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

How To Tell Others About Gluten Intolerance?


kellirae

Recommended Posts

kellirae Rookie

So I've been gluten free for about 6 months now and have done well telling family and friends what I can and can't eat. Our new boss decided it was a good idea to have a pot luck lunch next week and we passed around a sign-up sheet as to what we were going to bring. There wasn't anything on there I could eat for sure (not knowing what brands of sauces, etc. people would be using in their dishes). I obviously plan to bring something I can eat, but we're all (8 of us) going to eat together and I think it will look odd if I only eat my dish. Two people in the office know about my issue because they've seen me eating strange things and I've explained why. However, I don't really feel comfortable sharing my gluten intolerance with everyone and don't trust anyone to make something I could eat, so even if they tried I wouldn't eat it without seeing it made. I think some people I work with just think I'm fussy and snobby, when that's not the situation (but I've dealt with a lot being sick off and on for the last 5 years). Has anyone dealt with this? Any suggestions or advice would be great.

Thanks!!!

Kelli


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



Celiac.com Sponsor (A8-M):



mbrookes Community Regular

What you DON'T do is eat poison to be nice.

Depending on your personal style, comment on how good everything looks and how you would love to eat it all, but you have this goofy stomach (or however you usually talk... I always go for the joke)) If anyone asks questions, explain Celiac breifly and change the subject. No one is as fascinated with Celiac as we are!

If someone makes a snide remark (there's one in every bunch) just don't hear it.I think (and hope) you will be pleasantly surprised at how smooth things go.

luvs2eat Collaborator

I'm not understanding why you don't want to tell them about your gluten concerns? It might seem kind of fussy or snobby, when people offer you cookies or things you can't eat and you continually refuse... but it's really a serious health issue!

I remember feeling like people thought I was being fussy when they'd ask me, in sort of an impatient voice, "Oh geez... can't you just eat a LITTLE??" I used the old "rat poison" adage I read on here... "That's like me asking you if you can eat just a LITTLE rat poison. Eating a LITTLE gluten will make me very sick."

I am the same way when people say they'll make something gluten free for me. I thank them profusely, but explain that if I don't see it made, I just can't take the chance that I'll get glutened because it's really more involved than not using wheat flour and I'm more than happy to bring my own food. I laugh when they give me the pained look ... as if to say, "Oh you poor thing." I tell them it's not as hard as they think, although I've been doing it for years, and I NEVER starve... one only has to look at my body to see that!! ha ha

Jestgar Rising Star

I tell them, if I'm asked, and make some joke about being high maintenance, or a pain in the @ss or something. Just enough so people know I'm not snubbing their dish.

luvs2eat Collaborator
I tell them, if I'm asked, and make some joke about being high maintenance, or a pain in the @ss or something. Just enough so people know I'm not snubbing their dish.

Jestgar... I am CRACKING up at your photo!!!!

Jestgar Rising Star
Jestgar... I am CRACKING up at your photo!!!!

:D :D :D

I wasn't sure if it was too small to tell what it was.

serenitynerd Newbie

'fraid you may have to come out of the closet or folks might indeed think you are fussy or snobby-sad but true. i have found it most successful to say right out of the gate, matter of factly, that i have celiac's disease- most important part they hear then is disease (so not a fussy thing)- and that i can't eat any gluten at all, so if i avoid their dish not to be insulted. Usually then folks want to know what happens to me, so i just say there are little finger like structures in the digestive system called celia that allow the body to absorb nutrients. with celiacs gluten causes those structures get flattened out so i can't absorb nutrients and it can take a week or more for them to rebound. that has worked well in avoiding hurt feelings or misunderstandings in social dining situations.

now of course there can be many other effects of celiacs, but i limit my explanation to relevant facts and the seriousness of the condition, and that the reaction takes a while to correct itself so i have to meticulous. people will be curious, but i have found this tact prevents judgement, and since these are work folks, and you will have food related interactions in future, you may actually find that folks pay attention to what they put in the food in future, so they can either warn you off, or modify the dish so you can try their treat. strange but true, but often it seems to be a way that folks can show their interest concern and friendship.

also, as you begin to know what sauces do and don't have gluten, when they try and tell you the ingredients, you can better know yea or nay. for now if someone says their doesn't have any wheat in it, you can ask if it has any pre-bought sauces, and then explain that sometimes it sneaks in there....

i think that pretty covers what i have found to be helpful...hope that helps you too :)


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

Just say "I have food intolerances and really don't want to be sick over the holidays."

JillianLindsay Enthusiast

Too small? Oh, you're going to give poor santa a complex... coal in your stocking this year for insulting santa's "manhood"! :P

:D :D :D

I wasn't sure if it was too small to tell what it was.

JillianLindsay Enthusiast

I have no problem telling people I have celiac disease, but if I don't feel like getting into it (or it's not the right venue to give a fuller explanation), then I just say I have serious food allergies (I know it's not an allergy!! lol) and have to be very careful.

As everyone said, there's no point risking being sick over the holidays to avoid a bit of social discomfort at a work potluck. Do it in whatever way you're comfortable, just don't eat poison! :)

Just say "I have food intolerances and really don't want to be sick over the holidays."
Ahorsesoul Enthusiast

Yep, just tell them. You do not have to go into details. "I have food intolerances/celiac disease. If I eat something I shouldn't I'll be calling in sick tomorrow".

haleym Contributor

Oh, how I identify with you!

My clinic has regular potlucks, and I have NEVER eaten anything but a plain salad/veggie sticks from any of them! People always have commented about how healthy I eat, etc, and ask me if I'm vegetarian and stuff but I just say that I have a really really sensitive stomach and I know what I can and can't eat, and people dont really give me a hard time about it at all.

I haven't felt like getting into the whole gluten-intolerance thing. This sounds terrible but I dont want to tell people ''gluten-free'' because I don't think that you can really understand it until you have lived it, or done a lot of research. I dont want someone to give me meatballs that they say are gluten-free but contain breadcrumbs. Sometimes people who arent used to special diets don't know to pay attention to the less obvious things.

Thats my advice... ho[e that helps!

Haley

gfp Enthusiast
I'm not understanding why you don't want to tell them about your gluten concerns? It might seem kind of fussy or snobby, when people offer you cookies or things you can't eat and you continually refuse... but it's really a serious health issue!

I remember feeling like people thought I was being fussy when they'd ask me, in sort of an impatient voice, "Oh geez... can't you just eat a LITTLE??" I used the old "rat poison" adage I read on here... "That's like me asking you if you can eat just a LITTLE rat poison. Eating a LITTLE gluten will make me very sick."

I am the same way when people say they'll make something gluten free for me. I thank them profusely, but explain that if I don't see it made, I just can't take the chance that I'll get glutened because it's really more involved than not using wheat flour and I'm more than happy to bring my own food. I laugh when they give me the pained look ... as if to say, "Oh you poor thing." I tell them it's not as hard as they think, although I've been doing it for years, and I NEVER starve... one only has to look at my body to see that!! ha ha

As the one who started the rat poison adage I still struggle on the 'but surely you can eat a little' and such.

For me the worst situation is when people TRY ... you KNOW they don't get it but then they try and keep assuring you its fine. The pressure to try because they did just makes it all the harder for me.

kellirae Rookie

Thanks to everyone for your advice. I definitely don't plan to eat anything - just uncomfortable with sharing this information with people at work. But the ideas everyone shared were helpful!

gaingus Rookie

I've gone with the "selective" route. I tell them that I have a Gluten-Intollerance (since that is my official diagnosis for the time being), if I get a confused look and no question I tell them it is similar to a really bad food allergy and it gets left at that. If they actually ask what it meens, I simply tell them that I can't eat anything made out of wheat, barley, malt or rye. Of course being in the Navy the very first question after that is "You can't drink beer? That sucks" Usually followed by "I love potato bread, do you eat that?" Then I have to tell them that conventional potato bread still has wheat flour in it. It is by all meens a constant uphill battle.

It did take a little while to get to the point where I was comfortable telling people, of course there are still challenges and when I'm asked if I want something that has gluten I remind them that I can't eat that. I think it just comes with the final acceptance (Five stages of greiving). I went through all of these when I found out what exactly was "wrong" with me, everynow and then (especially with the hoidays) I get sad for the simple reason I haven't found replacements for certain foods, but I am getting there. In my experiance, when you are open with people about Celiac, the looks go away and you will find there are people out there that are willing to help you out.

One of my Daughter's behavioural therapists (my youngest has PDD-NOS) knows about my diet and when they had an art show with work from children with Autism Spectrum Disorders, the very first thing she asked me is if I noticed the Gluten-Free crackers they put out. There are studies that say our diet is good for them and has shown some help with my daughter, but for her to remember that I needed them as well was awesome. People will still respect you for not eating their food when they understand and some will try to help as much as possible.

mbrookes Community Regular

I have noticed recently that when my celiac disease comes up in conversation frequently someone will chime in with "Oh, my cousin has that" or "a girl I work with has that" As more and more of us are diagnosed, people are becoming more aware of celiac as a real disease, not a chosen diet like being vegitarian.

kellirae Rookie

Well, turns out I didn't need to be so worried about lunch after all. I ate my dish and we ordered a veggie tray so I snacked on some of those items and nobody said anything (which is a surprise considering how things usually go). Now I just have to get through tomorrow (my boyfriend's family is getting together for an early Christmas celebration and I know based on the menu I can't eat the main course or most of the side dishes so he suggested I bring my own food - his parents and siblings know, but this is at the grandparents and they're making the food).

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Wheatwacked replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      50

      Supplements for those Diagnosed with Celiac Disease

    2. - knitty kitty replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      results from 13 day gluten challenge - does this mean I can't have celiac?

    3. - knitty kitty replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      50

      Supplements for those Diagnosed with Celiac Disease

    4. - Florence Lillian replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      11

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    5. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      results from 13 day gluten challenge - does this mean I can't have celiac?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,355
    • Most Online (within 30 mins)
      7,748

    Amy Immerman
    Newest Member
    Amy Immerman
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Wheatwacked
      Raising you vitamin D will increase absorption of calcium automatically without supplementation of calcium.  A high PTH can be caused by low D causing poor calcium absorption; not insuffient calcium intake.  With low D your body is not absorbing calcium from your food so it steals it from your bones.  Heart has priority over bone. I've been taking 10,000 IU D3 a day since 2015.  My doctor says to continue. To fix my lactose intolerance, lots of lactobacillus from yogurts, and brine fermented pickles and saurkraut and olives.  We lose much of our ability to make lactase endogenosly with maturity but a healthy colony of lactobacillus in our gut excretes lactase in exchange for room and board. The milk protein in grass fed milk does not bother me. It tastes like the milk I grew up on.  If I drink commercial milk I get heartburn at night. Some experts estimate that 90% of us do not eat Adequite Intake of choline.  Beef and eggs are the principle source. Iodine deficiency is a growing concern.  I take 600 mcg a day of Liquid Iodine.  It and NAC have accelerated my healing all over.  Virtually blind in my right eye after starting antihypertensive medication and vision is slowly coming back.  I had to cut out starches because they drove my glucose up into the 200+ range.  I replaced them with Red Bull for the glucose intake with the vitamins, minerals and Taurine needed to process through the mitochodria Krebs Cycle to create ATP.  Went from A1c 13 down to 7.9.  Work in progress. Also take B1,B2,B3,B5,B6. Liquid Iodine, Phosphatidyl Choline, Q10, Selenium, D and DHEA.     Choline supplemented as phosphatidylcholine decreases fasting and postmethionine-loading plasma homocysteine concentrations in healthy men +    
    • knitty kitty
      @catnapt, Wheat germ has very little gluten in it.  Gluten is  the carbohydrate storage protein, what the flour is made from, the fluffy part.  Just like with beans, there's the baby plant that will germinate  ("germ"-inate) if sprouted, and the bean part is the carbohydrate storage protein.   Wheat germ is the baby plant inside a kernel of wheat, and bran is the protective covering of the kernel.   Little to no gluten there.   Large amounts of lectins are in wheat germ and can cause digestive upsets, but not enough Gluten to provoke antibody production in the small intestines. Luckily you still have time to do a proper gluten challenge (10 grams of gluten per day for a minimum of two weeks) before your next appointment when you can be retested.    
    • knitty kitty
      Hello, @asaT, I'm curious to know whether you are taking other B vitamins like Thiamine B1 and Niacin B3.  Malabsorption in Celiac disease affects all the water soluble B vitamins and Vitamin C.  Thiamine and Niacin are required to produce energy for all the homocysteine lowering reactions provided by Folate, Cobalamine and Pyridoxine.   Weight gain with a voracious appetite is something I experienced while malnourished.  It's symptomatic of Thiamine B1 deficiency.   Conversely, some people with thiamine deficiency lose their appetite altogether, and suffer from anorexia.  At different periods on my lifelong journey, I suffered this, too.   When the body doesn't have sufficient thiamine to turn food, especially carbohydrates, into energy (for growth and repair), the body rations what little thiamine it has available, and turns the carbs into fat, and stores it mostly in the abdomen.  Consuming a high carbohydrate diet requires additional thiamine to process the carbs into energy.  Simple carbohydrates (sugar, white rice, etc.) don't contain thiamine, so the body easily depletes its stores of Thiamine processing the carbs into fat.  The digestive system communicates with the brain to keep eating in order to consume more thiamine and other nutrients it's not absorbing.   One can have a subclinical thiamine insufficiency for years.  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function, so the symptoms can wax and wane mysteriously.  Symptoms of Thiamine insufficiency include stunted growth, chronic fatigue, and Gastrointestinal Beriberi (diarrhea, abdominal pain), heart attack, Alzheimer's, stroke, and cancer.   Thiamine improves bone turnover.  Thiamine insufficiency can also affect the thyroid.  The thyroid is important in bone metabolism.  The thyroid also influences hormones, like estrogen and progesterone, and menopause.  Vitamin D, at optimal levels, can act as a hormone and can influence the thyroid, as well as being important to bone health, and regulating the immune system.  Vitamin A is important to bone health, too, and is necessary for intestinal health, as well.   I don't do dairy because I react to Casein, the protein in dairy that resembles gluten and causes a reaction the same as if I'd been exposed to gluten, including high tTg IgA.  I found adding mineral water containing calcium and other minerals helpful in increasing my calcium intake.   Malabsorption of Celiac affects all the vitamins and minerals.  I do hope you'll talk to your doctor and dietician about supplementing all eight B vitamins and the four fat soluble vitamins because they all work together interconnectedly.  
    • Florence Lillian
      Hi Jane: You may want to try the D3 I now take. I have reactions to fillers and many additives. Sports Research, it is based in the USA and I have had no bad reactions with this brand. The D3 does have coconut oil but it is non GMO, it is Gluten free, Soy free, Soybean free and Safflower oil free.  I have a cupboard full of supplements that did not agree with me -  I just keep trying and have finally settled on Sports Research. I take NAKA Women's Multi full spectrum, and have not felt sick after taking 2 capsules per day -  it is a Canadian company. I buy both from Amazon. I wish you well in your searching, I know how discouraging it all is. Florence.  
    • catnapt
      highly unlikely  NOTHING and I mean NOTHING else has ever caused me these kinds of symptoms I have no problem with dates, they are a large part of my diet In fact, I eat a very high fiber, very high vegetable and bean diet and have for many years now. It's considered a whole foods plant based or plant forward diet (I do now eat some lean ground turkey but not much) I was off dairy for years but recently had to add back plain yogurt to meet calcium needs that I am not allowed to get from supplements (I have not had any problem with the yogurt)   I eat almost no processed foods. I don't eat out. almost everything I eat, I cook myself I am going to keep a food diary but to be honest, I already know that it's wheat products and also barley that are the problem, which is why I gradually stopped eating and buying them. When I was eating them, like back in early 2024, when I was in the middle of moving and ate out (always had bread or toast or rolls or a sub or pizza) I felt terrible but at that time was so busy and exhausted that I never stopped to think it was the food. Once I was in my new place, I continued to have bread from time to time and had such horrible joint pain that I was preparing for 2 total knee replacements as well as one hip! The surgery could not go forward as I was (and still am) actively losing calcium from my bones. That problem has yet to be properly diagnosed and treated   anyway over time I realized that I felt better when I stopped eating bread. Back at least 3 yrs ago I noticed that regular pasta made me sick so I switched to brown rice pasta and even though it costs a lot more, I really like it.   so gradually I just stopped buying and eating foods with gluten. I stopped getting raisin bran when I was constipated because it made me bloated and it didn't help the constipation any more (used to be a sure bet that it would in the past)   I made cookies and brownies using beans and rolled oats and dates and tahini and I LOVE them and have zero issues eating those I eat 1 or more cans of beans per day easily can eat a pound of broccoli - no problem! Brussels sprouts the same thing.   so yeh it's bread and related foods that are clearly the problem  there is zero doubt in my mind    
×
×
  • 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.