We have been on a journey with Angelman Syndrome for 9 1/2 years now, and see the daily struggles Kyla deals with. Many of you see her happy smile, but you don’t see the frustration, seizures, struggles with communication, sleep issues, educational struggles and being excluded from so many things that other kids her age enjoy. Today, five therapy strategies are in development to treat Angelman syndrome. Your donation to my page helps fund all of them. Please help me support this critical research by clicking the “Give Now” button and donating whatever you can. Every single dollar counts and is appreciated! 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.