Comprehensive care for neurodivergent populations represents a contemporary challenge for public health, particularly in view of communication-related, sensory, administrative, and institutional barriers that hinder access to and continuity of care. This essay aims to analyze the obstacles to and opportunities for organizing health services guided by equity, inclusion, and humanization. A theoretical and reflective approach was adopted, based on the critical interpretation of scientific studies, clinical guidelines, and international documents addressing rights, accessibility, and comprehensive care. The discussion encompasses the heterogeneity of needs, primary health care, mental health, transitions between care settings, professional competencies, reasonable accommodations, technologies, intersectoral collaboration, and social participation. It is argued that the uniform provision of procedures does not ensure equity when access and communication conditions remain unequal. Person-centered care is advocated as requiring attentive and responsive listening, organizational flexibility, shared decision-making, and institutional monitoring mechanisms. The need to recognize co-occurring conditions without attributing all forms of distress to neurodevelopmental factors is also emphasized. The essay concludes that comprehensive care depends on coordinated networks, continuing professional education, participatory evaluation, and public commitment to eliminating barriers. Transforming practices requires measurable indicators and sustained policies, rather than relying solely on individual initiatives to provide welcoming and supportive care. Future research should examine outcomes and experiences across different geographical contexts and levels of care.
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Platon et al. (2026) studied this question.
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