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The personal experience of parenting a child with Juvenile Huntington's Disease: perceptions across Europe
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience, Neurology.
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2013 (English)In: European Journal of Human Genetics, ISSN 1018-4813, E-ISSN 1476-5438, Vol. 21, no 10, 1042-1048 p.Article in journal (Refereed) Published
Abstract [en]

The study reported here presents a detailed description of what it is like to parent a child with juvenile Huntington's disease in families across four European countries. Its primary aim was to develop and extend findings from a previous UK study. The study recruited parents from four European countries: Holland, Italy, Poland and Sweden,. A secondary aim was to see the extent to which the findings from the UK study were repeated across Europe and the degree of commonality or divergence across the different countries. Fourteen parents who were the primary caregiver took part in a semistructured interview. These were analyzed using an established qualitative methodology, interpretative phenomenological analysis. Five analytic themes were derived from the analysis: the early signs of something wrong; parental understanding of juvenile Huntington's disease; living with the disease; other people's knowledge and understanding; and need for support. These are discussed in light of the considerable convergence between the experiences of families in the United Kingdom and elsewhere in Europe.

Place, publisher, year, edition, pages
2013. Vol. 21, no 10, 1042-1048 p.
Keyword [en]
Juvenile Huntington's disease, parent, qualitative
National Category
Medical and Health Sciences
URN: urn:nbn:se:uu:diva-210196DOI: 10.1038/ejhg.2013.15ISI: 000324727200009OAI: oai:DiVA.org:uu-210196DiVA: diva2:661520
Available from: 2013-11-04 Created: 2013-11-04 Last updated: 2013-11-04Bibliographically approved

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