Adolescents and young adults (AYAs), defined as individuals aged 15 to 39 years at the time of diagnosis, often face a complex and isolating experience when diagnosed with cancer. Many encounter delays in diagnosis, limited access to fertility preservation, gaps in psychosocial support, and fragmented transitions between pediatric and adult care. These challenges can have lasting effects on their physical health, emotional well-being, and future life planning. Despite these unique needs, adolescent and young adult patients often fall into a gap in cancer care systems—too old for pediatric models, yet not fully supported by adult oncology protocols.

Explore this curated collection of educational tools, clinical guidance, and support resources for providers and patients. Topics include cancer risk, screening and prevention, fertility preservation, psychosocial support, financial navigation, survivorship planning, and local referral options. These resources feature national best practices and community-based initiatives tailored to the unique needs of adolescent and young adult patients navigating cancer care.
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Explore evidence-based strategies to improve early detection, care coordination, and long-term support for adolescent and young adult (AYA) cancer patients. Led by multidisciplinary experts, each session highlights real-world models and actionable approaches to help providers deliver age-appropriate, equitable care across diverse settings.
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