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Encephalitis - My Brain and Me - Tahla's Story

Tahla had autoimmune, NMDA receptor antibody encephalitis when she was 15. She spent 6 months in hospital, losing her ability to walk, talk, eat, drink, as well as experiencing psychosis and aggression. As part of her treatment, Tahla needed to be intubated numerous times. These intubations led to issues with her throat, meaning Tahla was feeding through a tube, silently aspirating, on thickened fluids and a moderated diet for months. At the time, the damage done to Tahla’s throat by the intubations was so severe her voice was less than a whisper. Her voice is louder now after multiple surgeries, but she is still unable to sing as before, shout, and even minor infections can aggravate the damage and affect Tahla’s breathing, impacting her daily life and activities. Experiencing these medical emergencies and outcomes in her teens has had a profound impact on Tahla’s mental health. In this film, she shares her experiences of encephalitis, recovery, and friendships, as well as her tips on how she has supported and improved her mental health since her hospitalisation with encephalitis. If you are a young person affected by encephalitis, the Encephalitis Society can help. We have advice from other young people affected, young volunteers, videos about young people’s stories, and more... Visit https://www.encephalitis.info/young-p..., or reach out to [email protected] to learn more. If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/join-us If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/... Follow the Encephalitis Society: Facebook:   / encephalitissociety   Twitter:   / encephalitis   Instagram:   / the_encephalitis_society_   LinkedIn:   / the-encephalitis-society