As you probably know, we have lost many of our MSU group members throughout the past couple of years,...
This is a collection of user submitted content designed to promote awareness and education about living with the rare disease, Myositis and its subtypes of Polymyositis, Dermatomyositis, Inclusion Body Myositis, and the Juvenile forms of Dermatomyositis and Polymyositis.
As Jerry’s partner of 13 years, and spouse of 3 years, I think I have witnessed just about everything...
MSU Founder and President, Jerry Williams, shares his #MyositisLIFE. He shares his commitment to helping other Myositis patients...
Sage Filmore, 10 years old, interviews her mom, Emily Filmore, about MSU and what it is like to live...
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Dermatomyositis Patients with a Certain Type of Autoantibodies at Higher Risk of Skin Eruptions with Use of Hydroxychloroquine September 21, 2018
In this study, the researchers set out to determine if ...
Alexa, make a donation to Myositis Support and Understanding September 20, 2018
Amazon's donate feature is a part of the various tools ...