Telling People Much Much More



This chapter examines the inadequate communication about mental illness. Many users complain about insufficient information, often confusing and inaccurate. What are the obstacles to telling people much, much more? Why is relevant and accurate information often not sensitively given? Who else is entitled to know the personal and private details given to mental illness professionals and under what conditions?


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  1. Peter Allen and Kate Scales, Residents’ Rights — Helping People with Learning Difficulties Understand Their Housing Rights (Residents Rights Project, 1990).Google Scholar
  2. Jacqueline M Atkinson, ‘To Tell or Not to Tell the Diagnosis of Schizophrenia’, Journal of Medical Ethics (1989) pp. 21 ’4.Google Scholar
  3. J. M. Atkinson and D. A. Coia, ‘Responsibility to Carers — An ethical dilemma’, Psychiatric Bulletin (1990).Google Scholar
  4. B. R. Ballinger, ‘The Patient’s View of Psychiatric Treatment’, Health Bulletin, vol. XX1X no. 4 (October 1971) pp. 192-6.Google Scholar
  5. Virginia Beardshaw, Conscientious Objectors at Work — Mental Hospital Nurses — A Case Study (Social Audit, 1981) p. 81.Google Scholar
  6. Virginia Beardshaw, ‘Aiming to be Less of a Client, More of an Ally’, The Health Service Journal (1 September 1988) pp. 994-6).Google Scholar
  7. Peter Beresford and Suzy Croft, ‘Language for Service Users’, Social Work Today (11 August 1988).Google Scholar
  8. G. E. Bermak, ‘Do Psychiatrists Have Special Emotional Problems?’, American Journal of Psychoanalysis 37(1977) pp. 141–6.CrossRefGoogle Scholar
  9. William Bingley and Ronald Lacey, Inside Out (MIND, 1988).Google Scholar
  10. Anthony Bird, Jenny Cobb and Mohammed T. L. Walji, ‘Increased Patient Participation Using an Extended Consultation: An Inner City Study’, Journal of the Royal College of General Practitioners (May 1988) pp. 212 –14.Google Scholar
  11. A. and D. Brandon, Consumers as Colleagues (MIND, 1987).Google Scholar
  12. David Brindle, ‘The Resounding Call of the Whistle-Blower Nurse’, The Guardian (4 July 1990).Google Scholar
  13. British Association of Social Workers, Clients are Fellow Citizens (May 1980).Google Scholar
  14. British Medical Association, Handbook of Medical Ethics (1982).Google Scholar
  15. British Medical Association, Philosophy and Practice of Medical Ethics (BMA, 1988).Google Scholar
  16. M. Brost and T. Johnson (eds), Getting to Know You — One Approach to Service Assessment and Planning for Individuals with Disabilities (Madison, Wisconsin Council on Developmental Disabilities, 1982).Google Scholar
  17. J. P. M. Campbell and J. G. R. Howie, ‘Involving the patient in reporting adverse drug reactions’, Journal of the Royal College of General Practitioners (August 1988, pp. 370 ’1).Google Scholar
  18. Franklin D. Chu and Sharland Trotter, The Madness Establishment, Ralph Nader Study Group report on the National Insitute of Mental Health (Grossman, 1974).Google Scholar
  19. Nicki Cornwell, ‘On Record and Open to Question’, Social Work Today (18 January 1990).Google Scholar
  20. Department of Health, Working for Patients (1989) paragraph 1.13.Google Scholar
  21. Department of Health and Welsh Office, Code of Practice on the Mental Health Act, 1983 (HMSO, 1990).Google Scholar
  22. Paul Dolan, ‘Access to Personal Files: A Practical Guide to the Act’, Social Work Today (30 March 1989).Google Scholar
  23. Ronald Dworkin, ‘Autonomy and the Demented Self’, The Millbank Quarterly, vol. 64, supplement 2 (1986).Google Scholar
  24. Annie Faulkner, ‘How to catch the CAB’, Nursing Times (1 October 1986).Google Scholar
  25. Grant Gillett, ‘Informed Consent and Moral Integrity’, Journal of Medical Ethics 15(1989) pp. 117–23.CrossRefGoogle Scholar
  26. Larry Gostin, A Human Condition, vol. l(MIND, 1975) pp. 109–10.Google Scholar
  27. Janet Gregory, Patients’ Attitudes in the Hospital Service, Royal Commission on the NHS (HMSO, 1978, pp. 103–4).Google Scholar
  28. James D. Guy, The Personal Life of the Psychotherapist (John Wiley, 1987).Google Scholar
  29. V. Herbert, ‘Informed Consent — A Legal Evaluation’, Cancer 46, 4 (1988) pp. 1043.Google Scholar
  30. Roger Higgs in Michael Lockwood (ed.), Moral Dilemmas in Modern Medicine (Oxford Univ, 1985) p. 102.Google Scholar
  31. John Illman, ‘Medical Record You Can’t Forget’, The Guardian (5 Jan. 1990).Google Scholar
  32. F. J. Ingelfinger, ‘Informed (But Educated) Consent’, New England Journal of Medicine, 28(1972) pp. 465–6.CrossRefGoogle Scholar
  33. Richard M. Jones, The Mental Health Act 1983 with annotations by Richard M. Jones (Sweet & Maxwell 1982, p. 58).Google Scholar
  34. Elaine Kempson, Informing Health Consumers (College of Health, December 1987).Google Scholar
  35. Stuart A. Kirk and Herb Kutchins, ‘Deliberate Misdiagnosis in Mental’Health Practice’, Social Science Review (June 1988) pp. 223–37.Google Scholar
  36. L. S. Kubie, ‘Pitfalls of Community Psychiatry’, Archives of General Psychiatry, 18(1968) pp. 257–66.CrossRefGoogle Scholar
  37. Lambeth MIND, Thoughts of Home — The Views of Your Consumers (245a Coldharbour Lane, London SW9 8RR, 1988).Google Scholar
  38. The Lancet, ‘Write for Your Patient’(1989) no. 1, p. 1175.Google Scholar
  39. Jeremy Laurance, ‘Silencing the NHS’, New Statesman/Society (10 June 1988).Google Scholar
  40. Charles W. Lidz et al., Informed Consent: A Study of Decision Making in Psychiatry (Guilford Press, 1984).Google Scholar
  41. J. G. Looney et al., ‘Psychiatric Transition from Training to Career: Stress and Mastery’, American Journal of Psychiatry: 137(1980) pp. 32–5.Google Scholar
  42. Dave Lowson, ‘Successful Workers?’, IAMHW Bulletin, no 8 (1989).Google Scholar
  43. R. Masnik, ‘Telling a Schizophrenic Patient His Diagnosis’, American Journal of Psychotherapy 18(3) (1974) pp. 452–7.Google Scholar
  44. MIND, Understanding Caring (1989).Google Scholar
  45. MIND/Roehampton Institute, People First (1990).Google Scholar
  46. Ralph Nader (ed.), The Consumer and Corporate Accountability (Harcourt Brace, 1973).Google Scholar
  47. David Neville and Dick Beak, ‘Solving the Case History Mystery’, Social Work Today (28 June 1990).Google Scholar
  48. Florence Nightingale, Notes on Nursing (London, 1859).Google Scholar
  49. Clifton Perry, ‘A Problem with Refusing Certain Forms of Psychiatric Treatment’, Social Science and Medicine, vol. 20, no. 6 (1985) pp. 645–8.CrossRefGoogle Scholar
  50. Presidents Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioural Research, Making Health Care Decisions vol. 1, Report (October 1982) ch. 5.Google Scholar
  51. Lydia Sinclair, ‘A Plea to Access to Personal Files’, Social Work Today (17 Nov. 1986).Google Scholar
  52. Helen Smith, ‘Collaboration for Change’, in David Towell, Sue Kingsley and Tom McAusland (eds), Managing Psychiatric Services in Transition (King’s Fund College, 19S9).Google Scholar
  53. Kathryn M. Taylor, ‘Telling Bad News: Physicians and the Disclosure of Undesirable Information’, Sociology of Health and Illness, vol. 10, no. 2 (June 1988).Google Scholar
  54. Richard Titmuss, Essays on the Welfare State (Allen & Unwin, 1958) p. 127.Google Scholar
  55. Henry Walton (ed.), Education and Training in Psychiatry (King’s Fund, 1986) p. 54.Google Scholar
  56. World Health Organisation and United Nations Children’s fund, Primary Health Care — International Conference on Primary Health Care, Alma Ata, USSR (Geneva, WHO and UNICEF, 1978).Google Scholar
  57. World Health Organisation, Consumer Involvement in Mental Health and Rehabilitation Services (Division of Mental Health, WHO, 1989).Google Scholar

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© David Brandon 1991

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