Lifeline Fund

William

At five months William was diagnosed with a rare genetic disorder, a type of leukodystrophy called Krabbe Disease. In December 2014, William’s family moved from their home in Utah in order to prepare for his cord blood transplant at Children’s Hospital of Pittsburgh. Transplant is their only hope. In order to raise much-needed funds for the immense medical and living expenses they will incur during William’s treatment, Abbey and Robert have decided to team up with The Bone Marrow Foundation to help give William a second chance at life. Thank you!

The Bone Marrow Foundation relies 100% on private donations. Your generous Lifeline Fund donation will make a significant difference in the lives of patients like William.