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Richardson, JC; Ong, BN; Sim, J (2008)
Publisher: BioMed Central
Journal: BMC Musculoskeletal Disorders
Languages: English
Types: Article
Subjects: Research Article, Orthopedics and Sports Medicine, Diseases of the musculoskeletal system, RC925-935, R1

Classified by OpenAIRE into

mesheuropmc: human activities



Chronic widespread pain (CWP) affects 10% of adults and often causes significant disability in everyday life. Research on time in chronic conditions has focused on biographical disruption and perceptions of past and future. However, more mundane aspects of time are also disrupted in a condition such as CWP, which is uncertain on a minute-to-minute, day-to-day basis, as well as in the longer term. The results presented here are part of a wider study, the aim of which was to explore how people with CWP experience and give meaning to their 'condition'. This article focuses on how mundane, repetitive and taken-for-granted aspects of everyday life are disrupted for people with CWP.


Eight people aged 40–60 years living with CWP took part in multiple in-depth interviews, diaries and family interviews, exploring the meanings and interpretations of participants and individuals' experiences in a social context.


The findings illuminate the ways in which the experience of time is changed by CWP: carrying out the tasks of everyday life takes longer, routines are disrupted, and changes are needed in how time is managed. Some strategies for managing these tasks rely on ability to control one's time. However, this is not always possible and, for some, the experience of CWP becomes characterised by lack of such control.


This study explored the concept of controllable time in the experience of CWP. Regaining control over time is an important element in coping with chronic pain, and helping patients to regain such control has potential as a target for health professionals involved in pain management.

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    • 1. Felski R: The invention of everyday life. In Understanding everyday life Edited by: Bennett T, Watson D. Oxford: Blackwell; 2002:46-50.
    • 2. Bennett T, Watson D: Understanding everyday life Oxford: Blackwell; 2002.
    • 3. Bury M: Chronic illness as biographical disruption. Sociol Health Illn 1982, 4(2):167-182.
    • 4. Crossley ML: 'Let me explain': narrative emplotment and one patient's experience of oral cancer. Soc Sci Med 2003, 56(3):439-448.
    • 5. Charmaz K: Good days, bad days: The self in chronic illness and time New Brunswick: Rutgers University Press; 1991.
    • 6. Bury M: Health and illness in a changing society London: Routledge; 1997.
    • 7. Richardson JC, Ong BN, Sim J: Is chronic widespread pain biographically disruptive? Soc Sci Med 2006, 63(6):1573-1585.
    • 8. Richardson JC, Ong BN, Sim J: Remaking the future: contemplating a life with chronic widespread pain. Chronic Illn 2006, 2(3):209-218.
    • 9. Corbin JM: The body in health and illness. Qual Health Res 2003, 13(2):256-267.
    • 10. Macfarlane G, Croft PR, Schollum J, Silman A: Widespread pain: is an improved classification possible? J Rheumatol 1996, 23(9):1628-1632.
    • 11. Bury M: The sociology of chronic illness: a review of research and prospects. Sociol Health Illn 1991, 13(4):451-468.
    • 12. Bury M: Illness narratives: fact or fiction? Sociol Health Illn 2001, 23(3):263-285.
    • 13. Atkinson P: Narrative turn or blind alley? Qual Health Res 1997, 7(3):325-345.
    • 14. Charmaz K: Stories of suffering: subjective tales and research narratives. Qual Health Res 1999, 9(3):362-382.
    • 15. Elliott H: The use of diaries in sociological research on health experience. Sociol Res Online 1997, 2(2): [http://www.socreson line.org.uk/socresonline/2/2/7.html].
    • 16. Parry O, Thomson C, Fowkes G: Life course data collection: qualitative interviewing using the life grid. Sociol Res Online 1999, 4(2): [http://www.socresonline.org.uk/socresonline/4/2/ parry.html].
    • 17. Minichiello V, Aroni R, Timewell E, Alexander L: In-depth interviewing Sydney: Longman; 1995.
    • 18. Radley A: Social realms and the qualities of illness experience. In Qualitative Health Psychology Edited by: Murray M, Chamberlain K. London: Sage; 1999:16-30.
    • 19. Kelly MP, Field D: Medical sociology, chronic illness and the body. Sociol Health Illn 1996, 18(2):241-257.
    • 20. Lawton J: Lay experiences of health and illness: past research and future agendas. Sociol Health Illn 2003, 25(3):23-40.
    • 21. Radley A, Billig M: Accounts of health and illness: dilemmas and representations. Sociol Health Illn 1996, 18(2):220-240.
    • 22. Statement of ethical practice for the British Sociological Association. London British Sociological Association; 2002.
    • 23. NVivo qualitative data analysis program version 1.3. Melbourne: QSR International Pty Ltd; 2000.
    • 24. Smith JA, Jarman M, Osborn M: Doing interpretative phenomenological analysis. In Qualitative Health Psychology Edited by: Murray M, Chamberlain K. London: Sage; 1999:218-240.
    • 25. Moss P, Dyck I: Women, body, illness: space and identity in the everyday lives of women with chronic illness Lanham: Rowman and Littlefield; 2003.
    • 26. Williams G: Chronic illness and the pursuit of virtue in everyday life. In Worlds of Illness: biographical and cultural perspectives on health and disease Edited by: Radley A. London: Routledge; 1993:92-108.
    • 27. Reynolds F, Prior S: 'Sticking jewels in your life': exploring women's strategies for negotiating an acceptable quality of life with multiple sclerosis. Qual Health Res 2003, 13(9):1225-1251.
    • 28. Dyck I: Hidden geographies - the changing lifeworlds of women with multiple sclerosis. Soc Sci Med 1995, 40(3):307-320.
    • 29. Henriksson CM: Living with continuous muscular pain - patient perspectives 2. Strategies for daily life. Scand J Caring Sci 1995, 9(2):77-86.
    • 30. Charmaz K: Identity dilemmas of chronically ill men. In Grounded theory in practice Edited by: Strauss A, Corbin J. Thousand Oaks: Sage; 1997:35-62.
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