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  • Format: ePub

As individuals increasingly seek ways of accessing, understanding and sharing data about their own bodies, this book offers a critique of the popular claim that 'more information' equates to 'better health'. In a study that redefines the public, academic and policy related debates around health, bodies, information and data, the authors consider the ways in which the phenomenon of self-diagnosis has created alternative worlds of knowledge and practises which are often at odds with professional medical advice. With a focus on data that concerns significant life changes, this book explores the…mehr

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Produktbeschreibung
As individuals increasingly seek ways of accessing, understanding and sharing data about their own bodies, this book offers a critique of the popular claim that 'more information' equates to 'better health'. In a study that redefines the public, academic and policy related debates around health, bodies, information and data, the authors consider the ways in which the phenomenon of self-diagnosis has created alternative worlds of knowledge and practises which are often at odds with professional medical advice. With a focus on data that concerns significant life changes, this book explores the potential challenges related to people's changing relationships with traditional health systems as access to, and control over, data shifts.

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Autorenporträt
Celia Roberts is a Professor of Gender and Science Studies in the Department of Sociology at Lancaster University. Adrian Mackenzie is a Professor of Technological Cultures in the Department of Sociology at Lancaster University. Maggie Mort is a Professor of Sociology in the Department of Sociology at Lancaster University. She is also the Coordinator of the EC Horizon 2020 project, CUIDAR: Cultures of Disaster Resilience among children and young people.