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.
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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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
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Orange County Support Group (Hybrid)
This support group meets at the Josephine-Louise Public Library in Walden, NY and offers a virtual option. The library is inside of Walden's Municipal Building, and the community room is […]
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Central North Carolina Support Group
Virtual EventTopic: The Future of Lung Health and SSc, Guest: Dr. Murali Ramaswamy - Lebauer Pulmonology, Greensboro NC and Pulmonix - Clinical Trial Research CLICK HERE TO REGISTER IN ADVANCE
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.