Maureen, the Senior Group Administrator for MSU, and a patient living with Polymyositis, shares her #MyositisLIFE with MSU showing her artistic side and true strength when living with the rare muscle disease, Polymyositis.

“I was diagnosed with Polymyositis 10 years ago. It is a rare disease that people need to understand. You can visit to learn more.” – Maureen

See Maureen on our Myositis Network





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

1 Comment
  1. Sunshine Hughes 2 years ago

    You are the BOMB-DIGGITY! Thank YOU for sharing!

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