• J Palliat Med · Aug 2016

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

    • Brenda Bentley and Moira O'Connor.
    • 1 School of Health Professions, Murdoch University , Murdoch, Australia .
    • J Palliat Med. 2016 Aug 1; 19 (8): 857-62.

    BackgroundPeople 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.AimThis 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.DesignSemistructured interviews were conducted with 12 bereaved family carers of people who died from MND in WA. Thematic analysis was used to identify common themes.ResultsThe themes identified can be summarized into three main areas: accessing support, accessing information, and feeling prepared.ConclusionsThe findings indicate that increased access to specialist palliative care services by people with MND is needed to improve EOL experiences.

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