Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

They Can't Really Be Serious About This?


rgeelan

Recommended Posts

rgeelan Apprentice

I will have to buy new kitchen stuff??? If William comes back + for celiac disease I keep hearing that I will have to go get new thigns like a new toaster for his gluten-free bread only and I won't be able to cook his gluten-free food in the same containers that I use for regular food unless I wash them very well first... So I will have to make his food first if I dont want to buy a seperate set of pots and pans for him. And I should buy new seperate condiments for gluten-free food only. All this so that there is no chance of cross contamination by even a few crumbs of gluten getting in his food. Kris and I are 100% convinced that he has this allergy now because he hasn't had any Gluten since Thursday night and he is FINE! Not even a stomach ache!!! But when we tested it and gave him food with Gluten on Thursday night he threw up Friday morning again. I just keep praying that it is just an allergy because then he has hope of growing out of it where as if he has celiac disease he wont ever grow out of it and from what I keep reading even a little Gluten can cause major damage to him. The specialist was 75% positive that he has celiac disease just by the 1 blood test that came back but the base wont take that as a positive diagnosis...

I am beyond stressed at this point. We are so broke it isn't even funny... I splurged and bought Emma her coat.. It's furry like a dalmation print. She loves it... Cost $25 which I guess isn't all that bad for a winter coat but since we're broke it wasn't easy... Of course I also let William pick up a couple of cheep Star Wars toys he wanted. We're spoiling him this past week to make up for all the food we're saying no to and all the doctors he's seen and tests he had done...

I bought 3 books to help with this... 2 are cookbooks Wheat free and Gluten Free, 1 is normal food and 1 is just deserts. I figure if I can learn to make him good things like cookies and cakes then he won't be so upset over the things he can't have. I also got a book called Kids with Celiac Disease. It is good even if he doesn't have full blown celiac disease because the doctor said that if he doesn't have full blown celiac disease with the symptoms he had and how strong his allergy was it is very possible he could be a carrier still and have it show up later and he still has to follow the same diet because of his allergy. This book offers lots of suggestions for gluten-free foods and how to handle different situations which we are going through anyway becuase of his diet...

I just dont know what to do at this point... I keep reading and researching and even if he doesn't have celiac disease yet he at least has to have the same gluten-free diet because he has a strong allergy and all this stuff about needing a new toaster and things like that is just STRESSING ME OUT! We told our parents that from now on if they want to buy the kids something to buy food because we have enough toys and clothes for them but the food is killing us financially...


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

You absolutely cannot use the same toaster - there's no way to get all the crumbs out. (Then again, I never use a toaster, but you can get a $10 toaster from WalMart after saving up.) But, depending on your cooking implements, you may not really need new pots and pans. If you've got stainless steel that's in decent shape, then just washing well is fine, but if you're using cast iron, you'll need new pans. You definitely have to clean the pan between uses - if you've ever cooked pasta, you can see how much starch comes out in the water. And if you've ever made a PB&J sandwhich, you see crumbs come off on the butterknife and can see that they'd contaminate peanut butter or jelly, so yes, any shared condiments need to have a unique container for the celiac.

But you may find that sticking to the basics - lots of rice and corn - makes it cheaper. You don't need to buy specialty gluten-free stuff, for the most part.

celiac3270 Collaborator

Just stay away from specialty foods.......go through your grocery store and find all the foods that are gluten-free........rice, potatoes, veggies, some canned goods, etc. There are a lot of mainstream products, but it helps to know brand names going into it.....FritoLays, Hormel, Oscar Mayer, etc. and find out what products by each are gluten-free if possible. Remember that Kraft clearly displays gluten on their ingredients lists......here's a section of the site that has mainstream products/brands that are gluten-free:

Mainstream products that are gluten-free (celiac.com)

rgeelan Apprentice

Thanks guys... I laughed when I started reading my book that I bought and the lady who wrote it said how her first trip to the regular grocery store looking for food she left with a bunch of Fritos. LMAO! I did the same thing. I went looking for what I could buy and left with Fritos as the only "non specailty" food. The store I went to had a lot of natural and healt foods so I was able to find things like those Envirokidz bars that William likes...

I keep thinking I am getting ok with the idea of this new diet then it slaps me in the face again and I start freaking out again. William keeps asking for food he can't have and I keep telling him over and over why he can't have it but he laughs and says no, my tummy is fine... LOL! Of course he hasn't had Gluten since Thursday night...

I have to ask though... WHY a new toaster? My husband and I are going around in circles trying to figure this out. After all the crumbs fall down to the bottom and the bread just rests on a little metal wire so how is it getting contaminated?

tarnalberry Community Regular

Have you ever tried cleaning one out? You'll find that there really are crumbs all over the metal that the bread does touch. For $10, it's not worth the risk

dmbaird1230 Apprentice

my husband and I have a toaster oven and when I toast my gluten-free bread I put it on a piece of foil so that it doesn't touch the metal grate that the other bread has touched, do you think that's ok?

celiac3270 Collaborator

Well, it's better than just using the same toaster, but for $10 you could make things a lot safer and reduce the risk of contamination


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



Celiac.com Sponsor (A8-M):



debmidge Rising Star

I too thought we could get away without getting a new toaster....and I tried cleaning out the old one....cleaning it to the point of almost wanting to wash it out!! But my meticulous cleaning still couldn't dislodge all of the residue. There were layers of crumbs that unless I used a flashlight I couldn't see. I then realized that when using it for gluten-free toast, everytime the toast would pop up the residue would dislodge itself and get on the gluten-free bread. This would be unacceptable. I also purchased new wooden spoons and spatulas based on this same theory (that gluten gets into the worn out cracks and crevices).

I broke down and purchased a $10 toaster, but kept the old one for the gluten breads (but haven't used the old one since - my husband is celiac, not me).

Am I glad I purchased new? You bet! He was so sick that he didn't need any more risk factors for a reaction.

I do have a question for the long time celiacs, what about an aluminum pot that isn't stainless steel and was used to cook wheat macaroni? Would using a Brillo pad in it be sufficient to clean out gluten residue?

Pegster Apprentice

I'm not a long time celiac, but I've never had a reaction from using my same old pots and pans (aluminum, stainless, etc.) The only thing I bought was the same cheap $9.99 toaster that everyone else seems to have. Oh, I did buy a pasta pot with a strainer in the lid for my special pasta- but now my whole family has the gluten-free pasta with me.

tarnalberry Community Regular

I haven't replaced my pans either - though I no longer use my cast iron skillet, which I will have to replace as soon as I want to use one. We don't primarily use teflon anyway. (I've got a bird, and at high temperatures, non-stick coatings can give off toxic fumes. Birds are highly sensitive to these fumes (though they can harm humans, they hit birds way before that stage) and can die from very brief, very minimal exposure.) And the rest of our pots are either stainless steel or anodized aluminum, both of which clean well and have hardly ever seen wheat anyway (and not something that would relentless stick).

We do have one non-stick gridle, purchased after I went gluten-free, that is used for pancakes and corn tortillas only. We do use it for both gluten-filled and gluten-free pancakes, however, but I am extraordinarily anal rententive about no metal and no abrasive substance touching it, so the surface has not been scratched and I've never had a problem. While most non-stick surfaces can be porous, you're supposed to heat them well first, so that the non-stick chemicals on the surface of the pan expand and flow together, leaving no spaces between them. I've never had a problem from this pan. (I would, however, never cook something that would stick on it - once that happened, I'd replace it.)

You know, I haven't replaced my plastic strainer, but I probably should. I usually use a pasta cooker anyway (the pots with the built in stainless steel insert that acts as a strainer), and I feel confident about being able to fully clean that one.

I was also a bit worried when I read about pots and pans, but I think you really need to use some good judgement on this one. Well, first throw any considerations about money out the window - you don't want a biasing effect on your decision, and you can always find a way for the solution to fit into your budget. I decided that between the type of pots and pans that I've got and the type of cooking that I do, there was little chance for wheat to be stuck to my pots. In other situations, it may have been necessary.

I have stopped using my old bakeware, though kept a set of non-stick bakeware (and worry about my bird every time I use it, and only use it on lower temperature baking...) which I had purchased just before going gluten-free and had kept unscratched doesn't have any stuck on residue.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,062
    • Most Online (within 30 mins)
      7,748

    Robinlee
    Newest Member
    Robinlee
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I also want to mention that using prednisone would likely also make the endoscopy results invalid. This steroid will cause gut healing and could mask the damage caused by celiac disease. 
    • Jess270
      This sounds to me like histamine intolerance. Some foods have more or less histamine. processed or aged meats, fermented food like yoghurt or kimchi and bread (yeast), spinach, eggplant and mushroom are high in histamine. Other foods like tomatoes are histamine liberators, they encourage your mast cells to release histamine, which can also trigger the reactions you describe, flu like symptoms, joint pain, urinary tract irritation, rash, stomach upset, nausea, diarrhoea & fatigue. I had liver pain like you describe, as part of the intolerance is usually a sluggish liver that makes processing all the histamine difficult. There are multiple possible root causes of histamine intolerance, usually it’s a symptom of something else. In my case, leaky gut (damaged gut wall)caused by undiagnosed celiac, but for others it’s leaky gut caused by other things like dysbiosis. Some people also experience histamine intolerance due to mould exposure or low levels of DAO (the enzyme that breaks down histamine in the gut). I’d try a low histamine diet & if that doesn’t improve symptoms fully, try low oxalate too. As others have suggested, supplements like vitamin d, b, l-glutamine to support a healthy gut & a good liver support supplement too. If you’re in a histamine flare take vitamin c to bowel tolerance & your symptoms will calm down (avoid if you find you have oxalate intolerance though). Best of luck 
    • trents
      @GeoPeanut, milk is one of the better sources of iodine. Iodine is known to exacerbate dermatitis herpetiformis. Many people find that a low iodine diet helps them avoid dermatitis herpetiformis outbreaks. So, maybe the fact that you have limited your dairy intake of late is helping with that.
    • GeoPeanut
      Hi, I'm new here. Sorry for your troubles.herenis a thought to mull over. I recently was diagnosed with celiac disease,  and hashimoto's and dermatitis herpetiformis after getting covid 19. I eat butter, and 1/2 cup of Nancy's yogurt daily. I stopped all other dairy and  dermatitis herpetiformis is gone! I also make grass fed beef bone broth to help with myopathy that has occurred. 
    • trents
      Welcome to the forum, @KRipple! Sorry to hear of all your husband's health problems. I can only imagine how anxious this makes you as when our spouse suffers we hurt right along with them. Can you post the results from the Celiac blood testing for us to look at? We would need the names of the tests run, the numeric results and (this is important) the reference ranges for each test used to establish high/low/negative/positive. Different labs use different rating scales so this is why I ask for this. There aren't industry standards. Has your husband seen any improvement from eliminating gluten from his diet? If your husband had any positive results from his celiac blood antibody testing, this is likely what triggered the consult with a  GI doc for an endoscopy. During the endoscopy, the GI doc will likely biopsy the lining of the small bowel lining to check for the damage caused by celiac disease. This would be for confirmation of the results of the blood tests and is considered the gold standard of celiac disease diagnosis. But here is some difficult information I have for you. If your husband has been gluten free already for months leading up to the endoscopy/biopsy, it will likely invalidate the biopsy and result in a false negative. Starting the gluten free diet now will allow the lining of the small bowel to begin healing and if enough healing takes place before the biopsy happens, there will be no damage to see. How far out is the endoscopy scheduled for? There still may be time for your husband to go back on gluten, what we call a "gluten challenge" to ensure valid test results.
×
×
  • Create New...