This qualitative study explores informal caregivers’ experiences of supporting persons with dementia’s everyday life coping. In the future, there will be fewer health personnel, increased dementia prevalence and limited nursing home availability. Accordingly, close relatives may be compelled to assume greater care responsibilities. Knowledge concerning persons with dementia’s everyday coping from the perspective of informal caregivers remains insufficient, despite these people’s importance for those with dementia. This investigation analyses informal caregivers’ perceived challenges and pleasures in providing care, how home health care affects everyday life coping and the factors that are most important to informal caregivers in supporting care receivers.

这项定性研究探讨了非正式护理人员为痴呆症患者的日常生活提供支持的经验。将来，医护人员将减少，痴呆症患病率将增加，疗养院的可用性将受到限制。因此，近亲可能被迫承担更大的护理责任。从非正式照料者的角度来看，尽管痴呆症患者对痴呆症患者具有重要意义，但对他们的日常应对知识仍然不够。这项调查分析了非正式护理人员在提供护理方面所面临的挑战和乐趣，家庭医疗保健如何影响日常生活应对以及对非正式护理人员在支持护理接受者方面最重要的因素。