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Polymyositis
polymyositis Information
What type of disease is polymyositis?
I have looked at a bunch of different websites some say muscular, some say skeletal, and some say nervous. I am doing a report for biology, and I need to know what type it is.
Is there anyone with polymyositis that has gotten better?
I have recently been diagnosed with polymyositis and I am extremely weak. I want to get in touch with someone that has this disease and has regained strength back in their muscles. I would like to know what you have been through and the process it took to get there.
Is there any cure for polymyositis?
other than steroids, azothorpine, methotexrate ,immunoglobin ,is there any other treatment for polymyositis
Does anyone know what polymyositis means? does anyone know someone with polymyositis?
polymyositis is a disease that attacks the muscles. it is rare, only 1 in a 100,000 get this disease ech year. there is no found cause for the disease thus far. no one is known for living pass five years with the disease. there is no cure.
How are polymyositis and fibromyalgia similar?
First my dr said she thought I had fibromyalgia, then months later, she thinks it's Polymyositis. I feel I have all the symptoms of FM, and the meds the dr prescribed are ultram tramadol .
Got a shot of cortisone 5or6 days before labs for polymyositis will it effect results?
Can chemotherapy be used to treat polymyositis?
my dad has polymyositis. its been 3yrs now, hes done everything that could be done. now, 100lbs lighter, barely able to walk, and just entirely ready to give up, his doctors are trying chemo in pill form. someone have any kind of comment or ANYTHING. just hoping for someone to have had or heard of this before?? thank you for reading thank you Gary....VERY MUCH
Has anyone ever heard of polymyositis?
Or dermatomyositis? My dad was diagnosed in Dec. and then got septic shock infection and died in Feb. Has anyone else heard of this?
A person with polymyositis,collapse lung ,ashma,puemonia,and clog heart with only 20% workin can do surgery?
do you think it is possble for this person to have any type of surgeery without ending up on a ventilator or have a trach
What is dermatomyositis, polymyositis and inclusion body myositis?
Are there any cures for it?
Positive diagnosis (scleroderma, polymyositis) with negative blood tests?
Maybe someone out there can help me out on this one. Someone I know has been run through the mill so to speak ANA, Anti centromere, Anti dsdna, scl 70, CMP in addition to EMG and nerve tests, all has come back negative. She's in a lot of pain, and thinks it's either scleroderma or polymyositis. The doctor's she sees thinks she's stupid, and I feel for her. My question is could she possibly have some sort of blood test negative form of the above said diseases?Her symptoms are muscle loss, throat ulcer, rash on knuckles and arms, fatigue.
What type of a doctor treats polymyositis?
Ok, Tracolimus is an immunosuppressive drug and polymyositis an autoimmune disease.?
still the rationale to giving it to someone without the knowledge of a cause to their condition. polymyositis is with a BIG QUESTION MARK for the past 4 years.
Polymyositis anyone?
Does anyone have any ideas for non traditional or naturopathic treatments for polymyositis? My wife has been diagnosed but the treatment side effects are almost as bad as the disease. She is currently taking prednizone as well as some chemotherapy drugs and the side effects have her so depressed that she cries every day. Thanks for your time.
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