My Nonprofit Reviews

My son has Angelman Syndrome and is 25 yrs old. It took years of learning and working with him and years of parents hoping endlessly for something that could just help our children. It seemed hopeless listening to researchers and doctors and I left the community-sharing on line. However, when I returned, I found the FAST Organization and learned how starting with one mom (Paula Evans) brought together parents and professionals to the present day of current trials of a medication that may help our children. FAST makes a commitment of never giving up and they also continue to support us and our children. This is a GREAT Nonprofit!

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