Greetings all,
After a visit to my NS today, we have come to the conclusion that the MVD I had in January was a failure for controlling the TN2 pain. Iw as very hopeful that I would have a better outcome, but must now move on. My surgeon has suggested peripheral neuro stimulation to help control the constant burning pain in my scalp. I am interested to hear if any of you have had this, and would appreciate you sharing your experience with me. I did go to the neuro stimulators group, but did not find many posts.
As always, thanks for your insight and support.
Best
Christine
Bump
Did you type it in the search box?
Also put in
pain shield
seems good results with that here
Bump!
http://www.livingwithtn.org/forum/topics/peripheral-nerve-stimulator
http://www.livingwithtn.org/group/atypicaltrigeminalneuralgia/forum…
http://www.livingwithtn.org/profiles/blogs/has-any-one-had-a-periph...
http://www.livingwithtn.org/forum/topics/new-treatments?commentId=2...
Thanks Mimi!