
National Scleroderma Foundation
A relentless force in finding a cure and improving the lives of people affected by #scleroderma. The National Scleroderma Foundation's mission is to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support network. Our vision is to be a relentless force in finding a cure and improving care for people with scleroderma.

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1993
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National Scleroderma Foundation National Scleroderma Foundation Where to Start More than 300000 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 were advancing our mission faster than ever.
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Your voice can help shape the future of scleroderma research and care. Through our Patients as Partners program, you can share your journey and provide valuable insights that help guide clinical research and treatment development. Submit your form by November 15, 2025, to be considered for a 90-minute interview opportunity.
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