Cure JM Foundation™ is a 501(c)(3) nonprofit organization dedicated to finding a cure for Juvenile Dermatomyositis (JDM) and Juvenile Polymyositis (JPM), the rare and life-threatening autoimmune diseases collectively known as Juvenile Myositis (JM). Approximately 2 to 4 children in a million in the United States are diagnosed with JM each year.
Our mission is to provide support for families coping with JM, raise awareness of JM, and fund research that will ultimately lead to a cure.
“From the moment I made contact with Cure JM, they have made us feel like family members and have been with us every step of the way. No concern is too big or too small. Anytime I've had a question, someone has always been there to help.”
Parents, Grandparents, Patients, anyone... Become a member of Cure JM. It’s free to join and the best way to help find a cure.