Developments in technology, extension of life expectancy, decrease in birth rates, developments in health services, early diagnosis and treatment of diseases lead to an increase in the elderly population and the diseases seen in old age. One of these diseases is Alzheimer's disease, which is one of the most common types of Dementia. The disease is progressive, there is no cure, and as the disease progresses, the patient's addiction rate increases. This disease does not only affect the patient, but also the caregiver, the patient's family members, relatives, the environment and the entire society. One of the people most affected by the disease is undoubtedly the person or people who care for the patient. All areas of life of caregivers are negatively affected by the disease, and the care burden increases as the disease progresses. In this context, the aim of the research is to increase the knowledge and awareness of caregivers on the regulation of the patient's living conditions and communication, to draw attention to the problems they experience and to make suggestions for policies and services that can be created in this field. Caregiving for Alzheimer's patients is discussed within the framework of the empowerment approach. It is necessary to create policies and organize services that will center patients and caregivers, be agefriendly, prioritize the high well-being of the elderly and their caregivers, and increase their well-being.

Keywords: Alzheimer's, caregiver, empowerment approach, care, communication, social work