Literature DB >> 15124770

Caregivers of people with multiple sclerosis: experiences of support.

L P McKeown1, A P Porter-Armstrong, G D Baxter.   

Abstract

The aim of this phenomenological study was to gain an understanding of the experiences of a group of caregivers of people with multiple sclerosis (MS). Sixteen caregivers from Northern Ireland and the Republic of Ireland participated in focus group interviews. The theme of support, either sought or received, emerged as a major aspect of the experiences described. Caregivers' feelings about, and experiences of, support appeared to change over time. Four common phases that caregivers experienced in relation to support were identified as: 'rejecting', 'resisting, 'seeking' and 'accepting' support. This paper will present and discuss these four phases. The study findings highlight the complexity of issues surrounding a caregiver's decision to seek and accept support. It is hoped that the phases identified within this study are useful in depicting how caregivers of people with MS may progress through stages in their desire for, and acceptance of support. Findings from this study are useful to healthcare professionals who work with people with MS and their caregivers by increasing awareness that a caregiver's attitude toward and acceptance of support changes over time.

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Mesh:

Year:  2004        PMID: 15124770     DOI: 10.1191/1352458504ms1008oa

Source DB:  PubMed          Journal:  Mult Scler        ISSN: 1352-4585            Impact factor:   6.312


  11 in total

1.  Factors affecting employment among informal caregivers assisting people with multiple sclerosis.

Authors:  Robert J Buchanan; Chunfeng Huang; Zhida Zheng
Journal:  Int J MS Care       Date:  2013

2.  Informal caregivers assisting people with multiple sclerosis: factors associated with the strength of the caregiver/care recipient relationship.

Authors:  Robert J Buchanan; Chunfeng Huang
Journal:  Int J MS Care       Date:  2011

3.  The need for mental health care among informal caregivers assisting people with multiple sclerosis.

Authors:  Robert J Buchanan; Chunfeng Huang
Journal:  Int J MS Care       Date:  2013

4.  Caregiver burden in multiple sclerosis: the impact of neuropsychiatric symptoms.

Authors:  Nanna Figved; Kjell-Morten Myhr; Jan-Petter Larsen; Dag Aarsland
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-01-19       Impact factor: 10.154

5.  Longitudinal predictors of attitudes toward aging among women with multiple sclerosis.

Authors:  Tracie Harrison; Shelley Blozis; Alexa Stuifbergen
Journal:  Psychol Aging       Date:  2008-12

6.  Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditions.

Authors:  Michele Peters; Crispin Jenkinson; Helen Doll; E Diane Playford; Ray Fitzpatrick
Journal:  Health Qual Life Outcomes       Date:  2013-06-25       Impact factor: 3.186

7.  Patterns of Objective and Subjective Burden of Informal Caregivers in Multiple Sclerosis.

Authors:  E Bayen; C Papeix; P Pradat-Diehl; C Lubetzki; M E Joël
Journal:  Behav Neurol       Date:  2015-05-20       Impact factor: 3.342

8.  'You are just left to get on with it': qualitative study of patient and carer experiences of the transition to secondary progressive multiple sclerosis.

Authors:  F Davies; A Edwards; K Brain; M Edwards; R Jones; R Wallbank; N P Robertson; F Wood
Journal:  BMJ Open       Date:  2015-07-22       Impact factor: 2.692

9.  Is There an Association Between Social Support and Pain Among Individuals Living With Multiple Sclerosis?

Authors:  Khrisha B Alphonsus; Carl D'Arcy
Journal:  J Evid Based Integr Med       Date:  2021 Jan-Dec

10.  Anorectal dysfunction in multiple sclerosis: a systematic review.

Authors:  Sanober Nusrat; Elsie Gulick; David Levinthal; Klaus Bielefeldt
Journal:  ISRN Neurol       Date:  2012-07-29
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