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.