Epilepsy Foundation of America

Today, July 3, the U.S. House passed H.R. 1, the budget reconciliation package, & the legislation is expected to be signed into law by the President. We are devastated by the cuts and changes to Medicaid included in the reconciliation package. Read our statement in the images:

My daughter Avigail passed her driving test in January 2025, but after a return of seizures, her license was revoked in April. She graduated from high school in May and starts nursing school in July. Our family is supportive and offers her rides. Epilepsy isn’t stopping her!

If you’ve lost a loved one due to epilepsy, you’re not alone. Join our Bereavement Virtual Support Group on Wed, August 20—sessions available for adults & young adults. Email [email protected] for info & to register.

The ADA became law 35 years ago thanks to the advocacy and leadership of former Congressman Tony Coelho, its primary sponsor and a champion for people with epilepsy. Today, we honor that legacy and continue the fight for access, equity, and inclusion. epilepsy.com/stories/35th-a…

The Epilepsy Foundation proudly supports the 35th Anniversary of the Americans with Disabilities Act! On July 26, we commemorate this historic civil rights law that protects people with disabilities from discrimination, including those with epilepsy. epilepsy.com/legal-help/leg…

Being a young adult with epilepsy has been challenging, mainly a loss of independence that most people my age don’t experience. I want people to know they aren’t alone, and I believe epilepsy needs more awareness to help fund research. Share your story: epilepsy.com/eJourney?utm_c…

Managing life with epilepsy can be challenging. This International Self-Care Day, remember to prioritize your mental health and well-being. epilepsy.com/stories/ways-p…

Back-to-school season is right around the corner! Now is the perfect time to prepare your staff to support students with epilepsy. Check out our free Seizure Safe School courses for teachers, school nurses, and administrators at learn.epilepsy.com/?utm_campaign=…

Seizure emergencies can be scary, but knowing what to do can make a difference. The Epilepsy Foundation offers free #SeizureFirstAid training, so you can respond with confidence and help keep someone safe during a seizure. Be prepared: epilepsy.com/firstaid?utm_c…

You juice the lemons, and we'll handle the rest! From a convenient mobile app to printable yard signs and email templates, we've covered everything your stand needs to stand out! You can access all these resources and more on your participant dashboard.🍋 epilepsy.com/lemonadeforliv…

World Brain Day highlights the importance of awareness and education around neurological disorders. For our community, it’s a powerful reminder that no one faces epilepsy alone. We're here for you, offering trusted information, local resources, and supportive programs.

Understanding your diagnosis is essential for successfully navigating the challenges of living with epilepsy. Our toolkit for newly diagnosed individuals offers the information and resources you need to effectively manage your condition. epilepsy.com/tools-resource…

After life-changing experiences with seizures, Travis is speaking out for epilepsy awareness. He shares how stigma can make it easy to feel isolated or self-conscious, so he is empowering others to speak up, seek support, and never give up. More: epilepsy.com/stories/even-w…

Learn, Act, Save a Life. In just 30 minutes, you can become Seizure First Aid Ready! Our course provides you with the essential skills to assist someone during a seizure. It's interactive, informative, and suitable for everyone. learn.epilepsy.com/?utm_campaign=…

TJ, who lives with seizures, hosted a lemonade stand with his brothers to raise awareness and funds for epilepsy. Together, they raised over $900! 💜🍋 Thank you to TJ and his family for being powerful advocates in their community. Make a difference too: epilepsy.com/lemonadeforliv…

Considering medical cannabis for epilepsy? Start by having an open conversation with your health care team about the potential risks and benefits. Asking the right questions can help you make informed choices about your treatment. More: epilepsy.com/sites/default/…

I was diagnosed with juvenile myoclonic epilepsy when I was 13. Through the Epilepsy Foundation, I’ve read many stories that I can relate to and empathize with. Now, I have a club at school that advocates for students with epilepsy. Read more stories: epilepsy.com/eJourney?utm_c…

Tracking seizures is essential for managing epilepsy for you and your healthcare team. Recording details like duration, seizure type, and awareness level helps find patterns and improves treatment planning. For tools and info, visit: epilepsy.com/stories/ways-k…

Getting ready for summer camp? Nurse Jo explains why clear, open communication is one of the most important steps when sending your child with epilepsy to camp. Talking with camp staff beforehand helps everyone feel more confident and prepared. epilepsy.com/preparedness-s…

Make your classroom a Seizure Safe Space! Our free, age-appropriate toolkits help teachers and students learn about epilepsy and seizure first aid in a fun, simple way. Download now: epilepsy.com/sites/default/…

My son, Brooks, is my 1 in 26. He was diagnosed with epilepsy at 12 months old after multiple tonic-clonic seizures, and his journey has been full of ups and downs. His seizures were controlled, and then they weren’t. Brooks will forever be my hero and the bravest boy I know. 💜