"It's Like a Double Whammy!": A Photo-Phenomenological Analysis of the Experiences of Lesbian, Gay, Bisexual, and Queer People Living With Multiple Sclerosis.

IF 2.6 2区 医学 Q2 INFORMATION SCIENCE & LIBRARY SCIENCE
Qualitative Health Research Pub Date : 2025-04-01 Epub Date: 2025-04-02 DOI:10.1177/10497323241309583
Periklis Papaloukas, Iain Williamson
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引用次数: 0

Abstract

Multiple sclerosis (MS) is a neurological, autoimmune condition which affects the nervous system, creating several physiological and psychosocial issues. Simultaneously, there is an expanding body of research on lesbian, gay, bisexual, and queer (LGBQ) populations which indicates health inequalities due to heteronormativity. Despite this, research exploring chronic illness, neurological conditions, and MS within LGBQ contexts remains limited. Therefore, we aimed to investigate the experience of LGBQ people living with MS. We undertook a culturally responsive multi-method approach, employing verbal and visual data through phenomenological interviews and participant-authored photographs. Twenty-three LGBQ individuals from several countries took part. All data collected from the three groups were analyzed separately using interpretative phenomenological analysis (IPA). We created three interrelated themes: (a) (Loss and) the perceived incompatibility of MS and LGBQ Identities, (b) Multiple stigmas, estrangement, and discrimination, and (c) Surfacing through community, resistance, and resilience. It was revealed that from the moment of confirmed MS diagnosis, LGBQ individuals in this study appear to progress to an individual transformation of the self. Subsequently, the LGBQ persons living with MS typically experience an amended social exposure whereby they experience the enhanced force of multiple stigmas and incidents of discrimination. However, participants noted reaction and resistance against both the attack of MS on their identity and against the multiple discriminations. These different phases and stages are revisited and retouched dynamically and non-linearly, echoing the fluidity and episodic nature of MS. The findings have academic and real-world impact through recommendations for advocacy, policy change, future research, and healthcare.

“真是祸不单行!”对患有多发性硬化症的女同性恋、男同性恋、双性恋和酷儿人群经历的摄影现象学分析。
多发性硬化症(MS)是一种影响神经系统的神经系统、自身免疫性疾病,会产生一些生理和社会心理问题。与此同时,关于女同性恋、男同性恋、双性恋和酷儿(LGBQ)人群的研究也在不断扩大,这些研究表明,异性恋规范导致了健康不平等。尽管如此,在LGBQ背景下探索慢性疾病、神经系统疾病和多发性硬化症的研究仍然有限。因此,我们的目的是调查LGBQ人群与ms的生活经历。我们采用了一种文化响应的多方法方法,通过现象学访谈和参与者创作的照片使用口头和视觉数据。来自多个国家的23名LGBQ人士参加了活动。采用解释现象学分析(IPA)分别对三组收集的所有数据进行分析。我们创造了三个相互关联的主题:(a) MS和LGBQ身份的(损失和)感知的不兼容性,(b)多重耻辱,隔阂和歧视,以及(c)通过社区,抵抗和恢复浮出水面。研究发现,从被确诊为MS的那一刻起,本研究中的LGBQ个体似乎就进入了自我的个体转化阶段。随后,患有多发性硬化症的LGBQ人群通常会经历一种修正的社会暴露,由此他们会经历多重耻辱和歧视事件的增强力量。然而,与会者注意到对MS对其身份的攻击和对多重歧视的反应和抵抗。这些不同的阶段和阶段被动态地、非线性地重新审视和修饰,与多发性硬化的流动性和偶然性相呼应。研究结果通过对宣传、政策变化、未来研究和医疗保健的建议,具有学术和现实世界的影响。
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来源期刊
CiteScore
6.80
自引率
6.20%
发文量
109
期刊介绍: QUALITATIVE HEALTH RESEARCH is an international, interdisciplinary, refereed journal for the enhancement of health care and to further the development and understanding of qualitative research methods in health care settings. We welcome manuscripts in the following areas: the description and analysis of the illness experience, health and health-seeking behaviors, the experiences of caregivers, the sociocultural organization of health care, health care policy, and related topics. We also seek critical reviews and commentaries addressing conceptual, theoretical, methodological, and ethical issues pertaining to qualitative enquiry.
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