Don't let this rare illness isolate you from others. Becoming part of some autoimmune encephalitis support groups has not only done wonders for my mental health—it's equipped me with the info I've needed to advocate against dismissive doctors for diagnosis and treatment.

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This segment is part of the World Encephalitis Day countdown series, which culminates on February 22, 2021!

You can find more insight into my story on my blog, http://wherearemypillows.com/

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