Thanks to the continued generosity of Dr. Lorna Myers, Epilepsy Alliance America has a scholarship program for students with a diagnosis of psychogenic non-epileptic seizures (PNES). In June 2023 Epilepsy […]
Epilepsy Alliance America is committed to helping to grow the membership, reach and impact of the bipartisan Congressional Epilepsy Caucus. The Congressional Epilepsy Caucus brings together Members of Congress and […]
Epilepsy Alliance America is proud to have partnered with AJ Taylor, a patient advocate from Georgia, and the National Advocates for Seizure Safe Schools to advocate for the passage of […]
The Seizure Action Plan Coalition (managed by Epilepsy Alliance America) is proud to be distributing this educational program. For more information about this program – you can see the full […]
Epilepsy is a neurological disease that doubles or triples the risk of a person dying prematurely. Important causes of death among people with epilepsy include injuries, status epilepticus, and SUDEP, […]
Epilepsy Alliance America is proud to share that we have become the Managing Organization of the Seizure Action Plan Coalition as of January 1, 2023. We stand on the shoulders […]
Epilepsy Alliance America’s Board of Directors met in November 2022 and approved the nominations of new members of the Board of Directors as well as the officer slate for 2023. […]
What the EF (WTEF) is a podcast that discusses, points out, and chuckles at the ridiculous, poignant, heartbreaking, and sometimes funny sh*t that happens with epilepsy. By adding laughter to […]
Epilepsy Alliance America representatives attended the American Epilepsy Society Annual Meeting in Nashville, Tennessee on December 2-5, 2022. Board members, member organizations, and members of the National Professional Advisory Committee […]
Joyce Bender welcomed Patricia Dean, Epilepsy Network Liaison to her show, Disability Matters on November 22, 2022. Patricia Dean: Mission of Epilepsy Alliance America Tuesday, November 22, 2022 (voiceamerica.com) Epilepsy […]