SEARCH

SEARCH BY CITATION

References

  • American Heart Association (1999) Heart and Stroke Statistical Update.
  • Anderson, R. (1992) The Aftermath of Stroke: the Experience of Patients and their Families. Cambridge: Cambridge University Press.
  • Arber, S. and Evandrou, M. (1993) Ageing, Independence and the Life Course. London: Jessica Kingsley.
  • Becker, G. (1993) Continuity after a stroke: implications of life course disruption in old age, The Gerontologist, 31, 6319.
  • Becker, G. and Kaufman, S. (1995) Managing an uncertain illness trajectory in old age: patients’ and physicians’ views of stroke, Medical Anthropology, 9, 16587.
  • Bury, M. (1982) Chronic illness as biographical disruption, Sociology of Health and Illness, 4, 16782.
  • Bury, M. (1988) Meanings at risk: the experience of arthritis. In Anderson, R. and Bury, M. (eds) Living with Chronic Illness: the Experience of Patients and their Families. London: Unwin Hyman.
  • Bury, M. (1991) The sociology of chronic illness: a review of research and prospects, Sociology of Health and Illness, 13, 45168.
  • Bury, M. (1997) Health and Illness in a Changing Society. London: Routledge.
  • Carricaburu, D. and Pierret, J. (1995) From biographical disruption to biographical reinforcement: the case of HIV positive men, Sociology of Health and Illness, 17, 6588.
  • Charlson, M.E., Pompei, P., Ales, K.A. and MacKenzie, R. (1987) A new method of classifying prognostic comorbidity in longtitudinal studies: development and validation, Journal of Chronic Disabilities, 40, 37383.
  • Charmaz, K. (1991) Good Days, Bad Days: the Self in Chronic Illness and Time. New Brunswick, NJ: Rutgers University Press.
  • Corbin, J. and Strauss, A. (1987) Accompaniments of chronic illness: changes in self, biography and biographical time, Research in the Sociology of Health Care, 6, 24981.
  • Corbin, J. and Strauss, A. (1988) Unending Work and Care: Managing Chronic Illness at Home. San Francisco: Jossey-Bass Publishers.
  • Ellis-Hill, C. (1997) Biographical disruption, narrative, and identity in stroke: personal experience in acquired chronic illness, Auto/Biography, 1, 13144.
  • Ellis-Hill, C., Payne, S. and Ward, C. (2000) Self-body split: issues of identity in physical recovery following stroke, Disability and Rehabilitation, 22, 72533.
  • Foucault, M. (1973) The birth of the clinic: an archaeology of medical perception. New York: Pantheon Books.
  • Fujiura, G.T. and Rutowski-Kmitta, V. (2001) Counting disability. In Albrecht, G., Seelman, K. and Bury, M. (eds) Handbook of Disability Studies. Thousand Oaks, CA: Sage.
  • Good, B. (1993) Culture, diagnosis, and comorbidity, Culture, Medicine, and Psychiatry, 16, 42746.
  • Gubrium, J. (1993) Speaking of Life: Horizons of Meaning for Nursing Home Residents. Hawthorne, NY: Aldine de Gruyter.
  • Gubrium, J., Rittman, M., Williams, C., Young, M.E., Boylstein, C. and Faircloth, C. (2003 ) Benchmarking as everyday functional assessment in stroke recovery, Journal of Gerontology, 583, 920311.
  • Hart, E. (2001) System induced setbacks in stroke recovery, Sociology of Health and Illness, 23, 10123.
  • Hazan, H. (1994) Old Age: Constructions and Deconstructions. Cambridge, UK: Cambridge University Press.
  • Heikkinen, R. (2000) Ageing in an autobiographical context, Ageing and Society, 20, 46783.
  • Holstein, M. and Cole, T. (1996) Reflections on age, meaning, and chronic illness, Journal of Aging and Identity, 1, 722.
  • House, A. (2002) On-line citation. http://www.leeds.ac.uk.
  • Hýden, L.C. (1997) Illness and narrative, Sociology of Health and Illness, 19, 4869.
  • Kaufman, S.R. (1988) Illness, biography, and the interpretation of self following a stroke, Journal of Aging Studies, 2, 21727.
  • Kleinman, A. (1988) The Illness Narratives: Suffering, Healing and the Human Condition. New York: Basic Books.
  • Mansfield, C., Mitchell, J. and King, D.E. (2002) The doctor as god's mechanic? beliefs in the southeastern United States, Social Science and Medicine, 54, 399409.
  • Martin, J., Meltzer, H. and Elliot, D. (1988) The Prevalence of Disability Among Adults. London: HMSO.
  • Marr, J. (1991) The experience of living with chronic illness, Journal of Neuroscience Nursing, 23, 3259.
  • Mathieson, C.M. and Stam, H. (1995) Renegotiating identity: cancer narratives, Sociology of Health and Illness, 17, 283306.
  • Post, P., Stigglebout, A. and Walker, P. (2001) The utility of health studies after stroke: a systematic review of the literature, Stroke, 32, 142549.
  • Pound, P. (1996) [Lives with stroke]. Unpublished Ph.D. Dissertation. London: University of London.
  • 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, 489506.
  • Rajaram, S. (1997) Experience of hypoglycemia among insulin dependent diabetics and its impact on the family, Sociology of Health and Illness, 19, 28196.
  • Rosenfeld, D. (2002) Personal communication.
  • 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, 22753.
  • Schneider, P. and Conrad, P. (1983) Having Epilepsy: The Experience and Control of Illness. Philadelphia: Temple University Press.
  • Singer, E. (1974) Premature social aging: the social-psychological consequences of chronic illness, Social Science and Medicine, 8, 14351.
  • Web Health (2003) [on-line citation]. http://www.webhealth.co.uk
  • Williams, S. (1996) The vicissitudes of embodiment across the chronic illness trajectory, Body and Society, 2, 2331.
  • 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, 4067.
  • Williams, G.H. and Wood, P.H.N. (1988) Coming to terms with chronic illness: the negotiation of autonomy in rheumatoid arthritis, International Disability Studies, 10, 12833.