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The mission of the Scleroderma Foundation Minnesota Chapter is threefold: 1. To provide educational and emotional support to people with scleroderma and their families; 2. To stimulate and support research designed to identify the cause and cure of scleroderma as well as improve methods of treatment and; 3. To enhance the public’s awareness of this disease.
The Scleroderma Foundation Minnesota Chapter is a nonprofit organization serving as a voice for those in Minnesota who are afflicted with scleroderma. SFMC is d edicated to providing advocacy and support for its members; educating members, scleroderma patients, their caregivers, healthcare professionals, and the general public about scleroderma; and raising funds for research to identify the cause and a cure for scleroderma, while enhancing the quality of life for patients.