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

Gluten Free Kitchen


Kenster61

Recommended Posts

Kenster61 Enthusiast

I just read the Gluten Free Bible. The author says that if you live in a house with those who eat wheat that you have to get different utinsels. I didn't think about this issue but have been breaking out in DH even though I'm being very careful with my diet. Does this mean that wheat can get into silverware and things like that even after it's been washed? Has anyone had this experience with roomates and what did you do about it? thank you in advance.

Ken Ritter


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator
I just read the Gluten Free Bible. The author says that if you live in a house with those who eat wheat that you have to get different utinsels. I didn't think about this issue but have been breaking out in DH even though I'm being very careful with my diet. Does this mean that wheat can get into silverware and things like that even after it's been washed? Has anyone had this experience with roomates and what did you do about it? thank you in advance.

Not true. Just wash it well and you'll be fine. Oh, God. The minute I saw Gluten Free Bible I went nearly panicked :o . There have been rantings at Delphi on the inaccuracy of the book. First, Jax doesn't research carefully: she says that Cheetos and Tootsie Rolls aren't gluten-free--they both are. She has so many inaccuracies, suggesting that you eat something just so you don't offend your host, regardless of whether it contains gluten and suggesting that you take the wheat communion, hold onto it, and later feed it to the birds. She is more aware of contamination in this book than in the last, but I still wouldn't trust the book farther than I can throw it <_< . She still mentions removing the contents of a "normal" sandwich and putting it between two slices of gluten free bread and eating it -- if you are not "too sensitive."

TO OTHER READERS: Don't purchase that book!!! I highly recommend, instead, Wheat Free Worry Free by Danna Korn (the true gluten-free Bible) or Shelly Case's celiac book. Jax is too inaccurate. I apologize for this rant, but it's scary that such inaccuracies are out there.

Here is the review section at Amazon. It's basically a war between the newbies who like the writing style and assume the info. is correct and the old-timers who are warring against it:

Open Original Shared Link

angel-jd1 Community Regular
have to get different utinsels

Things that are poreous such as wooden spoons DO need to be replaced or only used on gluten free or gluten full foods. They can trap nasty things in them and make you sick.

-Jessica :rolleyes:

celiac3270 Collaborator

Right. Avoid wood and teflon. But in terms of regular, metal utensils, don't worry.

MySuicidalTurtle Enthusiast

Using a dishwasher is best when you share kitchen things, I find. Somethings that need to be hand-washed we have two of or just one clearly know to be only used for glutenfree foods.

Kenster61 Enthusiast

Thank you all for your thoughts. :lol:

kvogt Rookie

I use every utensil in our kitchen, wooden spoons, whatever, regardless of what it has touched before, with no problems. I wash well or run through the dishwasher.

You may find there won't be a lot of gluten around besides store-bought breadstuffs if you are doing the cooking


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

Wood absorbs everything even when wased and washed. Just because you don't get sick doesn't mean you are not getting gluten.

kvogt Rookie

MySuicidalTurtle,

I'd like to push back a little on your last statement... How do you know this? Has there been a study on it? Is there any proof? How do you/they/whoever know that a wooden spoon - washed and washed - still retains gluten and causes harm?

I've read posts on this topic which advocated virtually replacing everything in the kitchen. I don't believe this is practical advice. It is entirly possible to clean up most if not all of your kitchen.

KaitiUSA Enthusiast

I actually have to agree with everyone who said replace wooden spoons. It is true that wooden spoons retain gluten-they retain everything they are put into so if you used wooden items previously then they should be replaced.

celiac3270 Collaborator

Yes--I don't think anyone has tested how a wooden spoon retains gluten, but it's just generally known to...just as teflon is thought to.

plantime Contributor

Wooden spoons and cutting boards are also bacteria traps. Wood is a naturally porous product, it absorbs whatever it is in contact with.

cdford Contributor

Determine how sensitive you are. It varies for each of us. I have a friend who can cook for her non-celiac disease husband and kids with no apparent problems. I, however, am very sensitive. We also found that if non-gluten-free stuff was around, my daughter tended to snitch and cheat. No matter how much we preached, someone was always double-dipping in the butter or jelly or peanut butter. You get the picture. We finally went to a totally gluten-free house. It was not until we did that (even to the point of wiping down cabinets/shelving and shampooing carpets) that I stopped having symptoms regularly. I replaced my former pots and pans, threw out the wooden spoons, and replaced the appliances such as toasters and bread machines. It made a world of difference in both our health and our medical expenses.

christicrete Rookie

I have a quick question about dishwashers. I have a family that refuses to go gluten-free and my question is : When you wash dishes in a dishwasher (you know when a glass or plastic container gets turned upside down you get all that gritty junk inside) are you cross contaminating all your dishes? Then, would all restaraunts be off limits because no way in h#%& would they wash your dishes seperately. Also I have purchased those disposable ziploc containers and when I open a new jar of peanut butter and Jelly and other stuff I immediately put in containers for me and mark every lid with a marker. I have also adopted red as my official gluten-free color. I took red nail polish and put it on pan handles, cookie sheet lips and other things that are designated gluten-free. Also red duct tape on things that don't go in the oven. It helps even my 6 year old son, he asks when ever he sees red items if he can use it or not.

Just my questions and two cents

Christi :P

tarnalberry Community Regular
When you wash dishes in a dishwasher (you know when a glass or plastic container gets turned upside down you get all that gritty junk inside) are you cross contaminating all your dishes?

Then, would all restaraunts be off limits because no way in h#%& would they wash your dishes seperately.

Ideally, a good dishwasher will leave nothing behind - maybe clean water in an upturned container. If you're getting stuff left behind, you may want to 1) check the detergent you're using, 2) make sure there's no food particles going INTO the dishwasher, 3) check that the dishwasher doesn't need repair. (We've been dealing with this issue ourselves.)

As for a restaurant.... they don't use automatic dishwashers. Every restaurant I have been inside the kitchen of (and it's a few) washes dishes by hand. They have to be air dried, as well, from what I understand, for health reasons. (Drying with a towel can be problematic - studies have show that the towels, which stay damp when you use them so often, grow bacteria and mold fairly quickly.

christicrete Rookie

I have worked in many restaraunts and they all had automatic dishwashers that they changed the water in after 20 or so loads. they work differantly than your standard home dishwasher but they work on pretty much the same principles. As for washing by hand, we were not allowed to because the temperature of the water had to be hot enough to kill bacteria and you could not touch the water at those temps. The FDA would not allow hand washing. Everything had to be dishwasher safe. As for my dishwasher, it has a garbage disposal in it and chops the food material super fine. When my dishes are extra dirty I get grit on my dishes and have to wash them again. This is my question, wouldn't some of that grit be gluten since my household is not gluten-free, only me. and since there is some grit that is visible there of course would be residue that is not visible but from what I have read could still be potentially hazadouz to the celiac. OR am I just obsessing way too much and just live my life without over analizing everything, just being careful ;) (anyone ever notice that analizing has the word anal in it :rolleyes: ) I'm sorry for being so weird, just trying to figure how to feel better and not getting all the way there yet. I am also a little overwhelmed and still "grieving" my favorite gluten laden things.

Christi

tarnalberry Community Regular

Fascinating... my friends who had restaurants weren't allowed to have automatic dishwashers. Interesting difference. Of course, there may have been a prewashing area I forget about, but I remember the other one. Or maybe my memory is all twisted up...

Either way, in the home... I'm unfamiliar with that type of dishwasher that you note - I'd recommend cleaning the foodscraps off the plates thoroughly before putting them in the dishwasher if some particles get left behind. That's definitely not something you're too paranoid about! ;-)

christicrete Rookie

Must be the differances in state compliances. Icould not imagine washing all the dishes a restraunt generates by hand!!!! I have only worked in Minnesota and North Dakota restraunts, the laws were the same in both states. That is interesting, I have always wondered which way of doing dishes is best. I will stick with my dishwasher, easier! It does help having worked in a few rest. in the area because I know lots of the management and they are more willing to help out someone they know as far as special preparations. This will probably change down the road but for now, while I am learning, it is good!

debberdee Newbie

I am going back to the info that celiac3270 posted about the book by Jax and off the dishwasher talk (sorry) :wacko: Thank you celiac3270. I just recommended this book elsewhere and oh, my gosh! I feel so terrible! I just loved her writing style and chose to ignore the inacurracies! I now realize after reading your posting and also the comments at Amazon, that I should have never suggested this book. Thank you so much for your knowledge and insight. I read EVERYTHING that I can get my hands on about celiac disease and never realized that others may not read as much or the way I read and that some info in The gluten-free Bible could be damaging to those who don't disregard the 'untruths'. I have read many of your postings and want you to know that I think you must really be amazing! Thanks for your help!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,191
    • Most Online (within 30 mins)
      7,748

    teresa1955
    Newest Member
    teresa1955
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...