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.
National Scleroderma Foundation CEO, Mary J. Wheatley, IOM, CAE, joined the global scleroderma community at the 9th Systemic Sclerosis…
More than 1,000 clinicians and researchers joined together for the 9th Systemic Sclerosis World Congress. Organized by the World Scleroderma Foundation, the event runs…
The National Scleroderma Foundation and our network for patient advocates are preparing for our next Virtual Hill Days meetings….
Events
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Virtual Hill Days
Featured AdvocacyZoom 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. -->
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Austin Area Support Group
Virtual EventThis group will meet virtually on the 2nd Thursday of each month. CLICK HERE TO REGISTER
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Raynaud’s and Scleroderma, Dr. Ben Korman – Webinar
Virtual Event<!-- If you embed multiple forms on your page, only copy one of the lines. Otherwise, multiple copies of the form will appear. -->
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North Metro Support Group (MN)
Virtual EventTo register & for more information, please email uglchapter@scleroderma.org
