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

Please Help Me Figure Out What Is Glutening Us


hadabaday2day

Recommended Posts

hadabaday2day Explorer

I know I have seen a post like this before, but now I can't find it. My son and I have been gluten free since January and we were doing well for months. Now for the past month it seems we are constantly on again off again with symptoms. I pretty much feel like I did before I stopped eating gluten. I have indigestion EVERY time I eat. I am miserable all over again. I have been glutened twice that I know of since being gluten-free and both times I was incredibly nauseous. Now I am not nauseous, just indigestion, so I feel like I must be getting a steady stream of gluten if I am getting it. My son is on and off with very mild diarrhea after months of miraculous (to us anyway) solid poop. And his itchy bumps and eczema are back, just mildly, but he has been clear skinned since February. He says his tummy hurts every few days. He is only 3 so no much info from him other than what I can observe. I don't think I have introduced anything new into the house and our whole house is gluten-free so no CC. I have been doing my best to eliminate questionable things like Frito Lay products. I checked my floss, toothpaste, soap, all other toiletries are formulated gluten-free. I haven't checked the dishwasher soap, but I was pretty sure that Palmolive said all their products were gluten-free. Please correct me there if you know otherwise. I have been over and over all our food. We eat things mostly labeled gluten-free or if not I check carefully. Only things I question even though I have checked would be Hormel chili (only reg w/beans or Chunky no beans) Fritos, and tortilla chips (CC is possible I guess).

A week and a half ago I stopped getting anything to eat outside of the house besides coffee. And while I think it is very possible to get CC at Starbucks, I can't see it happening consistently now when it never happened before.

The only other reasonable thing I can think of is that it is purely coincidental that we are both getting "glutened." Maybe my stomach just hurts because my depression has been back for a month or so and my son has been attending daycare for about the same amount of time. His daycare provider is very knowlegible and I bring ALL his food, but CC is very possible just from playing with gluten covered kids.

Any ideas out there that I am missing. Feel free to ask any questions. Help please! We were feeling so good.


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



Celiac.com Sponsor (A8-M):



hadabaday2day Explorer

I forgot, we have also been eating a ton of Sour Patch Kids lately, but the ingredients looked okay.

RESO Apprentice

Just a thought, is it possible that you and your son are reacting to the dyes in the sour patch kids? The reason I am asking is that I have been finally starting to feel pretty good lately, but noticed when I ate pistachio ice cream that I got bloated and gassy, but not with any other flavor, so I'm pretty sure that the green dye is what did it.

Another thing to consider is that it takes a long time to feel better on a consistent basis. I say this based on my experience so far and based on many posts in this forum.

Would you be willing to try eliminating the sour patch kids for about a week to see if it makes any difference?

And a third thought, is there anything else you have introduced to your diet over the last month that you weren't eating before? Even if it's gluten free, you may be reacting to something else in the new food.

Good luck finding the right answer and I hope you and your son feel better soon.

FMcGee Explorer

I have gluten-like reactions to things like barbecue sauce, even if they're gluten-free, because they almost always have high fructose corn syrup in them, and I think that just doesn't sit well with me. Also, if I get too much sodium, I feel sick. I don't know if either of those are your problem, of course - just throwing it out there. Good luck, and I hope you feel better soon!!

Sassy-1 Newbie

Coffee may be the culprit for you. I have found that my system has become so sensitive that regular coffee on a daily basis just kills me. I have had to switch to low-acid coffee and have no problems.

Starbucks is also a major problem for me. Within a couple of hours of anything from Starbucks other than tea from a tea bag, I have the worst stomach issues that can be quite embarrassing if I'm around anyone.

Not sure what else it might be with your son. It has to be so hard with a little one. I would double-check with the daycare to be sure the kids aren't sharing snacks. They might think it's okay for him to have "just a taste". I know from personal experience that "just a taste" builds up over time and I end up sick sick sick.

Hope this helps a little. :)

darlindeb25 Collaborator

Maybe the two of you are super sensitive. Most grains have a measurable amount of gluten in them, although the amount is less than 20ppm, so it can be labeled gluten free. Many of us cannot eat gluten free cookies, crackers, and such for this reason. Some people will react to as little as 5ppm. There is not available testing for less than 5ppm, so who knows if there is any grain out there that really is gluten free.

Try staying away from processed foods for a while, see if that helps, then try one at a time, to find out what is effecting you.

You both may possibly have other intolerance's too, yet both having problems at the same time seems like maybe a little gluten is getting to you.

ang1e0251 Contributor

I agree with the PP. You said you are eating things labeled gluten-free but those can have those small amounts of gluten as she mentioned. I would stop eating all processed foods for awhile and see if you can't get your good health back. If you eat only whole foods you prepare yourself, then slowly add new foods, one at a time, you should be able to pinpoint the culprit.


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



Celiac.com Sponsor (A8-M):



Ahorsesoul Enthusiast

Do you take vitamins that might not now be gluten-free?

nutralady2001 Newbie

Have you checked the ingredients list of what you buy, could they have changed?

The first few months I stuck to fresh fruit/veg/meat chicken

hadabaday2day Explorer

Thank you to everyone who responded. First off, my vitamins are okay, my prescriptions, with the exception of one that said they add no gluten ingredients but can't guarantee anything, are ok. I check everything that goes into my shopping cart every time. Even if I buy it every week.

I have considered other intolerances, but if that is what it is then kill me now, I can't deal with anything else.

Daycare would never let my son have just one taste. I am positive on that one, but I know that kind of thing happens.

I would totally be willing to give up the Sour Patch Kids and all other food dyes and see if that helps. I have also eliminated all msg that I possibly can. And I plan on stopping with the coffee or at least making it at home to start and go from there.

We don't live off of prepackaged stuff, but we do eat some and while I wouldn't have a problem eating a whole food diet, my 3 year old is a different story. My kids are far from your typical "fast food era" kids even before gluten-free, but my son is kinda picky. We don't eat a lot of sweets or cookies, we mainly buy Chex, gluten-free crackers, white rice, pasta sauces, refried beans, chili, quinoa, potato chips (sometimes), yogurt, some canned veggies and fruit, but mainly fresh, hot dogs (nitrate free), bacon (nitrate free, uncured), turkey, corn tortillas, gluten-free bread, gluten-free baking mixes, potato flakes, and peanut butter. That is pretty much the extent of things that come in a package that reside in my house. I am not sure if "whole foods" means not eating rice and quinoa and corn tortillas or if it just limits things with more than a couple ingredients or un-natural ingredients. If someone could specify that would be great. I could probably get my son to do it if he had those options, but not without it.

Other than that I don't know. My son is more covered in hives by the day. My husband thinks I am a whack job. He tries not to, but he gets frustrated when I take away one thing after the other. My son is more covered in hives by the day, but it kills me to think of pulling him out of "preschool". He loves it so much and he just started. I really think I am missing something though because my stomach hurts about 60% of the time and feels normal the rest. It seems that whenever my stomach hurts, my son has new hives, or a stomachache too. I have a nagging feeling that it's right in front of my face.

Thanks for all your suggestions. I'm sure I will figure it out eventually.

tom Contributor
.. . .

Most grains have a measurable amount of gluten in them, although the amount is less than 20ppm, so it can be labeled gluten free.

Wow, that's a new one - except of course for oats.

darlindeb25 Collaborator
TOM...Wow, that's a new one - except of course for oats.

Isn't the implementation of gluten ppm in the future in the U.S.?

To begin with, they can't even test lower than 5ppm, so telling us gluten free is just a guess. Some celiac's/gluten intolerants can tolerate less than 20ppm, some less than 10ppm, some less than 5ppm, and some of us, none, we can't have gluten. If I eat 2 gluten free cookies, I will deal with it for at least 3 weeks. Even GIG will tell you, their verification of companies only goes down to 10ppm:

Open Original Shared Link

Does gluten-free certification guarantee that a product is gluten-free?

The mark assures that the product contains less than 10-ppm gluten (5-ppm gliadin) and similar proteins from rye and barley as measured by using testing methods that are accepted for gluten testing by analytical associations such as the Association of Analytical Communities (AOAC), testing researchers and other such agencies. No testing method is available that measures to zero.

So, hadabadday2day, it's possible your little guy is still reacting to the gluten in some of the products. IF you can bake, maybe you could make him almond flour cookies or something. I am not a good source for recipes...I do not eat any processed foods, only whole foods.

ang1e0251 Contributor

We don't eat a lot of sweets or cookies, we mainly buy Chex, gluten-free crackers, white rice, pasta sauces, refried beans, chili, quinoa, potato chips (sometimes), yogurt, some canned veggies and fruit, but mainly fresh, hot dogs (nitrate free), bacon (nitrate free, uncured), turkey, corn tortillas, gluten-free bread, gluten-free baking mixes, potato flakes, and peanut butter.

I see potential probelems in a few things. Potato chips, some brands like Lays, have no gluten in them but are made in a shared facility. I can eat them 10 times with no problem, then the 11th time whammy. I stopped eating them. Lays Stax are reported to be OK. Corn tortillas, in the beginning, I could eat the cheapest kind. Then I started reacting to something I was eating every day. It was mild but was building up. Someone wrote her son could only eat Mission tortillas or he reacted. I realized I was becoming more sensitive. When I stopped eating them, I was OK. Now I just eat Mission if I eat them. Now about gluten-free bread & mixes, as has been pointed out many of these have small amounts of gluten and sensitives will react to them. The other problem, for me anyway, is just too much grain does not sit well with me. I've cut way back on them and I feel really good.

That is pretty much the extent of things that come in a package that reside in my house. I am not sure if "whole foods" means not eating rice and quinoa and corn tortillas or if it just limits things with more than a couple ingredients or un-natural ingredients. If someone could specify that would be great. I could probably get my son to do it if he had those options, but not without it.

Whole foods would be foods that are complete as they come from nature; meat, fruit, vegetables, nuts, beans & rice. Also you want to use simple seasonings while you are in this transition. The point is that if you back off to eating whole foods for a time, your system should recover and you should regain your good health. If you still don't, then it's probably some other problem medically or another food intolerance like maybe dairy. If you do feel better, then after a month or so, start adding other foods back in but only one at a time. This should make the problem food clear to you. I don't know what you can get your son to eat but this is a clear and logical way to approach your problem. Otherwise, it's just hit and miss experimentation.

I have a nagging feeling that it's right in front of my face.

I have had more than a few of those moments. I hope you're able to pinpoint it.

TrillumHunter Enthusiast

What about Play-Do at the preschool? That's a no-no for gluten-free kids, right? Mine are past that stage so I'm not sure.

For you, what about your gallbladder? I struggled with nausea until I had it out. It was full of garbage and making me very sick.

I agree with the pp about some of those products but maybe there is another issue?

taweavmo3 Enthusiast

That's a tough one. I have some thoughts.....like the other poster said, coffee may be killing your stomach. I reluctantly gave it up four weeks ago b/c I couldn't figure out why my stomach was so sensitive. I gave up coffee, and feel a TON better. The first few days were rough, but I drank some Coke to tide me over until I could cut caffeine out completely. I won't lie, I still miss it, lol....but I'm not having stomach issues anymore and can eat more foods.

Also, I have a super sensitive daughter, and I really try to stay away from mainstream processed foods that aren't made in a gluten free facility. I have been right where you are, where I'm combing through everything b/c she's acting like she's been glutened, but can't find the hidden source. Sometimes, as frustrating as it is, even the products labeled gluten free still have gluten in them. Rice Dream is one example, it still has barley malt, but it is less than 20ppm so it can now be labeled gluten free (and they took barley malt off of the ingredients list despite it still being in there). Many people still react to any amount of gluten, even if it is supposed to be in the safe range. I stick with mixes from companies I trust like Namste, Enjoy Life, Kinnikinnick and Glutino.

Oh, also consider the Chex cereal. My dd does react to Chex. I'm not sure why, b/c it is gluten free, but she has been much better since I quit buying Chex. I have noticed a few others on here questioning the Chex cereal too, it seems some react and some don't.

Hope that helps! It is frustrating to cut out more foods, I know. I have found that this diet is a neverending learning process...we've been at this for 4 years, and still make mistakes or have to cut out another food that we thought was safe. That's why this board comes in so handy! Good luck to you.

wild fisher Rookie

I can eat them 10 times with no problem, then the 11th time whammy. Then I started reacting to something I was eating every day.

This happens to me and it makes me feel like I'm psychotic. Do you know why this happens. One example out of many. I ate a bannana with Natural peanut butter and honey. I felt fine for a couple of weeks then whamo my stomach is bloated to it's full compacity and painful. I've given up Soy and Dairy for the past few months. I felt great for about a week then right back to feeling like I've been glutened.

ksymonds84 Enthusiast

I've been gluten free for over a year and a half (except during the gluten challenge that I had to end recently) and have found that symptoms will pop up and you sometimes just can't find the cause. It could be hidden gluten such as reacting to 20 ppm or just that our system isn't completely healed (some adults can take 2 years or more depending on damage), or other intolerances that we haven't figured out. Lay's chips for instance is made in a shared facility and maybe 10 bags were okay but the 11th got some contamination. Its frustrating I know!

tom Contributor
If you do not believe me, believe them, they are the ones certifying our gluten-free foods.

I suppose I shouldn't be surprised that you've missed the point of my post, which wasn't about testing ppm, but rather this assertion:

Most grains have a measurable amount of gluten in them,
Mtndog Collaborator

Several people have posted that they react to the gluten-free Chex. I also can't eat Frito Lay products- I react to their chips, Fritos Cheetos- even though they are technically gluten-free. I eat Utz chips with no problem (and think they are even tastier!).

I've also had problems with Starbuck's and CC but since it's both you and your son reacting to something- I would eliminate all the processed foods you BOTH eat and go from there.

Hope you both feel better soon!

darlindeb25 Collaborator

A friend mentioned this in another forum, and I felt it may pretain to you:

My super, duper silly girl cannot be in a shared space without getting sick. She doesn't like church because it makes her sick. Just playing in the nursery is enough to get her reacting, even when no food is present. Playdoh is another huge issue that covers EVERYTHING. We are getting ready to give preschool a go, but we are working hard to make the space as clean as possible, and I have no idea if it will work. We have had issues with gluten exposure from caregivers that come to our home! We have had to implement protocols to ensure that the caregivers remain gluten free. When one of our babysitters started working at Huddle House and riding with her gluten eating dogs to work (again - that was against protocol because of earlier issues with gluten eating dog contact with the same clothes that she wore to work, but she had lost her car and was getting a ride from her mom that thought she was being a PITA), we started having gluten CC issues AGAIN.

TOM

(darlindeb25 @ Jul 11 2009, 05:14 AM)

If you do not believe me, believe them, they are the ones certifying our gluten-free foods.

I suppose I shouldn't be surprised that you've missed the point of my post, which wasn't about testing ppm, but rather this assertion:

I wasn't directing that statement at anyone...I have removed it, I guess you thought I was directing it at you...I wasn't. I was so disappointed when I found out about grains, and that the foods we trust can still contain gluten. I work so hard at being gluten free, and at every corner I run into a new intolerance. BUT, are they intolerance's or cross contaiminations? Two cookies can mess me up for 3 weeks, and I find it so unfair. I often say I wish I was ONLY celiac, and not so sensitive.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,961
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    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.