Mission & Values


The Epilepsy Foundation, in collaboration with our community and network partners, connects the people, data and resources needed to address challenging health problems associated with seizures and the epilepsies—and promotes education, policy, research and systemic change that will foster measurable and sustainable improvement for all people living with epilepsy.

Read the full 2025 Strategic Plan:

Improve the lives of people affected by epilepsy through education, advocacy, research, and connection. 

Only a small fraction of the 3.4 million Americans affected by the epilepsies are directly engaged with the Foundation network. People with epilepsy continue to experience stigma around the condition, and diminished opportunities for education and employment. Health disparities and unequal access to care plague our systems. Federal funds appropriated for epilepsy research lag in comparison to other diseases with far lower prevalence. After decades of new therapy development, we are still controlling the symptoms – the seizures – without modifying the course of the disease or preventing it from happening in those at risk. Year after year, we continue to see our loved ones with epilepsy suffer in myriad ways. Lost opportunities, injuries, depression, hopelessness. We lose loved ones with epilepsy, sometimes far too early.

“Fight for the things that you care about, but do it in a way that will lead others to join you. - Ruth Bader Ginsburg

The Foundation must rise to meet the serious challenges we face in a new way, with increased focus, greater scale and efficiency, and stronger partnerships with all organizations in the space that are equally committed to improving the lives of people living with the epilepsies. Here, we lay out a plan to harness the power of collaboration for our work over the next five years to End Epilepsy® Together.

Changes at the Epilepsy Foundation

The Epilepsy Foundation has undergone a dramatic transformation this year. As one of the largest and longest-standing non-profit organizations dedicated to improving the lives of people living with epilepsy, the Foundation and its nationwide network has long held a leadership role in advocacy, education, direct services, and research related to epilepsy.

But... we know that the organizational model that has supported our work over the last 52 years is not sufficient to meet today’s challenges, nor will it thrive over the next 50 years of improving the lives of people living with epilepsy. We are currently comprised of a national organization (EFA) which supports a network of local chapter offices and affiliated local 501c3 organizations. We have been in existence since 1968, and yet there are too many examples of where we are falling short of what the epilepsy community deserves.

The Foundation must rise to meet the serious challenges we face in a new way, with increased focus, greater scale and efficiency, and stronger partnerships with all organizations in the space that are equally committed to improving the lives of people living with the epilepsies. Here, we lay out the scope of the challenges, the way we see our new role in the landscape, and our strategic vision for our work over the next five years to End Epilepsy ® Together.

Our Challenges

Epidemiological data indicate that 10% of Americans will suffer a seizure at some point in their lives; 1-2% will have epilepsy. Epilepsy is characterized by re-occurring unprovoked seizures and affects 3.4 million Americans. At least 50% of the total population of individuals with epilepsy will have started having seizures at less than 20 years of age. Compared to the general public, people with epilepsy have higher rates of premature mortality, injury, cognitive impairment, depression, social isolation, and unemployment.

Our scientific understanding of seizures and epilepsy has grown dramatically over the last decades, revealing that epilepsy is not a single disease. Rather, it is a heterogeneous set of disorders with genetic and acquired etiologies better described as “the epilepsies.” There is a wide diversity of seizure types, epilepsy syndromes, outcomes and etiologies. For some, epilepsy is a manageable chronic illness -- affected individuals have risen to the highest echelons of professional success. However, for others, epilepsy is a devastating and progressive disease leading to developmental delay, regression and early death.

Wide variations in epilepsy care delivery and clinical practice may also contribute to poor individual outcomes. Achieving the best possible outcome and highest possible quality of life for every person with epilepsy requires a system with at least four components; high-quality medical care, accessible community services, supportive environments in which to live, learn, work, and play, and an activated individual and family. Unfortunately, today, the health promotion components that support people with epilepsy often do not function as a cohesive system. Healthcare and social support and self-management programs are isolated from each other, making it difficult for anyone to experience truly comprehensive care.

Health disparities create poorer outcomes for some groups within our community, driven in part by social determinants of health. For example, there are racial and ethnic disparities to comprehensive epilepsy care. We know that anyone with a brain can have a seizure or develop epilepsy; the epilepsies affect people of all ages, genders, races, ethnicities, and socioeconomic status. However, the impact of an epilepsy diagnosis is not equal.

The Foundation’s strategic vision for 2020 – 2025 has five objectives (the ‘Five Pillars’). These Pillars were identified through surveys and collaborative discussions with our stakeholders during 2018 – 2019 and were endorsed by our Board of Directors. They create a bedrock for the structure of our organizational priorities over the next five years.

For each Pillar, the Foundation’s executive staff leadership defined Key Results that will – if achieved over the five years of this plan – demonstrate dramatic progress toward the goal of ending epilepsy together.

In order to achieve the Key Results, staff leadership will identify specific, measurable, organizational priorities for each year of this plan, and will implement those priorities through the work of its cross-functional teams and partnerships. We will measure and report our progress quarterly, seeking to be transparent with our internal teams and external partners, and to adapt strategies as needed to achieve our goals.

In each year of this Strategic Plan, the Foundation will identify one or more organization-wide priorities for each of the Pillars. Achieving each organizational priority will culminate in achieving our Key Results for the Strategic Plan. The organizational priorities are intentionally cross-functional, requiring teamwork across the Foundation’s departments and with network partners and volunteers.

We will build Epilepsy Foundation 2025 for maximum impact over the next five years with strategic investments and measured progress on each of these critical building blocks.

Current organizational priorities include the following:

  • Seizure Safe Nation
  • Epilepsy Learning Healthcare System (ELHS) and Epilepsy Digital Experience Navigator (EDEN)
  • Volunteer Force
  • Epilepsy Venture Fund
  • Epilepsy Digital Engine

For more information about our 2021-2025 Strategic Plan download the PDF below.

on Friday, February 04, 2022
on Friday, February 04, 2022


Epilepsy Centers

Epilepsy centers provide you with a team of specialists to help you diagnose your epilepsy and explore treatment options.


Epilepsy Medication

Find in-depth information on anti-seizure medications so you know what to ask your doctor.


Epilepsy and Seizures 24/7 Helpline

Call our Epilepsy and Seizures 24/7 Helpline and talk with an epilepsy information specialist or submit a question online.


Tools & Resources

Get information, tips, and more to help you manage your epilepsy.