Literature DB >> 23464923

Exploring the transitional process from receiving a diagnosis to living with motor neurone disease.

Kriten Mistry1, Jane Simpson.   

Abstract

Motor neurone disease (MND) is a rapidly progressing neurodegenerative condition that results in a marked reduction in life expectancy. Currently, little is known about the experiences of people after they have received this diagnosis and the effect of this on their sense of self and identity. In this study, interpretative phenomenological analysis was used to explore both the personal and lived experiences of people with MND. Seven people diagnosed with MND within the previous six months were recruited. The three themes constructed from the participants' accounts were 'Then they dropped the bomb shell'; Receiving a diagnosis of MND; 'Getting on with it'; Learning to live with MND; and 'A lot of normal life is lost'; Experiencing progressive loss. Participants described receiving a diagnosis as a devastating experience but most participants were able to accept their diagnosis and employ adaptive strategies to cope with increasing levels of functional decline. However, in spite of this, the participants experienced functional changes that affected their identity, social status and social relationships.

Entities:  

Mesh:

Year:  2013        PMID: 23464923     DOI: 10.1080/08870446.2013.770513

Source DB:  PubMed          Journal:  Psychol Health        ISSN: 0887-0446


  6 in total

1.  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

2.  An exploration of the experience of Huntington's disease in family dyads: an interpretative phenomenological analysis.

Authors:  Caroline Maxted; Jane Simpson; Stephen Weatherhead
Journal:  J Genet Couns       Date:  2013-11-10       Impact factor: 2.537

Review 3.  Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis.

Authors:  Andrew Soundy; Nicola Condon
Journal:  Front Psychol       Date:  2015-05-12

4.  Exploring and Addressing 'Concerns' for Significant Others to Extend the Understanding of Quality of Life With Amyotrophic Lateral Sclerosis: A Qualitative Study.

Authors:  Hikari Ando; Rosanna Cousins; Carolyn A Young
Journal:  J Cent Nerv Syst Dis       Date:  2019-07-08

5.  Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre.

Authors:  Esther Hobson; Wendy Baird; Mike Bradburn; Cindy Cooper; Susan Mawson; Ann Quinn; Pamela J Shaw; Theresa Walsh; Christopher J McDermott
Journal:  BMJ Open       Date:  2019-10-22       Impact factor: 2.692

6.  Sharing and Empathy in Digital Spaces: Qualitative Study of Online Health Forums for Breast Cancer and Motor Neuron Disease (Amyotrophic Lateral Sclerosis).

Authors:  Sarah Hargreaves; Peter A Bath; Suzanne Duffin; Julie Ellis
Journal:  J Med Internet Res       Date:  2018-06-14       Impact factor: 5.428

  6 in total

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