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

Ate Tests Accurate With Children?


jmcbride4291

Recommended Posts

jmcbride4291 Contributor

My wife has atl east 10 symtoms. Night blindness, lumbar, skin, hair loss, vision, total loss of teeth emanmel, upset stomach, bathroom prob's.Her mother has Fiber Myasia, night blindness, diabetis, etc. Wifes sister, smae and colitis, ashma, weight problems, thyroid and her children have learnimg dis'a, orthopedic problems, and daughter only 18 cannot have children. All my children have skin probs.One of mine has had a fever 1 week of every month since 12/1/07. Her tonsils keep getting attacked but ENT said not problem. Other doctors do not know why. Could immune system be attacking her. Her liver came back with a high reading and she has pain on that side.. Had blood work for Celiac but no call from Dr. yet. How accurate are these tests with children? My other children have coordination prob's, one diagnosed with ADHD and as baby very colicy and vommited formula all the time and went through many brands and types. My wife refuses to pursue as if though this is the worst thing to have celiac disease and thinks their life would be no good. I feel if so will be much better. I am worried if test comes back negative will have a harder time getting this resolved. My wife will resist. How accurate can the blood work be and what else can I do besides diet change. And if diet change how long to see up swing in children?


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



Celiac.com Sponsor (A8-M):



lizard00 Enthusiast

Hi

Sorry to hear about the difficulties with their children. I hope you get some answers soon.

From what I have read, test results are more likely to be inaccurate in children, especially if they are really young. The reason for this is that 3 of 4 of the Celiac tests are IgA based, and children have a tendency to produce low amount of IgA. So, someone with low amounts would likely produce a negative test. Even if he/she has celiac disease. Your 18 y/o probably has a pretty good chance of having an accurate result, but it is not uncommon to have a false negative.

If it's your 18 y/o, and her tests come back neg, why not just have her do a gluten-free trial? She is old enough to make that decision. Then if she improves, maybe it'll help your wife to see that 1: this is nowhere near the end of the world and the diet is NOT that hard and 2: maybe she would also benefit from being gluten-free. Really, I would suggest that with any of your children who are old enough to make that choice and stick with it. But do remember, if you want any of the others to be tested, don't start a gluten-free trial with them until after the tests. Once gluten is removed, the body immediately starts to heal and even a week can make the numbers go down and give a false negative.

Also, try to nicely educate your wife. I'm sure she doesn't want to see her children suffer, and if, in fact, they DO have Celiac, they will suffer far greater in the long run. I have a 2 y/o and can think of nothing worse than seeing him suffer. There is a lot of information out there, see if you can get her to read it.

Wishing you the best!!!

kbtoyssni Contributor

The worst thing in the world would be to have undiagnosed celiac disease. This will eventually lead to the kids getting sicker and sicker until they're too sick to get out of bed. Or it could lead to cancer and other lifelong irreversible health conditions. Or early death. Cutting gluten out of a diet isn't easy, but the alternative is much much worse. Maybe getting your wife some books that talk about the long-term health implications of undiagnosed celiac disease would help? And I'm completely blanking on the name of my favorite book right now...

You could try enterolab testing. It can detect gluten intolerance long before blood tests and scopes can.

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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

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

    • Total Members
      132,914
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.