Synthroid symptoms and conditions

I was put on Yasmin several years ago to control symptoms caused by ovarian cysts. I was told this was pretty much the only solution. Against my better judgment, I went on it. Things were ok for a few months but I started having mild side effects. I didn't feel like myself and my sex drive was definitely gone. Two years ago I had my thyroid levels checked and found out my TSH level was very high. After doing some research, I found that birth control can affect thyroid levels. I contacted my general doctor and he confirmed my findings. I took Synthroid to control my thyroid for two weeks and had to get off of it. I was like a zombie. I called my general doctor back and asked about stopping everything. He said to contact my ob/gyn and if she ok'd it, then it was fine by him. They agreed but also said there is no connection with the pill and thyroid. Red flag #1. After being off of the pill, my sex drive has not returned. It has been two years now. I asked my ob/gyn to do a hormone profile and they said I was too young to be having any problems like that. Red flag #2. I was tired all the time and had no energy at all. My general doctor gave me pills for depression (which the main side effect is extreme drowsiness). I was so disgusted at this point, I went to a Homeopathic doctor. I was told I had adrenal fatigue (which can be caused by the pill). I have been on a course of natural supplements for a few months and have felt better than I have in a long time. However, the sex drive is still gone and due to the pill, may never return. This has been a horrible strain on my relationship. It's upsetting when you know you should be feeling a certain way and you just don't. I have given up on traditional medicine and the idea of pills being given out without knowing long-term side effects and causing even greater problems. Ladies, if you are experiencing problems on or off the pill, see your doctor. If they offer no help, find another doctor! Also, after looking up Yasmin in a pharmaceutical book, it is listed as one of the WORST pills and listed under definite do not take. Use this pill at your own risk.

I have been on this med for about 2 years. Until about 2 months ago, I had zero problems and it was great! About 2 months ago I started having SERIOUS issues. I had never had a palpitation or chest pain in my life and then I started having heart palpitations, chest pains, shortness of breath - sometimes it feels like I'm not going to be able to take the next breath. I was in the ER - they said it was my thyroid and gave me synthroid - that made everything worse so they gave me a beta blocker to cover up those symptoms. I quit taking ALL medication! I am not a pill taker and it doesn't make any sense to take a med and try to cover up those side effects/symptoms with the next med and so on. I can't find a good Dr. who will actually listen. I have been on the heart monitor and it found I was having PVC's all the time. I was then referred to a cardiologist - after a one thousand dollar visit with only an EKG he said my heart is fine - go home. I told every Dr. about Yaz - none of them could connect the dots! I thought I connected them....only by chance. I forgot to take my pill for a couple of days in the middle of all of this and stopped when I finally remembered to take one a couple of days later. I thought to myself.....hey - I've felt a little bit better the last couple of days. I was near the end of the pack so I QUIT taking them!! Best decision I ever made! Within 2 weeks my symptoms had pretty much disappeared! I thought I had it solved. I am 43 years old and in really good health. A few days ago my palpitations are back - but they are different this time. Before I had a "normal" heart rate but it felt like my heart was going to thump out of my chest. Now I have that PLUS a racing pulse! Chest pains are a part of daily life. Mornings and nights are the worst but I think it's going on all day - if I'm moving around I just don't notice it as much. These symptoms reappear a few days before I'm supposed to have my first period after quitting Yaz. I'm wondering if it's hormonal or menopause or if this stuff will just stick around for a while. I'm scared! I've read about people dieing and it's traced back to Yaz! I have a 6 year old precious daughter that I kiss good night and pray like heck that I get the next day with her! It's just not fair - I really wish I could find some answers. Anybody out there got any? Thanks.

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'm fed up. About 4 years ago I had a complete thyroidectomy and OMG my life has been a mess ever since, Yes, I needed the gland removed (it was a goiter pressing on my air way and esophagus), it needed to come out but OMG what a nightmare. Synthroid is a drug I can't figure out. I am convinced that this has ruined my life. I have developed chronic/non-stop head pain and pressure. My B.P. has gone up and now I'm on B.P. medicine. (still have severe head pain). It just never leaves me. E.R. visits/hospital stays and on and on. They treat me like I'm a complete lunatic because they can't seem to find anything organically wrong with me. Ummm-it hurts(my head). I am starting with a new Doctor who is a D.O. rather than an M.D. and I am praying that he finds what the **** is causing my pain. I feel like crap. The T.S.H. is in normal range but I have learned that the T.S.H. is not everything (even though my thyroid is gone). The isiots for lack od better description, are just too lazy to go the extra minute to find out what is wrong here. I just want to be able to function and this head pain will not let me do that. It is a nightmare and I have nothing but sympathy and empathy for anyone who suffers with pain on a daily basis.

The only constant is the Synthroid. Maybe I can't take this stuff. It has to be that my body just can't tolerate it and need something else or T3 added (I don't know). I just pray that this new doc can figure it out because I feel so helpless with this. My pain is always there squeezing and pressing. It is horrible. Maybe Synthroid is the culprit. Good luck to everyone.

I am 34 years old. Back in 1985 I had most of my thyroid removed, due to a tumor attached to it. Since I was 10 until my late 20s, I was on Synthroid. By age 19 I had 3 knee surgeries to remove arthritis. I have suffered most of my life with joint pains, dry skin, weight that is like a roller coaster, and being tired most of the time. In my 20s I was put on Levoxyl. I has been on Levoxyl for several years now. Since being on Levoxyl I have been fighting anxiety, racing heart, joint pain in fingers and ankles, sudden dizziness to the point where i have to sit or pass-out. I feel like I'm 80 and not 34. After reading this site I am printing all this out and taking it to my doctor. No telling how much damage has been done after all these years.

Has anyone had problems with their eyes on this medication, my have been going blurry and then I get a terrible headache.

weight-gain/ alternatives have been availalable.."Amour-thyroid" about.com any alternative medicine sites! Thy-Aid..etc,Synthroid does nothing for thy,roid issue Everything starts there! Bio-denticals deals w/ harmonal...read and learn..FDA lies! Alternatives have "Cured" ask "Breakthrough" Susann Sommers book w/ doctors! Larry King! Truth re: real cures for thyroid,not HRT's..yet another that has killed and/or close to from...Side-effects..alt's do not have side-effects.soon,if enough people stop being lazy and so afraid to take what will keep them alive and happy only then will ALT'S push the bad FDA approved poisons away! Both MUST be explored,but the FDA make billions w/ doctors who get kick backs from each script they write for the infamous SIN-Throid,made my life a horror..hypothyroid issue does not need syn! There are better natural things! Headaches,never get the right dose! Right thyroid tests? Endocrinologists will use those bio-denticals bec- hormone & Thy go together,for all of the idiots out there who think their doctors are sooo good,slowly they are killing them in many ways!

I thought my fatigue and mild depression symptoms were something separate but after reading these posts, it sounds like they could be linked to taking Synthroid? I've been on it for 2 years now. At first, I felt great. I started feeling tired again & my dr. upped the dosage. I just saw him today & complained of feeling tired, depressed, and getting light-headed and off balance at times. He wrote me a Rx for anti-depressants and changed my blood pressure Rx. I'm thinking about trying a Naturopathic Dr. to see if I can get the results I need without all the side affects. It couldn't hurt to get another opinion.

My symptoms started with aches in my ankles and I thought I should stop wearing heals for a while. But then the tingling pain moved up into my lower legs and then my arms/wrists over a period of a few days. I felt like I was having constant shin-splints. I was heavy joint/muscle pains. Then the back of my head hurt really bad on the left side, just at the top of my neck/bottom of my head, and was also really sore to the touch. Then massive headaches. Probably migraines, although I have never had them before. My MD immediately put me on celebrex, which did nothing. I was eating Advil and Tylenol like candy and couldn’t sleep. So the doc put me on steroids (prednisone). That took the pain away. After a few days, while at work, the vision in my left eye went in and out (perfect vision to completely gone). I have never had any issue with my eyesight before - perfect vision. Then at one point (actually while I was in for my first MRI) my vision never came back. No one thought it was serious enough until I demanded to go to the hospital. I spent three days in the hospital, where they ran tests after tests (including MRI, Lumbar Puncture, blood work, neurological tests, echogardiogram, dobblers, etc). Upon leaving the hospital actually diagnosed me with Optic Neurosis, and gave me a 15% chance of getting MS later in life. We were all relieved it was not MS, like they originally suspected. After going to the Eye Dr, they told me that was not the case. This kind of eye stuff only happens to people in their 80’s! I will never regain my vision. If my diagnosis had been optic neurosis, it would not explain the joint pain. I have seen specialist after specialist over the last two months, and they still have no idea. Every test I have undergone has come back clear and I am perfectly healthy. My doc said we might have to go with the retinal specialists theory - which was a piece of cholesterol that clogged the artery in my eye. I just don’t get why a piece of cholesterol would have caused me so much pain over the rest of my body. After viewing this site and the Mirena pamphlet that I found online they give to the doctors, I really think it was the cause. The packet even notes, if you have symptoms like visual loss and headaches/migraines for the first time, to remove it immediately! I did not get mine removed until a month after my vision loss. Every doc I have seen I have asked if it was Mirena and not one of them thinks that could be the cause. But it is ironic, that when you see someone for the first time, the first question they ask is if you are on birth control or any other medications! I think I need to show them this site, so they can read other women’s symptoms. I did also have all the other symptoms as well - weight gain, irritable, oily skin, cramps, moodiness, vaginal odor, gross discharge, headaches, nausea, low sex drive, hot flashes, anxiety, restlessness at times, fatigue, and the list could really go on and on.

Hello,
I posted earlier and here is an update "POST MIRENA"
It hurt for only about 20 seconds and it was over. EASY You can do it!
I had the mirena put in Oct. 2007 and nursed my daughter for a year until Sept. 2008. Just the last 6 weeks started having these symptoms and went to my MD/Osteopath because when I called my OB-GYN she said it has nothing to do with the mirena and to see my regular MD. He has been fabulous and I have had several tests that I have listed as well as taken the mirena out!
My symptoms:
Lower back pain
tingling in my arms, feet and lips
cramps
low energy
I had my mirena taken out on April 30, 2009 and am just starting to feel better post mirena. I had these tests:
* MRI on back/spine
* MS test(Vision Evoked Potential)
*blood work
*Thyroid (it's been low since Oct. so I'm taking Synthroid)
*Vitamin D
ALL NEGATIVE ...Thankfully!:)
You never know....I just pray I continue to improve and get my life back and feel healthy!:)) From other posts it sounds like it takes a little while. Does this sound familiar? Please respond....

You Can Now Boost Your Thyroid Function,

Eliminating Your Most Troubling Symptoms…

Without A Prescription and Without

Begging Your Doctor!

How? By adding a simple but vital supplement to your diet: Iodine.

Just how important is iodine? Consider this… about 25¢ worth is all that stands between an infant developing normally and one that’ll be severely mentally handicapped the rest of its life.

Iodine is essential to a proper functioning thyroid. But as we grow older, our thyroid starts slowing down. It just can’t metabolize the iodine it needs as efficiently, and that means the hormone produced (also known as thyroid) goes down as well.

There are 2 other reasons why most of us are iodine deficient:

Inadequate dietary intake, and
Exposure to toxic substances that displace iodine.

Iodine is a mineral, but one that is not abundant in the food we eat. Primarily found in very small quantities in seawater, soils are naturally deficient in iodine, especially the further away you get from the ocean.

Iodine is also fairly easily displaced from your body by toxins called toxic halides… fluoride, bromine and chloride.

Fluoride is by far the worst culprit. Found in toothpaste and in your water supply, every time you take a shower, brush your teeth or drink from the tap, your body gets a little exposure to fluoride, leeching out good iodine. And contrary to popular belief, fluoridated water is actually rather poor at preventing tooth decay.

Why is it in our water supply then? Poor science combined with corporate greed and political ignorance paved the way. Basically a toxic by-product of aluminum production, fluoridation was sold as a way to prevent cavities because some areas with natural fluoride in the water also had lower instances of tooth decay. Based upon that spurious observation, fluoridation began.

If You’re Human, You’re Most Certainly Iodine Deficient!

Because of these factors, 96% of all people tested are iodine deficient! This according to a study of 4000 patients conducted by Dr. David Brownstein, Medical Director for The Center of Holistic Medicine, and renowned author of several books on hormones, iodine and hypothyroidism.

The World Health Organization also concurs, estimating that 72% of the world’s population is being affected by iodine deficiency.

This trend is worsening. Over the last 30 years, the NHANES (National Health and Nutrition Examination Survey I) shows iodine levels have dropped 50% in the U.S.A. alone.

Everyone out there, try Armour Thyroid!!! I was changed to Synthroid (because my endo only believed in it) a few years ago, and put on 15 pounds and lost half of my hair. I work out at least 6 days a week, run 3-4 miles a day, and live on salad. I asked my regular MD to switch me to Armour, and in three weeks, my hair stopped falling out, and I'm losing weight. I was losing, yes, I counted, at least 45 hairs a day when I combed my hair after my shower (and I'm not counting the clumps that came out in the shower). Now, maybe when I wring my hair out in the shower, only one will come out and less than 15 in my comb. Ask you doctor to just try it, and if it doesn't work, you can always go back. I swear by it. I'm happy all the time again, where I have just been monotone for the last few years, and I'm thrilled. Good luck!!!

Someone PLEASE help or offer assistance! I have been on 50mcg Synthroid for about 1.5 yrs now and have gained about 25 pounds!! I am a very, very active triathlete, not just your 30 mins on the treadmill kind of girl. How about running 5-6 miles, riding my bike 40-50 miles, and swimming all about 3 times per week!! How can a human being continue to gain weight at this activity level? I am considering just stop taking it, cold turkey. Has anyone tried any of the supplements for thyroid support, or natural meds? If you've got any suggestions, I am open to just about anything at this point!!

lol im 22, ive been on this drug since i was 7-8ish I find this really interesting as I never have had any side effects.As a teen I even stopped taking the drug for weeks at a time, though my doctor advised me not to because he said my body would be all wacked out... i was a teen it was bound to happen. And there was no change in me, lol. Im so surprised you guys say you had this many side effects!!!!

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 had the mirena placed about 2 months ago, a year after my daughter was born. i was ready to start dating again and i figured this was a safe second protection for me. 2-3 weeks later i had a yeast infection, i've never had a yeast infection in my life, i'm 29yrs old. I was so scared i thought i had an STD. I scheduled an apt ASAP with my primary care Dr. yes it was a yeast infection but i did not think it was the mirena. After that my "girl" hasn't been the same. ive had this slight burning sensation all the time. my "girl" is swollen and irritated and i now have another yeast infection. I became concerned and started to research yeast infection and came across this site and instantly I knew what was wrong. i'm getting this thing out my body instantly. I'm also hypothyroid because of thyroidectomy surgery and thought my new symptoms were because my synthroid doses were being adjusted once again but now it seems the mirena is also to blame. Either way i'm getting the mirena out because of the yeast infection alone. this is making me crazy.

My mother is on Metoprolol Succ Er 50 MG Taast and Synthroid 100MCB @ 1 a day for thyroid. My stepfather told me he has been concerned about her for a long time. She seems to have episodes of delusion, paranoia & can occasionally be qiute vulgar and profane. These are far from characteristics of my mother. I told my step dad I would see what I could find out. Any info. on this would be greatly appreciated.

Desperate

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much rennin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued well for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turning straight and my incredibly (can't do nothing with) thick hair started to thin and become style able. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kind of job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... In December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not going to have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA or I would have lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing blood work from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much rennin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

I have been taking Synthroid 25 mcg for a year now, and here is a list of side effects that I have experienced. Appetite has gone nuts, Gained 15 lbs, ringing in my ears has gotten louder, here is some scary stuff-constant visual disturbances, and now moderate to severe vertigo of which I have never had before the medicine!

I have been on Synthroid for about five months. I started out on a relatively small dosage- 50 mcg. My Doctor upped me 50 mcg every month after he checked my TSH levels. They started out at 150, and right now they're at a 10. I hate this medication. Im now on a 250 mcg, and my side effects keep getting worse. I have probably lost about a third of my hair. I started to loose weigh, but i don't feel like i really am anymore. I am very moody, and also emotional. I lash out for absolutely NO reason whatsoever. Im hot, cold, but can never find a comfortable temperature. Im always tired, No matter if i just wake up, or if its time to go to bed. He's put me on Celexa, he said i was just depressed. But its not depression. Three months ago i wouldn't have lashed out for something as small as the mail didn't come. I hate to be this way, and i wish i didn't have to take this medication for the rest of my life.

I also gained weight, work out 4-5 days a week and havent lost a pound. I am now having a vibrating or shaking feeling through out my body that is worse at night. I tried to stop taking it but that was worse.

I can't believe I didn't find this sooner! I was on the Nuvaring for about 4 years and just last month traded it in for the Mirena.

At first, I was thrilled to find the Ring as I have a very hard time taking pills because I've always had a sensitive stomach. The patch was messy and sticky so I was excited to find the ring. For the first couple of years, the only problem I had was keeping it in place (it would continuously fall out) so I just got used to having to push it back into place every time I used the restroom. Every. Single. Time. But it was worth it because it made my periods much, much lighter and more manageable (i usually am down for the count for a few days). I also did the ring continuously without taking a week off because I still had some pretty terrible periods.

About two years ago, I started gaining weight uncontrollably, became very depressed, lethargic and achey. One day I came down with a terrible case of bronchitis and was put on a heavy duty round of antibiotics and steroids. After, I started having terrible heartburn and IBS symptoms which lead me to a gastroenterologist. Every test imaginable was performed, but nothing was found. I was told I had a nervous stomach. Unsatisfied, I got some bloodwork done and had abnormal blood glucose levels. My diabetic husband gave me a glucometer and I realized my blood sugars were totally out of range. I ended up at an Endocrinologist and all tests came back normal. I was also referred to a Rheumatologist for my achy body and joints. I found a list of symptoms of hypothyroidism and was convinced this is what I have, so I was put on a very low dose of Synthroid. At the same time, I was diagnosed with Fibromyalgia and put on a whole mess of anti-inflammatories and pain killers.

Unsatisfied with my diagnosis of Fibromyalgia and totally unwilling to admit this is something I have to live with for the rest of my life, I began working with a nutritionist who has helped me get off all the medications (except Synthroid). But still, I hadn't slept through the night in years (getting up 3-4 times a night to use the bathroom), I was terribly achy, irritable, nauseous, constipated and still gaining weight.

Recently, my insurance changed and I decided to get the Mirena. Within a few weeks, most symptoms have drastically improved, my family notices a major change. I actually slept through the night last week, only 3 weeks after using the Ring for the last time. I haven't lost any weight yet, but the fact that I even CAN exercise is monumental. More than anything, I'm thrilled at the prospect that everything was caused by the Ring, the one constant no matter what I tried, and maybe I won't have to live with Fibromyalgia for the rest of my life.

I can't say with total certainty that the NuvaRing caused all my problems, but it is absolutely astounding that all of us are experiencing the same terrible symptoms and none of our doctors have bothered to think that it could be the Ring. I'm angry about this. Why don't they know about these side effects??

Yes these side effects are listed in the package, but they're the same side effects from pretty much every medication... and I don't know about all of you but this thing came damn near close to ruining my life. I couldn't work, sleep, eat, exercise, clean my house, etc. etc. It's no heart attack or stroke, but definitely life altering.

I think health care providers need to be alerted to these symptoms and the possibility that the Nuvaring could be causing it all. It would have saved me thousands of dollars in medical bills and despair. Patients should be warned that the side effects are very real and can be debilitating. I'm almost sorry I found this so late (after I already got rid of it!) but I'm glad I found it nonetheless.

Good luck to all of you!

I have taken this Levothyroxine ever since I got Thyroid Cancer in 2006. And thank God I am free from cancer now. My main problem now is that, sometime I really don't know what was wrong with me and get confused over my own feeling. I do have cramps, sleep problem, headache, menstruation problem, mood swing, panic attack and always thinking of a negative thing eg like am I going to die. It has been bothering me since than. Please help I just wanna know is this really due to the medication or its really that I am going to die. I am very confused at times when feeling this side effect. =(

Oh My Gosh....I cannot believe I just stumbled across this site. Feeling so NOT LIKE MYSELF for quite sometime now made me decide to google Snythroid side effects, wondering if this medication I am on could possibly be the reason I am feeling so badly. I am 50-years old and started taking synthroid (Levythyroxine) about a year ago for hypothyroidism. I have been struggling tremendously with anxiety, mood swings, fatigue, more hot flashes, emotional instability, and sudden weight gain (about 10 lbs) since I started taking it. I never had any weight issues. I have just assumed this was all related to being "menopausal" (and I'm sure some of it is) and stress-related.....but here's the thing....BEFORE I started taking it, I felt "normal" emotionally, I never had a problem with my weight, and never really had any major "pre-menopausal" symptoms....in fact, I think I had A LOT LESS hot flashes and emotional turmoil, BRAIN FOG, etc., BEFORE I went on this stuff. I was technically POST MENOPAUSE two months ago. Okay, so symptoms should be subsiding now. Any menopausal symptoms would/should have been worse during pre-menopause. Again, I never remember having any major symptoms going through "the change" and felt blessed in that respect......so could it be possible that this hell I have been going through COULD be related to this fricken Snythroid????!?!? I want to just stop taking it to see if I feel normal again, but don't know if it's SAFE to go off all of a sudden. What is this Armour?? I cannot believe how many others out there are feeling like me. I hope this is the reason, so I can feel some hope. But now what do I do? I'm sure I still have to get my TSH levels or whatever regulated. Any suggestions out there? I'll try and make a doctor's appt and check levels again and see what my options are...I was told I probably had to stay on this stuff for the rest of my life. Thanks, everyone.

I started taking Lipitor in 2004 and by 2008 was taking 40mg daily. I'm not sure exactly when certain symptoms manifested themselves, as looking back they now seem insidious, but I do know they became bad enough in 2008 I went off the drug myself, especially after reading postings like those at this website. After being off the drug for a month, it was clear to me the most of the symptoms dissipated, but it did have a residual affect. I realized I had suffered a loss of range of motion (ROM) in my left arm (frozen shoulder) and have been in physical therapy for over a month to restored 80% of it. I could not have done this while staying on Lipitor as I was experiencing “deep” muscle pain and weakness. I still have some weakness and pain in my left arm and shoulder and don’t know if it is permanent.

I am Hypothyroid and take Synthroid and am currently going through menopause and am on partial HRT. I took no other meds other than the Lipitor. At one point, I thought my symptoms were stress related, but realized my symptoms were causing the stress. Aside from the muscle pain, spasms, tingling and numbness experienced in my left extremities, I experienced gastro intestinal disturbances, occasional vertigo, some lower back problems and other aching in other extremities (like that of flu symptoms). I also suffered recurrent mental fogs, which I initially attributed to some lack of regular exercise (although I lead a relatively an active life), but that was not the case, as even after aerobic activity the tingling and pain would resume.

When I told my physician I had stopped taking the Lipitor (at that time for nearly a month), he didn't blink an eye. I agree with previous blog; the idea of statins are to lengthen your life, but what kind of life is it when you are in misery and nothing short of ceasing the medication brings relief?

I'm not advocating everyone "doctor themselves. Listen to your physician, but most importantly listen to your body and trust your instincts when it comes to these types of medications. Symptoms listed about scripts described as "rare" are usually not that rare at all. You are not crazy.