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 is very excited to introduce Alison Fronning to the team. Alison joined the Foundation in…
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…
Events
-
-
Autoimmune & Scleroderma Support Group
Virtual EventTo register & for more information, please email pcollins@scleroderma.org
-
Denver Support Group
Hybrid EventThe Denver Mile High Support Group is hybrid and meets on the second Saturday of every month. Starting in January and through April, the meetings will only be held virtually. To register & for more information, please email rmchapter@scleroderma.org
-
Teal Hearts of Jacksonville Support Group
Virtual EventFor more information, please email floridaprchapter@scleroderma.org Use this link to register in advance: https://us02web.zoom.us/meeting/register/qWft8jCtQk6HUjt_qnfyrQ#/
-
Pacific Northwest Support Group
Virtual EventTo register & for more information, please email cfidalgo@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.