Gianna was diagnosed with Angelman syndrome (AS) when she was 15 months old. Matt and I were told that Gianna will never talk, might never walk, will have epilepsy, intellectual disability, sleep issues and severe anxiety. We were completely heartbroken and shocked. We felt completely helpless until we met several scientists that informed us of all the incredible scientific breakthroughs. We learned that AS HAS BEEN CURED several ways in the lab. The only thing preventing the cure being brought to market is money. Once we heard this we knew we had to be a voice for Gianna and the entire Angelman community. We are on a mission to raise awareness and money for FAST, the largest funder of Angelman syndrome research in the world. We are at the finish line and your donations will help eradicate a severe neurological disorder and allow kids like Gianna to have a much better life. Please help us on our mission!!!