Abstract
The insight that a diagnosis of chronic illness disrupted the structure of everyday life came to Mike Bury during his late 1970s fieldwork with people diagnosed with rheumatoid arthritis (Bury 1982). His analysis draws attention to the way illness interrupts ‘the expectations and plans that individuals hold for the future’, requiring ‘a fundamental rethinking of the person’s biography and self-concept’ (Bury 1982:169). Always alert to the effects of socio-economic circumstances, Bury (1982:177) explores how people may engage in a process of mobilising their resources to ‘normalise in the face of disruption’. Below we provide a summary of this initial elaboration of the concept, in the context of other contemporary work tending towards similar ideas about the impact of chronic illness: notably Strauss and Glaser on chronic illness (1975), Anthony Giddens on ‘critical situations’ (1979) and Kathy Charmaz (1983) on ‘loss of self. The concept of biographical disruption has proved durable and continues to inspire and challenge. We examine its legacy in four ways:
-
how Bury himself developed and refined his original work;
-
how other theorists have applied and adapted the concept in the field of chronic illness, including the recognition that biographical disruption may sometimes cause chronic illness;
-
challenges to the assumption of biographical disruption, including notions of biographical flow, continuity and reinforcement, ‘narratives of unconcern’, and the suggestion that disrupted and normal identities may co-exist; and
-
the extension of biographical disruption to a wider range of conditions and topics (including acute or se If-limiting conditions, terminal illness and cancer, and the experiences of family members).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
Becker, G. (1998) Disrupted Lives: How People Create Meaning in a Chaotic World. University of California Press: Berkeley.
Brown, J. (2003) ‘User, Carer and Professional Experiences of Care in Motor Neurone Disease’ Primary Health Care Research and Development 4:207–217.
Brown, G.W. and Harris T. (1978) Social Origins of Depression. Tavistock: London, New York.
Bury, M. (1982) ‘Chronic Illness as Biographical Disruption’ Sociology of Health and Illness 4(2): 167–182.
Bury, M. (1988) ‘Meaning at Risk: The Experience of Arthritis’ in Anderson, R. and Bury, M. (eds.) Living with Chronic Illness. The Experience of Patients and their Families. Unwin Hyman: London, pp. 89–116.
Bury, M. (1991) “The Sociology of Chronic Illness: A Review of Research and Prospects’ Sociology of Health and Illness 13(4): 451–468.
Bury, M. (2001) ‘Illness Narratives: Fact or Fiction?’ Sociology of Health and Illness 23:263–285.
Bury, M. (2005) ‘In Sickness and in Health: Working in Medical Sociology’ in Oliver, A. (ed.) Personal Histories in Health Research. Nuffield Trust: London.
Bury, M. and Holme, A. (1991) Life After Ninety. Routledge: London.
Canicaburu, D. and Pierret, J. (1995) ‘From Biographical Disruption to Biographical Reinforcement: The Case of HIV-positive Men’ Sociology of Health and Illness 17(1): 65–88.
Charmaz, K. (1983) ‘Loss of Self: A Fundamental Form of Suffering in The Chronically 111’ Sociology of Health and Illness 5(2): 168–195.
Charmaz, K. (1987) Struggling for a Self: Identity Levels of the Chronically 111’ Research in the Sociology of Health Care 6:283–321.
Conrad, P. and Bury, M. (1997) ‘Anselrn Strauss and the Sociological Study of Chronic Illness: A Reflection and Appreciation’ Sociology of Health and Illness 19(3): 373–376.
Davis, F. (1963) Passage through Crisis: Polio Victims and the Families. Bobbs-Menill, Indianapolis.
Davis, F. (1964) ‘Deviance Disavowal: The Management of Strained Interaction by the Visibly Handicapped’ in Becker, H. (ed.) The Other Side. Free Press: New York. pp. 119–138.
Exley, C. and Letherby G. (2001) ‘Managing a Disrupted Lifecourse: Issues of Identity and Emotion Work’ Health 5(1): 112–132.
Faircloth, C.A.; Boylstein, C; Rittman, M.; Young, M.E. and Gubrium, J. (2004) ‘Sudden Illness and Biographical How in Narratives of Stroke Recovery’ Sociology of Health and Illness 26(2):242–261.
Fisher, C. and O’Connor, M. (2012) ‘ “Motherhood” in the Context of Living with Breast Cancer’ Cancer Nursing 35(2): 157–163.
Frank, A.W. (1993) ‘The Rhetoric of Self-Change: Illness Experience as Narrative’ The SociologicalQuarterly 34(l):39–52.
Geertz, C. (1973) ‘Thick Description: Toward an Interpretative Theory of Culture’ in Geertz, C. (ed.) The Interpretation of Cultures: Selected Essays. Basic Books: New York. pp. 3–30.
Gerhardt, U. (1990) ‘Introductory Essay: Qualitative Research in Chronic Illness: The Issue and the Story’ Social Science and Medicine 30(11): 1149–1159.
Giddens, A. (1979) Central Problems in Social Theory. Macmillan: London.
Gillespie, C. (2012) “The Experience of Risk as Measured Vulnerability: Health Screening and Lay Uses of Numerical Risk’ Sociology of Health and Illness 34(2): 194–207.
Greenwood, N. and Mackenzie, A. (2010) ‘Informal Caring for Stroke Survivors: Meta-ethnographic Review of Qualitative Literature’ Maturitas 66(3):268–276.
Harris, M. (2009) ‘Troubling Biographical Disruption: Narratives of Unconcern about Hepatitis C Diagnosis’ Sociology of Health and Illness 31(7): 1028–1042.
Hubbard, G. and Forbat, L. (2012) ‘Cancer as Biographical Disruption: Constructions of Living with Cancer’ Supportive Care in Cancer 20(9): 2033–2040.
Jenkins, N.; Lawton, J.; Douglas, M. and Hallowell, N. (2013) ‘Inter-Embodiment and the Experience of Genetic Testing for Familial Hypercholesterolaemia’ Sociology of Health and Illness 35(4):529–543.
Larsson, A.T. and Grassman, E.J. (2012) ‘Bodily Changes Among People Living with Physical Impairments and Chronic Illnesses: Biographical Disruption or Normal illness?’ Sociology of Health and Illness 34(8):1156–1169.
Lawton, J. (2003) ‘Lay Experiences of Health and Illness: Past Research and Future Agendas’ Sociology of Health and Illness 25(3):23–40.
Locock, L.; Alexander, J. and Rozmovits, L. (2008) ‘Women’s Responses to Nausea and Vomiting in Pregnancy’ Midwifery 24(2): 143–152.
Locock, L.; Ziebland, S. and Dumelow, C. (2009) ‘Biographical Disruption, Abruption and Repair in the Context of Motor Neurone Disease’ Sociology of Health and Illness 31(7): 1043–1058.
McCann, L.; Ulingworth, N.; Wengstrom, Y.; Hubbard, G. and Kearney, N. (2010) ‘Transitional Experiences of Women with Breast Cancer Within the First Year Following Diagnosis’ Journal of Clinical Nursing 19(13-14): 1969–1976.
Mills, C.W. (1959) The Sociological Imagination. Oxford University Press: London.
Olsen, A.; Banwell, C. and Dance, P. (2013) ‘Reinforced Biographies among Women Living with Hepatitis C Qualitative Health Research 23(4):531–540.
Owens, C; Lambert, H.; Lloyd, K. and Donovan, J. (2008) ‘Tales of Biographical Disintegration: How Parents Make Sense of Their Sons’ Suicides’ Sociology of Health and Illness 30(2):237–254.
Pound, P.; Gompertz, P. and Ebrahim, S. (1998) ‘Illness in the Context of Older Age: The Case of Stroke’ Sociology of Health and Illness 20(4):489–506.
Rogers, A.; Bury, M. and Kennedy, A. (2009) ‘Rationality, Rhetoric, and Religiosity in Health Care: The Case of England’s Expert Patients Programme’ International Journal Health Services 39(4):725–747.
Sanders, C; Donovan, J. and Dieppe, P. (2002) ‘The Significance and Consequences of Having Painful and Disabled Joints in Older Age: Co-Existing Accounts of Normal and Disrupted Biographies’ Sociology of Health and Illness 24(2): 227–253.
Seeley, J.; Mbonye, M.; Ogunde, N.; Kalanzi, I.; Wolff, B. and Coutinho, A. (2012) ‘HIV and Identity: The Experience of AIDS Support Group Members who Unexpectedly Tested HIV Negative in Uganda’ Sociology of Health and Illness 34(3):330–344.
Sevon, E. (2012) ‘ “My Life has Changed, but his Life Hasn’t”: Making Sense of the Gendering of Parenthood During the Transition to Motherhood’ Feminism and Psychology 22(1)-.60–80.
Shepherd, M. (2010) ‘Stopping Insulin Injections Following Genetic Testing in Diabetes: Impact on Identity’ Diabetic Medicine 27(7):838–843.
Shostak, S. and Fox, N.S. (2012) ‘Forgetting and Remembering Epilepsy: Collective Memory and the Experience of Illness’ Sociology of Health and Illness 34(3):362–378.
Strauss, A. and Glaser, B. (1975) Chronic Illness and the Quality of Life, C.V. Mosby: St. Louis.
Tower, M.; Rowe, J. and Wallis, M. (2012) ‘Reconceptualising Health and Health care for Women Affected by Domestic Violence’ Contemporary Nurse 42(2):216–225.
Williams, G. (1984) “The Genesis of Chronic Illness: Narrative Reconstruction’ Sociology of Health and Illness 6:174–200.
Williams, S. (2000) ‘Chronic Illness as Biographical Disruption or Biographical Disruption as Chronic Illness? Reflections on a Core Concept’ Sociology of Health and Illness 22(1):4067.
Wilson, S. (2007) ‘”When You Have Children, You’re Obliged to Live”: Motherhood, Chronic Illness and Biographical Disruption’ Sociology of Health and Illness 29(4):610–626.
Wood, P.H.N. (1975) Classification of Impairments and Handicaps (WI-IO/ICD9/REV. CONFJ7S.15) World Health Organisation: Geneva.
Editor information
Editors and Affiliations
Copyright information
© 2015 Louise Locock and Sue Ziebland
About this chapter
Cite this chapter
Locock, L., Ziébland, S. (2015). Mike Bury: Biographical Disruption and Long-Term and Other Health Conditions. In: Collyer, F. (eds) The Palgrave Handbook of Social Theory in Health, Illness and Medicine. Palgrave Macmillan, London. https://doi.org/10.1057/9781137355621_37
Download citation
DOI: https://doi.org/10.1057/9781137355621_37
Publisher Name: Palgrave Macmillan, London
Print ISBN: 978-1-349-47022-8
Online ISBN: 978-1-137-35562-1
eBook Packages: Palgrave Social Sciences CollectionSocial Sciences (R0)