Experiences of Volunteers Supporting Parents Following a Fatal Fetal Anomaly Diagnosis

  • Stacey Power
  • , Keelin O’Donoghue
  • , Sarah Meaney

Research output: Contribution to journalArticlepeer-review

Abstract

Ireland has had a reliance on voluntary groups to provide peer-to-peer bereavement support. The aim of this study was to explore volunteers’, within these voluntary groups, experiences of supporting parents following a fatal fetal anomaly diagnosis. Purposive sampling was used to recruit volunteers (n = 17) and face-to-face interviews undertaken. NVivo12 was utilized to assist in the thematic analysis of the data. Five themes; “motivation for altruistic acts,” “being challenged,” “value of education and training,” “supporting volunteers to support others,” and “it is not a sprint, it is a marathon” were identified. Volunteers felt comfortable in their peer-support role but found the lack of knowledge regarding newly implemented termination of pregnancy (TOP) services challenging. The importance of education/training was identified, emphasizing the need for collaboration with health care professionals and other voluntary organizations for support. The findings illustrate the need for collaborative working between health care professionals and volunteers to assist them in supporting bereaved parents.

Original languageEnglish
Pages (from-to)835-846
Number of pages12
JournalQualitative Health Research
Volume31
Issue number5
DOIs
Publication statusPublished - Apr 2021

Keywords

  • abortion
  • bereavement care
  • congenital abnormality
  • interpretive descriptive approach
  • Ireland
  • peer support
  • perinatal mortality
  • qualitative research
  • volunteers
  • women’s health

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