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

Does anyone else have this problem?


Elizabeth Green

Recommended Posts

Elizabeth Green Newbie

I am new to this site so please be patient with me.

 I am a label reader, and careful with anything that triggers those ‘abdomen  issues’.
However, even when I have foods that do not list anything remotely gluten related, I still get an attack like I did.

Are there certain spices that can trigger issues as well?


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



Celiac.com Sponsor (A8-M):



trents Grand Master

Welcome to the forum, Elizabeth! There was an article on the forum recently outlining research about certain spices having proteins similar to gluten that cause reactions in some people with celiac disease. You might search for it using the forum search tool and also google it. I cannot remember the specifics. But aside from gluten and spices, there can be any number of ingredients in processed foods that cause GI distress for those with celiac disease. Things like xanthan gum, polysaccharides, lecithins, sugar alcohols, and on and on.

Scott Adams Grand Master

Here it is:

 

Wheatwacked Veteran
(edited)

 

Option 1:The Glute Contamination Ellimation Diet may be an effective therapeutic option for GFD-adherent NRCD patients. Response to this diet identifies a subgroup of patients, previously classified as RCD1, that is not truly refractory to dietary treatment. Preventing an inaccurate diagnosis of RCD1 avoids immunotherapy. Most patients are able to return to a traditional GFD without return of symptoms. Gluten Contamination Elimination Diet GCED Food Chart;  Table 1 Products allowed

Option 2: I've been sticking to Dr Haas's list of ingredients in THE VALUE OF THE BANANA IN THE TREATMENT OF CELIAC DISEASE SIDNEY V. HAAS, M.D. NEW YORK that was used for Celiac before they knew about gluten and it's helping. It was the first diet that worked back in 1920. Celiac Disease was called Infantilism. Of course now we know to never reintroduce wheat. "Ten cases are reported here ; eight of the patients were clinically cured by the form of therapy described below. The two patients not treated died" Back then they made their own cottage cheese (pot cheese) and the cows were all pasture fed. I am continuing to take large dose Thiamin, D3, Phosphatidyl Choline.

  • Whey protein
  • Cottage Cheese (Daisy 4% has no additives)
  • Bananas (ripe)
  • Oranges
  • Vegetables
  • Gelatin
  • Meat
Edited by Wheatwacked
Elizabeth Green Newbie

Wheatwacked:

I’m on the FODMAP diet. I have Celiacs and IBS-D.

The Banana treatment one you mentioned is not one that could work for me. There are way too many vegetables that I don’t have luck with. Even when others do.

Also, bananas cause me to throw up. I can’t handle cottage cheese. 🤢

I did another post that listed my 3 likely suspects. So, it would be one of them.

knitty kitty Grand Master

@Elizabeth Green,

Welcome to the forum!

I've found the Autoimmune Protocol Diet (AIP diet) to be extremely helpful.  Developed by Dr. Sarah Ballantyne because she and her children have Celiac Disease, the AIP diet has been shown in scientific studies to promote intestinal healing. Her book, The Paleo Approach, has been very helpful.  (Her website   https://www.thepaleomom.com is tied up in a ransom ware dispute and needs support to recreate it. Please consider buying her a coffee.)

The AIP diet eliminates some foods to reduce inflammation and calm the autoimmune response.  Relief is seen within three weeks to three months.

Nightshade vegetables (potatoes, tomatoes, eggplant, and peppers) are excluded as they promote leaky gut. 

Also excluded are spices from seeds like cumin, mustard, cardamum, and fenugreek (ingredients of curry powder).  Chili powder from chili peppers (nightshade) is excluded, too.  

Legumes (beans, lentils, peas, peanuts) are excluded. 

All grains, including corn, are not allowed. 

Nuts and seeds are excluded as well.

Dairy and eggs are also excluded.  

And no processed foods, including processed meats (like luncheon meats, sausages, chicken nuggets, etc) and gluten free cookies and such. 

Allowed foods are meat and nonstarchy veggies and some fruits.  Healthy fats like olive oil are allowed. 

I know it sounds drastic, but it really works.  I felt better and saw improvement within a few weeks.  I had to exclude high histamine foods like bananas, broccoli, avocado, fish and pork, bone broth and fermented foods.  

Foods are slowly added back into one's diet as one can tolerate after a trial period.  I waited three months to start adding foods back because my digestive system was so touchy (IBS-D).  

Hope this helps!  

Keep us posted on your progress!

Wheatwacked Veteran
Quote

 

I was diagnosed Celiacs and IBS-D probably 7 years ago. My question is in regards to spices in a dish called Butter Chicken. I had tried a really liked this about 3 or 4 years ago. I found a frozen one at the local store. I read the package and there wasn’t anything gluten in it.

So I have it narrowed down to these 3 spices listed on the package:

saffron, onion powder, curry

Are any of these known to trigger celiac issues? I still have a pack in the freezer.

 

I vote the onion powder, as it is not low fodmap.

Quote

 

Garlic and onion contain fructans. These are a specific type of carbohydrate. They’re not bad for your health in general, but they can sometimes trigger symptoms in people with IBS.

Realizing that garlic and onion give you IBS symptoms can be devastating. After all, they’re in almost every savory dish, and they take meals from “blah” to delectable. Turning to garlic powder and onion powder won’t help either. In fact, these might actually be worse because they’re more concentrated.   Cooking for IBS Without Garlic and Onion - HealthiNation

 

 


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



Celiac.com Sponsor (A8-M):



Wheatwacked Veteran
knitty kitty Grand Master

Nope, my vote is the spices from seeds in curry powder.  

Elizabeth Green Newbie
25 minutes ago, knitty kitty said:

@Elizabeth Green,

Welcome to the forum!

I've found the Autoimmune Protocol Diet (AIP diet) to be extremely helpful.  Developed by Dr. Sarah Ballantyne because she and her children have Celiac Disease, the AIP diet has been shown in scientific studies to promote intestinal healing. Her book, The Paleo Approach, has been very helpful.  (Her website   https://www.thepaleomom.com is tied up in a ransom ware dispute and needs support to recreate it. Please consider buying her a coffee.)

The AIP diet eliminates some foods to reduce inflammation and calm the autoimmune response.  Relief is seen within three weeks to three months.

Nightshade vegetables (potatoes, tomatoes, eggplant, and peppers) are excluded as they promote leaky gut. 

Also excluded are spices from seeds like cumin, mustard, cardamum, and fenugreek (ingredients of curry powder).  Chili powder from chili peppers (nightshade) is excluded, too.  

Legumes (beans, lentils, peas, peanuts) are excluded. 

All grains, including corn, are not allowed. 

Nuts and seeds are excluded as well.

Dairy and eggs are also excluded.  

And no processed foods, including processed meats (like luncheon meats, sausages, chicken nuggets, etc) and gluten free cookies and such. 

Allowed foods are meat and nonstarchy veggies and some fruits.  Healthy fats like olive oil are allowed. 

I know it sounds drastic, but it really works.  I felt better and saw improvement within a few weeks.  I had to exclude high histamine foods like bananas, broccoli, avocado, fish and pork, bone broth and fermented foods.  

Foods are slowly added back into one's diet as one can tolerate after a trial period.  I waited three months to start adding foods back because my digestive system was so touchy (IBS-D).  

Hope this helps!  

Keep us posted on your progress!

Hi Kitty Kitty,

The only issue I’ve had was when I ate this meal with these 3 spices in it.

Otherwise, I’m pretty good with the FODMAP diet.

The issue on some of the others is that the foods they want you to eat on them are:

1) foods I already cut out because I had an issue eating them. (and I don’t eat things like luncheon meats, etc anyway )

2) are foods I don’t like. That even the smell makes me nauseous. (fish for example) I cut bananas as they started making me sick. 
 

As someone on the FODMAP, I don’t eat things like broccoli anyway. Gas producers are a no-no. 
 

Thanks for the Welcome!

Elizabeth Green Newbie
22 minutes ago, Wheatwacked said:

This was really interesting. I knew not to do the Masala as it has onion. I don’t tolerate onion. (I also hate the smell and taste of them)

A friend also recently found that many people who have issues with IBS-D and or Celiac…also have issues with curry and with onions.

Sadly, things made Gluten-free, are still made with onions. (sigh)

Oh well. I try to make things for myself lately. 
Thanks!

MarElizabeth Newbie

Some spices are causing indigestion, bloating and sometimes stomach cramps.  As far as which ones. Gotta experiment.

Wheatwacked Veteran

As I understand it Masala is just a spice mix. Back when families made their own it varied with the family tradition, so different brands may have different mixes.

What Is Garam Masala? Here's What You Need to Know About the Spice Blend

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
  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,953
    • Most Online (within 30 mins)
      7,748

    ramonaja
    Newest Member
    ramonaja
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.