Autism between social ignorance and despair of affected families

Abstract

Introduction: The specific therapy for people with autism is not offered free of charge. The measures taken by the state are often insufficient. Purpose: Arguing the necessity to respect the principle of distributive equity of children with autism in specialized medical services funded by the state, improving the knowledge of health workers about this disease. Material and methods: Sources from medicine, medical and social bioethics. The methods that were applied: analyticdescriptional, bioethical, statistical and sociological. Results: On average, one of 150 children in the world is affected by autism. In our country, the principle of equity in treating children with such disorders is constantly violated. Conclusion: From a bioethical perspective, it is necessary for patients with autism to be treated as complex personalities who need continuous support from the state and community members, counteracting any form of discrimination and ignorance, ensuring equal chances in providing medical care.