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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.
“Know Scleroderma” is the National Scleroderma Foundation’s theme for June 2022 Scleroderma Awareness Month. Scleroderma is a rare rheumatic…
The scleroderma community is mourning the loss of Dr. Giuseppina Alessandra Farina, who passed away last week while in…
On April 21, 2022, the Foundation held a virtual brand launch event. It was great opportunity to unveil a…
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.
