Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/125139
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dc.contributor.authorHenderson ,Patricia C.
dc.date.accessioned2017-04-30T13:20:37Z-
dc.date.available2017-04-30T13:20:37Z-
dc.date.issued2011
dc.identifier.isbn9789089643599
dc.identifier.urihttp://hdl.handle.net/123456789/125139-
dc.description.abstractIn 2003-2006, Patricia Henderson lived in the South African province of KwaZulu-Natal where she recorded the experiences of people living with HIV/AIDS. In this illuminating study, she recounts the concerns of rural people and explores local repertoires through which illness was folded into everyday life. The book spans a period when antiretroviral medication was not available, and moves on to a time when the treatment became accessible. Hope gradually became manifest in the recovery of a number of people through antiretroviral therapies and 'the return' of bodies they could recognise as their own. This research implies that protracted interaction with people over time, offers insights into the unfolding textures of everyday life, in particular in its focus on suffering, social and structural inequality, illness, violence, mourning, sensibility, care and intimacy.
dc.language.isoeng
dc.publisherAmsterdam University Press
dc.relation.urihttp://www.oapen.org/record/408875
dc.rights.uriCC BY-NC (姓名標示-非商業性)
dc.sourceOAPEN
dc.subject.classificationHumanities
dc.subject.otherAnthropology
dc.subject.otherSociology
dc.titleAIDS, Intimacy and Care in Rural KwaZulu-Natal : A Kinship of Bones
dc.type電子教課書
dc.classification人文類
Theme:教科書-人文類

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