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

Practical Backpacking Tips?


ElseB

Recommended Posts

ElseB Contributor

Does anyone have any practical travelling tips? I've been reading crazy tips like bring your own breadmaker and toaster, ship things to yourself at your destination. I'm going backing packing in Australia, New Zealand and Europe for 6 months and will be staying mainly in hostels, and moving frequently. None of those tips are very practical. I've also heard people saying that its easy to find gluten-free products in these countries, but then I"ve also seen numerous posts from people who are travelling there and can't find any food! I'm worried about how to get carbs, without travelling with a sack of rice in my luggage.

To make matters worse, I was only just diagnosed this month, and leave in a month. I"m starting to think I should just cancel the whole trip because its so overwhelming.

Does anyone have any advice?


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



Celiac.com Sponsor (A8-M):



sallyterpsichore Explorer
Does anyone have any practical travelling tips? I've been reading crazy tips like bring your own breadmaker and toaster, ship things to yourself at your destination. I'm going backing packing in Australia, New Zealand and Europe for 6 months and will be staying mainly in hostels, and moving frequently. None of those tips are very practical. I've also heard people saying that its easy to find gluten-free products in these countries, but then I"ve also seen numerous posts from people who are travelling there and can't find any food! I'm worried about how to get carbs, without travelling with a sack of rice in my luggage.

To make matters worse, I was only just diagnosed this month, and leave in a month. I"m starting to think I should just cancel the whole trip because its so overwhelming.

Does anyone have any advice?

To tell you the truth, you're going to have to pack food in your backpack just in case you can't find food. I haven't traveled to Australia or New Zealand, so I can't say for those places. I have only traveled in Italy since going gluten-free and it wasn't hard to find gluten-free food to eat, but I went to sit-down restaurants and resigned to spending money on steak and that sort of thing. It's hard to grab quick "street food" that's gluten free, or at least it is in Italy. Trail mix is easy to pack, of course. Nuts, dried fruit, Lara bars (and I hear Clif Nectar is a new line of gluten-free bars that are tasty), fruit cups, are easy to pack. For carbs/energy, there are gluten-free pretzels that travel well, bag up some gluten-free dry cereal, rice/flax seed crackers, that sort of thing. It won't be easy, but I don't think you'll need to cancel the trip.

I was freaking out before my trip to Italy because I was still not feeling well (at all!) and the whole finding food outside of my home bit was really overwhelming and intimidating. Just plan ahead. Bring enough food with you to anticipate not being able to find food, but also realize that there are little markets with fruit and veggies all over the place. Carbs will take some planning ahead. Head to Whole Foods, buy some serving size baggies, and prepare to spend a whole lot of money on gluten-free version of normal snack foods, and you'll be all set. In fact, if you have a Whole Foods near you, the staff there are usually really knowledgable and helpful and you can set up a tour of the store with them showing you gluten-free items to buy and pack.

Sorry, that was long! Good luck! Wish I could come!

~Sally

Mango04 Enthusiast
Does anyone have any practical travelling tips? I've been reading crazy tips like bring your own breadmaker and toaster, ship things to yourself at your destination. I'm going backing packing in Australia, New Zealand and Europe for 6 months and will be staying mainly in hostels, and moving frequently. None of those tips are very practical. I've also heard people saying that its easy to find gluten-free products in these countries, but then I"ve also seen numerous posts from people who are travelling there and can't find any food! I'm worried about how to get carbs, without travelling with a sack of rice in my luggage.

To make matters worse, I was only just diagnosed this month, and leave in a month. I"m starting to think I should just cancel the whole trip because its so overwhelming.

Does anyone have any advice?

Ooooh, I've backpacked around Australia. It's very doable. When you get there, see if you can find a Coles or a Woolworths, and purchase a cooler bag (they're a few bucks - and about the size of a paper grocery bag). Fill it with things like peanut butter, Corn Thins, fruit, cans of tuna, Leeda bars, cans of beans, pre-cooked rice in microwavable bags, Orgran products etc. etc. If you throw a bag of frozen fruit in there, it will keep things cold for several hours.

It also helps to have some olive oil, salt and pepper, paper plates and eating utensils. Basically, every time you're at a stop with a grocery store, make sure to replenish your food bag.

If you're in a hostel, hard boiled eggs and fruit always makes a good breakfast, you can find gluten-free pasta everywhere (even in the tiniest of towns), and just stick to simple foods (garbanzo beans with veggies and olive oil, or steamed veggies and a potato cooked in a microwavable zip lock steam bag, with some tuna on the side for protein). I did occasionally use cookware in hostels, but only the stainless steel stuff (I just washed it very well before I used it).

I think it was me who posted that I couldn't find food there...I was having one frustrating jet-lagged day, but really, you will be fine.

Let me know if you have questions about specific places.

Phyllis28 Apprentice

I set out on a three month backpacking trip across Europe 3 months into a gluten free diet. I stopped at the grocery store nearly everyday and bought a days worth of food. In Europe most of the grocery stores are in the basements of the department stores. I ate a lot of yogurt, cheese, fruit, vegtables, juice and chocolate. Also, many of the major train stations have stores that sell fresh food.

In England ask if the grocery store has a "Free from" section, not all do. You can buy gluten free bread to put PB & J on. I agree with Mango04 bring along you own knife, fork, spoon and plate. You will need them when eating food purchased from grocery stores.

Pack along a small mat of blue ice and a small softsided lunch box. In a hostel with a kitchen you should be able to refreeze the blue ice wrapped in a paper towel. In addition to my backpack, I had a large purse with a shoulder strap the held my food and utensils.

Lastly, research the french fries from McDonald's in the various countries. I believe, I read that the french fries, including the oil, which has caused such controversy in the US, are gluten free in other countries. It is worth looking into because McDonald's are everywhere in Europe.

Have a super trip.

georgie Enthusiast

I haven't backpacked since being dx with Celiac but thought I would chip in and say that Australia is fairly Celiac aware these days. Most backpackers are in big cities, and near grocery stores and shopping malls - where gluten-free food, fruit and veges can be found. The ones in Adelaide are near Central Market where there are asian , italian and indian food galore. I have never had any trouble finding something to eat there and there is a stall that sells yummy savoury slices, and sweet cakes as well.

This list may be helpful for you. Open Original Shared Link

Also McDonalds has safe options. The chips are gluten-free ( ask for a dedicated fryer) and the beef patties are 100% beef too so you can have the burger without the bun ( put into a packing box) with all the normal salad. That is the same Australia wide. All foods are labelled in Australia by law, and if they contain wheat /gluten- they must state this on the label.And in Adelaide the Coeliac Society has its own shop that sells food to members - not sure but they may for travellers as well and other states are probably the same. Open Original Shared Link St Balflours have a great range of meals in a tin which are gluten-free and they are found in all supermarkets if you get tired of chocolate and fruit and pretzels.. You will probably have to carry food with you , and also may have to eat at restaurants more often than normal - but apart from that you should be fine.

ElseB Contributor
Ooooh, I've backpacked around Australia. It's very doable. When you get there, see if you can find a Coles or a Woolworths, and purchase a cooler bag (they're a few bucks - and about the size of a paper grocery bag). Fill it with things like peanut butter, Corn Thins, fruit, cans of tuna, Leeda bars, cans of beans, pre-cooked rice in microwavable bags, Orgran products etc. etc. If you throw a bag of frozen fruit in there, it will keep things cold for several hours.

It also helps to have some olive oil, salt and pepper, paper plates and eating utensils. Basically, every time you're at a stop with a grocery store, make sure to replenish your food bag.

If you're in a hostel, hard boiled eggs and fruit always makes a good breakfast, you can find gluten-free pasta everywhere (even in the tiniest of towns), and just stick to simple foods (garbanzo beans with veggies and olive oil, or steamed veggies and a potato cooked in a microwavable zip lock steam bag, with some tuna on the side for protein). I did occasionally use cookware in hostels, but only the stainless steel stuff (I just washed it very well before I used it).

I think it was me who posted that I couldn't find food there...I was having one frustrating jet-lagged day, but really, you will be fine.

Let me know if you have questions about specific places.

Thank you! Thank you! Thank you!!!! I"m feeling much better now!

georgie Enthusiast

Another link I have just found.

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



  • 3 months later...
mysecretcurse Contributor

This is a thread I was looking for.

I was actually thinking of starting one myself til I found this.

I find the gluten free diet easy for the most part, while having a home and cooking everything myself.

But come next spring at the latest Im quitting my job and giving up my apartment to take a year or more off

to travel, do volunteer work, visit friends, etc. Im gonna be traveling with nothing but the pack on my back

the whole time, so it's gonna be hard. I may have to walk long distances, hike, camp, etc.

Im really worried about how I'm going to get by.

If I wasn't a vegetarian it wouldn't be so bad as I would have a lot more options (plain steaks and what not) but my only main source of protien is quinoa, beans and rice. This would be ok if anything was PURE, as I could

get rice and beans at most restaurants, Im just scared the rice will have some sort of flavoring.

The stopping at supermarkets for peanut butter and fruit and stuff is a good idea. I need one

of those cooler bags!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.