Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I have had sweats aswell. The one that sticks out most is for about two weeks, maybe less, I had sweats from the neck up to the point of soaking one side of the pillow and the rest of my body was dry. I have other sweats where I have covers on my uper body while my legs have no covers and only my legs are sweating.
Kj
Matz...I had this problem too...in addition to being "Heat Intolerant!" I started noticing, that right after my total hysterectomy (all bodily hormones were instantaneoulsy thrown into utter CHAOS!)...that I could no longer sweat...not even with the Flu & 104 temp!! I lived/live in Oklahoma...where it often gets over 100 degrees in the summer! NOPE...that didn't do it either! I didn't EVER sweat again...until about 4 yrs ago...when all my MS symptoms started...that I started sweating again. I remember, bc I had come down with a bad case of the Flu (confirmed by a lab test) during this time...sending my symptoms through the roof...& I had noticed that for the 1st time, in almost 20 yrs..I WAS SWEATING!! I've been having these COLD, SHIVERING/HOT, SWEATING SPELLS ever since...only, they are gradually getting worse with time (were mild at 1st).
I've often wondered if going all these years, not sweating, has done something "permanent" to my internal temp system?? I kept asking docs about it...but they just kept "blowing me off!" I'm SOOOOO SICK of Doctors & their unsympathetic cold shoulders...trying to blame EVERYTHING on STRESS & ANXIETY!!! REALLY??? COME ON DOCS...GET REAL!!!!!!!!
(OK...SORRY...guess I'm through ranting for now!) {[hugs}}
~tj