Parents Who Have Lost a Child to Cancer: What Do They Really Need?
- 1 Department of Psychology, Laboratory of Psychopathology and Health Process, University of Paris Descartes, Boulogne Billancourt, France
- 2 Psycho-Oncology Department, Institut Curie, Paris, France
- 3 Medical Oncology Department Institut Curie, Paris, France
- 4 Pediatric Oncology Department, Institut Curie, Paris, France
- 5 Laboratory of Psychopathology and Neuropsychology, University Paris 8, Saint-Denis, France
Abstract
In a sample of parents who lost a child to cancer, we investigated their needs before and after their child’s death and how these needs were fulfilled. We met parents of AYA (adolescents and young adults) between 15 and 25 years old, who died in Curie Institute between 2000 and 2003. Twenty-one families agreed to participate in this study between October 2005 and April 2006. When a family agreed to participate, a semi-structured interview was held in the psycho-oncology unit of the Curie Institute. This interview was audiotaped and then retranscribed for analysis. Data were subjected to the Grounded theory method, a systematic and standardized method of semantic data analysis. Three prominent themes emerged from our thematic data analysis: first, the importance of psychological care during the terminal phase of the child’s disease and after the child’s death, reported by 95% of parents; second, the need to be listened to and to be understood by the medical team (97% of parents); third, the need for information from the medical team. A big discrepancy was observed between psychological support expectations and the proportion of parents who actually consulted or participated in bereavement groups. Our study clearly demonstrates that parents who lose a child through cancer have particular needs and therefore deserve special attention.
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