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My daughter Avigail passed her driving test in January 2025, but after a return of seizures, her license was revoked in April.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!

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.🍋

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.

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:

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.

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:.

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:

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:

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:

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.

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:

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. 💜

Managing epilepsy isn't just about medication, it's about teamwork, preparation, and staying informed. Learn how to track your seizures, manage triggers, and work with your healthcare team to take control of your seizures. To start your journey, visit:

Meet Livy, the inspiration behind the global Lemonade for Livy movement. 💜🍋1 in 26 people in the U.S. will develop epilepsy at some point in their lives. Make a refreshing difference with us:

Looking for local support? Your nearest Epilepsy Foundation office is just a click away! Whether you need resources, support groups, or just someone to talk to, our local offices are here to help. Find your local office at

Driven by her own experiences, Tatum is passionate about raising awareness. She aims to educate others about the different types of seizures and the realities of living with epilepsy, including mental health challenges and feelings of isolation. More:

The Epilepsy Learning Portal offers expert-led, on-demand courses designed to fit your schedule. Whether you're a healthcare professional or a caregiver, our courses provide the knowledge and confidence you need. Start learning today:

Community makes a difference! From local events to support groups and advocacy efforts, your local Epilepsy Foundation is here to help. Find the support you deserve at or call 1-800-332-1000 (1-866-748-8008 en español).

Understanding your risk for Sudden Unexpected Death in Epilepsy (SUDEP) is a key step toward prevention. Talk with your doctor about SUDEP and what you can do to lower your risk. Every question is important! Check out these tips to #StartTheSUDEPConvo: