GuitarStrummerBGM
Well-known member
Hello all,Some of you may remember me, some of you may not. I frequented these forums from mid-2007 to early 2008, at which point I received my no-ALS diagnosis. I started twitching in January 2007. Now, nearly 3 years after the onset of my twitching I have new worries and I will say they are not about ALS, but rather the other sclerosis that terrifies people; multiple sclerosis.First off, I'd like to say that I am in no way, shape, or form weak. Until recently, due to time commitments and being a senior in college, I've gone to the gym every day and have seen marked improvement in both muscle mass and strength. I still twitch, without exception, every day and the frequency hasn't decreased. However, I've developed some new sensory symptoms that concern me. The first were some paresthesia's... pins and needles feelings in my feet and hands. We've all had this. It went away and came back, and I haven't had it in a few days. What I have now is some more odd sensations - mostly warm or cold - in my hands and feet. Burning, hotness, etc. wouldn't be an accurate description, as it's not painful... just warm. I also have a slight headache right now, but no sign of blurry vision or dull color perception, which is normally the first real sign in MS. I also, on occasion, feel brief pains that feel like insect stings on my body, but when I look, no insect is to be found. These don't happen that often and I've had these a long time... I can remember these even well before I started twitching. I also have some pretty bad upper back pain, which I've had for a while. Do any of you experience anything like this?