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

Sensitivity To "oil" ?


loco-ladi

Recommended Posts

loco-ladi Contributor

OK, so a week or so ago I made homemade corn chips only ate a few as I was going to take them to work with me, used cut up corn tortillas deep fried in canola oil.... later had all the usual suspected symptoms on a "minor" scale. But as they did not store well at all was unable to eat the rest.

Bought a bag of fritos while shopping the other day and had "issues".....

Now call me stupid and smack me up side the head..... last night I made taco's for supper, used the store bought hard shell corn tortilla's and guess what, once more I feel like @#$%^&*

Now I am assuming oil is the suspect, its not the same feeling I get when I ingest gluten but it is simular. However I can eat corn without issues in other meals.....

anyone have an opinion on this? I am going with oil otherwise.


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

I get sick from Fritos and felt ill during a day I ate taco shells. Are you using gluten-free products? Also, when I was trying to find gluten-free cornmeal for cooking I had a terrible time locating some since cross-contamination is a big issue. So, I assume that companies do not go as far as I did and use cornmeal regardless of cross-contamination issues. I personally have tried to stay away from processed food made from cornmeal because of this. This could be why eating whole corn leaves you feeling fine while cornmeal leaves you feeling bad. Good luck, Loco_Ladi.

Kristina Marie

loco-ladi Contributor

thanks for the thoughts, will try a few "expiriments" and see what happens

Generic Apprentice

Is it possible that it is the corn? Maybe when it is ground up you digest it more, verses eating it whole. I know allot of people when they eat corn on the cob, out of the can, etc. that they don't really digest it well. And it will come out the "bottom" end pretty much intact.

Just a thought.

andreagrant Apprentice
Is it possible that it is the corn? Maybe when it is ground up you digest it more, verses eating it whole. I know allot of people when they eat corn on the cob, out of the can, etc. that they don't really digest it well. And it will come out the "bottom" end pretty much intact.

Just a thought.

Actually we do digest the kernel of the corn, it's just the yellow outer hull that slips off and is such a good 'tracer' of transit time.

ravenwoodglass Mentor
Actually we do digest the kernel of the corn, it's just the yellow outer hull that slips off and is such a good 'tracer' of transit time.

This depends on the person. For some of us the entire kernal will be present, insides and all.

On the original question, corn has a very high risk of CC, not just in the manufacturing process but also in the bins the dried corn is stored in and in the milling. I have been CC so many times by corn in chips and baked goods that I now won't touch it. It is IMHO just as much of a risk as oats. I don't usually mention it cause folks think I am a little overboard on the issue of processed food anyway. The less the better. Especially at first.

hathor Contributor

I guess you will just have to keep track of what you eat & how you react.

I have problems with fried or rich foods generally, but that's me. How are you feeling these days after having something high in fat other than fried corn products? Can you tell what kind of oil the storebought products had been fried in?

I ran across a list from a medical school a while ago that said that celiacs shouldn't use canola oil. However, it didn't say why. I posted here and no one really knew why the school would say that. Anyway, you can monitor how you react to oil and in particular canola.


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



Celiac.com Sponsor (A8-M):



Anonymousgurl Contributor

It's so strange...I react to ALL oils. If anything even has a drop of oil in the ingredients..I react. It's so odd. I'd love to hear if you've experienced more with oil, and I'd love to hear anyone else's perspective on issues with oil...because that's not really a common allergy.

akceliac Newbie

I have bad reactions to canola oil and I cannot eat fried foods either. I usually use safflower or sunflower oil in pancake batter and just "dry fry" them on a non-stick skillet.

I sure hope you can figure out what is ailing you.

loco-ladi Contributor

I did use canola oil for my homemade chips, as recommended by the living gluten free for dummies book (thats where I got the recipe for them)

The "frito's" says it uses corn oil

the Taco shells used "hydrogenated soybean oil"

I do realize corn is also a key ingredient in all three however I eat alot of corn, next to peas it would be my favorite veggie and I have not yet had a problem with "straight corn" thats why I am leaning towards the oils

I also do not use much other than olive oil or butter when cooking and that is in limited quanities and since this "oil" issue popped up I have stopped using that as well.

rsm Newbie

I have had problems with store bought tostada shells but have no trouble with corn tortilla's. I also think the oil is the culprit. I cook the tortillas on a smoking hot skillet with no oil and I'm ok.

I checked the shells, they are fried in cottonseed or corn oil. I think cottonseed seed oil is paint thinner, or is it linseed oil? Anyway, they had to go, cottonseed oil is not good.

I usually don't have problems with oils in moderation.

Generic Apprentice

I just had a thought. Maybe your gall bladder is starting to have some issues and isn't producing enough bile to help break down the oils....

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,431
    • Most Online (within 30 mins)
      7,748

    Dave162
    Newest Member
    Dave162
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Thoughtidjoin
      Can I wash gluten off dried chickpeas or green lentils when the packet says “may have been cross contaminated?” Has there been any research into this?  If so what are the results? If no research has been done why not? I am getting mixed advice from different sources, how serious is this or are the food manufacturer being over cautious? Many thanks Catherine
    • catnapt
      I've got some lab work results going back to 2010, various MRIs and CT scans and ultrasounds. I discovered two things that MIGHT be of interest to the GI doc tell me what you think? one is the results to an abdominal CT scan with contrast in 2013 that includes this:  "there is some thickening seen in the second and third portions of the duodenum"    Since this CT scan was for left lower quad pain, it was not followed up on   Then in May of 2024 I saw a foot specialist for problems with my feet. Some of that pain is due to a very obvious deformity of both of my legs- the right worse than the left. The dr suggested that my symptoms sounded like an auto immune condition (???) and I thought he was nuts but he ordered some lab work- it came back negative except for a weak positive on one test HLA-B27 and there was a follow up test recommended but that was never ordered and this dr gave me a useless Rx for custom insoles which he refused to address - and my calls to his office were never returned.   At that time I was having all over joint pains, plus some numbness in my feet (also stiffness) and some burning pain in my toes- esp the big toe on the right foot (the more deformed side of my body)   The last time I was eating any appreciable amount of gluten containing foods was in the period of Nov 2024 to around sometime in the summer of 2024. I regularly ate a barley soup that I loved and had subs and pizza and toast etc. I was no longer eating wheat pasta, had already switched to brown rice pasta but otherwise I had not yet made a clear connection between what I was calling 'refined grain products' and any symptoms that I had. And the symptoms were vague and could be attributed to other things.   I was referred to a neurologist in late 2023 for symptoms  of confusion/disorientation, that included loss of balance that I attributed, in part, to the inability to feel where my feet were. Some symptoms such as high spikes in blood pressure (some close to 200 over 100! scary stuff) were later determined to be due to covid or long covid (also had loss of sense of smell and taste)    I had periods of dizziness that did NOT include any spinning sensations, it was more of a feeling of lightheadedness as if my mind would go blank- very strange, never really got any answers about that but that eventually went away so not worried about that   WHAT OTHER THINGS from my past records might be good for the GI dr to know? I had my very first Vit D test done in 2023 and it was low at 23, supplements have gotten that up in the range of adequate but values varied up and down... most recent test was Nov 2025 and it was 45ish I think. That's on a min of 5000Ius per day (there are some fortified foods I eat sometimes that have added vit D)   I thought my serum calcium ran on the low side but it turns out that the reference ranges have changed for the labs that I use- one changed their RR back around er, 2014 I think? so I have no clue how to compare the results before and after those changes   calcium has never been below normal and most of my blood work looks "normal" except during illness or other issues like if I'm in afib- blood work looks insane LOL    I don't know what to make of all this but it sure will be nice to get some answers!         
    • catnapt
      just a few days off of that drug and my digestive system is finally getting back to normal stopping the gluten challenge was not enough to get back to normal, I was still horribly constipated with what seemed like a paralyzed digestive track- nothing was moving! but now, with a few mag citrate capsules that I had to order online and stopping the chlorthalidone, things are getting back to my usual "working well" digestion   so it's clear that the symptoms I had during the gluten challenge were compounded by the new med that was started the same day (I feel like the Dr really should have known better than to do those two things at the same time, add a new drug and start a new diet protocol... but I'm just the patient, what do I  know, right?)   I am going to do another 24 hr urine in a few weeks to see if lowering the dose of vit D gets my urine calcium down to a more tolerable level. that's the plan.  hope it works.  
    • Wheatwacked
    • catnapt
      oh geez!! i made a whole long detailed post and it didn't save it   I give up grrrrrrrrrrr  
×
×
  • 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.