This is a fundraising page for our sweet Everly. She was born with Angelman Syndrome. Everly is fully dependent on us as her parents. She is nonverbal, lacks the ability to walk, perform simple tasks and suffers from seizures. There is a cure on the horizon and we want to do our parts as her parents to help raise funds for that cure!There are breakthroughs being made by FAST including 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 our daughter'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 their impact, so please also spread the word by sharing this page with your contacts. Since AS is a rare disorder, we truly rely on the support of our friends and family members to fund this groundbreaking research. Thank you in advance for your generosity.