Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Dry Mouth When Glutened?


tiffjake

Recommended Posts

tiffjake Enthusiast

I had some gluten in my food last night and all day today I have been soooooo thirsty!!! Anyone else get dry mouth when they get glutened?????


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Absolutely!!

That's one of the symptoms that led me to find out I was gluten intolerant. It happened mostly when I had some rye bread. Even one slice would make me thirsty within an hour, probably like 20-30 minutes. It would last for an entire day, and no amount of water would relieve the thirst. Not even 12 full glasses, which was about as much as I could drink.

eeyor-fan Contributor
Absolutely!!

That's one of the symptoms that led me to find out I was gluten intolerant. It happened mostly when I had some rye bread. Even one slice would make me thirsty within an hour, probably like 20-30 minutes. It would last for an entire day, and no amount of water would relieve the thirst. Not even 12 full glasses, which was about as much as I could drink.

That's weird because I've had a very dry mouth since I went on the gluten-free diet! Always knew I was backwards! :blink:

jerseyangel Proficient

Yea--gluten does make me thirsty. The first couple of months gluten-free, I was thirsty all the time.

4getgluten Rookie

The last time I was really sick because of gluten (last August) I was so thirsty for about 24 hours. I couldn't stop drinking water. The extreme thirst was my first clue that I'd been glutened.

stef-the-kicking-cuty Enthusiast

Yes, it's with me, too. With us during the training drinking is allowed, but not during the belt tests. And I always tell my students to train for that. They look even more strange at me, when I drink during training, because I was glutened. But I'm incredible thirsty then, too. And my mouth is so dry, I can't speak to explain the exercises anymore. :blink:

Stef

Guest Viola

Dry mouth seems to be one of my first signs of gluten contamination. It does make it difficult to carry on a conversation :lol: It sounds funny when I speak.


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



Celiac.com Sponsor (A8-M):



Nashville Contributor

I have been thirsty all the time for the past three years. I was just diagnosed with celiac disease about 6 weeks ago, and the thirst has subsided some. Seems to be getting better each day. I had mono about 3 years ago and never really recovered. One of my mono-like symptoms, in addition to fatigue and headaches (the primary problems), was thirst. I often wake up feeling hung over. I feel better after a couple of glasses of water. I am hoping that all of my mono-like symptoms are gone after a few more months going gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,041
    • Most Online (within 30 mins)
      7,748

    GeoPeanut
    Newest Member
    GeoPeanut
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • GeoPeanut
      Hi, I'm new here. Sorry for your troubles.herenis a thought to mull over. I recently was diagnosed with celiac disease,  and hashimoto's and dermatitis herpetiformis after getting covid 19. I eat butter, and 1/2 cup of Nancy's yogurt daily. I stopped all other dairy and  dermatitis herpetiformis is gone! I also make grass fed beef bone broth to help with myopathy that has occurred. 
    • trents
      Welcome to the forum, @KRipple! Sorry to hear of all your husband's health problems. I can only imagine how anxious this makes you as when our spouse suffers we hurt right along with them. Can you post the results from the Celiac blood testing for us to look at? We would need the names of the tests run, the numeric results and (this is important) the reference ranges for each test used to establish high/low/negative/positive. Different labs use different rating scales so this is why I ask for this. There aren't industry standards. Has your husband seen any improvement from eliminating gluten from his diet? If your husband had any positive results from his celiac blood antibody testing, this is likely what triggered the consult with a  GI doc for an endoscopy. During the endoscopy, the GI doc will likely biopsy the lining of the small bowel lining to check for the damage caused by celiac disease. This would be for confirmation of the results of the blood tests and is considered the gold standard of celiac disease diagnosis. But here is some difficult information I have for you. If your husband has been gluten free already for months leading up to the endoscopy/biopsy, it will likely invalidate the biopsy and result in a false negative. Starting the gluten free diet now will allow the lining of the small bowel to begin healing and if enough healing takes place before the biopsy happens, there will be no damage to see. How far out is the endoscopy scheduled for? There still may be time for your husband to go back on gluten, what we call a "gluten challenge" to ensure valid test results.
    • kate g
      Ive read articles that there is stage 2 research being conducted for drugs that will limit damage to celiacs through cross contamination- how close are they to this will there be enough funding to create a mainstream drug? 
    • KRipple
      Hello, My husband has had issues with really bad diarreah for over nine months now. In mid November, he went to the doctor for what they thought was a bad cold, which two weeks later was diagnosed as bronchitis. A week later, in December, I had to take him back to urgent care and from there, to the emergency room cause his vitals were too low. They said he was having an Addisionan crisis and he spent five days in the ICU. Since my husband has Autoimmune Polyendocrine Syndrome Type II (type 1 diabetes, Addison's and Hashimoto's), I fought for a blood test to determine if he had Celiacs. Given the results of the test, he was told to go to a gastro for an endoscopy. It took two months to get his first appointment with the gastro. Still waiting for the endoscopy appointment. He stopped eating gluten in the hospital and has followed a gluten-free diet since. His diarreah continues to be as bad as before he stopped eating gluten. Still has a horrible cough that makes him hack. His energy is so depleted he pretty much goes to work, comes home and goes lie in bed. He is having issues regulating body temperature. He is barely eating (he's lost 20 pounds since mid-December). Body aches. Totally run down. He has been taking more prednisone lately to try to counter the symptoms.  Today, we went to his endo to discuss these things. She said to continue taking increased amount of prednisone (even though I explained that the increased dosage is only allowing him to do the bare minimum). According to the endo, this is all related to Celiacs. I am concerned because I know that both Celiacs and Addison's can have similar symptoms, but don't know if he would still be having these many symptoms (worsening, at that) related to the Celiac's after stopping gluten two months ago. If anyone in this group has a combination of Celiacs and Addison's, could you please share your experience? I am really concerned and am feeling frustrated. His primary care provider and endocrinologist don't seem to consider this serious enough to warrant prompt attention, and we'll see about the gastro.  Thanks.
    • cristiana
      Hi @Karmmacalling I'm very sorry to hear you are feeling so unwell.  Can you tell us exactly what sort of pain you are experiencing and where the pain is?  Is it your lower abdomen, upper abdomen etc?  Do you have any other symptoms? Cristiana
×
×
  • Create New...