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

Question About Kitchen


KimmyJ

Recommended Posts

KimmyJ Rookie

So I'm fairly new here - only dx about three months ago and I've been fairly successful at eliminating the big sources of gluten in my diet. So now I'm working on the less obvious stuff and I'm wondering what utensils/kitchen things I need to replace to prevent contamination from before I went gluten-free. Thanks in advance for the help!


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



Celiac.com Sponsor (A8-M):



NorthernElf Enthusiast

I have my own mayonaise, Becel margarine, etc. in the fridge since other dip their knives in and spread things on wheat bread and then "redip". Squeezables are another way to go - if it was just me & DH I would buy those (but I have 3 kids). So...I bought a small margarine and wrote "MOM" on it in permanent marker, I just refill it as I get a new larger one (that the family uses), cleaning it out once in awhile. When I buy a new peanut butter or jam or whatever I scoop out a bunch into a smaller container and write "MOM" on that too (or gluten-free). I have my own shelf in the pantry that has my gluten-free stuff on it too - I tend to put crackers in containers and write gluten-free on them too ! I also buy large packs of Mesa Sunrise cereal, Riceworks chips, etc. and repackage them - the chips & crackers in sandwich size ziplocs so I can take them to work. When I bake my stuff I package everything in sandwich bags and when I do wheat baking once in awhile I use the largest size freezer bags - everyone knows that stuff in small ziplocs is mine.

For bakeware I have my own silicone baking stuff - loaf pan, large & small muffin tin, and a silicone sheet to place on the regular cookie sheets. All my regular bakeware is nonstick (teflon) and that holds gluten. My stuff stands out since none of the 'regular' stuff is silicone. I have my own toaster, my own cutting boards, and my own nonstick fry pan - all is stored/placed in my corner of the kitchen.

I gotta tell you I fought this for awhile. I figured I could just eat gluten-free and not worry about bakeware if I washed it. However, I seemed to get more & more sensitive to gluten and finally had to change the bakeware too. When I bake my stuff I use the metal bowls, not the plastic ones. Oh, & I just bought my own silicone strainer since the holes are hard to clean.

Some of my current favs to bake - Kinnikinnick sunflower/flax seed bread mix (so good fresh I have to beat my family away!), Gluten Free Pantry truffle brownie mix, gluten-free chocolate chip cookies from recipezaar.com (I add ground flaxseed & psyllium husks), sorghum scones off the sorghum flour bag (Bob's Redmill - I add dried cranberries & chopped walnuts)...and that's it for now ! I don't like store bought cookies & such - homemade is always better.

cruelshoes Enthusiast
So I'm fairly new here - only dx about three months ago and I've been fairly successful at eliminating the big sources of gluten in my diet. So now I'm working on the less obvious stuff and I'm wondering what utensils/kitchen things I need to replace to prevent contamination from before I went gluten-free. Thanks in advance for the help!

We replaced anything porous or anything that had grooves or scratches that gluten could get wedged in. This includes: wooden spoons, cutting boards, colander, teflon pans, cake pans, cookie sheets. Also, think about anything that has multiple pieces, like a spatula thats head fits onto a handle made of a different material. Gluten canget into the groove where the 2 parts come together.

Think of anything your food will touch. If there is no way to imerse it in water and get it as clean as the day you bought it, I would replace it. A toaster is a good example. There is just no way to get all the crumbs out of it without ruining it. Same for a bread maker.

Hope this helps.

Gwen B Rookie
We replaced anything porous or anything that had grooves or scratches that gluten could get wedged in. This includes: wooden spoons, cutting boards, colander, teflon pans, cake pans, cookie sheets. Also, think about anything that has multiple pieces, like a spatula thats head fits onto a handle made of a different material. Gluten canget into the groove where the 2 parts come together.

Think of anything your food will touch. If there is no way to imerse it in water and get it as clean as the day you bought it, I would replace it. A toaster is a good example. There is just no way to get all the crumbs out of it without ruining it. Same for a bread maker

Hope this helps.

Surely not. My husband is rolling his eyes like I have become parraonoid about CC. However after feeling better the first month but this last week I have been plagued with less definitive but still uncomfortable stomach gas and bloating. I don't know why but maybe it is all the home cooking we have been doing. I still strain my gluten-free pasta in the same drainer as everyone elses (clean). We do have new anodized steel pans. Are they gluten-free friendly? How about wooden spoons?

Jestgar Rising Star
Surely not. My husband is rolling his eyes like I have become parraonoid about CC. However after feeling better the first month but this last week I have been plagued with less definitive but still uncomfortable stomach gas and bloating. I don't know why but maybe it is all the home cooking we have been doing. I still strain my gluten-free pasta in the same drainer as everyone elses (clean). We do have new anodized steel pans. Are they gluten-free friendly? How about wooden spoons?

NEW STRAINER!!!!

You cook gluten onto it every time you dump hot pasta into it!

Gwen B Rookie
NEW STRAINER!!!!

You cook gluten onto it every time you dump hot pasta into it!

OOPs! :huh:

I guess I'll get new boards and spoons too. This is just such a pain convincing my family to comply and I don't even know for sure if I have celiac. Many indicators point that way- family history, deteriorating gastirc issues, feeling better on this Gluten-free Casein-free diet but then I had a weird restaurant allergy incident (severe hives) and tested posative for soy (skin test). My Dr doesn't believe I have a problem(because I tested negative 18 months ago on a single tTg, my husband thinks it's just soy because that's what I've been tested (scientific type)for.

I just wanted to try going gluten-free for a while to see if it fixed me and maybe do a challenge to prove it. After the hives I am more wary but I don't see a choice.

Sorry this is too long a whine :(:(

this site is such a mine of information. thanks for all help!

kbtoyssni Contributor

New wooden spoons, too! Wood is one of the things I would absolutely replace along with the toaster. Other baking items are more of a judgment call.


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



Celiac.com Sponsor (A8-M):



Gwen B Rookie
New wooden spoons, too! Wood is one of the things I would absolutely replace along with the toaster. Other baking items are more of a judgment call.

Got a new toaster in Rite Aid yesterday for just $8.88! Bargain!

  • 10 months later...
imagine22 Contributor

I use a new toaster and have separate jams and butters etc. I only bake gluten free so I just thoroughly washed my existing baking goods etc.

I would throw out wooden spoons, chopping boards etc with cracks anyway as they are not hygienic :)

I use the same pots, pans and pasta strainer i use for gluten I just wash well each time and havent had any issues. (I have coeliac disease and have had repeated blood tests show Im back to normal range again)

Sinenox Apprentice

I may be really sensitive but I didn't get over the continuous low-level "yuck" feeling until I gave in to replacing everything and using exclusively my own new stuff - including non-scratched and non-porous materials such as baking sheets, plates and cutlery, plastic tupperware, etc. Just my two-cents.

aliciatakescare Newbie

I too have tried eating just gluten-free and using common cooking/eating stuff - since going to using only metal and glass prep/cook/bake kitchen stuff with my own new plastic/wood utensils I am finally starting to feel much better and have not had any symptoms for about a week (switched these things about 3 wks ago). I haven't replaced the toaster yet, but I don't have bread right now either - I bake my own in a new bread maker and just haven't made any in quite some time. I have my own cupboards (labeled gluten-free) with my kitchenware and food. I also have my own section in the deep freeze, regular freezer and fridge which are labeled as well. I keep all my condiments seperate as well (even the squeeze ones) because I am a single parent of 3 teens that get pretty messy when fixing their food.

This is definitely a challenging disease we have, but to me it is worth whatever it takes to stay healthy. I got glutened about 3 weeks ago (give or take) and not sure from what still, BUT it sent me to the ER once again and I was severely ill for almost a week before starting to feel the peace of healing. The research I have done has supported the thought that gluten intollerence gets worse with each and every glutening. Just my advice: Watch yourself very closely as my doctor told me that celiac disease is just as dangerous as any severe allergy and that I should take all precautions that I can. Best wishes!

mommaofthree Newbie
I too have tried eating just gluten-free and using common cooking/eating stuff - since going to using only metal and glass prep/cook/bake kitchen stuff with my own new plastic/wood utensils I am finally starting to feel much better and have not had any symptoms for about a week (switched these things about 3 wks ago). I haven't replaced the toaster yet, but I don't have bread right now either - I bake my own in a new bread maker and just haven't made any in quite some time. I have my own cupboards (labeled gluten-free) with my kitchenware and food. I also have my own section in the deep freeze, regular freezer and fridge which are labeled as well. I keep all my condiments seperate as well (even the squeeze ones) because I am a single parent of 3 teens that get pretty messy when fixing their food.

This is definitely a challenging disease we have, but to me it is worth whatever it takes to stay healthy. I got glutened about 3 weeks ago (give or take) and not sure from what still, BUT it sent me to the ER once again and I was severely ill for almost a week before starting to feel the peace of healing. The research I have done has supported the thought that gluten intollerence gets worse with each and every glutening. Just my advice: Watch yourself very closely as my doctor told me that celiac disease is just as dangerous as any severe allergy and that I should take all precautions that I can. Best wishes!

What about Silverware??? Does it matter that I run all of my baking pans and plates, etc through a VERY HOT dishwasher??? I was just dx 8 days ago and I am way in over my head!! However I have been feeling much better since I changed my diet, but I am a mom of 3 young children and don't want to take away their food either. How do you make part of your kitchen gluten free and the other part not? Any ideas?

Thanks

aliciatakescare Newbie

I washed the dishwasher with nothing in it twice and now I thoroughly rinse all dishes and then put them in the dishwasher together, except wood and plastic. I run it on pots and pans, high heat and always use an extra rinse cycle. I have 1 counter in the kitchen that holds all my gluten-free appliances (breadmaker, steamer, indoor grill and coffee pot), well marked areas in the fridge and freezers and then i have 1 cupboard that is gluten-free for food and 1 for my cutting board, storage, etc. I also have started cooking all my food first and puting it in the oven to keep warm while I cook the food for the kids. When my boyfriend is here, he usually helps in the kitchen and does the prep part of the regular food. It works very well for us.

wschmucks Contributor

If you do not have a dish washer I would just have your own seperate plates/ utencils that are washed with a different spounge.

I didnt start feeling better until i did this-- just imagine the gluten being washed on the spounge staying there and then you eating everything off that plate. Even if it was rinsed with water...I still think it would be contaminated. I might be crazy-- but I honestly did not start to feel better until i completely segreated all of my kitchen utencils, plates, bowls, cups, pans etc. Just not worth even having doubts-- better safe than sorry.

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. - asaT replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      nothing has changed

    2. - nanny marley replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

    3. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      45

      Supplements for those Diagnosed with Celiac Disease

    4. - par18 replied to Woodster991's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      9

      Is it gluten?

    5. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

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

    • Total Members
      133,342
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      Scott, I am mostly asymptomatic. I was diagnosed based on high antibodies, low ferritin (3) and low vitamin D (10). I wasn't able to get in for the biopsy until 3 months after the blood test came back. I was supposed to keep eating gluten during this time. Well why would I continue doing something that I know to be harmful for 3 more months to just get this test? So I did quit gluten and had the biopsy. It was negative for celiacs. I continued gluten free with iron supps and my ferritin came back up to a reasonable, but not great level of around 30-35.  Could there be something else going on? Is there any reason why my antibodies would be high (>80) with a negative biopsy? could me intestines have healed that quickly (3 months)?  I'm having a hard time staying gluten free because I am asymptomatic and i'm wondering about that biopsy. I do have the celiacs gene, and all of the antibody tests have always come back high. I recently had them tested again. Still very high. I am gluten free mostly, but not totally. I will occasionally eat something with gluten, but try to keep to a minimum. It's really hard when the immediate consequences are nil.  with high antibodies, the gene, but a negative biopsy (after 3 months strict gluten-free), do i really have celiacs? please say no. lol. i think i know the answer.  Asa
    • nanny marley
      I have had a long year of testing unfortunately still not diagnosed , although one thing they definitely agree I'm gluten intolerant, the thing for me I have severe back troubles they wouldnt perform the tests and I couldn't have a full MRI because I'm allergic to the solution , we tryed believe me  I tryed lol , another was to have another blood test after consuming gluten but it makes me so bad I tryed it for only a week, and because I have a trapped sciatic nerve when I get bad bowels it sets that off terribly so I just take it on myself now , I eat a gluten free diet , I'm the best I've ever been , and if I slip I know it so for me i have my own diagnosis  and I act accordingly, sometimes it's not so straight forward for some of us , for the first time in years I can plan to go out , and I have been absorbing my food better , running to the toilet has become occasionally now instead of all the time , i hope you find a solution 🤗
    • asaT
      I was undiagnosed for decades. My ferritin when checked in 2003 was 3. It never went above 10 in the next 20 years. I was just told to "take iron". I finally requested the TTgIgA test in 2023 when I was well and truly done with the chronic fatigue and feeling awful. My numbers were off the charts on the whole panel.  they offered me an endoscopic biopsy 3 months later, but that i would need to continue eating gluten for it to be accurate. so i quit eating gluten and my intestine had healed by the time i had the biopsy (i'm guessing??). Why else would my TTgIgA be so high if not celiacs? Anyway, your ferritin will rise as your intestine heals and take HEME iron (brand 4 arrows). I took 20mg of this with vitamin c and lactoferrin and my ferritin went up, now sits around 35.  you will feel dramatically better getting your ferritin up, and you can do it orally with the right supplements. I wouldn't get an infusion, you will get as good or better results taking heme iron/vc/lf.  
    • par18
      Scott, I agree with everything you said except the term "false negative". It should be a "true negative" just plain negative. I actually looked up true/false negative/positive as it pertains to testing. The term "false negative" would be correct if you are positive (have anti-bodies) and the test did not pick them up. That would be a problem with the "test" itself. If you were gluten-free and got tested, you more than likely would test "true" negative or just negative. This means that the gluten-free diet is working and no anti-bodies should be present. I know it sounds confusing and if you don't agree feel free to respond. 
    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
×
×
  • 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.