看见隐形:多发性硬化症隐形症状的生活与管理摄影探索

Leigh Parker, Gogem Topcu, Danielle De Boos, Clare Bale, R. das Nair
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引用次数: 0

摘要

在这项摄影选择研究中,我们探讨了多发性硬化症(MS)患者如何在日常生活中体验和处理隐形症状。12 名多发性硬化症患者在两周时间内制作了数字图像,以记录他们对隐形症状的体验。然后,参与者在半结构化访谈中讨论了他们的图像。我们对访谈进行了主题分析,并形成了三大主题,包括隐形症状概念化的困难,以及这给多发性硬化症患者带来的合法性冲突,在这些冲突中,他们隐形症状的真实性被他人否定,有时甚至被他们自己否定。参与者以动态的方式处理这些问题,根据具体情况选择将其症状融入生活或为其症状留出空间,这通常受到 "保持隐形 "或 "被看见 "的愿望的影响。我们强调了围绕多发性硬化症患者所经历的合法性冲突以及他们如何与隐形症状协商生活等问题为他们提供支持的临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Seeing the Invisible: A Photovoice Exploration of Living With and Managing the Invisible Symptoms of Multiple Sclerosis
In this photovoice study, we explored how people with multiple sclerosis (MS) experience living with and managing invisible symptoms in daily life. Twelve people with MS produced digital images over a 2-week period to capture their experiences of invisible symptoms. Participants then discussed their images in semistructured interviews. We thematically analyzed the interviews and developed three main themes that encompass the difficulties around conceptualizing invisible symptoms and the conflicts of legitimacy this presents for people with MS, in which the reality of their invisible symptoms is invalidated by others and sometimes for themselves. Participants navigated these issues in dynamic ways, choosing to fit their symptoms to their lives or make space for their symptoms depending on the context, often influenced by a desire to “stay invisible” or to “be seen.” We highlight clinical implications for supporting people with MS around the legitimacy conflicts they experience and how they negotiate living with invisible symptoms.
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