The Scleroderma and Fibrotic Diseases Foundation is deeply grateful to all of our partners. Together, we successfully leverage our resources to improve lives. Interested in partnering with The SFDF? Fill out the form below to get in touch!
Camp Diasozo is a unique camp working to enrich the lives of children with morphea and scleroderma (and their families) by offering a retreat-like environment for them to enjoy. For chronically ill children and their families, hope is an integral part of coping. Camp Diasozo strives to give that hope to those children by giving them a place where they can go to make new friends they can learn from and share with, a place for their families and others who struggle with the same health and social issues, and most of all- a place where they belong.
Sara Othon Foundation
Alex Othon is the President of the Sara Othon Foundation and husband of Sara, who has been suffering from Scleroderma for the last 12 years. The foundation was set up to spread awareness and collect funds for research about Scleroderma, and it hosts many events during the year. It has donated over 60K for research to the Johns Hopkins Scleroderma Center and Southeast Florida Scleroderma Foundation Chapter.