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

Feeling Sick After Eating Anything.


RideAllWays

Recommended Posts

RideAllWays Enthusiast

Lately I have been feeling sick after everything I eat. I don't get my gluten symptoms (bloating, D, vomit, etc) but I just feel really nauseated and my migraines are triggered. My depression and anxiety have been horrible lately. I have my own gluten-free kitchen (with the bf's occasional beer) so no utensils or anything are contaminated. Here is what I ate for dinner:

Salmon with lemon

Rice

Cooked carrots and peas

I don't know what could possibly bother me with that. For breakfast I had a rice cake and some turkey bacon, which has never bothered me before. Should I go back on an elimination diet? Keep a food diary? I don't really know how to keep a food diary, just write down what you eat?

Any ideas are appreciated!

Devon-Anne


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



Celiac.com Sponsor (A8-M):



i-geek Rookie

Sometimes rice gives me GI problems. Other times it's fine. I try to rotate my starches so that I'm not eating rice too often. If you've been eating a lot of rice lately, you could try a rice-free week and see if your symptoms improve.

And yeah, a food diary is pretty much just writing down everything you eat and when in the hopes of pinpointing problem sources. Easiest way is probably a small notebook that you can carry in your purse or pocket.

Ahorsesoul Enthusiast

A food journal would be a good thing. Make note of when bf drinks beer. Many people here say they are cross contaminated from kissing and from body fluids from people who consume gluten. Any new medications or new personal care products should be noted. Keep an eye out for oat contamination.

T.H. Community Regular

Yeah, I'd do a food log, too. Write down what you eat, at what time, and EVERY ingredient. Brand names of the foods can help, too, as some brands may have different processes, suppliers, etc... that affect your reactions. Then note every reaction and what time for that, too. After a couple weeks, or less, you may start to see a pattern. Maybe think about eating only certain foods for a couple days, then switch to completely different foods another day, see if it affects the reactions? (and you'd need different salt (one of them should be non-iodized), different oils, etc... for this to work well)

Rice could definitely do it to me, even though I was always told that rice was safe! It seems to be a little less safe for some of us celiacs, allergy-wise

I'd also look at anything else that might be in common in many of your meals?

--Was there salt in both meals? It can have anti-caking agents or corn for stabilizing, if it's iodized.

--Any oils that you used with both meals? Those are often problems for people developing seed or nut issues, due to cross-contamination. Nuts are ones that often give headaches, too.

--Oh! Do you have any allergies to antibiotics? I did, and once I went gluten free I started getting more sensitive to antibiotic residues in animal products! Farm raised fish has HIGH levels of residue, but bacon would probably have a little of it, too.

--Also, you might check out sulfite reactions and fructose malabsorption on-line. Those conditions can react to a wide range of foods, so it feels like reacting to everything.

Good luck - so sorry you are having difficulty!

Skylark Collaborator

Bummer. So sorry to hear you're depressed and anxious. I hate feeling like that.

Did you start any new meds lately, or start taking any supplements?

You do have a "big 8" allergen on that meal, the fish. A food diary is writing down everything you eat and how you felt that day. You look for patterns. It's hard to sort out delayed reactions though because you might have to sift through three days of foods. Did you feel better on your elimination diet? Maybe you missed a food you are reacting to because the reaction was delayed.

coryh5 Newbie

Lately I have been feeling sick after everything I eat. I don't get my gluten symptoms (bloating, D, vomit, etc) but I just feel really nauseated and my migraines are triggered. My depression and anxiety have been horrible lately. I have my own gluten-free kitchen (with the bf's occasional beer) so no utensils or anything are contaminated. Here is what I ate for dinner:

Salmon with lemon

Rice

Cooked carrots and peas

I don't know what could possibly bother me with that. For breakfast I had a rice cake and some turkey bacon, which has never bothered me before. Should I go back on an elimination diet? Keep a food diary? I don't really know how to keep a food diary, just write down what you eat?

Any ideas are appreciated!

Devon-Anne

I know exactly the feeling you are describing. My stomach is horrible after I eat ANYTHING. I am trying to pin point what the issue is but I haven't found the cause as of yet. It is very frustrating.

Cory

jackay Enthusiast

I good way to track your diet is using livestrong.com. Go to my plate and you can enter what you eat. There is a list of lots of brands, which is very helpful. It keeps track of calories, carbs, fats, etc. There is also a daily diary where you can enter how you feel, how you slept, notate what foods you suspect are bothering you, etc.

I used this when I was on an elimination diet and it was very helpful. It was a great way for me to keep track of how I felt. I was underweight and was able to consume enough calories each day because everything was calculated for me.


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



Celiac.com Sponsor (A8-M):



RideAllWays Enthusiast

Thanks, I'm going to have to try all of this. For breakfast I had an apple and a plum and felt sick for hours. D came later at work. wtf?

Skylark Collaborator

Apple and plum have fructose. Maybe you have fructose malabsorption. Try looking up a low FODMAP diet.

Mack the Knife Explorer

Apples are a big no-no with Fructose malabsorption. Plums are a stone fruit and should be ok.

But with fructose malabsorption it's all about the loading. When you eat something high in fructose, it may or may not be tolerated by you depending on how much other high fructose foods you have already eaten that day. This makes it hard to track down. Plus, everyone's tolerances are different.

Fructose malabsorption affects an estimated 33% of the population to some degree so it is quite possible this is your issue.

Try avoiding apples, pears, tomatoes, onions, garlic, artificial sweeteners and wheat (not that this is relevant to you anymore) for a while and see if it makes a difference.

looking4help Apprentice

I good way to track your diet is using livestrong.com. Go to my plate and you can enter what you eat.

Thank you so much for suggesting this site. I have been looking for something like this online to track my food diary! :)

kayo Explorer
Plums are a stone fruit and should be ok

Plums and the other stone fruits contain sorbitol which can bother you if you have a fructose intolerance. If you follow the FODMAP diet this is a fruit you'd avoid too.

FODMAP safe fruits: ripe bananas, strawberries, blueberries, raspberries (but not blackberries), oranges, mandarins, grapefruit, lemon, lime. Avocados and fresh tomatoes (in moderation) are ok too though we tend to think of them as veggies and not fruit.

Ahorsesoul Enthusiast

Too much Vit C can cause diarrhea.

Kathleen Smith Contributor

This happens to me too. I am a year and half gluten free. I just went to the Celiac Center in Columbia and my bloodwork is SO GOOD!!! No antigens showing I am ingesting gluten by cross contamination (or cheating as they would say). It doesnt show an immune response. All my vitamin defieciences were corrected!! I only need the mulit vitamin. So it all looked good, why so nauseos after eating???? They dont know. I had all kinds of tests done. My last endoscopy showed my intestines are still all scalloped but the doc said that is normal for only a year or so into diet. She also said not everyone heals a whole lot or at the same rates and they dont know why.

I guess the bottom line is they dont know why. Celiac has such varied symptoms......

Just wanted to share so you knew you werent alone

RideAllWays Enthusiast

Thanks Kathleen, it's always nice to know that we're not alone in all this. So for those who are on the FODMAP diet, gluten-free obviously, Soy-free, Dairy-free, and gonna try maybe corn and rice free...what do you eat? Rice cakes have been my saviour through this year and a half..and rice noodles, rice paper, rice tortillas, rice bread....

Are most veggies ok? If not, which ones are no-nos?

And thanks for the food list Kayo, anybody else want to add?

Thanks so much for your replies, doctors don't seem to be extremely helpful when I bring up this issue and I definitely don't have the money for a nutritionist (let alone for food itself lol), but I find that y'all know more from experience than these people anyways!

Muchly Appreciated :)

Skylark Collaborator

My mom has fructose malabsorption. She eats a lot of potatoes and white rice for starch. Also homemade cornbread or spoonbread with no added sugar. Brown rice has enough fructans to bother her. She eats a lot of leafy greens like kale and chard, and salads with limited amounts of other veggies with a little more fructose. Meats, nuts, eggs, and seeds are fine, and she can eat small servings of legumes with a little BeanZyme. She can also eat low-lactose dairy.

This is the best article I can find for you on a quick Google search.

Open Original Shared Link

It's partly about fructose load, which is why figuring out fructose malabsorption can be confusing. Half a plum with some cottage cheese might be perfectly fine, while a handful of prunes can be way too much sorbitol for your gut to handle. Mom can eat a bite or two of a high fructose food, but if she eats too much she's miserable all evening.

Mom also pays attention to the fructose:glucose ratio mentioned in the article. She keeps bulk dextrose around and can do things like sweeten her coffee with dextrose and then have a little fruit with breakfast.

  • 2 weeks later...
Dada2hapas Rookie

I have a similar story, but may or may not be related. I couldn't eat anything either. I had been gluten free for over a year, seeing a lot of improvement. However, in the last year, I was still sick far too often for it to be a cc issue. Food that was safe months previous would make me sick. Eating became like a minefield again. Becoming desperate & losing will to live, I read everything I could find that could possibly cause these terrible symptoms, and documented everything I ate. I went to see other specialists and asked a lot of questions. I was tired of having no good answer from my GI, who seemed to think it was not an allergy issue at all.

With a blood test, my new doc confirmed 'Mastocytosis' which sends my 'Oral Allergy Syndrome' thru the roof. My symptoms from that are very much like glutening. Gut anaphylaxis, with bloating, belching, vomitting, D, nausea, abdominal & musculoskeletal pain, immediate anxiety & depression. It's been a godsend to finally have a clue. For me, it's a 'seasonal' allergy to certain many fruit/veggies, etc. depending on what 'pollen' is in the air. Finally can eat, gaining weight again. Good luck to you!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,553
    • Most Online (within 30 mins)
      7,748

    Jennifer CCC
    Newest Member
    Jennifer CCC
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.