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

Should I Get Other Dd's Tested?


ptkds

Recommended Posts

ptkds Community Regular

I was just daignosed w/ celiac by a blood test, and my 17 m old dd was diagnosed by a blood test. We have 2 oder dd's ages 9 and 6. I really don't want to put them through the blood test but my dh does. He says he wants to have "proof" that they have celiac because he doesnt' feel comfortable telling people they have it without if being verified, especially for school.

My 9 yr old constanty gets stomach aches and diarrhea. She also gets dizzy at times and she is small for her age. My 6 yr old has occasional diarrhea, but she has a few behaviour problems (gets angry really easy and cries easily). She is also kinda small for her age and she has asthma.

So I made an appointment for wednesday to see their ped, but I just don't think it is necessary. I jsut wanted to test them by putting them on the diet and seeing if there is a difference. My dh is the one that wants to do the tests.

Any suggestions on what I should do? Which one of us is right??

Thanks,

ptkds


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



Celiac.com Sponsor (A8-M):



vampella Contributor

IMHO, you are RIGHT. why do the testing if there is such a strong history? Plus, the blood tests come up with false NEG's all the time.

There is no harm in getting them tested but, why does your DH care so much..if the diet works what other proof does he need?

I'm with you, let them be and put them gluten-free.

Char

Nikki2003 Contributor
IMHO, you are RIGHT. why do the testing if there is such a strong history? Plus, the blood tests come up with false NEG's all the time.

There is no harm in getting them tested but, why does your DH care so much..if the diet works what other proof does he need?

I'm with you, let them be and put them gluten-free.

Char

Nicole was diagnosed in july of 06. I had my older dd tested because they have a certain % of having it also,Plus when she was a bit younger she has issues with constipation. We did the blood work and hers it positive also. She is having her biopsy on the 27th of this month.

Celina

shayesmom Rookie
I was just daignosed w/ celiac by a blood test, and my 17 m old dd was diagnosed by a blood test. We have 2 oder dd's ages 9 and 6. I really don't want to put them through the blood test but my dh does. He says he wants to have "proof" that they have celiac because he doesnt' feel comfortable telling people they have it without if being verified, especially for school.

My 9 yr old constanty gets stomach aches and diarrhea. She also gets dizzy at times and she is small for her age. My 6 yr old has occasional diarrhea, but she has a few behaviour problems (gets angry really easy and cries easily). She is also kinda small for her age and she has asthma.

So I made an appointment for wednesday to see their ped, but I just don't think it is necessary. I jsut wanted to test them by putting them on the diet and seeing if there is a difference. My dh is the one that wants to do the tests.

Any suggestions on what I should do? Which one of us is right??

Thanks,

ptkds

I'm with you on this one. With strong family history like that, it's much SAFER to just get them all on a gluten-free diet as opposed to waiting for a positive dx with blood/biopsy. To be honest, I'd probably be telling dh that if he wants the other kids tested, he needs to go in too. This does tend to be genetic and just because you have tested positive doesn't mean that he also isn't passing on the genes for it. ;)

As for feeling comfortable about telling people about this.....if the children respond well to the diet, there is absolutely nothing dishonest or unjustified in simply saying that the children are gluten intolerant. And it may benefit them in the future when applying for their own health insurance to not have the positive Dx show up on record.

I know that this is fairly early in the game for the Celiac diagnosis and that there are a lot of conflicting emotions that come along with this. I'm sure that your dh is as frustrated as you have been throughout this. But at some point, acceptance will set in and eventually routine and then it becomes second nature. You don't have to get them tested to put them on the diet. Trust me, you and your dh will KNOW if gluten is a problem when you do the diet.

And if it's of any consolation, a little over a year ago....I was really torn about not having a Dx for my dd. But we've found doctors who have been willing to help us in dealing with the school and who are in agreement that dd has serious problems with gluten. Our GP told me 2 weeks ago that he wouldn't recommned the testing now that we've gotten everything under control and dd is thriving. As he put it..."Why go through all the tests just to get a slip of paper telling you to do the gluten-free diet? You're already doing it successfully and have all your answers. You don't need a doctor to give you any more common sense than you've exercised. Celiac or not, your dd cannot tolerate gluten. What else do you want to know?". :) Now THAT was a first for us! lol! But I definitely agree.

2Boys4Me Enthusiast

FWIW, after my younger son was diagnosed my husband, older son (7 at the time), my mom and I all had blood tests.

They all came back negative. (None of my in-laws, nor my brother or sister got tested.)

Guest nini

don't put them through testing... with such a strong genetic predisposition and obvious symptoms simply put your entire family on the diet (if hubby objects tell HIM to get tested and scoped but tell him the rate of false negatives is too high)

my daughter tested negative and putting her through the blood draws was VERY traumatic and I would NOT do it again if I had it to do over. I would have put her on the diet as soon as I suspected gluten intolerance instead of waiting for a Dr. to give me permission to NOT feed my child poison everyday.

Here's the thing, I tested positive for Celiac shortly before her 3rd birthday, it was another 6 months before we put her on the diet AFTER her test results were negative... when we put her on the diet, she got well within A WEEK. Proof enough for me.

chrissy Collaborator

i'd do the blood test if it were me. it is just a simple blood draw and the results come back pretty quick. i tested my whole family after we suspected one of the girls might have celiac---and we discovered that 3 of them actually have it. my oldest son has more symptoms than all 3 of the girls combined-----and he does not have celiac. there are other things that can cause symptoms.


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

a blood test really isn't that awful. I'd do a blood test, and after that, do the dietary challenge (take them gluten-free for a month). this, of course, is predicated on the assumption that you wouldn't bother with an endoscopy. if you would, then blood test, endoscopy if results warranted, or dietary challenge if tests didn't warrant the endoscopy. either way, blood and diet testing. why do I suggest the blood testing? because with kids there *is* an issue getting other institutions to believe you, and just your word may not be enough for them.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Jsingh replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

    2. - lizzie42 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

    3. - trents replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

    4. - trents replied to jenniber's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      Disaccharide deficient, confusing biopsy results, no blood test

    5. - Paulaannefthimiou posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,864
    • Most Online (within 30 mins)
      7,748

    Jojo3
    Newest Member
    Jojo3
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Jsingh
      Hi,  My 7 year daughter has complained of this in the past, which I thought were part of her glutening symptom, but more recently I have come to figure out it's part of her histamine overload symptom. This one symptom was part of her broader profile, which included irritability, extreme hunger, confusion, post-nasal drip. You might want to look up "histamine intolerance". I wish I had known of this at the time of her diagnosis, life would have been much easier.  I hope you are able to figure out. 
    • lizzie42
      My 5yo was diagnosed with celiac last year by being tested after his sister was diagnosed. We are very strict on the gluten-free diet, but unsure what his reactions are as he was diagnosed without many symptoms other than low ferritin.  He had a school party where his teacher made gluten-free gingerbread men. I almost said no because she made it in her kitchen but I thought it would be ok.  Next day and for a few after his behavior is awful. Hitting, rude, disrespectful. Mainly he kept saying his legs were shaking. Is this a gluten exposure symptom that anyone else gets? Also the bad behavior? 
    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
    • trents
      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
×
×
  • 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.