Epilepsy Alliance America will be SHARING SOLUTIONS this November in recognition of National Epilepsy Awareness Month.

SHARING SOLUTIONS amplifies our mission statement which was updated as part of our strategic planning process earlier this year.
Epilepsy Alliance America is A National Community, Building Local Solutions, for people impacted by epilepsy.

SHARING SOLUTIONS is in our DNA as an organization. 

As a collaborative of organizations dedicated to serving the needs of people who live with seizures and epilepsy every day our member organizations are always SHARING SOLUTIONS with each other.  Our member organizations work collaboratively, boldly advancing the mission and vision of Epilepsy Alliance America together.

As individual organizations, our member organizations and our partners, are SHARING SOLUTIONS with people with epilepsy and those who love them every day. The information they provide, the services they deliver, the connections they foster – all provide hope and  possibilities for individuals and families affected by epilepsy.

Together, with our member organizations, we are SHARING SOLUTIONS for…

Our member organizations provide connection points for people with epilepsy and their care partners so that they know they are not along.

The member organizations in our networks connect with each other, sharing tools, resources and information.  Connecting with each other they are building capacity in their organizations to provide better support to their constituents.

No one should face epilepsy alone. Through support groups, family outreach, and community programs, our network offers comfort, understanding, and hope.
Every day, organizations in the Epilepsy Alliance America network are connecting people with the care and compassion they deserve.

Through Seizure Response Training, Seizure Action Plans, Seizure Safety Tips we are SHARING SOLUTIONS for people with epilepsy and those who care for them.

We’re proud to help students with epilepsy and seizure disorders walk confidently through them. The Lorna Myers PNES Scholarship Fund provides financial support to students with Psychogenic Non-Epileptic Seizures (PNES), helping them pursue higher education and honoring their resilience and determination. Many of our member organizations also offer scholarship programs, expanding opportunities for students impacted by seizures across the country to thrive and achieve their goals. Together, we’re sharing solutions that empower students to learn, grow, and succeed.

Knowledge saves lives. Through Seizure Recognition and Response trainings, Epilepsy Alliance America and its member organizations provide school staff, law enforcement, and community groups with the tools to recognize seizures and respond with care and confidence.

Through information and Referrals we are providing education to patients and families so they can make the informed decisions about their epilepsy treatment.

Our National and state-wide advocacy efforts are all aimed at SHARING SOLUTIONS for people with epilepsy across the country – no matter where they live.  Across the country, our member organizations are working to shape policies, protect rights, and ensure that people living with epilepsy are heard, included, and protected - from the classroom to the workplace to the halls of Congress.