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  1. Too much thyroid meds can cause severe pain everywhere in your body as well. Anyone lowered their thyroid med and pain went away?

  2. Thank you for caring enough to tell people about this type of pain. If more people knew how to manage their pain there would be less overdoses.

  3. blank Sheri prieto says:

    I put my email address in there please email me I would love to talk to you

  4. blank Laura Suermann says:

    Thank you so much for this article. After MONTHS of searching for answers for chronic low back and pelvic pain, having scans (MRI/CT/Ultrasounds) and finding nothing and testing high for thyroid antibodies and reverse T3 (although docs REFUSE to treat it, saying it’s not that bad…uhmm!!!!!) I finally came across your site tonight. I realize this was posted a few years ago…but thank you for perhaps a better direction to pursue. I happen to be going to a D.O. tomorrow to review a few labs I’ve had recently and I will definately bring up the LDN and thyroid relation to the pain I’m having…I’m hoping that this is finally the answer. I’ve not been me for over a year, and keep getting misdiagnosed with things like fibromyalgia, chronic fatigue, etc…all of which could possibly be related to the Hashimotos and antibodies that are off the charts! So thank you. Have a good night. Laura

  5. blank Kelly Coley says:

    I’m begging and endless searching for help. Everything wrong with me falls under hypo or Hashimotos. I’m on my second endocrinologist and my labs are low, but in the normal range. I was just put on the lowest dose of synthesis. I can’t live like this anymore. I have often thought of suicide. Severe short and long term memory loss, the pain in every inch of my body, the burning tongue syndrome that started in April 2013. I feel like a hypochondriac. I’m passed fatigue. I cannot stay awake. I can read about two sentences the next thing I know is my book is on the floor and it does it all the time even if I don’t feel sleepy. I cry a lot. I cannot find a doctor to dx me with anything. I know this isn’t in my imagination. I was beginning to think I had that disease where you have everything wrong but it’s all in your head. The doctor’s are looking at me like I do have that disease. My new endocrinologist is in South Bend Indiana. I have four other specialist’s. I’m tired and drained. I need for someone to believe me that it is real. I wish I could take part in clinical studies. Do I go to Mayo, Chicago or throw in the towel. Lord help me.. I don’t even know who I’m sending this to.

    Sincerely,
    Kelly Coley

    S

    1. blank Kelly Coley says:

      In addition to my recent post I forgot to mention my body temperature. I’m soooo hot 95 percent of the time. NEVER cold. I don’t understand it, but it is severe. I take cool shower’s and when I’m done I turn it on colder and hold my head under it. When I dry my hair the sweat pours off of my face and I turn the dryer on cool and I have to coil down my scalp and face. Then I go set in front of a fan for ten min. I sleep with a fan on in the winter when the house temp is about 69. My sister is completely the opposite, she freezes. I do have family history of thyroid disease. I developed rosaceae. So I walk around with two lg red circles on each cheek. My heat problem bothers me the most.

      1. blank Esther Hunt says:

        I understand exactly where you are coming from. It took 3 years and still working on tiring to get healthy or at least a little bit of relief from a lot of what you are talking about. I have also changed Doctors a few times especially when they miss something that I caught. I did find some help from a Doc in South Carolina. She had me read a book called The Miracle of Bio‑identical Hormones: How I Lost My Fatigue, Hot Flashes, …
        Book by Michael E. Platt
        It made so much since. I have also started this therapy and I have started to feel better. I do still have my bad days here and there but more good than bad and I thank God for that. Don’t give up!!!! I took control of my medical all together. Every doc apt I ask for a complete print out of everything that was done and the solution. Every time they do blood work as well. I look up these test online and read as much as I can and If I have questions I ask the Doc and or nurse. They have started a patient portal for me to communicate with them thru e-mail. I also keep a journal of how I’m feeling and what I have eaten and drank that day. Life is too short to give up. To this day I have had or still have H. Pylori, premenopausal, Hashimoto’s, Hypothyroid and boarder line diabetic. I have had my gallbladder removed as well as a partial hysterectomy. I take meds for reflux as well. On my bad days I wake up with tight swollen hands. My feet numb along with my fingers. I stretch them out and wiggle them before I can even get out of bed. Then there is the cool feeling but with hot flashes so I change my clothes a few times a day to how I’m feeling. Then there is the joint and mussel pain. I try to exercise and do the normal house work but when I go to bed I’m sure to be in some major pain for the night. I just do my best make notes and let the doc know as soon as I can to see if any relief is out there for what I’m going thru. I am very luck that my husband is very supportive. Good luck and I hope putting all this out there can help someone if not you. feel better soon and keep your head up.

        1. blank Susan Holz says:

          Esther I live in SC. Could you tell me the name of the doctor you are seeing. I have been using bio-identical hormones since 2006. I was living in AZ. Moved here to SC and need to find a new doctor. No one does bio-identical hormones and I have also become hypothyroid.

      2. Dear Kelly
        I read your post tonight as I too search for answers. I have a long history of digestive disorders as a child and surgeries that cannot be rebersed. A fee years ago I was diagnosed with Hashimotos, adrenal
        Fatigue and chronic fatigue syndrome. I am so weary, worn and often sad – something that is so different than the ” real” me. I have high cortisol causing anxiety
        I just got 3 mri’s back with degenerative discs narrowing of spine opening causing numbness and pain. I am spiraling downward.
        I say all this to let you know you arent alone.
        As tired as I am you and I cannot give up. Who wants us better more than we do?
        You definitely have something wrong that is causing this pain and fatigue.
        I highly recommend going to a D.O. Who seed the body as a whole and mot just parts. Try going Gluten free for a few months or sugarfree
        I am convinced our answers lie in diet and food sensitivities. Simple but hard.
        I believe in a Good God who heals and delivers. Who gives wisdom and guidance. My prayers will with you and for you. Hoping you find this and we soon will proclaim these days far behind us.

    2. blank Sharon Brown says:

      I have had chronic pain in my right groin/hip area for 16 years. I know exactly how you feel. After 12 doctors and 5 surgeries (one for a double hernia that I don’t even think I had, Dr had a Hummer and I think he had a payment due), I finally gave up. I live with it and I am taking an anti-depressant to help me cope. You would think with today’s technology I would be able to find an answer. It is so frustrating. Hang in there!

      1. I have been telling my family doctor for over 2 years that I have been extremely tired and have widespread body pain. In January 2016 I had blood work done and my doctor said that my thyroid was low and he prescribed synthroid. I toss and turn about 10 to 15 times a night from pain and in the morning I am stiff and sore all over for nearly an hour. After seeing a rheumatologist, she said she thinks I should see an endocrinologist. I am sick and tired of appointments. I am 55 years old, I work part time and after 4 hours work, I feel like I could lie down and sleep for 9 hours. I walk at least 1/2 an hr to an hr a day because I have low bone mass and walking is good for it. I try to keep a positive mind and attitude but it is quite hard because I am used to feeling very energetic and well.

        1. blank Pamela Smith says:

          Hi Rita and all,
          Have you all tried LDN (low-dose Naltrexone) for the pain from Hashimotos?

          I had a surgery a few weeks ago and have been off the LDN for that time (and a week prior to the surgery) and I can tell you that I am going back on it tonight!!!

          I’d been on it for about a year and a half and did not fully recognize how much it helped with the daily pain. But now I am feeling that pain again and it is AWFUL. Hurts in my joints AND in my muscles.

          And not only does LDN stop pain, but it improves mood and reduces Hashimotos antibodies.

          I can not emphasize enough how you need to look into LDN and start it for pain relief and these other benefits!!

        2. blank Lisa Olivares McVey says:

          I have had hypothyroidism for many years and did very well on Unithroid until the last couple of years. I started having severe pain in my hips, ankles, feet, hamstrings, calves, shoulders, etc. I found through labsork I am well below normal on my T3. I’ve been given Cytomel but figuring out the dosage is difficult. I think I’m also having a reaction to the additives or fillers in Cytomel. I can tell my pain subsides with the addition of T3 but I cannot tolerate Cytomel so I’ve been referred to an NP who practices integrative medicine. She tests hormones and I’m hoping she can figure out exactly what I need and make a compound that is time-released pure T3. I can’t believe this has been so difficult to figure out. I don’t think doctors know their specialty like they should. I understand pain is common with hypothyroidism.

    3. I know this thread is old but did you ever resolve your issue. I am also from southbend!

      1. Nicole,

        Funny I was reading these old posts and thought the same thing. I hope you all found some answers and relief. I have had Hashimoto for apx 20 years, also have endometriosis inside my sigmoid colon (yes inside) so I’m on BCPs full time with no break until I go into menopause. Whenever that will be? I’m Going on 48. I will tell you all that Synthroid is not the best drug for Hashimoto. Look into something more natural like Armour thyroid which is what lifted the brain fog like day 5 of switching from Synthroid. Here is the difference… Synthroid is only comprised of T4 which has to go to your already compromised thyroid and convert to T3 which is needed for brain function, metabolism, etc., Armour thyroid has T4 and
        T3 although the ratio isn’t perfect for everyone but I will say it’s much better than just having T4 and expecting your body to convert it. Also a lot of the numbers and tingling in hands and feet can be contributed to B12 deficiency which a lot of people have and don’t know it. Get checked then go get yourself methylated b12 bioidentical form (not cyanocobalamin form, that’s synthetic) make sure it’s methylated and get sublingual tablets. D3 in 5000 IU is another lacking Vitamin that with low levels will cause brain issues, fatigue, severe depression and more. This can take a few months to feel a difference as it has to build up in the body and does take time. One last thing. Get yourself a good quality pre/probiotic w digestive enzyme included and take it everyday for gut health. Give up the gluten and sugar seriously. Your gut is the key to everything as it gets signals from the brain and visa versa. Once you give up the gluten and sugar and take your dig enzyme your gut health will thrive as you get rid of the yeast overgrowth that most Americans have and don’t realize it. Here is a link to my site where you can check out the “digestion plus” product we have. It’s a great product 3 in 1 ( prebiotic, probiotic and digestive enzymes) you will absorb so much more from your foods once your gut health is back in check. I have 3 friends who finally were able to lose weight because they took my digestive plus product and changed their eating habits. Good luck to you all. We really are our own health advocates. You have to take it into your own hands. Research and learn.
        http://Www.lauragreenawalt.arbonne.com

    4. blank Sheri prieto says:

      I feel your pain I’m right there with you I have chronic pain to start off with in my foot I accepted their answers with that but now they want to throw it in its neuropathy I think it’s my thyroid the more I keep looking and searching I didn’t know thyroid was inherited from your parents on my dad’s side it’s there I hurt all over my joints my knees my ankles and I think the doctors are ready to give up on me at Kaiser and the standard thyroid test doesn’t show s*** so now I’m waiting on my doctor to call me with it a phone appointment and I’m going to ask him to run the full gamut of thyroid testing that’s the only thing left to do I’m beside myself I’m only 55 I shouldn’t be in this much pain so it was nice to see somebody else is out there just like me writing this in tears

    5. Please have milk with a pinch of turmeric every morning and take a spoon of virgin coconut oil or include coconut oil in your cooking. Some of the healthy herbs and calm and believing in yourself will help you through this. I am in pain and I am trying a little. I see this as a way of going towards a healthier lifestyle. You can do it!! God is with you!! We can do this!

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