Mission & Vision
Our mission is simple. to share Jamie's memory, and to establish her legacy to aid in the funding for an eventual cure and treatment for all people with Angelman Syndrome.
The Foundation for Angelman Syndrome Therapeutics is an organization of families and professionals dedicated to finding a cure for Angelman Syndrome and related disorders through the funding of an aggressive research agenda, education and advocacy.
Where Your Donation Goes.
FAST's goal is to bring practical treatment into current medical practice as quickly as possible. It is our hope that grant we fund will lead to additional research support from government agencies and other funding sources.
Our volunteers
Volunteering
We have a wonderful group of dedicated volunteers, BUT, we always have room for more. If you have able hands, we want your help. Whether it's helping with check-in, selling mulligans, collecting donations, or just welcoming people as they finish their round, we need you!.
Such a joyful group to share the day with!! They truly have servants hearts.
Jamie's Family-Pictured left to right-Madison, Jackson, Mom (Cindy), Mekayla, Dad (Jason ), Rebekah and Lucas.
Mekayla and Rebekah also have Angelman Syndrome.
The Jamie Berkley Memorial Open is an annual event held in late september. The date of the event, is scheduled to coincide as close as possible with Jamie's Memorial Day. All profits raised are donated in Jamie's name to The Foundation for Angelman Syndrome Therapeutics (FAST) a Section 501(c)(3)non-profit, tax exempt organization designated under the Internal Revenue Code. F.A.S.T.'s EIN is 26-3160079.
www.cureangelman.org