Support line: +44 (0)1653 699599
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
Nearly a year ago, Annabelle was affected by encephalitis. Her parents wanted to do something to mark the occasion and represent the fight that Annabelle and others in a similar situation have to go through.Read 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
Lucy was affected by Anti-NMDA Receptor Encephalitis earlier this year. This short documentary tells her story.Read 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
Pete, from Scotland, was affected by viral encephalitis in early 2017. Here he tells us about the first seven months following his illness.Read more
Rafaela, 15, is an Anti-NMDA Receptor Encephalitis survivor. This is her story.Read more