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

Kitchen Make Over Help


Bella001

Recommended Posts

Bella001 Explorer

Hello all,

I'm trying to figure out what I need to do to get my kitchen gluten-free. I think I'm getting cc'd. I have Calphalon hard anodized pans/pots. Most are scratched. Should I get just start over and buy new? How about cookie sheets, cutting boards etc....I threw out my plastic measuring cup last night and replaced it with glass. My mixing bowels are metal/stainless.

Thanks!


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



Celiac.com Sponsor (A8-M):



shopgirl Contributor

Sorry, I must be 12 years old tonight but "mixing bowels" made me giggle.

I replaced: anything wooden, plastic, or metal. It was painful but I reasoned that it had to be done.

Rowena Rising Star

Mostly I replaced anything wood because the gluten gets absorbed by the wood. Also, anything that is not easy to clean or has a lot of holes, like a cheese grater or a toaster, I would replace (or just get an alternate one if you are doing the shared kitchen thing). As for anything else, I would say, if its beat up, even if you didn't have a problem with gluten, its probably time to replace it. I would also replace anything old. (Since we discovered my intolerance shortly after getting married, we didn't have to replace a whole lot. All the hand-me downs are getting or have gotten replaced though...) Oh and if something is textured, (like a glass cutting board we have lieing around somewhere) I would replace it too. And I think depending on how used they are, definitely replace cutting boards. Flour can get stuck in those cracks the knives make.

Of course, you also have to kind of test out a few things and such, because there is no foolproof way to make sure you have got rid of everything until you don't feel sick anymore. Every person is different.

SGWhiskers Collaborator

I had relatively new Calphalon non sticks when I went gluten-free. I didn't get rid of them partly from stubborness and partly from frugality. I scrubbed them with everything imaginable and soaked them in alcohol until I couldn't scrub stains out on a white cloth anymore. I was sick the first 3 months of gluten-free, but I was making all kinds of mistakes during that time.

So, if you are going for the full expense kitchen makeover, toss all tupperware and plastic cooking utensils. Toss the rolling pin, rusted metal items like the can opener. All wooden items like wooden spoons, cutting boards and salad bowls. Toss the pasta strainer. Really, toss all plastic, wood, and rusted items as well as scratched non-stick from your kitchen. Scrub the glass and metal bakeware until it looks new again. I replaced as much as possible with glass and cheap bamboo spoons because of what we are learning about the dangers of cooking with plastic. Also, the glass is easy to clean when my husband accidentally puts a gluten item in it.

OK, I said toss, but I really should have said donate to good will or transfer select items into a cupboard for family to use for gluten.

Now if you are like most of us, you won't be able to purge your kitchen entirely all at once.

Buy a large deep skillet for cooking, clean your glass bakeware, and line your nonstick bakeware with foil. Replace the can opener and cooking utensils. Buy a few of the paper thin plastic cutting boards and use the lid of a pot for straining your pasta. You can't use any of the plastics or wood, but you will probably find you can do without for a while.

appliances: no toaster or breadmaker. Others have said you can char and scrub the grill. I kept getting sick until I switched to tinfoil pouches or my own new cast iron grill pan. Also, I decided to get rid of my hand mixer because I knew it had years of flour blown into the vents and it would probably blow flour out the vents. I still have not replaced it because I've figured out that hand blending works just fine. Someday maybe.

Kitchen soaps: make sure your hand soap is gluten free. No good washing your hands then making burger patties with gluten soap.

Pet food: My bird's food got me sick on a number of occassions. Harvey's was the only gluten-free version I could find. We switched the cat to moist gluten-free right away. He was fat and dropped 20% of his bodyweight and turned into a kitten again.

The only things that my husband accidentally grabs from my gluten-free stash is the beer bottle opener and glass corning storage with the plastic lids. He drinks beer so rarely, he forgets it has gluten. We have so little plastic in the house, that he forgets that it can absorb gluten. Fortunately, I've caught him almost every time and the few times I didn't catch him, he didn't get anything on the lids.

Oh, and if you are stubborn like me and have to learn everything the hard way, learn from this one. I got a facebook post from a friend with newly diagnosed celiac who is stubborn and won't head to these boards stating she was miserably sick from eating a squash cooked in a tupperware that had once held cookies.

Keeping in mind that I'm desperately stubborn and cheap and I know this is bad advice, I would buy one skillet to use for the next few months while you get your diet under control. Scrub the calphalon to pieces and then try one plain safe meal in each pan and wait a few days to see if you have a reaction. I know how what an investment that calphalon is. Or you could play it safe and see if your sister or a friend would like a nice set. That's what I should tell you.

Good luck and have fun shopping!

SGWhiskers Collaborator

Oh, when you replace the can opener, they are all crappy these days except the OXO brand. I went through half a dozen before I found this one. The rest all die within 6 months or leave metal fragments in my can. Granted I didn't spend more than $15 or so on any of them.

Rowena Rising Star

SG~ I love oxo brand!!!! that's the best brand ever. I swear every other brand wears down far too quick and far too easy.

Tupperware.... is that what is getting me? Hmmmm.... I never thought about it but I guess that could be why I am often sick after eating leftovers from my parents and in-law's houses...

As for cheap way of replacing things, something I have done is replace a little bit every time I go to the store. IE one trip I replaced my wooden wares. The next trip I replaced the spatulas. It doesn't seem to drain the funds as much if you do it in bits and pieces. Though it can be frightfully annoying at first...

Oh that reminds me... a trip to Bed Bath and Beyond is in order... I need to replace pans... and get a toaster... And a stepstool... and a million and one other things... Darn it, why do I only have 30$ in gift cards?

cap6 Enthusiast

I got rid of all of my plastic containers and am slowly replacing them with glass - and ziplocs!


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. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,407
    • Most Online (within 30 mins)
      7,748

    H2HPizzaWagon
    Newest Member
    H2HPizzaWagon
    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
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.