Cure JM Foundation (@curejm) header
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Cure JM Foundation is a 501c(3) non-profit funding research for a cure for Juvenile Myositis. JM affects approximately 2-4 of every million children.

Leesburg, VA
Joined October 2009
Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)Photo by Cure JM Foundation (@curejm)
How do you stay on alert for your child without living on high alert? 💙 Our Mental Health Coordinator, Ronda Thorington, shares what she’s learned as a rare disease parent and five small steps for finding rest when things actually are okay. curejm.org/still-holding-you…
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Cure JM Pittsburgh Family Day brought 6 JM families together with @childrenspgh’s pediatric rheumatology team for art and music therapy, CAR-T research updates, and a $10,000 Miracle Grant to support innovation in JM care! 🎉 Thank you @upmcnews! #CureJM #JuvenileMyositis
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We’re on our way! 💙 Our goal is to bring 30 new families into the Holiday Challenge this year, and already 18 inspiring families have joined us. And right now, thanks to the Coffey Family Match, Holiday Challenge gifts are doubled. curejm.org/acurestartswithyo…
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Join us for our November Town Hall, Calcinosis in JDM. What we know, what we can do, and what questions remain. Dr. Belina Yi joins us Wed, Nov 18 at 8 PM ET with open Q&A. Register 👉 us02web.zoom.us/meeting/regi… #CureJM #JDM #juvenilemyositis
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What an incredible first for Michigan! 💙 Our inaugural Walk Strong Michigan raised more than $20,000 for Cure JM! 🎉 A huge thank-you to our amazing volunteers and everyone who showed up, participated, and supported our mission. You helped make this first walk one to remember!
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💙 Caring for a child with JM includes their emotional well-being, too. Our caregiver FAQs offer information on anxiety, depression, and finding support. curejm.org/mental-and-emotio…
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For children living with juvenile myositis, better treatment options can’t come soon enough. Your gift helps Cure JM keep research moving, and the Coffey family will match it dollar for dollar! That’s twice the support for work that can’t wait. 💙 curejm.org/acurestartswithyo…
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Changes in mood, sleep, energy or interest in play can be more than a rough day. Our guide helps families recognize the signs early, because spotting them early leads to support, and support helps kids thrive. Learn more 👉 curejm.org/signs-of-depressi…
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Find your people. Fuel your fight. 💙 Cure JM Family Days are coming to Los Angeles and Pittsburgh (Oct 24) and Orlando (Nov 7), with 25 planned nationwide this season. Register 👉 curejm.org/family-days/ #FamilyDayFriday #JuvenileMyositis
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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 📍 Berkeley, CA | Saturday, October 24 Register here: curejm.org/walkstrong/
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For seven-year-old Oliver’s family, research is personal. 💙 Meet the team rallying around him through Cure JM’s Holiday Challenge and hear why they’re supporting better treatments and a cure. curejm.org/holiday-challenge…
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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: curejm.org/impact/ #CureJM #JuvenileMyositis #autoimmunedisease #raredisease
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It was a gorgeous day in Austin, TX where families and friends gathered to Walk Strong for a Cure! A huge thank you to everyone who came out and supported! Next up: • Houston | October 17 • Northern California | October 24 Check our 2027 walk dates: curejm.org/walkstrong
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What can a Cure JM Family Day give your family? 💙 Expert guidance. Practical resources. A chance for children to meet others with JM. New people in your corner. 📍 New Orleans | October 17 📍 Los Angeles | October 24 📍 Pittsburgh | October 24 curejm.org/family-days
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JM has already asked too much of children and families. The Holiday Challenge is one way families answer back: raising awareness, funding better treatments, and turning their JM journey into hope for the next child diagnosed. What’s your reason? 💙 curejm.org/acurestartswithyo…
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Five Walk Strong events are coming this October! 💙 📍 Atlanta | Oct. 3 📍 Boston | Oct. 4 📍 Austin | Oct. 10 📍 Houston | Oct. 17 📍 Northern California | Oct. 24 Walk with us toward better treatments and a cure: curejm.org/walkstrong/ #WalkStrong #CureJM
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Caregivers can deeply love and feel grateful for their child while grieving the life they once imagined. Both can be true. 💙 Cure JM’s Ronda Thorington explores ambiguous grief in rare disease families: curejm.org/the-grief-no-one-… #CureJM #juvenilemyositis
🤖 Made with AI
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Cure JM Family Days are coming this October! 💙 📍 New Orleans | Oct. 17 📍 Los Angeles | Oct. 24 📍 Pittsburgh | Oct. 24 Meet JM experts and families who understand the journey. Register: curejm.org/family-days
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The Holiday Challenge is live. One story can change how people see JM, and how far we get toward a cure. Join today: curejm.org/acurestartswithyo…
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Our 2026 Impact Report is here! Research is opening new possibilities in juvenile myositis, and a powerful community is helping ensure that progress reaches the children and families who need it. Read the report: curejm.org/impact #JuvenileMyositis #autoimmunedisease
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