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

Need Help With Transitioning To Mostly Gluten Free Household


concernedmamma

Recommended Posts

concernedmamma Explorer

Hello everyone. We received our son's (age 4.5yrs) positive diagnosis of Celiac (from biopsy) on Tuesday, met with the dietician on Thursday and are now on our own. I am struggling with the best way to do everything. We have three other children and although we would love to go totally Gluten free in the house, but it just isn't financially feasible right now. For some things we are making the complete switch- pasta, soups, etc. The things that we aren't completely switching are bread, cereal etc. I am not sure what we are going to do about meats, crackers, etc.

What is the best way to set up our kitchen, pantry and fridge to avoid cross contamination? I am working on rearranging the pantry and fridge so that he will easily know which snacks, foods are safe for him to eat. I am realizing, though how many times during the making of one meal I am at risk of cross contaminating. My first real meal that I made for him was a grilled cheese sandwich. I did good at making his sandwich first, using 'clean' materials and supplies. I then made the other sandwiches, gave everyone gluten free pepperoni sticks, served lunch and realized we needed a fruit/veggie, so I grabbed a pear, headed for the cutting board and realized I couldn't use it because it was now dirty! I got out a new cutting board, but couldn't remember which knife was from his sandwich, so then got another one....... argh! Does this get easier?

Also-dishwasher question..... if we are washing our dishes with his, do we need to worry about the gluten food flecks getting left behind? what about the utensil drawer? It always seems to have some kind of 'flecks' that constantly appear.

I guess I am just looking for tips and tricks from those of you that are managing a combined household.

Well, one more question. Prior to diagnosis, we would have a few weeks of diarrhea then a week or so of almost-normal stools, etc. We started gluten free on thursday. His stools had been not bad, and remained that way until today. He got one of his baby sisters 'puffs' which are made of wheat. About 2 hours later we had explosive diarrhea. Do you think the gluten/gluten free diet was affecting him this quickly?

I will stop rambling on right now and wait with baited breath for all of your expert advice!!

Thank you!!!!!!!


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



Celiac.com Sponsor (A8-M):



Juliebove Rising Star

Our situation is a bit different in that we are dealing with allergies and not celiac. But pretty much the same diet.

What we did was to buy a little refrigerator for my daughter's food. We did this for a variety of reasons. She wasn't old enough to be able to read labels and figure out what was safe for her. My husband and parents (just in case they might babysit) couldn't seem to figure it out either. And also to avoid cross contamination. She had her own jam, nut butter, mustard, etc.

We also used a card table set up in a corner of the dining room for her speical foods that didn't require refrigeration. Why a card table? Because it's what we had. We have since bought some bins and shelves and hopefully one day will be able to afford a free standing pantry.

We have a very small kitchen and not enough cupboards the way it is. I do keep things like gluten-free pasta and rice in the regular cupboard. Her storage space just holds things that only she will eat like cereal, gluten-free crackers, bread, etc. I did replace all of my baking things. I have diabetes so didn't do much baking to begin with. And after she was diagnosed, I baked up a storm, trying to find things she could/would eat. I wound up mostly not baking and just buying pre-made stuff for her.

I did buy her a toaster just for her. A cheap one. I did replace some of my pans and other cooking utensils.

I do not use cutting boards. I use paper plates. Wasteful, yes. But no change of cross contamination there. I also use plastic knives for making sandwiches and other things. I just use one and throw it away. I buy these at Costco so they are cheap. I also look frequently at the local party store. For some reason they tend to put the knives on clearace for next to nothing. Yes, they might be odd colors, but I don't care!

We do not eat a lot of sandwiches at home. My daughter does sometimes take them in her lunch and I do make them a couple of times a week for her to eat after school and before dance class. If I were going to make them at home for us all to eat, I would make them all on paper plates. I would make hers first. Then mine (I also have food allergies but less than she does), then finally the one for my husband. I would use a plastic knife and use the same knife for hers and mine, then wipe it with a paper towel and use it for my husband's. He prefers mustard on his and we use fake butter on ours.

For dinners, I mostly try to make something we all can eat. Pasta. Or meat with rice or potatoes. Some kind of vegetable. I tend to cook things that are naturally gluten-free. Or I will make gluten-free gravy or sauce. Took some doing to come up with something to put in casseroles, but I finally came up with a "cream" of mushroom soup using fresh and dried mushrooms, rice milk and Nucoa, thickened with sweet rice flour.

My husband currently lives in another state (he's in the military) so when it is just my daughter and I here, it's not a problem. I rarely eat bread or crackers. I do eat peanut butter stuffed pretzels and sometimes regular pretzels. I just keep them by my computer. This is where I eat them.

My husband does eat bread, crackers, cookies, pie, cake, etc. I do not make these for him. I buy them. They are eaten on paper plates.

I find we generally do not have trouble at home with cross contamination. The main problem with that occurs at my parent's house where we go for holiday meals. People tend to pass gluteny things or other allergens over her plate. Or they expect her to touch things she is allergic to. Or don't understand that these things can't share a serving platter with her food. Or the same knife can't be used for different things. They think I am being silly and going overboard and poisoning her mind. They think a little bit of something can't hurt you.

When they say this... I give the example of a pill. I will ask them what the smallest pill is that they take. And they all take some kind of prescription med. They will then give me the name of the pill. So I will say, "Why don't you give Angela one?" To which I am met with a horrified look. I then reply, "Well... It's so small! A little bit can't hurt. Right?" You would think they would get it from that. But they do not.

  • 2 weeks later...
Bex326 Newbie

We have designated the pantry for all of my daughters gluten-free foods, we have also designated shelves in the fridge and freezer. We purchased new cooking utensils pots/pans, potholders, cutting boards and we got all of them in red. We tell everyone that only red items are to be used for her. We also designated a silverware draw for her to avoid crumbs since our draw is near the stove. We use a different part of the counter to prepare her foods (even though we use paper plates). We also buy our daughter her own butter, peanut butter, grated cheese, etc. I don't bake for anyone but my daughter so when I got the baking pans I dont need to worry about that. I don't cook for myself and my husband only for her (my husband still thinks I can't iron! LOL)

The hardest part is when she is not home. People just don't understand the importance of avoiding cross contamination or thinking it is OK to give her "just a little". I have tried books, lists, talking to them - only to find out that one of my babysitters was giving her french fries and sharing her sandwiches!

Keep reading, talking to your doctor keep & asking questions of those who are in your situation, I know I do. :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,005
    • Most Online (within 30 mins)
      7,748

    blessedwannab
    Newest Member
    blessedwannab
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
    • Scott Adams
      Exactly, everyone with celiac disease technically has an "intolerance" to these: Wheat: The prolamin is called gliadin. Barley: The prolamin is called hordein. Rye: The prolamin is called secalin. Around 9% of celiacs also should avoid oats (but around the time of diagnosis this may be much higher--some will have temporary intolerance): Oats: The prolamin is called avenin. I had to avoid this for 1-2 years after my diagnosis until my gut healed: Corn: The prolamin is called zein. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful:    
    • trents
      I think your question needs clarification. Are you asking who gets sick from consuming some of these prolamins are all of them? Everyone in the celiac/gluten sensitive community will get sick from consuming gliadin, hordein and secalin. Some will also get sick from consuming avenin. Apparently, some don't do well with any of them.
    • Bebygirl01
      Prolamins are a type of protein found in cereal grains. Different cereal grains contain different types of prolamins, which are named based on the grain they originate from.  Here's a breakdown by grain:  Wheat: The prolamin is called gliadin. Barley: The prolamin is called hordein. Rye: The prolamin is called secalin. Corn: The prolamin is called zein. Oats: The prolamin is called avenin. Rice: The prolamin is called oryzenin. Sorghum: The prolamin is called kafirin. Prolamins are a major component of cereal storage proteins and are known for their high proline and glutamine content and can get celiacs and non-celiac gluten sensitive individuals sick.
    • DebJ14
      Our son was put on Minocycline for his acne.  It did not solve the acne problem.  He developed drug induced lupus and pericarditis from it and missed an entire year of high school.  He literally went from playing football to bedridden in a couple of weeks.  His PCP tested him for genetic antibiotic resistance and he cannot take any drug in the Tetracycline family.  His gut microbiome was totally destroyed.  In fact he had a stool test done and had no good bacteria, whatsoever.   What did fix his (and his brother's acne) years after the Minocycline debacle was when I was diagnosed with Celiac disease and the kids were tested.  They were both put on a Gluten Free/ Caesin Free diet and within a week both kids were totally free of acne.  The family has now been on the diet 18 years and no acne, except for a teenage grandson who will not adhere.  The big clue that he is eating gluten is that his face breaks out!
×
×
  • Create New...