Thank you for visiting our Congenital Heart Walk team fundraising page for Molly! As many of you know, Molly was born with a critical CHD, called Tetralogy of Fallot with Pulmonary Atresia. She received life saving open heart surgery when she was just 5 days old, through The Children's Hospital of Philadelphia. Many people do not realize how important it is to fund CHD research because they have never been affected by it. There IS NO CURE for congenital heart defects. Those that are lucky enough to be treated face a lifetime of doctors, procedures, and surgeries. We are walking in honor of Molly, with hopes that money raised will go towards medical research that will end CHD and make life better for those that were born with it. Please consider making a tax deductible contribution to support my fundraising efforts on behalf of The Children’s Heart Foundation and the Adult Congenital Heart Association. All funds raised benefit CHD research and programs. I appreciate your support!