Literature DB >> 27539955

Living with uncertainty and hope: A qualitative study exploring parents' experiences of living with childhood multiple sclerosis.

Denise Hinton1, Susan Kirk1.   

Abstract

Background There is growing recognition that multiple sclerosis is a possible, albeit uncommon, diagnosis in childhood. However, very little is known about the experiences of families living with childhood multiple sclerosis and this is the first study to explore this in depth. Objective Our objective was to explore the experiences of parents of children with multiple sclerosis. Methods Qualitative in-depth interviews with 31 parents using a grounded theory approach were conducted. Parents were sampled and recruited via health service and voluntary sector organisations in the United Kingdom. Results Parents' accounts of life with childhood multiple sclerosis were dominated by feelings of uncertainty associated with four sources; diagnostic uncertainty, daily uncertainty, interaction uncertainty and future uncertainty. Parents attempted to manage these uncertainties using specific strategies, which could in turn create further uncertainties about their child's illness. However, over time, ongoing uncertainty appeared to give parents hope for their child's future with multiple sclerosis. Conclusion Illness-related uncertainties appear to play a role in generating hope among parents of a child with multiple sclerosis. However, this may lead parents to avoid sources of information and support that threatens their fragile optimism. Professionals need to be sensitive to the role hope plays in supporting parental coping with childhood multiple sclerosis.

Entities:  

Keywords:  Parents; children; chronic illness; family; multiple sclerosis

Mesh:

Year:  2016        PMID: 27539955     DOI: 10.1177/1742395316664959

Source DB:  PubMed          Journal:  Chronic Illn        ISSN: 1742-3953


  11 in total

1.  Uncertainty, hope, and coping efficacy among mothers of children with Duchenne/Becker muscular dystrophy.

Authors:  Megan Bell; Barbara B Biesecker; Joann Bodurtha; Holly L Peay
Journal:  Clin Genet       Date:  2019-04-03       Impact factor: 4.438

2.  Examining Uncertainty in Illness in Parents and Children With Chronic Kidney Disease and Systemic Lupus Erythematosus: A Mediational Model of Internalizing Symptoms and Health-Related Quality of Life.

Authors:  Jennifer L Petrongolo; Nataliya Zelikovsky; Rachel M Keegan; Susan L Furth; Andrea Knight
Journal:  J Clin Psychol Med Settings       Date:  2020-03

3.  Parent Experiences of Sanfilippo Syndrome Impact and Unmet Treatment Needs: A Qualitative Assessment.

Authors:  Katherine Ackerman Porter; Cara O'Neill; Elise Drake; Samantha Parker; Maria L Escolar; Stacey Montgomery; William Moon; Carolyn Worrall; Holly L Peay
Journal:  Neurol Ther       Date:  2020-12-02

Review 4.  Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions.

Authors:  Rebecca Maguire; Phil Maguire
Journal:  Curr Neurol Neurosci Rep       Date:  2020-05-22       Impact factor: 5.081

Review 5.  Needs and Experiences of Children and Adolescents with Pediatric Multiple Sclerosis and Their Caregivers: A Systematic Review.

Authors:  Shashank Ghai; Elisabeth Kasilingam; Roberta Lanzillo; Masa Malenica; Vincent van Pesch; Niamh Caitlin Burke; Antonio Carotenuto; Rebecca Maguire
Journal:  Children (Basel)       Date:  2021-05-25

Review 6.  A Scoping Review of Modifiable Risk Factors in Pediatric Onset Multiple Sclerosis: Building for the Future.

Authors:  Julie Pétrin; Max Fiander; Prenitha Mercy Ignatius Arokia Doss; E Ann Yeh
Journal:  Children (Basel)       Date:  2018-10-26

7.  Cancer patients' experiences with immune checkpoint modulators: A qualitative study.

Authors:  Kari Ala-Leppilampi; Natalie A Baker; Chris McKillop; Marcus O Butler; Lillian L Siu; Anna Spreafico; Albiruni R Abdul Razak; Anthony M Joshua; David Hogg; Philippe L Bedard; Natasha Leighl; Amit M Oza; Janet A Parsons; Aaron R Hansen
Journal:  Cancer Med       Date:  2020-03-02       Impact factor: 4.452

Review 8.  Paediatric Multiple Sclerosis: A Scoping Review of Patients' and Parents' Perspectives.

Authors:  Maria Luca; Nerea Ortega-Castro; Francesco Patti
Journal:  Children (Basel)       Date:  2021-12-25

Review 9.  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

10.  Parents' Expressions of Concerns and Hopes for the Future and Their Concomitant Assessments of Disability in Their Children.

Authors:  Niels Ove Illum; Mette Bonderup; Kim Oren Gradel
Journal:  Clin Med Insights Pediatr       Date:  2018-06-27
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