Reconfiguring time: optimisation and authenticity in accounts of people surviving with advanced cancer.

IF 2.5 2区 医学 Q2 HEALTH POLICY & SERVICES Health Sociology Review Pub Date : 2022-03-01 Epub Date: 2021-04-22 DOI:10.1080/14461242.2021.1918016
Stefanie Plage, Emma Kirby
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引用次数: 3

Abstract

Increasingly, people live longer with advanced cancer, despite having no prospect of full recovery. Ongoing survival is owed to early detection and effective disease management, yet experienced as highly precarious. In this article we explore how cancer chronicity brings into effect a pre-occupation with time, what time is to people with advanced cancer, and what socio-cultural norms inflect everyday practices. We analyse 20 interviews conducted in Queensland, Australia with 11 participants with advanced cancer, to trace the intersections of what time means, what people do with time, and what time feels like. Drawing on scholarship on the moralities around ill health, we discuss how awareness of time emerges in cancer chronicity and raises moral questions on how to live well. Here, imperatives of optimisation (urging people with advanced cancer to make the most of limited time) intersect with imperatives of authenticity (marked by emphasis on how to live one's own best life). These dynamics reveal expressions of living with advanced cancer in morally viable ways. Such ontological processes have implications for the lived experience of people with advanced cancer, their families and oncological care.

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重新配置时间:晚期癌症患者生存记录的优化和真实性。
尽管没有完全康复的希望,但晚期癌症患者的寿命越来越长。持续的生存归功于早期发现和有效的疾病管理,但经历了高度不稳定。在这篇文章中,我们将探讨癌症的慢性性如何影响人们对时间的关注,时间对晚期癌症患者意味着什么,以及社会文化规范对日常行为的影响。我们分析了在澳大利亚昆士兰州进行的20次访谈,其中11名参与者患有晚期癌症,以追踪时间的含义,人们如何利用时间以及时间的感觉。借鉴健康不良的道德方面的学术研究,我们讨论了时间意识是如何在癌症慢性中出现的,并提出了如何生活得更好的道德问题。在这里,优化的必要性(敦促晚期癌症患者充分利用有限的时间)与真实性的必要性(强调如何过自己最好的生活)交织在一起。这些动态揭示了晚期癌症患者在道德上可行的生活方式。这种本体论过程对晚期癌症患者的生活经历、他们的家庭和肿瘤护理都有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.50
自引率
0.00%
发文量
14
期刊介绍: An international, scholarly peer-reviewed journal, Health Sociology Review explores the contribution of sociology and sociological research methods to understanding health and illness; to health policy, promotion and practice; and to equity, social justice, social policy and social work. Health Sociology Review is published in association with The Australian Sociological Association (TASA) under the editorship of Eileen Willis. Health Sociology Review publishes original theoretical and research articles, literature reviews, special issues, symposia, commentaries and book reviews.
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