My Nonprofit Reviews

We received the diagnosis of Angelman Syndrome for our granddaughter in 2004. At the time of her diagnosis, both her neurologist and pediatrician provided outlooks on her future that were incredibly bleak. Through funding research and public awareness programs, FAST has given the families of the Angelman community hope. We are all observing a clinical trial of a medication that may yield positive results in treating some or all of the characteristics of Angelman Syndrome. This was unheard of in 2004! FAST gave us hope for a brighter future for our children. It is truly a wonderful organization!

More Feedback