Curly hair symptoms and conditions

I have been on fosamax for about three months. All of a sudden I noticed my hair falling out. I had very thick curly hair, and now I fear that it will all go away. I am in a state of panic right now. I am wondering how much hair will I be left with, and will it ever grow back? Can anyone tell me ?
I have stopped the fosamax a week ago, and will never take it again no matter what my doctor says. He is blaming the hair loss on hormones. But I have not had hormones for years. I am 57, had a hysterectomy at 28, took premarin for years, and stopped about 8 years ago. I have also been having pain in my shoulder which now that I read about other people having shoulder pain. could also be from the fosamax. Please tel me what to do about my hair loss! Will it grow back?

Wow. I am in awe. I lost my mother June 7, 2009. I plunged into severe depression. I was already on Paxil. I started the generic brand of Wellbutrin (Bupropion) around June 30th. I noticed a big difference neurologically. But on to why I am posting... I noticed last week my hands were shaking uncontrollably and I could not stop them. I ran out of Wellbutrin and waited a couple of days to pick it up. I noticed a lot of the symptoms stopped. I have also had off the chart vertigo. I am talking extreme. I had tremors this morning and thought something was under the pillows on my sofa and jumped up to look. I then wondered if I was going crazy. I then went to my desk to work and crossed my legs on top the desk and the tremors started again.

I had thick bit fat hair naturally curly hair (which I still have most of it) . I started seeing hair everywhere in the car seat, the desk chair, on the sofa, the floor blah blah. Everywhere! If pulled on the end to check for split ends and the freaking hair came out. I notice last night that I could see through the temples of my hair and freaked out. So now what? Am I going to have to have a Donald Trump comb over. Seriously I had enough hair on my head for two people. You know how people buy really bad wigs that have way too my hair on them. They are long bushy and you know they aren't real? Yeah well that's my natural hair. So when I looked last night and saw what I saw - I totally freaked. The tremors this morning did it along with the postings here. I just flushed my entire bottle. I had only taken 3 out of it. I'm over it. I like my too big nappy natural hair. I'm going to do everything I can to get it back. My dermatologist friend told me to go to Costco and buy Men's Rogaine gel form (I'm a chick). Can I just say I'm about to put my little dog in my purse and we are off to Costco. This is really, really, really the suck. So here are the choices; do you want to be sane and bald? Or do you want to be semi-crazy and shake like a junkie? I say screw it. Hey, I have cold turkied off Ambien before (it took 14 days but do not try this at home!). I'm done with Wellbutrin. No guts, no glory.

I took Wellbutrin XL 6bvyears ago and experienced weight loss but no other side effects. I recently started again. At the same time, I had the keratin protein treatment that make my curly hair straight. Recently, i noticed a lot of hair loss. I been attributing this to the hair treatment, but when I went to an acupuncturist about hair loss, he immediately said it was the wellbutrin. I couldn't believe it!!! 2 different doctors told me hair loss was not a side effect of Wellbutrin XL (300mg). But after the visit to the acupuncturist, I did a little more digging and found this sight. I can't believe what I'm reading. This wasn't my experience in the past when I took the drug. I will definitely stop this med ASAP. Good luck to you all.

I've been on the Nuvaring for about a year now. At first there were no symptoms and I actually felt a lot better since it made my periods shorter and lighter with less cramps. Recently, my skin has been acting up with rashes on my forearms and between my thighs and even sometimes on my face and lower abdomen! I've always had issues with my skin because I have eczema but it's never acted up this way before and the last time i had it anywhere but where my arm bends was when I was 12!
My attitude has also taken a turn for the worse, I used to be very active and play sports all the time, but since using the Nuvaring my body has changed so much! My flat stomach is gone. :( I feel like I'm always bloated and my weight went from 120 to 135. I attributed all these changes to maybe being disinterested in playing sports or maybe because I'm in a serious relationship, but after reading all these posts I'm sure I'm getting off of the Nuvaring. I haven't had a lessend sex-drive, but I don't orgasm as much as I think is normal. I also had really curly hair before, I thought it straightening out was maybe because I was straightening it too much, so I stopped using the straightener and started using a curl boosting shampoo and conditioner, its been 2 months and I still have not even one curl.

I had the Mirena inserted December 2007 and I thought everything was going great! Then the weight gain started it was like I gained weight in my sleep I went from a size 14 to a 20 and I hate it. My hair stopped growing and started shedding really bad. My face looks blotchy and rough and I've developed a skin rash that itches terribly. I'm irritable as HELL and my sex drive is completely gone. I hadn't had a period since I had the Mirena placed and three weeks ago I started cramping really bad I felt like I was in labor, I couldn't walk or stand up straight. I took some Advil laid down and woke up in a puddle of blood, by the time I could get to the bathroom I had started passing large blood clots. I went to the hospital and they did nothing gave me a prescription for Vicodin and Codeine. As of today I'm still having the same complications with no sign of getting better. Thanks to all the ladies and their post I now know that Mirena is the root of this evil. Thank you to everyone and hope you all find relief because I just called to have this thing removed first thing in the morning!!!!!

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 :(

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 renin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued good for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turing straight and my incredibly (can't do nothing with) thick hair started to thin and become stylable. 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 kinda 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 gonna 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 of 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 bloodwork 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 renin? 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 :(

My teenage daughter was taking generic Wellbutrin (manufactured by Watson pharmaceuticals) 150 mg. daily for about 3 weeks or so and started having serious hair loss on the top of her head. The prescribing psychiatrist told her to stop the medication and after about 2 weeks, the hair loss has stopped almost completely. I have read a number of blogs including this one that indicate that hair loss is a side effect yet the Wellbutrin trials only listed hair loss as a side effect for less than 1% of patients. Given the U.S. Supreme court ruling today that says that even if the FDA has approved a medication, a pharmaceutical company is still responsible for fully reporting side effects and can in fact be sued in individual states if they do not provide sufficient warning, I would be interested in hearing ideas of how we can put more pressure on the manufacturers of Wellbutrin and its generic equivalent so that they give better warning of this side effect.

I was on Aviane for about 2 years. During this time, I had very severe cramps during my period. This included majoe hot flashes, to a point where I would sweat! Just about every time I ate, I would have to go to the restroom with severe diarreha. All I wanted to do was to lay in bed, curled up in a ball, so nauseated from the pain! I was so miserable!! Not to mention my horrible mood. I was mean to everybody and I was so depressed that I would just cry for no reason. It almost caused my boyfriend and I to break up a few times because he couldn't take me anymore! Once my period ended, the mood swings ended, but I had no sex drive what so ever! It kept getting worse every month, and I am only 25 years old! So, I recently switched to Yaz. It costs a lot more, but so far is worth it. My sex drive is back, no PMS or mood swings! Cramps are very light and I haven't felt depressed at all. I am in such a better mood all of the time every day. Something else I noticed is that my sudden feelings of anxiety have disappeared! I thought it was just me, but now I believe that it was caused by Aviane. Also, It has made by breasts grow a whole cup size
with no weight gain! One more thing is that I used to have so much hair loss in the shower, and I thought it was from straightning my curly hair! Since I switched, it has dramatically lessened! Ooh! And one more thing...I have smoked for about 8 years...not a lot, just a few a day. Since I have been on this I have not had any cravings cir a cigarette.... maybe occasionally while having a drink or coffee. So maybe it is from Yaz as well! I am so glad I found this forum, and wish I found it sooner! Good luck everyone :)

I hate this pill! I don't know why I've been on it for so long. I am considering going off of it but I am afraid what I switch to might be worse. It has made me very anxious, its caused my curly hair to become straight, limp and dull and wearing my contact lenses is nearly impossible. If someone can recommend another option please do!

I am a 34 year old female and have been on wellbutrin for 3 yrs. taking 300mg a day. I have lost a bunch of hair. Half of my hair is gone and that is no exaggeration!!!!!! But the worst part of it is that I had no clue that my medication could be causing it. My mom is a hairdresser and she has been really concerned about my hair loss. We thought maybe we were just frying it with all of the chemicals we put on it---BUT after talking about it we ruled that out because we have ALWAYS done it. It wasn't until after LUCK of stumbling across this info on the net that we put 2 and 2 together. UUHHGG!!! I am sooo mad at my Dr. I even discussed my hair loss with her a YEAR AGO. She had bloodwork done for my thyroid and it came back normal. I have a check-up today concerning my meds. I'm going off it ASAP. Dont want to just stop completely because i heard it can be dangerous. But i recommend to anyone taking wellbutrin that likes having a full head of hair to stop taking it!!! The Dr.'s will tell you that it is not a side effect but believe me---IT IS!!! I can only hope now that mine will grow back.!!!!!

I have been on the NUVARing for 2 years and I'm 25. About 5 months ago I started having really really bad DRY EYE PROBLEMS. I have been to the ophthalmologist and I've been on restasis, refresh plus, Lotomax, and other ointment I put on my eyelids at night. The eye problem isn't getting much better. Has anyone else experienced this?

Also, I use to have super thick curly hair. I lose about a handful of hair a week and I don't think this is normal anymore.

I'm wondering if it is time to take out the ring. Any advice?

I have just been switched to Synthroid (by my Endocrinologist) after being on Armour for 4 years. I have to tell all you out there that think "Armour" is the save all drug..and believe me I am not an advocate of Synthroid either because I have not been on it long enough to know what possible side effects I might have..however when I first started on Armour I felt like I did before I had been diagnosed with Hypothyroidism ..then about 1 yr ago I started to gain rate rapidly like 40lbs in 6 months feeling sluggish, off and on skin problems, puffy hands, face, feet,hives, pimples in the back of my head almost hive like,some hair loss that is noticeable to me as I have had very thick curly hair all my life now it is getting noticeably thin and It is making me very nervous...My Endo put me on .75 mcg Synthroid and .5mcg Cytomel which she calls a "controlled Armour"..Armour does not stay consistent with your T4's and T3 levels and that is what cause my thyroid to become suppressed and these are the symptoms I was experiencing...she also put me on Spironolactone which is a mild diuretic to lose the puffiness in my face,hands,and feet and so far so good...Like I stated earlier, I am not an advocate of Synthroid or Armour our any drug for that matter, I just want to find what is right for me and stick with it..and if Synthroid doesn't work for me, then I will try something else...Just remember one very important thing.."You" are the only one who knows how you feel and Dr's are not God they can't fix everyone that is why its very important to read about your disease and find out what things might work for you..I suggest getting this book I bought that was recommended to me by my Endocrinologist called "Screaming to be Heard" Hormone connections women suspect and doctors still ignore written by Elizabeth Lee Vliet, MD...its a fabulous book and I am sure all you women can relate to this book...its all about us....Most important thing is to stay healthy eat a well balance diet and exercise..also find out about the foods that only worsen thyroid problems...

I was taking Aviane for 9 months - perhaps 9 months too long. I have experienced noticeable weight gain and TREMENDOUS HAIR LOSS. I USED TO have thick, curly hair. I have lost at least 25% of my hair since taking this pill. It is absolutely noticeable - even my hair dresser is shocked. I have checked the other misc prescriptions that I am on - allergies, acid reflux - and this bc pill seems to be the culprit. If you have not started this pill, think twice before doing so. I switched to another 'regular' pill a few weeks ago. I hope my hair grows back!

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.

Help me! I have stopped taking Yasmin for about 4 or 5 months because my husband and I want to conceive. I AM STARTING TO LOSE MY HAIR! I am so worried about this as I am losing at least double the normal amount everyday and this has been happening for about a week now. I have noticed the difference as my hair is not very thick. My husband has noticed. My friend says she can't tell, but if you look in my bathroom and my comb you would think I was undertaking radiotherapy. I went to my doctor two days ago and she thinks it could be thyroid or iron problems. She thinks it could be ceasing the pill but is unsure......PLEASE, is there ANYONE who has experienced this? And if so will it stop? I am so distressed about it.

I've had my Mirena for about 15 and a half months and I am having it removed today at 2 o'clock. At first I had sharp pains when I would sit down and I felt like the cords were poking me and irritating me. My OB/GYN requires patients to come back one month after having it put in so he can check it and make sure it is still in place. At this visit he also trimmed the cords although he acted like he didn't believe me when I told him that I could feel them poking me when I sat down and that it hurt. At first I didn't notice any bad side effects, but I did have one good one: my periods stopped, but I still had occasional and sporadic spotting. I didn't think to look for any bad side effects because I got the device under the impression that it had no bad side effects. I thought it only had a rare complication of perforating the uterus, but since mine was in place at the one month check, I didn't think about anymore until I started thinking about having another baby recently. I went online to see if I had to have a doctor remove the Mirena or if I could do it myself, and I found out that it's best done by a professional because bad things can happen and then you'd have to go to the doctor anyway. Plus, I didn't want to hurt my chances of having another baby. While online I discovered this whole world of message boards where women were having a lot of the same problems I'd been having in recent months and they all blamed their Mirenas. Some claimed that their problems had gone away since having it removed. I never thought to link my circumstances to the Mirena, but when I saw how many women are having the exact same problems as me I knew that I needed to go ahead and get mine out ASAP. Here is a list of my side effects, and I've found other women have had them as well with Mirena: weight gain, bloated stomach, depression, short temper with husband and daughter, acne, low sex drive, spotting, cramps, constipation, and back pain. There may be more, but I can't remember them all right now. Some of them may not even be related to the device, but I've read of so many women with Mirena who are having or have had the same issues, so I suspect a link between my problems and Mirena. I hope this helps someone out there looking for answers. God Bless!

well, after reading all of these posts,
i have hit a harsh reality. my husband has been right this whole time. My sex drive has hit ROCK BOTTOM....my fuse is so short i snap at him at absolutely NOTHING....our marriage is SUFFERING...and coincidentally...it all started right after i started taking topamax...i am only taking 75mg a day...2 in the morning, and 1 at night...
i was so excited because my migraines, that i was getting every single day, were FINALLY gone....and i lost 10 pounds...and i only had to suffer the change in taste in my sodas, the slightly irritating eye twitch in my left eye, and the tingling in my feet. i just thought the sex drive and mood swings were purely coincidental. now that i have read every single post from you guys, i am now forced to go to my husband with my tail between my legs and tell him i'm so sorry for blowing up on him every time he begged me to get off the topamax and i absolutely refused because i refused to go back to the pain of my daily migraines...
as far as the hair loss, i have thick curly hair and i already shed like a shaggy dog so i dont know if mine has really increased or not due to taking the medicine. looking at it now, i can probably say it has, a little, but not much.
i have always shed like crazy..lol
but mainly, my side effects were the change in taste with sodas and beer (beer aquired a "sweet" taste, sodas lost it's "fizz" on the front of my tongue if that makes any sense), my left eye had a constant twitch until i upped my dosage to 3 a day instead of 2, i get the tingling in my feet only, none in my hands or face like i've read, i started getting slight nausea when i added my birth control patch back into the mix with the topamax but that subsided once my body got used to everything.
Sitting here reading this has made me realize a lot about this medicine.

my curly hair is going completely straight!!! this is madness. happen to anyone else?

I started taking Fosamax in January, 2006. Have always had very thick, healthy hair and have noticed a marked thinning of my hair in this short time. Has anybody had the same symptoms and have they changed to another medication or treatment that does not promote hair loss? Thank you.

After reading about the side effects posted I am certain its not just me suffering from side effects from yasmin. I can relate to alot of other peoples side effects they have suffered. I have been on Yasmin for about 1 year now. I have always had really thick and really curly hair untill i started taking this pill, it started with Dianette, my hair went really thin and i hardely had any curls left. so i came off that pill and was switched to another pill, my hair got back to normal but i suffered terrible migraines, so my doctor switched me to yasmin. I have not suffered any weight gain but i have suffered from hair loss, and depression. I can get really low on this pill, another undesired side effects i am now suffering from it is a low sex drive. I have decided to get off this pill and switch to the mini pill. My doctor has pescribed me to Cerazette. I am afraid to go on to this pill after reading about the side effects, about hair loss. If anyone has experience in taking Cerazette please could you let me know.

Post your symptoms since stopping Yasmin!!!

Hey everyone it's Kay21 here and I just wanted to post my 3 month off Yasmin update. Because stopping the pill is a hard decision, I figured we should all post are updates here to help/support those who are planning to stop or who have recently stopped Yasmin.

I have been off of Yasmin since April 17. As some of you already know, I was experiencing horrible side effects while on Yasmin for 3 years (particularly stomach problems, vaginal dryness, muscle cramps, increased blood pressure and heart rate and anxiety).

The first 1 month off of Yasmin was okay. In fact, I felt the best I had ever felt in a while. My blood pressure and heart rate decreased and the migraines and muscle cramps went away. But when I hit the 2 month (8 week) mark, I felt HORRIBLE. I was severely depressed and anxious. I was crying all the time and felt a severe sense of DOOM! The physical symptoms also started to become problematic. The acne increased and I started growing more facial hair. The worse symptom, however, was that I started losing a ton of hair. I would lose stray hairs all day (probably about 200 a day). Since I have hit the three month mark, the hair loss has gotten MUCH WORSE! Now I am losing CLUMPS of hair all day. I have seen several doctors about this. Some say it's because of stress and a few (a derm, GYN and endo) say that hiar loss is common after stopping bcp. I have already loss about 1/3 of my hair.

I am also really concerned, because I have not had a period since April 22. So my doctor has put me on provera for 10 days to induce a period.

For those who have stopped Yasmin, what have your symptoms been (i.e. increased acne, weight gain, anxiety, etc.). Has anyone experienced hair loss? How long did it take to get a period???

Thanks...