Three-year-old Will and his race for a cancer cure, good health, and a bright future is nearing an end. His family is helping him finish his race, yet they also begin a new race: surviving life back at home.

Two 17-year-old boys. Angel and Jesu (“God saves”). Both have brain cancer — a high-grade glioma and DIPG. One lives in Charlotte, the other near Winston-Salem.

At Jane’s Fund, we think about celebrating the lives of children who have died of cancer a lot, because the ask for support comes often.

After cancer treatment initially worked and then failed, Rory returned home to North Carolina for end-of-life care. And then a miracle happened. Rory made a comeback.

The world abruptly changed this week for two families with a child battling cancer. In the same hospital. On the same day. Unexpected.

Jane's message to all of us as she accepted there would be no cure for DIPG and heaven would be her miracle: "Live and love fearlessly" because the world needs you.

“On behalf of my entire family, I want to express our deepest gratitude for the incredible blessing you have given us by helping us pay off our mortgage.”

When a cancer diagnosis changes everything overnight, hospital social workers help families navigate each step by solving problems and simply showing up.

A soccer fan for life, 15-year-old Josue has dreamt of attending a World Cup match. Unfortunately, DIPG, a brain tumor with no cure, continues to disrupt Josue’s life and his family’s plans.

For four-year-old Tizzy, diagnosed with terminal metastatic kidney cancer, the hardest wait began when treatment options ran out, her body grew weaker, and even breathing requires oxygen support.

Fixing, helping, and providing are what Dad does best, and nobody understands the anguish of not being able to solve a problem for their child better than our co-founder, Mike Harrell.

Thank you for helping us support 111 families with a child dying from cancer and sponsoring 37 funerals that gave hope for new life.

Mother’s Day at Jane’s Fund often looks different, because many moms are simply too busy carrying the weight of everyday survival.

Despite four treatment centers in four years, 16-year-old Lillie refuses to focus on her Ewing's sarcoma (bone tumor) diagnosis.

A rare and aggressive brain tumor diagnosis with impossible decisions to make, no right or wrong answers, becomes an instant reality. 

Onyx’s dad called him “The Mayor” because of how naturally he connected with people and made instant friends with complete strangers.