Thyroid disease symptoms and conditions

I have taken Yasmin for a year and a half. Since then I have gained 25 pounds, developed thyroid disease, and am very moody! I have taken several different types of BC because I have periods that last for two weeks and are very painful. I have to get off of this pill to see what happens. I can lose the weight, but I will be on medicine the rest of my life for thyroid disease. I also have headaches almost everyday and I have cramps for two weeks out of every month!

I am a 53 yr. old woman who had aortic Valve replacement surgery in April 2007. I had a St. Jude valve put in and have been on Warfarin ever since. I usually go for a couple months with a steady INR and then, for no apparent reason, it goes out of whack and I have to adjust the level (with repeated doctor visits) to smooth things out. I have gained 20 lbs since my surgery, and cannot lose it, no matter what I do! I ride an exercise bike an hour a day, or walk a 3 mile route. NOTHING helps. I have recently said that if I had it to do all over again, I would choose a Bovine valve (even with the knowledge that surgery would probably have to be repeated later in life) just to be able to avoid the side effects of Warfarin. I have also experienced light-headedness, left sided chest pain, fatigue, coarse thinning hair, but by far, the worst is the weight gain!!

OMG!

It's hard to admit this, but I thought the symptoms described here (forgetfulness, fog, inconsistency) were being HELPED by the drug. I gave up coffee and most caffeine as I got older, also.

Once upon a time I was extremely anxious- I took Ritalin for ADHD, it became too much, and tried some things before landing on WB about 10 years ago. I took it during my pregnancy (perfect child, BTW- so smart and beautiful, not just to his mama) after trying to go off. i just found out I have thyroid disease, and I suspect it's played a huge role in the lethargy and spaciness.

SO... I called my doc to go off. The key for me is getting enough rest and exercising, along with meditation to stay grounded. I will check back to let you know how it goes.

I do have to say- man-made drugs are the invention of Western medicine, and while they have no doubt saved lives, there are other cultures that use far more natural remedies that have been successful for centuries. Do your research- don't put your faith in one doctor or philosophy. Drive your own good health!

i have been on yaz for 8 days and for 8days i have had my period i had cramps so bad i couldn't get out the bed for 2 days constant headaches leg cramps tired but can't sleep dizzy sick stomach very moody i would not recommend this pill to anyone at all it would be a big mistake to take this pill

am having severe abdominal, pelvic, lower back and hip pain. I went to see my doctor who thought I might have a herniated disk in my back. Having no insurance I had to pay cash for the doctor visit and X-Rays and was told I may be suffering from a herniated disk in my back. X-Rays showed no such thing. I was given a muscle relaxer, pain meds and an anti-inflammatory med. Through the next week the pain began to intensify to the point I had to leave work. I went straight to the ER where I was given steroids and a stronger pain medication. By the way, pain medication has no effect on me so I have been suffering for quite a long time. The ER doctor did recommend I see a gynecologist right away. He thought for sure something was terribly wrong. This was just last night and after reading all the comments above, I am pretty certain this is my problem. Having no insurance my clinic would not see me so I have to go to another doctor who said I must pay $200.00 up front just to get in the door. I have had my Mirena for 2 years and was doing just fine other than having problems with the headaches, zero libido and uuuggghhh, that weight gain thing and a few other problems, but now I am convinced that no woman should use the Mirena. I have already been through all of the with the Norplant. Another horrible contraceptive. If it is indeed the Mirena, I will have to have it removed and most likely will need a hysterectomy. Wish me luck finding a doctor to that with no insurance.

toriintx

edrogers, sorry to hear about all your difficulties. Hair loss is a hallmark of Synthroid and any doc that tells you it isn't, is simply incompetent! I too am 110 and can't gain weight. After years of having tests, incl thyroid (I figured I had Graves), tests always came back normal. A year ago I had a large goiter that turned out to be non-cancerous but I had to have half my thyroid removed. I ended up on 50 mcg and now 75 mcg of Synthroid. Since the dosage increased 2 mos ago, I have had SEVERE leg and foot cramps that wake me up several times during the night. Plus when I wake up, I feel an aching in my legs and wonder if that is not "restless leg syndrome". I am not sure if that syndrome is related to thyroid disease or Synthroid. I have not read about that one anywhere so far. I hate the idea of being on this med from what I have read and am considering Armour.

Two things I have learned though are: 1. If you have thyroid disease, you MUST have your adrenal levels checked. Even the drug info states this must be done before any thyroid treatment and 2. if your doc doesn't listen to you, find a new one. The best article I have read for thyroid disease is Gail's Thyroid Tips. it is a real eye opener.

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. =(

I had my Mirena put in October 2006. I have gained 40 lbs since then. At first it was great I didn't have to worry about birth control, becoming pregnant again and periods. I started to have mood swings, became withdrawn, no sexual desire, problematic acne, discomfort in my abdomen and weight gain immediately. I asked my doctor repeatedly about the weight gain, acne and mood swings etc.... I have Hyper Thyroid disease and have never been over 145 lbs in my life. He said the weight gain and acne was not from the Mirena and the mood swings, feeling isolated and the rest of my symptoms would eventually wear off. My thyroid tests proved to be still overactive after a 25 lb increase in weight. A year ago I told him I was uncomfortable being so heavy, having acne and I still felt withdrawn from family and friends and wanted the IUD removed. He reassured me that it was NOT the Mirena and that the Mirena was best for me because I have 4 children and no desire to have more. I periodically checked the internet to check for complaints about the Mirena and never came across much until tonight. I am completely horrified that my doctor led me to believe these symptoms were my fault and not the Mirena's and I feel like I have been robbed of over 2 years of my life. I am making an appointment at another clinic with another doctor to have this removed immediately. I now weigh 185 pounds and have acne scars!!!

I had my Mirena inserted in July 2005 and removed 2 yrs afterward. Till this day the effects are still showing. I have facial hair that I never had before. And the hair loss is still onset. I have developed fibroid cystic breasts. I have also gained a significant amount of weight that I'm still battling. At first I thought I was leading an unhealthy life so I changed my eating habits, stopped smoking, stopped drinking (which both were extremely RARE!), and cut out the fast food and replace with a healthy lifestyle. My hormones are still so out of whack that I think hormone therapy will be the only thing that will control my mood swings and help with the breast tenderness. BTW!!! If you do experience this symptom limit your caffeine intake!!! It could cost you your breasts. Right now I'm trying to make the best of my life and spending lots of money in electrolysis. Do not think for a minute that this thing is safe because it is far from it. REMOVE IT OR OPT TO ANOTHER FORM OF BIRTH CONTROL!!!

I have been on Prednisolone about 4 times in recent years. the highest dose was last year when i was on 80mg reducing weekly by 5mg. I have had most of the side affects you all talk about above. I have severe colitis so the side-effects of this drug are something i have to put up with. at the moment i have all the classic side-effects i usually get, rapid hunger, swelling to my face (moon face), neck has layer of fat, swollen back (buffalo hump), bruising easily, horrible taste in my mouth, swollen stomach. the one good side effect is it gives me lovely smooth skin lol. anyway the point of my post isn't to rip this drug appart as i have to say for me its a wonder drug and this time has prevented me from having my bowel removed! from personal experience once you finish the steroid treatment after a few weeks you'll notice the swelling go, my hunger usually fizzles out quite quickly (altho i have a large appetite in the first place!!) none of the side effects are permanent, so please all rest assured you will go back to normal just try not to put on too much weight while on the drug.

Here is our daughter's story, and believe me the tears are pouring down my face as I am writing this.
Our daughter, who had completed her series of 3 vaccinations has been experiencing considerable hair loss. Her first shot was in May 24, 2007, the second on July 26, 2007 and the third and final on November 27, 2007.
Here are the other specifics....our daughter was 13 turning fourteen.
She has had every blood test imaginable to rule out the obvious which may cause hair loss such as thyroid disease, polycystic ovary disease, diabetes, and the list goes on and on. Everything came back negative. We even have a future appointment scheduled with a rheumatologist this coming November 08. We have seen the Endocrinologist and two dermatologists (a scalp biopsy proved negative to any infection, disease, etc. Granted, she had a typical amount of stress during the school year, as any young teen would, but nothing to cause this. Everyday our daughter says to us, "you should see how much hair fell out in the shower today". She's so afraid to brush or comb it because of the extreme shedding. She literally, to date has half the amount of hair she had one year ago. Let me tell you she had beautiful hair. The hair loss is becoming quite visible at the forward part of her scalp. This has been devastating, hair is everything to a teen. (to anyone this is devastating) We must also mention that her periods have been totally out of whack. She went 6 months at one point without one. It finally came back, but it is so sporadic, getting every two weeks, at times extremely heavy, etc...
She also complains of intermitent dizziness. We are reporting this to Merck today (the Co. who makes this horriffic vaccine), along with the FDA. If anyone else is experiencing anything close to what we are, we all need to pull together and make the public aware of what's happening so we can prevent this from happening to our loved ones.
Please share your experiences. Feel free to write me if someone you know is going through this same tragedy.

WEIGHT GAIN, NUMBNESS IN FINGERS AND FEET. LET PAIN. I ALREADY HAVE RHEUMATOID ARTHRITIS, MIXED CONNECTIVE TISSUE DISEASE, THYROID DISEASE AND AM MISERABLE ON THIS.

I GAINED 12 POUNDS IN TWO MONTHS. I'M IN A FOG AND CAN'T REMEMBER ANYTHING. HAVE REALLY BAD LEG PAIN TRYING TO EXERCISE.

I THINK THIS DRUG SLOWED MY METABOLISM.

I received my first shot of Gardasil in January 2007. It could have started sooner, but about a month later my hairdresser noticed a bald spot in the back of my head. I rushed back to my ObGyn and asked her if the Gardasil could be the cause as nothing else had recently changed. She said that she had not heard of this, but she referred me to a dermatologist. I asked him if my hair loss had anything to do with the Gardasil. He replied that I had Alopecia areata and one thing had nothing to do with the other. He advised that I continue with the Gardasil and that he would start treating me for the alopecia. I wish that I would not have listened. I don't know what would have happened if I had stopped then, but I didn't I proceeded with the treatment to the end now over half of my head is bald!!!
I don't know what to do. I keep going back to the dermatologist for treatments for the alopecia, but it just keeps getting worse.
If anyone has had a similar experience and would like to share or has found some other treatments that work, please post a reply.

Melissa

My thyroid troubles started in 1993. I am not sure how long before the discovery I had the problem. Mine started as a nodule on one side. I was immediately put on Synthroid and had to go see the Endo every 6 months for a biopsy. In 1995 I became pregnant. I had one more biopsy until after the birth of my daughter. The Endo told me he wanted to see me right away after she was born to do another biopsy. I had my suspisions, but didn't think anyhing until after she was born and went for my biopsy. Well, I had cancer. I went through the whole thyroidectomy, the 3 days isolation with radio-iodine, and every year to every few years after I had to go back and get the radio-iodine treatment, while not the high dose as the first time, it went with the complete body scan. In fact, I am due now, but don't have health insurance. My dose has been switched a lot, I have probably been on every dose from the lowest up to .200mcg, which has been the highest for myself.

Symptoms: pre-thyroid disease, I am 5'2. I was always 110-115 lbs, I was 22 yrs old and 120 lbs. when I married in 1993. I did notice gradual weight gain, probably because of my thyroid problems. I am sad to say that now I am around 180 lbs. I cannot seem to lose the weight unless I go on a total starvation diet. I managed to lose 10-15 lbs over the past summer, but unfortunately for me it has come back over the winter. I tried to stay as active as possible by going to stores and malls to walk around. I do for a fact notice that when my dosage for Synthroid goes higher, so does my weight gain. I was on .137mcg over the summer, and I think that was a good dose for me, that was through the regular dr. The Endo is the one who put me back up to .150mcg. My Endo told me the thyroid is a regenerative organ, so it CAN grow back. I guess they don't want that in case of cancer again, and I guess that is why he keeps me on higher doses.

I personally cannot stand it. I feel it is a horrible curse. I feel very robbed of my previous active life. I have been dealing with this now for 12 years not having a thyroid and being on this medication. I feel angry that I do not have the energy to do things with my 12 yr old and 3 yr old. I miss the way I was before having thyroid disease. I feel very sad when they come up to me asking to do certain things and they (nor anyone else I know for that fact) can understand that I just feel so whooped, and no energy. All I ever seem to want to do is take a nap. I have migraine headaches constantly, I am constantly tired. I cannot concentrate, I have some memory loss. My ex-husband, and my current husband too for that fact think I am just being lazy. Well, that is not so. There are moments when I do feel a burst of energy, but then, I have to use that burst to do the things I need to do around the house.

Pre thyroid disease I was always active, never tired, could do anything. After: TIRED, I was 24 in 1996 and felt like an old lady, dry skin, no matter how much lotion I put on. The tub is full of hair, while it doesn't come out in clumps and I still have thick hair, I have hair all over the place. Irritable, mood swings, happy to angry and the snap of a finger. I can have insomnia some nights, constipation, lots of the same stuff others have listed on this forum. Those side affects are the same no matter what dose I am on. And like I said the higher the dose for me, the more weight I pack on. It is instantanious. Over Christmas, and no, it wasn't from eating all the goodies, I gained a lot of the weight I had lost over summer back, and that was because a few weeks before, the Endo had put me on the .150 mcg.

I can't even describe how this website is making me feel. How could I be so stupid as not to consider my birth control as having large effects on my body. I was on Ortho Cyclen before and it was fine but I wanted to switch to something else because I gained weight on it. I switched to Yasmin and didn't notice much of a difference besides the annoying thing that I still get severe cramps and back pain during my period. In probably the last almost 2 years I have been suffering from depression and OCD symptoms that are very bad. I was not sure what was wrong with me! I have also developed IBS symptoms to the point that I can't even go out and eat dinner with my boyfriend or family without being anxious about having stomach pain, nausea, and having to run to the bathroom. I was tested for an ulcer (it's genetic in my family) but it has been confirmed otherwise. I am on Omeprazole (to decrease stomach acid) and feel at lest functional on it but still get severe stomach pain, nausea, and diarrhea. No one seems to understand!!! I also get dizzy spells and feel faint and weak frequently. I was diagnosed with a thyroid disease but have been on medication for that and never really felt many side-effects from that anyway. I am going to request a different medication the next time I see my gyno and hopefully I'll be back to the fun-loving spontaneous person I once was.

Been on Nuva Ring for about 1.5 years...just now starting to realize the potentially bad effects its having on me. 3 months ago i started having wierd issues going on with my body. Nervousness, shakes, racing heart, trouble breathing, FATIGUE, constant "floating" feeling/dizziness. I am in good/normal shape, exercise about 2 days a week, but have had no energy. I went to a dr and had some blood tests done. My Thyroid numbers came back unusually high. My Dr recommended an Endocronologist to check out the possibility of Hyperthyroidism (the Thyroid controls the metabolism and hormones in your body). Went to the Endocronologist and am waiting for test results to get back. She said that it is a big possiblity that Nuva Ring could be the cause but wanted me to do further blood tests. I am being opened minded to what the real reason to my symptoms are, but i know that putting any extra hormones in your body has an effect on you, regardless. I took the ring out about 45 min ago and i'm hoping for no bad side effects...cant be worse than what i've already had. I have a boyfriend and he was totally ok with it (encouraged me to take out the ring to see if it helps)....he doesn't like the thought of using condoms, but its a small price to pay to see if birth control with hormones (NR) are causing all these horrible symptoms. I'm going to look for other non-hormonal contraceptives to use!

I was born without a thyroid gland so I can't compare the way I feel now to the way I would've felt with a thyroid. I've been on Synthroid my entire life (22 years), and I'm up to 112 mcg now. I am very skinny (5'5", 104 lbs) and feel constantly fatigued no matter how many hours I sleep, what I eat, and how much exercise I get. I periodically get pain in my hip joints, heart palpitations, and intense mood swings. My thoughts race but I have very little physical energy. I feel restless and gloomy almost all the time for absolutely no good reason. My doctor tells me I'm depressed but I honestly have no reason to be depressed and I wish she would see it as a symptom instead of a diagnosis. I graduated from a good college, I've got a job I like, I have friends, I enjoy life and my hobbies, yet I feel overwhelmingly sad. This does not seem like depression to me.

I find that after I do aerobics I get a tightness in my chest, which makes me worry about my heart, but again my doctor doesn't seem to think this is cause for concern. I have been irritable/fatigued for YEARS and I suspect I'll feel this way for the rest of my life. The worst of it started when I hit 16 years old and started the 112 mcg. My tests are always normal and it frustrates me that my doctor disregards my symptoms. I've tried other doctors, but they always send me away with my 'normal' test results. Can anybody help?

I have had thyroid disease for 6 years. I just had my medicine increase less than one week ago from 125 mcg to 150 mcg. The endocrinologist did this with a lab result from over 6 months ago and I was never retested before he upped my dose. 2 days after my new dose I broke out in a rash head to toe. The next day I started itching and went to my doctor and she said I have no idea what is going on with you. Then I went to the Pharmasist and he said you are having an allergic reaction to the dye in the 150 mcg blue tablets (125 mcg are white). The following day I got new medication I now am taking 3 50 mcg tablets. But I now am swollen ankles to feet and elbows to hands. My hands are like balloons. When I go to bed at night my hands are completely numb. Has anyone else had any symptoms like this?? Help I cannot figure this out. I am thinking that I may be over medicated. Thank you Heidi

I HAD BEEN ON 80MGS. OF PREDNISONE FOR TREATMENT OF SEVERE SORIASIS. IT WORKED WONDERS FOR THE SKIN CONDITION. , I WAS SPEEDING MY BRAINS OUT , AND GOING 100 MILES PER HOUR. IT WAS SOMEWHAT EUPHORIC. I AM 45 YEARS OLD AND HAVE BEEN IN MENOPAUSE SINCE MY LAST CHILD WAS BORN 5 YEARS AGO. AFTER I TAPERED OFF THE PREDNISONE OVER A MONTH PERIOD... I STARTED TO HEMMORAGE. I HAD UNCONTROLLABLE VAGINAL BLEEDING, BLOATING , PAIN, MOOD SWINGS, DEPRESSION, ETC. THE BLEEDING DID FINALLY SUBSIDE AFTER BEING OFF THE DRUG FOR 10 DAYS. HOWEVER , NOW THE SKIN IS DETERIORATING, AND THE JOINT PAIN IS EXCRUCIATING. I CAN BARELY WALK. I AM A DANCE TEACHER, AND THIS IS BECOMING DEBILITATING. I ALSO HAVE A CANCER HISTORY, AND THYROID DISEASE. IT WAS AND IS ROUGH. I GUESS I HAVE A CHOICE BETWEEN HAVING HORRID, DISGUSTING SKIN ( AND UNABLE TO GET A PUBLIC JOB) AND BEING EMBARRASSED ALL THE TIME AND DEALING WITH THE VERY DIFFICULT SIDE AFFECTS OF THIS MEDICATION. I AM HOPING FOR A BETTER ALTERNATIVE. THE SUFFERRING IS UNBEARABLE. LIBBY B.

The chronicles of my nightmare:

First of all.... I have been on Yasmin about 3 years... I have been batttles for "3 YEARS" with being dizzy, fatigue, vaginal dryness, chronic yeast infections, chronic discharge, mood swings, panic attacks, anger issues, anxiety and stress, trouble sleeping at night, loss in sexual desire, depression, constint fluctuations in my weight (I swing 13 pounds), and gastrointestinal problems.... I have been to every doctor and tried every medication known to man.... (Well almost).... I started testing for thyroid disease cuz my mother has grave's disease... At first I test for hyper (Got put on meds), then went to hypo, then they thought it was hashimoto's thyroid disease, until I tested back to normal and have been normal for about 2 years now even though I have been feel all wacked out. But, during this wholefiasco I had been making regular visits to my OBGYN to see why I am in so much pain from sex and why I have cronic yeast infections.. (Visited two to three times a month to be exact)... I've takin dyflucan (yeast infection pill)... no less than 24 times... Never helping me, so I became immune to that, then we trying creams, which gave me an even worse yeast infection, then we tried a homopathic approach ("biotic acid sappasitories")... Which made me so inflamed and in pain tha I have had the same irritaion/ yeast infection for the past 6 months.... Where no one could help me and the most the Gyno could tell me to do was don't have sex or use tampons for a whole month, which I did... and it didn't help one bit... I tried everything from eating large amounts of yogurt (Which is quite painful cuz Im lactosintolerant).... I tried not shaving my gential area, shaving my genital area, changing body wash, changing detergent, not having sex, and changing lube.. Literally have tried everything... Then, they start sending me to different doctors.. They want to send me to an internal medicine doctor which told me the route of my problems was sleep and that would make everything better... SO, he gave me Xanax.. Which turned out to make me very angry, verbally abusive, and still could not get a good nights rest... Then, he told me I have to go to a physiatrist... Which I am still waiting on to see next month.... I thought all was lost and I would permanently be in pain forever until I thought I would give the practice of gynocology one more chance. Before my visit I decide to do some research on the one medicaton I take..."YASMIN".... I came to this very site and the testimonials blew me away. The side effects that many women were complaining about, were the same exact things that I was going through. I read every single page and went off to a new gyno doctor to explain my situation. She was the best doctor I have ever had.... She immediately said stop taking birth control! She also recommended taking a large about of vitiamins ( like calcium, vit. B complete, and vit. c)... She also said to take warm salt and olive oil baths to overall bring back the nature anatomy of my vagina. She also could'nt stress enough.... DON'T SHAVE! She said that the hair is there for a reason and shaving brings all sort of bacterialinto the fragile vagina... On other thing she said was to use a condom made out of something else, not rubber, latex, or goat skin... I forget what it's called... So, now that I have the knowledge from the doctor and this web site, hopefully my nightmare wll be over soon... I finish my birth control pack in a matter of days and I can't wait to start feeling better after 3 years!!!!!! I never knew that something as simple as a little pill can turn your life upside down and have your dragging for years.... Thank you so much ladies for all your help.... I really could have never found this out without you guys.... I hope I helped someone out there with my story... Has anyone else experienced this kind of horrific nightmare?

thyroid disease

i have rha,sle lupus and thyroid disease. i'm 51 yrs old and took a break from the prednisone hoping i'd be on a new med soon but, i can't get it done . So, it will be back to the pred..because it's the only thing that works for me so far. i don't know alot about it and would like to know how others handled taking it long term . i had the moon face, and weight gain and seemed was always angry and tired. anyhow, thanks .
Debbie

I just started taking methimazole today because i have a thyroid disease. I am only 20 years old and i have already lost alot of hair .. not from methimazole it just fell out on its own..i have one bald spot in the back of my head and my hair is breaking off every day.. What can I do about my hair loss?

I am a 16 year old female who has been on different thyroid medication for at least 3 years. Along with my thyroid disease I have type 1 diabetes also. Right now I am taking LEVOTHYROXINE. I have taken levoxyl, synthroid, and I cant remember any others. Over the years I have gradually increased my dose to 125 mcg. Instead of losing weight with these medications, I've actually gained 25 lbs, and Ive kept my slow metabolism. Ive experienced bloating, gas, fatigue, spaceiness-like out of it, unable to concentrate, increased appetite, and mild depression. I usaully am able to get fantastic grades, and catching on to things comes easy. But now ive lost interest in friends, sports and overall life. I am wondering if this thyroid medication or my other medication- Metformin has anything to do with how I feel or overeating?