(April 15, 2025): Epilepsy Alliance America is proud to have joined the 117 undersigned organizations – representing people living with epilepsy; caregivers and loved ones; physicians, care providers, and epilepsy […]
April 11, 2025 What Do Sweeping Government Budget Cuts Mean for Epilepsy? Federal health agencies have long funded epilepsy research and patient support. Now the future of those efforts is […]
EPILEPSY is not a red issue or a blue issue. It is a PURPLE Issue. Almost 3 million adults in the United States have epilepsy. About 456,000 U.S. children 17 […]
Epilepsy Alliance America is proud to support this legislation which was reintroduced in March, 2025. You can read the Press Release on Senator Booker’s website. (March 14, 2025) WASHINGTON, D.C. […]
Epilepsy Alliance America is proud to have joined the Partnership for Part D Access Coalition. The Partnership for Part D Access is dedicated to providing opportunities to bring awareness to […]
Red tape should never stand between a child and their treatment. That’s why we’re urging lawmakers to support the Accelerating Kids’ Access to Care Act. Every child deserves the best […]
Epilepsy Caucus Co-chairs, U.S. Senators Eric Schmitt (R-MO) and Amy Klobuchar (D-MN), along with U.S. Representatives Jim Costa (D-CA-21) and Greg Murphy, MD (R-NC-03) reintroduced the National Plan for Epilepsy Act […]
Epilepsy Alliance America is committed to keeping telehealth accessible. The goal is to protect telehealth as a lasting, meaningful tool for patients and health care providers. Epilepsy Alliance America recently […]
Episode 21 ~ Epilepsy Alliance America Voices for the Brain: American Brain Coalition Released just in time for November, Epilepsy Awareness Month…. Listen in as Katie Sale, ABC Executive Director […]
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 […]