Overview

Chronic Fatigue Syndrome (CFS or ME) is a problematic diagnosis which can be interpreted in conflicting ways by doctors, patients and others. Meanings of ME signals a paradigm shift in thinking about the illness by providing fresh perspectives from doctors, clinicians and those who have personal knowledge of CFS/ME.

Full Product Details

Author:   C. Ward
Publisher:   Palgrave Macmillan
Imprint:   Palgrave Macmillan
Dimensions:   Width: 14.00cm , Height: 1.40cm , Length: 21.60cm
Weight:   4.091kg
ISBN:  

9781137467317

ISBN 10:   1137467312
Pages:   231
Publication Date:   08 July 2015
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print  
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Table of Contents

Preface 1. Introduction PART I: WAYS OF SPEAKING 2. Personally Speaking: Experiences of Chronic Fatigue; Christopher Ward 3. Scientifically Speaking: CFS/ME in the Medical Literature; Christopher Ward 4. Diagnostically Speaking: how Should We Classify CFS/ME - and does it matter?; Hugh Rickards 5. Historically Speaking: Three Influences on the Way We Think About CFS/ME; Christopher Ward PART II: PERSONAL INTERPERSONAL AND PUBLIC MEANINGS 6. Symptoms into Words: How Medical Patients Talk About Fatigue; Penny Standen, Christopher Ward, Charlotte Beer and Laura Saunders 7. Meanings of CFS/ME in the Lives of Couples; Matt Horrocks and Christopher Ward 8. The self and others in CFS/ME: Reinterpreting Research Evidence; Christopher Ward and Matt Horrocks 9. The Public Meanings of CDS/ME: Making Up People; John Cromby PART III: PATIENTS, DOCTORS AND IDENTITIES 10. The Challenge of CFS/ME in Primary Care; Laura Saunders 11. The Said and the Unsaid: Ambivalence in CFS/ME; Christopher Ward 12. Stigma, Unspeakable Dilemmas and Somatic Symptoms - a Legacy of Suffering in CFS/ME and Fibromyalgia; James Griffith and Nancy Ryan 13. What Does the Diagnosis Say?; Christopher Ward 14. Ways of Not Knowing; Christopher Ward

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)

Author Information

John Cromby, Loughborough University, UK James Griffith, George Washington University, USA Matthew Horrocks, Nottinghamshire Healthcare, UK Hugh Rickards, University of Birmingham, UK Nancy Ryan, National Fibromyalgia and Chronic Pain Association, USA Laura Saunders, Derbyshire Healthcare, UK Charlotte Beer, University of Nottingham, UK Penny Standen, University of Nottingham, UK Christopher Ward, University of Nottingham, UK

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