Friends and family symptoms and conditions

i started taking it in January, for mild acne. Initially it worked wonders on my face, but eventually like three months ago I started feeling extremely depressed. I was not happy with myself and appearance, which ultimately lead to having a problem with eating. Every time I get near food my stomach cringes and I get nausea. I just got off the pill but was wondering if anyone has ever experienced this feeling. Beside my loss of appetite, I have secluded myself and have become more and more depressed. I thought it would get better but it hasn't. It has just made everything worse and more complicated. It has affected relationships with friends and family. Has anyone else felt the same way?

I had mirena put in nov 2007 after my son was born
at my 6 week appt it was the worse pain ever I bleed for
months had a uti with yellowish fawl smelly discharge
took 2 rounds of antibiotics before it was cleared up
about 6 months after having it inserted I hemriged real bad
made an appt with a interalist doctor. Under went 2 ultarsounds
blood work and an appt for a cat scan not never did test results came
back as cytes on my overies witch ruptured and indometreosis
this nov2009 will mark 2 years my friends and family think that
this mirena is the cause of all my issues every month I bleed at least 3 weeks out of every month and bleed heavily after sex every time I recently
got a real bad cold and was on antibiotics for 10 days had sex 4 times during this 10 days know I'm showing signs of pregnancy the pre milk from the breast as well as fatigue depression mood swings dizziness over all I think that mirena has a lot to do with all of this I will take aprego test in the morning and hope for the best

I had my Mirena removed two days ago and already feel a little more energy. I had it fitted in August 2006 and had major life changes about the same time. I moved to a new area and had a new job and my best friends moved 7 hours away from me...so when I started losing clumps of my hair, felt stressed out, tired all the time and depressed, I didn't think it was due to Mirena. I went to see a doctor and they told me it might be a thyroid problem so I had tests done and everything was fine. He said people lose their hair due to stress so I tried not to stress and all of my hair eventually grew back. I still felt tired all the time and would get angry easily and would have major depression episodes. I would stop talking to friends and family because I was this different person I didn't know how to tell them about. I was in college and my grades suffered because I would get so depressed I would get suicidal. I stopped taking a full load because I felt I wasn't mentally capable. I have always been very smart in school so for me to get bad grades made me feel even more depressed. I have had no drive to get out and do things that make me happy. I have had no sex drive. My boyfriend has been with me since a little before I had the Mirena inserted. I feel like he doesn't even know the real me. I feel so stupid for not adding this all up earlier and wasting 3 years of my life depressed. I told my doctor about all the symptoms before I had it removed and she said things in my life were most likely the reason not Mirena. I look at these posts and know she is wrong because people I know and family have seen me change for the worse and it has all been since I have had the Mirena. I was a person that would work all the time, take a full load of classes, go out with friends and family and enjoy life. Now I am a person that doesn't work, is taking 2 easy classes, most days stays in the room all day in bed on my computer and sleeps. This is ridiculous. I already want to leave the house. I am sure I am not back to normal already but I can see a spark there that wasn't there before. I am staying off birth control. I want my hormones to even out a little while before I even think of it again. Naturally we are supposed to have kids so when we take something to alter that we should be prepared for side effects. I would suggest getting this taken out because even if you think you may have no effects from it...later on you may realize you did. I will update with another post in a couple months to let you all know if my life has changed for the better. Good luck to you all.

I too have memory loss. It is humiliating not to recall events with friends and family and people I have been introduced to. I cannot conversations, movies and names of bands. I am 43 and have been taking this drug for seizures. The seizure disorder is gone due to the drug. I have gained weight, awaken with a severe headache on several occasions behind my right eye, feel tired and dizzy after an hour of taking the drug and blurred vision. I thought it was early onset of Alzheimer ( i forget how to spell it though I am in the medical field). My generalized Doctor and my Neurologist say this is not from the medication but from age and normal. The quality of life is not as I would like. I feel like I am missing out on my own life. Thank God I came across this blog! I have been researching this drug on the net and NOWHERE does it state this as a side effect. This is the only med I take.

I am 19 years old and I have depression. I had a Laparoscopy done in January to remove a rather large cyst... during the surgery they found that I have endometriosis mainly on my right side. After about two months of horrible pain (after the surgery) my doctor decided to put me through the 6 months of Depo Lupron. After a week the nausea was horrible and I actually vomited at work. The hot flashes have been horrible and my body hurts all over all the time. About a month or so into the treatment, my depression intensified to the point that I didn't want to live any more. I would sit up at night just thinking about how I could make it all stop. Crazily enough I stopped taking the depression medicine while one the shots and I felt a little better. I still have some bad days but it is better. The night sweats have gotten worse the past two months. I have a consult in a couple of weeks to figure out where to go from here in my treatment. I've read several "testimonials" and it seems that I'm not alone in the way I feel. My friends and family haven't exactly been understanding about it either. It's nice to hear that other people can sympathize with me.

For reference, I am 23 years old. I got the Mirena IUD put in 1/30/08 and I got it taken out today. For the first several months i bled and cramped a lot. Once that passed, i was doing good and only spotted every once and a while. Well, for the last 3 months i got my period. It was heavy and I cramped a lot. During this time I also started feeling distant from my close friends and family. I felt a horribly weird sensation of a fluttering in my uterus, almost like when you are driving really fast and go over a hill, how your tummy gets that weird feeling. It felt much like that except it was in my uterus and it started happening all the time. I have also gained like 20 pounds. I haven't been able to sleep at night. I was having sharp pains in my ovary areas. I had it removed today after 15 minutes of my dr. stalling almost as if he absolutly did not want to remove it. I just kept repeating myself until he finally called in the nurse to observe. I am not good at paps or anything else that has to do with strangers invading my lady parts to begin with. So i was sorta freaking out in my own little world while he poked and prodded away. He was good about asking me if I was okay and if it hurt, but im not one to go and answer these types of questions when im in that much distress so it's okay if they talk but i don't like talking to them back. I'd rather they just get it done and over with. Well, I felt him tug and after a few good ones he got it out. That was a Horrible feeling! I almost cried! Then he just started talking to the nurse and since he is foreign i have no clue what he was saying to her, WITH the thingy still stuck in me!! I was so worried and this went on for about two minutes.. Then i asked if we were all done and once he took it out I noticed that the IUD was in a container but there was another small container with a bloody chunk in it!!! sorry if tmi...when i asked what it was he said that "a bit of tissue came out with the IUD and they were going to send it to the lab. I could tell he was trying to act like everything was fine but if everything was FINE...why would tissue come out too? I'm in a state of panic right now and don't know quite what to think at this point. I would NEVER suggest anyone getting Mirena. The bad side effects plus the removal are NOT worth it at all. This should be banned! If i would have known what i do now i would never have gotten it to begin with. I am now dreading the "crash" hopefully it isn't as bad to me as others. I am a single mother of a child with disabilities...if i get this "crash" thing, things are get difficult fast. Hopefully I start feeling normal again soon.

I started taking this garbage in May of 2009. I would go to the Dr and my BP would be 180/110. Let me say im still on Lisinopril BUT stopping tomorrow. Let me tell you my story.

35 year old male, diabetic and HBP. After years of not taking care of my self i went to the doc, i started taking Lisinopril. With in weeks i got a hacking cough and my BP was still crazy high. They up'ed my dose to 20MG and then hell started.

Constant blinding chest pain, strange electrical shocks in my back and head, went to ER and was admitted, they said i may have had a PAST hart attack Weeks of in and out of the hospital a 3 day stay in the cardiac ICU! Then i had a CT angiogram with dye and that reviled MY HART WAS FINE. I still had this horrible pain in the chest and legs and hands and my gut, electrical shocks and night mares and freak out for no reason at all. Problems with erections and slow hart beat. Unreal panic attack that i think i was about to die or GO insane. The past few days i have had intense pains in my upped back and gut. I went to have some blood work done to see how my new diet is doing. All the numbers were amazing, BUT my LIVER IS HURTING! Now i do not see a doctor for 5 day to review it all BUT i know this pill has mad my life hell for the past 2 months. MY LIVER WAS FINE BEFORE i took this pill.

I was able to make my diabetes VANISH with diet, i must try that with HBP. STAY AWAY FROM THIS PILL.

OMG! Just reading these posts are giving me chills. I have had mine in since end of April 08. I had my son in March 08. I was prescribed Zoloft soon after having my son for post partum depression. It didn't help much and the doctor said it should go away by 6 months. It didn't. The symptoms have gotten worse and include thoughts of suicide often. I am EXTREMELY moody. I feel like I am psycho! I yell at my kids and hubby. I cut myself off from friends and family. For a while I was cautious everyday but not so much anymore. I have severe cramping, irregular periods, migraines, and I get that funny feeling like its something in my belly too. Worst of all is the weight gain. I have 3 children and I am naturally thin. After my 1st two I went back down in around 6 months. My son is almost 16 months and I am the same since after his birth! I am 5'7'' 160 lbs...normally 131. I look 4 months pregnant. I workout 5xs a week and have a strict diet..nothings working. Not to mention the dramatic loss of interest in sex. Me and my hubby were very frisky and now I just don't want to be bothered. When we do have sex there is pain and sometimes bleeding. After reading this post I have now realized these things have to be because of the Mirena, too many people have the same symptoms. I am suffering from low self esteem because of the weight gain and other issues and have become very paranoid. It may sound dramatic but I am suffering, my husband and children are suffering and I am making an appointment tomorrow to get it removed....

Signed the Mirena petition which all of you should too. So many people who are on it with no side effects as well as doctors do not believe us and it is very frustrating. Both my OB/GYN and the neurologist I have been seeing don't think the Mirena is responsible for my dizziness/foggy head, anger/anxiety/moodiness, body tingling, however my symptoms started exactly 3 weeks after I got Mirena inserted. Never had these issues before. Have had the Mirena removed and hope these horrible symptoms go away!

Ladies,

I hope you don’t mind a male posting on this forum but I do have a reason for doing so. I am a Coroner’s Officer in England. I will not at this time disclose whereexactly I am based as I need to protect the identity of the family. I would however like to use you as a sounding board in the hope that you can help me, help the family and perhaps, just perhaps, I can help you.

Sadly I am dealing with a suicide. The lady in question, who has taken her own life is in her 40’s, married and has children (all over 11 years). The lady has no history what so ever of any form of depression during her life.

The lady has described her life as being perfect with a family that loves her and who she loves in return and as the Investigator I believe she is truthful in that comment. She states she has been extremely happy until last week. She makes comments of - I am just very ill, cannot sleep, feel dizzy, cannot concentrate, sometimes lose my vision, feel sick all the time and sweat at night. She cannot understand, but it makes her feel bad. I am not myself, something has made me ill which means I can’t be my normal positive, active busy self. I can’t bring myself to do anything that I normally love, like gardening, cooking etc. I am losing my memory badly going fuzzy in the head.

Her final comment, which is the one that has prompted me to post on this forum (with the permission of the family) is ‘I just don’t understand this – I’m so sorry . I can’t understand myself or what is wrong with me or what I’m doing so sorry. Just remember I’m not myself somebody else has taken over – I don’t know if it is all the anti-histamine pills that has mixed up my chemical balance along with the Mirena coil or is it just me’.

The mention of the Mirena coil has therefore prompted me to investigate it. I am not, by any means suggesting that this is responsible but it would be wrong of me to discount it after having read the posts on this forum and other places on the Internet.

The lady in question had the coil inserted in 2004/5 and it would appear that there were no problems or side effects reported.

I am therefore looking for some help from you. Some comments on what I have posted etc. Some advice on where to obtain expert advice (although I am trying some avenues of my own).

I may also ask, depending on what help you can give me if you would be willing to identify yourself to me.

Thank you

P.

WOW! I have been feeling so bad lately, I decided to put my medications in google and do some research. I have been reading these peoples post like it was something that I wrote.I am only 36, but I feel 86. I thought I was loosing my mind. I have been on 40mg/day for 11 months now. In that 11 months, I have had to stop working, I can barely walk around because the pain in my ankles and knee. My right shoulder hurts all the time. I had been working 50+ hours a week for over 7 years. I pretty much have withdrawn myself from most friends and family, I just feel so bad all the time, I feel more like a burden than anything. The latest thing I have had going on is, this terrible pain in my upper right abdomen. Ive had blood work, Ultrasound, MRI all came back ok, with the exception of a small spot on my liver.(normal they say) I didn't refill the last Rx for about 2 weeks($$ issues) I actually was able to get outside and mow the yard, take a walk with my daughter, then 4 days ago I get it refilled and start taking it again. Now im back in the house, it hurts to walk again, I feel like im here but not here most of the time. I have asked my doctor about this and told her several times that I am not feeling right. She just tries to give me antidepressants! Yea just what I want more pills (NOT). I have also had terrible boughts with constipation and diarrhea. It was nice to see that I'm not loosing my mind here. My mother also takes this, I sent her a link to this site and we are both stopping this medication. Doctor says my chol. should be under 100 mine is 115, and she thinks she is gonna up my dose to 80mg/day. NOT! This is no way to live.

I don't want to scare all of you, but I thought I should share my recent experience. I am 40 years old and have never tolerated birth control pills very well. I experience major headaches that make the effects not worth the pain. As I was approaching menopause, I developed an ovarian cyst and dysfunctional bleeding and anemia. My periods could last up to 8 weeks at a time. I was desperate. I was put on Yasmin and was told to give it 3 months for my body to acclimate to this drug. I had a headache EVERY day that I was on this pill. 2-3 times a month it would flair up into migraine status. After 2 months and 1 week, I had one of those headaches that didn't go away. I went to the doctor 3 times to figure out what the problem was. I had a stroke and it was not diagnosed for 9 days due to the fact that I didn't have many outward stroke symptoms. I had a blood clot in my brain that blocked my sinus, sigmoid, and jugular veins. My neurologist said that most people would not have lived through this and that I was lucky to be alive. Please warn your friends and family. This is so dangerous. The only risk factors that I have are my age (40) and my weight (200 lbs) at 5' 7. I did not smoke, rarely drink, I'm not on medication for any other thing.

Reading these posts has given me a HUGE sigh of relief. I am desperate to find something else and get the hell off of Aviane. I think I've been on it since at least 2002 or 2003. Like many of you...I'm irritable, angry, cry, hungry, moody...an emotional basket case!! I start PMS 2 weeks before my period begins. I can flucuate at least 3-5 lbs a month. This month has been the absolute worst. I forgot to take a pill (totally normal for me to forget). I have had cramps, bloating, 5 lb weight gain ( I am training for a 25k, there's no way it's fat!), and actually have had my period for 1 entire week! I can not take it any more and I have a doctors appointment at 10:45 tomorrow morning! I will not leave there until I have a new prescription and an explanation.
SEX DRIVE- I am writing this in caps to get your attention. I'm 27 years old, married 2 years to my husband who I have been with for 7 years. I am completely and madly in love with him but have no desire for sex. We fight about it every day, without fail. For so long I felt that I was a bad person. I have no explanation for not wanting to have sex. I don't want to get used to feeling this way. Our sex life sucks. I wish it was better but part of me doesn't care because I don't crave it. BUT- i did before, so I know there's something wrong. I won't settle for this feeling and I don't want my husband to feel this way anymore! I want to show him that I love him. I can't wait to get off Aviane!
Did I mention that i'm always tired? I'm constantly finding ways to increase my energy. From coffee to red bull, hydroxycut, spark, you name it. My energy levels are pretty high while I'm busy or working out...but the minute I stop, forget it...I'm OUT! It's gotten to the point where I've fought with my friends and family. Did anyone else fall asleep at 10:30 on New Years Eve??- I'm 27, I have no kids....problem? I think so..
The only constant in my life is AVIANE! Gee....ironic? I don't think so. Thank you to all the women that have posted their experience with Aviane. I have read so many of them. I also read a lot of them to my husband to reassure him that it has to be my birth control that is making me "asexual" and crazy! I look forward to visiting with my doctor, forcing her to change my birth control and finally, looking forward to starting a new life...I HOPE! I will be happy to respond to this forum to share my new experience....tbd!
Thanks again to all you other bloated, irritable, crazy, emotional basketcases that aren't having sex more than twice a week! Gotta love being a woman!

I am a 65-year-old female. I was given Lipitor 10mg in Feb 07, which I appeared to tolerate, with the effect of reducing my high familial cholesterol. Because of a genetic enzyme problem, I am careful about my diet; having been a vegetarian for decades. I don’t smoke, and rarely have wine. By May that year my GP increased the dose to 20mg., but days later I was sent to A + E with cardiac concerns. The hospital adamant it had nothing to do with Lipitor.

By mid 2008 I told my GP of dizzy spells, and loss of balance, also swallowing difficulties, but after liver function tests I was reassured it couldn’t possibly be Lipitor.

Early October 08, saw me in hospital with a ‘stroke’, although the CAT scan and MRI were puzzling. I was sent home with no help or guidance after the Consultant insisted Lipitor was not a problem, and I should not reduce it, as it was already a very low dose. Unable to walk to the end of my street, my calf muscles feeling as though I’d run a marathon, and experiencing cardiac stress. Severe neck and shoulder pains, and confusion with words. Frequent muscle spasms in my feet, legs and hands, etc. etc. No energy for anything, and so difficult coping - living alone. End of Dec. a friend from out of town visited, and was alarmed, as she’d researched a web site for her brother, who was using a walking frame. I was astounded at the reports from users of Lipitor, so many suffering in the same way. Although my GP had arranged more laboratory tests for me, I was not prepared to wait.

On 6th January 2009, (almost 2 years later) I reduced my dosage to 10mg., and within days was experiencing improvement in many areas. By 17th January, I reduced to 5mg., (maybe a little hasty) and by 24th stopped it. By 28th my GP could see for himself, the considerable improvement generally, with a lower blood pressure reading.

By then, I could complete half, of what used to be my regular walking regime. To date, I am able to cover more than that, and hope I will eventually be able to cover the full distance. I’m hoping there will be no lasting damage, but am so thankful that my friend found this website. Its scary to think I had no quality of life, and doubt I would have survived more Lipitor. So I’m taking my chances with high cholesterol, and a near normal life.

M.

New Zealand

How much you wanna bet that if a commercial came on National TV that said: "If you have had or now have the Mirena IUC and are experiencing the following symptoms:...etc etc etc....please have it removed immediately", women by the hundreds of thousands would suddenly come out from under rocks and having been alerted to what was causing their problems, would have it removed and boy would there be a HUGE class action law suit. (I know there is supposedly one going on or was one but i cant seem to get a response from them.). I just know there are many many more of us but they just have no idea! I emailed everyone, I mean EVERYONE I know to pass along my story and you wouldn't believe how many people wrote back to me and said that they KNEW someone who had the Mirena and was having all those symptoms!! so ladies....put out an email bulletin to all your friends and family so people can be aware. Even if you saved one women, thats more than none!

I am so mad at my doctor! i feel like he knew about the mood swings and just opted not to mention it! my entire life my friends and family have joked about how im always laughing and smiling no matter what is going on. i am a VERY happy person....i was just prescribed doxycycline for my acne and have only been on it for a couple weeks. i thought i was possibly having a pms problem but it just continued after i was off my period, i am so easily irritated now i find that i cry over nothing and cant seem to get over anything.this morning i got in a huge fight with my dad and was more livid than i ever have been in my entire life all over nothing!! and when i say nothing i mean NOTHING.i screamed at him and left my house and told him i wasn't coming home and not to call me or talk to me and then i drove around crying angrily and hysterically for 3 hours.my dad is practically my best friend we never ever fight.ive been losing sleep and having depressing thoughts about life and where mine is going.i just started college and im bummed cuz the meds are effecting my grades already(or so i think they are) i feel physically incapable of getting up in the morning and i have a hard time keeping up in the easiest dance class ever.i always have thoughts about how screwed up EVERYTHING is and my mom and i myself noticed that in the last week every time i call her its to complain about something and i get all choked up about whatever im talking about.now after reading about all these other people having issues with the meds im pretty pissed that my doctor didn't give me any options.if u plan on going to the dermatologist for acne i would recommend mentioning what you've read about this drug before they waste your time and money.life is too short for this crap...seriously.

I had Mirena inserted in Feb 2007. The insertion was quite painful. I had severe cramping accompanied by light spotting for 2 or 3 days. After the cramping went away I didn't have any problems what so ever for several months (other than complaints from my husband of a pinching sensation during sex). I thought the device was wonderful, and regretfully have recommended it to several friends and family members. I had no bleeding at all, no period or spotting, for close to a year. Then one day after sex, when I got up to go to the bathroom I experienced heavy bleeding. The bleeding was so bad I was worried that the Mirena had punctured my uterus or something. I made a doctors appointment to have it checked and they said it was still in place and occasional unexplained bleeding was normal. Although it freaked me out I thought maybe it was a one time thing and said okay. Well, every since that day every time we have sex I spot, sometimes its very light and others quite heavy. Also my husband said he could no longer feel it during sex. I couldn't understand why if it hadn't moved as the doctor told me. The next side effect, well group of side effects, began not long after. I began having nausea, stomach pains, just feeling kind of blah. Then I started gaining weight. I thought "Oh my God, I am pregnant!" I took a pregnancy test and it was negative. I have thought that I was pregnant at least 5 times due to the increase in the nausea and being so emotional. I have gained about 30 pounds over the last 8 months and can not lose it. I have even taken Adipex, a prescription diet medication, no results. I have an appointment to have it taken out the 21st, if it's even still in there. I hope my body and my mind goes back to the pre-Mirena days.

DO NOT TAKE THIS POISON!! I have spent the last 4 years dealing with
adverse side effects of this medication. I have central nervous system damage, digestive disorders, anxiety, panic attacks, dizziness, achiness-it feels like a really really bad flu. My dad who is a doctor didn't believe that Levaquin was the cause at first however he had a chemist look up the compound makeup and was told to never prescribe this or any other fluoroquinolone again (cipro, avelox, etc!) Side effects can last long after you finish this medication. Also animals can get this stuff so it can be in the meat you eat which will make you feel worse or it could kill your beloved pets. Do your research. Warn friends and family-even strangers. Make a mediwatch report. Helpful sites if you are dealing with poisoning.
There is also a yahoo group.

I have been taking topamax for five months now. My friends and family have been so worried about me that they have accused me of doing hard drugs. I thought that some of the side effects I was experiencing were from stress in my life. I am a 26 year old girl who has battled migraines since puberty. Now I have about half my hair left, acne like you have never seen before, ( I have never ever had acne in my life!), depression, high levels of anxiety, and my vocabulary has shortened to that of a 6th graders. I have always been a thin girl, usually around 125 and I am 5'8. At this point, you can count every bone in my body, see every vein. it's pretty discussing. I am going to wean of 25 milligrams a week, and deal with my migraines in a different way, so that I can become the person I once was.

I have been on Celexa about 2 yrs now I am having a hard time dealing with the sexual side effects...I have no problem wanting sex...I am having a problem reaching orgasm...If I had known that this would be a real issue and how serious it is I would have never taken the drug...Please warn all friends and family about the serious sexual side effects of Celexa...I have little to no feeling in my clitoral area...It is so frustrating to me and my partner

I am 35 years old and LOVE my Mirena. I have NEVER felt better. All these "side effects" sound so crazy to me. I know 10 women who use this product and not one of the complain about anything. They all love it. Its their word of mouth that inspired me to look into it. I have had mine since March 06. I fear for all of you who are having "side effects" that you might be blaming this product, and ignoring that there can be some thing other than the IUD causing your problems. All of these comments are hell bent on blaming Mirena. I'm not saying that its not causing any of these side effects with some of you, but for some, I am wondering if your too busy blaming it, then finding out if there is really something else wrong. I didn't think it hurt that bad at the insertion, a little crampy, but nothing we as women couldn't handle. After I saw this site, I literally contacted the women that I know use it and they all were shocked that people were having such a hard time with it. You would think 1 out of us 10 would have something to say if there was a problem. The only thing in common that we all have is that we went to the same Dr. So maybe that could be an issue with some of you. I didnt bleed for weeks or months. And the pill NEVER could regulate me . Within 3-6 months I had a 90% decrease in my periods ( just like this product states it would do) i had used the vaginal ring before this and that caused some moodiness and was a bit odd during sex, But Mirena has made me feel free, not moody, no pain, no period, I have a strong sex drive ( mainly because I no longer have the worries such as did I remember my pill? Is the ring still in place or did it fall out?) My boyfriend never feels it or the strings ( and I have a short cervical neck!) Nor have I heard such things from my friends and family who do use it. I think if I was having some problems and stumbled across this website I would panic and blame Mirena as well. But in my opinion all these symptoms are things we as women will have happen due to stress, age or routine ob/gyn issues. i actually read in one of these comments someone asking about a lawsuit.... Are you kidding me??? If I were all you with these problems I would seriously check with your doctors and make sure there is nothing else causing your issues...Don't just blame a product with out making sure you know everything thats going on within your own body. I wouldn't take that chance but I am not the one with any problems. I'm sure this method isn't for everyone but my point is that I hope you don't overlook a more serious or undetected problem. good luck to all.

I am 28 years old and have always had terrible PMS, maybe could be considered PMDD, and I decided to try birth control pills for the first time in my life to help regulate it. My doctor prescribed Yasmin, and I took them for less than two weeks before I stopped. In that time, my face and back broke out in pimples worse than I've had in 15 years, I was so depressed, I saw the world differently. I cried uncontrollably when I listened to the news, I felt utterly helpless. I lost my sex drive completely, and saw my relationships in hopeless, negative terms. I had a sensation in my head that made me feel like banging it on the ground, and I understood what might make someone shoot themselves in the head - it was HORRIBLE! And scary, and I have never felt like that before. I bled a mysterious, odorless brown liquid the entire time. I've been off Yasmin for 2 weeks and still feel nauseous and tired but as soon as I stopped, felt instantly lifted and better. And it was expensive - it would have been sixty dollars a month. Of all my friends and family, only one said to stop taking it immediately, and I'm grateful to have listened to her. It's amazing that such a tiny little pill can have such a huge negative impact. The only thing I learned is synthetic hormones are bad for your body!!

hi all. thanks for writing your comments here. it has helped me today, another HORRIBLE day of prednisone hell. i have been seriously ill for 8 months been told ever other week I'm likely going to die from lung disease (i'm 35) and after a painful lung biopsy have been told my lung problems are almost all reversible... after a year on high dose prednisone. i was on 40mg a day for a month a while back and was so out of control from rage and crying and insomnia and panic/suicidality, ravenous appetite, that they lowered me to 30. then after biopsy they said i should be on 100mg to cure me, we settled at 60mg. it's been 24 days. The moon face started about one week in. i've gained 8 lbs. i am an emotional wreck. i have at least one rage filled attack per day where i am screaming and want to kill somebody or destroy something. some days i am so filled with hopelessness and worry i just want to die. my body changes (after just losing 30 lbs and being a work out fanatic my shortness of breath makes it impossible to walk up 2 flights of stairs without resting) face changes, acne, excess body hair (oh my god please make it stop i'm like a chia pet and i'm so afraid it is going to get worse) double chin, puffy eyes and cheeks, absolutely uncontrollable emotions and mood swings, inability to be logical or reasonable. i don't want to leave the house, i'm panicked and scared all the time. i never sleep. ambian gives me minimal relief (just started taking it) i feel like i'm losing everything, except my lung functioning is returning and i'm not going to die from this illness (they assure me THIS week) i understand light at the end of the tunnel, but living like this is unbearable most days, almost impossible the rest of the time. am i alone with the severity of this? or are all the others like me too busy hiding the sharps and crying in a corner to write on this board? thanks for listening :)

figures, forgot to mention what HELPS. no eating after 8 (7pm is better) no salt, no sugar, exercise, even just a walk every day, anything physical, i walk like a grandma on the treadmill but i still do it, sometimes it is the only thing that stops my crying. no alcohol, support and understanding from loved ones, it's not you, its the drugs. good luck.
figures, forgot to mention what HELPS. no eating after 8 (7pm is better) no salt, no sugar, exercise, even just a walk every day, anything physical, i walk like a grandma on the treadmill but i still do it, sometimes it is the only thing that stops my crying. no alcohol, support and understanding from loved ones, it's not you, its the drugs. good luck.

I was given this demon drug for a UTI, in May 2003. I have had severe skin rashes ever since. Cannot get in the sun at all. I have a beautiful back yard w/a pool. All my friends and family enjoy it, but not me.

I have had Mirena for almost 5 years...and am having it removed to put in a fresh one on Wednesday. I love it and have never had any negative side affects. I have recommended it to friends and family, all of whom have had no side effects either. I love it, love it, love it!