Dallas Congenital Heart Walk presented by Children's Health

Hi!

My name is Henry Kuntz, and I was born on October 11th, 2021 with my identical twin, Paul. I was born with multiple CHD defects including hypoplastic left heart syndrome, total anomolous pulmonary venous return, and pulmonary venous disease. As of right now, there are no cures for my heart problems. The doctors told me I was only going to live a few weeks to a few months, but I am still here and THRIVING because I am a FIGHTER!! I am walking everywhere and FAST without my walker! And sometimes on a good day I will nibble on some solid foods. My favorite things are snuggles with my mom and dad, playing with my brothers, swimming in the pool, playing with my hot wheels, and watching Wreck It Ralph or Soul when my mom puts it on :)

My parents have spoken with children's 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 that they can do to help me. We need your help to fund CHD research to find new cures to help kids like me and other families suffering from these disesases.

A message from Henry's parents - Henry has taught us to live life in the moment. Appreciate every smile, every laugh, every cry. He brings our entire family together and lifts us all up with his strength. We only pray for one more day with him. Please consider donating to help Henry and other families and individuals affected by these devesating diseases.

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

Henry Kuntz :)

Jennifer Kuntz

Henry's Fundraising Page

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