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

My Closed Minded,know It All Aunt


Guest cd&dhspruehead

Recommended Posts

Guest cd&dhspruehead

:angry: I have this aunt who has a husben with a wheat allergy and thinks he grew out of it.Now as we all know CELIAC is a life long pain in the butt that only a gluten free diet can make better.BUT SHE HAS TO BE RIGHT!!Now get this,he's not the only one with it.His cuz has a ''wheat allergy''to.My aunt's son is bracking out with theses lovely red spots whitch itch.She calls it hivs.ITS DH!!!This women is a know it all.Got a computer at home.I've told her about celiac disease.Laughs in my face.LETS her husben eat gluten foods.Tells me my doctor is crazy and so I'm I.

WE'VE had blows about this and realy don't want to be around her for the holydays or any other time.It's her family.Let her dell with the heart brake.I want to stay heathy.


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

Why not talk to her sun and husband instead of with her? They are the ones who need to know and belive about it, not her.

Guest cd&dhspruehead

I've tried but thay lessen to her.It's like thay don't have a brain of there own.My aunt loves to control poeple.If her son or hubby looks up any thing on the computer she looking over there sholders.

This lovely women has to be right.She thinks celiac disease is some made up thing.Her faverit line is''I DON'T THINK SO''.

CindyK Rookie

It sounds like you have tried to provide all of them with the information they need to improve their health and they are making the choice to disregard it. What a shame for them, but you really can't do anything about it. This woman is who she is. It may save you some frustration if you can aviod the topic with her. She clearly is incapable of listening to others when she believes she "knows" something. You could continue to provide information to her husband and sons in a discreet way but it is still out of your hands whether they will do anything with it or not.

I have found that people in my family are unwilling to even consider getting tested for this. Maybe they are afraid? I believe my Dad has it and I suspect my twin sister (fraternal) and older sister have it. They have never been rude and ugly acting like your Aunt sounds but they are really unwilling to even get the blood test!

I know it is hard to have her disregard something this serious. However, you can't control other peoples reactions. You have done the best you can do by sharing the information. What they do with it is up to them.

  • 2 weeks later...
stef-the-kicking-cuty Enthusiast

Yes, I have the same problem with a good friend of mine and her daughter. When that little girl was younger doctors told this woman her daughter can't have wheat. And she has this "oh, a little bit can't hurt attitude" and smiles in your face. When I refused to eat a strawberry with a little bit of that dip at one side once, she made fun out of me and said, what, a little bit like that already hurts? And if somebody treats me like that I get snappy real easy. And I said, yeah, because it's NOT an allergy. Next time eat a bit of rat poison and tell me how you feel afterwards. :angry:

And her daughter has DH, too. Well, i'm convinced, it is DH. She doesn't want to hear it. But I asked the same question on this message board about this woman and I was told: You only can lead a horse to water, it has to drink on its own. Or something similar. I think, that's sooo right. You just give yourself a headache. They have to live with the pain. I just try to avoid the subject and when I gave them their gifts for christmas I didn't get her any candy and her brother something wheatfree from Hershey's kisses, in case he offers her something.

Well, I think you've done your job. If I were you I wouldn't do more.

Stef

Carriefaith Enthusiast

That's too bad... It's really hard to believe that people can be that ignorant about the health of their loved ones. It's just sad actually... I would find it very hard to wtach someone act that way.

Does she know the long term complications of Celiac Disease if left untreated, like cancer (Lymphoma and adenocarcinoma), osteoporosis, seizures, anemia...

I know it may be harsh to say, but if I were you I would ask her how she would feel if her son or husband got seriously ill because of how ignorant she is being about the whole thing?

Just a thought...

Guest cd&dhspruehead

I saw my uncle this past cristmas.He had rashy thing all over his body.I know he was uncomfertable.My aunt only looks up things on the internet that she can sling at some one later with.The thing is is that there are others now in the famiely that think thay may have celiac disease and DH who want to be tested.They are now hearing her grip to.She got told off,but still thinks shes right.If Celiac is found to be true,shes going to have a duck.SHES not wanting to be tested so that's just tough.But that also means that my cuz has to tested.She likes her power trips and it don't matter who gets hurt in the cross-fire.


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
      131,685
    • Most Online (within 30 mins)
      7,748

    tdouglas2901
    Newest Member
    tdouglas2901
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I'd go with a vodka tonic, but that's just me😉
    • Rejoicephd
      That and my nutritionist also said that drinking cider is one of the worst drink choices for me, given that I have candida overgrowth.  She said the combination of the alcohol and sugar would be very likely to worsen my candida problem.  She suggested that if I drink, I go for clear vodka, either neat or with a splash of cranberry.   So in summary, I am giving ciders a rest.  Whether it's a gluten risk or sugars and yeast overgrowth, its just not worth it.
    • Inkie
      Thank you for the information ill will definitely bring it into practice .
    • Scott Adams
      While plain, pure tea leaves (black, green, or white) are naturally gluten-free, the issue often lies not with the tea itself but with other ingredients or processing. Many flavored teas use barley malt or other gluten-containing grains as a flavoring agent, which would be clearly listed on the ingredient label. Cross-contamination is another possibility, either in the facility where the tea is processed or, surprisingly, from the tea bag material itself—some tea bags are sealed with a wheat-based glue. Furthermore, it's important to consider that your reaction could be to other substances in tea, such as high levels of tannins, which can be hard on the stomach, or to natural histamines or other compounds that can cause a non-celiac immune response. The best way to investigate is to carefully read labels for hidden ingredients, try switching to a certified gluten-free tea brand that uses whole leaf or pyramid-style bags, and see if the reaction persists.
    • Scott Adams
      This is a challenging and confusing situation. The combination of a positive EMA—which is a highly specific marker rarely yielding false positives—alongside strongly elevated TTG on two separate occasions, years apart, is profoundly suggestive of celiac disease, even in the absence of biopsy damage. This pattern strongly aligns with what is known as "potential celiac disease," where the immune system is clearly activated, but intestinal damage has not yet become visible under the microscope. Your concern about the long-term risk of continued gluten consumption is valid, especially given your family's experience with the consequences of delayed diagnosis. Since your daughter is now at an age where her buy-in is essential for a gluten-free lifestyle, obtaining a definitive answer is crucial for her long-term adherence and health. Given that she is asymptomatic yet serologically positive, a third biopsy now, after a proper 12-week challenge, offers the best chance to capture any microscopic damage that may have developed, providing the concrete evidence needed to justify the dietary change. This isn't about wanting her to have celiac; it's about wanting to prevent the insidious damage that can occur while waiting for symptoms to appear, and ultimately giving her the unambiguous "why" she needs to accept and commit to the necessary treatment. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
×
×
  • 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.