Breck and I are supporting our friends Kevin and Jenni and their precious son Henry by participating in the Congenital Heart Walk on September 28th!

All funds raised support The Children's Heart Foundation and their crucial mission - advancing the diagnosis, treatment, and prevention of congenital heart defects through groundbreaking research.

We invite you to come walk or make a donation to drive forward life-saving research.

Thank you for your generosity!

About Henry

My name is Henry Kuntz, I was born on October 11, 2021 with my identical twin Paul. I was born with multiple CHD defects including hypoplastic left heart syndrome, total anomolyous pulmonary venous disease, and pulomnary venous disease, As of right now, there are no cures for my disease. The doctors told me I was only going to live a few weeks, but I am still here and THRIVING because I am a FIGHTER!! I recently have learned to walk with my walker and I am starting to nibble on solids. My favorite things are snuggles with my mom and dad, spending time with my siblings, and watching Nemo when mom puts it on :)

My parents have spoken with childrens' hospitals around the US and abroad. I even got to go on a trip to Boston Children's! But unfortunately, they all told us the same thing, which is there is nothing they can do to help me. We need your help to fund CHD research and help kids like me and other families suffering from these diseases. 

Did you know that the majority of money for heart research goes to adult heart research? We need more money for kids like me!! 

A message from Henry's parents - Henry has taught us to live life in the moment. Appreciate every smile, every laugh, every cry. We only pray for one more day with him. Please consider donating to help Henry and other families and individals affected by these devastating diseases.