This amazing video details how the Cure JM Foundation started. Twenty years later, Cure JM is the global leader in juvenile myositis (JM) research.
Today, Cure JM celebrates its 20-year commitment as a patient advocacy and juvenile myositis research leader, paving the way to better treatments for JM while improving the lives of families affected by the disease.
Learning that your child has Juvenile Myositis may feel overwhelming. Second opinions can confirm a diagnosis, help you understand different treatment options, and review your child’s current treatment plan to ensure it’s the right one for your family.
Research is vital to finding better treatments and a cure for juvenile myositis. Cure JM funds research studies through our Cure JM Centers of Excellence and the Cure JM Clinical Care Network.
The following brochures, handouts and posters are available for online viewing and printing. If you need professionally printed copies for an event, please contact us.
Membership is free and we’ll connect you with a network of support, encouragement, and resources.
To have your fundraiser matched, add “DIY Match” in the memo of your online gift or check.