When my symptoms began the end of February they resembled Restless Leg Syndrome. It was not until the end of May when some of them started to lessen that the burning,stabbing, pins and needle pain of neuropathy became clear and I saw a Neurologist who confirmed it. I had some tests (Not a biopsy yet) and the neurologist told me it was most probably length dependent SFN.
The beginning of August my night time twitches (which I am still not sure if those were RLS or neuropathy) stopped. (I still get the beginning of those occasionally.) My burning is not as bad and not as constant as it was. I am so afraid of becoming hopeful because I have read that symptoms change. One leaves, another comes. Does anyone have experience with this so I may know what I can watch out for. It is not my desire to drive myself crazy, I just want to stay informed.