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
Kelly Barch headshot
December 1, 2025
The Lilabean F oundation (LBF) is thrilled to announce the appointment of Kelly Barch as our new Executive Director. Kelly will work closely with our Founder and President, Nicole Giroux , to advance the mission of the Lilabean Foundation and deepen our impact for children and families affected by pediatric brain cancer. Kelly is a mission-driven leader with more than 20 years of experience building programs, strengthening teams, and driving meaningful change across organizations. She spent 16 years at the National Cancer Institute, where she led enterprise-wide recognition programs, executive recruitment efforts, high-profile events, and cross-functional workforce initiatives. In addition to her public service, Kelly is the co-owner of Clotacin, a family-owned wellness company providing high-quality nutritional support to individuals affected by blood disorders. She oversaw operations, customer experience, and brand development, helping expand the company’s reach and impact. A lifelong Washingtonian, Kelly lives in Kensington with her husband, Justin, their children, Taylor and Beau, and their dog, Boudreaux. Outside of work, she loves staying active with her family and cheering on her alma mater, the LSU Tigers. When asked what excites her most about this new chapter, Kelly shared: “I am honored to step into the role of Executive Director and excited to bring my passion for service to the Lilabean Foundation. The opportunity to fund critical pediatric brain cancer research and help raise awareness means so much to me, and I am truly grateful to be part of this mission.” Please join us in warmly welcoming Kelly to the Lilabean Foundation. We look forward to the leadership, energy, and heart she will bring to this work!
November 12, 2025
On November 1, 2025, the Lilabean Foundation for Pediatric Brain Cancer Research (LBF) hosted its 14th Annual Fall Ball at The Schuyler at the Hamilton Hotel in Washington, D.C., raising over $1.1 million to support vital pediatric brain cancer research. This fundraising milestone reflects the unwavering commitment of the foundation’s community and partners to improve outcomes for children diagnosed with brain cancer. The evening was one of celebration and remembrance, as we honored three cherished LBF Heroes—Cameron, Kasey, and Reed—though their lives were far too short, their strength, joy, and bravery continue to guide our mission and fuel our determination. The evening’s program was filled with heartfelt speeches that reminded guests of the night’s true purpose. LBF Founder and President Nicole Giroux opened the program, sharing, “Studies say that we can go weeks without food, days without water, minutes without oxygen, but we can’t LIVE a MOMENT without hope. Your presence here tonight gives me and so many others immeasurable hope. Hope is what propels us forward. Hope gives us strength to endure hardship and believe in a better future.” The first award of the night was the LBF “Cam’s Crew” Volunteer of the Year Award , presented to the Behr Family . Evan and Caitlin Behr, along with their family, have been deeply involved with LBF since 2021, generously sharing their time, expertise, and resources. LBF is deeply grateful for their unwavering commitment and generosity, which embody the spirit of this award, created in honor of LBF Hero Cameron Corno and her family. One of the most moving moments of the night was the presentation of the Jack Purssord Courage Award to Ben Bellavia-Cortezi , age 18, honoring his extraordinary strength and resilience throughout his battle with medulloblastoma. Ben’s remarks captivated the audience with their wisdom and grace. He shared, “Every single pediatric brain cancer patient and survivor is so much more than their diagnosis… I believe strongly that with more funding, researchers can develop better treatments- ones that not only save lives but also preserve the quality of those lives.” Ben is applying to colleges for next fall and plans to study mechanical engineering. The funds raised at this year’s Fall Ball will go directly toward groundbreaking research initiatives to discover new treatments and scientific advances for children with pediatric brain cancer. The Lilabean Foundation extends heartfelt thanks to all the sponsors, attendees, volunteers, and donors who made this year’s event such a success. As Ben so wisely put it, “Together, we can give more kids the chance to grow up, chase their dreams, and tell their own story.” Learn More and Get Involved For those unable to attend the Fall Ball, there are still many ways to be part of the Lilabean Foundation’s mission. To learn more about upcoming events, volunteer opportunities, or how to make a donation, please visit www.lilabeanfoundation.com . Together, we can continue to bring hope and funding to pediatric brain cancer research.
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