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What is AS?
- - Genetic Mechanisms of Angelman Syndrome
  - Normal 15 Chromosome
  - We each have two number 15 chromosomes, one inherited from our mother (M.) and one inherited from our father (P, paternal). The Angelman syndrome gene (UBE3A) is located at chromosome 15, band q12, as depicted. In the brain, the Angelman gene is primarily expressed from the maternally inherited chromosome 15. The diagrams below illustrate the four known genetic mechanisms that cause Angelman syndrome. Continue Reading →
  - Newly Diagnosed?
  - Has someone in your family been recently diagnosed with Angelman syndrome? Fill out this simple form if you would like to receive more information on AS.
  - Participate Today
Research
- - AS Funded Research
  - The Angelman Syndrome Foundation is the largest non-governmental funder of Angelman syndrome-specific research. It is our hope that these funded researchers, and their collaborators and peers, will bring forth new discoveries that ultimately lead to treatments and a cure.
  - Find out more.
  - Call for Proposals
  - The ASF conducts biannual calls for research proposals. Submission deadlines for review occur annually on October 15 and April 15 for one- or two-year grants.
  - See submission details
  - Families: Find out about participating in Research Studies.
  - Participating in Research.
Make an Impact
- - ASF Pop-up Shops
  - Unique ASF Merchandise
  - Back again soon!
  - Be the Cure
  - Ways to Donate
  - Fundraising for ASF
  - Volunteer Opportunities
  - Shop & Support ASF
  - How Donations Are Used
  - Purchase ASF Decals
  - Personal Fundraising Pages
  - From garage sales and golf outings to climbing mountains, people honor their loved ones in many ways. Create a Personal Fundraising Page that tells your story and generate donations for ASF.
  - Start now
Resources & Education
- - Resources
  - Family Resource Team
    International AS Resources
    Federal Resources
    State Resources
    Regional Representatives
    Professional References
    AAC & Technology
    Education Resources
    Employment Resources
    
    Financial Planning
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    Therapy Resources
    Travel Resources
  - Education
  - Communication Book by Dr. Calculator
    Communication Training Series
    Educational Webinars
    IEP Bank
    Angelman Syndrome A to Z
Events
- - Upcoming Events
  - Events
    
    Bank of America Chicago Marathon 2018
    
    October 7
    
    Center for Courageous Kids 2018
    
    October 19 - October 21
    
    2019 Research Symposium & Family Conference
    
    July 23, 2019 - July 27, 2019
    
    View All Events
  - ASF Events
  - Throughout the year, the Angelman Syndrome Foundation hosts, participates and receives support from events across the country.
  - Have an idea, or plan to host a local event in your area? Emailkmurphy@angelman.org with the details.
  - Fundraiser Search
AS Clinics
- - Partnership
  - The ASF has partnered with leading medical and research institutions, to found the Angelman Syndrome Clinics, a medical and psychosocial resource from birth through adulthood. Each clinic has its own unique capabilities that leverage the expertise and specialized care available from each partnering organization.
  - Read more
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Walk

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2018 Angelman Syndrome Foundation Walk

Thank you to everyone who participated in the 2018 Walk! Mark your calendars for May 18, 2019.

See photos from Walks around the country.

The ASF Walk raises essential funds for research to find treatments and a cure for Angelman syndrome, and provides resources and support services to families of individuals with AS.

Our ultimate goal: A CURE. Be the Cure!

See below for locations

Already registered? Login to your account here:

Participant/Team Search

2018 Walk Sponsors

Fundraiser Toolbox

Coordinator Login

2018 Walk Locations

Can’t find a location close to you?

Virtual Walker

Have questions? Contact Kitty Murphy kmurphy@angelman.org or 800-432-6435.