A new diagnosis can leave you with more questions than answers. Cameron Boyce Foundation and CURE Epilepsy are here to help you find your footing, connect with people who understand, and learn what comes next.
Join Support Groups ➡️
Connect with others living with epilepsy in a space built for honest conversation and real support.
Learn about Epilepsy ➡️
Clear, trustworthy information about epilepsy and what a diagnosis means for you.
Explore our Resources ➡️
Guides, tools, and materials to help you navigate everyday life with epilepsy, big and small.
Listen to the Podcast ➡️
Hear real stories and expert insight on living with epilepsy, straight from the community.
Epilepsy Facebook Support Groups
Connect with others who understand what you’re going through. These groups offer a safe space to share, ask questions, and find support from people who get it.
Epilepsy Support Group
A welcoming space for anyone touched by epilepsy to connect, share experiences, and support one another. Whether you’re newly diagnosed or have been navigating this for years, you’re not alone here.
Built for young adults living with epilepsy, this group is a place to talk openly about the challenges and wins that come with this chapter of life, surrounded by peers who truly understand.
Whether you’re newly diagnosed or supporting someone who is, these resources will help you feel prepared, informed, and connected to a community that understands what you’re going through.
Seizure Action Plan
A clear, shareable plan that outlines what to do before, during, and after a seizure, so caregivers, teachers, and loved ones know exactly how to help when it matters most.
Treating and living with epilepsy can add up fast. Explore medical and educational assistance programs designed to ease the financial burden and help you get the support you need.
With 1 in 26 people developing epilepsy in their lifetime, thousands of students head to college managing this condition. This guide helps them thrive, because epilepsy shouldn’t stand in the way of new experiences and friendships.
Festivals can bring seizure triggers like dehydration, lack of sleep, strobe lights, alcohol, and drug use. This toolkit gives you what you need to stay safe and enjoy the show, and helps everyone around you know what to do if a seizure happens.
Track seizures, triggers, and patterns over time to help you and your doctor spot what’s working and what needs to change. A simple habit that can make a real difference in your care.