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Abstract

This study explores the treatment journeys of pediatric cancer patients, focusing on the narratives of children, adolescents, and young adults. By employing a qualitative approach, we examine personal accounts to understand the emotional, psychological, and social impacts of cancer treatment at various developmental stages. Our findings highlight common themes, including resilience, support systems, and coping mechanisms, as well as the unique challenges faced by each age group. These insights can inform healthcare providers and support networks to enhance care strategies tailored to the needs of pediatric patients and their families.