SUKI Foundation is a not-for profit organization created in honor of our daughter, Sarah Katherine, affectionately known as Suki, following her diagnosis of Rett Syndrome at age two. In efforts to raise awareness and assist children in reaching their potential through early intervention services, SUKI Foundation is dedicated to improving the lives of those affected with RS and other neurological disorders. With early detection and diagnosis, the life of a child with RS can greatly be improved. Funds will assist families in early detection, and upon diagnosis, be instrumental in assuring Early Intervention by providing support, education, and the most therapeutic services possible through Early Learning Programs.