Literature DB >> 24214466

An exploration of the experience of Huntington's disease in family dyads: an interpretative phenomenological analysis.

Caroline Maxted1, Jane Simpson, Stephen Weatherhead.   

Abstract

Huntington's disease (HD) is a hereditary, late onset, neurodegenerative disorder. Children of affected parents have a 50 % chance of inheriting HD. Research into the psychological consequences of HD for the family has focussed on individual family members, but little is known about the ways in which its impact is jointly experienced by members of these families. This is particularly important due to the hereditary nature of HD. To address this, the current study examined the experiences of dyads within affected families. Seven parent/adult child dyads were interviewed jointly about their experiences and relationships with their family and each other and interpretative phenomenological analysis was used to analyse the resultant data. Identified themes were: "A spectre hanging over us": HD as a presence within the family, "Us against the world": Protection, knowledge and control, and "That could be me in 50 years": Cyclical changes in identity and role. These findings are examined in relation to previous research and indicate the need for an increased understanding of the needs of HD families. Clinical implications and suggestions for further research are discussed.

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Year:  2013        PMID: 24214466     DOI: 10.1007/s10897-013-9666-3

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  30 in total

1.  Perceptions of cause and control in people with Parkinson's disease.

Authors:  Fiona J R Eccles; Craig Murray; Jane Simpson
Journal:  Disabil Rehabil       Date:  2010-11-22       Impact factor: 3.033

2.  The impact of Juvenile Huntington's Disease on the family: the case of a rare childhood condition.

Authors:  Helen M Brewer; Virginia Eatough; Jonathan A Smith; Cath A Stanley; Neil W Glendinning; Oliver W J Quarrell
Journal:  J Health Psychol       Date:  2008-01

3.  A qualitative analysis of mindfulness-based cognitive therapy (MBCT) in Parkinson's disease.

Authors:  Lee Fitzpatrick; Jane Simpson; Alistair Smith
Journal:  Psychol Psychother       Date:  2009-10-19       Impact factor: 3.915

4.  Behavior in Huntington's disease: dissociating cognition-based and mood-based changes.

Authors:  Jennifer C Thompson; Julie S Snowden; David Craufurd; David Neary
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2002       Impact factor: 2.198

5.  Huntington disease as a dual diagnosis disorder: data from the National Research Roster for Huntington disease patients and families.

Authors:  Jason C Ehret; Patricia S Day; Ryan Wiegand; Joanne Wojcieszek; R Andrew Chambers
Journal:  Drug Alcohol Depend       Date:  2006-08-22       Impact factor: 4.492

6.  Attachment in families with Huntington's disease. A paradigm in clinical genetics.

Authors:  Lucienne Van der Meer; Reinier Timman; Wim Trijsburg; Marleen Duisterhof; Ruud Erdman; Thérèse Van Elderen; Aad Tibben
Journal:  Patient Educ Couns       Date:  2006-01-20

7.  Subtle changes among presymptomatic carriers of the Huntington's disease gene.

Authors:  S C Kirkwood; E Siemers; M E Hodes; P M Conneally; J C Christian; T Foroud
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-12       Impact factor: 10.154

8.  A hereditary disorder in the family and the family life cycle: Huntington disease as a paradigm.

Authors:  A Christine Brouwer-Dudokdewit; Anke Savenije; Moniek W Zoeteweij; Anneke Maat-Kievit; Aad Tibben
Journal:  Fam Process       Date:  2002

9.  Chronic illness and the life cycle: a conceptual framework.

Authors:  J S Rolland
Journal:  Fam Process       Date:  1987-06

10.  Avoidance as a strategy of (not) coping: qualitative interviews with carers of Huntington's Disease patients.

Authors:  Alison Lowit; Edwin R van Teijlingen
Journal:  BMC Fam Pract       Date:  2005-09-14       Impact factor: 2.497

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  7 in total

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

Authors:  Jessie S Gibson; Bethany A Rhoten; Sheila H Ridner; Daniel O Claassen
Journal:  West J Nurs Res       Date:  2021-02-05       Impact factor: 1.774

2.  What is the best way to keep walking and moving around for individuals with Machado-Joseph disease? A scoping review through the lens of Aboriginal families with Machado-Joseph disease in the Top End of Australia.

Authors:  Jennifer J Carr; Joyce Lalara; Gayangwa Lalara; Moira Smith; Jennifer Quaill; Alan R Clough; Anne Lowell; Ruth N Barker
Journal:  BMJ Open       Date:  2019-09-30       Impact factor: 2.692

3.  Using a Clinical Formulation to Understand Psychological Distress in People Affected by Huntington's Disease: A Descriptive, Evidence-Based Model.

Authors:  Maria Dale; Ashleigh Wood; Nicolò Zarotti; Fiona Eccles; Sarah Gunn; Reza Kiani; Amanda Mobley; Noelle Robertson; Jane Simpson
Journal:  J Pers Med       Date:  2022-07-27

4.  A qualitative study utilizing Interpretative phenomenological analysis to explore disclosure in adolescents with turner syndrome.

Authors:  Mhairi Nisbet; Rory O'Connor; Avril Mason; Elizabeth Hunter
Journal:  Br J Health Psychol       Date:  2022-02-14

5.  Irritability in Huntington's Disease: Factor Analysis of Snaith's Irritability Scale.

Authors:  John Maltby; Maria Dale; Mandy Underwood; Jane Simpson
Journal:  Mov Disord Clin Pract       Date:  2016-10-01

6.  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

7.  More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington's Disease.

Authors:  Nicolò Zarotti; Maria Dale; Fiona J R Eccles; Jane Simpson
Journal:  J Pers Med       Date:  2022-01-07
  7 in total

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