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

Can A Non-celiac Be Glutened?


Netzel

Recommended Posts

Netzel Rookie

My wife has been eating gluten-free with me for the past 2 months, since I was discovered to be Celiac. Can a person who has a 'clean' system but is not celiac show symptoms of being glutened when it is accidentally ingested?

She had some severe gastro issues tonight after eating out (Applebee's chicken Caesar salad, no croutons), which hit about an hour after the meal.

She several times over the past 10 or so years dieted via the Atkins method, which is very low-carb--high protein and felt physically terrific. I don't know if everybody gets a clearer head when dropping carbohydrate from their system, but she clearly felt a difference in this 'symptom' during those dieting times.

There is no history of celiac or any gastro problems in her family line. I don't think I have yet seen anywhere on this board a similar question. Has anyone else experienced this?


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



Celiac.com Sponsor (A8-M):



home-based-mom Contributor
My wife has been eating gluten-free with me for the past 2 months, since I was discovered to be Celiac. Can a person who has a 'clean' system but is not celiac show symptoms of being glutened when it is accidentally ingested?

She had some severe gastro issues tonight after eating out (Applebee's chicken Caesar salad, no croutons), which hit about an hour after the meal.

She several times over the past 10 or so years dieted via the Atkins method, which is very low-carb--high protein and felt physically terrific. I don't know if everybody gets a clearer head when dropping carbohydrate from their system, but she clearly felt a difference in this 'symptom' during those dieting times.

There is no history of celiac or any gastro problems in her family line. I don't think I have yet seen anywhere on this board a similar question. Has anyone else experienced this?

There have been posts by people who felt unexpectedly better gluten free and unexpectedly awful when they ate gluten after being gluten free. Others have posted the same thing about family members. It is not at all strange or unheard of.

In your wife's case, this situation could have been Applebee's, or it could have been gluten, or it could have been both, as Applebee's is generally unsafe. Nevertheless, given her history with Atkins, it would seem she would benefit being gluten free.

Ursa Major Collaborator

Scientists have evidence that 33% of people have celiac disease, but also that possibly up to 70% of North Americans are gluten intolerant without their villi being affected.

So, I believe that most people would benefit from a gluten-free diet. Your wife apparently is one of them. It sounds like you two need to be gluten-free together.

Rebecca's mom Rookie

Dear Netzel,

Has your wife been screened for Celiac Disease? Our youngest daughter, Rebecca (age 7), has Down syndrome. She had absolutely NO SYMPTOMS whatsoever. However, her pediatrician has a stepdaughter with DS, and when she was diagnosed with celiac disease last year, he started doing a lot of research on celiac disease and found that 1 out of every 8 people with DS has celiac disease. He took it upon himself to test all of his patients with DS for celiac disease. Thank goodness he did - her numbers were off the chart, and her intestinal damage was borderline Stage IV.

Because of Rebecca's diagnosis, I decided that our kitchen had to be gluten-free. After reading all of the information that I could get my hands on, I thought that I might have celiac disease, also. It does run in families. We all got tested, and 2 of our daughters and I were negative. My husband is still waiting on his results.

I found that once I went off of gluten I felt better than I did when I was a teenager. I also found that if I accidentally ingested gluten, I would start itching like crazy. So now I joke that I am Rebecca's "canary in the mine"! If something bothers me, I know that Rebecca got hold of gluten, too.

I also found out something odd today. I have been itching uncontrollably the past 2 days, and I KNOW that I haven't had any gluten, so I was at a loss as to what was causing it. I have had a couple of other itching spells in the past 2 months that we have been gluten free. The only thing that the items that I think caused these episodes had in common was that they all contained high concentrations of vinegar.

Now, vinegar is gluten-free, so I was stumped. I went out on the Internet and found out that some people who are allergic to mold have a severe allergic reaction to vinegar. I can honestly say that I NEVER would have made that connection! These same people may also be allergic to the Penicillin family of antibiotics. Who'da thunk it?

Chances are that your wife either has celiac disease or she may just be gluten-sensitive. Since she has been eating gluten-free with you, her tests may come back negative. I know there is a lab in Dallas that will test people's stool samples, and some people have had better luck with that. The test isn't covered by most insurance companies, though. You might have your wife ask her doctor what he/she thinks that she should do.

Good luck,

Teresa Koch

Fort Worth, Texas

ShayFL Enthusiast

It could be gluten or Applebees. A few years ago I got extremely sick (food poisoning) from Applebees. So bad, that I have never gone back. Gluten doesnt effect me that way, so I know it was bad food.

Tim-n-VA Contributor
Scientists have evidence that 33% of people have celiac disease, but also that possibly up to 70% of North Americans are gluten intolerant without their villi being affected.

That is significantly different than the 1 in 133 figure commonly cited on this site. Do yo have a link to that study?

urbancowboy717 Rookie

Have you ever heard about eating according to your blood type. As an O I should only consume sprouted wheat. I don't have any digestive issues with wheat but I feel better when I limit the amount I eat. In fact I have never really liked bread and unknowingly eaten pretty close to gluten-free all my life. I prefer rice noodles, corn tortillas and I absolutely hate bread. I started eating according to my blood type after seeing a nutritionist and I have never felt better.


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



Celiac.com Sponsor (A8-M):



purple Community Regular

Could it be the change from home cooked food compared to eating out. I am not allergic to gluten but my daughter is and I think it comes from her dad's side. I harldy ever eat out. I mostly eat homemade/gluten-free food. Yesterday I ate out at Carl's Jr. and my tummy hurt alot but I am sure it was from the coke I had b/c I only have one about once per month and my tummy couldn't handle it. I was a little shakey. It happens sometimes when I eat out. I can eat wheat and never have a problem. There is alot of chemicals, preservatives, food additives, germs, etc. in restaurant food. Could your wife have maybe a touch of food poisoning?? I am watching my whole families symptoms to be safe.

Ridgewalker Contributor
That is significantly different than the 1 in 133 figure commonly cited on this site. Do yo have a link to that study?

I just recently read that same percentage that Ursa mentioned... now I'm trying like heck to remember where. Will look at the most recent articles I've read again and see if I can find it.

tom Contributor

I've read that 33% have one or more of the genes involved, but of course most don't actually have celiac disease.

There are even identical twins where one has celiac disease and the other doesn't.

And the genetics research has quite a ways to go, as there are biopsy-confirmed celiacs w/ none of the usual markers.

Jestgar Rising Star

brief rant

Having the variant of a gene that predisposes you to a certain disease does not mean that you will get the disease. Finding out your genotype for Celiac or ANYTHING is merely interesting. It is not diagnostic, it is not suggestive, it does not define a course of treatment, it is only interesting, and probably only to you.

end of rant

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,563
    • Most Online (within 30 mins)
      7,748

    Bob Madden
    Newest Member
    Bob Madden
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.