Literature DB >> 26868176

A family matter--when a parent is diagnosed with multiple sclerosis. A qualitative study.

Katrin Boström1, Ylva Nilsagård2.   

Abstract

AIMS AND
OBJECTIVES: The aim was to explore and describe from a triple perspective--that of the ill parent, the healthy parent and the children--experienced issues that are important to acknowledge and act upon to make it easier for a child to cope when a parent is diagnosed with multiple sclerosis.
BACKGROUND: A chronic disease affects the whole family and has a substantial impact on the children. Traditionally, the focus is on the patient, and communication with other family members is not generally integrated into health care. Health care professionals need to be aware of a child's needs when a parent is diagnosed with multiple sclerosis.
DESIGN: A qualitative design using content analysis with an inductive approach was used.
METHODS: Nine focus group interviews were conducted with the ill parents, the healthy parents and the children separately.
RESULTS: Participants jointly indicated that family members need to be recognised, both initially and onwards in their everyday lives. Seven categories were defined: Prerequisites within the families, Initial reactions, Trying to adapt and manage, Developing strategies, Everyday life, Thoughts about the future and Support from health care providers. Together they constituted the theme that multiple sclerosis is a family matter. Both ill and healthy parents wished for support from health care professionals in addressing their children's needs.
CONCLUSIONS: Health care professionals need to pay attention to children as a parent's illness affects them. Not only the children would benefit, but so would their parents, as their worries for their children would be reduced. RELEVANCE TO CLINICAL PRACTICE: Staff can be advised to pay attention to the parenting role, how the parenting role and parent-child relationship may change as a result of a chronic disease. Parents may need reassurance and benefit from advice about how to talk to their children about their condition and its impact.
© 2016 The Authors. Journal of Clinical Nursing Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  adaptation; children; family; multiple sclerosis; parent; partner; support

Mesh:

Year:  2016        PMID: 26868176     DOI: 10.1111/jocn.13156

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  5 in total

1.  Understanding quality of life across different clinical subtypes of multiple sclerosis: a thematic analysis.

Authors:  Hikari Ando; Rosanna Cousins; Carolyn A Young
Journal:  Qual Life Res       Date:  2021-11-25       Impact factor: 4.147

2.  Mental health as perceived by Norwegian adolescents living with parental somatic illness: Living in an earthquake zone.

Authors:  Torill Eide; Anne Faugli; Elin Kufås; Nina Helen Mjøsund; Grethe Eilertsen
Journal:  Int J Qual Stud Health Well-being       Date:  2020-12

Review 3.  Young People's Response to Parental Neurological Disorder: A Structured Review.

Authors:  Lilian Hartman; Crispin Jenkinson; David Morley
Journal:  Adolesc Health Med Ther       Date:  2020-03-26

4.  Caregiver Involvement in MS: Duty or Disruption?

Authors:  Jürg Kesselring; Alexey Boyko; Alice Laroni; Trishna Bharadia; Pieter van Galen; Nektaria Alexandri
Journal:  Neurol Ther       Date:  2021-11-18

Review 5.  Intertwined like a double helix: A meta-synthesis of the qualitative literature examining the experiences of living with someone with multiple sclerosis.

Authors:  Anne Parkinson; Crystal Brunoro; Jack Leayr; Vanessa Fanning; Katrina Chisholm; Janet Drew; Jane Desborough; Christine Phillips
Journal:  Health Expect       Date:  2022-02-04       Impact factor: 3.318

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.