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Responsive neurostimulation (RNS) as an epilepsy treatment?

Posted by caseybach @caseybach, Sep 9, 2020

I am wondering what experiences people have had with RNS. My son has had seizures since he was 7, has tried several different sezure medications and is currently on Brivacta, Onfi, Oxycarbazepine & has a VNS. Still having 4-6 seizures a month. RNS is our next hope, so if anybody has any personal experiences or info. I would greatly appreciate it. Thank you Casey.

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absentsenior | @absentsenior | 2 days ago
In reply to @lisalucier "@absentsenior - just to let you know that for your own privacy and security, I've removed..." + (show)
Profile picture for Lisa Lucier, Moderator @lisalucier

@absentsenior - just to let you know that for your own privacy and security, I've removed your personal phone number and exchanged it for private messaging you on Connect. If you've not yet used it, you can find the little envelope between your profile and your notifications in the top right of any Connect page.

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@lisalucier
Thank you very much.I had not realized that would be published throughout the team.

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