The Foundation for a Cure for Mitochondrial Disease was established in November 2000, by Bill and Sandy Cunningham, who learned that their 10 year old daughter, Kelly, had Mitochondrial Disease. Unfortunately, she lost her battle in January 2005. Mitochondrial diseases are rare and insidious disorders with no clinically proven treatment, and premature death is currently the outcome. We are working hard to turn this around. The 501(c) 3 Foundation board is entirely made up of volunteers. Through the generosity of donors and golfers, all funds raised go to cutting-edge research to find a cure.
