Nurturing care is a holistic approach to supporting children in their earliest, most critical years. It brings together five essential components: good health, adequate nutrition, safety and security, responsive caregiving, and opportunities for early learning.
This approach maximizes every interaction with a child and protects them from the worst effects of adversity while producing lifelong and intergenerational health benefits. However, children with developmental delays and disabilities face increased risks: they are more likely to miss out on vaccinations or avoid accessing health services, more likely to be undernourished, more likely to experience severe physical punishment at home and less likely to have access to preschool or other early learning opportunities.
To support children with developmental delays and disabilities and ensure they receive nurturing care, this UNICEF and WHO brief urges actions at several levels:
- Governments should adopt policies, laws and national strategies that promote equitable access and deinstitutionalization—caring for children in community-based settings instead of institutional ones. Social benefit policies—including income support, health insurance and education assistance—can also ease the additional costs that families face.
- Prevention, promotion, early identification and intervention services should be culturally and linguistically appropriate, as well as offered in a confidential and ethical manner. The brief promotes a twin-track approach, which includes mainstream or universal services for all children and caregivers alongside targeted services for those requiring additional support.
- Communities can build inclusion for children with disabilities by challenging stigma and false beliefs, ensuring common spaces are accessible and welcoming and involving organizations run by persons with disabilities in co-designing solutions.
- Service providers should offer physical and mental health support to caregivers of children with developmental delays and disabilities, and identify central points of contact within communities to share information on available services and support for caregivers.
