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

Stupid Me.. Lucky Me!


Katrala

Recommended Posts

Katrala Contributor

I did a "Holiday Cooking Around the World" class with my students yesterday for an enrichment day. We were making different holiday dishes from different cultures.

I don't have any type of touch reaction from cooking gluten food, so I figured it wouldn't be a big deal. I made sure to eat a big breakfast before I left home, not wanting to eat even my brought lunch at school just because I figured I'd probably have gluten all over me.

So after thinking through all the precautions, I managed to negate them all by being a complete idiot.

Our first dish was Apple Kugel and we were boiling the egg noodles. I was explaining what "al dente" was and, just like I do with my gluten-free pasta at home and what I've always done with pasta, I took a piece out, popped it in my mouth to see if it was al dente yet - and then had them try it to see.

I didn't even think about it until I had swallowed it and thought, "You've GOT to be kidding me!"

I drank a good bit of water and was lucky - no terrible reaction other than my stomach gurgling some throughout the day.


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



Celiac.com Sponsor (A8-M):



srall Contributor

When I first went gluten free I still made gluten-filled food for my husband and daughter. It took so long before I was out of the habit of testing their food as I was cooking it. I'm glad you didn't have a terrible reaction.

BabsV Enthusiast

I'm so glad you didn't get really sick. I'm 4 months into the gluten-free lifestyle and I am paranoid about making this sort of mistake...being slightly distracted or busy and just popping something in my mouth without really thinking about it!

mamaw Community Regular

Happens to the best of us... I call it a brain fart!!!!!

Monklady123 Collaborator

Yes, pasta was the one thing I did that with several times before I managed to get over it. I think the pasta thing is more automatic than anything else I do in the kitchen... I mean, I never automatically added flour to things (I always used cornstarch even before celiac because it doesn't get lumpy like flour does), and I've never tasted my kids sandwiches (and now they make their own anyway), etc. But pasta...well besides tossing the spaghetti against the wall to test for doneness (lol) tasting is the only way I do it.

Now I've finally learned to call someone to taste it for me. :P

bumblebee-carnival Newbie

I totally understand. We had people over Saturday night and I was putting out crackers and cheese for them. Automatically I went to reach for a cracker to pop in my mouth. I "came to" before I actually grabbed it, but I just started laughing.

pricklypear1971 Community Regular

While I understand cooking gluten in a classroom, I think those of you who cook it at home for others are real troopers!

Around here I'm the gluten police, and very little walks through the door. And if they want it-THEY COOK IT!!!

But I'm not a nice person, and everyone knows this...


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



Celiac.com Sponsor (A8-M):



Takala Enthusiast

Now, now, prickly pear, there are plenty of "nice" people out there who are really passive- aggressive.... :wacko:bless their hearts. ^_^

srall Contributor

While I understand cooking gluten in a classroom, I think those of you who cook it at home for others are real troopers!

Around here I'm the gluten police, and very little walks through the door. And if they want it-THEY COOK IT!!!

But I'm not a nice person, and everyone knows this...

Oh that was only in the beginning. After my daughter was diagnosed the kitchen went mostly gluten free. (Sometimes I cannot contain my husband) But I will NEVER EVER EVER make something with gluten that neither my daughter or I can eat

Katrala Contributor

While I understand cooking gluten in a classroom, I think those of you who cook it at home for others are real troopers!

I do at home - we have a small section of the kitchen that is gluten-free.

Of course, I don't have any type of reaction from doing so. I learned early on that trying to do both at the same time (and make sure to wash hands in between, even) didn't work, so I had to either eat first or last. Well, that means I eat last when it's just me cooking.

I'm very fortunate in that my husband is an amazing cook and has been very supportive in making gluten-free foods. I only cook on the nights that he works (several times per week, but it's not too bad.) He and the kids still eat gluten, but our family meals are gluten-free and we have everything partitioned off.

I noticed today I was a bit "fuzzier" than normal and had a hard time in the faculty/student basketball game (I'm not normally talented at basketball by any stretch of the imagination, but today was noticeably more difficult.) This could be a reaction or it could just be a simple pure exhaustion from trying to wrap up the last few days of school before the break.

Monklady123 Collaborator

While I understand cooking gluten in a classroom, I think those of you who cook it at home for others are real troopers!

Around here I'm the gluten police, and very little walks through the door. And if they want it-THEY COOK IT!!!

But I'm not a nice person, and everyone knows this...

Everything else that they eat is gluten-free, since most foods are naturally gluten-free. But I do cook their pasta, and I do bake regular stuff for them from time to time. But it's always using a mix (I hate to cook or bake, lol) so I'm not dealing with sifting flour, etc. I've never had a reaction from it so I don't mind.

The reason I don't cook gluten free pasta for the rest of them is that it's too expensive! One of my pasta eaters is a teenage boy and if he has a friend over...well there goes a pound for just the two of them. lol..

LReynolds Newbie

I have only been diagnosed for about 5 days now, but I am just waiting for this to happen to me. Sorry to hear you didn't feel great afterward! Hope you feel better now!

red island Newbie

The first month or so after my diagnosis I had terrible nightmares about accidentally popping a regular cookie in my mouth, I'd wake up in a panic!

pricklypear1971 Community Regular

Everything else that they eat is gluten-free, since most foods are naturally gluten-free. But I do cook their pasta, and I do bake regular stuff for them from time to time. But it's always using a mix (I hate to cook or bake, lol) so I'm not dealing with sifting flour, etc. I've never had a reaction from it so I don't mind.

The reason I don't cook gluten free pasta for the rest of them is that it's too expensive! One of my pasta eaters is a teenage boy and if he has a friend over...well there goes a pound for just the two of them. lol..

Yes, I was pleasantly surprised when my son liked my gluten-free pasta. But he does eat a lot of it, and you're right it isn't cheap!

Poppi Enthusiast

I did that a couple of times too. On one memorable occasion I tasted a spoonful of vegetable noodle soup before I gave it to my daughter. Hubby and I were feeding the kids right before we set out on a weekend away so I panicked! I immediately did the only thing I could think to do and induced vomiting.

I don't cook gluten at all. We are lucky enough to have 2 kitchens in our house so we are set up like a kosher house. There is a gluten kitchen downstairs and my gluten free kitchen upstairs. Nothing goes between the two. The only exception is on pasta nights someone else cooks regular pasta downstairs and I cook gluten-free pasta and the sauce upstairs. My youngest son and I serve up our gluten free meals and then the rest of the family scoops their regular pasta downstairs and then comes up to get sauce and eat at the table.

Other than that no gluten comes up. Nothing capable of crumbs is allowed up here.

gfpirate Rookie

Hey... it happens! Sounds like just the kind of mistake I would make :P

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
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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.