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Angela previously served as VP of MSU and has had Juvenile Dermatomyositis since she was a young infant, so she knows no other life but this one. She has suffered a great deal but has also become a very passionate person due to her struggles. Myositis is a huge part of her existence. Learning different ways to cope while advocating for chronic illness has become her passion.

View more information: Angela Chami

1 Comment
  1. Jerry Williams 11 years ago

    This post makes excellent points especially that talking about Myositis will only do so much to truly promote awareness. What is awareness without action? Only through funding nonprofits dedicated to using those funds appropriately will anything truly get done. Don’t get me wrong, we still need to talk about it and share our stories with the world for better understanding.

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© 2026 Myositis Support and Understanding Association (MSU). All rights reserved. | View our Privacy Policy, Terms, and Non-Discrimination policy. MSU is a charitable organization with 501(c)(3) tax-exempt status. Federal ID #47-4570748.

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