Literature DB >> 16459890

The influence of social support on caregiver coping.

Norman Upton1, Val Reed.   

Abstract

Investigations into the act of proving care to a dementing family member typically approach the phenomenon from a stress/burden paradigm. Many studies have sought to highlight the relationship between of a range of dementia care factors (such as illness duration, patient symptoms/characteristics, service provision, etc.) and the experience of caregiver stress. Caregiving a spouse with dementing illness is complex and multidimensional (Gubrium, 1995) it is therefore not surprising that the vast majority of stressor-based approaches, though very revealing, have been largely equivocal in their findings. The relationship between the social support of family and friends and caregiver coping is no exception and therefore remains essentially unclear particularly in terms of its contribution in ameliorating stress (Thompson et al, 1993). Caregiver studies do however consistently highlight the pathogenic qualities of coping with an experience in which 'families are faced with often overwhelming and uncontrollable stress than can take a toll on their emotional health and well-being' (Zarit et al, 1998; Bourgeois et al, 1996). This article, emanating from a PhD study into caregiver coping (Upton, 2001), illuminates the study of caregiving from a different perspective. It highlights and describes how phenomenological exploration deepens our understanding of how and why spouse caregivers cope and uses the influence of social support as an exemplar of the value and need for such exploration both for its own sake and also to inform service providers. The results revealed a universal phenomenon of psycho-physical distancing by family and friends affecting all forty-six spouse caregivers included in this study. The implications of these finding are discussed along with what constituted social support for these carers. Other phenomenological insights are revealed, not least how the individual caregiver's relationship to time, space and their own identity shaped their caregiving experiences.

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Mesh:

Year:  2006        PMID: 16459890

Source DB:  PubMed          Journal:  Int J Psychiatr Nurs Res        ISSN: 0968-0624


  5 in total

1.  Expressive social support buffers the impact of care-related work interruptions on caregivers' depressive symptoms.

Authors:  Shannon Ang; Rahul Malhotra
Journal:  Aging Ment Health       Date:  2017-04-20       Impact factor: 3.658

2.  Caregivers had neighbourhood support but perceived it unsatisfactory and worsened: England Community Life Survey, 2012-2014.

Authors:  Ivy Shiue
Journal:  Environ Sci Pollut Res Int       Date:  2017-03-11       Impact factor: 4.223

3.  Being the Family Caregiver of a Patient With Dementia During the Coronavirus Disease 2019 Lockdown.

Authors:  Milena Zucca; Valeria Isella; Raffaele Di Lorenzo; Camillo Marra; Annachiara Cagnin; Chiara Cupidi; Laura Bonanni; Valentina Laganà; Elisa Rubino; Nicola Vanacore; Federica Agosta; Paolo Caffarra; Renato Sambati; Davide Quaranta; Valeria Guglielmi; Ildebrando M Appollonio; Giancarlo Logroscino; Massimo Filippi; Gioacchino Tedeschi; Carlo Ferrarese; Innocenzo Rainero; Amalia C Bruni
Journal:  Front Aging Neurosci       Date:  2021-04-20       Impact factor: 5.750

4.  Development of the caregivers attitude scale on home care of schizophrenics (CASHS).

Authors:  N Balasubramanian; T S Sathyanarayana Rao; Juliana Linnette D'Sa
Journal:  Indian J Psychiatry       Date:  2014-01       Impact factor: 1.759

5.  "When I hear my language, I travel back in time and I feel at home": Intersections of culture with social inclusion and exclusion of persons with dementia and their caregivers.

Authors:  Rossio Motta-Ochoa; Paola Bresba; Jason Da Silva Castanheira; Chelsey Lai Kwan; Shaindl Shaffer; Omega Julien; Meghan William; Stefanie Blain-Moraes
Journal:  Transcult Psychiatry       Date:  2021-05-06
  5 in total

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