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How much is too much gluten?


jkittyberry

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jkittyberry Newbie

I was diagnosed with celiac disease 2 years ago and have been strictly gluten free for a year and a half. Prior to my diagnosis I did not experience any gastrointestinal (or other) symptoms. Last month I decided to have a cheat day (bad, I know) and had no symptoms in the minutes, hours, days, weeks afterward. Basically, I've confirmed I have 'silent' celiac disease.

What I'd like to know is how much gluten will start to damage my intestines. I'm not talking about eating gluten bread again - I'll still stay away from large amounts - but on labels that "may contain" it. I know that it's voluntary for companies to include the "may contain wheat" label on their products so there are discrepancies there anyways, but will the amount of gluten in those products hurt my intestines? Or would it just cause the typical person with celiac to experience symptoms?

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AmandaWiggin Newbie

The way my GI doctor explained too me was that it depends on how advanced your Celiac is.   For example some people can tolerate a small amount of gluten and so it would take longer to have any effects.

but someone whose advanced and cannot tolerate any gluten, not even traces (me for example) I can't go out to eat because even something that says gluten-free it's still cooked in the same surface and becomes gluten laced.

 

someone like that it could affect them really fast... if continued to ignore and eat tons of gluten, it could injure the kidneys, liver, cause neurological issues and could cause cancer.

 

so it really depends on how advanced your celiac is.   For me it's been hard, I was just diagnosed in April and changing 30 years of eating habits is not exactly easy and quite depressing watching family eat out.   My celiac has had me on a severe weight loss pattern (18 lbs in 3 weeks) and a very small appetite.

 

be very careful.  Please feel free to message me and I'd be happy to share recipes and things ???❤️️

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GFinDC Veteran

Hi jkittyberry,

The FDA approved upper limit for foods to be labeled gluten-free in the USA is 20 PPM.  That is a very small amount of gluten.  The limit was set to a level where most celiacs won't experience symptoms/damage.  That doesn't mean there aren't people who will experience symptoms at lower levels though.

Welcome to the forum!

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jkittyberry Newbie

Thanks for the answers guys!

My problem is that I don't experience any symptoms. I know that it is a blessing in some ways, but it makes knowing what/where I can eat difficult. For example, I can't determine if a restaurant prepares gluten free meals properly or not from trial and error and have to base the assumption it's gluten free from the staffs assurances. Which means I don't know if I can eat there again.

I guess my question is if anyone knows if there is a "safe" amount of gluten people with celiac disease can eat before the body starts targeting the intestine. I've tried researching this myself, but most reports state that it varies from person to person and is usually fine until you start to notice your symptoms.

Since I have no symptoms it's difficult for me to determine safe foods/brands and unsafe ones. Up until now I have been extremely strict and will not go near anything that's even potentially contaminated but I am always hearing how some "may contain wheat" food items are suitable for (at least some) people with celiac. I just do not want to harm my body in the process.

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Ennis-TX Grand Master

Ouch, unsure if blessed or not, I can react to residue from touching a surface that had gluten then my food. Hyper sensitive, my issues is I sometimes do not know what caused the reactions, and depending on the form and how it was processed determines if  I get the initial lymph response in 30 sec or have to wait til the gut responds in 30mins. Top it off with all my other allergies >.>

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GFinDC Veteran

Hi again,

I usually leave those "may contain wheat " items on the shelf.  I translate that as may not be worth trying.  I suggest you search for celiac support groups in your area and see what restaraunts they recommend.  In my town Texas Roadhouse has been good for steaks, but I don't know about their other locations.

The damage in celiac disease is primarily caused by an immune system attack on the body.  That's the same immune system that protects you from microscopic germs by hunting them down and killing them dead, dead, dead.  When exposed to an antigen the immune system converts waiting non-specific immune cells into active killer cells for that antigen.  Then they go a hunting.  Your body is what they are hunting.  That's all bad for your gut lining (villi destruction) or skin (Dermatitis herpetiformis-DH), brain (gluten ataxia). liver or other organs that get in the way.

So the goal is always 100% avoidance of any dietary gluten.  Part of the immune problem is that your body doesn't give up making immune killer cells right away.  So you may eat some gluten today and have immune system damage going on for weeks to months.  Youch!

Other celiacs may be able to help in your area.  There are also thread on possible products issues on the forum.  You can search for a product name and see what pops up.

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squirmingitch Veteran

I also leave those "may contain wheat" items on the shelf. Really, my advice to you would be to continue as you had been before this "cheat day" and be very strict. I feel this is especially important for the very reason that you don't have reactions so you don't know when you've even been cross contaminated. Please don't take any chances!

I would say for eating out to check Find Me Gluten Free
Open Original Shared Link

for your area. If I were you I would only trust places with multiple, recent reviews by fellow celiacs.

How much is too much? 20 ppm is too much. Do you know how much that is? Unbelievably minute! Just think of grains of sand. 20 grains in a million grains. Or water..... 20 drops of water in a million drops of water.

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RMJ Mentor

I don't have symptoms either, so my doctor follows my antibodies (the whole panel was high when I was diagnosed).  That is not ideal, the scientific literature says antibody tests are great for diagnosis but not so accurate for followup.   At first I just read labels and avoided anything with gluten-containing ingredients.  Antibodies went down but two were still high.  Then I tried only eating if it was labeled gluten free (and on top of that mainly eating whole foods, meat, fruit, veggies, rice).  Antibodies down more but one still high.  I was due for my every ten year routine colonoscopy so my doctor decided to look at both ends.  I still have Marsh 3A damage.  So now if I eat prepared foods I only eat certified gluten free.  I rarely eat out and only go to a restaurant that is completely gluten free or trained by the gluten intolerance group.  I'm hoping my antibodies will finally be normal next year.  I've been at this for four years now.

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captaincrab55 Enthusiast

One needs to ask their own body what immune diseases, cancers, or other health issues it may decide to bless you with.    The  Medical Science Book for this disease isn't complete and there's no way that we can say what is safe for you.      Don't be foolish with so called, "Cheat Days".....

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GFinDC Veteran

Here's a video by Tricia Thompson that may help explain the gluten contamination risk.

Open Original Shared Link

 

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GF-Cheetah Cub Contributor

"What I'd like to know is how much gluten will start to damage my intestines."

I don't think anyone here or even the G.I. doctors can definitively answer your question.   But what you can do is shortly after your cheat day, go take a blood test, and see what your ttg and other celiac related numbers are.   If your ttg number is elevated, then without outward symptoms, your insides suffered.

My daughter is also a 'silent' celiac.   I have gluten test kits at home, and I test her favorite gluten-free restaurant meals regularly.   Anything tested positive, we would stop ordering that meal for her, or stop going to that restaurant entirely.

My daughter used to be very tall for her age.  But now, she is only 25 to 30th percentile of her height.   So we take her celiac disease very seriously.   If you are formally diagnosed with celiac, you should probably not cheat...

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    • Anmol
      Thanks this is helpful. Couple of follow -ups- that critical point till it stays silent is age dependent or dependent on continuing to eat gluten. In other words if she is on gluten-free diet can she stay on silent celiac disease forever?    what are the most cost effective yet efficient test to track the inflammation/antibodies and see if gluten-free is working . 
    • trents
      Welcome to the community forum, @Anmol! There are a number of blood antibody tests that can be administered when diagnosing celiac disease and it is normal that not all of them will be positive. Three out of four that were run for you were positive. It looks pretty conclusive that you have celiac disease. Many physicians will only run the tTG-IGA test so I applaud your doctor for being so thorough. Note, the Immunoglobulin A is not a test for celiac disease per se but a measure of total IGA antibody levels in your blood. If this number is low it can cause false negatives in the individual IGA-based celiac antibody tests. There are many celiacs who are asymptomatic when consuming gluten, at least until damage to the villous lining of the small bowel progresses to a certain critical point. I was one of them. We call them "silent" celiacs".  Unfortunately, being asymptomatic does not equate to no damage being done to the villous lining of the small bowel. No, the fact that your wife is asymptomatic should not be viewed as a license to not practice strict gluten free eating. She is damaging her health by doing so and the continuing high antibody test scores are proof of that. The antibodies are produced by inflammation in the small bowel lining and over time this inflammation destroys the villous lining. Continuing to disregard this will catch up to her. While it may be true that a little gluten does less harm to the villous lining than a lot, why would you even want to tolerate any harm at all to it? Being a "silent" celiac is both a blessing and a curse. It's a blessing in the sense of being able to endure some cross contamination in social settings without embarrassing repercussions. It's a curse in that it slows down the learning curve of avoiding foods where gluten is not an obvious ingredient, yet still may be doing damage to the villous lining of the small bowel. GliadinX is helpful to many celiacs in avoiding illness from cross contamination when eating out but it is not effective when consuming larger amounts of gluten. It was never intended for that purpose. Eating out is the number one sabotager of gluten free eating. You have no control of how food is prepared and handled in restaurant kitchens.  
    • knitty kitty
      Forgot one... https://www.hormonesmatter.com/eosinophilic-esophagitis-sugar-thiamine-sensitive/
    • trents
      Welcome to the forum community, @ekelsay! Yes, your tTG-IGA score is strongly positive for celiac disease. There are other antibody tests that can be run when diagnosing celiac disease but the tTG-IGA is the most popular with physicians because it combines good sensitivity with good specificity, and it is a relatively inexpensive test to perform. The onset of celiac disease can happen at any stage of life and the size of the score is not necessarily an indicator of the progress of the disease. It is likely that you you experienced onset well before you became aware of symptoms. It often takes 10 years or more to get a diagnosis of celiac disease after the first appearance of symptoms. In my case, the first indicator was mildly elevated liver enzymes that resulted in a rejection of my blood donation by the Red Cross at age 37. There was no GI discomfort at that point, at least none that I noticed. Over time, other lab values began to get out of norm, including decreased iron levels. My PCP was at a complete loss to explain any of this. I finally scheduled an appointment with a GI doc because the liver enzymes concerned me and he tested me right away for celiac disease. I was positive and within three months of gluten free eating my liver enzymes were back to normal. That took 13 years since the rejection of my blood donation by the Red Cross. And my story is typical. Toward the end of that period I had developed some occasional diarrhea and oily stool but no major GI distress. Many celiacs do not have classic GI symptoms and are "silent" celiacs. There are around 200 symptoms that have been associated with celiac disease and many or most of them do not involve conscious GI distress. Via an autoimmune process, gluten ingestion triggers inflammation in the villous lining of the small bowel which damages it over time and inhibits the ability of this organ to absorb the vitamins and minerals in the food we ingest. So, that explains why those with celiac disease often suffer iron deficiency anemia, osteoporosis and a host of other vitamin and mineral deficiency related medical issues. The villous lining of the small bowel is where essentially all of our nutrition is absorbed. So, yes, anemia is one of the classic symptoms of celiac disease. One very important thing you need to be aware of is that your PCP may refer you to a GI doc for an endoscopy/biopsy of the small bowel lining to confirm the results of the blood antibody testing. So, you must not begin gluten free eating until that is done or at least you know they are going to diagnose you with celiac disease without it. If you start gluten free eating now there will be healing in the villous lining that will begin to take place which may compromise the results of the biopsy.
    • Anmol
      Hello all- my wife was recently diagnosed with Celiac below are her blood results. We are still absorbing this.  I wanted to seek clarity on few things:  1. Her symptoms aren't extreme. She was asked to go on gluten free diet a couple years ago but she did not completely cut off gluten. Partly because she wasn't seeing extreme symptoms. Only bloating and mild diarrhea after a meal full of gluten.  Does this mean that she is asymptomatic but enormous harm is done with every gram of gluten.? in other words is amount gluten directly correlated with harm on the intestines? or few mg of gluten can be really harmful to the villi  2. Why is she asymptomatic?  3. Is Gliadin X safe to take and effective for Cross -contamination or while going out to eat?  4. Since she is asymptomatic, can we sometimes indulge in a gluten diet? ----------------------------------------------------------------------------------------------- Deamidated Gliadin, IgG - 64 (0-19) units tTG IgA -  >100 (0-3) U/ml tTG IgG - 4   (0-5) Why is this in normal range? Endomysial Antibody - Positive  Immunoglobulin A - 352 (87-352) ------------------------------------------------------------------------------------------------ Thanks for help in advance, really appreciate! 
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