I want to express my heartfelt thanks for taking a moment to visit my fundraising page.

As many of you know when Killian was born it came with many scary suprises. Hearing those words "its his heart" is something I will never forget. We watched a team come , pack up our baby, and take off to Akron Children's Hospital where at just 11 days old he had life saving heart surgery. Killian was born with whats called Coarctation of the Aorta along with a Bicuspid Aortic Valve. The Coarctation was fixed however the valve was left alone and is something killian gets checked on regularly.  He is no stranger to the heart center ?♥️

This year, I'm walking with extra purpose as The Children's Heart Foundation celebrates 30 incredible years of funding research that saves lives and changes futures. My commitment to making a difference has led me to participate in the Congenital Heart Walk, an event that carries immense significance for me—especially knowing that for three decades, CHF has been the leading force behind the treatments and surgical advances that help children with congenital heart defects thrive.

It's not just a walk; it's a stride toward the next 30 years of hope. This endeavor is all about supporting The Children's Heart Foundation's crucial mission—advancing the diagnosis, treatment, and prevention of congenital heart defects through groundbreaking research that improves survival rates, reduces complications, and helps Heart Warriors celebrate more birthdays than ever before.