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

Do People Try To Make You Prove Your Intolerance?


Juliebove

Recommended Posts

Juliebove Rising Star

I have not seen this too much here, thankfully.  But I sure have on other forums elsewhere and sometimes even in real life.  Things like...

 

Are you sure you can't have dairy?  Why don't you try it again!  Who diagnosed you?  Oh!  That's not a *real* Dr.  They did the wrong test!  That test is not legitimate!  Sorry to tell you this but you just wasted your money!  You can't believe those test results.  Too many false positives!  On and on and on like that.  Have even seen people attack other people for their symptoms and try to tell them that they are psychological and can't be related to food! 

 

This whole thing rather sickens and saddens me.

 

Sometimes we don't know the hows and whys of why something makes us sick.  We just know that it does.  Like me, with garlic.  I can handle a small amount of it.  I generally don't cook with it unless I am making something for my garlic loving Italian husband and often when I do it is just for him.  I am taking deodorized garlic capsules again.  Tried them years ago but can't remember why.  But after discovering bleeding in my eyes due to diabetes am trying anything and everything purported to strengthen the veins.  And so far so good in the stomach department.  But if I eat too much garlic, I get bad stomach pains.  It isn't an allergy and it isn't an intolerance.  I just know that I can't eat a lot of it.

 

But if a person tells me that a certain food doesn't agree with them, the reason why doesn't really matter to me.  Oh, I will listen if they want to tell me why.  Because stuff like this is of interest to me.  But I would never tell someone something like...  Oh but if you eat that, at least it won't *kill* you like *my* legitmate allergy would do to *me*!  Note that I am just repeating what I've heard others say or have seen written.  I myself do not have actual IgE allergies to food.  It just annoys me that some of these people think they are either better than *we* are because they have no food issues.  Or that their food issues are more serious than ours are.  And yes, I know that celiac does cause damage.  Celiac is not my issue.  In no way do I want to demean it.  I just think that for the rest of us with food issues, our food issues are just as real and serious to us (and by serious I do not mean necessarily damaging or life threatening but to be taken seriously) as yours are to you!  If you know what I mean.

 

Have you ever run across people like this?  They drive me nuts!


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



Celiac.com Sponsor (A8-M):



Adalaide Mentor

Weirdly enough, I ran into one on Saturday at the gluten-free Expo. I was checking out a shake which I shouldn't have bothered because they all have soy right? But I was like maybe one is in existence that doesn't and this is it and I can taste it for free and it won't taste like crap! Nope, soy.

 

Now, I'll explain quick what my problem is with soy. I have a condition called idiopathic intercranial hypertension. Part of my treatment is following a low tyramine diet and avoiding trigger foods that cause me to produce obscene amounts of cerebrospinal fluid (CSF) in a very short amount of time. One of those foods for me is soy. It's tricky for me because soy lecithin doesn't bother me, but soy oil does so regular allergen labeling is not accurate for me and I have to count on the actual ingredient list. (Soy oil is not required to be listed as an allergen which is terribly frustrating for me.) If an episode is triggered, I will get a blinding migraine, nerve pain beyond imagining down the left side of my body and will lose vision in my left eye. The key being the vision loss. My eye doctor has warned me that my blood vessels in my right eye are so intertwined and twisted around each other that if my condition ever starts affecting my right eye also it could be immediately and permanently catastrophic. (He didn't expound but I got the idea.) Without that complication, I am at risk of permanent vision loss in my left eye.

 

Keeping that in mind, one of the guys at the shake booth asked me what my problem is with soy. I rattled off the name of my condition, that it is managed with diet and said in a quite sarcastic but joking and light tone that it's "fun." He said he wouldn't use that word to describe it, it was as if sarcasm and humor were things he didn't understand. He then went on to explain all the health benefits of their shakes and how they have helped so many people and that maybe if I just tried them I would find out that the soy in them wouldn't be a problem because somehow magically because it's in that particular shake it wouldn't make my day the most horrid day ever. I've rarely ever wanted to hit someone so much in all my life. Instead I smiled and nodded and walked away and didn't let him ruin my day.

 

But yes, apparently if you put soy in a shake it magically won't make me blind for a day or 3 or risk permanent injury to me... I just can't fathom how it is that of all the places in the world I could run into this kind of twit, I managed to find one there. Besides, what kind of jerk tries to talk someone into eating food that will make them sick? None of us go around trying to talk people into eating rat poison, because just a little taste won't make you that sick.

1desperateladysaved Proficient

I  do get bothered when people question me in detail about my limitations, because they doubt them.  There is also the ones that give you dirty looks or out and out gasps when you need to ask about the ingredients in the foods!  Often, I think it does stem out of a honest concern for me.  Yesterday, I realized someone knew that I couldn't have grain.   He thought of a 10 grain cereal recipe and began with several grains.  I shook my head as he went down the list and in the end I could have flax and sesame.  He didn't have a malicious intent, I think it didn't register or he didn't understand it.  That is what I usually try to think when people make mistakes such as this.  They don't understand, so if I can drop the subject, I do.

 

 I have been thinking about this quite a bit lately and figure that I have been too concerned about what others feel about my reactions.  I think that I am the "expert" on my own reactions; I know when I have them.   I may not always understand them or where they come from, but nobody can tell me whether I had a reaction or not.  I can't afford to worry about whether people will trust me about it.  I need to make the decisions that make my healing possible.  It is working, so I can just trust my judgment!  When hearing about other people's strange reaction I just trust what they say and feel compassion or try to tell remedies that have worked for me.  Sometimes, a pat on the back or to know another has felt the same is all they need.

 

.

StephanieL Enthusiast

I think people think it's all or nothing is the thing. They don't get that there is a "spectrum" of food issues so to speak.  

That said, standard AND alternative testing for allergies and intolerances is really really really scientifically sketchy at best and quackery at worst.  I would trust someone saying "it doesn't agree with me" over some of the alternative testing because of my research on things but if they did the testing BECAUSE of how they were feeling, I would trust that. I *do* get frustrated that the words get muddled and lose meaning though.  Having a child who does suffer from several life threatening food allergies,when someone says they "get it" because they are lactose intolerant it's really frustrating.  It is NOT the same thing so please, don't suggest that it is.  My vegan in-laws pull this. I'm sorry but your lifestyle choice doesn't make me feel bad for you when you can't eat something when you are out. It's unfortunate there isn't an option but that is your CHOICE.  Obviously things like allergies, intolerances and other medical conditions are not the same but they do vary in severity.

IrishHeart Veteran

Having developed a problem with high histamine foods, soy, MSG, food dyes and other chemicals in foods  along with celiac, I can say that I do understand how difficult it is to try and explain things to people, especially when I have already explained what celiac is, what gluten is and why I simply cannot just "try something" they want me to try---when I do not know the source.

 

If the person seems interested, I will explain it briefly.

 

If the person is already yawning when I start my first sentence....I simply say

"I really can't try (fill in the blank) because it gives me grief .....but thanks anyway."

 

I really do not think any of us with health issues (or our children with health issues) owe anyone any explanations for why we

eat the way we do or why we turn down things offered to us.

 

We do it because we have to. As Stephanie points out, it's not a choice. 

bartfull Rising Star

"Are you sure you can't have dairy? Why don't you try it again! Who diagnosed you? Oh! That's not a *real* Dr. They did the wrong test! That test is not legitimate! Sorry to tell you this but you just wasted your money! You can't believe those test results. Too many false positives! On and on and on like that. Have even seen people attack other people for their symptoms and try to tell them that they are psychological and can't be related to food!"

 

If anyone said any of those things to me they would be shown the door. RIGHT NOW!

LauraTX Rising Star

With my myriad of health problems, I generally don't talk about them to strangers when I don't have to other than "I lack part of my immune system don't be sick around me."  People always read something on the internet or see a commercial on TV and that makes them an expert.  Their sister/friend/grandma/cat had that and they cured it with this magical treatment!  

 

People do this with every ailment.  My dad, bless his soul, passed away from ALS (Amyotrophic Lateral Sclerosis AKA Lou Gehrigs disease) a few years ago.  Before he looked visibly sickly and had to use a wheelchair, he would tell people what he had, saying it was a fatal illness with no cure or effective treatment.  Then people will say things like "Oh yeah I have weakness in one arm, too, I know how it feels."  You can really tell if people are actually listening or not due to some of their responses.  He couldn't comprehend how people can compare anything to his death sentence.

 

If you are in my house, you will respect the fact that you cannot have gluten, you will not smoke on my property because even the smell on you when you walk inside makes my asthma go off, and you need to wash your nasty hands so you don't get me sick, because a 2 day cold to you is 4 weeks of suffering to me.  I don't mind inquiries and dumb questions, I try to be patient, but if you are disrespectful of things I need to do for my health, I would show anyone the door, I don't care who it is.  Outside there is more I will tolerate, but when people start telling you their expert medical opinion I just tell them, I have it handled, I only take medical advice from professionals.  Usually that makes them hush.


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



Celiac.com Sponsor (A8-M):



Celtic Queen Explorer

Funny you should bring this up.  I am going through "an issue" with my mother in law right now.  I've been gluten-free for 2 years.  She knows this.  But lately she's been having issues with it.  Unfortunately we both have strong personalities and I have a feeling the whole situation will come to a head soon with a large fight.

 

Our house is semi-gluten free.  We only have bread and beer in the house and my family knows to be careful with both.  They don't mess with my peanut butter or my butter dish.  And if they want a sandwich, they have to make it themselves.  And they also know that anything I am cooking for the family will be gluten free.

 

I just got back from a week at the beach with my entire family. My son is seven.  At home when he wants a pb&j, either his father makes it for him or he makes it himself.  My husband had to leave early from vacation, so when DS wanted a sandwich, he had to make it himself.  He knows how.   My MIL threw a fit and acted like I was abusing the boy because I was making him fix his own sandwich.  And she doesn't get it why I don't want to touch bread in any way, shape or form.  I'd ask my husband to grab a bun for DS's hot dog and MIL will make snarky little comments like, "We need to go buy you some wipes so that you can touch the bread and then wipe your hands."  Ugh, like I would want to touch poison and "just use some wipes afterwards" to get it all off.  And hubby could care less about fixing sandwiches or grabbing buns.  He doesn't mind.  DS even knows to wash his hands afterwards and to try and not get me sick.

 

She also kept making little comments about what I was eating.  I brought a bunch of my own food with me, so I wouldn't have to worry about being cross-contaminated by the 5 gluten-eating kids who were there, plus all the adults.  So she would fix spaghetti and say, "I know you don't want any of this."  Ummm...no, I really don't because I'd rather not be sick for 6 weeks.  My SIL was watching all this go down.  We were in the car by ourselves one night and she said to me, "It seems like mom is testing  you about the gluten thing.  It's almost like she doesn't really believe that you can't eat stuff and have to be as careful as you are."   You would think after two years of watching me bring my own food with me, turn down food from people, asking about gluten free items every time we go out to eat, changing my eating habits, etc, you would think she would finally get it. 

 

But I also think part of the problem is that she glutened me one time and really hasn't gotten over that.  She was making her traditional Christmas eve dinner of shrimp.  It's naturally gluten free, but she served it in a bowl that she had used to make bread in before and I got sick on the way home from her house.  I can't remember if I mentioned it to her or if my husband did, but ever since then she's been a little crazy about the gluten thing.  Almost like she doesn't believe I got sick at her house.

YouAreWhatYouFeat Newbie

I have been diagnosed with Latent Celiac Disease and I had Leaky gut Syndrome. When I told everyone, I recieved comments like, "That's not even real....Iv'e never heard of it" and "Wow, a little won't kill you....you have had gluten for how many years?" Then I was in the store looking for yeast free bread since the protein in yeast is so similar to that in gluten that your body reacts the same way to it. My boyfriend of over 5 years said to me, "Oh god, this is just another little phase of yours." I think the problem is that there isn't enough education on Celiac or how gluten effects your body. This way, all of us with real isssues don't feel like we are making up a problem or something. Thankfully, my boyfriend and others around me have been alot more supportive recently! I guess the 6months pregnant look, gas, and other not so pretty symptoms finally proved to them why I need to be very careful about what I eat.

bartfull Rising Star

"Then I was in the store looking for yeast free bread since the protein in yeast is so similar to that in gluten that your body reacts the same way to it."

 

Actually, that is not true. You may, because of the leaky gut, have trouble with yeast but I assure you, many if not most celiacs can eat yeast with no problems.

Adalaide Mentor

Last I checked having a kid make their own sandwich isn't some sick, twisted form of child abuse. By the time my daughter was 5 she had pushed and pushed me so far with wanting to be self-sufficient that I was letting her use the microwave a little with some supervision. And... not super sharp paring knives to cut things like strawberries and other not super hard things. Aren't kids supposed to learn their way around a kitchen?

 

If my husband is home and he wants something that is gluteny I make him touch it. I'm not going to touch it then have to wash my hands. I'm already surprised that I don't have cracked and bleeding hands from how often I have to wash them. Wipes won't magically get rid of gluten in a way that washing your hands wouldn't take care of about a million times better. The whole point is, why bother if someone better suited to the task is standing right there. Your MIL sounds like a real winner. (I may have a lot of pent up MIL hate atm and am willing to aim it at any moderately apt target.)

IrishHeart Veteran

since the protein in yeast is so similar to that in gluten that your body reacts the same way to it.

 

I have never heard of this or found it in any medical literature about celiac, hon.,

"Then I was in the store looking for yeast free bread since the protein in yeast is so similar to that in gluten that your body reacts the same way to it."

 

Actually, that is not true. You may, because of the leaky gut, have trouble with yeast but I assure you, many if not most celiacs can eat yeast with no problems.

 

I agree!

YouAreWhatYouFeat Newbie

It is called cross confusion: Open Original Shared Link

 

Yeast, dairy, and corn are all suspects of this. I have heard this by a couple popular doctors in the Celiac community. Also, I know by how I feel when I eat all 3 that it's true lol

kareng Grand Master

I'm sorry if yeast, dairy and corn bother you, but it isn't a gluten reaction.

 

I think you should get your info from real doctors and Celiac researchers.

 

Open Original Shared Link

 

No  mention about not eating yeast, etc:

 

Open Original Shared Link

 

"What is the treatment for celiac disease?

There are no drugs to treat celiac disease and there is no cure. But celiacs can lead normal, healthy lives by following a gluten free diet. This means avoiding all products derived from wheat, rye, and barley.

What are the recommended blood tests to diagnose celiac disease"

 

 

Open Original Shared Link

IrishHeart Veteran

It is called cross confusion: Open Original Shared Link

 

Yeast, dairy, and corn are all suspects of this. I have heard this by a couple popular doctors in the Celiac community. Also, I know by how I feel when I eat all 3 that it's true lol

 

 

You really should understand that this man is not a doctor.

There is no validity to "cross-reactors" to gluten.

NONE.

 

And this is posted at the bottom of the page you reference on his website as "medical info" Check it out.

 

Disclaimer: The contents of this site are for educational purposes only. Nothing here should be construed as medical advice. Nothing here is a substitute for actual medical care. Consult a qualified healthcare professional.

bartfull Rising Star

Karen is right. There are TONS of celiacs who eat corn and soy and dairy and yeast with no problems at all! SOME of us have additional intolerances, but even if these foods make us feel crappy, they are not true gluten reactions. I, for example, am intolerant to corn. But my reactions to corn are skin related, while gluten has me running to the nearest restroom. And dairy? I eat plenty of white cheddar and a big dish of ice cream every night. No problems at all.

 

There is a lot of misinformation out there on the internet. We all need to get our info from reputable sources, such as the ones Karen posted. Plus, think about it - why would any company risk its reputation and its sales by selling "gluten-free" foods that contain corn or yeast or soy or dairy, if it were going to make celiacs sick? Wouldn't make any sense, would it? They'd be out of business in a hurry.

 

Stick around and read some of our stories. Check out the sites Karen posted. You'll learn a lot, and maybe we can even help you figure out your other intolerances. Some of us lose foods for a while, but once we heal we get them back. I hope this is true for you and that you will soon be feeling better. :)

YouAreWhatYouFeat Newbie

You really should understand that this man is not a doctor.

There is no validity to "cross-reactors" to gluten.

NONE.

 

And this is posted at the bottom of the page you reference on his website as "medical info" Check it out.

 

Disclaimer: The contents of this site are for educational purposes only. Nothing here should be construed as medical advice. Nothing here is a substitute for actual medical care. Consult a qualified healthcare professional.

All I am suggesting is that you keep an open mind about this before shutting it down. Have you researched this before you said it wasn't true? Have you tried eating corn, dairy, and yeast in one meal and documented any changes in how you feel? There are numerous sources of this information, not just from Dr.Clark. I am open minded to the fact that it isn't true, but let's make sure that it isn't before we shut it out. I am going to the gastroenterologist this week and will ask him. Here is another source of infor with the same thing. I will just keep finding more sources for you. There are foods that are cross confused with gluten. Here is a list of foods that can be confused:

 

Open Original Shared Link

Juliebove Rising Star

Weirdly enough, I ran into one on Saturday at the gluten-free Expo. I was checking out a shake which I shouldn't have bothered because they all have soy right? But I was like maybe one is in existence that doesn't and this is it and I can taste it for free and it won't taste like crap! Nope, soy.

 

Now, I'll explain quick what my problem is with soy. I have a condition called idiopathic intercranial hypertension. Part of my treatment is following a low tyramine diet and avoiding trigger foods that cause me to produce obscene amounts of cerebrospinal fluid (CSF) in a very short amount of time. One of those foods for me is soy. It's tricky for me because soy lecithin doesn't bother me, but soy oil does so regular allergen labeling is not accurate for me and I have to count on the actual ingredient list. (Soy oil is not required to be listed as an allergen which is terribly frustrating for me.) If an episode is triggered, I will get a blinding migraine, nerve pain beyond imagining down the left side of my body and will lose vision in my left eye. The key being the vision loss. My eye doctor has warned me that my blood vessels in my right eye are so intertwined and twisted around each other that if my condition ever starts affecting my right eye also it could be immediately and permanently catastrophic. (He didn't expound but I got the idea.) Without that complication, I am at risk of permanent vision loss in my left eye.

 

Keeping that in mind, one of the guys at the shake booth asked me what my problem is with soy. I rattled off the name of my condition, that it is managed with diet and said in a quite sarcastic but joking and light tone that it's "fun." He said he wouldn't use that word to describe it, it was as if sarcasm and humor were things he didn't understand. He then went on to explain all the health benefits of their shakes and how they have helped so many people and that maybe if I just tried them I would find out that the soy in them wouldn't be a problem because somehow magically because it's in that particular shake it wouldn't make my day the most horrid day ever. I've rarely ever wanted to hit someone so much in all my life. Instead I smiled and nodded and walked away and didn't let him ruin my day.

 

But yes, apparently if you put soy in a shake it magically won't make me blind for a day or 3 or risk permanent injury to me... I just can't fathom how it is that of all the places in the world I could run into this kind of twit, I managed to find one there. Besides, what kind of jerk tries to talk someone into eating food that will make them sick? None of us go around trying to talk people into eating rat poison, because just a little taste won't make you that sick.

I avoid most forms of soy because I had a thyroid condition.  Although I still have a goiter, I am not hypo or hyper like I used to be.  I used to eat a lot of soy too. 

 

Some lady handing out samples of something tried to give me one.  Can't remember for sure now what it was, but I do think it was shake which I wouldn't have taken even if I could have it because I don't like the texture of shakes. 

 

When I told her that I couldn't have soy, she asked why and then gave me a skeptical look and said that she didn't know of a connection between soy and thyroid.  And apparently it is a rather complicated one.  All I know is once I stopped the Tiger's Milk bars, the roasted soybeans, Boca burgers and soy bacon, my hypo and hyper problems went away.

Juliebove Rising Star

I  do get bothered when people question me in detail about my limitations, because they doubt them.  There is also the ones that give you dirty looks or out and out gasps when you need to ask about the ingredients in the foods!  Often, I think it does stem out of a honest concern for me.  Yesterday, I realized someone knew that I couldn't have grain.   He thought of a 10 grain cereal recipe and began with several grains.  I shook my head as he went down the list and in the end I could have flax and sesame.  He didn't have a malicious intent, I think it didn't register or he didn't understand it.  That is what I usually try to think when people make mistakes such as this.  They don't understand, so if I can drop the subject, I do.

 

 I have been thinking about this quite a bit lately and figure that I have been too concerned about what others feel about my reactions.  I think that I am the "expert" on my own reactions; I know when I have them.   I may not always understand them or where they come from, but nobody can tell me whether I had a reaction or not.  I can't afford to worry about whether people will trust me about it.  I need to make the decisions that make my healing possible.  It is working, so I can just trust my judgment!  When hearing about other people's strange reaction I just trust what they say and feel compassion or try to tell remedies that have worked for me.  Sometimes, a pat on the back or to know another has felt the same is all they need.

 

.

That multi grain thing really gets me!  I can't have rye or oats and daughter can't have flax.  If it's multi grain, chances are those things are going to be in there.  People also don't get that we won't eat things if we don't know what is in them.

Juliebove Rising Star

"Are you sure you can't have dairy? Why don't you try it again! Who diagnosed you? Oh! That's not a *real* Dr. They did the wrong test! That test is not legitimate! Sorry to tell you this but you just wasted your money! You can't believe those test results. Too many false positives! On and on and on like that. Have even seen people attack other people for their symptoms and try to tell them that they are psychological and can't be related to food!"

 

If anyone said any of those things to me they would be shown the door. RIGHT NOW!

Thankfully I don't get a lot of that in real life.  I do get some. But I have seen it a lot on the Internet.  I don't care if they don't believe in the testing methods I used.  I only know that since I stopped eating the various foods, I am no longer sick all the time.  Lots of maladies cleared up.  So clearly to me, I can't have those foods.

Juliebove Rising Star

Funny you should bring this up.  I am going through "an issue" with my mother in law right now.  I've been gluten-free for 2 years.  She knows this.  But lately she's been having issues with it.  Unfortunately we both have strong personalities and I have a feeling the whole situation will come to a head soon with a large fight.

 

Our house is semi-gluten free.  We only have bread and beer in the house and my family knows to be careful with both.  They don't mess with my peanut butter or my butter dish.  And if they want a sandwich, they have to make it themselves.  And they also know that anything I am cooking for the family will be gluten free.

 

I just got back from a week at the beach with my entire family. My son is seven.  At home when he wants a pb&j, either his father makes it for him or he makes it himself.  My husband had to leave early from vacation, so when DS wanted a sandwich, he had to make it himself.  He knows how.   My MIL threw a fit and acted like I was abusing the boy because I was making him fix his own sandwich.  And she doesn't get it why I don't want to touch bread in any way, shape or form.  I'd ask my husband to grab a bun for DS's hot dog and MIL will make snarky little comments like, "We need to go buy you some wipes so that you can touch the bread and then wipe your hands."  Ugh, like I would want to touch poison and "just use some wipes afterwards" to get it all off.  And hubby could care less about fixing sandwiches or grabbing buns.  He doesn't mind.  DS even knows to wash his hands afterwards and to try and not get me sick.

 

She also kept making little comments about what I was eating.  I brought a bunch of my own food with me, so I wouldn't have to worry about being cross-contaminated by the 5 gluten-eating kids who were there, plus all the adults.  So she would fix spaghetti and say, "I know you don't want any of this."  Ummm...no, I really don't because I'd rather not be sick for 6 weeks.  My SIL was watching all this go down.  We were in the car by ourselves one night and she said to me, "It seems like mom is testing  you about the gluten thing.  It's almost like she doesn't really believe that you can't eat stuff and have to be as careful as you are."   You would think after two years of watching me bring my own food with me, turn down food from people, asking about gluten free items every time we go out to eat, changing my eating habits, etc, you would think she would finally get it. 

 

But I also think part of the problem is that she glutened me one time and really hasn't gotten over that.  She was making her traditional Christmas eve dinner of shrimp.  It's naturally gluten free, but she served it in a bowl that she had used to make bread in before and I got sick on the way home from her house.  I can't remember if I mentioned it to her or if my husband did, but ever since then she's been a little crazy about the gluten thing.  Almost like she doesn't believe I got sick at her house.

Oh yes!  I get that too.  "It won't hurt you to TOUCH it!"  Well, yes.  I get a rash.  So I won't.

Juliebove Rising Star

I have been diagnosed with Latent Celiac Disease and I had Leaky gut Syndrome. When I told everyone, I recieved comments like, "That's not even real....Iv'e never heard of it" and "Wow, a little won't kill you....you have had gluten for how many years?" Then I was in the store looking for yeast free bread since the protein in yeast is so similar to that in gluten that your body reacts the same way to it. My boyfriend of over 5 years said to me, "Oh god, this is just another little phase of yours." I think the problem is that there isn't enough education on Celiac or how gluten effects your body. This way, all of us with real isssues don't feel like we are making up a problem or something. Thankfully, my boyfriend and others around me have been alot more supportive recently! I guess the 6months pregnant look, gas, and other not so pretty symptoms finally proved to them why I need to be very careful about what I eat.

Oh yes, the kill you thing!  Lots of things won't kill you.  But they are not pleasant.  I suppose I could stick needles in my eye.  That problably won't kill me either.  Why do people have to be so extreme?

IrishHeart Veteran

All I am suggesting is that you keep an open mind about this before shutting it down. Have you researched this before you said it wasn't true?

 

That's all I do is research, hon. :)

I have told you there is no evidence of foods "cross-reacting" like gluten. The leading celiac researchers have made this clear as well..

 

If you feel those foods bother you, don't eat them. 

But to say they are "cross-reactors with gluten" so celiacs cannot eat them--- is just plain incorrect.

 

Karen has provided the links for you to read.

If you wish to believe random blogs on the internet, that's your choice, of course.

 

I wish you all the very best as you heal.

kareng Grand Master

All I am suggesting is that you keep an open mind about this before shutting it down. Have you researched this before you said it wasn't true? Have you tried eating corn, dairy, and yeast in one meal and documented any changes in how you feel? There are numerous sources of this information, not just from Dr.Clark. I am open minded to the fact that it isn't true, but let's make sure that it isn't before we shut it out. I am going to the gastroenterologist this week and will ask him. Here is another source of infor with the same thing. I will just keep finding more sources for you. There are foods that are cross confused with gluten. Here is a list of foods that can be confused:

 

Open Original Shared Link

 

 

Yes.  I have eaten all those things in one meal and by  themselves.  No problem. 

 

On this Forum, we ask that you provide reliable research to back up any claims that are not widely accepted.  Posting random blogs and websites that sell a product are not medical or scientific proof.   I went to the International Celiac Disease Symposium because I wanted to learn more about my disease.  If you were there, you heard many times the doctors and researchers saying there is no valid scientific evidence for "cross-reactivity" in Celiac Disease.

Celtic Queen Explorer

 

Your MIL sounds like a real winner. (I may have a lot of pent up MIL hate atm and am willing to aim it at any moderately apt target.)

Adalaide, sounds like we need to get together over a few gluten-free glasses of wine and swap MIL stories :D 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,549
    • Most Online (within 30 mins)
      7,748

    Blough
    Newest Member
    Blough
    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.