Literature DB >> 31350304

What is the cultural value of dying in an era of assisted dying?

Naomi Richards1, Marian Krawczyk2.   

Abstract

Assisted dying is now a lawful and integral component of many societies 'death system', orienting individual and collective encounters with death and dying. While only a very small number of people living with terminal illness in these societies will opt for an assisted death, the choice, nevertheless, exists for those who satisfy the legal criteria. Theoretically, in these jurisdictions, this turns dying into an optional part of the human life cycle; a final phase of life that, until now, seemed a universal feature of life except in instances of sudden death. As anthropologists specialising in death and dying, we pose the question of how the various cultural scripts that have sought to give meaning to dying in post-industrial Western societies since the mid-20th century might be affected by the advent of assisted dying. We begin by building on both medical and social science literature to construct a working definition of 'dying'. We then identify four dominant cultural scripts: psychological growth, preparation for death, the suffering experience and the caring experience. After outlining each script, we discuss how it may (or may not) be affected by the increase in assisted dying legislation. We propose that it is the 'caring' script; the notion of affective, intergenerational bonds created through the experience of caring for people specifically in the last few months or weeks of their life, which are likely to be most affected. However, we find that access to these cultural scripts is already limited because of the widespread reluctance to recognise and name 'dying', and the challenges of doing so. Consequently, the various cultural scripts we identify are negated not by the increase in assisted dying, but rather by a combination of medical advances and institutional orthodoxies which limit opportunity for people to experience themselves, or others, as 'dying'. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  end of life care; medical humanities; palliative care; philosophy of medicine/health care; social anthropology

Year:  2019        PMID: 31350304     DOI: 10.1136/medhum-2018-011621

Source DB:  PubMed          Journal:  Med Humanit        ISSN: 1468-215X


  3 in total

1.  Practical and ethical complexities of MAiD: Examples from Quebec.

Authors:  Gitte Koksvik
Journal:  Wellcome Open Res       Date:  2020-11-23

2.  Travelling to die: views, attitudes and end-of-life preferences of Israeli considering receiving aid-in-dying in Switzerland.

Authors:  Daniel Sperling
Journal:  BMC Med Ethics       Date:  2022-04-30       Impact factor: 2.834

3.  Medicalisation, suffering and control at the end of life: The interplay of deep continuous palliative sedation and assisted dying.

Authors:  Gitte Hanssen Koksvik; Naomi Richards; Sheri Mila Gerson; Lars Johan Materstvedt; David Clark
Journal:  Health (London)       Date:  2020-12-11
  3 in total

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