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

Family Glutening Me In gluten-free Household


skullgrl

Recommended Posts

skullgrl Rookie

I was diagnosed 7 months ago roughly and I've been gluten-free ever since. Our household has been pretty much gluten-free since then (obviously the beginning was rocky). The only time there is gluten in the household is once in awhile my non-celiac family members will have something gluten-y and then promptly clean the area where they consumed it. Nothing is allowed in the kitchen. 

 

Anyways, I've gotten consistently glutened here in the past and December was actually a pretty good month. Last night I sat down at dinner and after I asked someone to grab a drink for me (I need an x-ray to confirm but the Dr. said my foot is probably broken). My Dad poured me a glass of ginger ale and he accidentally dropped the cap on the floor. So my Mom and I said don't put that back on the ginger ale and spoke for a minute about it. When we finished speaking my Dad reaches for the cap and goes to put it back on. We realize by the time its just touched the rim and told him no! Turns out he wasn't listening at all to us. So I said I wasn't going to drink from that one and that I couldn't. My brother said, "It only touched it a little, its fine." I reiterated that I couldn't.

 

Fast foreword to today, I was sitting on the couch and my brother grabs me a drink and I take a big sip and look down and see a ginger ale bottle without a cap and look over to the kitchen where the new bottle. There really should have been some sound effect for me realizing had just happened. I told my brother and he just said it would be fine. Well, positive thinking can't fix glutening. I have a very clean timeline to glutening - it pretty much always takes 30 mins so I know where it came from.

 

I live at my boyfriend's half the week and his apartment is not strictly gluten-free and even though I quite sensitive I've only gotten sick there once. (I touched his keyboard and absentmindedly touched my mouth) I just don't understand why I always have to come home and get sick. I can't remember whether it was Nov or Oct but I was sick 3/4 of the weeks. I also feel bad for my Mom who works really hard to try and keep me safe from my brother/dad. It's really hard trying to heal myself with this going on.

 

Thanks for reading :)


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I would wash the cap off if it touched the floor - germs, dirt, cat hair being more an issue than gluten. I live with 2 (3 during college breaks) gluten eaters. I don't get glutened from crumbs I cannot see on computer keyboards, etc. obviously, you wouldn't be touching things with big crumbs. I think the more likely is:

someone using the PB, as an example, and putting the knife back in a few times

Using the colander that drains gluten pasta

Someone forgetting and putting the spoon they are stirring gluteny pasta into the gluten-free pasta

Putting the top of the ketchup or BBQ sauce onto the gluten bread ( not squeezing or pouring an inch above the bread ( I tell them to pour onto the meat in case they slip) really, this habit is another germ issue and for everyone's protection).

Grabbing out cheese slices after they get the bread out instead of before

Eating something you assume is gluten-free and would be surprised to find out it isn't - corn flakes and Rice Krispies are 2 examples we see a lot on here.

skullgrl Rookie

I would wash the cap off if it touched the floor - germs, dirt, cat hair being more an issue than gluten. I live with 2 (3 during college breaks) gluten eaters. I don't get glutened from crumbs I cannot see on computer keyboards, etc. obviously, you wouldn't be touching things with big crumbs. I think the more likely is:

someone using the PB, as an example, and putting the knife back in a few times

Using the colander that drains gluten pasta

Someone forgetting and putting the spoon they are stirring gluteny pasta into the gluten-free pasta

Putting the top of the ketchup or BBQ sauce onto the gluten bread ( not squeezing or pouring an inch above the bread ( I tell them to pour onto the meat in case they slip) really, this habit is another germ issue and for everyone's protection).

Grabbing out cheese slices after they get the bread out instead of before

Eating something you assume is gluten-free and would be surprised to find out it isn't - corn flakes and Rice Krispies are 2 examples we see a lot on here.

 

All our food is gluten-free (and I don't buy anything that has a chance of CC) except for the occasional pizza the rest of the family orders when I'm not around. After which they clean the table. The problem is we don't have any of those things in our house.

kareng Grand Master

All our food is gluten-free (and I don't buy anything that has a chance of CC) except for the occasional pizza the rest of the family orders when I'm not around. After which they clean the table. The problem is we don't have any of those things in our house.

Then I don't see how they are glutening you. But, if they put dirty caps back on food, maybe you are getting a touch of food poisioning? Effects you worse right now because you need to heal? Normal guts process lots of germs everyday and don't get sick.

answerseeker Enthusiast

I've never heard of getting glutened from a cap touching the floor?

pricklypear1971 Community Regular

If the house of gluten-free except for takeout pizza, etcetera you should look into if people are bringing in gluten foods on the sly. My son does it (did it?). He'll shove half eaten bags on gluteny pretzels on his backpack (backpack goes on kitchen table, homework and crumbs pulled out together) or bring gluteny candy in the house and dump wrappers all over (including crumbs). I've found bags of chips in his jeans....crumbs falling out of pockets. I did get hit once this way - he was doing quite a bit of this and I cracked down on it.

In the beginning things are weird, but if you think you're getting glutened it's worth looking into. Of course, as Mom I have more authority than you do when it comes to handing down rules and consequences at home.

IrishHeart Veteran

I am trying to understand exactly  how you would be glutened from a bottle cap falling on the floor. Just can't be possible, hon unless the floor is filled with wheat flour or bread crumbs.

Just highly unlikely, IMO.

 

You mention there is "nothing gluten-y allowed in the kitchen" so then, the chances are pretty good there are no crumbs on that floor. 

 

Your family is not glutening you, based on what you have told us,  but perhaps something else is causing you to be ill. 


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

It sounds to me like your Dad is clueless about gluten, and your brother is actually "anti-gluten-free". With your brother's attitude, do you think it's possible he is deliberately sabotaging you? I agree with the others that the cap dropping on the floor shouldn't gluten you, but if your brother is annoyed by having to eat gluten-free in the house, maybe he is sneaking gluten into things just to try to get even?

Nikki2777 Community Regular

I agree ts not the bottle cap.. More likely its their attitude of "a little bit won't hurt you". being applied to gluten items.

IrishHeart Veteran

HUH? I still do not see how a (possibly dirty from hitting the floor briefly) bottle cap and a glass of ginger ale (which is G F) can be construed as her family "conspiring against her" to gluten her.

 

 

Seriously, let's be realistic here. This incident is hardly evidence of that kind of malicious behavior.

GottaSki Mentor

I guess I'm not understanding either...if the home is gluten free how did dropping the cap get gluten on it and when it dropped....how did anything get inside the cap?

 

If your brother said it only touched it a little...was he talking about it touching the floor? or obvious source of gluten?

 

Any family that has removed gluten to the extent mentioned for a family member that is only living there part time seems to be aware....even with awareness....none of us are perfect.  

 

You will likely be accidentally glutened as it does happen, but if you are having frequent reactions...I'd look to other possible food intolerances.  When I removed gluten I replaced glutenous items with other foods that I was unknowingly intolerant of.

dilettantesteph Collaborator

It is really hard when you can't be sure what caused your reaction.  You have to depend on other people to not expose you and you can't know if they have or not.  They don't take it seriously so they aren't careful.  They won't tell you if they may have exposed you to something because they don't believe that it could be a problem.  To figure out what is causing problems you need to have as few variables as possible.  Could you maybe set up a mini kitchen in your room with a dorm fridge and a microwave?  Don't go in the kitchen.  Then if you get sick, you will know that it something that you are eating and not a cap on the floor.  Then again, maybe it was your family and it will make you well.  I would get some crutches or hop around and get your own drinks.  I wouldn't trust people who might expose me to gluten.

 

I hope you feel better soon and stay that way.

skullgrl Rookie

Thanks for all the replies everyone! The community here is so amazing. I don’t think I was as clear yesterday with my post as I could have been so I will attempt to clarify. (Brain fog is no fun) I probably should have waited until my mind cleared a bit before posting but I was really angry and needed to vent.

I should first say that while my kitchen is gluten-free, the floor of said kitchen is probably not. Also, there were a lot of problems awhile ago with people not washing their hands before putting away the dishes. Mainly my father who would have a beer and then put away the dishes.

Kareng – That is a possibility and it actually happened with me once with mushrooms I didn’t wash as thoroughly as I thought I did. My boyfriend ate the exact same ones and was fine but I really wasn’t. I hope it was just that rather than gluten because the effects went away much quicker than those of gluten.

Pricklypear1971 – That could definitely be part of the issue. My brother wouldn’t be the cause of this but my Dad is likely the culprit if that is the case.

Bartfull/Nikki2777/IrishHeart – I don’t believe there to be any malicious intent, I’ve educated them both, and my mother has as well. I think it comes down to apathy or not thinking about the consequences of their actions. Most of the times I’ve been glutened (not including the beginning, because I had NO idea what I was doing. “Hey, Pizza Pizza has a gluten-free pizza, let’s order that.”) I can trace it back to one of them. Although mainly my father.

GottaSki – It took me a long time to figure out that dairy isn’t my friend right now. I think I might try looking to see if I have any others.

dilettantesteph Collaborator

I see that your reply was only minutes after mine, so you might not have seen it.  Please forgive me for reposting if you did.

 

It is really hard when you can't be sure what caused your reaction.  You have to depend on other people to not expose you and you can't know if they have or not.  They don't take it seriously so they aren't careful.  They won't tell you if they may have exposed you to something because they don't believe that it could be a problem.  To figure out what is causing problems you need to have as few variables as possible.  Could you maybe set up a mini kitchen in your room with a dorm fridge and a microwave?  Don't go in the kitchen.  Then if you get sick, you will know that it something that you are eating and not a cap on the floor.  Then again, maybe it was your family and it will make you well.  I would get some crutches or hop around and get your own drinks.  I wouldn't trust people who might expose me to gluten.

 

I hope you feel better soon and stay that way.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.