Overview
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Table of contents (15 chapters)
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Introduction
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Personal, Interpersonal and Public Meanings
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Patients, Doctors and Identities
Keywords
About this book
Reviews
“If you are a clinician or a member of the public who does not believe in the difficulties experienced by those with CFS/ME, as well as their families and carers, then I would recommend this book to you … . I would commend this book to you to help you understand the experiences of your patients and how your attitudes, demeanor, and behavior can so catastrophically influence a patient who presents with what is a significant and debilitating problem.” (Julia Newton, PsycCRITIQUES, Vol. 61 (24), June, 2016)
Editors and Affiliations
About the editor
Bibliographic Information
Book Title: Meanings of ME: Interpersonal and Social Dimensions of Chronic Fatigue
Editors: Christopher D. Ward
DOI: https://doi.org/10.1057/9781137467324
Publisher: Palgrave Macmillan London
eBook Packages: Palgrave Social Sciences Collection, Social Sciences (R0)
Copyright Information: The Editor(s) (if applicable) and The Author(s) 2015
Hardcover ISBN: 978-1-137-46731-7Published: 08 July 2015
Softcover ISBN: 978-1-349-69129-6Published: 14 June 2018
eBook ISBN: 978-1-137-46732-4Published: 14 July 2015
Edition Number: 1
Number of Pages: XI, 231
Topics: Health Psychology, Personality and Social Psychology, Medicine/Public Health, general, Medical Sociology, Community and Environmental Psychology, Popular Science in Medicine and Health