We're truly grateful for your visit to our team page!

The first year we came to this walk, I will never forget as we were checking in one of the volunteers asked "Who are you walking for" and I looked down pregnant belly, and said "My baby". This organization has a very special place in our hearts. This year will be our 5th year in a row walking to honor all of the incredible, brave, resilient Heart Warriors, like Eli. 

We have always told Eli that he was born with a special heart. That his heart is his superpower and he spreads love and light everywhere he goes. Anyone who knows Eli knows that this is exactly what his heart is, hence the name of our team. Ask Eli for some "heart light" and he'll give you the biggest, most special hug, and I guarantee you will feel it.

At my 20 week ultrasound, Eli was diagnosed with d-TGA. A type of congenital heart defect that effects roughly 1,153 babies in the U.S. each year. We were told we would need open heart surgery within the first week in order to survive. So before he was born, we relocated up to Boston. At just a day and a half old, he underwent an arterial switch operation at Boston Childrens Hospital. We are eternally grateful for his incredible surgeon and team that cared for Eli during his hospitalization. We are so fortunate that Eli was given a great prognosis, and we'll continue to follow up with his Cardiologist each year. 

But for now, you can catch Eli running around outside, being a great big brother to Kallie and Leo, playing soccer on Saturdays, making friends at the playground, being a typical 4 year old. From the outside you would never know, but his "super scar" underneath carries a story of strength and resilience that most will never see.

This year, I'm walking with extra purpose as The Children's Heart Foundation celebrates 30 incredible years of funding research that saves lives and changes futures. My commitment to making a difference has led me to participate in the Congenital Heart Walk, an event that carries immense significance for me—especially knowing that for three decades, CHF has been the leading force behind the treatments and surgical advances that help children with congenital heart defects thrive.

It's not just a walk; it's a stride toward the next 30 years of hope. This endeavor is all about supporting The Children's Heart Foundation's crucial mission—advancing the diagnosis, treatment, and prevention of congenital heart defects through groundbreaking research that improves survival rates, reduces complications, and helps Heart Warriors celebrate more birthdays than ever before.

I warmly invite you to become a part of this milestone journey by supporting my fundraising efforts. Together, we can raise the funds essential to continue the life-saving research that turns heartbreak into hope. Your contribution holds immeasurable value to me and to every family who needs CHF's support.

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