In May of 2018, our sweet girls, Kaia & Emma, were diagnosed with Angelman Syndrome (AS). If you've ever met them, you know they bring joy to all those around them. They inspire us every day with their ability to overcome any challenge.
Angelman Syndrome is a rare neurogenetic disorder that results in many challenges. Although AS is a devastating disorder, there is HOPE for a CURE and we need your help!
We are inspired by the breakthroughs being made by FAST and we're raising money to fund clinical trials for Angelman syndrome. 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 Kaia & Emma's 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 the impact, so please also spread the word by sharing this page. 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.