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Interpreting end-of-life experiences of the person with motor neurone disease

Published online by Cambridge University Press:  25 June 2021

Denise Andrea Harris*
Affiliation:
Faculty of Health, Psychology & Social Care/Nursing, Manchester Metropolitan University, Manchester, UK
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Abstract

Type
Letter to the Editor
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

Dear Sir/Madam,

Motor neurone disease (MND) is a progressive neurodegenerative disease with no known cure. At the time of diagnosis, a person has already experienced the degenerative nature of MND and the subsequent losses and uncertainty of life with the disease (Harris, Reference Harris2015; Harris et al., Reference Harris, Thomas and Thomas2018b).

Loss and uncertainty are recognized as existential concerns for people who are diagnosed with a terminal illness, such as cancer (Henoch and Danielson, Reference Henoch and Danielson2009). Breitbart (Reference Breitbart2017, 509) raises awareness that people facing death need support to explore their existential guilt, as a way to accepting a life that has already been lived in order to face death with “peace and equanimity.” It is important that we address the existential concerns of the terminally ill if we are to prevent people experiencing life in crisis and considering suicide or hastening death (LeMay and Wilson, Reference LeMay and Wilson2008). Saracino et al.'s (Reference Saracino, Rosenfeld and Breitbart2019) review acknowledges several best practices relating to psycho-oncology at end of life. However, in relation to MND care, there are still gaps in thinking that need to be addressed.

MND care should be provided through a multidisciplinary team (MDT) approach that is person-centered, focusing on the physical, emotional, social, and spiritual needs of the person (Foley, Reference Foley2011). Those MDT professionals who are more adept at addressing the existential concerns of people with MND are psychologists or palliative care professionals (Hogden et al., Reference Hogden, Foley and Henderson2017). It is known that psychologists are underutilized in MND care (Harris et al., Reference Harris, Jack and Wibberley2018a) and that people with MND are not usually referred to the palliative care specialist until the last weeks of their life (Flemming et al., Reference Flemming, Turner and Bolsher2020). This is too late for those who are suffering from life in crisis.

The person with MND's experience of their end of life may be vastly different from the way the provider of care experiences it, and the provider of care must be mindful of this. I propose a temporal model of care as a way of thinking about person-centered care through a temporal lens. Central to this model are three aspects of temporality — lived-through past, experienced present, and anticipated future.

The use of this temporal model of care will support professionals to focus their conversation on what is important for the person. This may be their lived-through past, or their experienced present, or their anticipated future. A person who has been diagnosed with MND, or any other terminal illness, will, through this model, be encouraged to direct the focus of conversation. MND care is complex, but the complexity can be reduced if those who provide MND care interpret the person's end-of-life experiences (Harris et al., Reference Harris, Jack and Wibberley2021).

Conflict of interest

The author declares no conflict of interest.

References

REFERENCES

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