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

Additional Food Intolerances - Poll


CR5442

Recommended Posts

CR5442 Contributor

Hi everyone

 

I thought it might be interesting for us all to list what we are intolerant too in addition to Gluten as so many of us seem to have problems after cutting gluten from our diet - we might be able to experiment on cutting certain foods based on the findings.  It might be interesting also to find out what symptoms you had with them which lead to you sussing out you were intolerant.  Here's mine:

 

Eggs - heartbeat/heat/irritability

Dairy - heat/irritability/massive water retention

Soya - heartbeat raised, water retention

Corn - hearbeat raised

Rice (? TBC) - heartbeat raised

Fish - itchy, water retention

Shellfish - itchy, water retention

Coconut - raised heartbeat, high irritability

Palm oil - heat, high irritability, water retention

Potato? - water retention


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



Celiac.com Sponsor (A8-M):



NoGlutenCooties Contributor

Oats.

Both my mom and my uncle have Celiac and neither can tolerate oats.  My uncle gets his typical glutening symptoms which include bloat, chills, cold sweats, diarrhea, and vomiting.  My mother gets dry, very itchy skin with an itchy/crawly sensation on her back and legs.  Given their experiences with oats I haven't touched them since going gluten free.

(And yes, these reactions were to the certified gluten free oats.)

bartfull Rising Star

Corn: similar to gluten but much more severe. D, nausea, weakness, brain fog, severe muscle spasms, and a drop in core body temperature. Oh yeah, and psoriasis flares.

 

Soy: Psoriasis flares, minor D.

 

Nightshades: Can eat a little. Too much and I get joint pain and psoriasis flares.

 

High salicylate foods: D and psoriasis flares.

 

Histamines? Not sure, but I have had the symptoms of MCAS all my life.

Salax Contributor

Corn & Rice - Colitis flares up, horrible intestinal pain, esp. in the morning. back and front

Cow's milk products - Horrible stomach pain, D, cramping, sick to my stomach

Large quantities of non-organic tomato (like a sauce or chili, etc) - Colitis flare up horrible intestinal pain, esp. in the morning. back and front (Oddly organic is fine, not an issue with organic)

Oats (gluten-free obviously) - Hives (Joy of itchy skin and welts)

GottaSki Mentor

Most Dairy, grains, legumes, nightshades, nuts (except almond), seeds, all histamine containing and inducing foods along with all sorts of things floating around in the air -- just call me bubble girl ;)

FruitEnthusiast Enthusiast

After going gluten-free, developed the same symptoms as with gluten to: rice, eggs, nightshades, coconut, soy. I haven’t tested any of them since because I’m still healing.

 

Symptoms: C, brain fog, blurred vision, nausea, fatigue, joint pain, occasional mild neuropathy in feet. Still get those at times, especially brain fog. In the first six months I also had irritability and anxiety but they went away.

 

Already sensitive to corn and mold (cultured/fermented foods) long before NCGI dx. Symptoms: sinus congestion, headache.

 

Recently maybe tuna (or it was mercury), I won’t know until I see an allergist. Symptoms: itchiness, eye irritation, insomnia, increased heartbeat.

CR5442 Contributor

This is amazing... to see that there are so many other things that we are reacting to... some of which are way away from gluten.  I was wondering if any of you had had a reaction to the components in probiotics.  I'm not sure how they make the cultures for dairy free ones.  Does anyone know?


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

In all fairness, I feel I must answer this.  I don't really have any other food issues.  Nothing I would call an intolerance.  I think it is normal for everyone , Celiac or not, to have some foods that might not work for them.  I know many people that are lactose intolerant, for example.  They don't have Celiac.  It is just a fact that adult mammals don't usually retain the ability to digest lactose.

 

Also, remember that Celiacs that are healed and happy and living their lives are not likely to be commenting here.  Forums like this attract people new to the disease and people with continuing problems.  Its just a fact of life.

 

Many times. these food "intolerances" resolve after the gut has healed and the GI system gets its self regulated and on track.  Just wanted t give a different view.

IrishHeart Veteran

I have a histamine intolerance because of lack of an enzyme called DAO in my gut. I hope it resolves entirely in time. My GI doc seems to think it will. He's been right about everything else in my recovery process so far, so I believe him! :) 

 

I have noticed that I am able to eat more foods with high histamine in them during the past few weeks (yaay!) and not have any symptoms, so I figure he's right. I do take probiotics and after all I have learned about the gut and or bodies being a microbiome, I firmly believe this has helped turn things around for me. I had an imbalance of bacteria (testing showed this after diagnosis and since then, I have dosed with proBs)

 

It's great to have bacon, chocolate and tomatoes back. I loves my bacon!

 

At one point, I could not tolerate dairy, eggs, soy, citrus and so many other foods. But my GI tract was a burning mess.

 

I still can't have MSG and food additives, nitrates, and corn is tough to digest for me, but I am not sure that has anything to do with celiac. 

 

Most people have  corn showing up in their (ahem....) well, you know. 

CR5442 Contributor

In all fairness, I feel I must answer this.  I don't really have any other food issues.  Nothing I would call an intolerance.  I think it is normal for everyone , Celiac or not, to have some foods that might not work for them.  I know many people that are lactose intolerant, for example.  They don't have Celiac.  It is just a fact that adult mammals don't usually retain the ability to digest lactose.

 

Also, remember that Celiacs that are healed and happy and living their lives are not likely to be commenting here.  Forums like this attract people new to the disease and people with continuing problems.  Its just a fact of life.

 

Many times. these food "intolerances" resolve after the gut has healed and the GI system gets its self regulated and on track.  Just wanted t give a different view.

Question is how long did it take for your gut to be healed?  I have been on a 'clean' diet for nearly three years and still have problems, though admittedly not as bad as previously.  However I still react to a bunch of things and I think that maltodextrin in my probiotic might be the next thing.

FruitEnthusiast Enthusiast

I have a histamine intolerance because of lack of an enzyme called DAO in my gut. I hope it resolves entirely in time. My GI doc seems to think it will.

 

I have noticed that I am able to eat more foods with high histamine in them during the past few weeks (yaay!) and not have any symptoms, so I figure he's right. I do take probiotics and after all I have learned about the gut and or bodies being a microbiome, I firmly believe this has helped turn things around for me. I had an imbalance of bacteria (testing showed this after diagnosis and since then, I have dosed with proBs)

 

Histamine issues are what I am dealing with also. Some may have celiac issues only, but many of us have leaky gut or other gut related problems which opens the door to many other food intolerances.

 

I’m seeing an allergist soon for allergy testing and I assumed that was where I would have my DAO enzymes checked. It sounds like I need to have my GI check that for me? Actually I’m not sure I have found the right GI yet. He’s the one who told me to go off gluten before testing me for celiac!!! I’m going to make an appt to see a GI at UCLA.

 

I’m taking good probiotics. Also glutamine for leaky gut, which I think has helped. My gut is messed up too, but my digestive symptoms are much better already, especially after cutting out histamine foods/liberators.

 

Thanks so much for posting about this!

GottaSki Mentor

Question is how long did it take for your gut to be healed?  I have been on a 'clean' diet for nearly three years and still have problems, though admittedly not as bad as previously.  However I staill react to a bunch of things and I think that maltodextrin in my probiotic might be the next thing.

 

This is a question I have asked many times.  The truth is no one can answer it for you personally.  It takes as long as it takes.  If it is taking more than six months to a year to see marked improvement, it is time to investigate other causes in addition to gluten.

 

Personally, I have had two periods of greatly improved health over the past five years which were followed by flares that were as bad or worse than prior to celiac diagnosis.  I am currently improving, but have learned to be very careful to assume I have found the complete answer to handle the damage caused by many years of living with undiagnosed celiac disease.

 

As Irish says..."every day is a healing day" -- there are days when I am having a horrid flare of symptoms that I don't believe it....but it is true as long as I keep looking for answers to solve my particular health puzzle.

cyclinglady Grand Master

I have had allergy issues (cats, mold, tree pollen, and some foods)  my entire life (so has my family).  I don't think it's related to Celiac Disease at all.  Just the luck of the draw! 

 

I forgot to add that my husband has NO allergies.  He's been gluten free for 13 years and enjoys good health!  It's no fair!!!!! :(

FruitEnthusiast Enthusiast

I have had allergy issues (cats, mold, tree pollen, and some foods)  my entire life (so has my family).  I don't think it's related to Celiac Disease at all.  Just the luck of the draw! 

 

I think some of us are inclined to have histimine issues for whatever reason. I'm the only one in my familiy with allergies though... bees, wool, cats, mold, dust...

cahill Collaborator

WOW I havent  though about listing this ,,, maybe be overwhelming

 

 

At one point in my journey I really really started to wonder if I was intolerant of EVERYTHING ,, I did an elimination diet and (pretty much) reacted to most every thing I ate,,, but as Irish says "every day is a healing day" Over time my gut healed ,I was able to reintroduce some foods with success but some are still troublesome

 

Current list looks something like this ;

 

Gluten ( of course ,lol)

Soy, mostly neurological issues & constipation

Potatoes,, at one point I was intolerant of all night shades but  am able to tolerate  (in limited amounts  ) all except potatoes

shell fish

Nuts,walnuts & almonds top the list

coconut 

peanuts  ,  but other legumes I can tolerate small amounts on occasion

corn but can tolerate small amount on occasion

most fruits  are hit and miss ,, so I rotate them in my diet

veggies well I mostly just dont eat them ,or if I do it is in  limited amounts here and there ,

chicken ( it just plain makes me sick ) not sure why I can tolerate turkey but not chicken :unsure:

histamine issues ??? not sure about this but  I am currently on loratadine daily and it seem to be helping .

seeds of any kind ( including flax ,chia pumpkin :(

 

 

 

At one point dairy and eggs but as I have healed I have successfully reintroduced them both :D( this was an important mile stone for me ,,, it makes life soooooo very much easier  :P  )

cahill Collaborator

In all fairness, I feel I must answer this.  I don't really have any other food issues.  Nothing I would call an intolerance.  I think it is normal for everyone , Celiac or not, to have some foods that might not work for them.  I know many people that are lactose intolerant, for example.  They don't have Celiac.  It is just a fact that adult mammals don't usually retain the ability to digest lactose.

 

Also, remember that Celiacs that are healed and happy and living their lives are not likely to be commenting here.  Forums like this attract people new to the disease and people with continuing problems.  Its just a fact of life.

 

Many times. these food "intolerances" resolve after the gut has healed and the GI system gets its self regulated and on track.  Just wanted t give a different view.

I have to agree

 

Most people come to these forum to seek help ,information and move on.

 

 

I am more of the exception then the rule  :wacko: 

IrishHeart Veteran

I have to agree

 

Most people come to these forum to seek help ,information and move on.

 

 

I am more of the exception then the rule  :wacko:

 

 

And some of us "veterans" hang around to "pay it forward" to the newbs. We just can't help ourselves. Could be the "mother hen" syndrome. :D

Adalaide Mentor

I also have a histamine intolerance. (thanks mom for beating me over the head til I learned my lesson :P) For me this has led to developing a full on allergy to heat which includes breathing problems when I get too hot, rashes when I'm in the sun and hives when exposed to extreme heat (like from a really hot oven). I also starting having oral allergy symptoms to avocados. Beyond that, I have learned how to live and eat on a regular low histamine diet, fitting some small amounts of everything into my diet without overdoing any single thing. For a long time tomatoes were always a huge, automatic hit for me no matter how small an amount I ate and now it seems I can tolerate them in small amounts. Yay!

 

I also generally avoid MSG because it is a migraine trigger for me. A few other things are too, that I can't think of off the top of my head now but that I would recognize on a food label.

w8in4dave Community Regular

This is a very interesting thread, I am Celiac and intolerant to Corn, Gas bloating the big"D" I think I can have some in very small amounts, but not HFCS . I am Lactose intolerant , I get the same way with Lactose I can eat some cheese and stuff but no milk. Or too much cheese. I am soy intolerant I don't even want a bite thank you anyway. I don't care if I ever eat that again. I hope I get my Corn intolerance back all the way :) It would be nice to eat a box of chocolate again :) Yea I did have some and yes it had corn. I ate some anyway and thought ohh well it was worth it! Suffer but worth it! I guess as long as I can eat cheese I am happy, I was never big on milk anyway. I don't have a problem with being Celiac it's the corn that bothers me! I hate being Corn intolerant! I don't know how some of you do it with all your intolerances. 

moosemalibu Collaborator

This is a very interesting thread, I am Celiac and intolerant to Corn, Gas bloating the big"D" I think I can have some in very small amounts, but not HFCS . I am Lactose intolerant , I get the same way with Lactose I can eat some cheese and stuff but no milk. Or too much cheese. I am soy intolerant I don't even want a bite thank you anyway. I don't care if I ever eat that again. I hope I get my Corn intolerance back all the way :) It would be nice to eat a box of chocolate again :) Yea I did have some and yes it had corn. I ate some anyway and thought ohh well it was worth it! Suffer but worth it! I guess as long as I can eat cheese I am happy, I was never big on milk anyway. I don't have a problem with being Celiac it's the corn that bothers me! I hate being Corn intolerant! I don't know how some of you do it with all your intolerances. 

 

Soy lecithin is also commonly used in chocolate.. just wanted to say that in case you are getting hit twice. I've never payed attention to corn so I don't know if that is a common chocolate additive.

w8in4dave Community Regular

Soy lecithin is also commonly used in chocolate.. just wanted to say that in case you are getting hit twice. I've never payed attention to corn so I don't know if that is a common chocolate additive.

I know Corn was listed in the ing. I am not sure if Soy Lecithin was or not. I have since gave up chocolate :) Lol maybe one day I can have some :) 

CR5442 Contributor

I can't have chocolate either in any form so I totally commiserate!

moosemalibu Collaborator

Just wanted to add that I figured out (no big surprise, it's common) that I'm intolerant to sugar alcohols. Removing them from my diet helped my chronic D significantly. It was sneaking in through a protein bar (I would bring 1/3 of a bar to work and eat it as a snack daily). Since removing it I am improving by leaps and bounds.

  • 2 months later...
across Contributor

 It would be nice to eat a box of chocolate again :)

enjoy life makes wonderful chocolate chips that contain only "Evaporated Cane Juice, Natural Chocolate Liquor (Non-Alcoholic), Non-Dairy Cocoa Butter."

They are made in a dedicated facility that doesn't process the major allergens. They really scratch the itch for chocolate.

dilettantesteph Collaborator

I have avenin enteropathy in addition to celiac disease, I believe based on a severe reaction to gluten-free oats. 

 

Other than that, other food issues seem to be caused by damage from glutening and are temporary until the gluten is removed from my diet and the damage has healed.  With frequent glutenings, there can be ongoing problems. 

 

I get most severe problems with dairy and high fat foods, but there are others that I haven't sorted out.

Archived

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

  • 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
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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.