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"Cancer Sucks," and Other Ponderings by Adolescent and Young Adult Cancer Survivors
Journal article   Peer reviewed

"Cancer Sucks," and Other Ponderings by Adolescent and Young Adult Cancer Survivors

Brad Zebrack, Erin E Kent, Theresa H. M Keegan, Ikuko Kato, Ashley Wilder Smith and Aya Hope Study Collaborative Group
Journal of psychosocial oncology, Vol.32(1), pp.1-15
01/01/2014
DOI: 10.1080/07347332.2013.855959
PMCID: PMC3902666
PMID: 24428248
url
https://escholarship.org/uc/item/6jm0m5zhView
Open Access

Abstract

As part of the National Cancer Institute's AYA HOPE study, 296 adolescent and young adults (AYAs) completed an open-ended survey item asking them to describe their medical care or experience with cancer. Patient, provider, and system-level characteristics all appear to influence AYAs' perceptions of their medical care. Participants attributed levels of satisfaction with care to the availability and communication of information, the management of side-effects, and the expediency and flexibility of treatments. Struggles with health insurance and finances were evident. Findings contribute to a better understanding of AYAs' cancer treatment experiences and will inform improvements to oncology care for this population.
adolescent medical care psychosocial qualitative research young adult

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