When you set out to cure an ‘incurable’ genetic disorder, you need three things: a comprehensive, well thought out plan; a dedicated and passionate community; and sufficient, often substantial, funding.

FAST feels strongly that we are in the final stages of bringing effective therapeutics to the clinic. We would not be at this point today if it were not for our unbelievably supportive community. The majority of research funds spent to date have come largely from our Angelman Syndrome parents and those who support us.

Please contact us with any ideas for fundraising.

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