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A Family’s Fight for Seizure Freedom
Some stories stay with you long after the conversation ends.
In this episode of The CortiCare Podcast, Brad Beauchamp sits down with Ty, Lisa, and Charlie O’Connor to share the reality of navigating a rare genetic epilepsy diagnosis, years of seizures, hospital stays, clinical trials, surgeries, and the constant search for answers.
Charlie is one of only a handful of children in the world living with a rare GABRA2 variant. His journey has included more than 30 medications, EEG monitoring, infantile spasms, ketogenic therapy, brain surgery, VNS therapy, and breakthrough moments that gave their…
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