AS In the News
My Daughter, My Angel
One physical therapist is determined to keep a child with Angelman Syndrome fighting to achieve m read more...
Medical family tackles rare genetic disorder
In fight against Angelman Syndrome, sisters help organize walk-a-thon.
For most children, read more...
ASF News and Announcements
2009 ASF National Walk-A-Thon
“…Saturday, May 16, 2009 the ASF National Walk-A-Thon will be held in 24 cities across the US. Today your participation is more critical than ev read more...
The 2008 ASF Walk Newsletter is now available for download.
The 2008 Walk Newsletter is a testament to the many donors, volunteers, sponsors and coordinators that hel read more...
Coveted 4-Star Rating Awarded to the ASF!
On behalf of Charity Navigator, I wish to congratulate Angelman Syndrome Foundation on achieving ou read more...
What is the Angelman Syndrome Foundation?
The Angelman Syndrome Foundation is a national 501(c)(3) organization of families, caregivers and medical professionals who care about those with Angelman Syndrome. Our mission 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.
