COVID-19 Statement
We at National Epilepsy Training are taking steps to ensure the safety of our staff and clients during the pandemic. Read more about this in our statement here.
Read NowAt National Epilepsy Training, we provide world class epilepsy training and care services to a wide range of organisations, practitioners, managers and individuals. We have one goal, to become the leading provider of epilepsy training and care in the UK.
At National Epilepsy Training, we provide a number of comprehensive services for our clients, including training courses, care services and expert witness and legal reports.
We provide training for epilepsy awareness and a wide range of other courses for healthcare professionals, educational staff, support teams and the general public. All of our courses are led by experts who provide a comprehensive understanding alongside solid learning outcomes.
Find out moreWe have a range of care services related to the successful management of epilepsy, including ensuring that an comprehensive care plan is in place. Our experts are passionate about high-quality health care and improving quality of life for people with epilepsy.
Find out moreWith a typical turnaround time of 6-8 weeks, our expert witness and legal report service is the ideal solution for law firms who want an impartial and thorough report. This includes primary evaluations, reports and if necessary court appearances.
Find out moreThe advice centre is our online resource for free information and advice on our services. Our blog posts cover a broad range of topics and knowledge that our clients may find useful.
Sturge-Weber Syndrome (SWS) is an extremely rare epilepsy syndrome that the most recent figures indicate only occurs in around 1 in 20,000 births, but could be as few as 1 in 50,000. With this syndrome, there is often a birthmark on one side of the face that’s often the first sign of SWS. This can…
Read moreUnverricht-Lundborg Disease (ULD) is a very rare epilepsy syndrome that research indicates only affects between 1 to 4 children in every 100,000. Most children with ULD will develop tit between the ages of 6 and 16. ULD is part of a group of epilepsy syndromes known as ‘progressive myoclonic epilepsies’ and is due to an…
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