Angelman syndrome is a rare neuro‑developmental disorder that affects one in 15,000 people.The Angelman Syndrome Foundation is advancing the awareness and treatment of Angelman syndrome through education, research, and support for individuals with Angelman syndrome and their families. They’re giving the community a reason to smile, with the ultimate goal of finding a cure. With us this morning to talk more about Angelman Syndrome Foundation and the work they are doing for people with Angelman syndrome is Katie Weber, the Chicagoland Area Walk Coordinator for the organization’s upcoming event.

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