These 2 diagnoses seem to go hand in hand. I have PN diagnosed by my neurologist (SFPN actually), and RSD diagnosed by my pain specialist (who implanted my SCS).

I'm wondering how others describe their pain.
Maybe this is a question that should be posted on the Chronic Pain forum, but some of our SCSers are wondering what the difference is because it might dictate whether or not they are considered a candidate for this implant.

I hope MrsD sees this so she can give her input.
I'll send out a pigeon with a special note to get her attention

Thanks
Rae