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

Any Way To Counter Act Gluten Once Accidentally Injested?


s-haas

Recommended Posts

s-haas Newbie

I am newly diagnosed with Celiac Disease. I was diagnosed after I finally became so sick I was hospitalized for a week. I have tried very hard to avoid Gluten since my symptoms are very severe. Most of my symptoms have disappeared since eating gluten free. Once in a while I accidentally injest gluten while at a restaurant or through hidden ingrediants. When this happens, within a few minutes I get asthma symptems and very nauseaus. Always the next day I will have extreme edema in my hands and legs. Is there any way to counter act or stop the adsorption of the gluten when you realize that things start to go wrong? I hope some of you who are more experienced with eating gluten free might have some advice. Again, I am not eathing gluten on purpose and I wish gluten would just disappear from my world. It is a bit frightening when the symptoms come on and I feel helpless when I don't know what to do except take an inhaler and hope for the best. Thanks for your help and advice.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

First off mention the asthmatic symptoms to your doctor. You may have a true allergy to wheat in addition to celiac. If that is the case your doctor might want to have you carry an Epi-pen.

Unfortunately there isn't much that we can do once the gluten reaction starts. I find Pepto Bismal helps with the stomach pain I get and I take for sure gluten-free asprin to help with the inflammation. Drinking lots of water might help but for the most part for me time is the true healer.

You may want to avoid restaurants for a bit till you have healed more. Also if you can go with unprocessed whole foods that are naturally gluten free that will help also.

tarnalberry Community Regular

Ditto everything ravenwood said. Right on the money!

CGally81 Enthusiast

I'd always taken L-glutamine. It definitely seemed to help. Chewable, gluten-free (of course), L-glutamine. It seems to stop the symptoms in less than an hour, even the "brain fog" symptoms.

It can't hurt. It's only bad for you if you have kidney or liver problems, otherwise, it only has health benefits. The only side effect is that it's been known to reduce appetite for starch and sugar (which is in fact another reason it's used - to help dieters and alcoholics reduce cravings).

Reba32 Rookie

the other night I felt all bloaty and couldn't figure out why, and then I had some homemade yogurt for dessert and a short time after that I didn't feel so bloaty. I don't know for certain if I got glutened, but something wasn't quite right, but the yogurt seemed to help for some reason. Maybe the bacteria in it.

gaingus Rookie

I agree with a lot of what everyone has posted. Some other things I do also is take gas-ex, just make sure to read the label, there is one that doesn't have "hidden gluten" in it. I also take some benadryl (sp) and tylenol. Other than that lots and lots of water to flush out my system.

JustLovely9216 Rookie

Just my random ideas of what I do that makes me feel better:

Ginger tea and yogurt to aid with digestion.

Exercise to release toxins and aid in digestions.

Warm bath with Epsom salt toxins.

Don't know why, but they do help me!


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



Celiac.com Sponsor (A8-M):



Reba32 Rookie

CGally, what brand of L-Glutamine do you use? And do you use tablets or powder drink mix?

Vitacost.com has diet and sport aids on special, and there are a few options for L-Glutamine. I couldn't find any locally, but I think I might like to try it and keep it around in case of future glutenings.

Are there other benefits to using it? I'm a lot carb-er anyhow, so I don't eat starch or sugars!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,900
    • Most Online (within 30 mins)
      7,748

    tessycork47
    Newest Member
    tessycork47
    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

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for 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.