Vida L Kennedy1, Mari Lloyd-Williams. 1. Academic Palliative and Supportive Care Studies Group, School of Population, University of Liverpool, Liverpool L69 3GB, UK.
Abstract
OBJECTIVE: When parents are diagnosed with cancer, children experience significant distress. There is little information regarding the nature of this distress and how children cope, particularly when a parent is diagnosed with advanced cancer. This study aimed to explore how children cope, and to identify areas where there may be barriers to children accessing support to enable them to cope. METHODS: Semi-structured interviews were conducted with ill parents with advanced cancer and well parents and/or any children above the age of 7. Interviews were recorded and transcribed fully, and analysed using a constructionist grounded theory approach. RESULTS: Twenty-eight family participants were interviewed. Four major themes emerged from the data including response to diagnosis, mechanisms of coping, life changes, and positive aspects. Children described being distressed by their parents diagnosis and having concerns related to their parents and their own health. Distraction and maintaining normality were described as the dominant strategies of coping for children, and increased responsibilities and decreased social activity were considered to be the most noticeable of life changes. Parents did not recognise the impact on children to the same degree as described by children and focused on limiting the impact by maintaining normality. Positive aspects described by children and parents included strengthening of relationships and learning to value family members and the important things in life. CONCLUSIONS: Open communication within the family may lead to more effective coping and a positive experience for children whose parents have been diagnosed with advanced cancer.
OBJECTIVE: When parents are diagnosed with cancer, children experience significant distress. There is little information regarding the nature of this distress and how children cope, particularly when a parent is diagnosed with advanced cancer. This study aimed to explore how children cope, and to identify areas where there may be barriers to children accessing support to enable them to cope. METHODS: Semi-structured interviews were conducted with ill parents with advanced cancer and well parents and/or any children above the age of 7. Interviews were recorded and transcribed fully, and analysed using a constructionist grounded theory approach. RESULTS: Twenty-eight family participants were interviewed. Four major themes emerged from the data including response to diagnosis, mechanisms of coping, life changes, and positive aspects. Children described being distressed by their parents diagnosis and having concerns related to their parents and their own health. Distraction and maintaining normality were described as the dominant strategies of coping for children, and increased responsibilities and decreased social activity were considered to be the most noticeable of life changes. Parents did not recognise the impact on children to the same degree as described by children and focused on limiting the impact by maintaining normality. Positive aspects described by children and parents included strengthening of relationships and learning to value family members and the important things in life. CONCLUSIONS: Open communication within the family may lead to more effective coping and a positive experience for children whose parents have been diagnosed with advanced cancer.
Authors: Maximiliane Burgmann; Kerstin Hermelink; Alex Farr; Friederike van Meegen; Annika Heiduschk; Jutta Engel; Thomas Kolben; Tom Degenhardt; Nina Ditsch; Sven Mahner; Nadia Harbeck; Rachel Würstlein Journal: Breast Care (Basel) Date: 2018-02-01 Impact factor: 2.860
Authors: Eliza M Park; Devon K Check; Mi-Kyung Song; Katherine E Reeder-Hayes; Laura C Hanson; Justin M Yopp; Donald L Rosenstein; Deborah K Mayer Journal: Palliat Med Date: 2016-08-06 Impact factor: 4.762
Authors: Franziska Kühne; Thomas Krattenmacher; Corinna Bergelt; Johanna C Ernst; Hans-Henning Flechtner; Daniel Führer; Wolfgang Herzog; Kai V Klitzing; Georg Romer; Birgit Möller Journal: BMC Palliat Care Date: 2012-10-30 Impact factor: 3.234