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:
    Join eNewsletter
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    2. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    3. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    4. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    5. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,832
    • Most Online (within 30 mins)
      7,748

    Duhgirl
    Newest Member
    Duhgirl
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
×
×
  • 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.