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

Cross Contamination Question?


LisaaaNoel

Recommended Posts

LisaaaNoel Explorer

I'm currently sharing a kitchen with someone who isn't gluten-free, but doing everything she can to keep me from getting glutened. She often eats gluten-free with me, but I have a couple of questions. Say if she is cooking pasta on a burner next my gluten-free pasta, is there a risk of CC?

And if we are using an oven at the same time and her food contains gluten but mine doesnt and they are in separate pans, is it likely that I will get glutened?

If we share a microwave, does it have to be cleaned after every time she uses if he food contains gluten? :(


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



Celiac.com Sponsor (A8-M):



WW340 Rookie

I would think that you could avoid contamination in all of those cases by using caution or a lid.

If the boiling water is splattering over in to the other pan, then yes, you could get contamination cooking pasta in seperate pans on the same stove. However, if you make sure there is no splatering, it should be ok. I would put as much separation between them as possible. There are splatter tops available for frying foods, which you could use to cover your pan if you are concerned that there is gluten in the condensation that might contaminate your food. The splatter tops would allow the pan to vent.

Cooking in the oven - Again, I personally would use a cover whenever possible when cooking near gluten, either in the oven or on top of the stove.

My husband and I share a microwave. He has a plastic cover made for the microwave to cover all food that he cooks there. I use a paper plate to cover any food I cook there. We clean the microwave frequently, and always immediately if there are any splatters.

dilettantesteph Collaborator

It really depends on how sensitive you are to trace gluten. Some can handle shared households and some (like me) can't.

gfp Enthusiast
I would think that you could avoid contamination in all of those cases by using caution or a lid.

In most cases but sooner or later an accident will happen.

I once subscribed to this and was cooking for a friend, different pan, spoons etc.

Somehow when i served the pasta one of his had found its way into mine... did I use the wrong spoon? I guess I must have but I really couldn't remember!

After this I stopped having any gluten in the house AT ALL.

Soon after this I actually found all those nagging things the last 10% of the puzzle sorted itself out.

Some problems I hadn't even realised I had (they had crept up so slowly over years)

StacyA Enthusiast

I'd suggest getting two different spoon rests: one for you and one for her, so you don't use the wrong spoon or rest your spoon in a puddle of gluten.

Ditto on the other suggestions. You do need to watch the microwave. My first week of having to go gluten-free my husband microwaved some BBQ wings for my son and I noticed the splatters in the ceiling of the microwave - just waiting to drip into my food. Always cover her stuff and your stuff - with different covers, of course.

(And I hope you have your own margarine and jelly and peanut butter - those are magnets for crumbs - and you watch out for crumbs in your silverware drawer.)

Lanie940 Newbie
I'd suggest getting two different spoon rests: one for you and one for her, so you don't use the wrong spoon or rest your spoon in a puddle of gluten.

Ditto on the other suggestions. You do need to watch the microwave. My first week of having to go gluten-free my husband microwaved some BBQ wings for my son and I noticed the splatters in the ceiling of the microwave - just waiting to drip into my food. Always cover her stuff and your stuff - with different covers, of course.

(And I hope you have your own margarine and jelly and peanut butter - those are magnets for crumbs - and you watch out for crumbs in your silverware drawer.)

We just bought a new 4 slice toaster, I will have my OWN SIDE that I will use. My son and husband will use the other side ONLY.

Chrissyb Enthusiast
We just bought a new 4 slice toaster, I will have my OWN SIDE that I will use. My son and husband will use the other side ONLY.

I am not sure what anybody else thinks on this one but I would of bought two toasters. You are still putting yourself at risk for CC with the slots that close. I bought myself a little $8 toaster and it works great just for me. I guess with crumbs I am pariond just ask my son and husband lol.


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



Celiac.com Sponsor (A8-M):



nasalady Contributor
I would think that you could avoid contamination in all of those cases by using caution or a lid.

If the boiling water is splattering over in to the other pan, then yes, you could get contamination cooking pasta in seperate pans on the same stove. However, if you make sure there is no splatering, it should be ok. I would put as much separation between them as possible. There are splatter tops available for frying foods, which you could use to cover your pan if you are concerned that there is gluten in the condensation that might contaminate your food. The splatter tops would allow the pan to vent.

What if your husband wipes all the crumbs off a counter but there's still enough gluten stuck to the surface to contaminate your food? What if wheat flour is suspended in the air and lands on your salad...or you breathe it in?

What if you have a four-year-old who scatters gluten-y crumbs all over the place no matter how careful you try to be?

I don't know how all you people manage to live in the same house with gluten but more power to you!! :)

For those of you that can't do it, don't feel bad.....I can't either. I tried it and just about died from constantly being glutened. :blink:

I posted more about this in an earlier thread, but I don't mind repeating it....I don't think it's doing your families any harm by having them eat gluten-free. After all, your children are related to you....it's highly possible that they too have a problem with gluten or will develop one! Your spouse is not related to you but it doesn't mean that he/she is not gluten sensitive/celiac. My husband turned out to be celiac; we never would have known if he hadn't gone gluten free with me and then tried gluten again a few weeks later (beer during Super Bowl Weekend). Poor guy broke out all over with DH!! :(

I do all the cooking, and I've learned how to make almost *anything* gluten free (even grain free now!!). My family is NOT suffering!

For those who have roommates, etc., it's a different story of course.....best of luck to you!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Ibuprofen

    2. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      My only proof

    3. - Scott Adams replied to wellthatsfun's topic in Coping with Celiac Disease
      1

      still struggling with cravings

    4. - Scott Adams replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Oh my goodness medication causing pain !!!!

    5. - Scott Adams replied to Me,Sue's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Knowing what to do when feeling unwell.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,871
    • Most Online (within 30 mins)
      7,748

    GR82BNTX
    Newest Member
    GR82BNTX
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      Hi Colleen Are you supplementing B12/having injections? I have learned recently that sometimes when you start addressing a B12 deficiency, it can temporarily make your symptoms worse.  But it is important not to stop the treatment.  Regarding your problems with anxiety, again that is another symptom of a B12 deficiency.   I didn't know what anxiety was until it hit me like a train several months before gastrointestinal issues began, so I can certainly relate.   Two books which helped me hugely were At Last A Life by Paul David (there is a website you can look up) and The Depression Cure: The Six-Step Programme to Beat Depression Without Drugs by Dr Steve Llardi.  Although his book is aimed at people who have depression, following the principals he sets out was so helpful in lessening my anxiety.  Llardi suggests we need to focus on getting enough: - physical exercise - omega-3 fatty acids - natural sunlight exposure - restorative sleep - social connectedness - meaningful, engaging activity   ... and we should feel a lot better. That is not to stay you must stop taking medication for depression or anxiety if you have been prescribed it, but adopting the changes Dr Llardi sets out in the book should really help. Can I just ask two more questions:  1) you say that you are B12 deficient, did they test your iron levels too?  If not, you really ought to be checked for deficiency and, 2) did they check your thyroid function, as an overactive thyroid can be cause rapid heartbeat and a lot of coeliacs have thyroid issues? Cristiana        
    • Jmartes71
      Hello still dancing around my celiac disease and not getting medically backed up considering Ive been glutenfree since 1994.All my ailments are the core issue of my ghost disease aka celiac disease. Im angery because the "celiac specialist " basically lightly dismissed me.Im extremely angery and fighting for a new primary care physician which is hard to do in Northern Cali.So currently without and looking.Im angery that its lightly taken when its extremely serious to the one who has it.My only evidence is a brochure back in the days when I got news letters when I lived at my parents.It was published in 1998.I was diagnosed before any foods eliminated from my diet. Angery doctors don't take seriously when Im clearly speaking.I did write to the medicine of congress and have case number.
    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
×
×
  • 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.