Chronic illness, self-management and the rhetoric of empowerment

New Directions in the Sociology of Chronic and Disabling Conditions: Assaults on the Lifeworld

Volumn , Issue , 2016, Pages 161-179

  Bury, Mike ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 85015004927     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1057/9780230297432_9     Document Type: Chapter

References (46)

1. ABC (2007) The Health Report ABC National Radio, 29 January.
2. Anderson, R. and Bury, M. (eds) (1988) Living with Chronic Illness: The Experiences of Patients and Their Families. London: Unwin Hyman.
3. Barnes, C. and Mercer, G. (2003) Disability. Cambridge: Polity Press.
4. Bunker, J. (2001) Medicine Matters After All: Measuring the Benefits of Medical Care, a Healthy Lifestyle and a Just Social Environment. London: The Nuffield Trust.
5. Bury, M. (1982) Chronic Illness as Biographical Disruption. Sociology of Health and Illness 4(2): 167-82.
6. Bury, M. (1991) The Sociology of Chronic Illness: A Review of Research and Prospects. Sociology of Health and Illness 13(4): 451-68.
7. Bury, M. (1996) Defining and Researching Disability: Challenges and Responses. In C. Barnes and G. Mercer (eds), Exploring the Divide: Illness and Disability. Leeds: The Disability Press.
8. Bury, M. and Taylor, D. (2008) Towards a Theory of Care Transition: From Medical Dominance to Managed Consumerism. Social Theory and Health 6: 210-19.
9. Buszewicz, M., Rait, G. et al. (2006) Self Management of Arthritis in Primary Care: Randomised Controlled Trial, British Medical Journal 33: 879.
10. Carricaburu, D. and Pierret, J. (1995) From Biographical Disruption to Biographical Reinforcement: The Case of HIV-Positive Men. Sociology of Health and Illness 17(1): 66-88.
11. Cayton, H. (2006) The Flat-Pack Patient?: Creating Health Together. Patient Education and Counselling 62: 288-90
12. Charmaz, K. (2000) Experiencing Chronic Illness. In G. L. Albrecht, R. Fitzpatrick and S. C. Scrimshaw (eds), The Handbook of Social Studies in Health and Medicine. London: Sage.
13. Corbin, J. and Strauss, A. L. (1985) Managing Chronic Illness at Home: Three Lines of Work. Qualitative Sociology 8: 224-47.
14. Corbin, J. and Strauss, A. (1988) Unending Work and Care: Managing Chronic Illness at Home. San Francisco, CA: Jossey Bass.
15. Davis, F. (1963) Passage through Crisis: Polio Victims and Their Families. Indianapolis, IN: Bobbs-Merrill.
16. Department of Health (DoH) (2004) The NHS Improvement Plan: Putting People at the Heart of Public Services. London: Department of Health.
17. Department of Health (DoH) (2005) Creating a Patient-Led NHS: Delivering the NHS Improvement Plan. London: Department of Health.
18. Donaldson, L. (2003) Expert Patients Usher in a New Era of Opportunity for the NHS. British Medical Journal 326: 1279-80.
19. EPP evaluation team (2005) Process Evaluation of the EPP - Report II. University of Manchester: National Primary Care Research and Development Centre.
20. Faircloth, C. A., Boylstein, C., Rittman, M., Young, M. E. and Gubrium, J. (2004) Sudden Illness and Biographical Flow in Narratives of Stroke Recovery. Sociology of Health and Illness 26(2): 242-61.
21. Frank, A. (1995) The Wounded Storyteller: Body, Illness and Ethics. Chicago, IL: University of Chicago Press.
22. Gerhardt, U. (1990) Introductory Essay: Qualitative Research in Chronic Illness: The Issue and the Story. Social Science and Medicine 30: 1149-59.
23. Gravelle, H., Dusheiko, M. et al. (2007) Impact of Case Management (Evercare) on Frail Elderly Patients: Controlled Before and After Analysis of Quantitative Outcome Data. British Medical Journal 334: 31.
24. Ham, C., York, N., Sutch, S. et al. (2003) Hospital Bed Utilisation in the NHS, Kaiser Permanente and the US Medicare Programme: Analysis of Routine Data. British Medical Journal 327: 1257-60.
25. Jordan, J. E. and Osborne, R. H. (2007) Chronic Disease Self-management Education Programs: Challenges Ahead. Medical Journal of Australia 186(2): 84-7.
26. Kelly, M. and Field, D. (1996) Medical Sociology, Chronic Illness and the Body. Sociology of Health and Illness 18(2): 241-57.
27. Kennedy, A., Reeves, D., Bower, P., Lee, V., Middleton, E., Richardson, G., Gardner, C., Gately, C. and Rogers, A. (2007) The Effectiveness and Cost Effectiveness of a National Lay-led Self Care Support Programme for Patients with Long-term Conditions: A Pragmatic Randomised Controlled Trial. Journal of Epidemiol and Community Health 61(3): 254-61.
28. Lorig K. (2002) Partnerships between Expert Patient and Physicians. Lancet 359: 814-5.
29. McKinlay, J. and Marceau, L. D. (2002) The End of the Golden Age of Doctoring. International Journal of Health Services 32: 379-416.
30. Mullean, P. (2000) The Imaginary Timebomb: Why an Ageing Population Is not a Social Problem. London: I.B. Tauris.
31. Newbould, J., Taylor, D. and Bury, M. (2006) Lay-led Self-management in Chronic Illness: A Review of the Evidence. Chronic Illness 2: 249-61.
32. Newman, S., Steed, L. and Mulligan, K. (2004) Self-management Interventions for Chronic Illness. Lancet 364: 1523-37.
33. Oliver, M. (1996) Defining Impairment and Disability: Issues at Stake. In C. Barnes and G. Mercer (eds), Exploring the Divide: Illness and Disability. Leeds: The Disability Press.
34. Osborne, R., Wilson, T., Lorig, K. R. and McColl, G. J. (2007) Does Self-management Lead to Sustainable Health Benefits in People with Arthritis? A 2-year Transition Study on 452 Australians. The Journal of Rheumatology 34: 1112-7.
35. 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.
36. Rogers, A., Hassell, K. and Nicolas, G. (1999) Demanding Patients? Analysing the Use of Primary Care. Buckingham: Open University Press.
37. Rogers, A., Bury, M. and Kennedy, A. (2009) Rationality, Religiosity and Rhetoric in Health Care: The Case of the Expert Patients Programme. International Journal of Health Service 39(4): 725-47.
38. Roland, M., Dusheiko, M., Gravelle, H. et al. (2006) Follow Up of People Aged 65 and Over with a History of Emergency Admissions: Analysis of Routine Admission Data. British Medical Journal 330: 289-92.
39. Roth, J. A. (1963) Timetables: Structuring the Passage of Time in Hospital Treatment and Other Careers. Indianapolis, IN: Bobbs-Merrill.
40. Salter, B. (2004) The New Politics of Medicine. Palgrave: London.
41. Shakespeare, T. (2006) Disability Rights and Wrongs. London: Routledge.
42. Strauss, A. (1973) America: In Sickness and in Health. Society 19: 33-9.
43. Strauss, A. (1975) Chronic Illness and the Quality of Life. St Louis: Mosby.
44. Taylor, D. and Bury, M. (2007) Chronic Illness, Expert Patients and Care Transition. Sociology of Health and Illness 29: 27-45.
45. Wanless, D. (2002) Securing Our Future Health: Taking a Long Term View. London H M Treasury.
46. Williams, S. J. (2000) Chronic Illness as Biographical Disruption or Biographical Disruption as Chronic Illness? Reflections on a Core Concept. Sociology of Health and Illness 22(1): 40-67.