Literature DB >> 22149179

MS and me: exploring the impact of multiple sclerosis on perceptions of self.

Louise Mozo-Dutton1, Jane Simpson, Julia Boot.   

Abstract

PURPOSE: The aim of this qualitative study was to explore the impact of multiple sclerosis (MS) on perceptions of self as well as the emotional, social and practical implications of any self-reported changes.
METHOD: Twelve participants were interviewed and interpretative phenomenological analysis used to analyse the data. Participants were recruited from a MS hospital clinic in the north-west of England.
RESULTS: Four themes were identified although for reasons of space and novelty three were discussed, (i) 'my body didn't belong to me': the changing relationship to body, (ii) 'I miss the way I feel about myself': the changing relationship to self and (iii) 'let's just try and live with it': incorporating yet separating MS from self.
CONCLUSIONS: The onset of MS was seen to impact upon self yet impact did not necessarily equate with a loss of self but rather a changed self. Self-related changes did, however, carry the potential to impact negatively upon a person's mood and psychological functioning and consequently, clinicians are encouraged to consider issues relating to self as standard.

Entities:  

Mesh:

Year:  2011        PMID: 22149179     DOI: 10.3109/09638288.2011.638032

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  9 in total

1.  Understanding quality of life across different clinical subtypes of multiple sclerosis: a thematic analysis.

Authors:  Hikari Ando; Rosanna Cousins; Carolyn A Young
Journal:  Qual Life Res       Date:  2021-11-25       Impact factor: 4.147

2.  "Putting one foot in front of the other": a qualitative study of emotional experiences and help-seeking in women with multiple sclerosis.

Authors:  Joanna Blundell Jones; Sue Walsh; Claire Isaac
Journal:  J Clin Psychol Med Settings       Date:  2014-12

3.  Body Esteem Among Women with Multiple Sclerosis and its Relationship with Demographic, Clinical and Socio-Psychological Factors.

Authors:  M Wilski; T Tasiemski; A Dąbrowski
Journal:  Int J Behav Med       Date:  2016-06

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.  The impact of an online Facebook support group for people with multiple sclerosis on non-active users.

Authors:  Jacqui Steadman; Chrisma Pretorius
Journal:  Afr J Disabil       Date:  2014-11-21

6.  Cerebellar ataxia and intrathecal baclofen therapy: Focus on patients´ experiences.

Authors:  Shala Ghaderi Berntsson; Anne-Marie Landtblom; Gullvi Flensner
Journal:  PLoS One       Date:  2017-06-27       Impact factor: 3.240

7.  What Are the Participants' Perspectives of Taking Melatonin for the Treatment of Nocturia in Multiple Sclerosis? A Qualitative Study Embedded within a Double-Blind RCT.

Authors:  Rafiyah Khan; Alan Uren; Luke Canham; David Cottrell; Marcus J Drake; Nikki Cotterill
Journal:  Mult Scler Int       Date:  2018-10-18

Review 8.  'It struck at the heart of who I thought I was': A meta-synthesis of the qualitative literature examining the experiences of people with multiple sclerosis.

Authors:  Jane Desborough; Crystal Brunoro; Anne Parkinson; Katrina Chisholm; Mark Elisha; Janet Drew; Vanessa Fanning; Christian Lueck; Anne Bruestle; Matthew Cook; Hanna Suominen; Antonio Tricoli; Adam Henschke; Christine Phillips
Journal:  Health Expect       Date:  2020-06-24       Impact factor: 3.377

9.  Experiences of quality of life in people with Multiple Sclerosis who are in a wheelchair.

Authors:  Stine Torp Løkkeberg; Gunnar Thoresen
Journal:  Nurs Open       Date:  2021-05-30
  9 in total

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