Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births or 500,000 people worldwide. It is caused by a loss of function of the UBE3A gene in the 15th chromosome derived from the mother.

In this episode we hear from Amanda Moore, CEO of the Angelman Syndrome Foundation, speak on her personal connection with Angelman and all the incredible efforts their Foundation has going.