Literature DB >> 19669170

"Now we have to cope with the rest of our lives". Existential issues related to parenting a child surviving a brain tumour.

Ulla Forinder1, Annika Lindahl Norberg.   

Abstract

AIM: The aim of the paper was to explore the existential issues expressed by parents of children who had been treated for brain tumours.
BACKGROUND: A brain tumour in childhood is an event that triggers acute traumatic stress and it has long-term consequences for the child as well as for the parents. Due to advanced treatment techniques, more children survive brain tumours today. However, for most survivors a brain tumour is associated with sequelae and uncertainty about the future.
METHOD: Eleven parents of seven children successfully treated for brain tumours were interviewed in 2006. The semi-structured interviews were conducted by two licensed psychologists. The Inductive Thematic method was used to analyse the data.
FINDINGS: Consequences of a perceived threat, uncertainty and loss were described in terms of grief and sadness, loneliness, changes in the conditions for parenting, and changed views regarding identity and meaning. A traumatic experience is typically followed by an existential crisis, i.e. a process of restoring the person's assumptive world. As summarized by one parent: "Now we have to cope with the rest of our lives". The statement can be seen as a metaphor for the reconstruction of everyday life - a new picture including the child's disease and its sequelae, as well as the uncertainty about what the future might be like.
CONCLUSION: The findings underscore the importance of the social network, validating and supporting parents through this process. Moreover, in this social network the paediatric oncology and neurology care is a significant part.

Entities:  

Mesh:

Year:  2009        PMID: 19669170     DOI: 10.1007/s00520-009-0678-3

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  21 in total

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4.  The long-term psychosocial effects of cancer diagnosis and treatment on children and their families.

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5.  Pediatric brain tumor patients: their parents' perceptions of the hospital experience.

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6.  Experiences of parents of children surviving brain tumour: a happy ending and a rough beginning.

Authors:  A Lindahl Norberg; S Steneby
Journal:  Eur J Cancer Care (Engl)       Date:  2009-05-21       Impact factor: 2.520

Review 7.  Late neurocognitive sequelae in survivors of brain tumours in childhood.

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  3 in total

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2.  Patterns of family management for adolescent and young adult brain tumor survivors.

Authors:  Janet A Deatrick; Lamia P Barakat; George J Knafl; Wendy Hobbie; Sue Ogle; Jill P Ginsberg; Michael J Fisher; Thomas Hardie; Maureen Reilly; Elizabeth Broden; Jennifer Toth; Nicole SanGiacomo; Kathleen A Knafl
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Review 3.  Existential distress among caregivers of patients with brain tumors: a review of the literature.

Authors:  Allison J Applebaum; Maria Kryza-Lacombe; Justin Buthorn; Antonio DeRosa; Geoff Corner; Eli L Diamond
Journal:  Neurooncol Pract       Date:  2015-12-08
  3 in total

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