Health Care Analysis

, 17:331 | Cite as

Story in Health and Social Care

Original Article

Abstract

This paper offers a brief consideration of how narrative, in the form of people’s own stories, potentially figures in health and social care provision as part of the impulse towards patient-centred care. The rise of the epistemological legitimacy of patients’ stories is sketched here. The paper draws upon relevant literature and original writing to consider the ways in which stories can mislead as well as illuminate the process of making individual treatment care plans.

Keywords

Story Health and social care 

References

  1. 1.
    Aldiss, B. (1999). When the feast is finished. Reflections on terminal illness. London: Little Brown.Google Scholar
  2. 2.
    Burke, L. (2008). The country of my disease: Genes and genealogy in alzheimer’s life-writing. The Journal of Literary and Cultural Disability Studies, 2(1), 63–74.Google Scholar
  3. 3.
    Davison, C., Davey-Smith, G., & Frankel, S. (1991). Lay epidemiology and the prevention paradox–the implication of coronary candidacy for health promotion. Sociology of Health and Illness, 13(1), 1–19.CrossRefGoogle Scholar
  4. 4.
    Davison, C., Frankel, S., & Davey-Smith, G. (1992). The limits of lifestyle: Reassessing ‘fatalism’ in the popular culture of illness prevention. Social Science and Medicine, 34(6), 675–685.CrossRefPubMedGoogle Scholar
  5. 5.
    Demicheli, V., Jefferson T., Rivertti, A., & Price, D. (2005). ‘Vaccines for measles, mmps and rubella in children’, The cochrane database of systematic reviews, 4. (Art. No.: CD004407).Google Scholar
  6. 6.
    Elwyn, G., & Gwyn, R. (1999). Narrative based medicine. Stories we hear and stories we tell: Analysing talk in clinical practice (Education and debate). British Medical Journal, 318, 186–188. (16 January).PubMedGoogle Scholar
  7. 7.
    Frank, A. (1995). The wounded storyteller: Body, illness and ethics. Chicago: Chicago University Press.Google Scholar
  8. 8.
    Gillman, M., Swain, J., & Heyman, B. (1997). Life history or ‘Case’ history: The objectification of people with learning difficulties through the tyranny of professional discourses. Disability and Society, 12(5), 675–694.CrossRefGoogle Scholar
  9. 9.
    Goodley, D. (1996). Tales of hidden lives: A critical examination of life history research with people who have learning difficulties. Disability and society, 11, 333–348. (Issue September 1996).CrossRefGoogle Scholar
  10. 10.
    Greene, R. (1971). Sick doctors. London: Heinemann Medical.Google Scholar
  11. 11.
    Greenhalgh, T. (1998). Narrative based medicine in an evidence based world. In T. Greenhalgh & B. Hurwitz (Eds.), Narrative based medicine: Dialogue and discourse in clinical practice. London: BMJ Books.Google Scholar
  12. 12.
    Greenhalgh, T., & Hurwitz, B. (Eds.). (1998). Narrative based medicine. Dialogue and discourse in clinical practice. London: BMJ Books.Google Scholar
  13. 13.
    Hilton, S., Petticrew, M., & Hunt K. (2007). Parents’ champions vs. vested interests: Who do parents believe about MMR? A qualitative study. BMC Public Health, 7:42. Accessed June 03, 2009, at http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1851707.
  14. 14.
    Hunter, K. M. (1991). Doctors’ stories: The narrative structure of medical knowledge. Princeton, NJ: Princeton University Press.Google Scholar
  15. 15.
    Illich, I. (1976). Limits to medicine: Medical nemesis, the expropriation of health. London: Boyars.Google Scholar
  16. 16.
    Kearney, R. (2002). On stories. (Series: Thinking in action). London: Routledge.Google Scholar
  17. 17.
    Moerman, D. (2002). Meaning, medicine and the ‘placebo effect’. Cambridge studies in medical anthropology. Cambridge: Cambridge University Press.Google Scholar
  18. 18.
    Oakley, A. (1980). Women confined: Towards a sociology of childbirth. Oxford: Martin Robertson.Google Scholar
  19. 19.
    Porter, R. (1997). The greatest benefit to mankind: A medical history of humanity from antiquity to the present. London: Harpercollins.Google Scholar
  20. 20.
    Prendergast, C. (2008). The unexceptional schizophrenic: A post-postmodern introduction. The Journal of Literary and Cultural Disability Studies 2(1), 56–62. Accessed on June 03, 2009, Available at: http://jlcds.lupjournals.org/default.aspx?content=0201prendergast.
  21. 21.
    Rose, S., Bisson, J., Churchill, R., Wessley, S. (2002). Psychological debriefing for preventing post traumatic stress disorder. Cochrane database systematic review: 2. (Art no CD000560).Google Scholar
  22. 22.
    Stein, D. J., Seedat, S., Iversen, A., & Wessley, S. (2007). Post traumatic stress disorder: Medicine and politics. Lancet, 369, 139–144.CrossRefPubMedGoogle Scholar
  23. 23.
    Sacks, O. (1986). A leg to stand on. London: Pan.Google Scholar
  24. 24.
    Salter, B. (2004). The new politics of medicine. Basingstoke: Palgrave Macmillan.Google Scholar
  25. 25.
    Scheper-Hughes, N. (2002). Coming to our senses. Anthropology and genocide. In L. Alexander (Ed.), Annihilating Difference. The Anthropology of Genocide (pp. 348–381). Hinton: University of California Press.Google Scholar
  26. 26.
    Sinclair, C. (1998). A soap opera from hell. Essays on the facts of life and the facts of death. London: Fourth Estate.Google Scholar
  27. 27.
    Strong, P. (1979). The ceremonial order of the clinic: parents, doctors and medical bureaucracies. London: Routledge, Kegan Paul.Google Scholar

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  1. 1.Department of SociologyUniversity of WarwickCoventryUK
  2. 2.School of Human and Health SciencesUniversity of HuddersfieldQueensgateUK
  3. 3.NESTALondonUK

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