Amanda Moore,  —

Amanda Moore is the CEO of the Angelman Syndrome Foundation (ASF). After her son Jackson was diagnosed with Angelman syndrome in 2016, she joined the ASF board before becoming CEO in 2019.

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When the world forgets our children

This article was provided by our partner, the Angelman Syndrome Foundation. It has been reviewed by Bionews for accuracy and relevance. The views and opinions expressed are those of the author and do not necessarily reflect the views of Bionews or Angelman Syndrome News. I’m writing this because I don’t…