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angel-jd1 Community Regular
Don't misunderstand me. I'm not recommending eating mainsteam oats as a breakfast cereal. My point was that there is probalby so little oatmeal in the Taco Bell hard tortillas that many celiacs will not be bothered by the miniscule amount of CC on an occasional basis. At least, that is my experience when eating at Taco Bell.

Steve

Knowingly contaminating yourself is just not a smart idea. You are suggesting that people contaminate themselves? ANY amount of gluten that you are ingesting into your system can/will cause damage to your intestines. I personally don't care to cause myself harm on purpose. Please don't suggest that others try!

-Jessica :rolleyes:


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trents Grand Master
Knowingly contaminating yourself is just not a smart idea. You are suggesting that people contaminate themselves? ANY amount of gluten that you are ingesting into your system can/will cause damage to your intestines. I personally don't care to cause myself harm on purpose. Please don't suggest that others try!

-Jessica :rolleyes:

My, we're getting hostile, aren't we? My conviction is that Celiacs vary in their sensitvity. Just trying to be practical that's all. A celiac may be in a situation where they have to chose between Taco Bell and going hungry.

Steve

BeckyW Contributor

BTW: If you have an egg allergy TELL YOUR ANESTHESIA PROVIDER!

Just wondering Russ, what is the importance of the egg allergy with the anesthesia?

penguin Community Regular
My, we're getting hostile, aren't we? My conviction is that Celiacs vary in their sensitvity. Just trying to be practical that's all. A celiac may be in a situation where they have to chose between Taco Bell and going hungry.

Steve

You have fun with that. Even the COMPANY tells you to stay away from it, and it's not good enough for you. I'm assuming that in this scenario where the celiac has to choose between the taco or going hungry, Taco Bell no longer makes pintos and cheese or steak bowls with no jalepeno sauce?

I agree with Jessica, you're free to knowingly ingest gluten, but please don't suggest to others that they do the same. Taco Bell does have gluten-free options.

Rikki Tikki Explorer

I personally cannot eat oats in any form but I think what Steve is saying is that studies have shown that oats can be safe for celiacs. Many people have posted on here that they eat oats without a reaction and I think he was just posting his thoughts. I have also read research that suggests oats are safe, so while I cannot have them some people seem to be able to tolerate them

angel-jd1 Community Regular
My, we're getting hostile, aren't we? My conviction is that Celiacs vary in their sensitvity. Just trying to be practical that's all. A celiac may be in a situation where they have to chose between Taco Bell and going hungry.

Steve

Nope not hostile at all. Just saying that if you care to damage yourself that is fine. Please do not suggest to others that it is a good idea.

-Jessica :):rolleyes:

elonwy Enthusiast

The FACT remains that commercially grown oats in the united states are not safe for celiacs because of cross contamination during growth and processing. For those Celiacs who can tolerate oats there is at least one company who grows and processes them in such a way that they are free of contamination here in the US, and McCanns in Ireland also has safe growth/process requirements and regulary tests for contamination.

Other than that, no other oat products should be ingested by Celiacs, whether they react or not.

I can eat oats, but I only eat McCanns.

As far as the taco bell tacos, they are fried in oil that is shared with other items that have gluten, and should not be consumed on that basis alone, whether or not they contain oats. This is not safe, and should not be recommended to anyone. The tostado shell does not contain oats, and is not fried.

Elonwy


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RKB-MD Rookie

Couple o' things:

First: A HUGE thank you to this board and the link to the meal cards! I just went to a local Peruvian restaurant. I brought my Spanish language diet card and had a wonderful meal that I, in no way, am "worried" about. It was so nice being able to go out to eat, and not fear every bite. I can't wait to use it at all sorts of other places. Thai, Indian, Japanese, HERE I COME! Basically, everything I have a hard time cooking myself...

Next: For those with Egg and Soy allergies. Let your anesthesiologist know. Reason is that one of the main drugs we use is called Propofol (fabulous for endoscopy sedation). It is a drug that is used for sedation procedures, but also is used to induce a state of anesthesia for total anesthesia. Propofol is delivered in a lecithin and soybean oil suspension. There are substitutes, we just need to know.

Last: I am going to side on the part of those who say - don't do it, with regards to foods with any ppm of wheat-gluten/ giladin content. If you can avoid it, do so. There are obviously people around who are so sensitive that they cannot even deal with food that has contacted giladin-containing foods. Personally, I'm pretty sensitive, but I have not (knock on wood) had a problem if I have to separate a sandwich to get the "goods" out. However, I would not KNOWINGLY consume foods that contain giladin.

OK: time to go do another "happy dance" about the meal cards... :D

trents Grand Master
The FACT remains that commercially grown oats in the united states are not safe for celiacs because of cross contamination during growth and processing. For those Celiacs who can tolerate oats there is at least one company who grows and processes them in such a way that they are free of contamination here in the US, and McCanns in Ireland also has safe growth/process requirements and regulary tests for contamination.

Other than that, no other oat products should be ingested by Celiacs, whether they react or not.

I can eat oats, but I only eat McCanns.

As far as the taco bell tacos, they are fried in oil that is shared with other items that have gluten, and should not be consumed on that basis alone, whether or not they contain oats. This is not safe, and should not be recommended to anyone. The tostado shell does not contain oats, and is not fried.

Elonwy

Actually, the hard taco corn torilla shells are not cooked with other gluten containing foods, at least not in the TB restaurants. They are precooked and in the TB restaurants themselves they are taken out of a bag and just warmed. I confirmed that just now by calling one of my local franchises. Whether or not they are deep fried with other gluten containing foods when they are being produced I don't know but it seems unlikely that would be the case. I would think things like that being produced in mass quantity probably have a dedicated vat.

Thanks for the info about the tostado shells. That's good to know.

Steve

Helena Contributor

Russ,

Thanks for the heads up about the Propofol. I'm actually trying to figure out the safe alternatives to diazemuls and fentanyl (sp.?) right now . . . both of which my GI doctor was going to give me for the flexible sigmoidoscopy and gastroscopy that I'm scheduled for. Good thing I researched this---I'm anaphylactic to egg and soy so diazemuls will be out.

What would be alternatives for the diazemuls/fentanyl combination? (My GI doctor is on vacation right now so I can't ask him, and in any case, I need to research the meds on my own and then consult with my allergist because my allergy situation is complicated.

I also wanted to provide another perspective on the trend towards banning peanuts on commercial flights about which you commented. I can understand why people with celiac would be frustrated with the pretzel snacks . . . but for people with severe peanut allergies, the issue isn't that they will be deprived of food if peanuts are being served but that their health can be put at risk if everyone around them is opening vacuum-sealed bags. I know that whether people can react just when peanut butter is being consumed in their vicinity is controversial . . . but there has only been 1 medical study on this. (Some doctors accept the possibility. Others, like my allergist, do not. However, both of my sisters do react, and they are not alone. )

*But* allergists do recognize that when those packages of peanuts are opened that some peanut protein becomes airborne which can cause hives, wheezing, eye swelling, etc. There was a study done (published in the Journal of Allergy and Clinical Immunology) in which researchers obtained air filters from a commercial plane and discovered that there was an appreciable amount of peanut protein.

The only way to treat anaphylaxis is a shot of epinephrine followed by *prompt* treatment in the hospital (the epinephrine in many cases is not enough. Very rarely people die even when medical treatment is available).

So peanuts on board airplanes really do put peoples' lives at risk . . . of course there is the argument that people with peanut allergies should just stay home. But that is discriminatory.

eKatherine Apprentice
Russ,

Thanks for the heads up about the Propofol. I'm actually trying to figure out the safe alternatives to diazemuls and fentanyl (sp.?) right now . . . both of which my GI doctor was going to give me for the flexible sigmoidoscopy and gastroscopy that I'm scheduled for. Good thing I researched this---I'm anaphylactic to egg and soy so diazemuls will be out.

What would be alternatives for the diazemuls/fentanyl combination? (My GI doctor is on vacation right now so I can't ask him, and in any case, I need to research the meds on my own and then consult with my allergist because my allergy situation is complicated.

I also wanted to provide another perspective on the trend towards banning peanuts on commercial flights about which you commented. I can understand why people with celiac would be frustrated with the pretzel snacks . . . but for people with severe peanut allergies, the issue isn't that they will be deprived of food if peanuts are being served but that their health can be put at risk if everyone around them is opening vacuum-sealed bags. I know that whether people can react just when peanut butter is being consumed in their vicinity is controversial . . . but there has only been 1 medical study on this. (Some doctors accept the possibility. Others, like my allergist, do not. However, both of my sisters do react, and they are not alone. )

*But* allergists do recognize that when those packages of peanuts are opened that some peanut protein becomes airborne which can cause hives, wheezing, eye swelling, etc. There was a study done (published in the Journal of Allergy and Clinical Immunology) in which researchers obtained air filters from a commercial plane and discovered that there was an appreciable amount of peanut protein.

The only way to treat anaphylaxis is a shot of epinephrine followed by *prompt* treatment in the hospital (the epinephrine in many cases is not enough. Very rarely people die even when medical treatment is available).

So peanuts on board airplanes really do put peoples' lives at risk . . . of course there is the argument that people with peanut allergies should just stay home. But that is discriminatory.

I think they should just stop serving snacks if they're just going to decide to sock it to another sensitivity group, one that is larger than those with peanut allergies. The flight attendant always looks at me like I have two heads when I give her back the packet of stale pretel bits and say I can't eat them.

Nantzie Collaborator

I'd much rather not have something to eat than put other people at the risk of anaphylaxis.

But maybe that's just me.

DingoGirl Enthusiast
Are you really a doctor? :lol::lol::lol::lol:

Tavi - :lol::lol::lol:

balsamic vinegar.....WHAT?? I eat it all the time.....just skimmed these pages but h ad to ask....

Doctor - welcome - Peruvian restaurant - exotic - we don't have that in these parts.... :lol:

Anasthesia....loved it the two times I had it (appendectomy, age 40, endoscopy/colonoscopy this year)...anything that can take me to my Magic Place.....always good..... :rolleyes::lol:

happygirl Collaborator

https://www.celiac.com/st_prod.html?p_prodi...-35106112548.2a

balsamic vinegar is safe. it is the flavored "vinagrettes" that could be in question. hope this helps.

Rikki Tikki Explorer

There you are Susan, I have been scanning the boards hoping to see you! Even asked about you in Rachelville 2. Hope all is well :D:D:D

DingoGirl Enthusiast
https://www.celiac.com/st_prod.html?p_prodi...-35106112548.2a

balsamic vinegar is safe. it is the flavored "vinagrettes" that could be in question. hope this helps.

Whew! thanks! I have never had a problem with regular or white balsamic....

There you are Susan, I have been scanning the boards hoping to see you! Even asked about you in Rachelville 2. Hope all is well :D:D:D

TAvi! I have not been posting as much, been quite busy in painting house etc. and have friends here for three days. but, I am most often found in that crazy "tazorac" thread that Cecile has hijacked, and which has nothign to do wtih my face peelign any more. Come visit! I sometimes show up in R2 - -

(oops - sorry - guilty again - complete digression of topic) :ph34r:

gfp Enthusiast
I'd much rather not have something to eat than put other people at the risk of anaphylaxis.

But maybe that's just me.

No I agree but I agree with eKatherine too.

It goes a bit further, I don't want the person next to me eating a crusty roll and spilling crumbs over me either. I don't have two heads!

Helena Contributor

Yeah, it would be great if people would be more aware of dietary restrictions and provide appropriate alternatives . . . And thanks for the support on the allergy issue.

by the way, peanut allergies are not rare or not rarer than celiac disease. it affects 1% of US adults and 3% of American children . . . that's not taking other food allergies into account. Allergists are agreed that allergies are on the rise . . . I went to a lecture where a researcher explained that it isn't just allergies---it is all autoimmune diseases. It would be difficult to know about whether celiac is on the rise because it is so underdiagnosed . . . but I bet it is.

eKatherine Apprentice
Yeah, it would be great if people would be more aware of dietary restrictions and provide appropriate alternatives . . . And thanks for the support on the allergy issue.

by the way, peanut allergies are not rare or not rarer than celiac disease. it affects 1% of US adults and 3% of American children . . . that's not taking other food allergies into account. Allergists are agreed that allergies are on the rise . . . I went to a lecture where a researcher explained that it isn't just allergies---it is all autoimmune diseases. It would be difficult to know about whether celiac is on the rise because it is so underdiagnosed . . . but I bet it is.

While peanut allergies may not be rarer than celiac disease, they are certainly rarer than gluten intolerance.

And I am certain that there is more celiac than ever and at earlier ages because people are eating more gluten than ever in the typical American diet.

gfp Enthusiast
While peanut allergies may not be rarer than celiac disease, they are certainly rarer than gluten intolerance.

And I am certain that there is more celiac than ever and at earlier ages because people are eating more gluten than ever in the typical American diet.

I agree .... but it is also an awareness thing.

Those seats on planes are awfully close together.... back in the "carry on days" i would take my own food and have someone next to me from my perspective "throwing" bread crumbs into my carefully prepared gluten-free meal.

Hence I learned to wait .... then ask the person to please be careful, I have an allergy.

Sometimes it works and sometimes you have two heads!

The difference is try asking the steward to change seats because of celiac .... if it was a peanut allergy then they would respond but celiac? never heard of it.

eleep Enthusiast
Couple o' things:

First: A HUGE thank you to this board and the link to the meal cards! I just went to a local Peruvian restaurant. I brought my Spanish language diet card and had a wonderful meal that I, in no way, am "worried" about.

What is Peruvian food like? I have a friend coming back from Peru soon and he's promised to cook a meal with me because he claims it's a very celiac-friendly cuisine.

eleep

gfp Enthusiast
What is Peruvian food like? I have a friend coming back from Peru soon and he's promised to cook a meal with me because he claims it's a very celiac-friendly cuisine.

eleep

Roast guinea pig?

jerseyangel Proficient
Roast guinea pig?

:lol::lol::lol:

lonewolf Collaborator
Roast guinea pig?

Yeah, either that or seviche made with octopus. (Seviche is raw fish or octopus that is soaked in a very strong acidy liquid like lime and lemon juice.) We had a house guest from Peru once and he made us seviche from octopus as a way to say thanks for our hospitality :o .

eKatherine Apprentice
What is Peruvian food like? I have a friend coming back from Peru soon and he's promised to cook a meal with me because he claims it's a very celiac-friendly cuisine.

eleep

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    • tiffanygosci
      Thank you for sharing all of this, Knitty Kitty! I did just want someone to share some commonality with. I did not know This one Deficiency was a thing and that it's common for Celiac Disease. It makes sense since this is a disorder that causes malabsorption. I will have to keep this in mind for my next appointments. You also just spurred me on to make that Dietician appointment. There's a lot of information online but I do need to see a professional. There is too much to juggle on my own with this condition.<3
    • RMJ
      I think your initial idea, eat gluten and be tested, was excellent. Now you have fear of that testing, but isn’t there also a fear each time you eat gluten that you’re injuring your body? Possibly affecting future fertility, bone health and more? Wouldn’t it be better to know for sure one way or the other? If you test negative, then you celebrate and get tested occasionally to make sure the tests don’t turn positive again. If you test positive, of course the recommendation from me and others is to stop gluten entirely.  But if you’re unable to convince yourself to do that, could a positive test at least convince you to minimize your gluten consumption?  Immune reactions are generally what is called dose response, the bigger the dose, the bigger the response (in this case, damage to your intestines and body). So while I am NOT saying you should eat any gluten with a positive test, the less the better.  
    • knitty kitty
      @Riley., Welcome to the forum, but don't do it!  Don't continue to eat gluten!  The health problems that will come if you continue to eat gluten are not worth it.  Problems may not show up for years, but the constant inflammation and nutritional losses will manifest eventually.  There's many of us oldsters on the forum who wish they'd been diagnosed as early.    Fertility problems, gallbladder removal, diabetes, osteoporosis and mental health challenges are future health issues you are toying with.   To dispel fear, learn more about what you are afraid of.  Be proactive.  Start or join a Celiac group in your area.  Learn about vitamins and nutrition.   Has your mother been checked for Celiac?  It's inherited.  She may be influencing you to eat gluten as a denial of her own symptoms.  Don't let friends and family sway you away from the gluten-free diet.  You know your path.  Stick to it.  Be brave. 
    • knitty kitty
      @tiffanygosci, Hello.  I apologize for your thread being hijacked.   I recognize your symptoms as being similar to what I experienced, the migraines, food and chemical sensitivities, hives, nausea, the numbness and tingling, joint pain, tummy problems, sleep problems, emotional lability, and the mom brain.  My cycle returned early after I had my son, and I became pregnant again with all my symptoms worsening.  Unfortunately, I lost that baby.  In hindsight, I recognized that I was suffering so much from Thiamine deficiency and other nutritional deficiencies that I was not able to carry it.   Celiac Disease affects the absorption of nutrients from our food.  There's eight B vitamins that must be replenished every day.  Thiamine Vitamin B1 becomes depleted first because it cannot be stored very long, less than two weeks.  Other B vitamins can be stored for two months or so.  But Thiamine can get low enough to produce symptoms in as little as three days.  As the thiamine level gets lower, symptoms worsen.  Early symptoms like fatigue and anxiety are often attributed to life situations, and so frequently go unrecognized by medical professionals who "have a pill for that".   I used to get severe migraines and vomiting after gluten consumption.  Thiamine and the other B vitamins are needed to turn carbohydrates, fats and proteins into fuel for our bodies.  With a large influx of carbohydrates from gluten containing foods, the demand for Thiamine increases greatly.  Available thiamine can be depleted quickly, resulting in suddenly worsening symptoms.  Emotional stress or trauma, physical activity (athletes and laborers) and physiological stresses like pregnancy or injury (even surgery or infection) increase the need for Thiamine and can precipitate a thiamine insufficiency. Pregnancy requires more thiamine, not just for the mother, but for the child as well.  The mother's Thiamine stores are often depleted trying to meet the higher demand of a growing fetus.  Thiamine insufficiency can affect babies in utero and after birth (autism, ADHD).  Having babies close together doesn't allow time for the mother to replenish thiamine stores sufficiently.   Thiamine insufficiency can cause migraines, pins and needles (paresthesia), and gastrointestinal Beriberi (gas, bloating, diarrhea or constipation, back pain).   Thiamine deficiency can cause blurry vision, difficulty focusing, and affect the eyes in other ways.  Thiamine deficiency can damage the optic nerves.  I have permanent vision problems.  High histamine levels can make your brain feel like it's on fire or swelling inside your cranium.  High histamine levels can affect behavior and mood.  Histamine is released by Mast Cells as part of the immune system response to gluten.  Mast Cells need Thiamine to regulate histamine release.  Mast Cells without sufficient thiamine release histamine at the slightest provocation.  This shows up as sensitivities to foods, smelly chemicals, plants, and dust mites.  Thiamine and the other B vitamins are needed to lower histamine levels.  Vitamin D is needed to calm the immune system and to regulate our hormones.  Menstrual irregularities can be caused by low Vitamin D.   Celiac Disease is a disease if Malabsorption of Nutrients.  We must take great care to eat a nutritionally dense diet.  Our bodies cannot make vitamins.  We must get them from what we eat.  Supplementation with essential vitamins and minerals is warranted while we are healing and to ensure we don't become deficient over time.  Our bodies will not function properly without essential vitamins and minerals.  Doctors have swept their importance under the rug in favor of a pill that covers the symptoms but doesn't resolve the underlying issue of malnutrition. Do talk to your doctor and dietician about checking for nutritional deficiencies.  Most blood tests for the eight B vitamins do not reflect how much is available or stored inside cells.  Blood tests reflect how much is circulating in the blood stream, the transportation system.  Blood levels can be "normal" while a deficiency exists inside cells where the vitamins are actually used.  The best way to see if you're low in B vitamins is to take a B Complex, and additional Thiamine and look for improvement.   Most vitamin supplements contain Thiamine Mononitrate, which is not easily absorbed nor utilized by the body.  Only thirty percent of thiamine mononitrate listed on the label is absorbed, less is actually utilized.  This is because thiamine mononitrate is shelf stable, it won't breakdown sitting on a shelf in the grocery store.  It's so hard to breakdown, our bodies don't absorb it and can't turn it into a form the body can use.  Take Thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) which the body can utilize much better.  (Ask for an Erythrocyte Transketolace Activity test for Thiamine level.  Though not accurate, this test does better picking up on a thiamine deficiency than a blood test.) Are you keeping your babies on a gluten free diet?  This can prevent genetically susceptible children from developing Celiac Disease.   P. S. Interesting Reading  Thiamine deficiency in pregnancy and lactation: implications and present perspectives https://pmc.ncbi.nlm.nih.gov/articles/PMC10158844/ Descriptive spectrum of thiamine deficiency in pregnancy: A potentially preventable condition https://pubmed.ncbi.nlm.nih.gov/37458305/ B vitamins and their combination could reduce migraine headaches: A randomized double-blind controlled trial https://pmc.ncbi.nlm.nih.gov/articles/PMC9860208/
    • trents
      @Riley, on this forum we sometimes get reports from people with similar experiences as you. That is, their celiac disease seems to go into remission. Typically, that doesn't last. At age 18 you are at your physical-biological peek in life where your body is stronger than it will ever be and it is able to fight well against many threats and abuses. As Wheatwacked pointed out, absence of symptoms is not always a reliable indicator that no damage is being done to the body. I was one of those "silent" celiacs with no symptoms, or at least very minor symptoms, whose body was being slowly damaged for many years before the damage became pronounced enough to warrant investigation, leading to a diagnosis. By that time I had suffered significant bone demineralization and now I suffer with back and neck problems. Please, if you choose to continue consuming gluten, which I do not recommend, at least get tested regularly so that you won't get caught in the silent celiac trap down the road like I did. You really do not outgrow celiac disease. It is baked into the genes. Once the genes get triggered, as far as we know, they are turned on for good. Social rejection is something most celiacs struggle with. Being compliant with the gluten free diet places restrictions on what we can eat and where we can eat. Our friends usually try to work with us at first but then it gets to be a drag and we begin to get left out. We often lose some friends in the process but we also find out who really are our true friends. I think the hardest hits come at those times when friends spontaneously say, "Hey, let's go get some burgers and fries" and you know you can't safely do that. One way to cope in these situations is to have some ready made gluten-free meals packed in the fridge that you can take with you on the spot and still join them but eat safely. Most "real" friends will get used to this and so will you. Perhaps this little video will be helpful to you.  
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