The burden of the carergivers of copd patients. A qualitative research.

Introduction: COPD is one of the primary causes of death for thousands of adults dying annually. The typical model for those living with COPD is the implacable decline of the pulmonary function as well as the attenuation of their quality of life. Many members of the family take responsibility for the patient’s provision, without being fully aware of the burdens connected with this role. Aim: This purpose of this qualitative research is to engage the caregivers in a dialogue concerning their experiences and living with a COPD patient; to seek reason and meaning in the provision; and, to manage through the process to detect hint potentially threatening their lives directly or indirectly. Materials and Method: A total of 46 caregivers of COPD patients participated in this qualitative research. Data were collected through structured interviews. The interviews were conducted both in the General University Hospital of Larissa and in