Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Very Bad Night Sweating...what Could It Be?


shendler

Recommended Posts

shendler Rookie

Hey

So for as long as I can remember vie also had very bad night sweats. I dont have this problem during the day just at night. It isn't the temperature in the room that is causing the problem nor is it from wearing hot clothes.

It's getting very bad and when I wake up in the middle of the night Im soaking wet. What could it be?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



lucia Enthusiast

If it's getting worse (& I can see that you've been off gluten for over a year), then I would suggest talking to a doctor.

Sorry, I know that's not helpful. It's just that it could be a symptom of something serious. Or not.

Although if the M.D. doesn't find anything, I will say that a holistic health practicioner (Chinese herbalist/acupuncturist, ayurvedic doctor) would still find it to be a serious indicator that something is awry with your body.

Wolicki Enthusiast

Have you been strict with your diet? The reason I ask is because I suffer horrible night sweats (buckets!) when glutened, and it was awful before going gluten free. It has miraculously stopped, as long as I don't get accidental gluten.

How old are you? Could it be perimenopause or menopause?

kenlove Rising Star

I used to go through 6 or 7 t-shirts a night they were so wet. Had been off gluten for 3 or 4 years at that point too. The docs could not figure it out but ordered a total blood work up and found I was again without a number of hormones and vitamins. A month on supplements and it was fine. Still happens once or twice every 4 or 5 months if I get glutened.

Good luck

Hey

So for as long as I can remember vie also had very bad night sweats. I dont have this problem during the day just at night. It isn't the temperature in the room that is causing the problem nor is it from wearing hot clothes.

It's getting very bad and when I wake up in the middle of the night Im soaking wet. What could it be?

shendler Rookie

I am not eating gluten. I prepare all my food in a gluten free kitchen. Plus when I do eat gluten I can tell within 30 minutes based on how tired I get. I've been to the doctor but there is nothing in my blood that indicates a problem. I'm only 25 so I do not think it is menopause. Plus it only happens at night.

'lynrn Apprentice

There are many conditions not related to gluten that can cause night sweats, one of which is TB/Tuberculosis...yes it is still very much alive and around us...not saying it is...but early infections, this included, can cause severe night sweats. Go back to your doctor. TB can often be ruled out by a simple skin test or a chest x-ray. Night sweats tell you SOMETHING is going on....

kenlove Rising Star

I would try to get additional blood test for micronutrients and hormones. As a celiac the body does not get everything it needs. Also Sweats can be from other allergies you get after celiac. It was 5 years but now I'm off of all dairy too.lots of changes can happen so for me it was a matter of bugging the doc to give me as many tests as he could think of and then get the appropriate supplements.

good luck

ken

I am not eating gluten. I prepare all my food in a gluten free kitchen. Plus when I do eat gluten I can tell within 30 minutes based on how tired I get. I've been to the doctor but there is nothing in my blood that indicates a problem. I'm only 25 so I do not think it is menopause. Plus it only happens at night.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



GFinDC Veteran

I tend to think it could be caused by a low-level fever, possibly a food intolerance reaction. There are lots of things other than food intolerances that could cause night sweating I think, but it is a as good a place to start looking as any.

undiagnosedillness Newbie

I'm not 100% sure but I've been told Thyroid problems can cause night sweats. I get them too and day sweats (dreadful things, not looking forward to summer this year) and I have a goitre, yet thyroid function blood tests always normal for me

Maybe ask for thyroid testing?

Samantha :)

kenlove Rising Star

HAve them check the parathyroids by ultrasound too. That regulates something with calcium which also affects my sweating.

good luck

I'm not 100% sure but I've been told Thyroid problems can cause night sweats. I get them too and day sweats (dreadful things, not looking forward to summer this year) and I have a goitre, yet thyroid function blood tests always normal for me

Maybe ask for thyroid testing?

Samantha :)

Open Original Shared Link

minniejack Contributor

Hey

So for as long as I can remember vie also had very bad night sweats. I dont have this problem during the day just at night. It isn't the temperature in the room that is causing the problem nor is it from wearing hot clothes.

It's getting very bad and when I wake up in the middle of the night Im soaking wet. What could it be?

Initially, that's what the #1 complaint that we kept going to the doctors for my DS now 15. He ended up with vomiting, ADHD, diarrhea, acne.... He's been gluten-free for almost 2 yrs and no night sweats, stomach issues gone, ADHD gone--we're just dealing with normal teenage issues. Amen!

Oh and at first we had to eliminate sulphites and milk products--his body can handle them now, though.

  • 2 weeks later...
up late Newbie

I get them too, oddly more when it's cold, it's when I get shivering with them I go to the Dr.

Low grade fever could cause night sweats. Did the dr check your urine for a urinary tract infection? They can be chronic and don't always have pain with them.

Lizking531 Rookie

Yeah - I used to get horrible night sweats as well. That was one of the indicators originally to go to the doctor. When I originally got my bacteria overgrowth issues under control, my waist slimmed down a lot & the seat went away. Now many symptoms have crept back in, but luckily, the sweats have stayed away for the most part.

For me, it felt like more of a response, like something was going on to create the heat that being dissipated thru my sweat & it would make sense that intolerable foods & bacterias were having a party & heating things up in there.

  • 2 weeks later...
BoydBT Apprentice

I would try to get additional blood test for micronutrients and hormones. As a celiac the body does not get everything it needs. Also Sweats can be from other allergies you get after celiac. It was 5 years but now I'm off of all dairy too.lots of changes can happen so for me it was a matter of bugging the doc to give me as many tests as he could think of and then get the appropriate supplements.

good luck

ken

All this I never knew, thank God I joined this forum. The stupid Doctors have no time to really go into all this. But I too have night sweats , I get soaked.

It doesn't happen often now but yes but a few times a week. I must be more careful.

What does CC mean exactly. Crappy Celiac.

I am glad to have found out why, now.

  • 3 years later...
Jess27 Newbie

Hi,

 

I to get very bad night sweats, Iv had it for about a year and a half and its every night! I wake up all the time drenched in sweat from head to toe and it stinks! I have been to the doctors and have had so many blood tests. I have been tested for Diabetes, HIV, Thyroid problems, and TB. They all came back negative. The doctor has also ruled out early menopause and a few other things. I have also been tested for celiac but that came back negative to and they wont do a biopsy. My little sister has been diagnosed with chronic celiacs but her blood tests came back negative as well, it wasn't until she had a biopsy that she was diagnosed. I went gluten free for about a month and the sweating halved. So im guessing that i really should go gluten free to see if the sweating stops al together?   

kenlove Rising Star

My sweating comes and goes even though i've been  gluten free for almost 9 years. It is less than it was before I went gluten-free but it still happens. Now I think its tied into the supplements I take which also might cause frequent urination.  It cant hurt you to go gluten-free unless you plan to get  certain tests. I also need a endoscopic exam to confirm celiac.  good luck

Hi,

 

I to get very bad night sweats, Iv had it for about a year and a half and its every night! I wake up all the time drenched in sweat from head to toe and it stinks! I have been to the doctors and have had so many blood tests. I have been tested for Diabetes, HIV, Thyroid problems, and TB. They all came back negative. The doctor has also ruled out early menopause and a few other things. I have also been tested for celiac but that came back negative to and they wont do a biopsy. My little sister has been diagnosed with chronic celiacs but her blood tests came back negative as well, it wasn't until she had a biopsy that she was diagnosed. I went gluten free for about a month and the sweating halved. So im guessing that i really should go gluten free to see if the sweating stops al together?   

  • 1 month later...
Aleka Munroe Rookie

I have  21 years diagnosed with celiac disease and am religious about eating gluten-free. I went through heavy night sweats through peri menopause and menopause then they stopped post menopause. About a year ago the sweats started again, I began to notice an extremely dry mouth (worse than ever before) and as time went on I had a constant bad taste in my mouth. Additionally I noticed my blood pressure levels became erratic. I reported all of this to my three specialists and one primary doctor, the last of which was doing a CBC every three months. In September my primary care referred me to a nephrologist due to abnormal creatinine levels in my blood, although my urine had no negative test results. Days after I met the nephrologist he put me in the hospital with a diagnosis of Stage 5 (End Stage) Renal Failure. When I left a week later they had gotten it down to Stage 4. Since then I've had a kidney biopsy. My kidneys are permanently damaged due to scarring with 50% functioning. There is no known reason for this. Tests prior to January of 2013 showed no creatinine disfunction. My nephrologist told me there is growing research showing a correlation between Chronic Kidney Disease and Celiac Disease. Given my situation, I suggest you have your creatinine levels tested and GFR calculated. Request that you be followed carefully and frequently if your creatinine is lower than 95. 11 months ago mine was 90 and my physician did not note it until it dropped to 40. I don't know if he or I had known this sooner my kidney disease perhaps would not be at Stage 4 now. This means I must go on dialysis and will need a transplant eventually.

kenlove Rising Star

Thanks so much for posting this and warning us about creatinine levels. Goimg to send the info to my Kaiser doc now. Good luck!

 

I have  21 years diagnosed with celiac disease and am religious about eating gluten-free. I went through heavy night sweats through peri menopause and menopause then they stopped post menopause. About a year ago the sweats started again, I began to notice an extremely dry mouth (worse than ever before) and as time went on I had a constant bad taste in my mouth. Additionally I noticed my blood pressure levels became erratic. I reported all of this to my three specialists and one primary doctor, the last of which was doing a CBC every three months. In September my primary care referred me to a nephrologist due to abnormal creatinine levels in my blood, although my urine had no negative test results. Days after I met the nephrologist he put me in the hospital with a diagnosis of Stage 5 (End Stage) Renal Failure. When I left a week later they had gotten it down to Stage 4. Since then I've had a kidney biopsy. My kidneys are permanently damaged due to scarring with 50% functioning. There is no known reason for this. Tests prior to January of 2013 showed no creatinine disfunction. My nephrologist told me there is growing research showing a correlation between Chronic Kidney Disease and Celiac Disease. Given my situation, I suggest you have your creatinine levels tested and GFR calculated. Request that you be followed carefully and frequently if your creatinine is lower than 95. 11 months ago mine was 90 and my physician did not note it until it dropped to 40. I don't know if he or I had known this sooner my kidney disease perhaps would not be at Stage 4 now. This means I must go on dialysis and will need a transplant eventually.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,856
    • Most Online (within 30 mins)
      7,748

    Sonya Haskin
    Newest Member
    Sonya Haskin
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.