[HParks]

Hi Micki!

You’ll have to excuse the slowness of my reply. However, I’ve had the same problems with night sweats for the last couple of years. I’ve had problems with flushing from my Tecfidera and so I’ve always told people that I’m going through “the change”. Never mind that I’m a male (at least the last time I checked). I’ve started sleeping on a huge bath towel every night so the sheets aren’t completely soaked! My wife, God bless her, put some sheets and pillow cases that will prevent everything from getting soaked down so we don’t have to change the sheets every two days.

I’ve never heard of this being an symptom of MS, but nothing surprises me anymore.

Praying for both of us,

Howard

[HParks]

I’m sorry Ed. I just read the attached link you sent referring to your “no-sweat” situation. Very interesting what you posted!

[HParks]

Thanks for the reply, Ed! I wouldn’t mind switching to the “no sweating” for awhile. I’ve been trying to do some research on the cause of the “excessive” or “non sweating” phenomenon. Does it have to do with lesion location, or is it just the course of the disease. Why? I’m going to keep diving into this and will let everyone know what I find out, from a reputable source.

Thanks again!