Introducing the NEW Myositis Support Community! The Myositis Support Community is similar to Facebook, however, it provides a more...
MSU has come a long way since the beginning in 2010 with our first Facebook support group and subsequent...
Myositis patients, join us Saturday, October 20th at 2 PM Eastern for our live, online video support session. Meet...
Myositis patients, join us Thursday, October 11th at 7 PM Eastern for our live, online video support session. Meet...
Myositis patients, join us Saturday, September 22nd at 2 PM Eastern for our live, online video support session. Meet...
Myositis patients, join us Wednesday, September 12th at 7 PM Eastern for our live, online video support session. Meet...
Explaining myositis (Idiopathic Inflammatory Myopathy) and how it affects our lives is difficult. There isn’t a simple, clear-cut answer...
Learn more about the different types of Myositis Live Online Video Support, Education, and Activity Sessions we offer, how...
I think we often neglect to hear what our children and younger family members think about us living with...
If Myositis prevents us from seeking our dreams and goals, it wins. We must follow our true passions...
Yvette shares her #MyositisLIFE, “Imagine That!,” a glimpse into being perfectly healthy and then becoming disabled in the blink...
There are many challenges faced by patients living with a rare, chronic illness like Myositis. These can include: medication...
Diagnosed with Dermatomyositis in 2012, I was looking for an easy (and interesting) way to share my story with...
At MSU, our passion translates into action As promised, the brand new Myositis Support and Understanding Association website is...
For a nonprofit organization that is only a few months old, Myositis Support and Understanding has had an amazing...
My disease is worse than your disease: Why comparing our struggles damages us all
, , Autoimmune Disease
My disease is worse than your disease Why comparing our struggles damages us all In conscious living, people work...
My new life,with Polymyositis by guest author, Sandra Hello my name is Sandra. I have a rare autoimmune disease...
NONPROFIT NEWS: Five years ago Jerry Williams founded “Polymyowhat: Understanding Myositis” as a Facebook group and blog. At the...
by Emily A. Filmore How many times have you found that you were viewing yourself as, predominantly, a person...
Understanding Myositis, a part of Myositis Support and Understanding (MSU), and its related Facebook support groups and social media...
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Upcoming Events
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A Day of Remembrance
May 26 @ 2:00 pm - 3:00 pm EDT -
Skin findings seen with myositis autoantibodies and treatment of skin in dermatomyositis
May 28 @ 4:00 pm - 5:00 pm EDT
