This is a glimpse of my simple but fulfilling life with Myositis.
In December 2003 I began complaining about a burning sensation in my lower legs, so bad that it would...
Emily Filmore, Vice President of MSU and author of "The Marvelous Transformation: Living Well with Autoimmune Disease" shares this...
Maureen, the Senior Group Administrator for MSU, and a patient living with Polymyositis, shares her #MyositisLIFE with MSU showing...
2015 - Photos and Video of Myositis patients, friends, and family supporting MSU and Myositis Awareness.
Before Dermatomyositis I was a pretty healthy guy. I was in good shape, went to the gym 7 days...
Myositis Awareness Day And My Husband’s Diagnosis by Guest Author, Barbara Naturally Speaking It’s been almost three years since...
Myositis Awareness Day 2015 video is a story in photos and music that shows the support that MSU fosters...
Day-by-Day is the Myositis Way! Myositis Support and Understanding Association’s theme for Myositis Awareness Day 2015, and our ongoing...
It was an exciting day in the State of Delaware Tuesday, September 2nd. I had the honor to meet...
