International Angelman Day: What’s on & what you can do
This International Angelman Day. The goal is to raise awareness of Angelman syndrome worldwide, mobilize people to action, encourage fundraising, promote r
Boston on FIRE
What do you do when you are told your child has a rare and debilitating condition and that the science suggests it can be treated or cured, but the researche
Make it Happen
The Federal Government’s Combined Federal Campaign (CFC) season has kicked off and FAST; the Foundation for Angelman Syndrome Therapeutics (CFC #5105
Moms Rock!!!!
On May 11th in Castle Rock, Colorado, approximately 400 participants came out for the first-ever “Moms Rock 5K” for FAST! A virtual run was also held w
The Ripple Effect
My name is Alex McFee; I am a senior at Western Michigan University and am an active member of my sorority Sigma Kappa. Each year for Greek Week the frater
FAST Announces The 2nd Annual Global Summit on Angelman Syndrome
The Foundation for Angelman Syndrome Therapeutics (“FAST”) is pleased to announce that the 2nd Annual Global Summit on Angelman Syndrome will take place
Lite the Night on FIRE, a benefit for FAST
Please join us for a unique fundraising event on Friday, Sept. 11th, 2015 at Boston Harbor Hotel from 7:00-11:30pm. Enjoy great food & drinks, dancing t
More than just a wheelbarrow
Most parents of a child with Angelman syndrome (AS) would do whatever it takes to create a new, brighter future for their children and a great deal of us cho
Extraordinary measures
“It is good to have an end to journey toward; but it is the journey that matters, in the end.»~Ernest Hemingway To families of individuals with Angelman S
Making the Bank Pay
A monumental amount of training is required to tackle an Ironman, our community, with two dedicated running groups; Miles for Smiles and Angel Runners is ete