Burden of disease in parents and caregivers of children and adolescents diagnosed with disability-related disorders

Abstract

A disability diagnosis will always impact the family and not only financially in terms of access to health services, but also at the emotional, mental, and psychological level. So it is worth asking What has been the contribution of research on the burden of the disease in parents and caregivers of children and adolescents diagnosed with disability-related disorders? This systematic review article will seek to answer this question, emphasizing the need to study this concept from Clinical Psychology based on a qualitative methodology.\n\nUn diagnóstico de discapacidad siempre impactará en la familia y no solo económicamente en cuanto alacceso a los servicios de salud, sino también a nivel emocional, mental y psicológico.