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

Explaining Celiac To People Without Talking About Poop?


colfax

Recommended Posts

colfax Newbie

Hi. After doing a lot of internet research, I tried going gluten-free in July and after a week my belly started feeling better. A lot of other nagging physical problems have been getting better since then, and that combined with the fact that I've had a couple of accidental glutenings--with unpleasant results--that have convinced me that I'm right to avoid gluten. I don't have good insurance right now though, so I'm not planning on getting officially diagnosed any time soon.

My parents and inner circle of friends have been really supportive. But how do I talk about it with random acquaintances who invite me out to lunch? Or other people--like potential dates--who I don't really want to go into the gory details with? Having diahrrea for years and then having it stop completely after 2 months gluten-free (except for the accidental glutenings) is pretty conclusive proof to me, but like I said, that's not something I want to talk about with everyone.

So what do you tell people? How do you convey the seriousness of this disease without talking about poop or pulling out a very long health history? Lately I've been trying to explain it to people and I've been getting responses like, "Oh, I couldn't live without bread. If I had gluten-intolerance, I'd just eat it anyway and deal with the consequences," and that sort of makes me want to scream. I'm sorry if this sort of question has been asked before.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I tell people that gluten causes the destruction of my small intestine. If people want more detail I can explain about antibodies, mal- absorption of vitamins, etc.

Skylark Collaborator

I tell people that eating gluten gives me symptoms like having food poisoning. It's reasonably polite and everyone completely understands what I mean.

pricklypear1971 Community Regular

Dead Bread-heads.

You can't explain it other than saying you have an autoimmune disease that destroys your GI system, and glutenous foods make you very ill. I find it's more your ability to say it with a certain tone and move on in conversation that does the trick. Of course, I can't convey that on here....other than to say its a matter-of-fact, no-nonsense, it isn't up for discussion tone.

If you get to know someone well enough you can get into the crappy (ha!) details.

bartfull Rising Star

You could just say that it causes severe digestive problems that eventually lead to vitamin deficiencies, neurological problems, thyroid diseases, and cancer, if not addressed.

Takala Enthusiast

My symptoms were supposedly "atypical," so this isn't a problem for me. I will tell people if they have a "need to know" that I have food allergies and intolerances. And this isn't a lie as there is other stuff I'm avoiding.... ;) They hear the word "allergy" and that conveys the seriousness. This disease damages the gut and causes malnutrition. THAT causes the other problems.

I doubt anyone would actually want to hear the entire saga of symptoms, so I just say "neurological symptoms" and I'd rather not have my eyes crossing and a migraine or dizziness start up, or go into an arthritic flare. Or I'd rather not have kidney damage, or I'd rather not have liver damage, or I'd rather not have more bone loss or I'd rather not have brain fuzz or I'd rather not have an asthma attack..... I'd rather not walk with a cane, and I'd rather not be using a wheelchair at this age, so I'm really not motivated to eat what I shouldn't be eating.

Deal with the consequences ? :ph34r:

If they really had gluten intolerance, and some of the symptoms I have had in the past like repeated infections, and getting literally knocked down by gall bladder symptoms (oh, I forgot the ob- gyn ones! how about nearly passing out from bleeding and back pain from endometriosis & cystic ovary more than once ?) they wouldn't be so flippantly announcing they couldn't give up mere wheat breads. Wonder if they've ever actually been hurt by anything, that sounds like addictive behavior.

rosetapper23 Explorer

All great advice to choose from....but I liked Bartfull's explanation the best, and it's closest to what I tell servers and acquaintances. I say that I have an autoimmune disease where gluten destroys the lining of the small intestine, which can result in nutritional deficiencies, neurological problems, and cancer if I don't follow a strict, gluten-free diet.

In your case, I realize that what you most experience with gluten exposure is diarrhea, but you don't have to disclose that part of it. Usually, people "get" it when I mention the destruction of the lining of the small intestine. I think you'll find over time that many people are genuinely interested in knowing more about celiac and gluten sensitivity, not so much out of curiosity, but more out of self-interest. Whenever I attend a conference and have a "special" meal served to me, people at the table want to know why I'm eating something different (since it doesn't look like a vegetarian meal). I give everyone a brief rundown on what celiac is and the symptoms it can cause. Invariably, everyone gets quiet...and one by one they'll volunteer that either they suffer from these symptoms or they know someone who does. As for the "poop" part, I just mention "digestive complaints" in my list of symptoms.


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



Celiac.com Sponsor (A8-M):



YoloGx Rookie

All good. I like to mention the auto immune response attacks my villi resulting in neurological and kidney damage, migraines and food poisoning symptoms. Just cross contamination completely knocks me out for at least a day if not three or more. Also by avoiding the gluten I no longer get sick for weeks on end like I used to. I only say more now if they are truly interested and think they might have something like it too. The quick and easy response to their question is that it makes me ill for a week...

MissHaberdasher Apprentice

I just simplify it to the max (if it's someone I'm not likely to run into again) with "Thanks, but I'm allergic to bread".

Surprisingly, a lot of people say, "Oh, you mean celiac's?" YES thank you, official new friend!

Monael Apprentice

I have described it by saying that it gives me gastrointestinal problems. You really don't need to go into detail. If you say you can't have gluten because you have celiac disease or you are gluten intolerant, most people don't really ask what symptoms you have. At least that has been my experience. I have also said that it gives me all sorts of problems. Most people really don't care, to be honest. But I keep it pretty low key. I have a man in my life who has been there for many years so he knows the problems I have had with the big D, so I didn't need to tell him that part...and he has noticed a difference since I went gluten free so that helps (imagine how embarrassing that conversation was :lol: ) If I were to start dating all over again, I think I would only go on dates that didn't involve food until I knew that we were going to be dating for a while.

chai Newbie

I find that people are pretty skeptical of my allergies to the point where they do ask what happens if i eat gluten and don't just accept that I'm allergic to it. If it happens I give them the whole explanation to make them as uncomfortable as possible....

I like to think it might help the next person they meet with celiac. :D

Monael Apprentice

I find that people are pretty skeptical of my allergies to the point where they do ask what happens if i eat gluten and don't just accept that I'm allergic to it. If it happens I give them the whole explanation to make them as uncomfortable as possible....

I like to think it might help the next person they meet with celiac. :D

OMG I can't imagine what I would say to someone if they pressed me for details. Your idea is pretty funny! But honestly, if someone is skeptical or doesn't accept what I tell them then I really don't care. It's really none of their concern. I know it can be tough sometimes when we are dealing with people we have to work with or get along with. I have told people straight out, in a calm non-confrontational way, that I don't want to talk about it (not about gluten but other personal questions people sometimes ask) and I have had good responses to that. But then again, maybe if I encounter someone skeptical of my gluten intolerance, I will give them the gory details just to see the look on their faces :lol:

HS7474 Apprentice

I'm amazed that so many people can get away with not having to explain the symptoms! As soon as I mention it, 4 out of 5 people ask "So, what happens when you eat it then?". 3 years in and I still don't have a good answer. It's not the most feminine or attractive thing to say "Well, I bloat up like I'm 8 months pregnant and have gas that would clear this room and have the bio-hazard team in here within seconds." :P I think the food poisoning comment is a great idea! I'll try that one out next time.

pricklypear1971 Community Regular

I have pics of my rash on my iPhone. I guess I could whip them out if needed.

I won't advise others to take pics of GI issues, but assume there's at least one jerk who deserves to have such pics tossed in his/her face for pressing for details.

notme Experienced

I have pics of my rash on my iPhone. I guess I could whip them out if needed.

haha - i took pictures of my rash, too - it would disappear by the time i could get an appointment w/dermatologist! i showed it to my GI doc and she said "yup" but never could get it biopsied. AND no matter how many times i erased them off my camera, there they were..... :ph34r: at the most embarrassing times, naturally.....

Skylark Collaborator

I find that people are pretty skeptical of my allergies to the point where they do ask what happens if i eat gluten and don't just accept that I'm allergic to it. If it happens I give them the whole explanation to make them as uncomfortable as possible....

I like to think it might help the next person they meet with celiac. :D

Hehee. I've done this too for people who wouldn't take NO for an answer.

colfax Newbie

Thanks for your thoughts, everyone. It's really helpful to hear about how other folks deal with this conversation. Maybe I just have really nosy acquaintances, or maybe a lot of my socializing just revolves around food, but thus far every time the gluten-free thing has come up, people have wanted to know more about it. It's usually just in a casually curious sort of way though. I like the food poisoning analogy as a way to answer the question without really answering it.

srall Contributor

I also have pictures of my rash on my phone, and before and after pics of my 8 year old with her various rashes (hives and white pimply bumps) as well as her deep sunken eyes with black circles, scabs all over her mouth and lips and dried brittle thinning hair (she was 7 at the time). In 2 years I've only had one "friend" who pushed me so hard that I whipped those pictures out. She was very skeptical that I had diagnosed both of us (because the doctors weren't helping) and even though both her doctor and my doctor were completely supportive, my friend just thought I was being overly protective crazy mama.

Most people will accept food allergy, or celiac (people are catching on), or food poisoning symptoms...I like that one. I even say GI problems and nausea...I had so many other symptoms that resolved I could keep someone "entertained" for several minutes. I do agree that if you think something is personal you don't have to talk about it. The one thing I'll say is I have a couple of people who when asking me questions started to look at their own symptoms. One girlfriend is now also gluten free/soy free and dairy free, and another friend is TRYING to be gluten free. It's just such a hard commitment and until you're convinced that the gluten is what is making you sick, there is heavy denial.

Good luck to you. It sounds like you have figured out a good reply. Food poisoning was my favorite also.

lovegrov Collaborator

Tell them about anemia, severe fatigue, and fogginess so bad that you can't function mentally.

richard

aeraen Apprentice

It does make me chuckle,sometimes, at how free we all are here in discussing a subject that most would never think to bring up outside this forum :o . Its nice to have a comfortable place to ask questions that we could not ask anywhere else. :)

When I don't want to go into a litany of woes, I simply say that the long-term consequences of gluten intolerance are vast and can, eventually, be deadly. But that the short-term effects of being glutened can be (here, I pause slightly for dramatic effect) "inconvenient". Believe me, EVERYBODY understands what I mean.

HS7474 Apprentice

It does make me chuckle,sometimes, at how free we all are here in discussing a subject that most would never think to bring up outside this forum :o . Its nice to have a comfortable place to ask questions that we could not ask anywhere else. :)

When I don't want to go into a litany of woes, I simply say that the long-term consequences of gluten intolerance are vast and can, eventually, be deadly. But that the short-term effects of being glutened can be (here, I pause slightly for dramatic effect) "inconvenient". Believe me, EVERYBODY understands what I mean.

Brilliant! :D Thanks to the OP for asking this, I can't believe it never occurred to me. I think a worry-weight has been lifted off of my chest after reading these responses.

Chad Sines Rising Star

Butt, butt (spelling intended), why would you not want to talk about poop?? Everybody poops. :)

I like the food poisoning explanation. I usually just say upper and lower GI issues. If they probe more, I say that I start out nauseous and it does not end (emphasis added) well.

Ironically, just saying "I have celiac. Eating anything with gluten in it makes me really sick." works 99% of the time except for those who honestly want to know more about it. Many often know friends or family members with it.

lynnelise Apprentice

If pressed I say eating gluten is like giving myself dysentery. They can draw their own conclusions from that. lol

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    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
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.