Synthroid and hyperthyroidism

Hi everyone! Well, I was just diagnosed with Hyperthyroidism..The doctors say it is really bad ..they prescribed 10 mg of Tapazole..I am trying to get as much info - loaded as I can because I already know that I have to fight my own doctors to keep them on their toes...however, I do believe after all I have read so far ..I may be beat before I even start the fight...It appears I may have had this for a little while ...I have been so sick....serious vertigo...My head is not mine at all...I live in virtual unbalance...always floating...and the heat from the sweats is killing me..then there is the freezing although I refuse to let that bother me..I am tired all the time and get the vertigo every time I try to do anything strenuous and even if I just get up from bed or sitting position....I have some nausea..I refuse to let depression set in although It tries real hard...but I laugh at all my sickness as much as possible and just ask Is there anymore..I am sure I haven't got enough..haha....bring it on..I have been really sick before with the Meniers but this is just as bad..Of course I have Meniers disease, Fibromialgia, and am Peremenopausal...among other smaller problems..so it was really hard to discover thyroidism...I think I got it all....My throat was not swelled ..just throbbed and gave me serious headaches all over my face and especially in my ear....It was hurting so bad and was terribly sore to swallow or even turn my neck...but they did the test and I had one more disease to add to my growing list...go figure...why not ..I am thinking...I am very miserable..and don't trust doctors at all...they like to play to many games with peoples lives...what can I do..I am getting lost..I don't want to live like this..I want someone who really cares...Is it really to much to ask..

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 am was diagnosed with Hyperthyroidism about 2 years ago. I took the radiation treatment and was placed on Synthroid. Every 4 weeks the dosage was adjusted until my Dr doc determined 0.125mcg worked best for me. Well, at the time I was diagnosed I weighted about 150 pounds. Two years later I am at 180. I'm 5'8 so my doctor(s) tell me my weight is in portion to my height. Well, the extra weight is centered around my stomach and hips, I am extremely fatigued and lethargic, I have brain fog and would like to exercise but I'm just too tired. I heard about Armour but from reading some of the other experiences, it doesn't appear to be the 'cure all' solution either.

I am a female and was diagnosed with Hashimoto's three years ago (looking at old childhood photos I've probably had this all my life) and have taken Levoxyl and Synthroid in escalating doses over time. Initially 25mcg for about a year and that was the endo plan until bloodwork indicated a need for more. I quit taking it after a year as it seemed I was gaining weight. After a few months went to a different endo and he started the treatment again with 25 (I weighed 160 at the time) and now has worked it to 100mcg (I now weigh 178!!!). I thought that with the higher dose I would have more of a weight loss effect (definitely not weight gain) and thought I'd have more energy, better brain function and happier outlook. I am experiencing the complete opposite. The last time I visited the endo and he looked at my weight gain he just said to "stop it". I work out almost every day for 45 minutes to 2 hours, have a job that at times requires arduous work, I eat a very healthy diet full of fiber, low in fat, low in carbs. I'm always hungry and feel like eating to make up for a lack of energy. I come home from work exhausted. This isn't living. I've had it with the Synthroid and any form of T-4 alone. I'm going to see a natural healthcare professional to try Armour because none of the medical doctors I've seen will prescribe it or synthetic T-3.

I been on Synthroid now for 10 years. Almost right after I started the medication i started to have headaches. I had / have headaches every single day , all day long. Before the Syntthroid i NEVER had headaches, EVER. It has been 10 years and i still complain. I have spent so much money and wasted time on exams and doctors. All the doctors tell me is that i am stressed or its sinus or something else . Which i don't think i am . I have CT scans a few times. I am not crazy, i know what i am saying. Doctors don't listen. I looked on online and saw that headaches are a side effect. I went back to my doctor and explained. The doctor(s) insist that the Synthroid is not a cause of my headaches. With headaches every single day a person can not function normally.

I ran across this website and in a way i felt better knowing that this symptom is real and other people are experiencing the same thing. On the other hand it upset me that all these people are complaining and no one is listening.

Is there no solution?

I suggest to anyone that has Hashimoto's Thyroiditis (type of Hypothyroidism) to have a blood test done for Celiac Disease. There has been research done linking Celiac Disease and Hashimoto's Thyroiditis. Celiac Disease can be controlled by a gluten-free diet (wheat, rye, and barley free). In the US, not many doctors recognize/know of this link. I have been hypothyroid for 20 years (had Hodgkin's Disease (cancer) - radiation/chemo at age 16) I have 2 sisters with Hashimoto's Thyroiditis and were iron and B12 deficient. I was diagnosed with Hashimoto's Thyroiditis 3 months ago with iron and B12 deficiency. I have been on a gluten-free diet for 2 months now. My dosage of synthroid (levothyroxine) was 175 mcg and now is down to 137 mcg. I hope that I am one of the lucky ones that will have their antibodies to their thyroid normalized (no more synthroid!) I have a couple of days left before my next blood test and I hope that it goes down more. I am feeling better now than I have in a very long time. I have attached a link for those of you interested. It is an endocrine article from Finland outling the link between Celiac Disease and Hashimoto's Thyroiditis (among other things). I hope that this helps some of you. http://edrv.endojournals.org/cgi/content/full/23/4/464

Hello, I had a TT two weeks ago. I had hyperthyroidism. I was diagnosed three years ago after ending up in the hospital because I had a thyroid storm. I started taking synthroid the day after my surgery. I feel like a nut job! I don't know if it is because of the medication or because of the TT. Could it be a combination of both. I don't remember my numbers but I know that I was in a hyper state when I went in for surgery. Since I have been home...I can not fall asleep without meds, can not stay asleep, my day starts around 4:30 AM, have night sweats (big time) and chills (although, that symptom seems to be improving), I have been so irritable that I can't stand myself, my husband and kids are ready to kill me. I know that my behavior is totally unreasonable but I can not seem to control myself. I feel crazy! I see my Endo next week, I just hope that I can make it until then. I feel like I need to pack my bags and head to a hotel and spare my family from me! Please someone tell me that this will get better.

hello everyone
i am a full time college student and I believe that i have some side effects from synthroid. As i was reading everyones blog i notice that some people feel the same way that i do. At times i feel that i'm normal but if something upsetting happens i get really tired, depress, and I have a never time concentrating at school and home. My body hurts all the time. especially my joints and i feel that i don't want to do anything. I have about a year left until i graduate and its the going to be hard. I cry sometimes for no reason. help! i'm going to talk to my doctor but if any body else feels the same way please reply.

Originally, i was diagnosed with hyperthyroidism. This was about 6 years ago. I was on a beta-blocker for 3 years. Afterwards i was diagnosed as being hypothyroid (about 2.5 years ago). I've been taking synthroid ever since. At first my dosage was .075 mg. It was changed to .05 mg a year ago. I haven't gained any weight since i became hypothyroid, but i've had many other problems. Some of them include, difficulty swallowing and breathing, heaviness in throat area, memory loss, insomnia, lack of focus. These are the most serious problems.

I took 75 cmg of Synthroid after having my thyroid destroyed by radiation, then two months later dropped to 50 cmg. Within a month I was hospitalized for atrial fibrillation. The Synthroid was reduced to 37 cmg by my physician. I am experiencing dramatic hair loss and want an alternative to this poison that has ruined my heart as well as my appearance. In less than two weeks, I have gained 3 pounds. I should have left the thyoid alone but three "experts" said the hyperthyroidism would kill me. I had lost 14 pounds and had a thick gorgeous head of hair. Thanks to Synthroid, I am fatter and have gross hair loss. What hair I have is dry and thinning.

I have been between 110 - 115 lbs most of my adult life. I tried everything to gain weight, but it didn't work. I was diagnosed with Graves Disease when I was pregnant with my son. I took PTU for the duration of the pregnancy. I was symptom free for about 4 years. About two years ago, I started to experience symptoms related to Graves Disease. I saw an Endo doctor who told me that I have a non-cancerous goiter that needed to be removed. I have thyroid surgery 8 months ago. I started taking Synthroid shortly thereafter. I have been trying to explain my symptoms of Hair Lost, Dry skin and nails, Insomnia, weight lost, lost of appetite, and leg cramps to someone for 6 months. Nobody listens. They just discount my symptoms. Today I decided to do some research to find out if I was alone. I AM NOT ALONE. I've been taking Synthroid for 8 months. My hair is so thin that you can see my scalp. Combing my hair makes me upset because I have chunks of hair in the comb. I too called my doctor and he replied,"I can't believe that your symptoms are related to your synthroid use." Reading these articles helped to prepare me for his responses. I insisted that I didn't want to take Synthroid anymore. He ordered blood work and advised that I have to continue taking this medication. I don't want to feel this way for the rest of my life. I have a 6 years old son who is full of life. I don't have the energy to keep up sometimes. I felt better before my Thyroid Surgery. (34 years old Woman, post Thyroid Surgery for an Enlarged Goiter and Hyperthyroidism). Where is the support????

I have been diagnosed with having hyperthyroidism. I have lost 70 lbs as a result. My doctor has just informed me that he is ultimately going to kill my thyroid and subsequently put me on synthroid. All of the symptoms reported here are scaring the hell out of me.......

I am 23 and found out just a month ago that I had graves disease, hyperthyroidism and a cold nodule that they couldn't determine if it was begning or not so I just had my thyroid removed last week and I started synthroid a few days laterl. I've noticed that I'm a little
shaky, i thought maybe it was from my parathyroid glands not producing enough calcium but even though my calcium levels have gone up i'm not visibly shaky just feel shaky,
I also don't want to sleep I feel like I have more energy but at the same time i've been weepy. Is this normal?
I really haven't had a chance to ajust to any of this it's all been happening sooo fast.
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