
EAN works to help individuals with epilepsy and seizure disorders by promoting community education and awareness. Their services include, but not limited to, First Aid training, support groups and helping to obtain seizure alert devices.

Founded by parents who lost their son to SUDEP. Their main mission is to prevent death caused by seizures. Their vision is that healthcare providers proactively communicate about the risk of SUDEP. They help in awareness, support and obtaining devices.

Their mission is to improve the lives of people affected by epilepsy through education, advocacy, research and connectivity. Their vision is that no one has to go through their Epilepsy journey alone.

Founded by parents who lost their daughter to SUDEP. They believe education starts in the Dr's Office. They are committed to patients & caregivers obtaining information about SUDEP & the SAD's so that they can make informed decisions about their unique diagnosis.
The Butterfly Effect
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