Carers’ experiences of the transition of people with dementia into residential aged care: a narrative analysis

Author:

Wright Faye1,Breheny Mary2,Gibson Rosemary1

Affiliation:

1. Massey University, New Zealand

2. Victoria University of Wellington, New Zealand

Abstract

This study represents the experiences of informal carers of people with dementia concerning periods of transition into formal care. Retrospective interviews with 18 carers identified the key narratives: ‘This is why I had to’, ‘They said I need to’ and ‘It was a last resort’. These indicate a sense of carers’ responsibility in decision making and the undesirable assumptions around the move. However, the narrative of ‘I made the right decision’ was common after transition. Findings represent the nuanced carer experience around transitions, providing insight into the experiences of families living with dementia and informing future care planning.

Publisher

Bristol University Press

Subject

Public Health, Environmental and Occupational Health,Health Policy,Sociology and Political Science,Health (social science)

Reference49 articles.

1. Factors associated with caregiver distress among home care clients in New Zealand: evidence based on data from interRAI Home Care Assessment;Abey-Nesbit, R.,2022

2. Achieving a Dementia Friendly New Zealand: Alzheimers NZ Strategy 2015–2025,2015

3. Recruitment of individuals with dementia and their carers for social research: lessons learned from nine studies;Beattie, E.,2018

4. Examining trust in health professionals among family caregivers of nursing home residents with advanced dementia;Boogaard, J.A.,2017

5. Likelihood of residential aged care use in later life: a simple approach to estimation with international comparison;Broad, J.B.,2015

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1. Editorial;International Journal of Care and Caring;2024-09-02

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