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The moral experience of illness and its impact on normalisation: Examples from narratives with Punjabi women living with rheumatoid arthritis in the UK
Author(s) -
Sanderson Tessa,
Calnan Michael,
Kumar Kanta
Publication year - 2015
Publication title -
sociology of health and illness
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.146
H-Index - 97
eISSN - 1467-9566
pISSN - 0141-9889
DOI - 10.1111/1467-9566.12304
Subject(s) - ethnic group , context (archaeology) , psychology , causation , narrative , attribution , social psychology , sociology , political science , anthropology , law , paleontology , linguistics , philosophy , biology
The moral component of living with illness has been neglected in analyses of long‐term illness experiences. This article attempts to fill this gap by exploring the role of the moral experience of illness in mediating the ability of those living with a long‐term condition ( LTC ) to normalise. This is explored through an empirical study of women of Punjabi origin living with rheumatoid arthritis ( RA ) in the UK . Sixteen informants were recruited through three hospitals in UK cities and interviews conducted and analysed using a grounded theory approach. The intersection between moral experience and normalisation, within the broader context of ethnic, gender and socioeconomic influences, was evident in the following: disruption of a core lived value (the centrality of family duty), beliefs about illness causation affecting informants’ ‘moral career’, and perceived discrimination in the workplace. The data illustrate the importance of considering an ethnic community's specific values and beliefs when understanding differences in adapting to LTC s and changing identities.