Literature DB >> 12823429

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

Hennie R Boeije1, Mia S H Duijnstee, Maria H F Grypdonck.   

Abstract

As is expressed in the term 'caregiving career', caregiving is a dynamic phenomenon. The present study addresses the total care phase in which spouses give direct and ongoing personal care to their partners with multiple sclerosis (MS). The dyadic nature of caregiving is stressed by examining the roles which both spouses play in establishing a commitment that results in the continuation of caregiving. For this purpose, 17 couples facing MS were selected in the Netherlands and Belgium. Ten females and seven males were disabled, and all were living with partners who provided a full range of care. Both partners were interviewed separately about their motivation to give care, dependency on help, the continuation of caregiving and their relationship. The analysis consisted of fragmenting and connecting the data, and involved close reading and constant comparison. The present findings support those previous studies, i.e. that continuation of caregiving is the result of an interchange between the partners. The commitment that is established can be expressed in terms of inevitability, shared misfortune, reciprocity and the desire to prevent admission to a nursing home. Three aspects appear to contribute to the creation of commitment and the ensuing continuation of caregiving: namely, marital loyalty, and the arbitrariness of the disease and its serious nature. For community care, it is important to consider the negotiations between partners and the impact of caregiving on their relationship.

Entities:  

Mesh:

Year:  2003        PMID: 12823429     DOI: 10.1046/j.1365-2524.2003.00422.x

Source DB:  PubMed          Journal:  Health Soc Care Community        ISSN: 0966-0410


  7 in total

1.  Ready or not: planning for health declines in couples with advanced multiple sclerosis.

Authors:  Hannah Chen; Barbara Habermann
Journal:  J Neurosci Nurs       Date:  2013-02       Impact factor: 1.230

Review 2.  [Coping with multiple sclerosis in partnerships: a systematic review of the literature].

Authors:  A-K Busch; R Spirig; W Schnepp
Journal:  Nervenarzt       Date:  2014-06       Impact factor: 1.214

3.  Avoidance as a strategy of (not) coping: qualitative interviews with carers of Huntington's Disease patients.

Authors:  Alison Lowit; Edwin R van Teijlingen
Journal:  BMC Fam Pract       Date:  2005-09-14       Impact factor: 2.497

Review 4.  The Relational Impact of Multiple Sclerosis: An Integrative Review of the Literature Using a Cognitive Analytic Framework.

Authors:  Joanna Blundell Jones; Sue Walsh; Claire Isaac
Journal:  J Clin Psychol Med Settings       Date:  2017-12

5.  [Motives and perceptions of family care for dependent elderly].

Authors:  Antonio Frías-Osuna; Sara Moreno-Cámara; Lourdes Moral-Fernández; Pedro Ángel Palomino-Moral; Catalina López-Martínez; Rafael Del-Pino-Casado
Journal:  Aten Primaria       Date:  2018-11-10       Impact factor: 1.137

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

Authors:  Nic Hughes; Louise Locock; Sue Ziebland
Journal:  Soc Sci Med       Date:  2013-08-06       Impact factor: 4.634

7.  Getting back or giving back: understanding caregiver motivations and willingness to provide informal care.

Authors:  Mikołaj Zarzycki; Val Morrison
Journal:  Health Psychol Behav Med       Date:  2021-07-13
  7 in total

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