Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/25979
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dc.contributor.authorWatchman, Karenen_UK
dc.contributor.authorJanicki, Matthewen_UK
dc.contributor.authorUdell, Leslieen_UK
dc.contributor.authorHogan, Maryen_UK
dc.contributor.authorQuinn, Samen_UK
dc.contributor.authorBerankova, Annaen_UK
dc.date.accessioned2018-02-15T04:33:26Z-
dc.date.available2018-02-15T04:33:26Z-
dc.date.issued2019-06-01en_UK
dc.identifier.urihttp://hdl.handle.net/1893/25979-
dc.description.abstractThe International Summit on Intellectual Disability and Dementia held in Scotland in 2016 covered a range of issues related to dementia and intellectual disability, including the dearth of personal reflections of persons with intellectual disability affected by dementia. This paper reflects on this deficiency and explores some of the personal perspectives gleaned from the literature, from Summit attendees, and from the experiences of persons with intellectual disability recorded or scribed in advance of the two-day Summit meeting. Omission of the perspectives of persons with intellectual disability in both policy and practice limits understanding of the experience of dementia. It leads to an overreliance on proxy reporting; something considered by the Summit to be a backwards step in person-centred work. The Summit recognised that the perspectives of persons with intellectual disability must be considered whenever interventions and supports are discussed with planning required at an earlier stage for advance directives that guide medical treatment, and for advice or counselling around relationships, the continuity of social networks, and when securing dementia-friendly housing. Systemic recommendations included reinforcing the value of the involvement of persons with intellectual disability in (a) research alongside removing barriers to inclusion posed by institutional/ethics review boards, (b) planning groups that establish services and supports for dementia, and (c) peer support efforts that help adults with intellectual disability who are affected by dementia (either directly or indirectly). Practice recommendations included (a) valuing personal perspectives in decision-making, (b) enabling peer-to-peer support models, (c) supporting choice in community dwelling arrangements, and (d) wider availability of materials for persons with intellectual disability that would promote understanding of dementia.en_UK
dc.language.isoenen_UK
dc.publisherSAGEen_UK
dc.relationWatchman K, Janicki M, Udell L, Hogan M, Quinn S & Berankova A (2019) Consensus Statement of the International Summit on Intellectual Disability and Dementia on Valuing the Perspectives of Persons with Intellectual Disability. Journal of Intellectual Disabilities, 23 (2), pp. 266-280. https://doi.org/10.1177/1744629517751817en_UK
dc.rightsWatchman K, Janicki MP, Udell L, Hogan M, Quinn S, Berankova A, Consensus statement of the International Summit on Intellectual Disability and Dementia on valuing the perspectives of persons with intellectual disability, Journal of Intellectual Disabilities (23.2), pp. 266-280. Copyright © The Author(s) 2018. Reprinted by permission of SAGE Publications.en_UK
dc.subjectdementiaen_UK
dc.subjectDown syndromeen_UK
dc.subjectintellectual disabilityen_UK
dc.subjectpersonal perspectivesen_UK
dc.subjectself-advocacyen_UK
dc.titleConsensus Statement of the International Summit on Intellectual Disability and Dementia on Valuing the Perspectives of Persons with Intellectual Disabilityen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1177/1744629517751817en_UK
dc.identifier.pmid29343166en_UK
dc.citation.jtitleJournal of Intellectual Disabilitiesen_UK
dc.citation.issn1744-6309en_UK
dc.citation.issn1744-6295en_UK
dc.citation.volume23en_UK
dc.citation.issue2en_UK
dc.citation.spage266en_UK
dc.citation.epage280en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusAM - Accepted Manuscripten_UK
dc.author.emailkaren.watchman@stir.ac.uken_UK
dc.citation.date17/01/2018en_UK
dc.contributor.affiliationHealth Sciences Stirlingen_UK
dc.contributor.affiliationUniversity of Illinois at Chicagoen_UK
dc.contributor.affiliationWinnserv Incen_UK
dc.contributor.affiliationFamily Advocateen_UK
dc.contributor.affiliationUniversity of the West of Scotlanden_UK
dc.contributor.affiliationCharles University in Pragueen_UK
dc.identifier.isiWOS:000469388400010en_UK
dc.identifier.scopusid2-s2.0-85045914521en_UK
dc.identifier.wtid516677en_UK
dc.contributor.orcid0000-0003-0000-3589en_UK
dc.date.accepted2017-09-29en_UK
dcterms.dateAccepted2017-09-29en_UK
dc.date.filedepositdate2017-10-16en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionAMen_UK
local.rioxx.authorWatchman, Karen|0000-0003-0000-3589en_UK
local.rioxx.authorJanicki, Matthew|en_UK
local.rioxx.authorUdell, Leslie|en_UK
local.rioxx.authorHogan, Mary|en_UK
local.rioxx.authorQuinn, Sam|en_UK
local.rioxx.authorBerankova, Anna|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2018-01-17en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||2018-01-17en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/all-rights-reserved|2018-01-17|en_UK
local.rioxx.filenameRevised Perspectives of Persons with ID.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1744-6309en_UK
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles

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