Journalism student, Abi Simpson knows exactly what it is like to have NEAD having been diagnosed with the condition in 2013. When asked to do an assignment for her University course, Abi jumped at the chance to research more into NEAD. You can read Abi’s resulting article here.
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On this page, people have been kind enough to share their stories. Some are people who have NEAD and some are from people who care for people with NEAD. We
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We have been asked to take part in a new research project. Study title The Effects of Repetitive Thoughts and Feelings in People with Chronic Seizure Disorders Institution The University of Sheffield About the study The project aims to explore two main areas: 1. People who suffer seizures often worry about these and have […]
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