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Postcolonial Language Politics and Practice
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This edited book addresses ways in which ''bodies'' conceived broadly – get languaged, and ways in which ideas of ''normalcy'' and ''normal'' bodies are held in place and reproduced. The articles show how it is through this medium that people with ailments or ''unusual'' bodies get positioned and slotted in certain ways. The present volume represents a departure from other works in at least two ways. First, it brings in discourses around bodies per se into language-related research, a realm that previous research has not directly engaged. Second, it ushers in discussions about bodies by critically addressing the language by which experiences around bodily breakdowns and ailments occur. Calling attention to a host of discourses – biomedical, societal, poststructuralist – and drawing on a variety of disciplinary perspectives, critical theories, ethnographically gathered materials, and extant data, the chapters pierce the general veil of silence that we have collectively drawn regarding how some of our most intimate body (dis)functions impact our everyday living and sense of "normalcy".
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This book critically addresses the role of language in our collective construction of ‘normal’ bodies. Addressing a range of concerns linked with visible and invisible, chronic and terminal conditions, the volume probes issues in and around patient and caregiver accounts. Focussing on body conditions associated with breast cancer, Alzheimer’s disease, (type-1) diabetes, epilepsy, partial hearing and autism, the book draws on a range of critical theories to contest collectively assembled notions of ‘abnormality,’ ‘disability’ and ‘impairments.’ It also addresses the need for applied sociolinguists to take account of how our researching practices - the texts we produce, the orientations we assume, the theoretical grounds from which we proceed-- create ‘meanings’ about bodies and ‘normalcy,’ and the importance of remaining ever vigilant and civically responsible in what we do or claim to do.
1 841 kr
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This book critically addresses the role of language in our collective construction of ‘normal’ bodies. Addressing a range of concerns linked with visible and invisible, chronic and terminal conditions, the volume probes issues in and around patient and caregiver accounts. Focussing on body conditions associated with breast cancer, Alzheimer’s disease, (type-1) diabetes, epilepsy, partial hearing and autism, the book draws on a range of critical theories to contest collectively assembled notions of ‘abnormality,’ ‘disability’ and ‘impairments.’ It also addresses the need for applied sociolinguists to take account of how our researching practices - the texts we produce, the orientations we assume, the theoretical grounds from which we proceed-- create ‘meanings’ about bodies and ‘normalcy,’ and the importance of remaining ever vigilant and civically responsible in what we do or claim to do.
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This book offers a critical exploration of the role of English in postcolonial communities such as India. Specifically, it focuses on some local ways in which the language falls along the lines of a class-based divide (with ancillary ones of gender and caste as well). The book argues that issues of inequality, subordination and unequal value seem to revolve directly around the general positioning of English in relation to vernacular languages. The author was raised and schooled in the Indian educational system.