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Becky, who had encephalitis when she was 16, in May 2012, shares her story with us. She talks openly about her after-effects, and shares her advice for adapting after encephalitis. This film is part of our My Brain and Me Project. You can check out Becky's blog, all about her life after encephalitis, here: https://myencephalitisnotepad.co.uk ------------------------------------------------------------------------------------------------------------------------------------------------------------------ If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in... Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate ------------------------------------------------------------------------------------------------------------------------------------------------------------------ Follow Encephalitis International: 📢 Facebook: / encephalitisinternational 📢 Instagram: / encephalitisinternational 📢 LinkedIn: / encephalitisinternational