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

This is for our boys! For those who don't already know, Evyn was born with Pulmonary Stenosis. To date, he has not had to have any procedures YET! Just monitoring, echoes and ekgs every 6 months. Because of his stenosis, Tavish's Bicuspid Aortic Stenosis was detected through a fetal echo. When he was 4 days old, he had his first cath ballooning procedure. He had his 2nd cath ballooning at 4 months old. At 11 months old, after both procedures failed, he underwent open heart surgery where the Ross Procedure was performed. Along with Evyn, he goes every 6 months for monitoring, echoes and ekgs. 

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.