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. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,956
    • Most Online (within 30 mins)
      7,748

    Crismedin
    Newest Member
    Crismedin
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.