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How Long Does It Take For Symptoms To Develop After Eating Gluten?
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So I think I accidently got glutened today, but I'm not sure.

My sister dropped her roll in my soup, but I ate it even though I thought I saw a few crumbs in it (I was being lazy and didn't want to go get a new bowl).

I have stomach pains and I'm a little bloaty/gassy now, but I'm not sure if it's because of the gluten, or becaues I do actually get these symptoms occasionally for no reason.

I started getting the pains about 2 and 1/2 or 3 hours after dinner. I'm not sure how long it takes for the body to start reacting to gluten. So I'm wondering if I have pain because of the minute amount of gluten I ate. If so, I will definitely try to be more careful in the future.

Any insight would be great. Thanks guys!

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Reaction time varies from person to person. For some people it is almost instantaneous. In my case it takes 3 to 6 hours. Some of us take longer than that.

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With me, I'm not so sure, as my symptoms are differant than others. I get mood swings and am extremely... irritable. My mom took 15 minutes. Since I'm a moody teenager, It's hard for me to tell.

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For me it takes 4-12 hours for the awful digestive symptoms to occur. In my opinion, the longer it takes for the reaction to occur, the harder it is because it's harder to find out what made you sick. :(

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for me it usually takes about 10-15 mins but it varies for each of us some take hours and sometimes days to feel the full effects. Feel better soon!

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It usually takes me a couple hours to react.

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That is a loaded question. Bowl reactions are usually within min. and last forever! I also suffer with DH. That usually takes a great deal longer to show up. Also, minor cross contaminations will not affect my bowls, but the DH will show up sometimes weeks later. Then the miriad of symptoms can happen from immediately to weeks. Hard to tell what causes the problem.

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My symptoms show up either in the evening if I got glutened that morning, or in the morning if I got glutened the night before...my reaction has never been immediate.

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it takes me a few seconds and i feel like crap for a week.

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Any insight would be great. Thanks guys!

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That is a very good question that I am looking for the answer to aswell...

My son was diagnosed in Oct with celiac (blood test confirmed)...he was never really sick, diarrhea ('D') once or twice a week, compained of a sore stomach once or twice a week...when he has 'D' it is a one time thing - he goes to the bathroom once has 'D' and then he is fine for another week. They sent him in for a whole battery of tests, (celiac was only one of them) so they weren't really looking for it, it was just on the list of tests they scheduled him for.

....regardless he has been gluten free since the diagnosis but he isn't really getting any better. We have been to a nutruitionist, dietician, pediatrician, allergist and now a surgeon. He was put on the disacharide - no lactose or succrose - and that didn't change the weekly visit to the bathroom either. It actually made him worse - no energy, very pale etc...he has had extra blood tests to check his levels - iron, hemoglobin, white, etc and they all came back normal.

He has eaten gluten by accident but never reacted to it until 3 1/2 days later. Now honestly I can't say that he was reacting to the gluten or he was just getting his weekly bout of 'D'. He also ate an Oreo at a friends house and didn't react at all.

Now the surgeon has scheduled him for a biopsy so he is eating gluten. And when I say he's eating gluten - I mean everything in sight!! He started the new diet on Tuesday afternoon and ate a whole lot of gluten for 4 1/2 days before he got his weekly bout of 'D'. Now he has eaten a whole lot more and he seems fine again.

My question is - is this normal??? Everything I read on here the reaction is almost immediate (5 mins to 12 hours) but his syptoms don't seem to fit the norm...anyone else out there been thru this??? If so, do you have any advise???

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That is a very good question that I am looking for the answer to aswell...

My son was diagnosed in Oct with celiac (blood test confirmed)...he was never really sick, diarrhea ('D') once or twice a week, compained of a sore stomach once or twice a week...when he has 'D' it is a one time thing - he goes to the bathroom once has 'D' and then he is fine for another week. They sent him in for a whole battery of tests, (celiac was only one of them) so they weren't really looking for it, it was just on the list of tests they scheduled him for.

....regardless he has been gluten free since the diagnosis but he isn't really getting any better. We have been to a nutruitionist, dietician, pediatrician, allergist and now a surgeon. He was put on the disacharide - no lactose or succrose - and that didn't change the weekly visit to the bathroom either. It actually made him worse - no energy, very pale etc...he has had extra blood tests to check his levels - iron, hemoglobin, white, etc and they all came back normal.

He has eaten gluten by accident but never reacted to it until 3 1/2 days later. Now honestly I can't say that he was reacting to the gluten or he was just getting his weekly bout of 'D'. He also ate an Oreo at a friends house and didn't react at all.

Now the surgeon has scheduled him for a biopsy so he is eating gluten. And when I say he's eating gluten - I mean everything in sight!! He started the new diet on Tuesday afternoon and ate a whole lot of gluten for 4 1/2 days before he got his weekly bout of 'D'. Now he has eaten a whole lot more and he seems fine again.

My question is - is this normal??? Everything I read on here the reaction is almost immediate (5 mins to 12 hours) but his syptoms don't seem to fit the norm...anyone else out there been thru this??? If so, do you have any advise???

This sounds like 'constipation' with D after. I found my children with gluten problems had to cut out MILK for a while. The milk (once the digestive system is damaged) caused them to 'back up' to the point in my youngest one of needing a suppository. Then the 'plug' would come out and have massive D.. enough to come out of the clothes on my one year old (and all over!!). About every 4-5 days they would then go to the bathroom. After cutting out gluten (and milk for about a month or two) they now go every day like clockwork and have normal bowels. Doctors don't like to 'cut out' milk because they say it's essential - what good does drinking milk do if your intestines are damaged and you don't absorb it? We used organic soy milk for a while to get the calcium into them... now we use broccoli and cheese. We STILL don't give them plain milk because it seems to cause issues - maybe because cows eat wheat? (dunno!). I know my kids do best limiting dairy intake to just cheese.

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He has normal bowel movements inbetween the weekly 'D'...I have asked him if he is constipated and he says no...he has a BM once or twice a day like clockwork...like I said above, we cut out milk and sugar but it left him pale and without any energy so the doctor told us to go back to the normal gluten free diet.

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That is a very good question that I am looking for the answer to aswell...

My son was diagnosed in Oct with celiac (blood test confirmed)...he was never really sick, diarrhea ('D') once or twice a week, compained of a sore stomach once or twice a week...when he has 'D' it is a one time thing - he goes to the bathroom once has 'D' and then he is fine for another week. They sent him in for a whole battery of tests, (celiac was only one of them) so they weren't really looking for it, it was just on the list of tests they scheduled him for.

....regardless he has been gluten free since the diagnosis but he isn't really getting any better. We have been to a nutruitionist, dietician, pediatrician, allergist and now a surgeon. He was put on the disacharide - no lactose or succrose - and that didn't change the weekly visit to the bathroom either. It actually made him worse - no energy, very pale etc...he has had extra blood tests to check his levels - iron, hemoglobin, white, etc and they all came back normal.

He has eaten gluten by accident but never reacted to it until 3 1/2 days later. Now honestly I can't say that he was reacting to the gluten or he was just getting his weekly bout of 'D'. He also ate an Oreo at a friends house and didn't react at all.

Now the surgeon has scheduled him for a biopsy so he is eating gluten. And when I say he's eating gluten - I mean everything in sight!! He started the new diet on Tuesday afternoon and ate a whole lot of gluten for 4 1/2 days before he got his weekly bout of 'D'. Now he has eaten a whole lot more and he seems fine again.

My question is - is this normal??? Everything I read on here the reaction is almost immediate (5 mins to 12 hours) but his syptoms don't seem to fit the norm...anyone else out there been thru this??? If so, do you have any advise???

Yes, it is very normal! There will be times when he will appear to be normal, but each bout will be more severe and more damage is done. He will have weeks of normalcy, then days of illness. Back and forth until eventually he is malnourished and has all sorts of problems from anemia to heart or liver problems. Plus he may develop all sorts of autoimmune problems.

The gluten free diet alone does not work for everyone. Check out the specific carbohydrate diet. It is the original cehiac gluten free diet. It's a diet that heals the intestines, and eventually one will get bettter.

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about 10 minutes

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I came across this, while googling "how long after eating gluten it takes for effects to take place" because I ate some thai sandwhiches 2 days ago. I was noticing slight stomach ache. My reason for responding is that I used to have very strong stomach pains, allways in the same spot, in the middle above the belly button. Worst was about every day or every other, sometimes so bad I could only go to sleep. I went to doctors who perscribed different medicine, but nothing helped. One day I was having the regular upset stomach, when I decided to attend my Korean yoga class. There were these stomach exercises they do there. And I thought that I woulnd't be able to do them or that it would be bad. On the contrary, the instructor made me do them, and in 10 minutes the ache was gone. So whenever I have the ache coming, I do the excercise, even if it takes an hour, it goes away. I tried to find video, but so far couldn't find one. You lie on your back, breath deep in and out. Make big stomach when inhale, and then when you exhale, make it small. Also when exhaling with your thumbs make downward motion across your belly. You do four phases, one with legs straight, one with legs bent, and third with rump off the floor while legs are bent, and fourth, back down with legs straight and just gentle breathing. Each phase about 5 min. Eventually your belly will start to make gurgling noises during the excercise, the more the better. So this helped me, and I still don't know what my problem was, but maybe this may help others. :)

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For me it can be anywhere from 2 hours until late the next day. I get D and my abdomen becomes distended and bloated. I feel tired/weak, and nauseous. Before I was gluten-free I had difficulty sleeping, and when I eat gluten I have a terrible time sleeping that night or the next; I wake up every hour, and am super tired the next day!

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With me it's about 3 days but my Grandma has always found it takes her 8 days. To the hour. Ha. All different :) .

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For me  some reactions appear within an hour after consuming gluten accidently. First it's mouth sores and then gas and   bloating. Stomach cramps takes some time and stays there till the next day.

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Greetings! I am new to the boards. I have been gluten free since August 2015. My doctor has suggested that I get the blood test...I have not yet done so but I noticed that since I began cutting out gluten I feel much better. However,  yesterday I was at a going away party for some friends and I ate imitation crab, which apparently is loaded with wheat. I am dying today!! It usually takes me between 8 - 14 hours to have a major league reaction and it takes me between 6-12 days to recover completely. I know a lot of people that are celiac and some are gluten sensitive the majority of us have very similar symptoms when we've been gluten-slapped. I know I get foggy brain, I get clawing pain in my stomach, bloating, diarrhea, fatigue and a headache. When I am eating gluten-free normally I have 2-3 BM a week. I tend to just try to wait it out. I'll eat bland foods, lay off the fats, drink plenty of fluids and ginger ale or ginger to soothe my tummy.

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    • Thanks for posting this Adrien, it's a great list and I and others will appreciate the effort and the thought behind it. I loved my time in Malaysia and I'm glad I sampled all the food I could whilst I was still on an unrestricted diet. The good thing is that, like you say, some of the nice Malay foods are still ok. As a backpacker I survived on a lot of nasi goreng and laksa, nice to think if I return there I could still do the same Terima kasih!
    • I have posted on here before. DQ2, brother with celiac, DGP iGA was the only mildly elevated test. Was gluten-free so did 6 week challenge last winter. Negative biopsy. I am gluten-free now but do go out to eat. Prior to the challenge my health was good. Since then I have: Chest pain, pain between shoulder blades, periods of shortness of breath, heart palpitations, one instance of a heart arrythmia episode, neck is tender to touch on one side (they kept saying sinuses or TMJ which my dentist vetoed) ear ache, bowels never sink. Numbness and tingling. Blood pressure variations. Could be doing chores and feel dizzy and it might be 84/52.  not super low, but not typical for me if I'm running around the house.While other days I am mildly hypertensive. Recently lost 5 lbs in 8 days without trying. Recently electrolytes were low, alkaline phosphatese was low. Ferritin started dropping so started liquid iron 2-3 times per day 4 months ago. Primary watching that, I am not anemic but we are nowhere near iron overload either.  GI doc was a dick. Did not even know DGP replaced older tests and he was very condescending When I begged him for help recently and told me to get a second opinion which is exactly what I plan on doing.  I now have pain in my upper GI area. It is tender to touch. I had my gallbladder out in 97 along with a stone and infection in my bile duct. It hurts in this area. Pancreatic enzymes look fine, liver enzymes fine. Pancreatic ultrasound fine. I will now be doing a EUS Soon to look at bile duct, pancreas and liver.   so a typical day for me is that I might feel fine for a while and then suddenly feel like I'm going to pass out. really dizzy, numbness in odd places, like my body has been hijacked. I will typically eat a bunch of food something high protein and in about an hour or so I start to feel better. However, then my upper stomach starts to hurt in place of the passing out feeling. blood sugars are also normal. After getting the " it must be panic attacks" and condescending looks a million times my primary finally ordered an ultrasound of my sore neck and there is an abnormality in my thyroid which she says looks like possibly Hashti's. Except for one time, all my serum TSH tests were normal. We have more blood work on Monday. As I have not put on any weight and there are other symptoms that are closer to Graves.  Has anyone else had any thyroid issues that followed doing a gluten challenge?  where is your stomach pain? Do you have it above or below your belly button? Mine feels like it's in the pancreas area, like 2-3 inches above the belly button and when I push on it it's tender, but not all the time. sometimes i feel it in my back. 
    • Thanks for sharing with me.  I really appreciate it.  Honestly, after a glutening last summer (still do not know what glutened me), I did not eat out for a year!  The risk was too great as my healing time took 3 months (for symptoms to subside) and six months to regain lost weight.  Our recent vacation to Europe was worth the risk  as we traveled with our entire extended family, but we were extra cautious and ate only at celiac-approved places.  Otherwise, we "dined" at markets or ate the food we brought from home.  Thankfully, we did not get glutened (at least we don't think so!)  
    • I do not struggle with this and I was brought up the same way as you. I don't struggle because for many years off & on we didn't have a bathtub, only showers as well as this being therapy or medicinal for the skin - heck even for the muscles as I age. I figure I've earned my right to luxuriate or medicate with baths any time I've a mind to. My husband saw just how bad my dh got & NEVER begrudges me a nice long soak in the big soaking tub we now have.
    • Hi, No, I do not have celiac  disease. I have an ankylosing spondylitis which is an auto-immune disease provoking an inflammation of the joints. Under the advice and supervision of my doctor and the professor at the hospital I follow a gluten free & casein free diet, which is extremely successful in preventing inflammatory events. And I've been doing so, strictly, for more than 6 years. So I'm not Celiac, but I can tell you that I react strongly every time I take gluten even in small amounts. Even soya sauce, which according to this website has an almost zero dose of gluten, is a lot too much for me. Nevertheless I allow myself to eat food which has been processed in a factory which processes gluten. To conclude, I would say that when you are travelling, especially in a country where celiac disease is scarcely known, you should be twice as careful as when you're going out at home. In the end you can never guarantee that the cook has cleaned his pan after using soya sauce and so on... You can only bet
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