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

What Is Your Worst Symptom When Glutened?


Googles

Recommended Posts

bartfull Rising Star

Interesting about the TMJ. It was one of the first things they ruled out though in my case. I have an egg sized, hard as a rock lump on my jawbone, about halfway between my chin and the hinge of my jaw. It never goes away, but from time to time that whole side of my face swells like a chipmunk, I can't open my mouth wide enough to even get the baby toothbrush I bought inside, and I have a constant throbbing pain, like a bad toothache, interspersed with severe stabbing pain in my jaw and my ear.

It has been acting up again lately. I finally got a prescription for Tylenol,made without gluten, corn, or salicylates. That makes things so much easier. For a while there I was relying on warm compresses for the pain, and frankly they didn't help at all. At least the Tylenol knocks it back a little.


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Interesting about the TMJ. It was one of the first things they ruled out though in my case. I have an egg sized, hard as a rock lump on my jawbone, about halfway between my chin and the hinge of my jaw. It never goes away, but from time to time that whole side of my face swells like a chipmunk, I can't open my mouth wide enough to even get the baby toothbrush I bought inside, and I have a constant throbbing pain, like a bad toothache, interspersed with severe stabbing pain in my jaw and my ear.

It has been acting up again lately. I finally got a prescription for Tylenol,made without gluten, corn, or salicylates. That makes things so much easier. For a while there I was relying on warm compresses for the pain, and frankly they didn't help at all. At least the Tylenol knocks it back a little.

OMG! you sound like me--right down to the referred pain in my ear! It hurts like heck.

I have those hard knots and swelling--and yes, they can be the size of an egg. These are called trigger points. (not to be confused with tender points of fibromyalgia) They are hyper-irritable knots in taut muscle bands and they can cause pain locally or refer to other places, in this case, the ear or the temple. They can prevent you from opening your mouth and cause tooth pain, when there is no tooth problem.

Oh hon, I have this pain. If you have been Xrayed and there is nothing showing like arthritis in the jaw, it could be muscular. It MIMICS TMJ dysfunction. I can tell you more if you want as I have had a significant reduction in pain from massage and exercises. I was in agony from this for 2 years and no doctor could help me.

I read about trigger points and how they are perpetuated by things like vitamin deficiencies and food intolerances and that's how I knew why I had so much darn pain in my body.

You may wish to read about trigger points, myofascial pain and TMJ pain. See if you can find a massage therapist to help you out. I wish you well. I really do know how much this hurts!

  • 1 year later...
Glutenfreegibbon Newbie

I just recently found out that I have celiac disease.. my symptoms are broad I tend to eat more at night and this causes insomnia and projectile vomiting along with extream anxiety and depression.. I'm imbarrassed.. I know its nothing I can help but I hate being a pain for others to deal with.. after the initial explosion I get the gluten head as I have heard others talk about and stomach cramps that make me in pain and ill for hours.. I have a job that requires me to be on the ball and I have been noticing that I will randomly hit a wall and everything becomes much more difficult. Which is hard for me.. I don't seem to get a break and I often hear that this really is not that bad and I should not make it more than it is. I honestly don't feel like I am... does anyone have

lovechild Rookie

I haven't been diagnosed with Celiac disease but I have been avoiding gluten for 2.5 months now. My worst symptom when glutened is extreme exhaustion about 10 minutes after I eat the offending food. 

 

It is so interesting that you mention that TMJ is associated with Celiac Disease. I have TMJ and have to wear a splint at night. I have been bad for the past 6 months and haven't been wearing my splint and I know that I have been clenching my jaw at night because I have had some dreams where I was biting into something and I got lock-jaw and couldn't open my mouth in my dreams. Now the past two months I have not only jaw pain but pain into my ear canals and the rest of my head feels like it has a blood pressure sleeve around it 24/7 squeezing my brain. Do any of you also have these same symptoms? I think I need to make a point of wearing my splint again so I can make these headaches go away. 

 

It's great to talk to others with similar symptoms. I feel that I am not alone in this. :)

1desperateladysaved Proficient

Fatigue and brain fog are my most troubling symptoms.

w8in4dave Community Regular

I have the GI symptoms, as soon as I start getting that familiar pain I better start heading towards the bathroom!! Yes someone said it was embarrassing and believe me it is!! Also fatigue, I cannot tell you how wonderful it is not to be so danged tired all the time!! It isn't all gone yet!! But it is slowly leaving!! Thank goodness!! :) 

Mr. GF in Indiana Newbie

Pre-diagnosis: All of the worst of almost every physical and psychiatric symptom you can think of, worsening month to month for 60 years, but especially from age 50-60, bone pain from celiac-caused tumor of the parathyroid, and muscle wasting/neuropathy.

Post celiac diagnosis 2010: residual dementia, neurologic damage, which is both disabling and terribly painful. The dozens of other problems, are now almost entirely fixed, controlled, ignored, or surgically repaired, so there's that.

The moral: Where would we be without the invention of the internet? (especially pubmed.com) and all the wonderful posters everywhere who shared their agony, mistakes, and successes without which my journey to this point would have been almost impossible. So thank you.


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



Celiac.com Sponsor (A8-M):



w8in4dave Community Regular

Pre-diagnosis: All of the worst of almost every physical and psychiatric symptom you can think of, worsening month to month for 60 years, but especially from age 50-60, bone pain from celiac-caused tumor of the parathyroid, and muscle wasting/neuropathy.

Post celiac diagnosis 2010: residual dementia, neurologic damage, which is both disabling and terribly painful. The dozens of other problems, are now almost entirely fixed, controlled, ignored, or surgically repaired, so there's that.

The moral: Where would we be without the invention of the internet? (especially pubmed.com) and all the wonderful posters everywhere who shared their agony, mistakes, and successes without which my journey to this point would have been almost impossible. So thank you.

Amen!!! TY I feel the same way!! 

VeggieGal Contributor

Mine is brainfog, can't concentrate properly and forget what I'm supposed to be doing and feel unmotivated. My arms ache and feel heavy like the starting of flu and I suffer with fatigue. I'm pretty sure my eyesight is effected too and goes blurry.

Fire Fairy Enthusiast

Migraine, fatigue and a feeling of defeat.

w8in4dave Community Regular

I ate 2 cookies yesterday , after the fact (because I am new to this) I was like "Ohhhh Noooo!! I ate cookies!!" I totally forgot about Celiac!! So today!! I had a very embarrassing  moment!! Lucky for me I don't think anyone noticed! I did make it home to shower and do laundry! So NO MORE GLUTINIZED cookies for me!! That was horrid!! That familiar pain hurts!!!! Still feeling the after effects!! 

Fire Fairy Enthusiast

I have re-occurring nightmares like that. :wacko: (((hugs))) Now, never do that again.

quincy Contributor

many are complaining of jaw pain and neck muscle aching.  TMJ and jaw pain are closely related to fibromyalgia which has a high incidence in the celiac population.  I have chronic muscle and tendon pain even after going gluten-free for 3 years, though I have to say I eat out alot and I now have to curb my eating out because inevitably I am being glutened alot.....

Greebo115 Rookie

Brain fog/neurological symptoms are the hardest to cope with.

 

A few hours after glutening I can barely speak. My mind is halted, I can't think, remember ANYTHING or make basic decisions....my coordination goes completely (I walk into door frames, burn/cut myself when prepping food - smacked myself in the face with a door REALLY hard a while ago, resulting in bruised nose and 2 black eyes) and it takes 3 weeks to become clear-minded again.

People try to complete my sentences (incorrectly) when I can't think of a word and I get FURIOUS trying to get my meaning across, or when people (poor hubby) ask me the most basic of questions (E.g. tea or coffee?).

Work comes to a halt (I left my job as a teacher before I knew I needed to be gluten-free) and I'm now self employed so if I don't work, then I don't get paid.

I started to wonder if I was depressed (as the doctors kept suggesting), because I didn't want to go out in case someone talked to me...now I realise it was because I had times when it was it was just so hard to speak!

 

The "C", the "smells", then later "D", I can cope with because my "office" is the bedroom next to the toilet, lol,

 

Edited to add: The severe insomnia also turns my life upside down as I don't sleep at all at first...then sleep 16 plus hours as I begin to recover.

w8in4dave Community Regular

I was having hallucinations , usually in the wee hrs. of the morning, one morning hubbs came over to give me a kiss before he left for work (I make him) lol anyhoo I said OMG look at the size of that spider!! He looks up and say's "I don't see a spider!" I mean this thing was the size of a crab!! So I said pointing my finger : "OMG you cannot see that? It's huge!! It is right there!!" he looks and say's "nope! I don't see it" I got up grabbed a shoe and at this point the spider was right over my head so I smacked it and as my shoe was about ready to hit the ceiling I noticed it vanish.. Like it disappeared ... SO I said "That was weird" He kinda raised his brows and said "Well I hafta go to work now" I said " how am I supposed to go back to sleep now?" The spider thing happens alot! I know it is hallucinations so I don't let it bother me, i just turn over and go back to sleep. What in the heck would make someone hallucinate like that? Is it Celiac? Or some kind of vitamin deficiency ??

klisja Rookie

I am not sure I am celiac or gluten intolerant but I don't tolerate gluten (but I can eat rolled oats, not quick). I think my problem is that my colon is so damaged from intolerance that there are few things I can tolerate for now. 

 

But eating rye and barley make my colon shake and squeeze (don't now how to describe properly) but fine wheat and spelt make me extreamly tired, I kinda just fall allt the way to the bedroom and my bed grabs me.

 

I don't know how not to have brainfog, lethargy or hyperactivity (getting better) so that's in second place.

BelleVie Enthusiast

I have re-occurring nightmares like that. :wacko: (((hugs))) Now, never do that again.

 Fire Fairy, I just started a gluten challenge a week ago, and have had troubling dreams and nightmares EVERY night since. I haven't had nightmares in years! It's really interesting, because my mother has always struggled with "night terrors." I'm convinced she's celiac and am begging her to get tested! Maybe going gluten free will solve her nightmare problem too! 

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.