I was diagnosed with juvenile myoclonic epilepsy (JME) at 15 years old after experiencing two tonic-clonic seizures in high school. What started as a typical morning quickly turned into a defining ...

The National Epilepsy Walk returns to the iconic National Mall on March 15, bringing together one of the largest epilepsy communities in the country. Don’t miss your chance to be part of this powerful ...

The Epilepsy Foundation Iowa provides programs and services that support people and families impacted by epilepsy. With the strength of a national organization and network of epilepsy experts, EFIA ...

In her book, The Spirit Catches You and You Fall Down, Anne Fadiman tells the story of Lia Lee, a young Hmong girl whose epilepsy was diagnosed in Merced, California. The title of Ms. Fadiman's book ...

Join us for Purple Day ® on March 26 to harness the Power In Purple, the Epilepsy Foundation’s 2025 theme emphasizing the strength and resilience of the epilepsy community. Together, we can turn ...

The Epilepsy Foundation South Dakota provides programs and services that support people and families impacted by epilepsy. With the strength of a national organization and network of epilepsy experts, ...

This support group provides an opportunity to meet other adults living with epilepsy and to share your experience with others. This is open to anyone and virtual.

Epilepsy is the fourth most common neurological disease in the world, affecting over 3.4 million people in the United States. Epilepsy is considered rare when the underlying cause affects less than ...

This virtual group is open to parents & caregivers from the Southwest- Arizona and New Mexico. It provides a place to share experiences, provide encouragement and offer support through the epilepsy ...

This group supports parents and caregivers and provides a place to share experiences, provide encouragement, and offer support for each other through this epilepsy journey. The group takes place on ...