I have been on Vytorin 10/40 for the past two months and started getting muscle pains within the first month.The pains have intensified and my CPK result is 228.Previously I was on Lipitor and had...
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I am into considering IBM as a metabolic disorder, not an "autoimmune disease". I was offline for about a year, but about two years ago had started using DMSO, a laboratory solvent whic...
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I don't think this is the right place for me... but maybe someone can help or point me in the right direction....
have had chronic pain for the last 5 months. I am hoping someone will know wh...
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what kind of Doctor to treat the VDRL
...
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Hi,
Im a 20 year old male, and have recently been diagnosed with Polymyositis about 6 weeks ago.
I noticed a big drop in muscle strength and had muscle weakness that was getting worse. My ...
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Hi,
Will my tummy go back down after I get off prednisone? I never had a stomach in my life, always in good shape, but now with the autoimmone disease it's hard for me to even exercise..I'm tr...
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Anyone with DM have trouble with lung blood clots?
I was in the hospital last week for 5 days due to multiple and massive clots in my lung. They did not find any in my legs....so they don't...
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Is there anyone out there that has this diagnosis?
...
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When do side effects go away
...
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Would love to talk to people who have been diagnosed with DM. Family and friends are very supportive but it would be nice to share experiences with people who understand the uncertainty and the lo...
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was diagnosed with dermatomyositis about 1 year ago. Didn't realise how hard I would be hit by depression.Is anyone else suffering? Thought I could cope with most things but find I am struggling....
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Just wanted to give everyone a little encouragement. My hubby was finally diagnosed with dermatomyositis last year. He lost use of his throat and had to have a feeding tube put in. Today after ...
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I was diagnoised 5 year ago with skin form of Lupus. After several years of problems and my hands kept getting worse I was sent to a dermatologist who specailized in Lupus. After one look at my ...
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New to the board. My dad was diagnosed with IBM or polymyositis (the doctors continue to debate which one). Thankfully it is slow digression, but it is still difficult to watch him slowly get wo...
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Hello,
In 2003, I was misdiagnosed with eosinophilic fasciitis - an inflammation and hardening of the sheathing covering the muscles. Earlier this year, I was finally correctly diagnosed with ...
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I have just been diagnosed, through a muscle biopsy, with mild myopathy consistent with polymyositis. The neuro didn't seem concerned, just handed me a script for prednisone and said I needed to ...
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To make a very long story short ... i started treatment of High Cholestrol (which runs in my family) nearly 12 yrs ago! Well over 300 and ratio's and triglyc were also out of whack. Started on Zoc...
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hello every 1, i had a cpk of 8000, im down to 4200 now, i have problems with stairs and lifting. how long does it take to get back to climbing stars without using the rails? i have had myositis s...
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I am greatful to have found this site but so sad the many out there suffering. For aprox 20 years, have had this dreadful monster "they" call OM orbital myositis. Is there anyone else wi...
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I have a daughter who is 17years old. She was tested on polymyositis. But the results of all the tests which included electroneuromyography came out negative. Yet she still has symtoms like mustle...
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I was wondering what meds you are on and if they are helping. I'm on predinisone and doesn't seem to be helping. I did the IVIG, the first treatment looked promising but the second i was off the...
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Firstly thank you to the responses to my first posting on this board it is much appreciated.
I have some questions and since I will be seeing my rheumatologist on the 24th I want to get them a...
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Has anyone ever seen a naturalist for their condition? I have been dealing with this diease for 3 years now and was in terrible shape. THe prednisone and all the other perscriptions to care for th...
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Hi there all, well I've yet to see anyone with my problem. Even doctors are floored. I was diagnosed with chronic focal myositis. Just wondering if anyone out there has it too.Mine is rare it star...
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I am a 35 yr old mother of 2. My symptons started in 2005 with tripping, followed by difficulty walking up stairs, then difficulty standing up and walking, now i can't walk at all and my arms and...
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