'What is it like to have ME?' The discursive construction of ME in computer-mediated communication and face-to-face interaction

Abstract: ME (Myalgic Encephalomyelitis) or CFS (chronic fatigue syndrome) is a debilitating illness for which no cause or medical tests have been identified. Debates over its nature have generated interest from qualitative researchers. However, participants are difficult to recruit because of the nature of their condition. Therefore, this study explores the utility of the internet as a means of eliciting accounts. We analyse data from focus groups and the internet in order to ascertain the extent to which previous research findings apply to the internet domain. Interviews were conducted among 49 members of internet groups (38 chatline, 11 personal) and 7 members of two face-to-face support groups. Discourse analysis of descriptions and accounts of ME or CFS revealed similar devices and interactional concerns in both internet and face-to-face communication. Participants constructed their condition as serious, enigmatic and not psychological. These functioned to deflect problematic assumption

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Postprint
begutachtet (peer reviewed)
In: Health ; 11 (2007) 1 ; 87-108

Ereignis
Veröffentlichung
(wo)
Mannheim
(wann)
2007
Urheber
Guise, Jennifer
Widdicombe, Sue
McKinlay, Andy

DOI
10.1177/1363459307070806
URN
urn:nbn:de:0168-ssoar-226102
Rechteinformation
Open Access unbekannt; Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
25.03.2025, 13:54 MEZ

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Beteiligte

  • Guise, Jennifer
  • Widdicombe, Sue
  • McKinlay, Andy

Entstanden

  • 2007

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