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

traveling on a school trip on a tour of europe


lucy power

Recommended Posts

lucy power Rookie

I am going to europe next summer and this will be my first time traveling overseas. i am not sure if the plane provides a gluten free meal or if i am allowed to pack snacks in my carry on bag. i have read a lot that italy is very accommodating to celiac disease, but i am also going to france, england, and switzerland. i'm going with EF tours so they pick the restaurants i'm pretty sure.  i'm not sure if i will be allowed to stop at stores even though they said they try their best to accommodate to dietary restricts i feel like meals we eat at the hotels will not be safe. the train rides to each country confuse me to. i was hoping for any guidance with traveling to europe with celiac disease or any experience with EF tours with celiac.


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



Celiac.com Sponsor (A8-M):



RMJ Mentor

My only experience is with the air travel part.  You should be able to get gluten free meals, but they must be requested from the airline in advance.  You can take plenty of “dry” snacks on planes. The only food limitations would be on liquids.

There are cards available in various languages that one can show to a waiter  to request gluten free food.  Hopefully someone with more knowledge of those will chime in.

lucy power Rookie

thank you, yes i saw the cards, i am definitely getting some.

Kurlykaitlyn Explorer
On 10/21/2023 at 10:17 AM, lucy power said:

I am going to europe next summer and this will be my first time traveling overseas. i am not sure if the plane provides a gluten free meal or if i am allowed to pack snacks in my carry on bag. i have read a lot that italy is very accommodating to celiac disease, but i am also going to france, england, and switzerland. i'm going with EF tours so they pick the restaurants i'm pretty sure.  i'm not sure if i will be allowed to stop at stores even though they said they try their best to accommodate to dietary restricts i feel like meals we eat at the hotels will not be safe. the train rides to each country confuse me to. i was hoping for any guidance with traveling to europe with celiac disease or any experience with EF tours with celiac.

I can only speak for air travel and being the UK. 
i always pack my own snacks and meal to carry on. I haven’t had problems bringing my own but I have kept it limited. Bars and nuts are great for an extra snack or supplement of calories. 
i found it to be quite easy to eat in the UK! I traveled a few weeks and did become sick once and that was a risky chance with a restaurant. Better safe than sorry! Listen to your gut and don’t risk it, otherwise you may end up on a hotel toilet that hopefully has a fan to block out sounds. 
i found great success in going into grocery markets and keeping a load of snacks and easy things to carry around. Things like a jar of pesto and gluten free crackers to enjoy together. Also nut butter and bananas. This worked for me so that I had food in my bag everywhere I went. I wasn’t very picky when I was there because I cared more about having fun and exploring the country while not falling sick. Tasty food was low on my list. I was able to eat in a couple restaurants that were very reassuring about celiac safety. Hotels only had bananas or some other fruit which isn’t enough. 
Use your judgement, trust your gut, and focus on calories and nutrition over taste. 

Scott Adams Grand Master

We have some excellent travel articles that might be helpful for you which are here:

https://www.celiac.com/celiac-disease/gluten-free-travel/ 

lucy power Rookie
9 hours ago, Scott Adams said:

We have some excellent travel articles that might be helpful for you which are here:

https://www.celiac.com/celiac-disease/gluten-free-travel/ 

thanks!!

On 10/22/2023 at 10:04 PM, Kurlykaitlyn said:

I can only speak for air travel and being the UK. 
i always pack my own snacks and meal to carry on. I haven’t had problems bringing my own but I have kept it limited. Bars and nuts are great for an extra snack or supplement of calories. 
i found it to be quite easy to eat in the UK! I traveled a few weeks and did become sick once and that was a risky chance with a restaurant. Better safe than sorry! Listen to your gut and don’t risk it, otherwise you may end up on a hotel toilet that hopefully has a fan to block out sounds. 
i found great success in going into grocery markets and keeping a load of snacks and easy things to carry around. Things like a jar of pesto and gluten free crackers to enjoy together. Also nut butter and bananas. This worked for me so that I had food in my bag everywhere I went. I wasn’t very picky when I was there because I cared more about having fun and exploring the country while not falling sick. Tasty food was low on my list. I was able to eat in a couple restaurants that were very reassuring about celiac safety. Hotels only had bananas or some other fruit which isn’t enough. 
Use your judgement, trust your gut, and focus on calories and nutrition over taste. 

thank you so much! that made me feel much better because i was super worried about the UK

Scott Adams Grand Master

Do you know yet which countries you will visit? 


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



Celiac.com Sponsor (A8-M):



patty-maguire Contributor

Wow!  Sounds like an amazing trip!  Enjoy!

I've travelled in Italy, France and UK.  Italy is amazing for gluten-free.  France and UK are very good too.

Others mentioned printing off dining cards.  Definitely do that.

On overseas flights you can usually order a gluten-free meal.  Check the airline's website.

I always bring food on the plane.  Nuts, cheese & crackers, granola bars, sandwich or wrap.  Be careful of liquids or gels, they must be under 100ml or 3.4oz.  I had hummus confiscated once.  You can bring an ice pack to keep your food cold so long as it's under the liquid allowance.  Bring an empty water bottle.  You can fill it up after you go through security.

I also recommend the Find Me Gluten Free app.  They cover many cities around the world.  If your tour group is booking the restaurants you can check to see if there are any reviews. If you can't influence the restaurant choice, at least you'll know what to expect and if you need to eat in advance or bring your own food. 

You may be pleasantly surprised about hotel meals.  Check their websites and email in advance so you know what to expect. 

Same with trains.  You may be pleasantly surprised, but they will have a websites too and like airlines, you may need to order in advance or bring your own food.

Look for celiac associations for the countries your travelling to.  The often have good tourist info.  The Italian Celiac Association website is very good and they also have an app.

Enjoy!  This sounds like the trip of a lifetime.

  • 2 weeks later...
lucy power Rookie
On 10/22/2023 at 10:04 PM, Kurlykaitlyn said:

I can only speak for air travel and being the UK. 
i always pack my own snacks and meal to carry on. I haven’t had problems bringing my own but I have kept it limited. Bars and nuts are great for an extra snack or supplement of calories. 
i found it to be quite easy to eat in the UK! I traveled a few weeks and did become sick once and that was a risky chance with a restaurant. Better safe than sorry! Listen to your gut and don’t risk it, otherwise you may end up on a hotel toilet that hopefully has a fan to block out sounds. 
i found great success in going into grocery markets and keeping a load of snacks and easy things to carry around. Things like a jar of pesto and gluten free crackers to enjoy together. Also nut butter and bananas. This worked for me so that I had food in my bag everywhere I went. I wasn’t very picky when I was there because I cared more about having fun and exploring the country while not falling sick. Tasty food was low on my list. I was able to eat in a couple restaurants that were very reassuring about celiac safety. Hotels only had bananas or some other fruit which isn’t enough. 
Use your judgement, trust your gut, and focus on calories and nutrition over taste. 

thank you i'm glad the grocery stores had stuff!

On 10/25/2023 at 12:58 PM, patty-maguire said:

Wow!  Sounds like an amazing trip!  Enjoy!

I've travelled in Italy, France and UK.  Italy is amazing for gluten-free.  France and UK are very good too.

Others mentioned printing off dining cards.  Definitely do that.

On overseas flights you can usually order a gluten-free meal.  Check the airline's website.

I always bring food on the plane.  Nuts, cheese & crackers, granola bars, sandwich or wrap.  Be careful of liquids or gels, they must be under 100ml or 3.4oz.  I had hummus confiscated once.  You can bring an ice pack to keep your food cold so long as it's under the liquid allowance.  Bring an empty water bottle.  You can fill it up after you go through security.

I also recommend the Find Me Gluten Free app.  They cover many cities around the world.  If your tour group is booking the restaurants you can check to see if there are any reviews. If you can't influence the restaurant choice, at least you'll know what to expect and if you need to eat in advance or bring your own food. 

You may be pleasantly surprised about hotel meals.  Check their websites and email in advance so you know what to expect. 

Same with trains.  You may be pleasantly surprised, but they will have a websites too and like airlines, you may need to order in advance or bring your own food.

Look for celiac associations for the countries your travelling to.  The often have good tourist info.  The Italian Celiac Association website is very good and they also have an app.

Enjoy!  This sounds like the trip of a lifetime.

thank you i didn't even think about trains! i was worried about francs

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • 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. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    2. - par18 replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    3. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    4. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

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

    • Total Members
      133,339
    • Most Online (within 30 mins)
      7,748

    Teresa King
    Newest Member
    Teresa King
    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

    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
    • par18
      Been off this forum for years. Is it that important that you get an official diagnosis of something? It appears like you had a trigger (wheat, gluten, whatever) and removing it has resolved your symptom. I can't speak for you, but I had known what my trigger was (gluten) years before my diagnosis I would just stay gluten-free and get on with my symptom free condition. I was diagnosed over 20 years ago and have been symptom free only excluding wheat, rye and barley. I tolerate all naturally gluten free whole foods including things like beans which actually helps to form the stools. 
    • trents
      No coincidence. Recent revisions to gluten challenge guidelines call for the daily consumption of at least 10g of gluten (about the amount in 4-6 slices of wheat bread) for a minimum of 3 weeks. If possible, I would extend that two weeks to ensure valid testing.
    • SilkieFairy
      Thank you both for the replies. I decided to bring back gluten so I can do the blood test. Today is Day #2 of the Challenge. Yesterday I had about 3 slices of whole wheat bread and I woke up with urgent diarrhea this morning. It was orange, sandy and had the distinctive smell that I did not have when I was briefly gluten free. I don't know if it's a coincidence, but the brain fog is back and I feel very tired.   
    • knitty kitty
      @Jane02, I hear you about the kale and collard greens.  I don't do dairy and must eat green leafies, too, to get sufficient calcium.  I must be very careful because some calcium supplements are made from ground up crustacean shells.  When I was deficient in Vitamin D, I took high doses of Vitamin D to correct the deficiency quickly.  This is safe and nontoxic.  Vitamin D level should be above 70 nmol/L.  Lifeguards and indigenous Pacific Islanders typically have levels between 80-100 nmol/L.   Levels lower than this are based on amount needed to prevent disease like rickets and osteomalacia. We need more thiamine when we're physically ill, emotionally and mentally stressed, and if we exercise like an athlete or laborer.  We need more thiamine if we eat a diet high in simple carbohydrates.  For every 500 kcal of carbohydrates, we need 500-1000 mg more of thiamine to process the carbs into energy.  If there's insufficient thiamine the carbs get stored as fat.  Again, recommended levels set for thiamine are based on minimum amounts needed to prevent disease.  This is often not adequate for optimum health, nor sufficient for people with absorption problems such as Celiac disease.  Gluten free processed foods are not enriched with vitamins like their gluten containing counterparts.  Adding a B Complex and additional thiamine improves health for Celiacs.  Thiamine is safe and nontoxic even in high doses.  Thiamine helps the mitochondria in cells to function.  Thiamine interacts with each of the other B vitamins.  They are all water soluble and easily excreted if not needed. Interesting Reading: Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/ Safety and effectiveness of vitamin D mega-dose: A systematic review https://pubmed.ncbi.nlm.nih.gov/34857184/ High dose dietary vitamin D allocates surplus calories to muscle and growth instead of fat via modulation of myostatin and leptin signaling https://pubmed.ncbi.nlm.nih.gov/38766160/ Safety of High-Dose Vitamin D Supplementation: Secondary Analysis of a Randomized Controlled Trial https://pubmed.ncbi.nlm.nih.gov/31746327/ Vitamins and Celiac Disease: Beyond Vitamin D https://pmc.ncbi.nlm.nih.gov/articles/PMC11857425/ Investigating the therapeutic potential of tryptophan and vitamin A in modulating immune responses in celiac disease: an experimental study https://pubmed.ncbi.nlm.nih.gov/40178602/ Investigating the Impact of Vitamin A and Amino Acids on Immune Responses in Celiac Disease Patients https://pmc.ncbi.nlm.nih.gov/articles/PMC10814138/
×
×
  • 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.