Survivors of pediatric cancer are prone to late effects which require ongoing medical care. Young adult survivors often transition from specialist pediatric care to adult-oriented or community-based healthcare. This study aims to describe the attitudes and experiences of survivors and their parents towards transition barriers and enablers.

Beeshman S. Nandakumar, Joanna E. Fardell, Claire E. Wakefield, Christina Signorelli, Jordana K. McLoone, Jane Skeen, Ann M. Maguire, Richard J. Cohn on behalf of the ANZCHOG Survivorship Study Group

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