Please join us and walk with Coco on June 10th 8:30-12 in Chicago! It's always an amazing time for the whole family with lots of music and activites!
Research goes to helping kids like Coco. For those of you who don't know- Coco was born with HLHS (hypoplastic left heart syndrome). This means her left ventricle in her heart never formed, therefore her right atrium doesn't work... so her half-heart is beating twice as hard doing twice the work. You'd think this would slow her down... but thanks to this research and medical advances... and of course by the Grace of G-d it doesn't!
One ventricle children, like Coco, are in danger of other organs failing because they too are working twice as fast to keep up with their hearts. Typically they transplant other organs before being eligible for a heart transplant. Research is developing ways to protect one ventricle kids and their other organs.
Come walk with us and/or start your own page to fundraise and support children like Coco! ? Go Team Coco!
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. 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.
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.
