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

Other Types Of Natural Chemicals In Food


bartfull

Recommended Posts

bartfull Rising Star

The latest thing I have reacted to is nettle tea. I assumed it must be high in sals, but then I read where it is used to COUNTERACT high sals foods.

I DO react to a lot of high sals foods, but not all. I can eat a great big sweet potato with broccoli every day and have no reaction. That should be a no-no.

So I looked up amines and oxalates. Nope. A lot of the foods high in these chemicals don't bother me while some of the one's that are low do.

So is there something I'm missing? Is there another chemical in foods that I might be reacting to?

Here is what I can eat:

meat

dairy

eggs

white rice

broccoli

cauliflower

summer squash

carrots

sweet potatoes

white potatoes

bananas

avocadoes

sea salt

coffee

cornstarch

sunflower oil

safflower oil

What I know I can't eat:

corn meal

blueberries

grapes

corn oil

chocolate

apples

leafy greens

brown rice

every vitamin supplement I have ever tried

Things I like but haven't tried yet:

citrus

tomatoes

eggplant

bacon

camomile tea

There are probably others I've tried that didn't work but I can't think of them right now. And I know there are others I would like to try, but those on the list are the ones I would MOST like to eat. And even more important to me would be finding a vitamin and mineral supplement I could tolerate. Sweet potatoes have a lot of nutrition, but a person can get mighty sick of eating them every single day!

Thanks for any help or suggestions.


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

Sweet potatoes have a lot of nutrition, but a person can get mighty sick of eating them every single day!

My intolerances tend to be to high lectin foods. I can and do eat sweet potatoes, but I don't really care for them - they also leave me feeling "heavy" so I limit them to once a week or so.

I make many, many batches of butternut squash fries. They are a pain to cut up - into very thin fry shapes, but oh so worth it. I cut up the whole squash and use 1/4 at a time tossed with oil, salt and pepper. Bake at 350 - between 20-40 minutes depending on thickness of fry. Store the unused fries in ziplocks in the frig at the ready for a quick treat or side dish.

I also bake one half of a spaghetti squash to keep the "noodles" ready in the frig to toss with something for a quick meal.

I was never a squash fan, but now have them coming out my ears and I haven't tired of them - yet :)

bartfull Rising Star

According to what I have read, white potatoes are high in lectins and they don't bother me. I haven't tried any winter squash yet because I don't like them. It's tough because I never really liked vegetables much. Broccoli, cauliflowers, eggplant, and summer squash are the only ones I ever liked besides corn (which I will never eat again.)

I forgot, I can also eat walnuts and cashews, but not almonds. That was one of the reasons I suspected sals. I can eat pistashios too, but have to limit them to 10 a week, so what's the point?

GottaSki Mentor

was just checking the sal content of squash - didn't want to recommend something you shouldn't be eating - and found this blurb on the page of sal content I was looking at:

"Essential Sugars and Plant Lectins

Dietary lectins are associated with some intolerance reactions to food. Lectins are not considered a part of the food chemical intolerance syndrome, though they can cause similar negative reactions in vulnerable people. The effects of lectins are dose-related, and lectins can produce illness in any individual."

Only found one reference to butternut squash - it called it "moderate" for sals - sweet potato was also listed as "moderate" on the same page:

Open Original Shared Link

I didn't know pumpkin was high in salicylates - I learned my something new for the day :D

edit: was typing this when you posted you think you are ok with lectins ;)

ciamarie Rookie

Possibly sulfites?

Open Original Shared Link

And here:

Open Original Shared Link (note where it mentions dried herbs and spices.)

shadowicewolf Proficient

According to what I have read, white potatoes are high in lectins and they don't bother me. I haven't tried any winter squash yet because I don't like them. It's tough because I never really liked vegetables much. Broccoli, cauliflowers, eggplant, and summer squash are the only ones I ever liked besides corn (which I will never eat again.)

I forgot, I can also eat walnuts and cashews, but not almonds. That was one of the reasons I suspected sals. I can eat pistashios too, but have to limit them to 10 a week, so what's the point?

Two words: acorn... squash... it has a similar texture to a sweet potato (though more squashy) and can be doctored the same.

I'm burnt out on sweet potatos sadly :(

GFinDC Veteran

Alkaloids in nightshades are a possible problem.


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



Celiac.com Sponsor (A8-M):



Juliebove Rising Star

Maybe there is no connection? I test as intolerant to a variety of things. And yet there are other things that I can't eat or can't eat much of because they bother me for other reasons. Chocolate sets off my GERD. Too much garlic gives me stomach pains. I can't seem to have mashed potatoes now. They make me sick to my stomach. But I can eat baked or fried. That makes no sense. Most fruit gives me horrid stomach pains but apples and pears do not. And then there are the things I simply can't digest. Like broccoli and large amounts of salad. I do love salad. I can have a small bowl a couple of times a week but any more than that is pushing it. Steamed beets? No good. Canned beets? Fine. I don't try to analyze it any more. If I react badly to it, I just don't eat it.

dilettantesteph Collaborator

Have you tried different sources of the same thing? That might be helpful to see if you are reacting to the item itself, or something used in it's growth, harvesting or processing. I found that to be the case for me. I was fine with things from some sources but not others. That lead me to be able to find safe sources of some things that I can eat, rather than having to cut everything out.

Good luck.

bartfull Rising Star

I should have mentioned that most of these foods that I can't tolerate don't cause much in the way of digestive symptoms. They cause psoriasis flares. I STILL don't know if each time I get a psoriasis flare I am also damaging my gut.

I hate this! I need my hands!

shadowicewolf Proficient

I should have mentioned that most of these foods that I can't tolerate don't cause much in the way of digestive symptoms. They cause psoriasis flares. I STILL don't know if each time I get a psoriasis flare I am also damaging my gut.

I hate this! I need my hands!

enviormental perhaps? I know when a new weather front comes in, my knee aches like mad.

Juliebove Rising Star

I should have mentioned that most of these foods that I can't tolerate don't cause much in the way of digestive symptoms. They cause psoriasis flares. I STILL don't know if each time I get a psoriasis flare I am also damaging my gut.

I hate this! I need my hands!

Ah, interesting! I haven't a clue what is causing my psoriasis. I just started the nettle tea. Too soon to tell if it is helping.

bartfull Rising Star

I am sure it's not environmental Shadow, because when I am strictly on my original 11 safe foods the psoriasis clears up completely. It's only when I branch out and try something new that I get in trouble. And the insomnia always comes with it. And my feet swell. And I get grumpy. And my jaw swells and hurts so bad I sometimes whimper. Kinda like right now, "*#%*@*, whine". :lol:

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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.