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

What Level Of Sensitivity To Trace Amts Is This?


sreese68

Recommended Posts

sreese68 Enthusiast

I've had a person with celiac and a person with gluten intolerance say I sound "really sensitive" when I've told them the following, and I'm wondering if I am or if I'm more on the "normal sensitivity" end. I KNOW I'm not super sensitive after reading some of the posts by the people who really ARE super sensitive! Anyway, on July 4th, my daughter spent a long time in the petting zoo at our local fair. She fed the animals a lot. Without my knowledge, she opened, drank out of, and closed our shared water bottle. Unfortunately, I drank right after her and got glutened, which lasted about 6 days. So her glutened hands touching our water left enough of a trace to get me.

I ate my usual diet at home, and we have a gluten-free home, so no risk of cc there. And I know I didn't react to another food because gluten gives me neuro problems - no other food does. I've only been gluten-free for a few months. Does this level of sensitivity sound normal? Oh, I may have gotten the smallest of trace amounts on Thursday while drinking my coffee from home in the crumb-filled waiting area at my kids gymnastics class. Or maybe from the grocery store afterwards. I only reacted for a couple of days that time. Not sure, but won't bring my coffee again!

And will my sensitivity decrease as I heal??

Thanks! Sorry to go on for so long! Can't seem to be able to keep my posts short! LOL!


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



Celiac.com Sponsor (A8-M):



Harpgirl Explorer

I've had a person with celiac and a person with gluten intolerance say I sound "really sensitive" when I've told them the following, and I'm wondering if I am or if I'm more on the "normal sensitivity" end. I KNOW I'm not super sensitive after reading some of the posts by the people who really ARE super sensitive! Anyway, on July 4th, my daughter spent a long time in the petting zoo at our local fair. She fed the animals a lot. Without my knowledge, she opened, drank out of, and closed our shared water bottle. Unfortunately, I drank right after her and got glutened, which lasted about 6 days. So her glutened hands touching our water left enough of a trace to get me.

I ate my usual diet at home, and we have a gluten-free home, so no risk of cc there. And I know I didn't react to another food because gluten gives me neuro problems - no other food does. I've only been gluten-free for a few months. Does this level of sensitivity sound normal? Oh, I may have gotten the smallest of trace amounts on Thursday while drinking my coffee from home in the crumb-filled waiting area at my kids gymnastics class. Or maybe from the grocery store afterwards. I only reacted for a couple of days that time. Not sure, but won't bring my coffee again!

And will my sensitivity decrease as I heal??

Thanks! Sorry to go on for so long! Can't seem to be able to keep my posts short! LOL!

Honestly, it may depend on the perspective of the person you are talking to. I read in Living Gluten-Free for Dummies that even people with celiac can handle a certain amount of gluten, but that amount is a fraction of a crumb. My grandmother has celiac, but apparently only thinks of it as a GI issue. When I told her about my reactions (I too got sick after drinking from a straw that I didn't realize my hubby drank from), she said the same thing, "Oh, you're extra sensitive." However, I can see now that she has always had brain fog and severe joint/muscle pain, and she is not at all careful about cc. She has even gone back to taking regular wheat communion at church because its not enough to make her "sick". After reading more in these forums as well, I think that if she had been truly gluten-free for longer, her GI symptoms may have become more intense with each glutening. My last glutening lasted 2 more days than the previous one (5 days). But I've only been gluten-free for about 5 weeks.

GlutenFreeManna Rising Star

I really think it is all relative. There isn't really a "normal" level of sensitivity but what you described are things I have experienced (the water bottle thing and stray crumbs in a non-gluten-free environment). I consider myself to be very sensitive but I know there are people MORE sensitive and LESS than I am. The thing is, with people you talked to that said you were more sensitive than they are it could be one of two realities: 1. You really ARE more sensitive than them and need to be more careful OR 2. They don't take their diet as seriously and still think certain symptoms are "normal" for them or attribute those symptoms to another health condition they have. In my opinion number 2 reality is more likely. Not many people are willing to go to the lengths some of us go to avoid CC and many people diagnosed with celiac have other health conditions that can cause similar symptoms. A few people may be asymptomatic and so they don't avoid cc as much but in my experience most of the celiacs I meet in real life are not as careful with their diet as I am with mine and they attribute symptoms to other things. I knew someone once that only had DH as a symptom. She was completely gluten-free when she made her own food but if she went to someones house and they offered her something that "looked safe" (no visible flour, bread, etc) she would eat it. She had multiple miscarriages and a host of other health issues and she could never figure out why. I tried to explain to her that gluten can cause other things besides DH or digestive problems. She looked at me like I was crazy and said she wasn't that sensitive so I never brought it up again. People can get really defensive when you try to tell them how to eat. I think the best you can do is tell people YOU are supersensitve, explain all that YOu have to avoid and (if they are interested) gush about all the symptoms that have gone away since you went "strictly gluten-free".

love2travel Mentor

CC makes me paranoid. Nearly OCD in a way. I am the strictest celiac I know (in person, not on these boards because most of us are VERY strict!). As I have been asymptomatic as far as GI symptoms go it is difficult because I do not know yet whether I have been glutened. (I was once accidentally a few months ago but did not get sick at all. I only found out after a company that had told me on the phone their product was safe and it was only after I consumed it they contacted me to apologize - it was NOT gluten-free after all!) I cannot tell and am terribly in tune with my body. As I suffer from other ailments (i.e. chronic pain, insomnia and fibromyalgia) I am in constant pain. I just cannot ever escape it. However, I do believe they are linked to celiac so am really praying I see an improvement in all these in the future. So, although I may not be as sensitive as others I treat it as though I am. And there is no way I am deliberately ingesting gluten to see how I would react. It is not worth it to me. Nope - cannot do it! People on this board frequently seem to become more sensitive as time goes on and I am not willing to find out just how sensitive I am.

anabananakins Explorer
I am the strictest celiac I know (in person, not on these boards because most of us are VERY strict!)

This. And it's actually quite scary because we're only a teeny fraction of the people out there. I ate lunch with two people with celiac in the months before I went gluten free. Looking back now, at how they handled that, I don't think I'd want to eat at one of them's house. On the other hand, I have a friend who I do trust even though she's not gluten free, because she's demonstrated time and again that she gets it and she never makes me sick.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,023
    • Most Online (within 30 mins)
      7,748

    Tubbybooboo
    Newest Member
    Tubbybooboo
    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
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.