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

Immediate Family Members Should Be Tested!


VegasCeliacBuckeye

Recommended Posts

VegasCeliacBuckeye Collaborator

She had the blood test and she tested positive for Celiac (at least the gene) . She just had the EGD tests done and is awaiting those...

I don't know whether to feel bad or relieved for her...

At least now she will want to join me for the Holiday meals and not the family...

Bronco


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



Celiac.com Sponsor (A8-M):



Kaycee Collaborator

Bronco, it is good that your mother got tested. And I can understand your mixed feelings, I think we all can understand them.

All I want is my immediate family to get tested (not all of them have) so that they know either way whether they have the disease or not. If they all got tested, I would be able to rest a little easier for them. It is not because I want someone to share the disease with, I just want them to be a bit more responsible about their own health, and to do their own worrying and not leave it up to me.

Cathy

jayhawkmom Enthusiast

Good for your mom!!!

Since my daughter was the first one DX - I was the next one to be tested. Now, I'm practically begging MY first degree family members to be tested, but they all think I'm nuts. =(

I wish they'd wake up and stop ignoring the health issues that have plagued them their entire lives. Their lives could be so much better if they'd just stop consuming gluten!!!

Lisa Mentor

Chris

Of anyone, what is the exact name of the gene test. I would like to have my girls tested and hopefully they will agree.

Thanks, Lisa

taweavmo3 Enthusiast

That's great your mom got tested.....kind of bittersweet that she is positive though. At least now she can take control of her health and prevent any further complications.

I wish my family would get tested, but no one will. Even my brother who has been really sick since he was a child refuses to believe he may have it. It's driven us apart somewhat. Last time he came over, he had a few beers and immediately was in the bathroom for the rest of the night. I try to hold my tongue most of the time about how skinny he looks, but when he got sick all over my bathroom, I felt like that gave me the right to say something! It did not go well, he really thinks he's fine.

Hope everyone else has a family who takes celiac a bit more seriously!

Gentleheart Enthusiast

Sorry, it's been posted before, but I have forgotten. Would someone please clarify exactly what constitutes a "first degree relative" or a second or third, etc.? And also the likelihood for them genetically having celiac/gluten intolerance (either your observed personal opinion or statistics). Thanks!

Grandparents = ?

Parents = ?

Siblings = ?

Children = ?

Cousins, Aunts, Uncles = ?

TestyTommy Rookie

My understanding is that a first degree relative is a parent, sibling or child of yours.

And if you have the celiac gene, it had to come from somewhere. That means either your mom or dad is carrying it.

Any advice on how to convince family members to get tested? Like some of you, my mom and sister absolutely refuse to get tested. My sister just tells me that she doesn't want to give up eating cookies and muffins! It's kinda ticking me off. . . . .


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



Celiac.com Sponsor (A8-M):



VegasCeliacBuckeye Collaborator

My mom is a nurse, so she kinda accepted it when I brought it up. She is also a logical and reasonable person.

My brothers will be tougher. I can see my eldest brother getting his kids tested before he will. He is the kind of guy that loves Guiness, Pasta, French Bread, etc.

My other brother might be easier, but he will still go kicking and screaming.

Bronc

Gentleheart Enthusiast
My understanding is that a first degree relative is a parent, sibling or child of yours.

And if you have the celiac gene, it had to come from somewhere. That means either your mom or dad is carrying it.

Any advice on how to convince family members to get tested? Like some of you, my mom and sister absolutely refuse to get tested. My sister just tells me that she doesn't want to give up eating cookies and muffins! It's kinda ticking me off. . . . .

My family won't be tested either. In our case it would require Enterolab type testing and money is an issue there. But the main reason is that they honestly don't want to know. I'm afraid it will have to wait until they get sick enough to be out of choices. Another sad reason is that they honestly think this is all a bunch of hooey.

chrissy Collaborator

lisa, through prothethius lab, our ped gi ordered celiagene and celiaplus.

happygirl Collaborator

Lisa: Your doc should know what the "name" of the panel is, depending on which lab they use. All they need to know is that they want to be tested for the presence of "Celiac genes" which are HLA-DQ2 and HLA-DQ8.

Like Chrissy mentioned above, many use "Prometheus" as their lab of choice for that type of testing.

VegasCeliacBuckeye Collaborator

Well,

Mom just got back the test results from the endoscopy. She has Celiac! She alsso has elevated IGA and IG levels.

I told her "welcome to the club" and if she has any questions, I am here.

Once she gets her new computer, she will be coming on this site.

BB

p.s. No, you cannot ask her any potentially embarrassing questions about me - LOL

:)

Lisa Mentor

thank you crissy and laura...

In my notebook.

Lisa

mouse Enthusiast

What do you mean, in that I cannot ask her any embarassing questions about you? I just started a list. You mean I have to throw it away - that sucks big time.

Guest AutumnE

Im sorry your mom has it too. Me, my daughter, my sister, my bil, my niece and nephew all have it.

My parents have the gene at least if not the antibody due to me and my sister both having a double gene, they didnt get tested themselves but obviously we get it from somewhere ;)

My husband still needs some coaxing to get tested even though he basically eats gluten free anyways.

Unfortunately not everyone sticks to their diet faithfully but I hope they come around soon. My mom, dad, and bil dont stick to it at all, I would call them more gluten lite than gluten free. It helps tremendously with holidays though since everybody makes gluten free dishes.

jerseyangel Proficient
What do you mean, in that I cannot ask her any embarassing questions about you? I just started a list. You mean I have to throw it away - that sucks big time.

So-o- funny! :D

Well Bronco, I'm sorry that your mom is positive, but as we all know, it's best that she know so she can heal and be as healthy as she can. :)

I look forward to meeting her on the board!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,017
    • Most Online (within 30 mins)
      7,748

    Sjcucinotta
    Newest Member
    Sjcucinotta
    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

    • 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.
    • knitty kitty
      Please do more research before you settle on nicotine. Dr. Paul New house is a psychiatrist.  His latest study involves the effect of nicotine patches on Late Life Depression which has reached no long term conclusions about the benefits.   Effects of open-label transdermal nicotine antidepressant augmentation on affective symptoms and executive function in late-life depression https://pubmed.ncbi.nlm.nih.gov/39009312/   I'm approaching the subject from the Microbiologist's point of view which shows nicotine blocks Thiamine B1 uptake and usage:   Chronic Nicotine Exposure In Vivo and In Vitro Inhibits Vitamin B1 (Thiamin) Uptake by Pancreatic Acinar Cells https://pubmed.ncbi.nlm.nih.gov/26633299/   While supplementation with thiamine in the form Benfotiamine can protect from damage done by  nicotine: Benfotiamine attenuates nicotine and uric acid-induced vascular endothelial dysfunction in the rat https://pubmed.ncbi.nlm.nih.gov/18951979/   I suggest you study the beneficial effects of Thiamine (Benfotiamine and TTFD) on the body and mental health done by Dr. Derrick Lonsdale and Dr. Chandler Marrs.  Dr. Lonsdale had studied thiamine over fifty years.   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/ I suggest you read their book Thiamine Deficiency Disease, Dysautonomia, and High Calorie Malnutrition.     Celiac Disease is a disease of malabsorption causing malnutrition.  Thiamine and benfotiamine: Focus on their therapeutic potential https://pmc.ncbi.nlm.nih.gov/articles/PMC10682628/
    • sleuth
      Thanks for your response.  Everything you mentioned he is and has been doing.  Tobacco is not the same as nicotine.  Nicotine, in the form of a patch, does not cause gastrointestinal irritation.  Smoking does. He is not smoking.  Please do your research before stating false information. Dr. Paul Newhouse has been doing research on nicotine the last 40 years at Vanderbilt University Medical Center.  
    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
×
×
  • 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.