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

Process For 4 Year Old?


StephHappens

Recommended Posts

StephHappens Rookie

I was just diagnosed (positive blood work and positive endoscopy) right before the new year. My gastroenterologist said my mom and daughter should be tested. My daughter is just about to turn 4. What is the process to get a 4 year old tested? My husband doesn't want her to have to get blood drawn. Should we do it now or wait to see if she has symptoms?

What was the process for those of you with younger children?

Thanks!


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



Celiac.com Sponsor (A8-M):



Dixiebell Contributor

There is no other way. She will need to have the blood test for celiac. This is a good time to do it because she is on a gluten filled diet. I believe it is recommended to have them done once a year. It is better to catch it early.

Most children are not too afraid of getting blood drawn. I am more afraid than my son.

salexander421 Enthusiast

Did you have any genetic testing done? If you did you could have your daughter tested to see if she carries the same gene as you. I believe some do it with a cheek swab. If she carries the same gene/genes as you then I would go ahead and suggest the celiac panel. If she does not carry the same genes as you then she most likely does not have celiac. There are people that have celiac with out carrying the classic celiac genes but I think it's only like 5% of people with celiac, so very small chance. Hope that helps!

divamomma Enthusiast

My daughter (also 4) had bloodwork and a scope/biopsy. She has no problems with either.

Roda Rising Star

Both my kids do fine getting their blood drawn. My youngest son(6) has been screened twice Two years apart and was neg on blood testing after I was dx but just 2 months ago was positive. My oldest has been screened three times and all neg but the numbers are slowly inching up. He will probably be gluten free soon since his allergist feels that he is either celiac that is not showing up on blood work or at least gluten intolerant. I'm probably going to get a referral to a GI soon so for now he is still eating a regular diet.

StephHappens Rookie

Ok. Thanks. I think my husband is more scared of having blood drawn or seeing blood drawn. He almost passes out every time. I might have to take her. She isn't showing any signs, but I didn't either at her age. I think mine became active right after she was born. She has an appt on Friday. Fingers crossed all goes well.

mushroom Proficient

Ok. Thanks. I think my husband is more scared of having blood drawn or seeing blood drawn. He almost passes out every time. I might have to take her. She isn't showing any signs, but I didn't either at her age. I think mine became active right after she was born. She has an appt on Friday. Fingers crossed all goes well.

No need to worry. Nurses/phlebotomists know how to deal with young children, and it really is a relatively painless procedure. If you wanted to prepare her, you could practice tying something around her arm above the elbow so she will get used to the feel of it and explain to her that they do this to make it easier. There are a lot of people who cannot stand the sight of blood/faint upon seeing it. It is not at all uncommon and your husband should not feel embarrassed about it, just accept it. (And he doesn't have to look when they draw his blood :D )


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



Celiac.com Sponsor (A8-M):



irish daveyboy Community Regular

Journal of Pediatric Gastroenterology & Nutrition 12th Jan 2011.

Objective:

Small intestinal histology is the criterion standard for the diagnosis of celiac disease (celiac disease).

However, results of serological tests such as anti-endomysium antibodies and anti-tissue transglutaminase antibodies (tTGA) are becoming increasingly reliable.

This raises the question of whether a small intestinal biopsy is always necessary.

The aim of the present study was, therefore, to investigate whether a small intestinal biopsy can be avoided in a selected group of patients.

Conclusion:

Pediatric patients with a tTGA level

salexander421 Enthusiast

Journal of Pediatric Gastroenterology & Nutrition 12th Jan 2011.

Objective:

Small intestinal histology is the criterion standard for the diagnosis of celiac disease (celiac disease).

However, results of serological tests such as anti-endomysium antibodies and anti-tissue transglutaminase antibodies (tTGA) are becoming increasingly reliable.

This raises the question of whether a small intestinal biopsy is always necessary.

The aim of the present study was, therefore, to investigate whether a small intestinal biopsy can be avoided in a selected group of patients.

Conclusion:

Pediatric patients with a tTGA level

Lunabell Apprentice

I am considering getting the genetic testing done for my 6 year old. It would take a team to hold her down for a blood draw and at this point in her life, she has zero symptoms. Getting the genetic test is a compromise. It is painless for her and will let us know how much we should worry about testing her.

I did have my 10 year old tested. She is disabled and cannot talk, nor does she show pain until it is dire. She has always had some digestive issues, so we decided we needed to know for sure. She was negative, but we will keep an eye on her.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,933
    • Most Online (within 30 mins)
      7,748

    Kazwal
    Newest Member
    Kazwal
    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

    • Wheatwacked
      The discovery of the vitamin D receptor in multiple immune cell lineages, such as monocytes, dendritic cells, and activated T cells credits vitamin D with a novel role in modulating immunological functions and its subsequent role in the development or prevention of autoimmune diseases.  The Implication of Vitamin D and Autoimmunity: a Comprehensive Review
    • Wheatwacked
      Definitely get vitamin D 25(OH)D.  Celiac Disease causes vitamin D deficiency and one of the functions of vitamin D is modulating the genes.  While we can survive with low vitamin D as an adaptation to living in a seasonal environment, the homeostasis is 200 nmol/L.  Vitamin D Receptors are found in nearly every cell with a nucleus,while the highest concentrations are in tissues like the intestine, kidney, parathyroid, and bone.  A cellular communication system, if you will. The vitamin D receptor: contemporary genomic approaches reveal new basic and translational insights  Possible Root Causes of Histamine Intolerance. "Low levels of certain nutrients like copper, Vitamins A, B6, and C can lead to histamine build up along with excess or deficient levels of iron. Iodine also plays a crucial role in histamine regulation."  
    • AnnaNZ
      I forgot to mention my suspicion of the high amount of glyphosate allowed to be used on wheat in USA and NZ and Australia. My weight was 69kg mid-2023, I went down to 60kg in March 2024 and now hover around 63kg (just after winter here in NZ) - wheat-free and very low alcohol consumption.
    • AnnaNZ
      Hi Jess Thanks so much for your response and apologies for the long delay in answering. I think I must have been waiting for something to happen before I replied and unfortunately it fell off the radar... I have had an upper endoscopy and colonoscopy in the meantime (which revealed 'minor' issues only). Yes I do think histamine intolerance is one of the problems. I have been lowering my histamine intake and feeling a lot better. And I do think it is the liver which is giving the pain. I am currently taking zinc (I have had three low zinc tests now), magnesium, B complex, vitamin E and a calcium/Vitamin C mix. I consciously think about getting vitamin D outside. (Maybe I should have my vitamin D re-tested now...) I am still 100% gluten-free. My current thoughts on the cause of the problems is some, if not all, of the following: Genetically low zinc uptake, lack of vitamin D, wine drinking (alcohol/sulphites), covid, immune depletion, gastroparesis, dysbiosis, leaky gut, inability to process certain foods I am so much better than late 2023 so feel very positive 🙂    
    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
×
×
  • 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.