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

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

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