Hi everybody, I'm new here, just wanted to pop in and say Hi first thing. I've had RRMS since 1996. One of the most irritating things I've experienced, and am currently experiencing, is the numbness I have blocking symptoms of illnesses. I recently ended up in the ER with blood in my urine because I had no idea I have a pretty bad UTI. I always let physicians know that my scale of 1-10 when they ask about illness or pain is not going to reflect reality due to MS. My 2 may be a 6 to somebody else and vice versa. Anybody else experience this kind of thing? It's no fun.