Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Cross-Contamination Realities- Grits


Finally-45

Recommended Posts

Finally-45 Contributor

I've posted another question here,I'm basically just trying to figure out if I'm in the super sensitive Celiac category, should I act like one for a little while, or if I can relax since this is all so new to me.

I had grits this morning from a cafeteria and it occured to me I should see what the gluten-free community says about grits even though it's made from hominy. Most people seem to worry about cross-contamination.

I don't feel anything with the grits, but I did feel nauseated when I ate a cold cereal, which was listed less than 20ppm of gluten. I've had steel-cut oats, no problem. (I've avoided all other oats with little effort.) I felt sick from Chinese food, and decided to give it up. There is no doubt that I don't tolerate caramel color at all, even from a single cough drop.

The great thing is that I know what to look for now. Should I go to the paranoid level and try to eat all fresh foods that I prepare or are from a reputable gluten-free source?

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



T.H. Community Regular

It seems to be a matter of preference in the beginning. IMO, there's two ways you can go:

1. Go super gluten free from the beginning, eating only whole, fresh foods or reputable gluten free grains. Then when symptoms resolve, slowly add foods back in and see what you tolerate.

or

2. Go gluten free with whole foods and gluten free products, and then if things do not resolve, slowly take things out until you stop having reactions.

Right now, it sounds like you're probably following a slightly risky gluten free diet, not quite as gluten free as #2. Some examples.

Steel cut oats, if they aren't tested to be gluten-free, are a huge risk. They are almost always contaminated (to the point that scientists thought for a while that oats had some similar proteins to wheat, when it was just cross-contamination).

Chinese food (like fried rice) often has soy sauce added, and soy sauce has wheat as an ingredient. Unless you made it yourself with gluten-free soy sauce, of course.

Grits might be cc'd (many tolerate them fine) but if you didn't discuss your dietary needs with the chef at the cafeteria - avoiding gluten cross-contamination - then that's a more likely cause of gluten cc than the grits themselves.

So as to what to do, I guess I'd say you should decide what matters more, at this point. The diet challenges or the symptoms challenges. For me, the symptoms were so debilitating that the diet challenge of going super gluten free was better than living with the symptoms. My father was the opposite.

Link to comment
Share on other sites
Skylark Collaborator

If you're in the US and don't tolerate carmel color, it's not a gluten issue. It's made from corn or the package has to declare wheat.

I agree with T.H. that you really don't quite have the diet right yet. You have to get certified gluten-free steel cut oats. Bob's Red Mill makes them. Chinese food is always a no-go. Even if you order a dish without the soy sauce (which is usually made from wheat and soy) it will be CC'd from the seasoned woks. I worry less about grits, although you can never be 100% sure about gluten CC with any grain.

I don't think eating fresh foods you prepare and sticking to tested gluten-free grains is "paranoid". I think that's the celiac diet. I rarely eat out, and if I do it's at a restaurant with a gluten-free menu. For bread, I buy brands like Rudi's and Udi's. I get my flours from Bob's Red Mill, who tests for gluten.

Link to comment
Share on other sites
padma Newbie

I've posted another question here,I'm basically just trying to figure out if I'm in the super sensitive Celiac category, should I act like one for a little while, or if I can relax since this is all so new to me.

I had grits this morning from a cafeteria and it occured to me I should see what the gluten-free community says about grits even though it's made from hominy. Most people seem to worry about cross-contamination.

I don't feel anything with the grits, but I did feel nauseated when I ate a cold cereal, which was listed less than 20ppm of gluten. I've had steel-cut oats, no problem. (I've avoided all other oats with little effort.) I felt sick from Chinese food, and decided to give it up. There is no doubt that I don't tolerate caramel color at all, even from a single cough drop.

The great thing is that I know what to look for now. Should I go to the paranoid level and try to eat all fresh foods that I prepare or are from a reputable gluten-free source?

Chinese food has been off my list for a long time. Too risky. Even "wheat free" soy sauce usually has some wheat! Ugh!

Eating in a cafeteria that is not committed to be gluten free is dangerous. The chef can stir one pot of gluten with a spoon and use the same spoon in another "gluten free" pot.

The same goes for tortillas in Mexican food places. I ask them to use a clean pan to warm up the corn tortilla and NOT to put it on the stove where they warm up the flour tortillas.I ask them to wash their hands or change their gloves. I about drove a man crazy last weekend trying to explain what i needed. I didn't get sick, so he did a great job. I get so frustrated sometimes in ordering, especially if there is a language barrier, that I almost cry. I didn't use to persist because i was embarrassed, but not anymore.

The longer you are totally free of gluten the easier it will be for you to sort out where it is hiding. Also, as you find the other things you are allergic to, it will get easier.

Some candy is made on conveyor belts that have gluten on them and they don't have to list that because it is not an ingredient. I don't eat any candy except for dark chocolate without dairy or nuts made in a facility without gluten. I don't eat cough drops.

I got really tired of accidentally getting glutened by eating a product that wasn't really gluten free, so I'm rarely eating them anymore. My episodes of getting sick have diminished to an exposure only once in a very great while. My digestion is back to normal and no more pain. This site with everyone's helpful ideas is what got me over the hump. Good luck. You'll figure it out. Be patient with yourself.

Link to comment
Share on other sites
Skylark Collaborator

Some candy is made on conveyor belts that have gluten on them and they don't have to list that because it is not an ingredient. I don't eat any candy except for dark chocolate without dairy or nuts made in a facility without gluten. I don't eat cough drops.

Can you substantiate this, please? I believe it's a rumor and no manufacturers have said anything about belts with gluten when we have written and asked about CC.

Link to comment
Share on other sites
Finally-45 Contributor

Thanks, everyone. The caramel color is still an outstanding issue. There seems to be some disagreement, I just know that when I eat caramel color products, I get terrible indigestion and a swollen throat, so quickly that I could easily connect it to caramel color. But on the other hand, I do recall sometimes having a cola and not being bothered and just wondering if I was just having a "good" day.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,045
    • Most Online (within 30 mins)
      7,748

    Averyreed8
    Newest Member
    Averyreed8
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      Hi Katie I am so sorry you had two miscarriages in the past.  Try not to worry, though, because it could be that they were unrelated, perhaps? Well done for contacting your GP.  Is it possible that you can speak to your midwife in the meantime for a chat?    Cristiana  
    • Katiec123
      @cristiana hi!  the things I’ve read online about having untreated coeliac disease whilst pregnant has really scared me and made me very hesitant to continue eating it. I feel like the best option might be to eliminate gluten from my diet now and then continue with testing after I’ve given birth. I’ve got in touch with my gp and am due to get a phone call back on Monday. Really worried now as I’ve had 2 miscarriages in the past 
    • cristiana
      @Katiec123 Welcome to the forum. I started to have symptoms related to coeliac disease (mouth ulcers, aura migraines etc) but no gastric symptoms during my first pregnancy.  That went to term, in fact, I was 10 days over and had to be induced.  But my second baby, born 21 months later, arrived at 33 weeks.  He's now doing well, and taller than all of us - it was just an earlier than expected arrival! I agree, it would not be wise to eat gluten  if there is any suspicion that you have coeliac disease during a pregnancy.   It would of course be good to know for sure, one way or another, because I believe coeliacs receive extra monitoring during pregnancy in many countries.   I think it may be well worth asking your GP if you can be referred to a gastroenterologist for a formal diagnosis asap.   By the way you spell 'coeliac' I'm guessing you are posting from the UK?  If that is the case, the NHS may rush things along for you, I suspect they will.  If it appears that they cannot refer you urgently, if you have the money for a private consultation it might be well worth it, as there is a trend here in the UK (I'm British) to diagnose coeliacs without the need for an endoscopy if the blood test results are compelling. Sounds like this is the case for you.  If you can see a gastroenterologist privately s/he might be able to diagnose you there and then (make sure you take a printout of your blood tests). Generally, there is a lot of support for coeliacs through the NHS, with a nutritionist, annual reviews and blood tests to check for diet compliance and health related issues, DEXA scans to check bone density, extra vaccinations where indicated and in some areas, certain gluten free food available on prescription.  So for lots of reasons, if you can get a diagnosis it's worth it. I hope all goes well with your appointment, let us know how you get on.
    • Shireen32
      Hi , since being gluten free I am still having bad stomach problems . Such as constant gas in my stomach 24/7 ,burning, constant bubbling noises coming from my stomach and gurgling sounds that never stop .Pain under the left side of my rib cage when ever I eat and just always there’s pain there  .  My symptoms have not improved at all since being gluten free.  Could this be refractory coeliac disease ?? How is that even diagnosed or confirmed  ?  I had tests recently and this is what they say :Endomysial abs (IgA) -Positive  TTG abs (IgA)U/ml : My result is : 0.9 U/ml The Range:0 - 10 U/ml What does this mean pls ??? How can I still test positive for Endomysial abs when I am gluten free and am very careful about cross contamination? Do I even have coeliac disease I’m convinced some other digestive disorder is causing these symptoms .   I also have not had a endoscopy and now the gastroenterologist calls me after one year ( I’m from the uk and have free healthcare which has been such a nightmare with all this and never help me  )  so as I am gluten free the gastroenterologist advised me to start eating gluten again to be referred for a biopsy .. Is a biopsy even worth me doing ? The only proof I have is when I was eating gluten I could never get my ferretin , vitamin d and folate levels up . And since being gluten free these have gone up a little bit  . But that doesn’t always mean coeliac as I know gluten stops absorption in even normal people  . Pls can anyone shed some light it’s much needed ! And share some advice or answer my questions above . I have no idea with this whole coeliac stuff and am very much struggling .Much Appreciated .  
    • knitty kitty
      Vitamin D deficiency.  Not enough Omega Threes. Another autoimmune disease like arthritis, maybe.    
×
×
  • Create New...