I want to express our heartfelt thanks for taking a moment to visit Liora's fundraising page.

In September of 2024 we discovered that Liora had a rare congenital heart defect. She was diagnosed with an anomalous right coronary artery. This defect is only present in  0.1% of the population. Because this defect is so rare, there is much that is unknown about how to best treat and care for Liora. We have spent the time since her diagnosis doing lots of testing, monitoring, and speaking with committees of specialists. Like others living with CHD, she has a long and uncertain road ahead. But we are committed to walking alongside her and doing all that we can.

Our commitment to making a difference has led us to participate in the Congenital Heart Walk, an event that carries immense significance for Liora. It's not 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 - advancing the diagnosis, treatment, and prevention of congenital heart defects through groundbreaking research.

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

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