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

Cross Contamination?


Bubba's Mom

Recommended Posts

Bubba's Mom Enthusiast

I just got my diagnosis after an endoscopy. I saw the Dr. yesterday. She said the biopsy confirmed Celiac Sprue. She said the damage to my mucosa and villie are severe.

She ordered up a slew of blood tests to check for vitamin deficiencies, a bone density test, and a repeat of the CT scan I had in March that showed enlarged lymph nodes in my belly...the first test that showed a problem. My primary care Dr had me pegged as a hypochondriac and told me to eat Tums for my belly pains.

After I had the scope she gave me pics of my upper intestines and a tentitive diagnosis of C. Sprue. I looked it up and found out what it was and decided to stop eating gluten while waiting for the test results.

I checked the labels on everything before eating it, but then found out the "sneaky" names for gluten in an ingredient list. What I thought was gluten free wasn't.

The specialist I saw yesterday said.."don't eat gluten". That's all she said. I'm reading what I can online and I'm thankful for finding this forum.

I've been seeing things like..seperate cutting boards, pans, wooden spoons, etc. Do I really have to scrub the dickens out of everything? Not handle dog food?

It's going to be tough. I opened the container of Olivio spread to add it to my potato yesterday and found toast crumbs in it from my husband. I told him he can't leave crumbs in things and he laughed at me and told me to "scrape it off".


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

Sensitivity levels vary from individual to individual. Here's what I know after eleven years.

The effect of gluten on your system is a function of the *total* amount of gluten actually ingested. You can eat a slice of "gluten-free" bread at 10 ppm, or two slices at 5 ppm--the amount of gluten you ingest is the same.

What you need to do is keep the total gluten ingestion small enough that the autoimmune reaction does not overtake the continuous healing of the body. Every bit counts, so the more you can prevent the better.

Some things are porous, and can not be cleaned effectively: wooden cutting boards and spoons come to mind. Any material with visible scratches fit here, too.

Some things are impossible to clean of crumbs effectively: you can not share a toaster.

Most things can be washed thoroughly and safely used. Cutlery, metal pots and pans in good condition (cast iron is a special case), plates, glasses would be in this group. An automatic dishwasher is effective for this. If you are worried, a double wash may make you feel safer. When we had a mixed kitchen, we only used the single wash cycle, and I never had any problems.

These may also be of help:

Unsafe ingredients: https://www.celiac.com/articles/182/1/Unsaf...ents/Page1.html

Safe ingredients: https://www.celiac.com/articles/181/1/Safe-...ents/Page1.html

A list of companies that has a clear gluten policy. If you don't see "wheat, rye, barley, barley malt, oats" on the labels, its not there, or hidden in "flavors, starches, etc." Open Original Shared Link This makes shopping MUCH easier.

GFinDC Veteran

Yep, trace amounts will get cha! Celiac is an auto-immune disease, and the damage is caused by your own bodies immune cells attacking the tissues. Your immune system like germs not so very much, and so it attacks and kills them. It also keeps attacking for a while. Celiac makes your immune system think your gut lining is an invader when their is gluten stuck in it.

Shared toasters are crumb warehouses, with lots if gluten packages waiting to get in your gut and trigger a reaction. Shared condiments like butter or peanut butter, jelly etc are mine fields also. Shared pots and pans that aren't well washed are a problem, and so are wooden utensils that are rough and porus. The gluten molecules can get stuck in little places and come out later.

okieinalaska Apprentice

Bubbas mom I wondered the same thing and after confirming it for myself the hard way i can say Yes, you do have to watch for contamination. However, I don't worry about handling the dog food or if there is gluten in my shampoo. But I do have my own toaster, peanut butter jar etc...and I wash everything in the dishwasher. The contamination adds up.

Best wishes,

Darn210 Enthusiast

Yep, from my daughter's perspective, I see it as an accumulative effect. In general, I don't think my daughter is overly sensitive to contamination, but once she triggers a reaction, it takes a long time to return to "normal". I look at it this way, I prevent every possible crumb that I can see because I don't know how much she is ingesting that I can't see. I can see those crumbs in the butter so she has her own. I can't see how they handled her food in the restaraunt or how many ppm her store bought food contains.

Bubba's Mom Enthusiast

Thanks so much for your answers.

I guess I'm going into overwhelm at the changes I have to make? I can get a new toaster, maybe a couple of small frying pans too? A new cutting board shouldn't be hard, and some spoons? I think the hard part will be getting my husband and son to take contamination seriously? I shopped for some kind of pasta I can eat and it was pricey. I hate to give up spaghetti though. My hubby said I should just make both kinds of pasta and keep the pricey one for myself. It sounds like it might be better to just go all gluten free instead?

I'm wondering if once the gluten is out of my system, being exposed to it will give me a more severe reaction?

I've had such trouble sleeping I was taking a Xanax and Melatonin an hour before bedtime and two Benadryl just before hitting the hay. I just read the bottles last night. The Melatonin and Benadryl both have starch. No wonder it wasn't working!

mushroom Proficient

I've had such trouble sleeping I was taking a Xanax and Melatonin an hour before bedtime and two Benadryl just before hitting the hay. I just read the bottles last night. The Melatonin and Benadryl both have starch. No wonder it wasn't working!

Starch is not necessarily from wheat; it could be cornstarch - these are the two most common fillers. Unfortunately, you have to check with the manufacturers to find out which because they are not required to tell you (sometimes they don't even know themselves because they have purchased product ingredient from another company which did not specify). It can be a real pain checking meds. With scrips, sometimes the pharmacist will do it for you. You can call their 800 number or email the company to find out. I am in the process of doing that myself right now. :)


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



Celiac.com Sponsor (A8-M):



Bubba's Mom Enthusiast

Thanks..I'll call. I just assumed starch meant gluten.

I just got diagnosed and I called my pharmacy right away. I told them to add gluten to my allergy list and had them do a quick check to see if any of my current meds had gluten. They didn't..so that's good!

There are so many details to attend to!

sa1937 Community Regular

There are so many details to attend to!

Yes, it seems to be overwhelming at first but after awhile, it becomes automatic and so much easier. We do have to major in Label Reading 101. :lol:

Bubba's Mom Enthusiast

I'm so glad I mentioned the ingredients. I was told that dextrose meant gluten, but when I called about the Melatonin I was told it was from corn.

The generic Benadryl said starch only. It took two phone calls to track that down and I found out it's corn starch.

Maybe I'll get some sleep tonight? :blink:

Bri69 Newbie

i was told by my doctor that it doesnt matter if its a trace or a slice of bread. the same damage is happening even if you dont feel the pain.

GlutenFreeManna Rising Star

I'm so glad I mentioned the ingredients. I was told that dextrose meant gluten, but when I called about the Melatonin I was told it was from corn.

The generic Benadryl said starch only. It took two phone calls to track that down and I found out it's corn starch.

Maybe I'll get some sleep tonight? :blink:

Brand name Benedryl is gluten-free. My husband is sensitive to dyes and has different reactions to generic versus brand name meds. Some meds that make me sleep (like Benedryl) make him stay wide awake. So you might just try the name brand and see if it helps you more than the generic.

psawyer Proficient

i was told by my doctor that it doesnt matter if its a trace or a slice of bread. the same damage is happening even if you dont feel the pain.

For most of us, there is a definite relationship between the amount ingested and the magnitude of the reaction and recovery time. Your doctor's perspective is dangerous because it leads to the idea, "I've eaten one bite by accident, so now I might as well finish the whole thing."

Bubba's Mom Enthusiast

That's just what I thought! :o Surely the more you're exposed to, the bigger the reaction should be?

GlutenFreeManna Rising Star

For most of us, there is a definite relationship between the amount ingested and the magnitude of the reaction and recovery time. Your doctor's perspective is dangerous because it leads to the idea, "I've eaten one bite by accident, so now I might as well finish the whole thing."

My reactions are the same whether I get a few crumbs or a large amount. I have NEVER thought "might as well eat the whole thing" if a little gets me by accident. I don't think that's what the dr was implying at all. I think it's just as dangerous to think that crumbs don't matter. Even people that don't get major reactions from small amounts may notice a culmulative effect over time. It's better to be overly cautious than to not worry at all about cc.

GFinDC Veteran

I don't know if the name brand Benedryl is really safer. The Feds took over control of the factory where it is made a while back because of quality concerns. So maybe it is ok now, with the Feds running things. Hmm, doesn't sound real believeable tho.

Bubba's Mom Enthusiast

Isn't it scary when you hear they could mess up medicines? :o For now, I'll stick to the generic. They were very nice about finding the ingredient info for me, and I'm glad I can still take it. It helps me sleep, but it also helps with my allergies. My son recently moved back home and brought his two dogs with him. I'm allergic to dogs.

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. - Hmart replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    2. - trents replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      10

      Help I’m cross contaminating myself,

    4. - DebJ14 replied to Jhona's topic in Introduce Yourself / Share Stuff
      30

      Does anyone here also have Afib

    5. - Hmart posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,924
    • Most Online (within 30 mins)
      7,748

    Mckshane
    Newest Member
    Mckshane
    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

    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
    • Hmart
      The symptoms that led to my diagnosis were stomach pain, diarrhea, nausea, body/nerve tingling and burning and chills. It went away after about four days but led me to a gastro who did an upper endo and found I had marsh 3b. I did the blood test for celiac and it came back negative.  I have gone gluten free. In week 1 I had a flare-up that was similar to my original symptoms. I got more careful/serious. Now at the end of week 2 I had another flare-up. These symptoms seem to get more intense. My questions:  1. How do I know if I have celiac and not something else? 2. Are these symptoms what others experience from gluten?  When I have a flare-up it’s completely debilitating. Can’t sleep, can’t eat, can’t move. Body just shakes. I have lost 10 pounds since going gluten free in the last two weeks.
    • Serena Rodriguez
      You've already identified the issue. You cannot have ANY gluten in your home EVER. It's not optional for everyone who lives with you to have a dedicated gluten free diet! And anyone who comes to visit you cannot bring anything gluten-containing into your home. All gluten containing items need to be thrown away, beauty/bath products included. All pots/pans, dishes, utensils need to go through the dishwasher. Anything too porous or delicate for the dishwasher needs to be thrown away and replaced. Your toaster needs to be thrown away and replaced. Your oven, stovetop, and all surfaces throughout your home (bedrooms and bookshelves too) need to be thoroughly washed. All of this needs to happen in the same day because you risk contaminating other parts of your home if you do only part of the job. There's no such thing as a "safe" amount of gluten in your home. Not putting your foot down means greater risks into the future for vitamin deficiencies, diabetes, damage to your thyroid, cancer, rheumatoid arthritis, and more.
×
×
  • 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.