
Our mission is to ensure that the voices, values, and lived experiences of children with cancer and their families guide pediatric oncology research. Through our advisory board, we partner with clinicians and scientists to review research priorities, study designs, and outcomes so that every project is grounded in what matters most to patients: better treatments, improved quality of life, and hope for a cure.

We value open dialogue, critical review, and shared understanding. We are committed to carefully examining pediatric cancer research, asking the questions families would ask, and working with researchers and clinicians to ensure studies are transparent, relevant, and focused on what matters most to children and their families.

We work to bring the voices and needs of children with cancer and their families directly to state leaders. By translating complex pediatric cancer research into clear, compelling information, we advocate for increased, sustained funding and evidence-based laws that accelerate discovery, expand access to cutting‑edge care, and improve outcomes and quality of life for every child facing cancer.
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