Our son Matthew was diagnosed with Prader Willi at birth. He was born at 32 weeks & almost didn't make it. He was on every machine imaginable. After Matthew's birth he was transferred to Women & Children's Hospital. Upon building strength from blood & platelet transfusions, it was confirmed that Matthew had Prader Willi Syndrome. During his two month stay, we often heard the doctor's & nurses say, "It couldn't happen too two better parents." Well Matthew is 5 years old now & is a loving & very happy little boy. He melts everyone's heart when they meet him. He always has a smile on his face. So I am helping to raise money for the Foundation for Prader-Willi Research & to strive for a better life for Matthew & other children living with syndrome. So it is very important that you give. All proceeds from the One SMALL Step walks go to fund the Prader-Willi Syndrome Research. Please Donate Today! To Learn more about PWS and this event at http://www.fpwr.org/.