Be Informed

Patient Education

Trusted, free guides for living with epilepsy — from the Epilepsy Foundation, the American Epilepsy Society, and other organizations we trust.

These materials are for general education — always talk with your own care team about what applies to you.

New to seizures & epilepsy

A new seizure or epilepsy diagnosis brings a lot of questions at once. These starter materials from the Epilepsy Foundation explain what seizures and epilepsy are, how treatment usually works, and how to stay safe and organized in the early months — whether the diagnosis is yours or a loved one's.

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Seizure first aid

Helping someone through a seizure is simpler than many people expect. These free guides teach the basic steps the Epilepsy Foundation calls Stay, Safe, Side — along with when to call 911. They are worth a few minutes of your time even if you never need them, because someone nearby might.

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Understanding SUDEP

SUDEP (Sudden Unexpected Death in Epilepsy) is the topic many families wish someone had explained sooner. It is rare, but doctors bring it up because some of the risk can be lowered. These materials explain what SUDEP is, who is most at risk, and the practical steps and questions that help.

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Functional (non-epileptic) seizures

Functional seizures — also called non-epileptic or dissociative seizures — look like epileptic seizures but have a different cause, and they are real, involuntary, and treatable for many people. If you or a loved one has received this diagnosis, or if seizures have not responded to anti-seizure medication, these resources explain what is happening and where to find genuine support.

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Seizure safety & planning

Seizures are hard to predict, but you can plan for them. This page gathers free tools for building a seizure action plan, tracking seizures, caring for the everyday habits that affect them — like sleep and stress — and thinking through whether a seizure alert device makes sense. These materials are for people living with seizures and for the family, friends, and caregivers who support them.

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Driving in California

Driving is one of the first questions many people ask after a seizure diagnosis. California has its own rules for how doctors, the DMV, and drivers handle seizures — and losing your license is not automatic or always permanent. These resources explain, in plain terms, how the process works and what to expect.

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Paying for & managing medication

For most people with epilepsy, taking anti-seizure medication (ASM) every day is the main treatment — but paying for it, refilling it on time, remembering doses, and dealing with side effects can all be real challenges. These free flyers offer practical help with each one, including programs that lower medicine costs and simple systems for staying on schedule. Two of the flyers are also available in Spanish.

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Women & epilepsy

Epilepsy can affect a woman's health differently at every stage of life — from monthly hormone changes to birth control, pregnancy planning, and menopause. This page collects plain-language resources on the questions women and girls with epilepsy most often bring to their care teams, and how to make sure those questions get asked.

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Teens becoming adults

Sometime in the teen years, epilepsy care starts moving from a children's neurologist to an adult one. Planning that move early — instead of scrambling at 18 — makes it much smoother. These roadmaps from the American Epilepsy Society show what to work on at each age, whether your teen is headed toward full independence or will continue to need a caregiver's support.

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