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Pacific Northwest Angelman Syndrome Foundation


Who Are We?

Pacific Northwest Angelman Syndrome Foundation (PNWASF) was formed in 1994 to increase public awareness of Angelman Syndrome (AS) and to support and serve as a resource for individuals with AS and their families in the states of Washington, Oregon and Alaska.


PNWASF is currently in the process of renaming the foundation to Angelman NW.  The foundation has an all-volunteer board of directors elected by the members. Our members and their families volunteer countless hours to make the organization a success while raising children with AS. Thank you to all of them for their hard work and dedication. 


Board of Directors


Membership in the Foundation connects you to a local community of individuals with similar challenges and experiences. Members are able to participate in all activities including Great Wolf Lodge, camps and the family retreat/business meeting. As a member you also have the opportunity to receive a scholarship for the ASF conference. Becoming a member is a quick and easy process. Membership is on a yearly basis and it is open to individuals, families and medical professionals. Become a member for the first time or renew your membership online or by mail.


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