The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.
To assist the growing number of families needing support, the ASF created the ASF Family Resource Team, a group of experts in their respective fields that are helping families handle a variety of needs. Each member of the ASF Family Resource Team has a family member with AS, so each is personally familiar with AS and have experience in overcoming challenges faced by families and individuals with AS and in improving the quality of life for all involved.
Online Only Service
|Type of Organization||Nonprofit (501c3)|
|Categories||Disability Specific, Emotional Support, Medical, Other|
|Spanish Services Offered?||No|
|Child Care Available?||No|
|Age Range||All ages|
|This organization pertains to all disabilities?||No|
|This organization pertains to these specific diagnoses||Angelman’s Syndrome|
|Is this a statewide service?||Yes|
|Contact Name||Elizabeth Jalazo, Clinical Director|
|Email Address||[email protected]|