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

Corn Tortillas


crittermom

Recommended Posts

crittermom Enthusiast

Hi Everyone,

Well I haven't been here in awhile, things have been crazy however thanks to all of your help, my little lady is doing wonderfully! However we had a setback today, first one since she was diagnosed back in early September. Tonight she had bloodin her stool again and it the stool itself is changing color again and she is complaining of stomach upset. The only thing that has changed in her diet is the introduction of corn tortillas. Based on the ingredient list there are no celiac based ingredients nor are there any that I would have to call on such as food starch or flavorings.

My question is this, if these are cross contaminated by being made in the same factory as the flour (which is not mentioned as per 2006 FDA regulations) could they cause a problem and if so, she hasn't had one since friday would it take this long to produce the effects she was having before the diagnosis? How long would it take to see adverse reaction to something? She is getting a blood test done tomorrow as a follow up to her diagnosis so I guess that will give us the true answer but it takes a couple of weeks to get them back.

Does anyone have a corn tortilla that they use successfully? Thanks for you help in advance!

Melissa


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



Celiac.com Sponsor (A8-M):



AmandaD Community Regular

Ortega hard corn shells or El Paso corn tortilla have both worked fine for me. I hear that Mission corn tortillas are also gluten free.

4getgluten Rookie

I eat Mission corn tortillas all the time with no problems. The are labeled gluten-free. I believe Mission corn tortillas are made at the same plant as flour tortillas, but on different lines.

Guhlia Rising Star

Mission corn tortillas are awesome for soft tortillas. They are so much better than the other ones on the market. I haven't had any problems with these and I'm relatively sensitive. As for fried tortilla shells, I often fry my own with Mission. They also make fried ones. Yum.

rlemmon Apprentice

great value brand from walmart. They say gluten free on the bag. :)

Yenni Enthusiast

I got sick from Corn tortillas. The hard kind. It said on the bag that they were gluten free but they make wheat stuff in the same place so I am guessing it was cross contamination. For now I stay away from products like that.

grantschoep Contributor

Mission Corn products are gluten free, and yes, they are produced in the same facility, but they are produced on separate lines. Actaully, the above 3 statements are actually FAQs off their website, hadn't checked their website in awhile. I don't remeber all that being there before.

Open Original Shared Link

(select Food Allergens from the drop down)

I've never got sick off them, and they seem to be pretty serious about the allergen thing. I've called them before and they know what I am talking about immediatly, and do state they put a lot of controls in place to prevent cross contamination. So, I trust them.


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



Celiac.com Sponsor (A8-M):



BRUMI1968 Collaborator

Was she eating corn prior to that? Or is adding the tortilla's the same as adding corn?

jaten Enthusiast

My word is to be careful with the corn tortillas. Others eat Mission, Great Value, and other brands successfully. I get sick from every brand I've tried. I am not corn intolerant, and do not react to On the Border tortilla chips.

If you search you'll see where I posted of my glutenings from tortillas from the beginning of this for me. For a long time I couldn't figure it out because everyone else eats them. But recently, someone else posted that they broke out with DH after eating Mission tortillas. To my knowledge we are the only 2 who suffer from tortillas, but for me there is no doubt...I am glutened by them, and it must be the cross-contamination. It sounds like your daughter may have the same degree of sensitivity.

teankerbell Apprentice

El Milagro are gluten-free. I checked with the manufactuer. They use seperate machines to produce flour and corn tortillas, because both are different sizes.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,137
    • Most Online (within 30 mins)
      7,748

    Jamy
    Newest Member
    Jamy
    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

    • Sarah Grace
      Dear Kitty Since March I have been following your recommendations regarding vitamins to assist with various issues that I have been experiencing.  To recap, I am aged 68 and was late diagnosed with Celiac about 12 years ago.  I had been experiencing terrible early morning headaches which I had self diagnosed as hypoglycaemia.  I also mentioned that I had issues with insomnia, vertigo and brain fog.   It's now one year since I started on the Benfotiamine 600 mg/day.  I am still experiencing the hypoglycaemia and it's not really possible to say for sure whether the Benfotiamine is helpful.  In March this year, I added B-Complex Thiamine Hydrochloride and Magnesium L-Threonate on a daily basis, and I am now confident to report that the insomnia and vertigo and brain fog have all improved!!  So, very many thanks for your very helpful advice. I am now less confident that the early morning headaches are caused by hypoglycaemia, as even foods with a zero a GI rating (cheese, nuts, etc) can cause really server headaches, which sometimes require migraine medication in order to get rid off.  If you are able to suggest any other treatment I would definitely give it a try, as these headaches are a terrible burden.  Doctors in the UK have very limited knowledge concerning dietary issues, and I do not know how to get reliable advice from them. Best regards,
    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
×
×
  • 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.