Soutenir les personnes atteintes d’épilepsie aves des outils pour réduire la stigmatisation

La stigmatisation affecte tous les aspects des soins de l’épilepsie, du diagnostic au traitement en passant par la législation et aux allocations budgétaires. Elle affecte la vie des personnes atteintes d’épilepsie lorsqu’elles n’ont pas un accès égal à l’éducation, à l’emploi et aux mêmes droits sociaux.

Empowering people with epilepsy to lead the way in reducing stigma

Stigma affects all aspects of epilepsy care. It affects the lives of people with epilepsy when they are not given equal access to education, employment, and social opportunities. In a US study, one-third of respondents identified stigma—not seizures—as the most difficult part of living with epilepsy.

How can primary health care help to close the epilepsy treatment gap? A journey through Andhra Pradesh, India

Hours from the nearest city in India, down a pothole-studded road framed by fish farms, primary care centers in Andra Pradesh provide service to tens of thousands of people. How do these centers care for people with epilepsy, and what challenges do they face?

Epilepsy education in India: Teacher training project aims to address stigma, increase inclusion

Schools can be important for epilepsy screening, as well as awareness of seizure first aid and basic knowledge. In a rural area of Punjab, a three-year project of surveys and training activities aimed to increase knowledge and dispel myths and misconceptions.