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 Celiac.com!
    eNewsletter
    Donate

Roomates & Friends


ehrin

Recommended Posts

ehrin Explorer

I just recently bought a house with a friend of mine and another friend of ours is renting a room. We used to each prepare a few meals and go on with our lives...but now I either have to run down their ingredient list or make my own meals. I'm only on day 3 of being gluten-free free and am having a hard time driving the point home to my friends.

Do you have any suggestions on how to help them understand that one iota of gluten can not touch anything that will go into my mouth?

I am going to create a "safe" cabinet of foods that I can eat...and I will get my own utensils and mark them gluten-free - but I fear they think I'm being neurotic and just don't understand how sensitive the issue is.

Any advice is appreciated.

Thank you,

Ehrin

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Noelle126 Apprentice

I live with my boyfriend and I think him reading this site has helped...since I think I just snapped one day and was like "ok I'm 100% doing this!" and I think he got a better understanding with reading the message boards but also it is a learning process, we are trying to eat more meals that are naturally gluten-free instead of substituting...it seems to be working more and I have made a shelf in the pantry all gluten-free and he has his shelf of all the stuff I can't eat. We are eating more fruits and veggies than we were before...which is healthier anyway.

Link to comment
Share on other sites
MySuicidalTurtle Enthusiast

Like Noelle126 said, there are naturally glutenfree meals. If you have a safe cabinet and they are doing the meal they should only use the safe foods, bowls, and such. Having them read the message board would help, yes. Just let them know that gluten destroys your villi! It just doesn't make you sick! They are your friends and if they do not understand, well, you will just have to not participate with them. You need to take care of yourself first. You can make your meal and they can make theirs but I do think they will understand since you are friends and are living together. Good luck!

Link to comment
Share on other sites
aikiducky Apprentice

This might sound a bit extreme but... my experience has been, and I've noticed many other people's here as well, that people you live with will REALLY get it once you've been thoroughly sick from glutening once. <_<:o I'm not suggesting that you purposefully eat something with gluten, but it's just hard to understand for other people, until they see the results with their own eyes. Then suddenly they get it! So whatever you do, IF you get glutened and feel sick, don't put a brave face on and hide your symptoms. Preferably throw up noisily where your housemates can hear you... :D

Pauliina

only slightly tongue in cheek

Link to comment
Share on other sites
Lisa Mentor

I live with my husband and college age daughter.

I have green round "dots" that I put on things that are mine to use and not to cross cantaminate. They know that those with the stickies are mine and they should not use them. I have also bought squeese jellies and mayo that will not touch the bread.

Put dots on your things and they will know that it is special just for you.

Maybe this will help.

Link to comment
Share on other sites
nettiebeads Apprentice
I just recently bought a house with a friend of mine and another friend of ours is renting a room.  We used to each prepare a few meals and go on with our lives...but now I either have to run down their ingredient list or make my own meals.  I'm only on day 3 of being gluten-free free and am having a hard time driving the point home to my friends. 

Do you have any suggestions on how to help them understand that one iota of gluten can not touch anything that will go into my mouth?

I am going to create a "safe" cabinet of foods that I can eat...and I will get my own utensils and mark them gluten-free - but I fear they think I'm being neurotic and just don't understand how sensitive the issue is.

Any advice is appreciated.

Thank you,

Ehrin

<{POST_SNAPBACK}>

My dh isn't celiac disease, and eats nongf foods. He tries to be careful and clean regularly, but I decided that I'd rather be paranoid and prepare my foods on paper plates, paper towels, whatever it takes to keep any hidden crumbs from cross contaminating my foods. Okay, so what if they think you are over reacting. Have them read up on what gluten does to those with celiac. And how if you don't go gluten-free, you'll have a higher chance of all kinds of problems - neurological, physical, cancers.... KatieUSA (I think) mentioned putting cleanser on a piece of pizza, rinsing it off and then handing it to her non-gluten-free friends to eat. They refused and then finally got the message that gluten is poison to us special people.

Link to comment
Share on other sites
ehrin Explorer

Thank you all very much.

They seem to be understanding, but just don't get that it's like poison.

I suspect I've had celiac disease for a few years now, so they're used to my gas and bloating as well as belly aches - it's me being healthy they're not used to.

I think being a diabetic, nearly my whole life, and being raised not able to eat processed foods is helping me immensley. Meaning, I already read labels due to being T1 and I don't eat many things with "crap" in them because I took the mentality from my parents that it's not worth eating if it's full of chemicals.

Thankfully I also love to cook, and have been cooking for myself, and friends, for years now - it'll just be a bit different now!

One of my roomates made shepherd's pie last night and ran the ingredient list by me first...so perhaps I should give them more credit!

thanks again...

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      120,987
    • Most Online (within 30 mins)
      7,748

    happydays
    Newest Member
    happydays
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • TessaBaker
      It sounds like you're dealing with a complex situation, and I can understand how frustrating it must be not to have a clear answer. Gut health can indeed play a significant role in various aspects of our well-being, including hair health.
    • Celiac16
      I have found similar benefits from thiamine. I was diagnosed with celiac at 16 and never really recovered despite strict gluten and dairy free diet and no detectable antibodies on checkup bloodworks. I’ve tried stopping the b1 but start to feel bad again- I wanted my doctors to do more extensive testing for the different thiamine transporters and enzymes which would be a better indication if I was deficient or dependent on it but everyone dismisses it (there are know genetic mutations where you need to take it daily for life). I have looked into Thiamine Responsive Megablast Anemia and I have a lot of the more mild symptoms of the disease that manifest when thiamine isn’t given to the patient such as optic neuritis… I just find the parallels interesting. i think that celiacs could be a side issue of inflammation that resulted from vitamin deficiencies. I was eating a lot of sugar leading up to my diagnosis and since eating gluten free didn’t make me feel much better, I’m wondering if this was more the underlying issue (sugar heavily depletes b1). I usually take 1.5g thiamine a day.
    • Fluka66
      Thank you for your welcome and reply.  Yes I've been carefully reading labels looking for everything in bold and have been amazed by what I have seen. However Heinz tomato and basil soup is wheat free so I m thinking I already have ulcers?  The acid could be causing the pain . My pain always starts in one place then follows the same route through me . GP confirmed that is the route of our digestive system.  So much pain from stabbing to tearing. If I throw in milk with lactose it's horrific.  Many years of it now, won't go into details but been seeing a consultant for a supposedly different problem . Wondering what damage has been done over the years. Many thanks for your reply. Wishing you the very best.    
    • trents
      Welcome to the forum community, @Fluka66! Did you realize that the vast majority of all canned soups use wheat starch as a thickener, including such common commodities as Campbell's tomato soup?
    • Fluka66
      Hello. Any help would really steady my nerves right now. I realised recently that certain food left me in agonising pain so eliminated from my diet. I also have a swollen lymph node. My very caring Dr did some blood tests and I went back the other day to see another equally caring Dr . She looked at the test results one result has come back with something wrong. It came very fast so I'm afraid I didn't catch what it was. Anyway the urgent referral to ENT. She did say as I had already eliminated gluten it wouldn't say anything on the results and neither Drs nor I were prepared to reintroduce gluten . I've just had some tomato soup and again in agony only thinking this must have aggravated maybe existing problems. Does anyone know what I'm facing now ? My swollen lymph node , pain when eating gluten and lactose and I'm assuming the acidity of tomatoes triggering pain.  I'm trying to stay calm and to be honest I've been in intolerable pain at times rendering me unable to stand up straight but I've always just got on with it . Guess I'm reaching out and would really appreciate any wise or unwise words at this stage. Wishing you all the very best as you live with this illness. Fluka66  
×
×
  • Create New...