Peer Support

Peer Support

Cure JM is an organization of parents, patients, and clinicians whose mission is to fund JM research, care, and support.  We offer peer-support for every member of the family to help them thrive in their daily life with JM, comply with medication instructions, and connect with other families.

We invite all clinicians of pediatric or adult JM patients to share these resources with their patients.  

Click here for resources on how to start your own JDM Clinic 

Click here for resources to share with your patients and families 

Clinicians, researchers, and HCP’s click here to receive Cure JM’s quarterly Medical News. You will receive a quarterly summary of JDM updates and be invited to our quarterly medical symposia on Zoom.


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Pioneering JM Care – Integrating Research With a Multidisciplinary Approach to Care

Dr. Jessica Turnier of the University of Michigan / Mott’s Children’s Hospital is dedicated to creating new directions for JM research and wider perspectives on how it is treated. About the University of Michigan, she states, “When I came to Michigan, there were a lot of myositis patients, and I just developed a really strong connection with those patients.”

Cure JM January 2025 – Virtual Summit

In January, the Cure JM Clinical Care Network was pleased to invite juvenile dermatomyositis healthcare professionals to join us virtually for the latest presentations from world-leading researchers and clinicians on advancements in basic research, translational studies, and best-practice clinical care in juvenile dermatomyositis. 

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?

We’re here to help!

To have your fundraiser matched, add “DIY Match” in the memo of your online gift or check.