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.
For more than 20 years, Lisa dedicated her career to helping children learn and grow. A Tampa-area teacher, wife,…
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…
Events
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West Metro Support Group (MN)
Virtual EventTo register & for more information, please email westmetrosupport_ugl@scleroderma.org
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Texoma Scleroderma Support Group
Virtual EventFor more information, please email dcharlton@scleroderma.org Use this link to register in advance: Meeting Registration - Zoom
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Stepping Out to Cure Scleroderma – South Bend, IN
Potawatomi Park - Pavilion 2 500 S. Greenlawn Avenue, South Bend, IN, United StatesRegistration starts at 9:00 AM. The walk at 10:00 AM. Walk begins outside, across the parking lot at the park pavilion and then the walk ends inside the Potawatomi Zoo! 🦁🐒🦓 T-shirt deadline is August 5, 2026. CLICK HERE TO REGISTER
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Northern Colorado Support Group
To register & for more information, please email rmchapter@scleroderma.org This group meets on the fourth Saturday of even months.
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.
