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I can do that on my own!” On the relevance of subjective factors to the use of formal support, from the perspective of people with dementia

Bibliographic Data

ID15216994
AuthorsKristin Illiger (0000-0001-9815-2341, Section Technology and Health for Humans, Jade University of Applied Sciences Wilhelmshaven Oldenburg Elsfleth, corresponding author), Ulla Walter (0000-0002-0709-2206, Institute of Epidemiology, Social Medicine and Health System Research, Hanover Medical School), Frauke Koppelin (0000-0002-1827-9279, Section Technology and Health for Humans, Jade University of Applied Sciences Wilhelmshaven Oldenburg Elsfleth)
Year2021
Volume42
Issue11
Pages1298-1320
Publication date2021-03-01
Open AccessNo
TypeARTICLE
VenueHealth Care For Women International (JOURNAL)
Journal identifiersISSN: 0739-9332 • E-ISSN: 1096-4665
PublisherTaylor & Francis (PUBLISHER • GB)
DOI10.1080/07399332.2021.1876064
PMID33646088
OpenAlexW3134971851
LanguageEN
References cited44

Our aim was to reach a better insight of the disposition of people living alone with dementia toward the use of care and support services. In biographical narrative interviews, women and men with dementia communicated to us their opinions, needs, and subjectively perceived level of resources regarding their everyday life and care. Both individual and gender-specific differences concerning the use of formal support become evident in their narrations. We offer indications for a future healthcare practice that is specific to dementia. To fully exploit the potential of participatory research, study designs specific to dementia should be developed further

Citizen journalism · Dementia · Disease · Exploit · Narrative · Perspective (graphical · Political science · Relevance (law · Computer Science · Dementia and Cognitive Impairment Research · Geriatric Care and Nursing Homes · Intergenerational Family Dynamics and Caregiving · Medicine · Psychology · Gerontology

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