Literature DB >> 24237139

Caregiver roles in families affected by Huntington's disease: a qualitative interview study.

Merete Røthing1, Kirsti Malterud, Jan C Frich.   

Abstract

AIM: The objective of this study was to explore family caregivers' experiences with the impact of Huntington's disease (HD) on the family structure and roles in the family.
METHODOLOGY: We interviewed 15 family caregivers in families affected by HD, based on a semi-structured interview guide. The participants were recruited through hospital departments and a lay organisation for HD in Norway. Data from the interviews were analysed with systematic text condensation.
RESULTS: Huntington's disease could have a substantial impact on the family system, the shape of roles among family members and the hierarchical order between spouses, partners, and parents and children. The relationship between spouses and partners changed during the course of the disease. A reciprocal relationship was difficult to maintain, as the role as carer overshadowed other roles. Children of an affected parent could compensate for impairments by taking on adult responsibilities, and in some families, a child had the role as main caregiver. The increasing need for care could cause conflicts between the role as family member and family caregiver. The burden of care within the family could fragment and isolate the family.
CONCLUSIONS: Huntington's disease has a major impact on family systems. Caregiver roles are shaped by impairments in the affected family member and corresponding dynamic adoption and change in roles within the family. Making assessments of the family structure and roles, professionals may understand more about how to care for and support individuals in their role as family members and caregivers in different stages of the disease and family life cycle.
© 2013 The Authors. Scandinavian Journal of Caring Sciences published by John Wiley & Sons Ltd on behalf of Nordic College of Caring Science.

Entities:  

Keywords:  Huntington's disease; caregiver role; chronic disease; family caregiver; family dynamics

Mesh:

Year:  2013        PMID: 24237139     DOI: 10.1111/scs.12098

Source DB:  PubMed          Journal:  Scand J Caring Sci        ISSN: 0283-9318


  8 in total

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2.  Perceived Effects of Neuropsychiatric Symptoms on Functional Status in Early-stage Huntington Disease.

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4.  Exploring the Reliability and Validity of the Huntington's Disease Quality of Life Battery for Carers (HDQoL-C) within A Polish Population.

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5.  Experiencing the care of a family member with Crohn's disease: a qualitative study.

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6.  Health Care Delivery Practices in Huntington's Disease Specialty Clinics: An International Survey.

Authors:  Jan C Frich; Daniela Rae; Richard Roxburgh; Zofia H Miedzybrodzka; Mary Edmondson; Erika Bjorklund Pope; LaVonne Goodman; Monica S Haddad; Joe Giuliano; Eugene C Nelson; Mark Guttman; Martha Nance
Journal:  J Huntingtons Dis       Date:  2016-06-27

7.  Families Affected by Huntington's Disease Report Difficulties in Communication, Emotional Involvement, and Problem Solving.

Authors:  Celine M H Jona; Izelle Labuschagne; Emily-Clare Mercieca; Fiona Fisher; Cathy Gluyas; Julie C Stout; Sophie C Andrews
Journal:  J Huntingtons Dis       Date:  2017

8.  Another Perspective on Huntington's Disease: Disease Burden in Family Members and Pre-Manifest HD When Compared to Genotype-Negative Participants from ENROLL-HD.

Authors:  Jannis Achenbach; Carsten Saft
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  8 in total

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