Seizures do not always look like convulsions. Less talked-about signs can include changes in the senses, body signals, and ...

Epilepsy Foundation offers support for caregivers through SAGE, Epilepsy & Seizures Helpline, local services, and more. Navigate epilepsy with less stress.

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

Autumn is here and if you are like us, you are ready for cooler weather, warm apple cider and gourds and pumpkins everywhere! This fall, the Epilepsy Foundation needs your help to raise awareness and ...

We established the Jeanne A. Carpenter Epilepsy Legal Defense Fund to help people with epilepsy get the legal help they need. Our goal is to end epilepsy-related discrimination through public ...

Myoclonic atonic epilepsy (MAE), typically known as Doose syndrome, is an uncommon childhood epilepsy syndrome. I accounts for 1 to 2 out of 100 (1 to 2%) of all childhood-onset epilepsies. Genetics ...

The Legal Defense Fund has prepared a series of fact sheets and advocacy materials to educate the public about the legal rights of people with epilepsy. If you are facing discrimination because of ...

Social media can be a powerful part of your epilepsy journey. Whether you’re a person with epilepsy or a caregiver, it can connect you with others going through the same things you are. You can share ...

As many as two-thirds of people with epilepsy face some change in sexual desire, behavior, or activity as a result of their seizures. Even if this kind of problem has affected you, you may not have ...

New Approaches to Seizure First Aid This first video in the series introduces the other videos and explains what viewers will learn and why it’s important. [scald=17141:sdl_editor_representation] Care ...