My Nonprofit Reviews

As a parent of a child with Angelman Syndrome, there are just not enough ways to express my appreciation for the work that F.A.S.T is doing. They are the driving force behind AS awareness and the advances in research that we have seen over the last few years. There is absolutely just no stopping F.A.S.T. in their mission to find a treatment for Angelman Syndrome. In addition to their work in research, they have developed an amazing community of parents/caregivers/educators/scientists that supports each other unconditionally. F.A.S.T. is most definitely making the lives of people living with AS and the world in general a much better place.

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