Literature DB >> 27143577

Examining the Experiences of Fathers of Children with a Life-Limiting Illness.

David B Nicholas1, Laura Beaune2, Maru Barrera3,4, Jonathan Blumberg5, Mark Belletrutti6,7.   

Abstract

Families who have a child diagnosed with a life-limiting illness (LLI) face substantial challenges resulting from the complexity and devastating impact of the condition and potential closeness of death. The experiences of fathers of a child with LLI have been understudied; therefore, this study explored the stresses, experiences, and strategies of these fathers, including their perceptions about support needs. Based on grounded theory, in-depth semi-structured interviews were conducted with 18 fathers of children with LLI. Six fathers had experienced the death of their child. The overarching themes were stresses, means of coping, and perceived needs for support. Generally, fathers in this study struggled relative to discursive and internalized notions of fathers as providers and protectors for their children, combined with an inability to ease their child's vulnerability to LLI. Participants were engaged in the care of their child with LLI, but several felt marginalized by health care providers in care planning and staff/family communication. Some fathers recognized and valued their support network while others had few supports. Some described personal growth and desired to help other fathers. Practice implications and recommendations include renewed application of family-centered care, overcoming presumptions about fathers' roles, and recognizing the impact of LLI beyond physical health.

Entities:  

Keywords:  Bereavement; caregivers/caregiving; children/pediatrics; health care; palliative care

Mesh:

Year:  2016        PMID: 27143577     DOI: 10.1080/15524256.2016.1156601

Source DB:  PubMed          Journal:  J Soc Work End Life Palliat Care        ISSN: 1552-4264


  9 in total

1.  Parent-Child Communication and Adjustment Among Children With Advanced and Non-Advanced Cancer in the First Year Following Diagnosis or Relapse.

Authors:  Madelaine C Keim; Vicky Lehmann; Emily L Shultz; Adrien M Winning; Joseph R Rausch; Maru Barrera; Mary Jo Gilmer; Lexa K Murphy; Kathryn A Vannatta; Bruce E Compas; Cynthia A Gerhardt
Journal:  J Pediatr Psychol       Date:  2017-09-01

Review 2.  Parents as informal caregivers of children and adolescents with spinal muscular atrophy: a systematic review of quantitative and qualitative data on the psychosocial situation, caregiver burden, and family needs.

Authors:  Maja Brandt; Lene Johannsen; Laura Inhestern; Corinna Bergelt
Journal:  Orphanet J Rare Dis       Date:  2022-07-19       Impact factor: 4.303

3.  "You Never Exhale Fully Because You're Not Sure What's NEXT": Parents' Experiences of Stress Caring for Children With Chronic Conditions.

Authors:  Stephanie Smith; Mary Tallon; Carrie Clark; Lauren Jones; Evalotte Mörelius
Journal:  Front Pediatr       Date:  2022-06-27       Impact factor: 3.569

4.  The Association of Perceived Social Support with Anxiety over Time in Parents of Children with Serious Illnesses.

Authors:  Jackelyn Y Boyden; Douglas L Hill; Karen W Carroll; Wynne E Morrison; Victoria A Miller; Chris Feudtner
Journal:  J Palliat Med       Date:  2019-11-07       Impact factor: 2.947

5.  Consulting with a folk deity before making decisions: spiritual practices in parents facing end-of-life decisions for their child on life support with brain stem dysfunction.

Authors:  Shih-Chun Lin; Mei-Chih Huang
Journal:  Int J Qual Stud Health Well-being       Date:  2020-12

6.  The Many Roles of the Rock: A Qualitative Inquiry into the Roles and Responsibilities of Fathers of Children with Brain Tumors.

Authors:  Jacob E Robinson; David Huskey; Jonathan Schwartz; Meaghann S Weaver
Journal:  Children (Basel)       Date:  2019-10-11

7.  A meta-ethnographic study of fathers' experiences of caring for a child with a life-limiting illness.

Authors:  Gianina-Ioana Postavaru; Helen Swaby; Rabbi Swaby
Journal:  Palliat Med       Date:  2020-12-18       Impact factor: 4.762

8.  Grieving Experiences of Parents with Children in End-of-Life Care-A Qualitative Review Protocol.

Authors:  Maria Eduarda Correia; Tânia Melo; Joana Nobre
Journal:  Nurs Rep       Date:  2022-06-22

9.  Differing needs of mothers and fathers during their child's end-of-life care: secondary analysis of the "Paediatric end-of-life care needs" (PELICAN) study.

Authors:  Tanja Leemann; Eva Bergstraesser; Eva Cignacco; Karin Zimmermann
Journal:  BMC Palliat Care       Date:  2020-08-04       Impact factor: 3.234

  9 in total

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