A Pioneering Community Model for Lifelong Childhood Cancer Survivorship
This white paper is intended for a broad and cross-sector audience within—and connected to—the childhood cancer community, including:
Children and adolescents diagnosed with cancer.
Survivors of pediatric cancer across all stages of life.
Parents, siblings, and extended family members.
Bereaved families and those living with loss.
Physicians, nurses, social workers, psychologists, child life specialists, and allied health professionals.
Hospital leadership and survivorship program directors.
Patient associations and advocacy organizations.
Foundations and philanthropic institutions.
Academic and research institutions focused on pediatric oncology and survivorship.
Industry partners and life sciences organizations engaged in pediatric cancer.
Impact investors, mission-aligned donors, and family offices.
Policymakers and ecosystem leaders shaping pediatric health systems.
Beyond these groups, this document is intended for anyone committed to understanding, strengthening, or supporting the long-term well-being of children and families affected by cancer.
White Paper
February 15th , 2026 | International Childhood Cancer Day