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

Dorm Life


justjane

Recommended Posts

justjane Rookie

Hey all!

This is my second year of college and will be my first one gluten-free. The school I go to used to have cooking apartments, but recently we moved so now the dorms are just a room and a bath and all residents of the dorm must purchase a meal plan. I am not really worried about living in the dorm, because I did it last year and everything turned out fine. It's cheaper and closer in the long run than anywhere else. What I *am* worried about is the meal plan!

As I have not *officially* been diagnosed with anything other than Irritable Bowel Syndrome, I know that it might be hard for me to tell the school that I cannot eat anything containing gluten in it. The school I go to is very small, and last year didn't even have a nice cafeteria. Just remembering what they served last year though, I couldn't eat it now. They had wraps, sandwiches, the normal lunch food and that was pretty much it.

The school told me that they would try to help me out in every way, but I just can't see it happenening sinse the school is soooo small and I really don't have anything to *prove* that there is anything wrong with me!

I have two other options. Sinse college is out of state for me I can either find an apartment to live in with a roommate and risk cc, or live with my cousins in the basement where I'd have my own kitchen.

I'm going to the doctor to talk with him in July. Should I ask for a doctor's note? How did you guys manage in college? Have any suggestions?

Thanks!


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



Celiac.com Sponsor (A8-M):



jmengert Enthusiast

I was in college pre-gluten-free, but I have taught at a university for six years now, so I'm still around college life constantly. I would definitely get a fridge and microwave for your dorm room (I had both when I lived in the dorm). In my dorm, we had a kitchen we could share on each floor--will you dorm have one of those? If so, buy yourself some pots that you can use and keep them in your room. You can then go down to the kitchen and make whatever you want, and keep your supplies in your own fridge and room.

If you don't have a kitchen in your dorm or on your floor, I would invest in a single burner (Walmart, Target, etc. sells these) and a rice cooker, as well as a small George Forman Grill. You can do a lot with these alone.

I would then have a doctor's note to give to the university. They should have to cover your needs in the dining hall to a reasonable degree. Hopefully you can at least get plain meats, cheese, eggs, salad, etc., and if necessary, I would do most of my eating in my room.

Good luck--but your school should be able to help you if you have a doctor's note.

MySuicidalTurtle Enthusiast

You should go to your doctor so that you can prove your Celiacs or gluten sensitivity. By law your school has to help you by either giving you gluten-free food with the meal plan or not making you take the meal plan and allowing you to cook your own food. However, without any proof they don't have to do this. Do what's best for you because it's hardto get through classes and life being sick.

kbtoyssni Contributor

I don't know how small your school is, but they should still be able to make accomodations for you. Have you called the cafeteria manager and asked if they can do anything for you? My brother goes to a college with about 6000 students, and they have a special fridge filled with gluten free food. There are about five students with celiac, and they are allowed to go in the back and prepare their own food in one of the ovens, microwaves, etc. When I visited I wanted scrambled eggs, and they gave me real eggs because they weren't sure about the egg-powder mix stuff that everyone else has to use. If you go to school there, the staff is more than willing to sit down and talk to you about ingredients. I'd ask, it's not like food intolerances/allergies are uncommon.

gymnastjlf Enthusiast
I don't know how small your school is, but they should still be able to make accomodations for you. Have you called the cafeteria manager and asked if they can do anything for you? My brother goes to a college with about 6000 students, and they have a special fridge filled with gluten free food. There are about five students with celiac, and they are allowed to go in the back and prepare their own food in one of the ovens, microwaves, etc. When I visited I wanted scrambled eggs, and they gave me real eggs because they weren't sure about the egg-powder mix stuff that everyone else has to use. If you go to school there, the staff is more than willing to sit down and talk to you about ingredients. I'd ask, it's not like food intolerances/allergies are uncommon.

Not that it's a competition, hehe, but I go to an even smaller school than your brother. My school only has about 1400 students. I was the first to bring up gluten-free diets, but somehow word got around, and by the end of the year there were a couple of us that were eating the gluten-free stuff (we ordered from ener-g). We aren't allowed to prepare our own food, however the chefs are good about knowing what they put in the dishes that were already on the buffet line. And, a lot of them were really cool about making sure there was something we could eat. For instance, they knew that I always wanted some type of potato/rice with dinner. If they were making scalloped potatoes (which I couldn't do because of the cheese sauce), they'd usually hold just a few boiled potatoes to the side for me. Same with meat-- if they weren't sure if whatever sauce they were making for the day was gluten-free, they'd just keep a piece of meat off to the side for me until I said no I can eat the sauce (in which case the plain piece just went into the sauce with the next batch)! And the best part, everyone seemed pretty willing to learn about the diet! I agree though, just talk to them and don't give up if they're not too willing at first. I had to get the dean involved, and after one conversation, the dining services decided to help out real fast!

tarnalberry Community Regular
Not that it's a competition, hehe, but I go to an even smaller school than your brother. My school only has about 1400 students. I was the first to bring up gluten-free diets, but somehow word got around, and by the end of the year there were a couple of us that were eating the gluten-free stuff (we ordered from ener-g). We aren't allowed to prepare our own food, however the chefs are good about knowing what they put in the dishes that were already on the buffet line. And, a lot of them were really cool about making sure there was something we could eat. For instance, they knew that I always wanted some type of potato/rice with dinner. If they were making scalloped potatoes (which I couldn't do because of the cheese sauce), they'd usually hold just a few boiled potatoes to the side for me. Same with meat-- if they weren't sure if whatever sauce they were making for the day was gluten-free, they'd just keep a piece of meat off to the side for me until I said no I can eat the sauce (in which case the plain piece just went into the sauce with the next batch)! And the best part, everyone seemed pretty willing to learn about the diet! I agree though, just talk to them and don't give up if they're not too willing at first. I had to get the dean involved, and after one conversation, the dining services decided to help out real fast!

My school was 600 when I graduated. They're at 800 or so now. :-)

I wasn't gluten-free at school (I don't believe I developed celiac until a year after college), but did a lot of cooking. See if they have dorms with a kitchen - which might allow you to get off the meal plan - or look into getting a small set of items to cook with electrically. For instance, an electric skillet, a microwave, and a steamer (and maybe a small electric grill) can cook you almost anything in a pinch. You'd need a mini-fridge too, and (for safety purposes), I'd do most of my cooking outside on a coffee table (if the kitchen was full).

But do talk to the dean of students. They can help you deal with the food services people properly.

Archived

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

  • 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.