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Alzheimer's disease – the experiences of national voluntary organisations

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) on the experiences of national Huntington's disease (HD) organisations in Britain, Holland, Ireland, New Zealand, and the USA. The Australian experience was discussed later (Kapp, 1990; O'Shea, 1990). The earlier paper supported the contention (Black, 1988) that the medical profession in general was not supportive of HD voluntary groups. I also expressed concern that the lobbying of voluntary groups representing far more common disorders was “bound to dilute the impact that Huntington societies may have.”

Type
Original articles
Information
Psychiatric Bulletin , Volume 16 , Issue 11 , November 1992 , pp. 689 - 690
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, 1992

References

Black, M. E. (1988) Self help groups and professionals – what is the relationship? British Medical Journal, 296, 1485–1486.Google Scholar
Kapp, R. (1990) Huntington's disease associations in Australia. Psychiatric Bulletin, 14, 93–94.CrossRefGoogle 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 associations in Australia. Psychiatric Bulletin, 14, 94.CrossRefGoogle Scholar
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