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

One More Quick Question....do I Need New Pans?


Guest taweavmo3

Recommended Posts

Guest taweavmo3

I don't have non-stick cookware, everything I currently have is stainless steel. Food sticks to these pans pretty bad, no matter how much I scrub. Is it possible to get all the gluten off of stainless steel or no?

I read in Kids with Celiac that you should have high quality non-stick cookware. What's everyone's take on this and what do you all do?


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

A couple materials are bad: teflon (especially), plastic, wood (such as in wooden spoons), etc. With steel, you can get new pots/pans if you want, but you don't have to. I personally would, but if you make sure that it's ALWAYS cleaned very well, you should be okay. Things you should replace:

- Collander (no matter what material it's made out of, it's too difficult to make sure all the crumbs are out of it.

- Anything wooden, such as a wooden spoon.

- Spatula

I would recommend that you have a set of gluten-free pots/pans and a set of regular--that can be easily distinguished between--but it's not essential.

jcgirl Apprentice

Great question, I was wondering that myself. I must have posted at same time celiac3270 did, thanks for the answer.

Boojca Apprentice

I've changed collanders, wooden and plastic utensils, and we have a separate butter dish for "his" butter...but other than that everything is the same.

Bridget

celiac3270 Collaborator

Oh, that reminded me....separate condiments are good...it's too easy to forget that you can't double-dip on the jelly/butter/peanut butter with a knife that's already touched regular bread....

minibabe Contributor

The one thing that my nutritionist said to me was to change my Toaster. I have a seperate one from the rest of my faimly. but the collander and anything wooden are great ideas also. :)

angel-jd1 Community Regular

I make sure to label my containers of butter, jelly and such. I just use a magic marker and put my name on them or something silly like "NO GLUTEN ALLOWED". At my parents house I also get one of the drawers in the fridge to put "my stuff" so it doesn't get mixed up with everyone elses.

-Jessica :rolleyes:


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

Yes :)....I usually write with a Sharpie on the lid or label: GLUTEN FREE or gluten-free or celiac3270'S...although one time, on a peanut butter lid I wrote "celiac3270's...All Mine!!! Hahaha!!" [the hahaha is an evil laugh]....yeah...that was in one of my weird moments :lol:

And a new toaster is ESSENTIAL. If you buy nothing else new, buy a new toaster.

all4gals Newbie

I actually used a sharpie to write Gluten Free all over our new toaster for my daughter. Even then when my sis was babysitting she accidentally put a regular waffle in it. She bought us a new toaster before we got home. :) Sent her husband out. So sweet! If we double dip I use a sharpie to write contaminated on the jar and lid. I wonder if that scares my visiting family. "why do they have contaminated stuff in their fridge?" :lol:

I love the squeezable bottles for condiments...mayo, jelly etc. But with just me and my dh cooking for now it's easy. We spoon everything out.

It's amazing how we adapt for our kiddos health huh?

Nicole

celiac3270 Collaborator
I actually used a sharpie to write Gluten Free all over our new toaster for my daughter. Even then when my sis was babysitting she accidentally put a regular waffle in it. She bought us a new toaster before we got home. :) Sent her husband out. So sweet! If we double dip I use a sharpie to write contaminated on the jar and lid. I wonder if that scares my visiting family. "why do they have contaminated stuff in their fridge?" :lol:

I love the squeezable bottles for condiments...mayo, jelly etc. But with just me and my dh cooking for now it's easy. We spoon everything out.

It's amazing how we adapt for our kiddos health huh?

Nicole

lol...that's great :D. I've done the same thing--with a few containers of Duncan Hines icing that were used for regular cupcakes for my brother's birthday...I wrote contaminated all over them with a Sharpie, just like you do. I also write gluten-free or Gluten-Free or celiac3270's Only on certain things that I keep in a gluten-free cabinet (peanut butter, etc).

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. - Wheatwacked replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      12

      Blood Test for Celiac wheat type matters?

    2. - trents replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    3. - JudyLou posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    4. - marzian commented on Scott Adams's article in Diagnosis, Testing & Treatment
      5

      A Future Beyond the Gluten-Free Diet? Scientists Test a New Cell Therapy for Celiac Disease (+Video)

    5. - Jmartes71 posted a topic in Related Issues & Disorders
      0

      Medications

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

    • Total Members
      133,144
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Wheatwacked
      no argument. Never take the pills sold for Nuclear events, except in a nuclear event when instructed to by authorities.  Some of these go up to 130 milligrams per pill. 5000 times the strength of the dietary supplement.  130 times the safe upper limit.  130 mg = 130,000 mcg. Dietary supplements like Lugol's Solution and Liquid Iodine are 50 micrograms per drop.  It takes 20 drops to reach the safe upper limit. In the US the Safe upper limit is 1100 mcg.  In Europe 600 mcg and in Japan 3000 mcg ( 3 mg).
    • trents
      Welcome to the celiac.com community, @JudyLou! There are a couple of things you might consider to help you in your decision that would not require you to do a gluten challenge. The first, that is if you have not had this test run already, is to request a "total IGA" test to be run. One of the reasons that celiac blood antibody tests can be negative, apart from not having celiac disease, that is, is because of IGA deficiency. If a person is IGA deficient, they will not respond accurately to the celiac disease blood antibody tests (such as the commonly run TTG-IGA). The total IGA test is designed to check for IGA deficiency. The total IGA test is not a celiac antibody test so I wouldn't think that a gluten challenge is necessary. The second is to have genetic testing done to determine if you have the genetic potential to develop celiac disease. About 30-40% of  the general population have the genetic potential but only about 1% actually develop celiac disease. So, genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out. Those who don't have the genetic potential but still have reaction to gluten would not be diagnosed with celiac disease but with NCGS (Non Celiac Gluten Sensitivity).  Another possibility is that you do have celiac disease but are in remission. We do see this but often it doesn't last.
    • JudyLou
      Hi there, I’m debating whether to consider a gluten challenge and I’m hoping someone here can help with that decision (so far, none of the doctors have been helpful). I have a history of breaking out in a horrible, burning/itchy somewhat blistering rash about every 8 years. This started when I was in my early 30’s and at that point it started at the ankles and went about to my knees. Every time I had the rash it would cover more of my body, so my arms and part of my torso were impacted as well, and it was always symmetrical. First I was told it was an allergic reaction to a bug bite. Next I was told it was eczema (after a biopsy of the lesion - not the skin near the lesion) and given a steroid injection (didn’t help). I took myself off of gluten about 3 weeks before seeing an allergist, just to see if it would help (it didn’t in that time period). He thought the rash looked like dermatitis herpetiformis and told me to eat some bread the night before my blood tests, which I did, and the tests came back negative. I’ve since learned from this forum that I needed to be eating gluten daily for at least a month in order to get an accurate test result. I’m grateful to the allergist as he found that 5 mg of doxepin daily will eliminate the rash within about 10 days (previously it lasted for months whether I was eating gluten or not). I have been gluten free for about 25 years as a precaution and recommendation from my doctor, and the pattern of breaking out every 8 years or so remains the same except once I broke out after just one year (was not glutened as far as I know), and now it’s been over 9 years. What’s confusing to me, is that there have been 3 times in the past 2 years when I’ve accidentally eaten gluten, and I haven’t had any reaction at all. Once someone made pancakes (they said they were gluten-free, they were not) and I ate several. I need to decide whether to do a gluten challenge and get another blood test. If I do, are these tests really accurate? I’m also concerned that I could damage my gut in that process if I do have celiac disease. My brother and cousin both had lymphoma so that’s a concern regarding a challenge as well, though there is a lot of cancer in various forms in my family so there may be no gluten connection there. Sorry for the ramble, I’m just doubting the need to remain gluten free if I don’t have any reaction to eating it and haven’t had a positive test (other than testing positive for one of the genes, though it sounds like that’s pretty common). I’d appreciate any thoughts or advice! 
    • Jmartes71
      Hello, just popped in my head to ask this question about medications and celiac? I have always had refurse reaction to meds since I can remember  of what little meds my body is able to tolerate. I was taking gabapentin 300mg for a week,  in past I believe 150? Any ways it amps me up not able to sleep, though very tired.However I did notice it helped with my bloating sibo belly.I hate that my body is that sensitive and medical doesn't seem to take seriously. Im STILL healing with my skin, eye, and now ms or meningioma ( will know in April  which)and dealing with this limbo nightmare. I did write my name, address ect on the reclamation but im not tech savvy and not sure if went through properly. I called my city representative in Stanislaus County and asked if theres a physical paper i can sign for proclamation for celiac and she had no clue about what I was saying, so I just said I'll go back on website. 
    • Scott Adams
      I'm not saying that some celiacs won't need it, but it should be done under a doctor's supervision because it can cause lots of problems in some people.
×
×
  • 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.