“…Long-term responsibility for a disabled child, combined with a necessity to face adversities and challenges associated with handling the child, frequently leads to negative emotions, such as anxiety, sadness, anger, hopelessness and distress, experienced by the person, and adversely affecting the functioning of the parents and the entire family [13,14,15]. The most common effects of long-lasting caregiver burden include depressive and anxiety disorders of varied intensity [1,6,16,17,18,19,20,21,22,23,24,25,26]. However, intensity of anxiety and depressive symptoms in the parents is not related exclusively to predictors associated with the child’s disability, but is also linked to personal, social and economic variables resulting from the parents’ needs and health status as well as factors occurring in the family; this fact reflects the multidimensional effects of these determinants in health-related quality of life (HRQOL) in individuals taking care of children with CP [27].…”