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Alzheimer’s disease (AD) is a chronic degenerative disease that compromises the physical, mental and social integrity of the elderly, and therefore leads to an increasing dependence on care, and almost always linked to family dynamics and performed at home. Objectives: The main objective of this research is to analyze the daily lives of family caregivers of patients with AD. Methodology: The qualitative approach was used. Data were collected in the municipality of Tamandare/PE, through semi-structured interviews with ten family caregivers of patients with Alzheimer’s disease. In addition to the interview, a structured questionnaire with closed-ended questions was applied, referring to the general and personal characteristics of each interviewee. For data analysis, the verbatim reports were fully transcribed, where relevant aspects were observed and organized into two categories: impact of diagnosis and challenges in caring. Results: The results showed that all coexistence and adaptation to this new reality modify the style and quality of life of those involved. The changes are significant and need to be understood and incorporated into the family routine. Negative emotional reactions involving impotence, fear and anger are common, besides a deep feeling of injustice. Conclusion: The study showed the need for assistance that includes all affected family members. The nurse should support and contribute to overcoming the difficulties faced from the moment of diagnosis to the most advanced stages of the disease.

PSYCHIC DIAGNOSIS OF THE FAMILY CAREGIVER OF THE ALZHEIMER: CASE STUDY OF A BASIC HEALTH UNIT