Epilepsy Alliance America joined 23 organizations representing people and families living with and affected by, the epilepsies urging Congress to maintain the Orphan Drug Tax Credit (ODTC). In late November, […]
Epilepsy Alliance America proudly exhibited at the 75th Annual Meeting of the American Epilepsy Society in Chicago, Illinois on Friday, December 3 through Monday, December 7, 2021. Epilepsy Alliance America […]
Lisa Gallipoli, Epilepsy Alliance America COO, hosted a virtual Expo Table at (virtual) Epilepsy Awareness Day in November 2021 and shared a little about ‘who we are and what we […]
Baton Rouge, LA: Epilepsy Alliance America announced today that it will be providing 3,000 Seizure ID products to people with epilepsy who need them through a one-of-a-kind campaign in the […]
Epilepsy Alliance America is a proud member of the Infantile Spasms Action Network (ISAN) – a collaborative network of 30+ national and international entities dedicated to raising awaress for IS. […]
Baton Rouge, LA, November 12, 2021 – Epilepsy Alliance America (EAA), a nationwide network of community-based epilepsy organizations dedicated to providing direct care, education and support services to people living […]
Thank you to Joyce Bender, Epilepsy Alliance America Board Member, for having Allison DeBattista and Liza Gundell, fellow Epilepsy Alliance America Board Members, as her guests on DISABILITY MATTERS on […]
Epilepsy Alliance America is a proud member of the International Bureau for Epilepsy. In recognition of November as Epilepsy Awareness Month, the North America region of the International Bureau for […]
Call to action: Are you a parent or caregiver of a child with epilepsy? Help researchers at Duke University understand how healthcare providers can best communicate information about Sudden Unexpected […]
Epilepsy Alliance America is proud to be supporting Safe Step Act (HR 2163 / S464) This legislation would provide patients and providers with a clear and transparent appeals process when subject […]