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.
Heidi Jacobe, MD, MSCS, will serve as chair of the Department of Dermatology at Duke Health beginning in December….
National Scleroderma Foundation leadership is aware of the pause in two CAR-T clinical development programs and is closely following…
The National Scleroderma Foundation joins the scleroderma community in mourning the passing of Dr. Thomas A. Medsger Jr., a…
Events
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Granite State Support Group
To register & for more information, please email NEchapter@scleroderma.org
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Mid-Atlantic Support Group
The Mid-Atlantic support group is meeting on Saturday, October 31st at 11:00am ET. Please register in advance here: https://scleroderma.org/MidAtlantic-SG-Oct31 Questions? Email: Mid-AtlanticSG@sclerodermavolunteer.org
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#TealTalk: Raynaud’s, Winter & You
FeaturedZoomVirtual EventAs temperatures drop, Raynaud’s can become more challenging for people living with scleroderma. Join us for this #TealTalk to learn practical tips for managing Raynaud’s symptoms, protecting your hands and […]
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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 […]
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.
