All Family Resources
All Clinician Resources

May 2024 Symposium

The Spring Cure JM Medical Symposium in partnership with Duke University happened May 23rd, 2024, 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 (pending 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.

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Walking Strong, Empowered by unity

Walking Strong – Empowered by Unity

Like other teens new to the JM journey, Catie Beth Caldwell and Madi Cook were two individuals who felt alone at the beginning of their journeys. Catie Beth was diagnosed just before the Covid-19 pandemic took hold of the world as we knew it. With this came feelings of isolation and loneliness. These emotions were commonplace for many teens but were only compounded by teens new to a rare disease diagnosis. These first years of the “new normal” were difficult to navigate.

Unveiling the Future of Hope, Malloy and Heaton, September Town Hall 2024

Unveiling the Future of Hope

This expert-led presentation is for parents about how to help their kids and themselves when their kids express high levels of emotional distress. Our presenters will talk about ways parents can calm themselves, share tips for talking to kids with age-appropriate information, and know when to find help from a professional. There will be a Q&A session immediately following the presentation.

Family holding a Cure JM sign on a beach

Our Story

Cure JM was founded 19 years ago by a small group of volunteers who wanted to change the world for children with a rare disease few had ever heard of—juvenile myositis, or JM.

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

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