Thanks Vanna!
I was hoping to hear from SCS patients.....i see that the last posts were clear back in Sept. I hope they come back to share, I'd like to get to know them and to see, how they are doing with their's.
Good that you brought up the 'scar tissue' issue <--- cool rhyme!
That is one of the things that are a potential problem from what I've read.
I wonder if there are any 'preventative measures' a person could do ?
Probably not.
Too bad there isn't a way they coulda wired both your units into ONE battery so that you don't have to carry around 2.
I'm waiting for insurance approval. Did you have a hard time getting yours covered by insurance? I did the psyche eval and the doc wrote in a letter of "medical necessisty"......so we'll see where that leads.
There's still a small part of me (cold feet) that is wondering if this truly is what i need to do. I keep hoping that I'll have some phenominal 'breakthru' and find out that i was simply gluten sensitive or something.
I was tested twice for Lyme, amongst other 'toxicity' blood draws....i guess i'll never actually know the real cause of the PN.

I hope to hear from the others soon and i hope they are doing well with their implants.
TTYS
Rae