Centre of Diaconia and Professional Practice, VID Specialized University, Oslo, Norway.
Department for Interdisciplinary Health Sciences, University of Oslo, Oslo, Norway.
Int J Qual Stud Health Well-being. 2023 Dec;18(1):2223420. doi: 10.1080/17482631.2023.2223420.
The condition known as chronic fatigue syndrome or myalgic encephalomyelitis (CFS/ME) is poorly understood. Simplified medical models tend to neglect the complexity of illness, contributing to a terrain of uncertainty, dilemmas and predicaments. However, despite pessimistic pictures of no cure and poor prognosis, some patients recover.
This study's purpose is to provide insight into people's experiences of suffering and recovery from very severe CFS/ME and illuminate understanding of how and why changes became possible.
Fourteen former patients were interviewed about their experiences of returning to health. A narrative analysis was undertaken to explore participants' experiences and understandings. We present the result through one participant's story.
The analysis yielded a common plotline with a distinct turning point. Participants went through a profound narrative shift, change in mindset and subsequent long-time work to actively pursue their own healing. Their narrative understandings of being helpless victims of disease were replaced by a more complex view of causality and illness and a new sense of self-agency developed.
We discuss the illness narratives in relation to the disease model and its shortcomings, the different voices dominating the stories at different times in a clinically, conceptually, and emotionally challenging area.
慢性疲劳综合征或肌痛性脑脊髓炎(CFS/ME)这一病症尚未被充分理解。简化的医学模型往往忽略了疾病的复杂性,导致不确定性、困境和困境的出现。然而,尽管存在没有治愈方法和预后不良的悲观情况,但一些患者确实康复了。
本研究旨在深入了解人们在经历非常严重的 CFS/ME 后的痛苦和康复经历,并阐明理解这些变化是如何以及为什么成为可能的。
对 14 名前患者进行了有关他们恢复健康的经历的访谈。进行了叙事分析,以探讨参与者的经历和理解。我们通过一个参与者的故事来呈现结果。
分析产生了一个共同的情节线,其中有一个明显的转折点。参与者经历了深刻的叙事转变、思维方式的改变以及随后长时间的努力,积极追求自己的康复。他们对疾病无助受害者的叙述理解被更复杂的因果关系和疾病观点以及新的自我代理意识所取代。
我们将这些疾病叙事与疾病模型及其缺陷联系起来进行讨论,在临床、概念和情感上具有挑战性的领域,不同的声音在不同的时间主导着这些故事。