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Ciara's Encephalitis Story
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A rare brain disease changed my life.
In May 2022 I was 25 years old and I got diagnosed with a rare brain disease called Anti-NMDA Receptor Encephalitis.
I have posted a long version and a short version of my story, so get yourself a cup of tea and feel free to read as much as you want.
I have also added a short video if anybody is interested in seeing some pictures and videos.
Thank you for reading my story.
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For more information on Encephalitis and how you can help please visit https://www.encephalitis.info/
This is my experience with Anti-NMDA Receptor Autoimmune Encephalitis.
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