Q&A with LBF Hero, Zoe FitzGerald

LBF Hero Zoe Fitzgerald

We are so excited to have had the opportunity to virtually sit down with our April LBF Hero, Zoe Fitzgerald, for a Q&A. A reminder that you can read all about her cancer journey, written by Zoe herself, here but read the Q&A below for even more info on just why Zoe is so clearly a Hero to so many and already making an impact for other kids diagnosed with brain cancer.


Q: You have mentioned that until recently you were very private about your cancer journey, can you let us know what made you change that? 

A: What helped me to be able to open up more about my journey was coming to terms that a brain tumor is so much bigger than just my struggles, and I know that my healthy condition while having a brain tumor, I knew I could use my position to help others


Q: How do you think your diagnosis has affected your life?

A: I think my diagnosis has made me more aware and given me a perspective that I wouldn’t have had otherwise, I have a clearer understanding of the effects of childhood cancer and can more easily empathize with others struggling with illness. I have made some amazing friends that I wouldn’t have even met if not for my diagnosis.


Q: In addition to LBF, how have you been advocating and raising funds and awareness around pediatric brain cancer?

A: Last summer I started a non profit organization called Books4Brains to raise money for brain tumor research! It was a read-a-thon during the month of May (Brain tumor awareness month) and people were able to donate funds which went to children’s hospital pediatric brain tumor research.


Q: What do you think is important to help the next generation of children diagnosed with Pediatric brain cancer?

A: I think continued research and new treatments being made is so important, because there are so many children who either don’t have treatment options or their medicine can be toxic/harmful to their body.


Q: What advice would you have for a child diagnosed with pediatric brain cancer today as a child who has gone through this?

A: I think one piece of advice would be to let yourself feel all your emotions; it's okay to feel sad and not okay, it’s important to let your emotions out.

LBF Hero Zoe Fitzgerald on the boardwalk
Title text on dark blue: “Memories from a Hero’s Grandpa” by Jay Spitulnik
August 10, 2026
August marks one year since we lost Kasey Vivian Zachmann. She was 10 years old. Over the course of four years, Kasey endured 10 surgeries, 45 proton radiation treatments, multiple rounds of chemotherapy, and two clinical trials, and through all of it, she never lost her smile. To mark this anniversary, we are honored to share a reflection written by Jay Spitulnik, Kasey's maternal grandfather. Jay's words carry the kind of love and clarity that only comes from someone who was there, someone who watched Kasey light up every room she entered, and who has spent the past year learning to carry both grief and pride in equal measure. The Kasey Zachmann Fund for Medulloblastoma Research was established in her honor to ensure her fight advances the science for every child who comes after her. We hope Jay's reflection touches your heart as it has ours.
Blue title card reading “Driving Hope, Coming Full Circle” by Kelly Barch.
By Kelly Barch, Executive Director of the Lilabean Foundation July 29, 2026
Thirteen years ago, my dad passed away from cancer. Long before that, he'd spent years at Herson's Honda teaching sales after starting his second career. When I was old enough to drive, my very first car was a Honda Civic from that same lot.
Trip to See My Daughter text in yellow on blue background
May 15, 2026
Recently, members of the Lilabean Foundation team had the opportunity to visit Children’s Hospital of Philadelphia (CHOP) and spend time with researchers and leaders from the Children’s Brain Tumor Network (CBTN).
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