People with dementia and their relatives: personal experiences of Alzheimer's and of the provision of care.

Little is known about the experiences of people with dementia, as there has been relatively little research carried out that includes their perspectives. In the past, user perspectives on experiences of dementia and on services have mostly been solicited from family carers, rather than from people with dementia themselves. It has been suggested that these studies may lack information and insight into the experiences of people with dementia. This study aimed at eliciting the views and feelings of people in all stages of dementia, as well as those of their relatives, on care services and on experiences of dementia. Twenty-seven people with dementia from residential and day care settings were interviewed and their daily lives videotaped. Interviews were also conducted with next of kin. This article reports on findings and issues arising from the study.

[1]  E. Muir‐Cochrane The context of care: Issues of power and control between patients and community mental health nurses , 2000 .

[2]  G. Martin,et al.  Anti oppressive practice: a route to the empowerment of people with dementia through communication and choice. , 2000, Journal of psychiatric and mental health nursing.

[3]  J. Moriarty Use of community and long-term care by people with dementia in the UK: A review of some issues in service provision and carer and user preferences , 1999 .

[4]  R. Tappen,et al.  Communicating with individuals with Alzheimer's disease: examination of recommended strategies. , 1997, Archives of psychiatric nursing.

[5]  R. Cheston,et al.  Inhabitants of a Lost Kingdom: A Model of the Subjective Experiences of Dementia , 1997, Ageing and Society.

[6]  Pam Enderby,et al.  What Does it Mean to Listen to People with Dementia? , 2001 .

[7]  M. Bourgeois Enhancing conversation skills in patients with Alzheimer's disease using a prosthetic memory aid. , 1990, Journal of applied behavior analysis.

[8]  Kirsten Stalker,et al.  Eliciting user perspectives on what works , 1999, International journal of geriatric psychiatry.

[9]  P. Kaminski,et al.  Ignorance is not bliss. , 2000, Nursing times.

[10]  Rom Harré,et al.  The Construction and Deconstruction of Self in Alzheimer's Disease , 1992, Ageing and Society.

[11]  J. Lindesay,et al.  The quality of interactions schedule (QUIS): Development, reliability and use in the evaluation of two domus units , 1993 .

[12]  Murna Downs,et al.  The Emergence of the Person in Dementia Research , 1997, Ageing and Society.

[13]  G. Proctor Listening to Older Women with Dementia: Relationships, voices and power , 2001 .

[14]  D. Brooker,et al.  The efficacy of Dementia Care Mapping as an audit tool: Report of a 3-year British NHS evaluation , 1998 .