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Your stories help to raise awareness of encephalitis among the general public and encourage and inspire others whose lives are only just beginning after encephalitis.
We also welcome short films, vlogs, music and more - if you would like to submit any media to us for consideration, please email [email protected] or call +44(0)1653 692583.
Alan's wife, Celia, fell ill with a rare form of encephalitis called Subacute sclerosing panencephalitis (SSPE). Here he shares their story and his reasons for supporting The SocietyRead more
Imogen's life changed when she was affected by Limbic Encephalitis at the age of 17Read more
James, a brewery owner from Yorkshire, fell ill with encephalitis in 2016Read more
Maddilyn was a typical five-year-old girl when she was affected by Anti-NMDA Receptor Encephalitis. Her mom, Tricia, writes about the devastating impact the condition has had on her daughter.Read more
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