I’m Tyler Wilson and I want to thank you for visiting my website. I am 11 years old and live with my Mom, Dad, Sister, and my service dog, Anamarie in Dublin, CA. I was diagnosed with Angelman Syndrome, a rare neuro genetic disorder, when I was 1 year old.
Despite my many mental and physical challenges I am a happy kid who loves swimming, horseback riding, listening to music and being silly with my friends. In addition to my family I’m supported by 2 amazing caregivers, Shannon and Christina, who help me and my parents on a daily basis.
Family & friends,
We have created this page because we are inspired by the breakthroughs being made by FAST, and we 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 our 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.
Love, Reini & Ina