Epilepsy Alliance America is a national organization, launched in 2018, dedicated to providing support, care, and service to those with epilepsy.
For more than 50 years, the Epilepsy Foundation has shone a light on epilepsy by promoting awareness and understanding, advocating for laws that matter to people with epilepsy, and funding epilepsy research.
A broad coalition of consumer, governmental, health professional, and advocacy organizations working to improve care for and advocate for people with epilepsy and their caregivers.
A website with comprehensive public and professional information concerning psychogenic non-epileptic seizures.
A registry for research to determine the safety of anti-epileptic drugs for pregnant women and their babies.
A network representing patients with rare epilepsy designed to establish a registry that will allow for patient-centered research.
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