Abstract
Families of dying children are profoundly impacted by numerous interactions with health-care providers before, during, and after their child’s death. However, there is a dearth of research on these families’ direct, qualitative experiences with health-care providers. This study presents findings from interviews with 18 family members, predominantly parents, regarding their experiences with health-care providers during a child’s terminal illness, from diagnosis to death. The importance of compassion emerged as a salient theme, manifested in myriad ways, and connected to participants’ perception of caregiver presence in multiple domains. Families were likewise negatively affected by a wide variety of situations and behaviors that represented individual or institutional abandonment or nonpresence, and thus compounded the experience of loss. Specifics and implications for practice are explored.
Original language | English (US) |
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Pages (from-to) | 404-420 |
Number of pages | 17 |
Journal | Omega (United States) |
Volume | 78 |
Issue number | 4 |
DOIs | |
State | Published - Mar 1 2019 |
Keywords
- bereaved parents
- bereavement
- cancer
- pediatric palliative care
- trauma
ASJC Scopus subject areas
- Health(social science)
- Critical Care and Intensive Care Medicine
- Life-span and Life-course Studies