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...
- Inclusion Body Myositis Functional Rating Scale (IBMFRS) January 14, 2019
- Inclusion Body Myositis Specialty Clinic at Washington University, St. Louis January 10, 2019
- The first step when approaching a patient with muscle weakness – Differential diagnosis of idiopathic inflammatory myopathies in adults January 9, 2019
January 25 @ 4:00 pm - 5:30 pm EST
February 6 @ 7:00 pm - 8:30 pm EST