Why I Fundraise for CHD Research

Hi, my name is Gabby and I was born with aortic valve stenosis. I have undergone two open heart surgeries to repair my aortic valve, had a pacemaker (named Finnegan) implanted, and became the 4th person at St. Louis Cardinal Glennon Children's Hospital and 110th person in the nation to receive the HAART 200. I want to express my heartfelt thanks for taking a moment to visit my fundraising page.

My commitment to making a difference has led me to participate in the Congenital Heart Walk, an event that carries immense significance for me. As someone living with a CHD, this isn't just a walk; it's a stride toward changing lives. This endeavor is all about supporting The Children's Heart Foundation and their crucial mission to advance the diagnosis, treatment, and prevention of congenital heart defects through groundbreaking research. It's because of research supported by organizations like CHF that I have hope for my future, and the future of those born with CHD.

I warmly invite you to become a part of this significant journey by supporting my fundraising efforts. Together, we can raise the funds essential to drive forward life-saving research. Your contribution holds immeasurable value to me.

Thank you for your generosity, and for standing beside me in this mission. Your support means the world.

- Gabby

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