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dc.contributor.authorLewis, P
dc.contributor.authorMooney-Somers, Julie
dc.contributor.authorJordens, C
dc.contributor.authorBennett, David
dc.contributor.authorPatterson, P
dc.contributor.authorMcDonald, F
dc.contributor.authorKerridge, I
dc.date.accessioned2014-09-03
dc.date.available2014-09-03
dc.date.issued2014-09-03
dc.identifier.urihttp://hdl.handle.net/2123/11741
dc.description.abstractMany adolescent and young adult (AYA) cancer survivors live with ongoing adverse consequences of their cancer experience. While an increasing number of these young Australians have direct access to care in the specialised Youth Cancer Service, many continue to receive care in diverse, non-specialised settings. It is important that health professionals in specialised and non-specialised settings are aware of the continuing diverse consequences of cancer, including the challenges created for negotiating family, peer and intimate relationships. This paper draws together insights derived from qualitative studies into the experiences of AYA who have survived cancer, with a focus on our recent Australian study of young people diagnosed during adolescence and young adulthood. We describe how members of multidisciplinary teams (MDT) can help young cancer survivors maintain their social relationshipsen_AU
dc.description.sponsorshipARCen_AU
dc.language.isoen_AUen_AU
dc.relationARC Linkage Grant LP0883632en_AU
dc.titleCaring for young people with cancer: Practical implications of qualitative engagement with cancer survivors and those who care for themen_AU
dc.typeArticleen_AU
dc.type.pubtypePost-printen_AU


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