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Voluntary schizophrenia organisations

Attitudes and experiences

Published online by Cambridge University Press:  02 January 2018

Brian O'Shea
Brian O'Shea*
Affiliation:
Newcastle Hospital, Greystones, County Wicklow, Ireland
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I previously reported (O'Shea, 1989, 1992) on the experience of national voluntary Huntington's disease (HD) and Alzheimer's disease (AD) organisations. This series of enquiries stemmed from an observation of Black (1988) that the medical profession in general offered little support to voluntary groups, a statement which has been largely supported for both HD and AD organisations in the first two parts of this trilogy. This final paper examines the experiences and attitudes of (mostly national) schizophrenia organisations.

Type
Original papers
Information
Psychiatric Bulletin , Volume 18 , Issue 1 , January 1994 , pp. 32 - 35
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © Royal College of Psychiatrists, 1994

References

Black, M.E. (1988) Self help groups and professionals – what is the relationship? British Medical Journal, 296, 1485–1486.Google Scholar
O'Shea, B. (1989) Huntington's disease – the experiences of voluntary organisations. Psychiatric Bulletin, 13, 409–411.Google Scholar
O'Shea, B. (1990) Huntington's disease association in Australia. Psychiatric Bulletin, 14, 94.Google Scholar
O'Shea, B. (1992) Alzheimer's disease – the experiences of national voluntary organisations. Psychiatric Bulletin, 16, 689–690.Google Scholar
Roberts, G.A. (1986) Burnout: psychobabble or valuable concept? British Journal of Hospital Medicine, 36, 194–197.Google Scholar
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