I’ve been diagnosed with RRMS for about 2 years now. I haven’t been put on any medication yet, though we’ve come to a decision to get me on Tecfidera in the next few months. However over the last 8 months I’ve had regular night sweats and I just wondered if this is another ‘common’ symptom that other MS’ers get? He’s running blood tests to rule out other things before I go on Tecfidera, but my doctor didn’t seem to think it was that common a symptom.
I seem to go to bed with extremely cold feet and hands (plus tips of my nose) most nights despite being warm everywhere else, and then awake in a pool of sweat around my face and torso. Lovely!
Does anyone else have this problem?
Thanks in advance!
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