Striving for balance between caring and restraint: young adults' experiences with parental multiple sclerosis
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Abstract
Suggested Citation
DOI: 10.1111/jocn.13587
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References listed on IDEAS
- Katrin Boström & Ylva Nilsagård, 2016. "A family matter – when a parent is diagnosed with multiple sclerosis. A qualitative study," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(7-8), pages 1053-1061, April.
- Torild Mauseth & Esther Hjälmhult, 2016. "Adolescents' experiences on coping with parental multiple sclerosis: a grounded theory study," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(5-6), pages 856-865, March.
Citations
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Cited by:
- Camille Bou, 2023. "Factors Associated with the Quality-of-Life of Young Unpaid Carers: A Systematic Review of the Evidence from 2003 to 2019," IJERPH, MDPI, vol. 20(6), pages 1-15, March.
- Hinke M. van der Werf & Marie Louise A. Luttik & Alice de Boer & Petrie F. Roodbol & Wolter Paans, 2022. "Growing up with a Chronically Ill Family Member—The Impact on and Support Needs of Young Adult Carers: A Scoping Review," IJERPH, MDPI, vol. 19(2), pages 1-16, January.
- Bou, Camille, 2023. "Factors associated with the quality-of-life of young unpaid carers: a systematic review of the evidence from 2003 to 2019," LSE Research Online Documents on Economics 118357, London School of Economics and Political Science, LSE Library.
- Giulia Landi & Kenneth I. Pakenham & Silvana Grandi & Eliana Tossani, 2022. "Young Adult Carers during the Pandemic: The Effects of Parental Illness and Other Ill Family Members on COVID-19-Related and General Mental Health Outcomes," IJERPH, MDPI, vol. 19(6), pages 1-18, March.
- Russell, Helen & Smyth, Emer, 2024. "Caregiving among Young Adults in Ireland," Research Series, Economic and Social Research Institute (ESRI), number RS168.
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