This study aimed to investigate and understand the experiences and feelings lived by people with an ICD. Qualitative study, semi-structured interviews were conducted with a sample of 16 patients, during the annual follow-up. A hermeneutical analysis of the interviews was carried out to identify the themes. Four main themes were classified: “My heart falls asleep,” highlighting a reduced awareness of the pathology and ICD installation; “But what is this thing. . .?” underlining the lack of information and fears related to the device and its functioning; “I cannot hug the microwave” which describes the changes brought about by the surgery; “And with this one I am alright for the rest of my life”, involving hopes and life expectations. This study highlighted the patients’ need for major support from health professionals while processing their new life conditions.
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