Long Island Congenital Heart Walk

Will the Warrior

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

Our son William was born with a Double Outlet Right Ventricle with TOF physiology. He had life saving open heart surgery at 2 months old. They were unable to spare his pulmonary valve, and he currently does not have one. We are hoping that research continues to advance so that when the time comes for Will to get a pulmonary valve, it can be a procedure and not open heart surgery. We walk for William, and all of the other heart warriors and angels. We are so grateful that William is thriving today.

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.

I warmly invite you to become a part of this milestone journey by supporting my fundraising efforts. Together, we can raise the funds essential to continue the life-saving research that turns heartbreak into hope. Your contribution holds immeasurable value to me and to every family who needs CHF's support.

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