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Avoidance as a strategy of (not) coping: qualitative interviews with carers of Huntington's Disease patients.
Lowit A, van Teijlingen ER.
BMC Fam Pract. 2005 Sep 14;6:38.PMID: 16162290 [PubMed - indexed for MEDLINE]Related articlesFree article
Huntington's disease: seldom seen--seldom heard?
McGarva K.
Health Bull (Edinb). 2001 Sep;59(5):306-8.PMID: 12664744 [PubMed - indexed for MEDLINE]Related articles
The emotional experiences of family carers in Huntington disease.
Williams JK, Skirton H, Paulsen JS, Tripp-Reimer T, Jarmon L, McGonigal Kenney M, Birrer E, Hennig BL, Honeyford J.
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Young people's experiences of growing up in a family affected by Huntington's disease.
Forrest Keenan K, Miedzybrodzka Z, van Teijlingen E, McKee L, Simpson SA.
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Caring as worrying: the experience of spousal carers.
Cheung J, Hocking P.
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Caring for a person in advanced illness and suffering from breathlessness at home: threats and resources.
Gysels MH, Higginson IJ.
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Caring for the carers: quality of life in Huntington's disease.
Aubeeluck A.
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Companions through cancer: the care given by informal carers in cancer contexts.
Thomas C, Morris SM, Harman JC.
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Exploring supportive care for individuals affected by Huntington disease and their family caregivers in a community setting.
Soltysiak B, Gardiner P, Skirton H.
J Clin Nurs. 2008 Apr;17(7B):226-34.PMID: 18578798 [PubMed - indexed for MEDLINE]Related articles
Living with Huntington's disease: need for supportive care.
Dawson S, Kristjanson LJ, Toye CM, Flett P.
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Parents and partners: lay carers' perceptions of their role in the treatment and care of adults with cystic fibrosis.
Lowton K.
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Huntington's disease. Part 3: family aspects of HD.
Aubeeluck A, Moskowitz CB.
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Formal support of stroke survivors and their informal carers in the community: a cohort study.
Simon C, Kumar S, Kendrick T.
Health Soc Care Community. 2008 Dec;16(6):582-92. Epub 2008 Mar 27.PMID: 18371168 [PubMed - indexed for MEDLINE]Related articles
A theory to guide families and carers of people who are at risk of suicide.
Sun FK, Long A.
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Huntington's disease--falling through the net.
Shakespeare J, Anderson J.
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Caregiving at the end of life: perspectives from spousal caregivers and care recipients.
Jo S, Brazil K, Lohfeld L, Willison K.
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Informal caring in late life: a qualitative study of the experiences of older carers.
McGarry J, Arthur A.
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Home-based palliative care in Sydney, Australia: the carer's perspective on the provision of informal care.
Zapart S, Kenny P, Hall J, Servis B, Wiley S.
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Caring for a child with Juvenile Huntington's Disease: helpful and unhelpful support.
Brewer HM, Smith JA, Eatough V, Stanley CA, Glendinning NW, Quarrell OW.
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Caregiver coping in dementing illness--implications for short-term respite care.
Upton N, Reed V.
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