I think the surgeon did a bad job, it's not the stimulator. When he implanted the first one it took him a hour longer because of the condition of my spine. Who knows what he cared not to do the second time. Obviously I will not have that surgeon for the third one. I understand my pain management doc is going to do it.
I have just done some research on two of my conditions, small fiber neuropathy and complex regional pain syndrome. They are both on the move. It seems my left butt is the latest conquest. That makes the whole left leg and foot united in SFN and much also in CRPS. I was told today that my left vagus nerve is non-functioning. Rather unique way that was discovered. My PT took a course this past weekend on the vagus nerve. She asked me to open my mouth and say ah three times. The left side of my uvula did not move. Thus my non-functional vagus nerve. She put a patch of kinesio
tape in my left ear. Fascinating stuff. Also was given homework. I need to sing to help get my diaphragm moving! Sure beats meds.
I still believe the stimulator is effective simply from my first. While disappointed with my current one, I do get relief in several areas. A trial should cement your decision. It's not that terrible a process.
Thanks for getting back to me. Would like to stay in touch.