Respirator symptoms and conditions

I was on remicade for 2 months and contracted pneumonia. It kept getting worse for 8 weeks until I had to go hospital. None of the antibiotics were working. I almost was dead and they considered a heart and lung transplant and I was on a respirator in a coma. Finally somebody figured out I had eosinophilic pneumonia and treated it with cortisone. I began to improve but was still in hospital 4 months and after almost 2 years I'm still on oxygen and can't walk right. Many people develop this and die without a diagnosis. I won't take remicade ever again.

My son has been on Singulair for about a year and a half...it really seemed to help his allergies...at least at first. This winter has been very dry and I have been having to give him other over the counter allergy medication as the Singulair isn't helping much. He also started losing weight..just not hungry. At first that was ok as he needed to lose a little but then he was getting too thin. He wasn't eating much at school but refused to take a lunch from home. I took him to the doctor just recently to see if he was physical ok since I didn't know what was causing the weight loss. The blood testing showed everything was normal and I just told him he had to start eating better...he has somewhat...but also he finally told me he has been feeling very depressed...seriously depressed and having suicidal thoughts too due to some kids picking on him at school.

I knew there were problems as he complained alot but I had no idea it was this serious. I have taken him out of that school. Right now I don't know if the Singulair could be adding to this depression or if its all just due to the bullies. While he complained a lot he never acted as if it was bothering him that badly or I would have gone to the school about it. Anyway I stopped the Singulair and am going to see if his mood improves or not. After reading some of the scary posts on here regarding the side effects I am wondering if this is a good idea stopping it or not. I am waiting for a call back from his doctor on it. Since its once a day..its kind of hard to wean them off of it...but I could cut it in half ..do that for a few days, then cut it smaller and so forth. His is chewable so I could do that with no problems. He is 13.

I am being treated for ulcertive colitis. I have been on prednisone since Sept of 08. I started out on 40 mg. In late Oct. my doctor started tapering me off 5mg per month. Each month following the tapering date, I would get sick. As I look back, all the signs of withdrawal were there. This Jan. I tapered once again, but the window was only 3 weeks. I hit rock bottom. If there was a symptom, I have it. Nausea, burning in my digestive tract, diarrhea every time I eat, muscle ache, numbness in my legs, swollen feet, sore bones and joints. ( The worst was in my feet. I ended up seeing a podiatrist. He thought plantar faciaitis until I told him about being on prednisone. The small bones in my foot were swelling, The muscles in my calf were buning they were so sore. That was last week. Today my other foot started. I can hardly walk. In addition to that, I am lightheaded, have elevated blood pressure, and fatigue. I also had some vision problems that sent me to the doctor. I went through a ton of testing which all were negative. It seems that pseudotumor is another symptom of withdrawal. I have a history of that. It would have been nice to know that. As I look back each month, I had different muscle and joint pain that lasted about a week. I was put on an acid reducer in Dec. to help my stomach, but in all of this time, I was not told that these all may be withdrawal symptoms. I have been off work for two weeks now in addition to the days I missed each month. My physician is now controlling the tapering procedure. They up the dose to 10 mg again. They plan on weaning me by 1mg doses. This has been a terrible experience for me. I have only been severely sick one other time in my life. This pain is awful. It is chronic. This drug may be beneficial, but it is like poison too. Anyone who takes this should really ask a lot of questions, and be careful..

Had 8 infusions that helped a lot,but then things took a turn for the worst. During my treatment I GOT BUTTERFLY RASH ON MY FACE(drug induced lupus). I had small red bumps everywhere I have hair. My body then and still year latter always feel tired and ache. In April of 06 I went to have my colon removed, because the Remicade stopped working, and took my immune system down to nothing. My body could not fight off the infection. Four day after the colon came out my doctor had to open me back up. I was full of infection, it poured out of me. They took my innards out and washed them. Remicade and a weak immune system gave me sepsis infection. The infection clogged my heart and gave me a major heart attack. I was put in a coma for 4 days. They had to continually flush me with water and antibiotic. I did not remember the first 3 weeks of the nightmare. I had a respirator to keep me breathing for 3 weeks. Then a track for two more weeks. I had to be feed threw a tube, go to the bathroom using a catheter. I lost a total of 85 pounds and spent 41 days in the hospital, because of infection. My wife and daughter had to help me up two steps to get in my house. I was suppose to have my surgery April 06, get second surgery June 06 to get rid of the bag and use the pouch the doctor had constructed. Its 7 months later and the healing posses, because of the REMICADE has been so slow I am still waiting. I have a scope up my butt every 6 weeks to check the progress. I thank the Lord , doctor and my wonderful wife I am alive today. Remicade can be deadly, as my family doctor said its like playing with fire cracker. By the way I am 42 years old, my name is Mike H. from Lake city, MI. If you are on Remicade please keep a very watchful eye. If you get a infection , REMICADE has lower you body's ability to fight back. I wish the best for all who suffer from illness, GOD BLESS.

I was a 2:42 marathoner. I used a synthetic varnish containing isocyanates, pentanedione, organic solvents, in one 7-hour session; the company-recommended respirator did not in fact prevent transmission: Severe chemically- induced asthma, plus neuropathy, plus, plus.

I've used Advair 500/50 for six years. There have been many diverse effects from the chemical exposure; I'd not questioned any being Advair side effects. But the raised blood pressure was not initial, and certainly not a priori. Diminished hearing, diminished eyesight, anxiety. Again, not to lump in, but these questions are new for me. But the point I'd like to bring before this group is this: In August I was diagnosed with ehlichiosis , and was prescribed 28 days on doxycycline. They recommend eliminating many possible antagonists to the doxycycline. My respiratory capacity had been continually diminishing. My ongoing physician said this was to be expected and recommended only the next more powerful steroid. Not a good solution. Before all this I was strong; repaired myself. In the absence of constructive answers, wondering if the Advair was weakening me, making me dependent, I quit the Advair as well on beginning the doxycycline. Today is eleven days post-doxycycline. Eight days ago there began with increasing severity, a terrible wracking deep cough producing dark yellow mucus. Painful. No fever. Grevious throat from the wracking, but I question whether this is a cold or infection. It's just in my lungs. Maybe it's as though I've thrown off an epithelial coating. These past two days the quantity of deep yellow mucus is not as ready, but the wracking and coughing is more severe. And my lung capacity, my respiratory capacity, is frighteningly diminished. Until these past two days I'd considered this an infection, especially post-doxy. But it doesn't feel like an infection. And I'm scared. Is this because I quit the Advair abruptly after long regular use? Have any of you had a similar experience. Can you discuss the effects of abruptly discontinuing Advair. Have you stayed off it. What's happened to your respiratory capacity. Have you any professional studies, trials or experience to recommend. Thanks.

OH TO ADD TO MY PREVIOUS POST, THE COUGHING ALL NIGHT KEEPS HER UP, DRS TOLD US AT HOSPITAL ITS DUE TO THE TUBEING FROM RESPIRATOR... ANY ADVICE PLEASE EMAIL ME AT ***

In 1980, my neice was given Anectine anesthesia during a D & C procedure. Her side effects were: blood pressure dropped dramatically, could not breathe on her own, no feeling in extremities. Weakness continued for several days after returning home. It was discovered her father's mother had the same symtoms. After testing other sibs, they found all girls in that family was allergic to Anectine but NOT the boys. This was declared to be hereditary and the girls had a less than normal amount of pseudocholinesterase which did not allow the Anectine to be broken down in the body.

It took doctors and nurses approximately 7 hours to get me to come out of the effects of Anectine. When I first came to realize I was aware of my surroundings, I was completely paralyzed and was on a respirator. While I laid in recovery after I became aware of my surroundings, a nurse would yell my name and rub my shoulders extremely hard to make me feel pain so I would come out of the effects. Once I did, I gagged on the respirator and it was removed, however, I was groggy for several days and stayed in the hospital. By the way, I was in the hospital for a 15-20 minute surgery to have my throat scrapped (tonsils grew tags or were not removed completely at age 8). I was 18 years old at the time. Talk about a raw throat with a respirator being pulled out of it. I didn't eat anything for 3 weeks. My children are not allowed to have Anectine either, because there is no test that can be performed to see if they would have the same reaction as I. It is not an allergic reaction, but one that is brought on by one gene from my mother and one from my father that caused me to react as I did. I was told if I was to be under an anesthetic longer than 20 minutes and Anectine were used, I would die.

PLEASE HELP FIND AN ANTIDOTE TO REVERSE THE DAMAGE CAUSED BY LIPITOR. IT CAUSED MY MOTHER MOTOR NEUROPATHY, THEREFORE SHE IS ON A RESPIRATOR & NOW IN A COMA.
THERE MUST BE SOMEONE OUT THERE OR THE PHARMACY COMPANY WHO MANUFACTURERS LIPITOR TO REVERSE THIS TERRIBLE SIDE EFFECT.
HELP BEFORE IT IS TOO LATE.
******

MY MOTHER IS NOW ON A RESPIRATOR SINCE ASPIRATING BECAUSE HER MUSCLES BECAME SO WEAK FROM 40-60MG OF LIPITOR CONSUMED FOR 2 PLUS YEARS. SHE DEMONSTRATES MOTOR NEUROPATHY WHICH MIMICS A.L.S. BUT IS DUE TO MURDEROUS LIPITOR.