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

Will Villi Heal If I'm Still Borderline Iga 20 On A Strict gluten-free Diet?


inmygenes

Recommended Posts

inmygenes Apprentice

First diagnosed and eating gluten my IgA was 100+ about 6 months later on a strict gluten free diet it was IgA 29 borderline and now a year and a half later without gluten it's 20 which is still borderline. Does this mean my intestines are still being damaged with tiny amounts of gluten contamination, will they be able to heal? What is your experience with healing?


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



Celiac.com Sponsor (A8-M):



Emilushka Contributor

From a medical standpoint, the lower you can get your IgA (closer to normal) the better for your chances of healing. I don't know what the magic number is that will allow you to heal, but higher antibody levels mean that there's a response to SOMETHING, and unfortunately with Celiac, the response is the problem. So my guess is that you'd need to get your IgA to normal range to heal fully.

However, you may have a personal "normal" range that is higher than other people. It's a possibility. If that were the case, you might heal just fine with your IgA at 20.

How do you feel? Do you have symptoms still?

Skylark Collaborator

You may need to try a very strict diet where you're not eating processed foods. Also, some celiacs react to oats and casein as if they were gluten so stop eating oats, and consider removing dairy from your diet as well. I'm not diagnosed so no experience to share, but I generally feel better if I don't eat processed "gluten free" cookies, breads, and so forth as they all have a chance for minor CC.

BoydBT Apprentice

You may need to try a very strict diet where you're not eating processed foods. Also, some celiacs react to oats and casein as if they were gluten so stop eating oats, and consider removing dairy from your diet as well. I'm not diagnosed so no experience to share, but I generally feel better if I don't eat processed "gluten free" cookies, breads, and so forth as they all have a chance for minor CC.

What is CC?

psawyer Proficient

What is CC?

Cross contamination: the unintentional contamination of a product from another product or source.

Skylark Collaborator

Cross contamination: the unintentional contamination of a product from another product or source.

Thanks, Peter. The board expands the letters G F to gluten-free but I forget it doesn't expand CC. That might be something nice to add.

There was a recent study showing that some flours that would normally be gluten free, like rice or soy, had enough gluten to cause problems for celiacs. The study didn't sample enough products to make any guesses about how often it happens. It's probably a result of manufacturers not cleaning mills well enough, or maybe grains of wheat getting into other foods in grain elevators and trucks. Even the so-called gluten free breads and baked goods are usually tested to be below a cutoff of 10 or 20 ppm, as that is low enough for the tests to be reliable and to not bother many celiacs. I'm sure a lot of their food has less gluten, but the occasional 20 ppm loaf may be enough to keep you from healing.

We had one fellow here who didn't heal until he went to a completely whole foods diet and stopped eating processed foods entirely. Another person has to grind her own flours from grains she gets from certain suppliers who do not process wheat at all. Also, not all celiacs can tolerate things like distilled vinegar or whiskey, even though they do not have detectable amounts of gluten.

inmygenes Apprentice

From a medical standpoint, the lower you can get your IgA (closer to normal) the better for your chances of healing. I don't know what the magic number is that will allow you to heal, but higher antibody levels mean that there's a response to SOMETHING, and unfortunately with Celiac, the response is the problem. So my guess is that you'd need to get your IgA to normal range to heal fully.

However, you may have a personal "normal" range that is higher than other people. It's a possibility. If that were the case, you might heal just fine with your IgA at 20.

How do you feel? Do you have symptoms still?

I think I'm very sensitive to gluten and sometimes get stomach pains and bloating. It's hard to tell as I never had extreme symptoms but was always malnourished and full of toxins. Now I'm much healthier and my mineral levels are normal so I'm absorbing better which is a good sign. According to my natropath I'm no longer full of toxins from undigested food. I'm going to try and get the result lower than 20 but my doctor said that it's almost impossible to get it lower than that.


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



Celiac.com Sponsor (A8-M):



inmygenes Apprentice

You may need to try a very strict diet where you're not eating processed foods. Also, some celiacs react to oats and casein as if they were gluten so stop eating oats, and consider removing dairy from your diet as well. I'm not diagnosed so no experience to share, but I generally feel better if I don't eat processed "gluten free" cookies, breads, and so forth as they all have a chance for minor CC.

Yes I think you're right and I do get a reaction to oats and have stopped eating them. I try and only eat my own bread and cakes etc but even the flour sources are sometime dubious. Recently I've been considering giving up dairy as I get some negative effects from it. So I think gradually I'll weed out potential sources and triggers.

inmygenes Apprentice

Thanks, Peter. The board expands the letters G F to gluten-free but I forget it doesn't expand CC. That might be something nice to add.

There was a recent study showing that some flours that would normally be gluten free, like rice or soy, had enough gluten to cause problems for celiacs. The study didn't sample enough products to make any guesses about how often it happens. It's probably a result of manufacturers not cleaning mills well enough, or maybe grains of wheat getting into other foods in grain elevators and trucks. Even the so-called gluten free breads and baked goods are usually tested to be below a cutoff of 10 or 20 ppm, as that is low enough for the tests to be reliable and to not bother many celiacs. I'm sure a lot of their food has less gluten, but the occasional 20 ppm loaf may be enough to keep you from healing.

We had one fellow here who didn't heal until he went to a completely whole foods diet and stopped eating processed foods entirely. Another person has to grind her own flours from grains she gets from certain suppliers who do not process wheat at all. Also, not all celiacs can tolerate things like distilled vinegar or whiskey, even though they do not have detectable amounts of gluten.

Thanks Skylark this is interesting to read. I read recently that gluten flour can take 2 hours to settle out of the air. It gets everywhere! I try and eat a whole food diet but do have a few processed things. I didn't know about the whiskey and distilled vinegar, that's worrying. I guess it's just trial and error finding out what works.

SYBERBUNNI Newbie

Yes I think you're right and I do get a reaction to oats and have stopped eating them. I try and only eat my own bread and cakes etc but even the flour sources are sometime dubious. Recently I've been considering giving up dairy as I get some negative effects from it. So I think gradually I'll weed out potential sources and triggers.

When you guys are talking oats. Are you talking about non gluten-free oats or oats in general?

Skylark Collaborator

Oats in general. Oats have a gluten-like protein called aveenin. A few celiacs react to aveenin as if it were gluten.

Oats that weren't specially grown and processed to be gluten-free are a problem for all celiacs.

BoydBT Apprentice

What about Bob's Red Mill Oatmeal?

Skylark Collaborator

If you tolerate oats, the Bob's Red Mill oats are pretty carefully grown and tested so they should be safe.

inmygenes Apprentice

Oats in general. Oats have a gluten-like protein called aveenin. A few celiacs react to aveenin as if it were gluten.

Oats that weren't specially grown and processed to be gluten-free are a problem for all celiacs.

I've found I react to pure oats (uncontaminated) and recently read that the Canadian government are doing a study to see if oats cause intestinal damage in celiac patients that react to them. I'm very interested to hear the result.

Skylark Collaborator

There are rather a lot of studies on oats already done. Most celiacs tolerate them, but there are very clear examples of people with activated T-cells, anti-avenin antibodies, and mucosal damage from oats that were tested and gluten-free. I would guess from the literature that maybe 10% of celiacs cross-react to oats. My number may be high as it's a gut feeling and I haven't done a proper meta-analysis. Unfortunately, if the Canadian government uses a small cohort they may not catch the oat-sensitive people. Another problem with the way clinical trials are structured is that celiacs who react to oats tend to feel ill and drop out of the studies.

  • 2 months later...
inmygenes Apprentice

There are rather a lot of studies on oats already done. Most celiacs tolerate them, but there are very clear examples of people with activated T-cells, anti-avenin antibodies, and mucosal damage from oats that were tested and gluten-free. I would guess from the literature that maybe 10% of celiacs cross-react to oats. My number may be high as it's a gut feeling and I haven't done a proper meta-analysis. Unfortunately, if the Canadian government uses a small cohort they may not catch the oat-sensitive people. Another problem with the way clinical trials are structured is that celiacs who react to oats tend to feel ill and drop out of the studies.

Here are some recent studies by the Canadian Government on the safety of Oats. It seems a little inconclusive but generally as you also said most people with celiac can handle them but a small minority are intolerant to oats. I do wonder about the ppm in pure oats as some people react to anything over 10 ppm;

Open Original Shared Link

I've stopped eating oats as I always get a reaction when I eat them and I tend to eat more that the recommended 1/4 cup.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,551
    • Most Online (within 30 mins)
      7,748

    Newest Member

    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
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.