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Fulfilling a sense of duty

How Men and Women Giving Care to Spouses With Multiple Sclerosis Interpret This Role

Bibliographic Data

ID2171968
AuthorsHennie R Boeije, Hennie Boeije (0000-0002-7540-2114), Anneke Van Doorne-Huiskes, Anneke Van Doorne‐huiske
Year2003
Volume6
Issue3
Pages223-244
Publication date2003-12-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueCommunity Work & Family (JOURNAL)
Journal identifiersISSN: 1366-8803 • E-ISSN: 1469-3615
PublisherInforma UK Limited (PUBLISHER • GB)
DOI10.1080/1366880032000143438
OpenAlexW2111354854
LanguageEN
Citations received9
References cited3

This qualitative study examines how spouses experience caregiving when predominantly motivated by a sense of duty and addresses whether any differences between female and male caregivers can be detected. For our purpose semi-structured interviews were conducted with eight male and five female caregivers providing total care to their spouses who are disabled as a result of multiple sclerosis (MS). The analysis consisted of fragmenting and connecting the data and involved close reading and constant comparison. Participants involved in this study maintain caregiving despite the unfavourable changes they have noticed in their relationships. They interpret caregiving as something they just have to do. Males and females develop different perspectives on caregiving, which are illustrated by two exemplary case stories that can be summarized respectively in the phrase ‘You have to be satisfied with it’, and as ‘I have to become harder and less self-sacrificing’. Explanations for these outcomes are sought in differences in moral orientations between women and men and in gender differences regarding their feelings of duty and rights. The results shed light on previous findings that female caregivers report more stress than male caregivers and as such pertain on the discussion on home health care

Developmental psychology · Duty · Feeling · Phrase · Qualitative research · Reading (process · Ethics and Legal Issues in Pediatric Healthcare · Ethics in medical practice · Medicine · Patient Dignity and Privacy · Psychology · Clinical Psychology · Social Psychology

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  • A systematic review of relationship sacrifices from 2002 to 2021

    Open Access•M A Curran, Valerie J Young et al.•Personal Relationships•2023

  • Men Doing “Women's Work

    Open Access•R Russell•The Journal of Men s Studies•2007

  • Continuation of caregiving among partners who give total care to spouses with multiple sclerosis

    Open Access•Hennie R Boeije, Hennie Boeije et al.•Health & Social Care in the…•2003

  • Multiple sclerosis caregiving

    Open Access•Roshanth Rajachandrakumar, Marcia Finlayson•Health & Social Care in the…•2021

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    Open Access•Victoria Team, Milica Markovic et al.•Health & Social Care in the…•2007

  • Eldercare in the Transnational Setting

    Open Access•Iftekhar Amin, Stan Ingman•Journal of Cross-Cultural…•2014

  • Personal identity and the role of 'carer' among relatives and friends of people with multiple sclerosis

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  • Learning From Strangers

    Robert S Weiss•Learning From Strangers•1995

  • Qualitative Researching

    Jennifer Mason•Qualitative Researching•2018

  • Encountering the downward phase

    Open Access•Hennie R Boeije, Hennie Boeije et al.•Social Science & Medicine•2002

Unique citing works9
Citations per year0,39
Citation span2003 - 2026 (24)
Citation velocitycurrent
Highly citedNo
Citation typesNeutral: 9

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