The Epilepsy Foundation and partner patient groups applaud the newly released final rule on Section 1557 of the Affordable ...

According to the Centers for Disease Control and Prevention, racial and ethnic minorities represent more than 40% of the 3.4 ...

10% of other races, including Asian Americans and Pacific Islanders, receive surgery as children, compared to 60% of Whites, ...

My name is Liv. I was diagnosed with epilepsy around 10 years old, and it has been quite a journey. I have been diagnosed with generalized epilepsy and Jeavons syndrome. Growing up, it was an obstacle ...

The Walk is a fun-filled community event – with a serious cause – that gives everyone an opportunity to share their story of epilepsy, learn more about epilepsy, and connect with others affected by ...

This virtual group is open to Young Adults living with Epilepsy. It provides a place to share experiences, provide encouragement and offer support through the epilepsy journey. The group meets the 4th ...

Join us in-person or virtually to raise awareness and funds to END EPILEPSY. With each step taken and dollar raised, we're closer to reaching our goal: a world free from epilepsy and free from fear of ...

A memoir of discovery, acceptance, and hope, this book chronicles Kristin’s tenacious fight for a seizure-free life.

The Epilepsy Foundation of Michigan is thrilled to invite you to the Epilepsy Innovation Round Table! We hope you can join us in Grand Rapids, Michigan on April 27th for this time of learning and ...