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ABSTRACT
The aim was to increase understanding of parents’ experiences of having a child with a cochlear implant (CI) and to explore how these related to children’s use of CI. Twelve parents of children, full-time users or limited users of CIs, participated in the study. Qualitative content analysis showed that the parents of children who used their CI differed from the parents with limited users in how they handled stressors. Support from health care professionals was seen as insufficient. Parents need to get involved in dynamic processes in which health care resources promote parental coping.
Acknowledgment
We gratefully thank all participating parents for taking part in this study.