because they are dramatic and in complications of epilepsy (eg, gingival hypertrophy following phenytoin use or intellectual disability). 8 Stigma scores are highest in the poorest people, in children with unemployed parents, and in urban areas. Stigma scores might be higher in older children, who have more awareness of stigma. Other context-specific devalued statuses might add com plexities to epilepsy stigma in children (eg, race and gender issues in India or HIV-orphanage residence and poor economic status in Africa). 9 Stigma affects the quality of life of children with epilepsy, but few studies formally assess this interaction. A child with epilepsy might be refused admission to school, with Guinean children citing embarrassment due to seizures as reason for nonschool attendance. 10 However, school attendance can also be affected by other epilepsy-related factors (eg, intellectual disability). Stigma exacerbates psychiatric comorbidities in children with epilepsy, and in a survey of parents of children with epilepsy in India psychological stress due to fear of shame and rejection was cited if they divulged their child's diagnosis. 4 Epilepsy stigma might deter parents from seeking care for their children for fear of being discriminated against by the community. Stigma is associated with poor self-efficacy management in children with epilepsy by their parents and can persist even after seizures are controlled by anti-seizure medication.Interventions for epilepsy stigma should be multicomponent, cost-effective, scalable, and directed towards tackling forces that engender and sustain stigma (self, the public, and institutions) and to those stigmatised (child and family or caregivers). Most intervention studies in LMICs are fraught with bias, and criteria for evaluation of efficacy should be robustly defined. Peer support groups have reduced internalised stigma in adolescents, and traditional health practitioners offer psychosocial support to victims of stigma in LMICs. Epilepsy stigma should be addressed by joint efforts of epilepsy stakeholders, such as National Epilepsy Coordinating Committees, whose role includes awareness creation, advocacy for policy change and practice, and promotion of responsible journalism.We declare no competing interests.