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  1. The TSH test alone doesn’t tell you much. My daughter (an RN) had graves and her TSH test came back, just fine. She insisted on the FT 3 and FT 4 and sure enough, graves!! Now she just gets tested whenever she feels like it because we know how we feel.

    I really got tired of the doctor’s claiming I’m okay on not enough Synthroid. I finally stopped going( 2008) because I found a OTC supplement that works for me.

  2. So how do I KNOW if I am hypothyroid? If my labs are normal, how do I KNOW that the symptoms aren’t from some other disease, like a vitamin deficiency or poor sleep? To just assume and start taking different thyroid medications seems a bit nuts. I’m sure speed would make me feel better too, but that doesn’t mean I should do it. It’s all so confusing!

    1. The idea is to use the blood TSH level, as well as visible clinical signs, and the patient’s report of their symptoms, as sources of evidence for diagnosis. Your TSH level won’t be high if everything’s working as it should.

      Once treatment begins, though, low TSH isn’t to be relied on as evidence that you’re well.
      Medication with Levothyroxine, synthetic T4, suits most people. However, those users who can’t break down T4 to its useable form, T3, or can’t get T3 into the cells, won’t trigger high levels of TSH, because TSH responds to what’s in the blood. It doesn’t tell us what’s going on in our brain or liver or other essential parts.

      You can have low TSH, plenty of blood T4, and still be starving.

  3. blank Lauren Smith says:

    My thyroid was tested 3 times when I was younger. It was normal but I very much had hypothyroidism. The fact that my hypothyroidism went untreated for so many years because of unreliable test results has had major psychological effects. I will never be able to trust any tests. Also I lost 60 pounds over the past few years. My synthroid has not been lowered but my thyroid is still normal. Further proof of how unreliable the test is.

  4. blank Margret Stahl says:

    Thank you for helping educate and inform. After reading your information I asked my Dr to retest everything. He hasn’t had my levels checked for over a year and I struggle with numerous symptoms. I feel terrible. I have never had any test except TSH and I have been taking the same T4 medication and dosage for 12 years.
    I left and took my labs to another Dr. I got the same thing. “Your numbers are normal”. I can’t get in to see the endocrinologist for 6 months. I won’t have any more hair if I have to wait that long. Why is it so hard to get help?

  5. I live in Puerto Rico and was diagnosed with thyroid cancer in 2014. Had a thyroihitemic in September 2014. Had been taking Synthroid since then upping a lowering my dosage. I feel worse everyday. Have headaches, dizziness, weakness. Endocrinologists here in PR are so busy with so many patients with thyroid problems and it is very hard to find doctors available to seek different opinions. I’ve read before about different treatments for thyroid problems but haven’t been able to find a doctor here to discuss my options for different treatment.

    1. My only advice would be to call Mind Body Spirit Care in Tampa Fl. Ask them for T150. Take it like other thyroid meds (30 minutes before eating or drinking anything in the morning). I saw vast improvements with Xymogen T150 (desiccated thyroid, spleen, pancreas, etc…). My depression went away and I now have so much energy in spite of the fact I don’t work out like I should.

  6. This is so shocking! I’m italian and endocrinologists here prescribe only T4
    Thanks to this and others blogs I’ve been able to understand that I wasn’t crazy and my symptoms were real
    I fortunately live in Rome and some pharmacies supply NDT from Vatican State
    Is like going abroad for a simple medicine not available in my country
    And most shocking is that 3/4 endocrinologists in all the entire country are open minded about a different approach to hipothyroidism

  7. blank Claire Zippilli says:

    Just had my thyroid removed after 5+ years of being tested and medicated , gained weight every year . After an accident a nodule was discovered . After a failed biopsy , could not be aspirated we opted for surgery . Upon going in there they discovered it was cancerous. No surrounding lymph nodes were cancerous . I already have dropped 7 lbs. I am now on 100 mg of synthetic thyroid meds, Os Cal with vitamin D and trying yo keep levels high to have strength . Persist in asking what is wrong , 3 drs, all told me we will continue to monitor it every 3-6 months . No way was I leaving a nodule that was over half an inch long and wreaking havoc on my chokestral , edema , weight gain, foot pain,etc. Find someone to do what you want to solve this .

  8. blank Sigrid Saradunn says:

    I had Grave’s Disease in 1980 which was treated with radioactive iodine. I then became
    hypothyroid and have been on synthroid ever since.
    My question, as a patient, and health care professional, (RN), I am curious if the treatment doses … determined by blood work, not on how I feel (when I feel like I can get my life together, my weight is responding to my food plan appropriately, the medication is usually increased to bring the level down and then I gain wt even after adjusting the food plan to less carbs and calories. My exercise regimen is nil due to exhaustion even with plenty of sleep.
    .
    Needed to vent… thanks for the place to do so.

  9. I am extremely frustrated with my doctor. I had my TSH tested in April and it was slightly elevated, as well as my cholesterol. My doctor proscribed Synthroid, but it gave me unbearable side effects… so he took me off. Then he sent me for another blood work T4 and T4 , which came back within a normal range.
    Having said all of this, I have a lot of symptoms of hypothyroidism….. now I am left hanging.
    I don’t know what to do, as I also suffer from PTSD, Anxiety, Chronic Pain since the two MVA in 2013. Besides all of this my heart rate has been elevated for the past 6 months.
    I am going crazy now…..
    Not sure what to do.

    1. Go get a second opion i also suffer from thyroid issues and sure know how u feel never feel 100 percent even with meds but they do help

  10. blank Angela Navarro says:

    Hello,
    I am new to support groups… are we allowed to speak our mind about what we are going through, what we went through and how we feel about this dreadful disease?

  11. Excellent article. Glad that the author said all treatment options
    should be available, because you never know what might work
    for someone. I’ve had years of bad health because in 1982-83, they
    quit making the version of Synthroid that really helped me. The company
    wanted to be “cost-effective,” as one University thyroid professor told me–and the new version was not required to be tested for safety & effectiveness
    on anyone before being released in the marketplace. I had over
    six good years on the old version when I was a teen, but lots of trouble
    ever since despite being tried on all sorts of different thyroid drugs & doses.
    Having a little more success with NP thyroid right now, but
    it’s still a struggle. I wish drug companies couldn’t just discontinue
    making a version of a thyroid drug that was helping people. I wasn’t
    the only one affected by Synthroid’s changes ‘way back, and I still
    feel if they ever could duplicate the old version, maybe some people
    would have a better outcome with their thyroid treatment. Other
    thyroid drugs have made changes and affected some patients badly,
    too, over the years–Armours and a couple in Europe, I think. This
    kind of thing needs to stop, and if I ever get in a position to do
    something about it, I will. The author is right in that sometimes
    an older way of doing something has some real merit, whether it be
    an older version of a drug, or an older approach to treating a thyroid
    patient, which would include really looking at one’s symptoms.

  12. I can gain weight nut i have all the symptoms. My blood work is normal so what should i do

    1. blank Elizabeth says:

      Check out Stopthethyroidmadness.com
      It will tell you the right way to look at labs and what labs are needed. This site has 17 years of patients experiences and wisdom.

  13. blank Den Demron says:

    I was having horrible symptoms for over 4 years. Endo’s were the worst. NOT ONE ever asked how I was feeling. They would just read the freaking lab report and say take more or take less. I hated, absolutely HATED going to see one. The idea of having to live this way for the rest of my life was depressing as hell. Where does one gone where they don’t don’t know where to go? One day I was in a Sam’s club and I had the idea of asking one of the pharmacists behind the counter for help. As I approached the desk I thought who would have the names of doctors who prescribe NDT and or T3 more that a pharmacist? So I asked one of them for a name of a doctor that prescribes T3 or NDT? She went to the back and came out with a name of a DO GP that worked with her patients using NDT. I immediately made an appointment and saw her the next week. I was in bad shape, hopelessly tired and I could feel myself cratering. I saw her and gave her my latest labs. She looked at me and said “I don’t treat numbers, I treat people.” “How are you feeling?” She got me back on my feet and living life again. Don’t get me wrong – it’s not perfect but I am soooo much better than I was when I was seeing those Endo’s who thought they hung the moon. They couldn’t give two cares about how I was feeling – just “Take two of these a day and come back in 2 months.” Screw that. Don;t give up – go talk to a pharmacist.

    1. Where are you located? I’d love to see this doctor as well

  14. blank Melissa Fields says:

    I don’t mean to be judgmental but no where on Here do I see you mention the factor of taking your medication on an empty stomach. My NP and a bottle of water is on my night stand. I take my medication every morning when my eyes open. And I wait 2 hours before consuming ANYTHING. I have suffered with thyroid since I was 15, I’m 55 now. I had a lobedeitomy.
    When I am diligent with this practice my body thanks me. I was informed by my GP (back in the 1970) to always follow this practice. Don’t get me wrong, I have systems of my Thyroid not functioning properly but for the most part those are mild.
    I’m one of the blessed ones, my Nurse Practitioner listens to my body.

  15. So are there any doctors who will treat according to symptoms? I am being treated but my endocrinologist treats me strictly by my lab results. Yet I still have many symptoms. It’s so frustrating.

    1. Have had that exact same issue EXCEPT when I was treated in Portland, Oregon. Seeing another new endo soon. I hope he listens to me first, and labs second!

    2. I don’t know where you’re located, but the McMinn Clinic in Birmingham, Al will greatly consider symptoms in addition to labs.

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