The Kendall Burrows Foundation was founded by the Deb and Dave Burrows to honor the memory of their daughter, Kendall, who passed away from Evan’s Syndrome in 1996. The Kendall Burrows Foundation advocates, educates, and contributes to research for Evan’s Syndrome and similar autoimmune blood disorders; raises awareness and increases donations of whole blood and platelets with the American Red Cross; and creates loving and healing environments for children facing long-term hospital stays. Kendall’s memory serves as the inspiration, standing for all children who must face incredible odds and yet do so with a smile on their face.