The Power of Reconnection and Collaboration in the Face of Childhood Brain Cancer

By Nicole Giroux, Founder and Executive Director of the Lilabean Foundation for Pediatric Brain Cancer Research


Life can present startling coincidences. In the early 1990s, Meg Cortezi and I were high school classmates and teammates at Notre Dame Preparatory School in Baltimore, MD. Little did we know that a friendship that started in the halls of NDP would be rekindled in the halls of Children’s National Hospital in Washington, DC, thirty years later. Our former mutual worries about mundane high school things suddenly transitioned into the shared terror of having a child with brain cancer. 


In 2015, when Meg’s son Ben was diagnosed with medulloblastoma, an aggressive malignant brain cancer, my family was already several years into our daughter Lila’s brain cancer journey. Lila was diagnosed in 2009 at 15 months old with inoperable low-grade glioma. Several years later, my husband and I started the Lilabean Foundation for Pediatric Brain Cancer Research (LBF). Our foundation's singular mission is to fund collaborative and innovative research to discover safer and more effective treatment options for children with all types of brain cancer. Thirteen years later, I am proud to share that LBF has raised over $5 million and has funded some of the world’s top neuro-oncology institutions. 

I was completely shocked to learn of Ben’s diagnosis. What are the odds that two friends from a small class of 75 women both have children with brain cancer? This disease is so often categorized as ‘rare,’ and it’s instances like these that remind us that, in reality, it is far too common. The bonds formed in high school allowed us to reconnect immediately. Ben was in the throes of toxic treatments and there was no time to be wasted. Meg was quick to realize the importance of funding research to identify treatment options for kids like Lila and Ben. It wasn’t long before she became an incredible advocate and involved her family, friends and colleagues at TEKsystems in her advocacy.

TEK Systems quote at AWS Summit in white text and light blue background

In 2019, Meg became an LBF board member. Soon thereafter, TEKsystems began partnering with LBF more frequently and intentionally. Since 2020, TEKsystems has supported our mission and has acted compassionately towards the objectives of our foundation. TEKsystems has played an important role in raising awareness about the severity of childhood brain cancer and the dire need for private funding. For instance, most people don’t know that approximately 11 children are diagnosed with a malignant brain tumor every day in the United States.

TEKsystems’ support is helping to educate communities on these alarming statistics. And even though brain cancer is the deadliest form of cancer in children, the pediatric brain cancer landscape is grossly underfunded. TEKsystems continues to help LBF fill the federal funding gap with private support for institutions, including the Brain Tumor Institute at Children’s National Hospital, where Lila and Ben remain patients. The relationship between TEKsystems and LBF is an excellent example of the impact that is possible when partnerships are prioritized. 


Ben and Lila are two of many LBF HEROES. Their stories inspire. Meg’s willingness to share her family’s story has paved the way for LBF to connect with other families including TEKsystems’ colleague, Tim Brown, whose daughter Abby also suffers from low grade glioma brain cancer.

The Lilabean Foundation Heores Lila and Ben

At our 30 year high school reunion, Meg hosted a cocktail party for our NDP classmates to learn more about LBF. It was powerful to connect with old friends and share our stories of heartbreak and resilience.


It is surreal to think that Ben and Lila are now the same ages that Meg and I were when we first met. I am so grateful for Meg’s friendship and commitment to the Lilabean Foundation. Our partnership with TEKsystems is a testament to the power of turning suffering into hopeful action.


May is brain cancer awareness month and we hope that you will consider becoming an 11for11 member in honor of those approximately 11 children who are diagnosed with brain cancer each day. Please join us in our mission to give hope to children and families suffering from this terrible disease.

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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