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
by Timothy Misiak My cousin’s daughter Kyla was diagnosed with a rare neurodevelopmental disorder called Angelman Syndrome (AS) when she was only 22
In an Australian first, the opportunity to hear about Angelman Syndrome research being conducted overseas was showcased at a scientific symposium at the Roya
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 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
Written by Becky Rubenow Howard, Mom to Erinn. This year, over 60 parents, grandparents, siblings, aunts, uncles, friends, caregivers and angels boarded a t
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
From my first encounter with the Foundation for Angelman Syndrome Therapeutics (FAST), shortly after my youngest son’s diagnosis of Angelman Syndrome in No
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
The Foundation for Angelman Syndrome Therapeutics (FAST) is proud to announce the launch of the most aggressive, novel and innovative research program to dat
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