Brain Fever Podcast

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Mother, psychiatrist, and one of the four co-founders of the Autoimmune Encephalitis Alliance, Dr. Helen Egger, talks about having a child with AE and gives hope to other AE parents.

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In this episode, Jackie welcomes Caterri Woodrum, CEO of the AE Alliance. They discuss AE statistics, and how the AE Alliance can help patients and carers.

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This episode of Brain Fever commemorates Jackie's second year of remission since her diagnosis with AE. Special guest Dr. Ava Easton, CEO of The Encephalitis Society, joins Jackie to discuss recovery and rehabilitation post-encephalitis. Dr. Ava is the author of the book, "Life After Encephalitis," and she speaks at conferences and lectures around the world on various aspects of encephalitis and its consequences for patients. Her expertise also extends to neuro-narratives, narrative medicine, and patient and public engagement.

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In our final episode, Jackie interviews Sean about Jackie's Autoimmune Encephalitis....from beginning to end. I wasn't really looking forward to this...not my favorite subject, but, I know there are some caregivers out there that are going through or have went through a similar process.

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Today, we took questions from listeners from our listeners for Jackie.

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Jackie describes her stay at the Sanford Psychiatric Ward, St. Alexius Hospital after her Grand Mal Seizure and her 4 visits to the Mayo Clinic. Also, a few funny stories on the road to recovery.

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In our first episode, Jackie talks briefly about the beginning stages of her Autoimmune Encephalitis. AE is different for everyone, so, Jackie is sharing her experience.