We've created this page for our oldest daughter Aubrey who has Angelman Syndrome. She is 12 years old and has never spoken a word. She battles seizures and has challenges in her daily life that require constant supervision.
Her younger sister Molly is a cancer survivor and was able to survive because of the money and research poured into Leukemia over the past 50 years. We want to give Aubrey and all the other Angelman Syndrome patients that same chance for a cure. Given Angelman Syndrome is so rare - we need your help.
We're excited by the research breakthroughs being made by FAST, and want to do our part by raising money to fund clinical trials for Angelman syndrome (AS). FAST researchers know exactly what causes AS and have already cured it in the laboratory.
Today, five therapy strategies are in development to treat Angelman syndrome. Your donation to my page helps fund all of them. Please help us support this critical research by clicking the “Give Now” button and donating whatever you can. Every single dollar counts and is appreciated!
The more people that know about FAST, the greater their impact, so please also spread the word by sharing our page with your contacts. Since AS is a rare disorder, we truly rely on the support of friends and family members to fund this groundbreaking research. Thank you in advance for your generosity.