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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.
The National Scleroderma Foundation community shined bright during the 2026 National Scleroderma Conference and Baltimore, Maryland. The conference celebrated…
The National Scleroderma Foundation is excited to announce that scleroderma will be part of the expanded Accelerated Medicines Partnership…
The National Scleroderma Foundation, a relentless force in finding a cure and improving the lives of people affected by…
Events
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Wisconsin Scleroderma Support Group
Virtual EventPlease click here to register in advance. To register & for more information, please email uglchapter@scleroderma.org
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Caregivers Support Group
ZoomVirtual EventThe Caregivers Support Group meets on the 4th Thursday of the month at 7:00 p.m. ET. Click here to register. A link to the Zoom meeting will be sent after […]
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Granite State Support Group
To register & for more information, please email NEchapter@scleroderma.org
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Southwest Support Group
Virtual EventTo register & for more information, please email rmchapter@scleroderma.org