Know Our Work:
SCLERODERMA FOUNDATION
The Scleroderma Foundation is thousands of individuals across the United States engaged in a great undertaking to provide support and education to individuals and families affected by scleroderma while funding more than $1 million in research to discover the cause, to understand the mechanisms, and to overcome the symptoms of scleroderma. Our National Patient Education Conference is a hallmark of patient outreach and our highly respected Peer-Review Grant Program helps establish research careers and facilitates innovation by established investigators. Locally, 20 chapters manage support groups, host patient education workshops and fundraise to fuel our threefold mission: support, education, and research.