Rare Disease Day at NIH 2022: Cure JM Session

Our Journey with NIH — How One Rare Disease Organization Forged a Transformational Research Partnership

Jim Minow, Executive Director of Cure JM Foundation, moderates this rare disease day session at NIH—National Institutes of Health.

The presentation’s objective is to share how one small rare disease organization that funds research to find better treatments and a cure impacts in part on creating effective partnerships with leading research hospitals and, most notably, with NIH.

Learn about the Cure JM Foundation and how it evolved to where they are today.

Jim’s 2024 Resolutions

Each January, I share with our community a few personal New Year’s resolutions for the year ahead. I believe these resolutions help us keep a keen focus on the priorities that matter most—better treatments, better care, and a cure for JM.

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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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