Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Cheat days?


Aevintiri

Recommended Posts

Aevintiri Rookie

Does anyone here just completely go rogue on days and consume gluten like normal people? I have been gluten free for about 3 years now since my diagnoses. I have really been craving a Jets Deep Dish pizza which was my favorite meal prior to diagnoses. Who does cheat days and if so are the symptoms the same as before or are they worst since your body hasn’t had gluten in so long?


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



Celiac.com Sponsor (A8-M):



twilatexas Newbie

No. I have been glutened accidentally enough times in the past. There is nothing that could make me cheap. Not enough upside to warrant the days of illness that would make days of illness worth it.

trents Grand Master
5 hours ago, Aevintiri said:

Does anyone here just completely go rogue on days and consume gluten like normal people? I have been gluten free for about 3 years now since my diagnoses. I have really been craving a Jets Deep Dish pizza which was my favorite meal prior to diagnoses. Who does cheat days and if so are the symptoms the same as before or are they worst since your body hasn’t had gluten in so long?

Most of us who have been gluten free for long periods of time find that when we get a significant amount of gluten (talking more than cross contamination, here) we react much more strongly than before gluten free when we were eating gluten regularly. We lose whatever tolerance to it we once had. Speaking personally, when I mistakenly eat something with a full load of gluten in it (like when I accidentally ate my wife's wheat biscuits instead of the gluten-free ones she made me) I get violently ill. Two or three hours of gut wrenching cramps with vomiting followed by a few hours of diarrhea. No way am I going to give into my craving with that kind of reaction.

cristiana Veteran

The last time I ate something loaded with gluten by mistake - a slice of cake - within two hours I had severe chills, was unable to stand, threw up two or three times (first time I'd been that sick since childhood), palpations, nearly blacked out, and then had days of gastritis like symptoms and a feeling of sea sickness.  So I'm not tempted to cheat.

I cannot believe how severe my reaction to gluten is these days, yet a friend's brother has gone back to eating gluten after years of not eating it and has had no reaction at all.  I can't understand how this can happen.  I do wonder if he was misdiagnosed as coeliac as a child?

Aevintiri Rookie
21 minutes ago, cristiana said:

The last time I ate something loaded with gluten by mistake - a slice of cake - within two hours I had severe chills, was unable to stand, threw up two or three times (first time I'd been that sick since childhood), palpations, nearly blacked out, and then had days of gastritis like symptoms and a feeling of sea sickness.  So I'm not tempted to cheat.

I cannot believe how severe my reaction to gluten is these days, yet a friend's brother has gone back to eating gluten after years of not eating it and has had no reaction at all.  I can't understand how this can happen.  I do wonder if he was misdiagnosed as coeliac as a child?

Did he start slow kind of like starting a new medication or eating meat after being vegan? I recently started eating steak again after being vegan for years and ate small portions with a zofran but aside from some light nausea, I had no stomach upset. I plan on keeping it going slowly. My gastro said the same thing can work with a lot of celiacs people. Your body is just shocked at a new thing and naturally want to reject it. 

41 minutes ago, trents said:

Most of us who have been gluten free for long periods of time find that when we get a significant amount of gluten (talking more than cross contamination, here) we react much more strongly than before gluten free when we were eating gluten regularly. We lose whatever tolerance to it we once had. Speaking personally, when I mistakenly eat something with a full load of gluten in it (like when I accidentally ate my wife's wheat biscuits instead of the gluten-free ones she made me) I get violently ill. Two or three hours of gut wrenching cramps with vomiting followed by a few hours of diarrhea. No way am I going to give into my craving with that kind of reaction.

Did you eat multiple biscuits or just one?

trents Grand Master

Two biscuits, if I recall correctly. I'm fine for about two hours after getting glutened but as soon as the stomach starts to empty into the small bowel, the agony begins. I believe I have also experienced a similar reaction when getting glutened from cross contamination on occasion. Happened once after ingesting a shake with some chia seeds in it that came from India and were not advertised as gluten free. Made me sicker than a dog.

cristiana Veteran
15 minutes ago, Aevintiri said:

Did he start slow kind of like starting a new medication or eating meat after being vegan?

I have no idea.  

But returning to eating gluten for coeliacs can lead to serious health complications.  I can understand it must be more tempting to take risks if one doesn't have any obvious side effects from eating gluten, but it could still be making one ill.

I do sympathise though - cravings are awful.  I even fancy eating a McDonald's or a KFC meal when my family indulge - even though I never really liked them much before my diagnosis!

I've never been that fond of pizza but I really miss doughnuts and a certain chocolate biscuit we have here in the UK called a "Penguin". But I tell myself that soon these things too will be available in the gluten-free aisle and that helps.  And it is true -  time and time again since my diagnosis things I thought I would never eat again have now appeared in the gluten-free aisles: gluten-free cornflakes, Weetabix type biscuits, and more recently, iced currant buns! 

I don't know the brand of pizza you are speaking of - tell me, what is it that you like so much about it?  Is it possible you could try making something like it yourself?


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



Celiac.com Sponsor (A8-M):



trents Grand Master

Your question to Cristiana about whether or not her friend started slow and built up to it suggests to me you are considering more than just an occasional impulse indulgence. Starting slow implies systematic cheating.

Aevintiri Rookie
1 minute ago, cristiana said:

I have no idea.  

But returning to eating gluten for coeliacs can lead to serious health complications.  I can understand it must be more tempting to take risks if one doesn't have any obvious side effects from eating gluten, but it could still be making one ill.

I do sympathise though - cravings are awful.  I even fancy eating a McDonald's or a KFC meal when my family indulge - even though I never really liked them much before my diagnosis!

I've never been that fond of pizza but I really miss doughnuts and a certain chocolate biscuit we have here in the UK called a "Penguin". But I tell myself that soon these things too will be available in the gluten-free aisle and that helps.  And it is true -  time and time again since my diagnosis things I thought I would never eat again have now appeared in the gluten-free aisles: gluten-free cornflakes, Weetabix type biscuits, and more recently, iced currant buns! 

I don't know the brand of pizza you are speaking of - tell me, what is it that you like so much about it?  Is it possible you could try making something like it yourself?

Yeah I am aware that it does harm us but from what I understand is that, it doesn’t do significant damage unless consumed regularly. So I am curious how like once a month would actually effect our intestines. Unfortunately there is no replicating the pizza gluten free. It is kind of similar to like a Chicago deep dish. The slices are about 3-4 inches tall and the flavor can’t be rivaled for me. I don’t know how you could get anything gluten free to match up. 

Aevintiri Rookie
10 minutes ago, trents said:

Two biscuits, if I recall correctly. I'm fine for about two hours after getting glutened but as soon as the stomach starts to empty into the small bowel, the agony begins. I believe I have also experienced a similar reaction when getting glutened from cross contamination on occasion. Happened once after ingesting a shake with some chia seeds in it that came from India and were not advertised as gluten free. Made me sicker than a dog.

Hmmm very interesting. I wonder what would happen if you took Imodium and zofran prior to eating it. 

Aevintiri Rookie
4 minutes ago, trents said:

Your question to Cristiana about whether or not her friend started slow and built up to it suggests to me you are considering more than just an occasional impulse indulgence. Starting slow implies systematic cheating.

I guess I am just trying to find out if celiacs can naturally reintroduce gluten without causing harm or severe illness. I can’t find any documentation online about it so looking for answers from others who may have experienced it

cristiana Veteran
(edited)

from Coeliac UK:

"Coeliac disease is a lifelong autoimmune condition and the gluten free diet is the only treatment for it. If gluten is introduced back into the diet at a later date, the immune system will react and the gut lining will become damaged again.

Once you develop coeliac disease, you must avoid gluten for the rest of your life."

https://www.coeliac.org.uk/information-and-support/coeliac-disease/coeliac-disease-faqs/

The problem is, as it is a lifelong autoimmune condition, the immune system will continue to react to gluten - even if it isn't obvious.

Out of interest, was your own coeliac disease asymptomatic and an incidental finding?  In my own case, I was very ill indeed at diagnosis and perhaps because of that I am keener than others on wanting to remain on the "straight and narrow".  I would hate to return to the poor health I had ten years ago.

 

Edited by cristiana
trents Grand Master
(edited)
39 minutes ago, Aevintiri said:

I guess I am just trying to find out if celiacs can naturally reintroduce gluten without causing harm or severe illness. I can’t find any documentation online about it so looking for answers from others who may have experienced it

It might be possible to reintroduce gluten gradually without causing severe illness but that would not avoid harm to the villi of your small bowel. Some celiacs are "silent" when it comes to symptoms but the damage done to the small bowel lining is universal. It's what defines celiac disease. Celiac disease does not "go away". It's not an allergy that you might outgrow. It's an autoimmune disorder that is baked into your genes. I get the impression you are in denial about the reality of your diagnosis.

And I would point out that you aren't the only celiac who struggles with cravings for real wheat bread products. We all struggle with that at times. Do we eat to live or do we live to eat? That is the question.

Edited by trents
Scott Adams Grand Master

I don’t think anyone here would recommend that someone with celiac disease eat any gluten, but polling has shown that perhaps 25% of celiacs do cheat on their diets. I suspect that those who do this may be more in the asymptotic group, but this isn’t clear.

If you go this route I would recommend follow up blood panels and endoscopes to monitor possible damage. Let us know how it goes for you.

LCAnacortes Enthusiast

For me the price of poker is intestinal pain followed by explosive, uncontrolled diarrhea. Definitely not worth it.  

MADMOM Community Regular
11 hours ago, Aevintiri said:

Does anyone here just completely go rogue on days and consume gluten like normal people? I have been gluten free for about 3 years now since my diagnoses. I have really been craving a Jets Deep Dish pizza which was my favorite meal prior to diagnoses. Who does cheat days and if so are the symptoms the same as before or are they worst since your body hasn’t had gluten in so long?

cheat days are just like going back to day 1 - you’re destroying your villi

and it can cause major things / there are great gluten-free options in the pizza world too 

RMJ Mentor

A vaccine booster challenges the immune system with a protein that the body hasn’t seen for a while, with the purpose of increasing antibodies. I envision eating gluten in the same way. Since I don’t want my autoimmune antibodies increased, I would never knowingly eat gluten-containing foods.

captaincrab55 Collaborator

One small slice of the wrong pizza will do me in for the rest of the day/night.   On top of that I have DH and the itch will follow for days.   IMO a cheat day is like playing a game of suicide with your health.   Good luck finding your real self, because I'm not playing a game with my health.

 

TurtleSeaba Newbie

I was diagnosed 5 years ago, and I went all in Gluten free immediately. About 6 months in I had a breakdown and devoured a variety of doughnuts. I regretted it immediately, and it strengthened my resolve to be completely gluten free.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,960
    • Most Online (within 30 mins)
      7,748

    PMcCauley
    Newest Member
    PMcCauley
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Once you've completed testing and still don't have improvement, start a trial gluten free diet.  Looking for imprvement that may indicate Non Celiac Gluten Sensitivity, which is 10 times more prevalent than Celiac Disease. Deficiencies in vitamins B6, B12, D, and C can manifest as skin rashes.  Virtual guaranty you are deficient in vitamin D.
    • cameo674
      So those rs numbers tell researchers where the dbSNP is located in a Genome so that other reasearchers or an AI system can look in that specific spot for that Snip of information.  You can look those rs # s by pasting the numbers after rs into the lookup on this page https://www.ncbi.nlm.nih.gov/snp/ right under the Blue header bar at the top of the webpage.  Since you are not a researcher, I do not know how this will help you though.
    • cameo674
      So I posted here once before, and everyone advocated that I get into a GI doc.  I finally got into my functional health appointment on 6/16 to get my blood results evaluated and get the Gastro referral. I was told that I would be fortunate to see a gastro doctor by December, because of the number of people waiting to get in, but they did believe that I needed to see a GI doc among others.  Well, the stars aligned. I got home. I looked at MyChart and it showed an appointment available for later that same day. I never clicked so fast on an appointment time. The gastro doc ran some additional blood work based off the December values that had confirmed my daughter's suspicion that I have undiagnosed stomach issues.  Gastro has also scheduled me to get an upper endoscopy as well as a colonoscopy since it has been 8 years since my last one. She said it would rule out other concerns if I did not show Celiac per the biopsies.  Those biopsies will not occur until August 29th and like everyone here stated, Gastro wants me to keep gluten in my diet exactly as everyone suggested. To be honest, I was barely eating any gluten since I figured I would have plenty of time to do so before testing.  Doc is also looking for the cause of the low level heartburn that I have had for 30 years.  I have mentioned the heartburn to PCPs in the past and they always said take a tums or other OTC drug.  The upper endoscopy is for ruling out eosinphilic esophagitis, h. pylori, and to biopsy the duodenal bulb and second portion to confirm or exclude celiac. The colonoscopy will have random biopsies to rule out microscopic colitis. I didn't really catch her reasoning for the bloodwork.  Doc looked at the December numbers and said they were definitely concerning for Celiac.  She also said, “Hmm that’s odd; usually it’s the reverse”, but I did not catch which result made her say that. She seems very through.  She also asked why I had never bothered to see a GI before.  To be honest, I told her I just assumed that the heartburn and loose stool were a part of aging.  I have been gassy since I was born and thought constantly passing gas was normal?  Everyone I know with Celiac have horrible symptoms that cannot be attributed to other things.  They are in a lot of stomach pain.  I do not go through that.  I attribute my issues to the lactose intolerance that comes with aging, but have slowly been eliminating foods from my diet due to the heartburn or due my assumption that they did not agree with a medication that I was prescribed. I have already eliminated milk products especially high fat ones like ice cream; fats like peanut butter; acids like citrus and tomatoes; chocolate in all forms; and breads more because it is so hard to get in 100 grams of protein if I eat any foods that are not a protein.  I would not have even done the testing if my daughter had not brought up the fact that she thought I might have an undiagnosed condition since she has issues with bloating and another sibling has periodic undiagnosed stomach pain that GI docs throw pills at instead of helping.  Who knew that Bristol scale 5 and 6 were not considered normal especially multiple times a day? I watched my MIL go through basically the same bowel changes starting at 50 so to be honest, I really did think it was normal before this week's appointment.   December 2024's blood tests ran through Quest Labs were:  Deamidated Gliadin (IgA) 53.8 U/mL Above range >15.0 U/mL; Deamidated Gliadin (IgG) >250.0 U/mL Above Range >15.0 U/mL; Tissue Transglutaminase (IgA) 44.0 U/mL Above range >15.0 U/mL; Tissue Transglutaminase (IgG) <1.0 In range <15.0; Immunoglobulin A (IgA) 274 mg/dL In range 47-310 mg/dL 6/16/25 bloodwork:  Until today, I did not really know what all the four tubes of blood were for and since I did not understand the results, I got into the clinical notes to see what was ordered, but it did not exactly explain why for everything. Immunoglobulins IGG, IGA, IGM all came back in range:  IGG 1,010 mg/dL In range 600-1,714; IgA 261 mg/dL In range 66-433 mg/dL; IGM 189 mg/dL In range 45-281.  How do these numbers help with diagnosis? Google says she checked these to see if I have an ongoing infection? I do have Hashimoto's and she did say once you have one autoimmune disease others seem to follow. Celiac Associated HLD-DQ Typing: DQA1* Value: 05; DQA1*DQA11 Value: 05; DQB1* Value: 02; DQB1-DQB11 Value: 02; Celiac Gene Pairs Present Value: Yes; Celiac HLA Interpretation Value: These genes are permissive for celiac disease.  However, these genes can also be present in the normal population. Testing performed by SSOP.  So google failed me.  I think these results basically say I have genes, but everybody has these genes so this test was just to confirm that there is a vague possibility?  Maybe this test result explains why I do not have the horrible symptoms most individuals with celiac have?  I told the GI my assumption is that I am just gluten intolerant since I do not have the pain? So maybe this test explains why I have antibodies? Comprehensive Metabolic Panel: Everything was in the middle of the normal range.  Google says this just says I am metabolically healthy. Tissue Transglutaminase ABS test results – Done by the Mayo Clinic’s Labs –  T-Transglutaminase IGA AB --Value: 3.1 U/mL – Normal Value is <4.0 (negative) U/mL; Tissue Transglutaminase, IgG -- Value: 15.3 U/mL High -- Normal Value is <6.0 (Negative) U/mL – Interpretation Positive (>9.0) – These are the only labs the GI did that have been labeled Abnormal.  I am confused at how/why these came back different than the December labs? Because these numbers seem to be the opposite of what the were in December and I know I have eaten less gluten.  They were definitely measured differently and had different ranges. This must be why she said they are usually opposite? Molecular Stool Parasite Panel said I was Negative for Giardia Lamblia by PCR; Entamoeba Histolytica by PCR and Cryptosporidium Parvum/Hominis by PCR.  So at least I do not need to do a parasite cleanse like everyone on TikTok seems to be doing. So I guess, I am just really asking why the Tissue Transglutaminase numbers are different.  Was it because they were truly different tests? Is it because I have not consumed the crazy amount of gluten one is suppose to eat prior to testing? To be honest, I thought that was only for the biopsy testing. I generally only eat twice a day, and the thought of eating the equivalent of 6 slices of bread is daunting. Even in my youth, I probably only consumed the equivalent of maybe 3 slices a day. Like I said before, now I usually focus on trying to eat 60 gram of protein.  I am suppose to consume 100 grams, but have failed to succeed. I will focus on eating gluten starting in July now that I know my procedure date.
    • Scott Adams
      I agree with @trents and wiping down the spot you eat your lunch, and eating the food your brought from home should be safe for even sensitive celiacs. Gluten can jump on your food, so it would likely better better for you to continue eating where you prefer.
    • Scott Adams
      This article might also be helpful, as you could have DH: https://www.celiac.com/celiac-disease/understanding-dermatitis-herpetiformis-the-skin-manifestation-of-celiac-disease-r6361/
×
×
  • Create New...