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Unveiling the Future of Hope

In this town hall, you can hear the latest updates on Cure JM research and discover what these advancements mean for you and your family. This session covered groundbreaking research developments, the progress of ongoing studies, and how these findings are paving the way for better treatments and improved quality of life for those affected by juvenile myositis. Whether you’re a patient, caregiver, or supporter, this is your chance to get informed and understand how these research efforts are bringing us closer to a cure.

Research Achievements

A task that seemed daunting 20 years ago, to change the world for patients diagnosed with juvenile myositis, is now within our reach.

Balancing Work and Caregiving: Strategies for Working Parents of Children with Juvenile Myositis

Balancing Work and Caregiving: Strategies for Working Parents of Children with Juvenile Myositis

Balancing the demands of a career with the responsibilities of caregiving is a challenging task for any parent. For those with a child diagnosed with juvenile myositis (JM), a rare autoimmune disease affecting children, the challenge is heightened. Juggling work commitments while providing the necessary care and support for a child with JM can be taxing. In this article, we hope to provide you with a few effective strategies and insights to help working parents navigate this delicate balance.

Getting the Diagnosis. Megan Curran, MD

Getting the Diagnosis

It often takes a bit of time for children with juvenile myositis (JM) to get a proper diagnosis. This is due to the fact that

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

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