Literature DB >> 23336121

Experiences of living with motor neurone disease: a review of qualitative research.

Dikaios Sakellariou1, Gail Boniface, Paul Brown.   

Abstract

PURPOSE: This review sought to answer the question "what is known about people's experiences of living with MND?".
METHODS: The review followed the guidelines of the Centre of Reviews and Dissemination. Twenty articles met the inclusion criteria and their results were analysed thematically. Data were managed and coded using the software package NVIVO and the analysis was performed in two stages, with the first stage aiming to develop descriptive themes offering an overview of the included data. During the second stage, analytical themes were developed with the explicit aim to answer the review question.
RESULTS: The themes that emerged point to the following: (a) people with motor neurone disease (MND) develop experiential knowledge that helps them to live with the disease and (b) while people with MND believe they do not have any control over the disease, they try to have control over their lives through active choices, e.g. how and when to use adaptive equipment.
CONCLUSIONS: This review highlights the decision-making and knowledge generating processes used by people with MND. Further research is required to explore these processes and their implications for the care of people with MND. IMPLICATIONS FOR REHABILITATION: Decision-making process by MND patients regarding their care is complex and takes into account the social elements of the disease as well as the medical. Exploring the practical knowledge that patients develop can offer insights on appropriate care for MND patients.

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Mesh:

Year:  2013        PMID: 23336121     DOI: 10.3109/09638288.2012.753118

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


  4 in total

1.  How Narrative Journalistic Stories Can Communicate the Individual's Challenges of Daily Living with Amyotrophic Lateral Sclerosis.

Authors:  Jørgen Jeppesen; Jes Rahbek; Ole Gredal; Helle Ploug Hansen
Journal:  Patient       Date:  2015-02       Impact factor: 3.883

2.  Emotional distress and well-being among people with motor neurone disease (MND) and their family caregivers: a qualitative interview study.

Authors:  Cathryn Pinto; Adam W A Geraghty; Lucy Yardley; Laura Dennison
Journal:  BMJ Open       Date:  2021-08-17       Impact factor: 3.006

3.  Lung volume recruitment improves volitional airway clearance in amyotrophic lateral sclerosis.

Authors:  Stuart Cleary; John E Misiaszek; Sonya Wheeler; Sanjay Kalra; Shelagh K Genuis; Wendy S Johnston
Journal:  Muscle Nerve       Date:  2021-09-28       Impact factor: 3.852

4.  The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review.

Authors:  Kate Flemming; Victoria Turner; Samantha Bolsher; Bill Hulme; Elizabeth McHugh; Ian Watt
Journal:  Palliat Med       Date:  2020-04-14       Impact factor: 4.762

  4 in total

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