Who Are We?
Pacific Northwest Angelman Syndrome Foundation 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 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.
Membership in the Pacific Northwest Angelman Syndrome 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 adult 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.