Hello there!

We have another forum here at NT that might provide you with even more info regarding SCS for face pain/Trigeminal Neuralgia. Our good friend "Burntmarshmallow" will no doubt have some good insight to offer. You'll see her name when you get over to that forum. Be sure to check out the upper part of the page there in the "Sticky" section. VERY helpful stuff that Burntmarshmallow has provided.

Here is the link to get you to that forum:

http://neurotalk.psychcentral.com/fo...aysprune=&f=26

I bet you can appeal your insurance's denial. Hopefully you'll get feedback on this. Hang in there and we'll round up some help, K!
Keep us posted

Rae