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. - knitty kitty replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    2. - Jane02 replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    3. - knitty kitty replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    4. 0

      Penobscot Bay, Maine: Nurturing Gluten-Free Wellness Retreat with expert celiac dietitian, Melinda Dennis

    5. - Scott Adams replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

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

    • Total Members
      133,335
    • Most Online (within 30 mins)
      7,748

    johnfreirefr
    Newest Member
    johnfreirefr
    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

    • knitty kitty
      @Jane02, I hear you about the kale and collard greens.  I don't do dairy and must eat green leafies, too, to get sufficient calcium.  I must be very careful because some calcium supplements are made from ground up crustacean shells.  When I was deficient in Vitamin D, I took high doses of Vitamin D to correct the deficiency quickly.  This is safe and nontoxic.  Vitamin D level should be above 70 nmol/L.  Lifeguards and indigenous Pacific Islanders typically have levels between 80-100 nmol/L.   Levels lower than this are based on amount needed to prevent disease like rickets and osteomalacia. We need more thiamine when we're physically ill, emotionally and mentally stressed, and if we exercise like an athlete or laborer.  We need more thiamine if we eat a diet high in simple carbohydrates.  For every 500 kcal of carbohydrates, we need 500-1000 mg more of thiamine to process the carbs into energy.  If there's insufficient thiamine the carbs get stored as fat.  Again, recommended levels set for thiamine are based on minimum amounts needed to prevent disease.  This is often not adequate for optimum health, nor sufficient for people with absorption problems such as Celiac disease.  Gluten free processed foods are not enriched with vitamins like their gluten containing counterparts.  Adding a B Complex and additional thiamine improves health for Celiacs.  Thiamine is safe and nontoxic even in high doses.  Thiamine helps the mitochondria in cells to function.  Thiamine interacts with each of the other B vitamins.  They are all water soluble and easily excreted if not needed. Interesting Reading: Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/ Safety and effectiveness of vitamin D mega-dose: A systematic review https://pubmed.ncbi.nlm.nih.gov/34857184/ High dose dietary vitamin D allocates surplus calories to muscle and growth instead of fat via modulation of myostatin and leptin signaling https://pubmed.ncbi.nlm.nih.gov/38766160/ Safety of High-Dose Vitamin D Supplementation: Secondary Analysis of a Randomized Controlled Trial https://pubmed.ncbi.nlm.nih.gov/31746327/ Vitamins and Celiac Disease: Beyond Vitamin D https://pmc.ncbi.nlm.nih.gov/articles/PMC11857425/ Investigating the therapeutic potential of tryptophan and vitamin A in modulating immune responses in celiac disease: an experimental study https://pubmed.ncbi.nlm.nih.gov/40178602/ Investigating the Impact of Vitamin A and Amino Acids on Immune Responses in Celiac Disease Patients https://pmc.ncbi.nlm.nih.gov/articles/PMC10814138/
    • Jane02
      Thank you so much @knitty kitty for this insightful information! I would have never considered fractionated coconut oil to be a potential source of GI upset. I will consider all the info you shared. Very interesting about the Thiamine deficiency.  I've tracked daily averages of my intake in a nutrition software. The only nutrient I can't consistently meet from my diet is vitamin D. Calcium is a hit and miss as I rely on vegetables, dark leafy greens as a major source, for my calcium intake. I'm able to meet it when I either eat or juice a bundle of kale or collard greens daily haha. My thiamine intake is roughly 120% of my needs, although I do recognize that I may not be absorbing all of these nutrients consistently with intermittent unintentional exposures to gluten.  My vitamin A intake is roughly 900% (~6400 mcg/d) of my needs as I eat a lot of sweet potato, although since it's plant-derived vitamin A (beta-carotene) apparently it's not likely to cause toxicity.  Thanks again! 
    • knitty kitty
      Hello, @Jane02,  I take Naturewise D 3.  It contains olive oil.   Some Vitamin D supplements, like D Drops, are made with fractionated coconut oil which can cause digestive upsets.  Fractionated coconut oil is not the same as coconut oil used for cooking.  Fractionated coconut oil has been treated for longer shelf life, so it won't go bad in the jar, and thus may be irritating to the digestive system. I avoid supplements made with soy because many people with Celiac Disease also react to soy.  Mixed tocopherols, an ingredient in Thornes Vitamin D, may be sourced from soy oil.  Kirkland's has soy on its ingredient list. I avoid things that might contain or be exposed to crustaceans, like Metagenics says on its label.  I have a crustacean/shellfish/fish allergy.  I like Life Extension Bioactive Complete B Complex.  I take additional Thiamine B 1 in the form Benfotiamine which helps the intestines heal, Life Extension MegaBenfotiamine. Thiamine is needed to activate Vitamin D.   Low thiamine can make one feel like they are getting glutened after a meal containing lots of simple carbohydrates like white rice, or processed gluten free foods like cookies and pasta.   It's rare to have a single vitamin deficiency.  The water soluble B Complex vitamins should be supplemented together with additional Thiamine in the form Benfotiamine and Thiamine TTFD (tetrahydrofurfuryl disulfide) to correct subclinical deficiencies that don't show up on blood tests.  These are subclinical deficiencies within organs and tissues.  Blood is a transportation system.  The body will deplete tissues and organs in order to keep a supply of thiamine in the bloodstream going to the brain and heart.   If you're low in Vitamin D, you may well be low in other fat soluble vitamins like Vitamin A and Vitamin K. Have you seen a dietician?
    • Scott Adams
      I do not know this, but since they are labelled gluten-free, and are not really a product that could easily be contaminated when making them (there would be not flour in the air of such a facility, for example), I don't really see contamination as something to be concerned about for this type of product. 
    • trents
×
×
  • 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.