Does any body else get severe night sweats with langerhans cell histiocytosis! Last night I woke up wet thru, as if I had been in a bath! 😩😩also the tiredness I get is unbelievable! 12 hours at night straight thru then another 3 hours in the afternoon! ShTtered!! 😩😩😩
Ugh night sweats!: Does any body else... - Lung Conditions C...
Ugh night sweats!
Don't know what langerhans cell hitiocytosis is but I can certainly relate to the rest of your post. I'm getting soaked at night recently - not hot, just sweaty. It's horrible. And I keep nodding off in the day, but manage to sleep at night. I'm wondering if latest medication is to blame. I've started taking stuff for bone strengthening. Are you on anything like that?
Hello. I had severe night sweats for a few months when I had a lung infection in 2012 (5 hospital visits for intravenous antibiotics). I had the idea of putting a tower around my pillow and underneath me in bed and that did help to keep me a bit less wet. Of course the towels, and pyjamas, had to be washed every day but I didn't have to wash bed sheets every day. The hospital very kindly gave me towels to sleep on.
Oh at least I'm not the only one! 😳