Drawing on patients' accounts, Graham Scambler examines the experience of both epilepsy and the stigma that can accompany it and illuminates the contribution that social science can make to understanding and managing the illness.
In examining the social and psychological aspects of epilepsy, the author takes not only the perspectives of individuals and their families, but also popular conceptions of the disorder. The result is an illuminating account of the social reality of epilepsy that demonstrates the distinctive contribution that the social sciences can play in understanding illness.
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