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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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Ciara's Encephalitis Story - Short

2022 started off as a normal year. I was 25 years old; I had the perfect life with my boyfriend Joe, a nice job and the best friends and...

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Ciara's Encephalitis Story - Long

Before 2022 started off as a pretty normal year. Me and my boyfriend Joe had been together for over 4 years and we had not long moved...

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