Multiple sclerosis : living the reality and experiences of hope

This thesis is divided into three parts: a meta-synthesis of qualitative research, an empirical report and appendices. Part one is a descriptive meta-synthesis reviewing the contribution of phenomenologically informed qualitative literature regarding the lived experience of Multiple Sclerosis (MS)....

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Main Author: Blamires, Charity
Published: University of Hull 2013
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613478
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spelling ndltd-bl.uk-oai-ethos.bl.uk-6134782015-12-03T03:18:49ZMultiple sclerosis : living the reality and experiences of hopeBlamires, Charity2013This thesis is divided into three parts: a meta-synthesis of qualitative research, an empirical report and appendices. Part one is a descriptive meta-synthesis reviewing the contribution of phenomenologically informed qualitative literature regarding the lived experience of Multiple Sclerosis (MS). The meta-synthesis aimed to provide insights for healthcare professionals working in person centred MS services, in addition to reviewing literature relating to the empirical paper. Individuals living with MS have diverse healthcare needs and person centred care offers a holistic approach to meeting these needs. Six broad themes regarding the lived experience of MS were identified following synthesis of findings from seven qualitative studies. Deficits in person centred care are highlighted and implications for future service provision are discussed. Part two is an empirical study investigating a deficit in person centred care highlighted in the meta-synthesis: the concept of hope. The study examines the subjective experience of hope by exploring what generates, diminishes, or maintains hope for individuals living with Relapsing-remitting MS (RRMS) who confront relapses and remission of MS symptoms over time. Six individuals were interviewed and interpretative phenomenological analysis (IPA) was used to identify themes from their narrative accounts of hope. The study considers the importance of family systems and relationships in the experience of hope in RRMS, in addition to exploring illness experiences which result in losing hope. Clinical implications are discussed including the role of hope-fostering interventions for individuals living with RRMS adopted from the Recovery Model currently operating in mental health services. Part three consists of appendices relating to the research, including a reflective statement discussing the process of research from conception to results.616.89Clinical psychologyUniversity of Hullhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613478http://hydra.hull.ac.uk/resources/hull:8019Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 616.89
Clinical psychology
spellingShingle 616.89
Clinical psychology
Blamires, Charity
Multiple sclerosis : living the reality and experiences of hope
description This thesis is divided into three parts: a meta-synthesis of qualitative research, an empirical report and appendices. Part one is a descriptive meta-synthesis reviewing the contribution of phenomenologically informed qualitative literature regarding the lived experience of Multiple Sclerosis (MS). The meta-synthesis aimed to provide insights for healthcare professionals working in person centred MS services, in addition to reviewing literature relating to the empirical paper. Individuals living with MS have diverse healthcare needs and person centred care offers a holistic approach to meeting these needs. Six broad themes regarding the lived experience of MS were identified following synthesis of findings from seven qualitative studies. Deficits in person centred care are highlighted and implications for future service provision are discussed. Part two is an empirical study investigating a deficit in person centred care highlighted in the meta-synthesis: the concept of hope. The study examines the subjective experience of hope by exploring what generates, diminishes, or maintains hope for individuals living with Relapsing-remitting MS (RRMS) who confront relapses and remission of MS symptoms over time. Six individuals were interviewed and interpretative phenomenological analysis (IPA) was used to identify themes from their narrative accounts of hope. The study considers the importance of family systems and relationships in the experience of hope in RRMS, in addition to exploring illness experiences which result in losing hope. Clinical implications are discussed including the role of hope-fostering interventions for individuals living with RRMS adopted from the Recovery Model currently operating in mental health services. Part three consists of appendices relating to the research, including a reflective statement discussing the process of research from conception to results.
author Blamires, Charity
author_facet Blamires, Charity
author_sort Blamires, Charity
title Multiple sclerosis : living the reality and experiences of hope
title_short Multiple sclerosis : living the reality and experiences of hope
title_full Multiple sclerosis : living the reality and experiences of hope
title_fullStr Multiple sclerosis : living the reality and experiences of hope
title_full_unstemmed Multiple sclerosis : living the reality and experiences of hope
title_sort multiple sclerosis : living the reality and experiences of hope
publisher University of Hull
publishDate 2013
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613478
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