Construction of identity in individuals with inflammatory bowel disease across the lifespan.

IF 1.9 3区 心理学 Q2 PSYCHOLOGY, MULTIDISCIPLINARY
Psychology & Health Pub Date : 2025-07-01 Epub Date: 2024-01-03 DOI:10.1080/08870446.2023.2299243
Jasmine Kobrosli, Kenzie Tapp, Kendall Soucie
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Abstract

Inflammatory bowel disease (IBD) is a chronic illness that affects 10 million individuals worldwide; however, Canada has the highest rates of IBD per capita in the world. Presently, 0.7% of Canadians are diagnosed with IBD, which is expected to rise to 1% by 2030. Disease onset is typically between the ages of 15-45 years old. This is a crucial period for identity development and growth; however, IBD symptoms often disrupt these processes and cause individuals to abandon or reconstruct parts of their identity. As a result, changes in individuals' life plans and health status may cause them to grieve their former pre-IBD identities. In this qualitative narrative study, we captured the lived experiences of IBD, with a focus on what individuals have lost, gained, or accomplished across various avenues (e.g. relationships, education, and future scripts). Thirteen participants constructed IBD narratives using a holistic-form narrative approach, a method that captures various plot formulations and discourses that emerge through storytelling. We found three main plotlines: The 'journey to acceptance', which detailed a route to acceptance wherein individuals integrated IBD into their identity, 'the ambivalent story', which exemplified individuals who were unsure of IBD and the resulting impacts of the diagnosis on their identity, and 'the grief story', which outlined grief and loss surrounding one's pre-IBD self. These results illuminate the role of narrative in shaping meaning-making and identity processes over the life course. We urge future researchers to explore narrative inquiry as a route to further understand the integration of IBD into one's life story/identity.

炎症性肠病患者在整个生命周期中的身份构建。
炎症性肠病(IBD)是一种慢性疾病,影响着全球 1 千万人;然而,加拿大是世界上人均 IBD 患病率最高的国家。目前,0.7% 的加拿大人被诊断患有 IBD,预计到 2030 年,这一比例将上升至 1%。发病年龄通常在 15-45 岁之间。这是身份发展和成长的关键时期;然而,IBD 症状往往会扰乱这些过程,导致患者放弃或重建部分身份。因此,个人生活计划和健康状况的改变可能会使他们对自己在 IBD 之前的身份感到悲伤。在这项定性叙事研究中,我们捕捉了 IBD 患者的生活经历,重点关注他们在各种途径(如人际关系、教育和未来剧本)上失去了什么、获得了什么或取得了什么成就。13 名参与者使用整体形式叙事方法构建了 IBD 叙事,这种方法可以捕捉到通过讲故事而产生的各种情节表述和论述。我们发现了三个主要情节:接受之旅 "详细描述了个人将 IBD 纳入其身份认同的接受途径;"矛盾故事 "体现了个人对 IBD 的不确定以及诊断对其身份认同造成的影响;"悲伤故事 "概述了与 IBD 前的自我有关的悲伤和失落。这些结果阐明了叙事在塑造生命过程中的意义生成和身份认同过程中的作用。我们敦促未来的研究人员探索叙事调查,将其作为进一步了解 IBD 与个人生命故事/身份认同相结合的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.30
自引率
3.00%
发文量
95
期刊介绍: Psychology & Health promotes the study and application of psychological approaches to health and illness. The contents include work on psychological aspects of physical illness, treatment processes and recovery; psychosocial factors in the aetiology of physical illnesses; health attitudes and behaviour, including prevention; the individual-health care system interface particularly communication and psychologically-based interventions. The journal publishes original research, and accepts not only papers describing rigorous empirical work, including meta-analyses, but also those outlining new psychological approaches and interventions in health-related fields.
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