Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Eating At Other People's Homes


katiekay

Recommended Posts

katiekay Explorer

My husband and I ate at the inlaws tonight. We both have horrible stomach ache. I ate something that I can't imagine had gluten in it so must be cross contamination.

We've been invited to someone's home next weekend and wedding meal tomorrow... how do you guys handle?! I can't imagine grilling someone when invited to their home to eat but this is awful.

What do you guys all do? We don't have a diagnosis and I am sure they think I am a hypochondriac (although I've never mentioned health issues before).

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



iamsarar Rookie

I am interested in this too. I am going to a family dinner and when I talked to my aunt about hte food she thought being "that careful" was silly but said she cooks some gluten-free meals for her husband. She said she would make the gluten free dish first and them make the other things. I still don't trust it but trying to figure out how to handle it without making everyone mad.

Link to comment
Share on other sites
jerseyangel Proficient

All I can tell you is what I do. I've been at this for almost 6 years and right at the beginning made it clear that I would bring my own food. I simply told people that I was insanely sensitive, and that I didn't want to put them to the trouble of trying to cook for me.

I was polite but firm--and after a few times everyone just accepted it and now it's not even an issue.

Link to comment
Share on other sites
kareng Grand Master

All I can tell you is what I do. I've been at this for almost 6 years and right at the beginning made it clear that I would bring my own food. I simply told people that I was insanely sensitive, and that I didn't want to put them to the trouble of trying to cook for me.

I was polite but firm--and after a few times everyone just accepted it and now it's not even an issue.

Ditto.

I try to find out what they are serving and bring something similar if possible. Then I borrow the microwave or I take mine hot and put it in a small cooler if we are eating soon after arriving. If it's a help yourself & stand around type of party, I just eat first and stick something really good (Snickers), that I don't eat often in my purse. In case I feel left out.

What has worked for my family is " my doctor said..". Even though he didn't cause he doesn't know.

Link to comment
Share on other sites
playin-d-fiddle Newbie

My good friends know of my dire situation so they take it upon themselves, after a learning process highly facilitated by me, to make sure that I am safe (special cutting boards for me, calling to read me ingredient lists from packages, etc), but those not as close as they are might not completely understand, or 'get it'. That means that it is my responsibility to take care of myself that night and ensure that I am safe (until the world is a better place and we're not such a SHOCK to everyone).

If I am uncomfortable inserting myself into the necessary food conversations, or perhaps it's not entirely appropriate for whatever reason (that's up to you to decide), I make sure I am either not hungry or I bring my own food. Whether you're diagnosed or not, stating a "severe reaction to certain foods" should be enough to start the pertinent conversations. You'll get more comfortable with those conversations the more you have them. Eventually you might even get to the point where the explanation includes "if you want anyone else to be able to use the restroom this evening it might be a good idea for us to talk about the menu"!, for those who still have reservations. Talking to the chef, organizer, caterer, those are all requests that are not unheard of, nor are they asking too much :)

Often it can be difficult to accommodate our extreme sensitivities, which is why I always have food in my purse. Sure, you're going to miss out on some awesome food here and there, but you won't be sick afterward! I don't like to take any risks so unless I can talk to someone who cooked it, I won't touch it. The people around you will be curious and ask why you're not eating, or why you just pulled a small meal out of your bag. That gives you the opportunity to educate people that might not otherwise learn about the difficulties the gluten sensitive/allergic/intolerant face in these situations that others might just take for granted.

Hope that helps? Good luck!!

Link to comment
Share on other sites
hawkgirl98 Newbie

I always ask ahead of time about what will be served and specific ingredients and I've found people to be really understanding. Sometimes it turns out some things are already planned that are naturally gluten-free. Went to a party a few weeks ago where spinach dip was on the menu - the dip itself was gluten-free, but would be accompanied by pita bread. I talked to the host and she prepared a separate bowl of the dip for me to have with veggies & tortilla chips to avoid any cross-contamination. Similarly, at the holidays, my aunt usually makes a salad with nuts that are processed in a facility that also processes wheat. She just separated out a portion of the salad for me before adding the nuts for everyone else.

The holidays were actually a pleasant surprise for me - the only non gluten-free dish was stuffing. My aunt made the gravy with cornstarch instead of flour and then everything else - veggies, potatoes, meat - was naturally gluten free. To be extra safe, I went through the buffet line first to avoid people possibly mixing up serving spoon for the stuffing with the veggies or potatoes.

Anyway, I also always volunteer to bring something myself that I know will be safe to eat.

Link to comment
Share on other sites
katiekay Explorer

thanks for all the great advice!!!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



mushroom Proficient

I have let a few people cook for me, but not many :ph34r: Usually take my own, with apologies.

Link to comment
Share on other sites
GlutenFreeManna Rising Star

I just take my own food. I don't let anyone else cook for me except my mom and even then I'm in the room when she does it and she is using my pots and pans. She doesn't live with me and doesn't have to cook like this all the time so I can see how it would be easy to make a mistake even if she was trying to be careful. I would feel so bad if I ate something someone else made and I got sick. I wouldn't want to tell them I got sick, but I would have to tell them so it didn't happen again. I would rather just avoid that whole possible situation by eating my own food. It's really only awkward for the first meal or two. Then people just accept that that is the way it is. I DO drink soft drinks or tea and things that they offer and use their plates, silveware, etc. I just don't eat the food. I also try to bring something I can share (but make sure mine is portioned out ahead of time to prevent cc)--dessert is always a big hit ;)

Link to comment
Share on other sites
rosetapper23 Explorer

Thankfully, many of my relatives also have celiac (including my mom), so family members are well versed in serving gluten-free meals. I even let a few, select friends cook for me (VERY short list). However, if anyone else invites me to lunch or dinner, I always respond, "I'm sorry, but I can't eat at other people's homes because I have celiac disease and don't feel safe unless the kitchen is a dedicated gluten-free one. I hope you'll understand." Usually, when this happens, the person immediately states that we can meet up at a restaurant instead. If people don't understand how dangerous celiac can be, I explain what the slightest contamination can do to me....they then seem even more frightened of having me eat at their home than I am at the prospect of eating there.

Link to comment
Share on other sites
annegirl Explorer

I so ditto the watching family members cook. I walked into the kitchen just in time to see my dad put garlic salt (soy) on the hamburger patties. He rarely cooks (and he's the only one that puts garlic salt on hamburger patties) so if I hadn't seen it I would have thought they were safe and ended up being sick.

Even when people try their hardest it's tough to think of every single thing that could have a "bad" ingredient....especially when you have several intolerances.

Link to comment
Share on other sites
katiekay Explorer

yea, it would be alittle much to expect others to keep track of all of it.

Link to comment
Share on other sites
Darissa Contributor

We either bring our own food or snacks, or we just eat at home prior, and go over to visit. That seems to be the best for us. We have tried to eat at other peoples houses, and it just ddoesn't work out for us. My daughter and I are both very sensitive to CC. We go to dinner parties to socialize and visit, and not to eat. I make sure the host knows prior that we will not be eating, but we will come to visit. Eventually you get used to not eating, while watching everyone else eat!! I will often times bring a desert to share, so that way we can have something too. Or, if it's going to be a long evening, we offer to bring a main dish, so we have something safe to eat too.

Link to comment
Share on other sites
MindytheOrganist Enthusiast

My hubby has had celiac for a little over a year, but he has been Type 1 Diabetic for over 30. All our friends and family think nothing of our bringing food to supplement what is being offered, because that's all they've known.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      120,985
    • Most Online (within 30 mins)
      7,748

    Leenacut
    Newest Member
    Leenacut
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • TessaBaker
      It sounds like you're dealing with a complex situation, and I can understand how frustrating it must be not to have a clear answer. Gut health can indeed play a significant role in various aspects of our well-being, including hair health.
    • Celiac16
      I have found similar benefits from thiamine. I was diagnosed with celiac at 16 and never really recovered despite strict gluten and dairy free diet and no detectable antibodies on checkup bloodworks. I’ve tried stopping the b1 but start to feel bad again- I wanted my doctors to do more extensive testing for the different thiamine transporters and enzymes which would be a better indication if I was deficient or dependent on it but everyone dismisses it (there are know genetic mutations where you need to take it daily for life). I have looked into Thiamine Responsive Megablast Anemia and I have a lot of the more mild symptoms of the disease that manifest when thiamine isn’t given to the patient such as optic neuritis… I just find the parallels interesting. i think that celiacs could be a side issue of inflammation that resulted from vitamin deficiencies. I was eating a lot of sugar leading up to my diagnosis and since eating gluten free didn’t make me feel much better, I’m wondering if this was more the underlying issue (sugar heavily depletes b1). I usually take 1.5g thiamine a day.
    • Fluka66
      Thank you for your welcome and reply.  Yes I've been carefully reading labels looking for everything in bold and have been amazed by what I have seen. However Heinz tomato and basil soup is wheat free so I m thinking I already have ulcers?  The acid could be causing the pain . My pain always starts in one place then follows the same route through me . GP confirmed that is the route of our digestive system.  So much pain from stabbing to tearing. If I throw in milk with lactose it's horrific.  Many years of it now, won't go into details but been seeing a consultant for a supposedly different problem . Wondering what damage has been done over the years. Many thanks for your reply. Wishing you the very best.    
    • trents
      Welcome to the forum community, @Fluka66! Did you realize that the vast majority of all canned soups use wheat starch as a thickener, including such common commodities as Campbell's tomato soup?
    • Fluka66
      Hello. Any help would really steady my nerves right now. I realised recently that certain food left me in agonising pain so eliminated from my diet. I also have a swollen lymph node. My very caring Dr did some blood tests and I went back the other day to see another equally caring Dr . She looked at the test results one result has come back with something wrong. It came very fast so I'm afraid I didn't catch what it was. Anyway the urgent referral to ENT. She did say as I had already eliminated gluten it wouldn't say anything on the results and neither Drs nor I were prepared to reintroduce gluten . I've just had some tomato soup and again in agony only thinking this must have aggravated maybe existing problems. Does anyone know what I'm facing now ? My swollen lymph node , pain when eating gluten and lactose and I'm assuming the acidity of tomatoes triggering pain.  I'm trying to stay calm and to be honest I've been in intolerable pain at times rendering me unable to stand up straight but I've always just got on with it . Guess I'm reaching out and would really appreciate any wise or unwise words at this stage. Wishing you all the very best as you live with this illness. Fluka66  
×
×
  • Create New...