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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.

Is There A "team" For People Who Have Gotten A VNS? I Am Considering It, And Curious To Hear About People's Experiences

A MyEpilepsyTeam Member asked a question 💭
Denver, CO
August 10
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A MyEpilepsyTeam Member

I am getting VNS on the 20th. No meds are working for me. So this is the next step for me

August 12
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A MyEpilepsyTeam Member

I believe the VNS website has an online chat group. Last time I was on the VNS website I had seen a chat group for support. I know there are private groups on Facebook for VNS that assist others who can answer questions. I also noticed that Liva Nova has a chat group that can assist answering questions.

August 10 (edited)
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