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The National Scleroderma Foundation is a 501(c)(3) nonprofit organization founded in 1998 to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support networks. Supported by a network of thousands of individuals across the United States, the Foundation helps those living with scleroderma by providing support and education at the same time that it funds peer-reviewed scleroderma research. Since its founding, the Foundation has committed over $30 Million to discover the cause, understand the mechanism, and overcome scleroderma forever. The Foundation is home to the National Scleroderma Conferencethe only educational program...
Scleroderma,systemic sclerosis,localized scleroderma,medical research,disease awareness,rare disease,autoimmune disease,raynaud's phenomenon,patient support,patient advocacy,continuing medical education,orphan disease,research grants,pediatric scleroderma,scleroderma centers,treatments and medication,national scleroderma conference,scleroderma voice magazine,and chronic disease
National scleroderma foundation operates in the Non-profit organizations industry.
National scleroderma foundation's revenue is 11m - 100m
National scleroderma foundation has 51 - 200 employees.
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