My Nonprofit Reviews

My daughter was diagnosed with Angelman Syndrome in 2007 when she was just over one year old. The information we received was incredibly bleak and we were devastated. Not long after we discovered F.A.S.T and were given wonderful information and discovered they were hopeful that a treatment would be found in the near future which would improve our childrens lives. Since then we have been full of hope, and are incredibly excited about the current trial in Florida. Thank you F.A.S.T for everything you do for our Angel Families. Anne Gribbin

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