Roller coaster symptoms and conditions

Googled and found this site. Could not believe all that I read! I've been taking Lamictal for several years for Bi-Polar disorder. I also have GAD for which I control with another drug BUT...I guess it's been so long since I began taking Lamictal that I had forgotten, or did I ever even know, the side effects of it. First if all, the memory loss is incredible! Not being able to complete a sentence...never able to find a "word" that should be so simple to remember...going somewhere and within 2 seconds, forgetting what in the world I'm doing or where I'm going...happened today TWICE!
And to top it all off, my eyes are so bad...I didn't even attribute the L to this until I came to this site but it makes PERFECT sense! I feel such a sense of loss in my eyesight that it has begun to really scare me. I have not been to eye doc yet but plan too.
Also, someone mentioned in here that they feel the med just wears off before next dosage and that is exactly what I've been telling my doctor so at first, we just upped the dosage until I was on 450mg a day but even the, it still was not working. SO...now I'm decreasing and the doc added Depakote Er 250mg. But doc says I have to be almost completely off L to get fully on D. So...feel like crap a lot of the time!!
I'm like someone else on here who said, "just start fresh" and that is what I'd like to do but how do you go "cold turkey"? I know it isn't good! Even decreasing this L for the last several months has been hell!
I have been on a roller coaster of meds for 10 yrs. Have yet to find the "combo" that works! Sometimes I wonder if the diagnosis of BP was/is even correct.
Another person in here said he feels like he may have some side effects of OCD and I feel that way too. Nothing major but...enough for me to notice.
Damned either way, right?
One thing I DO KNOW is that I cannot take this eye problem anymore and now that I know my memory and all that other stuff has to do with L, I'm getting off it no matter what! I'm calling my doc tomorrow and we HAVE TO MAKE A PLAN!!!!!!!
I'm only 42 but my memory is that of an 80-yr old (except for my grandmother who died at 96 and could remember details of when she was 4 yrs old...lol) I guess it's good I can kinda laugh at all this but I DEF know it is not funny!!!
Anybody out there with insight to diff. meds...combo of meds?? I really am worn out!!
Right now, I am down to 375 mg of L and this has taken me several months now to decrease from 450mg...don't see the D working that well yet but it's only 250mg so...
I really am worn out!! My anxiety shoots through the roof bc of all of this! Esp. when I feel the L wearing off around 5p or so...
I'm game for any advice ( I did see where the one woman talked about changing the time you take this in the morning but that won't work for me)
Thanks!!

been taking atenolol amlodipine and lisinopril for quite a while but BP has been on the increase so GP has increased my dose of lisinopril to 30mg a day oh my god i feel like i have been on the drink my head was swimming,felt like i was on a roller coaster when i closed my eyes felt nauseous had a headache and had to go to bed feel reluctant to take another dose does anyone think that these symptoms will decrease with use cause i really don't want to feel like that all the time

I was on Yasmin for 6 months and all i can say is get off this pill! I was on linessa before. my doctor then said that if i switched to Yasmin it would clear up my acne, (which isn't that bad to begin with, have very mild break outs around that time of month and then that is it) so i thought hey way not give it a try cause who wants acne in their late 20's. well since i switch i gained 30 pounds in under 2 months and went up 3 sizes in my pants! how can this happen when I eat healthy?!? and never put on this kind of weight with the other pill (which i was on since being in my late teens) Also in the last 2 months of being on Yasmin, my emotions have been so out of control, i freak out about everything I can't control my anger, then when i'm all by myself i just brust out into tears, i felt like i was on a roller coaster and wasn't able to get off. And the finally straw that made me switch was the never ending period! it started off normal then after 5 days i thought hey its going to stop but sure enough i still had clots and deep red blood, this continued for a month finally stopped for a couple of days and then started all over again! my doctor suggested to take 2 pills a day! i laughed and cried due to having no control over my emotion and then when to another doctor who finally listened to me and put me back on my old pill, now everything is back to normal well almost still trying to lose all that extra weight i put on!

I am 34 years old. Back in 1985 I had most of my thyroid removed, due to a tumor attached to it. Since I was 10 until my late 20s, I was on Synthroid. By age 19 I had 3 knee surgeries to remove arthritis. I have suffered most of my life with joint pains, dry skin, weight that is like a roller coaster, and being tired most of the time. In my 20s I was put on Levoxyl. I has been on Levoxyl for several years now. Since being on Levoxyl I have been fighting anxiety, racing heart, joint pain in fingers and ankles, sudden dizziness to the point where i have to sit or pass-out. I feel like I'm 80 and not 34. After reading this site I am printing all this out and taking it to my doctor. No telling how much damage has been done after all these years.

I have had Mirena for five months now since Oct. 2008. I seriously thought I was making the best decision after begin told by my doctor that I could not get my tubes tied because I did not inform her before my six week check-up. And she totally talked me into getting mirena. I waited a week to read up on mirena on the official website and i heard nothing but good reviews.Since I had mirena inserted I have had some periodic cramping which did not seem so bad. Yester was the first day i experienced my period since mirena. To my surprise I had no sanitary napkins (pads) available I only had tampons. I was afraid and a little reluctant to use the tampons b/cause I was not sure if it was safe to do so with the IUD in plac, so i decided to research it on the website I google for mirena side effects and my results wer the official website along with tons of others. I decided to check the official site b/cause I thought that they would best be able to answer my question an address my concern about the tampons. Well the did answer my question and said that there was no risk and it was safe to use iI just needed to pay close attention as to how I removed it so as to not remove the device instead. Well anyway I used the tampon and when dear hubby returned from work I rushed to the store to get some sanitary napkins (Pads) b/cause I was still a little scared with the tampons. That whole evening the situation pondered me and I started to think about all the other sites that i came across but never pulled them up and thought that maybe I should b/cause one sub heading caught mu attention which said" I finally got Mirena removed Yeaaa!!!". Anyway this morning I got up and started my research I was shocked by the things I was reading about the side effects which were all things that I was experiencing but had no idea and no clue that the mirena was the cause . Here goes, I experienced the cramping, very uncomfortable at times. Oh my God the extreme hair loss, which i was told that due to increased hormones during pregnancy it happens shortly after giving birth when the hormones are leaving the body and decreasing. Bull shit I am almost six months postpartum hormones are all gone and still i have excessive hair loss. The tiredness and depression I thought was due to me being at home all day. I never have the strength to do simple chores around the house even when I take vitamins. I am always sleepy and sleeping. And the weight gain I thought It was shame on me I had gained over 30lbs since my six week check up. I am always hungry can never seem to stick to a diet or exercise regimine. Pre pregnancy with my last child which I have three I weighed 125 lbs and have always been a fitness fanatic with six pack abs!!! Now I have a barrel so to speak. Which I did not have after giving birth until i started the weight gain that I thought was due to being at home and being stressed with so much going on in my life within the last two years. little did I know MIRENA made me FATTT!!!!!!. I have also had problems with back and chest pain and also total body pain. I have stairs in my recent new home which it literally hurts me to go up and down the stairs b/cause my whole body is in pain I just thought I was fat and out of Shape but I constantly walked pre and post pregnancy so no it's not me its MIRENA!!!. I have also experienced very bad blurry vision. Hell! I thought i was going blind! I could never focus my eyes and they are always cloudy and blurry.I also experience a very annoying ringing sound in my ear like a radio which sometimes last very long. I am so happy to have found this site and realize that nothing is wrong with me it is MIRENA that is the problem and I am going to waste no time to fix it my plan was to have mirena for at least two years then get my tubes removed b/cause I do not want any more kids but I am not waiting any longer I am going to make an appointment to have it removed ASAP!!!! I need my life , my energy, appearance and my happiness back so long MIRENA. I wil;l not miss you one bit I will let you all know how it turns out fell free to comment and ask questions. I think I experienced it all and poor me I did not know. Thank you all so much for this site and information. Oh! my husband will be happy to know that his sexy little house wife did not just happen to deteriorate for no reason!!!!!! he will be reading this site.

I haven't had ANY problems taking Aviane. I've been on it for almost 4 months now. I don't know why everyone else is having so many problems with it? Aviane has actually decreased my appetite of sweets, which has made me lose about 10lbs. My Period only last about 3 days, and it's way lighter than what it was w/o BC. Also, Aviane helped my face acne A LOT! I was on a different BC before this and it made me EXTREMELY crabby/mood swings and it didn't help with the bleeding..it made it worse. I'm satisfied with Aviane and recommend it to anyone.

I read with interest several of the posts here. I have been on Lipitor for about 5 years. I have been experiencing leg pain, back pain, neck, and hand pain for likely 4 of the last 5 years. I have arthritis, I thought. Two weeks ago I ran out of Lipitor. I read several other forums where Vitamin C and Omega 3 were suggested as a possibles to replacing the Lipitor along with generous amounts of water. I said, What the hell, I will give that a try. Within days of stopping the Lipitor, most all the pain has subsided to the extent that I have not had to take any other Pain management medications at all. I was prescribed Perocet for the pain I have been experiencing. Two weeks ago, I had a tough time opening a bottle of soda, or even a relish or pickle jar. Today I can! Coincidence, I think not!!

I am so glad I found this site, as well, by typing in Mirena causing acne. I workout regularly and at first, didn't have any noticeable weight gain. Really, I am still within my 10lb roller coaster but have also went from 135 to about 148 and it will not go down no matter what I do! And the acne! I too have been using proactiv to no avail when it worked fine before. I cry when I look in the mirror, the scarring and the huge pimples are embarrassing and hideous! They're not normal either, having like 2 heads per bump and I am now breaking out on my back, which I didn't ever do. I haven't had any other side effects, it's actually made me nicer than I was when I was on the pill for 10 years. I have enjoyed the periodlessness, but at what cost? My self esteem is plummeting and I am going to get it removed tomorrow. I first thought it was Hydroxycut side effects but it has been too long and it didn't take me longer than perhaps a year to realize this is the only thing I have changed in my lifestyle. On to the removal! And to any woman who's doctor will not remove it, YOU ARE PAYING THEM! They have no right to tell you that you must keep a voluntary form of contraception inserted! Change doctors for crying out loud! If your doctor is trying to run, or ruin, your life you have a choice!

Hi my name is Ari. I'm 20. About a month ago an on-call gyno prescribed me YAZ. For the 2 weeks I was taking it I felt like my brain was up my butt. I was anxious and easily agitated. I was with one of my friends 3 Fridays ago and I got these random heart palpitations. I had no idea what was going on bso I had to have my friend rush me to the ER. By the time I got there my heart rate was at 127 bpm. The nurses and doctors told me it wasn't the pill, it was anxiety. They gave me some shrinks numbers and told me I needed therapy... I say horseshit. That's never happened to me before. I'm quite the happy kid and I'm not depressed. Needless to say, I stopped taking it that night. For the next week I still had random heart palpitations. I was trying to shop for a new cel phone with my bf and my heart started racing again. For no reason. I waited for another week to see if they would stop and it didn't. I went to a PCP and she told me the same thing. She didn't even give me a chance to explain to her what had happened. She just said I was stressed and go see a shrink.

Please somebody help me. These heart palpitations aren't stopping and its been over 2 weeks that I haven't taken YAZ. I'm in the process of finding an endocrinologist to see which of my glans this medicine messed up. I even tried to get a hold of my OBGYN and twice, the receptionists told me if I stopped taking it and I got my period then the drug is out of my system... not too comforting considering they're not a doctor. Not only that but they wouldn't let me talk to my doctor! Coffee, tea and marijuana make the heart palpitations worse (I smoke occasionally). I can't exercise either without my heart racing uncontrollably. I would greatly appreciate someones help. =)

I have been on Topamax for about two years for migraines, and was very pleased that after the first month or two, most of the noticeable side effects (dizziness, flat-tasting soda, etc.) disappeared, and the Topamax has been very effective in cutting my migraines in half. However, I've recently begun to question whether other health problems I've been experiencing are actually Topamax side effects and I just didn't realize it.

The first is intermittent stomach troubles that have been ongoing for the last year. Starting last January, I started experiencing diarrhea, stomach pain, and other persistent gastrointestinal problems, and through online research, I decided that it was probably either a spastic colon or Irritable Bowel Syndrome. I lost 15-20 lbs. in the spring and summer, but the problems would always recede before I took them to my doctor, then resurface just long enough to irritate me before disappearing again. It never occurred to me until recently that these could be Topamax side effects.

The other possible side effect that I assumed was an unrelated problem is interruptions to my sleep pattern. I have been experiencing some occasional bouts of sleep paralysis, and which researching this, read that in normal sleep patterns, one is supposed to enter REM sleep (when dreaming occurs) after about 90 minutes. I frequently enter into dream sleep in as short as a 20-30 minute nap, which does not seem to be normal. Again, researching this, the only two explanations that came up were narcolepsy, which I obviously do not have, and that my normal sleep patterns are being interrupted "by medication." So I'm back to wondering if it's the Topamax. Has anyone experienced similar sleep symptoms?

I took Wellbutrin 300 mg for two years before to quit smoking and for mild depression. After the initial (weeks 2-4) side effects of nausea, dizziness and headaches - I felt great. Not drugged and not overly emotional. I had been crying all the time and felt hopeless. I felt much better (and didn't want to smoke at all). I quit it for about 2 years and now I am back on Wellbutrin for the last 7 months. I started with Cymbalta - but hated the loss of sex drive (not able to orgasm - so who wants to have sex, right?) and felt drugged. So Wellbutrin was a welcome "old friend" I didn't have bad side effects with switching and have been pretty happy. EXCEPT for the one very scary side effect that I have experienced just a handful of times - but I really am curious if anyone else has had this HEAD TRIP WHILE DRIVING: It has happened when I'm on the interstate and/or bridge when I am driving at fast speeds, and my head feels whoozie all of the sudden and my brain seems to shift sideways - like on a roller-coaster, up and down, sideways - and I am amazed that my hands don't go with it and drive me into the wall! It takes intense concentration and wheel gripping to get myself where I can pull off the road. What the?? I don't want to ever experience this again - but it is so OCCASIONAL. The only variable I can think of is that I have not been faithfully taking the WB at the same time everyday (I'm more and more forgetful) and have skipped a day. Has ANYONE ELSE had a similar experience???

I've been on 200 mg Lamictal for 2 months now, after 4 month titration up from 25mg; Going off Lithium 900mg titration to 450mg this week. Since 1st day of lower Lithium, all the common Lamictal symptoms went from mild to extreme. Whole body muscle aches (like 24 hours after a heavy weightlifting workout) worse in neck & back/shoulders/calves, bad headaches, swelling in hands & feet, extreme blurred vision, loss of memory, halted speech while trying to figure out what to say, fuzzy. I called the Clinic to simply ask which NSAID (aspirin? ibuprofen? Excedrin? naproxin?) to use to manage the pain. They all freaked and made me come in for a blood test to check Lithium levels. I explained I wasn't "overly" concerned about it at this point, but just looking for a recommendation, and that they may be over-reacting (even though I did appreciate their concern). I also reminded them that I had just **decreased** Lithium when it happened, so I wasn't having a Lithium Toxic attack (I'm well-versed in that, having been on Lithium for 7 years). It didn't do much good to tell them I thought their diagnosis was a little off. I'll find out the blood test results today, but I'm pretty sure I know what they'll be. They also wanted me to see my PCP since it could be something else. Again, the problem was a ramp-up of existing symptoms the next morning after I lowered Lithium (the only change), so I'm conviced everything centers around that. I think they're a little inexperienced with this med. (Lamictal/Lamotrigine) and if they'd just read this blog they'd probably learn a lot. They had never heard of the muscle ache side effect. Pretty hard to believe after reading all of your comments! My theory is that Lithium was somehow holding back the side-effects of Lamictal and now they're expressing themselves more fully. I haven't read anything like this on any internet discussion, so maybe my body is very different. But maybe my experience will give someone else some insight in a similar situation.
I might also mention something that happened to me I have only seen (kinda) in one other "blog" about follicle (sweat gland) cysts. Yeah, I definitely got the jawline acne starting at the Lamictal 50mg level & increasing at 100mg. But I also got my first ever "cyst" that concerned me and sent me to my dermatologist for the first time in 30 years (I'm 47 and saw the old guy when I had acne at 17!). It started as a blind pimple on my chest the week I increased Lamictal to 200mg (final dose), but didn't go away. It continued to grow (not diminish) over 4 weeks to 3/8 inch round/pink/solid/itchy/burn-when-rubbed. So off to the "Doctor" like my father used to do on a regular basis (I know I'm getting old now) and scalpel/pop/stitch it was out. But it was real, not my imagination or hypocondria, and the timing of its appearance was right when Lamictal changed to full steam. Since acne appears to be a common effect with so many, it seems it's not unreasonable that this occurs occasionally as well to others. Let me be the 2nd to mention it. No "official" verification, but....
I'm not bagging on Lamictal, and have been very hopeful that this would be better than Lithium. It has eliminated the GastroIntestinal problems I had on Lithium, but I am getting discouraged that it has all the brand new symptoms that are discussed in this blog. Your "stuff" is real. I wish the Docs/Nurses/Case Workers would spend 5 minutes checking your comments out. It might bring about a better informed conversation than the shiny Glaxo flyers provide. That is all.

Hey, I cycle, so who knows if some of this is the meds or the BP roller coaster..

What I do know:

• Memory Loss ***
• Rash like Poison Oak if I increase too quickly *12.5 mg
• Heart Racing + Mind Racing (part of all this right)

GROUCHY at work regardless of meds.

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 am 35, and my doctor recently prescribed me Loestrin 24 Fe to regulate my periods. (I was bleeding/spotting for almost 2 weeks out of the month) and to help with my PMDD. Well, I just finished my 2nd week of pills, and let me tell you, I feel horrible. I'm bloated, have gained 3 lbs(I'm on Weight Watchers, plus exercise 4 times a week) , have insomnia (I've never had a problem sleeping) I am extremely moody (just ask my poor husband and kids) and have more pimples now than I did as a teenager. Since I"m not taking the pill as a form of birth control, (my husband has had a vasectomy), as of tomorrow, I am finished taking this pill. I would rather deal w/2 weeks of bleeding, than the the emotional/physical roller coaster I have been on for the past 2 weeks. Just my opinion..hope this helps someone!

My mother is on Toprol-XL, and she has complained of being so fatigued, she sleeps so much, and this is someone who has always had a tremendous amount of energy. The other thing, and I would love a reply to this - she said she's experienced something at night while sleeping that feels like a seizure. She describes this as follows, "like my brain is shaking or trembling inside my head and my hands are trembling too." Has anyone else experienced this? Please let me know.

hi, im not sure what to do. my 3 1/2 year old daughter was today given the prescription for singulair. i voiced my concerns to the doctor after my friend telling me its no good due to the side effects.she said that there are risks and side effects with any drug you take but for some reason i don't feel right about this. don't doctors know better than this. anyway Would like to know if all the people who take singulair suffer some sort of side affects or is it minimal? or going by this side it looks like its probably best not to give it to her at all.

I am a 32 year old sane woman with a degree in Psychology. I was prescribed levaquin for walking pneumonia. This is day 7, and I am in tears because I truly thought I was having a psychotic break for the past 5 days. My roller-coaster of symptoms include emotional instability, paranoia, violent thoughts, thoughts of hopelessness and suicide, overwhelming gloom, facial numbness, insomnia, and the feeling of tingling in my mouth and throat. I am going to stop taking this medicine right now, and I've already called my doctor. I just wish I would have linked this to the only medicine I'm taking much sooner.

Hi all.

I just found this site and all of your posts. I *never* connected my Mirena with all the health issues I've been having. I've had the Mirena in since about August/September 2006. Within 6 months I started having side effects. Due to other things going on in my life I thought my problems were related.

Now I am seriously thinking it's all related to the IUD. I've had chronic fatigue, increased hair falling out, acne that won't go away, uterine cramping, pelvic sensitivity, mood swings, ridiculous irritability, decreased focus and concentration, increase in my depression, weight gain of about 50 pounds within 1 year, decreased libido down to next to nothing, increase in pain and length and frequency of migraines, and that annoying string. I seriously never related all these things to the Mirena. In fact, if you had asked me a week ago, I would have raved about it and sung it's praises. I do love that I don't have to worry about pregnancy and not having to think about the birth control every day and so on. I also love, love, love that I don't have a period at all but for maybe 2 times a year.

I have sought the help of a Doctor in trying to figure out what all these symptoms might mean. This is not the same doc who inserted the IUD, she quit the practice. My new doctor at first thought my thyroid must be messed up so we had it tested. Ummmm, nope. Then she did some more thinking about it and had me tested for diabetes. Nope again!

I'm sick and tired of feeling sick and tired and I think I want this fool thing taken out. I'd rather have periods again than have all these other things wrong with me. I'm normally very energetic almost to the point of being hyper and I now sleep about 16 hours a day. I'm not being a good parent to my daughters, and I'm trying to go to Nursing school and it's wrecking my ability to make it to class and get homework done. At this point I think the worse thing that can happen is I have it removed and nothing changes and I'm really sick with something we haven't identified. Best case scenario, it fixes the majority of these problems. I don't expect some things to go away. I've always had migraines, but maybe they will be less severe. I've had depression for as long as I can remember but maybe now it will go back to being controlled as it was before. I hope to have my energy increase again and to gain my focus and concentration.

I can't tell you just how incredibly thrilled I am for having stumbled onto this website and to be able to read all your comments and thoughts. Even though we don't know each other and we're likely spread all over the United States, and perhaps other countries, we've managed to come together and share. Thank you all.

Clarissa S.

I have itching, pain in the abdominal area, sometimes panic attacks, and sometimes drowsiness.
The pain I took it for has gone away now, but I still keep taking it cuz I feel like crap when I get up in the morning, runny eyes and nose, and an anxious feeling, with no energy. I take a perc and drink some coffee and I'm good to go. Think I'm addicted? I do.

moody/depression, stomach pains, lack of energy, some weight gain, but lighter regular periods

Yaz has been driving me crazy. I keep having these mental break downs and before my period I hate myself and everyone around me and just walk around and cry to myself and stressing out. I've had times of extreme fatigue as well, but that may or may not be due to the pill. I lost weight first, then put some on and my chest grew, then gained again, but lost in my chest. There are other side effects that I also have a hard time to blame on Yaz, but even doctors have very little way of explaining them. It's a horrible roller coaster for me since I switched from Orthotricylen Lo in AUG2007. I am jealous of those who have had a successful experience with Yaz, however, I believe I am NOT one of them.

I Have ms I just found out. They thought I had a brain tumor and the admitted me to the hospital and started treating me immediately with Prendisone.It has just been horrible do you hear me horrible!! after I weened off of them the moon face became horrible. I have knee pain and they swell. my legs and feet and stomach. I have swelling in my back that looks like a buffalo hump. It is horrible.please help me. I feel so unattractive I just cant help it. I am very grateful that it has helped me. I was numb on my entire right side that is another reason why they put me on it. I am glad that is gone, but I almost think I would rather deal with the numbness than I would all of this. It is really scary because nobody said anything to me about how it was going to effect me. Actually the nurses said that there were no side effects to worry about. well let me tell you it has been one roller coaster; i was pumped full of the Prednisone through an IV for thirteen days straight in the hospital,, then was sent home and was given the pill form. all together I have been on the Prednisone for 26 days straight. I will just be so grateful when all of this subsides.All I want for Christmas is to get this swelling off of me and get rid of the moon face and the joint pain. is that tooooo much to ask my goodness. I am so glad that I found this site. it has really been most helpful. I hope everyone out there has better luck with this than I have. it sounds like allot of people have problems. thanks

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.

I am glad to have read the post below me.

From the majority of posts on this forum, it makes it seem as though Yasmin is an evil poison that the medical community is using to destroy women. I was seriously frightened after reading all the comments. While I do believe all these women about the negative effects of Yasmin, there must be some out there who are pleased with this pill. Everyone's body is different. I have been on it for only 5 days now, so I can't really say anything yet.

I will report back after 3 months or so, unless I have gone bald, blind, insane and bed ridden with head-to-toe pain at that time. I guess that could happen but I really hope it will simply calm my awful menstruation and help my husband and I delay pregnancy while we work on being able to afford to at least take care of ourselves.

I have been on Loestrin fe 24 for 6 months for peri-menopause symptoms. It seems to work better for that than for younger women who are used to higher hormone levels. It sounds like to me, from reading above, that the dose is too low for child bearing women, and you're getting peri-menopausal symtpoms while on this.

My hormones were already low, especially my progesterone being 48, so this medicine gave me huge relief from mood swings, insomnia, mid month periods with terrible cramping and even lifted my libido just a tiny bit. It did not stop the hair loss. I never had complexion problems and never got any with this either.

After I had been on it for 4 or 5 months, I started getting the mid month cramping again, then almost every day, felt like I was having a period. The depression came back, just like it was before I started.. So I don't know WHAT happened. It felt like it did me good for a few months, then suddenly
I felt like I did before taking it and now I have gained 15 pounds!

I dont know if this was because of having to take Rhinocort for 3 months for allergies or what, it seemed to all go bad after that. Now I don't know what to do.

But from everything I have read, it does not seem to be the pill for younger women as it lowers your hormones too much. Peri-menopausal, yes it does have it's benefits because it lifts your hormones a bit and keeps them evened out during the month instead of the roller coaster which happens during peri.

Good luck
TD.