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

Breakroom/work Issues


Katsby

Recommended Posts

Katsby Apprentice

Ok a little backstory: I work in an area with a very small breakroom that has 1 microwave, 1 fridge, and 1 table for 3 small depts to share (about 15 or so people coming and going on my workshift at various break times). That microwave is filthy and covered with spagetti sauce and all sorts of other disgusting things. I simply cannot bring myself to use it. We cannot have a toaster due to fire issues. If I have something that needs microwaving I basically go downstairs to the 3 microwaves near the cafeteria (I work at a hospital) and use the ones the general public does to pop their popcorn, etc from the snack machines. It seems ten thousand times cleaner since the housekeepers keep it clean. The microwave in my breakroom hardly ever gets cleaned. I never really used it before until I found out I was gluten intolerant and started bringing more prepared meals to work (rice + chicken, etc) that I need to heat up. The breakroom table is scary with sticky stuff, crumbs, etc. It's cleaned every day by housekeeping despite how dirty it gets. I just work with a bunch of pigs I think.

Anyway I don't want to have to clean the microwave every single day to use it, so I am unsure what I could bring to work that would not require heating up. Also do you think people would get offended if I left a note on the microwave to please make sure to cover your food and if you make a mess please clean it up? I can easily wipe down the table when I eat so that's not a huge deal. It's just that people are so messy and sometimes after I eat I still get gassy/bloated and I wonder if it's not cc. I don't really want to explain to people my food issues because I feel it's none of their business (I have only told my boss and 2-3 coworkers, but they still don't understand the importance of cc). I don't want to put anyone out and it's kind of at the point where I just don't eat up there anymore.


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

A good large Thermos can go a long way. Heat at home and put in Thermos so it is still warm at lunchtime.

cruelshoes Enthusiast

When I use our work microwave, I put a paper towel below and over the top of my food. They both go promptly in the trash when I am done. I sort of reach in between them and slide my food out so none of the detritus from the microwave contaminates anything. I have my own toaster at my desk that I keep locked up. It is labeled with my name and a skull and crossbones so nobody tries anything funny. :lol: You can try putting a sign on the microwave if you want, but I really don't think it will do anything. Unless there is a mandate from HR, nobody in our office will change anything. Wher I work, HR had to put signs up with threats of termination to get people to stop stealing lunches out of the refrigerator.

You could also put a paper towel under your food in the breakroom. People might think you are OCD or a neat freak, but it would help prevent CC.

People are just pigs in the lunchroom. It amazes me what people will do, and I know they aren't that disgusting at home ( at least I hope so).

Katsby Apprentice
It is labeled with my name and a skull and crossbones so nobody tries anything funny. :lol: You can try putting a sign on the microwave if you want, but I really don't think it will do anything. Unless there is a mandate from HR, nobody in our office will change anything. Wher I work, HR had to put signs up with threats of termination to get people to stop stealing lunches out of the refrigerator.

lol the skull and crossbones is a great idea. We also had people in the past stealing lunches. If someone steals my carefully prepared gluten-free lunch I may well just freak out lol

Katsby Apprentice
A good large Thermos can go a long way. Heat at home and put in Thermos so it is still warm at lunchtime.

That's a great idea :)

home-based-mom Contributor

This must be a universal problem One place I worked put up a big sign that read.

"YOUR MOTHER DOESN'T WORK HERE. PLEASE PICK UP YOUR OWN MESS."

But alas, that didn't work, either. Sigh. :(

WW340 Rookie

I agree with everything said so far. The only thing I have to add is that I have a thermal lunch box that will either keep things cold with a cold pack so I don't have to use the fridge, or will keep things warm, esp. if I use the thermos. I try to stay as totally independent as possible. I can keep my lunch with me and then I know it has not been messed with. If I should have to use the microwave, I do the paper towel liner as well. I also carry my own silverware with me. The lunch room is a disaster. I spray down my eating area and use paper towels as a place mat.


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



Celiac.com Sponsor (A8-M):



margiemakes Newbie

I have the same issues at my work. I have always washed the cutlery before I use it but one time I saw someone slice bread with a knife and then put it straight back into the drawer and ever since then I have been extremely vigilant about bringing my own cutlery with me that I store in my office, and washing it before and after I use it just in case.

Also to use the microwave I always put paper towel down and only loosen the lids on my containers and not actually take them off inside there.

I also eat at the tables either off my own plate/lunchbox that I bring in and out or off paper towel (or both).

Another big source of CC that I worry about is the communal dishbrush thing which is one of those ones with detergent in the handle and a sponge on the end, and I hate to think about how much gluten is lurking in that sponge let alone the germs etc so I just put fresh detergent on and use my hands to wash, dry with paper towels instead of the communal tea towel ( or use a new one from the drawer) and even that is if i bother to wash them at work, usually I just take my dirty lunchbox home and wash it there.

People at work all know about my intolerance though and we there is someone else here who is also intolerant so nobody looks at me funny. Mostly they are just worried about whether what they are doing would affect me so that's pretty lucky I guess.

kera87 Newbie

When I go to work I try to bring cold things or foods that don't need to be heated up. For example I bring tuna fish already made in a ziplock container, as well as fruit, gluten-free bars (i like bumble bars), gluten-free lunchmeat (from Wegmans), salads made at home, and there are great gluten-free bagels out there that you could also bring. I'm a bit of a snacker so I like to bring a bunch of small things but you could always made a sandwich on gluten-free bread and bring that. I usually bring a lunchbox thing and an ice pack and everything stays fresh. Also, get plastic silverware to bring so you never have to worry about someone else using a utensil.

Lockheed Apprentice

BTW you can file with your HR person that you have a disability and that you require a clean working microwave to accommodate your disability and then they are supposed to provide that to you.

gfp Enthusiast
BTW you can file with your HR person that you have a disability and that you require a clean working microwave to accommodate your disability and then they are supposed to provide that to you.

or they might just take the Microwave away altogether ????

Katsby Apprentice
BTW you can file with your HR person that you have a disability and that you require a clean working microwave to accommodate your disability and then they are supposed to provide that to you.

Well I can't prove that I have a disablity because I haven't been diagnosed with celiac just gluten intolerance. I don't want to take it that far anyway. Even if we had another microwave that I could use I don't really trust my coworkers to not use it.

There were a lot of good suggestions in the topic so thanks everyone :)

Fifi Newbie

I am new to this forum. I just joined today. I have had celiac disease for 7 moths now and been G F for that long. I can agree with the way people leave the break rooms and bathrooms. I can't understand if they don't do that at home why on earth would they do that any where else??? It just doesn't make sense to me. But I am still in the learning stage and I can't get enough information.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,311
    • Most Online (within 30 mins)
      7,748

    SWilson
    Newest Member
    SWilson
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, Linda! Many on this forum can sympathize with you. It can be extremely difficult to get reliable information about gluten when it comes to meds, supplements and oral hygiene products. This is especially true since so much of this stuff is generic and comes from over seas. I will deflect with regard to your question about meds and oral products but take you in another direction. Have you tried a low iodine diet. Iodine is known to exacerbate dermatitis herpetiformis and some find that a low iodine diet helps reduce the number of outbreaks. By the way, have you had your celiac antibodies retested recently? If they are elevated that might be a clue that you are getting gluten in your oral hygiene products or meds.
    • Itsabit
      Hi. I’m 70 years old, and a 22 year survivor of head and neck cancer treated with chemo-radiation, which resulted in non-existent submandibular salivary glands and extreme dry mouth and altered oral mucosa. I have been using dry mouth toothpaste, Rx oral dentrifices and moisturizers for years.  I’ve recently been diagnosed with severe celiac dermatitis herpetiformis. I was being treated with oral Dapsone, but it was not effective and I developed some serious side effects. So, the medication was stopped and I was started on Doxycycline (another antibiotic) for inflammation. I’ve been using Rx Betamethasone steroid ointment with little to no effect. I have tried every oral and topical antihistamine treatment available OTC. None have touched this horrible relentless itching. That is my history.  Now to my question. Does anybody know about gluten free toothpastes and mouth moisturizers? I ask because a very common dry mouth brand stated to me that they were indeed gluten free. But as I am not getting any better with my dermatitis herpetiformis, I was wondering if I was getting glutenized some way other than diet as  I have been following a strict clean gluten free diet, but I am not seeing any improvement at all. So, I started looking up the toothpastes and moisturizer ingredients individually and nine (9) of the eleven (11) or so listed showed up as   containing gluten or that may have gluten! Am I getting glutenized orally by these products?  As an aside, I checked on my favorite lavender scented baby lotion which is supposed to be gluten free, but many of those ingredients when investigated separately, show they  do contain or may contain gluten as well. I stopped using the lotion. But I cannot forgo my dental care. I was unable to get any information from the manufacturer of my current brand of chewable multivitamins either. They told me to check with my doctor. If THEY don’t know what’s in their product, how do they think a PCP will?  In light of all this, I am confused and angry that I might keep getting contaminated with gluten through products I am using that are supposedly gluten safe. *I should also state that I have a nickel allergy since I was about 12-13 years old. And I developed a contact allergy to latex (gloves) when I was a student nurse at 19 years old.  I know and I’m sorry that this is so lengthy. I’m trying to do everything I can to combat this condition, and I’m feeling very confused, anxious and angry about not getting adequate information as I try to educate and advocate for myself. I’m hoping someone here is more knowledgeable than me of how to navigate through all of this. Can anyone offer any advice?  Thank you for your time.  Respectfully,  Linda
    • trents
      Welcome to the forum, @Cathijean90! I went 13 years from the first laboratory evidence of celiac disease onset before I was diagnosed. But there were symptoms of celiac disease many years before that like a lot of gas. The first laboratory evidence was a rejected Red Cross blood donation because of elevated liver enzymes. They assume you have hepatitis if your liver enzymes are elevated. But I was checked for all varieties of hepatitis and that wasn't it. Liver enzymes continued to slowly creep up for another 13 years and my PCP tested me for a lot of stuff and it was all negative. He ran out of ideas. By that time, iron stores were dropping as was albumin and total protein. Finally, I took it upon myself to schedule an appointment with a GI doc and the first thing he did was test me for celiac disease. I was positive of course. After three months of gluten free eating the liver enzymes were back in normal range. That was back in about 1992. Your story and mine are more typical than not. I think the average time to diagnosis from the onset of symptoms and initial investigation into causes for symptom is about 10 years. Things are improving as there is more general awareness in the medical community about celiac disease than there used to be years ago. The risk of small bowel lymphoma in the celiac population is 4x that of the general population. That's the bad news is.  The good news is, it's still pretty rare as a whole. Yes, absolutely! You can expect substantial healing even after all these years if you begin to observe a strict gluten free diet. Take heart! But I have one question. What exactly did the paperwork from 15 years ago say about your having celiac disease? Was it a test result? Was it an official diagnosis? Can you share the specifics please? If you have any celiac blood antibody test results could you post them, along with the reference ranges for each test? Did you have an endoscopy/biopsy to confirm the blood test results?
    • Cathijean90
      I’ve just learned that I had been diagnosed with celiac and didn’t even know. I found it on paperwork from 15 years ago. No idea how this was missed by every doctor I’ve seen after the fact. I’m sitting here in tears because I have really awful symptoms that have been pushed off for years onto other medical conditions. My teeth are now ruined from vomiting, I have horrible rashes on my hands, I’ve lost a lot of weight, I’m always in pain, I haven’t had a period in about 8-9 months. I’m so scared. I have children and I saw it can cause cancer, infertility, heart and liver problems😭 I’ve been in my room crying for the last 20minutes praying. This going untreated for so long has me feeling like I’m ruined and it’s going to take me away from my babies. I found this site googling and I don’t know really what has me posting this besides wanting to hear from others that went a long time with symptoms but still didn’t know to quit gluten. I’m quitting today, I won’t touch gluten ever again and I’m making an appointment somewhere to get checked for everything that could be damaged. Is this an automatic sentence for cancer and heart/liver damage after all these symptoms and years? Is there still a good chance that quitting gluten and being proactive from here on out that I’ll be okay? That I could still heal myself and possibly have more children? Has anyone had it left untreated for this amount of time and not had cancer, heart, fertility issues or liver problems that couldn’t be fixed? I’m sure I sound insane but my anxiety is through the roof. I don’t wanna die 😭 I don’t want something taking me from my babies. I’d gladly take anyone’s advice or hear your story of how long you had it before being diagnosed and if you’re still okay? 
    • trents
      Genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out and also to establish the potential to develop celiac disease. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop it. To develop celiac disease when you have the genetic potential also requires some kind of trigger to turn the latent genes "on", as it were. The trigger can be a lot of things and is the big mystery component of the celiac disease puzzle at this point in time with regard to the state of our knowledge.  Your IGA serum score would seem to indicate you are not IGA deficient and your tTG-IGA score looks to be in the normal range but in the future please include the reference ranges for negative vs. positive because different labs used different reference ranges. There is no industry standard.
×
×
  • Create New...