Kendall Burrows Foundation

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. During her lifetime, Kendall was an inspiration for how she lived with grace and strength despite intermittent and sometimes lengthy hospital stays. She stands for all children who must face incredible odds and yet do so with a smile on their face. Out of heartbreak, The Kendall Burrows Foundation was born to: 1. Create loving and healing environments for children facing long-term hospital stays and critical illness 2. Raise awareness and increase donations of whole blood and platelets 3. Advocate, educate, and contribute to research for Evan’s Syndrome and similar autoimmune blood disorders To support the number one piece of our mission, The Kendall Burrows Foundation has partnered with the Johns Hopkins Children’s Center to support the Harriet Lane Compassionate Care program (palliative care). We raise funding to support families and children with critical and terminal illness at the Johns Hopkins Children’s Center.