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


mamaloca2

Recommended Posts

mamaloca2 Apprentice

I am new to all of this. I self-diagnosed about a month ago and I have been getting progressively better but not completely. I have occasional bouts of diarrhea which I didn't have before, and my cracked lips will almost completely heal and then get worse again for a couple days. I am pretty sure I am getting gluttened by not sure how. I try to use separate peanut butter jars, ect...but don't have separate pots and pans. Do I really need to go to that length? You would think the heat would destroy any leftover gluten protein...but I don't know. I guess what I'm asking is, could my diarrhea and persistent dry lips be a sign I am not completely gluten free, or could something else be the cause? I have heard people talk about casin sensitivity also. How do you know if you have a problem with that?


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



Celiac.com Sponsor (A8-M):



Nantzie Collaborator

Yes, you need seperate pots and pans. If you have stainless steel ones, you should be able to clean them very, very, VERY well and use them. You also need a new cutting board, new wooden spoons if you use them, sometimes new plastic utensils and plates if they're really scratched up, a new strainer, etc.

Heat does not kill gluten. It is not a living thing, so can't be killed. Gluten is a protein, not a bacteria or virus. Imagine you were allergic to strawberries for example. You could cook them for hours and they wouldn't change - they'd still be strawberries.

Gluten is also very sticky (remember making paste out of flour and water as a kid?) and will stick into every little scratch and crevice it can.

The way someone explained it to me when I first started was to think of it like raw chicken. We all know about raw chicken and cross contamination. Anything the chicken touches and anything you touch with chickeny fingers has to be washed. Just think of gluten the same way.

Other things you need to check are your personal care products. Shampoos, haircare products, lotions, makeup, lip balm, nail polish.

Also, if your husband or boyfriend eats gluten or drinks beer, you will get glutened by kissing. If he brushes his teeth really well it's fine, and if it's been a few hours it's fine. My husband sometimes has gluten for lunch, but by the time he gets home from work it's been long enough that I don't make him go brush his teeth. :)

Hope that helps. Don't worry. You'll get the hang of it.

I'm glad you're feeling better.

Nancy

jambo massive Apprentice
Yes, you need seperate pots and pans. If you have stainless steel ones, you should be able to clean them very, very, VERY well and use them. You also need a new cutting board, new wooden spoons if you use them, sometimes new plastic utensils and plates if they're really scratched up, a new strainer, etc.

Heat does not kill gluten. It is not a living thing, so can't be killed. Gluten is a protein, not a bacteria or virus. Imagine you were allergic to strawberries for example. You could cook them for hours and they wouldn't change - they'd still be strawberries.

Gluten is also very sticky (remember making paste out of flour and water as a kid?) and will stick into every little scratch and crevice it can.

The way someone explained it to me when I first started was to think of it like raw chicken. We all know about raw chicken and cross contamination. Anything the chicken touches and anything you touch with chickeny fingers has to be washed. Just think of gluten the same way.

Other things you need to check are your personal care products. Shampoos, haircare products, lotions, makeup, lip balm, nail polish.

Also, if your husband or boyfriend eats gluten or drinks beer, you will get glutened by kissing. If he brushes his teeth really well it's fine, and if it's been a few hours it's fine. My husband sometimes has gluten for lunch, but by the time he gets home from work it's been long enough that I don't make him go brush his teeth. :)

Hope that helps. Don't worry. You'll get the hang of it.

I'm glad you're feeling better.

Nancy

oh my god just read your advice i never knew cross contam was that bad, is that just for people that get really bad symptems or everybody??

nikki-uk Enthusiast
oh my god just read your advice i never knew cross contam was that bad, is that just for people that get really bad symptems or everybody??

Afraid it is for all coeliacs !

Oh - and a separate toaster IS A MUST!!

Nantzie Collaborator

Yep. Everybody as far as I've ever seen. I don't even have official celiac (borderline blood test, negative biopsy) and I have to be very careful about all that stuff.

There are people who choose not to guard against second-hand gluten (cross contamination), but they usually have never tried it. I would compare it to getting a really bad flu (life during undiagnosis), then there's that day where you start feeling better and aren't throwing up and in the bathroom all the time (stopping eating obvious gluten) and can go to work. But then theres that week or so where you're still not feeling right, tired, sneezy, coughy, can't sleep well.

Just stopping at not eating the obvious gluten is like living your life in the time after the flu where you're still sick. But calling it healthy. Yes, it's way better than the worst of the flu, but you're still sick.

If you've got a diagnosis in hand and you KNOW for sure your villi are trashed, it's especially important to guard against second-hand gluten because your intestines won't heal if you're getting gluten. Even in minute amounts.

If you're self-diagnosed like so many people here are, and you're not sure if the damage was just not caught by the tests (very common), or you may have one of the other forms of gluten problems that doesn't create villi damage, in my opinion, you STILL should guard against all cross contamination.

Like I mentioned, I was self-diagnosed and had negative tests. But I had almost all of the lovely classic celiac symptoms, as well as neurological symptoms to the point I could barely walk and daily headaches. I was pretty much house-bound.

At first, I figured since my tests came back negative, I wouldn't have to worry about second-hand gluten, but I have found that the opposite is the case. I'm just as sensitive to it as someone with an official diagnosis.

That's why I always encourage people, even if they're not sure or don't believe it could be a problem, to at least TRY it. It's really something that you have to experience on your own.

To be honest, when I was first learning, I figured there were some people who were very sensitive, but that most people were just being paranoid. Little did I know... :lol: If I hadn't tried it for myself, I don't think I ever would have believed it.

Nancy

connole1056 Rookie

I disagree completely about using separate pans! I use a separate strainer/colander, but not pots and pans. Washing them well after using them with foods with gluten is all that is needed. It is weird to see the responses saying to get different pans beause NO ONE in the support groups where I live recommend that.

I do use different toasters for gluten-free and non-gluten-free foods though because it is very difficult to get every crumb out of a toaster. However, I do know some people who use a toaster oven instead of a toaster because clening the rack of the oven well is simple. I also use two bread makers for gluten-free and non-gluten-free foods. Basically, I think anything with small, hard to clean crevices may harbor gluten after being washed. Other than that it is fine to use the same pans. Obviously you shouldn't be taking the same utensils from pan to pan while cooking gluten-free and non-gluten-free food at the same time.

I do want to mention that if you think you actually do have celiac disease you should get a biopsy to know for sure. You could feel better going gluten-free, but what if you have a different condition that is not diagnosed and you do not know it because you are assuming it is celiac disease? You could be missing detection and treatment of something else.I advise you to get a biopsy to be safe. Then you will know the true story and whether or not you need to investigate further. There are many people on these boards who are self-diagnosed and do feel better after going gluten-free but I worry they may have another condition they do not know about. I know they feel they have made the correct diagnosis, but I would not trust anything but a biopsy. Plus this diet is SO restrictive and expensive I think it is ridiculous to follow it if you do not have to.

Also, you mentioned you have been following the diet for only one month. Some people do take a long time to be completely symptom free. Some lucky people see results almost immediately, but you may not be one of those people. So I advise you to get a proper diagnosis and then go from there. And GOOD LUCK!!

blueeyedmanda Community Regular
I disagree completely about using separate pans! I use a separate strainer/colander, but not pots and pans. Washing them well after using them with foods with gluten is all that is needed. It is weird to see the responses saying to get different pans beause NO ONE in the support groups where I live recommend that.

I do use different toasters for gluten-free and non-gluten-free foods though because it is very difficult to get every crumb out of a toaster. However, I do know some people who use a toaster oven instead of a toaster because clening the rack of the oven well is simple. I also use two bread makers for gluten-free and non-gluten-free foods. Basically, I think anything with small, hard to clean crevices may harbor gluten after being washed. Other than that it is fine to use the same pans. Obviously you shouldn't be taking the same utensils from pan to pan while cooking gluten-free and non-gluten-free food at the same time.

I do want to mention that if you think you actually do have celiac disease you should get a biopsy to know for sure. You could feel better going gluten-free, but what if you have a different condition that is not diagnosed and you do not know it because you are assuming it is celiac disease? You could be missing detection and treatment of something else.I advise you to get a biopsy to be safe. Then you will know the true story and whether or not you need to investigate further. There are many people on these boards who are self-diagnosed and do feel better after going gluten-free but I worry they may have another condition they do not know about. I know they feel they have made the correct diagnosis, but I would not trust anything but a biopsy. Plus this diet is SO restrictive and expensive I think it is ridiculous to follow it if you do not have to.

Also, you mentioned you have been following the diet for only one month. Some people do take a long time to be completely symptom free. Some lucky people see results almost immediately, but you may not be one of those people. So I advise you to get a proper diagnosis and then go from there. And GOOD LUCK!!

That's odd, my support group spoke very highly about seperate pots, pans, and other kitchen items.


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



Celiac.com Sponsor (A8-M):



nikki-uk Enthusiast
I disagree completely about using separate pans! I use a separate strainer/colander, but not pots and pans. Washing them well after using them with foods with gluten is all that is needed.

Yep, I do think it depends on your type of equipment.

My pots and pans are stainless steel - I hand wash them and then put them in the dishwasher & my 2 coeliacs have never had any problems.

Whereas plastic containers used in the microwave tend to get scratched and (IMO) could 'hold onto' gluten so my coeliacs use pyrex for that.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

    2. - TheDHhurts posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      need help understanding testing result for Naked Nutrition Creatine please

    3. - cristiana replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

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

    • Total Members
      133,107
    • Most Online (within 30 mins)
      7,748

    Maggie1349
    Newest Member
    Maggie1349
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      @cristiana,  I react the same way.  Dairy consumption flushes out my digestive system within an hour, too! As casein is digested, it forms casomorphins that bind to opioid receptors in our bodies.  This is similar to digested gluten peptides being able to attach to opioid receptors in our bodies.   We have opioid receptors throughout our bodies including lots in the digestive tract. Casein raises tTg IgA antibodies just like gluten consumption does, which leads to further intestinal damage and continuing inflammation.  No wonder our bodies react to it by pushing the "emergency evacuation" ejection seat button! The mother of my childhood friend was British and introduced me to drinking tea properly with milk or cream.  I miss it so much.  And chocolate ice cream.  Not worth the after effects, though.  I've found taking Omega Three supplements (flaxseed oil, sunflower seed oil, evening primrose oil) helps shake those dairy cravings.   Green leafy veggies like broccoli, kale, and greens (mustard, turnip, collards) are great sources of calcium.  Avoid spinach as it is high in oxalates that block calcium absorption and may cause kidney stones.  Yes, more leafy greens are needed to reach the same amount of calcium in a glass of milk, but the greens have other benefits, like increased dietary fiber and polyphenols that act as antioxidants, reduce inflammation, and promote health.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards.  The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.   Some people in remission report being able to consume gluten again without consequence.  Another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.  
    • TheDHhurts
      Hi, I bought Naked Nutrition Creatine. It lists itself as gluten free but is not certified. (It used to be, but they dropped it in the past year or two apparently.) I wrote the company and asked them what testing results they had for creatine and they sent me the attached, which says the test result for gluten is <0.025MCG. I'm used to seeing test results as ppm, so I'm not sure what <0.025MCG means. Can it be converted to ppm easily? I want to confirm that it is safe to use.
    • cristiana
      When I was still recovering my gastroenterologist suggested I bought lactofree product as I was very bloated.  So I bought some from the supermarket and from memory, I drank a nice big glass of milk - and it went right through me literally within an hour or so, if my memory serves correctly.  I came off dairy completely next and it worked like a charm, but started to reintroduce quite gradually it as I missed it! To this day, if I overdo dairy products, they work like a mild laxative.  I've never wanted to give up milk completely as I like it so much, and my mum had osteoporosis and it's an easy way of getting calcium.  But it doesn't really 'sit' well with me.   You may need to experiment a bit as when I was healing certain dairy products were worse than others - I could cope with one brand of Greek yoghurt, but I got extremely and painfully bloated with another brand of live British yoghurt.  
    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for you.  
×
×
  • 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.