Clarify CACNA1A

Welcome to the CACNA1A Foundation blog: updates on current research, advocacy efforts,
therapy options, community activities and real life experiences of caregivers.

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CACNA1A Foundation at AES2020

This past weekend we hosted a booth in the nonprofit section of the virtual exhibit hall at the American Epilepsy Society’s (AES) annual meeting. This conference is the largest meeting and exhibition in the world for those who share the common scientific and clinical interests of epilepsy and clinical neurophysiology. AES typically attracts more than 5,000 attendees dedicated to improving the quality of life for people living with epilepsy. Our booth’s visitors included clinical neurologists, researchers, pharmaceutical companies, other rare disease groups and various epilepsy-related corporations. We made some excellent introductions and formed new relationships that will further our mission of accelerating CACNA1A research.

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