The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives

Background: People with motor neuron disease (MND) face barriers when accessing palliative care. There is a lack of research about how these barriers affect the end-of-life (EOL) and death experiences of people with MND. Aim: This study examined the perceptions of EOL experiences of family carers of...

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Main Authors: Bentley, B., O'Connor, Moira
Format: Journal Article
Published: Mary Ann Liebert, Inc Publishers 2016
Online Access:http://hdl.handle.net/20.500.11937/32995
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author Bentley, B.
O'Connor, Moira
author_facet Bentley, B.
O'Connor, Moira
author_sort Bentley, B.
building Curtin Institutional Repository
collection Online Access
description Background: People with motor neuron disease (MND) face barriers when accessing palliative care. There is a lack of research about how these barriers affect the end-of-life (EOL) and death experiences of people with MND. Aim: This study examined the perceptions of EOL experiences of family carers of people with MND in Western Australia (WA) to identify unmet needs and gaps in EOL support for people with MND and their family carers. Design: Semistructured interviews were conducted with 12 bereaved family carers of people who died from MND in WA. Thematic analysis was used to identify common themes. Results: The themes identified can be summarized into three main areas: accessing support, accessing information, and feeling prepared. Conclusions: The findings indicate that increased access to specialist palliative care services by people with MND is needed to improve EOL experiences.
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spelling curtin-20.500.11937-329952017-09-13T15:27:13Z The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives Bentley, B. O'Connor, Moira Background: People with motor neuron disease (MND) face barriers when accessing palliative care. There is a lack of research about how these barriers affect the end-of-life (EOL) and death experiences of people with MND. Aim: This study examined the perceptions of EOL experiences of family carers of people with MND in Western Australia (WA) to identify unmet needs and gaps in EOL support for people with MND and their family carers. Design: Semistructured interviews were conducted with 12 bereaved family carers of people who died from MND in WA. Thematic analysis was used to identify common themes. Results: The themes identified can be summarized into three main areas: accessing support, accessing information, and feeling prepared. Conclusions: The findings indicate that increased access to specialist palliative care services by people with MND is needed to improve EOL experiences. 2016 Journal Article http://hdl.handle.net/20.500.11937/32995 10.1089/jpm.2015.0538 Mary Ann Liebert, Inc Publishers restricted
spellingShingle Bentley, B.
O'Connor, Moira
The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
title The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
title_full The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
title_fullStr The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
title_full_unstemmed The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
title_short The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
title_sort end-of-life experiences of people with motor neuron disease: family carers' perspectives
url http://hdl.handle.net/20.500.11937/32995