Epilepsy Foundation

Public health plays a vital role in supporting the epilepsy community, from educating about seizure first aid to ensuring access to quality care. It all starts with YOU—your ability to make a meaningful impact in your local community. When we come together with local Epilepsy Foundations, support groups, and participate in epilepsy events, we create stronger, more resilient communities. At the city and state levels, we can make a difference by implementing seizure-safe schools and training first responders. On a national scale, investing in research and expanding healthcare access will pave the way for a brighter future for all. This #NationalPublicHealthWeek, let’s unite to ensure that no one faces epilepsy alone. 💜 https://lnkd.in/e3eMz8EE

Growing up, Lyzet often lacked the support of her family in her search for answers regarding her epilepsy diagnosis. Now, she’s sharing her journey to highlight how online support groups have made a difference in her life. By telling her story, she hopes to remind others that they are not alone and to help #ChangeOurEpilepsyStory. You can also help challenge the stigma surrounding epilepsy and seizures by sharing your journey so others can feel supported, too: https://lnkd.in/eQ3RVWTF

In celebration of the 30th Anniversary of National Public Health Week, the Epilepsy Foundation of Greater Chicago is hosting a virtual Health Equity Week! This event will explore key topics impacting individuals with epilepsy. Don’t miss this opportunity to learn, connect, and advocate for health equity. Learn more and register: https://lnkd.in/eKry4Fac

Losing the ability to drive due to epilepsy can feel like losing a piece of independence, but innovation is creating new possibilities. For one advocate, discovering Waymo’s autonomous driving technology was more than just a transportation solution; it was a gateway to freedom, privacy, and regained time. Hear how technology is helping people with epilepsy navigate life on their terms. Read the full story here: https://lnkd.in/eGCHcTwA

Make a difference in your community. Are you a coach, caregiver, or someone who engages with the public? Becoming Seizure First Aid Certified equips you with the tools to assist people in need. This course covers everything from recognizing seizures to understanding when to seek medical help. Get started today! https://lnkd.in/eckZmFGY

Join us on Thursday, April 24 at 1 p.m. ET for the Law Enforcement Informed Training on Recognizing and Responding to Seizures. This free, virtual session will teach you how to identify seizures, administer first aid, and ensure the safety of individuals with epilepsy during public safety encounters. Register now: https://lnkd.in/e9u7NadU

Supporting her brother Paul through tonic-clonic seizures, Anna uncovered a passion for advocating change and building a brighter future for people with epilepsy. Their journey has inspired them to raise awareness, ensuring that others with epilepsy feel supported and included. Read their story or share yours: https://lnkd.in/eDtmtyXx

Join PACES, our program dedicated to enhancing self-management, building confidence, and improving the quality of life for individuals with epilepsy. Explore this and other valuable programs available through the Managing Epilepsy Well Network: https://lnkd.in/e4DEg2k6

A Seizure Action Plan (SAP) is crucial for ensuring everyone knows how to respond when a seizure occurs. Whether you’re living with epilepsy or caring for someone who is, having a plan in place and being prepared can make all the difference. Access our free SAP form: https://lnkd.in/e5wtBH-Q

I am a mother of two who was diagnosed with broad-spectrum epilepsy after undergoing IVF and experiencing seizures in 2015. We are blessed to have adopted our beautiful daughter and then to get pregnant after years of trying. However, the pregnancy, hormone cycles, and triggers such as flashing lights and lack of sleep only worsened the frequency and variety of seizures I was experiencing. In 2023, after trying numerous medications, specialists performed a Stereo EEG, and I spent 10 days in the hospital to study my brain. A Deep Brain Stimulator was eventually implanted. My biggest journey has been learning to accept my new reality. I accept not being able to drive or work and struggling to watch movies with my kids or attend concerts. I also accept the many challenges epilepsy brings, such as memory loss, brain fog, and nerve pain and numbness on one side of my body. Read more stories and share yours: https://lnkd.in/eZJE7rvS