Titlebook: Meanings of ME: Interpersonal and Social Dimensions of Chronic Fatigue; Christopher D. Ward (Emeritus Professor) Book 2015 The Editor(s) (

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Implicit

残忍

Historically Speaking: Three Influences on the Way we Think about CFS/MEthe diagnosis of CFS/ME and its nineteenth-century equivalent, neurasthenia. In each case our thinking has been influenced by three historical/cultural processes: (1) medicalisation, which brings human troubles into the medical sphere; (2) medical theorising; and (3) medical professionalisation, whi

glisten

Fulsome

Symptoms into Words: How Medical Patients Talk about Fatiguest, does the way people use fatigue-related language reflect distinctive patterns? Second, is there a particular pattern characteristic of CFS/ME? These questions can be asked with various theories of language and meaning in mind, as we discuss. Our orientation is towards the intersubjective realiti

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gustation

The Self and Others in CFS/ME: Reinterpreting Research EvidenceE are developed between individuals and others. We begin with a critique of the cognitive-behavioural model of illness and suggest how it might better take account of connections between human relationships and illness. Using examples from Chapter 7 and elsewhere we then review research literature i

Explosive

The Public Meanings of CFS/ME: Making Up Peoplele; these changes then ‘loop back ’ to influence the nature of the classification itself. The present chapter describes a study of the way websites, as sources of public knowledge, might contribute to the ‘making up ’ of people diagnosed with CFS/ME. For some (although not all) people the internet c

harbinger

The Challenge of CFS/ME in Primary Careexperience of people with medically unexplained fatigue than is possible in other medical contexts. General practitioners (GPs) are exposed to emotional tens ions which are reflected in a wide range of attitudes towards patients with the symptoms of CFS/ME. I describe some of the emotional responses

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