Synthroid neuropathy

Common Questions and Answers about Synthroid neuropathy


I switched to Armour from <span style = 'background-color: #dae8f4'>synthroid</span> and on the first day (during napping) I awoke to servere pain originating from my skin. There is no discolorations, just pain to the touch. It is located below my armpit and across my back and toward my chest. This is unchanged now for 4 days. Could this be neuropathy? Will it subside?
I was diagnosed with Hashimotos a year ago and have been gradually upping my dose of <span style = 'background-color: #dae8f4'>synthroid</span> since then because I have angina and can't take a big dose yet. I have started to get <span style = 'background-color: #dae8f4'>neuropathy</span> in my feet and my heels burn also. Is this Thyroid related? My doctor says yes, but I wanted to check with this forum and see if anyone has that with their Thyroid condition. I also have red and burning knees and feet. Does anyone else have this?
You are correct in stating that numbness in the hands can be due to <span style = 'background-color: #dae8f4'>neuropathy</span>. However, the generalized <span style = 'background-color: #dae8f4'>neuropathy</span> (involving most nerves in the body) related to diabetes and several other metabolic and nutritional disorders most often starts in the feet, not the hands. In a diabetic with thyroid disease, numbness in the hands would raise concern for another type of neuropathy: carpal tunnel syndrome. The median nerve can be injured anywhere along its course.
i have been taking with water and 2 tramadol for <span style = 'background-color: #dae8f4'>neuropathy</span>..after taking, i immediately down 2- cups of coffee..all this time labs were great and still are.i am off tramadol now 2 wks i think lol..i am experiencing brain fog and fatigue whereas before i didnt..i belienow i am wondering if i should just cut my dose in half and take as before ,or should i do the same at nite. or should i continue .088 and go to nitetime dose.i believe withdrawals are over......went to dr today ..
I AM HASHIMOTO HYPO WITH UNDERLYING <span style = 'background-color: #dae8f4'>neuropathy</span> IN FEET.. TAKE .088 <span style = 'background-color: #dae8f4'>synthroid</span>...BEEN HAVING PROBLEM FOR 4 DAYS WHERE WHEN I TAKE MY synthroid MY BP GOES UP T0 150/100 FROM 118/80.. NEVER HAD BP PROBS..I AM TAKIN HYDROXYZINE STARTING YESTERDAY 1-23-13...SEEMS LIKE MAYBE TRAMADOL WAS canCELLING OUT MY synthroid WHILE I WAS TAKING IT AND NOW , WHEN I TAKE JUST synthroid BP GOES UP FROM NORMAL AT WAKING..
I believe I have Hypothyroid <span style = 'background-color: #dae8f4'>neuropathy</span>. PCP agrees I have <span style = 'background-color: #dae8f4'>neuropathy</span>. My T3 levels are in and below of low normal and probably have been a long time. I can't get to see an endo for 1.5 months! Will bringing T3 to mid normal range help fix the neuropathy? How do I do this if my TSH is 0.1? Should reverse T3 be known? Do you see much hypothyroid neuropathy and does it go away after how long? This is something I never expected and has me very concerned?
The current dosage of <span style = 'background-color: #dae8f4'>synthroid</span> is 75mcg. In January my test results were T4 13.4 T3 uptake 32 Free Thyroxine Index 4.3 TSH 0.358 When is blood work was done I was on 88mcg then dosage was lowered. Is this correct?
I have most of the symptoms of hypopituatary and have <span style = 'background-color: #dae8f4'>neuropathy</span> in my feet. I had 8 mos of chemo about a year ago and am clear for now. I take .75 synthroid and that is my only medication.
I am hoping to get a bit of advice: I was diagnosed as severely hypothyroid and hashimotos about 3 months ago after my TSH level was >150. I have been put on 200mcg of synthroid and it seems to be helping my symptoms a bit. Recently (over the past 2 months) I had noticed some tingling and numbness in my face, hands, feet, arms and legs.
The cancer doctors say it has nothing to do with the Thyroid cancer. P.A.'s and naturopaths say it is being on only <span style = 'background-color: #dae8f4'>synthroid</span>. An internist told me in fact if I go on Cytomel it will cause the cancer to return. I also have Hep C. Is there anything natural I can do to help stop the pain in my legs? Is ther a cure for this? Are there any vitamins that help?
I was DX'D with Hashimotos in 2011 and was given <span style = 'background-color: #dae8f4'>synthroid</span> . I started with .25mcg and had difficulty right away with angina. The Endo then slowly titrated the dose up, but I still had some difficulty although thanks to Gimel's suggestion, I'm now taking the doses in quarters and find it helps a little with the chest pain. However I still feel really fatigued and still have all my Hypo symptoms.
Is it possible that exposure to several different herpes viruses could cause <span style = 'background-color: #dae8f4'>neuropathy</span>? For example, if you have been exposed to HSV-1 (Cols Sores), HSV-2 (Genital Herpes), Chicken Pox, Mononucleosis and possibly HHV-6, do you run more of a risk for neuropathy? (I know for sure I have or have had the first four). Recently, I have been using acyclovir because I was having genital herpes outbreaks almost every month right before my period.
I am a 29 year-old female with the following primary symptoms: 1. <span style = 'background-color: #dae8f4'>neuropathy</span> with “half-numbness” as well as various types of pain in all four limbs, with fatigue; “half-numbness”/altered sensation started mid-May, while the pain started mid-June and has continued. The level of severity of pain appears to be related to the amount of rest and activity I get. 2. Hypotension: My blood pressure dropped last week after I felt like I was going to pass out, and remained low.
Hi people, my question is to anyone who has thyroid problems and has ever been diagnosed with <span style = 'background-color: #dae8f4'>neuropathy</span>. I was diagnosed with hyperthyroid 5 yrs ago and off and on I would get treated for it, I say off and on because I'm uninsured and can't afford testing, medications, and Dr. visits, by the way I can't afford a specialist so I go to my family Dr. who treats me when I can afford to go.
60 yr WM. Diagnosed hypothyroid age 50; taking <span style = 'background-color: #dae8f4'>synthroid</span>. 2002 diagnosed peripheral neuropathy in feet; 2005 Mayo Clinic said cause unknown. Lab tests in 2004: TPO=1200, Antigliadin IGA=100, IGG=70. Anti TTG normal and biopsy for Celiac normal. Allergic to cats, house dust, and wasps. Other allergy tests negative. When eat milk products especially cheese my feet hurt much more. Questions: Underlying autoimmune reason for peripheral neuropathy? Why are Antigliadin IGA and IGG so high?
(Not to mention the <span style = 'background-color: #dae8f4'>synthroid</span>) I haven't had leg <span style = 'background-color: #dae8f4'>neuropathy</span>. Maybe stopping the Cytomel will stop the leg problem. With a shift in your hormones of that magnitude, you are bound to get some symptoms, and neuropathy may be one. I get sensory overload to varying degrees when my levels shift. Hope it stops bothering you.
MD prescribed 50mcg of <span style = 'background-color: #dae8f4'>synthroid</span>. After several weeks on 50mcg I was just beginning to feel a LITTLE better. My TSH was still not in normal range(5.3 I think), so last week MD increased dosage to 75mcg. Now I'm actually feeling WORSE!!! I'm more tired in the evening, feeling depressed (depression is s brand NEW symptom for me), still constipated, still have tingling feet, and now I have carpal tunnel in hands/wrists!!! Has anyone else felt worse after their synthroid dose was increased??
How many of you out there have <span style = 'background-color: #dae8f4'>neuropathy</span> problems along with Thyroid? If you do give a breif description of the problems and what type of thyroid problem you have. If enough of us out there suffer from this then maybe the Endo's would relate to it, as we can print this out and take it to the Doctor with us. Thanks for participating.
The doctor has again recommended <span style = 'background-color: #dae8f4'>synthroid</span>.(0.025 mg to start). He made no mention of Cytomel. I have read that some people take both. I haven't take any pharmaeuticals since 1993 and the thought of having to take one for the rest of my life is unsettling! How does the doctor decide whether to prescribe synthroid, Cytomel, or combination of both? On December 9, 2013 my Ferretin was 39 ug/L and the reference ranges for reduced iron stores is 31 - 79 ug/L.
in the past several months, he's developed <span style = 'background-color: #dae8f4'>neuropathy</span>. they've done scans, checked him for diabetes, etc. all have come back neg. however, his tsh has consistently been 5. the neurologist and gp insist thyroid has nothing to do with neuropathy. they haven't check thyroid antibodies. do you think they should be going down the thyroid path? maybe try synthroid?
I just started a small dose of <span style = 'background-color: #dae8f4'>synthroid</span>- I am almost 1 month post tt and 7 days post RAI and have major leg pains and leg cramps, but I think mine is due to a high tsh and little relief- I'm on 75mcg of synthroid. Tuesday was the first day I started any meds. I was hoping for some relief. Maybe you need to let your body adjust. Sorry I am not experienced enough to help out.
What are the symptoms or the feeling of hypothyroidism <span style = 'background-color: #dae8f4'>neuropathy</span>? I have a TSH that has ranged from 2.2 to 3.14 and a Free T4 .9 to 1.1. My antibodies come back negative TPO and TGab. The doctors insist I do not have a thyroid problem.
So now my doctor started 75mcg or Levoxyl and 10mcg Cytomel to see that help but still have sysmptoms of fatigues/dry skin which create itchy skin and hives also /still have trouble sleeping because of peripheral <span style = 'background-color: #dae8f4'>neuropathy</span>. I am wondering if some one share their thoughts about Hashimotos and PM connection , would i get better ever on muscles spasm / muscles weakness/ cold burning sensation. My TSH value last time 1.24, FT4 1.68 and FT3 2.
I was on trial of <span style = 'background-color: #dae8f4'>synthroid</span> for 3 months ,did not really seem to help me with my symptooms, It did bring my tsh down to .1,but I did not stay at that level very long before I decided to go off drugs. I was starting to get heart palp's. My question is my tsh now is 3.73 just got results today,and wondering if it will go down on it's own or should I start the drugs again and stay on them for at least 6 months.
I have been diagnosed with Hashimoto's Disease and currently on 100mcg thyroxine (<span style = 'background-color: #dae8f4'>synthroid</span>). - my bloods look good but I am waiting to trial some T3 soon (cytomel). I have had some tests for celiac disease and I am waiting on the results at the moment. I have neuropathy and parastheisas on my entire right side, head to toe, and no one can tell me the cause. Had a couple of MRIs and a CT scan - seen 2 neurologists etc and am seeing and excellent thyroid specialist.
Taking too much vitamin B6 can be as harmful (if not more harmful) than not taking enough, too much vitamin B6 can cause a <span style = 'background-color: #dae8f4'>neuropathy</span>; a lot of these multivitamins that provide you with super high doses of the vitamin Bs can be more harm than good, and only the necessary amount should be taken. A lot of the teas and other herbal supplements which are advertised as being "natural" are in fact harmful to more than one organ system, and excesses of them should be avoided.
Does anyone have these issues more in cold weather? I have been diagnosed with peripheral <span style = 'background-color: #dae8f4'>neuropathy</span>. No one has been able to tell me what the underlying cause might be. I don't have diabetes though I have strong family history of both type 1 and 2. I did have a high A1c result (6.1) which my neurologist thought was high for someone without diabetes, but I did pass the Glucose Tolerance Test.
I did not know that a thyroid problem coutd cause <span style = 'background-color: #dae8f4'>neuropathy</span>. I am on 25 mcg of <span style = 'background-color: #dae8f4'>synthroid</span> and for the last 4 years have had terrible burning in my thighs and now my feet as well. It has worsented over the years and a yeat ago I was diagnosed with small fiber neuropathy. Three months ago, I read that nerves need vitamin B so I started taking the liquid 5000 mcg of Ultra B-12 a day and the neuropathy has gone away. If I forget to take the B for a day, I know it by night as mild burning returns.
If there are NO symptoms of hypothyroidism, but TSH levels are high (T3/T4 normal), is it O.K. not to take Levothyroxine (or other thyroid treatment)? Husband is happy, peaceful, energetic, healthy, in shape, etc. Only "symptoms" of hypothyroidism are high cholesterol and peripheral neuropathy. Both are usually from something else and neither goes away when he takes Levothyroxine.
I am 52 years old and have been taking <span style = 'background-color: #dae8f4'>synthroid</span> for hypothroid. Lately, I have had burning, tingling on tops of hands, cheeks, and scalp. During these times I get mild to severe anxiousness. When it goes away I am fine. Any thoughts? This discussion is related to <a href='/posts/show/297675'>Facial Tingling with Bulging C6-C7?</a>.
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