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

Dealing with Symptoms in College


eturnquist

Recommended Posts

eturnquist Newbie

I am a college junior and was just recently diagnosed with celiac disease in June, two months before I went back to college. I was feeling great initially, but now I am living with 3 people who are not gluten free, and so I have been having issues with cross contamination. I've been trying to pinpoint the cross contamination, but sometimes my roommates use utensils or contaminate my food when I'm not there because they just don't think about it. Does anyone have any tips for avoiding cross contamination?

Also, I've been dealing with symptoms off and on for about two weeks now. Diarrhea, fatigue, brain fog, achy joints, all of it. I've really been struggling attending classes and studying because I feel so sick all the time. Although some teachers are accommodating, some just don't understand and think that because I look fine, I must be fine. How do you deal with symptoms in college and does anyone have any tips for overcoming the symptoms?

Thanks!


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



Celiac.com Sponsor (A8-M):



Taras Light Rookie

Hello eturnquist,
Sorry you are being cross contaminated! 1st I would suggest you keeping your cookware in your own room. Better safe than sorry because cross contamination still causes damage to your body, which makes healing take that much longer all over again.
2nd, take care of yourself after being sickened. Rest as much as you can, even sleep, because it gives your body less to deal with while healing. Water will be a good friend too if you don't drink enough.


I relate to you with the brain fog being in college. Same here. Things take like 2 days longer than they should some times because my brain wont work.

GFinDC Veteran

Hello eturnquist,

I live with 2 people who are pretty gluten unaware.  There is plenty of gluten everywhere.  So I assume any dishes or silverware might be contaminated.  Quick rinse is all it takes to clean a little flour off.  I keep most of my food in a separate large dorm size refrigerator.  That is simple and works well.  If you take a little extra effort you should be fine.  I generally avoid the kitchen when pies, or bread etc is being baked.

Ennis-TX Grand Master

Freezer Paper you prep surfaces, use your own cooking appliances, your own fridge, and disposable plates and utensils when you can. Keep a stash of gluten-free Safe snacks like from GERBs or Enjoy life around for munching. Wash your hands before cooking or eating anything, gloves might help with this. And a safe meal replacement shake to take with your if you need for emergency safe meals while out in a shaker bottle. Call me paranoid but when you got to get stuff done you have to take a bit of extra precautions to avoid getting sick. Perhaps drill into your roommates about your issues, they might be emphatic and work on your with compromises or ground rules about keeping things in certain areas.

  • 1 month later...
rugenzj Newbie

Hey man, im a Junior in college living in a fraternity house, as you can imagine its not easy.

I keep all my plates and silver ware in my own room and wash everything in the sink myself.  That way i know its clean and i don't have to worry about anything. I can clean everything right when i'm done using it, let it dry, and be done with it.

Be careful with people drinking out of your drinks or drinking out of other peoples drinks. that can cause a lot of cross contamination. 

as for the symptoms, i've typically dealt with everything through the liberty of using cannabis, provided by my roommate.  as many would not suggest this method, it does help make your stomach feel better, and sometimes let you sleep everything off.  i know thats probably not what you wanted, but thats my honest opinion. 

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
      133,340
    • Most Online (within 30 mins)
      7,748

    Abbyyoung417
    Newest Member
    Abbyyoung417
    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

    • 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.