Alan's Story

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

Annabelle's story

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 Story

Imogen's life changed when she was affected by Limbic Encephalitis at the age of 17Read more

James' Story

James, a brewery owner from Yorkshire, fell ill with encephalitis in 2016Read more

Lucy's story

Lucy was affected by Anti-NMDA Receptor Encephalitis earlier this year. This short documentary tells her story.Read more

Maddi's story

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's story

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's story

Rafaela, 15, is an Anti-NMDA Receptor Encephalitis survivor. This is her story.Read more