The things we do for love – Virtual 5k
by Timothy Misiak My cousin’s daughter Kyla was diagnosed with a rare neurodevelopmental disorder called Angelman Syndrome (AS) when she was only 22
News
Generating support in the search for a cure – building partnerships
In an Australian first, the opportunity to hear about Angelman Syndrome research being conducted overseas was showcased at a scientific symposium at the Roya
Talking Science – Gala Scientific Round Table
After a wonderful party at the 5th annual FAST Gala on Saturday night, December 1, 2012, and a fantastic brunch sponsored by Yahoo! Sports and Union Pacific
FAST Grant-In-Aid Award: Potential new roles for UBE3A in Angelman Syndrome (AS)
FAST is pleased to announce a new Grant-In-Aid award in the amount of $41,460 to Dr. Zafar Nawaz at the University of Miami for his project entitled, “E6-A
Anyone can hustle
Written by Becky Rubenow Howard, Mom to Erinn. This year, over 60 parents, grandparents, siblings, aunts, uncles, friends, caregivers and angels boarded a t
It’s a Beautiful Day in the Neighborhood
In the Angelman Syndrome community, we often get to hear heartwarming stories of the good in other people. Maybe it’s the perspective we gain from lo
What the Gala means to me
From my first encounter with the Foundation for Angelman Syndrome Therapeutics (FAST), shortly after my youngest son’s diagnosis of Angelman Syndrome in No
A message from the Chair
This is normally my very favorite time of year. December brings with it the FAST Gala and Christmas all in one month. It is a time filled with so much c
Lighting a fire; FAST Integrative Research Environment (FIRE)
The Foundation for Angelman Syndrome Therapeutics (FAST) is proud to announce the launch of the most aggressive, novel and innovative research program to dat
Dogsledding in Sweden
by Alistair Blackburn Back when my son Callum (del +) was born, two great friends (Giles Derry and David Drake) kindly agreed to be his godfathers. They prob