I had my first seizure at 17. I was diagnosed with JME. I learned what triggers my seizures is sleep deprivation and heavy stress. I've been in denial and embarrassed because I don’t want to be judged. I am sharing my story to educate others and to learn more about myself.

Your journey to managing seizures starts with understanding your unique needs. From tracking seizures to managing triggers, discover the tools and resources to help you live confidently with epilepsy. Learn more at epilepsy.com/manage?utm_cam…

Becoming #SeizureFirstAid Certified equips you with the tools to help people in need. This course covers everything from recognizing seizures to knowing when to seek medical help. Get started today! epilepsy.com/firstaid?utm_c…

We hosted a Lemonade Stand for Remyngtyn to share our story and raise awareness. Remy had his first seizure in October 2023 and it has been a long road. We have tried many different medicines, but he still has seizures almost daily. Remy is a hero to many people and perseveres.

I am Peter S. I have lived with epilepsy my whole life, but I am not to be ashamed. I have experienced headaches, fainting, and trouble sleeping, but it is my goal to overcome. Sometimes people with epilepsy are ignored or treated poorly. Stay strong and encourage one another!

Honor the memory of your loved one. Stories and photos from our community will be featured on the Memory Wall at the Partners Against Mortality in Epilepsy (PAME) Conference this December and on Facebook. Share pictures and stories here: bit.ly/3oGPwXN

We hosted our lemonade stand this past weekend to share our story and raise awareness. Our son Cameron was diagnosed with infantile spasms and focal epilepsy at 19 months. The Epilepsy Foundation was one of the first resources we turned to. We're thankful to those who gave $7K!

Don’t miss It’s All Your Fault, Tyler Price! A powerful musical that follows Jackson, a middle school boy who stands up against bullying to defend his sister, Lucy, who has epilepsy and learning challenges. Get your tickets now: tylerpricemusical.com

As the seasons change, our virtual support group continues to be a steady source of strength, connection, and understanding. Join us as we navigate the epilepsy journey together—your presence truly makes a difference! epilepsy.com/?utm_campaign=…

Join us live for #SeizureFirstAid Training and Certification this month! Knowing how to help during a seizure can save a life. Learn how to recognize seizures and provide the right care when it matters most. Register: epilepsy.com/firstaid?utm_c…

The Epilepsy Foundation's national office is closed for the holiday. If you need assistance finding resources or support, our 24/7 Helpline is available at 1-800-332-1000 (1-866-748-8008 en español) or visit epilepsy.com/247-helpline

Olivia from Texas is sharing about the challenges of her young son Carter's epilepsy diagnosis and the uncertainty it brought to their family. Building a supportive community has been a crucial part of their journey. Read more: epilepsy.com/stories/buildi…

Join us and the International Bureau for Epilepsy in the Global Epilepsy Needs Study (GENS). Your experiences can help us better understand the challenges faced by individuals with epilepsy and their caregivers across the globe. qualicis.eu.qualtrics.com/jfe/form/SV_2l…

People with epilepsy can experience emotional challenges, including stress and anxiety. Speak with your doctor if stress and anxiety are negatively impacting your life, and learn about available tools and resources to improve mental health care: bit.ly/3sGlJnQ

Help end discrimination against people with epilepsy! Urge Gavin Newsom to sign SB 357 into law to remove discriminatory language, increase access to care, and protect the doctor-patient relationship. Take action immediately by visiting gov.ca.gov/contact

I’m a survivor of abusive head trauma as an infant. I was diagnosed with epilepsy at age 21 after two unprovoked tonic-clonic seizures. The support of friends and therapy is essential. I’m open about my health and am an Epilepsy Awareness Ambassador, which I hope can help others.

Emergencies may impact access to resources like medications and transportation. People with epilepsy and their caregivers should consider what they may need during an emergency- before disaster strikes. Learn how to prepare: epilepsy.com/preparedness-s…

Sarah was diagnosed with epilepsy when she was 8 years old and has had many kinds of seizures. We finally seem to have found the right combination of medications and have good seizure control! We celebrated 3 years seizure-free on September 1.

Did you know seizure dogs are the most searched public safety topic through the Epilepsy Foundation’s 24/7 Information and Referral Services? Discover how these incredible service dogs support people living with epilepsy. youtu.be/PP4lmtoAlx4?si… #NationalServiceDogAwarenessMonth

September marks #SuicidePreventionMonth—a time to honor the lives lost to suicide, support those who have faced suicidal thoughts, and recognize the individuals, families, and communities affected. Remember, you're not alone. Help is available 24/7. Call or text 988. #SPM24