A Chance Encounter…A Forever Friend
I don’t think a day goes by when a board member of FAST isn’t asked why or how we volunteer so much of our time and energy to this organization. The an
Moms Rock 5K for FAST
Meet 3 year old Anna. Anna is an adorable Castle Rock preschooler and the oldest daughter of two Active Duty Air Force parents. Anna is a big sister with
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
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
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
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
Science is on our side
Anniversaries are typically a date in which we celebrate achievements, important, happy milestones-yet often anniversaries can also mark pivotal times in our
Little Things That Inspire…
by Jason Berkley Cindy and I had been together just a little over five years when Jamie was born. We already had a 4-year-old son Luke and a 2-year-old daugh
Community Nominates FAST for Chase Giving Contest
Great news!!!! The Angelman community has nominated the Foundation for Angelman Syndrome Therapeutics (FAST) to be a part of the 2012 Chase Community Givin