This was more like "A Month in the Life" since I filmed almost every day this month for Myositis...
This is a collection of user submitted content in the form of videos 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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- Myositis Awareness, September 2020
- Myositis Empower Walk, Join us 9/19/20
- The Grieving Project
- Explore Myositis
- Financial Assistance Program
- #ItsMyTurn: Becoming a Plasma Donor Hero
- Myositis Clinical Trials
- Myositis Webinars
- Upcoming Events
- Donate today!