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

Questions Re Shared Toaster Oven, Initialisms


KikiB

Recommended Posts

KikiB Explorer

I'm still doing a gluten challenge before my endoscopy, but I'm trying to only eat gluten at night because it makes me so sick. This morning at work I made my gluten-free English Muffin in the shared Toaster Oven -- as I have done for the past week.

I always lay foil down on the shelf before I put the muffin in so it's only touching brand new foil.

But I got sick soon after (for me it's massive fatigue and muscle weakness, and have been sick all day. Could I have been glutened by the toaster oven even though I used my own new foil over the shelf?

(Apologies in advance if this is a dumb question!)


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



Celiac.com Sponsor (A8-M):



  • Replies 68
  • Created
  • Last Reply
shadowicewolf Proficient

mmm i'm thinking its more of touching the oven (gluteny hands and whatnot) that might have gotten you.

KikiB Explorer

Can I get glutened by touching the toaster handle?

GottaSki Mentor

Can I get glutened by touching the toaster handle?

Yep...I use a paper towel to open and close the microwave at work.

Admittedly, I am a super-sensitive silly-yak.

Couple other thoughts:

Was this the first time you had that particular brand of gluten-free english muffin? Some gluten-free items can be difficult on your system.

It is also possible that you reacted to your previous gluten consumption - it's going to be very difficult to figure these things out until you are gluten-free - heck, it's difficult to figure them out even when you've been gluten-free for years ;)

KikiB Explorer

Was this the first time you had that particular brand of gluten-free english muffin? Some gluten-free items can be difficult on your system.

It is also possible that you reacted to your previous gluten consumption - it's going to be very difficult to figure these things out until you are gluten-free - heck, it's difficult to figure them out even when you've been gluten-free for years ;)

They are Glutino English Muffins and I have been eating them for breakfast for the last week and a half without problems.

Maybe I am reacting to the previous day's gluten, hadn't thought of that. Although I felt ok until I ate that muffin. I kind of feel like I am getting worse by the day the last few days. Sigh.

I will use your suggestion of the paper towel and won't touch the handle or buttons anymore. Thanks!

Lisa Mentor

We have a shared toaster oven at home. I use the top rack and husband uses the bottom....so far without issue (after several years). I clean the tray often. But, then I'm not that sensitive. What may work for me, may not work for others, as Lisa.

Everyone will vary in severity and duration. And some will react to many things, gluten or non-gluten until some healing can take place. If you're still on a gluten challenge, it could be anything.

Oh..and I wanted to add that when I get zapped, I feel it about 22 hour later. But, as I said, everyone will vary.

Hopefully, you will have some answers soon. AND, there are no dumb questions here. B)

KikiB Explorer

Everyone will vary in severity and duration. And some will react to many things, gluten or non-gluten until some healing can take place. If you're still on a gluten challenge, it could be anything.

Oh..and I wanted to add that when I get zapped, I feel it about 22 hour later. But, as I said, everyone will vary.

Hopefully, you will have some answers soon. AND, there are no dumb questions here. B)

Thank you!


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



Celiac.com Sponsor (A8-M):



Gemini Experienced

Yep...I use a paper towel to open and close the microwave at work.

Admittedly, I am a super-sensitive silly-yak.

Couple other thoughts:

Was this the first time you had that particular brand of gluten-free english muffin? Some gluten-free items can be difficult on your system.

It is also possible that you reacted to your previous gluten consumption - it's going to be very difficult to figure these things out until you are gluten-free - heck, it's difficult to figure them out even when you've been gluten-free for years ;)

I really feel the need to clarify this......you cannot be glutened by merely touching something that may be gluten containing. It has to find it's way into your GI tract. If you had licked the toaster handle, OK, that would be a problem but you don't do that! No one does that. :o Gluten can be handled by even the most sensitive of Celiacs (of which I am one) but you have to remember to wash your hands, always, before eating, or always after touching something you are unsure of. Everyone should be doing that, not just the Celiac population. It's a hygiene issue.

GottaSki Mentor

I really feel the need to clarify this......you cannot be glutened by merely touching something that may be gluten containing. It has to find it's way into your GI tract. If you had licked the toaster handle, OK, that would be a problem but you don't do that! No one does that. :o Gluten can be handled by even the most sensitive of Celiacs (of which I am one) but you have to remember to wash your hands, always, before eating, or always after touching something you are unsure of. Everyone should be doing that, not just the Celiac population. It's a hygiene issue.

Gemini is correct - you can't get glutened by touching surfaces containing gluten. In the shared "kitchen" of our office there was no sink - so rather than trudge down the hall to wash after warming my food I decided to use a paper towel to open/close the micro. It is far better to wash each time you encounter gluten - just not always convenient.

IrishHeart Veteran

Not a dumb question at all, Kiki!

I am thinking you are having a reaction from gluten ingestion, period, so it is difficult to blame the toaster or the muffin or anything, for that matter. I just blame the gluten.

Under a gluten challenge, who can say when/how you will feel worse? None of us. Inflammation from gluten/celiac can last a long time.

For example, even after my DX and being gluten-free, I was still very ill for quite some time.

Unfortunately, until you are gluten-free entirely, you may feel pretty rotten, hon. Sorry. :(

Gemini Experienced

Gemini is correct - you can't get glutened by touching surfaces containing gluten. In the shared "kitchen" of our office there was no sink - so rather than trudge down the hall to wash after warming my food I decided to use a paper towel to open/close the micro. It is far better to wash each time you encounter gluten - just not always convenient.

Thanks for clarifying that, GottaSki! I KNOW you know your stuff with regards to Celiac and I didn't want to annoy anyone but if you don't clarify that, you know what will happen! ;):o

GottaSki Mentor

Didn't annoy me in the least - I often add CYA statements and am glad you were covering mine this time when I was unclear -- Thanks!

GFinDC Veteran

I'm still doing a gluten challenge before my endoscopy, but I'm trying to only eat gluten at night because it makes me so sick. This morning at work I made my gluten-free English Muffin in the shared Toaster Oven -- as I have done for the past week.

I always lay foil down on the shelf before I put the muffin in so it's only touching brand new foil.

But I got sick soon after (for me it's massive fatigue and muscle weakness, and have been sick all day. Could I have been glutened by the toaster oven even though I used my own new foil over the shelf?

(Apologies in advance if this is a dumb question!)

Hi Kiki,

The immune system reaction doesn't stop after a few hours. It will keep going as long as you are eating gluten. Your symptoms may vary during the challenge, getting better or worse at times. If you are eating gluten every day for the challenge, your reactions each day are kind of unpredictable. It is possible they will get progressively stronger over time, or they may plateau for a while or even taper off. Everyone has their own experience and it is not something standard for each person. Some people have no symptoms at all but still have damage to their gut going on.

KikiB Explorer

I really feel the need to clarify this......you cannot be glutened by merely touching something that may be gluten containing. It has to find it's way into your GI tract. If you had licked the toaster handle, OK, that would be a problem but you don't do that! No one does that. :o Gluten can be handled by even the most sensitive of Celiacs (of which I am one) but you have to remember to wash your hands, always, before eating, or always after touching something you are unsure of. Everyone should be doing that, not just the Celiac population. It's a hygiene issue.

Lick the toaster handle. LOL!!! I am already super germ conscious because I have such a weak immune system. Not going to catch me licking anything in that kitchen. :)

KikiB Explorer

Not a dumb question at all, Kiki!

I am thinking you are having a reaction from gluten ingestion, period, so it is difficult to blame the toaster or the muffin or anything, for that matter. I just blame the gluten.

Under a gluten challenge, who can say when/how you will feel worse? None of us. Inflammation from gluten/celiac can last a long time.

For example, even after my DX and being gluten-free, I was still very ill for quite some time.

Unfortunately, until you are gluten-free entirely, you may feel pretty rotten, hon. Sorry. :(

That makes sense. Since I usually react so quickly to food, I just assumed it was the breakfast muffin.

Gemini Experienced

Lick the toaster handle. LOL!!! I am already super germ conscious because I have such a weak immune system. Not going to catch me licking anything in that kitchen. :)

I figured that would get your attention! :P

KikiB Explorer

Hi Kiki,

The immune system reaction doesn't stop after a few hours. It will keep going as long as you are eating gluten. Your symptoms may vary during the challenge, getting better or worse at times. If you are eating gluten every day for the challenge, your reactions each day are kind of unpredictable. It is possible they will get progressively stronger over time, or they may plateau for a while or even taper off. Everyone has their own experience and it is not something standard for each person. Some people have no symptoms at all but still have damage to their gut going on.

Thanks! I would hope for a tapering off, but not happening so far.

Chiana Apprentice

They are Glutino English Muffins and I have been eating them for breakfast for the last week and a half without problems.

Maybe I am reacting to the previous day's gluten, hadn't thought of that. Although I felt ok until I ate that muffin. I kind of feel like I am getting worse by the day the last few days. Sigh.

I will use your suggestion of the paper towel and won't touch the handle or buttons anymore. Thanks!

When I did a challenge it was a slow, downhill progression of worsening fatigue, brain-fog, and depression. It wasn't any one thing, and I would feel better or worse in a fashion seemingly unconnected to what I had just eaten. All I knew was that after 4 or 5 days, I felt like I was carrying around a bag of bricks. For some of us, it is cumulative.

IrishHeart Veteran

When I did a challenge it was a slow, downhill progression of worsening fatigue, brain-fog, and depression. It wasn't any one thing, and I would feel better or worse in a fashion seemingly unconnected to what I had just eaten. All I knew was that after 4 or 5 days, I felt like I was carrying around a bag of bricks. For some of us, it is cumulative.

This the most descriptive explanation of a gluten challenge I have ever read. Glad you saw the thread and posted!

Sorry you had to go through it :( but it does clarify the impact on the human body --for readers of this thread and for the OP and for me---as I know I could never withstand such a thing and was relieved my GI doc did not ask me to do it. I feel this way after a minor CC incident and cannot imagine doing it for any length of time.

KikiB Explorer

This the most descriptive explanation of a gluten challenge I have ever read. Glad you saw the thread and posted!

Sorry you had to go through it :( but it does clarify the impact on the human body --for readers of this thread and for the OP and for me---as I know I could never withstand such a thing and was relived my GI doc did not ask me to do it. I feel this way after a minor CC incident and cannot imagine doing it for any length of time.

That was a great description and exactly how I feel. Only throw in extras like, yesterday I had a 1/2 of a cookie in the afternoon, and then halfway through my commute was unsure if I was going to make it home in time. So I don't know if it was the cookie -- or like Chiana said, a cumulative reaction.

What does OP stand for? I'm sure it's really obvious, and I'll feel stupid after you tell me, but for the life of me I can't figure it out. :)

mushroom Proficient

OP refers to the original poster who started the thread. :)

KikiB Explorer

OP refers to the original poster who started the thread. :)

Thanks!!

IrishHeart Veteran

....and not for "Old Person" which I most definitely would not like to be called.

GottaSki Mentor

....and not a stupid question at all...I scratch my head regularly over abbreviations here - FWIW - took me way too long to figure out ;)

IrishHeart Veteran

....and not a stupid question at all...I scratch my head regularly over abbreviations here - FWIW - took me way too long to figure out ;)

Me too... hmm.. "filled with ice water"?

But the one that stumps me still is

SIL -- is it son- in- law or sister- in -law?

and DD--well, at first, I thought it was really, really bad Diarrhea--like "disastrous diarrhea".

and when Sylvia says this to me : "Pffft!"

it makes me laugh and I know she is really saying "Psshaw" or piffle!

...us OP (older people) with brain frogs take longer to learn these new things and we are easily amused.

:)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,962
    • Most Online (within 30 mins)
      7,748

    Roieliu
    Newest Member
    Roieliu
    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

    • Wheatwacked
      Hello @CeliacNew, If you are Vegan to help you feel better, reconsider returning to omnivore.  Actually, since you are already on a very restrictive diet, transitioning to gluten free might be easier for you.  Read the ingredient labels, Particularly vitamin D and Choline require supplements for vegan diet because our primary source is sun, eggs and beef.  B12 also.
    • Wheatwacked
      Once you've completed testing and still don't have improvement, start a trial gluten free diet.  Looking for imprvement that may indicate Non Celiac Gluten Sensitivity, which is 10 times more prevalent than Celiac Disease. Deficiencies in vitamins B6, B12, D, and C can manifest as skin rashes.  Virtual guaranty you are deficient in vitamin D.
    • cameo674
      So those rs numbers tell researchers where the dbSNP is located in a Genome so that other reasearchers or an AI system can look in that specific spot for that Snip of information.  You can look those rs # s by pasting the numbers after rs into the lookup on this page https://www.ncbi.nlm.nih.gov/snp/ right under the Blue header bar at the top of the webpage.  Since you are not a researcher, I do not know how this will help you though.
    • cameo674
      So I posted here once before, and everyone advocated that I get into a GI doc.  I finally got into my functional health appointment on 6/16 to get my blood results evaluated and get the Gastro referral. I was told that I would be fortunate to see a gastro doctor by December, because of the number of people waiting to get in, but they did believe that I needed to see a GI doc among others.  Well, the stars aligned. I got home. I looked at MyChart and it showed an appointment available for later that same day. I never clicked so fast on an appointment time. The gastro doc ran some additional blood work based off the December values that had confirmed my daughter's suspicion that I have undiagnosed stomach issues.  Gastro has also scheduled me to get an upper endoscopy as well as a colonoscopy since it has been 8 years since my last one. She said it would rule out other concerns if I did not show Celiac per the biopsies.  Those biopsies will not occur until August 29th and like everyone here stated, Gastro wants me to keep gluten in my diet exactly as everyone suggested. To be honest, I was barely eating any gluten since I figured I would have plenty of time to do so before testing.  Doc is also looking for the cause of the low level heartburn that I have had for 30 years.  I have mentioned the heartburn to PCPs in the past and they always said take a tums or other OTC drug.  The upper endoscopy is for ruling out eosinphilic esophagitis, h. pylori, and to biopsy the duodenal bulb and second portion to confirm or exclude celiac. The colonoscopy will have random biopsies to rule out microscopic colitis. I didn't really catch her reasoning for the bloodwork.  Doc looked at the December numbers and said they were definitely concerning for Celiac.  She also said, “Hmm that’s odd; usually it’s the reverse”, but I did not catch which result made her say that. She seems very through.  She also asked why I had never bothered to see a GI before.  To be honest, I told her I just assumed that the heartburn and loose stool were a part of aging.  I have been gassy since I was born and thought constantly passing gas was normal?  Everyone I know with Celiac have horrible symptoms that cannot be attributed to other things.  They are in a lot of stomach pain.  I do not go through that.  I attribute my issues to the lactose intolerance that comes with aging, but have slowly been eliminating foods from my diet due to the heartburn or due my assumption that they did not agree with a medication that I was prescribed. I have already eliminated milk products especially high fat ones like ice cream; fats like peanut butter; acids like citrus and tomatoes; chocolate in all forms; and breads more because it is so hard to get in 100 grams of protein if I eat any foods that are not a protein.  I would not have even done the testing if my daughter had not brought up the fact that she thought I might have an undiagnosed condition since she has issues with bloating and another sibling has periodic undiagnosed stomach pain that GI docs throw pills at instead of helping.  Who knew that Bristol scale 5 and 6 were not considered normal especially multiple times a day? I watched my MIL go through basically the same bowel changes starting at 50 so to be honest, I really did think it was normal before this week's appointment.   December 2024's blood tests ran through Quest Labs were:  Deamidated Gliadin (IgA) 53.8 U/mL Above range >15.0 U/mL; Deamidated Gliadin (IgG) >250.0 U/mL Above Range >15.0 U/mL; Tissue Transglutaminase (IgA) 44.0 U/mL Above range >15.0 U/mL; Tissue Transglutaminase (IgG) <1.0 In range <15.0; Immunoglobulin A (IgA) 274 mg/dL In range 47-310 mg/dL 6/16/25 bloodwork:  Until today, I did not really know what all the four tubes of blood were for and since I did not understand the results, I got into the clinical notes to see what was ordered, but it did not exactly explain why for everything. Immunoglobulins IGG, IGA, IGM all came back in range:  IGG 1,010 mg/dL In range 600-1,714; IgA 261 mg/dL In range 66-433 mg/dL; IGM 189 mg/dL In range 45-281.  How do these numbers help with diagnosis? Google says she checked these to see if I have an ongoing infection? I do have Hashimoto's and she did say once you have one autoimmune disease others seem to follow. Celiac Associated HLD-DQ Typing: DQA1* Value: 05; DQA1*DQA11 Value: 05; DQB1* Value: 02; DQB1-DQB11 Value: 02; Celiac Gene Pairs Present Value: Yes; Celiac HLA Interpretation Value: These genes are permissive for celiac disease.  However, these genes can also be present in the normal population. Testing performed by SSOP.  So google failed me.  I think these results basically say I have genes, but everybody has these genes so this test was just to confirm that there is a vague possibility?  Maybe this test result explains why I do not have the horrible symptoms most individuals with celiac have?  I told the GI my assumption is that I am just gluten intolerant since I do not have the pain? So maybe this test explains why I have antibodies? Comprehensive Metabolic Panel: Everything was in the middle of the normal range.  Google says this just says I am metabolically healthy. Tissue Transglutaminase ABS test results – Done by the Mayo Clinic’s Labs –  T-Transglutaminase IGA AB --Value: 3.1 U/mL – Normal Value is <4.0 (negative) U/mL; Tissue Transglutaminase, IgG -- Value: 15.3 U/mL High -- Normal Value is <6.0 (Negative) U/mL – Interpretation Positive (>9.0) – These are the only labs the GI did that have been labeled Abnormal.  I am confused at how/why these came back different than the December labs? Because these numbers seem to be the opposite of what the were in December and I know I have eaten less gluten.  They were definitely measured differently and had different ranges. This must be why she said they are usually opposite? Molecular Stool Parasite Panel said I was Negative for Giardia Lamblia by PCR; Entamoeba Histolytica by PCR and Cryptosporidium Parvum/Hominis by PCR.  So at least I do not need to do a parasite cleanse like everyone on TikTok seems to be doing. So I guess, I am just really asking why the Tissue Transglutaminase numbers are different.  Was it because they were truly different tests? Is it because I have not consumed the crazy amount of gluten one is suppose to eat prior to testing? To be honest, I thought that was only for the biopsy testing. I generally only eat twice a day, and the thought of eating the equivalent of 6 slices of bread is daunting. Even in my youth, I probably only consumed the equivalent of maybe 3 slices a day. Like I said before, now I usually focus on trying to eat 60 gram of protein.  I am suppose to consume 100 grams, but have failed to succeed. I will focus on eating gluten starting in July now that I know my procedure date.
    • Scott Adams
      I agree with @trents and wiping down the spot you eat your lunch, and eating the food your brought from home should be safe for even sensitive celiacs. Gluten can jump on your food, so it would likely better better for you to continue eating where you prefer.
×
×
  • Create New...