We've created this page in honor of our son Cooper because he is our HERO. He inspires & motivates us to be better people. FAST is working hard for Cooper & his friends with AS & is close to a cure. Breakthroughs are being made by FAST,& we want to do our part by raising money to fund clinical trials for Angelman Syndrome. We are no longer hoping for a miracle; we are planning for it. 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 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 & is appreciated! The more people that know about FAST, the greater their impact, so please also spread the word by sharing my 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.
This is our son Cooper.
He smiles often & through many challenges .
He has the ability to turn most peoples moods around with his compassion, actions & kind heart.
He has the best judge of character & shows it if he chooses you as one of “his people” .
He has a way of spreading his love & how he feels about you without saying a word.
He has always enjoyed particular interests music & has dance moves like no other.
He doesn’t care about money, politics & nonsense.
He isn’t vain & doesn’t care about what others think of him.
He doesn’t stress about what the future may bring for him.
He is my son. He is my hero! He is my confidant. He is my world.
With countless possibilities that lie ahead for Cooper to talk, to live a life without fear of seizures, to lead a life of independence, to tell us his plan for world domination, to sing to his hears content. To hear his voice.
Right NOW there are significant & unequivocal scientific strides happening to make certain that Cooper will live to see a cure for AS in his lifetime.