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

Shared Kitchens: How do you label your kitchenware?


Pepper88

Recommended Posts

Pepper88 Explorer

Hi everyone. I share a kitchen with 3 other non-celiacs. I have my own storage cubbies and color code some of my things if possible.

I was also wondering how folks labeled their kitchenware - pots, pans, baking sheets, kitchen utensils, etc. I'm failing to think of a method that is heat and water resistant. I've thought about nail polish or sharpie marker but not sure if they would actually stick well. 

Has anyone else played around with this and care to share what has worked for them?

thank you!


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

Many say to buy them in a different color or put tape on the handle. You can buy casserole pans and enameled pots in a unique color also...baking sheets I guess you could engrave the lip? Parchment paper, foil lining and crackpot liners might be a extra precaution.....or set up a camp kitchen in another room so you have a dedicated place. IE induction cook top and pans, toaster oven combo, microwave, on a table, minifridge and bus bins to wash stuff in and dump in the tub,

I honestly just got all my own stuff and moved to my own dedicated living space, before that I used nordic ware microwave cookware and just kept my baking dishes separate in a different location...I did have 1 pot and a skillet get used for gluten food after...I honestly snapped after and bent the skillet in half after getting sick....no one used my stuff again.

Pepper88 Explorer

Yikes, I'd be SO angry if someone used my stuff. I just re-bought a whole kitchen set and would definitely be breaking things if I had to buy another. Unfortunately having my own kitchenette is not feasible at this point. I do have color coded utensils and did take your tape idea to tape up the rest of my stuff with the color green. Thanks Ennis ?

kareng Grand Master
20 hours ago, Pepper88 said:

Yikes, I'd be SO angry if someone used my stuff. I just re-bought a whole kitchen set and would definitely be breaking things if I had to buy another. Unfortunately having my own kitchenette is not feasible at this point. I do have color coded utensils and did take your tape idea to tape up the rest of my stuff with the color green. Thanks Ennis ?

I mostly just kept an eye on my cookie sheets/ oven stuff & put away as soon as possible.   I may have used nail polish on the edge of a cookie sheet at the beginning.  

There are paints you can get at the hobby store that you bake on coffee cups or glass.  Might work for a cookie sheet?  

Jenny8413 Rookie

When I tried a "shared kitchen" with my husband, we kept entirely separate areas to store items and I bought red colored cooking utensils etc.  Orange duct tape went on food jars etc.  But I realized that my husband was transporting gluten everywhere, setting items in his crumbs and then setting them on my cutting boards and on my areas in the fridge.  Also visitors were using the gluten sponge when cleaning shared glass bowls and leaving sticky stuff in them (so I was always re-washing shared items before using them and my hands were cracking from so much washing), and when I wasn't home who knows where the gluten was ending up.  So now we are trying 100% gluten free, and I am 1000% more relaxed without worry (or cracked hands).  If sharing a space, I hope you can block off dedicated free space for all of your items and put a big red ribbon on it to remind gluten'ers to stay out.  I'd want my own mini-fridge because I know no one else is careful enough to prevent cross contamination here.  

Pepper88 Explorer

Thanks for the suggestions folks. I may look up the baked on paint if the tape doesn't hold up. Duct tape sounds like a good idea - right now I'm using packing tape over green mascing tape.

I totally resonate. I find myself rewashing things excessively and washing/ drying/ putting away all my things immediately after eating. I do have my own cupboards that are clearly marked. All that said and done I'm still anxious. I've been training my partner to rewash cutlery before dipping into our shared spreads and dips (and to not double dip of course etc) He finds it a chore but is trying. 

Thats great that your husband is  going gluten-free with you. Ideal situation for sure!

notme Experienced

my kitchen is 99% gluten free.  I keep spaghettios and some gluten snacks for the kids, lunchables, etc.  but the gluten-free is enforced - wash your hands after you eat gluten!!  husband has regular rye bread, but we make his sammiches for lunch together and he touches the bread and I throw lunch meat at it ha ha 

all my cookware is stainless except I keep a Teflon frying pan he can do whatever he wants with.  he also gets his own strainer and colander and cutting board.  when I go out of town, he makes himself a big ole pot of regular gluten spaghetti and puts it in freezer boxes.  I never get sick, so he must be cleaning everything up very well.  I am super lucky he is so on board with the whole thing but he saw how sick I was before I was diagnosed.  he thought (and I did too!) I had cancer or something.  it was starving me to death!  keeping my food and kitchen safe and clean is a small change and thank goodness for that  :) 


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



Celiac.com Sponsor (A8-M):



Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,127
    • Most Online (within 30 mins)
      7,748

    Steve715
    Newest Member
    Steve715
    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

    • knitty kitty
      Just wanted to add that checking B12 and Vitamin D only is not going to give an accurate picture of vitamin deficiencies.   B12 Cobalamine needs the seven other B vitamins to work properly.   You can have vitamin deficiency symptoms before the B12 blood level changes to show deficiency.  You can have "normal" B12, but have deficiencies in other B vitamins like Thiamine and Niacin, for which there are no accurate tests. Take a B Complex supplement with all the B vitamins.  Take additional Thiamine B 1 in the form Benfotiamine which has been shown to promote intestinal healing.  Thiamine Mononitrate found in most vitamin supplements is not easy for the body to utilize.  What makes thiamine mononitrate not break down on the shelf also makes it hard for the body to absorb and utilize.  Thiamine and Niacin B 3 deficiency symptoms include anxiety, depression and irritability.  The brain uses more Thiamine than other organs.  Take the B Complex and Thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) and look for health improvements in the following weeks.
    • knitty kitty
      Hello, @rei.b, Ehlers Danlos syndrome and Celiac Disease can occur together in genetically predisposed individuals.  Losing ones gallbladder is common with celiac disease. I'm glad Naltrexone is helping with your pain.  Naltrexone is known to suppress tTg IgA and tTg IgG production, so it's not surprising that only your DGP IgG and DGP IgA are high.   Have you tried the Autoimmune Protocol diet designed by Dr. Sarah Ballantyne, a Celiac herself?  The AIP diet helps lower inflammation and promotes intestinal healing.   The AIP diet is a Paleo diet that eliminates foods that can cause intestinal inflammation until you heal on the inside, then more foods can be added back in.  The low histamine AIP diet will help reduce inflammation further.   Histamine is released as part of the immune response in celiac disease.  Foods also contain various amounts of histamine or provoke histamine release.  Lowering the amount of histamine from foods helps.  The body, with help from B vitamins, can clear histamine, but if more histamine is consumed than can be cleared, you can stay in an inflammatory state for a long time. Cutting out high histamine foods is beneficial.  Omit night shades which contain alkaloids that add to leaky gut syndrome found with celiac disease.  Night shades include tomatoes, peppers including bell peppers, potatoes and eggplants.  Processed foods like sausages and gluten-free processed products are high in histamines.  All Grains are removed from the diet because they are inflammatory and provoke histamine release. Blood tests for deficiencies in B vitamins are notoriously inaccurate.  You can have vitamin deficiency symptoms before blood levels show a deficiency.  Blood levels do not accurately measure the quantity of B vitamins stored inside the cells where they are utilized.  The brain will order stored vitamins to be released from organs into the blood stream to keep the brain and heart supplied while deficiency occurs inside organs, like the gallbladder.  Gall bladder dysfunction is caused by a deficiency in Thiamine Vitamin B 1 and other B vitamins.   The eight essential B vitamins are water soluble and easily lost with diarrhea and constipation, and the malabsorption and inflammation that occurs with celiac disease.  Because they are water soluble, the body can easily excrete any excess B vitamins in urine.  The best way to see if you are deficient is to take a B Complex and Thiamine in the form Benfotiamine and look for health improvements in the following weeks.  Most B Complex supplements contain Thiamine Mononitrate which is not bioavailable.  The body has a difficult time utilizing thiamine mononitrate because it doesn't break down easily.  Benfotiamine has been shown to promote intestinal healing.   Remember your intestines are in a damaged, permeable state.  Treat them tenderly, like you would a baby until they heal.  You wouldn't feed a baby spicy bell peppers and hard to digest corn and nuts.  Change your diet so your intestines can heal.   I use a combination of B12 Cobalamine, B 6 Pyridoxine, and B1 Benfotiamine for pain.  These three B vitamins have analgesic properties.  They relieve pain better than other otc pain relievers. 
    • Mari
    • trents
      Sorry, I think I got you mixed up with another poster.
    • rei.b
      I hadn't been eating gluten free before having the antibody test done. I started eating gluten free after having the test done because the gastro PA told me to eat gluten-free for 6 months. I'm now 3 months in.
×
×
  • 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.