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.

Anna Ramsey – “Doing Something About It”

Anna Ramsey has lived with juvenile myositis for most of her adolescent and adult life. Over the years Anna has been actively involved in Cure JM as a fundraiser, an advocate, and most recently the first ever patient on the Board of Directors.

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.

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.

Interested in DIY fundraising but need help?

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