About Us

Founded in 2003, Cure JM is a family of families seeking a future when every child is free from JM.  Learn about our founders and inspirational Stories of Hope from around the country.

Three sets of hands with Cure JM bracelets on

Our Mission

To find a cure and better treatments for juvenile myositis and improve the lives of families affected by JM.

Cure JM actively supports families, patients, and the JM research community!

Families

We provide JM education, resources, and support to parents and other family members.

Patients

We provide resources to teens and young adults living with JM, opportunities to connect with other teens, and resources to learn how to manage their care as they move into adulthood.

Research

Cure JM offers grants to researchers and clinicians to find better treatments and a cure for JM.

Stories of Hope

Learn from other Cure JM families about their journey with juvenile myositis.

Smiling family holding "Team Choys R Us" sign

Together, We Are Making a Difference

Connecting and supporting 3,000 families and patients in 40 countries
Invested over $21 million in research and education
Funded more than 195 research studies to improve treatment and care for patients
Development & advancement of up to 10 clinical trials
Established 20 Clinical Care Network locations and five Cure JM Centers of Excellence to advance care for patients
Created more than 20 regional chapters across the U.S.
Large gathering of people attend a fundraiser to advance juvenile myositis research.
Walk Strong Event - Chicago
Cure JM is led by a passionate team of volunteers, staff, and medical experts in juvenile myositis research and care.

Leadership

Meet our board of directors, medical advisory board, and staff.

National Leadership Council

The Cure JM National Leadership Council is the organization that leads the charge to raise funds and advance Cure JM’s mission in communities across the country and beyond.

A family participates in a Cure JM event.
Family holding a Cure JM sign on a beach

Our Founders

Cure JM was founded in 2003 by a small group of volunteers—parents and grandparents—who wanted to change the world for children with a rare disease few had ever heard of—juvenile myositis, or JM.

The founders came together with the same determination to find better treatments and a cure for juvenile myositis that drives Cure JM today. Our accomplishments today are still driven by engagement from our families.