A wife, sister, soldier, student, and a daughter. Life was great. 22 years old and nothing seemed impossible. The...
Watch and read as patients, caregivers, family members, friends, and others show and write about their lives living with the rare disease, Myositis.
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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- Explore Myositis
- Financial Assistance Program
- #ItsMyTurn: Becoming a Plasma Donor Hero
- Myositis Clinical Trials
- Myositis Empower Walk
- Myositis Webinars
- The Grieving Project
- Upcoming Events