Fisher-Wallace CES Stimulator Device
 

Hey out there! It's nice to be back, I've been away from NT for quite some time... Got stuck in a rut, I guess. But I've found something that excites me for the first time in a LONG time. I have hope again! A friend has helped me discover the idea of CES devices (CRANIAL ELECTROTHERAPY STIMULATION) and I found the website for the Fisher Wallace CES device, and I'm telling ya, it sounds like a miracle! I only know what I've read/heard online so far, but I'm hoping that in conjunction with my current meds, that it could be exactly what I'm looking for (at least while I fight the good fight for ketamine w/my ins. and decide if I really want an SCS, very hesitant).

Anyway, if anyone has used this, or another CES (or similar) device, please let me know- any input is greatly appreciated! Will be seeing doc tomorrow, so I'm hoping to get much more info then.

Thanks everyone!

~C

There is a long thread on TDCS. Which sounds similiar to what you have described. Check it out. And welcome back.