Email symptoms and conditions

I have been taking Wellbutrin 300 xl ( i believe - here comes the "Brain Farts" i attribute to Wellbutrin ) for seven years. I can tell you that i have noticed a small very very small amount of hair loss compared to most people but as i read thru these posts it appeared to me that MOST of them stated generic Wellbutrin. I will say i have had more hair than i am comfortable with appearing in my shower and bathroom floor and sink from drying my hair BUT i have NOT had the scary experiences that i have read here. I came to this site because i had to quit taking my Wellbutrin cold turkey because of some changes in the law in my state i have to drive 50 miles away to see my N.P. and because the office i was going to and the one she works in act like they have to send fire signals to each other instead of email and i am out of meds! so i was searching for side effects i could expect until i can get my meds back. i will tell you it is nice to see that i am not alone but i think it sucks that any of us have to decide if taking the medication and side effects are worth it! i also have problems with memory, spelling,speech, following thru with my thoughts much less getting them out of my head and making sense to someone else. did that make sense? ! ? i personally didn't notice any weight loss. my husband says i have the patience of a flea and really dislike " hate" a lot of things. i don't notice this but go back a couple of sentences and you will understand :)
After being here and reading all that i have i am afraid to continue taking this medication so i think i will just let it go and see what happens. i am also taking lamictal and seroquel and xanax and i am pretty sure i would be just as afraid of them if i went and looked them up but i have the choice as i am sure most of you do ...... do you take the meds and deal or go off the meds and well ... die?

I have been taking Lisinopril for years. Also I've taken numerous tests to find out why I'm so fatigued, sleep all day and more tired afer sleeping even,severe knee pain at night when laying down only... I had also put on a huge amount of weight in a month or two when I started taking it now that I come to think of it. Oh my gosh. As I continued reading everyone's posts I wanted to cry. Has this been my problem after all these years? I sleep my life away for the last few years and I'm only 40. Before I started taking it, I worked out extreme 36 hours a week and worked 50 to 60 hours a week. Now my day is trying to get up to make it to work on time for 8 or 9 hours! I've already sent an email to my endocrinologist to request a different prescription and I am not using Lisinopril anymore!! Are there any class action suits for this? This has really taken a lot from me. I only hope this is my answer, which it sounds like it is! Thank you so much for sharing your stories. I will return after time to reveal my results!

I've been taking doxy for lyme disease. tomorrow nov.2 is my last day of a 30 day cycle. my dizziness is gone, but still getting rapid heartbeat, and feel very weak..does any one feel better after their done with doxy or has any one fully recovered ?? please post reply...

I'm a 22 year old female who is pending a lawsuit against Avelox. This drug ruined my life. I was a full-time student hoping to get into Duke University in Fall of 2010; it looks like all of my dreams have been destroyed after taking this deadly drug. I was diagnosed with pneumonia (pretty much walking-pneumonia) on August 8th, 2009...I have no slept since; it has been about 2 and 1/2 months. I did not get to go to school this Fall Semester to pursue my 15.5 units honors classes. I'm currently being told by the doctors of KAISER that I'm gong crazy, bipolar, psychosis, anything but a victim of this terrible drug. Please, help me with this lawsuit. I will let everyone know the status and hopefully we can bring many people to my court case and support!!!! my email: ******

Please do not ever take this drug!

-Brittany

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..

****KENALOG CLASS ACTION LAWSUIT****
Need a list of people that want to join Kenalog class action lawsuit A.S.A.P Please email me with name,state and all side effects. Include if you were treated for the side effects from a Doctor and/or hospitalized.
******

My good friend is on Topamax and Trileptal for epilepsy seizures. She has developed severe paranoia. We cant call her on her phone or send her an email as she believes that her phone, computer and house are all "bugged". I have written a letter to her doctor to let him know what is occurring in her personal life as Im sure that he is unaware of her behavior. She lives in a world of fear and her medication needs to be changed.

My 62 year old husband has had Parkinson's for about 10 years now. The other day he was prescribed Prednisone (20 mg tablets, twice a day) for 5 days. After the first day his pinched nerve problem was greatly improved, and as a side effect, his Parkinson's symptoms disappeared completely and he was like normal again! This is a miracle to us and we are looking for medical research to help prescribe Prednisone for Parkinson's', or some agent similar. Did the Prednisone make the other Parkinson's drugs more effective; or did the Prednisone fix the Parkinson's on its own. We don't know. For 5 days, it was bliss; I hope we can get someone to weigh the side effects against the miracle of being normal without any Parkinson's symptoms!

My 9 year old daughter got her first shot in Dec. 2008 and her second in Feb. and the last in June. We have have been to the doctor a lot of times due to headaches with the doctor's opinion being that it's "allergies". She is now on allergy shots with still no relief from the headaches. I listened to her pediatrician and got her the shots. I feel so bad now after reading all the problems others are having with this vaccine. She also has had a change in her attitude aggression,moodiness,cries often, and she says she's depressed. If anybody has any suggestions for us please let me know. I love my little girl and know I'm worried.

How Many parents would be willing to go to the FDA headquarters and picket to get this drug relabeled?The official location is in Maryland.Contact me on this site via-private Email.K. M.

Update. I received a response from my Gynecologist regarding my email listing the symptoms I have been experiencing since having the Mirena placed. She said some people are sensitive to the hormone that is in the Mirena even though it is a low level. She acknowledged the headaches could be related, but didn't think the weight gain was (I was told the same thing about the pill, yet the weight literally FELL OFF once I stopped taking it). She said she doesn't know about the joint pain - that it's not usually a side effect, and that there shouldn't be an odor to the discharge. She wants to evaluate the discharge & said I can have the Mirena removed at that time if I am more comfortable with that. I just don't understand how there can be SO MANY WOMEN who have these symptoms yet the doctors aren't aware of them being side effects! I truly believe the only research they do is read the literature the manufacturers supply them with and that's that. I am going to print out as much info as I can to present to her and tell her she needs to look into it further. And yes, I am having it removed on that visit because I CAN'T STAND the hip pain any longer.

I am 20 and I have been on Loestrin 24 Fe for almost 6 months now. Before that I was on Lybrel for almost a year. I started taking Lybrel because I had always had awful periods to the point where I would sometimes faint from the pain of the cramps and would pretty much couldn't function normally. Lybrel was fine for the first couple of months but I began to spot after 6 months and decided to try a different one. I was put on Loestrin and like other pills I have been on I had intense mood swings, felt more anxious, depressed, and had night sweats for the first 3 months. I had light periods, 2 or less days and then about 3 months ago, I stopped getting a period all together. I have had no spotting and recently I have started to have cramping around the time I should be getting my period, breast tenderness and bloating. These are all symptoms I have had on past BC too. I take my pill every day around the same time and have never missed a day. I like not getting my period but it does concern me a bit because my doctor didn't tell me that I would not get a period at all, he actually warned me that I probably have spotting for a while. Does anyone else not get their period on this pill?

I am 14 years old, and have had all three Gardasil shots. Now, this may not be much in comparison to what some of you are going through, and im very sorry for you. however, it seems that a very common side effect of Gardasil is a sore arm. I had my first two shots already, and i recently received my third. as the nurse was administering the shot, i heard the words "oops" escape her lips. Needless to say, this worried me. I was also getting another shot that day, so my sore arm on the day of did not worry me. However, in the days after the shot, slowly the bump from the *other* shot went down, as the one from the Gardasil remained. It is as sore as can possibly be, and has recently become quite itchy. I do not want these other side effects to occur, especially since i am going away to camp very soon. Should i be terribly worried?
please respond to this comment or email at ****** (no space... an htm just isn't allowed.)

Hello... I started taking Levothyroxine last July for slight hypothyroidism. I felt great for the first 6-7 months, but then in January the problems started for me. I was getting severe anxiety which the doctor said was stress and he also thought I was depressed. I knew I wasn't, but he put me on Ativan and Prozac. The week I took prozac was the worst week of my life. I thought the effects I had were from the prozac, but now I know now it was my thyroid spiking, which the doctor never checked my levels during this period. My heart rate doubled, I had insomnia, was gagging, sick, felt like my body was on speed and wanted to die. I was prescribed a beta blocker for my anxiety previously which I had never taken, but decided to take when my heart was racing, which helped me feel a bit better for the week, but I knew something was wrong. I had this happen again recently for about a week (and I was on nothing but levothyroxine). I know what anxiety is and I have never had anxiety or depression my whole life until these episodes that happen when taking this medication. By the time I went to the doctor to get labs done, I had been feeling a bit better and he said my levels were fine. I am now wondering if it's side effects from the meds or if it is spikes in my levels making me hyperthyroid instead. All I know is that I cannot live like this!! I have a 3 yr old and I need to be happy and healthy like I used to be before this medication... no more heart racing, racing thoughts, anxiety, and insomnia. Please help!!

Please help me. I have had the Mirena for a little over a year now and I have been miserable ever since. I just yesterday one of my very frequent depressive states. I has become so bad that I often think about hurting myself. I am very petite, 4'11 to be exact and I have never weighed anything over 115lbs. I just recently went to the doctor and I weigh 147lbs. I have always eaten healthy and I couldn't explain my weight gain. It has become so depressing I refuse to take pictures and I no longer want to look in the mirror. I have horrible headaches and my periods are longer. I am now going through a divorce and I don't have a job or health insurance. I really need to take the Mirena off but I don't know what to do!! Every day that passes by I keep getting more and more depressed. I am afraid for myself...help me

Ironically, when I was in high school, I was sick for 2 years; I had migraines so bad I couldn't read, write or even watch TV. I was nauseated every day.. felt a bit better in the evenings. But my eyes were so sensitive to movement, if i was to move my eyeballs just to look at something move on the TV screen, I would be in agony. At the time, my mother was so worried about me, she took me to see every specialist there was in the city (Winnipeg), I missed 2 years of high school. After seeing about 50 doctors, finally one asked me if I was on the birth control ill and told me to get off it. 3 months later I was completely cured! Since then, i have been so afraid about birth control. i have used nothing but condoms.. until my son was born, my maternity doctor recommended the Mirena. I was skeptical because it had hormones in it, but she assured me they were different hormones then what were in the BC pill, and she said the risks were so low. I thought I would try it, and be on the look-out for the same symptoms I had with the pill. But I didn't have any. No visual problems, no nausea, no headaches... so I thought it was the greatest thing on the planet. Meanwhile, I was miserable, angry at my husband all the time, had no interest in sex whatsoever, was not sleeping.. I thought it was post-partum hormones. We decided our son needed a sibling so i had Mirena removed to get pregnant, and after our daughter was born in Dec '07, i had it put back in... again, thinking I had post-partum depression or something. Even 6 months later after I quit breast-feeding, I still couldn't lose the weight. I was eating chocolate and peanut butter by the cup every single day, crying all the time, had no energy to look after my kids and wanted to nap all the time, and cried when I couldn't! Then a few months later all of a sudden my joints started hurting. My wrists, elbows (like tendinitis), then a couple of days later I was limping because my hip or my knees hurt or my ankles felt swollen and weak. I felt like a hypochondriac because I was always complaining of something. Did I mention the hair loss?
So, sorry for the long story. But most of my symptoms have disappeared since removal if the Mirena this past Valentine's day 2009. However, as I was forewarned, I have recurrent symptoms every month while PMSing. I have never suffered from PMS in my life, until I had Mirena removed. I get depressed, eat more, and my joints hurt so bad, and sex repulses me. My poor husband; A couple of weeks ago I got so grossed out during sex that I made him feel like a creep.
These last 2 weeks, I wasn't supposed to have joint pain, because i wasn't PMSing anymore. But it has gotten worse. That's when I put up my post asking if anyone else has this pain. I was beginning to think I had Fibromyalgia. I also have very dry burning eyes, which is also a symptom on Fibromyalgia. I saw my doctor twice last week, and she thinks I may have it too. Is anyone out there in a similar boat?

My daughter was prescribed Doryx for mild acne- 150mg a day. At Track Meets she is complaining that she is dizzy (seeing black spots) after races. Now she says she has tingling in her hands and lips. They feel like they are on fire also. I had her stop the meds immediately and am waiting for the dermatologist to call back. If anyone had these symptoms how long does it take for them to go away?? email me: ******

I had my daughter in Sept. 2009. 6 weeks later I had the Mirena put in. I would first like to say that I was told it would not hurt going in. I screamed and cried at the top of my lungs it hurt sooo bad. The OB blamed it on a tilted cervix. I have since been irritable, always in a fog, very crampy, constipated, terrible acne (that I've never had before), developed hemorrhoids, Weight gain, and I have no sex drive. Now new symptoms occur. I am exhausted. I struggle everyday to get out of bed. I have a 2 year old and a 8 month old. Sadly this is affecting my parenting. I am having severe headaches. Now I am constantly nauseous. After I eat I am getting very sick for like an hour. I am extremely weak and can barely even walk. I shake uncontrollably also. Please, anyone with any info. please let me know. I am getting this thing out ASAP, but I am scared to death of the pain when it comes out and I am extremely worried that it has done some damage to my body. my email is fireflies10105 at yahoo. please I need advice!!

been on the patch 50 mg for nine yrs now i don't seem like i get no relive at all its like the patch is not working at all,it fell like i have to take a piss. and then i have to force it out

I had the Mirena put in December of 2008. My baby was 6 months old at the time, and I am a fertile mertile! lol so i had it put in so i wouldn't run the risk of getting pregnant too quickly again! i am happily married, but as of lately i have had trouble with my husband. i have no LIBIDO what so ever. I have no desire to have sex or make love with my husband. i have gained a ton of weight, and i feel depressed and tired ALL THE TIME. i feel like i don't get enough sleep. does anyone else feel the way i do? please send me an email at ******. i would love to hear the feed back, because i may have it removed, because my marriage is more important.

I am just in shock. I have been on Avelox for 7 days now, and I can tell you that the side effects are not worth it. I still feel sick and have the bad cough. Now, I also have Thrush. But the weirdest and most upsetting part of this was that I didn't notice any of the other symptoms. So I went all week, talking a mile a minute, sweating, dry mouth, hallucinations, etc. Then on Saturday, a few of my friends staged an intervention. They actually believed that I was taking Crystal Meth - ICE. I was heartbroken, confused, and mad. I knew I had not done any illegal drugs, but several of my friends were convinced.

I went to the doctor today and found out that it was the Avelox. However, I had already taken today's dose. I even told the doctor about the situation with my friends and asked if this drug could be related. He said no, it must be the steroids and sent me on my way. As luck would have it, the pharmacist saw me in the store and approached. I asked him if Avelox could make me feel the way I was feeling. He told me that I should have never been prescribed Avelox and Effexor as they had drug interaction issues. He also told me that my symptoms were disclosed on the pamplet. The problem was that I got the Avelox as samples after the Augmenton didn't work.

So, I came home took the meds for the Thrush and watched tv. I haven't slept since Thursday, nor have I eaten since Saturday. I am hearing and seeing things. Now I am scared to go to sleep because I may not wake up. My heart is beating fast, I can't stop talking, dizzy, blurred vision, disoriented but extremely happy given the circumstances, paranoid, jittery, extremely thirsty even though unable to pee.

This is just horrible. I am not a drug adict and do not do Meth/Ice or any drug like that, but now my best friends are doubting me. They don't understand or believe that an antibiotic could do this and how am I supposed to prove it to them? It looks like, just because I got sick, I may lose some of my closest friends... Remember, most drug adicts and alcoholics DENY it first. Great, huh. Now everyone is going to be watching me to see if I am on drugs. I feel violated because evidently I got all high on this antibiotic, didn't enjoy it, and now am suffering the consequences.

What makes it worse is that people I love now don't trust me, and I didn't even know what was going on

LOL- EVERYONE! I'M SITTING HERE SEARCHING FOR SIDE EFFECTS FOR MIRENA AFTER REMOVAL. I HAD MIRENA FOR 1 1/2 YEARS, AND I REMOVED IT ABOUT 2 MONTHS AGO. I HAVE EXTREMELY HEAVY BLEEDING SO I FIGURED I WOULD SEARCH IF IT HAD SOMETHING TO DO WITH THE REMOVAL. WHEN I HAD MIRENA INSERTED, I HAD ABSOLUTELY NO PROBLEMS! THE ONLY SIDE EFFECT I HAD THE ENTIRE TIME WAS EXTREMELY LIGHT PERIODS FOR 2 DAYS, BUT I GOT THE PERIODS EVERY OTHER WEEK! WHEN IT WAS REMOVED, I FELT ABSOLUTELY NOTHING! NO PROBLEMS! I WAS IN SHOCK BECAUSE I THOUGHT IT WAS GOING TO HURT. THE ONLY REASON I DECIDED TO HAVE THE MIRENA REMOVED IS BECAUSE MY HUSBAND AND I PLANNED A TROPICAL VACATION, AND I DIDN'T WANT TO BE BLEEDING ALL THE TIME, SO I FIGURED-GET IT REMOVED AND GET THE DEPO ( I HAD DEPO FOR 9 YEARS AND HAD NO PROBLEMS, AND NEVER GOT MY PERIOD). WELL, HERE'S A FUNNY STORY!! THE REASON THIS VACATION IS IMPORTANT IS BECAUSE I AM CONSTANTLY DEPRESSED, ALWAYS CRYING, EASILY AGGRAVATED, LOST ALL MOTIVATION, LAZY-I STOPPED CLEANING/ COOKING, I DON'T GO OUTSIDE WITH MY LITTLE ONES- MY HUSBAND DOES, ALONG WITH EVERYTHING ELSE. NO SEX!! MY HAIR IS FALLING OUT , EXTREMELY BAD ACNE (RESULTING IN MANY TRIPS TO THE DERM. AND SHORT HAIR CUT), I SOMETIMES FEELS PINS AND NEEDLES ON THE RIGHT SIDE OF MY BODY FOR DAYS! I WENT TO THE DR. AND SHE SAID I WAS EXTREMELY OVERWHELMED, STRESSED AND DEPRESSED! I ALSO HAD A THYROID TEST. MY THYROID IS FINE, AND AS FOR THE MEDS THAT WAS PRESCRIBED FOR DEPRESSION- I NEVER TOOK THEM ( I'M NOT A PILL TAKER-CAN'T REMEMBER!) SO AFTER ALL A TROPICAL VACATION IS JUST WHAT I PROBABLY NEED TO SNAP ME OUT OF WHATEVER MY PROBLEM IS! WELL, AFTER READING THIS , ALL I COULD DO IS LAUGH!! YOU SEE, LOOKING BACK----IN THE PAST 2 MONTHS- I HAVEN'T CRIED, I AM FILLED WITH TREMENDOUS JOY WITH LOTS OF ENERGY. I TOOK MY KIDS TO THE PARK AND FOR LONG WALKS NUMEROUS TIMES. I CLEANED THE ENTIRE HOUSE AND IT'S STILL SPOTLESS, COOKED ALMOST EVERY NIGHT, I HAVEN'T HAD A SISSY FIT, OR FELT SOME TYPE OF ANNOYANCE YET, MY FACE IS CLEARER, MY HAIR HASN'T FALLEN OUT AND GREW LONGER. AND MOST IMPORTANT I LOST 34 POUNDS! ( 174-140). RIGHT NOW AT THIS CURRENT MOMENT I FEEL BETTER THAN EVER! MIRENA BEING THE CULPRIT NEVER ONCE CROSSED MY MIND. I SUMMED UP MY PROBLEMS TO BEING STRESSED FROM MARRIAGE, 3 HIGHLY ACTIVE CHILDREN AND RUNNING A BUSINESS. SO I SIT HERE IN MY GLORY AND CHUCKLE TO MY SELF THINKING ABOUT ALL MY POINTLESS NAGGING & CRYING & BLAH BLAH BLAH. AND I THANK YOU WOMEN FOR OPENING UP AND BEING HONEST BECAUSE I NOW KNOW WHAT WAS WRONG! THANK YOU.

Hi ! I'm French and bipolar 2 rapid cylcing (every 2/3 months for about 3 weeks each taking anafrani)l. I'm 50 years old and I had lithium for many years. Since July I have lamictal. It's very recent in France and my doctor doesn't know if my problem to sleep I get since I have lamictal will go away or not and if lamictal is responsible.
I describe the problem : I have difficulty to get asleep, I wake up during the night and I wake up very early in the morning even if i go to bed late. So I'm obliged to go to bed before 10 pm. It's very hard but since I take lamictal I had no down since September (6 months it's wonderful for me)
I only had some variations during the day at the beginning but it seems to be better. I feel really better than with lithium. But there is this problem of sleeping. In France nobody could answer to me and my doctor told me to go on internet with USA of Canada where you use for long time lamictal. Do you know something about that and do you know if it can be better after a few month more ?
Could you please answer me here or on my email : ******
Thanks a lot in advance and sorry for my bad English. I hope you will understand me.
Kind regards
N.

I had a 103 fever Thursday went to my doctor Friday she prescribed this to me and I started taking it same day - that day - hardly any side effects until later that night...took a shower and I looked like I had spider webs all over me - then the real fun started...I started to swell up, I have not slept since that first night and needless to say, I have stopped taking the Avelox now. My fingers are so swollen they are like coctail weenies and it is hard to type - my legs are so swollen it hurts to wear shoes and I have bright red dots all over from my knees down. Is this permanent???? I'd rather not have this look for summer. : ( I feel like I am all "craked out" for lack of a better term but I am exhausted form the no sleep, etc. Oh yeah and the best part of this whole thing, I am so itchy I want to peel my skin OFF. Who the h*** lets this remain on the market?? Better yet - why do doctors keep prescribing it knowing all this - oh yeah I forgot MONEY...
I really hope all of this goes away? I am terrified cause most of the posts I have read thus far say most people deal with this for weeks +!!!!

This is amazing to me to hear all of these side effects from the yaz. I have been experiences all of them but really didn't make the connection. I have been experiencing knee joint pain since I have been on these pills but really didn't make the connection. I only started researching this since I received an email from someone about yaz and the warnings about it. This message went into my spam out of the blue, and I opened it to read it. That was about a month or so ago, and I am scheduled to see my doctor in a month or so and I don't want to abruptly discontinue without having a plan. I am 46 years old and was an anemic due to heavy periods, so this was the solution to get my blood count up to what it should be. This was a real issue because I had to have emergency surgery but had to have 2 units of blood before the surgery. So after that, it was suggested that I take bc to control my periods. I really didn't want to do this but I had to for the mean time and I have been on them for about 8 months. My blood count is back to normal now but I have to figure out what else I am going to do because I cannot continue on these pills now that I see what it is doing. I will be going into menopause soon also, but that's probably not until 5 more years and I am not going to take these all that time. I have some decisions to make.