Blog
The advice centre is our online resource for free information and advice on epilepsy and our other services. Our blog posts cover a wide range of topics and provide valuable knowledge that our clients and others may find useful.
When a child is diagnosed with epilepsy, one of the first questions asked by parents is often “What does the future look like? Will my child always have epilepsy?”. Epilepsy is extremely varied and can affect each person diagnosed in different ways. Some people with epilepsy will have a handful of seizures in their entire…
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As you may already know, here at National Epilepsy Training, our epilepsy awareness training courses are designed to ensure that anyone who may need to be is aware of epilepsy and knows how to react in emergency situations. This could include parents, teachers, employers, carers or nurses and other healthcare professionals. In this post though,…
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Unfortunately, the misdiagnosis of epilepsy is fairly commonplace and it can have a significant impact on the person who has received the misdiagnosis. Epilepsy misdiagnosis continues to be a huge problem, as it’s estimated by the World Health Organisation (WHO) that up to 70% of people living with epilepsy could be seizure-free, but only if…
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The MCT diet is sometimes used to help treat epilepsy in children and reduce the frequency and severity of seizures. The diet is similar in many ways to the classical ketogenic diet, but the MCT simply refers to an oil called medium chain triglyceride that makes the diet more varied and allows the child to…
Read moreCategory: Education, Living with Epilepsy
Recently, we wrote a blog article on the genetic factors of epilepsy. We also mentioned that in many cases there are no genetic factors to epilepsy, which is known as acquired epilepsy. Acquired epilepsy can be used to describe a number of causes that are not genetic in nature, this means they were not passed…
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Stigma in epilepsy can mean a number of things, whether it’s people believing untrue myths, people being disqualified from activities they feel they could take part in or simply just being treated differently due to having epilepsy. Stigma and discrimination take many forms. A common example might be children being left out of school activities…
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