November is National Epilepsy Awareness Month (NEAM), a time to stand united for the 3.4 million people in the U.S. living with epilepsy. 💜 This year, we’re "All In" for connection, understanding, and change. Join us throughout November: https://t.co/9Wis4fwjNJ 💪 #NEAM2025

By joining EmpowER&D, you help create a living dataset that drives discoveries and advocacy. Be the breakthrough. Sign up today: https://t.co/YxjYBAfNwm

Langston University is going purple for NEAM! 💜 Dr. Desmond Delk, a Seizure First Aid Instructor, has brought epilepsy education to campus. LU Basketball wore purple, and students are spreading awareness with PSAs and info tables at their games.

I was recently diagnosed with epilepsy. I experienced three tonic-clonic seizures. I felt like my whole life had turned upside-down, but I am pursuing my dream of going to nursing school. I try to stay positive even when I'm not feeling well. More stories: https://t.co/Od18fjN0pA

Going all in looks different for everyone. Whether you’re hosting a game night, running a race, or celebrating a birthday, every effort counts. 💪💜 When you Fundraise Your Way, every act of giving matters. Start today: https://t.co/fdNYcb1UQQ #NEAM2025 #AllInForEpilepsy

Every story has the power to change how the world views epilepsy by promoting conversations, helping others find support, & breaking down misconceptions. In partnership with the Epilepsy Foundation of Greater Chicago, we're proud to share Michael’s story.

For Mike, being All In means fully committing to understanding epilepsy and seeking the best resources, treatments, and support available for children like his son George. He's constantly learning about what is often a complex condition. #NEAM2025 #AllInForEpilepsy

Being All In for epilepsy awareness means showing up every day with passion, purpose, and persistence. It means lifting the voices of those living with epilepsy and locking arms, united in this mission!

My 1 in 26 is our daughter, Elin. In utero, she was diagnosed with multiple brain malformations that gave her a higher proclivity to developing epilepsy. Elin is now 22 months old and is thriving! She walks, talks, reads, and is an inspiration to every single person she meets.

My efforts embody the spirit of being All In because I don’t just want to raise awareness; I want to make a difference. Through my art, voice, and advocacy, I am committed to showing what epilepsy truly looks like: resilience, creativity, and strength that refuse to be silenced.

The Epilepsy Foundation’s national office is closed today in observance of the holiday. If you need resources or support in the meantime, our AI Epilepsy Assistant, Sage, is available 24/7 to help guide you. You can connect with Sage anytime at https://t.co/23FJbzq6HR

Keep an eye out in LA, Phoenix and San Francisco where 1 in 26 Waymo vehicles will feature an Epilepsy Foundation decal to recognize the 1 in 26 people who have been or will be diagnosed with epilepsy in their lifetime. #NEAM2025

See your journey with fresh eyes. EmpowER&D brings your medical records and lived experiences together in one place. You can spot trends, track patterns, and use that knowledge to guide your next steps. Join today: https://t.co/mOZ13b7GU1

Through her challenges with photosensitive epilepsy, Anzli found freedom in dance and co-founded EpiArts Alliance. Her question, "When do flashing lights occur?" sparked the FlashCue Project, making theatre more accessible. Be inspired & share your story: https://t.co/NHzBA746KP

Open Enrollment for a #Marketplace health plan runs now through January 15! #GetCovered by visiting https://t.co/Km9BmDAgjQ and check if you qualify for savings to make coverage more affordable.

Encourage your workplace, school, or community group to get Seizure First Aid Certified! It takes just 90 minutes to gain knowledge and confidence to recognize seizures and respond safely. Sign up at https://t.co/L8veAcGXEN and earn a 2-year certification. #NEAM2025

Applications are open for the Research Ambassador Program! Empowering patients, caregivers & advocates to shape epilepsy research. Selected participants invited to the Research Ambassador Bootcamp in Minneapolis, MN, April 11-12, 2026. Learn more & apply: https://t.co/zCAy1RlXhk

Michael was diagnosed with epilepsy when he was 5 years old. While it impacts how he lives, it hasn't stopped him from building a life filled with love, purpose, and strength. Read more about his journey and help #ChangeOurEpilepsyStory: https://t.co/W9cPUZ96FC

EmpowER&D reveals the connections between your symptoms, treatments, and experiences. Claim Your Data. Sign up today: https://t.co/ZtRrOrHmCe

Before the holiday hustle begins, check your medication supply. Having your prescriptions filled and organized brings peace of mind. If you need assistance, our Epilepsy & Seizures Helpline is here for you. Call 1-800-332-1000 (8AM–8PM ET) or visit: https://t.co/ScapvXSJg0

Sabrina had her first seizure when she was just 2 years old, and it had a big impact on her as she grew up. She often felt different from other kids her age. As she got older, she realized that while epilepsy is a part of her, it doesn’t define her. More: https://t.co/CQ6ZXXI3F4