Every year more and more people (many of whom were previously led to believe they had epilepsy) are being diagnosed with NEAD. This can be a particularly unsettling time for sufferers and their carers, as very little is known about the condition. Even worse, there is no known medication as - although the seizues may LOOK like epilepsy - there is no link to the electrical currents in the brain and AED's are ineffective.
Anyone looking for information is invited to visit our website at http://nead-scotland.org where we have a large amount of information freely available along with links to other organisations who may be able to offer further support. Come and visit us, sign our guestbook and join our forum. All welcome.