Flashes
I need some advise! I was diagnosed with Multiple Sclerosis back in November of 2025 also with a spinal stroke, I went paralyzed from the chest down no feeling in my stomach area or half way down my back or my legs and feet…but praise GOD my left leg is holding me still dealing with the right leg weakness don’t have any sensory felling back yet…it’s been such a crazy roller coaster 🎢 and it’s like every day it’s something different! But the hot and cold flashes to me is just unbearable at times! From my back to my head my skins fells like it’s on fire with no relief and my legs and feet feel like they’re frozen from frostbite. But if you touch my skin everything feels normal burning during the day but at night I’ve been told by my family they can feel the heat coming off me without even touching my skin! Im constantly sweating or shivering. Im on Dimethyl fum for the MS plus the medication for muscle spasms. Is there anything for the flashing help so worn out from this issue 😭
I share that! My body thermostats broken too 🫠I have to wear as close to 100% cotton clothing as I can get. It keeps me from having to change sweaty wet clothes so often. I have a personal rechargeable fan and always have my body covered. If I get too hot I expose my stomach or reface my fan towards my face. Having short or no hair on my body also relieves the feeling of the crawlys when my hair moves and help with the prickly heat feeling. Plus I cover my head with a hat or beanie 24/7. I take it off to let my scalp breathe otherwise I get cradlecap bad.