Hello to fellow Neuropathic POTS patients,
I'm curious as to the trajectory of your POTS. Here, by Neuropathic, I presume the existence of small-fibre neuropathy and its associated features (burning sensations, pinpricks, electric shocks, goosebumps, etc). Some studies have said that neuropathic pots patients had a higher rate of recovery, some others draw no conclusion. As a result, I have two main questions
1). Has your POTS stayed the same, worsened, or progressed?
2). For each of the above, does the small fibre neuropathy correlated with it (less tingling and burning if its