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

Italy...suggestions?


luvrdeo

Recommended Posts

luvrdeo Apprentice

I'm flying to Italy in 3 weeks, have yet to venture out since being diagnosed with celiac so this should be an adventure! I guess I'm looking for more snack ideas than anything...and any great restaurants anyone has tried? I'll be in the Tuscan region - Florence, Venice, Siena, Cinque Terre. Also...due to my serious issues with colitis lately, I'm pretty much on a "mush" diet, which works fine once I get to Italy...but what on earth can I take for the 20+ hour plane ride that will stay for that long? Ahh the joys of being a newbie!! ;)


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



Celiac.com Sponsor (A8-M):



love2travel Mentor

I've been to Italy many times and three times since my diagnosis 1.5 years ago. It is known to be one of the easiest countries in which to travel with celiac. I'm getting ready for a trip to Paris and then Croatia myself so unfortunately have no time to give you specific resto recs. To me the tricky part of travel is the airports and flights because of delays, etc. I take crackers, nuts, Skittles, Kind bars, a few slices of bread and peanut butter. Usually I do not eat that much processed food but it can be tricky on flights that disallow cheese, meats and so on. I also take two loaves of bread each trip for making into sandwiches, etc. at our destination.

Frequent markets for fresh vegetables and fruit.

Are you staying in apartments? That is easier as you can prepare your own meals. I have been to every place you mention - you are sure to fall in love with Italy! Nice time of the year, too - far less crowds.

BabsV Enthusiast

Once you get to Italy it will be no problem...but the international flights are a pain. The last international trip I took (24+ hours of travel time door-to-door) I took my Kindle and a backpack full of food!

I had apples slices, carrot and celery sticks, beef jerky, some gluten-free cookies, peanut M&Ms, Kind bars, hard boiled eggs (for first thing in the morning when we took off), tuna in a pouch in case I was stranded and needed more protein, some gluten-free crackers (Schar I think...), boullion cubes, etc. I know of people who've frozen chicken or other types of meals in small containers and then eaten them after they'd thawed on the trip...I wasn't that desperate because we were heading back to the US and I knew if I ran into trouble in DC or San Francisco I'd be calling friends to come get me and the food situation wouldn't be nearly so dire.

I packed everything in small amounts and in either ziploc bags or small disposable plastic containers (like the eggs.) As I finished items I would pitch the container or bag. I also brought a few plastic spoons just in case I would need them.

I passed through security without a single problem despite the picnic in my bag (even in Munich, Germany which is notorious for having tons of security hurdles...) I picked up a Go Picnic meal at one of the newstands in DC -- my first ever. Not great but at least I had a little more variety and didn't have to worry about not having anything to eat on the flight from DC to SFO -- which was good because they actually ran out of food about 3/4 of the way back through the rows. The people all around me were pissed off they couldn't even get some overpriced Pringles!

Basically you have to look at what you can eat and then try to fit that into small packages that won't arouse suspicion from security if at all possible. I was even tempted to get a note from my doctor to explain why I had all the food but didn't get around to it.

CeliacAndCfsCrusader Apprentice

All good tips so far.

Remember to download some Italian phrases regarding having Celiac and take them with you to show to waiters, etc.

Also, pharmacies or drug stores can usually be found quite easily in Italy and often stock a selection of gluten-free food (pasta, bread, snacks, etc). I saw this prior to being diagnosed myself and wondered "why do they have a small display of groceries HERE?"

Well, it's because Italians take care of their Celiac citizens better than just about anyplace in the world (including testing, subsidies, etc). They treat it as a real public health concern.

Because they test each child, many more are properly diagnosed. Awareness breeds familiarity which equals great support for you!

Have a blast. We can't wait to go back.

Lisa Mentor

I just spent a week in Italy, returning home last week. Other than choosing well, the key to my success was an Imodium before lunch, daily. It helped with the anxiety of an "issue". If you are touring, bathrooms are few and far between, with long lines and no toilet paper. Imodium is a must, in my opinion.

Most grocery stores or restaurants are familiar with "Gluten Free" or "Celiac" - it transcends the language barrier. But, Google on line "I am Celiac" in Italian and print it out. I never used mine, and had great pasta's and wonderful service. But I was on an arranged tour and our wonderful tour guide made previous arrangements for me. Dining on our own was not an issue either.

And a Caprese Salad will be your best friend for lunch.

Enjoy your stay and savor your experience. It's a lovely place. :)

luvrdeo Apprentice

Thanks for all the great advice! We will be mostly traveling on our own, so I'd imagine I'll use the "celiac" card often! Unfortunately, immodium doesn't touch my "D" issues, no matter how much I take! Could make for an interesting 10 days... :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,544
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.