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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 is proud to announce the recipients of the 2026 Pre-Doctoral Fellowship awards. The Pre-Doctoral Summer Fellowship…
During the 2026 National Scleroderma Conference in Baltimore, the National Scleroderma Foundation proudly recognized the extraordinary volunteers, advocates, healthcare…
The National Scleroderma Foundation community shined bright during the 2026 National Scleroderma Conference and Baltimore, Maryland. The conference celebrated…
Events
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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
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Utah Support Group
Virtual EventTo register & for more information, please email rmchapter@scleroderma.org
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Tampa Support Group
Virtual EventTo register & for more information, please email floridaprchapter@scleroderma.org
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Scleroderma and Endometriosis Support Group
Virtual EventThis support group will meet every other month on the 1st Saturday at 6:00 pm CT. To register in advance, please email achadwick.scleroderma@gmail.com.
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.