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Anyone Got Sick From Canola Oil?


Yenni

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trents Grand Master
(edited)

A gluten allergy would be scientifically defined since allergic reactions engage the immune system in specific ways. Intolerances are typically conditions that cause lower GI distress, as in lactose intolerance. Gluten sensitivity falls short of celiac disease but is usually viewed as creating some sort of toxic reaction that has a more systemic effect and can manifest itself in various ways such as brain fog and neurological problems. It does not damage the mucosa of the small bowel like celiac disease does. This is my understanding of the differences between these gluten-related medical conditions. The problem isn't so much differentiating them medically and scientifically but rather the confusion of the terms in the populace as driven by the indiscriminate use of these terms by marketing and pop science, which tends to lump all of them under the heading of "gluten intolerance" or "gluten allergy." Gluten sensitivity may be a precursor to celiac disease.

"Leaky gut" is the result of the damage done to the SB mucosa and is the chief defining characteristic of celiac disease. Dermatitis Herpetiformis is also considered to be a certain indicator of celiac disease. So if you have leaky gut I would certainly be tested for celiac disease since celiac disease does in fact have a genetic basis. We know the genes responsible. But it takes both the genes and a triggering event such as a viral infection to wake up the genes and produce an active condition of celiac disease. Otherwise, it remains in a latent form. Many people with the genes do not experience a triggering event and therefore the genes are not expressed in active celiac disease. Once you develop active celiac disease it does not go away. You will always need to avoid gluten entirely. Celiac disease is classified as an autoimmune disease since the ingestion of gluten by people whose celiac genes have been activated by a stressor (such as a viral infection) causes inflammation in the small bowel mucosa that damages the villi. In other words, the body is attacking itself. This in turn causes leaky gut and poor absorption of nutrients. Poor absorption of nutrients in turn causes a host of other medical conditions over the course of time. The turning on of the genes to wake up the latent celiac disease can happen at any time in life. Many with active celiac disease do not experience dramatic GI symptoms, at least at first. We call them "silent celiacs." Various medical conditions down the road typically develop, however.

The first stage of diagnosis of celiac disease is to get a serum celiac antibody panel done. The damage to the small bowel produces some characteristic antibodies. If the serum antibody panel is positive for celiac disease, especially if the results are not strongly indicative, the physician may order an endoscopy and biopsy of the small bowel to check for microscopic villi damage. Sometimes the damage is so severe the doc doing the scoping can see it even before sending the biopsy to the lab for analysis.

I would suggest you look into this. By the way, the inability to absorb fats is very common in celiac disease because of the damage to the SB mucosa and so people with celiac disease often see oily/fatty residue in their stools until the gluten free diet allows their villi to heal. That may take a year or more. I mention that in connection with your OP about canola oil.

Edited by trents

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raspberryfirecracker Contributor
9 hours ago, Hoody123 said:

pathology courses in massage therapy school

This is not the same as being a diagnostician; knowing a disease exists doesn't make anyone a medical doctor trained to diagnose diseases.

9 hours ago, Hoody123 said:

I was diagnosed with IBS and leaky gut in college when I first developed these reactions. I was not born with them. Therefor I do not have a genetic disease

This isn't an accurate understanding of celiac disease, Hoody. You are born with the genes, but genetic diseases can either be active from birth, get triggered in adolescence, or get triggered in adulthood. People who have genes for Huntington's for example, will start developing nerve damage in their 30s and 40s. 

9 hours ago, Hoody123 said:

I believe celiac to be . . . (one of the strongest on the scale). I do not know if my understanding is correct

It's not correct. Celiac disease is not "the strongest" response to gluten on a scale of symptom severity. Someone who has a severe allergy to wheat gluten might go into anaphylaxis and die from exposure to a breadcrumb, and someone who has celiac could get a rash, mild bloating, and a headache and have no idea it's because of what they ate.

It's genetic in that, you inherit genes which come with these instructions to the immune system: If you find the presence of gluten, produce antibodies. Those antibodies are what do the damage, to our own tissues. Celiac is an autoimmune disease, and is one of the "great imitators." Stress makes any autoimmune disease worse, and easing stress makes any disease easier to live with, but it doesn't stop the underlying illness.

Your descriptions sound exactly like so many people here before we accepted we might have more than "an intolerance" which we could control by just living better. I count myself in that group. What you wrote is frightening, because we know that kind of denial, and we know how bad the disease sometimes has to get before people in denial are forced to acknowledge it. The truth is celiac disease is a silent killer. The truth is anyone with gluten intolerance should be evaluated by a doctor who can test for the antibodies, genes, and a biopsy if necessary (they're starting to diagnose without the biopsy if other tests are overwhelmingly positive) because it will get worse. Undiagnosed people just get diagnosed with other, seemingly unrelated diseases that never needed to occur if they'd have stopped ingesting gluten sooner. There is no easier time to live gluten free than right now. I wish you the best.

raspberryfirecracker Contributor

(And what trent said--sorry I didn't see there was a page two until I'd already replied!)

  • 4 years later...
gailc Newbie

I get coughing and choking from canola oil. I cough up stuff.  Symptom is like bronchitis.  I have gluten intolerance, maybe celiac.  the choking persists for about a week, it simulates a cold.  I got it from the gluten free menu at Outback too, that time I got cramps for 25 hours. the cramps start about 20 minutes after finishing eating.

 

  • 1 month later...
SoBannaz Rookie

No I use canola oil all the time never had a problem (yet) my body is so crazy who knows. But yes I can use canola oil and olive oil. I stay away from vegetable oil because of the soy, soy makes my throat tight it’s the reason I no longer eat chicken unless it’s from krogers because I noticed it made my throat tight looked up on their website majority of those chicken companies feed their chickens soy. The only brand I can tolerate is the one in Kroger’s Simple Truth. 

trents Grand Master

@SoBannaz, how are you using the term "vegetable oil"? I think all the oils you mentioned in your above post would be considered vegetable oils since they aren't made from animal tallow.

gailc Newbie

I avoid soy because of the link to breast cancer. I have had some scares and two biopsies. Not cancer.


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    • trents
      Certainly, it would b wise to have a gene test done if your physician is open to it as it would provide some more data to understand what's going on. But keep in mind that the genetic test for celiac disease cannot be used as to diagnose celiac disease, only to establish the potential to develop active celiac disease. About 40% of the general population possess one or both of the primary genes known to be associated with the development of active celiac disease but only about 1% of the population actually develop active celiac disease. So, the gene test is an effective "rule out" tool but not an effective diagnostic tool.
    • Roses8721
      Had Quaker gluten-free oatmeal last night and my stomach is a mess today. NO flu but def stomach stuff. Anyone else?
    • Roses8721
      So you would be good with the diagnosis and not worry to check genetics etc etc? Appreciate your words!
    • Scott Adams
      As recommended by @Flash1970, you may want to get this: https://www.amazon.com/Curist-Lidocaine-Maximum-Strength-Topical/dp/B09DN7GR14/
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      For those who will likely remain gluten-free for life anyway due to well-known symptoms they have when eating gluten, my general advice is to ignore any doctors who push to go through a gluten challenge to get a formal diagnosis--and this is especially true for those who have severe symptoms when they eat gluten. It can take months, or even years to recover from such a challenge, so why do this if you already know that gluten is the culprit and you won't be eating it anyway?  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS--but those in this group will usually have negative tests, or at best, elevated antibodies that don't reach the level of official positive. Unfortunately test results for celiac disease are not always definitive, and many errors can be made when doing an endoscopy for celiac disease, and they can happen in many ways, for example not collecting the samples in the right areas, not collecting enough samples, or not interpreting the results properly and giving a Marsh score.  Many biopsy results can also be borderline, where there may be certain damage that could be associated with celiac disease, but it just doesn't quite reach the level necessary to make a formal diagnosis. The same is true for blood test results. Over the last 10 years or so a new "Weak Positive" range has been created by many labs for antibody results, which can simply lead to confusion (some doctors apparently believe that this means the patient can decide if they want more testing or to go gluten-free). There is no "Weak Negative" category, for example. Many patients are not told to eat gluten daily, lots of it, for the 6-8 week period leading up to their blood test, nor asked whether or not they've been eating gluten. Some patients even report to their doctors that they've been gluten-free for weeks or months before their blood tests, yet their doctors incorrectly say nothing to them about how this can affect their test, and create false negative results. Many people are not routinely given a total IGA blood test when doing a blood screening, which can lead to false negative interpretations if the patient has low IGA. We've seen on this forum many times that some doctors who are not fully up on how interpret the blood test results can tell patients that the don't need to follow a gluten-free diet or get more testing because only 1 of the 2 or 3 tests done in their panel is positive (wrong!), and the other 1 or 2 tests are negative.  Dermatologists often don't know how to do a proper skin biopsy for dermatitis herpetiformis, and when they do it wrongly their patient will continue to suffer with terrible DH itching, and all the risks associated with celiac disease. For many, the DH rash is the only presentation of celiac disease. These patients may end up on strong prescriptions for life to control their itching which also may have many negative side effects, for example Dapsone. Unfortunately many people will continue to suffer needlessly and eat gluten due to these errors in performing or interpreting celiac disease tests, but luckily some will find out about non-celiac gluten sensitivity on their own and go gluten-free and recover from their symptoms. Consider yourself lucky if you've figured out that gluten is the source of your health issues, and you've gone gluten-free, because many people will never figure this out.    
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