Jump to content
  • 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):

Salivary Glands


Moongirl

Recommended Posts

Moongirl Community Regular

About the same time i was dx with celiac disease...i started feeling this funny 'lump' underneathe my jaw on my right side.

after about 2 years to the ENT dr, and the dx of dry salivary gland, it seems to begetting worse. So i was for a CT scan to rule out a stone.

And I got the all clear, nothing is there.

So my question is, could it be only dehydration? I noticed when i was eating sour candy i had much relief. Also when he was checking for the saliva secretion under my tongue, there wasnt much.

so my next phone call to the dr, i kinda want to have an idea what to ask him what my next steps are...

any advice or comments would be greatly appreicated.

Thanks :)


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



Celiac.com Sponsor (A8-M):



jewi0008 Contributor
About the same time i was dx with celiac disease...i started feeling this funny 'lump' underneathe my jaw on my right side.

after about 2 years to the ENT dr, and the dx of dry salivary gland, it seems to begetting worse. So i was for a CT scan to rule out a stone.

And I got the all clear, nothing is there.

So my question is, could it be only dehydration? I noticed when i was eating sour candy i had much relief. Also when he was checking for the saliva secretion under my tongue, there wasnt much.

so my next phone call to the dr, i kinda want to have an idea what to ask him what my next steps are...

any advice or comments would be greatly appreicated.

Thanks :)

I have a question, then, for you. Does your mouth/tongue annoy you? That is my BIGGEST problem! I always think I feel little lumps underneath my jaw.

Moongirl Community Regular
I have a question, then, for you. Does your mouth/tongue annoy you? That is my BIGGEST problem! I always think I feel little lumps underneath my jaw.

Nope Ive never had a problem with my mouth or tongue. its just my salivary gland on one side...i cant seem to figure out whats causing the lumpiness....they keep saying it dehydration, but i dont think thats the only thing. <_<

Katydid Apprentice

I couldn't believe it when I saw your post about salivary gland issues. My husband, who has been celiac for 20 years gets a 'lock jaw' like syndrome. He goes to the doctor and they call it a salivary gland inflamation. They give him antibiotics and it goes away. I never dreamed it might be celiac related.

CDFAMILY Rookie

Well, this is definitely my area. I had my left gland swell so bad I was sent to the ER. I was in for 3 days to get the swelling down on drips, steroids and antibiotics. They were afraid the swelling would close my airway. That was last April 2006. I would periodically get swollen glands since then. By January of this year this happened again and called doctor and got a prescription but nothing helped and I ended up in the ER begging for morphine. My gland was huge, my tongue was swollen and I was running a 102 fever. By evening, out popped a 4mm stone.

My Xray in April of 2006 showed nothing but of course now I know I had a stone just waiting to come out. I have had my glands swelling for years and always thought it had to do with my body trying to fight an infection, but now I know it was really a stone.

They tell me to suck on sour candy which helps if it is barely swelling, but once the stone starts moving, and the gland becomes inflamed, you really can't suck on anything let alone eat.

Gemini Experienced

I posted on another thread about this but you need to be tested for Sjogren's Syndrome. Sjogren's is another autoimmune disease that Celiac's often get also. Causes dry eyes and dry mouth AND causes

swelling of the salivary glands as a result of the inflammation. I never had the swollen glands but have the dry eyes and mouth. I believe stones are also a problem for some.

Tests are blood work and are called SSA and SSB. Doctor's rarely get this right and dehydration is not the cause. There are products to use that can make the symptoms easier to deal with but, of course, there is no cure. I am now on Restasis eye drops and they have made a HUGE difference in my eyes.

Sorry to bring more bad news but I felt I should tell you all this so you can be tested and get some relief. Otherwise, you'll just be plied with antibiotics and other meds that won't do anything long term.

Good luck to all!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      11

      Celiac flare years after diagnosis

    2. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      11

      Celiac flare years after diagnosis

    3. - Peace lily commented on Scott Adams's article in Latest Research
      2

      New Study Reveals How the Immune System Learns Which Foods Are Safe to Eat

    4. - nancydrewandtheceliacclue replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      11

      Celiac flare years after diagnosis

    5. - Jmartes71 replied to Jmartes71's topic in Dermatitis Herpetiformis
      4

      Skin issues

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      134,061
    • Most Online (within 30 mins)
      10,442

    Francisco1007
    Newest Member
    Francisco1007
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Aretaeus Cappadocia
      @nancydrewandtheceliacclue, you are welcome. After looking at this thread again, I would like to suggest that some of the other comments from @Russ H are worth following up on. The bird-bread may or may not be contributing to what you are experiencing, but it seems unlikely to be the whole story. If you have access to decent healthcare, I would write down your experiences and questions in outline form and bring this to your Dr. I suggest writing it down so you don't get distracted from telling the Dr everything you want to say while you have their attention.
    • Aretaeus Cappadocia
      @Russ H, I partly agree and partly disagree with you. After looking at it again, I would say that the slick graphic I posted overestimates the risk. Your math is solid, although I find estimates of gluten in white bread at 10-12% rather than the 8% you use. Somewhat contradicting what I wrote before, I agree with you that it would be difficult to ingest 10 mg from flinging bread.  However, I would still suggest that @nancydrewandtheceliacclue take precautions against exposure in this activity. I'm not an expert, I could easily be wrong, but if someone is experiencing symptoms and has a known exposure route, it's possible that they are susceptible to less than 10 mg / day, or it is possible that there is/are other undetected sources of exposure that together with this one are causing problems. At any rate, I would want to eliminate any exposure until symptoms are under control before I started testing the safety of potentially risky activities. Here is another representation of what 10 mg of bread would look like. https://www.glutenfreewatchdog.org/news/wp-content/uploads/2019/10/10mgGlutenCrumbsJules.jpg Full article that image came from: https://www.glutenfreewatchdog.org/news/what-does-10-mg-of-gluten-look-like/
    • nancydrewandtheceliacclue
      @Aretaeus Cappadocia thank you for your reply and the link, that is very helpful to get a visual of just how small of an amount can cause a reaction. I know I am not consuming gluten or coming into contact with gluten from any other source. I will stop touching/tossing bread outside! My diet has not changed, and I do not have reactions to the things I am currently eating, which are few in number. My auto immune reaction just seems so severe. The abdominal pain is extreme. It takes a lot out of me. I guess I will be this way for the rest of my life if I ever happen to come into contact with gluten? I appreciate the help. 
    • Jmartes71
      Thankyou I did find out the Infectious disease is the route to go rather than dermatologist. I did reach out to two major hospitals and currently waiting on approval for one of them in Infectious Diseases to call me. I also did have implants ( I didn't know and sense not properly in my medical. Neither did surgeon)in 2006 and there was a leak 2023 during the same time I was dealing with covid, digestive issues, eyes and skin.Considering I " should  be fine" not consuming gluten/wheat, taking vitamins for sibo and STILL feeling terrible.It has to be parasites. I also take individual eye drops prescribed, could there be an issue there? Anyways my pcp thinks I need therapy because again they don't acknowledge my digestive issues because in my records it shows im fine, hintz the reason I had to go back to bay area hospital:(  I thought skin issues maybe sibo related but I feel and have seen and seriously trying not to think about it because it's disgusting. 
    • Aretaeus Cappadocia
      oops. I didn't see that before posting or I would have at least referenced it. The two recipes are pretty similar, but I think the newer one is a little simpler/faster. Next time though I will search more before posting.
×
×
  • Create New...