Cure JM Foundation

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Cure JM Foundation Cure JM Foundation's mission is to find a cure and better treatments for Juvenile Myositis (JM)

Founded in 2003, Cure JM is the global leader in juvenile myositis (JM) research. We are paving the way to better treatments for JM while improving the lives of families affected by the disease. The mission of the Cure JM Foundation is to find better treatments and a cure for juvenile myositis while improving the lives of families affected by JM. 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. The Cure JM Foundation is a 501(c)3 non-profit organization in the USA.

Find your people. Fuel your fight. 💙Cure JM Family Days bring JM families together at leading children's hospitals to le...
10/16/2026

Find your people. Fuel your fight. 💙

Cure JM Family Days bring JM families together at leading children's hospitals to learn from expert physicians, hear the latest in JM research and care, and connect with families who get it.

Coming up soon
📍 Los Angeles • Oct 24
📍 Pittsburgh • Oct 24
📍 Orlando • Nov 7
📍 San Diego • Feb 6

Learn more and register at: https://www.curejm.org/family-days/

Lace up, Cure JM family! 👟💙Two Walk Strong to Cure JM events are coming up, and there is still time to join us.📍 Houston...
10/15/2026

Lace up, Cure JM family! 👟💙

Two Walk Strong to Cure JM events are coming up, and there is still time to join us.

📍 Houston, TX
Saturday, October 17 at Camden Park Westchase
📍 Berkeley, CA
Saturday, October 24 at Shorebird Park

Every step raises awareness and funds research and support for kids and families living with juvenile myositis. Walk with your team, cheer on a JM warrior, or come meet the community. Register here: https://www.curejm.org/walkstrong/

For Oliver’s family, the need for better treatments became personal when he was diagnosed with juvenile dermatomyositis ...
10/15/2026

For Oliver’s family, the need for better treatments became personal when he was diagnosed with juvenile dermatomyositis at age seven.

Now, family, friends, coworkers, and others are rallying around them through Cure JM’s Holiday Challenge to support research.

Read his mom Marianne’s perspective on turning a difficult diagnosis into a reason to get involved:
https://www.curejm.org/holiday-challenge-spotlight-meet-olivers-team/

Help spread the word by sharing, or join the Holiday Challenge at the top of the article!

23 years of asking what more we can do for kids with JM. And a community that keeps answering.See the progress you’ve ma...
10/14/2026

23 years of asking what more we can do for kids with JM. And a community that keeps answering.

See the progress you’ve made possible: www.curejm.org/impact/

10/10/2026

It was a gorgeous day in Austin, TX where families and friends gathered to Walk Strong for a Cure! A HUGE thank you to Haley and Diana for your time, creativity, and energy! And thank you to everyone who came out to spread awareness and build our community.

Next up:
📍 Houston | October 17
📍 Northern California | October 24

And be sure to check our 2027 walk dates: www.curejm.org/walkstrong

Just a few of the many reasons to join the Cure JM Holiday Challenge.What's your reason? Let us know what drives you to ...
10/08/2026

Just a few of the many reasons to join the Cure JM Holiday Challenge.

What's your reason? Let us know what drives you to join and spread awareness! We have already made so much progress to learn and combat this rare disease, and it's all thanks to this utterly remarkable community of families, friends, and medical professionals.

We're here to help you get started on being part of the road to a cure: www.curejm.org/acurestartswithyou

Three Walk Strong events are rounding out this October! 💙Walk with us toward better treatments and a cure: https://www.c...
10/07/2026

Three Walk Strong events are rounding out this October! 💙

Walk with us toward better treatments and a cure:
https://www.curejm.org/walkstrong

📍 Austin | October 10
📍 Houston | October 17
📍 Northern California | October 24

Every step makes an impact.

What can a Cure JM Family Day give your family? 💙Expert guidance. Helpful resources. A chance for children to meet other...
10/06/2026

What can a Cure JM Family Day give your family? 💙

Expert guidance. Helpful resources. A chance for children to meet others living with JM. New connections with families who truly understand.

Upcoming Family Days:

📍 Los Angeles | October 24
📍 Pittsburgh | October 24
📍 Orlando | November 7

Learn more and register: https://www.curejm.org/family-days

We do not talk enough about the grief that can accompany a rare disease diagnosis.Caregivers can deeply love and feel gr...
10/05/2026

We do not talk enough about the grief that can accompany a rare disease diagnosis.

Caregivers can deeply love and feel grateful for the child in front of them while still grieving the life they once imagined for their child and family. Both can be true. 💙

In a deeply personal new article, Cure JM’s Mental Health Coordinator Ronda Thorington explores ambiguous grief, the losses that often go unnamed, and why acknowledging them can be an important step toward healing.

Read the blog here:
https://www.curejm.org/the-grief-no-one-warned-me-about/

Address

19309 Winmeade Drive
Leesburg, VA
20176

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