds?

      Maybe a break from the T?

      Maybe more T3?

      It’s all related, and we’re all very individual. Hope your new doc can help!

  37. help! hashi’s patient. taking 65mgs Nature Throid. now losing hair. test results last wk :
    TSH .728
    FREE T4 71
    T3 202.60

    I have asked the doctor if there could be something up w/ my hormones. She didn’t answer and offered to lower my Nature Throid and put me on T4 med.

    I’m going to be bald soon! HELP!

  38. Hi I don’t have a thyroid because its been removed which is the best meds you recommend synthroid or naturthroid. I’ve been taking so many different meds going higher & lower that I just stopped taking everything & now starting from scratch again so now I’m taking 75 MCG synthroid. Its only been about a week 1/2 I started with 1/4 every 3 days then 1/2 & so on to work up to now 75 MCG but I’m not losing much weight & lots of hair is falling even m,y eyebrows is this from synthroid or just being hypo from being off all meds for 2 months. However as soon as I got on syhthroid I noticed the hair loss. Should I just go back to naturthroid?

  39. Dear Barb,

    My mom is having Hypothyroidism and her latest reports read as : T3 – 62.35, T4 – 9.40, TSH – 2.50 & Anti Thyroglobulin Anti bodies – 369. She has been on Elctrocxin 75 for past 6 months. Pls advice

    • Sounds like you live in another country, where lab results are very different. However, even one antibody is TOO MANY, because rigorously screened, healthy volunteers with healthy thyroids had ZERO antibodies–they were undetectable. “Thyroid” antibodies aren’t evidence of “thyroid” disease; they are evidence of autoimmune disease that attacks the thyroid FIRST. They prevent whatever T3 your Mom has available (regardless if ingesting or secreted) from getting INto the cells. There is NO lab test result that reveals how much T3 is actually getting INto the cells.

      Left unchecked, antibodies go on to attack other organs/systems. I suggest your Mom read and re-read the above article and all the comments by everyone until she understands. I’ve suggested other resources in other comments as well. I’m not a doctor or a nurse; but most doctors and nurses aren’t living without a thyroid, and the ones I’ve met who have “hypothyroidism” are settling for abuse and neglect from their doctors with a T4-only med that shortens their lifespan. I wish you education and a medical professional who is willing to be educated so your Mom can feel better, regardless of what her lab results might be.

  40. deration.

    I have a question, i take synthroid since i have 12 years old ( im now 26), but i forget sometimes to take it.
    do you know if there is another form to take the hormones? like for birthcontrol, now we can use implanon – a chip full of birthconrols hormones that stays in your arm 3 years, until u change it.
    does anyone know if such thing already exists for thyroid hormones?

    • Not to my knowledge, but it sounds nice.

      Sunthroid is T4-only; in general, for most people, it takes seven to ten days to get to your liver, get converted into Free T3 and get back out to your cells, so missing one dose, one day, probably won’t hurt you. If it does, you probably won’t notice until a week later.

      You deserve to replace the T3 not converted from T4 as well. Clinical outcomes prove that the T3 converted from T4 is not enough to restore and maintain health. If you have no antibodies, you might do well on an NDT.

  41. I have a question, i take synthroid since i have 12 years old ( im now 26), but i forget sometimes to take it.
    do you know if there is another form to take the hormones? like for birthcontrol, now we can use implanon – a chip full of birthconrols hormones that stays in your arm 3 years, until u change it.
    does anyone know if such thing already exists for thyroid hormones?

    • Hello, Thyroidless Barb, are you still receiving replies from this site? I am at my witts end and you seem so much more knowledgeable than anyone I have found yet. If you can help me too I would be so grateful, I am so close to giving up this fight, no matter what I try NOTHING works…

      If you don’t mind, my issue is I had half of my thyroid removed by UNEDUCATED Endocrinologists and then was put on 30 mcg/mg? of Synthroid, then MONTHS of getting worse and worse. I found another doctor who allowed me to try Synthroid + cytomel….still no change. She then let me try Armour…..I felt much better (scale of 0 to 10, “10” being how I felt BEFORE Hashimotos problems, so with Armour 180 I felt like I had gone from 0 to 6.) However I still had/have MAJOR memory problems, anxiety, and inflammation NO MATTER the dose or T4 T4/t3 combo..This “better feeling” was short lived, and then we looked at my low adrenals (24 hr saliva tests), she put me on 400mg of Spironolactone and I started to feel better for a few months then I began to feel HYPER, so we lowered the 180 Armour to 120, which right away made me VERY HYPO, so 4 months later I had to go back on the 180 dose!!! I have done all of the allergens test, for 18 months I took out ALL of the foods that “could cause problems”, and that make life worth living, did the gut and candida tests, all negative….A few months into taking the Spironolactone I began having NON STOP UTI’s, I knew it was the Spiro DESPITE the UNEDUCATED KNOW IT ALL DOC’s online who claim Spironolactone DOES NOT cause UTI’s as a side effect, but weeks of research prove that using Spironolactone causes UTI’s IN MANY WOMEN, NOT JUST ME !!! I decided to wean off of the Spironolactone because NON-stop UTI’s is simply unbearable, BUT weeks later I had the HORRIBLE acne again and all over weakness and body pain. I then started back taking 200 MG of Spirono but 200 had little affect on the acne and NO effect on the inflammation/pain. I am now feeling the HYPER again, and my doc told me to start back on 400 mg of Spirono, but it DOES NOT help with the inflammation, it DOES cause non-stop uti’s, it ONLY helps with my chronic pain and acne…..

      I have read SO MUCH for SO long, most things are contradictory to other things, I know about the rt3 etc but I can’t find CUT AND DRY information to print off for my doc…..seriously, if we have Hashimotos we MOST likely can’t concentrate, focus, remember the info from 40 different “thyroid” sites…….I have just become TOO overwhelmed, my doctor will try anything to help me, BUT she is VERY over worked due to being the ONLY doctor who will listen to patients, so I NEED to be able to get the CLEAR info on what to try next from someone like you who really knows her stuff!!

      I am so sorry to bother you with this, I just don’t know where else to turn, the information is all so spread out and contradictory from one of these sites to another and my going , SEEMINGLY, ALL the way back to square one….I don’t want to keep living like this if there is some other thing to help me…Thank you so so so very much, I hope to hear from you, and I hope you have a wonderful week.

      • Oop’s Sorry I forgot to add my current syptoms and dosages:

        I take 400 mg Spironolactone (was on 200 until yesterday) (been taking Spironolactone for 9 months now)

        180 mg of Armour

        I have been “Hypo” for 4 years now as far as always having all over inflammation, edema, unable to lose weight, brain fog (more like brain dead), weakness, all over pain, headaches almost daily, sore neck, dry eyes, constant white goop in my eyes often making my vision blurry, acne on face, neck, under chin, upper back (but only if im taking less than 400 mg Spironolactone), MAJOR anxiety, easily winded just walking from one side of house to the other, and HOT, I am ALWAYS SO HOT, I sweat almost non stop and stay HOT no matter what,(since May, before May it just was night sweats and almost daily HOT FLASHES, I have been dealing with the EASILY STARTLED issues for YEARS now (7 years), and it has NOT improved AT ALL taking nothing more than sudden movement to send me to the ceiling, and noise is worse and the “freight” makes me MAD angry at the one who caused me to startle, I am SAD, but not depressed, I feel helpless and hopeless, I feel like crying but have NO tears, and NO saliva anymore (Spirono side effect) I STILL have TMJ and recently my plantar fasciitis returned so walking HURTS in the mornings especially, dry hair dry skin, and weird individual bumps that are skin colored, sometimes itch for a day but can go weeks without itching, they sart as an itch I MUST scratch and slowly grow to a 2/3cm bump kind of like a skin colored pimple…In the past year I have gotten 7 of these, one on my breast, 3 on thighs, and 2 on legs, one on my knuckle on right hand middle finger and I can’t find info on what they are? I am SURE there are more symptoms but I can’t remember right now. My skin is still sagging more and more especially on my thighs and chin/face, It started in late 2010 I was 32 yr old 117 lbs 5’4″ tall…..NOW I am 36 yrs old BUT I LOOK 56 yrs old, I weigh 136 and CAN’T LOSE NO MATTER WHAT I TRY….

        I would like to try LDN for the inflammation because I cant wear shoes AT ALL, and I haven’t been able to wear a wedding ring for 3 years….but with NOTHING else getting better, I am at a wall….I just don’t know what to do? Again, thank you so much!

        • Yes, I’m still here, periodically. I still can’t afford the internet at home.

          Most people I know who ingest an NDT also ingest synthetic T3 as a supplement, as needed or daily with extra as needed. The T3 in one grain (60 mg) of your NDT acts the same way as synthetic T3–it gets to work in about 30-45 minutes after dissolving it in your mouth and wears off 3-6 hours later. I ingest my T3 doses about every three hours. I DO have “thyroid” antibodies (autoimmune disease) even though i have no thyroid.

          There’s an LDN facebook page; they “treat” themselves based on lab results, comparing their lab results to the reference ranges provided by their lab (which are based on sick and suffering people who have dysfunctional thyroids). I haven’t tried it, so I can’t help with that.

          IF you’re converting the T4 in the NDT (and it’s about 80% T4) into RT3 instead of FT3, that means the T3 in the NDT (about 15%) isn’t enough for all your cells.

          IF autoimmune disease caused your “hypothyroidism” in the first place, that needs to be treated as well as replacing the thyroid hormones your thyroid can no longer produce since you had it removed. Same with calcium since your paras were removed.

          A healthy thyroid makes about 94-110 T4 and 10-22 T3, so, ingesting an NDT, you’ll need 3-5 grains (180 mg is 3 grains) for replacement. Congrats on getting a doc to prescribe 3 grains! Dissolve them in your mouth at 3 different times per day (not all at once)!

          It takes 7-10 days for the T4 to get to your liver, get converted and back out to your cells, so changing dosing times and amounts, usually, takes about two weeks for you to notice any difference.

          I think ALL of your symptoms are related to under-replacement of thyroid hormones, even if you are converting the T4 to FT3 instead of RT3. The imbalance really screws with our reproductive hormones. When I have an estrogen spike, a separate dose my of OTC progesterone cream helps. Women even have estrogen spikes AFTER menopause.

          As the ovaries shut down (during the sometimes ten-plus years of menopause), progesterone levels decrease quicker than estrogens’ levels, so supplementing or replacing progesterone becomes that much more important. Usually, adrenals pick up the slack as the ovaries shut down, but with thyroid problems comes adrenal problems. Women ovulate for an AVERAGE of 40 years, so take your age when you started and don’t let any doctor bully you into removing your parts! Menopause is more about FLUCTUATING levels of reproductive hormones than it is in dramatically dropping levels. Intense fluctuations, as the adrenals learn to compensate for the ovaries, cause symptoms. Those symptoms can be less intense IF your cells are getting the T3 they need.

          Here’s a blog written by someone else named Barb (I’m not writing blogs yet). If I had written it, it’d be a lot longer!

          http://www.tiredthyroid.com/blog/2014/08/07/why-t4-only-treatments-do-not-work-why-we-cant-dose-by-tsh-and-why-we-need-t3/

          Bottom line, for me: a healthy thyroid is EXQUISITELY self regulating. Providing this exquisite self regulation from the OUTside IN is NOT easy! You have to know how a healthy thyroid works so you can replicate that health for your individual body. The only site I know that summarizes all this information is http://www.eaware.org.

          Hope this helps!!!

          There are multiple articles on my timeline on facebook set to “Public” view so you don’t have to be my friend to read them. Most of those articles appear in January for “Thyroid Awareness Month”. Barb Shultz (Barb Boston), my profile pic is a white tiger cub.

  42. How do you find a dr to test your labs and treat hashimotos? I’m desperate to find a dr that can help me. I feel like I’m dying…

  43. Hi Barb,

    Great insight you have there. It is difficult to find information for those who no longer have a thyroid. Can I ask what you take now that your RT3 problem is at bay? Do you take T4/T3 or just T3?

    Thanks,
    Rachel

  44. I am a 66 year old female. I am tired; sleep great at night; can’t lose any weight; walk everyday 2 plus miles. Last TSH in October 2013 5.75. I have been on the high side for several years. Do I need thyroid replacement therapy?

    • Only YOU can make that decision. If I were you, I’d get more tests FIRST, to figure out WHY your TSH is so high. Maybe you have thyroid antibodies, which is evidence of autoimmune disease, not thyroid disease? Maybe you’re no longer converting your own T4 into the Free T3 your cells need, in which case, you need a T3-only med instead of a T4-only med. TSH results, just like Free T3 results, fluctuate during the day, so what TIME of day is your blood drawn (both results are highest in the morning, lowest at 3-4 pm for “most people”)? Mr. Kresser won’t answer your questions; I suggest you make an appointment with a functional medicine doctor who also happens to be an integrative medical doctor, it will probably be cheaper to order your own tests from an on-line laboratory, and get more results, get more info on how a healthy thyroid works and THEN decide if and which thyroid hormone you might need to supplement or replace. 🙂

      Rigorously screened, healthy volunteers tested as follows, so ignore any labs’ reference ranges:

      TSH .4-2.5 (yes, 5.+ anything is too high!)
      Free T4 .7-1.8
      Free T3 for women 4.25-6.19
      Free T3 for men 2.0-5.0
      Reverse T3 ZERO
      Antibodies ZERO! UNdetectable!!!
      (There are four antibody tests.)

      Good luck!!!

      • Barb,

        I have appreciated reading your comments. My father had thyroid cancer many years ago and it is now becomming clear to me that his medication for NO THYROID has been terrible mis-managed for a long time. I am trying to educate myself so I can hopefully steer him in the right direction to get the help he needs. The internet seems to be focused primarily on treating hypothyroidism rather than treatment for no thyroid. Would you be willing to give me your perspective if I ask you some questions?
        If so, my email is [email protected].

        First question: Is the reason you are unable to convert T4 to T3 because you have no thyroid or a different unrelated issue?

        • Mark:

          I sent you an email.

          We think I was only converting T4 into Reverse T3, but there’s no way to tell since we just started me on T3-only and never looked back. eaware.org, under Thyroid on the left, under RT3, says that ingesting T4 for a long period of time causes Reverse T3, so that’s probably also a part of my previous problem. Since RT3 can only be made from T4, I won’t ever have that problem again.

          On the other hand, ingesting T4-only when I needed the T3 not converted from T4 also caused “other issues”.

        • First, you need to know the test measurement. (Get a copy of ALL your lab reports; they show your result, the test measurement and the reference range your lab is using.)
          Second, you need to realize that Free T3 only measures the Free T3 IN your bloodstream, NOT how much is actually getting INTO your cells.
          Third, in the USA, healthy women with healthy thyroids test between 4.25-6.19 pg/mL, so, if that’s your test measurement, someone is misreading the result as high, OR, everyone being tested by your particular lab is really, really sick and suffering. (I’d be nearing my deathbed if my FT3 result was 2.anything!)
          Fourth: RT3 and antibodies can prevent the Free T3 in your bloodstream from getting INto your cells, but there is NO blood test to measure how much FT3 your cells are actually receiving.
          Fifth, the time of day your blood is drawn affects your result (it’s highest in the morning and lowest in the afternoon for “most people”).

          Doctors will say it means you are “hyperthyroid” or you have Graves Disease. Graves is autoimmune disease, not thyroid disease, so destroying your thyroid won’t address the underlying cause. I’ve listed elsewhere the antibody tests.

          You can order your own tests from an online lab if you can’t get anyone to re-order (or order more) tests.

          If they want you to swallow radioisotopes or ingest an anti-thyroid med, get a second opinion first!!!

  45. Hi!! so glad i came across this board, Thyroidless Barb, I have sooo many questions for you…. I have no thyoird, had rt3, 8 weeks at t3 only, plus low cortisol, at cross road, should i have antibodies checked before I make a switch??

    • I would get my antibodies checked, remembering that one is too many regardless of which reference range the lab provides. There are four antibody tests:

      Hashimoto’s Disease:
      Thyroid Peroxidase Antibody (TPOab)
      Anti-Thyroglobulin (TgAb)

      Grave’s Disease:
      Thyroid Stimulating Immunoglobulin (TSI)
      Thyroid Receptor Antibody (TrAb)

      This might help:

      LOW thyroid (short version):

      We get what appear to be hyPER symptoms when labs prove we are hyPO. What occurs is that when the body senses the metabolism slowing due to low thyroid hormones, in it’s effort to maintain homeostasis, the adrenals are given the signal to increase catecholamine output (adrenalin) which revs up the heart rate and BP, causing anxiety, heart racing and palps.

      NO thyroid:

      We get what appear to be hyPER symptoms AND lab results when we are hyPO. What occurs is that when the body senses the metabolism slowing due to low thyroid hormones, at the CELLULAR level (not in the bloodstream), in it’s effort to maintain homeostasis, the adrenals are given the signal to increase catecholamine output (adrenalin) which revs up the heart rate and BP, causing anxiety, heart racing and palps. Low T3 at the cellular level also stops production of progesterone (elevating estrogen unopposed by progesterone) and increases cortisol. Progesterone is a KNOWN component of converting T4 into FT3, and I notice my T3 works better when I use my OTC progesterone cream.

      Labs will always be higher and the TSH lower when ingesting thyroid hormones, especially when ingesting T3, because you must ingest more than a healthy thyroid secretes to get the same effect at the cellular level….

      My TSH and FT4 are completely suppressed; my FT3 is too high; my RT3 is non-existent, since it can only be made from T4; and my antibody levels/results vary/fluctuate, depending on what, when and how much I eat. I trying to do all organic, no GMOs, but it’s not cheap!

      I’m also not a doctor or nurse. We’re all VERY individual!

  46. Thank you so much for your article, I wondered why I couldn’t tolerate NDT and now I appear to have the answer. Unfortunately, I think I’m one of those subsets of Hashimoto’s patients that not only have antibodies to thyroid tissue but to the actual thyroid hormones themselves, as ANY thyroid medication makes the soreness in my throat worse. Is there a way to test this – what are the antibodies called, just anti-T4 and anti-T3? If anybody knows the names of all the antibodies associated with the thyroid, please can you let me know because I’m having a blood test this week and want to make sure I get the right tests!

    • Antibodies and their tests are:

      Hashimoto’s Disease:
      Thyroid Peroxidase Antibody (TPOab)
      Anti-Thyroglobulin (TgAb)

      Grave’s Disease:
      Thyroid Stimulating Immunoglobulin (TSI)
      Thyroid Receptor Antibody (TrAb)

      Again, any positive result is evidence of autoimmune disease.

      NDTs are, in general, better than a T4-only med, because of the T3 in them. What the famous thyroid advocates DON’T tell you is that a healthy thyroid secretes tiny bits of T3, all day every day, the synthetic version of T3 is called Cytomel, and those with antibodies, in general, won’t be able to tolerate an NDT (they need the synthetic T3).

      ThyroidLESS patients’ experiences PROVE that the T3 converted from T4 is not enough, precisely because they need and DESERVE replacement of the T3 not converted from T4. If you can’t convert T4 into FT3, you DESERVE 100% replacement of your T3.

      Ingesting T3 is different than ingesting T4; you can’t just take it once a day.

      • Thank you for your replies to my few postings on here, and your quick response, Barb. That’s so interesting about NDT, I wish I’d known that before reading Janie Bowthorpe’s book and spending over 200 quid (of money I couldn’t really spare) importing it to the UK! On my test last year a doctor told me I appeared to be a good converter of T4 to T3. I hope this is true. I’ve never had a Reserve T3 test as I was told it was a specialised test that wasn’t available to me due to me being bed/housebound (with a neurological disease not thyroid, although I think low thyroid might be contributing/overlapping with that.)

        What you said higher up in your other reply to me about increased heartrate/palpitations – so do these effects dissipate as your metabolism and body adjusts, meaning it’s worth persevering with the meds? I will be asking my GP about adding Cytomel then now if necessary when we know my latest results. Do you think it’s worth pursuing meds when I get this increased throat soreness – it feels like a double-edged sword: Increased energy, brain fog lifting, better sleep etc but increased soreness in thyroid and tendency of heartrate to increase. I don’t want to make matters worse by increasing the autoimmune attack, and I already have heart failure. Maybe I just need to go slowly and give my body time to adapt. Anyway, please don’t feel a need to respond as I don’t want to be an imposition! 🙂 You were already kind enough to answer the other questions.

        • You are NOT a bother!!!

          Ingesting T3 will teach your thyroid to shut down (suppressing your TSH), teach your body to depend on what you ingest. Ingesting thyroid hormones, even synthetic ones, is NOT a treatment for antibodies. Experimentation with low dose naltrexone is ongoing, but I decided against it, for me. Ingesting T3 “resolved” my congestive heart failure, within ten days of ingesting full replacement doses, not “supplemental” doses. IF you choose to ingest T3: Start low, build up. http://www.eaware.org suggests (not ingesting any T4), 12.5 mcg, twice a day, increasing by 12.5 mcg every 5-7 days. I increased every three days; a friend who still has his thyroid increased every eight days. We are ALL too individual for me to suggest what you should do; just know that considerable experimentation on yourself, by yourself, will be necessary. Read from the websites I listed; learn how a healthy thyroid works, so you can be your own thyroid from the outside in, if you so choose. Best wishes!!!

  47. Have found the protocols of NUTRI-SPEC.NET to be the most complete.Progesterone by mouth is useful ,as in PROGEST-E.
    The endocrine/immuno/neuro sisters are so interrelated that only chasing T: 3/4/glandular may be too focused .You probably need more saturated fat. The best gut flora supplement is FLORASTOR .Your body wants to heal.
    Z

    • Thank you!!! Most patients appreciate doctors who can still learn from patients (at least I do). What my doc found most interesting: it is a punishable CRIME (cruelty) to “practice” the “acceptable” standard of “care” on chimps. Yet the AACE continues to mandate that every doctor in every specialty “practice” this same cruelty on humans (at least one in every eight women). From my perspective, without a thyroid and being unable to convert T4 into FT3, this cruelty “practiced” on me is not only cruel, it is abusive, neglectFULL, and deadly. I sat in a wheelchair, dying of congestive heart failure, which cardiologists were unable to explain. Within ten days of ingesting replacement doses of T3, my wheelchair was gone and so was my CHF. Coroners are no longer trained to notice accumulated mucin in the heart due to INsufficient T3 at the CELLULAR level, so, now, one in three women dies of “heart disease”….

    • Doctor, I hope by interesting you also mean scary. Interesting in that I think there needs to be an internet presence of integrative and endocrine physician specialists and researchers willing to listen to the voices of thyroid sufferers and then more research needs to be done. This little gland is a powerhouse and really affects quality of life for many. There needs to be more attention paid and then there also needs to be a calming and authoritative voice from the people who dedicate their lives to endocrine research- not just a bunch of us sick from it pretending to be doctors. I am a nurse but I fully respect that I didn’t do 4 years medical, followed by residency and fellowship followed by lifetime of practice. There is too much CRAP advice on the internet regarding thyroid. With that said however, where there is smoke, there is fire…

      • I agree. A lot of the information I have found has caused (me personally) more harm than good. The NDT so heavily promoted on Janie Bowthorpe’s website and book and the T3 it contains was too much for me, I was soon having high heart rate and palpitations. This article finally explains why y I couldn’t tolerate that, even though NDT is so heavily promoted by some as being THE BEST choice for EVERYONE.

        • LOW thyroid:

          We get what appear to be hyPER symptoms when labs prove we are hyPO. What occurs is that when the body senses the metabolism slowing due to low thyroid hormones, in it’s effort to maintain homeostasis, the adrenals are given the signal to increase catecholamine output (adrenalin) which revs up the heart rate and BP, causing anxiety, heart racing and palps.

          NO thyroid:

          We get what appear to be hyPER symptoms AND lab results when we are hyPO. What occurs is that when the body senses the metabolism slowing due to low thyroid hormones, at the CELLULAR level (not in the bloodstream), in it’s effort to maintain homeostasis, the adrenals are given the signal to increase catecholamine output (adrenalin) which revs up the heart rate and BP, causing anxiety, heart racing and palps. Low T3 at the cellular level also stops production of progesterone (elevating estrogen unopposed by progesterone) and increases cortisol. Progesterone is a KNOWN component of converting T4 into FT3, and I notice my T3 works better when I use my OTC progesterone cream.

          • you sound like a fellow woman warrior as I was.. or am… I would like to talk to you about a few things… but im still recovering from thyroid cancer surgery and parathyroid surg… you wouldn’t believe my story.. my health issues that were ignored for years.. even when I presented them with info and test results.. I would love your insight if you get a chance.. thanks jackie

            • Thanks jackie. There are, literally, millions of us.

              When doctors remove the paras with the thyroid, you will need calcium replacement for “the rest of your life”. The thyroid makes calcitonin, which opposes PTH. So, PTH tells the body “make calcium” and calcitonin, from the thyroid you’re now missing, says “ok, but not too much”. Some surgeons are smart enough to leave paras intact; some patients adjust to not having calcitonin; and some don’t. I’m lucky: I “only” swallowed RAI, which destroyed my thyroid (literally, disintegrated it), and I adjusted to not having any calcitonin.

              The reference range for serum calcium is very narrow for a reason: too little or too much can kill you in just a few days.

              “Thyroid” problems can also CAUSE parathyroid problems, which is yet another story from someone I know that you “won’t” believe!!!

              I don’t have the internet at home or on my phone, but there are lots of groups on fb where you can gain info. I listed several websites above in other comments. On fb, FTPO has multiple groups, one for each problem encountered by most people with “thyroid” problems. There are very few groups for those of us withOUT a thyroid, but they do exist!

              I wish you a speedy recovery from surgery and a knowledgable doc who will be truthful (i.e., one who says “I don’t know” when they don’t know).

  48. I am having major Thyroid symptoms but normal tests…i believe I have estrogen dominance but have yet to find a doctor who diagnosis this let alone who cares! So frustrating!!

    • Sure is!!! 21st Century medical SCIENCE has PROVEN that progesterone is a known component of converting your own or ingested T4 into the Free T3 that every individual cell in the body and the brain NEEDS. I ingest T3 only and have proven that progesterone is also necessary for my cells to use my T3 (it works better). I use an OTC progesterone cream, because doctors don’t know how much prescription progesterone is absorbed, and they “think” it’s half life is “about 17 hours”. Estrogen, especially when elevated, but definitely when UNopposed by equally elevated progesterone, CAUSES excess stress (more frustration)! Stress uses up the supply of Free T3 quicker than any other drain, and a healthy thyroid even interprets food as stress. Left untreated, even a mild thyroid problem wreaks havoc on ALL other hormones, especially for women. Get a Free T3 test done from blood drawn at 3-4 Pm when it’s lowest, and know that healthy women who were tested created a reference range of 4.25-6.19. Of course, the lab won’t use that reference range, because they are basing their reference range on sick and suffering people. Then, find a doctor who treats symptoms, not lab results, and soon, because excess estrogen creates fibrous tumors in various parts of the body. I have one on my left adrenal gland, so I’m short more than just progesterone. Surgery to remove it would only replace the tumor with scar tissue and I’d still have the same problem: only one functioning adrenal. If you develop uterine fibroids, know they go away on their own once you start replacing your progesterone. YaY!!! You don’t “need” a hysterectomy OR “ablation”. If you develop one of these tumors in a breast and start getting radiated every year to “check it”, KNOW the radiation WILL eventually turn it into a malignant tumor. Mandate a sonogram and bypass the mammogram altogether. Radiation also destroys thyroids, but you won’t hear that from ANY radiologist or endocrinologist! They aren’t sufficiently educated about how women’s thyroids function or the connection between T3 and every other hormone, much less the connection between one in every eight women being radiated annually and being diagnosed with a “thyroid problem”. If you haven’t gotten “thyroid” antibodies tested, that’s a good idea as well. “Thyroid” antibodies aren’t evidence of thyroid disease; they are evidence of autoimmune disease that attacks your thyroid FIRST.

  49. Don’t you just love people who post articles like this, anticipating multiple comments and questions from the millions of people suffering? All so those suffering people can be ignored by the author of the article, and actual doctors, because the suffering people don’t have endless supplies of money??? SMH, and whoever moderates comments should be, too….

    There’s TONS of articles like this! They are all directed at people who still have their thyroid. If you are thyroidLESS, please understand you are NOT “hypothyroid” and you deserve 100% replacement of T3 for ALL your cells. IF you can convert T4 into FT3, great! You still need that T3 not converted from T4.

    • At last! Something that makes sense. Sheesh it’s so hard to find info on thyroidless people like myself!
      Thank You!

      • You’re welcome! Please know that labs’ reference ranges change every 2-3 years and they are based on the sick and suffering people that lab is testing; rigorously screened, healthy volunteers haven’t been tested since 2002. 🙁 Lab tests’ results become irrelevant once you are ingesting ANY version of T3, because 21st Century medical SCIENCE has PROVEN that you need to ingest more than a healthy thyroid would secrete, just because you are INGESTING it. If your doc doesn’t understand this, then your results will be compared to the labs’ reference ranges, based on those sick and suffering people who still have a thyroid that’s not working.

  50. Any advice would be helpful… Unfortunately at the beginning of the year I haven’t been able to see my doctor due to new insurance and I don’t even know where to go now… Trying to get him nominated on my new insurance but I’m not sure how long it will take

    • eaware.org, from Thyroid on the left
      21centurymed.com, Hypothyroidism tab
      hypothyroidmom.com
      recoveringwitht3.com
      stopthethyroidmadness.com
      thyroidchange.org

      .org sites are not-for-profit but may request donations
      .com sites are selling services, time, books, and/or products

  51. I’m so confused. I went to the doctor because my neck felt swollen and my ears have been ringing. My ears look okay but I have mild hearing loss got an MRI and my brain was okay… My doctor thought the swelling in my neck was an infection. Antibiotics took it away. Them I got an ultrasound of my neck I have a small cyst that’s beign on my thyroid. Doc checked my tsh level iodine and other things. Low levels of iodine so I went on iodine pills. Then next blood work check tsh levels again checked for that auto immune disease and t3 and t4. Don’t have any antibodies or immune disease. But after taking iodine for a little under 3 months my tsh got higher. It went from 2.8 to a little over 3 so he decided I was hypothyroid. Now that I’m taking armour thyroid my hair has increasingly started falling out my skin feels even drier. And he told me to keep taking iodine. I feel like everything he’s put me on has made my thyroid even slower I don’t get it. I’m about a couple days away from stopping the armour thyroid and just started going gluten free to try and see if that helps my thyroid. I’ve always had random spurts of weight gain and loss. Hair was falling out before the armour thyroid but now I can see my scalp and I lose a bunch of hair everyday to the point where my scalp is starting to feel weird. Can anyone suggest anything? I just want my hair to stop falling out, I can deal with feeling tired I’ve been like that since I hit pueberty.

    • Sounds like MAYBE, the T3 in the Armour isn’t enough, or you’re not ingesting enough Armour, or maybe(?) you’re allergic to a filler in the Armour, or maybe(?) you’re allergic to porcine or GMOs (Armour is made from pigs’ thyroids and the pigs are ingesting, exclusively GMO feed), or you’re not converting the T4 in the Armour into Free T3, but Reverse T3 instead, or you MAY have a pituitary problem. Pituitary tumors are rare, but they DO exist.

      Were the tests FREE T3 and FREE T4? Total T3 and Total T4 really, tell your doc nothing. You need copies of ALL your lab results in YOUR hands, always. Example: you may need to make copies of your copies for a different doc.

      Iron, B12, D3, Cortisol could all or individually be too high or too low, causing the T4 in the Armour to convert to RT3 instead of FT3.

      Read here: http://www.eaware.org, from Thyroid on the left. It has lists of symptoms, causes of conversion problems and treatments.

      You can order your own tests if you have an endless supply of money; you can order your own NDT made from range-fed cows in New Zealand if you have an endless supply of money. Insurance won’t reimburse you for either, usually. All NDTs are about 80% T4, so IF there is a conversion problem, you’ll need a T3-only med. There are ways to order that, as well, without a prescription, if you have endless supplies of money without insurance reimbursement. Unless you understand how a healthy thyroid works, I don’t suggest this means of self-treatment.

      It’s clear from your individual symptoms that the “cyst” on your thyroid is depleting the T3 available to your cells, and every individual cell NEEDS T3, converted and not. Congrats on getting your doc to prescribe an NDT!!! That indicates more knowledge of how a healthy thyroid works than most docs can demonstrate. 🙂 YaY! For you having no antibodies!!!!!!! Make sure all four antibodies were tested….

      Lists of symptoms are also here: http://www.21centurymed.com, Hypothyroidism tab and scroll down

      And here: http://www.hypothyroidmom.com.

      Hope you get in to see a doctor soon!

  52. What do you think is best for someone who doesn’t have a thyroid? I had a thyroidectomy 10 years ago and take Synthroid. I’m not sure if this is optimal, though. I’m wondering if perhaps something with T3 would be better?

    • Thyroidless patients’ experience proves that the T3 converted from a T4-only med (your Synthroid) is NOT enough. In most cases, ingesting a T4-only med, by itself, too long causes a Reverse T3 problem (the T4 gets converted to RT3 instead of/in addition to Free T3). Cells can’t use RT3, so massive, systemic illness is the result of cells not getting enough FT3, and the FT3 isn’t enough in the first place. Yes, please get either some Cytomel to ingest in addition to your Synthroid, or switch to an NDT. Neither Cytomel nor an NDT are ingested only once a day like your Synthroid, so, please educate yourself. 🙂

      • Barb, you are putting a lot of misinformation out here. You should know better than all this. No body is the same!!! Some people have hashi and do fine on T4, some need T3, some go well with Armour, some don’t. Not everyone has rT3… has the internet gone nuts?

        • She clearly states that she has NO thyroid. ThyroidLESS patients’ experiences (clinical outcomes) PROVE that the T3 converted from T4 is NOT enough.

          Even people with healthy thyroids convert their own T4 into RT3; the difference is, they HAVE A THYROID to make the T3 not converted from T4, AND the EXTRA T3 they need to clear their RT3. Again, she clearly stated she has NO thyroid.

          Just because a doctor can control a PITUITARY lab test result, even when there is no thyroid with which the pituitary can communicate, does NOT mean that a thyroidLESS patient is “optimal” when ingesting a T4-only med. It just means that ill-educated doctors can continue to blame “other causes”, refer us to multiple specialists who also “can’t figure out” what’s wrong, until, ultimately, we are all but bankrupted, and get referred to a psychiatrist who assures us WE are to blame for our “lifestyle” choices. ALL, 100% LIES, based on 20th century medical MYTH.

          The “practice” of 20th century medical MYTH is a punishable crime when applied to chimps; otherwise, we’d have gender-specific thyroid hormones’ (plural) replacements because we humans are so closely related to chimps. I think we humans deserve better than cruelty, so I share MY clinical outcome (among others’), not “misinformation”. Based on my experiences since 1998, doctors and the nurses they educate are spreading the “misinformation” provided to them by Big Pharma, whose sole goal is profit, and lots of it.

          I wish you, with Hashis, much better education, and continued health! I sincerely hope you learn what you need to know to take good care of you, an individual. Maybe you’re more likely to be treated as an individual human being (rather than as an individual, annual, pituitary lab test result once you have NO THYROID) than most, because you are a nurse? I don’t know….

  53. My experience is that my cells use whatever they will use (Cytomel), and any excess gets processed out as waste. There are NO “side effects” to taking “too much T3”. I can’t afford to waste my money or my Cytomel. I also have “thyroid antibodies” (yes, with NO thyroid). Ingesting thyroid hormones of any kind is NOT treatment for antibodies. Since I can’t convert T4 into T3, I NEED 100% replacement of my T3. I’m not gluten sensitive, dairy sensitive, etc. I AM processed foods sensitive, food-laced-with-chemicals sensitive, etc.

    • Barb,

      That’s NOT true. Excess T3 will make you go hyper and runs a risk of tachycardia and atrial fibrillation, panic attack and a bunch of other oddities… I should know, excess T3 landed me in hospital with both. 🙁 I was on 75 mcg T4 nd 18 mcg T3 when I went into sinus tachycardia followed by a-fib. I am 36 y/o female and VERY fit. Scary. Doctors took me off T3 and kept me on T4 at 75mcg only. 9 months later the T4 only stopped working at that dose and they had me alternating 88mcg and 75 mcg in a variety of combinations before trying me on 75 mcg T4 and 2.5 mcg T3. So far, so good. Really good. It’s been a week. Minimal to no palpitations on low dose T3 (a little morning jitter) and energy is good. Blood pressure immediately dropped 10 mmHg systolic. Fascinating isn’t it? Sign me Hashimoto Kris.

      • Sorry you were fed the same lies (and apparently believed them) as I was, Hashi Kris, but everything I state is 100% true, FOR ME. MY tachycardia, a-fib, and congestive heart failure were a direct result of NO T3 at the cellular level, precisely because I wasn’t converting the T4 into anything but RT3. RT3 is not the ONLY conversion problem, it’s just the most common.

        There is no blood test for how much T3 is actually making it INto the cells, only for how much is circulating in the bloodstream. There IS extensive “evidence” that the reference ranges being used by the labs are based on sick and suffering people with dysfunctional thyroids; there IS extensive “evidence” that once you are ingesting thyroid hormone(s), you will need more than what a healthy thyroid secretes; and when doctors in every specialty treat women who have no thyroid based on lab results compared to reference ranges established by testing sick and suffering people, there IS extensive “evidence” those thyroidless women have a shortened lifespan and die of “heart disease”, currently, one in three. (Coroners are no longer trained to detect accumulation of mucin at the cellular level, namely, in the heart, due to insufficient T3 AT the CELLULAR level.

        I wish you better education than you are being spoon-fed by, apparently, ill-educated doctors; especially if you have NO thyroid.

        I agree, we are all EXTREMELY individual!!! Unfortunately, doctors and the labs don’t distinguish between those who can successfully ingest only a storage hormone and those who need the active hormone, so they, essentially, know nothing about the active hormone when it’s ingested (as opposed to when it’s secreted).

  54. Hi Chris.

    I found the information very interesting. However, I have Hashimotos and have been on Levothyroxine for 1.5 years. I am so depressed and unwell still, its not working. I live in the Channel Islands and its so difficult to get a GP to entertain the idea of supplemental T3. I noted you also said that people with Hashimotos can fluctuate between hyper/hypo which I never knew, so T3 may not be helpful? However if the issue is a conversion problem from T4 to T3 then surely it would be necessary? Also, can your GP tell if your issue is not enough free T3 by your blood test results? It’s such a minefield of information that I feel a little lost…. Any ideas on how to approach my GP with all this would be really very helpful….. I just want to feel well again.

    Many thanks.

    Clare

    • Fluctuating between hyper & hypo = antibodies are taking bites out of your thyroid, dumping large amounts of hormones into your bloodstream. Taking T3 suppresses your TSH, which will “teach” your thyroid to shut down and depend on the T3 you ingest instead. If there is a conversion to RT3 problem, yes, you will need to take T3-only, AND figure out what is causing the RT3, to resolve it. No, a Free T3 result ONLY tells what is AVAILABLE TO YOUR CELLS, not what is actually getting INto your cells. Thyroid hormone(s) are not a treatment for antibodies.

      • Do you know the names of the antibodies that attack the thyroid hormones themselves (that he discusses in the article) – are they just anti-T4 and anti-T3? You sound like you might know. Any chance you can let me know all antibodies associated with the thyroid as I’m having a blood test this week and want to make sure they test the right stuff!

        • Antibodies and their tests are:

          Hashimoto’s Disease:
          Thyroid Peroxidase Antibody (TPOab)
          Anti-Thyroglobulin (TgAb)

          Grave’s Disease:
          Thyroid Stimulating Immunoglobulin (TSI)
          Thyroid Receptor Antibody (TrAb)

          Again, any positive result is evidence of autoimmune disease.

  55. I was born with my thyroid gland not functioning. I have taken many different medicines and I have been increasing in weight all my life. I have considered Bariatric surgery which I really don’t want to do but I am at a loss as to being able to lose weight. The only time I lost weight easily was when my medicine was off and I was wired and full of energy, but happy. I have diabetes now as well as sleep apnea and I really want to lose weight in a healthy effective way. I am on many medications and I am wondering how to figure out if some medications are hindering my attempts at weight loss.

  56. Hi, Chris

    I have Hashimoto’s and gluten allergy, I take Synthroid 75mcg but I have some many side effects like my breasts hurts a lot my headaches are others make me kind funny feeling, I have foggy brain everyday and I honestly I see some of this other people say about if you take medication you are more at risk to have dementia and other mental illness someone told me why I just take iodine and thyrosine instead of all that stuff but I get so worry to do something like that because once in a while I get anxiety attacks too, I honestly I just want something to make me be here for some time I got pregnant in 2010 with hashi already and it was a miracle to have my son now I’m worry no to be here for him he is 2years 11 months by march 6 he will be 3 and have Autism spectrum disorder is so sad for me to see me at my age 41 and with my thyroid bad I have my others kids 26,22, 19, I didn’t have this sickness before can you give some advised what lab should ask to my dr. thank you

    Janeth

  57. Addendum
    I forgot to mention in previous email I also experience hairloss, muscle fatigue ana pain and joint pain. uric acid levels are normal. i also take Seacure aprocessed fish supplement for protein & Omega 3 and Methyl Protect by Xymogen with B12, Folate and Betaine.
    sorry my mind can’t stay on track these days to finish a thought.
    thanks,
    Bykerchic

  58. Hi Chris,
    I have chronic Fatigue Immune Dysfunction/Fibromyalgia. I was diagnosed in 1996. unable to work since 2000. I finally found a Dr after years of searching that specialized in FM/CFIDS/CFS treatment. I had <0 Cortisol level when tested and low thyroid. took Compounded Cortisol starting low an increasing to 20 mg BID then gradually decreasing over the years. i have been off the cortisol about a year now.Duriing that time and up till now she and my new Dr have tried every combination treatment of thyroid available including compounded T3 SR for those sensitive to fillers. Everytime I take any thryoid tx I feel better at first although the first time I took the compounded T3 we slowly worked up to 20 mcg BID and I felt normal for the first time ever in my life for about 3 months then I crashed and have never recovered. Now when I take thyroid meds I start having worsening symptoms of hypothyroidism if I increase or decrease the dose or leave it the same such as brittle hair /nails and intolerance to cold and just freeze all the time no matter how hot it is. I also I start developing painful (nodules??) in my abdominal area and have to eventually stop the thyroid tx because they become unbearable. no one can or wants to explain or find out what the reason is or what they are. I also start breaking out with pimple/boil type sores on my chin, groin and buttocks. I had one so severe on my chin I had to go to the ER and get IV antibiotics and have it lanced.
    Do you have any idea what is causing this when taking thyroid meds and any suggestions on how to be able to tolerate thyroid meds??? I can't sleep and am always exhausted and sleepy and pretty much spend most of my life in bed or on the couch these days
    My current meds are: Valium 8 mg poqhs, Vivelle Dot Patch 0.375 mg and GcMaf 0.05 mg every 7 days. Tried testosterone 200 ml 0.05 ml weekly but makes me feel even worse. Compounded Progesterone does the same to me as the thyroid medscausing the nodules.
    Please any help would be greatly appreciated. I am desperate to find someone that can help.
    Thanks,
    Bykerchic

  59. Chris
    Thanks for all your fantastic information on Hashimoto’s Thyroiditis. After my insistence to be checked for Hashis, i was diagnosed in 2006. My doctor actually told me his specialty was diabetes and he didn’t know that much about the thyroid. After seven years under his care, I decided to change doctors. My new doctor immediately found a nodule through ultrasound and poor conversion from levothyroxine for my T3. She put me on Synthroid 75mg and scheduled a biopsy. I find that I have several things going on because of the Hashis. I wonder now if my adrenals are working normally. In 2006 I was also diagnosed with breast cancer. In 2009 had a double mastectomy. Estrogen related. Can I safely take a licorice supplement? My GYN has me on a grain-free diet and has given me natural progesterone 75mg for my sleep problems. I’m also on Spironolactone 50mg and 500 mg of Azithromycin for cystic acne. I’ve heard of something called low dose naltrexone that calms the AI but no one will prescribe it since it hasn’t been approved by FDA for Hashimoto’s treatment. I think the root cause of AI should be treated but guess we are all stuck with treating the devastating results of Hashimoto’s. Thanks again for your web site.

    • I have the all that you mention and finally went to a specialist that does the LDN route. So far so good but I will know more in one more month after blood tests. The specialist I found was Dr. Holtorf in Torrance – They push their supplements which is annoying BUT their website is LOADED with information for “us”.

  60. I am so happy that I found your site while searching for explanations of my husband’s cholesterol tests and results. My question, though is about my hypothyroid condition. I moved many states away while in the beginning stages of treatment for Adrenal Fatigue and thyroid issues. It took me 5 years to find a practitioner who actually knew more than I did on both issues, and I am far from being an expert. My practitioner added iodine and selenium to my regiment and increased my D3 intake and told me to take calcium – I actually lost 1 1/2″ in height over the last 5 years. Upon retest, my thyroid results (don’t remember which specifically) were higher than previous results. It was explained to me that this was due to the iodine and selenium and my thyroid meds were reduced. Is this an expected result of adding the selenium and iodine?
    Thank you for making your website available to the general public and for your great explanations of so many issues.

  61. I am such a loss. No one that I have seen seems to understand what is causing my inflammation. I am positive for tpo antibodies and I would like to not take any meds if possible. If hashimotos is an immune system problem wouldn’t it make sense to fix the malfunction in the immune system rather than take medications? If you lower your antibody levels doesn’t the immune system attack stop? Why not just focus on that and not take any meds?

    • I would suggest you research NUTRI-SPEC.NET for thyroid. He gives the most complete paradigm I’ve found in 24 years of natural medicine. Low progesterone /hi estrogen could be a problem (progesterone not progestin)…Chris’ diet suggestions also are key
      Dr Z

    • Sk, I have been under treated by an endocrinologist for Hashimoto’s thyroiditis about 20 years. In all that time my TSH would gradually inch up and the Synthroid would be increased about every two years. Not once did the doc try to get at the root of the problem (inflammation), or alternative treatments. I started seeing a functional internist and one of the first things he checked was a genetic marker MTHFR, which indicates an inability for the body to methylize certain B vitamins, such as B12. This can be causing systemic inflammation and everyone with an autoimmune disease should get this test.. Treatment: methalized B – complex vitamin supplements. Positive MTHFR can indicate problems with preterm pregnancy losses, as well as elevated homocysteine levels.

      I hope this helps!

  62. Great series of articles. In my practice I use the protocols of NUTRI-SPEC.NET, which see. This site seems to be very much in line and the above referenced site would be added info. Reverse T3 can also be a factor as well as the microsomal antibodies (TPO) mentioned. Another factor I’ve found useful is to use oral progesterone (not progestin ) in the form of PROGEST-E from the work of Dr. R. Peat…I don’t agree w/ everything Dr. Peat says but his progest-E product is great. Low thyroid is often caused by low progesterone &/or high estrogen. Finally, studies have been done on animals where the pituitary gland
    ( THE MASTER GLAND OF THE ENDOCRINE SYSTEM) was removed…as long as high doses of thyroid were given , the animal continued to function. The point being throwing enough thyroid substance as a mammal can cover as a lot of deficits. Am not recommending this as good medicine, just that putting women on thyroid can often give relief, yet at a high cost. Thanx again for a great site about truth in medicine.
    Ezra Edgerton, DC (ND) No. Carolina

  63. The “starch” in brand name Cytomel is from corn not gluten. Pfizer who now owns King / Monarch verified that none of the ingredients contain gluten. But they will not guarantee any cross contamination in manufacturing. But then again no pharmaceutical company guarantees that anymore in my experience. Hope that helps because there is a lot of disinformation out there on the Internet.

    • Not completely true. I verified this with Pfizer after getting an itchy, blistering DH rash from Cytomel. Cytomel contains trace gluten; the amount is below 20 ppm, so it is considered gluten free. Those of us that are sensitive to very low levels of gluten will react to it.

  64. k,

    My heart goes out to you. Although his bedside manner leaves something to be desired (I’ve seen him myself), were I in your shoes, I would definitely call/email Dr. Ted Friedman with the synopsis you wrote above, any lab data you can email or, and ask if there’s a way he’d be willing to treat you if you could find a way out to see him. Cushing’s is his specialty, so he’s very up on pituitary issues: http://www.goodhormonehealth.com/ (good hormone health dot com).

    Then, based on his response, and any feelings you have on whether he’d be of assistance to you, I’d get to borrowing funds, even selling off my belongings, until I could afford the airfare. Don’t give up! Keep reaching out everywhere you can, even though it gets exhausting and dispiriting. Eventually, you will find a good practitioner fit for your health issues and you will be back on the path to equilibrium. No use spending any more time with practitioners who aren’t giving you the help you deserve.

    Wishing you well,
    trillium

  65. Hi. I really like your articles – very informative. I’m combing through the one about the gut and hypothyroid. I was diagnosed with hypothyroid after the birth of my second child in October 2011. I’ve been told by two doctors (a GP and a homeopathic doc) that I have Hashimoto’s. I’ve never been sure of this. How can I find out the ‘source’ of my hypothyroid? Should I see an endocrinologist? My docs just give me medicine and send me on my way with a ‘well, it won’t kill you’ attitude and don’t want to go any further.

  66. Love this article. It is so great that I included it in my post at Hypothyroid Mom this week “Which Is The Best Thyroid Drug For Hypothyroidism”. I was so curious about what you wrote about Cytomel having modified food starch that contains gluten. I am very curious about this because I’ve tried different brands and feel my best on natural desiccated thyroid. When I tried a combination of Levothyroxine and Cytomel, I just didn’t feel as good as on natural desiccated thyroid. I know we are all individual in how we respond to these drugs but I had no idea that Cytomel had a modified food starch that contains gluten. This would explain why some hypothyroidism sufferers report not feeling great on Cytomel.

  67. Chris – I was just diagnosed with Hashimoto’s on Saturday. I love your site – but I honestly don’t know where to go from here. I know you have info on gut dysbiosis etc. – but everything is so detailed I don’t even know how to start! I can’t imagine trying to figure out the Omega 3 vs. 6 issue today…but I know I need to get this all right. What is my next step?

    • S, I would suggest contacting NUTRI-SPEC.NET to find s Dr. near you….searching their site about thyroid would also make you more informed than most endo docs

  68. I have been in and out of the hospital for three years now after first having a botched pituitary tumor removal that resulted in coma and damage to the pituitary, then follow up brain radiation to shrink it (damaging the pituitary further) and one month after that I was diagnosed with an aggressive thyroid cancer and had a complete thyroidectomy. Since then, I have had cortisol readings all over the place, prolactin levels at 150+, stroke events that cause complete left side paralysis which eventually just go away, massive migraines that supposedly cause these migraines, and constantly fluctuating thyroid levels regardless of the brand or dose of medication. My cortisol level is very low as well, and my endocrinologist wants me to take hydrocortisone as well now. I feel like crap, can barely function, and now I am suffering from extreme panic attacks which I have never had before – they are very frightening and feel like full blown heart attacks. Nobody can quite figure out what is wrong with me despite test after test and doctor after doctor. I also have gluten intolerance and arthritis, nobody has ever told me if I have Hashimotos or if that can even be possible once the entire thyroid is removed, I am at my wits end and I don’t know what to do anymore. I am about to be tested for ACTH cortisol corsytropin stimulation next week, my doctor suspects adrenal insufficiency. Regardless of that, why is it so difficult to get my thyroid levels regulated since I don’t have a thyroid to compete or throw off the medication? I am confused, faced with only ONE endocrinologist within 50 miles, and he and his partners are rude (literally yell at me sometimes when the meds don’t work the way they say they will) and they do not seem interested in getting to the bottom of things…they just spend 10 minutes or less and don’t listen. I have no health insurance and cannot work from the issues my health causes, and I can’t afford to keep seeing doctors without getting some solutions. I hate taking so many meds, and I prefer more natural solutions when possible. Anybody have any ideas? I would literally travel hundreds of miles if I thought I could see a doctor who would look at all the information and really treat ME, not just a few numbers on a lab report.

  69. I have been on Levoxol 50-75 mcg since 2001. What a nightmare. I feel exhausted
    ALL the time. My once thick long nails are
    tissue thin as is my hair. there are no specialists where I live that address just thyroid tx. When 1st put on meds I was only
    borderline hypo…any suggestions?

  70. Chris,
    This is a very helpful article. I wondered if you could answer the question about Cytomel being or not being gluten-free. I have a letter from the manufacturer (to me) stating that it is gluten-free. If there is any evidence that it is not, I should not be taking it as I have Celiac Disease.

  71. T3-only is also best for those with reverse T3 issues because as long as there’s T4 available, the body will continue to convert T4 -> rT3 and the person will never get better. Doesn’t matter if it’s natural, unnatural, or your own T4, when your body gets into the “mode” of making rT3, it ekeps doing it.

    I do not have Hashi’s and as far as I know have a perfectly normal thyroid gland. However, due to diabetes and adrenal insufficiency, I wound up literally bedridden with severely elevated rT3. Hydrocortisone fixed up the AI, and very large doses of T3 (enough to suppress both TSH and FT4 entirely) cleared the rT3.

    I now maintain on a very low dose of T3, just enough to keep the rT3 at bay and have “normal” bloodwork.

  72. Debbie,

    Yes, if you can achieve the results you want with licorice or other natural adrenal tonics that would be best. As I’m sure you’re aware, corticosteroids have adverse effects on the immune system, bone health, weight regulation and cardiovascular function – among other things. Taking them over the long-term should be avoided if possible.

  73. Chris,
    I’m hoping you answer my question from 9/23, but in the meantime I’ve dropped down to 25 mg. Cortef and 1 or 2 Isocort pellets before bedtime.

    • Hello Chris, I have been taking Armour Thyroid all of my life since I was 3 and I am going on 57 and when I take the other like Levothyroid and Synthroid it is like I am not taking nothing at all and my got up and left me I will not take anything else I was on 90 mg . 1 1/2 grain and now they are decreasing they found a cyst on each side of my Thyroid Gland and they said the 90 was suppressing the TSH and I want to know more about the RT3 I was adviced to go with sites that ended in endu and gov that I needed to be careful with the other information given out !!!!!!!!!!!!!

      • I have been on Armour for 5 years and have been feeling much better.
        Recently my 21 year old daughter was diagnosed with hyperthyroidism and the doctor said that Armour was going to be discontinued and that it is not good for you. I was looking for information on this, I have not found any? Also, I was interested in what other meds address both T3 and T4?

        • Wow. So wrong. The company making Armour changed again not too long ago; they may change the fillers, but they will continue to produce it.

          There are lots of NDTs (Natural Desiccated Thyroid meds), most of them have a generic, and some are available over the internet and in health food stores. Prescription NDTs are all FDA-approved and legally available, just like synthetic T4 (Synthroid is the brand, Levothyroxine is the generic) and T3 (Cytomel is the brand, Liothyronine is the generic). Each med has different fillers.

          21st century medical science has proven that the T3 converted from T4 is not enough. Prescription NDTs are made from pigs’ thyroids, and they also have T2, T1, and calcitonin, just like human thyroids.

  74. Chris,
    Your comment:  I don’t recommend people take hydrocortisone in general. It’s preferable to take natural compound like licorice extract to boost endogenous cortisol production than to take cortisol directly.
    I had several tests that determined I have secondary adrenal insufficiency and am currently on 35mg Cortef since my body doesn’t produce enough. Are you saying that licorice would still be preferred to supplemental hydrocortisone?
    Really great post (and blog).  Thanks!

  75. Thanks so much, this sheds a lot of light on some things for me. I tried bioidentical thyroid medication for over a year, and it did nothing to help my thyroid symptoms. So I went back onto synthetics (both T3 and T4) and saw an immediate improvement. My doctor prefers the bioidentical, but said to use what works. He wasn’t really sure why synthetics worked better for me. This is the first time I have read anything that gives a clue to why!

  76. Spectacular stuff. It’s amazing what kind of disorders improve with good nutrition, good eicosanoid balance, gut flora, and eliminating stuff like wheat. I’ll share this series like I do all your other ones.

  77. Chris,
     
    Something to think about before taking the conventional way (synthetic T4):
     
    Hypothyroid persons using conventional treatment (synthetic T4) usually have higher levels of free T4 and lower levels of free T3 than normal persons (see Pubmed 20693806 for a comparation in pregnant women).
     
    Hypothyroids taking thyroid medications progressed more rapidly to a diagnose of Alzheimer’s than hypo not taking thyroid medications (Pubmed 19666883).
     
    Higher total and free T4 levels are associated with increased risk of dementia and Alzheimer’s (Pubmed 17870208, 17136019, 17132968, 16636121).
     
     

  78. Wow Chris,

    a truly penetrating look into an issue that proves so frustrating for so many patients AND M.D.s   Thyroid disease is rampant,  thyroid misdiagnosis is rampant, and thyroid mis managment is rampant. 

    As illustrated in your article there is a reason for all this……it is a very complex issue that needs careful testing, managment and observation. 

    I am going to bookmark this and send it to many patients.

    Thank You

  79. Read the comments to one of your previous posts where you mentioned panax ginseng treatment for adrenal fatigue. That sounded interesting, but I have already been recommended to take hydrocortisone tablets for those problems. How do these two substances work toghether, is it possible to combine them?

    • I don’t recommend people take hydrocortisone in general. It’s preferable to take natural compound like licorice extract to boost endogenous cortisol production than to take cortisol directly.

      • Licorice has more of a mineralcorticoid effect than a corticosteroid effect, so should not be taken by those with high bp.

        Also, whether it’s effective is going to depend non how low cortisol someone is. For example, if you have high cortisol in the morning, and low at noon, licorice in the morning is very effective as it extends the life of cortisol in your body.

        However, if your body flatout can’t make enough cortisol, you need hydrocortisone (or another steroid, though I think HC is best as it can be dosed in a diurnal pattern).

        Really, you can’t determine the best treatment for someone without a 4x diurnal saliva test to see the specific pattern of dysfunction.

        For example, many folks who are low all day wind up high at night with insomnia. This is because the pit keeps putting out ACTH in response to the low all day and the adrenals can’t keep up, but they can produce enough to go over range at night. So… a person with this pattern may need doses of HC at 7AM, 11AM and 3PM but then need PS at night to lover cortisol to allow sleep. (Though usually when on enough HC during the day, the sleep problems will dissipate).

        Lots of info here: http://adrenalsweb.org

      • Hello
        I have been taking 25 of synthroid for the past couple months my hair has fallen out really bad. I have seen so many doctors and they say that the synthroid would not cause my hair to fall out, but it’s a side effect on the label. Have you ever heard of synthroid causing hair to fall out? My hormone levels are:
        TSH 3.51
        T3 free 2.9
        T3 UPTAKE 29
        T4 6.4
        Thank you 🙂
        T3 TOTAL 91

        • Rigorously screened, healthy volunteers tested between .4-2.5 for TSH results. Your result is too high (meaning, you deserve some help). 25 mcg T4-only is not much help. Unfortunately for you and millions of others, it IS the “acceptable” standard of “care”. I suggest you learn how a healthy thyroid works, then self-treat, if you can’t find a doctor who runs appropriate tests. Appropriate tests are TSH (if you still have a thyroid with which your PITUITARY can communicate), Free T4, Free T3, Reverse T3, and antibodies (plural). There are four antibodies. Antibodies are evidence of autoimmune disease, not thyroid disease. Ingesting thyroid hormones isn’t treatment for antibodies. 🙁

          • How can we self-treat? Don’t I have to get the prescription from the doctor? Mine tests only for tsh and keeps saying I’m too high even though his low dose sent me into a deep depression that was “miraculously” cured when I upped my own dose. After ten days the depression lifted. But when I went to get a refill, he tested me again, again said I was too high even though I had low-thyroid symptoms all over the place, and I’m having trouble finding a doctor in my area who will prescribe according to how I feel. If I just take extra, this doctor will know I’ve run out too early.

            • Google Thyroid-S, ThyroGold. These are over the counter NDTs like Armour. They contain T4, T3, T2, T1, calcitonin and fillers. Joining one of the “FTPO (For Thyroid Patients Only) groups on Facebook will connect you with someone who can help you self treat.

              You noticed a difference after ten days because your T4-only med takes 7-10 days to get to your liver, get converted and back out to your cells. The T4 you ingest today isn’t used by your body until sometime next week. The T3 in an NDT works the same as the T3-only meds: it gets to work within 30-45 minutes of dissolving it in your mouth, and wears off 3-6 hours later. Women need more T3 than men; our TSH and Free T3 fluctuates during the day; and our T3 needs to fluctuate during our cycle with our other hormones’ fluctuations. If you don’t know your body and you don’t understand how a healthy thyroid works, I don’t suggest self-treating.

              To try to find a doctor who “deviates” from the “acceptable” standard of “care”, you call ahead and ask, does he/she prescribe T3 and/or an NDT. Sometimes, ob/gyns are more willing; sometimes your primary care doc will help if you copy articles for them, present your case with your documentation of symptoms. If neither of those options exist, try a DC’s office or a naturopath, or an integrative physician.

              Thyroidchange.org has a list of doctors who support their efforts….

              • Thankyou, that helps a lot. I didn’t realize the difference of dispersal between the T3 and T4. I know my body pretty well but have had trouble understanding how the replacement hormones work. So many books written about it, I read them and it seems so complicated, but maybe I’m just seeing it that way.
                Thank you for taking the time to explain a bit to me. Will look for a new doctor for sure.

                • Karen,
                  I’ve found a great doctor that takes full panels and treats based on symptoms. I found her by going to worldhealth.net and searching in my state. Then I picked the one with the most accreditations in integrative medicine. I live in MS.

                • Thankyou, Leigh, I will check that site. I don’t guess the doctor you found is in south MS? I’m in the FL panhandle.

        • Hello. My hair fell out before i was medicated and once i was put on synthroid it got even worse. It is from the synthroid!!!! Not sure if it is the meds itself or just not being at an optimal level and that is why it happens. I have been on Levo, then synthroid brand name, then combo of Synthroid and generic cytomel, then armour and then back to synthroid only and now armour again…..all different doses too. NDT i have found is best for most people because it is the closest to what our own body secretes, however there are a small % that do better on T4/T3 combo of synthetics. My hair stopped falling out once i got on NDT.

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