Hypothermia and MS
Does anyone go thru random Hypothermia when your body can't adjust to the temperatures? Man does it hurt and I freeze til I can get warm,this happens all year long depends on room or outside temps and wind really I don't understand how to control this
Well Weirdest thing ever is my body tempreture I have white skin yes white arab My skin ia so thin Tempreture heee is 9 in saudi arabia my feet are burning because im wearing sucks When i was in edinburgh during winter i felt as if i was walking on lava just because i was wearing shoes during the winter in edinburgh scotland i was off treatment back then didnt use ti believe dmt is effective I have neuro burny sensation and its the worst I got a fan to wear on my neck My weight is 46 on 157cm Skelton i know lol i drink a lot of caff and not eat much
I feel this in my bones (or at least my feet and hands hahah). I've always been the type of person who runs cold - give me a shower that's a few degrees short of boiling and I'll be comfortable :P Post diagnosis, my hands / feet will go completely numb pretty quickly. I haven't figured out a way to really "control" it - but if it's really bad (especially with my feet) I'll stand in my bathtub and run warmish water on them till the feeling returns. I also do try to get up and move to keep my blood moving if I start feeling the tingle in my toes. I've got a couple pairs of really thick hiking socks that I throw on once I'm warmed up - and I've got a little rechargable hand warmer that I keep on me at all times. It's not a perfect solutions, but I've found it helpful. I know how painful it can be both feeling that cold and the process of warming back up T_T, but you're absolutely not alone!!