Epilepsy guides and research in plain English
Clear explanations for adults living with epilepsy, parents, caregivers, and people supporting someone. Start with the question that matters today, then explore the research when you are ready.
Start with what you need now
You do not need to read everything. Choose one useful starting point for yourself or someone you support.
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Help someone having a seizure
Find first-aid steps, when to call 911, and a free one-page guide to print or share.
Practical guide
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Get ready with a seizure action plan
Understand what a personal plan covers and what to ask about rescue medicine if it has been prescribed.
Practical guide
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Understand an EEG and its results
Learn what the test records, what to expect, and what its results can and cannot tell you.
Practical guide
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Prepare questions after a first seizure
Find questions for the care team and a research review about the chance of another unprovoked seizure.
Care-team questions and research summary
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Learn about breathing changes during seizures
Read what a research review says, how its limits affect the findings, and questions to discuss with the care team.
Research summary with safety links
Explore recent research summaries Β· Get the weekly newsletter
More topics when you need them
Important: Epilepsy Policy & Research
ποΈ National Plan for Epilepsy Act (S. 494): Plain English Summary ποΈ
A clear, caregiver-friendly explanation of a bipartisan bill designed to improve epilepsy research, care coordination, and long-term outcomes in the United States.
Browse All Topics
Explore the full list of topic hubs to find what matches what you are dealing with right now.
Latest Epilepsy Research Summaries
New summaries are added regularly. Each post explains what the study asked, what researchers found, and what it may mean for real life decisions.
Epilepsy Explained FAQ
Epilepsy Explained brings together practical epilepsy guides and plain-language summaries of published research. It helps people living with epilepsy and those supporting them understand safety, tests, treatment questions, and new findings.
This site is for parents and caregivers, teens and adults living with epilepsy, and anyone trying to understand seizures and epilepsy care without medical jargon.
No. This site is educational and cannot replace medical care. Always talk with your neurologist or epilepsy specialist about diagnosis, treatment changes, or urgent symptoms.
We focus on studies that answer common real life questions about seizures and epilepsy. We prioritize topics like safety, medications, tests such as EEG and MRI, seizure triggers, sleep, quality of life, and what helps families day to day.
Most summaries explain what the study asked, who was included, what researchers measured, what they found, and the main limitations. We also add a βwhat this may mean for youβ section with practical, careful takeaways.
New epilepsy research summaries are added on a regular schedule. The easiest way to stay updated is to join the newsletter.
We base our summaries on published research and aim to describe findings accurately and clearly. Research can be complex, and no single study should guide a major decision by itself. Use the summaries to learn and to prepare better questions for your clinician.
We cover major epilepsy topics such as pediatrics, genetics, drug resistant epilepsy, SUDEP, status epilepticus, safety and first aid, imaging and EEG, devices and neuromodulation, ketogenic diet, pregnancy, lifestyle and sleep, and common comorbidities.
Use the Start Here section to choose what you need now: first aid, a seizure action plan, EEG explanations, questions after a first seizure, or research about breathing changes. You can explore one topic at a time and take your questions to the care team.
Yes. If there is a question you keep running into, you can send it through the newsletter page or contact option. We use suggestions to plan new topic guides and future evidence overviews.