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Washing Dishes


mtdawber

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mtdawber Apprentice

Hil all, I got glutened again and I'm being really stupid careful. It's very frustrating. I noticed that a bunch of people talk about hand washing their dishes separate from everyone. Can you tell me - do you bleach them or how do you make sure that you dishes are extra safe in a house full of gluten loving, eating people?

Thanks for you help.


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nikki-uk Enthusiast

I have 2 coeliacs out of 5 in my house.

I always rinse every thing off under the tap before putting it in the dishwasher.

If it's a saucepan that's had gluten pasta in for example I wash properly with soap and and a scourer before putting in the dishwasher. ( :lol: what's the point of a dishwasher )...but it works for us :)

Viola 1 Rookie

I rinse all the dishes that go into the dishwasher and use only gluten free pasta. That's the one thing that my hubby eats gluten free. :rolleyes:

I also make sure I use paper towels, or a clean plate under any of my food that I prepare on the counter.

I think the biggest problem is making sure that no crumbs get stuck to coffee cups and glasses.

BTW ... you really need to check the cup before your coffee is poured in a cafe or restaurant as well. I've seen some with crumbs stuck to them out of the dishwasher. :(

Guest Kathy Ann

Even with a high quality dishwasher, I notice that if I run my finger around on the inside of coffee cups, glasses and cereal bowls, there is frequently a gritty residue. It doesn't always show. I rinse the dishes before putting them in the dishwasher too. But these new high efficiency dishwashers don't use much water. Open it up halfway through the cycle and look how gunky the water is. If that dirty water doesn't efficiently rinse off and then gets "baked" back on in the drying cycle, it could be a problem I would think. I'm fighting the same thing. I'm extremely careful, but live in a house with all gluten eaters. I'm getting glutened all the time. So as hard as it will be, I'm planning to separate everything and use my own dishes and handwash all my stuff. It isn't working the way it is.

happygirl Collaborator

I am an extremely sensitive Celiac, and any gluten food gets wiped into the trash can with a papertowel/napkin. Gets rinsed well, and either washed or put in the dishwasher. If it goes in the DW, it gets rinsed a little extra. It seems to work well for us.

jkmunchkin Rising Star

I rinse everything off before it goes in the dishwasher. However trying to get my husband to do that, well you'd think I'm asking him to jump off the Empire State Building.

We also have 2 scrubby brushes. So if I'm washing a pot that had gluten stuff in it, I use the gluten brush.

Viola 1 Rookie
I rinse everything off before it goes in the dishwasher. However trying to get my husband to do that, well you'd think I'm asking him to jump off the Empire State Building.

We also have 2 scrubby brushes. So if I'm washing a pot that had gluten stuff in it, I use the gluten brush.

Yes, hubbys aren't very cooperative for the most part. Mine gets very deffensive if I say anything about cleaning up his crumbs or what ever. :( But as we've been married for 40 years this spring, he isn't about to change now. :rolleyes:

So, it's up to us to make sure we stay as healthy as possible.


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4getgluten Rookie

I am gluten-free, but my husband is not. He is pretty good about cleaning up his crumbs, but I am still forever cleaning the counters. I also have two different sponges to clean my dishes. One for gluten dishes, for gluten-free dishes. I change my gluten-free sponge frequently, and rinse it with soap and water everyday. I also rinse and scrub all my dishes before I put them in the dishwasher.

One other thing to mention, have you invested in gluten-free cooking tools? I keep a gluten-free cutting board, gluten-free wooden spoons, measuring cups, spoons, spatulas, and stainless steel pots and pans. I have them all in a special spot. I also don't use my non-stick coated pan to cook any gluten-free meals. It's just too risky. It seems no matter how much I scrub those pans; they still have a residue on them. I only use my stainless steel pans to cook gluten-free meals.

Cross-contamination happens really easily. In addition to cooking utensils, try to keep separate gluten-free mugs, plates, glasses, and silverware if you can. It will help cut down the risk.

Guest cassidy

I am very, very sensitive and I have separate pots & pans, strainer for pasta, can opener and kitchen scissors. Other than that we share all silverware, cups, plates, tupperware. I never get myself sick at home and I don't do anything special with the dishes. My husband (the gluten eater) isn't very good at rinsing the dishes before he puts them in the dishwasher and most of the time there is at least one plate/fork with food stuck on it. I wash that again along with anything it could have touched, but that is all I do. We share a sponge for hand washed dishes and I've never had a problem. I do wipe down the counters a lot, along with fridge and microwave handles and I never put my food directly on the counters just in case.

So, you have to do what makes you most comfortable. I like having my own pots & pans but I do fine without worrying about the rest of it. I'm sure other people do things differently, but I don't think it is 100% necessary to keep everything separate if you are washing it normally. Hopefully, you will find a system that works for you.

emcmaster Collaborator

We have four separate dish brushes: 1 for gluten-y dishes that are going in the dishwasher, 1 for gluten-y dishes that get handwashed (the idea of using a dirty brush to "handwash" something that isn't going in the dishwasher irks me), 1 for gluten-free dishes that are going in the dishwasher and 1 for gluten-free dishes that are being handwashed. This is probably a little too much, but it seems to work for us.

My husband is terrible, terrible about putting his dishes in the dishwasher. It drives me up a wall! But when he does, he's pretty good about cleaning them off well enough.

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • 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 😁.
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      @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 
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