The discursive context of medical aid in dying: A paradox of control?

Agency Biopower Control End of life choice Euthanasia Freedom Medical aid in dying New Zealand

Journal

Social science & medicine (1982)
ISSN: 1873-5347
Titre abrégé: Soc Sci Med
Pays: England
ID NLM: 8303205

Informations de publication

Date de publication:
12 2021
Historique:
received: 01 12 2020
revised: 31 08 2021
accepted: 19 10 2021
pubmed: 31 10 2021
medline: 4 1 2022
entrez: 30 10 2021
Statut: ppublish

Résumé

Individual agency is central to late modern and neoliberal concepts of the self and notions of a good death. Assisted dying can be understood as a reflection of these ideas in that control over death resides with the individual. The aim of this article is to explore individual agency and control and employ concepts of biopower and freedom to illustrate the paradoxes inherent within assisted dying. Assisted dying is currently of wide interest due to legislative change. At the time of research, the New Zealand Parliament was passing the End of Life Choice Act, yet there had been no research with people approaching the end of life about assisted dying. Through the media we recruited and interviewed 14 people approaching the end of life who would have considered choosing assisted dying if it were available to them. Interviews were analyzed using an immersion/crystallization thematic analysis. Assisted dying appealed to participants because it offered control. This article examines the discursive context of control as well as the participants' perception of control to offer insights into how paradoxically, a medical regime of assisted dying reinforces health professionals as in control of the circumstances of dying. We argue that although legalized medical assisted dying is highly regulated and monitored, thus limiting freedom, the option of assisted dying also increases freedom for the dying person. Within this paradox of control, there is still scope for choice and an ethical making of the self, although limited by the biopolitical regime, that equates to a degree of freedom for participants.

Identifiants

pubmed: 34717285
pii: S0277-9536(21)00833-9
doi: 10.1016/j.socscimed.2021.114501
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

114501

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Jessica E Young (JE)

Department of General Practice and Rural Health, University of Otago, Dunedin, New Zealand; School of Health, Victoria University of Wellington, Wellington, New Zealand. Electronic address: jessica.young@vuw.ac.nz.

Chrystal Jaye (C)

Department of General Practice and Rural Health, University of Otago, Dunedin, New Zealand.

Richard Egan (R)

Department of Preventive and Social Medicine, University of Otago, Dunedin, New Zealand.

Janine Winters (J)

Bioethics Centre, University of Otago, Dunedin, New Zealand.

Tony Egan (T)

Department of General Practice and Rural Health, University of Otago, Dunedin, New Zealand.

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