Houston Congenital Heart Walk

My Story.

First I would like to express my heartfelt thanks for taking a moment to visit my fundraising page.

As you may know I was born with a very unique heart. Hypoplastic Right Heart Syndrome, mom didn't know what or how life would be. She definitely knew I would be loved beyond measure. As most of you have followed my story from day one, some of you may not have.

My birthday is July 22nd, on day 2 of life I had my first open Heart surgery. We spend almost 3months in the hospital. I came come with oxygen & weekly doctors visits. At 6 months I had my second open Heart surgery. This one took a little more time to heal from. We spent a few weeks in the hospital and came home with a feeding tube. Definitely not fun. Nevertheless, the tube was gone before I turned 1. In August 2023, I turn 3yrs old I had my 3rd open Heart surgery. This time I bounce back fast! We spend a few days in the hospital & came home with a new piece of equipment.... A pacemaker. We have learned our new normal, which is as normal as anyone else.

The Congenital Heart Walk, is an event that carries immense significance for me and my family. It's not just a walk; it's a stride toward changing lives. The Children's Heart Foundation and their crucial mission - advancing the diagnosis, treatment, and prevention of congenital heart defects through groundbreaking research.

I 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 and my family. Without all the amazing research that's been done before me, I may not have been able to come this far. Let's help the research continue.

We would like to Thank you from the bottom of our hearts for standing beside me in this mission. Your support means the world to us!