This is a collection of personal, user submitted stories.
We learn from the experiences of others, so we want Myositis patients, caregivers, family members, and friends to share their stories of what life is like living with the rare disease, Myositis, and its subtypes.
Hi, I’m Sage and I am nine years old. My mommy has dermatomyositis. I have a list about the...
The week after all the double lung transplant evaluation testing is a long one. Our hospital meets on Tuesdays,...
Life with JDM, by Cathelina V. Sharing her experience living with Juvenile Dermatomyositis
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