Living with/out Dementia in Contemporary South Korea

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Standard

Living with/out Dementia in Contemporary South Korea. / Lee, Jieun.

I: Medical Anthropology Quarterly, Bind 33, Nr. 4, 2019, s. 501-516.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Lee, J 2019, 'Living with/out Dementia in Contemporary South Korea', Medical Anthropology Quarterly, bind 33, nr. 4, s. 501-516. https://doi.org/10.1111/maq.12532

APA

Lee, J. (2019). Living with/out Dementia in Contemporary South Korea. Medical Anthropology Quarterly, 33(4), 501-516. https://doi.org/10.1111/maq.12532

Vancouver

Lee J. Living with/out Dementia in Contemporary South Korea. Medical Anthropology Quarterly. 2019;33(4):501-516. https://doi.org/10.1111/maq.12532

Author

Lee, Jieun. / Living with/out Dementia in Contemporary South Korea. I: Medical Anthropology Quarterly. 2019 ; Bind 33, Nr. 4. s. 501-516.

Bibtex

@article{575cc4b62f9b40d09f6df4a9e78e49ab,
title = "Living with/out Dementia in Contemporary South Korea",
abstract = "While the debate on diagnostic disclosure is often based on the premise that knowing about one's condition (the diagnosis and its prognosis) is essential in securing the patient's autonomy, many people with dementia in Korea are not told directly about their diagnosis. This article concerns the laborious and ethically contentious post-diagnostic living undertaken by the families of people with dementia, which I call “living with/out dementia.” This is a paradoxical form of living that has emerged through the increasing biomedicalization of dementia, the socialization of elder care, and an enduring fear of dependency in old age. Attending to how living with/out dementia comes to be initiated and maintained through efforts of care, I argue that nondisclosure entails a kind of ethical process through which dementia is un/done in the caregivers{\textquoteright} struggle to truthfully engage with the person with dementia while actively hiding the diagnostic truth from him or her.",
keywords = "bioethics, care, dementia, diagnostic disclosure, Korea",
author = "Jieun Lee",
year = "2019",
doi = "10.1111/maq.12532",
language = "English",
volume = "33",
pages = "501--516",
journal = "Medical Anthropology Quarterly",
issn = "0745-5194",
publisher = "Wiley-Blackwell",
number = "4",

}

RIS

TY - JOUR

T1 - Living with/out Dementia in Contemporary South Korea

AU - Lee, Jieun

PY - 2019

Y1 - 2019

N2 - While the debate on diagnostic disclosure is often based on the premise that knowing about one's condition (the diagnosis and its prognosis) is essential in securing the patient's autonomy, many people with dementia in Korea are not told directly about their diagnosis. This article concerns the laborious and ethically contentious post-diagnostic living undertaken by the families of people with dementia, which I call “living with/out dementia.” This is a paradoxical form of living that has emerged through the increasing biomedicalization of dementia, the socialization of elder care, and an enduring fear of dependency in old age. Attending to how living with/out dementia comes to be initiated and maintained through efforts of care, I argue that nondisclosure entails a kind of ethical process through which dementia is un/done in the caregivers’ struggle to truthfully engage with the person with dementia while actively hiding the diagnostic truth from him or her.

AB - While the debate on diagnostic disclosure is often based on the premise that knowing about one's condition (the diagnosis and its prognosis) is essential in securing the patient's autonomy, many people with dementia in Korea are not told directly about their diagnosis. This article concerns the laborious and ethically contentious post-diagnostic living undertaken by the families of people with dementia, which I call “living with/out dementia.” This is a paradoxical form of living that has emerged through the increasing biomedicalization of dementia, the socialization of elder care, and an enduring fear of dependency in old age. Attending to how living with/out dementia comes to be initiated and maintained through efforts of care, I argue that nondisclosure entails a kind of ethical process through which dementia is un/done in the caregivers’ struggle to truthfully engage with the person with dementia while actively hiding the diagnostic truth from him or her.

KW - bioethics

KW - care

KW - dementia

KW - diagnostic disclosure

KW - Korea

U2 - 10.1111/maq.12532

DO - 10.1111/maq.12532

M3 - Journal article

C2 - 31206771

AN - SCOPUS:85069944990

VL - 33

SP - 501

EP - 516

JO - Medical Anthropology Quarterly

JF - Medical Anthropology Quarterly

SN - 0745-5194

IS - 4

ER -

ID: 226531096