Cure JM Leader Publishes New JDM Research

Tracy Van Ness

Cure JM is proud to share exciting news from our community. Dr. Tracy Van Ness, DHSc, PA‑C, has published a new peer‑reviewed article, Juvenile Dermatomyositis: Multisystem Impacts and Evolving Treatment Paradigms, contributing important insights to the scientific understanding of JDM. 

Access the article

Dr. Van Ness is a standout leader in the JM community — serving as a Director on the Cure JM Board of Directors, a member of the Research CommitteeCo‑Chair of Walk Strong New York, and a dedicated JM mom. Her work bridges clinical expertise, research leadership, and lived experience, making her voice especially meaningful in advancing care for children, teens, and young adults with JM.

This publication highlights Dr. Van Ness’s commitment to improving outcomes for JM families and strengthening the research foundation that drives better treatments and long‑term health.

Cure JM celebrates this achievement and is grateful for the many ways Dr. Van Ness helps move our mission forward.

May 2025 Town Hall, Dr. Ardalan

Tapering Medication

Cure JM hosted a special Town Hall featuring Dr. Kaveh Ardalan, Co-Director of the Duke Children’s Myositis Center, a Cure JM Center of Excellence. The

Nathanael’s Story

Nathanael was an active 7-year-old. In the summer of 2014, he played baseball under the Southern California sun, and that’s when the rash started. “He

Lemons to Lemonade for Kids Logo

Lemons To Lemonade For Kids

Our Story – Humble Beginnings In 2003, Cure JM co-founders Tom and Shari Hume set up the Foundation’s first-ever DIY fundraiser to seed important new

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.