Angela Chami shares her video “A Day in the Life of Someone with Myositis” for Myositis Awareness Month and the MSU #MyositisLIFE project.

This was more like “A Month in the Life” since I filmed almost every day this month for Myositis Awareness :). I am extremely fortunate to have the support that I do. I hope you enjoy my #MyositisLIFE!

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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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PIONEER, Idera clinical trial for dermatomyositis

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