Losing my hair symptoms and conditions

Has anyone been LOOSING their HAIR on this pill. My daughter is taking to regulate her periods and so far she has turn from a sweet layed back princess to a hateful unbearable wench!!!! She has had all of the symptoms I'm reading about PLUS one!!!! She has been LOOSING her HAIR and its BREAKING OFF along the hairline making it look like someone is cutting it off and this, as a 14 yr teenager, is worse (for her) than all the other symptoms put together!!!! Of course, she's not affected by her thinking the world is coming to an end and arguing about everything she can and thinking I'm the dumbest person in the world!!! Wait! You think that has something to do with her age? lol In all seriousness if anyone is experiencing hair loss tell me about it. I'd like to make sure it is the medicine. Thanks!

I can't attribute this directly to my cortisone shot - however, I've noticed that the past few months I have been losing my hair. I can pull it out virtually by the handfuls anymore! I am only 24 - this doesn't seem normal and the only change I could point to is the shot. HAS ANYONE ELSE HAD HAIR LOSS THEY CAN TIE TO A CORTISONE SHOT?

I also noticed a change in my period. Nothing as extreme as I'm reading here - but I'm so glad to have read this - puts my mind more at ease to know have a cause for that.

I have tried other remedies - but the cortisone shot has been the only thing to actually work. Any other ideas?

I'm 18 and had my first son June 4, 08; I got the mirena put in late june 08. This is the worst choice I've ever made health wise. It started when it was inserted - severe cramping like I was having a miscarriage or something. They made no mention of this before hand. I started having spotting and constant light cramping since the day I had it put in for the first 3 weeks. When the time comes for my regular period I get severe cramps that nothing relieves. I've used ALL the ibuprofen and Norco pills that have been prescribed to me in 2 weeks. I'm out of all OTC ibuprofen even though it offers no relief. I called the OBGYN and they say the cramping is normal and just to take two ibuprofens (the ones I had which were 300 mg each) EVER 6 HOURS.

When I went in for a check up, they said it was normal and it would hurt for the first 2-3 months. I then told them that I took all my prescribed Ibu. and then moved to the norco which seemed to be the only relief as I've tried warm baths, Alieve, Advil, Motrin, sleeping in different ways, hot and cold compresses and nothing. He offered to prescribe me ANOTHER form of Ibuprofen as if he didn't hear me mention I have been taking 600 mgs of Ibu EVERY 6 hours since I had it in. Then he told me all he could say was to try Noproxem and that it was just Alieve. He then just told me as I left pissed off to give it more time.

I'm now passing big clots and bleeding in shades of brown and bright red, have severe cramping bleeding through OVERNIGHT maxi pads that you can supposedly wear for up to 8 hours. But he says everything is normal and just give it time. I'm down to begging my mom for her prescription Hydrocodone and she's beginning to think I have a drug dependency problem even if I go for a few days without mention or thought of one at all. Because of this I'm in pain all the time, losing my hair, constantly tired, depressed because there's nothing I can do for the pain, and I'm gaining back all my pregnancy weight. I'm also a pain to be around because I now have severe mood swings that I didn't even have when I was pregnant. And now I have to wait to get my medicaid again to have it removed. As of right now the cramping is so bad I'm on the edge of going to the ER to get it taken out.

The commercials are a lie and every user comment of mirena are just like mine or worse. I would not recommend this to ANYONE (unless I hated them enough). Mirena is a form of torture.

How interesting to find this site! I, too, was diagnosed with temporal arteritis on February 29 (no more leap years for me!). Because I was already blind in one eye (had no idea) and losing sight in the other eye, I was put on 100 mg daily of prednisone. I had no idea of what I was in for. Since that time I have been able to taper down to 42.5 mg daily, but I don't think I've missed a single side effect. Horrific headaches. A 25-pound weight gain so rapidly it was unbelievable, moon face like I've never seen, was thrown into diabetes right away. My blood pressure went haywire, my cholesterol went haywire (had never had problems with either of them). I think I agree that the most debilitating has been the muscle weakness and leg cramps. I have no balance, have had 3 serious falls. The latest is my skin is breaking down and I'm losing my hair. What hair I have is like somebody held a match to it and frizzed it. I'm short of breath, keep trying to exercise and it's like climbing a high-altitude mountain. Swelling of my feet to where I can wear NO shoes except for Crocs in about three sizes bigger than I ever wore in my life. Now I have a liver problem, am being sent to an "ultra-specialist" for this. The good news is that my remaining eyesight has been stable, and I am very thankful for that. I have been assured by multiple specialists that I would have been blind by now if not for the prednisone. Although it is very difficult for me to read by the time night arrives, and that was my chief "hobby." The other part of this whole sad saga (ha) is how much money my husband and I have been out this year -- unbelievable. Lab tests or doctors every single week and sometimes every single day. I am now under the care of 5 different specialists (ophthalmology, rheumatology, cardiology, hepatology and internal medicine), and it has been so incredibly expensive. This is even with fairly decent insurance. I have been told that I have at least six more months to go on this treatment, and then possibly another year on methotrexate. Thank God I have NOT experienced the depression that seems to be a common thread here. I am trusting in Him to get me through this itme and to come out on the other side completely cured. But it does get difficult in the meantime.

HEY EVERYBODY, IVE BEEN ON FEMCON FE FOR THE PAST 6MNTHS AND I HATE IT. MOST OF THE SYMPTOMS ALL YOU LADIES HAVE, I HAVE HAD AND DIDN'T EVEN REALIZE IT COULD BE THE PILL: WEIGHT GAIN, DIZZINESS, LEG CRAMPS, GROWTH AND TENDERNESS OF THE BREAST, NO SEX DRIVE, ACHNE, AND THE WORST OF ALL AND THAT WORRIES ME THE MOST IS THE GREAT AMOUNT OF HAIR LOSS IM EXPERIENCING!!! IM 22 AND FEEL THAT I SHOULDN'T BE HAVING THIS PROBLEM. IM JUST WONDERING IF ANY OF YOU HAVE HAD THIS PROBLEM AND IF YOU HAVE WHEN YOU GOT OFF THE PILL, DID YOUR HAIR COME BACK? YOUR REPLY IS GREATLY APPRECIATED!!!

i too have went through losing my hair through gardasil a lawyers office is handing gradasil cases and if enough people come forward they will investigate this and that action please help yourself and our young women and children and call 1800lawinfo and let them know what your going through thanks

Oh my I am not alone.. I have tiredness muscle pain and am losing my hair.. has anyone else experienced this side effect.. I am only on this medication and I know it has to be the medication causing the hair loss.. Dr. says none has been reported but yet here I am.. I have a red bumpy like rash on the upper part of my legs that will not go away.. I am so glad for this site.. am calling doctor tomorrow --off this stuff now!

I was on birth control pills for about 12 years when I decided to stop taking them about three months ago. For the past two weeks I have been experiencing some hair loss so I made an appointment w/my MD and she said that hair loss can occur when stopping hormones and she suggested Nuvaring. I didn't even have the thing in for 24 hours before I took it out! My head hurt so bad I thought I was going to die! I also got extremely queasy and sensitive to the smell of food so much that I couldn't be around my coworkers heating up their lunch. I had to give a presentation and felt the whole time that I might throw up in front of everyone. I also became extremely irritable and was ugly to a patient I saw that day and yelled at my husband for no good reason. My head felt like it was in an awful fog and I felt like I couldn't think clearly. I never experienced anything like that on BCP's. I will NEVER try Nuvaring again. It was awful. I'd rather keep losing my hair and go bald then take Nuvaring!

My psychiatrist started me on Topamax 2 yrs ago for depression from being 75 lbs overweight. Started at 25 mg/day up to 50/day for 2 yrs. Lost 70 lbs and kept off with only minor side effects. Also took 150/day Wellbutrin during this time. (For being kind of a neat freak and washing my hands a lot.- didn't affect my social or work life much) Have slowly started gaining the weight back (+12 lbs). Seem to have built up an immune to the 50/day dosage over the 2 yrs. So he added 25 in the am in addition to the 50 I've been taking in the evening. (1 mo. ago) Having some strange reactions. My memory seems to be taking a real hit. I am a CPA (passed these exams 15 yrs ago) and now I'm studying for the Cert.'d Internal Auditor exams. I am having a great deal of trouble trying to memorize for these 12 hour long tests! I feel fatigued every day. My blurred vision (that requires reading glasses) has gone crazy. I can't read the song book at church at all. And I'm only 47!. I've had acne like bumps all around my nose and face. How could such a slight increase cause so much change? Also sometimes my heart feels like it is going to beat out of my chest. And I'm losing patience w/my 13 yr old son who's pushing my buttons to see how much he can get away with. He seems to sense that I'm not at my best. But if I go off this Topamax and gain back my 70 plds I know I will plunge into a DEEP depression. Has any one talked to their doctor about the possibility of these side effects going away after time? My tingling hands and feet did and my slight hair loss did. And my weight loss is trying to go away but I don't want that. I'm majorly concerned about the memory loss and blurred vision eventually going away. DALIAL

Inserted 2-25-08
Insertion uncomfortable but would do it again for 5 years of birth control with little to no period and not having to worry about taking the pill or paying $50 and up a month for it.

Now the down side: am losing my hair little by little and my blood pressure is sky high. Two years ago my pressures were perfect through my whole pregnancy and now as high as 140/90. Have been working out 3 times a week and can't seem to lose the baby belly. After reading these posts am wondering if Mirena is the culprit there too.

Called the doctor today to ask to have it removed. Appt. scheduled for mid August. Wish the side effects weren't there because it would be wonderful otherwise.

nausea, headache, anxiety, hairloss, hairloss, oh yea; major hairloss, light headed. I was on yaz for 3 months, all side effects had went away except for the hair loss. I stopped taking the pill mid pack, i was scared of losing my hair. My Dr. said to go back on my pill, that the hair loss would get worse if I went off. My Dr.also told me that the pill was most likely not the cause of my hair loss and that if I stayed on the pill it would eventually correct itself. I went back on the pill after being off for only 2 weeks. This is my first week back on the pill and I think I am losing my mind, and my dinner. I remember this feeling only lasted for a few weeks the first time I took the pill. At this point, I just want to keep my hair, so I am back on the pill and just started using Nixion products. I will keep you posted. The side effect that never went away was yaz made my oily skin dry. On the positive, I lost weight, and my small breasts grew a cup size. Any advice on the hair situation?

Hi all, I have had the Mirena since May of 08. I had twins in Feb of this year and was given the little plastic ring for birth control. That gave me TERRIBLE migraines. i hardly ever even have headaches let alone migraines. It was impossible to take care of twin infants along w/migraine pain. I really shouldn't be on estrogen anyway because of a clotting problem in my family. So my doctor recommended the Mirena. I wanted it anyway because I can't remember to take pills now, (I'm a little busy.) Since I had it put in I have been losing my hair in unbelievable amounts which my doctor attributed to my just having twins. My depression and anxiety meds are NOT working anymore. My fourth and fifth toes on my right foot are completely numb and stiff, almost like I have arthritis or something. I have NO interest in having sex w/my husband. But after taking care of twins, who does?? Just kidding. I am not very happy with this IUD, but have decided the alternative (being pregnant) is not a better option at this time. So, for now I will continue to be a bitchy, balding, arthritic, celbate mother of two. Good luck to everyone else

Saw Levaquin on the news yesterday. I was very pleased to see that they are putting a warning on this med. I thought it was just me with a problem with Levaquin. I have allergies to antibiotics anyways so I attributed my problems to just another allergic reaction to an antibiotic. Wow!
I took Levaquin in April 3 years ago for a respiratory infection of some kind. I then had the same experience I have with allergies where my tongue felt swollen. I called the nurse and she told me to take the next dose anyway. I did so and my chest/esophagus felt like it was on fire. I couldn't breathe. I went into the Emergency room and they gave me a lidocaine/maalox combo that would take the pain away for a while and diagnosed me with reflux.
I went on some reflux medications later that caused more problems for digestion. The more we tried to solve it the more my system reacted. I ended up in the emergency room about 5 times that year. Two were for chest pain from the esophagus and two were from severe allergic reactions (anaphylaxis). I became allergic to many categories of food and lost down to 110 lbs. I went to naturopaths and other specialists and none of them could pinpoint any problems. I was tested for Celiac and had two upper GI and one lower GI that year alone, My Dr. bills totalled more than $5,000 for that year.
The next year I had given up. The only doctor that I would go to was the allergist and the new GI doctor I had found. I still worked but was in such severe pain that I did nothing but sleep when I got home. I cried and begged God for death or healing all night long. I was losing my hair in great handfuls. They put me on ativan and I became addicted to the stuff. I was allergic to most foods. I had a diet of about 6-10 foods that I would cook homemade and I would never eat out unless I knew what and how the food was prepared. I took vitamin c in very high doses and that took the pain away.
I slowly re-introduced food back to my system. Now I have a less restrictive diet but it still is limited. I am now allergic to all nuts, rice, sunflower seeds (sunflower oil is used in most potato chips), some other grains, and melons. I still have problems with legumes and some other foods.
It took 2 years for the pain to subside and I still have digestive problems with diarrhea on and off. I am fine just as long as the pain stays away. I don't mind being limited on my diet.
I had noticed that my legs and joints hurt during that time too- but the other pain was so severe and my diet was so limited that I attributed that to diet.
If there is a class action lawsuit on this stuff I would like to be involved.

Also reading other people's side effects... when i started the pill i had my period for a month and a couple of days.... THAT ISN'T NORMAL.. i don't care what people say that your body has to get used to the pill... that just does notttt seem healthy to me at all! and i too noticed cellulite on my legs i was horrified!!!!!!!!! so many bad things happened to me because i was on it.. i too was losing my hair.. and still am .... my mom even noticed and was making a huge deal out of it.. whatever i HATE that pill whenever anyone brings it up .. i only have terrible things to say about.. good for you if it works for you.. because i think it sucks!

I started Topamax in November of 2007 the usual 25mg and worked my way up to 150mg. I have always had pretty thick hair and now have hair loss in the widows peak and top part of my hair. Needless to say I am devastated. I have cut myself down to 50mg in the am and 50 mg in the pm. My Neurologist states that she has not heard of hair loss but even this web site and the drug company states that it can cause hair loss. I have with the help of a very good massage therapist determined that my migraines are cervical so I am seeking a second opinion and taking myself off this drug. Not worth the hair loss if I don't need to be on this drug.

My mother and I have both been diagnosed with Hashimoto's Thyroiditis and we both take levothyroxine. We both experience extreme pain and she has been diagnosed with fibromyalgia. I have not been diagnosed with fibromyalgia but I experience the pain body also. Another thing. I have been losing my hair. No reason, it's falling out from the root and I have some serious thinning. Memory...what memory. I can't remember anything. Has anyone received advise from a MD? Thanks

Please let me know if a class-action lawsuit is ever filed against this Pharm Co because I will file a suit to get this dangerous drug off the market. Yasmin/Yaz almost took my life in January 08. My OB/GYN put me on Yaz in Oct 07 for bad periods and cysts on my overies. Within a month my entire personality changed and I started losing my hair. I experienced a complete loss of sex drive, became depressed and was either constanting crying or raging at someone. However, my adult acne did clear up. On 1/27/08 I experienced extreme pain in my calf that moved up to my thigh within 48 hrs. I went to the ER and was told that no only did I a condition called DVT (Deep Vein Thrombisis-blood clot) in my leg but that the clot had broken off and moved into both of my lungs and I had bi-lateral pulmonary embolism. I can't even describe how incredibly painful this was. I was admitted into the hospital for 1 week and was put on powerful blood thinners, which I will be on for about a year. It's now been nearly 6 months since I was diagnosed and the DVT and it is still in my uppper thigh. But am grateful to be alive. If you would like to contact me I would be glad to answer any questions regarding this situation and my email addy is ****** PLEASE DO NOT TAKE YAZ OR YASMIN OR LET ANYONE IN YOUR FAMILY TAKE THIS MED, IT COULD KILL YOU.

I've been on Yasmin for four months. With all of the side affects from Yasmin it is the only pill that makes me feel somewhat normal. Just to name a couple I've been on Levlen, Tricyclen and they all caused major infections, depression and mood swings. I am only on the pill because I have a cyst on my ovary and the doctors will not operate because it is not big enough to remove but big enough to cause a lot of discomfort. Every month when I start Yasmin the first couple of days I am very moody and then I am okay until the week before my period thats when i am depressed and grouchy. Now I've started losing my hair, not cool. I'm sure it's Yasmin because i am not on any other medications and I take really good care of my hair. I just hoping it will pass.

I posted back in early March 2008 and figured I would update my experience with Mirena. I had many symptoms that most posted on here but not all. I figured I would give this option a few months and if the symptoms continued, I would have it removed. After a month, all symptoms have disappeared. Periods are lighter, no pain during intercourse and I can breathe a sigh of relief. No longer do I have to worry about pregnancy ( I always used natural planning going by my body cycle). I did have slight weight gain but started exercising more to offset the extra calories I was taking in with the sudden cravings for food. All and all, I am glad I stuck with it and let my body adjust to Mirena. Good luck to all of you.

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.

Doing an article on Yasmin, INFO WANTED on Side Effects that occur after you stop taking the pill

Hey okay so I'm doing an article on Yasmin, the side effects that occur when you stop taking the pill, and would like more information on it. I would like to interview ex users of the pills that have experienced either hair loss, lack of period, severe headaches, and just about anything that resulted. I need to write this article ASAP! All experiences are helpful. I too used to be on the pill, and ever since I stopped taking it my cycle has been out of whack. Please contact me either via email gator924@ufl.edu or through AIM: lipsfullbittin or via phone: 786-239-8751.

While most people know some of the side effects of taking the pill, few know the side effects that occur when you stop taking it. It would be a helpful article to any users or future users of the pill, don't you agree?

I am also experiencing hair loss and have been on Topamax about 2 months. I had no idea this was a side effect. I initially lost weight which was wonderful, but then my weight dipped so low my family and friends thought I was anorexic. I was finally wearing a size 3 pants. I normally am in size 8's. I am on it for bi-polar and to help with binge-eating. But I cannot deal with the hair loss. I don't think that being skinny is worth losing my hair for. No other meds have helped my depressive moods without making me gain weight and at this point I just don't want to take any drugs. I would rather try some therapy...that has become less common. The doctors just want to give you a pill now-a-days.

hi. everyone. I just had Mirena put in a week ago and already experiencing the dry skin, acne, losing my hair, feeling tired all the time, i just don't feel like myself. My blood pressure went up extremely high after i had my son and they put me on a pill made bp go into stroke range so my doctor suggested this. If i would have know how painful it was just to get the thing inserted i don't know if i would have gotten it. I am now on bp medicine and it is still elevated, i am still having discharge, which my doctor said would be normal but for how long?? Sex is sure not the same. My boyfriend doesn't complain but i sure can tell a huge difference. Its not even pleasurable anymore. What is really scary is my bp. I 20 yrs old and already have to take bp meds n it still hasn't gone down to a range that i am comfortable with. I honestly cant say if i will be able to keep this merena. I will be calling my doctor for the next appt available.

I took Yasmin for 2 years and about 6 months after starting Yasmin I started getting migraines at least 3 x per week and sometimes 5 x per week (before not even really getting many normal headaches). I thought it might be my birth control and saw my OB who referred me to a Neurologist who put me on a medicine for migraines. About another 5 months later I noticed I had a small bald spot in my hair line. Saw a Dermatologist who diagnosed it is alopecia. I immediately stopped Yasmin and migraine meds and decided to get an IUD (GREAT CHOICE!) My migraines stopped almost immediately, however my hair loss continues to progress. I now have 3 additionally bald spots on my head and areas on my scalp that are very thin. I feel great otherwise, no headaches, no depression (other than losing my hair), no anxiety, appetite is normal. I'm so desperate to find someone else that has had this specific problem as no one believes the hair loss is connected to Yasmin. I just pray after awhile the hair will grow back. Please if anyone has experienced this same situation please post what might have helped you get through it and if it does ease up! One more thing - I have scalp pain, like burning on the front and top and back part of my scalp, wide spread, not only in the bald areas.

I've been taking Yasmin for 7 months now...at first it was brilliant! i have had trouble with other pills in the past and Yasmin seemed totally different.
however, after settling down with it, i am starting to experience some side effects. i appreciate that obviously they may not be related to Yasmin but after reading other people's experiences I'm thinking that they probably are!

my hair falls out more than is normal...i used to have really thick hair and now it's getting pretty thin.
i have developed a cyst on the side of my head?!
i get weird pains in the right of my chest and stomach as if I've been exercising too much or sitting balled up for hours.
i have gone off food.
my sex drive is none existent! my boyfriend and i used to do it pretty much every day and now i never want it. we haven't really had any proper sexual contact in over a month.
i had complete loss of vision in one eye.
I'm getting seriously anxious about things that are important, but overly so.
i feel permanently tired and drained no matter how much sleep i get.
i cry 24/7 over absolutely anything... songs, adverts... its ridiculous!?

if i come off Yasmin it'll be the 3rd pill that doesn't agree with my body. I'm gonna have to try something new i think...