Lucky one symptoms and conditions

I have had no side effects!!
Well I have been taking Avelox 400mg for 5 days now, and had no side effects whatsoever. I asked my doctor to give me this prescription for upper respiratory infection, and after two days of taking it, I felt 200% better. It is now 5 days, I feel great, and not one side effect. This goes to show that what may be a terrible experience using Avelox for one person, it may be a great experience for another person. I was a lucky one that have not had any side effects at all. I have never recovered so quickly from taking an antibiotic in my life and I'm 38 years old. I do though recommend doubling up on a 30 day treatment of Acidophilus. This will help you replenish the Good bacteria in your body that was also killed off when taking a strong antibiotic such as Avelox 400mg. This antibiotic kills the bad bacteria causing the infection and the good bacteria in your body as well. Acidophilus after treatment is highly recommended. Other than taking Acidophilus after the treatment, I found this antibiotic to be the best that I have ever taken. Take care, Joe.

Never had any problems with my mirena and i'm very surprised to read all the above complaints. I guess i'm a lucky one of the bunch. I had Mirena inserted in November of 2006 and still going strong. My hair is beautiful, I did gain some weight, but I like it i've always been skinny! I can't imagine having all those negative side affects. I also experienced mild acne at times, but who doesn't? Best wishes to you all and hopefully things workout.

Well ladies, after reading about all of your experiences with mirena, I'm a little concerned to say the least. I have had mirena inserted for about 4 months now and really haven't had any problems with me personally. I did check out the website to see if any of your husbands/boyfriends had any complaints. My husband said that he could feel the strings during intercourse and they were painful. I went back to my ob/gyn to have her trim them but they are still "pricking" him. My libido is great but what good is that if my husband is afraid to have sex with me?? Anyone else having this probelm or am I the lucky one?? By the way, insertion was absolutely painless for me but I am 32 with 2 children

If you are considering getting the Mirena don't read this site it will scare the hell out of you....lol I believe every person is different. I would say about 95% of the comments on here are negative so I decided to give my experience. I had my IUD inserted about a 1.5 month ago. Really the insertion process to me hurt like hell, but it was worth a try if I would not have a period for years at a time. The day after insertion cramping was barable. I still continue to have sharp cramps every now and then, but from my understanding my doctor said this may occur up to 6 months. I had a very light 2 week cycle after insertion. I have not experience much spotting since then. I have NOT had many of the symptoms like hair loss, lack of libido, acne. I did experience a bit of depression due the transition from the pill I believe.

My experience with NuvaRing

I started NuvaRing when I was 40 years old and got married not to long ago. I have two kids and they are in there late teens. My new husband does not want to have any kids, so I've been on NuvaRing for two years because I was always really bad about remembering to take the pill so the NuvaRing is GREAT for me and I love it!!! It's very convenient, being able to just forget about birth control for a month. But for some reason I think that I got a hold of a bad batch and I am having problem with them. If you have experienced the following symptoms, please consult with your doctor:
Depression: because I thought that I was pregnant, so I hit an extreme low.
The first time I used the ring I had itching, discharge, burning and yeast infection.
Headaches, Mood swings, bloating, gas, cramps, emotional, pelvis pain, hair loss, my vision has change, constant fatigue and lack of motivation and I have gained about 20 pounds. I get headaches all the time. I'm CONSTANTLY tired, but I do have to get up to go to work. My experience the first time using the ring was an infections and burning and it went away after the second time I used it. I didn’t know the ring was the cause of the infections it until now. After two years I have been passing blood clots and bleeding know for three weeks, I even thought that I was pregnent and I lost the baby and for three days and I was very diprest, afraid that I really miscarried a baby and on Friday I took a pregnancy test and it came negative. I made an appointment with my OB/GYM doctor and he also did a pregnancy test and it came negative and we didn’t know the reason why I was bleeding for so long and he also gave me medicine to stop the bleeding and also gave me iron pill for my anemic, since I lost so much blood. He told me he would do some test and find out why I am bleeding so much, so he did other test and schedule a Tran’s vaginal ultra sound sonogram test. The doctor found out that I have 3 fibroids in the uterus and the doctor suggested having D/C uterine scraping, so that I don’t get any cancer in my uterus. I talk with my husband and also decided to do a hysterectomy. Surgery went well, I am still here. I schedule the surgery on a Friday and back to work on Monday. Now I am concentrating on getting better and try to loose the weight. NOTE: I have read that soo many of you have problems in the libido or sex drive. I never had a problem in that department. I meet a great man and we both love having sex, before I started the NuvaRing and during using the ring and after the operation have not lost the edge of having sex two to three times a day. I think many of just don’t find the time, too busy with work or busy with the kids, lost that loving feeling. I am too in love and love doing it.
I hope this was helpful.

Okay...so I first posted the day I had Mirena inserted, Oct. 1. ( and had wished i found this site prior to installment)
It has now been two weeks. So lets up date:
I bled for only a few days, maybe 5 days tops. Which was great, I just thought " hmm maybe I'm a lucky one, maybe they put it in right, or maybe my body is handling it better than I though it would" But then 5 days later I started bleeding again.
Like I said, I have had this thing in for TWO WEEKS.. and I've had sex.... TWICE! I don't even want to have sex, no wonder it is so good for birth control.
The first time was great. My boy friend didn't feel anything, and was enjoyable for the both of us.
Needless to say, the second time was great... until it was over.
The second it was over, I was doubled over in pain. Literally, 30 seconds after sex, I had a severe hot flash, and felt like i couldn't breathe. I started shaking, and started crying. I felt like the " insertion part" was happening allllll over again. ( insertion, is miserable.. that alone makes me not want to recommend it to ANYONE) I thought i was going to pass out, and standing felt impossible, I couldn't even roll over. A few minutes later I stood up and went to the bathroom, I was nauseated and felt sick. I tried to pee, and couldn't. It just burned and felt like my whole body was trying to squeeze this thing out.
I went back to bed and layed there for about 45 minutes in agonizing pain. My fiance was so sad, he felt completely guilty that he "caused" the pain... he thinks it should be removed immediately. And so do I.
The one word to describe this pain was INTENSE.

To add, I have noticed dry, itchy skin. And my skin is now sooo fragile. My scalp is sooo itchy that when I scratch I actually bleed and scab.. it is DISGUSTING. And yes, my hair is slowly getting worse. Everyday I notice a little bit more shedding than usual. My complexion is not getting WORSE, but the few pimples I have are deep, painful, and are actually scaring. Never before did I scar.

I also feel the extreme fatigue, and occasional mood swings, I will admit, I have Always had an attitude but this is a little more than even I am willing to except.
I have not gained any weight, but it's only been TWO WEEKS and, I have intentionally weighed my self everyday... and I am now fluctuating 6 lbs a day in water weight.My belly is 23/7 bloated. The only time I am not bloated is after the first pee in the morning for about 45 minutes, and then it starts allllllll over. People have noticed my fingers are chubbier, and are sore. For 2 days my toes and feet were a light blue-ish color... that "symptom" was enough to make me WANT to go to the E.R. but I opted not, as there was no discomfort.
A major discomfort, like i said was sex, and the random times throughout the day when I bend over or wiggle into a chair... it just feels like it is STABBING the right side of my body. There is truly no comfortable way to sit without favoring my right side.
It is weird, painful, and is getting really old.
I tried calling my doctors all day today, and it was still left on their " night time recording" so, I am a little angry.
I thought about pulling it out myself, but this time I read " REAL PEOPLE INFORMATION" and apparently its not a good idea. SO DON'T, if your thinking about it. lol.
Anyone that has had it removed, is it painful? Does it feel anything like the insertion? I am scared to death.. and I am a little upset that i have to continue to wait to get through to my nurse practitioner. I just want this to be over with. The last thing I need is to have it get " lost" like so many other women.
I tried, but I'm listening to my instincts, and this just isn't right.

my acne has gotten a lot worse. I never had zits in highschool and stuff i was a lucky one but since i started these its just out of control. The kind of acne thats like 3 zits in one spot and they hurt. It also seems like im more emotional than i was before im not 100% that its the pill doing though.

Doctors should realize that we continue to learn something new every day. Nobody should ever believe that we know the answers. Everything should be constantly questioned.

My life is an example of "who knew" but I am the miracle, the lucky one. I was born pre-mature, very small for almost 60 years ago. Another baby was also born on that day pre-mature. We were placed in the incubator together. No one really knew the dangers of oxygen levels and the eyes. The baby who was next to me has lived as a permanently blind -- never saw anything about the world. I somehow never opened my eyes. I wasn't breathing well and was more knocked out. But one baby lived normally and the other didn't. So there will always be a "who knew."
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I have been concerned that the fact that Singulair binds with a leukotriene receptor on the mast cell and blocks one of it's function has possibly opened up a pandora's box of other problems. As I said before, there is communication between several receptors on the mast cell that determine how it performs it's normal function. I finally found an abstract written pretty clearly that does reference some of these concerns.

J Allergy Clin Immunol. 2004 Jul;114(1):21-7. Links
Mast cells in innate immunity.Marshall JS, Jawdat DM.
Dalhousie Inflammation Group, the Departments of Pathology and Microbiology & Immunology, Dalhousie University, Halifax, Nova Scotia, Canada. jean.marshall@dal.ca

Mast cells have been most extensively studied in their traditional role as an early effector cell of allergic disease. However, in the majority of individuals, it might be the role of this cell as a sentinel in host defense that is most important. Mast cells have been repeatedly demonstrated to play a critical role in defense against bacterial infections, and evidence for their involvement in early responses to viral and fungal pathogens is growing. Mast cells are activated during innate immune responses by multiple mechanisms, including well-established responses to complement components. In addition, novel mechanisms have emerged as a result of the explosion of knowledge in our understanding of pattern-recognition receptors. The mast cell shares many features with other innate immune effector cells, such as neutrophils and macrophages. However, a unique role for mast cells is defined not only by their extensive mediator profile but also by their ability to interact with the vasculature, to expedite selective cell recruitment, and to set the stage for an appropriate acquired response.
Copyright 2004 American Academy of Allergy, Asthma and Immunology

In other words, mast cells play a key role in the development of the immune system. The child's immune system is changing and developing every day. If we block one of the mast cell's receptors, what are we doing to the entire system.

I have been looking for studies that addressed the long term effects of Singulair on the immune system in other animals like pigs. I am still searching.

I've been on Topamax since Sept 2007 and the only side effects I have had were at the beginning were the tingling in the hands and feet when I was brining my dosage up. Soda tastes awful but I no longer drink it and that is a godsend after being a heavy drinker of it for years. I do find there are time when I can't find the right word to say, or I forget what I was doing, but I deal with it. I have lost 20 pounds since being on the medication. After being on it for 6 months the tingling is gone, I usually counteracted it by drinking plenty of water in the morning, that got rid of it. The drug has taken away the migraines, and regular headaches I have suffered from for years. It has also stabilized my moods and taken away my anxiety issues. I'm 36 and have never felt better. Topamax is definitely not for everyone. For those that are suffering, please do contact your doctors and try to get off the medication.

I have read a ton of the posts in this category. I have been taking Lisinopril as an addition to my regular blood pressure medication for approximately 3 years, with absolutely no problems. My 10mg was increased to 20mg a week ago. Still no problems. It has only helped me. If there are any changes, I will definitely post it. I believe that symptoms can arise from reading an article. I actually know a couple people who read things, and suddenly they are convinced they have the problem or disease referenced. I call it an Epidemic of Diagnoses. Always seek a doctors advice before stopping medications. Stopping suddenly on certain drugs, can be more dangerous than taking them.

This is all very interesting, but it's all anecdotal! Can you PROVE that Singulair is responsible for all this stuff?

What other meds are you all taking? In what doses? Under what conditions? Do you have a family history of ? Are you under stress? Or are at least SOME of you just hypochondriacs who, reading this stuff, say to yourself, "Say, I get headaches -- sure, it's gotta be the Singulair!" C'mon, now -- hair loss?!

I've been taking Singulair for over 10 months, and if I'd been as damaged as you all, I think I'd know it.

Without rigourous medical studies to show what is REALLY going on, you lot are just gossipping.

This site is obviously trolling for a class-action suit.

I have been on 10mg eoday prednisone for years to counter my psoriatic arthritis. I guess I'm the lucky one because I've had no side effects. Psoriatic arthritis is like rheumatoid, but has skin problems associated. A round of arava kicked the arthritis into remission and the pred kept it there, and I've been pretty happy. I decided to try to get off of it, but now all of my joints ache again, so I'm deciding to go back on--although, you-all are scaring me! Maybe I'll rethink this!

I was prescribed Levaquin (500mg x 10 days) for bronchitis and ear infection. I'd already taken heavy regimen of Augmentin a few weeks prior, but my symptoms only abated temporarily and then returned 'full force'. My case is a little different from the typical poster, as I was not ignorant of the possible nasty s/e of this drug. In fact, when the Levoquan was first prescribed for me, I read this message board (among others) and was scared enough by what I read that didn't start this medication right away. I went back to my MD to discuss my concerns; he acknowledged that some people do experience some bad side effects from this drug but indicated that these effects tend be pretty rare and didn't think I would have a problem - given my age (32) and otherwise good health.

After waiting a few days and debating whether to try this medicine, my upper respiratory infection worsened and my ear pain became so tormenting that I finally decided it was worth the risk to at least try Levaquin...hoping I'd be one of the lucky one who experienced few, if any, side effects.

After taking the first pill yesterday, everything seemed fine for several hours. In fact, I almost immediately noticed improvement of my URI and ear ache. However, last night before bed I noticed that both of my knees felt swollen and walking felt uncomfortable. I also noticed an audible "clicking" sound in my knee joint when using stairs. Today, I called my MD to report my symptoms. My doctors nurse called me back and suggested I not taking any more doese until she was able to discuss this matter with the doctore (who was out of the office but due to return tomorrow). By the time the nurse gave this advise, I'd already taken the second dose of Levaquil earlier in the day. Tonight, my knee pain (especially right) is much worse and it hurts to get up and walk around. I'm starting to feel like an old man. I've never had any joint problems or tendonitis prior to taking this medication. Tomorrow I intend to ask my doctor for advice. I don't plan on taking any more of this medication. I do fee a little conflicted though, because now after taking the second dose of Levaquin, my upper respiratory infection seems almost gone and my ears have completely stopped aching.

If anyone has any suggestions, it would be appreciated. Should I expect that my knee pain will resolve in a few days after stopping this med? Again, I'm a health 32 year old male, and hope that this drug hasn't done anything irreperable (sp?). Thanks for listening.