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

When Do You React/how Soon?


CMCM

Recommended Posts

CMCM Rising Star

I'm just wondering...when you eat something with gluten, how soon do you get an identifiable reaction? Same day? Hours later? Next day? And what kind of things do you feel first? And then, when you do react , how long does it typically last?


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator
I'm just wondering...when you eat something with gluten, how soon do you get an identifiable reaction?  Same day?  Hours later?  Next day?  And what kind of things do you feel first? And then, when you do react , how long does it typically last?

<{POST_SNAPBACK}>

That seems to vary widely from person to person. For me, some things would cause a reaction in like minutes. Other things very slowly and more subtle, such that detection isn't so easy. It can take days for certain foods if you already have a crippled digestive system. So if you are catching it early, before much damage has been done, then the reaction would be different I think. Therefore, over time, the reactions could change.

The things I'd get first depended on the food too. For the rye bread I was eating, I'd get a dry mouth in less than an hour, even just minutes. That would last over 24-36 hours, even with one slice. No matter how much water I'd drink, there was a thirst that could not be quenched. Sometimes 8 to 12 full glasses of water, and still thirsty as if I'd been dehydrated for a day or more. Pasta was more subtle. Mostly digestive issues, which would last a few days or more. It seemed to also depend on what I ate along with the gluten-containing food.

Now, for how long it lasts, again it depends on the food, but for me typically a few days or so.

The important thing is that you know to avoid certain foods, so reactions hopefully won't normally be a problem. That is unless you actually plan to ignore the gluten intolorence because you think you can put up with the symptoms. I hope nobody resorts to that, because this is not like an allergy. It's a serious problem that requires a life-long commitment. You only get one body. Any gluten will cause damage if you are gluten intolorent. It won't matter if you don't notice the reaction. Over time, that damage is what causes Celiac Disease.

pixiegirl Enthusiast

I react quickly, in 20 minutes or so and if I got a big does of gluten it lasts for a long time... a good 2 weeks.

Susan

tammy Community Regular
I react quickly, in 20 minutes or so and if I got a big does of gluten it lasts for a long time... a good 2 weeks.

Susan

<{POST_SNAPBACK}>

For me, it seems to be relatively consistent. If I accidently ingest gluten, even a tiny amount, I will have a subtle wheeze within about 20 minutes. Then my stool will be pencil thin for about a week. I don't remeber what I was like when I ate a whole slice of bread. I react to casein as well. I find that a little butter daily causes no reaction however a glass of milk or a serving of ice cream does. I feel sluggish the next day and my stool is weird the second day. :unsure:

elisabet Contributor

My son reacts between 1-4 hour,he will have very itchy skin and a tight nose during the night.It will reduce during 1-2 weeks.

darlindeb25 Collaborator

Each person is different and sometimes reactions are different---I get flu like symptoms and I generally will not feel well again for weeks. Now barley doesnt cause a reaction at all with me, but it still is doing the same damage. Most gluten incident will cause diarrhea for me--I havent been glutened too many times. Soy/corn on the other hand cause constipation. Everyone is different. Deb

jerseyangel Proficient

I'm gluten-free almost 6 months now and up until recently, I'd begin to get symptoms within 1-2 hours. Mostly D, cramping, fatigue and anxiety. It would go on for 5 days or so. Last week, I think I had a reaction--I don't know how it got into me--but I felt anxious and depressed and had mild cramping but no D. Maybe it wasn't from gluten--I'm super careful--but I think it probably was. As you can see from the replys, we're all different and even our own reactions can vary.


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

I usually feel it instantly and the reactions usually last a good 2 weeks. Everyone is different though.

Carriefaith Enthusiast

My typical reaction is:

Brain fog within a few hours, this lasts for days

Skin outbreaks within 12-24 hours

Bm problems within 24-48 hours

Upper abdominal stomach pain within 3-4 days

CMCM Rising Star

I'm finding your replies MOST interesting. I've also noticed that many people on these forums are also lactose intolerant. I thought for YEARS that the lactose was my only problem....and in fact, I've never been much of a dairy person, perhaps instinctively. But because I could eat wheat without the sort of reaction my seriously celiac mom did, I thought I had escaped the wheat thing and I just never thought I could have some degree of celiac disease for most of my life until recently. The two must be connected, though....because when I don't eat wheat I seem to be able to tolerate dairy fairly well. I went on the Atkins diet several years ago (didn't eat much "fat" stuff because I don't like/can't handle it), but basically ate chicken, fish, small amount of cheese, and salads. I felt GREAT, and I could hardly believe it. I attributed it all to the lack of sugar in my diet, although I did wonder if the lack of grains had anything to do with it. Now I know it must have been the fact that I had zero grain of any kind for the 6 weeks I did the diet.

cookiedog Newbie

I have only recently started a gluten free diet, and boy it's nice to feel better. Not 100% but any bit is better. I have been lactose intolerant for years. I know within a minute if i have eaten gluten. Major headache between my eyes, brain fog (I just learned that's what I've been having), and then within an hour or so bm/cramping for days and days.

Carriefaith Enthusiast
I've also noticed that many people on these forums are also lactose intolerant. I thought for YEARS that the lactose was my only problem....and in fact, I've never been much of a dairy person, perhaps instinctively. But because I could eat wheat without the sort of reaction my seriously celiac mom did, I thought I had escaped the wheat thing and I just never thought I could have some degree of celiac disease for most of my life until recently. The two must be connected
Most people with celiac disease are temporarily lactose intolerant until they are on the gluten-free diet. Gluten antibodies destory the tips of the villi in the small intestine which contain the enzyme to break down lactose. So whenever lactose is ingested, the person gets really sick because they can't digest the lactose. Within time on a gluten free diet, however, the villi heal and are able to digest lactose again. Other people with celiac disease, like myself, seem to be intolerant to the milk protein casein. I don't know a whole lot about the connection between celiac disease and casein, but I have recently found out on these forms that the milk protein casein is quite similar to gluten, which would explain a few things ;)
RiceGuy Collaborator
I went on the Atkins diet several years ago (didn't eat much "fat" stuff because I don't like/can't handle it), but basically ate chicken, fish, small amount of cheese, and salads.  I felt GREAT, and I could hardly believe it. I attributed it all to the lack of sugar in my diet, although I did wonder if the lack of grains had anything to do with it.  Now I know it must have been the fact that I had zero grain of any kind for the 6 weeks I did the diet.

<{POST_SNAPBACK}>

I'm curious then, what made you stop after 6 weeks if you felt GREAT?

RiceGuy Collaborator
Most people with celiac disease are temporarily lactose intolerant until they are on the gluten-free diet. Gluten antibodies destory the tips of the villi in the small intestine which contain the enzyme to break down lactose. So whenever lactose is ingested, the person gets really sick because they can't digest the lactose. Within time on a gluten free diet, however, the villi heal and are able to digest lactose again. Other people with celiac disease, like myself, seem to be intolerant to the milk protein casein. I don't know a whole lot about the connection between celiac disease and casein, but I have recently found out on these forms that the milk protein casein is quite similar to gluten, which would explain a few things  ;)

<{POST_SNAPBACK}>

Thanks for that excellent explanation! I know some people who need to have this info.

Carriefaith Enthusiast
Thanks for that excellent explanation! I know some people who need to have this info.
Thanks :) I'm glad I could help.
CMCM Rising Star
I'm curious then, what made you stop after 6 weeks if you felt GREAT?

<{POST_SNAPBACK}>

Well, I was doing Atkins to lose a few lbs, and I just burned out on the restrictive nature of the diet....not a lot of veggies....just one salad a day etc. I really missed fruit, stuff like that. So I went off the diet and the bad grain stuff crept back in.

RiceGuy Collaborator
Well, I was doing Atkins to lose a few lbs, and I just burned out on the restrictive nature of the diet....not a lot of veggies....just one salad a day etc.  I really missed fruit, stuff like that.  So I went off the diet and the bad grain stuff crept back in.

<{POST_SNAPBACK}>

Ah, ok.

I need my veggies for sure. I eat literally pounds of them per day. Like at least three or four, unlike most people I know who barely touch any in an entire week. No wonder they all have chronic issues...

I couldn't get any more restrictive without seriously crippling my overall mood. So many things off limits already. If I have to strike anything more off my list I'll go bananas.

I gotta have rice and potatoes too, because those and veggies constitute like 99.9% of my diet! My daily decisions for a meal is like "hmmm...do I have rice and veggies, or potatoes and veggies?" As an "extra special treat", I'll have rice pasta. Oh Boy!

OK, that's nearly all off topic...oh well...

Rusla Enthusiast

It depends on what I have eaten. Yesterday it took no more than 20 min for me to get so tired and have my face break out with just one cookie. If I eat bread it can be very drastic and fairly quick with crackers it can take an hour or so, and some times less. So times it takes longer with more extreme longer lasting effects and some times it happens fast with either minor or nasty effects that can last longer than two weeks or last two days. It also depends on what I eat the next day on how bad the breakouts get. I also get the brain fog and get very nauseous and sometimes dizzy.

I have noticed extreme fatigue very quickly and instant relapse with washroom issues.

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. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,155
    • Most Online (within 30 mins)
      7,748

    lfedas
    Newest Member
    lfedas
    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

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.