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.

Lemonade, popsicles, cookies, and more have organically appeared over the years in the form of lemonade stands supporting Jane’s Fund each summer.

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.

Because of you, more families will be supported in their hardest moments. Because of you, more students will be seen, encouraged, and given opportunities they never thought possible.

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.

On March 5, community came together to celebrate three years of Jane's Fund, and it was a true miracle to experience the power of strangers laughing and crying together in one space.

Every single one of you who gives, volunteers, attends, shares, and believes is part of our why, and the reason we have many miracles to share each Monday.

Some miracles aren’t loud. They don’t arrive with cheering crowds or flashing lights. They arrive quietly in the form of time. In the form of presence.

Dying of brain cancer in just five months at age 17, Jane challenged us to finish life strong. “Change the world as you go,” she advised, so you don't regret at the end having lived your life wrong.

Watching four-year-old Carter dress up as a fairy princess, twirling around their home, Ms. Ford—Carter’s Mom—never imagined that Carter’s subtle loss of balance was caused by DIPG.