Night Sweats?

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Does anyone else have problem with really bad night time sweating? Last few night i have had to change my sheets at least once or twice or sleep with a towel due to massive sweating. I checked my temperature and it may have been because of the sweating and the cool air but it was at 95.9 which is WAY below normal temp... Any ideas?
 
When I was flaring really badly, I would get horrible night sweats. I could literally wring my sheets out in the morning, regardless of what the room temperature was. My GI told me that night sweats are a result of your body trying fight inflammation.

Since I have been in remission. The sweats have pretty much disappeared. The only advice I can offer is to make sure to drink a lot of fluids, so you don't get dehydrated. I couldn't really figure out any way to reduce the sweating, while I was flaring.
 
yes, i get night sweats... it seems to be in my neck area the most... the collar of my shirt will be pretty wet halfway through the night... i wouldn't say it's horrible, bt noticeable and slightly uncomfortable.

i also wake up frequently to use the washroom, but it's not the big D, it's just peeing like 4 times a night. not sure why. it's been like this even before meds.
 
well mine have been to the point of where it seems like someone has poured water on my bed, and of course when i get up to go to the bathroom and i come back the cool air has hit the sheets and turned cold as hell so i either have to throw some towels down or change the sheets. I'm thinking about just using towels instead of sheets, seems much easier.
 
I get these when I have had a rigorous physical workout. I think it is just the repair process.

If you are not working out physically, that is something different. The only other time I have this is if I have virus or something of that nature.

Dan
 
i get night sweats too, like i've been dunked in cold water. i know what you mean about wanting to sleep on towels instead of sheets! when i'm flaring i change my pajamas every time i wake up.
 
Yes, I get night sweats too. I thought I was too young for menapause and my mother didn't start going though menapause until way late in life. Usually you follow the trend of your mom.

I wake up soaked behind my knees, my back, neck. I have to lay with the covers off for a while to let my body cool down. I think you may be right and it could be linked to a flare.:ylol2:
 
E Cameron said:
I get night sweats pretty often. Nothing too bad, though... just like Cheeky, it's uncomfortable and a little annoying.

I think it's mostly because of the Prednisone, though. I get them much more often when I'm on that stuff.


yeah true, i think my nightsweats did get worse while on pred, so now that i'm off of it, we'll see if there's a change.
 
yup im a big night sweater too. i wake up at least 3 times during the night to go to the bathroom and i have to change my soaking wet tshirt almost everytime. im not on pred right now either, but i think when i was on it it made them worse.

i dont really have any advice except wear as cool clothes as you can to bed, even if its freakin cold out. i wear shorts and a tshirt no matter what season it is. you can always pile on the blankets and then take them off when you heat up to try to avoid sweating too much.
 
yeah, i just wear boxers.... so the overheating due to clothes isn't the problem. hahaha, and i keep the overhead fan on at night. I wasn't on prednisone when the night sweats started. Sunday i got to the point of having to call my doctor to get something to help me make it to wed. They gave me 30 mg prednisone to take for a while. But i have to say that the sweating has gotten less and less last few nights. So hopefully i am getting a little better with the prednisone
 
Yes, I have had this Really bad before. Pred does it to me. I've soaked my sheets through and had to sleep on a towel some nights.

It should pass in time. :)
 
I have had night sweats since my first flare. Now they are much better since I am in remission, but I still occasionally get them. I have found that it doesn't matter what the temp. is in the room or what I wear to sleep in. I sweat no matter what. I have checked my temperature too and there seems to be no correlation. When I told my GI about it he just said it was probably due to the body fighting inflammation. Who knows! It is really annoying though. Good thing I own a lot of pajamas cuz I have to change them like every night.
 
well, day 3 of me being off of pred, and i noticed that last night i didn't get sweaty. so this confirms it's the pred for me.
 
Didn't know it was a crohn's thing, but yes I do a lot. Not to the point where I actualy have to change my sheets or anything, but enough to be anoying
 
I wish I could get rid of my night sweats with prednisone. I can't take more than 20mg at once with psychotic reactions so it's off the list for me. I have horrible drenching night sweats though. I somewhat think it's from the tylenol pm's I take (GI says they're safe) to help wth the joint pain I have. If only he wasn't too lazy to fill out my humira patient assistance form. Them mabye I'd get real help. Anyway, I get drenching, outlining my body and soaking (I sleep only in boxers) everything below and somehwhat above me, like evey pore in my body wet itself. I'll just get up and sleep another 3-4 hrs in my recliner than hop by into the dry side of the bed when i wake up wet again. MY GI and general practitioner and psychiatrist have no ideas...i just am trying to get used to it. I think it's the meds though........my 2 cents anyways......
 
wow! your question was an answer to a question I have had for a while now! Im on pred and have really bad night sweats and sweat in general. Up till now I used to think I had no sweat glands because no matter what I'd never sweat or when i did it was very little. :lol: Stupid meds, i must say that no matter what , a person just can't seem to get things right with this disease. If it isn't one thing it is another eh?
 
When I was first ill a couple years ago I would sweat like a fiend, as others have mentioned I'd wake up soaking wet, have to change the sheets if I had a fresh set and change my t-shirt. I'd run the A/C and a fan and still wake up soaking wet like as if I had just taken a shower. I got to bringing a towel to bed with me so when I woke up I could dry off and just ended up sleeping in boxers most of the time. I was on Pred for 7 months and AP (after pred) I didn't get them so much anymore. Every once in awhile I'll get them for a couple nights then they disappear again.
 
drew_wymore said:
and just ended up sleeping in boxers most of the time.
NICE!
Oh - what was the question? I never had night sweats, even on pred. I do remember felling comfortable for the first time though in the winter. I am usually freezing, and I stay a little warmer when I am on pred.
 
My night sweats are more like cold sweats when I think about it, I am usually freezing but covered in sweat at the same time.
 
i'm getting them a lot just now.. have been for weeks without a break - i thought they were hormonal (as i've been told i've been hurtling into premature menopause for years) but i am wondering if they are more Crohns related than hormone.... i dunno. i just know i get these horrid episodes about 10 times each day, 4 or 5 in the night, where my heart suddenly speeds up, bangs, i feel ill for a few seconds, then i start to heat up from my toes to my scalp.. my face blushes (which is embarrassing - was talking to a male shop assistant and i had a hot flush.. i am sure he thought i was blushing for his benefit haha).. and then the sweat comes. i hate hate hate it!!
 
ding, does this also happen when you get PM's from certain people?

(sorry, back to sensible thread now)

:D:D:D

also, did you get any discount from the shop assistant?

again, sorry.....
 
jed said:
ding, does this also happen when you get PM's from certain people?

yes, it even happens when i just see certain people's usernames on the forum. like now. omg. :blush:

jed said:
also, did you get any discount from the shop assistant?

again, sorry.....

no. lol
 
hmm, that sounds alot like what happens to me, but mine are more of really bad dizziness with the heart speeding up episodes... then at night I'll wake up in a cold sweat... can't say it has all happened at once, then again like you said 10+ times a day and seriously I am usually just happy when it is all over with, I am 24 tho.. far from menopause state far as I know
 
Cold Sweats - No Meds

i never knew crohn's affected so many non-GI parts of the body. i have been dealing with the night sweats for years, never making the connection (i was only diagnosed a few months ago). but i am like mark33180 and mrae85 in that my night sweats are cold sweats and my temp is low when this happens! it is an annoyance that wreaks havoc with the sleep deprivation, but could be worse i suppose. i just keep spare towels and moisture-absorbing t-shirts (found in the exercise clothing) close by.

i am concerned about the tachycardia with mrae85 - this needs to be addressed by your doctor more closely. i've heard of joint pain (my next post) and the night sweats, but not heart problems with crohn's. you're far too young. good luck.
 
Before my resection, I would get night sweats every night. Not enough to soak my pj's or sheets, but enough that it was freaking annoying, and kinda gross...mostly behind my neck, and between my knees and thighs...

I still get them now, even though I'm in remission, but only once every couple of weeks. My husband loves a cold room when he sleeps, so even in the dead of winter, we're sleeping with a window open, and a fan going. I think he may be menopausal...anyone agree?
 
I posted something about this a few weeks ago, wondering if it had something to do with the Entocort. The 1st time it happened, I had been out drinking & I thought I peed the bed. LOL Opps! It has happened a few other times since then, but the other times I had not been drinking LOL
 
I get night sweats every now and then, too. It seems I go to bed freezing and wake part way throughout the night being all sweaty and usually hot.
Although when I flip off the covers I end up with a chill.
I am hoping this is just preparation for menopause....LOL
 
I had it very bad too before i was diagnosed, like it had rained inside my bed!!
I woke up drenched, even my hair was soaked. I never got hot though, i would just wake up freezing cold. It went away when i went into remission, so i guess it is due to the inflamation.
xXxXxXx
 
i have them too not real bad just enugh to make me uncomffy my mom keeps the ac on at night and its down on like 60 plust the vent is right on me and i still cant have my blankets on but as soon as i ake them off im cold and i have to switch on and off thrughout the night its really annoying lol
 
Flare-ups with odd symptoms

Hello - I have a question about some odd symptoms. I was diagnosed in 1986 and had a resection in 2003. Since the surgery, I have been taking Entocort, Lomotil and Imuran and for the most part, normal symptoms are under control. I had an CT Scan about six months ago and was told I have no active disease. However three or four times a year, I end up having what seems like a minor flare with gas, left-side abdominal pain and some minor diarrhea. What I find out of the ordinary is that it's always coupled with exhaustion and joint pain. These symptoms tend to last three to fours days and then disappear one their own, without any change in medication. The only change that I an call out is that I tend to become more conservative with my diet... but nothing significant. I find this strange because back when my diesase was active, I didn't have these predictable short-term flares and I never had the joint pain.

After this happened the last time, it occured to me that one of the things I did just prior to getting these symptoms was that I started taking a high protein, high vitamin supplement. And I never put two and two together, but I've done this before, with different supplement types and I think maybe there's a correlation between the supplements and these symptoms.

Has anyone ever found this type of reation to high vitamin intake? I have a friend with Lupus who mentioned that she can't take vitamins because it causes her joints to ache even when the Lupus is inactive and she said it's a given that it will happen to her. It made me wonder whether there's something with people who have autoimmune disorders; perhaps taking vitamins that are intended to boost the immune system cause the immune system to become overly active.

Anyway, I'm just theorizing about that. I'm wondering if other people have these short flare-ups even when symptoms are seemingly under control, and that include the joint pain?

Thanks you!

Gary
 
I've noticed night sweats lately as well. Since surgery I've had a few nights, not every night though, where I've woke up sweating. So far it hasn't been bad enough to the point where I've had to change clothes or anything, but still a nuisance. I've always been the kind of girl that sleeps in sweats and sweatshirt and lots of blankets and never got hot ... now ... not so much. ;) I get too hot and sweaty. ugh.
 
lol, i really do believe men go thru some kind of change themselves. It would only be fair, lol...BTW i still have night sweats, usually on my neck legs & thighs. Havent figured out what causes them but still looking for more info.
 

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