I recommend to notice if anything else may have contributed to the feeling. Diet, exercise, may be factors. My hands and feet were numb/tingling right before I was diagnosed. The tingling in my feet went away but my hands have tingled (sometimes it was very noticible and others not as much) for almost 3 years. I think of the tingling as one of the things I track and discuss with my neurologist (along with my other symptoms).

@jessa my personal experience over the past few months of having these symptoms was... scared shitless like urself, wondering what was going on and what is going to happen. Now a few months down the line i think ok so this is now part of life, it irritates the fcuk outta me but stressing makes it feel worse and possibly brings on more symptoms. So now, I try ignore it, it's here for life and the burning, tingling, cramps, numbness, coldness, foggy eye (my main day to day symptoms) is just there it's a part of me and now I just have to manage it and that way I find I forget about it most days. So my advice for you, make notes, seek advice from the professionals if ur worried or if it's a new symptom uv not felt before, learn to manage your ms by not over doing it and as mcgilligan above said think of diet, exercise etc n anything that may have contributed to make it worse or what may make u feel better then include or illuminate it! Just Try not to stress about these things as they will make it worse, carry on with life be strong and fight it :D