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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Utah Support Group
Virtual EventTo register & for more information, please email rmchapter@scleroderma.org
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Tampa Support Group
Virtual EventTo register & for more information, please email floridaprchapter@scleroderma.org
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Curling for a Cure
The National Scleroderma Foundation - Lower Great Lakes Chapter brings you Curling for a Cure. A 2 1/2-hour event in which you’ll learn the basics of curling with qualified instructors […]
$70 -
Supporting Your Loved Ones – Webinar
FeaturedVirtual EventThe National Scleroderma Foundation invites caregivers and loved ones of people living with scleroderma to a special, peer-led panel discussion focused on navigating the unique challenges of caregiving. Caring for […]
Free
