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

I'm Afraid My Kitchen Will Be Toxic


chrissy

Recommended Posts

chrissy Collaborator

the more i read, the more worried i get. i don't know if it will be possible to keep my kids from getting glutened in my own house!! with so many kids around, someone is always leaving a mess in the kitchen---plus, we have a great room (if you can call it that) so the kitchen and family room are basically one room, so crumbs are dragged everywhere---even if i vaccum several times a day. everyone is in and out of the pantry and leaving crumbs as they go. we would be safest to have a totally gluten free kitchen, but i think i would have trouble with dh on that one-----i don't think he "get's" this disease yet. i must be making some headway with him, though, because he did go and get the blood test done. i am having a hard time with the realization that even a crumb of gluten is too much (and i have been doing alot of reading on celiac) i can see how he wouldn't understand. can you REALLY cross contaminate food if you handled something with gluten and then touched something else---even without crumbs??!!

christine


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



Celiac.com Sponsor (A8-M):



par18 Apprentice

Chrissy,

I understand your concern. In my situation it is just my wife and myself. We made the decision in May after my Dx to try to make the kitchen as gluten-free as possible. Even though she still has a few items with gluten for the most part we eat the same things. As a matter of fact even though I am the one with celiac disease she is starting to go gluten-free with me. After complaining of headaches she is trying to change her diet to see if that helps. I have not been glutened one time since going gluten-free in May. I think the biggest reason is the effort of "both" of us. In your case I don't know how many persons we are talking about but the more that can get on board the better. Good luck.

Tom

Smunkeemom Enthusiast

I try to keep my house as gluten-free as possible. We don't cook gluten meals at all, and any gluten snacks are eaten when the kids are away. After a while you don't really miss the gluten, sometimes you find out that the gluten-free stuff is actually better.

My only other suggestion is to make a "gluten free special place" in the kitchen, with new stuff that has never been "glutened" (like toasters, and spaghetti pans, and mixers and such) and try to explain to everyone that gluten is poison for someone with celiac disease and that if they wouldn't leave arsenic down for a baby then they can't leave crumbs around in your house. It's everyone's job to be "gluten scouts" and you can be their leader. :D

Nadtorious Rookie

I live with a couple of twenty something guys that eat gobs of gluten. I have never expected them to change their eating/cooking habits for me, so I have found ways around cross contamination.

I use only non-porous cooking utensils-glass cutting board, stainless steel pans, etc. I "hide" my good knives, I use plastic cutlery, etc. I use the dishwasher to wash my dishes, usually seperate from theirs, and I don't put my colanders in the dishwasher (those suckers catch everything!). Everything gets prewashed before I start cooking. From the sink to my food, I don't touch anything, including turning off the faucet with a paper towel. Yes, I'm paranoid, but I haven't been glutened by cross contamination in this house yet (knock on wood :huh: ).

As far as having kids with celiac disease, I'm clueless. Maybe stress the importance of handwashing before each meal? That will hopefully eliminate the issue of crumbs on the hands.

Good luck!

Nadia B)

Merika Contributor

Hi Chrissy,

If I recall, you have several newly gluten-free kids, several eat-anything kids, and dh eats gluten? I would be tempted to make the house gluten-free as much as possible. For us, this means dh MUST eat his gluten at the kitchen table, and wash his hands afterwards. No more crumbs around the house.

See if you can work towards making all the kids gluten-free in the house. Maybe dh can eat gluten-free too in the house, or at least confine gluten to when the kids aren't around. I only advocate being sneaky like this if dh insists on eating gluten because the mess kids make vs. the mess adults make is pretty different. And it would be nice if it appeared everyone were on board, so to speak.

Worst case, everyone should be taught that all food gets eaten in the kitchen. At least then the rest of the house is "safe" - especially if they remember to wash their hands after eating.

Our extended family just celebrated our 3rd xmas with a celiac diagnosis, but this is the first year we've had a completely gluten free xmas meal. :) :) Yay! And it was delicious. :)

Merika

Guest nini

my husband is the only one that eats gluten in our house. for a very little while he tried to go gluten free with us but developed such an attutude problem about it... I think he was very angry and resentful of us... (blaming us that he couldn't have his favorite foods and that he doesn't like what we eat... makes nasty comments about how gross it is) that he has resorted back to his gluten-y ways and has even gone overboard with carrying his crumby stuff EVERYWHERE in the house and leaving a mess all over the kitchen and even using my designated gluten free pans for gluten. I was so proud of him when he initially went gluten free with us all on his own, but this going back to eating gluten and being blatantly messy and not caring about it is really starting to get to me. I don't think it's fair for me and my daughter that he doesn't give a rip if he contaminates us with his gluten. I even get mad in the grocery store if he throws his donuts on top of my gluten-free stuff (even if it's sealed)... I don't know which one of us is being less rational about this. Sorry for the rant, I'm just really upset about this. I just went to make gluten-free bagels for me and my daughter, and I had to TAKE APART THE TOASTER OVEN so that I could clean it before toasting our bagels.

angel-jd1 Community Regular

When I visit my parents, I sometimes find myself being a gluten natzi. However, I figure it's ME who has to deal with the puking and diarrhea when I get contaminated, not them. If you don't take care of yourself, and take responsability for your health, nobody else is going to do it. Stand up for what you need and make it very clear!! It is the only way to stay healthy.

-Jessica


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Hey Nini--I hear ya. Could it be that maybe he is doing these things to "prove" that "just a crumb" won't hurt? Like if there are crumbs around, or if your food touches his a little bit, and you don't get sick (outward symptoms, anyway), then he can say--see, you have been overreacting! Even though in reality, you're running around after him like a crazy woman to keep your stuff safe. My experience is that men have a need to "fix" problems. Maybe he is just frustrated that he can't fix it, and this is how he is showing it.

Guest nini
Hey Nini--I hear ya. Could it be that maybe he is doing these things to "prove" that "just a crumb" won't hurt? Like if there are crumbs around, or if your food touches his a little bit, and you don't get sick (outward symptoms, anyway), then he can say--see, you have been overreacting! Even though in reality, you're running around after him like a crazy woman to keep your stuff safe. My experience is that men have a need to "fix" problems. Maybe he is just frustrated that he can't fix it, and this is how he is showing it.

I don't know, but it's making me mad... I've been getting glutened at home A LOT lately which probably explains my mood... and my daughter has been complaining of an upset tummy for a week now... I think he's just being a butt.

jerseyangel Proficient

Yea--I'd be pi--ed off, too. You and your daughter sick like that :angry: --hope you guys get some things worked out.

Guest nini

me too... oh and the night before last she was even running a temp of 100.2, not high enough to be too concerned, but enough to make her uncomfortable, and her tummy was cramping really bad... after a bout of "D" she started feeling better... :angry: This has GOT to stop.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,953
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    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

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.