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Experiences Following the Deaths of Disabled Foster Children

“We Don't Feel Like ‘Foster’ Parents”

Bibliographic Data

ID13629188
AuthorsAnn Fudge Schormans (0000-0002-7892-3599, University of Toronto, corresponding author)
Year2004
Volume49
Issue4
Pages347-369
Publication date2004-12-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueOMEGA - Journal of Death and Dying (JOURNAL)
Journal identifiersISSN: 0030-2228 • E-ISSN: 1541-3764
PublisherSAGE Publishing (PUBLISHER • US)
DOI10.2190/pmpx-5jww-7lab-c9le
OpenAlexW2068078096
LanguageEN
Citations received10
References cited17

Foster parents in the child welfare system occupy a unique position in our culture. While expected to parent and provide safe, loving, and normative family experiences to a child removed from her/his family of origin, they are, simultaneously, expected to remember that they are not the child's biological parent. Increasingly, foster parents are being asked to care for children with severe disabilities that sometimes precipitate an early death. How do foster parents experience the death of a foster child with disabilities in their care? Semi-structured interviews with bereaved foster parents revealed foster parents' self-identification as “parents” who shared “parent/child” relationships with foster children whom they considered to be part of their families. The foster parents' experience of the death of the foster child with a disability was reported comparable to the death of a birth child, however, their identification as legitimate grievers was often disenfranchised by others

Developmental psychology · Foster care · Foster parents · Identification (biology · Normative · Welfare · Child Welfare and Adoption · Grief, Bereavement, and Mental Health · Medicine · Migration, Health and Trauma · Nursing · Psychology

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Unique citing works10
Citations per year0,53
Citation span2007 - 2024 (18)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 10

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