让事情切实可行:印度城市中父母主导的自闭症倡导中的关怀关系

IF 2.2
Shubha Ranganathan, Jayaprakash Mishra, S. V. Chetan, Bindhulakshmi Pattadath
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引用次数: 0

摘要

本文以民族志为基础,对印度成年自闭症患者的父母进行了深入的在线访谈,重点介绍了五位对话者的经历,以考察在印度COVID-19的背景下,以及更广泛地说,在残疾领域,对残疾、家庭和护理的细微理解。该研究立足于女性主义关怀哲学框架,解决了两个关键问题。首先,它探讨了受访母亲的叙述如何挑战护理的规范性表述。其次,它说明了涉及自闭症的护理关系具有相当大的相互依赖的特点。在以其固有的多样性为特征的印度自闭症倡导领域中,本文强调护理、依赖和亲属关系的问题更多地是由个人的社会位置决定的,而不是由西方的包容和护理理论决定的。本文为正在进行的关于残疾、家庭和护理的讨论做出了贡献,为2019冠状病毒病大流行在印度的特定背景下自闭症成年人母亲的生活经验提供了丰富的见解。研究结果对护理关系中固有的复杂性提供了更广泛的理解,并倡导采用更具包容性和文化敏感性的方法来支持印度城市自闭症患者的家庭。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Making things work, practically: Care relations in parent-led autism advocacy in urban India

Drawing on ethnography that involved in-depth online interviews with parents of adult autistic individuals in India, this article focuses on the experiences of five interlocutors to examine the nuanced understanding of disability, family, and care in the context of COVID-19 in India and, more broadly, in the realm of disability. Anchored in a feminist philosophical framework of care, the study addresses two pivotal questions. First, it explores how the narratives of the mothers interviewed challenge normative articulations of care. Second, it illustrates that care relations involving autism are characterized by considerable interdependence. Within the realm of autism advocacy in India, which is characterized by its inherent diversity, this article emphasizes that questions of care, (in)dependence, and kinship are shaped more by individuals’ social locations than by Western theorizations of inclusion and care. This article contributes to the ongoing discourse on disability, family, and care, providing rich insights into the lived experiences of mothers of autistic adults in the specific context of the COVID-19 pandemic in India. The findings offer a broader understanding of the complexities inherent in care relations and advocate for more inclusive and culturally sensitive approaches to support families of individuals with autism in urban India.

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