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 Feel Like I'm Nagging


Roda

Recommended Posts

Roda Rising Star

I really am beginning to think I am nagging all the time to my husband. I live in a shared household where I am the only one gluten free. Everything appeard to be going alright, until recently when I did some observation during my time off. My husband has his area on the counter that he can do his and the boys' gluten stuff. They have their own shelf in the pantry. The condiments are shared as are the lunch meats/cheese (We buy packaged gluten free). The issue I am having with him is that I observed him getting out his bread to make a sandwich, then he opened up the lunchmeat/cheese and grabbed what he wanted, made his sandwich, sealed it up and put it away. Anybody see the problem here? When I asked him not to do that or at least wash his hands after the bread and before opening/closing the packages, his response was "I'm only touching what I am going to eat." Don't get me wrong he is understanding and takes this serious, I just didn't realize he was taking shortcuts with that stuff. If he cooks dinner it is always gluten free and he is always good, since I am always home. He eats sandwiches almost daily for lunch and since I was off I was privey to his practices. How can I get my point across without seeming like I am nagging? He won't give up certain things, which I am ok with he just needs to me more careful. As for the condiments I usually wash after touching the outside of the containers (most are squeezeable) and before touching my food. I know the handle of the fridge is an issue so I make sure to wash after it also.


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



Celiac.com Sponsor (A8-M):



The Fluffy Assassin Enthusiast
I really am beginning to think I am nagging all the time to my husband. I live in a shared household where I am the only one gluten free. Everything appeard to be going alright, until recently when I did some observation during my time off. My husband has his area on the counter that he can do his and the boys' gluten stuff. They have their own shelf in the pantry. The condiments are shared as are the lunch meats/cheese (We buy packaged gluten free). The issue I am having with him is that I observed him getting out his bread to make a sandwich, then he opened up the lunchmeat/cheese and grabbed what he wanted, made his sandwich, sealed it up and put it away. Anybody see the problem here? When I asked him not to do that or at least wash his hands after the bread and before opening/closing the packages, his response was "I'm only touching what I am going to eat." Don't get me wrong he is understanding and takes this serious, I just didn't realize he was taking shortcuts with that stuff. If he cooks dinner it is always gluten free and he is always good, since I am always home. He eats sandwiches almost daily for lunch and since I was off I was privey to his practices. How can I get my point across without seeming like I am nagging? He won't give up certain things, which I am ok with he just needs to me more careful. As for the condiments I usually wash after touching the outside of the containers (most are squeezeable) and before touching my food. I know the handle of the fridge is an issue so I make sure to wash after it also.

In the first place, have the boys been tested? There is either a 1 in 7 or a 1 in 10 chance that immediate family members of celiacs are also celiac. I'm assuming that they've been tested, but if they haven't that's the first priority.

As to the lunch meat, just sit down with him and figure it out. If he wants to make sandwiches that way, you'll just have to have your own lunch meat separately labeled and segregated. But of course that'll cost more. If he wants to pay more for his own convenience, let him. If he wants to take the trouble to watch his hands carefully every time, thereby saving some money, that's good, too. (You might want to get him to read up on cross-contamination, though.)

Crayons574 Contributor

What I have had to do is, when one of us gets back from the grocery store, I am the first to take out some of the lunch meat and snacks or what have you, and then I will put that in a separate plastic bag that has my name on it, and a "do not touch unless you have washed your hands with Gluten-Free soap" sign on it. Also, I have had to get my own condiments and put my name on them as well.

It's a bit more of a hassle to do this, but no one is going to be as careful about things as you are--even if they mean well. Sometimes, it might not cross their mind to wash their hands after they have touched bread and are reaching for the lunch meat.

So, I would say to put your lunch meat and condiments in completely separate, labeled containers. You will have to worry a lot less and perhaps it will allow your husband to be more aware of your concerns without having to verbalize it anymore. Hope that helps :)

Roda Rising Star

The Fluffy Assassin--

Yes my boys have been tested and were negative. I had them tested Nov. 08 when the youngest was almost 4 and the oldest was going on 8. Their ttg was 1 and 2 respectively ref. range >20 positive. I did think at one point the oldest was at least gluten intolerent, but for now I have rethought this. He is doing good and I believe his sx (moodiess and minor behavior) are from his seasonal allergies. The youngest is growing like a weed and has shown no signs yet.

I don't really like the idea of buying two different packages of the lunchmeat/cheese, since I will have a lot more waste.

Crayons574--

I guess something that simple never occured to me. Thanks for the suggestion it will make things simpler. Sometimes the simplest things allude me like I have a permanant brain fart. :lol:

ranger Enthusiast

Glad to see someone use the term brain fart! Once again, this forum makes me feel like I'm not alone! LOL

ang1e0251 Contributor

That's like when your spouse demolishes the tooth paste container. Just get your own toothpaste. No one likes to be nagged.

I really liked the suggestion someone made on another thread. She said get a plastic box to go in your fridge for all your gluten-free stuff. That made a lot of sense. It's very obvious and a no brainer for the rest of the family. We need no brainers in my family.

Billygean Apprentice

Are you feeling well? If you are, I wouldn't worry about things like this, especially if you only noticed it on your days off - if you are feeling okay try not to stress. You cannot have absolute control over your environment and arguably having a few molecules of gluten here and there will help you if you ever want to eat out and there's a risk of CC> If it's not affecting your health I wouldn't bother, I spent a lot of time stressing but as long as you've got the big things down - no shared toasters, butter, etc - then I wouldn't nag.


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



Celiac.com Sponsor (A8-M):



Ariauna Apprentice

No one likes to nag or to be nagged about anything but this is your health and all of us here know what you will go through if you get cc'd and it is horrible. Although it is impossible for your family to remember the hand washing all the time and for them to think about cc everytime they go into the fridge for some food or the cupboards we can ask them to be thoughtful.

My kids/husband their own cupboards I don't even do shelves. I have about 3 cupboards that are mine and they have about 4 that are theirs, the rest are used for dishes ect... I keep all my food, pans and dishes in my own gluten-free cupboard. I also have my own silverware/drawer and the counter above it is never used for preparing normal foods. If my family prepares food they do it on the table and then wipe if off immediately. I pretty much prepare my own food and as far as my food in the fridge goes I have a snap tight container that I keep my items in. All these things help to eliminate the possibility of being cc'd.

The only issue that I worry about is our oven as of course we don't have two of... we just make sure we clean it out a couple times a week. Our microwave oven I am just sure to wipe it out before I use it... a bit time consuming but worth it to me :)

Roda Rising Star

I can truthfully say that this was the only thing I was complaining about. He generally does a good job. I do have to admit sometimes I can get onto something and he just has to come out and tell me to be quiet about it. :lol: I guess we all need our checkes and balances. Thanks everyone for the insight and help. It is greatly appreciated.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,130
    • Most Online (within 30 mins)
      7,748

    Tony White
    Newest Member
    Tony White
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
×
×
  • 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.