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 are the symptoms of being "Glutened"?


SteveB

Recommended Posts

SteveB Rookie

Since last October 2016, my stomach has been feeling like it's full all the time (or constant pressure may be a better word here), and it seems like it's constantly rumbling and I have more gas coming out of both ends. I was diagnosed with Celiac a couple of weeks ago and since I've changed my eating habits, the constant rumbling in my stomach has subsided. The pressure hasn't let up at all yet but I'm hoping that will.

My question: When folks who are in this situation and have been eating good and feeling better, what exactly happens when you do eat something with gluten in it?

What can I expect if I eat something with gluten in it, by mistake, now that I'm starting to feel better? Will the rumbling come back, and if the pressure ever eases up in my stomach, will that pressure come back?

Or will my symptoms be much worse?

I realize it's probably different for everyone but can some of you tell me what to expect if I eat Gluten by mistake? And once the gluten has been ingested, how long will it take for those symptoms to appear?

 

Thanks and much appreciated,

Steve in Central Vermont


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



Celiac.com Sponsor (A8-M):



Mrsjinx Newbie

I totally know how you feel. I went gluten-free 4 months ago and just started getting the same symptoms you describe. I recently developed an egg allergy as well as lactose intolerance, and once I cut those out the symptoms definitely improved. I also get those same symptoms if I've eaten rice or quinoa a couple days in a row. My symptoms start within 1/2 hour of eating. It may be different culprits for you, Steve, but those are mine. For now, anyway ;)

 

SteveB Rookie
21 minutes ago, Mrsjinx said:

I totally know how you feel. I went gluten-free 4 months ago and just started getting the same symptoms you describe. I recently developed an egg allergy as well as lactose intolerance, and once I cut those out the symptoms definitely improved. I also get those same symptoms if I've eaten rice or quinoa a couple days in a row. My symptoms start within 1/2 hour of eating. It may be different culprits for you, Steve, but those are mine. For now, anyway ;)

 

I hope I don't get other food allergies because of Celiac disease!!!!

Egg allergy?!?.......Sigh

Just from the short time I've been connected to this Web site, it seems that there are many symptoms people have that can "show their ugly face", and those symptoms vary.

Thanks for the words of encouragement Mrsjinx. Good luck with your progress.

Ennis-TX Grand Master

This differs from person to person, note you will have huge up and downs til your system regulates and your antibodies decrease on a gluten-free diet. Should regulate in 1-2 months and improvements in 4-6 in overall health should be noticeable. NOTE keep a food journal of everything you eat to help nail down any other culprits that might crop up causing you issues.

As for symptoms, I have a gluten ataxia on top of just plain celiacs, for me it depends on the kind, amount, of exposure. Straight bread/gluten.....swollen lymph nodes, extreme gut wrenching pain, violent vomiting, loss of motor control, and later rotating D&C along with brain fog and numbness for a week or two. Slight exposure is normally just brain fog, a twitch, numbness, lymph nodes, and and can vary from just vomiting mildly to the D&C rotation. I also have a response to inhaling flour where it causes the numbness, and brain fog.   The brain fog leads to confusion and random outburst of extreme anger I refer to as Hyde. Check the about me in profile for my other issues I had crop up.

Since your new we normally suggest a whole foods diet only of greens, fresh meats, potatoes, etc. for the first month or so. And dropping oats, dairy, and limiting grain intake, this will boost the healing process. Now if your having gas issues limiting the grains/carbs/sugars will really help out til you regulate to the new diet.

Few helpful links to get you started .

https://www.celiac.com/forums/topic/91878-newbie-info-101/

https://www.celiac.com/forums/topic/117090-gluten-free-food-alternatives-list/

^very nice list of where to get alternatives, ingredients, foods, etc. and how to get them.

OH and many of us find that damage caused malabsorbtion issues, you need to check about seeing getting tested for different deficiencies you might have, common ones are magnesium, iron, b-vitamins, calcium, vitamin D, vitamin E and a few others. I will give you a example page of foods and supplements I take to manage stuff.

https://www.celiac.com/forums/topic/116482-supplement-and-foods-you-take/

 

SteveB Rookie

Ennis, thanks for the reply and info.

I've done a lot of reading and I must have missed the info on eating no oats. I purchased Bob's Red Mill gluten-free Quick Cooking Rolled Oats (Whole Grain) and some Udi's gluten-free Original Multi Grain Hot Cereal. I mix about 1/4 cup of each with hot water and add about a tablespoon of pure Vermont maple syrup to it.

I've been eating whole foods since my diagnosis except for breakfast when I eat the oats/oatmeal.

And from the sounds of what you've been going through, your Celiac disease is much worse than mine. I wish you the best of luck in your journey through this problem....

Thanks for your input.

 

Ennis-TX Grand Master
1 hour ago, SteveB said:

Ennis, thanks for the reply and info.

I've done a lot of reading and I must have missed the info on eating no oats. I purchased Bob's Red Mill gluten-free Quick Cooking Rolled Oats (Whole Grain) and some Udi's gluten-free Original Multi Grain Hot Cereal. I mix about 1/4 cup of each with hot water and add about a tablespoon of pure Vermont maple syrup to it.

I've been eating whole foods since my diagnosis except for breakfast when I eat the oats/oatmeal.

And from the sounds of what you've been going through, your Celiac disease is much worse than mine. I wish you the best of luck in your journey through this problem....

Thanks for your input.

 

You might be alright to reintroduce them later. But some celiacs react to oats just as bad as gluten containing grains. There is also the huge industry issues with oat purity issues and being gluten free.  I personally have a minor reactions to oats, and quite minor. It took someone else harking on me to point it out actually. Luckily I do not have to worry about oat CC making me sick in my gluten-free bakery lol. So just avoid them for now til you stabilize your diet and system in a month or two then try them for a few days and record how they make you feel both mental and body wise.

  • 4 months later...
Rhotitar Apprentice

I am not sure if it's new symptoms or I may just be more aware of it but I now know when I accidentally eat gluten I get migraines, insomnia, irritability, and fatigue in addition to my hallmark symptom of intense right uppper abdominal pain. Also someone I know who also has had celiac since she was a child developed herpetiformis dermatitis after being an adult that's scary. 


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



Celiac.com Sponsor (A8-M):



plumbago Experienced

This is in many ways a key question in understanding celiac disease, and one I have never really been able to satisfactorily answer in myself or understand the pathophysiology of in general, especially neurological symptoms (I mean, really understand).

First of all, it's always hard for me to make a definitive connection of possible symptoms to something I've eaten. One or two times after eating out in a restaurant, I suspect I was "glutened," but again do not know for sure. The reaction I had was a flushed feeling, warmth all over (I may have spiked a little fever) and then, once, D. But it's that flushed inflammatory reaction I've felt a couple of times.

On the other time, there've been occasions when I ate something that I later learned actually had gluten in it, but had no reaction at all.

Great question.

Plumbago

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,607
    • Most Online (within 30 mins)
      7,748

    Noniangie
    Newest Member
    Noniangie
    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

    • Scott Adams
      It seems like you have two choices--do a proper gluten challenge and get re-tested, or just go gluten-free because you already know that it is gluten that is causing your symptoms. In order to screen someone for celiac disease they need to be eating gluten daily, a lot of it--they usually recommend at least 2 slices of wheat bread daily for 6-8 weeks before a blood screening, and at least 2 weeks before an endoscopy (a colonoscopy is no used to diagnose celiac disease). Normally the blood panel is your first step, and if you have ANY positive results there for celiac disease the next step would be to take biopsies of your villi via an endoscopy given by a gastroenterologist.  More info on the blood tests and the gluten challenge beforehand is below: The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate. Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:   Not to discourage you from a formal diagnosis, but once you are diagnosed it may lead to higher life and medical insurance rates (things will be changing quickly in the USA with the ACA starting in 2026), as well as the need to disclose it on job applications. While I do think it's best to know for sure--especially because all of your first degree relatives should also get screened for it--I also want to disclose some negative possibilities around a formal diagnosis that you may want to also consider.  
    • Wheatwacked
      Yes.  Now, if you hit your finger with a hammer once, wouldn't you do your best not to do it again?  You have identified a direct connection between gluten and pain.  Gluten is your hammer.  Now you have to decide if you need a medical diagnosis.  Some countries have aid benefits tgat you can get if you have the diagnosis, but you must continue eating a gluten-normal diet while pursuing the diagnosis. Otherwise the only reason to continue eating gluten is social. There are over 200 symptoms that could be a result of celiac disease.. Celiac Disease and Non Celiac Gluten Sensitivity  both cause multiple vitamin and mineral deficiency.  Dealing with that should help your recovery, even while eating gluten.  Phosphatidyl Choline supplements can help your gut if digesting fats is a problem,  Consider that any medications you take could be causing some of the symptoms, aside from gluten.        
    • trents
      Welcome to the forum, @Ben98! If you have been consciously or unconsciously avoiding gluten because of the discomfort it produces then it is likely that your blood antibody testing for celiac disease has been rendered invalid. Valid testing requires regular consumption of generous amounts of gluten. The other strong possibility is that you have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms with celiac disease but does not have the autoimmune component and thus does not damage the small bowel lining. It is 10x mor common than celiac disease. There is currently no test for NCGS. Celiac disease must first be ruled out. Some experts in the field believe it can be a precursor to the development of celiac disease. Having one or both of the primary genes for developing celiac disease does not imply that you will develop active celiac disease. It simply establishes the potential for it. About 40% of the population has the genetic potential but only about 1% develop active celiac disease. 
    • Ben98
      TTG blood test and total IGA tested on many occasions which have always remained normal, upper GI pain under my ribs since 2022. I had an endoscopy in 2023 which showed moderate gastritis. no biopsy’s were taken unfortunately. genetic test was positive for HLADQ2. extreme bloating after eating gluten, it’ll feel like I’ve got bricks in my stomach so uncomfortably full. the pain is like a dull ache under the upper left almost like a stitch feeling after a long walk. I am just wanting some advice has anyone here experienced gastritis with a gluten issue before? thank you  
    • Wheatwacked
      "Conclusions: The urinary iodine level was significantly lower in women with postmenopausal osteoporosis, and iodine replacement may be important in preventing osteoporosis"  Body iodine status in women with postmenopausal osteoporosis Low iodine can cause thyroid problems, but Iodine deficiency will not show up in thyroid tests.  Iodine is important for healing, its job is to kill off defective and aging cells (Apoptosis). Skin, brain fog, nails, muscle tone all inproved when I started taking 600 mcg (RDA 150 - 1000 mcg) of Liquid Iodine drops. Some with dermatitis herpetiformis, Iodine exacerbates the rash.  I started at 1 drop (50 mcg) and worked up to 12 drops, but I don't have dermatitis herpetiformis.
×
×
  • 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.