Sage Filmore shares her interview with Emily about Life with Myositis and why #MyositisAwareness is important for Myositis Awareness Month and MSU’s #MyositisLIFE project. 

Sage Filmore, 10 years old, interviews her mom, Emily Filmore, about MSU and what it is like to live with Myositis.

Author: Sage Filmore


 

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Myositis Support and Understanding Association (MSU) is a 501(c)(3) nonprofit organization with a mission to improve the day-to-day lives of Myositis patients. MSU is a patient-centered organization, founded by Myositis patients, for Myositis patients, and believes education, support, advocacy, and assistance are key to helping patients and caregivers. As a nonprofit, we rely on donations for funding and volunteers to help manage our fast growing organization.

View more information: Myositis Support

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