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

I Think I’Ve Been “Corned”


FruitEnthusiast

Recommended Posts

FruitEnthusiast Enthusiast

I think there has been hidden corn in my diet from something I new nothing about: Plastic made from corn!

 

I’ve been sensitive to corn for decades, I’ve avoided it entirely since my gluten problems started. For the last week or two I’ve been itchy from a newly developed fragrance intolerance. I’ve been getting all new fragrance free products, but not feeling better really. I kept thinking that I still almost felt like I was feeling itchy from the inside out. Even my eyes were burning off and on.

 

Then I just learned on this site (thanks Bartfull :)) about corn being used to make plastic to avoid the harmful BPA problem, including in the lining inside canned food!!! I didn’t even know cans were lined with plastic!

 

I usually eat non-processed whole foods and I was starting to feel a lot better lately. Until the last couple weeks when I added something new to my diet: Wild Planet canned tuna, the healthiest, lowest mercury tuna in a can. I think it corned me!!!  I was eating some canned fruit too.

 

I’ve been having trouble sleeping, which usually doesn’t happen. I feel terrible. I’m really overwhelmed from a lack of sleep and I’m starting to lose it. No more canned anything. I need to research my bottled water now, especially since most of my drinking water comes in liter-sized clear plastic from Trader Joe's. The cloudy water containers are supposed to be better (thanks again to Bartfull for the info :)).

 

This gluten thing along with all the other food reactions has turned out to be a very complicated, ongoing, twisty-turvy bugger! I don’t know what I would do without this site. I hope this info helps others too.


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

FruitE, have you checked your medications and supplements? Almost all pills and capsules contain corn starch. As I told you, corn starch doesn't have the protein that other corn byproducts do, but it might not hurt to check.

 

Another biggie is "citric acid" and "ascorbic acid". You would THINK these came from citrus fruits, but alas, they can get them from corn and usually do because it is cheaper. The last time I got corned it was from some vitamin C capsules. The guy at the health food store researched them for me and the best info he could get from the company didn't mention the corn. I tried them and it was the worst reaction I have ever had to ANYTHING! I honestly thought I was going to die.

 

Anyway, that means you should avoid bagged, ready-to-eat salads or carrots in the grocery store. Most are washed in a citrus (corn) wash. My grocer even sells bottles of the stuff and yes, the ingredients label says "citric acid from corn". Restaurant salads MIGHT be washed in this stuff too.

 

If you have any corn questions at all, please feel free to PM me. My celiac is just a mild inconvenience compared to my corn intolerance, but I have learned how to avoid it most of the time.

FruitEnthusiast Enthusiast

Thanks Bartfull! I have many things made of plastic around here too that I'm wondering about, like plastic baggies for example. I probably will have questions for you as soon as my head stops spinning.

 

I developed my corn problem when I worked in Kansas City for three years and that was twenty years ago! I actually had to move back to the CA coast away from the corn crops it made me so sick, and it's been a problem for me ever since. To me corn is just nasty stuff that's way too cheap and easy to use for everything, so not likely to go away...unfortunately.

 

But like you say about your guitar, I can still make my artwork, and that's all that matters!

catmaus6 Newbie

I was diagnosed gluten intolerant. I stopped eating gluten and started feeling better. Quickly I replaced my flour and started buying gluten-free products. Pasts and cereal. I was having burning in my belly and was horribly bloated. I went to a nutrition store and was told to try pancreatic enzymes which seemed to help. Then I had a bowl of honey nut chex. Bam horrible pain. Lasted for a week. I couldn't eat. The doctors were no help. No positive test. Lipase and amalyses negative. Couldn't sleep and no bathroom activities. So I started writing down what I was eating and how I felt. Every time I eat bread (gluten-free) I got sick and bloated. gluten-free stir fry sauce I got sick. Everything had corn in it. I cut put the corn 2 days ago.... Omg the bloat is going away. The burning stopped. I can go to the bathroom. What else do I have to cut out? And why don't doctors know about this corn/ gluten issue. I'm working this out on my own. Any suggestions would be appreciated, thanks!

FruitEnthusiast Enthusiast

Hi catmaus6,

 

Welcome to the site :) There is a lot of support here.

 

The foods that give each of us trouble are as individual as we are. Not everyone is sensitive to corn, but it's good that you found some relief by cutting it out. One important thing to know is that not all foods labeled "gluten free" are created equal. Some brands can be trusted but others are not authentic. Also grains in general can be a problem for many of us when newly diagnosed.

 

The best suggestion I can give you at this point is to check out the information on this site under the "Celiac Disease - Coping with" heading. Look at the "Newbie info 101" posting. There is very helpful info there. Take some time to read that info then if you have more questions, you can start a new topic with questions you may have, so that more members can see your questions and respond.

 

It's confusing at first, learning all the new information, but you'll get the hang of it!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      3

      Related issues

    2. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      3

      Related issues

    3. - MogwaiStripe replied to annamarie6655's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Airborne Gluten?

    4. - knitty kitty replied to Midwestern's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      16

      Gluten Issues and Vitamin D


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,255
    • Most Online (within 30 mins)
      7,748

    BeccaLynn
    Newest Member
    BeccaLynn
    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

    • Jmartes71
      I had the test done by one of the specialist through second pcp I had only a few months because he was saying I wasn't.Even though Im positive HLA-DQ2 .My celiac is down played.I am with new pcp, seeing another girl doctor who wants to do another breathe test next month though Im positive sibo this year.I have high blood pressure not sure if its pain from sciatica or sibo, ibs or hidden gluten. Im in disability limbo and I should have never been a bus driver because im still suffering and trying to heal with zero income except for my husband. This isnt fare that my health is dictating my living and having ti beg for being revalidation of my disregarded celiac disease. Its an emotional roller coaster I don't want to be on and the medical made it worse.New pcp new gi, exhausted, tired and really fed up. GI doctor NOT girl..
    • Mari
      Hi Jmartes, It sure is difficult to get useful advice from medical providers. Almost 20 years  ago a Dr suggested that I might have Celiacs and I took a Celiac Panel blood test. No gluten challenge diet. On that test the tTG was in normal range but an alpha antibody was very high. I went online and read about celiac disease and saw how I could investigate this low tTG and still have celiac disease. Normal tTG can happen when a person had been reacting for many years. Another way is that the person has not been eating enough gluten to raise the antibody level. Another reason is that the tTG does not show up on a blood but may show up on a fecal test. Almost all Celiacs inherit at least one of the 2 main Celiac genes. I had genetic tests for the Celiac genes at Enterolab.com. I inherited one main Celiac gene from one parent and the report said that the DQ gene I inherited from my other parent, DQ6, could cause a person to have more problems or symptoms with that combination. One of my grandmother's had fairly typical symptoms of Celiacs but the other grandmother had severe food intolerances. I seem to show some problems inherited from both grandmothers. Human physiology is very complex and researchers are just beginning to understand how different body systems interact.  If you have taken an autosomal DNA test you can download your raw data file and upload it to Prometheuw.com for a small fee and search for Celiac Disease. If you don't find any Cekiac genes or information about Celiac disease  you may not have autoimmune gluten intolerance because more than 99% of Celiacs have one or both of these genes.  PLEASE ASK QUESTIONS IF YOU WANT TO KNOW EHAT i HAVE DONE TO HELP WITH SYMPTOMS.  
    • MogwaiStripe
      I can't prove it, but I truly believe I have been glutened by airborne particles. I used to take care of shelter cats once per week at a pet store, and no matter how careful I was, I would get glutened each time even if I wore a mask and gloves and washed up well after I was done. I believe the problem was that because I'm short, I couldn't do the the tasks without getting my head and shoulders inside their cages, and so the particles from their food would be all over my hair and top of my shirt. Then I had to drive home, so even if I didn't get glutened right then, the particles would be in my car just waiting for me to get in the car so they could get blown into my face again. I gave up that volunteer gig and stopped getting glutened so often and at such regular intervals.
    • knitty kitty
      Hello, @MogwaiStripe, Vitamin D is turned into its activated forms by Thiamine.  Thiamine deficiency can affect Vitamin D activation. https://pubmed.ncbi.nlm.nih.gov/14913223/ Thiamine deficiency affects HLA genes.  HLA genes code for autoimmune diseases like Celiac, Thyroiditis, Diabetes, etc.  Thiamine deficiency inside a cell triggers a toggle switch on the gene which in turn activates autoimmune diseases carried on the gene.  The reference to the study is in my blog somewhere.  Click on my name to go to my page, scroll down to the drop down menu "Activities" and click on blogs.  
    • knitty kitty
      Hello, @annamarie6655, Yes, there's many of us who react to airborne gluten!   Yes, animal feed, whether for chickens or cats or dogs, can release airborne gluten.  I can get glutened from the bakery section at the grocery store.   The nose and mouth drain into the digestive system and can trigger systemic reactions.   I find the histamine release in response to airborne gluten will stuff up my sinuses and bother my eyes.  High histamine levels do cause anxiety and migraines.  The muscle spasms can be caused by high histamine, too.  The digestive system may not manifest symptoms without a higher level of gluten exposure.   Our bodies make an enzyme, DAO (diamine oxidase), to break down histamine.   Pyridoxine B 6, Cobalamine B12, Vitamin C, copper, zinc, and iron are needed to make DAO.  DAO supplements are available over the counter.  Taking a B Complex supplement and additional Thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) helps reduce the amount of histamine being released.  Mast cells without sufficient Thiamine have an itchy trigger finger and release histamine at the slightest provocation.  Thiamine helps mast cells refrain from releasing their histamine.    I find taking additional TTFD thiamine helps immensely with neurological symptoms as TTFD can easily cross the blood brain barrier without a carrier.  High histamine in the brain can cause the muscle spasms, anxiety and migraines.  Vitamin C really helps with clearing histamine, too.   The Digiorno pizza mystery reaction could have been caused by a reaction to the cheese.  Some people develop lactose intolerance.  Others react to Casein, the protein in dairy, the same as if to gluten because Casein resembles the molecular structure of gluten.  An enzyme used in some dairy products, microbial transglutaminase, causes a gluten reaction because it is the same as the tissue transglutaminase our bodies make except microbes make it.  Those tTg IgA blood tests to diagnose celiac disease measure tissue transglutaminase our bodies release as part of the autoimmune response to gluten.   You're doing great!  A Sherlock Holmes award to you for figuring out the connection between airborne gluten and animal feed!!!  
×
×
  • 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.