T4 levels symptoms and conditions

I had a baby in May.I had the mirena inserted in the beginning of August. I began having night sweats and noticing a lot of hair loss at the beginning of Sept. I went to my Ob/gyn who said it couldn't be the mirena causing the symptoms. So I thought that maybe I had a thyroid issue.(After my last pregnancy I had post-partum thyroiditis, which caused my hair to fall out and night sweats). I had my levels checked, and sure enough my t4 levels were high. So, now I am waiting for my t4 levels to go back to normal and hope that's what was causing my symptoms, not the mirena. I have also read that the mirena can cause thyroid problems, so who knows what is REALLY causing my symptoms. My most recent symptom is numbness and pain in my wrist/hand. I'm thinking it is possibly carpal tunnel syndrome which can be caused by hypothyroidism. If you just had a baby and are having the night sweats, hair loss, heart palpitations, weight gain etc.... I would recommend getting your thyroid checked.

Just want to survey everyone and ask for responses for the following 3 questions:

1. how long did you keep your Mirena and if you no longer have it, why did you have it removed?

2. how many of you had your thyroid checked? who's came back abnormal? what were the levels?

(I'm a medical student doing research on this one since I believe the levonorgestrel affects our thyroid hormone. My TSH was elevated to 5.2 which is considered "subclinical HYPOthyroidism". This was mid cycle when my natural progesterone AND synthetic progestin were cumulatively high. When I had it rechecked 6 weeks later (around my period when any natural progesterone level is gone) it was normalized at 1.5. So I think that the P+P screws up our thyroid and can throw us into a high TSH and "hypothyroid state". The opposite effect may be true during menstruation and we can become HYPERthyroid for a few days... hence the really bad anxiety?!)

3. where is everyone from? perhaps we can have support group meetings?

I've been on levothyroxine 150mcg for about 3 months before that it was 100mcg and so on. I have gain lots of weight and tired all the time. depression also, headaches. I hate this gaining weight, sleepy all the time and depression is from gaining weight. I thought this med is to up boost my thryiode but it doesn't seem to be working. my dr. said I'm on the highest dose there is. I don't know what to do any more. I was thinking about taking myself off this but not sure what will happen if i do. I hope there is someone out there that might be able to let me know if they are going through the same things what they are doing and how they feel now.

Boy, this could take a while. Have been on generic Levoxyl for more than 7 yrs(can't say exactly how long since I stay "fuzzy headed" all the time). Anyway, about a yr ago I became so depressed I went off all my meds -- I'm a diabetic on insulin and also have high blood pressure. I felt good!To try and make this story a little shorter, I went on a diet and lost 70 lbs -- went from 310 down to 240. Then I went back on meds. In less than a yr, have regained all the weight I lost. Also, my legs swell and ache so badly it makes walking painful. Hands, wrists and knees throb constantly. Intermittent headaches so bad I have to wear sunglasses just to tolerate indoor lighting. Hair loss is so severe I'm considering a wig. Skin is dry and itchy and lotions help not at all. Any work I have to do I must accomplish before noon because by early afternoon the fatigue is debilitating. I'm currently on 300mcg of Levothyroxine (up from 250mcg 2 months ago) and doctor wants to increase dosage even more. Had no idea there were other people suffering the same problems until I stumbled upon this site. I take the medication as prescribed (with perhaps less than the recommended full glass of water) but plenty of coffee. Discovered on another site that the coffee may be inhibiting the drug's absorption. I feel so helpless/hopeless. Am considering going back off the Levothyroxine but am seriously worried about high T3/T4 levels. Thanks for listening; guess I just needed to vent.

Hi I have severe lower-back cramps and ache going all he way up to my shoulder blades.
I guess its from the Euthyrox 25micro grams(Livothyroxine sodium) which I am taking now for over a week.
I was diagnosed for hypothyroidism and my T3, T4 levels were marginally high so my practitioner started me on the lowest dose.

But this side effect is quite disturbing and need to get rid of this to handle the work pressure in the office.

thanks
Abhishek

I was prescribed 25 MCG tabs of levothyroxine (generic for Levoxyl) by my MD for my hypothyroid. (I was tested at a 4.5 reading -- just below a normal 5 reading). After 60 days of taking levothyroxine EXACTLY as prescribed (i.e.; on an empty stomach, 1st thing in the morning with a glass of water; no vitamins for at least 4 hrs afterward), I started to have symptoms that I've never experienced before: my hands began hurting so bad with joint pain; my lips felt numb; and I was sweating more than I ever had in my life. I decided to stop taking the medication due to these symptoms, and in about 7-10 days from stopping, ALL these symptoms had disappeared and have not returned to date. I relayed this information to my MD who told me that my symptoms had nothing to do with Levothyroxine and that I needed to continue taking the drug. It's more than strange to me how some MDs will not listen to his/her patient -- even more so now that I've read other info on the internet where many other people have had these same side effects taking levothyroxine!! On my own, I am now looking into taking an all natural alternative that I found on wellness resources called "Thyroid helper". I will not take Levothyroxine again if I can avoid it by taking an alternative. Has anyone else out there had success taking "Thyroid Helper"?

I have been on Levoxyl for 4 months now. Started at 100 mcg and then to 125 mcg and have just had my dosage of Levoxyl increased to 150 mcg and I have been experiencing a heartburn like tighness in my chest since the day after the increase to 150 mcg. I was wondering if anyone else has experienced this side effect. I felt fine at 125 mcg but my T4 levels were still way below normal. Does any one have any insight?