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

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


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.

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!

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

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.

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.

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...


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
      131,176
    • Most Online (within 30 mins)
      7,748

    Ceekay
    Newest Member
    Ceekay
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
×
×
  • Create New...