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December Town Hall – Live from Giving Tuesday

This Giving Tuesday, families and supporters joined us for an exciting update on the breakthroughs accelerating JM research and care.

Executive Director Jim Minow walked through the newest developments in emerging therapies, clinical trials, and next-generation CAR-T approaches.

Dr. Brian Feldman outlined why many clinicians believe we are entering a collaborative breakthrough era for JM treatment.

Live updates from a global JM research meeting in the United Kingdom brought news on JAK inhibitors, clinical trial progress, and innovations that may shape future treatment options.

The event celebrated the momentum in JM science and the impact of our community in driving these advancements.

Cadence’s Story

Cadence was only 18 months old when she was diagnosed with juvenile dermatomyositis. Her mother took her to their pediatrician’s office multiple times, only for

Parrish Story of Hope

Parrish’s Story

We would like to introduce a one-of-a-kind, competitive, and determined young man, named Parrish. His story of resiliency and hope is one that will resonate with many of us in the Cure JM family. Parrish faced many challenges in his journey with JM, but found hope and support in his family and the Cure JM community. We are pleased to now share his experience to help others facing the same struggles during Myositis Awareness Month.

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

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