National Epilepsy Awareness Month

 

All In theme graphic for national epilepsy awareness month
november is neam graphic

Sharing facts about epilepsy helps raise awareness and stop stigma surrounding seizures. By educating the public, we can promote understanding and encourage support for individuals living with epilepsy. Knowledge empowers communities to provide better care, offer assistance during seizures, and create a more inclusive and compassionate environment. We've compiled some facts about epilepsy and seizures for you to share on social media or with your friends and family to help them learn more. 

  • 1 in 10 people will have a seizure and 1 in 26 will develop epilepsy during their lifetime.  

  • There are approximately 3.4 million people living with epilepsy in the United States; about 456,000 of them are children. 

  • Epilepsy is a neurological disorder that can affect any one of us regardless of race, age, or gender.  

  • Seizures are a symptom of epilepsy. Not all seizures are the same. Many people with epilepsy have more than one type of seizure. 

  • Misunderstanding and misinformation about seizures contribute to continued feelings of stigmatization and negative outcomes for people with epilepsy.1 

  • People with epilepsy may experience "felt" stigma, which leads to shame about their condition and fear of discrimination if they talk about it.2 

  • Felt stigma was linked to higher seizure frequency, younger age at epilepsy onset or longer duration, lack of knowledge about epilepsy, and younger age.5

  • Felt stigma can reduce the quality of life even when seizures are well controlled.6 

References: Epilepsy & Behavior 2015 1, Epilepsia 2007 2, Epilepsia 2022 5, Epilepsy & Behavior 2021 6  

Epilepsy affects everyone, everywhere. Here's how we continue to help the epilepsy community: 

Programs and Education 

From live On-Demand certification courses to 30-minute basic steps training, our seizure first aid program educates the public on approved procedures for recognizing seizures and responding to someone having a seizure. We will be hosting a Seizure Recognition and First Aid Certification Training in recognition of NEAM on November 4.

Advocacy

We advocate to improve the lives of people affected by epilepsy through education, advocacy, research, and connection. Now more than ever, it is critical for the entire epilepsy community to SPEAK UP and speak with ONE VOICE to try and protect epilepsy programs and research. Take action through our tool to email your members of Congress about your concerns. We strongly encourage advocates to personalize these messages by sharing information about their own experiences as a member of the epilepsy community. You can take action on a variety of issues, including funding for epilepsy research and programs.

Research and Innovation 

Our epilepsy research ecosystem covers all parts of therapy, from ideas to market. It includes innovation programs that test new concepts; engagement programs that improve communication; digital tools that support research infrastructure; and funding that supports young researchers. 

Authored By:

Epilepsy Foundation Communications

on Wednesday, September 17, 2025

Resources

Epilepsy Centers

Epilepsy centers provide you with a team of specialists to help you diagnose your epilepsy and explore treatment options.

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Epilepsy Medication

Find in-depth information on anti-seizure medications so you know what to ask your doctor.

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Epilepsy and Seizures Helpline

Call our Epilepsy and Seizures Helpline and talk with an epilepsy information specialist or submit a question online.

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Tools & Resources

Get information, tips, and more to help you manage your epilepsy.

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