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
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
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
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