The Angelman Syndrome

The Angelman Syndrome Foundation improves the lives of people with Angelman syndrome, and their families by providing: 

Research to Find Treatments and a Cure for Angelman Syndrome: 

• http://www.angelman.org/research/

Learning and Educational Opportunities: 

• Educational Webinars: http://www.angelman.org/get-involved/educational-webinar-series/
• Educational Conferences: http://bit.ly/1sVfpgf
• Resources and Resource Team Support: http://www.angelman.org/understanding-as/resources/

Angelman Syndrome Clinics for Comprehensive and Specialized Care: 

• http://www.angelman.org/about/angelman-syndrome-clinics/

Behavioral Support for Careproviders and Educators: 

http://www.angelman.org/understanding-as/angelman-syndrome-behaviors-informational-series/

Annual National Walk to Raise Awareness and Financial Support: 

• http://bit.ly/1fki2r9
• 3rd Weekend Each May (May 19, 2018 - Lisle, IL!)
• More than 40 locations, including Canada and Mexico
• Largest Angelman fundraising and awareness event world-wide
• Raises funds to support ALL aspects of our mission 

The Angelman Syndrome Foundation is a national 501(c)(3) non-profit located in DuPage County, Aurora, IL. We serve thousands of people with Angelman syndrome, and their families, in DuPage County and in all 50 states plus over 50 countries world-wide. We are a dedicated group of parents and professionals who daily support all people with Angelman syndrome, and their families, through research, education, information, support and advocacy. 

Established in 1989 and incorporated in 1992, the Angelman Syndrome Foundation is the largest, most established Angelman organization in the world. We are the largest non-government support of Angelman-specific research and to date we have provided funding support for over $8 million in Angelman research to find viable treatments and a cure for Angelman syndrome. 

http://www.angelman.org/research/