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.
Myositis-specific antibodies (MSAs) are associated with certain symptoms in JM patients. In some cases, knowing the MSA of a patient may help clinicians look out for certain symptoms and guide treatment decisions.
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.
Membership is free and we’ll connect you with a network of support, encouragement, and resources.
