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 Containimation


Chris Anne

Recommended Posts

Chris Anne Newbie

I am still having problems while eating gluten-free. Do I really need to go out and buy my own plates, utensils etc. And I am having a problem with family members understanding about this disease.


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



Celiac.com Sponsor (A8-M):



Raining Skittles Rookie

I wish I had an answer for you. All I can give you right now is the comfort that you are not alone. People are not understanding of why I'm doing this either. They keep asking "isn't gluten free that new fad diet?" And I got into an argument about grocery shopping last night.

I don't know about separate utensils and dishes as I'm just learning all this myself. Hopefully we can learn together.

bartfull Rising Star

Sorry you are both having problems with family members. From what I have read here, that happens a lot. They need to be educated. If you can get them to read some of the info here it would help, but if not, just compare it to peanut allergies. Everyone knows by now that the tiniest exposure to peanuts can kill a person with a peanut allergy.

Or compare it to poison. Even a microscopic bit of cyanide is deadly. For you, gluten is the poison, and though it won't kill you instantly, over time it CAN. And every time you get cross contaminated it sets you back.

So, yes, you really DO have to be vigilant about CC. Seperate dishes, toaster, condiments, sponges and dish towels, and all of the other things you have read about here. And if you can get your family to read here they will see that celiac runs in families. Chances are some of THEM have it and don't know it. Symptoms vary so much and many of us don't have digestive issues. But you know what? So-called silent celiacs are still at risk for all of the nasty things like cancer, neurological problems, lupus, thyroid problems, vitamin deficiencies, and a host of other things they DON'T want.

Get them educated, and then get them tested. If they still refuse, you need to do everything in your power to at least make sure YOU are safe.

dani nero Community Regular

My family did not take me seriously, until I told them the following:

For a food to be labeled gluten-free legally, it's gluten content must be less than 20ppm (parts per million). So a single breadcrumb of gluten in a loaf of bread will cause a reaction.

I actually want to make an informative illustration to help people visualize this.

irish daveyboy Community Regular

My family did not take me seriously, until I told them the following:

For a food to be labeled gluten-free legally, it's gluten content must be less than 20ppm (parts per million). So a single breadcrumb of gluten in a loaf of bread will cause a reaction.

I actually want to make an informative illustration to help people visualize this.

This may help, there are 1 Million dots in the following and each small square contains 100 dots.

Open Original Shared Link

kareng Grand Master

I don't have separate dishes, plates, spoons, forks, etc. I do have separate pans because we wanted new ones anyway. We have separate colander for gluten pasta. A separate cutting board for gluten bread. A separate toaster. I have new gluten-free cooking utensils like stirring spoons. I have new "Tupperware" stuff for gluten-free. We have 2 dish sponges that we dish washer every day. ONe is blue and the gluten-free one is pink.

Basically, if its easy to clean, you can use it. For example - Colanders have lots of little holes and its hard to get the pasta out, so you need a gluten one & a gluten-free one for everything else. My stuff is usually red or I put red tape on it - Red cooking utensils, plasticware with a red lid or red piece of tape, red toaster, red colander, red tape on my butter tub, etc.

We keep the gluten bread, pretzels, etc to one separate counter in our kitchen.

What makes this work at our house is:

-people are willing to follow the rules

-my kids were teens when I was diagnosed.

- We have an excellant dishwasher.

-We can afford new kitchen things (we don't eat out twice a week like we used to so we saved money there)

- Red kitchen utensils are in style and available at Walmart and Target

If you can't trust the people you live with, it may be best to have some of your own stuff & keep it safe or re-wash everthing before using. You could switch to paper plates and disposable silverware for a few months, until everyone gets the hang of it.

Adalaide Mentor

If you can't trust the people you live with, it may be best to have some of your own stuff & keep it safe or re-wash everthing before using. You could switch to paper plates and disposable silverware for a few months, until everyone gets the hang of it.

I can't trust the people (or person now) I live with. My husband I trust 100%, my MIL I can't trust at all. For this reason I share literally nothing in the house. She will get out a spoon or fork and leave the silverware drawer just a little bit open which then leads to a drawer full of crumbs. I was still getting sick all the time and couldn't figure out why and just said I'm done. I got my own silverware, plates, cups, everything. (I already had all my own cooking stuff, hers was all scratched up teflon junk and melted plastic spoons.) I went from still having GI symptoms nearly all the time to several months without a hitch.

Know what made me sick? Frozen chicken soup I had made with veggies I cut up the week after my MIL had set a pizza stone on top of my cutting board. That is all it takes. A pizza stone on a cutting board, I washed that cutting board but the veggies I cut on it still made me sick. Think of how little gluten that is. Maybe your family will say I'm a nutjob, but maybe they'll take it to heart and realize that they need to be on your side.


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



Celiac.com Sponsor (A8-M):



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. - olivia11 replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      26

      My journey is it gluten or fiber?

    2. - olivia11 replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      26

      My journey is it gluten or fiber?

    3. - olivia11 replied to olivia11's topic in Gluten-Free Foods, Products, Shopping & Medications
      4

      suggest gluten free food

    4. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      26

      My journey is it gluten or fiber?

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

    • Total Members
      132,791
    • Most Online (within 30 mins)
      7,748

    blondebomber
    Newest Member
    blondebomber
    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

    • olivia11
      This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too color coding and baking G F first makes a lot of sense. This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too color coding and baking G F first makes a lot of sense. This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too color coding and baking G F first makes a lot of sense.   You are not confusing yourself  you have got it right. Thiamax (TTFD) plus a B-complex, and if you want benfotiamine, the Life Extension formula covers that at ~100 mg.
    • olivia11
      High fiber can definitely cause sudden GI distress especially if it’s a new addition but accidental gluten exposure can feel similar. Keeping a simple food/symptom log and introducing new gluten-free foods one at a time can really help you spot the pattern. This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too; color-coding and baking gluten-free first makes a lot of sense. This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too; color-coding and baking gluten-free first makes a lot of sense. This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too; color-coding and baking gluten-free first makes a lot of sense. This is really helpful  I had not considered sugar alcohols or inulin as triggers. Thanks for the practical baking tips too; color-coding and baking gluten-free first makes a lot of sense.
    • olivia11
      Thanks for asking  I’m mainly looking for gluten-free staples and snacks. Any recommendations for brands or go-to items would be appreciated.
    • xxnonamexx
      sorry a bit confused so I should take my B complex along with Objective Nutrients Thiamax for TTFD but what about a Benfotiamine to take. The Life extensions contains Benfotiamine and Thiamine together or im confusing myself. I am trying to see if I take Thiamax what should I take for Benfotiamine. Thanks EDITING after further research I see ones water soluble ones fat soluble. So I guess 100MG as you suggested of Life Extension contains Benfotiamine and Thiamine Hydrochloride. and the Objective Nutrients Thiamax contains TTFD.     would work for me.
    • Rogol72
      I put on over 12kg by eating protein with every meal, 3 to 5 times a day. Eggs, Chicken, Tuna, Turkey etc. I stay away from too much red meat as it can be inflammatory. Scott is correct. I've come across a bunch of Coeliac PT's on Tiktok and Instagram. They all say the same thing, the key is getting enough protein and consistency.
×
×
  • 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.