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

Cooking In Microwave And Cross Contamination


kimis

Recommended Posts

kimis Collaborator

I know this might sound dumb....but I just heated up some gluten filled lasagna for my boyfriend in the microwave. When I took it out I noticed condensation inside the microwave from it. Does that condensation contain gluten because it came from a gluten source? Do I need to get my own microwave?


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



Celiac.com Sponsor (A8-M):



sa1937 Community Regular

I would think the condensation is steam but something like lasagne could also splash as it's getting zapped...but whenever I heat up anything in my microwave, I cover it. I've used everything from wax paper, plastic wrap, a paper towel or a plastic cover that fits over a dinner plate (depends on what I'm heating up). I got some plastic plate covers at the dollar store and I've also seen them in Wal-Mart.

ETA: I don't think you'd need your own microwave if you take precautions heating things up.

kwylee Apprentice

I always cover with parchment paper just to be safe because an errant flying bit of pasta attached to the microwave ceiling could always drop down into your tea.

But I often wondered about that ominous microwave "steam" as well, for example if it's from zapped pasta or something buttery that will make me react, and I DIDN'T cover my plate and put it in directly afterward, could that be an issue of CC?

kareng Grand Master

I have small plates that I turn over on top of a bowl. We tend to have exploding chili beans! They stick to the roof. Get a couple of paper towels and wipe the inside down. I think it would be worse at a shared office microwave. At home you can keep it clean.

Make BF some lasagna with gluten-free noodles. No one at my house notices and you don't have to cook the noodles first.

Marilyn R Community Regular

I really appreciate this thread. I rely on communal microwaves for all of my lunches, and have seen some really yucky ones, even in hospital cafeterias. I try to remember to pack a piece of parchment paper in my lunch to use in the microwave. If I forget to pack the parchment paper, I use a napkin or deli paper to wrap up my food, or wash the plastic cover that was used before.

That being said, I've never suffered consequences from a microwave that was used by gluten eaters. I'd insist on separate toasters, and the gluten toaster located away from your kitchen, but I'm okay with sharing a microwave.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,350
    • Most Online (within 30 mins)
      7,748

    JohannesW85
    Newest Member
    JohannesW85
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Itsabit
      Hi. Yes. I’m awaiting my Biopsy results. I had B12 and other labs drawn on Mon, including Thyroid levels, as I am on Levothyroxine for radiation-induced hypothyroidism. Those levels should indicate any iodine issues. We had discussed the urine iodine, but he went with the thyroid instead. We’ll see.  I never had any of those Pellagra skin changes, or Casal’s necklace. Just itchiness in the supraclavicular hollows on both sides of my neck, and the anterior aspect as my neck radiation site.  The hollows had no changes until I scratched them, then I got the rash on those areas like the ones I have now scattered in different areas, usually on both sides with the exception of my anterior thighs. My right is affected, my left isn’t. I am 70 and have all my teeth as well - amazingly after having had max dose radiation in 2002. 😂 Unfortunately, because of long term changes in my oral mucosa because of it I can’t use mouthwashes - even non-alcohol ones, as they all burn my mouth like fire. Toothpastes burn as well, but not nearly as bad. I have an electric toothbrush but it is getting more difficult to use due to increasing trismus. Some days I cannot open my mouth wide enough to get the electric brush between my back teeth, so on those days I use a regular one. Gotta do what you gotta do.  Thank you for your input. Any insight I can get into this is appreciated. So, for now it’s the waiting game for test results, then we can form a treatment plan going forward. 
    • James47
      Hiya..I was 48 when diagnosed two years ago and I was in right bad way but strict gluten-free diet you will recover I promise x
    • James47
      Hi everyone I'm James, I hope you are all feeling well??. Accidentally had gluten at weekend and I've had severe diarrhea since sat night. My question is ,the longer someone like myself has been following a strict gluten-free diet will the exposure to gluten be lot more extreme as body now has been free of it well over a year ? Any information be much appreciated and any tips on how to stop the constant diarrhoea I have currently also be appreciated guys x
    • Cathijean90
    • Wheatwacked
      I use Listerine.  Rinse first to soften the tarter, then brush with Oral B electric toothbrush super sonic.  The $15 ones at the supermarket.  At 73 I still have all my teeth.  While a blood test can measure iodine levels, it's not the most accurate method for assessing iodine status, and urinary iodine excretion is considered a better indicator.  Have any of your dermatologists ever done a biopsy for dermatitis herpetiformis?  I may have missed it.  Note the similarity of Casal's necklace to one of your symptoms. Pellagra rash is a characteristic skin manifestation of niacin (vitamin B3) deficiency. It typically presents as:  Erythema: Red, sunburned-like areas of skin, often on the face, neck, arms, and legs.  Scaliness: Dry, flaky skin that may become thickened and crusty.  Hyperpigmentation: Darkened patches of skin, particularly in sun-exposed areas.  Casal's necklace: A dark, pigmented band around the neck.  I am currently taking these} Vitamin D 10,000 IU (250 mcg) DHEA 100 mg 500 mcg Iodine  10 drops of Liquid Iodine B1 Thiamin 250 mg  B2 Riboflavin 100 mg B3 Nicotinic Acid 500 mg 4 times a day for hyperlipidemia. B5 Pantothenice Acid 500 mg Vitamin C 500 mg     Selenium 200 mcg  Several times a week
×
×
  • Create New...