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 Be A Gracious Guest And Remain Gluten Free?


hilwacat

Recommended Posts

hilwacat Rookie

I am newly diagnosed and leaving for Ireland in 3 weeks to visit my boyfriend's extended family. His family is large and live on beautiful farm in a rural part of Ireland. The good news is that, as I remember from my last visit, there will be ample potatoes. What I don't know is how they will be prepared or if gluten-containing ingredients will be used. Also, I have become lactose intolerant as well. (I am hoping that it isn't permanent)

His family is so gracious and I don't want to be a burden during this visit. They are feeding a lot of people and I don't want them to buy expensive gluten-free ingredients or change the menu around for me. But truthfully, I am dreading the "tea and toast" breakfast or pasta dinner where I may not be able to eat anything at the table.

Is it more rude to impose dietary restrictions or to bring one's own food and not eat what is provided?

Also, any tips for food that I can pack with me that will make a real meal if I am hungry (rice cakes and nuts aren't going to cut it if we have been hiking all day)

Thanks for any input!


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



Celiac.com Sponsor (A8-M):



ArtGirl Enthusiast

I think it is just too difficult to fully educate people on gluten-free cooking. And, there's always a problem with cross contamination in other people's kitchens.

I always bring my own food. I warn people ahead of time that I will be doing that. I tell them not to worry about me and my food that I'll take care of it and they don't have to do anything special for me. While most people would be willing to make an effort, they accept this about me and it is not a problem.

Potatoes should be easy to add to your meals if they're baked (wrapped in foil and not handled by anyone but you) in an oven or even a microwave (without foil, of course, but protected with a paper towel). Cold, baked potato travels well, sliced and spread with margarine, salt and pepper - one of my favorites!

I don't know what will be available to you in local grocery stores, but canned green beans and beets can be eaten cold (at least, I like them that way).

If the kitchen contains stainless steel pans, you could scrub one out and use that to warm up a can of baked beans, and even fry up a piece of meat.

If you have room in your luggage, I found that a small electric grill just perfect for cooking a chicken breast (coat with oil and add Italian herbs and sprinkly with lemon juice). It takes less than 10 minutes as the grill cooks both sides at the same time.

Of course, raw veggies and fruit are always good. (a great, quick dip for veggies that is dairy free - slightly watered down mayonnaise, a spash of vinegar, dried dill, salt & pepper, onion powder and sugar to taste).

There are some gluten-free jerky packages available - I saw them at Whole Foods.

I hope you have a good time and a great visit.

CarolAnne Apprentice

I'd advise talking to the family if at all possible. You'll be absolutely amazed at how aware people in Ireland are of Celiac Disease and staying Gluten-Free. I was there for a week...and everything in the grocery is clearly marked "Celiac Safe" and even the restaurants understood "Celiac Diet" when I was there. We were in Dublin and County Cork. I was able to enjoy my vacation like a real person and didn't get sick once. Shopping for gluten-free food is super easy...even in some of the smaller counties.

As for your airline...call them and ask for a Gluten-Free meal. Here in the states they may say they can't do that...but ask for a manager anyway. They need to become more aware of people who need to stay gluten-free. In Ireland call the airline again and ask again before any flight...they can accomodate you without any problems. And don't forget to check with the Flight Attendent on all flights...they are very helpful.

You can also pack your own sandwiches and snacks too. Just remember no containers of jams/jellies or liquids!! They will serve you drinks and fresh fruit on board if you ask.

sallyterpsichore Explorer

Are you sure that they are completely unaware of the gluten-free diet? I hear from my friendly Irish bartenders that Celiac (Coeliac there) is very common and highly prevalent in Ireland. Then again, it may be a rural/urban thing; like Dubliners know about Celiac, but out in the country they have no idea of what you're talking about.

I still struggle with the being a gracious guest vs. getting sick thing. So far, people who truly care about me and want me to spend time with them, go way out of their way to provide food for me. Those who don't get it have wanted to learn and have done things like buy me fresh fruit, Blue Diamond Nut Thins, and hunk of amazing cheese for snacks. I am assuming that they know that you have Celiac, but you don't really mention that in your post.

Absolutely do bring some of your own food, especially for the hiking. There are fruit and nut bars like Lara Bars (which I hate, honestly) but they provide you with solid nutrition for a day of hiking. Also, dried fruit from Trader Joes is good. As ArtGirl mentioned, there's gluten-free jerky available. Eat a big protein-filled meal in the morning before your hike, that'll help. If you're taking a cooler, roll up a couple of slices of gluten-free deli meat with some avocado or tomato in a big Boston lettuce leaf and munch on that.

Try not to worry too much, but definitely don't be too shy to explain your dietary situation to your boyfriend's family. The good thing is that they live on a farm and you can eat most stuff straight from the farm (plain grilled meats, veggies, etc.) so you just skip the gravy and you might very well not have to deal with it too much.

elonwy Enthusiast

Its less rude to bring your own food, I think. Also, gracious guest or not, nobodies feelings are worth getting sick over, as far as I'm concerned. I always bring my own food, and then if cooking is happening, I volunteer to assist in the kitchen and watch everything like a hawk. Even if they go on and on about wanting to make sure I don't feel "left out" or whatever, I don' t cave about not eating something I'm not comfortable with.

In Ireland the produce is absolutely stunning. Fruits and veggies are amazing, and in abundance in the country. I'm sure as long as you offer to help out during all the stages, no one will mind your issues. Walking in and asking them to do special shopping and cooking without lifting a finger... that is ungracious. (Not to say you would, just making my point).

The last time I went to Europe, half my suitcase was food. I took a box of cereal, bread, all the things I felt I needed. I found stuff in the stores to supplement, and ate a lot of fruit and veggies. gluten-free bars were a constant go-to no matter where I went. The thing is, the trips not about the food, its about the trip, and the people. Take some crackers in your bag for the gluten-free tea, or just have cucumber sandwiches the way I like them, putting the filling between slices of cucumber, not bread, etc. If you're creative and show that you're in charge and not "suffering" protests will die down after the first few days if they are there at all.

HTH.

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. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    2. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    3. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    4. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over

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

      Recovery from gluten challenge


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,290
    • Most Online (within 30 mins)
      7,748

    Joycemarie
    Newest Member
    Joycemarie
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
    • Scott Adams
      Hopefully the food she eats away from home, especially at school, is 100% gluten-free. If you haven't checked in with the school directly about this, it might be worth a planned visit with their staff to make sure her food is safe.
×
×
  • 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.