Do people with RRMS have sensory symptoms that come and go without qualifying as relapses? Ever since I had my first and only relapse 1.5 yrs ago (numbness in one foot which cleared completely never to return) I've had various sensory symptoms in different body parts. Examples are tingling, icing, burning, pain, buzzing, and vibration with a duration from seconds to weeks. In my case the longer-lasting symptoms often fluctuate during the day and hence are not consistently present. Some such symptoms have disappeared, but I never know if they will reappear after months. All these symptoms are very mild and not clinical. Nothing has been as dramatic as my initial relapse where I experienced persistent numbness for three weeks. BTW I'm on Copaxone.
Does anyone else experience intermittent symptoms similar to mine? How often do you have relapses?
Thanks in advance.
Does anyone else experience intermittent symptoms similar to mine? How often do you have relapses?
Thanks in advance.
Comment