Taylor was born with a rare syndrome called Cri du Chat syndrome. We got her diagnosis when she was just 9 days old. We were told she would never walk, talk or live to be a teenager. She is walking, talking and she is a healthy 19 year old. The money raised will go to the 5p- Society. The 5p- Society is the national support group for families that have a child with Cri du Chat or 5p- syndrome. For more information about the syndrome, check out the website at www.fivepminus.org