慢性斗争:理解慢性疼痛和边缘化的新框架

F. Webster, Laura Connoy, K. Rice, J. Katz, Abhimanyu Sud, C. Dale
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引用次数: 0

摘要

医学常常忽视健康经验的社会方面。应用健康的社会决定因素的镜头并没有完全减轻西方医学侧重于生物原因和药物解决方案的倾向。目的:我们呈现了26名慢性疼痛患者的故事,他们被现有的不平等制度和结构以加剧痛苦的方式在社会、经济和政治上边缘化。我们认为,他们的多样化和多方面的经验是更好地理解术语“慢性斗争”,而不是“慢性疼痛”,从而去中心的医疗方面的人的经验。研究设计:制度人种学(IE)是一种越来越多地用于健康研究的社会学方法。IE从有生活经验的人的角度出发,把他们看作是经验方面的专家。IE分析遵循一系列的行动,由一个信息提供者的采访引导到下一个或一个文本进行分析。通过这个过程,我们将参与者的微观体验与宏观系统和结构联系起来。设置或数据集:参与者通过在线空间(如Twitter和Kijiji)和我们在加拿大几个省的多学科研究团队的现有网络进行深度电话采访。研究人群:我们的研究重点是18岁以上、英语流利、自我认同患有慢性疼痛和边缘化的人群。结果:我们的研究结果呼吁人们关注复杂性和“日常紧急情况”(Millar, 2014;Mitchell, 2020)来塑造和定义一个人的慢性疼痛经历。我们的主题捕捉了疾病、精神疾病、成瘾和贫困的层叠和相互关联的经历,因为它们是由有生活经验的人描述和理解的。综上所述,我们意识到慢性疼痛并不是定义一个人生活的关键困难——一种传记性的破坏——而是生活中一个额外的困难,而这个困难总是由健康和社会复杂性所定义的。结论:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic struggle: A new framework for understanding chronic pain and marginalization
Medicine often ignores the social aspects of health experience. Applying the lens of social determinants of health has not fully mitigated the tendency of Western medicine to focus on biological causes and pharmaceutical solutions. Objective: We present the stories of 26 people living with chronic pain who have been rendered socially, economically, and politically marginal by existing systems and structures of inequity in ways that exacerbate suffering. We argue that their diverse and multi-faceted experiences are better understood by the term “chronic struggle” rather than “chronic pain”, thus de -centering the medical aspects of people's experiences. Study Design: Institutional ethnography (IE) is a sociological approach increasingly used in health studies. IE begins in the standpoint of people with lived experience and considers them as experts of that experience. IE analysis follows sequences of action, with one informant’s interview leading the way to the next or to a text for analysis. Through this process, we linked participants’ micro level experiences to macro level systems and structures. Setting or Dataset: Participants were recruited for in-depth telephone interviews in online spaces (e.g. Twitter and Kijiji) and through existing networks of our multi-disciplinary research team across several provinces in Canada. Population Studied: Our study focuses on people who are over the age of 18, speak fluent English and who self-identify as living with chronic pain and marginalization. Results: Our findings call attention to the complexities and ‘everyday emergencies’ (Millar, 2014; Mitchell, 2020) that come to shape and d efine one’s experiences with chronic pain. Our themes capture the cascading and inter - related experiences of illness, mental illness, addiction and poverty as they are described and understood by people with lived experience. Combined, we are made aware of how chronic pain is not the key defining difficulty of one’s life— a biographical disruption — but rather one additional difficulty in a life that is always already defined by health and social complexities. Conclusions: As
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