10th Annual Cure JM Medical Symposium

10th Symposium for Clinicians and Researchers - Juvenile Dermatomyositis


The 10th Annual Cure JM Medical Symposium in partnership with Duke University happened May 13th, 2023, virtually, with presentations from world-leading researchers and clinicians on advancements in basic research, translational studies, and best practice clinical care in juvenile dermatomyositis.

For clinicians, researchers, and healthcare professionals unable to attend the event, we are honored to share the full virtual symposium recording. This video features presentations in order, with the recording separating each presentation topic into YouTube chapters.

3.0 CME Credits are available through Duke University by watching the recording.

Additional peer support resources for clinicians of juvenile myositis patients and families can be found at www.curejm.org/clinicians.

For questions regarding the Cure JM Medical Symposium, please email Andrew Heaton, CSO, Cure JM Foundation, at andrew.heaton@curejm.org.

Myositis and You

This comprehensive guide to juvenile dermatomyositis features over 450 pages with contributions from over 80 experts and medical professionals.

Emotional Health Recognized as Vital Component of JDM Care

Caring for a child with juvenile myositis (JM) goes beyond managing flares and medications—it means supporting their whole well-being, including mental and emotional health. Research shows that children with chronic illnesses like JM are at a significantly higher risk for anxiety, depression, and emotional distress. These challenges can affect not just day-to-day life, but also treatment outcomes and long-term health

Doctor with parent and juvenile myositis patient.

Treatment Plans for Juvenile Myositis

A treatment plan is based on many factors, including the severity and expression of the juvenile dermatomyositis (JDM). Each case is different and the symptoms can change over time.

Join Cure JM

Membership is free and we’ll connect you with a network of support, encouragement, and resources.

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

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