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
  - Available again in the Fall
  - Purchase ASF Decals
  - Be the Cure
  - Ways to Donate
  - Fundraising for ASF
  - Volunteer Opportunities
  - Shop & Support ASF
  - How Donations Are Used
  - 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
    Household Resources
    Inclusion Resources
    Recreational Resources
    Seizure Resources
    Special Needs Safety
    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
    
    My Marathon 2019
    
    September 1 - September 30
    
    27 Hours of CrossFit for Cameron
    
    September 28 @ 6:00 am - September 29 @ 9:00 am
    
    Bank of America Chicago Marathon 2019
    
    October 13
    
    CCK Angelman Family Retreats 2019
    
    October 18 - October 20
    
    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
Conferences
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Make an Impact

Name: CCK Angelman Family Retreats 2019
Start: 2019-10-18T00:00:00+00:00
End: 2019-10-20T23:59:59+00:00
Location: Center for Courageous Kids

Home / Make an Impact

Make a Difference for Angelman Syndrome

Thank you for wanting to support our mission! The Angelman Syndrome Foundation (ASF) has funded the most Angelman-specific research of any nongovernmental organization and is the leading source of information about Angelman syndrome research, support, education, and therapies.

Be the Cure for Angelman Syndrome

Be the Cure by staying involved with ASF.