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Daughters and sons as caregivers for their demented and non-demented elderly parents. A part of a population-based study carried out in Sweden

The study focuses on adult children (n = 81) having the main responsibility for parents with dementia (study group). They were compared with children (n = 102) of nondemented parents (reference group). The children were interviewed about burden experienced. The interviews also secured information ab...

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Published in:Scandinavian journal of public health 1997-12, Vol.25 (4), p.289-295
Main Authors: Jansson, Wallis, Grafström, Margareta, Winblad, Bengt
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Language:English
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container_title Scandinavian journal of public health
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creator Jansson, Wallis
Grafström, Margareta
Winblad, Bengt
description The study focuses on adult children (n = 81) having the main responsibility for parents with dementia (study group). They were compared with children (n = 102) of nondemented parents (reference group). The children were interviewed about burden experienced. The interviews also secured information about the children's co-operation with the informal and formal network and their willingness to remain as caregivers during the progression of the disease or ageing process. The results showed that the daughters reported feeling more affection in their caregiving role than the sons. About one third of the participants in the study could not get relief from someone else. Eighty-nine per cent of the children in the study group and 76% of the children in the reference group were not willing to care for their parents in the family home during the progression of the disease, even if they were employed as caregivers.
doi_str_mv 10.1177/140349489702500412
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A part of a population-based study carried out in Sweden</title><title>Scandinavian journal of public health</title><addtitle>Scand J Soc Med</addtitle><description>The study focuses on adult children (n = 81) having the main responsibility for parents with dementia (study group). They were compared with children (n = 102) of nondemented parents (reference group). The children were interviewed about burden experienced. The interviews also secured information about the children's co-operation with the informal and formal network and their willingness to remain as caregivers during the progression of the disease or ageing process. The results showed that the daughters reported feeling more affection in their caregiving role than the sons. About one third of the participants in the study could not get relief from someone else. 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Hygiene</subject><subject>Public health. 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Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Social consequences</topic><topic>Social Support</topic><topic>Specific populations (family, woman, child, elderly...)</topic><topic>Sweden</topic><topic>Sweden - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jansson, Wallis</creatorcontrib><creatorcontrib>Grafström, Margareta</creatorcontrib><creatorcontrib>Winblad, Bengt</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Scandinavian journal of public health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jansson, Wallis</au><au>Grafström, Margareta</au><au>Winblad, Bengt</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Daughters and sons as caregivers for their demented and non-demented elderly parents. 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About one third of the participants in the study could not get relief from someone else. Eighty-nine per cent of the children in the study group and 76% of the children in the reference group were not willing to care for their parents in the family home during the progression of the disease, even if they were employed as caregivers.</abstract><cop>London, England</cop><pub>Scandinavian University Press</pub><pmid>9460143</pmid><doi>10.1177/140349489702500412</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0300-8037
ispartof Scandinavian journal of public health, 1997-12, Vol.25 (4), p.289-295
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language eng
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source Applied Social Sciences Index & Abstracts (ASSIA); JSTOR Archival Journals
subjects Adult
Adult children
Aged
Aged, 80 and over
Biological and medical sciences
Caregivers - psychology
Caregivers - statistics & numerical data
Carers
Dementia
Dementia - epidemiology
Dementia - therapy
Elderly people
Family Relations
Female
Homes for the Aged
Humans
Male
Medical sciences
Medicin och hälsovetenskap
Middle Aged
Nursing Homes
Prevention and actions
Public health. Hygiene
Public health. Hygiene-occupational medicine
Social consequences
Social Support
Specific populations (family, woman, child, elderly...)
Sweden
Sweden - epidemiology
title Daughters and sons as caregivers for their demented and non-demented elderly parents. A part of a population-based study carried out in Sweden
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