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 UnderstandingMyositis.org to learn more.” – Maureen

See Maureen on our Myositis Network

 


 

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Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization Empowering the Myositis Community. Founded by Myositis patients, for Myositis patients, MSU provides education, support, advocacy, access to research and clinical trial matching, and need-based financial assistance.

View more information: Myositis Support

1 Comment
  1. Sunshine Hughes 3 years ago

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

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