Hyperthyroidism symptoms and conditions

i discovered that i had hyperthyroidism which was from grave's disease and grave's thyroid eye disease in jan. 2009. at the end of march i had my thyroid removed. never let anyone use the radiation treatment if it is in your eyes. my surgeon said if we had waited another week i would have been dead. they started me on 75 mcg of levoxyl. it made me mean, i prayed to God to let me die in my sleep every night. the dosage was changed to 88 mcg. my hair was falling out by the handfuls. i kept calling my dr. and being told it was normal. i lost 75% of my hair mass almost to non reversible. i have been on appearex and women's rogaine once a day and am using nioxin hair cleanser and conditioner for 2 months. i have new growth thank goodness. my toes almost froze off my feet, the headaches cannot even be described, i gained 40 lbs, this will be the 3rd time in 7 mos. they need to change my dosage to 100 mcg. my body cannot take it. today i am starting synthroid. until i found this site today i had no idea most of my agony was from levoxyl and it's side effects. thanks so much for all the information. good luck to everyone.

I had just gotten married and never been on any type of birth control. i decided that since i was a forgetful person the best option was the nuvaring and my husband agreed. my gyno gave me the script and i swear not 8 hours after i put the thing in i was more sensitive. i stayed on the nuvaring for 8 months. i had serious depression, i slept the majority of the day, i'd even sleep at work. i had no sex drive, which doesn't make since, b/c i was a newly wed. i would be angry with my husband if he didn't say i love you in the right way. i had never had any problems in the vag department, and then all of a sudden i had cramps that you couldn't imagine, yeast and bacterial infections and itching that could not go away. i thought my body was just transitioning or something. i had to eat like 24/7... i was always snacking and i have hyperthyroidism so its hard to gain weight but i gained like 15 pounds one week then dropped 20 the next. i hated my life and my family. when my husband would ask me what was wrong i just couldn't tell him b/c i barely knew who i was.

ive been on sronyx for about 3 weeks, and besides forgetting to take it here and there, i am back to my old self, i can have fun and i don't cry if someone tells me i look nice. lol i would definitely caution anyone who is even thinking about the nuvaring, to really do your research!

I've posted here before right after I removed my mirena. Well it's been 27 days since I've had it out. At first I felt great. I had a period two days after I removed it. That period lasted a week long. Right after my period I CRASHED MAJORLY!!!! I had severe depression, severe anxiety and really bad leg and joint pain. All of that lasted about a little over a week. I got put on clonazapam and 20 mg. of celexa. So far I'm doing pretty good. I still get a little leg and joint pain, but not as bad and it doesn't last as long. I feel 90 % better and am expecting my second period on the 9th. I really hope I don't crash again. It was awful!! While on the mirena I had high blood pressure, fast heart rate, low grade fever, joint and leg pain, anxiety and depression, bloating like I was 4-5 months pregnant, nausea, heartburn, headaches, body aches (like I was sick), carpul tunnel syndrome (which I only get when i'm pregnant just like the heartburn) and more! Everything went down or completely away within a couple of weeks of having it removed. All except my heart rate. I am on a low dose of beta blockers to keep my heart rate from going over 100. Just like many of you I have been tested for many things like lupus, rheumatoid arthritis and so on. i have also been suspected of having hyperthyroidism, but with negative results from blood work. We are experiencing a major hormonal imbalance from this mirena. I just hope and pray our dr.'s will do their research and realize we are all right about our experiences and something can be done about this IUD. There is hope. Your bodies will regulate. It's only been about 4 weeks for me, but I am feeling better so far since my crash. Don't hesitate to tell your dr.'s about any depression and anxiety you may be experiencing as those are very serious side effects and can be treated even if it's just temporary to get you through the crash. I also take a one a day multi vitamin. So maybe that will help to.

37 - Dx'd w/ Hyperthyroidism at 20 and have been on levoxyl since then. I started at .075 and was increased to .1 when I got pregnant w/ my 1st child at 29. I always thought I had anxiety so until I started reading the posts I didn't put it together. I was always shaky and nervous and super skinny before I was dx'd with hyper and after the treatment I was still anxious so I thought it was a different problem.

The anxiety has gotten much worse in the last few years w/ pressure, family, and career so I went to a psych last week and he gave me lexapro and klonopin. The klonopin had done nothing and I was treated 10 years ago with Zoloft which made things MUCH worse so I won't take the lexapro.

I recently switched to Synthroid .1 because I thought maybe the generic meds didn't work as well. I developed a small rash on my elbow a week or 2 later, then a week after that I got 2 big patches on my back over my kidneys. A bout 2 weeks later I developed a HORRIBLE itchy rash over my whole body. I thought the itching would drive me insane. I saw a dr who gave me prednisone (made me feel awful), after I took the dose pack it came back like crazy. I went to the ED and the dr gave me scabies medication (I was mortified) but nobody else in the house had anything. I went to the derm and they biopsied two areas and a week later have not given me the result. Meanwhile, I'm back on levoxyl and the rash is slowly getting better. It must have been the cause. Anybody else get that??

Hi, my name is Eva and I am 27 years old.
I am a mother of 2 and had Mirena IUD inserted a few months after my 2nd daughter was born. This was 3 1/2 years ago.
Since then I have developed Eczema on my hands (which is the least of my concerns). More importantly I was diagnosed with Graves' Disease (hyperactive thyroid function) last year.
I had developed a goiter on my neck (enlarged Thyroid) , my hair was very brittle & my eyes were always dry and itchy.
Since then I have undergone Radioactive iodine treatment to destroy my thyroid. Reading all of your posts seriously made me angry and I teared up because I definitely think that there is a link between Mirena and thyroid problems. It makes sense that your body would try and fight off any foreign object in your body and maybe that send the thyroid into a out of whack mode ?
I am currently researching if there are any clinical studies out there on this possible connection. If anyone would like to join me - pls. contact me at ******
I have an appointment to have my Mirena removed in a few days, I sincerely hope that it will make a difference in my health.
Best regards,
E.

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..

Hello Again. I'd like to correct my earlier statement regarding the migraine. The terminology is "migraine with aura" (it still hurt like a son of a b*^$& no matter what you call it). I'd also like to update you all with an interesting finding from my Dr. app the other day...it appears that I have "hyperthyroidism" which can, in fact, cause many of the symptoms that I've been experiencing. It may be a good idea, for those of you who haven't already done so, to have a complete blood workup, including thyroid tests, to rule out possible root causes for many of these symptoms. I need to undergo further testing (which is just how a Mom wants to spend her precious "free-time" eh?) but I'm still keeping Mirena high on my list of culprits! Best of luck!

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.

OMG!! This is insane, I thought I was going crazy, I started YAZ about 2 weeks ago, I usually try to maintain healthy and workout a lot, but in 2 weeks i gained like 10 lbs out of nowhere!!! I am freaking out! I completely lost sex drive and as well as other said completely dry, nothing can make me wet, I also notice that I started getting a really heavy discharge everyday, Oh and depression (mood swings, snap at everything I feel like I don't want to live anymore, I don't care for my job as I used to or school...I feel helpless) I stopped YAZ 2 days ago and so far i haven't notice any change...I am still very moody and SSSOOOO tired, I can sleep all day and all night with no problem and when I do try to get up is like a magnet that's keeping me in bed, its awful!!! When does it get better???? Anybody knows??? I am falling apart!!! HELP PLEASE!!!

I was on the Nuvaring for about 9 months before I decided to go off it. At first it was great, but around the 3rd month I noticed that whenever I would put in my new ring I would feel extremely nauseous for the next day or two (as the hormones kicked in, I'm guessing). Then the longer I used it, I was VERY emotional and would cry all the time. I was constantly getting upset - which was terrible because I had gone on birth control b/c I was getting married. The last two months I was on it I also had terrible insomnia, and that was the last straw. Me and my husband couldn't take my moods anymore, the poor guy...
I'm 5'1" and about 100lbs, and i think that had a lot to do with it. The Nuvaring is one dosage for everyone, and I think being a smaller person had a worst effect on me. The plus for the ring, I have to say, was that my periods were barely there. They were very light when they came & I knew exactly when to expect them. But it's not worth it!!

Hi, I have been taking lisinopril 2.5 mg for a little over a year now. I am 20 years old and had high blood pressure for my age so my doctor prescribed me to a low dose (2.5 mg) of lisnopril. I didn't think much of it at first because I figured my doctor had prescribed it and knew what was best for me, so I have been taking it over a year now.
The past couple days, I've started to think more about things and am wondering if the lisinopril has anything to do with it. I have definitely noticed that my hairline is receding faster and my hair, especially in the front of my head, is thinning. I have also gained weight over the past year and cannot seem to get any weight off. I never had these problems of losing hair or gaining weight before I started lisinopril.
My question is could the lisinopril, even with the low dose of 2.5 mg that I'm taking, actually cause these types of things to happen?
If anyone reading this could please reply to me and let me know, I would appreciate it so much because I am really worrying about this. Thanks.

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?

Hello I'm a 41 year old female, and I took Lipitor 20 mgs for 6 months about two years ago. When I called my doctor's office to complain about side effects they told me it couldn't be the Lipitor because I had been taking it for a month already, and would have had problems before that. I eventually took myself off of the drug 5 months later. Here are some of the side effects I experienced:
Itchy fingertips, increased blood pressure, 30lb weight gain, shaky hand writing, acne, poor driving skills, poor memory, hair loss, "frozen joints", IBS, incontinence, low grade fever, itchy feet, numb toes, numb hands, foggy brain, joint pain, muscle pain, foot pain, plantar pain, dizzy, jaw pain, back and neck pain, week ankles and wrists, nasal allergies, skin rashes, migraines, heartburn, Increase in Astham, heart palpitations, knee pain, difficulty standing up from sitting position, difficulty climbing stairs, water retention alternating in feet, hands, arms and legs, almost constant taste of bile in my mouth.
These are only the ones I can remember. Two years down the road everything but the muscle and joint pain and weakness is gone. even those have improved a lot. I stopped taking the Lipitor and lost all 30lbs I had gained on it, without dieting, in a months time. I still have two toes on each foot that are partially numb. I have trouble climbing stairs, and getting up from a sitting position. I can do both, but I move slowly while doing them. The pain in my muscles and joints drives me crazy, but I'm grateful that the rest of the symptoms have cleared up. My doctor never believed me about my symptoms, and neither does my new doctor really. Went to the emergency room for asthma that was not responding to my inhaler, and they were about to let me go home when I mentioned to the doctor that I had been on Lipitor. Suddenly a huge battery of tests were ordered including a CT scan and a stress test. When I asked the doctor why he said that they just wanted to be sure that it wasn't something other than asthma. Why did they do that after hearing about the Lipitor? Do they know something? Are there doctors who believe that statins are killing and seriously injuring people? I'm so angry. Even as I sit here typing I know when I stand up I will have massive amounts of pain that I will have to "walk off". My quadriceps have not recovered, and remain ridiculously weak.
If I can stop one other person from going through this I will be happy. Thanks everyone for taking the time to list your symptoms. It makes me feel better to know that someone believes me, and knows what I am going through.

My now 17 year old daughter was prescribed Yaz back on 7/12/07. Since then she has had an extreme problem with constipation. She has been to the doctors several times, and is now seeing a gastrointestinal specialist because she can only have a bowel movement if she takes a laxative. The pediatric doctor had her on miralax from April to October trying to get this problem under control. It has not worked. We are seeing the specialist and they are running her through a battery of tests, which will now possible include a colonoscopy (at 17 !!!!). She has been extremely moody and aggravated - which I attributed to her age of course. She is no longer extremely athletic, she doesn't really do a lot. She is not the same person, definitely is a homebody now - never going out hardly with friends,etc. She has also had a 20 pound weight gain and for a tiny girl, this has had a huge effect on her. I have watched all of this, and never really thought about the yaz connection until today when a friend sent me this email with a link to this site:
******

that is when I got scared thinking maybe her problems were all caused by yaz. of course her acne cleared up, but her periods are still irregular and spotty. has anyone else experienced the bowel problems???

I have had a merina in for 12 months to reduce heavy periods as tehre was no change I went back to the doctors to have it removed only to find it had been out of position, so had another one inserted and some blood tests as i was feeling unwell, depressed,weight gain,itching eyes, feeling cold, insomnia,heart palpitations,headaches the tests showed i had hyperthyroidism yet i had more symptoms of hypothyroidism i feel this was caused by mirena but the doctors deny it yet looking into different sites the above symptoms are very common so i don't know if i feel unwell due to the merina of the thyroid will be going to the specialist this week hopefully to find out has anyone else had hyperthyroidism diagnosed while on mirena

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 am a 45 year old black female. After the death of my father, I started experiencing blood pressure problems and headaches. I was diagnosed with obstructive sleep apnea 2 years ago. Not having bought a CPAP yet has contributed to a lot of the blood pressure and headache problems. But, my GP put me on Toprol in June '08. I am having difficulty sleeping.Every time I eat, I have severe gas and my chest is hurting off and on. There has got to be a better solution. I started exercising and using Isagenix (******). It is simply wonderful - I have lost weight and toxins. When I go to my doctor on tomorrow, I am going to ask him if I can get off of Toprol. I do not like the way this medication makes me feel.

I am a 34 y/o male who started taking 10mg/day of lisinopril on May 15th. My blood pressure at the time was 140/118, pretty high I guess! I was feeling it too in the form of headaches. The doc wrote the script for me and I filled it that night. I should also mention that this is not the first time I have taken Lisinopril. I stopped taking it back in March because the script ran out. I don't seem to recall any kind of side-effects the first time, but I could be wrong. Anyway, I also take Levoxyl for my hypothyroidism, and it is a pretty hefty dose, 225mcg a day.

So, for the first week, I was doing pretty good on it. No coughing, or any of the listed side effects listed for the med. Then, about a week into it, I started having numbness in the right three toes on my right foot. When I say numb, I don't mean I could not feel anything, it was like touching your skin with a t-shirt over it. I could feel it, just kind of topically numb. I had a 'patch' of this numb skin right behind those same three toes and several other areas up the front and back of my right calve. I delt with this for a few days, thinking it was my shoes I was wearing at work. They were pretty worn out on the outer edges. I got new shoes on Monday, June 2nd. I wore them to work on the next day. At the end of the day, my calves felt kind of tired. The next day, they felt kind of tired still. I found this sort of weird. From that point on, my high anxiety really kicked in. I don't want to mention the thoughts I am having about what it could be that is causing this. I forgot to mention that I have not been sleeping well lately either since I started taking the Lisinppril again. I guess overall, I feel exhausted and weak. More so in my legs. To add to it, my lower back hurts like mad. I have two herniated discs and mild arthritis in it from damage from years ago. Also, for the past week, a pain has been developing in my left shoulder blade in my back. It is worse in the morning, and had gradually been getting worse for about a week. Today, it was awful.

I have ready a lot of the messages about the side effects different people are having. My question is, has anyone ever been on the lisinopril, gone off of it for whatever reason, having had no bad side effects, then gone back on it only to start having these bad side effects that you did not have before?

I have stopped taking the lisinopril on the 5th and have a doctor's appointment on the 9th to find out what is going on. I don't feel good at all. Can anyone relate?

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

I have been taking kelone for 20 yrs due to palpitations and a rapid HR the pappitations got worse over the last few months and I was panicky so I went to the dr and this is what happened!

I was put on metoprolol 25mg 2x's a day and it didn't work. I found myself in the hospital with a rapid HR and not feeling well. I had been on kerlone/betaxolol for more than 20 yrs and my NEW Dr was not familar with it so he swithched me. I went to fill the RX and was told by the PharmD that it had a very short half life compared to my old med. I asked the Dr. he said lets try it. Well like I said I was in the hospital within 2 days. I wanted to know what you all think about switching from generic to Toprol Xl and what should my does be? I was raised to 50mg metoprolol 2x's a day and it still doesn't seem to work. I know it is wearing off and I feel crappy! I am 38 with a hx of type 2 Diabetes which is controlled and I take Metformin 500 mg er. I also take Crestor 20 mg all other things are ok but I can't excercise or do any activity due to the feeling my heart is going to POUND out of my chest.
Any and all advice is welcomed since I am new to this med and dont't know if I go back to the palpitations I had with my old one or feel like crap with the new one.

Hi guys, I'm just curious as to whether and Paxil users developed hyperthyroidism?

I am trying to wean off of Atenolol bc it makes me tired and I feel as though my metabolism has slowed down. I have been on it for one year due to a fast heart beat. I did not have hbp when prescribed and I don't now. I was suffering from anxiety due to katrina and quit smoking. sometimes I feel sick to my stomach. has anyone gotten sick to their stomach from this med. also, I found that if I take it at night I am not tired during the day but I do have strange dreams.
my real question is how can I wean myself off this drug. I am afraid that if I stop it I will be somewhere and my heart will jump out of my chest.

I have been on toprol for two weeks. I was on atenolol before that for about10 months. Does anyone get head pressure from this stuff. I have constant head pressure. I also get depression and very dry mouth makes it hard to swallow.
I want to go off. I am only on 25 mg once a day. Doctors act like they don't want people off meds. I only went on cause I started with anxiety a year ago and makes my blood pressure wacky but not to high. Like 140/85 I use to always have low blood pressure. I got to get off cause it's causing me anxiety with the side affects.