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

Toaster Oven And Cross Contamination?


eblue

Recommended Posts

eblue Apprentice

Hey everyone,

I was diagnosed with Celiac a few weeks ago and have been wondering about using the same toaster oven as people at work who eat gluten. I have replaced all of my at home kitchen supplies, but I am confused about using the break room stuff at work... 

 

I like to bring my breakfast to work with me, and would like to bring these gluten free frozen waffles I found at a health food store. Here is my question: If I put foil down and wipe down any crumbs on the door of the toaster oven to ensure that my waffles are not touching any crumbs, can I still get glutened? Would it be safe? or should I skip the waffles altogether for the risk of cc? I know that my waffles wouldnt be touching anything, but still, the thought of using it makes me nervous because I can visibly see bread crumbs everywhere in the bottom of the oven. What do you guys think?

 

What about using the break room microwave? Could I get glutened from that too?


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



Celiac.com Sponsor (A8-M):



notme Experienced

if you use the microwave, i would make sure it's covered - people explode things in the microwave (lolz ok *i* explode things..)  and there might be stuff that could get into your stuff.  toaster oven........  i would, i think.  just make sure you put down foil like you said.  you know everybody who uses it and they're not baking cakes or anything in it, right?  just make sure your waffle doesn't come in contact with any crumbs.  and you'll be right there while it's toasting to keep a hawk's eye on it i hope!

Adalaide Mentor

I would be nervous about it, and frankly... I'm not into sharing appliances with strangers... but I'm not sure it would be a problem if you made a little foil thing to put your waffle on.

 

But, as was pointed out the microwave is a whole other story. I was sharing a microwave at home with 3 gluten eaters. It was on me to keep MY food covered because the other 3 people didn't and so the inside of the microwave was always questionable at best. If a cover slipped off my food went in the trash. Finally one night I missed my cover slipping off and wasn't paying attention... got sick. (I get sick for about 6 weeks. Fun times.) We now have two microwaves in the kitchen and if anyone ever lays a hand on mine it'll start WWIII. Microwaves are viscous, dangerous creatures when shared with gluten eaters.

cyclinglady Grand Master

For $10 you can buy a cheap toaster at Walmart and keep it in the original box and stash it at your desk.   How about becoming the microwave monitor?  Keep it clean yourself and make sure your food is covered with one of those plastic plate covers (again at Walmart).  That will insure that it won't slip off.  

 

You might score brownie points for keep the kitchen neat!  

 

 

eblue Apprentice

For $10 you can buy a cheap toaster at Walmart and keep it in the original box and stash it at your desk.   How about becoming the microwave monitor?  Keep it clean yourself and make sure your food is covered with one of those plastic plate covers (again at Walmart).  That will insure that it won't slip off.  

 

You might score brownie points for keep the kitchen neat!  

That is a good thought. I never thought about buying a cheap toaster and keeping it at my desk. Thanks!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,172
    • Most Online (within 30 mins)
      7,748

    Vickie Cavitt
    Newest Member
    Vickie Cavitt
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Hello, @Kwinkle, How are you doing?   Have you tried adding a Magnesium supplement?   The B Complex vitamins need magnesium to work properly, especially thiamine vitamin B 1.   Magnesium deficiency symptoms and Thiamine deficiency symptoms both include gas and bloating.  Thiamine deficiency symptoms also include loss of appetite and fatigue.   My gas and bloating resolved rather quickly when I took Benfotiamine (a form of thiamine shown to promote intestinal healing) and Magnesium Glycinate in addition to my B 50 Complex (all twice a day plus the following...).   I found Magnesium L-Threonate or Magnesium Taurate are better when taken with a form of thiamine called TTFD (Tetrahydrofurfuryl dusulfide) because all of these cross the blood brain barrier easily, which corrects the loss of appetite, fatigue and anxiety.    Like @Celiacandme said, keeping a food/mood/poo'd journal is a big help in finding problematic foods, and for making sure your diet is not carbohydrate heavy.  If you're eating a lot if processed gluten free facsimile foods, be aware they do not have vitamins and minerals added to them like their gluten containing counterparts.  For every 1000 kcal of carbohydrates, we need an extra 500 mg of thiamine to turn them into energy and not store them as fat.   Let us know how you're doing!
    • Scott Adams
      Yes, if you had symptoms when eating gluten ruling out celiac disease won't necessarily mean you'll be able to eat gluten again, although it might mean that you may be able to be less strict with your gluten-free diet. 
    • trents
      Have you considered the possibility that you might have NCGS (Non Celiac Gluten Sensitivity) rather than celiac disease? They share many of the same symptoms, the difference being that NCGS does not damage the lining of the small bowel. It is 10x more common than celiac disease. There is no test yet available for NCGS. Celiac disease must first be ruled out. In view of your genetic profile, I would give it consideration.
    • Kj44
    • mariamccl
      Hi, 25f who recently had a endoscopy procedure to diagnose celiac disease. Mum and uncle are both diagnosed celiacs. I've had symptoms over the past year - headaches that have become debilitating and frequent, feeling faint and nauseous with high heart rate, diarrhea and constipation, anemia, and recently my periods have become almost non existent. My doctor sent me a letter yesterday saying this " biopsies from the duodenum show some very mild features that could be in keeping with celiac disease but also could be due to other causes". I am waiting on an appointment to see him in the clinic to discuss this but in the meantime I wanted to check if anyone else has experienced this? I was eating plenty of gluten before my camera test and for the past 2 weeks have completely cut it out of my diet and I'm seeing changes in my bowel movements for the first time in my life! Headaches, dizziness etc are still there but maybe it takes longer for them to go away? Any help would be so appreciated -  I feel so lost in this whole process!! 
×
×
  • Create New...