You’re not alone.

The breaking of that awful feeling of isolation is the greatest gift one Angelman family can give to another . . . Those of you who will share your experiences will do it because in the Angelman family, that is what we do.  Whatever problems you have to meet, others not only understand, but have found a solution.  Whatever road you have traveled, others have traveled before you, so there is no need to travel alone.

Audrey Angelman

What Now? 

Families sometimes don’t know where to turn once they’ve received a diagnosis. It is life-changing and can be overwhelming. The ASF has been supporting Angelman families for over 25 years. We and our network of families are here for you. 

Start with these easy steps: 

  1. Please fill out the form below and we will send you a packet about AS and information about ways the ASF can help as you begin this journey.
  2. Use this website to help you become acquainted with Angelman syndrome and some of our services, like the Family Resource Team.
  3. Connect with the world-wide Angelman community through our social media channels. 

4.  Have a specific question and want to contact the ASF right away?  Call us at 800-432-6435 or email us at

Parent First Name (required)

Parent Last Name (required)

Spouse First Name

Spouse Last Name

Email (required)

Phone number (required)

Address (required)

Address 2

City (required)


Country or Province (required)

Zip or Postal code (required)

Relationship to Individual with AS (required)

Information About Individual with Angelman syndrome

First Name (required)

Last Name (required)

Date of Birth (required)

Gender (required)

Date of Diagnosis (required)

Genotype (required)