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Rns Device Implant
A MyEpilepsyTeam Member asked a question 💭

I'm going to have the RNS implant in March. And all I want to know is has anyone else had it done and dose it work . I go in March to Vanderbilt medical center in Nashville Tennessee.

posted October 27, 2022
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A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member
I have had the RNS for several years now. I mainly had it implanted because I had previously had a lot of surgeries where the doctors wanted to gather information on my seizures but I didn’t have any of my bigger ones for them to see so they were all a waste. I have had seizures for 31 years now and I usually will just have 1 or 2 seizures per a month so I wasn’t expecting the RNS to make me seizure free. I chose to do it because now I can send seizure activity to my doctors everyday. Now if you have seizures more often it could possibly slow your seizures down. The RNS records my brain activity 24/7. Whenever I do have a seizure my mom touches my head with a magnet and that marks the spot where I had a seizure. Right before I go to bed I turn on the RNS monitor and stick a wand on my head. It will take a couple minutes for it to download. When it’s done I hit send and all of the info goes to the doctors. When I go see the doctors they get out their computer and can see everywhere I had a seizure and everywhere someone touched my head with a magnet. They gather information about my seizures too. Since I have continued to have seizures the doctors have raised the amps on the RNS. To do that I just have put their wand on my head while they do some adjusting on their computer. I never feel any vibrations or other things with the RNS. So hopefully it will help slow your seizures down and your doctors get more info on your seizures.

posted October 27, 2022 (edited)
A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member

posted October 27, 2022
A MyEpilepsyTeam Member

I have had the RNS for 4 years 1 battery replacement and a ton of adjustments. When I first got it i was having 12-14 seizures a month. Now I'm down to 4-6 so cut in half and some of them I barely even know I have.

posted October 30, 2022
A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member , You can reach out to @A MyEpilepsyTeam Member & get feedback from him because he has the RNS. I hope it works out well for you. Wishing you all the best. 🙏 Your friend in Texas, Becky

posted October 27, 2022 (edited)
A MyEpilepsyTeam Member

My MDS said RNS not for me. I will pray you have success with your implant. Vanderbilt is a great hospital! 🙏🏻✌️🙂👣🐾🐾

posted October 27, 2022
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