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:

Summer camp should be exciting—not overwhelming. Nurse Jo is here to help you feel confident and prepared as you get ready to send your child with epilepsy to camp. A little preparation can go a long way in making camp a safe and empowering experience.

Managing epilepsy looks different for everyone. Some explore options like medical cannabis or CBD alongside traditional treatments. Learn more:

CDSMP is a free virtual workshop for adults living with chronic conditions such as epilepsy. The upcoming session begins on July 15 and is available to adults aged 18 and older nationwide. To register, please visit:

My daughter, Piper, is my 1 in 26. She has focal awareness seizures and is incredibly strong and resilient. She has not let epilepsy define her or hold her back, and she helps others with epilepsy and neurological disorders. She is my hero. 💜

Join us on Thursday, July 10 at 1 p.m. ET for the Law Enforcement Informed Training on Recognizing and Responding to Seizures. Register now:

Looking to squeeze more fun into your summer?🍋 Host a lemonade stand to raise funds & awareness for epilepsy! It's easy:.1️⃣ Register at 2️⃣ Create your personalized page to share your story & spread the word.3️⃣ Host your lemonade stand & make a difference

Haley is sharing her experiences living with seizures from the challenges she’s faced at school to the search for the right treatment. By sharing her story, she hopes to help others feel less alone in their own journeys. Read her story and share yours:

Take our 90-min on-demand course to earn a 2-year Seizure First Aid Certification. The skills you gain could save a life. Start today:

Educators, school nurses, and administrators—access free, age-appropriate resources to teach students about epilepsy and seizure first aid. Let’s create safer, more inclusive classrooms together! Get your toolkit now:

I was diagnosed with epilepsy in June of 2023, after months of not knowing what was going on. I went to see a neurologist and was prescribed an anti-seizure medication. After many trials and errors, I am now almost 4 months seizure-free. More stories:

The Epilepsy Foundation’s national office is closed for the holiday. As you celebrate, be sure to stay safe, especially if you or a loved one has photosensitive epilepsy. Read our safety tips: If you need support, our 24/7 Helpline is here for you.

Before your child goes to summer camp, ensure their Seizure Action Plan is ready and shared with camp staff. This personalized plan helps counselors, nurses, and other caregivers know exactly what to do if your child has a seizure. Learn more:

July 3 is Bereaved Parents Awareness Day. If you lost a child, please know that you are not alone. We are here to support you with resources, connection, and care. Visit to help navigate your journey.

If you or a loved one are unsure about the type of seizures you're experiencing or are having difficulty managing them, visiting an epilepsy center may be helpful. To find a center near you, use the locator tool on our website:

A year ago, I started my day like any other, trying to get as many tasks done as I could. Suddenly, everything changed. I woke up with my husband beside me, telling me to stay still because I had hit my head during a seizure. I’m proud to say I’ve been seizure-free for a year.

URGENT: Congress is moving quickly to pass a budget reconciliation bill with cuts to #Medicaid that would be devastating for millions of Americans, including people living with epilepsy. Help #ProtectMedicaid by contacting your Representative today at

Lemonade for Livy is BACK! 🍋💜 This summer, turn something sweet into something powerful. Help raise critical funds and awareness for epilepsy right from your own neighborhood! ➡️ Register today at and pour your heart into making a difference.

Strength in numbers. When we unite, we empower each other. Find an epilepsy support group near you and surround yourself with people who understand your journey:

After being diagnosed with epilepsy, Morgan refused to let seizures define his future. From losing his driver’s license to navigating treatment challenges, he stayed determined to chase his dreams. Now, he’s sharing his journey: