Impact of Juvenile Myositis on Mental Health

Drs. Kaveh Ardalan, Andrea Knight, and Alison Manning discuss juvenile myositis’ impact on mental health and how parents can address them.

Family News

Family News

The Cure JM Foundation produces a monthly newsletter with the latest news and updates about juvenile myositis. Please click to read past issues of the Family News.

GCOM 2024, Executive Director Update

GCOM 2024 Round Up

Recently, Cure JM’s Jim Minow was able to attend the Global Conference for Myositis. This conference was not only informational, but was a most impressive day for Cure JM. The conference brings together leading myositis researchers from around the world to share results and collaborate on future projects leading to better care and improved treatments for our JM kids.

Rare Disease Warriors

Since it is Rare Disease Month, we would like to take a moment and shine the spotlight on some of our amazing JM warriors.

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Cure JM supports families, patients, and the juvenile myositis research community.

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