In loving memory of Charlie's great grandmother, Beatrice Clark. Thank you for stopping by to learn more about Charlie and Angelman Syndrome. 

Charlie is a 3 year old girl who loves all things typical little girls love, stickers, music, her friends, and her baby brother Lincoln. One thing that is different in Charlie, is she is missing a single gene on her 15th chromosome, which makes motor movements challenging and is why she does not speak. Charlie uses a talker (ipad) to communicate, but deserves more. 

FAST researchers know exactly what causes Angelman syndrome (AS) and have already cured it in the laboratory. Together we CAN cure Angelman syndrome. 

Much of this pioneering, critical research was funded, one dollar at a time, by members of our FAST community- people like you! Today, this research has led to the announcement of several revolutionary clinical trials that hold the potential to treat, and ultimately cure, this rare disorder.

Your donation to my page helps fund critical research and ensures all promising treatments reach every individual with AS.Please help us support critical AS research by clicking the Give Now button and donating whatever you are able to. Every single dollar is appreciated and gets us closer to our goal! The more people that know about FAST, the greater the impact, so please also spread the word by sharing this page with your contacts.

Please help me reach this goal. Thank you in advance for your generosity.