45 years symptoms and conditions

I am 45 years old. I have had Mirena out for 3 weeks now (had it in for 9 months). At removal I went right back on the BC pill so there was no break in hormone levels. I have never had problems with the pill. I know some of you cannot use them. But for those who say "I just can't remember to take it every day..." consider the alternative of getting this IUD or keeping it inside you. The side effects alone are not worth it. In 3 weeks time that horrible facial/body acne has cleared up, the bloating is gone and my jeans fit much better although I'm not sure I've actually lost weight. A lot of it was just inflammation. The emotional issues just seem to have "vanished". I feel happy again. Imagine that (sarcasm intended). Libido much much better, with no pain or cramping. I started my period for the first time just this week. I thought it would be the period from "hell", getting revenge on my body for not having one for so long. But so far it is fine, and I'm glad it's back to tell the truth! Instead of spotting all the time or who knows when, I'll go back to light periods 3 days a month. Again, it beats the alternative. And a trick to try for taking the pill: put the pack somewhere around your bathroom sink area (away from kids of course) and just take it every morning after you brush your teeth. I mean you never "forget" to brush your teeth in the morning, so take the pill right after you rinse! It never fails. Also, you can tell yourself that if you did have a serious medical condition that required daily medication, insulin, for example, you would be good to your body and make it a priority. As long as the pill doesn't give you any problems, it's 99.9% effective and makes your periods very short and light, but predictable and right on time. No awful surprise breakthrough bleeding. The reliability of it is great. You just have to TAKE it. I'm only writing about the pill because it is the only other option I've tried and it worked well for me. If it's only a matter of inconvenience, try the toothbrush trick. It really works! Hope this helps some of you who are looking for other alternatives. Good luck!!

I am 45 years old. I get the impression many of the ladies here are younger, as they speak of having younger children, so I will tell my side from a bit more "mature" (ie older!) perspective:

Had Mirena for a little over 9 months. My two MAIN side effects were a development of terrible cystic acne on my face, back, shoulders, hairline, behind my ears and straight down my spine, ending in a nice lovely rash just above my tailbone. These things were deep, solid knots under the skin, not average little pimples. Worse acne I've ever had, and at my age too!

Second, profuse sweating under my breasts and lower back, again just at my tailbone, right above my butt. After drying off from a shower, I'd run my hand back there and still feel soaked. This did not seem related to hot flashes. Just sweating, and I think that contributed to the acne, which was beginning to leave scars it was so deep.

I do feel like I gained weight, my pants were much tighter and I just felt bloated all the time.

Fortunately, no hair loss or emotional side effects. I've had anxiety for years and take Ativan (lorazepam) which keeps it pretty much under control. No loss of sex drive either. It seems there are a distinct set of side effects, and some get them in different combination than others, but we're ALL getting them one way or the other!

OBGYN said as the Mirena is only progesterone, I was missing the estrogen which were the 2 components of the pill I took for years with no trouble. He gave me a Rx for a low dose of estrogen. Now I am getting what I had in the pill in 2 separate forms, and having these awful side effects on top of it. It didn't help.

So I had Mirena removed 6 days ago. Luckily he found the strings, told me to cough, and pulled it out, no pain! I immediately went back on Alesse BC pill that same day, so no break in hormones, but I handled the BC pill fine all those years, so I"m just going back on it. Have been bleeding ever since removal, but I figure that is just my body "getting back at me" for not having periods for months. My first real one, due in about 3 weeks following the pill schedule will probably be the period from hell. Ok, I accept that. My uterus wants to get this poison toxic mess out of me, and I'm ok with that.

I'm crossing my fingers that I will miss the "crash" I've read so much about. As it seems to be mostly psychological, and I didn't have those side effects to begin with, maybe it won't be so bad, or at all. Of course that could just be wishful thinking on my part! So far, 6 days of having it out of me and I already feel 100% better! My face cleared up in a matter of days. The sweating stopped immediately. My pants are looser, although I still weigh the same. The bloated feeling is gone. I just feel thinner. Before, my profile in the mirror looked like I was 4 months pregnant! That too is going down quick. Good luck to all who have it removed. Things can only get better!

And don't let any doctor tell you you can't have it out! It's your body! You can demand whatever you want, especially if you feel like it is making you sick! Do not take no for an answer. You don't even owe them an explanation. Just a "Sorry, it's not for me..." at the most.

Good luck to all....

I'm 45 years old and I have been on Nuvaring for about 2 years, and I think I will stop this month when my cycle is over. I have had severe depression, mood swings, crying incessantly at times, mad about everything, wake up in the middle of the night, hot flashes (that's probably pre-menopausal), but for the most part, have had weight gain, insomnia, and a lot of the other symptoms other people on this board are describing. I'm not going to have kids, so I think going back to condoms will be the best option for me and my spouse, he's been very worried about my mood swings lately, as they always happen the week before I take out the ring. When I asked my doctor about it, he said that's probably not the cause, but he's not experiencing what I am going through, so I have to attribute this problem to the Nuvaring. I have also lost all my sex drive and have dryness and need lube for intercourse, which never happened to me until I got on the Nuvaring, I'm done with this crap too!

I started using Yasmin one month ago after using Yaz for a year. I had no problems on Yaz, but have had a multitude of problems that I believe are related to Yasmin. One of the side effects I'm having that I don't see listed by anyone else is insomnia. I am 45 years old and have never had any problems going to sleep initially or when I wake up to go to the bathroom in the middle of the night. Before Yasmin, I would get up once in the middle of night to urinate, and now, I'm getting up 4 or 5 times a night and then sometimes, it takes me an hour to go back to sleep. I have also been feeling depressed and more anxious than usual. During the second week of Yasmin, I had gastritis that lasted for about a week. Gastritis is something I typically get 3 or 4 times a year, but I'm thinking it's another side effect caused by Yasmin. I've also had more nausea and bowel problems this month than normal. I have breast tenderness and I had unexplained rib pain for a few days. Finally, my belly seems to be more bloated than normal. I have an appointment with my doctor tomorrow and I WILL be switching to another pill.

45 years old, female, diagnosed bipolar II in 2006. On Lamictal for 2 years. Initially, very positive effects of Lamictal - felt "normal" and stable for the first time in years. Didn't notice any side effects. Gradually increased from 200 to 400 mg per day 6 months ago as I still experienced mood swings with a tendency towards depression. I have been on 400 mg/day since August 2008. It is difficult to say what are the side effects of the medication, and what are "natural causes". Since doubling the dosage, I experience memory loss and increasing cognitive problems (slow thought process, difficulty putting together coherent sentences in discussions, fumbling for words. I have spent more than one hour on this posting!). I sometimes wake up during the night drenched in sweat. It could be that I'm menopausal, but I find it unlikely. Mood swings have perhaps become less pronounced, but I would like to regain my mental capacity. I plan to cut back to 200 mg of Lamictal - and perhaps some day learn to live with bilpolar II without medication and a lot of help from my friends and loved ones.

I am a male 45 years and used simivastin another statin for three and a half years. Over this time i had severe muscle pain at time then about 4 months ago the muscle pain in my legs came on with a vengeance. It started in both thighs then calfs got very tight sore ankles feet and eventually got in to my arms. A deep achey sort of a pain and an irritability that casesa feeling like a toxin in my inside elbows that makes me want to stretch all the time. I feel very weak compared to my former self. I tried many things to alleviate the pain but nothing really took the pain away or even decreased it much. sometimes i would lay and groan in agony. I especially noticed that draghts and weather changes made me feel worse????. I stopped taking the simivastin 6 weeks ago. I have not had a lot of improvement but must admit thet i have been trying to push my self over this and probably done more damage. My ck levels are normal but my liver enzyme is increased a little. I started also to take q10 and L- carnitine along with magnesium. I might be improving a little each day but nothing definite. I saw a rheumatologist who has no diagnosis and isn't to committal on whether the statin is to blame. He put me on celebrex which has finally given me some relief. Can anyone relate to the worsening of symptoms with cooler changes in weather? and is there anything else i could do to hasten recovery? Thank you to all contributors on this board although it is the first time i have contributed this board has been a scores of help to me.

I began having right hip pain a month after the mirena was inserted. I assumed it was from running. All the doctors I have seen for the past year stated I strained a muscle. They ordered MRI's and physical therapy. I have completed all, but still have the same hip pain-over a year now. Has anyone had hip pain due to the mirena? And did your hip pain stop completely after your mirena was removed? I am considering getting it removed. Although the doctors tell me they are not connected, I can't help but think there is a coincidence.

First off, your OBGYN is a moron if they told you it only takes a month to adjust to the pill. It is more common for the body to regulate to the pill at a minimum of 2 months and 3 months is not uncommon. So it can easily take 3 months for your body to adjust to your pill. And sometimes longer if you were on another pill and switched to another OC.

Amenorrhea(no Period) can happen on Loestrin 24. Notice the first for letters of amenorrea are AMEN. Is that a bad thing? To put this in the most basic lay terms....Birth Control tricks your body into thinking its pregnant. Thats it!!! Do pregnant women have periods? ..Of course not.

Regarding your lack of sex drive comment...that is ridiculous. The progestin in Loestrin 24 is norethindrone acetate. That is androgenic...it is one of the few pills that increases your sex drive.

I suggest if you want a pill that lowers your sex drive try yaz or Yasmin. It is anti-androgenic and lowers sex drive. It also is the ONLY pill that has extra warnings by the FDA for hyperkalimia. ...basically extra dangers if you take it my Advil, Tylenol or ANY NSAID. REMEMBER THIS PILL HAS only been around for 10 years and has been tied to several deaths in Europe. Google search yaz or Yasmin +death.

Loestrin has been around for 45 years. tried and true.

ALSO if anyone is a smoker and takes birth control you are guaranteed to have Bleeding and spotting.

I have had the Mirena for four months. I am 45 years old and finished having children. I cannot take the birth control pill because I'm a smoker. I talked with my physician about a tubal ligation versus Mirena. She actually recommended the tubal ligation but I was afraid of the general anesthesia. However, after the side effects I have experienced, I will be calling my physician soon to schedule a tubal ligation and have the Mirena removed. I have always been fortunate to have three, light days of a period each month. After the insertion of Mirena, I have 20 days or more a month of spotting which necessitates the wearing of a mini pad daily. I would rather have three days of light bleeding every 25-28 days than 20 days of pesky light spotting. Also, my knees are killing me. I feel like I'm 95 years old. I can hardly walk up and down steps without pain. This was not an issue prior to the insertion of Mirena. Within the last couple weeks, I've noticed an increase in acne. I have NEVER had acne problems so the three or four zits on my face now is very unusual and I can only attribute that to Mirena. I guess I need to overcome my fear of general anesthesia and get those tubes tied and end my birth control woes!

My husband is 46 years old. He has been taking Lipitor for over 8 years. He has had several of the side effects mentioned. He has had memory loss, pain in his feet and joints. He also has had problems sleeping.

In the past two months he has developed a rash. It first started on his left leg. He went to his doctor and told him of his problem. The doctor told him to just try an over the counter medicine for rashes. He tried this and it did not help. The rash is now all over his body. He has been going to a skin specialist for the last three weeks.

The doctor took him off of the Lipitor and the rash has started to clear up. It is going to leave black spots all over his body. Has anyone else out there had any of these side effects?

Hi. I went on Lamictal April 2007 after being diagnosed w/ BiPolar. The key issue that brought me to the psychiatrist to begin with was acute depression following a divorce, move cross country, losing my job and my only son going off to college. All the big stress factors - short of death in family. Nonetheless, I was nervous that one year after all these crises that I was, if anything, feeling worse. I had been able to handle all the changes during them, but now that they were over all I wanted to do was sleep all day.... Anyway, I had been on Paxil for years re anxiety, and my psychiatrist decided to keep my on the Paxil till I tolerated the Lamictal, then get me off the Paxil..... Well, the 20 mg of Paxil and the 100 mg of Lamictal worked great, I thought; the Lamictal really raised the bottom.... BUT, apparently Paxil fuels mania, so after a few months, I was taken off the Paxil completely and my Lamictal went up to 200 mg. Almost IMMEDIATELY upon going to 200 mg Lamictal my ankles / feet / legs got enormously swollen. Plus, I noticed that my hair started to fall out // thin out.... Plus -- and I don't know if this is the Lamictal or the absence of the Paxil, but I sob uncontrollably almost 24/7. The sobbing and anxiety and sense of dread and sadnessness has persisted even when the Lamictal was dropped to 100 mg and the shrink added first Clonazepam .5 mg, then when that wasn't calming me, changed me to 1mg Xanax -- each as needed. The Xanax isn't helping me either, and now I also feel paranoid. So, in short: Lamictal at 200 mg makes my feet / ankles / legs swell or suffer edema; Lamcital as low as 100 mg makes my hair thin out; and either the Lamictal or the loss of the Paxil or these anti-anxieity meds (Clonazepam or Xanax) are making me paranoid, profoundly sad and depressed, panicked, anxious, stressed out and, most urgently, make me sob uncontrollably 24/7... My shrink says that we should use anti-depressants with bipolar, and that Paxil fuels the mania, but I tell you, I'd rather be manic and screaming at everyone than so depressed that I'm fearful and sobbing constantly.... Any answers out there: Any anti-depressants for your bipolar?

Right after I started taking Lisinopri in May 2007, I had a major flare-up of my Psoriasis. I have had Psoriasis for over 35 years and it was only in certain areas, now it has completely spread over my entire body. I also have constant ringing in my ears, never thinking it could be related to the Lisinopril. Sometimes it works to lower my blood pressure and other times it seems not to help. Occasionally I experience dizziness. These are all symtoms I never had before, I am not overweight and do not smoke. I had been healthy except for borderline hypertension prior to taking Lisinopril. I am not taking any other medications. My dermatologist is pressuring me to start Raptiva and I have agreed, not realizing that maybe just stopping the Lisinopril might ease the symptoms of my psoriasis. I just started researching Lisinopril in the last few days when someone I work with casually mentioned that there may be a link between Lisinopril and Psoriasis flare-ups.

I also am having a difficult time with memory loss. I have a very short term memory. I never used to be this way. Before I started taking Lamictal, I was taking Depakote. I haven't been on Lamictal for that long, so I do not know if my previous medications have caused my memory loss. I also get dizzy sometimes and I'm feeling out of breath lately. Some other medications I've taken are: Zyprexa (which gave me type I diabetes); Abilify; Risperadol; Adavan...the list goes on, unfortunately. I have been taking anti-psychotic drugs since I was 16, and I am 37 years old now. God help me!

Hi everyone, I have been on Loestrin fe for 8 months and I am 45 years old - taking the pill again after a four year absence. I have found that all of the posted side effects are true - but are greatly minimized by taking the pill EXACTLY at the same time every day.... if you are off by even a half hour you WILL have breakthrough bleeding - sometimes with clots and with drawl-like headaches... my gyn says no way - but I actually tested my own theory this month - much to my regret - I am right... I am ready to quit as I am at the end of my rope. Fortunately for me my blood count has come back into the normal range after the last two years of horrific bleeding every 11-26 days without a break.

I am going to go off next month - and I may have RESET MY SYSTEM so to speak - if no I will take a hysterectomy please... straight up with a tummy tuck to match!!!!!!!!!!!! Please email me if you ever want to discuss - I am a nurse anesthetist and have a great deal of sympathy for all of you out there. I am not sure if this drug is a bad one - but I think it is so low dose that timing must be precise for it to work properly. I have stayed on it only to reduce the bleeding (perimenopausal/estrogen dominant I am sure) twice a month periods that last 7-8 days. It has worked for me in that regard - but the first 7 months were plagued by horrific (and I mean really bad) right sided headaches that scared me. I had relief from NSaids (Motrin) so I almost overdosed on that stuff. Not good. My next strategy is to do saliva testing for cyclic hormones OFF the pill to see what kind of hormonal swings I really am having - and to adapt a more natural approach - possible progesterone cream to alleviate the misery of it all....
Much Love, Ellen M

I am 45 years old, just started to take Singulair, seems to be working OK, but I get a constant dull ringing in my ears...Starts to go away by the time I need to take the dosage again....but comes back an hour later after taking dosage.

I have been on Levothyroxine 50 mcg
for six months I have really bad leg cramps
and in the morning when I wake up I can
barely bend my ankles to walk I am 45 years old I have also gained 10 pounds since
I have been on this medicine. My Doctor is sending me for more blood test, she says
it may be hormonal.
A.R Chicago

I have been taking Topomax for quite some time.Tried it several years ago, the mgs were not high enough (only 25mg/day).My doctor didn't really know the prpoer dosage.It didn't help the migraines.My new doctor has me on it again.50 mgs/day.Here's the good - NO MIGRAINES! Here's the bad: Acne at 45 years old, tingling doesn't even describe my legs or face, ringing in the ears, remembering names and places just doesn't happen, I'm eating less but gaining weight quickly,& one last thing- Itchy spots that I would describe as "hot spots" if I were speaking of my dog. Still sticking with it because I don't have the migraines.I tried to slowly take myself off and the headaches came back.What choice is there?

I HAVE BEEN TAKING LEVOXYL FOR 22YRS AND I FEEL LIKE I CAN NEVER GET SLEEP,I TAKE MY PILL IN THE MORNING AND CAN'T SLEEP ALL NITE AND AM TIRED OF IT,I WISH THEY HAD AN ALTERNATIVE.THAT WAY I CAN SLEEP AND NOT BE DEPRESSED ALL THE TIME

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

I went for a physical in about September of 2000 because i was going to go back in the gym and workout.... Doctor said i was very healthy but did prescribe Levaquin for a small amout of Fluid on one lung he said showed up on an Xray... I think i took two maybe 3 of them but was sick the next day... He worked with me for the next 4 months trying to figure out what happend. Then i finally had to go to a specialist/Rheumatologist becuse i was loosing weight, tired and very tired, no appetite, sleepy etc... finally i was diagosied with Lupus Myositis (not sure about some of the spelling). Anyway i have been battleing with this from Sept. 2000 until now... August of 2007... I do pretty decent most of the time but am tired alot and cant do the things i did before... I am now 45 years old...

I was diagnosed with asthma 8 months ago at 45 years old. It was quite a shock considering I never had sympthoms untill recently. The doctors thought that abulterol would be enough to control it but unfortunately the events become too frequent. They then swictched me to Singular. Wow, what a mistake that wa! Yes, my breathing improved but the side effects were frightening and painful. After only two or three days my arms, hands and fingers were numb and tingling...constant pins and needles...and virtually useless. At night I had the worst most vivid nightmares I've ever had. And I was unable to fall asleep because my mind was constantly racing. It's almost enough to make one psychotic. Plus I had sudden, very painful ear and tooth aches.

All this cleared up a few days after stopping Singualr.

This drugs is suppose to interfere with your body's signals to produce inflammation but it has to be doing so much more, and most of that not good. It seems clear based on my side effects and others I've read about it has a huge impact on the central nervous system too.

This is not a safe drug. I wouldn't be surprised if someone, some day uses it as an excuse for some really bad behaviour. In fact, I'm shocked that this is given to kids at all. If I had to take this for months I would go insane.

BTW, months later, on advice of my doctor, I tried it again with the intent of taking it every other day to limit dose. Nice idea, but no cigar. After just one dose I was once again "flipping out" in bed.

If you have really bad asthma and singular works for you without side effects that's great news. But I'd still ask myself what kind of impact is it having on your body if it does so much damage to so many other people. How safe can it really be?

If you have kids, and they're taking it, please keep a close eye on them. Sometimes kids don't have the communication tools to explain to parents what they're experiencing. Don't make them suffer...and don't let them be punished at school because their behaviour is uncontrollable. It could very well be this med.

I was on Celexa for a year and a half and gained 40lbs!!! Has anyone else experienced this? It was a great anti-depressant but did make one somewhat lethargic. I also kept having small fits of depression here and there despite the meds. I just switched to Wellbuterin and its making me alternately spacey and moody, but i've only been on it four days. Does it get better?

I HAD BEEN ON 80MGS. OF PREDNISONE FOR TREATMENT OF SEVERE SORIASIS. IT WORKED WONDERS FOR THE SKIN CONDITION. , I WAS SPEEDING MY BRAINS OUT , AND GOING 100 MILES PER HOUR. IT WAS SOMEWHAT EUPHORIC. I AM 45 YEARS OLD AND HAVE BEEN IN MENOPAUSE SINCE MY LAST CHILD WAS BORN 5 YEARS AGO. AFTER I TAPERED OFF THE PREDNISONE OVER A MONTH PERIOD... I STARTED TO HEMMORAGE. I HAD UNCONTROLLABLE VAGINAL BLEEDING, BLOATING , PAIN, MOOD SWINGS, DEPRESSION, ETC. THE BLEEDING DID FINALLY SUBSIDE AFTER BEING OFF THE DRUG FOR 10 DAYS. HOWEVER , NOW THE SKIN IS DETERIORATING, AND THE JOINT PAIN IS EXCRUCIATING. I CAN BARELY WALK. I AM A DANCE TEACHER, AND THIS IS BECOMING DEBILITATING. I ALSO HAVE A CANCER HISTORY, AND THYROID DISEASE. IT WAS AND IS ROUGH. I GUESS I HAVE A CHOICE BETWEEN HAVING HORRID, DISGUSTING SKIN ( AND UNABLE TO GET A PUBLIC JOB) AND BEING EMBARRASSED ALL THE TIME AND DEALING WITH THE VERY DIFFICULT SIDE AFFECTS OF THIS MEDICATION. I AM HOPING FOR A BETTER ALTERNATIVE. THE SUFFERRING IS UNBEARABLE. LIBBY B.

I MYSELF HAVE NEVER TAKEN PITRESSIN HOWEVER MY GRANDMOTHER WAS ON IT FOR YEARS TO TREAT HER DIABETES INSIPIDUS. NOW 45 YEARS LATER HERE I AM TRYING TO FIND OUT WEATHER THIS COULD HAVE CAUSED THE HEARING LOSS OF MY MOTHER AND MY TWO AUNTS AT SUCH A YOUNG AGE. IF YOU OR ANYONE HAS ANY INFORMATION ON THIS MATTER PLEASE E-MAIL ME BACK.
THANK YOU
ERICA ***

i have been on advair since august o5, i have gained a lot of weight, i am in extreme pain at all times, i can hardly get out of chairs & out of bed, because of the pain im in, my hands go numb With hot tingling sensations, & have to walk with a cane now, & can barely stand for very long!!! i have c.o.p.d. & im on 250-50, the only good thing is i can breathe!!! im 45 years old, im gonna try & stop this medication, i dont know what will happen, but i guess ill find out.....................