Aislinn’s Wish Foundation is a non-profit organization created to improve the lives of children diagnosed with the rare, genetic, terminal disorder known as Sanfilippo Syndrome. The Foundation strives to promote awareness and contribute to scientific research, with the goal of finding a cure for Sanfilippo Syndrome.
Amy and Brian Fadden founded Aislinn’s Wish in May 2016 in honor of our daughter Aislinn Delaney Fadden.