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

Gluten pizza party in my house?


GFAnnie

Recommended Posts

GFAnnie Explorer

This will probably sound like a silly question but bear with me! My children and I all have celiac, therefore, my outnumbered husband stays pretty much 100% gluten free at home, making our entire home gluten free. Holiday entertaining is about to begin here, and I have a large group coming next weekend. I would like to keep it simple and order out pizza. There's no way I can afford gluten free pizza for all, which leads me to the idea of ordering regular old gluten pizzas for the guests, but it kind of freaks me out to fill my kitchen with all that gluten.  I will add that we are NOT sensitive, at all, so this shouldn't result in weeks of serious gluten symptoms. However, exposure is exposure, right? So what do you think? Would you do this? Any special precautions you would take? I have a pretty small kitchen so it would be hard to contain anything to one area.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

There is no way in h$)& that I would allow a gluten pizza party in my house.  Instead, I would opt for something like salad and chili, tacos, a baked potato bar, stew....the list is endless and cheap.  All can be easily thrown together and prepped during the week.  

I do get the desire to just order out though.  But to risk being miserable for Christmas holidays seems really risky to me!   But that may be just me.   

Gluten is just not allowed in my house.  No one has ever complained. Well, once we had burgers and I offered no buns.  We just used iceberg lettuce to wrap.  Oh, those gluten folks complained, but whil they were eating, I overheard them saying  it was the best burger they ever had!  

 

kareng Grand Master

I would and have done something like that. I get sick from a little cc, but this has worked for me.   It costs too much to give everyone gluten-free pizza.  I have a big enough kitchen to keep my gluten-free pizza or whatever away from the gluten stuff.  You could use paper plates.  Then scrub up after.  If ÿou are serving salad or something else, keep some separate for the Celiacs.  Serve a gluten-free  dessert, but know that, unless you hand each serving to people, the Celiacs can't have the  leftovers.  

kareng Grand Master

Just saw the small kitchen comment - put the gluten pizzas on a table in the living room when the pizza comes, or something  like that & keep the gluten-free stuff in the kitchen?  Or serve dinner in the basement rec room?  If your kids aren't old enough to know not to eat the gluten stuff, then this probably won't work too well.  

Ennis-TX Grand Master

FREEZER PAPER, stuff is a life saver, also disposable table cloths. IF YOU can opt for outdoor entertaining and doing it outside that way you do not have to worry about gluten crumbs everywhere in the house, on the door knobs, couches, chair arms etc.  IF you can not do it outside get disposable everything, cups, plates, utensils, serving platters, table cloths, and line everything to keep your place safe and make cleanup a breeze.

Udream2 Newbie

My daughters school ordered pizza for the whole school b/c power went out and she got glutened, she did not eat any. I feel Pizza is a huge risk as flour is airborne more easily. Plus pizza is greesy, messy and crumb crust. I personally couldn’t do that in our safe home. I do see your point though about making it easy but the gluten can stick around a long time after the party and exposing your family. 

kareng Grand Master
1 minute ago, Udream2 said:

My daughters school ordered pizza for the whole school b/c power went out and she got glutened, she did not eat any. I feel Pizza is a huge risk as flour is airborne more easily. Plus pizza is greesy, messy and crumb crust. I personally couldn’t do that in our safe home. I do see your point though about making it easy but the gluten can stick around a long time after the party and exposing your family. 

But I don't think they were making the pizza - so the flour from making the crusts wouldn't be flying around  in her house or the school.


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master
1 hour ago, kareng said:

But I don't think they were making the pizza - so the flour from making the crusts wouldn't be flying around  in her house or the school.

The issue with pizza is you pick it up by hand....you pick up grease coated gluten, you then touch door handles, desk, arm rest on chairs, counters, chairs, remotes, switches, water facets.....spreading gluten residue with sticky grease everywhere. Then someone else touches then touches their gluten free food, or their lips...BAM glutened .....pizza is one of those high risk foods for CCing stuff. The grease + flour/gluten residue makes it spread, does not help if people eat it with their bare hands not a utensil.....Sorta why I suggested a outdoor party over indoor....

Victoria1234 Experienced
13 minutes ago, Ennis_TX said:

The issue with pizza is you pick it up by hand....you pick up grease coated gluten, you then touch door handles, desk, arm rest on chairs, counters, chairs, remotes, switches, water facets.....spreading gluten residue with sticky grease everywhere. Then someone else touches then touches their gluten free food, or their lips...BAM glutened .....pizza is one of those high risk foods for CCing stuff. The grease + flour/gluten residue makes it spread, does not help if people eat it with their bare hands not a utensil.....Sorta why I suggested a outdoor party over indoor....

Exactly the same reason I wish I could wear a hazmat suit when I have breakfast duty at the elementary school! Pancakes, waffles, cereal, muffins, corn dogs, all spread everywhere with messy dirty little hands, ugh. I wash my arms up to the elbows after that.

Ennis-TX Grand Master
2 minutes ago, Victoria1234 said:

Exactly the same reason I wish I could wear a hazmat suit when I have breakfast duty at the elementary school! Pancakes, waffles, cereal, muffins, corn dogs, all spread everywhere with messy dirty little hands, ugh. I wash my arms up to the elbows after that.

Why I had to quit the standard food industry years ago after dia. I semi joke about working in a standard restaurant etc or helping out but going in with a Open Original Shared Link

Although after your mentioned hazmat I can think of serving food in this and and the looks you would get.
Open Original Shared Link

Victoria1234 Experienced
23 hours ago, Ennis_TX said:

Why I had to quit the standard food industry years ago after dia. I semi joke about working in a standard restaurant etc or helping out but going in with a Open Original Shared Link

Although after your mentioned hazmat I can think of serving food in this and and the looks you would get.
Open Original Shared Link

It doesn't come in purple so I can't wear it, lol. God these little kids and all their germs I really should be wearing that suit. 

cap6 Enthusiast

Wouldn't!  Couldn't!   Shouldn't!   Oh my!  I hear  what some are saying about keeping areas clean, but no way.  I get not wanting to cook for a big group but a couple pretty easy, and cost effective, thoughts are a simple crock pot or two of chili, taco bar, potato bar or a salad bar.  I just did a Xmas party for 22 people, only 4 of us are gluten free, and did crock pots of chili.  for bread I bought gluten free hamburger buns, sliced them and then quartered them.  It made great bread garlic bread.. 

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • 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
×
×
  • 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.