I walk for my daughter. I walk for my heart hero. Our story begins on May 11th, 2018. My daughter was born with a severe congenital heart defect called Tetrology of Fallot with Pulmonary Atresia. We were prepared but also unprepared. On May 24th, 2018 our daughter went for her first surgery and it didn't go as planned. She ended up having a second open heart surgery in her room. She ended up on ECMO for 5 days and we were being prepared for the worst but our daughter fought and pulled through. She went on to have her 3rd open heart surgey in August where they discovered yet another abnormality with her heart which would require another surgey. We spent over 200 days in the children's hospital and mad lots of friends who became our heart family. Our heart hero is the definition of a miracle but she isn't the only miracle. We meant so many kiddos who fight like she fought, we meant kiddos who won the fight and gained their angel wings. My wife and I's mission is to raise awareness for these kids because there is no cure that will fix thier disease. My why is simple, its Kaeli. 1 out of 100 children will be born with a Hear Defect. My daughter is that 1, she's the 1 percent of the 1 percent, she's my miracle kiddo but most importantly she's my HEART HERO!