Narratives of professionals in Uruguay on bereavement in Intellectual Disabilities

Abstract

People with Intellectual Disabilities (ID) face significant barriers to accessing health care due to stigma and exclusion processes. This reality occurs despite new approaches and regulatory frameworks that promote the improvement of the quality of life (QoL) of this population and their families. This study analyses the strategies of psychologists and social workers in Uruguay to address bereavement in people with ID, using a qualitative approach based on semi-directed interviews. Work perspectives, available resources and the main difficulties encountered in this task were identified. The results reveal a lack of specific training, limited resources for referral and care and a low prioritisation of the topic in professional training and academic production.