blobWho are we?
blobNEAD in numbers
blobHow this site works
blobContact us
blobWhat are non-epileptic attacks?
blobAre NEAs common?
blobWhat do NEAs look like?
blobWhat do NEAs feel like?
blobWhat about my other symptoms?
blobHow are NEAs diagnosed?
blobDo I have epilepsy?
blobHow to feel about the diagnosis
blobWhat causes my attacks?
blobEarly life factors?
blobWhy do NEAs start?
blobWhat can trigger further attacks?
blobWhy have the attacks not stopped?
blobHow do these factors act together?
blobHow can stress cause symptoms?
blobWhat if people don't believe me?
blobWhat do I tell people?
blobWhat should people do?
blobWhat can I/my family do to help?
blobHow can I help myself get better?
blobShould I stop doing anything?
blobWhat can my family do?
blobWhat if I get worse?
blobIs there any treatment for NEAs?
blobWhat can help?
blobWhat is psychological treatment?
blobDifferent types of psychotherapy?
blobWho can help?
blobWill I recover?
blobHow can I find out more?
blobCan I drive with NEAD?
blobCan I still claim benefits?
blobAre there any support groups?
blobYour personal stories
blobFurther Support
blobGlossary

Your personal stories

What is it like to live with non-epileptic attacks?

The mother of a NEAD sufferer:

Our daughter was referred to the Neuro team where they decided the seizures leaned towards a condition called NEAD. We were totally unaware of the existence of this condition and then had to 'educate' ourselves about it, as I believe the more knowledge gathered makes you less fearful of what is a very scary, frightening and isolating situation.
Seeing someone in a full 'Tonic Clonic' seizure is a scary thing to witness, the feelings of being powerless and not able to help is beyond upsetting. Still with these seizures ongoing, our daughter has now just completed a block of dynamic psychotherapy, which is thought to be helpful for this condition of NEAD. We can only keep our fingers crossed and be hopeful and glad that this is a positive step and something in the way of support.

 

The story of a 64 year old female sufferer:

Approximately 7 years a go I saw a consultant neuropsychiatrist and a consultant psychologist and together with the epileptologist an answer for the seizures, the blackouts the amnesia the depersonalisation and ‘splitting’ as it was described to me, was finally diagnosed as dissociation.
Since the diagnosis and the treatment many things have surfaced which I had kept locked in behind a door deep within my mind.  I am not receiving any more treatment. It seems that there is nothing more to offer. I have been recommended for counselling but I am still waiting as it appears not every professional in the counselling field would be happy taking on a case such as mine. The thing I hate most about this disorder is not just the effect it had and still has on me but on all those people who over the years have lived their life's alongside me.

 

S’s daughter aged 13 has recently been diagnosed with NEAD:

2 weeks ago Jade had 12 seizures in one day and after her 2nd seizure she lost all feeling in her arms and legs for 12 hours.  Again we were taken into hospital via ambulance.  The A&E staff were amazing. Then the paediatric consultant came into A&E and asked myself and my husband if we knew what was going on and his answer was "WELL SHE'S FAKING THIS". Well you can imagine our reaction!  Jade has now been excluded from school of which she was attending 2-3 hours a day as the staff can't cope. We really feel that with NEAD there is just no help and not enough information out there.  THIS IS NOT FAKE THIS IS VERY VERY REAL and affects everyone's life around the person suffering.

 


We would very much like to hear your personal stories about how NEAD has affected your life. You might be a patient, a family member or friend. Let us know your story by contacting us here.

 


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