06/20/2026
A National Plan for Epilepsy Act is moving through Congress, and families, caregivers, and clinicians can help push it across the finish line!
This legislation would direct the federal government to build a coordinated national strategy for preventing, diagnosing, treating, and curing epilepsies, while improving quality of life for people and families living with them. That means more research, better access to specialized care, stronger data collection, and real efforts to reduce SUDEP and other epilepsy-related deaths.
At CNF, we believe every child with a neurologic condition deserves a system that's built to support them. That’s why we're raising our voice alongside the broader epilepsy community and asking you to do the same.
It takes less than five minutes to contact your Members of Congress and ask them to support S. 494 and H.R. 1189, and personal messages from community members can make a REAL difference.
Share your voice today: https://tr.ee/ZL47AzWcX2