A delicate equilibrium: living with Huntington's disease

Background: People with Huntington’s disease (HD) can be affected by motor, cognitive and behavioural symptoms. The length of the illness trajectory can result in patients receiving care at home for extended periods during which the contribution from family caregivers is invaluable. There has been l...

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Main Author: Wilson, Eleanor
Format: Thesis (University of Nottingham only)
Language:English
Published: 2013
Online Access:https://eprints.nottingham.ac.uk/13487/
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author Wilson, Eleanor
author_facet Wilson, Eleanor
author_sort Wilson, Eleanor
building Nottingham Research Data Repository
collection Online Access
description Background: People with Huntington’s disease (HD) can be affected by motor, cognitive and behavioural symptoms. The length of the illness trajectory can result in patients receiving care at home for extended periods during which the contribution from family caregivers is invaluable. There has been little research into patient or carer perspectives on needs or how these should be met, and how these correspond to professional viewpoints. Objectives: To gain an understanding of living with, caring for and working in the field of HD. Study design: A collective case study approach was used to gather data from the person with HD, their family carer and a nominated healthcare professional to build 15 cases involving 33 individuals and 115 interactions (68 interviews and 47 observations) over three years of study participation. Findings: Living with HD requires continued readjustment to maintain balance between increasing disability, diminishing cognition and living well at home. Patients and carers were challenged to cope with: the diagnosis; an impulse to secrecy and a duty to share knowledge; autonomy and decision making; the transformation of homes to hospitals; and a shift in the burden of care when the patient moved to a residential care home. Examination of services showed how multidisciplinary working, a keyworker approach, disease, person and service specific knowledge alongside continuity of staffing contribute to quality care. Conclusion: This is the first qualitative study of living with HD incorporating multiple perspectives over time. It explored the complexity of living with HD and the ways in which care can be provided in the community. The study identified a number of daily challenges for both family and professional carers when changes in capacity occur slowly over time. Holistic, multidisciplinary and flexible care is shown to be essential for those trying to balance the delicate equilibrium of living with HD. nb. The journal articles and book extracts in appendix A have not been included in the electronic version for copyright reasons.
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spelling nottingham-134872025-02-28T11:25:26Z https://eprints.nottingham.ac.uk/13487/ A delicate equilibrium: living with Huntington's disease Wilson, Eleanor Background: People with Huntington’s disease (HD) can be affected by motor, cognitive and behavioural symptoms. The length of the illness trajectory can result in patients receiving care at home for extended periods during which the contribution from family caregivers is invaluable. There has been little research into patient or carer perspectives on needs or how these should be met, and how these correspond to professional viewpoints. Objectives: To gain an understanding of living with, caring for and working in the field of HD. Study design: A collective case study approach was used to gather data from the person with HD, their family carer and a nominated healthcare professional to build 15 cases involving 33 individuals and 115 interactions (68 interviews and 47 observations) over three years of study participation. Findings: Living with HD requires continued readjustment to maintain balance between increasing disability, diminishing cognition and living well at home. Patients and carers were challenged to cope with: the diagnosis; an impulse to secrecy and a duty to share knowledge; autonomy and decision making; the transformation of homes to hospitals; and a shift in the burden of care when the patient moved to a residential care home. Examination of services showed how multidisciplinary working, a keyworker approach, disease, person and service specific knowledge alongside continuity of staffing contribute to quality care. Conclusion: This is the first qualitative study of living with HD incorporating multiple perspectives over time. It explored the complexity of living with HD and the ways in which care can be provided in the community. The study identified a number of daily challenges for both family and professional carers when changes in capacity occur slowly over time. Holistic, multidisciplinary and flexible care is shown to be essential for those trying to balance the delicate equilibrium of living with HD. nb. The journal articles and book extracts in appendix A have not been included in the electronic version for copyright reasons. 2013-12-11 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/13487/2/A_delicate_equlibrium_Living_with_Revised.pdf Wilson, Eleanor (2013) A delicate equilibrium: living with Huntington's disease. PhD thesis, University of Nottingham.
spellingShingle Wilson, Eleanor
A delicate equilibrium: living with Huntington's disease
title A delicate equilibrium: living with Huntington's disease
title_full A delicate equilibrium: living with Huntington's disease
title_fullStr A delicate equilibrium: living with Huntington's disease
title_full_unstemmed A delicate equilibrium: living with Huntington's disease
title_short A delicate equilibrium: living with Huntington's disease
title_sort delicate equilibrium: living with huntington's disease
url https://eprints.nottingham.ac.uk/13487/