Wack symptoms and conditions

I have had the Mirena in since I was 12 weeks postpartum. My daughter is now five months old. I have had so many side effects that I also thought were due to just having a baby and the life changes that follow (plus my kids are 12 months and 1 day apart so who knows what's out of wack once you've been pregnant for two years straight!). I've had some headaches, sleeplessness, so many pregnancy symptoms I took a pregnancy test and had the doctor do one, incredible moodiness, I hate being touched (I felt this way with both pregnancies), no libido...all of these have made in incredible strain on my marriage. If things don't improve between us a few months after I get this hell-stick IUD removed we're going to couples therapy! I was diagnosed with depression at 14, but it has been under control since then. However, since Mirena I have been incredibly depressed. I have been on birth control since 14 due to terrible periods/cramping etc and never had an issue. I am going to switch to the copper/hormone free IUD and just pray my periods have changed now that I've had two children. Wish me luck!!!!!!!!!!!

cannot believe how many stories I have read about mirena and hair loss etc..etc.. etc.. I have experienced many of the side effects that everyone is mentioning.. I actually feel I could live with most of them if it weren't for the hair loss. I have had ( copying from other post.. ridiculous right?)Tired all the time ~ Depression ~ Hungry all the time ~ leg cramps ~ HAIR LOSS TO THE POINT OF BALDING IN SEVERAL AREAS ~ oily skin and bad breakouts ~ Mood swings (huge...yelling fits at my husband and the kids) ~ fluttering in uterus~Sore breasts.. I have medium thick hair that is about 10 inches. I noticed a bald spot in June and now have discovered 4-5 others starting. I just had the iud removed today and my OB pretty much tried to convince me that there is no way that the IUD is causing my issues. I have never had any of these issues before. I got the Mirena on 4/30 of 08 and noticed slowly but surely all of the side effects mentioned. My OB told me that the progesterone could not be causing my issues because it is such a small dosage that it would be comparable to spitting in the ocean as far as the amount that is in my blood stream. She said because I am black and 35 that I may have an autoimmune disorder and that I should stop reading blogs. I told her that all of my research wasn't from a blog and that ALOPECIA is a side effect just not mentioned in my pamphlet that I can find. I understand what she is saying and that she is the one that is the dr. but nobody knows my body better than I do.. I am in it!! I have !never had any problems and have been healthy my entire life. There is no history of autoimmune disease in my family. I am going to my primary care doctor.. to have some blood tests done. I think that the mirena has caused an autoimmune response in my body.. it may not necessarily be the progesterone..although I don't rule it out no matter what she says . the progesterone is synthetic and has an androgynous like activity that is similar to testosterone the main thing that causes male pattern baldness. also Mirena is made out of Silicone.. perhaps those of us that are having hair loss are having it due to our body trying to fight off the foreign invader of the IUD itself. I was going to go and have the Paragard inserted.. because i was thinking it may just be the progesterone.. nope... I read that many women are complaining of ACNE and HAIRLOSS even with that because its made out of copper. So with that being said.. not sure what to do.. may have to go back on Yasmin.. didn't seem to have any problems with that.. I really just don't want to risk putting another hormone in my body.. We all need to get together and look into a class action suit because I am tired of being made to feel crazy by doctors.. sometimes what seems to not be possible is .. especially when there are so many women having the same problem. Feel free to e-mail me re: a class action suit.. if they took depo off Mirena needs to come of too. It seems like it has really screwed a lot of peoples system up.. Hopefully I won't find out I know have a thyroid problem etc.. etc..

I had the Mirena inserted in November 2007 after having my third child. The first 6 months I had bleeding everyday. The insertion was painless. For the last year I have been trying to figure out what is wrong with me. I really didn't pay much attention to it until about 4 months ago when I started having anxiety attacks. I figured it was due to stress of a new job. I have been so tired that I can barely function. I have no interest in even leaving the house. It is even hard to come to work everyday because I am exhausted. I don't sleep well. I wake up soaking wet from sweat. I have a lot of joint pay in my legs, arms, and hands. My arms stay numb most of the time. I too experience the moodiness and I can sit and cry over nothing. I have experienced hair loss since having the Mirena. As far as sex drive it is nonexistent, even if it was there I would be too tired to even do anything. I have blurry vision sometimes. I have gained so much weight it isn't funny. I thought maybe my thyroid was out of wack so I went to the doctor for blood work. My blood work came back great. After researching some more I found this site and apparently Mirena is the cause of my problems also. I go to my GYN doctor tomorrow for my annual exam and I am going to request that the Mirena be removed. I have three children 15,10, and 22 months so I can not live my life like this. I am glad that I found this website and I plan to pass it along for those women that are having problems that they may be blaming other things for. If you have the Mirena you definitely need to read this site. I'll keep everyone posted once the Mirena is removed.

I had been on Yasmin for about seven years. I decided to get on the pill because I used to experience HORRIBLE menstrual cramps and pretty bad acne. For seven years, I thought that Yasmin was the BEST thing that ever happened to me. My cramps went away, my acne cleared up and my hair seemed healthier than ever.

In January, I decided to give my body a break and get off of the pill. I figured that seven years was a long time to be dependent on a drug. Since I have gotten off, I have had a RIDICULOUS amount of hair loss, terrible mood swings, hints of depression, wacky appetites, increased acne and my menstrual cramps are getting worse with each cycle. I have been off of the pill for 5 months now and I am wondering how long it takes before the drug is completely out of my system. Can anyone help?

I've been taking Aviane for a month now and I must say it has been the BEST birth control that I have ever taken! When I was a senior in high school I started taking birth control, Apri (I think that's how you spell it idk), for my mind-numbing cramps and horrible PMS. While it did fix that my mood swings were out of wack, I got horrible acne, and I was hungry 24/7. My body was constantly hungry and I ate SSOO much and ended up gaining 35lb.
Then after a year and a half of that I went to Yaz. Yaz helped my acne and my periods, but made me moody, still hungry, and it KILLED my sex drive. The decreased sex drive was definitely the worst part of the Yaz. I was so dry 'down there' that sex was painful and I was never turned on.
Now that I'm on Aviane my sex drive is INCREDIBLE. I love having this feelings again for sex and my boyfriend definitely loves it lol. Also, it has decreased my appetite and I've already lost 10lb. from being on it. I will admit that when I started taking it I was a little moody, but now I feel fantastic.
Different birth controls have different effects on everyone, but I'm more than happy that I found one that works for me :)

After having my third child in Aug 08 I wanted to try the mirena since I always forgot to take the pill. I have 3 friends that have this piece if crap it and they are fine but me I feel like I'm going down hill. I had it inserted on thanksgiving eve 08 and about two weeks later I started with a rash on my neck, shoulder, and arm. My doctor told me it was the shingles. He also did blood work on me cause I haven't been in the doctors in awhile and my test came back that I had severe hypothyroidism in which I didn't feel any symptoms of it. My doctor started me on 100mcg of levothyroxin and every since than its been down hill. He decreased my amount to 50mcg due to heart palpitations, anxiety, depression, diarrhea, weakness, muscle aches (especially in the neck and shoulders) and fatigue. I really wonder if the Mirena cause my thyroid to be out of wack and currently even with only a week of being on 50mcg I am experiencing anxiety everyday that my doctor prescribed me Xanax in which I was scared to take because I do not do drugs. After reading all these forums I am having mine removed on Tuesday Feb 3rd and hopefully this is really the cause of my problems. Has anyone else experience the same as me. I hate not feeling myself and not being able to take full care of my children. This sucks and the Mirena should be off the market.

I went from a rational non-emotional women to a crazy person!!! I feel awful. I would rather have pain than feel this way. I can't sleep though constantly fatigued. Achy body, headaches. Everything tastes like cardboard so I'm not eating well though I have gained a few pounds. I am severely emotional. I almost left my husband this weekend whom I adore, can't stop crying, very depressed and irritable. I want nothing more than to be alone and sleep, which no one can live that way. I am a mother of 3, a wife, and have a full time job. I can't function properly. I will never undergo hormone treatment after I get through this! I am currently on Lupron, just had laporoscopy 2 weeks ago for the 5th time all for endometriosis and I'm only 25. I started Premarin today to assist this anxiety and mood swings. Wish my family and I luck.

I have been on Toprol 25mg XL for over three years now and I personally think it's a great drug. My doctor prescribed it to reduce my heart work load after I had a quadruple heart bypass at 47yrs old - not over weight. Initially, I felt tired, lacked motivation to do anything, dizziness when I abruptly stand up - still do, weird dreams, lack of sex drive including less rigid erection and less intense ejaculation, depression and also gained over fifteen pounds. Anyway, things have improved since, I started working out every day and quickly lost the excess weight. All the side effects have gone except for the occasional dizziness and the sex part. I can feel my heart go out of wack if I don't take the med. Stay away from the generic that you have to take twice a day - not as effective.

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK THIS LINK AND COMPLETE THE FORM: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities.

Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

My gyn wants me to get the mirena. I am 28 and have a blood clotting disorder for which I take blood thinners. I had an embolism while on Nuvaring in March. Anyway, because of the blood thinners I bleed 25 days out of a 28 day cycle and there is nothing they can do about it...so the gyn suggested MIRENA. I'm a bit scared because I have not had any babies yet and I DO want to get pregnant within the next 5 years and start a family. The gyn assured me that I would not have any fertility problems and that Mirena was a wonderful device. I am still skeptical. What if I become depressed? What if the cramping is too much? It seems like a lot to go through ...the insertion, the risks etc. and what if I hate it? I am leaning towards asking for the mini-pill instead (progestrin only). The idea of having something inserted into my uterus frightens me.

I started taking Yaz 2 years ago after my son was born. I didn't have any side effects for a long time and was generally happy with the pill. About a year after being on Yaz I started getting horrible anxiety and depression. It was really beginning to interfere with my life. I always felt on edge, my heart was constantly racing, I felt down, starting binge eating, etc. I also started noticing that my blood sugar was out of wack. I became hypoglycemic and had to eat little snacks every hour to keep myself from having my blood sugar drop too low. I sometimes even had to take a glucose tablet. My thoughts were always racing. I felt like I was going crazy. After going to my PCP and a psychiatrist and not getting any relief from the way I was feeling, I took it upon myself to stop taking Yaz to see if that made a difference. Well, since stopping Yaz my anxiety, depression, and hypoglycemia has completely disappeared. I feel happy again, normal and healthy. I have gained a few pounds and my skin is an oily mess, but I would much rather deal with that than the hell I was dealing with before. I'm not big on taking medicine unless I absolutely have to and this experience has only made me feel stronger about that. I think I will go back to using condoms and give my body a break. (forever)

Let me start by giving you some history.

My sister is a 22 year old girl who worked full time and was never seriously ill until this summer.

During the last full week of June my sister started having headaches. She told me that these headaches were like none she had ever had before. Days later she started complaining that her legs and wrists hurt. She said that her legs were so tired and achy she could barely walk up the stairs. At that time I dismissed what she was saying. My sister constantly wears heels and I chalked up the complaint to a pair of shoes that were not yet broken in.

By July 4th, the headaches were so intense that she went to urgent care. The physician she saw in urgent care gave her an antibiotic and sent her on her way. By July 7th, she was having difficulty standing up and walking was almost impossible. My sister started complaining about severe joint pain. Her ankles began to swell and her stomach appeared distended.

On July 8th, my sister went to her primary care physician. I believe he sent her for an x-ray and said that she had a cyst on her sinus cavity which was causing her to have severe headaches. He then gave her another antibiotic and referred her to a rheumatologist never even thinking that these two symptoms may be related.

On July 10th, my sister saw the rheumatoid arthritis doctor her pcp referred her to. He dismissed her complaints saying that she probably has some form of arthritis, but that there are over 800 forms and it would takes months to pin point exactly which one she has. He then gave her a prescription for Celebrex and sent her on her way. She spent the entire week in bed because her joints were so swollen and achy that she could not move. She actually crawled to go to the bathroom.

By the middle of the following week, my sister's stomach began to burn. She contributed it to being a side effect of the Celebrex and stopped taking it on July 21st. We had no idea that the pain was so bad. My sister's last normal meal was on July 22. By the 23 she had no appetite and could not go to the bathroom. On July 24, the stomach pain was so bad that she could not work, or sit, or function. All she did was cry. She went back to her primary care physician who then prescribed her prevacid to help with the so called indigestion. He told her if the pain continues she could call him. On July 25th the pain became unbearable. My sister called her PCP as directed and he told her to go to the ER. Never once did he say he would meet her there! I brought my sister to the ER where they did an x-ray and cat scan of her stomach. They found nothing. At that time my sister had not gone to the bathroom or had anything to eat since the 22nd. The physician in the ER said that she was literally "full of shit" and needed to go home and take a liquid laxative. My sister is only 22 and my parents were away on vacation. We were stupid and didn't know any better and were so happy that they didn't find anything that we accepted his findings and got out of there.

My sister took the liquid laxative prescribed by the ER physician as soon as we got home. We waited anxiously for it to relieve her stomach pain. After many hours the laxative did not work and my sister ended up back in the ER. This time she was screaming in pain. One of the doctors there told her that if she couldn't calm down she needed to leave her ER. My sister did just that. At this point my parents (back from vacation) took my sister home and called Digestive Disease. A doctor there told my mom to give my sister 2 Enemas. He said that should relieve her pain. My mother followed the doctor's orders, but the pain did not stop. Sunday, July 27th my sister was right back in the ER - this time at another hospital. This time my sister was admitted to the hospital for severe stomach pain. After 5 days and numerous tests my sister was discharged. The doctors found nothing in her cat scans, x-rays or ultra sounds. The pain was more manageable (she was on morphine every 2 hours) and they said she was ok to go home.

August 1st my sister had a great day. She was sitting up in bed and seemed to be in good spirits. The following day she couldn't get out of bed. This time it was neck pain. My sister said the pain in the back of her neck was so severe that she could not lift her head up or move it side to side. By August 4th she was admitted to the hospital again. This time we brought her to University Hospital in Syracuse, NY. We were sure to get some answers there...or so we thought. As soon as my sister arrived in the ER they started treating her with antibiotics. They were certain she had an infection. They then told us they would have to do a lumbar puncture to check her spinal fluid for infection. We thought we would finally have an answer to what was wrong with my sister, so we agreed. The spinal fluid came back fine - no infection. At that time they admitted her to the hospital. While at University Hospital my sister was treated by a team of doctors. They tested my sister for lyme disease, west nile, lupus, leukemia etc. They performed a spinal tap, cat scans, x-rays, ultra sounds, blood smears, etc. All of these tests came back negative. The doctors could find nothing abnormal except for an elevated white blood count -22,000 (it was also very high during her last hospitalization), an elevated C reactor and a very high SED rate. After 4 days of numerous tests and pain killers (first morphine, then Dilaudid, then Dilaudid with a fentanol pain patch) they discharged my sister. The head doctor told her that he believed she had viral meningitis and that it would eventually work its way out of her system. By this point my mother and I were skeptical. We did the research and viral meningitis should only last approximately 10 days. Mig had been sick since the last week in June. No one was putting all these symptoms together. On the day of her discharge my sister started getting her stomach pain back. The pain was mostly on the left side of her lower stomach - under her belly button. Again she was told the pain was due to constipation and she should buy some Miralax when she got home.

My sister was home for a mere 2 days before she would be hospitalized again...for the 4th time. Her stomach pain was back and worse then before. My family could not believe this was happening. My sisters spirits were down and the excruciating pain was making her mentally unstable. This time the ER physician recommended a hematologist come in to see my sister. We just wanted answers so we agreed. This hematologist, Dr. R stated that she believed my sister had drug induced lupus. We were shocked as my sister was tested for lupus twice before and both times the test came back negative. Dr. R explained that she believed my sister got drug induced lupus from the Gardasil shot. My entire family was shocked. We had never heard of any severe side effects like this from the Gardasil shot. Dr. R asked my sister for her permission to test her again. My sister agreed and a week later my sister learned that she was positive for drug induced lupus. My entire family was so happy that my sister finally had a diagnosis and could begin treatment. We were told that after a 6 week steroid treatment (Prednisone) my sister would be back to her old self. We were ecstatic!

My sister was home from the hospital and on the steriod treatment for 10 days when things started to go wrong again. The doctors were very concerned with the dosage of Prednisone that my sister was taking (80mg. I'm not sure how many times a day). They cut the dosage down in half over the course of a few days to prevent kidney damage and other side effects. Once the Prednisone was decreased, my sister started getting sick immediately. Her forearms were very weak - she could not put any pressure on them. Her shoulders would tingle and she would get shooting pains down her right arm. One of her doctors believed she was developing fibromyalgia and prescribed her lyrica. Shortly after my sister began taking lyrica she started seeing stars. She had double vision and a migraine that would not go away. My mother called her doctor and told him about this. His answer was for my sister to stop taking the Lyrica. She did immediately.

On August 29th, my sister still had a migraine. This was day 3 without a break. She woke up early Saturday morning and began vomiting every 30 minutes. After a few hours of non stop vomiting my mother called her doctor. His nurse practitioner was on call and she told my mother to take my sister to the ER immediately. My mother went back into my sister's room to tell her they had to go back to the hospital and she found my sister having a seizure. My sister has no history of seizures. My mother called 911 and the ambulance came to bring my sister back to the ER...her 5th hospitalization.

Shortly after arriving at the ER, my sister had another seizure. Immediately after the seizure the ER doctor ordered my sister to have an MRI. My sister had one during her last hospitalization only 2 weeks before. That MRI was normal. This one was not. There are lesions all over my sister's brain. The neurologist told us that he cannot believe she does not have permanent damage. According to him there is no oxygen going to her brain.The neurologist also explained to us that her brain looks as though she has been poisoned. He said that her MRI is very similar to an MRI of a patient who has been poisoned with antifreeze. Later I learned that Gardasil has both aluminum and sodium borate (which is in both rat poison and cockroach killer). However, according to the doctor once your brain looks like my sister's all the poison is out of your body. My sister's team of doctors started debating as to whether this could all still be from the Gardasil shot...my sister's last shot was on 02/22/08. Some believe that the side effects started off as mild, but since they were left untreated for so long they've turned into a serious neurological problem. They told my family the only way to truly know what is going on is to do a brain biopsy.

Yesterday, my sister was transferred to Mass General in Boston. We were hoping for a bigger hospital, better technology, more seasoned doctors. So far my sister has been treated badly. When my mother told the doctors' about the Gardasil shot and the devastating effects it has had on my sister they dismissed it. When my mom asked the doctors to test my sister for heavy metal toxicity they completely ignored her. I fear that she will never get the proper care.

I had my Mirena IUD removed on Monday, May 5, 2008. I had it inserted on November 10, 2005. I was having major side effects from the birth control, and every doc I went to said that there is no way that Mirena would cause the side effects I was having because the "progesterone amounts are too low to cause these side effects". I have had the following side effects:
WEIGHT GAIN
JOINT PAIN
LUMPS IN BREASTS
BREAST TENDERNESS
HUNGER (as if i were pregnant)
DEPRESSION
LOSS OF SEX DRIVE
HAIR LOSS
SWOLLEN ABDOMEN (BLOATED?)
HEADACHES
GROUCHY/ON EDGE
ACNE
CYST (had a couple weeks ago... i was on vacation in Vegas and had a cyst burst.. never had these issues... this was the last straw)
STABBING PAINS IN ABDOMEN AND IN AREA OF OVARIES
PMS SYMPTOMS EVERY OTHER WEEK FOR TWO YEARS
BREAST GROWTH D TO DD
VAGINAL BLEEDING AFTER INTERCOURSE
FATIGUE
TENDERNESS OF ABDOMEN
BACK PAIN
HIP PAIN

As of today, Friday, May 9, 2008 (4 days after Mirena has been removed) I have lost 9 pounds. I am sure this is probably water weight? I am feeling a little better every day. The night I got home from having it removed, I had major mood swings... would be happy one minute and crying my eyes out the next!!! I would not recommend this IUD to ANYONE.. not even on my worst enemy (if I had one). This needs to be taken off the market. It is not safe! I have spent thousands of dollars on ultrasounds on my breasts (thinking i could have cancer because the lumps i had in my breast) and on other doctors bills to figure out what was wrong with me.. only to find out that "Mirena is not the cause"!!!!

Hi, I wish I would have found this site a long time ago! I had Mirena put in in Dec 2005 after the birth of my son. I was nursing and was told that the birth control that I could take and would not interfere with my milk was "not as forgiving" as regular pills (and, I definitely did not want to get pregnant again at that time) So, I went with the Mirena. It seemed great in the beginning. I had the strings trimmed a little after my husband felt them and got freaked out and then everything seemed great.
It's funny how this has worked out for so many of us because after having a baby, your life is so changed and your body is so out of whack that it's hard to say what could be causing it. I ended up becoming extremely hypothyroid after having my son (I wonder if Mirena may have had anything to do with it!??!?!) Even though I take thyroid medication now and seem to have it very under control, I still have no sex drive, have tremendous mood swings even though I am on antidepressants, my acne is worse than it was when I was a teenager, and what I consider to be worst of all, tremendous eczema! Last summer I became so covered in eczema, my face, neck, chest and arms, that my mother said I looked like a burn victim. I was insanely uncomfortable and extremely self-conscious. After going to all kinds of doctors who only kept prescribing topical creams and steroid pills, I started going to an awesome alternative medicine nutritionist and realized that there was something internal going on causing my skin to react like this. After seeing him for months, we came to see a pattern between my eczema flare-ups and my period. I always seemed to start getting really itchy around the time of ovulation and we also discovered that during that same time I would be gluten-sensitive. I had all the tests done and I do not have Celiac disease.
I can't believe that I am only reading about all of this now. Thank you all so much for confirming my hunch that it might be the Mirena. I am going to call my Gyno today and have it removed.

I took one injection of Lupron for fibroids in Nov. 2001. It totally changed my life, I am no longer the same person I was before. It started with severe migraine headaches for 14 days straight and attacks of nausea, lack of appetite. I used to have a strong stomach - now I was very easily nauseated. I never went for the second shot. I began to have panic attacks regularly (I had not had them for over 20 yrs). I was tired all the time, and a person who used to work out at the gym 5 days a week - eventually I quit. Now I just walk. I feel about 65 yrs old (I am just 49). I look old, my face began to droop, my hair thinned. I had bouts of depression coupled with general anxiety. My migraines worsened. My sex drive dropped to zero, I feel almost "sexless". I used to be confident, now I was afraid of everything. I now suffer from irritable bowel syndrome - with bouts of diarrhea, bloating and severe gas pains. I have trouble eating sometimes.. I have had all the tests and no one can find anything wrong with me,and none of the doctors think all these problems are due to Lupron. But, I know - I was NOT like this before Lupron. It ruined my life. I just wish my doctor would have informed me of all the terrible side effects - she only told me about hot flashes. I looked into suing her for malpractice but the lawyers said they could not build a case with no real medical evidence that my symptoms are caused by Lupron. I just wish I had known then what I know now. I tell everyone - NEVER take Lupron. Six years later and I still feel like this. Oh what I wouldn't give to have not taken that drug.

When a class action lawsuit is filed, let me know....this drug should be taken of off the market immediately. We started all of this with an OB/GYN that prescribed this “miracle pill” and now have had to go not only to our primary doctor, but also a psychiatrist, gastrenologist, college campus counselors, psychologists, psychiatrist, and the campus medical doctors; All the while, accumulating enormous doctor bills. All the doctors say, "No, Yasmin won't cause those problems" (except the college campus doctors..wonder why? Hmm.. could it be that they are not in private practice?)....well, I beg to differ. Everyone needs to give this website to their doctor so the doctors can hear from the patients that have taken this drug, and not listen to the pharmaceutical companies that are pushing this drug to be the "miracle pill". Maybe if enough people complain and go to the media, we can get rid of this drug!
My daughter who is 18 was put on Yasmin because of irregular periods, hormonal imbalance, etc. We were told it was the new “miracle pill”. It will make you loose weight, regulate your periods, clear up acne, you name it, it will fix it. Yeah, right.
She started taking this pill in March 2007. She was off at college but called to tell me she was experiencing horrible headaches, behind the eyes. She complained about her stomach hurting, but we just figured it was the stress of freshman year at college. Then she said she got where she couldn’t eat when she went to a restaurant. When she came home in May for the summer, I noticed a total personality change. For example, she was always a neat freak, and now she wouldn’t clean her room. The first day when she drove home, she started crying she was so mad about the traffic. Yes, she has always had a little road rage, but this was ridiculous.
By June, not only could she not be in crowds, like at a restaurant, but now she is having full blown panic attacks and IBS. We called the OBGYN and they said, “Yasmin won’t cause this, go see your primary doctor”. I knew that the only thing that had changed with her was taking the YASMINE. I knew it had something to do with all of this so I “Googled Yasmin” and this website (http://www.medications.com/se/yasmin) was the first one I looked at. All of her symptoms matched everyone else’s! I am so glad we found this website, it explained everything and I had her to stop Yasmin immediately.
So we went to the primary doctor, explained about the Yasmin and how we thought it was the culprit of everything. Of course this doctor also says, “Yasmin won’t cause that”. We told him to look it up on the internet and see how there are over 3000 complaints on this drug, more than any of the other drugs on the market.
Besides the emotional problems she starting having, her pulse and blood pressure was sky high, so he puts her on medicine for that, and puts her on an anxiety medicine and sends her to a psychiatrist. She is very thirsty all the time, and develops IBS. She can’t eat without having pains in her stomach. So, now we’ve have gone from having just irregular periods, to all of the above, plus a psychiatrist.
The psychiatrist doubles her medicine (and puts her Pamine for the IBS) because the panic attacks are gone, but she still is having a lot of nervousness, anxiety, can’t sleep at night, crazy thoughts, worrying all the time, etc. A month later he changes her medicine again, to Effexor. The first 2 weeks, she does okay, but the packet doubles the strength after 2 weeks. It takes 4 weeks for it to take full effect. Right after she doubles this medicine, it is like her senses are on hyper-mode. She can taste everything that is in her food (chili powder, seasonings, etc…), taste the metal in water, and she can hear someone’s phone vibrating, in another room.
Then she goes back to college at the end of August 2007, and it’s horrible. The Effexor is having bad, bad side effects. We called the psychiatrist that she was using at home and he doubled the dose. That was the worse thing they could’ve done. The side effects were worse than ever. I had her to immediately go to a psychiatrist on campus. She told him the whole story and he believed her! Needless to say we switched doctors. He then lowered her dose back down to ½ a dose and hopefully can slowly get her off of all this medicine.
The newest thing she has developed is being hypoglycemic. The campus psychiatrist sent her to a campus medical doctor and he told her that they would get to the bottom of this. He tested her for everything under the sun. Low blood sugar is the only thing they found. But, she hasn’t taken the Yasmin since May. No telling what the results would have came back like if it was done at the time she was taking Yasmin.
Thank goodness she has counselors and doctors there at the campus that believes that Yasmin can cause all of these problems, and are working with her. From what I have read from the people that have used this medicine, although most doctors do not agree, Yasmin takes like 6 months to get out of your system. I think I am going to believe the testimonials of the people who take this medicine, over a doctor who prescribes it.
If everyone goes to the media, their doctors, the FDA, congressmen, and make them aware of these horrible effects, surely we can get this drug off of the market! Does anyone know a class action lawyer that would pursue this? For my child to have to go through all of this is ridiculous, not to mention costly. What do we know of the long term effects this drug will have if it is doing all of this when you first start taking it?
If you have the same concerns as me about this drug, and would be interested in looking into a class action lawsuit, please email: ****** I would be interested to see how many would want to pursue this.

I am sooo relieved that I found this site. OMG. I was on the NR before for about a year and 3 months. I didn't have any side effects whatsoever. I went of the NR because my boyfriend and I broke-up and I wasn't having sex. About 4 months later, I developed 2 ovarian cysts that ended up rupturing in my right ovary. BTW, I turned 30 in the same month. I was in so much abdominal pain, hot flashes, painful menstrual cycle, passing huge blood clots, depression, crying all the time, thoughts of suicide, anxiety attacks, very irritable, easily frustrated, inability to concentrate, and nausea. I had NEVER had any bouts of depression, crying all the time, thoughts of suicide, anxiety attacks in my life before. NEVER! My OB/GYN told me my hormones were all out of wack and that I should go back on the NR to regulate my hormones. So, I went back on the NR, my cysts went away and I felt 100% better immediately. Now it's 2 months later and I'm having all the same symptoms I had before the NR, although, it’s not as bad as it was before. Apparently, I'm still ovulating while on the NR although the NR STOPS ovulation. I have developed more cyst(s), haven't gone for the ultrasound yet, in my right ovary, even though my last ultrasound showed that the last 2 cysts went away. Right now, I am emotionally drained and physically in a lot of pain. I think that if I get off the NR my symptoms would be a lot worst. I’m allergic to the patch because of the adhesive, coming off of depo caused too much pain, and I forget to take the pill. So I don't know what to do.

Stomach cramps, night sweats which stopped when I forgot to take them on a long weekend away.

I started taking Advair 500/50 about 3 years ago in October. In October of 2004 I was about a size 9/10 and in the past years I am over 200lbs and wearing a size 16. I know that weight gain is normal with getting older but my diet plan would allow me to gain almost 55lbs in 3 years. On top of the weight gain I almost always get a sore throat and im always coughing up something. (Gross I know) MY moods are so wack..I have the weridest moodswings. I came by this website trying to find answers to why I couldnt loose all this weight and now I think that I have the answer. I have decieded to gradually take myself off Advair.

I had been on nuvaring for 6 weeks. I usually don't do well with any birth control pills so when I heard about nuvaring I was excited to try it. The first few days I felt some light body ache as if I were getting sick. I noticed I was feeling depressed, but I thought it was because of some problems in my personal life. Then I went on a trip to Brazil to visit my family. I always have a great time. This time I wasn't having fun at all. I was always super depressed. I was always tired and never felt like doing much. Some days I just felt like crying. Some nights I would wake up in the middle of the night, think about my problems and just start crying, something that is not like me. My emotions were totally out of wack. I was not in conrol of my emotions, which is not a good feeling. I also had this horrible pain/feeling in the middle of my chest. More like an emotional pain as if you were missing someone super bad, as if someone had died, a very weird feeling. These symptoms subsided a little with a vitamin b complex. I read that vitamin B6, about 100 mg is good for depression. I would take a multivitamin and with it a vitamin B complex. On the days I would forget I felt the difference, the symptoms were worse. Two times during my trip when I was having one of those days my grandmother then my father asked if everything was ok, that I looked pale. The second time when he asked me, I thought to myself, this is not normal. I feel horrible. I came on to the web and found this sight. The same day I took out my ring. I was on my second month starting my third week. It has been two days. That pain in my chest has gotten much better and also my mood is getting better. About the sex drive I am not sure, because I have been away from my husband since I started the ring, but I haven't thought about sex at all. I think it was the right choice to take it out. Another thing about a week and a half ago my breasts have been very tender. My breast are still very tender, maybe a little worse, probably because I took olut the ring a week earlier, but I am glad I did. Hopefully now I will enjoy the rest of my trip. All these products for birthcontrol with hormones is like poison to our body. Well at least I have noticed it has been for mine.

Developed Systematic Candiasis, dry mouth, etc. It put some things out of wack. Asside from that I wouldn't say anything horrible as a result of this medication.

Hi Dejay

Its me Kim
Dejay and I have had parallel symptoms now for weeks we have cried many tears over thephone.
I have been off Yaz for 5 weeks now and everytime I think Iam feeling better getting better I have a setback. I have had the worst with anxiety and feeling of vibration under my skin. Recently I have had disrupted sleep I dose off for thirty minutes wake up and Iam wide awake I can do this for days?????
I dont understand why my sleep is worse now than 3 weeks ago??
I had a good day yesterday than today had terrible weird headaches I never had headches before yaz.

My doctor insists it was not the ;ill and Iam just experiencing stress!! I want to scream
I too like Dejay had my Thyroid go out of wack that was the worst.

Iam just not myself have spent 7 weeks now sufferring and in and out of the ER and doctors office just to be told Iam fine.
Iam not me Iam not fine I want to be normal not have good days and bad days.
Also it seems like my right eye was affected it feels a little twitchy now anyone else have this??

What can I do to sleep? My eating patterns are horrible too. I have no appetite most days than will get sudden appetite and eat than lose it again.

Please when will we be normal??

I don't know if this counts as a side effect or not.
I stopped taking Yasmin on the 6th of October and got my period on the 11th of October. I want to try and have a baby but I don't know what is going on with my body. It is now the 9th of November and no period. I don't know if my period is delayed or not, or if I am pregnant.
I went to the doctor last week to see if I was pregnant and the blood test results came back negative. So I am guessing that my side effect is that my period has not returned because I don't think that I am pregnant.
This is very frustrating because I want to concieve and my period is not present and I can't determine when I ovulate so this is a pain in the butt.
That is my side effect of yasmin. You stop it withdraw bleed and then your body is out of wack for ages and no sign of period which makes you think that you are pregnant. But then again maybe I am and I don't know it!

Ive been on topral for 3 months and I still have the same symptoms from MVP. I had a sore throat for 2 months and neck stiffness. Thyroid levels got off wack. Keep gaining weight and even quit smoking. I am more miserable than before I got on the Topral. IS there any cure to MVP other than medicine?

I have been onthe nuva ring for a few weeks. and i have a history of birth control use too. first off, u DONT gain weight from birth control. if anything its water weight such as bloating and such. and yes ur breasts to get bigger.
YOU ALL must understand that birthcontrol makes ur body think u are pregnate!!! HELLO! that it why ur boobs get bigger, and u have abdominal pain, and ur horemones go wack. might i add that u also wanna eat a lot??? but birth control ALONE does NOT make u gain weight. u choose to eat.
unfortunatley birthcontrol isnt for all women b/c of chemical imbalances. which is another story.
but i havent had any problems with nuva ring except some abdominal pain.

Make wise choices, and take care of ur body. u choose to eat, and u choose ur birth control. be well everyone!