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?


BrittLoves2Run

Recommended Posts

BrittLoves2Run Apprentice

How serious do you take Cross contamination at your home? Should I have separate pots and pans? colander? What about dish sponges? What thinks should I think about replacing? My family think i'm crazy when I talk about this saying "I'm sure it's not THAT bad" and things like that

What items do you keep separate at your house??


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



Celiac.com Sponsor (A8-M):



navigator Apprentice

My house is completely gluten free. My husband eats gluten out of the house but at home he is gluten free to ensure that there is no cross-contamination. My son-in-law does the same. It's a huge issue and will prevent healing taking place. It's a steep learning curve and a lot for you and your family to get your heads around. I found the cross-contamination issue the most difficult one to get people to really understand and take seriously but it's all about perseverance and education. Good luck!

lynnelise Apprentice

If your pots and pans are scratched then yes you should buy new. Definitely a new colander, toaster, and dish sponges. My house is 95% gluten free. For the most part if my family wants gluten they can eat it outside of the house. Occassionally my husband will buy a gluten snack but it's always in single serving containers and he is careful not to contaminate anything with it.

sa1937 Community Regular

Brittany, you might want to check this recent thread for additional ideas: http://www.celiac.co...you-get-rid-of/

BrittLoves2Run Apprentice

Thanks everyone!! I will buy new things for myself! I don't know that i'll be able to get my house 100% gluten free as my boyfriend is obviously fine. And Sylvia, I will check out that thread!

domesticactivist Collaborator

We decided to make our house 100% gluten free for simplicity's sake last year. It made a huge difference in our son's health. He stopped getting glutened all the time!

The past two months I have been doing a gluten challenge. While I tried to be super careful and obviously was up to date on all the details of being gluten-free and not contaminating things, I managed to gluten my son a couple times. I felt so bad for having made him sick with my carelessness.

Even if your bf wants to keep eating gluten, it would be better if he could stick to keeping gluten safely at restaurants and friend's houses, and eat gluten free at home. (and of course remember to wash up when he gets home, brush his teeth before kissing you, etc)

BrittLoves2Run Apprentice

We decided to make our house 100% gluten free for simplicity's sake last year. It made a huge difference in our son's health. He stopped getting glutened all the time!

The past two months I have been doing a gluten challenge. While I tried to be super careful and obviously was up to date on all the details of being gluten-free and not contaminating things, I managed to gluten my son a couple times. I felt so bad for having made him sick with my carelessness.

Even if your bf wants to keep eating gluten, it would be better if he could stick to keeping gluten safely at restaurants and friend's houses, and eat gluten free at home. (and of course remember to wash up when he gets home, brush his teeth before kissing you, etc)

I checked out the link about getting your house gluten free. WOW. What an overwhelming piece of information!! It seems like so much. I know it has to be done, but WHEW! I emailed a restuarnt today about how they prepare those gluten free items then I get from family members "well it's not like your going to stop breathing!" I've only been reading about Celiac for about a month and discovered I had it 5 days ago, but I understand that you should not ingest ANY! I feel like my family will NEVER understand this. *grumble*


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Show them some info from Celiac Experts:

Open Original Shared Link

Q: Is it ok if I ingest some gluten if I do not experience any symptoms?

No. The majority of patients with celiac disease experience no symptoms when they ingest gluten, either intentionally or unintentionally. This led to the concept that patients, especially children may grow out of the disease. In addition, patients also consider that it is doing no harm to them. However the ingestion of even small amounts of gluten results in damage to the small intestine--regardless of the presence or absence of symptoms--and puts the patient at risk for resulting complications including malignancies and osteoporosis.

Open Original Shared Link

The gluten-free diet is a lifetime requirement. Eating any gluten, no matter how small an amount, can damage the intestine. This is true for anyone with the disease, including people who do not have noticeable symptoms. It can take weeks

Katrala Contributor

We use tape (duct tape with peace signs and fun designs) to identify equipment that is gluten-free only.

You need separate just about everything. Definitely sponges. We buy colored "fun" ones for gluten-free and the plain ones for gluten. Each have their own plastic basket to sit in.

And, yes, it's that bad. But also no, it's not. You can't spend your life worrying that some tiny bit of gluten has made its way into your food. If you take good precautions the problems will hopefully be few and far between.

domesticactivist Collaborator

It will get less overwhelming as time goes on. You'll make some mistakes at first, but it will get easier. Cut yourself some slack - while no gluten is safe, a tiny bit of cross-contamination as you get things figured out is not the end of the world. Some cc from time to time is inevitable. Gluten is all over the place! The idea is to do your best to minimize your exposure so that when you do get it by accident that's *all* that you've gotten.

As for those relatives, once you have all the details straight in your own head you'll be able to better communicate with them. No doubt they've seen plenty of "gluten-free" people cheat and don't really know to take it seriously yet.

If you do get symptoms, they may not be as instantly dramatic as "not breathing" but they are serious nevertheless. It wasn't very long ago that they used to think people "outgrew" celiac, or that it was ok to eat it if your symptoms were mild. Now we know that there are serious long term health consequences for celiacs who continue eating gluten. My friend's dad was one of those folks, he ended up dying of a cancer specifically associated with celiac. Here is a fact sheet from the University of Chicago that your relatives may take more seriously: Open Original Shared Link

Some people never get it. You just have to learn to set your own boundaries and take responsibility for your own food.

Monklady123 Collaborator

I have decided not to stress about it too much. I definitely have my own colander since it's practically impossible to get a metal colander completely clean. Mine is pink. B)

We use a toaster oven so there isn't the same worry about crumbs as there would be in a regular toaster. I put my toast on a piece of foil just in case, but I don't worry about it more than that.

We take cold cereal out of its original boxes and put it in tall plastic containers. I have my own labels "gluten free container". Even if it's empty no one is allowed to put any other cereal in there.

I have my own peanut butter, my own jelly,and my own margarine. That's about it.

wildwood Apprentice

In our house, any kitchen item that is to be used for gluten free only (colander, storage containers, whisk, etc) is red in color. I got the idea on this forum. It has worked out very well in our home. I write gluten free on the lids with marker for peanut butter, jelly, etc. It was a little easier in our home because there are no young children so we all understand how important it is not to cross contaminate/mix things.

MomGoneRunning Rookie

This forum was so helpful and full of good ideas to help prevent cross contamination! Thank you all responders ans OP for posting the question. :D

Adalaide Mentor

I know that without a gallbladder I have no business using a deep fryer. Last week I found a really nice one on sale though and my husband needed a new one so we just bought 2 so I can have french fries occasionally. I just used pink nail polish to mark the dial on mine and the handle of the basket.

After noticing yesterday morning that the new non-stick frying pans look like someone took a fork to them (out of 4 adults I'm the only one who knows that it is never okay to use metal in non-stick pans) I decided I needed my own pots and pans. Now, instead of lamenting the fact that I have no oven save cookware I have a shiny new set of copper bottom stainless steel pans. I figure if someone else uses them at least I can get them clean, unlike non-stick which if scratched up I can never use again.

I haven't gotten around to getting a toaster yet, but it is on my list for when I find one I like. I'm not a huge toast eater so it isn't a priority for me.

I won't touch a blender anyone else uses because even if it's glass it has that rubber seal on the bottom. I picked up a bullet style blender that I can use for smoothies and such.

Other than that, just some basics like cutting boards, measuring cups and spoons, pyrex for storage, dishcloths and my own space in a pantry. Also all of my own containers of anything spreadable. (PB&J, butter, mayo) I tell myself I won't stress about it but it is something I worry about. I don't want to be doing everything I am for no reason at all. If I don't worry about CC sharing a kitchen with 3 other adults I may as well just stuff a loaf of bread in my face.

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. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    5. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,084
    • Most Online (within 30 mins)
      7,748

    bigwave
    Newest Member
    bigwave
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.