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Striving for balance between caring and restraint: young adults' experiences with parental multiple sclerosis

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  • Julie Y Moberg
  • Dorte Larsen
  • Anne Brødsgaard

Abstract

Aims and objectives To explore and describe how young adults between 18–25 years of age experienced growing up with a parent with multiple sclerosis and how these experiences continue to influence their daily lives. Background Chronic parental illness is occurring in about 10% of families worldwide, but little is known about how the children experience growing up with a parent with multiple sclerosis during their childhood and into young adulthood. Design We chose a qualitative design using a phenomenological approach based on Giorgi. Methods Exploratory and open‐ended interviews with 14 young adults were conducted. Results The essence of the phenomenon of having a parent with multiple sclerosis was synthesized into ‘Striving for balance between caring and restraint’ from two themes ‘caring’ and ‘restraint’ and eight subthemes. Participants’ experiences of caring for parents with multiple sclerosis continued influencing their other close relationships, in which they tended to assume responsibility while concealing some of their feelings and desires. Most participants showed restraint among parents with and without multiple sclerosis, friends and partners. Conclusion It seems that one of the greatest challenges of having a parent with multiple sclerosis is achieving a balance between caring for others and asserting one's own desires. Relevance to clinical practice Healthcare professionals can support the family by encouraging family members to participate in consultations and to assist the parents in providing information about multiple sclerosis and its symptoms to the children. Parents might need assistance in applying for help with domestic chores or referrals to support groups for their children or other family members.

Suggested Citation

  • Julie Y Moberg & Dorte Larsen & Anne Brødsgaard, 2017. "Striving for balance between caring and restraint: young adults' experiences with parental multiple sclerosis," Journal of Clinical Nursing, John Wiley & Sons, vol. 26(9-10), pages 1363-1374, May.
  • Handle: RePEc:wly:jocnur:v:26:y:2017:i:9-10:p:1363-1374
    DOI: 10.1111/jocn.13587
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    References listed on IDEAS

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    1. 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.
    2. 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.
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    Cited by:

    1. 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.
    2. 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.
    3. 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.
    4. 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.

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