Tsh symptoms and conditions

I had Mirena placed 2 months ago. After experiencing all of the symptoms you have all talked about, I went in and demanded it be removed, despite my physicians resistance. She said that all of my symptoms sounded like a thyroid problem. I got my TSH tested, at the same time Mirena was removed. Just today got a call from my Dr. and my thyroid level is through the roof!!! Normal range is up to 4.0 My thyroid level is 131!!!!! I 100% believe that Mirena directly impacted this result, as the symptoms did not start until Mirena was placed. OMG!! 131!! I HIGHLY do not recommend Mirena....

I am 57 years old, male, and active, and have been on Warfarin since 1987 post Aortic Valve Replacement. I was quite happy with the dosage up till 2001, when I had an episode of TIA due to a malfunctioning thyroid and when my heart rate went down to 30 bpm. Since then, I have also been on a daily dosage of thyroxine, just enough to get my TSH up to normal levels.

Since then, I have a creeping condition of body aches and back pain, which has now, after 7 years, become chronic. This does not seem to alleviate with change from the Eltroxin from Glaxo, to Thyronorm from Ranbaxy. I have now accepted to live with this sometimes-chronic pain.

I tried some experiments with my dosages of the medications, and so I reduced my Warfarin to 5mg from 8mg. Within a week I was plagued with cramps and aches, and I got scared and went back to my old dosage.

Has my body, my heart, my arteries, adjusted to the thin blood over this time since 1987? Due to this thinning of the blood, will the detection of constriction of arteries and veins be more difficult? And consequently the detection of angina pectoris and atherosclerosis? Or can it be just old age catching up?

If any of you are on a similar combination of these two drugs and with similar symptoms, I would appreciate a line.

I have burning sensation on hands, weak legs and watery eyes. I take 50mcg on alternate days. My latest TSH is 37.8. My medic has asked me to take 25mcg on Sun, Tue, Thu, and Saturdays and 50mcg on the remaining days of the week. I have yet to start this regimen

I am a 48 year old woman, 5'1" (now 145 pounds). I had Mirena inserted almost exactly 5 years ago, and am scheduled to have it removed in 2 weeks. I gained 25 pounds over the course of the last three years; prior to that, my maximum weight for my whole (non pregnant) life was 123 (I was at 120 when Mirena was inserted, four years after the birth of my second child). I have always been very healthy, never abnormal blood tests except during my two pregnancies was tested as pre-gestational diabetic and had to watch my carbs.

I never put it together with Mirena until just recently, when I started doing research on hypothyroidism after a friend told me that my symptoms could be due to that problem. Depression, hair loss, acne on my back, and the terrible weight gain. I went to see my G.P. who referred me for blood work. I hoped to see evidence of low thyroid function (actual TSH value, 3.12 -- I was told this is normal on a range of .4 to 4.5). I also discovered that I now have high cholesterol (269 triglycerides, 251 total cholesterol, 46 HDL, and 151 LDL). My fasting (14 hours) glucose # is 99 (I was told this is normal on a range of 65-99 mg/dL), and my vitamin D, 25-OH is 21 (also was told this is still normal but low on a range of 20-100 ng/mL). I tried to give blood six months ago, and was turned down because of anemia, so I've been eating a lot of spinach, greens, and more red meat than I normally would, so I was interested to see if I am still anemic -- the red blood cell count is 3.8 (told it was normal on a range of 3.8-5.1 mill/uL). I mention these specific results because although I was told they were normal (except for cholesterol), when I physically went to the doctor's office and requested a copy of the results and did some research online I see that my thyroid IS actually low-functioning -- according to guidelines revised six years ago, anything over 3.0 is considered hypothyroid and should be treated. Plus, isn't a fasting glucose of 99 pretty high? Yet my doctor's only suggestion: diet and exercise. Good grief, I've been on a diet since I had my first child, 13 years ago. True, I don't exercise regularly (I'm a teacher and mom of 2; I never seem to have the me time.) I guess I have an excuse to get a gym membership now.

Also, for the last year I've had increasing pain in my shoulder (I couldn't lay on my side, for example, and lately I can't reach behind me or over my head). An x-ray turned up mild bone degeneration, but not enough to cause the pain I've been having. I was referred to an orthopedist, who today diagnosed a shoulder rotator cuff injury (I've had no injury; he says it is a common degenerative complaint in the over-40 crowd). He gave me a cortisone injection and I'll be on PT for a while to see if the pain goes away. If not, I'll have to have an MRI and surgery to correct the tear.

I'm posting all of this in case it might be useful to someone out there who might be going through the same thing. I had a thyroid test done about six years ago at my OB/GYN, and it was normal then (though I don't have the number; I'll get it in 2 weeks at the OB/GYN). It will be interesting to learn whether my thyroid level has gone up since Mirena. Also, although my research suggests that the effects of these synthetic hormones do not wear off for some time, possibly even years, I will finally feel like there may be hope if my symptoms improve over the next few months when Mirena is gone. If so, I will share it with you.

If you are reading this, perhaps you have a similar story. I wish I had been more aggressive about checking out the possible causes of my many symptoms, but I let them go for years because, I guess, I just figured I'm a healthy woman who is no longer young. (Oh, one more thing: for the first year or even two years that I had Mirena, I had incredibly heavy periods. The blood flow was similar to that during the day or two after the vaginal births of my daughters. Don't know if that's significant, but it took a couple of years for my periods to get fairly normal on Mirena.)

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?

Sometimes the symptoms of depression, anxiety, headaches, short temper and hot flashes are due to out-of-balance TSH and your medication may need to be adjusted. That's been the case with me in the past and it has worked. Usually the doctor increases the dosage and things go back to normal. However, my last increase has produced opposite results. I am on 0.137 now and I feel very, very anxious, fearful, and get easily upset. I feel hot flashes as I get angry and generally feel quite depressed. I've also gained about 6 pounds in the last two months, which should is bizarre, as higher dosage usually means higher metabolism rate and weight loss. I am confused. Should I go back to my old dosage where I felt better, except for the onset of weight gain.

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.

I have only been on Synthroid for 2 months, but my appetite is out of control. I read that gaining weight might be a side effect of Synthroid. You would think that you would lose weight with it since it makes your thyroid run more efficiently. My TSH is 4.3, still normal, so I don't guess I really need it yet. I am going off of it and going to the health food store and take Thyroid support.

I have always had and currently have the side of effect of extreme fatigue associated with the use of synthroid and now Armour thyroid replacement as well.
Whenever my tsh reaches normal levels I become increasingly fatigued. Now I an hardly stay out of the bed and yet my levels are normal.
I have Hashimoto's Disease and am menopausal with severe insomnia to cloud the issue. But the fatigue associated with thyroid replacement is longstanding and has occurred for about 15 yrs. For many years, I would stop taking the medication because of it. My doctors do not believe that the fatigue is related to Synthroid which I find utterly frustrating. Will be looking for another endocrinologist soon. Has anyone out there experienced this side effect of extreme fatigue?
Any input would be greatly appreciated.

I was on LIPITOR for 5 weeks. Am fit 60 year old Nurse. I had pain in my heel like a spasm and also near my Hip. Tiredness, Lack of concentration blurred vision and a level of deafness. I stopped taking Lipitor 1 week ago and energy levels returned to normal already. No more spasm pain. However still have blurred vision and the deafness. Anyone know how long this may take to improve?
I am on Oroxine for low thyroid function and maybe this is a contributing factor.

As most of you, my TSH always came back normal/border line as well. However, due to all of my symptoms - every single one for Hypothyroid - they went ahead and did an ultrasound. I had a nodule 15mm x 5mm on the left lobe and 5mm x 4mm on the right. Because I had the constant "turtleneck" feeling around my throat, it was getting hard to swallow and sounded like I was an 11 year old boy gowing through puberty again, because of the hoarseness, I had Total Thyroidectomy last week. My surgeon put me on 150mg of Synthroid. So far so good with the side effects, granted it's only been 6 days. I actually have more energy, and a decrease in appetite. I've already lost 5 lbs. Not real sure if my energy level has gone up because I no longer have a thyroid to bring it down or if it is from the medication. Either way I hope my side effects stay as they are, I could stand to lose another 50 lbs - haha

Hello, I have been on synthroid since 1999. I am hypothyroid with hashimotos. Endr. docs couldn't seem to get any levels right so I went to my Intergretted doctor . and he put me on 1/4 grain armour so I took anywhere from 50mcg to 100mcg of synthroid in the AM and 1 armour at night. It worked but after a short while I felt terrible. Then I had to start taking high blood pressure presc., it was about 170/116 after I had some shots in my back for pain, never had hp. before these shots. In Sept. of this year I stopped the Topralxl because I felt my heart was pounding out of my chest which I was in hospital for they said I was having a heart attack, had anigram, but I didn't have a heart attack and and angigram came out good. Then this summer they put me on 2 Topralxl. My heart was pounding with 4 extra beats so with a ultra sound{echo]of my heart and 24 hour halter it was all good, so I figured it had to be something I am taking. So that lead up to the stop of Topralxl which I researched and took a few things from Health Food store and got my pressure down to 140/80. My heart quit racing and beating so hard, but still felt depressed, puffed up, confused, teeth felt loose, urinated a lot, gained weight, rashy on my neck, tired all day, did not sleep good, eyes were always red and watery, skin and hair dry, blemishes on my face{ I am'56 yrs. old] just didn't feel good and the list goes on. Came across this site and read them all. Realized so much from you all. Sythroid only has T4 which your cells should be able to covert T3 out of that. T4 stores in your body and T3 is used up as the day goes on. But some peoples bodies don't convert the T3. Several people have talked about TSH which is your thyroid stimulating hormone which comes from your Pituitary Gland. When you thyroid or your meds. don't give you enough thyroid of what you need the Pituitary kicks in there to tell your thyroid gland to to produce more. It's not good for your TSH to be high so Docs. put you on a higher dose of Sythroid or whatever you take for the pituitary to stop producing TSH. So I want to say I am not a doc. but have felt so terrible and researching what I could I quit my Synthroid on the 29 of Dec. and started taking my armour thyroid 1 AM, 1 late afternoon and 1 PM on my own cause I figured I am still getting my T4 and T3. I went to my Endr. Doc. yesterday and told him I went off my Synthroid and just taking Armour. and told him I felt so terrible, after stopping the Topral heart felt great but the rest of me felt drugged, I just felt desperate and horrible. So again it had to be something I was taking. Well I have to say that I feel 100% better than I was. I am much more alert with my surroundings and whatever i am doing, sleep so good, teeth feel good, no rash, urinate normal, not confused, face cleared up, eyes not red or watery, pretty much I already feel normal again. Working at my job is not exhausting, my neck, which I didn't mention before quit hurting. In a whole it was the right thing for me but maybe not for everyone. I just felt that it was slowing taking me out. Blood Pressure, Thyroid issues are to be concerned about but seems like a person should feel better not worse with the meds. So this is the information I have learned and I'm sure there is much more. So good luck to you all and listen to your body and talk to your doc.about how you feel. It can be very scary when you are diagnosed with something but we are all different in what our body needs and our side effects.

Here' what it says..

10/28/2008 7/1/2008 2007 2006
TSH 1.41 1.71 4.08 4.28

TUP 36.1

FTI 9.96

T4 11.02

Am I still low enough to have the dry brittel hair and al the hair loss and wieght gain?

I have hypothyroid. Have been taking Synthroid for about a year, 0.075MG a day. Had my levels checked 3 times since on the meds and still have never gotten to normal, but a lot closer. I have gained 20 pounds that I can't get rid of, which for me, is crazy. I have never had a problem dropping weight, and for the past month or so, I have started losing my hair. Not just losing it, but the texture and everything has changed. No matter what I do it looks dry and flat, and even when I condition it and also use a leave in conditioner, it still knots up and tangles. I have NEVER had a problem with tangles. It's coming out in handfuls. Im not taking any other meds, so I imagine it has to be the Synthroid. My problem is..What else can I take? I mean, I have Hypothyroid, so I can,t just leave it untreated, But I have no wish to be fat and bald either. Please...anyone know of others meds without these side effects?

I have had great experiences with Levothyroxine. I am no longer tired, achey, grumpy, constipated. I feel great. I am only 27 years old and got my hypothyroidism from having my first child. I am excited that my levels are now normal after 3 months (TSH was 25.89). I was on .50 mcg now I am on .75. Feel great!
I am a medical technician and have found that a lot of people who start on a certain medication for hypothyriodism, such as Synthroid - do not fair well if they have to switch. My doctor always says NOT to switch...not EVER. She repeats over and over again to check my prescription every time I receive it. That means checking the pills against each other, because hypothyroidism medication is one of the highest missed - filled prescription. If I were anyone who has had to switch, I would demand to be put back on your original meds. Have your physician write up your symptoms with the new meds and make a recommendation to the insurance company that you NEED synthriod.

I am a 27 year old who has been on birth control for the past 11 years. I was on Ortho Tri Cyclen for the majority of that time until my sophomore year of college when the doctor suggested I switch to the "shot". Depo Provera caused me to bleed continuously for several months on end and I was then switched back to pills by my new gynecologist. He placed me on a generic form of the ortho which again worked wonders for several years. At 25, I started bleeding constantly from the generic and was switched to several Loestrin 24 which completely stopped the breakthrough bleeding... initially. After a year of it, we were back to constant bleeding. The ONLY side effect I have ever experienced from birth control is breakthrough bleeding. I moved cities and with a new town came a new doctor who thought Femcon might work. I was prescribed it in May and have been taking it for nearly 6 months. Over that time I have been so happy with it as there is no bleeding except when there should be. That is until I read today that my increased anxiety (I have a diagnosed anxiety disorder to begin with), vivid, realistic nightmares, and 15 lb weight gain could be caused by this pill. I am getting married in January and my dress barely fits at this point because of the weight gain. I go to the gym 5 days a week for cardio and weight training yet keep getting fatter... I thought I was stressed out by the wedding and that is what was causing my emotional imbalance... I really thought I was losing it. I just called my gyno and left a VM asking if this could be the reason... Don't quit taking a birth control based on other peoples reports, they are all going to react differently to different people and all meds come with an initial side effect that goes away once your body is accustomed to having that hormone or chemical in it. Initial nausea is common... I have always had it when I started a new medication, especially birth control. It goes away after a couple of weeks. Will keep you posted.

Sitting here with heat on thigh fm severe muscle cramp. Had one earlier in hand. Have had many probs with hands lately; thought it was carpel tunnel but pain seems to be randon in hand and fingers. The muscle cramps are unbelievably severe; didn't know about the loss of Calcium and B - good to know. Was taking Levothyroxine .25 with seemingly no effects but when TSH was still over 4.0, MD changed to .50 Levoxyl. Have been on it a month and have had nausea, bowel disturbances; irritable eyes; bloating, depression (which MD is offsetting with antidepressant), and SEVERE muscle cramps in places you wouldn't expect... hands, neck when I yawn, things, stomach, waist... it's awful. After hearing everyone else, I'm weaning off and doing more research. Thanks to everyone for sharing.

I am a 48-year-old male that is still pretty active playing competitive soccer several times per week. I am in good health except that my BP was considered a little high back four years ago and was originally put on a diuretic which made me cramp up easily on the soccer field. I asked my doctor for something different and was changed over to Atenolol. I have been living with the Atenolol side effects for that time and finally had enough. I had recently moved and changed doctors. Now was a good time to complain about the restless nights that I attribute to Atenolol (insomnia is one side effect). My new doctor knowing that I am an athlete suggested Lisinopril.
Again, my research is after the fact and was really spurred by a trip back home and a chat with my brother who is 49 and was just recently put on Liprinopril too. He described some bazaar conditions that he believed were Lisinopril side effects. When researched, he was right. He experienced the blackness or tunnel vision and the feeling of passing out while at work. He felt that he couldn’t drive as the effects where hampering his ability to do so. He stopped taking the drug and started a regiment of fish oil with his other daily supplements. This was two months ago and he is doing great. He too is still an athlete and runs in Masters Track & Field.
For me, it was a little different. I started Lisinopril on a Friday as my Atenolol had just run out on Thursday. I asked the Pharmacist if there was an issue with starting Lisinopril after stopping Atenolol only one day apart. She said there were no issues. 5 days later, Wednesday, while at work I developed an incredible lower back pain on the left side. I began to have nausea and heavily salivate as if I was going to throw up. I ran to the bathroom where I sat on the toilet for a half hour rubbing my back & hip believing it was some intestinal issue or gas. To no avail… When I felt stabile enough, I left work only to sit in my car wondering if was going to be able to drive and if I could should I drive home or to the hospital. Well, I drove home and went to bed for a couple of hours before I felt well enough to function normally. It’s been two weeks and the dull lower back pain that feels similar to a back strain persists. I’ll be heading back to the doctor with this information and will start the fish oil with my daily supplementation program.
Thanks to this website because I was able to find at least five examples out of about the first twenty postings that matched my suspected side effects.

After a year and a half of synthroid because of removal of my thyroid for cancer, I feel worse than I have ever felt in my life. Many tests have shown that there is no recurrence of the cancer. I would think I had fibromyalgia if it weren't that I read the blogs from other sufferers like me. I now take 150 mcg on most days. Some days I have to cut it down or skip it because I just cannot bear the body pain, weakness, brain fog, constant awakening in the night, severe cramping knee and leg pain, and muscle aches (there's no word strong enough to describe this pain -- 'aches' just doesn't do it). On the days I don't take synthroid I begin to feel like my old self. But my old self was 40 pounds thinner and losing. My old self walked three miles a day and hiked into the back country with my son. And my old self felt energetic and woke up every day with happy plans. Now I feel like an invalid. Some days I can barely walk. I cannot stand for longer than 5 minutes. I have tried cytomel, unithroid, and armour with varying problems. Synthroid is all that is left. Those of us who are dependent on this drug really need some good research on its effects. And we also need compassionate physicians who do not dismiss our pain and, it is not overdramatic to say, suffering.

I was on Levoxyl .175 for 6 years and found it was the only one that worked for me. I do have pain in my joints ,but defiantly have arthritis, I have anxiety and panic but have had this stuff my entire life. About 4 months ago my doctor had me cut my .175 in half despite my level was in the normal range,all it did was wack my thyroid out and now my TSH is 18.4 .Instead of giving me my .175 back he felt I may be getting to much with it (though my levels were always normal on it) and put me on .100.
I did notice when he changed it,I felt nervous and bad for a week now its been 2 weeks and I feel like I always did so far the only difference is im having trouble with constipation and stomach pain and I have nausea ..Not sure though if its the Levoxyl or something else going on.

I have been on Topamax since Jan of 08 for complex partial seizures. I was very pleased with it at first but started having
some more unpleasant symptoms. My hair recently started falling out about two months ago in massive handfuls! I was
and am very upset about it. I did have the tingling in the hands and feet when I first started taking it and I don't drink sodas
at all which I did all the time before. I did not lose weight at first but did a couple of months ago when I got very ill with a GI
problem. I actually lost about 20 lbs in about a month. This is when my hair started falling out. I have had a lot of labs
drawn and my TSH was undetectable but my thyroid levels (T3 and T4 are normal) and my antibodies are normal as well so,
there is no telling what is going on?? I just want off of this medication before I am bald!!

Hello Ladies....I am 56 and diaged Hashimotos disease 3 years ago.At the moment on 112mcg of synthroid....dosage started off low and have gradually worked up....So angry with drs...was seeing endo, but moved and using family practice...so frustrated with weight gain approx 25lbs since diag. Also does the word sweat ....mmmm perspire for all us ladies, mean anything? I can't even wash dishes without breaking out in to a sweat...mmm beads of perspiration....Dry skin, I own stock in Aveeno....Also....does anyone get "boil type" skin eruptions in the nether region...butt, inner thighs etc? Does anyone or has anyone done any serious research on Iodine? I try to eat as well as I can, was doing Weight Watchers and gained weight do ya hear me? I am questioning my idodine intake or lack of....Presently take mulit vit with 150mcg. Considering uping it and dc ing my synthroid...cuz docs have been useless....eat less, (how much more less?) exercise more...I swim so much I look like a freaking prune....Any comments?

I was on synthroid for 10 years after getting treated with Radio Active Iodine. As the years went by my period was all all over the place. They were heavy the first three days and lasted 9 days or more days. I spotted all the way through the month. Other times I was so late that I thought I was pregnant. I had PMS two weeks before I started and was irritable. I had low grade depression. I had anxiety and heart palpitations. My skin was dry and rough. I went to the doctor and had my blood test. He checked for TSH and T4 and T3 levels. He insisted they were normal and that something else is wrong wth me (he wanted to give me sleeping pills, anxiety pills, depression pills) and that it had nothing to do with my thyroid. He sent me to an endo to get a second opinion and he said my levels were normal too. I ended up going to a holistic doctor (paid over 1000 dollars for two visits plus meds) that checked under my feet (yellow) and my reflexes. She checked my reverse T3 and my free T3 and T4. It turns out that my body was not converting T4 to T3 the way they said synthroid (T4 only med) should. My diagnosis was hypothyroid. I was put on Armour and felt the difference in my skin. It was softer and moist! My teeth felt strong compared to before I felt like my teeth were getting loose. My stamina last longer and can run on the treadmil 45 min at six miles per hour. I am less nervous and my low grade depression seems to be lifting. My days are brighter and less anxious. My hair is falling less. I know I have a long way to recovery because my Adrenal glands need some healing and I am still being optimized. I might still need to be raised on the dose that I am in. I will never go back to synthroid! My period has improved drastically as soon as I started on Armour! I am down to 4 days of period and less heavy. I still spot on day 5 and 7 but it is nothing compared to what I went through when I was on synthroid (T4 med only). My gynecologist wanted to burn my uterus to control the menstrual flow. He said that he could also pull it out. It seems like main stream doctors are more interested in treating the symptoms than looking to see what is the problem that is causing the symptoms.

extremely depressed after a week of taking levoxyl. Also face is swollen, eye swollen and red and face and eyes burn. These were the same symptoms after taking synthroid after a week. What's next? I am close to being suicidal after having survived lung cancer, surgery, chemo and radiation. To get another primary cancer and have things slide downhill after such a remarkable recovery, I can do nothing but cry after making the decision to have a cancerous thyroid removed that could have served me for years and years since it was such a slow growing cancer. I should have followed my instincts and just left it alone. Now all I want to do is lie on the couch and cry.

I started taking thyroxine about 6 weeks ago - i went to the doc with tingling fingers, bloods showed tsh 34 so doc gave me 50mg thyroxine. Felt awful within a few days i was getting palpitations and felt like my skin was crawling. I couldn't bear even the slightest noise. I had diarrhea (cant spell) fast heart rate, the shakes and couldn't handle lots of people in a room. I am a teacher so it became difficult for me to work. I went up to 100 it got worse, until in the end I decided to stop them.
I am going to wait and see but I would rather be hypo than have these symptoms, my doc said you will feel great soon, pah what a load of c%%%