Hey,

I have not been diagnosed yet. I have an appointment in London in 2 weeks with a autonomic neurologist.

I had a lot of cold tingle feelings all over my face a year or two ago, then it went away but I still get an odd tingle on my legs or sometimes random places now and again, so I assume my POTS is some form of PN.

I dont sweat as much as I should in certain areas, and I sweat loads on my hands, arm pits and feet. Not sure if healing the nerves can sort this out or if its permanent?

My main concern is getting some sort of relief from my POTS.