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This book is an attempt to understand the cultural roots of non-medical representations of disability and HIV/AIDS in KwaZulu-Natal. It argues that the way in which people are prone to think about and respond to disability and HIV/AIDS, exposes people with disability to a particularly high risk of infection while simultaneously decreasing access to treatment and care. While unfolding hidden meanings and notions about disability and HIV/AIDS, this book analyses both phenomena on a macrocultural, microcultural and individual level in todays South African society.

Produktbeschreibung
This book is an attempt to understand the cultural roots of non-medical representations of disability and HIV/AIDS in KwaZulu-Natal. It argues that the way in which people are prone to think about and respond to disability and HIV/AIDS, exposes people with disability to a particularly high risk of infection while simultaneously decreasing access to treatment and care. While unfolding hidden meanings and notions about disability and HIV/AIDS, this book analyses both phenomena on a macrocultural, microcultural and individual level in todays South African society.
Autorenporträt
Dr. Jill Hanass-Hancock has graduated at the Humboldt-University in Berlin. She joint the Health Economics and HIV/AIDS Research Devision in Durban South Africa in February 2008. Since than she has been leading various studies in the area of HIV and AIDS and its relation to disability, sex education, gender and agriculture.