Abstract
Fatigue, which is the central symptom of CFS/ME, is notoriously difficult to define. We describe an investigation in which we raise two questions. First, 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 realities revealed by language, rather than towards the neurological substrate of fatigue.
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© 2015 Penny Standen, Christopher D. Ward, Laura Saunders, and Charlotte Beer
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Standen, P., Ward, C.D., Saunders, L., Beer, C. (2015). Symptoms into Words: How Medical Patients Talk about Fatigue. In: Ward, C.D. (eds) Meanings of ME: Interpersonal and Social Dimensions of Chronic Fatigue. Palgrave Macmillan, London. https://doi.org/10.1057/9781137467324_7
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DOI: https://doi.org/10.1057/9781137467324_7
Publisher Name: Palgrave Macmillan, London
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