Emotional Repercussion and Changes Experienced by Family Caregivers of Individuals with Alzheimer's: A Study in the Southern Region of Tocantins, Brazil
Camila Rocha de Oliveira
School of Psychology Service - Sepsi, University of Gurupi-Unirg, Avenue Rio De Janeiro, Nº 1585, Sector Central, Gurupi, 77403-090, Tocantins, Brazil.
Ellen Fernanda Klinger
School of Psychology Service - Sepsi, University of Gurupi-Unirg, Avenue Rio De Janeiro, Nº 1585, Sector Central, Gurupi, 77403-090, Tocantins, Brazil.
Daniely de Sousa Prado *
School of Psychology Service - Sepsi, University of Gurupi-Unirg, Avenue Rio De Janeiro, Nº 1585, Sector Central, Gurupi, 77403-090, Tocantins, Brazil.
Larisse Aires Moreira
School of Psychology Service - Sepsi, University of Gurupi-Unirg, Avenue Rio De Janeiro, Nº 1585, Sector Central, Gurupi, 77403-090, Tocantins, Brazil.
*Author to whom correspondence should be addressed.
Abstract
Alzheimer’s disease is the most common dementia among the elderly, but unfortunately, the early symptoms are mistaken for natural aspects of age. Thus, knowledge is an excellent tool to get a diagnosis still in the early stage.
Aims: Therefore, this article addresses the psychological reactions of family caregivers of individuals with that disorder and coping conditions experienced by them.
Methods: To this end, an exploratory descriptive study of qualitative approach with semi-structured interviews with primary caregivers of individuals with Alzheimer took place, and some of the participants were appointed by indicated Regional Tocantinense Association Brasilian Alzheimer’s - ABRAZ, not exceeding the expected number, the researchers received help in the indication of caregivers who were already part of this research.
Results: Regarding the coping conditions, there was family resilience, some resorted even psychological aid, since the change in routine was essential for the welfare of the elderly. Five respondents knew little about the disease before diagnosis, however, they began to delve into the matter with a view to aid in the treatment. Thus the knowledge acquired over time only came to add, thereby contributing to an improvement in the quality of life in both parties.
Conclusion: The look of psychology facing the coping experienced by caregivers of individuals with Alzheimer’s is of paramount importance, as well as knowledge of caregivers about the disease, although acquired over time, contributed to an improvement in the quality of life of both parties.
Keywords: Illness, resilience, family, Alzheimer's disease