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

Camp


roo#9

Recommended Posts

roo#9 Newbie

hey

Have any of you guys every been to a summer camp or something. Did you bring your own food or what? :unsure:


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

You might want to pm flagbabyds. She's been to summer camp. She hasn't spent as much time on the message board as she used to, but I'd bet she can answer your questions if you pm her.

MJS Rookie

l

MJS Rookie

Hey roo#9,

I attended an overnight summer camp last summer for 2 weeks. what i did was bring a couple boxes of cereal for breakfast, gluten-free bread and pb&j for lunch, and some frozen meals for dinner. usually there was something gluten-free i could eat in at least one of the meals (like eggs for breakfast, potatoes and salad at lunch and dinner). i also brought a few boxes of crackers to keep in my cabin just in case.

Just be sure to bring enough food! I was new to the diet when I went to camp, so i wasn't that good at label-reading and stuff. I also didn't bring enough food and my dad had to drive down and bring me a loaf of bread and frozen dinners (luckily it's only an hour away from home). Bring a variety, too. I got so sick of my millet bread by the end of the second week that I couldn't eat it for months afterward.

Also call ahead and tell the director or whoever's in charge about your problem. Then they can plan on where you will keep your food and stuff like that. And talk to the food staff once you're there about the food that they are preparing in advance. Out of two weeks, I was able to eat 3 of the main dishes at dinner.

I really hope this helps! It is hard to do, but you can be gluten-free at camp and still have a great time! (I have to warn you--kids are inherently nosy and rude, so don't be surprised when half the camp asks you about the "weird" food you're eating and why)

Kassie Apprentice

what kind of camp will you be goin to? i am goin to a girl's camp in the 2nd week of june, its a church thing so there wont be tonz of people and i know everyone and they know my condition. Make arrangments before hand to know what sort of cooking devices will be available and bring food for the meals you cant eat also ask ahead of time (like a week before camp) if they know whats goin to be on the menu. good luck

roo#9 Newbie

MJS - Thanks for all the help! I will keep all of those things in mind. Ya, people have said my food looks weird before, it kind of gets annoying. I don't know anybody my age with celiac (I only know like 3 people who have it) So, where are you from?

Kassie - I am going to a church camp too! I am super excited. it is actually a family camp but I am volunteering there. Thanks for all the help, I will tell them about my allergies before I go.

MJS Rookie

hey, i'm glad to help!

i'm from gainesville, florida (home of the gators :P ), just a couple hours north of orlando. the camp i go to is really awesome, i've been going since 2nd grade and we do pretty much every activity ever invented. i'm going to an adventure camp this summer where we canoe down a river and camp out for a week. finding a way to bring food will be hard, but i'm really excited.

yeah, i don't really know any people with celiac. except for one of my friends who is a year older than me was diagnosed a month ago. the funny thing is that we've gotten a lot closer this past month just because we can relate. it's great having someone to talk to about things with.

well, hang in there! btw, where are you from? what is the camp like that you're going to?


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



Celiac.com Sponsor (A8-M):



Run-4-Jesus Rookie

A few summer's ago I went to a Christian camp and my mom and I explained to all the directors about my situation. We brought lots of gluten-free food and they cooked it for me. So when everyone else was lining up to go through the food lines, I just went back to the kitchen and this really nice lady had my food all ready for me. Most of the kids asked why I was eating weird, different stuff simply because they're curious. But everyone at my camp was really nice about it after I told them why. They all asked about a million questions though, example: Oh my gosh, how do you live without eating bread? What happens if you eat it? Have you never tried an oreo...a biscuit...spaghetti...and the list went on and on. :lol:

Then two summer's ago I went to cross country camp. I didn't explain my situation to anyone there because the camp was held on a college campus and we got to eat the food from the cafeteria at the college. There was always a variety of salads, lunch meats, veggies, and fruits that I could eat - so the only things I had to bring from home was a loaf of bread and some cookies!

HAVE FUN AT CAMP!

  • 2 weeks later...
marriedtoceliacman Newbie

Hey you all! Just wanted to share a funny story! My husband has had celiac disease since the mid 1980's. He was a young child when he was diagnosed. He went to camp one summer and ahead of time his mom called and confirmed that they would feed him gluten free diet. So he gets to camp ( he was probably around 10 years old) And every time they served bread or something he couldn't eat they would give him rice cakes. He ate rice cakes at almost every meal! Now look back 15 years ago, we all laugh together about his week of rice cakes. The world has really changed and improved since then and there are so many great gluten free products!

GF Family of 4 Since 2002 Newbie

Roo,

I'm glad to hear that you are attending a family camp. Does this mean that your Mom (or someone) will be there with you to help w/food?

I do such camps with my kids (age 10 and 12) - we are all gluten-free. So, I am able to prepare our meals, and the camp directors have always been helpful. I use the kitchen ahead of time, when the cook isn't there. I bring my own equipment, and food. Then wash my dishes after all the others are done.

Sometimes we are able to use camp-supplied food, that I get from the cook before the meals are prepared. I try to get the menu ahead of time, and make similar meals to the other campers. Then our food doesn't look so wierd - just different.

Consider a propane stove, or bring gluten-free dedicated electric appliances, even dutch-oven cooking with charcoal is fun.

There are also gluten-free-Summer camps offered around the country. One is a Family Camp, offered here in New Mexico. We went last year - it was great to not have to prepare mels for 5 days straight !!!! UNPRECEDENTED !!! Chk out the www.celiac.com calendar for July to see the details.

Have Summer Fun, Lori -Haley, Jack - and Mike.

  • 8 months later...
Eesha Newbie

I know this post is old, but for anyone looking for camp advice:

I did a sleepaway camp for three weeks at Vassar College in NY. Since it was a college campus (not woods camping) I didn't really have a problem with the diet.

I spoke to the coordinators ahead of time and they told me to bring gluten-free food. I brought bread, cookies, crackers and pretzels. They let me store my bread in the dining hall fridge, so all I had to do was ask one of the attendants to get it for me whenever I wanted some. The snacks and such I just kept in my dorm room.

Breakfast wasn't that much of a problem, but it did get boring eating the same thing everyday. I stuck to scrambled eggs, potatoes and fruit. For lunch I usually ate some gluten-free bread and they had a cold cut bar so I made sandwiches. For dinner, I ate salad and maybe some chicken (if it wasn't breaded or anything).

The kitchen staff was really nice and answered all of my questions about the food and looked up ingredients for me. I don't think I got too sick because of gluten contamination (maybe a little stomach ache once or twice). But I did get food poisoning!! I ate hot dogs at the 4th of July bbq and I guess they had been sitting out for too long, or undercooked? I'm not sure, but it wasn't because of gluten. Other than that, camp was really really fun. No one really bothered me about the diet. The first few days the kids at my dining table asked why I was eating different looking bread and such. But after I explained everything, it wasn't a big deal at all. Also, my birthday came during camp and my counselors and friends got gluten-free ice cream to celebrate (instead of cake). It was really sweet.

Email me if you have any questions: moonstruck_eyes@yahoo.com

  • 8 months later...
eeyore Collaborator

I went to a week-long camp a few weeks after I was diagnosed as gluten and casein sensitive...I brought homemade, frozen lunches and dinners (the nurse had a microwave in her cabin) and gluten-free bagels and cereal, and rice milk for breakfast. For snacks I took corn/tortilla chips and homemade chocolate chip cookies...The trip took two days to make, and for on the way there and back I would find extras of what I had or had eggs cooked in coconut oil.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      2

      Gluten related ??

    2. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    3. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      2

      Gluten related ??


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,079
    • Most Online (within 30 mins)
      7,748

    Terra33
    Newest Member
    Terra33
    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

    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
    • Russ H
      This treatment looks promising. Its aim is to provoke immune tolerance of gluten, possibly curing the disease. It passed the phase 2 trial with flying colours, and I came across a post on Reddit by one of the study volunteers. Apparently, the results were good enough that the company is applying for fast track approval.  Anokion Announces Positive Symptom Data from its Phase 2 Trial Evaluating KAN-101 for the Treatment of Celiac Disease https://www.reddit.com/r/Celiac/comments/1krx2wh/kan_101_trial_put_on_hold/
×
×
  • 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.