Jump to content
  • You are not alone. Join Celiac.com for trusted gluten-free answers and forum support.



  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):

How Do You Handle Cross-contamination At Home?


mythreesuns

Recommended Posts

mythreesuns Contributor

If I'm really going to stick with this, I need to figure out how to keep my kitchen "clean." Impossible, I know, but if you're the only one gluten-free, how do you keep yourself free from contamination? Any and all tips welcomed!


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



Celiac.com Sponsor (A8-M):



kabowman Explorer

I am the only one with this many restrictions - my boys have food intolerances but not on this level and we don't use onions any more in cooking for my husband who can no longer tolerante any onions, at all.

I have several things:

-Safe counters and shared counters

-gluten-free foods only pots, shared pots (like stainless steel), only their pots (we each have our own cast iron)

-gluten-free pantry section - nothing but my stuff goes in there

-Mixed pantry - just bottles

-Their pantry

-gluten-free 'fridge shelf - including my own condiments

-Constant cleaning, rinsing, cleaning, rinsing, etc.

-gluten-free sponges for handwashing gluten-free pots, and mixed sponges for washing their stuff

-Separate towels - if you are touching my food, my stuff, wash your hands and dry them on my towel, use the other for everything else.

-Don't share the toaster

I don't keep any regular flour in the house BUT we do have some flour containing mixes in the house for gravy and pancakes - those are poured into a bowl, with the overhead fan OFF, on the desk in the kitchen, where we don't prepare food, then it is cleaned, rinsed, cleaned, rinsed, etc.

We replace the main teflon 2 skillets each year but the old ones go to the camping box.

jmengert Enthusiast

I'm the only one gluten-free in my house, so here's what I do:

I keep my food in a separate cabinet in the kitchen.

I keep my pots/pans/utensils in a separate cabinet.

I keep separate condiments--mayo, mustard, jelly, etc.--anything that touches bread, basically.

My boyfriend has to keep his "scary" foods (i.e. foods with crumbs--cookies, breads, etc.) on a separate table that I never go near.

I cover all my foods in the microwave with a plastic plate or paper towel.

That's all I can think of for now. I've been doing this for 2 years, and so far, not a problem. My boyfriend was a bit clueless for awhile (he never used my food or pots), but he was known to leave crumbs on the counter for a bit, but it's been awhile since that has happened. I also wash my hands a lot when cooking, since I know gluten is in my kitchen. I feel that as long as you are viligant, it can be done.

Good luck, and let me know if you have any other questions!

happygirl Collaborator

here's my two cents---and it's just me and my husband, who is super careful

separate butters, mayos, peanut butters, sour cream (anything dip-able!)...label "GLUTEN FREE ONLY" and then label the other one as "other" or something to identify it clearly as having potential crumbs.

Get lots of cooking utensils--this way, if something gluteny is being cooked, you have enough spoons, spatulas, etc to keep one per pot (no dipping a contaminated spoon in gluten-free food)

we have a bread box that he keeps his bread in (so that its not laying out everywhere)

if he makes anything gluten-filled, he has to make it on a plate so that it can go in DW right away....and wipes down counter so there are no crumbs.

separate toasters

to make things easier, we buy a lot of things that are naturally gluten free---we'll buy a bbq sauce that is naturally gluten-free, so then we don't have to have two.

if he is making something gluten-filled, he has to wash his hands thoroughly if he is getting ice out (of the bin) so there are no crumbs (or he does it before he makes it)

no kissy kissy if he has had beer or other gluten sources...only kisses on the cheek til he brushes real well.

lots of wiping things down, cleaning, washing, etc just to be extra careful.

hope this helps and gives you some ideas. good luck!

kabowman Explorer

Oh, separate wooden cooking utensils - I came home and a neighbor boy, used one of my good wooden utensils to make his gluten filled soup with - I tried to use it, got really really sick and had to give it to good will. Hated to do that when I paid quite a bit for the handmade, cherry spatula.

penguin Community Regular

All gluten in my house is prepackaged in the form of Kraft dinners, cheerios, and saltine crackers. I don't keep bread in the house (we just don't use it) so that eliminates all the cc condiment issues. I also don't make anything or handle anything that isn't gluten-free. Since I do all the shopping, everything I buy is gluten-free.

DH has his own pot to make mac and cheese (rare) or oatmeal fudge (rare), and his own cooking utensils for that. He's not as good at keeping the cheerios contained as he used to be, but we're working on it. He's more or less gluten-free at home (with the exception of saltines and cheerios) because it's easier. If he wants gluten, he can eat it at work or at a restaurant.

It's a family disease, and everyone in the house needs to help out to keep the celiac healthy.

Nantzie Collaborator

I do a lot of the above, but here's how I handle kitchen towels. I have two hooks above my kitchen sink. One is for the gluten-free hand towel, and one is for the gluten-free dishrag. There is a gluteny hand towel on the counter on the other side of the sink if anyone needs it. I also keep a ton of dish towels and dish rags, so that if I or anyone else accidentally contaminates one of them, we can just quickly throw the cc'd one in the hamper and put out a new one.

I also take out a clean plate to put my cooking utensils on while I'm cooking. That way, I don't have to worry about having a clean place on the counter to put my cooking spoons and such. We have tile counters (stupid grout...) and so I don't entirely trust my counters to be gluten-free. Nothing ever just gets put on the counters. I use a plate or paper towel to create clean a surface, depending on what I'm doing.

Nancy


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



Celiac.com Sponsor (A8-M):



NoGluGirl Contributor
I do a lot of the above, but here's how I handle kitchen towels. I have two hooks above my kitchen sink. One is for the gluten-free hand towel, and one is for the gluten-free dishrag. There is a gluteny hand towel on the counter on the other side of the sink if anyone needs it. I also keep a ton of dish towels and dish rags, so that if I or anyone else accidentally contaminates one of them, we can just quickly throw the cc'd one in the hamper and put out a new one.

I also take out a clean plate to put my cooking utensils on while I'm cooking. That way, I don't have to worry about having a clean place on the counter to put my cooking spoons and such. We have tile counters (stupid grout...) and so I don't entirely trust my counters to be gluten-free. Nothing ever just gets put on the counters. I use a plate or paper towel to create clean a surface, depending on what I'm doing.

Nancy

Dear Nantzie,

I am so glad you all posted these tips! I am gluten - free but my parents are not. I am constantly worrying about being glutened. I use the same pans as they do, and now realize that needs to stop. My dad is more understanding about it than my mother. They don't either understand that there are so many precautions you need to take. The reflux I get is so bad, it is just not tolerable. I need to make sure everything is safe from now on. This may be why the reflux did not go away completely yet. I was doing so much better, then it started up again. I know what you mean with the bloating. I have had a very hard time with that. I get reflux and stomach cramping, and feeling out of it all the time when I have gluten. Again, thank you for your tips.

Sincerely,

NoGluGirl

mythreesuns Contributor

Thanks so much, everybody!!

I did get my own cookie sheets and utensils, but I haven't used them yet because I can't figure out how to store them properly.

I use stainless-steel pots, and I don't put them or the cooking utensils in the dishwasher anymore, I hand wash them. Is that sufficient? Although, I don't have a strictly gluten-free washrag, so that will change as soon as I get home. LOL

I stay far away from the towels, as it is just too hard to figure out what's really on them. I wash my hands frequently in the kitchen these days, and I use only paper towels.

I do have a "safe zone" on my counter, but it's hard to keep gluten-free, so I scrub it, wipe it, and wipe it with a paper towel before I use it (which means putting my gluten-free cutting board on it).

I did get my own toaster. I have my own shelf in the pantry, too. I have my own butter and peanut butter, but I suspect I'll need my own jelly as well. Everything else is a squirt bottle, so assuming no one touches their food with the bottle I'm safe, right?

Thanks again for all the tips! With the kids using the kitchen, I can't rely on anyone else to keep my stuff clean.

Nantzie Collaborator

I have a plastic bin that I put on a higher shelf where I put my cooking untensils and stuff. I also have a small cutting board up there

I definitely recommend going with a dishrag rather than a sponge. You can wash it if it gets contaminated, and you're all set again. Once someone accidentally uses your gluten-free sponge on a gluten thing, there's no way to get all that stuff out of those little sponge holes.

I use a lot of paper towels too. A few months ago someone on the board thought to contact Bounty (I think...) and ask whether their paper towels were gluten-free, and it turns out the glue that they use to put the paper towels on the cardboard roll has some gluten in it and they said that it might effect the last few towels on the roll. So when I get down to the last several on the roll, I just transition that roll to the bathroom and use the rest of the roll for cleaning in there. I've never had a problem with the rest of the roll. I use Viva, not Bounty, but I'm guessing the possibility is the same with all brands.

For jelly, I use Welch's grape, which comes in a squeeze bottle. Even if you don't like that brand/flavor, you could always have your kids use it, then clean it out really well, relabel it, and reuse it to keep your gluten-free jelly in.

Nancy

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. - trents replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    2. - cristiana replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    3. - trents replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    4. - knitty kitty replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    5. - knitty kitty replied to kevert93's topic in Gluten-Free Foods, Products, Shopping & Medications
      4

      Having issues with chips

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      134,185
    • Most Online (within 30 mins)
      10,442

    Dennis E. Schertz
    Newest Member
    Dennis E. Schertz
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Cristiana asks a very relevant question. What looks normal to the naked eye may not look normal under the microscope.
    • cristiana
      Hello @CC90 Can I just ask a question: have you actually been told that your biopsy were normal, or just that your stomach, duodenum and small intestine looked normal? The reason I ask is that when I had my endoscopy, I was told everything looked normal.  My TTG score was completely through the roof at the time, greater than 100 which was then the cut off max. for my local lab.  Yet when my biopsy results came back, I was told I was stage 3 on the Marsh scale.  I've come across the same thing with at least one other person on this forum who was told everything looked normal, but the report was not talking about the actual biopsy samples, which had to be looked at through a microscope and came back abnormal.
    • trents
      My bad. I should have reread your first post as for some reason I was thinking your TTG was within normal range. While we are talking about celiac antibody blood work, you might not realize that there is not yet an industry standard rating scale in use for those blood tests so just having a raw number with out the reference scale can be less than helpful, especially when the test results are marginal. But a result of 87.4 is probably out of the normal range and into the positive range for any lab's scale. But back to the question of why your endoscopy/biopsy didn't show damage despite significantly positive TTG. Because they took the trouble to take seven samples, it is not likely they missed damage because of it being patchy. The other possibility is that there hasn't been time for the damage to show up. How long have you been experiencing the symptoms you describe in your first post? Having said all that, there are other medical conditions that can cause elevated TTG-IGA values and sometimes they are transient issues. I think it would be wise to ask for another TTG-IGA before the repeat endoscopy to see if it is still high.  Knitty kitty's suggestion of getting genetic testing done is also something to think about. About 35% of the general population will have one or both genes that are markers for the potential to develop active celiac disease but only about 1% of the population actually develop celiac disease. So, having a celiac potential gene cannot be used to definitively diagnose celiac disease but it can be realistically used to rule it out if you don't have either of the genes. If your symptoms persist, and all testing is complete and the follow-up endoscopy/biopsy still shows no damage, you should consider trialing a gluten free diet for a few months to see if symptoms improve. If not celiac disease, you could have NCGS (Non Celiac Gluten Sensitivity). 
    • knitty kitty
      @CC90, Your Lansoprazole is a proton pump inhibitor and has immunosuppressive effects!!!!  This is why your endoscopy didn't show much damage to the intestinal lining!!  The Lansolprazole is suppressing tTg IgA antibodies in the intestines, but those antibodies are getting into the blood stream and causing inflammation and damage in other organs.   Proton pump inhibitors cause intestinal damage in the long run.  If you get off the Lansoprazole for a few months so your immune system is not blocked, then do a gluten challenge, and an endoscopy, THEN they would see intestinal damage. Sheesh!  Doctors can be so ignorant.  I've seen this so many times it's frustrating! Take the B Complex and Benfotiamine.  Get off the Lansoprazole.  Go with the DNA test results.   Welcome to the tribe! P.S. B vitamins are needed to correct anemia!  Not just iron.  
    • knitty kitty
      Hi, @kevert93, Those Gluten Assist enzymes digest carbohydrates, not just gluten specifically.  Eating a high carbohydrate meal can deplete Thiamine Vitamin B 1 causing digestive symptoms like you describe.  You could also be having difficulty digesting the oils used in those chips.  Thiamine in the form Benfotiamine can help. We need the eight B vitamins to digest our food, carbs, fats and proteins.  Poor digestion can cause symptoms like vomiting and stomach pain, brain fog, headaches, exhaustion.  Try taking a B Complex with the activated forms of the B vitamins (Life Extension's Bioactive B Complex is great!) and additional Benfotiamine.  The B vitamins are used to make digestive enzymes and will allow your digestive system to function properly.  The B vitamins also will improve headaches, exhaustion, and brain function.  Taking Thiamine in the form Benfotiamine will improve digestive symptoms and lower inflammation, too.  Benfotiamine and the B vitamins are safe.  The B vitamins are chemical compounds found in whole foods, not in highly processed foods like chips.   The body cannot make the B vitamins, so supplementing is beneficial.  Benfotiamine is safe and nontoxic even in high doses.
×
×
  • Create New...