“…Previous studies have shown that parents can provide valid information about the quality of life of children with CP when self-reporting is not feasible. 32,34,35 The mean HRQoL score was low, with greater impairment of physical capacity, followed by school, social, and emotional aspects. Low scores and greater impairment of physical ability compared to psychosocial aspects were also found in the pediatric population with CP in the United States, 32,33 Canada, 34 China, 35 Thailand, 36 and Turkey, 14 despite the social and cultural differences of each locality.…”