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

Teflon, Plastic


Yenni

Recommended Posts

Yenni Enthusiast

A woman with Celiac deseas told me to get new frying pans and stuff if they have Teflon. She sais that if gluten had been used in it it can have gotten cooked into it. I have read that it is safe to use the same pots and pans. What is the right thing to do?

Thanks!


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



Celiac.com Sponsor (A8-M):



Guest Robbin

I just boiled water in mine. If they are scratched badly and you are worried about it, what the heck get some new ones. I read on here that with each washing 80 % is removed, so keep washing. I mean really, that is an expensive prospect if they are not damaged.

Yenni Enthusiast

My problem is that I live ina household where everyone else eats glutenand lots of it. So with me being in this situation I should probably get my own?

What about plastic containers and stuff? Is it just the cooking that is the danger?

Thanks for the reply!

This might be a weird quetsion, but what about microvawe ovens? Are they safe to share with such a gluten crazy family that I live in?

ebrbetty Rising Star

I'm the only gluten-free person in my house, I bought all new pans and only use glass baking dishes

kabowman Explorer

I originally tried to share pans be finally realized (after about a year) I was getting sick each time so now we have gluten-OK teflon and non-gluten teflon pans. My kids and hubby like their mac & cheese which I can't have anyway any my youngest loves his ramon noodles (ick but hey). So we have a few of their pots and pans and a few of my pots and pans.

We have all new wooden utensils. We have separate cast iron skillets.

I sometimes get sick from using shared plastic containers so will be buying dedicated containers and keeping them that way; I will put a big K on them so nobody else uses them. The problem is, since I take my lunch and morning and afternoon snacks to work each day, I will need quite a few. Most of the stuff I store in the 'fridge is in glass containers.

I am the only gluten-free person in our house (soy, dairy, yeast, etc. too) but hubby cannot have beans or onions, my oldest cannot have processed meats (me either) or cinnamon, and my youngest cannot have lactose. Meals consist of non-onion stuff, baked goods are made with my milk and no cinnamon, etc.

gfp Enthusiast
My problem is that I live ina household where everyone else eats glutenand lots of it. So with me being in this situation I should probably get my own?

What about plastic containers and stuff? Is it just the cooking that is the danger?

Thanks for the reply!

This might be a weird quetsion, but what about microvawe ovens? Are they safe to share with such a gluten crazy family that I live in?

If you continue in that household like that you will end up getting glutened anyway. (I'm basing this on how you say it :D)

Is it just the cooking that is the danger?

No the danger is that a single speck of gluten so small you can't even see it can make you sick.... this includes washing sponges and tea towels and everything else including the hoover if its used to hoover gluten.

HOWEVER

What you are experiencing is VERY NORMAL.....

Most of us started off like this ... and most of us took a long time to finally accept it.

I realise this sounds paranoid and that is what I thought .....

The best thing you can do if its your family is get them on board.... I'm sorry but this is the way it is.

Please search here on CC (cross contamination).....

Read it yourself and let it sink in.....

I wish I could GIVE you my experience .. really but I can't and your questions are really really common.

Please.. do the search and read .... listen to those of us who really have found this out the hard way and try and see if you can't accept that. Believe me; I'm one stubborn SOB and I was so going to be a "mild" celiac when I was diagnosed.... but wise people like those here told me and told me again and again until I actually TRIED...

You can't be a bit celaic just like you can't be a bit pregnant... you either are or are not.

Its not like "having a bit of a cold" .. and even if you don't react externally you are still doing damage.

Yenni Enthusiast

Thanks so much for your replies.

Yeah, I need to read more on here. I have read a couple of books, but it is all so overwhelming..

I feel like some stuff doesn't say in books either. For example that charcoal briquetts have gluten. Toothpaste...I have read about it all here.

I am trying hard to make sense of all of this. I just ordered tests from Enterolab too. Gonna get checked for gluten, milk, soy, egg and yeast.

I feel I need to get some answers.

I feel I keep on getting sick so often. And every time I seem to figure out one more thing that I have missed. I have heard it is common to have it this way until you figure it all out.

Well, today my husband got me some new pots and pans and stuff.

I am working on it. ;)


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



Celiac.com Sponsor (A8-M):



gfp Enthusiast
Thanks so much for your replies.

Yeah, I need to read more on here. I have read a couple of books, but it is all so overwhelming..

I feel like some stuff doesn't say in books either. For example that charcoal briquetts have gluten. Toothpaste...I have read about it all here.

I am trying hard to make sense of all of this. I just ordered tests from Enterolab too. Gonna get checked for gluten, milk, soy, egg and yeast.

I feel I need to get some answers.

I feel I keep on getting sick so often. And every time I seem to figure out one more thing that I have missed. I have heard it is common to have it this way until you figure it all out.

Well, today my husband got me some new pots and pans and stuff.

I am working on it. ;)

You already sound like you are way ahead of the curve....

You will keep making mistakes, view them as learning and validation and go forwards....that is what we have done and soon you will be posting what we just did to someone in your situation.

Aussie Peg Rookie

hello!

i ended up getting my own pots and pans, cutlery and crockery which means i dont have to worry about scrubbing the gluteny equipment like a mad woman before i can use it, i know if something isnt cleaned perfectly it doesnt matter as no gluten has touched it! I also have my own spatula and other cooking utensils and a few months ago bought my own plastic microwave dishes as i was getting mystery glutenings which turned out to be the old ones - must have had sneaky gluten embedded in the plastic, especially the dishes with scratches. I have my own dish sponge and bench spaces too which no-one is allowed to use :)

This has helped so much with avoiding glutenings! good luck! :)

Yenni Enthusiast

Thanks guys! :)

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. - trents replied to Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - Russ H commented on Scott Adams's article in Latest Research
      5

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,373
    • Most Online (within 30 mins)
      7,748

    Alexis Parker
    Newest Member
    Alexis Parker
    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

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • 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.