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
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
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
“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
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
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
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
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
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