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.

10th Symposium for Clinicians and Researchers - Juvenile Dermatomyositis

10th Annual Cure JM Medical Symposium

The 10th Annual Cure JM Medical Symposium in partnership with Duke University happened May 13th, 2023, virtually, with presentations from world-leading researchers and clinicians on

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.