I've created this page because I'm inspired by the breakthroughs being made by FAST, and I want to do my 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 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! 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.
Our son Naveen has been diagnosed with Angelman Syndrome in his 18 months. We were devasted to know this news. But he his our angel. His smile and loving hug makes our each day a best one. Naveen still cannot walk and are not able to make any word. He likes music, books, and water, his favorite toy is iPhone, favorite person is his sister, best time of the day is when daddy comes back from work, do not like the word "Goodbye", and only food he likes is Mac'N'Cheese. His life is full of therapies now. With your donation may be scientist will get a cure for our son and may be he will be able to walk, talk, eat by himself, or go to bathroom by himself. Please donate whatever you can. Please share this message with your friends, families, and colleagues. Try to double your donation by taking advantage of your company's corportate matching program. Also, pray for our son so that he can cope up with his challenging life ahead.