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

Biting Inside Of My Cheeks


mamaloca2

Recommended Posts

mamaloca2 Apprentice

Does anyone kno wif there is a connection between Celiac disease and habitual biting of the inside of the mouth. I have done it since I was a kid and now my son who is only four does it. Does anyone else have this problem?


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



Celiac.com Sponsor (A8-M):



chrissy Collaborator

sounds more like an obsessive-complulsive behavior-----and OCD can run in families.

jennyj Collaborator

Wow. I have done this as long as I can remember. My dad used to say "Jenny stop it," all the time. I tend to do it when I am very nrevous or watching TV. I don't know if there is a connection but you are not alone.

Kellygirl Rookie
Wow. I have done this as long as I can remember. My dad used to say "Jenny stop it," all the time. I tend to do it when I am very nrevous or watching TV. I don't know if there is a connection but you are not alone.

Yep I am obsessive complusive and I do it all the time, even while sleeping. I am celiac too, but I never really questioned if they go together or not!

Kelly

mamaloca2 Apprentice
sounds more like an obsessive-complulsive behavior-----and OCD can run in families.

I don't have any other traits that are OCD. And I only really bite them when a am stressed. I just noticed when I got glutened that I did it much more, and thought there could be a connection.

mamaloca2 Apprentice
Wow. I have done this as long as I can remember. My dad used to say "Jenny stop it," all the time. I tend to do it when I am very nrevous or watching TV. I don't know if there is a connection but you are not alone.

Us too! Even if it's not related to celiac, seems like there's got to be something more to it. Thanks for your reply!

RiceGuy Collaborator

I used to have similar sorts of stuff happen, but by accident. Usually it was my lip that got chomped :angry: Thankfully, this has subsided/disappeared, and I believe the key was a sublingual methylcobalamin (vitamin B12) supplement. Either that or it just took time, but I notice that my teeth are straighter too, and no longer have the aching that would come and go.

Still a bit of teeth clenching, but not as bad as it used to be.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I actually trained myself to do this. On gluten or under great stress I am a teeth grinder. I have broken them in my sleep, those good old celiac teeth, and I do it to keep from grinding. Perhaps a mouth guard might help you and your son, your dentist can give you one with the best fit. Another thing that helps, at least for me, is a hot compress on my cheek before bed. When I get glutened it helps my muscles to relax and I don't do as much grinding and biting. Plus it feels very soothing.

cmom Contributor

I used to accidentally bite the inside of my mouth and once I did it, it seemed like I did it several times, each time very painful. Hadn't thought much about it until reading these posts. That's a good thing cause that means it "ain't " happenin' anymore!!!!!!

zakismom Newbie

I used to do this all the time! I also used to bite my lip until it turned into a bump. I don't do it as much but I do know that if I get glutened I get a mouth sore.

Rusla Enthusiast

I do this all the time, although it could be not just an ocd but in some cases a tourettes thing.

Stargirl* Newbie

Hi.

I am a long time lurker, first time poster. ;)

My daughter bites the inside of her cheeks and lips. I have put it down to the mouth ulcers she used to have until the gluten intolerance diagnosis.

  • 4 weeks later...
mwahlman Newbie

You may be refering to TMJ. I was recently diagnosed with this by my dentist, around the same time as my Celiac Diagnosis.

I am unsure if the two are directly related, or if I just have been lucky finding medical professionals who arent qwacks lately.

"TemporoMandibular Joint and muscle disorders" The following article goes over the specifics:

Open Original Shared Link

Does anyone kno wif there is a connection between Celiac disease and habitual biting of the inside of the mouth. I have done it since I was a kid and now my son who is only four does it. Does anyone else have this problem?
lob6796 Contributor
Does anyone kno wif there is a connection between Celiac disease and habitual biting of the inside of the mouth. I have done it since I was a kid and now my son who is only four does it. Does anyone else have this problem?

Interesting, I would have never connected the two. I do it alot (ugh the scars!), and my mom, who never knew she did it, went to a special dentist the other day and the lady goes "wow, you really bite your mouth alot, huh?" The dentist said she is probably doing it in her sleep without realizing it. I have Celiac, and she is suspected of having it.

Guhlia Rising Star

I am mildly OCD and I compulsively scratch my lips with my teeth. I'm assuming this is about the same as what you guys are talking about. Luckily, most of my OCD symptoms disappeared when I went gluten free. Unfortunately, this one hasn't gone away completely. It has gotten better though since going gluten free. I think there's definitely a connection with OCD and gluten.

Ursa Major Collaborator

I have Tourette's syndrome and Asperger Syndrome, and I have always done that, too. It isn't possible to determine if in my case it is a tic, OCD (which I have mildly, but not enough for a separate diagnosis, as EVERYBODY with TS and AS has some compulsive behaviours) or a stim (self-stimulating behaviour, typical for people on the autistic spectrum).

But I do know that I don't do things like that as much as I used to when still eating gluten, and my tics have decreased as well.

JamiD Apprentice

*reluctantly raises hand*

Gawd, I'm doing it right now.

I've habitually chewed/bit my inside cheeks and lips since I was a teen. I do it more when I'm not physically busy.

Never been diagnosed w/ OCD and I would say that if I have it, it is mild.

  • 3 weeks later...
glutenfreek Newbie

Add one more person with celiac and bites their tongue...literally. I have wondered about OCD, never been diagnosed, but that doesn't mean much. Like others have mentioned I remember doing this as a child, my grandmother did it and so does my father. I have tried to stop numerous times, hence why I am on this site right now, seeing if anybody has ever been successful in kicking this nasty habit. I used to grind my teeth too and my dentist made me a mouth guard, (Wal Mart sells a mouth guard that you mold to your teeth at home, fairly easy to do and only $20). This stopped my grinding but I am having trouble with biting my tongue still. It is sooooo irritating, I do it in my sleep and sub consciously. I don't understand why I do this, I absolutely hate it, my tongue is sore all the time and looks repulsive I want to stop! Any suggestions or advice would be appreciated.

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. - trents commented on Scott Adams's article in Kids and Celiac Disease
      2

      New Study Reveals Age and Racial Gaps in Pediatric Celiac Testing

    2. - Russ H replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Positive biopsy

    3. - Scott Adams replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Positive biopsy

    4. - Scott Adams commented on Scott Adams's article in Latest Research
      3

      New "Glowing Bacteria" Pill Could Transform Gut Disease Detection (+Video)

    5. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

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

    • Total Members
      133,001
    • Most Online (within 30 mins)
      7,748

    bonniebeebe143
    Newest Member
    bonniebeebe143
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Russ H
      What you describe is seronegative villous atrophy (negative antibody tests but positive biopsy). It is uncommon in coeliac disease, and there are other causes, but the most common cause is coeliac disease. I would pursue this with your healthcare provider if possible. Based on clinical history, test results and possible genetic testing for susceptibility to coeliac disease it should be possible to give a diagnosis. There is a bit more here: Seronegative coeliac disease
    • Scott Adams
      If you are still eating gluten you could get a celiac disease blood panel done, but I agree with @trents and the gold standard for diagnosing celiac disease would be your endoscopy results. Is it possible they did do a celiac disease panel before your biopsy? This would be the normal chain of events. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
×
×
  • 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.