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 delighted to be participating in the Rare Disease Week and Rare Disease Day activities…
The National Scleroderma Foundation is very excited to introduce Chrissy Geimann to the team. Chrissy joined the Foundation in…
The EACH/PIC Coalition has released an updated, patient-led analysis that sheds light on how people across the U.S. actually…
Events
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Bereavement Support Group
Zoom Meeting link available after registrationVirtual EventIf you have lost a loved one to scleroderma, you may find support and solace in speaking with others who are grieving. Our monthly bereavement support group will be on […]
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Morphea/Localized Scleroderma Support Group
Zoom Meeting link available after registrationVirtual EventThe Virtual Localized Scleroderma Support Group will meet at 7 p.m., Eastern, 3rd Tuesday of each month. Click here to register in advance. A meeting link will be shared after […]
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Texoma Localized/Morphea Support Group
Virtual EventFor more information, please email support@scleroderma.org
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#TealTalk | Advocacy in 2026 – Updates & How to Get Involved!
Zoom Meeting link available after registrationVirtual Event<!-- If you embed multiple forms on your page, only copy one of the lines. Otherwise, multiple copies of the form will appear. -->
