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dc.contributor.authorTolhurst, Edward*
dc.contributor.authorCarey, Malcolm*
dc.contributor.authorWeicht, Bernhard*
dc.contributor.authorKingston, Paul*
dc.date.accessioned2018-05-24T15:24:42Z
dc.date.available2018-05-24T15:24:42Z
dc.date.issued2018-05-21
dc.identifier.citationTolhurst, E., Carey, M., Weicht, B., & Kingston, P. (2018). Is living well with dementia a credible aspiration for spousal carers? Health Sociology Review, 28(1), 54-68.
dc.identifier.issn1446-1242
dc.identifier.doi10.1080/14461242.2018.1475249
dc.identifier.urihttp://hdl.handle.net/10034/621144
dc.descriptionThis is an Accepted Manuscript of an article published by Taylor & Francis in Health Sociology Review on 21-5-18, available online: https://doi.org/10.1080/14461242.2018.1475249
dc.description.abstractIn England there has been substantial policy development and an academic drive to promote the goal of ‘living well’ for people with dementia and their family members. This article critically evaluates the feasibility of this intention, with reference to the experience of those caring for people with the condition. Qualitative data are utilised from a study which explored how couples negotiate relationships and care. The focus of this paper is the perspectives of spousal carers and the challenges they encounter within their caring role. Views were obtained via semi-structured joint interviews where the carer participated alongside the person with dementia. The extent to which living well with dementia is a credible aspiration for carers is examined via three themes: identity subsumed under care responsibilities; the couple as an isolated family unit; and barriers to professional support. The findings highlight that experience of caring is highly complex and fraught with multiple practical, emotional and moral pressures. It is asserted that research into dementia and care relationships must avoid a zero sum situation, prompted by living well discourses, where attempts to bolster the position of people with dementia compound the marginalisation and stigmatisation of informal carers.
dc.language.isoenen
dc.publisherTaylor & Francisen
dc.relation.urlhttps://www.tandfonline.com/doi/full/10.1080/14461242.2018.1475249en
dc.rights.urihttp://creativecommons.org/licenses/by-nd/4.0/en
dc.subjectCareen
dc.subjectCouplehooden
dc.subjectDementiaen
dc.subjectIntergenerational relationshipsen
dc.subjectSpousal relationshipsen
dc.titleIs living well with dementia a credible aspiration for spousal carers?en
dc.typeArticleen
dc.contributor.departmentStafford University; University of Chester; University of Innsbruck
dc.identifier.journalHealth Sociology Review
dc.date.accepted2018-05-03
or.grant.openaccessYesen
rioxxterms.funderUnfundeden
rioxxterms.identifier.projectUnfundeden
rioxxterms.versionAMen
rioxxterms.versionofrecordhttps://doi.org/10.1080/14461242.2018.1475249
rioxxterms.licenseref.startdate2019-05-21
html.description.abstractIn England there has been substantial policy development and an academic drive to promote the goal of ‘living well’ for people with dementia and their family members. This article critically evaluates the feasibility of this intention, with reference to the experience of those caring for people with the condition. Qualitative data are utilised from a study which explored how couples negotiate relationships and care. The focus of this paper is the perspectives of spousal carers and the challenges they encounter within their caring role. Views were obtained via semi-structured joint interviews where the carer participated alongside the person with dementia. The extent to which living well with dementia is a credible aspiration for carers is examined via three themes: identity subsumed under care responsibilities; the couple as an isolated family unit; and barriers to professional support. The findings highlight that experience of caring is highly complex and fraught with multiple practical, emotional and moral pressures. It is asserted that research into dementia and care relationships must avoid a zero sum situation, prompted by living well discourses, where attempts to bolster the position of people with dementia compound the marginalisation and stigmatisation of informal carers.
rioxxterms.publicationdatehttp://doi.org/10.1080/14461242.2018.1475249


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