How many of you experience a "dripping water sensation" or "cold spot sensation"

Hello, curious do alot of MS patients also experience the feeling that there is water dripping on a part of your body or feel like there is a sensation of a draft on a part of the body that is not exposed to any cold or wet? Thanks!

I have had that type of feeling before. Most of my symptoms in my legs especially are sensory and the last time I had problems they were completely numb for a couple of months. When they started getting better I had that "wet" kind of feeling. It's kind of hard to describe, but I do remember thinking I could pee my pants or spill something on me and would not have even been able to tell. I was worried my legs might not ever get back to normal again but after my first dose of Tysabri those symptoms resolved (and have not come back for six months now, YAY!).