Seizure Tracker

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Seizure Tracker

Seizure Tracker empowers people living with seizures to take control of their own healthcare.

02/03/2026

After a seizure ends, recovery doesn’t always happen right away.

The postictal state is the period after a seizure when someone may experience confusion, memory gaps, fatigue, headache, emotional changes, or temporary weakness. These symptoms can look different from person to person and they can take time to resolve.

Tracking what happens after a seizure is just as important as tracking the seizure itself. Postictal symptoms can offer valuable context for caregivers and clinicians when reviewing seizure patterns and recovery.

Learn more about tracking seizures and recovery with Seizure Tracker: https://seizuretracker.com/

01/29/2026

When your seizure data is easy to share, care can move faster.

Seizure Tracker’s EHR integration allows patient-reported seizure data, including medications, therapies, and seizure activity, to be shared directly with participating electronic health record systems.

That means fewer gaps between visits and clearer conversations with your care team, using the data you already track every day.

Learn how Seizure Tracker supports EHR integration:
https://bit.ly/4qBAtNS

01/28/2026

Seizure tracking and brain-responsive therapy work better together.

Seizure diary information recorded in Seizure Tracker can be combined with data from the NeuroPace RNS System for Epilepsy, giving doctors a more complete view of what’s happening between visits. When seizure details from daily life are paired with device data, care teams gain clearer insights to guide treatment.

By tracking seizures consistently, you’re doing the one thing your doctor can’t: capturing what life with epilepsy actually looks like day to day.

Learn more about how Seizure Tracker works with the RNS® System:
https://bit.ly/45sgmsV

01/27/2026

How do you share seizure data with your doctor?

With Seizure Tracker, you can turn your seizure diary into clear, easy-to-understand reports. These reports can be shared digitally or printed for appointments, helping your doctor see seizure patterns, medications, and changes over time.

Sharing real data helps support more productive conversations and informed care decisions.

Learn more about sharing your data: https://bit.ly/3YTtwvm

01/22/2026

Seizure counts don’t tell the whole story.

A peer-reviewed study in Epilepsia found that most quality-of-life priorities for adults with drug-resistant epilepsy extend beyond seizure frequency and severity highlighting the importance of tracking cognitive, emotional, and daily life impacts.

Patient-reported data helps make epilepsy care more meaningful and complete.

Full study: https://bit.ly/4sIU28k

01/20/2026

Managing seizures is hard enough; language shouldn’t be a barrier.

Seizure Tracker supports multiple languages, making it easier for individuals and families around the world to record seizure activity clearly and accurately. When seizure details are logged in a language you’re comfortable using, information is easier to understand, share, and act on.

Clear communication supports better care and stronger collaboration with your care team.

Learn more about Seizure Tracker’s language support:
https://bit.ly/3YH4lvS

01/15/2026

A new peer-reviewed study using Seizure Tracker data looked at a question many people with epilepsy worry about: Does missing a single medication dose immediately increase seizure risk?

In this prospective study, adults with frequent, drug-resistant epilepsy tracked seizures and medication use over nearly a year. Researchers found that occasional missed anti-seizure medication doses did not measurably increase short-term seizure risk for most participants.

That doesn’t mean medication adherence isn’t important, it absolutely is. But these findings suggest that brief, infrequent lapses are unlikely to trigger seizures right away, which may help reduce anxiety and guilt around the occasional missed dose.

This study highlights the power of real-world, patient-reported data to answer meaningful clinical questions and support more informed conversations between patients and care teams.

Read the full study: https://bit.ly/4jHkDP0

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01/14/2026

Every epilepsy journey is different, but shared data can help communities move forward together.

Seizure Tracker works with advocacy partners to create condition-specific resources that help families, clinicians, and researchers better understand seizure patterns over time.

See how community data supports:
🔹 Tuberous Sclerosis Complex: https://bit.ly/4sCTbpH
🔹 Lennox-Gastaut Syndrome: https://bit.ly/4sJdBNW

01/13/2026

Managing seizures often means managing medications, too.

Seizure Tracker’s Medication Management tool helps you log anti-seizure medications, dosages, and timing, then view that information alongside seizure activity. By tracking medication changes and seizures together, patterns become easier to see and discuss.

Clear records support better conversations with your care team and more informed treatment decisions.

Learn more: https://bit.ly/3NkF0W2

01/08/2026

For caregivers, confidence matters, especially when it comes to seizures.

Mark tracks his daughter’s seizures so her data is secure, accessible, and ready to be analyzed for patterns that may help tailor her treatment. Having reliable seizure records means better conversations, clearer insights, and more informed care decisions.

Your story could empower someone else.

Share how tracking helps you and join the conversation:
https://bit.ly/4ou1P7A

01/07/2026

A new study published in Epilepsia examined seizure forecasting using Seizure Tracker e-diary data to see whether advanced models could reliably predict seizures.

Researchers found that none of the five tested machine learning models performed better than a simple moving average approach, often called the “Napkin method,” for predicting seizure risk over the next 24 hours.

This study highlights why rigorous evaluation matters when developing seizure forecasting tools and the important role patient-reported data plays in advancing epilepsy research.

Study link: https://bit.ly/4q5jl2R

01/06/2026

Managing seizures often involves a team, and the Seizure Tracker Valet system helps keep everyone connected.

With Seizure Tracker Valet access, you can share a secure “Valet key” with caregivers, medical providers, or school staff. Each person receives only the tools you allow, whether that’s recording events, reviewing data, or generating reports.

You stay in control, and your support network stays informed.

Learn more: https://bit.ly/4p3rqUg

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Alexandria, VA
22310

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http://www.SeizureTracker.com/

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