Family Support & Trusted Resources from the Child Neurology Foundation

You’re not navigating this alone.

When a child is living with migraine or another neurologic condition, families are often navigating medical care, school accommodations, insurance questions, and long-term planning all at once. Finding clear, trustworthy information shouldn’t add to that stress.

This page brings together free, family-centered support resources curated by Migraine at School in partnership with the Child Neurology Foundation, a national nonprofit dedicated to improving care for children with neurologic conditions. The downloadable handouts below are designed to help families better understand neurologic care, prepare for appointments and school conversations, connect with support networks, and navigate key transitions over time.