Where to Start
More than 300,000 Americans live with some type of scleroderma. Today, the face of scleroderma includes people of all ages, genders, and backgrounds. Scleroderma can affect young parents, children, grandparents, and teenagers. Thanks to the passion and dedication of countless volunteers, scientists, and supporters, we’re advancing our mission faster than ever.
One of the most challenging things about scleroderma is that it presents differently in each person. Find the right resources for you.
Most people with autoimmune conditions already keep their own records: a spreadsheet of results, a running list of medicines…
Heidi Jacobe, MD, MSCS, will serve as chair of the Department of Dermatology at Duke Health beginning in December….
National Scleroderma Foundation leadership is aware of the pause in two CAR-T clinical development programs and is closely following…
Events
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Austin Area Support Group
Virtual EventThe Austin Area Support Group meets on the 2nd Thursday of each month at 10:30am CT. The Austin Area group is a hybrid group, which also has monthly in-person meetings. […]
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North Metro Support Group (MN)
Virtual EventTo register & for more information, please email uglchapter@scleroderma.org
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Stepping Out to Cure Scleroderma – Houston
Join us on November 14 for Stepping Out to Cure Scleroderma - Houston, honoring Jacob Giovanna. Register by October 23 to guarantee a t-shirt. Date: November 14, 2026 Registration Time: 9:00 a.m. CT Walk Time: 9:45 a.m. Location: Houston, TX - More details to come. Click here to register in advance.
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Autoimmune & Scleroderma Support Group
Virtual EventTo register & for more information, please email pcollins@scleroderma.org
The Foundation’s peer-reviewed research grant program is a leader in scleroderma research. Learn more about how this program accelerates the search for better treatments, and ultimately, a cure.
