Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Celiac In The University Setting


Beth in NC

Recommended Posts

Beth in NC Contributor

My son is a Junior at NC State University. He has lived off campus his entire college experience thus far so hasn't had too much difficulty. But it has been a challenge none the less. He wants to meet with the "higher ups" and attempt to get some changes made and some gluten-free awareness there on campus for other students, because he knows they are out there.

Do ANY of you have any stories, experiences, etc of similar situation where people worked on the ground level to get things changed like this? I would appreciate anything you can offer to help.

Thank you.


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



Celiac.com Sponsor (A8-M):



Mtndog Collaborator

When I was in college, I was not gluten-free. But I taught/attended a university once gluten-free. The most important suggestion I would make is that he make an appt to met with the head of Dining Services. I believe that celiac does fall under the Americans with Disabilities Act (ADA) and that universities must, in some way, accommodate it.

I know some universities have "accommodated" it by not requiring students to buy the meal plan, but others have embraced it and tried to offer a gluten-free option at every meal. The university I taught at did this after students approached the head of Dining Services.

If he can put up flyers around campus and try to get in touch with others on campus who have celiac, then maybe they can meet as a group. Power in numbers!

jenngolightly Contributor

Do ANY of you have any stories, experiences, etc of similar situation where people worked on the ground level to get things changed like this? I would appreciate anything you can offer to help.

Thank you.

I work for a university and am vocal about my gluten-free needs whenever there's a function going on. Not quite the same as for a student, but anyone who works for a college or university can be a change-agent. Our campus has an on-campus caterer who does both the student food services, and the catering for staff and faculty functions. I suppose that means I might be bringing some education to those who feed students. Unfortunately, what I'm getting is really disgusting food - yes, gluten free, but very disgusting. Last Friday I was at a conference and the lunch was greens with chicken breast and fresh peppers, asparagus, and other greens. They had ordered 8 vegetarian meals and 2 gluten-free meals (didn't see who got the other one). The vegetarians got the salad with tofu instead of chicken, the gluten-free ones were salad and tofu (why do they always assume we're vegetarians?). However, the gluten-free ones had no salad dressing and had obviously been made in the morning and sat under heat lamps. GRODY. Wilty greens and no salad dressing. I asked about the dressing and they said they weren't sure of the ingredients. Grrr.

I really should know better by now and bring my own food, but 2 years ago they didn't even have gluten-free options. Of course I complained, but their reaction was typical - they were very concerned for my health and wanted to give me the safest lunch possible. Like they were saints or something! My letter to the department reflected my disappointment and how much the lunch made me gag.

If your son's campus has an on-site food service provider - I urge him to go see the director of that department. It pays to confront the system directly. People want to keep you safe and are most likely willing to give you safe food - even if it's just salad at first. Baby steps.

I hope you get other suggestions about a movement. I can only do my part because I don't know a lot of celiacs. The kids here are so young - and most people aren't diagnosed until much later.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,847
    • Most Online (within 30 mins)
      7,748

    askJO
    Newest Member
    askJO
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Awol cast iron stomach
      "...hemorrhoids, constipation and diarrhea" . Heard of indeed. Experienced too. In hindsight, I can remember from age 2 having, and trying to convey my issues. I went 38 years misdiagnosed. So yes one can have these issues. I did have to go back on gluten for a gluten challenge. I failed that challenge and 6 days in they give me permission to stop, and I proceed with my scopes as scheduled. Post those 6 days I had gained 13 intolerances. I had to remove many foods, and reintroduce them back in. Nine years later I have two that remain gluten, and corn. I found it helpful to follow a whole foods diet. I also found autoimmune (AIP) protocol diet/recipes, and Paleo diet/recipes helpful. I still enjoy many of those homemade version recipes. I still continue to make my own salad dressings even if I can find a gluten-free store bought version. Fresh taste best to this palate now.  I did give up many grains I was off many and reverted to coconut flour and almond flour as work arounds .  I still remember the first time my gut experienced the reintroduction of quinoa. It wasn't sure if it wanted to flare or not. In 30 minutes it reported back ok this will pass. Many foods were removed post gluten challenge for me for 2 years and 4 months. At the 2 year 4 month mark is when my body said ok let's eat again, but don't ever feed me gluten again! I wish you the best.   
    • Scott Adams
      if you have already learned that Gluten is the cause of your symptoms, of course there is no need to add it back into your diet— your decision could save you a lot of needless suffering. One thing to consider is that if you do have celiac disease, your first- degree relatives may also need to get screened for it, because, like diabetes the disease is genetic, although many of its triggers seem to be environmental factors. You may want to consider getting a genetic test for celiac disease, so you can at least warn your relatives if it turns out that you do carry a celiac gene.
    • lookingforanswersone
      Thanks everyone. I've decided to do a gluten challenge (4 slices of bread a day for 3 months) and then do a full gluten panel of all the tests that can be done, just to rule it in or out for sure. I think otherwise psychologically it will keep bothering me 
    • Suze046
      Thanks Scott. Those articles are really interesting. I’m cutting out gluten for 6 weeks but honestly I’m not sure I even want to reintroduce it! I ate at a restaurant for the first time on Wednesday and then Thursday was really uncomfortable and had a few trips to the loo.. wonder if there was some cross contamination 🤷‍♀️ if that’s how my body reacts after not eating it for 3 weeks I’m not sure it’s worth reintroducing it and re testing for celiac! It might have been a coincidence I realise that I’m not going to feel better all of a sudden and my gut is probably still trying to heal. Thanks for your supportive message! 
    • RMJ
      Reference range 0.00 to 10.00 means that within that range is normal, so not celiac. There are other antibodies that can be present in celiac disease and they don’t all have to be positive to have celiac.  I’m sure someone else will post a link to an article describing them! Plus, if you are IgA deficient the celiac IgA tests won’t be accurate.
×
×
  • Create New...