个人身份和耻辱不平等:来自卢旺达足癣患者经验的见解。

IF 4.1 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Jean Paul Bikorimana, Josephine Mukabera, Gail Davey, Peter John Mugume, Papreen Nahar
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引用次数: 0

摘要

足癣病是一种影响热带地区贫困人群的皮肤被忽视热带病(SNTD)。虽然对足癣病相关的耻辱感有了实质性的了解,但基于个体身份(如性别、阶级、年龄、位置和身体能力)的足癣相关的耻辱感却知之甚少。由于与这些身份相关的权力差异,个人经历不同的健康问题,导致健康差异。本文旨在讨论由于个体身份导致的足癣病病耻感相关的不平等,为减少足癣病病耻感相关的不平等提供政策和实践信息。方法:本文采用定性研究方法,探讨个体身份如何影响足癣病患者的病耻感。采用定性方法,包括参与观察、访谈、焦点小组讨论以及与受影响者、家庭成员、社区卫生工作者和代表的关键线人访谈。对数据进行主题分析。结果:我们的研究结果揭示了根植于个体身份的足癣病耻辱相关不平等的复杂性。我们确定了三个主要主题:(1)文化规范和传统在塑造社会定位中的重要性;(2)不均匀的耻辱经历;(3)一个人的社会定位在应对足癣病引起的耻辱方面的重要性。某些被污名化的个人或群体比其他人面临更高程度的污名化。受影响的个人通常与文化定义的身份有关。由于与阶级、能力、性别和年龄相关的文化解释,那些具有压迫性身份的人比具有积极身份的人经历了更多的耻辱。贫穷的已婚妇女和男子、年轻女孩和患有足癣病的残疾人比他们的同龄人更容易受到耻辱感。结论:足癣病的病耻感不平等与个体的性别、年龄、经济地位和身体能力相关的身份形成有关。具有压迫性身份的个体比其他人承受更多的耻辱。这种不同的病耻感经历加强了对与足癣病或其他sntd相关的病耻感差异如何支持卫生不公平的理解。这些见解建议将干预措施与其他干预措施相结合,以减少足癣病的耻辱感,例如性别平等教育、经济赋权方案、培养积极的身份和社会包容,从而减少差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Individual identities and stigma inequalities: insights from the experience of people affected by podoconiosis in Rwanda.

Introduction: Podoconiosis is a Skin Neglected Tropical Disease (SNTD) that affects impoverished individuals in tropical regions. While there is a substantial understanding of the stigma associated with podoconiosis, little is known about the podoconiosis-related stigma experience based on individual identities, such as gender, class, age, location and physical ability. Due to the power differentials associated with these identities, individuals experience health problems differently, resulting in health disparities. This paper aims to discuss the inequalities related to podoconiosis stigma due to individual identities, informing policies and practices to reduce podoconiosis stigma-related disparities.

Methods: This paper draws on a qualitative research approach to explore how individual identities shape the experience of podoconiosis stigma among affected people. Qualitative methods, including participant observation, interviews, focus group discussions, and key informant interviews with persons affected, family members, community health workers, and representatives, were employed. Data were thematically analysed.

Results: Our findings reveal the complex nature of podoconiosis stigma-related inequality rooted in individual identities. We identified three main themes: (1) the importance of cultural norms and traditions in shaping social positioning, (2) Uneven stigma experience, and (3) the importance of one's social positioning in coping with stigma due to podoconiosis. Certain stigmatised individuals or groups face higher levels of stigma than others. Affected individuals are often associated with culturally defined identities. Those with oppressive identities experience significantly more stigma compared to those with positive identities, because of cultural interpretations linked to class, ability, gender, and age. Poor married women and men, young girls, and disabled individuals with podoconiosis encounter greater stigma than their peers.

Conclusion: This paper illuminates that the podoconiosis stigma inequalities are shaped by individuals' identities related to gender, age, economic status, and bodily ability. Individuals with oppressive identities endure more stigma than others., and this differential stigma experience enhances the understanding of how disparities in stigma associated with podoconiosis or other SNTDs underpin health inequities. Such insights suggest integrating interventions to reduce podoconiosis stigma with others, such as gender equality education, economic empowerment programs, fostering positive identities and social inclusion, thus reducing disparities.

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来源期刊
CiteScore
7.80
自引率
4.20%
发文量
162
审稿时长
28 weeks
期刊介绍: International Journal for Equity in Health is an Open Access, peer-reviewed, online journal presenting evidence relevant to the search for, and attainment of, equity in health across and within countries. International Journal for Equity in Health aims to improve the understanding of issues that influence the health of populations. This includes the discussion of political, policy-related, economic, social and health services-related influences, particularly with regard to systematic differences in distributions of one or more aspects of health in population groups defined demographically, geographically, or socially.
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