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What's The Best Way To..


futuredvm24

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futuredvm24 Rookie

What is the best way to eliminate CC in my kitchen if my family isn't gluten-free? I feel like I need to clean the entire kitchen and ziplock bag everything that may contain gluten..or maybe ziplock all my gluten-free stuff. My mom got me gluten free granola..and put it in the baking cabinet where there's loose flour and everything. Everyone is so messy with their bread crumbs so I have to Lysol the counter before I make anything and rewash anything that I'm going to use. The fridge makes me paranoid as well. I'm going crazy!! Any tips/words of encouragement appreciated! :D


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shadowicewolf Proficient

i don't even bother making stuff on the counter. I've pretty much gone to making stuff on plates and such because a certain family of mine does not know how to clean up their messes :angry:

NorthernElf Enthusiast

I live in a family of 5, I'm the only gluten-free one.

The top shelf of the pantry, the fridge, and the freezer are "mine" - gluten-free stuff only. Any muffins, cookies or whatever in smaller ziplocs are mine in there - the gluteny stuff is always in big freezer bags. I label my stuff "gluten-free" anyway.

All the counters are mine (gluten-free) - I bought an island at walmart with drawers that is across the kitchen and that's where everything gluteny is. In the drawers are the gluten measuring cups, mixing spoons, plastic containers (a different brand than my gluten-free ones). All gluten sandwiches are made on the island.

It's not perfect - the sink is a mix up of gluten & non gluten dishes, the cloth I clean with can be mixed up too. But cutting boards, strainers, measuring cups & large utensils, fry pans, are all separate. It works pretty well.

I use a lot of plastic containers for food for work - but they are all different than the one DH or the kids use & everyone knows whose is whose.

Oh, we have two toasters too - one on the island, and mine on the counters. I even put a gluten-free label on my toaster (we do have company once in awhile). Be firm but figure out your own system - it is so worth it - I was getting contaminated a lot.

FWIW, I am the cook & shopper in the house so I can keep pretty good control on things - and I'm not a happy camper when I get glutened - EVERYONE knows that, haha !

kareng Grand Master

We have a "bread" counter for the gluteny bread & crackers. I use red for stuff that is for gluten-free use. I put red duct tape on my PB & butter tub. I have red cooking utensils, red colander, red cutting board, etc. I have plastic containers with red lids. I use plastic baggies and will write on them my name if its only for me. I write "not gluten-free" on baggies of stuff that has been cc'd that should be gluten-free (like a bag of cheese slices someone forgot & touched after the bread).

Because most stuff is gluten-free, I don't put red tape on everything like the milk, cheese, etc. We get sandwich stuff out & put it on a plate first then get the gluten bread. Or I plop it on for them if we are all making sandwiches together.

If the folks in your house won't becareful like my family, I would suggest getting the colored tape & sticking it on everything that is for you only. Seal anything gluten-free that is open in baggies or containers with your colored tape. Maybe you could have a section or big box for your stuff only? If they miss bright red, pink or green tape on the top, they need to get an eye exam or they are just the rudest & meanest people ever! You can tell them I said that! ;)

kareng Grand Master

Forgot -

If you are newly gluten-free, it is not recommended that you eat oats, even gluten-free ones. It appears that about 10% of celiacs re-act to oats like gluten. It is recommended that you not try them until you have healed. I have seen it said that is 6 months to 2 years.

futuredvm24 Rookie

Thanks everyone! I am definitely going to try the color coding..that should make it simple enough for other people to understand..hopefully ;)

As far as the oats go, I am definitely not eating them for awhile..just sticking to whole foods for now!

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    • 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. 
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      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.
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