Our CC4C supporters help provide critical resources, hope, and community to families navigating the uncharted challenges of rare diseases like Noah's.

Noah was born with Hypoplastic Left Heart Syndrome (HLHS), a rare and severe congenital heart defect. By the age of 3, he had already endured three open-heart surgeries and a heart transplant. Over the years, he’s faced additional diagnoses including kidney failure and the need for a feeding tube (G-tube). Despite it all, Noah is one of the most vibrant, resilient kids you’ll ever meet.

With a big personality and an even bigger love for fast cars and thrilling adventures, Noah finds joy in anything that gets his heart racing—in the best way. He brings laughter and energy wherever he goes, teaching those around him how to find light even in the darkest moments.

Noah is a proud big brother to two sisters, Elodie and Izabela, and he inspires everyone with his strength, determination, and heart. His journey is a powerful reminder that joy and courage can exist even in the hardest circumstances.

“No matter what he’s facing, he never gives up. His smile lights up the darkest days.” — Noah’s Mom & Dad

Every day, our families face uncertainty about their child's health, financial burdens, and isolation.

Every day, new families face an overwhelming diagnosis, unsure of where to turn. 

Your year-end gift ensures families won’t face this journey alone. With your help, we can continue offering life-changing programs, advocacy, and support for Noah's family and many more.

Together, we can make 2025 a year of hope for families who need it most. Please consider a tax-deductible donation today and help us reach our goal of raising $67,000 for CC4C's mission.