摘要：The evolution of a social model of care has been accelerated by a range of factors such as new technology, a change in political parties, and lobbying activity. Further complicating the emergence of the new paradigm is the fact that providing effective care within the community requires an understanding of the context that surrounds the family and the ill person, who must often cope with illnesses that require specialized services and the caring for another person's basic human needs. Using the relational sociology perspective, this study aims to better understand the care trajectory of caregivers of people with Alzheimer's disease. We have adopted a methodologically innovative approach that explores two life histories from the viewpoint of social networks, social representations and action sequences. Only once researchers and policy-makers better understand help-seeking processes in the unpredictable context of chronic illness and social life, can they hope to develop social policies adapted to a population whose multiple needs require long-term community care.
