Aspirated symptoms and conditions

I had the Mirena inserted in March of this year (2008)! I hate it! Shortly after having it inserted I developed huge painful cysts on my ovaries. The doctors insit that the Mirena didn't cause the cysts but b/c there isn't enough hormones in the Mirena, they cyts aren't going away on their own. I had the cyst aspirated which caused the remainder of the fluid to leak out causing an infection in the lining of my abdomen. They put me on a heavy dose of antibiotics and hormoned to get rid of the cyst. For about a week I felt better until the pain came back worse. The cyst had not only come back but gotten bigger. I have to take a double dose of birth control pills now to get rid of the cysts.
For the past week I have been having pain again and not wanting to tell anyone b/c I know they are just as tired of this as I am! I can't sleep at night which makes it nearly impossible to get through the day. My doctor had given me pain medication the first time I had the pain to sleep at night but they are gone and I'm afraid to ask for more at the risk of sounding like a drug addict! I can't take these pills during the day b/c they make me loopy and tired and I am a single mother of a 3 year old little girl plus I work full time! What kills me is the that I had the Mirena inserted b/c I can't handle the extra hormones or remember to take the pill everyday! I can't deal with it anymore. I have gained almost 12 pounds in the last 2 months and I am afraid to exercise b/c of the cysts. I am hungry like I was when I was pregnant and tired all of the time and don't enjoy the things that I used to do. I cry at everything..good or bad...and I just can't take it anymore.
I will post back more when I have this thing removed and hopefully will have some good news.
I do feel like I have to say that I hear about Mirena from a co-worker who absolutely loves it!! She has had no side effects and has had it in for 7 years now! So it's not for everyone...but if you feel side effects...listen to your body and have it removed!!

I was put on Advair 500/50 about 2 monhs ago. I was in the mild asthma category. I use Albuterol as a rescue inhailer, and I have used Singulair for some time. A spoot showed on my lung. I then had a brochoscopy done, which showed that I had aspirated some vegetable matter. (I also have GERD). I developed a severe cough and could hardly walk, at first unable to raise much sputum, and had pleanty of audible heezing. Finally, I got put on MethylPrednisolne 4mg tablets (6 days). That took care of the asthmatic end. However, I still coughed pleanty, and could hardly move or take care of myself. I started coughing up huge amounts of pus looking sputum and also yellow-green sputum.My throat hurt, my ears hurt, and I was exhausted. I went to the ER, where they did a Chest X-Ray and a blood test. The next day, I went to my pulmonary specialist. I have pneumonia, and thrush, still couging up pleanty of stuff. I am on Nystatin for Thrush and Augmentin for infection, some other stuff for cough. I think that most of our doctors sincerely want to help us. However, this wining and dining of our doctors from the pharmeceutical companies has to stop!!! It is causing A LOT OF PROBLEMS FOR BOTH DOCTORS AND PATIENTS. I am still on the Advair. I would like to get off it.

I am a South Florida female, now 61, who started taking 10 mg daily Lipitor in 2000, when aged 55, for high cholesterol. Lipitor worked. My cholesterol dropped from 270 to 207 and stayed there for 5 years.
Early 2006, I began feeling unsteady in the mornings so started taking Lipitor at bedtime, instead. Also began taking CoQ10 along with it.
Then I started feeling oddly foggy, mentally, but was under a lot of stress at home, so discounted it. I became clumsy, dropping things and stumbling. Had a bad fall in February and injured my left knee. As the left leg got better I realized I was also limping on the right leg. Soon I had to use a cane to get about and needed to use my arms to get up out of a chair. I was slurring my words. I sounded drunk and was tired all the time. I couldn't turn keys or door handles. Emotions were near the surface. I would burst into tears over a newspaper cartoon.
Before long I was so weak I could only stagger around my house by hanging onto the furniture. Still no pain whatsoever, (apart from horrible nightime cramps and spasms throughout my whole body) just increasing muscle weakness and being in a constant daze. I was having difficulty swallowing and often aspirated bits of food. I began worrying about having MS or ALS, or having had a stroke, so made an appt to see my doctor. Suddenly the possibility of it being the Lipitor dawned on me at last and I stopped taking it the first week of April 2006. (I now know I should really have eased myself off it in case of sticky platelet rebound.)
Within a week of stopping the Lipitor I felt so much better and brighter. By the time my doc's appt came around in May my mental fog was lifting and I was walking a bit better, but dragging my right foot. My right calf was wasting just as my right thumb muscle had. My doc diagnosed a dropped right foot and a claw hand and referred me to a neurologist. She also sent me for a brain tumor MRI, which was negative
I had for years been waking at 5am every morning to urinate. Within two weeks of stopping Lipitor I was sleeping through till 7am and having no problems during the day. Bladder muscles must be able to regain their strength quickly. I also noticed that the dry mouth that for years had plagued me was gone. Instead of constantly chewing gum and carrying bottled water I have regained a normal saliva flow, something I had completely forgotten ever having. The muscle cramps completely stopped, and also the awful nightmares.
Two months later I seemed to reach a plateau in improving, so decided to see the neurologist in July 2006. He dismissed my theory that it was Lipitor, saying he'd never such seen such side effects and sent me for two MRIs of my spine. The neurologist thinks it's probably ALS as he observed some muscle twitches and has referred me to a specialist in Miami. I haven't made an appointment as I am convinced it was the Lipitor and hope no permanent damage has been done and that I will eventually regain muscle mass and strength.
Lipitor is a poison derived from toxic mold -- red yeast rice. And though it may be safe for some, I believe there are many people suffering needlessly from taking it and the other statin drugs.
I was lucky enough to have a home pc and discover others are in the same boat, but what about all the old folk and working moms and dads taking Lipitor who don't have the time, ability or resources to research this? They are alone in their Lipitor fog, stumbling and slurring, many being diagnosed with dementia and neuropathies, having no idea that their medication is causing such horrible side effects.
Yes, my cholesterol shot up without Lipitor, but I am now on an organic, glutamine-free diet, mainly vegetables, fish and fruit, oatmeal every day, CoQ10, Omega 3 and lots of vitamin C and hoping to keep it somewhat under control.
Any other South Florida sufferers of similar statin-induced myopathy are welcome to e-mail me. Let's get the word out and some support groups going.