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.
With Scleroderma Awareness Month just a week away, the National Scleroderma Foundation is incredibly excited to share some news…
Advocates from the National Scleroderma Foundation traveled to Washington, D.C. this past weekend to participate in Hill Day 2026…
The National Scleroderma Foundation is proud to announce the 2026 Scleroderma Research Grant Award recipients. To date, the National…
Events
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Scleroderma Awareness Month
Featured Scleroderma Awareness MonthJune is Scleroderma Awareness Month. We know that every person’s experience with scleroderma is unique. Each June, the National Scleroderma Foundation shines a light on individual journeys with scleroderma by […]
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Boardman/Youngstown Support Group
Hybrid EventThe Boardman/Youngstown Support Group holds hybrid meetings on the first Monday of the month. The meetings are on Zoom and at Davidson's Restaurant on Canfield Rd. in Canfield. To register & for more information, please email lglchapter@scleroderma.org.
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Working Through Scleroderma Support Group
Virtual EventJust like each of our lives are different, so are our lived experiences with scleroderma. One thing we all seem to have in common is that at some point in this journey we have found the need to advocate for ourselves, whether it has been with family, friends, in our jobs or in a medical […]
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Pulmonary Arterial Hypertension Support Group
ZoomVirtual EventThe Pulmonary Arterial Hypertension Support Group meets on the first Tuesday of the month at 3:00 p.m. ET. Please click here to register in advance. A meeting link will be shared after registration. For more information, please email PAH@scleroderma.org.