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

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Exploring the transitional process from receiving a diagnosis to living with motor neurone disease. / Mistry, Kit; Simpson, Jane.
In: Psychology and Health, Vol. 28, No. 8, 2013, p. 939-953.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Mistry K, Simpson J. Exploring the transitional process from receiving a diagnosis to living with motor neurone disease. Psychology and Health. 2013;28(8):939-953. doi: 10.1080/08870446.2013.770513

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Mistry, Kit ; Simpson, Jane. / Exploring the transitional process from receiving a diagnosis to living with motor neurone disease. In: Psychology and Health. 2013 ; Vol. 28, No. 8. pp. 939-953.

Bibtex

@article{35f4e388d6d640c2838f36b5219f412d,
title = "Exploring the transitional process from receiving a diagnosis to living with motor neurone disease",
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{\textquoteright} accounts were {\textquoteleft}Then they dropped the bomb shell{\textquoteright}; Receiving a diagnosis of MND; {\textquoteleft}Getting on with it{\textquoteright}; Learning to live with MND; and {\textquoteleft}A lot of normal life is lost{\textquoteright}; 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.",
keywords = "Activities of Daily Living, Adaptation, Psychological, Aged, Female, Humans, Male, Middle Aged, Motor Neuron Disease, Qualitative Research, Self Concept",
author = "Kit Mistry and Jane Simpson",
year = "2013",
doi = "10.1080/08870446.2013.770513",
language = "English",
volume = "28",
pages = "939--953",
journal = "Psychology and Health",
issn = "0887-0446",
publisher = "Routledge",
number = "8",

}

RIS

TY - JOUR

T1 - Exploring the transitional process from receiving a diagnosis to living with motor neurone disease

AU - Mistry, Kit

AU - Simpson, Jane

PY - 2013

Y1 - 2013

N2 - 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.

AB - 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.

KW - Activities of Daily Living

KW - Adaptation, Psychological

KW - Aged

KW - Female

KW - Humans

KW - Male

KW - Middle Aged

KW - Motor Neuron Disease

KW - Qualitative Research

KW - Self Concept

U2 - 10.1080/08870446.2013.770513

DO - 10.1080/08870446.2013.770513

M3 - Journal article

C2 - 23464923

VL - 28

SP - 939

EP - 953

JO - Psychology and Health

JF - Psychology and Health

SN - 0887-0446

IS - 8

ER -