Hey everybody! I haven't been around too much lately (been hanging around health anxiety boards instead) but I thought I'd come back and rehash some conversation with some members that I've gotten to know this past year. It was around this time last year when I stumbled upon this site. Between the muscle twitches and sensory issues, I was convinced I had MS/ALS. Fast forward 1 year, 6 neurologists, and 2 Brain MRI's later, I'm still here. However, that doesn't mean I feel any better. If anything, I feel as if I've deteriorated more. Being that it is summer, I've definitely noticed an increase in my symptoms, be it the twitches, the fatigue, and the parasthesia. My question to everyone here is, do you guys notice an increase in any type of symptoms when exposed to the hotter temperatures of summer? This truly drives me crazy and makes me feel so isolated. I specifically brought up this heat intolerance to an MS specialist I'm seeing but he did not seemed too concerned, as he told me that he wouldn't call it heat intolerance (I told him my left leg/left arm begin tingling when i sweat/am hot). What do you guys think? Normal or not normal?