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Real members of MyEpilepsyTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Does Anyone Have The Neuropace Rns System? If So What’s Your Opinion On It?

A MyEpilepsyTeam Member asked a question 💭
Van Buren Twp Michigan
April 25
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A MyEpilepsyTeam Member

Thank you for your input.

April 25
A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member can you tell me how long the surgery was, what was recovery like, how long were you in the hospital and how long were you off work?

May 25
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A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member , Reach out to @A MyEpilepsyTeam Member , he has the RNS. Your friend in Texas, Becky

April 25 (edited)
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A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member
I was in the hospital for about a week when I had the RNS surgery. I couldn’t tell you how many hours I was out. I wasn’t able to work or lift anything heavy for about 10 or 11 weeks. The recovery was kind of painful. It hurt to even lay my head down on a pillow so I got one of those neck pillows. I laid the scar over the open hole so it didn’t put pressure on the womb. I wish you luck.

May 25 (edited)
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A MyEpilepsyTeam Member

@Ibrokenshire
I have had the RNS system for about 5 years. Before I got it I had so many EEG’s, including a surgical one, where I didn’t have any big seizures so they were a waste. The RNS not only helps reduce seizures but it also records your brain information everyday. Whenever I have a seizure or aura someone touches my head with a magnet and that marks that spot important. Before I go to bed, every night, I turn on the RNS and place a wand on my head. It will take a minute or two for it to download any seizure information. When it’s finished downloading I hit “Send” and all of the information goes to my doctors. When I go see my neurologist and RNS squad they get out a monitor and can see everywhere I had a seizure or aura and everywhere we used the magnet. Most of the lines are level but when they go to a spot I had a seizure the lines get bouncy ———wwwww——-. They write down whatever information. Since I still have some seizures the doctors have risen the power many times. To do that they just place a wand on my head and make some adjustments on their computer. I never feel anything. I do still have seizures but I think they’ve decreased. I only have 1 or 2 seizures per month but if you have more seizures you’ll probably see a bigger decrease. So I’m happy I go the RNS.

April 25 (edited)
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