Meet Our 2024 LBF Fellow, Jian Li, PHD

 Meet our 2024 LBF Fellow, Jian Li, PhD


The LBF Fellowship Fund is a program that was established in 2018 with a mission to fund the next generation of researchers in the pediatric brain cancer space. The goal of this program is to provide seed funding to recruit and retain young, talented researchers and clinicians who plan to dedicate their careers to improving the lives of children with pediatric brain cancer. In order to advance the field of pediatric brain cancer research we believe that it is vital to support the next generation of researchers and clinicians. We are thrilled to be funding the work of Jian Li, PhD at Children’s National Hospital in Washington, D.C. in 2024. Read below to learn more about our 2024 LBF Fellow and the work he is doing to advance research for pediatric brain cancer. 

Jian LI, PHD Profile Pic

Can you tell us a bit about what you do and your role at the Lab at Children’s National Hospital? 

I'm a staff scientist in Dr. Pei's lab. I started working here last July. My work mainly focuses on Medulloblastoma. Since the recurrence and metastasis tumors always have poor prognosis, we generated a mouse myc-amplified group3 tumor and mimicked the treatment on patients by treating the tumor-bearing mice with radiation and find mice developed recurrence and metastasis tumors. We are now generating CAR-T cells to target these tumors, and try to figure out the tumor microenvironment, and whether we could manipulate TME to enhance immunotherapy. My role is to lead the project, design, and conduct experiments, organize and interpret data, and write papers and grants.


What led you to specialize in pediatric brain cancer research/ treatment?

I believe cancer could be the biggest hazard to human health, now and in the future. Brain tumors are the deadliest childhood tumor.


Can you share a fun or interesting fact about yourself that people might not know?

Before I went to university, my dream was always to be a machine engineer and create machines like transformers. However, I ended up studying bioengineering at university and was fascinated by elegant tiny machines like ATP synthase, so I decided to continue my journey with these bio-machines.


What do you hope to do in the future?

I hope to develop therapeutics that can eventually eliminate cancer cells.


What continues to drive you to do this research in pediatric brain cancer research?

Knowing that my research could eventually help kids battling such a terrible disease.

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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