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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.
On March 21, the National Scleroderma Foundation announces the return to in-person meetings and events. The Board of Directors…
Registration OPEN for National Scleroderma Conference Join us at July 14, 15 and 16, 2023 for the National Scleroderma Conference…
Registration for the 2023 National Scleroderma Conference is now open. Join us July 14-16, at the Signia by Hilton…

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.