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

"how Sensitive Are You?"


BlessedMommy

Recommended Posts

BlessedMommy Rising Star

As you know, this is usually a question from people who want to know if you will purposefully eat food that's been contaminated.  :rolleyes:

 

My situation is that given the severity of my high levels of gluten response, I would prefer not to tempt fate by being careless with lower levels. I did get a headache and a low grade fever the other day though after what I think was a slight gluten exposure. Sometimes I wonder though if that was gluten or something else.

 

So I do seem to get some responses to low level contamination but certainly not a rush trip to the ER. 

 

So, what's a meaningful and concise way to answer that question that doesn't give people too much detail but also doesn't lie? 


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

As you know, this is usually a question from people who want to know if you will purposefully eat food that's been contaminated.  :rolleyes:

 

 

 

Honestly, no. I do not know a single person in my life who would ask me if I would purposefully eat food that's been contaminated

with gluten. 

 

No one I know would ask such a stupid question of me. 

BlessedMommy Rising Star

I read your testimony, and yes, I agree that any person who would ask you a question like that, would be pretty silly. If it would be like asking someone if they would eat rat poison on purpose. 

IrishHeart Veteran

It's as ridiculous as asking you that question.

BlessedMommy Rising Star

So pretty much treat it like a dumb question? 

IrishHeart Veteran

So pretty much treat it like a dumb question? 

^_^

 

who is asking this question of you? 

BlessedMommy Rising Star

My cousin once asked me that question, when referring to a restaurant that stated as a disclaimer that cross contamination may occur. 

 

I sort of bumbled through an answer which boiled down to, "I use my common sense, ask questions, ask for accomodations, and avoid the chips made in the shared frier." 

 

On another occasion, I refused to eat my own dish at a potluck after someone CC'ed it. Someone said, "Well maybe you're not THAT allergic." 


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Hon, you want my very best advice about this whole thing?

 

Say it once to everyone and never explain yourself again.

 

 

"Gluten tried to kill me. I can't eat it. Not a single speck. Understand? "

 

Then, smile .......and let it go.

BlessedMommy Rising Star

I love it! That really gets the point across. 

IrishHeart Veteran

I have said it (but with swear words).

 

 

Yes, your rat poison analogy also works. My husband usually says  strychnine. 

BlessedMommy Rising Star

I think that people just do not understand how ridiculous it is to mess around with something that could destroy your ability to function independently and speak correctly.

 

Of course, in this society, almost everybody seems to subscribe to the "a little won't hurt" mentality.  :blink:

IrishHeart Veteran

 

 

Of course, in this society, almost everybody seems to subscribe to the "a little won't hurt" mentality.  :blink:

 

well, that depends on what "that little something" IS... ^_^

cristiana Veteran

I don't know about you but one of my problems pre-diagnosis was liver function test results that my doctor didn't like the look of.  I often get the impression that people think I am taking this gluten-free diet too far but when I say that gluten affects my liver they don't say any more.   

NatureChick Rookie

I think there is a huge difference between risking a slight cross contamination and eating a meal that you know contains an ingredient that has gluten. For me, a minor cross contamination could mean feeling lousy for a few days. A full-on glutening could mean all-over pain for weeks. 

I generally don't risk either, but everyone I know in real life who is gluten free (three total) takes many more risks than I do, eating out at restaurants that have gluten-free items on their menu, trying the food a coworker claims to be gluten free, eating the home-made foods friends gave them. And I know from their experience that they are not gluten-free because they call me for sympathy or send pictures of their break outs when they are in the middle of their reactions. 

But they do honestly believe (hope) that the foods will be gluten-free before they eat them. I don't know if I'm less trusting or just less willing to lose a few days to recovery that the risks just don't seem worth it. The last risk I took was eating food prepared by my cousin at Thanksgiving. The contamination really wasn't that bad because I only tried the foods that I thought would be okay (watched how they were prepared), and I slept through most of my reaction over on a long weekend ... but I definitely brought my own food at Christmas. Plus, who wants to quiz their host about every ingredient?

 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    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

    • 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
    • DebJ14
×
×
  • 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.