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 Much Food Should I Bring On My Trip?


Guest cassidy

Recommended Posts

Guest cassidy

I'm headed to Paris next month. I travel monthly for business and have traveled gluten-free internationally before and typically bring all my food with me or make a trip to WH at my destination. I am very sensitive and rarely eat in restaurants because I usually get sick, although I never get sick at home. We are renting an apartment in Paris for a week. DH would be fine eating every meal at McDonalds so he won't be upset if I choose not to eat restaurant food. We will also have our 15 month old with us, he has never had gluten and pretty much eats off my plate and nurses. I don't eat much meat and never eat meat when I'm traveling.

So, I'm trying to figure out how much food I should bring with me. A loaf of WF bread and a bag of Tinkyada would have us set. Since we could buy eggs, fruits and veggies I could make us omlettes for breakfast, cheese sandwiches for lunch and veggie pasta for dinner.

Or, I saw that Schar and Valpiform only make gluten-free food and have tons of stores in Paris that sell their products. I do love to try new gluten-free foods so I'm trying to figure out if I should just buy those brands over there. The Schar website tells you what stores are top sellings of their products so I can map out health food stores in relation to our apartment and where we will be sightseeing each day. Is there stuff good? How does it compare to WH bread and Tinkyada?

We really don't eat cookies or sweet treats but my son likes pretzels and perkyO's - little dry snacks throughout the day.

I'm not going to take chances because getting glutened while being a mom on vacation isn't fun, but I do like the idea of trying new gluten-free goodies.

Any advice on how much food I should bring with us?


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

I would just take what you normally would, but try the new stuff while there. Nothing wrong with returning home with what you took. :)

missy'smom Collaborator

We purchased things online from a source in country and had it shipped to our temporary residence. It was nice to try a few new things and we brought back what was left over and are still enjoying them. My husband doesn't have celiac disease but got a little shop happy ordering :lol: If I remember right, on the way home we even put glass bottles of sauces in the suitcase wrapped in plastic bubble wrap and placed in plastic ziplock bags. Security stopped us on the way into the US(dept. of agriculture). We were honest and said I had food allergies and had food and they opened our bag but let us go through. They were mostly interested in meats and fruit. We also brought an inexpensive fry pan with us. The things that came in handy the most in my situation were the snacks and emergency foods that I had brought. On the way home I was served a gluten-free meal on the plane but didn't feel well and didn't feel like eating it so I snacked on my own stuff. I also brought some of it when we were out and about there. The night we came back to our home sweet home DS and DH got MCD's and I nuked my Tastybite meal out of the suitcase cause we weren't up to fixing dinner. I ended up bringing home the pasta and pancake mix I had brought with. Be sure to sample some of the local fare, at least fruit and veg that are better than or varieties that we can't get here.

Phyllis28 Apprentice

Below is the list of foods I usually bring:

One or two loafs of gluten free bread (for just me I bring along 1 loaf per week)

1 box of gluten free cereal, I have had trouble locating gluten free cereal when traveling internationally so I bring my own.

Gluten free bars (Glutino, Lara, Enjoy Life are examples) I bring along enough for two each day.

A small jar of peanut butter

A small jar of jelly/jam

Gluten free salad dressing. I use a homemade sunflower oil and rice vinegar dressing with salt, garlic powder, pepper and oregano. It does not require refrigeration. I pack it in a "Leak Proof" container and place it into two ziploc sandwich bags. I like the leak proof bottles available from the Container Store.

I also bring along the following non-food items so I can pack a lunch each day.

Insulated lunch bag

Plastic knives, forks and spoons

Ziploc sandwich bags

A few Ziploc quart and gallon bags to store food in.

Blue Ice to keep the lunch cold.

A small day backpack to carry the lunch any everything else I need for the day out.

My typical traveling lunch consists of a PBJ sandwich, fruit, juice, yogurt, cheese and a gluten free bar.

Hope you have a wonderful trip.

AMQmom Explorer

We have not traveled internationally, but we find it very helpful to pack a cooler with staples and ice packs and check it on the plane. We also put a clear note on top of the food items explaining that the food it gluten free and requesting that gloves be used if items need to be searched. I go to the extreme of explaining why - but it is up to you! Enjoy your trip!

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. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,411
    • Most Online (within 30 mins)
      7,748

    Rebekah1922
    Newest Member
    Rebekah1922
    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

    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.