Saturday, May 18, 2024*
*in most locations
We’re celebrating the 25th Anniversary of the ASF Walk
The ASF Walk has raised $19.5 million since 1999. Those funds have made an enormous impact on the lives of those impacted by Angelman syndrome. From the ASF Clinics and groundbreaking research to the ASF Family Fund and free counseling services!
Join us to celebrate the trail blazers in the AS community who started a ripple of impact. We will raise funds to support the ASF mission and have a great time doing it.
Registration Opens
January 10
Save $5 on ALL FEES
Through January 14
January 15 – May 18
Adult – $30
Child – $20
Virtual Participant – $30
Free for Individual with AS
How it All Began
The very first ASF Walk was coordinated by neighbors of an Angelman family. Al and Barbara Kelkoff convinced Eileen and Tom Braun, daughter of Kaitlin who is diagnosed with AS, that a walk would be a great way to raise money for Angelman research, create community and raise awareness.
The initial even raised $26,000 and hosted people from 5 states around the Chicago area.
GOAL: $1.24 Million
ASF Walk Locations
Virtual participant options available at every location.
Allows you to join a team, even if you can’t be there in person.
Don’t see a location near you? Register for the Virtual Location.
Arizona
Phoenix (May 11)
Arkansas
Hot Springs
California
Capitola
Los Angeles
Sacramento
San Diego
Colorado
Colorado Springs
Connecticut
Cheshire
Delaware
Dover
Florida
Sarasota
Georgia
Atlanta
Illinois
Chicago
Iowa
Bettendorf (May 19)
Indiana
Indianapolis (May 19)
Kansas
Olathe
Kentucky
Louisville
Louisiana
Gonzales (April 27)
Maryland
Baltimore (May 25)
Garrett County
New York
Buffalo
Westchester
North Carolina
Charlotte
Oklahoma
Oklahoma City
Pennsylvania
Centre Hall
Philadelphia
South Carolina
Upstate
Tennessee
Memphis
Smoky Mountains
Texas
Austin
Dallas-Fort Worth
Houston
Utah
Salt Lake City
Washington
Seattle
Wisconsin
Oshkosh
Thank you ASF Walk Sponsors!
Thank you to all of our ASF Walk Sponsors! You make a direct impact on the lives of individuals with Angelman syndrome and their families.