August 2026 Town Hall – First Steps Forward for the Newly Diagnosed

Families received clear, compassionate guidance during this session, designed to support those newly diagnosed or looking for fresh perspective. Dr. Angela Chun broke down the basics of JM, explained common treatments and medications, shared practical tips on sun protection and managing medical records, and offered strategies for working effectively with a healthcare team.

Dr. Chun is an Attending Physician in Rheumatology at Lurie Children’s Hospital in Chicago and an Assistant Professor of Pediatrics (Rheumatology) at Northwestern University Feinberg School of Medicine. She also serves on the steering committee of Cure JM’s Clinical Care Network.

Rare Disease Warriors

Since it is Rare Disease Month, we would like to take a moment and shine the spotlight on some of our amazing JM warriors.

Clinician's September Summit 2024

Cure JM September 2024 – Virtual Summit

We are pleased to invite all juvenile dermatomyositis healthcare professionals to join us virtually for the latest presentations, sharing clinical best practices to help providers diagnose, treat, and care for juvenile myositis patients.

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.