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

Camping Food- What Kind Of Protein?


munchkinette

Recommended Posts

munchkinette Collaborator

I want to get into backpacking. (in the woods, with just a pack, no car) I have a friend who has offered to teach me, who knows nothing about gluten free foods.

What do I do for protein? I would normally do something like pouches of tuna when I travel, but the empty packets would attract animals from miles around. I love trail mix, but I really don't feel full unless I eat enough to be sick.

Suggestions?


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

I want to get into backpacking. (in the woods, with just a pack, no car) I have a friend who has offered to teach me, who knows nothing about gluten free foods.

What do I do for protein? I would normally do something like pouches of tuna when I travel, but the empty packets would attract animals from miles around. I love trail mix, but I really don't feel full unless I eat enough to be sick.

Suggestions?

You can still use packets of tuna (not cans, but the pouches). You just have to put them in your trash bag (usually a good ziploc) and hang your trash with your food anyway. (BTW, an Ursak is GREAT for food.) (ALL food you bring is going to attract animals. Hence food is put in its own bag, and hung from a tree. I use a combination of odor proof bags and an Ursak and haven't had a problem. Of course, there are a few places - Olympic National Forest, Yosemite - where you are REQUIRED to use a bear canister.)

I just make my regular meals and dehydrate them. Chili is GREAT for this. A lot of friends bring cheese. Some folks bring beef jerky (there are a few gluten-free ones, but I prefer the homemade stuff :) ). Eggs dehydrate well for breakfast, and if you can do dairy, you can buy freeze dried eggs. Nuts and seeds can also provide protein.

Wolicki Enthusiast

peanut butter :D

I don't care for it, but beef jerky might be a good option.

Have fun!

tgrahek Newbie

We camp up in the Boundary Waters near Canada where there are plenty of bears. We use packets of chicken and make meals like chicken tacos and chicken and rice. We also make grilled peanut butter sandwiches on Udi's bread and eat Gluten Freeda's gluten-free oatmeal packets for breakfast. We wrap the garbage up well and hang it from a tree in a 5 gallon paint bucket. This is what we pack our food in for the canoe, so it works really well.

mamaw Community Regular

Gary West Meats has several gluten-free meat sticks.... protein bars, Comfort Bars, Zing Bars, Pure-Fit bars are wonderful. Freeze-dried survival foods also just select the gluten-free varieties. Granola. hth

munchkinette Collaborator

Thanks! I didn't know some of the prepared meals were gluten free. Where would I find the right brands? REI?

How on earth would I dehydrate chili? Does something liquidy like that work in a food dehydrator? Maybe I should get one.

tarnalberry Community Regular

Thanks! I didn't know some of the prepared meals were gluten free. Where would I find the right brands? REI?

How on earth would I dehydrate chili? Does something liquidy like that work in a food dehydrator? Maybe I should get one.

I make my chili rather thick, and there are teflon sheets you can put on trays (or use saran wrap or wax paper) so nothing leaks through if you like. It takes about two days to dry, but reconstitutes fabulously. (I tend to do "freezer bag cooking". Boil water in your stove, pour into freezer ziploc bag, insulate (with fleece or what have you) for 20 minutes, eat. Cleanup is as easy as closing the bag! No pot to clean, no plate to clean - which also means no smelly cleaning water on the ground, even if you are eating a couple hundred yards away from your campsite.)

Chicken rice soup (again, cooked thick) works. I've also done thin rice noodles with a bit of boullion, dried veggies (you can get them at some healthfood stores - it's just mixed dehydrated veggies, you can also use "Just Veggies" which are freeze dried, but more expensive), and dried tofu (harder to find, but still available). I tend to alternate between eggs and potatoes (again, dehydrated at home) and hot cereal (usually a combination of cream of rice, quinoa flakes, flax seed, a bit of brown sugar, and cinnamon) for breakfasts.

I generally don't cook lunch, so gluten free crackers (homemade flax crackers are great for fat/protein, and you can doctor them with whatever you like), dried fruit, almonds (I generally don't mix them together for trail mix, though), some variety of bar form food (I'll do things like LaraBars, but I try to also get ones like Zing that have more protein), and chocolate.

For me, the packaged meals tend to not work - if they don't have gluten, they have dairy. And they tend to be bulky and expensive - I'm small enough that my pack is *not* that large, and trying to get five days worth of food in that thing with the rest of my gear is reaching it's limit! :)

That means I have to make more of my own backpacking food, which takes time, but you can make large batches at once. (When I prepared for my last five day trip, I ended up with enough food for about 10 days. I have stored the extra in the freezer, and I'm ready to use it... aside from the whole baby thing. :P)


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



Celiac.com Sponsor (A8-M):



  • 3 weeks later...
Char Apprentice

Tastybites are great -- they don't use up too much fuel to heat (just put into a pot and boil with some water that you can use to cook instant rice or pasta with) and have protein already in them.

Hard cheese (like a block of cheddar) works well too -- it'll be ok for a few days, although I wouldn't bring it to the desert (ok for at least up a few days in NE August summers).

Otherwise, I echo what everyone else here has said -- you'll probably have to bear bag anyway, so I think using tuna packets shouldn't be a huge issue (depends where you go, of course).

Have fun!

Reba32 Rookie

practice tying up your food in a tree before you go! That's the trickiest part to backpacking. ;) It's got to be high enough up that a bear standing on it's hind legs can't reach it, (and remember, black bears can climb trees!) and it's got to be a sturdy enough bag/canister that a raccoon can't climb into it and eat all your food while you're asleep!

Archived

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

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

    • Total Members
      133,640
    • Most Online (within 30 mins)
      7,748

    JennaK23222
    Newest Member
    JennaK23222
    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)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Jmartes71
      Thats the thing, diagnosed in 1994 before foods eliminated celiac by biopsy colonoscopy at Kaiser in Santa Clara  now condo's but it has to be somewhere in medical land.1999 got married, moved, changed doctor's was with former for 25 years told him I waz celiac and that.Fast forward to last year.i googled celiac specialist and what popped up was a former well known heard of hospital. I thought I would get answers to be put through unnecessary colonoscopy KNOWING im glutenfree and she wasn't listening to me for help rather than screening me for celiac! Im already diagnosed seeking medical help.I did all the appointments ask from her and when I wanted my records se t to my pcp, thats when the with holding my records when I repeatedly messaged, it was down played the seriousness and I was labeled unruly when I asked why am I going through all this when its the celiac name that IS what my issue and All my ailments surrounding it related. I am dea6eoth the autoimmune part though my blood work is supposedly fabulous. Im sibo positive,HLA-DQ2 positive, dealing with skin, eye and now ms.I was employed as a bus driver making good money, I loved it for the few years my body let me do until I was yet again fired.i went to seek medical help because my body isn't well just to be made a disability chaser. Im exhausted,glutenfree, no lawyer will help and disability is in limbo thanks to the lax on my health from the fabulous none celiac Google bay area dr snd team. Its not right.
    • trents
      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
    • Scott Adams
      Here are some articles on cross-reactivity and celiac disease:      
    • knitty kitty
      @HectorConvector, Here are some articles about "dry Beriberi" and neuropathy.  I hope you've been able to acquire thiamine hydrochloride or Benfotiamine.  I'm concerned.   Dry Beriberi Due to Thiamine Deficiency Associated with Peripheral Neuropathy and Wernicke's Encephalopathy Mimicking Guillain-Barré syndrome: A Case Report and Review of the Literature https://pubmed.ncbi.nlm.nih.gov/30862772/ Dry Beriberi Manifesting as Acute Inflammatory Demyelinating Polyneuropathy in a Patient With Decompensated Alcohol-Induced Cirrhosis https://pmc.ncbi.nlm.nih.gov/articles/PMC7707918/ A Rare Case of Thiamine Deficiency Leading to Dry Beriberi, Peripheral Neuropathy, and Torsades De Pointes https://pmc.ncbi.nlm.nih.gov/articles/PMC10723625/
    • cristiana
      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? Cristiana
×
×
  • 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.