Young adults' experiences of biographical retrogression whilst living with long COVID.

IF 2.7 2区 医学 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Sociology of health & illness Pub Date : 2024-11-01 Epub Date: 2024-06-12 DOI:10.1111/1467-9566.13798
Kate Hunt, Alice Maclean, Louise Locock, Callum O'Dwyer, Sarah Nettleton, Sue Ziebland, Cervantee Wild
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引用次数: 0

Abstract

During the early years (2020-2021) of the COVID-19 pandemic, relatively little attention focused on experiences of people with long-lasting symptoms, particularly young adults who were commonly understood to be invulnerable to serious effects of the virus. Drawing on narrative interviews with 15 adults in their twenties and living in the UK when they became ill with long COVID, we explore contextual factors which made their long COVID illness experience, and the wholescale disruption to their lives, challenging. We propose that existing adaptations of the concept of biographical disruption are problematic for this group, and instead suggest that 'biographical retrogression' may more accurately reflect these young adults' experiences. For many of these young adults, their illness occurred at a crucial stage in forming or solidifying (presumed) adult trajectories. Secondly, the recency of long COVID did not allow for comparison with an existing 'grand narrative' of recovery, so the future course of their illness was not just unknown for them as individuals; there was no prognostic map against which to assess their symptoms. Thirdly, the lives of people with long COVID have been disrupted in the context of global societal disruption by the same virus, rendering their experiences both topical yet invisible.

青壮年在长期 COVID 生活中的传记倒退经历。
在 COVID-19 大流行的最初几年(2020-2021 年),人们对症状持续时间较长的人的经历关注相对较少,尤其是通常被认为不会受到病毒严重影响的年轻人。通过对 15 名 20 多岁、居住在英国的成年人进行叙事性访谈,我们探讨了导致他们长期感染 COVID 的背景因素,以及对他们生活造成的全面破坏。我们认为,现有的 "传记中断"(biographical disruption)概念对这一群体来说是有问题的,而 "传记倒退"(biographical retrogression)可能更能准确地反映这些年轻人的经历。对这些年轻人中的许多人来说,他们的疾病发生在形成或巩固(假定的)成人轨迹的关键阶段。其次,COVID 病程较长,无法与现有的康复 "宏大叙事 "进行比较,因此他们不仅不知道自己未来的病程,也没有预后图来评估自己的症状。第三,长期慢性阻塞性肺病患者的生活是在全球社会被同一种病毒破坏的背景下被扰乱的,这使得他们的经历既具有现实意义,又不为人所见。
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来源期刊
CiteScore
6.10
自引率
6.90%
发文量
156
期刊介绍: Sociology of Health & Illness is an international journal which publishes sociological articles on all aspects of health, illness, medicine and health care. We welcome empirical and theoretical contributions in this field.
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