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

College Life For New Celiac


gZimmiZ

Recommended Posts

gZimmiZ Rookie

I just wanted to share a wonderful experience I had a few days ago as an encouragement to those of you who are the 'support staff' to your celiac family.

I phoned the private university where my child attends, with my students permission, and spoke to the cafeteria manager. I explained the new diagnoses and the gluten-free diet. The manager asked lots of questions. I explained that I would be happy to bring some food to the cafe freezer to help out. I was thrilled when she replied, "Isn't your student on a meal plan?" I said, "Yes". She said, "Well, I am happy to have you bring food and I will store it for you, but it is my responsibility to provide safe meals! " I almost cried.

God is so Good!


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



Celiac.com Sponsor (A8-M):



byuiemily Newbie

That's wonderful! I am in my sophomore year of college, and even though I don't use the cafeteria, it's still music to my ears to hear that universities and specifically those in charge of the cafeterias are really stepping up to the plate as far as catering to the students' needs go. I remember just 2 years ago when I was first diagnosed, my high school was less then excited about the possibility of having to accomodate for me, and I heard other such stories, but I truly believe that things are starting to make a turn for the better and that is a great miracle. Worrying about whether or not the college you want to attend will work with you to meet your health needs in the last thing a person should have to agonize over. Again, wonderful to hear that the cafeteria manager at your child's Uni. is being so helpful :)

Guest ~wAvE WeT sAnD~

gZimmiZ,

I am impressed! I'm a Junior who will have a confirmed diagnosis in one week. I attend a small Liberal Arts College that makes accommodations for those with dietary restrictions. I'm not quite sure what this entails, but it's amazing that the college is letting your daughter have a reasonable amount of control over what is being put in her body. I hope the Food Services director and I can work out a similar agreement.

I was wondering, what in particular does this cafeteria do to prevent Gluten cross-contamination? It is my biggest concern.

Thank you for listening,

gZimmiZ Rookie

Cross Contamination!!! I understand this can be a big nightmare! She told me she would plan on putting aside meat prior to seasoning and bake in a separate pan and would do the same for pasta. On that topic, our conversation stopped there. We are going to make an appointment and talk on campus. We are reading and making notes out of Danna Korns book, Wheat Free Worry Free, about concerns and needs, a separate toaster etc. She did ask where she could go to buy gluten-free bread!

Does anyone have any ideas for us? We are so new at this I appreciate any ideas. Thanks!

angel-jd1 Community Regular

A while back I had done some research into college food service programs. You can find that info here: Open Original Shared Link

Hope it helps someone.

-Jessica :rolleyes:

  • 3 weeks later...
starlitgrl27 Rookie

I'm starting my sophomore year of college and i was just last week told i was gluten-intolerant. the private university i attend uses Sodexho food services which i really popular on campuses across the country. I just placed a phone call to the dining hall services on my campus and they're setting an appointment for the first week back for me with a dietician! I was so happy considering my recent change in diet has been a kick in the butt. They said that they would be more than happy to help. I figure since Sodexho and my school has been so good to me that maybe other schools might do it too.

Archived

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

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

    • Total Members
      133,225
    • Most Online (within 30 mins)
      7,748

    Paulyw
    Newest Member
    Paulyw
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • xxnonamexx
      I noticed eating gluten-free or CGF foods have higher sugar and sodium some. No added sugar protein bars I found better with plant fiber. I wanted to know what are you go to besides whole fruits/veggies that you find are healthy for you where you can feel eating normal without hurting yourself or health. I was looking into subscription based like Thrift to see if there is something that is healthier CGF that can make me feel normal. Thanks
    • Jmartes71
      Thankyou because I met up with K B with well known bay area hospital once and she said she knows I don't like to take meds, I said thats incorrect, I have issues.Thats the one that said I was deemed " unruly " when she admitted I was celiac when I asked why am I going through this.
    • cristiana
    • trents
      Cristiana, that sounds like a great approach and I will be looking forward to the results. I am in the same boat as you. I don't experience overt symptoms with minor, cross contamination level exposures so I sometimes will indulge in those "processed on equipment that also processes wheat . . ." or items that don't specifically claim to be gluten free but do not list gluten containing grains in their ingredient list. But I always wonder if I am still experiencing sub acute inflammatory reactions. I haven't had any celiac antibody blood work done since my diagnosis almost 25 years ago so I don't really have any data to go by.   
    • cristiana
      I've been reflecting on this further. The lowest TTG I've ever managed was 4.5 (normal lab reading under 10).  Since then it has gone up to 10.   I am not happy with that.  I can only explain this by the fact that I am eating out more these days and that's where I'm being 'glutened', but such small amounts that I only occasionally react. I know some of it is also to do with eating products labelled 'may contain gluten' by mistake - which in the UK means it probably does! It stands to reason that as I am a coeliac any trace of gluten will cause a response in the gut.  My villi are healed and look healthy, but those lymphocytes are present because of the occasional trace amounts of gluten sneaking into my diet.   I am going to try not to eat out now until my next blood test in the autumn and read labels properly to avoid the may contain gluten products, and will then report back to see if it has helped!
×
×
  • 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.