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

殘忍

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

運動吧

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

Libido