vns therapy

Welcome to the Coping With Epilepsy Forums

Welcome to the Coping With Epilepsy forums - a peer support community for folks dealing (directly or indirectly) with seizure disorders. You can visit the forum page to see the list of forum nodes (categories/rooms) for topics.

Please have a look around and if you like what you see, please consider registering an account and joining the discussions. When you register an account and log in, you may enjoy additional benefits including no ads, access to members only (ie. private) forum nodes and more. Registering an account is free - you have nothing to lose!

I would suggest taking the time to read through the prior discussions (from the link Cint posted). There is a lot of information and personal experiences already shared in the forum.
 
I also have a VNS and I'm very happy with it. I've had it since 2007.

I'm unable to have surgery so my neuro suggested it. I'm still having seizures but not as many. I was having around 5 a week before it now I'm having maybe 5 a month at most. They aren't as bad as they were before either. I am still taking medicine too.

It takes awhile to get the settings right so don't expect to walk out of the hospital seizure free once you get it. The 'voltage' (I don't know what it's actually called) has to be increased gradually, and you have to find the right settings for you. I'm still having to get it adjusted every so often if my seizures start to increase.

If I feel the seizure coming on I can stop it. The only problem is that my auras are usually short. So sometimes by the time I realize that I'm having one it's too late. If I do know I'm having one and use it I won't have the seizure.

If I'm having a seizure and there is someone there with me they can use the magnet on me and it will bring me out of the seizure faster.
 
Back
Top Bottom