The mission of the Scleroderma Foundation is: 1)To help patients and their families cope with scleroderma through mutual support programs, peer counseling, physician referrals, and educational information. 2) To promote public awareness and education through patient and health professional seminars, literature, and publicity campaigns. 3) To stimulate and support research to improve and ultimately find the cause and cure of scleroderma and related diseases.
The Foundation distributes numerous scleroderma books, specialized brochures, videos, and other information. Serial publication: Magazine, quarterly. Electronic Newsletter, Weekly.
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