At five months William was diagnosed with a rare genetic disorder, a type of leukodystrophy called Krabbe Disease. In December 2014, Williamâ€™s family moved from their home in Utah in order to prepare for his cord blood transplant at Childrenâ€™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 Williamâ€™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.