Ty Louis Campbell

Ty Louis Campbell, nicknamed “SuperTy” at the onset of his diagnosis, was a bright, courageous, and funny little boy whose life continues to inspire others. Born in 2007, Ty was diagnosed with ATRT -- a rare and aggressive brain tumor -- at the age of 2. From that moment, he faced a difficult but undeniably brave journey.

Over the next two years, Ty endured numerous surgeries, rounds of chemotherapy, radiation treatments, infections, shunt revisions, and other extraordinary medical challenges. Despite it all, his spirit never dimmed. He had a constant smile, a love for superheroes, dreams of jumping in muddy puddles, and a contagious laugh that reminded others of just how simple it is to bring joy to a child.

On October 17, 2012, at only five years old, Ty passed away—free from suffering but deeply missed. Even though his physical journey ended, his legacy lives on in the work that is happening in research labs around the world.

Ty’s parents, Cindy and Lou Campbell, turned his memory into action by founding the Ty Louis Campbell Foundation (TLC). The foundation supports innovative research into childhood cancer—especially the deadliest, most aggressive brain tumors—and also helps lift the burdens of families when a child is in treatment.

The Muddy Puddles Project is a fundraising platform for TLC that has garnered major national media over the years for its simple message, which encourages kids “being kids” in honor of those who can’t.

Ty will always be remembered not just for how he approached life despite his illness, but for the joy he brought to ordinary moments. Forever a superhero in his own right, his story reminds us of what’s precious in life, and why we must keep fighting for safer, more effective treatments for children.

In Loving Memory — Ty Louis Campbell