You are not alone. 馃挏 Connect with others who understand the challenges of living with epilepsy. Join a support group today and find strength in community. ow.ly/W6pX5102gkN
I鈥檓 inspired by the many friends I know living with epilepsy, the families and caregivers who stand beside them, and the researchers, clinicians, advocates, and partners I鈥檓 fortunate to work alongside. This community gives our work both direction and urgency.
Are you Seizure First Aid Certified? This #NEAM2026, spark hope by joining our free virtual training on Nov. 3 at 4 p.m. ET. Learn how to support people with epilepsy and register now: ow.ly/ma8A5102e8A#WhereCommunitySparksHope
It鈥檚 National Epilepsy Awareness Month! Together, we can spark hope through understanding, support, and awareness. Learn more at ow.ly/xCYn51029xL, share this post and help us spread the word. #NEAM2026#WhereCommunitySparksHope
Daylight Saving Time ends tonight! Don鈥檛 forget to set your clocks back one hour before bed. For people living with epilepsy, a consistent sleep schedule and taking medications on time are essential for seizure management. Learn more: ow.ly/m2Wg5102uuI
Medicare Open Enrollment runs now through Dec 7! This is the time to review your choices for health & prescription drug plans. Costs & benefits change yearly & some plans may not be available or there may be new ones. Pick the right plan at ow.ly/CiiQ5101Kgk. #MedicareOE
I started having seizures when I was 17, and it felt like nobody believed me. Even after showing my medical records to family and friends, I still faced doubt and disbelief. Take epilepsy seriously. Every minute counts. Read more stories and share yours: ow.ly/IBFe5101KiJ
Turn your pumpkin purple this Halloween to raise epilepsy awareness! Every purple pumpkin supports the 1 in 26 people who will develop epilepsy. Help us reach our goal and register today: ow.ly/8uyO51024Uz 馃挏 #PurplePumpkinProject
This #HealthLiteracyMonth, feel empowered to understand the health information your provider shares. Come prepared with questions, ask for clarification, repeat key points back, and take notes. The power is in your hands. ow.ly/kzPX51017l0
Trust in science starts with transparency. Caitlin Grzeskowiak, Chief Research and Innovation Officer at the @EpilepsyFdn addresses what it means to translate complex science for patients and meeting them where they are.
Caitlin participated in a #BIOPACE26 panel on trust in science last week, moderated by BIO Executive Vice President and Chief of Global Health Phyllis Arthur. Both were joined by Sean Clements, Principal at SPC Strategies, and Amar Duggirala, Board Chair and Immediate Past President of the Maryland Academy of Family Physicians.
Why is my pumpkin purple? 馃巸馃挏 Because I'm a mom raising a little boy with epilepsy. Purple reminds me of the moments that changed our lives, but also of the strength, hope, and courage of my son. I'm raising awareness for TJ and every family living with epilepsy.
For Adam, sharing his experience is more than telling his story. It's a way to advocate for the epilepsy community. He hopes his story offers encouragement, builds understanding, and reminds others that they are not alone. Read more and share your story: ow.ly/q5Ec5100YlS
I鈥檓 participating in the Purple Pumpkin Project because I am a mom to a son with epilepsy. He is in college studying neuroscience and has been navigating his uncontrolled, medication-resistant epilepsy since he was 8 months old.
This National Disability Employment Awareness Month, we鈥檙e highlighting the importance of workplace safety for people living with epilepsy. Creating safe, supportive environments helps everyone thrive
Honored to be nominated for the inaugural Prix Galien Patient First Award in Honor of Michael J. Fox! This recognizes our commitment to patient-centered care and innovation. Winners announced Oct 29 at the Galien Patient Summit. Details: ow.ly/loaC51014vK
Happy National Pumpkin Day! Have you joined the #PurplePumpkinProject yet? Watch Effie and Helen as they paint their pumpkins and share important Halloween safety tips for people living with epilepsy. Let's raise awareness and help make Halloween safer! ow.ly/6J8o5100Zzn
Our 1 in 26 is our 3-year-old daughter, Kloe. She was diagnosed at just over 1 year old. She proves that, day in and day out, epilepsy does not define her; she defines epilepsy.
Last call to apply for the 2027 Research Ambassador Bootcamp! People with epilepsy, caregivers, healthcare professionals, and advocates can help shape the future of epilepsy research. New for 2027: A bilingual Spanish-speaking cohort! Apply by October 30: ow.ly/rgsf50ZZM9M