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

Help Please


momzilla

Recommended Posts

momzilla Newbie

I need some advice. My 12 year old son has had digestive problems since infancy. He was recently diagnosed as having lactose intolerance and irritable bowel syndrome and GERD. Treatment initially worked, but lately he has been worse than before. His gastroenterologist said blood work for wheat came back negative, and as far as his endoscopy/colonoscopy that was normal also. My health insurance is not the best and I know that most of my concerns are brushed aside. I put my son on a gluten free diet and for that time he was a normal kid again. All his symptoms (headache, grouchiness, diarrhea, tiredness, gas) have disappeared. Two days ago he had a major stress and a minor digestive upset but he is back to normal now. My question is could he be gluten intolerant even though his medical tests say no because the gluten free diet has really changed him. Sorry for the long post but I'm at my wits end. Thank you!


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



Celiac.com Sponsor (A8-M):



3boyzmom Newbie

Yes, he could be gluten intolerant even though he tests negative for Celiac's disease. Currently doctors are not testing for anything short of having damaged villi in the small intestines and having full blown Celiac's disease. If your son's tests fell short of that criteria, then you would not have been advised to try a gluten free diet.

I have been finding more and more people who have tested negative on the Celiac blood tests panel and have found major improvement in their physical health going gluten free.

Do you have copies of the blood work done on your son? I am curious if his IgG was elevated and not the rest. This would have indicated a gluten intolerance but not Celiac's disease.

If it makes him feel better and you see the difference, then I think you have your answer. Join the gluten-free club and know that you are doing the right thing by modifying his diet to alleviate his symptoms!

Priscilla

gf4life Enthusiast

There are a few articles here at Celiac.com that talk about the blood tests not being accurate. Here are some links to a few of them.

False Negative Serological Results Increase with Less Severe Villous Atrophy

https://www.celiac.com/st_prod.html?p_prodi...-43104177172.cf

The patient should also have the celiac antibodies blood testing, but the diagnosis is still established on the biopsy pathology. In Dr. Greens experience, about 30% of celiacs have negative antibodies at diagnosis, so positive antibodies are not required to make the diagnosis.  Antibodies testing often helps establish the need for a biopsy, but they also have great value in establishing a baseline so that an assessment can be made on how the patient is doing later on. All the antibodies should normalize, in time, when gluten is eliminated from the diet.

The full article can be found here:

https://www.celiac.com/st_prod.html?p_prodi...-41104189220.0e

I personally tested negative on every blood test. My kids tested negative on all but the IgG Gliadin tests. When we did the stool tests we all had antibodies present in the iintestines, and two of my kids had moderate to significant malabsorbtion. But fortunately not severe malabsorbtion. We have all been steadily improving on the diet for most of this year. So needless to say, I am not a big supporter of the blood tests. They just are not sensitive enough to pick up the lower levels of antibodies.

If your son improves on the diet, then you should consider that he is most likely having problems with gluten.

God bless,

Mariann

momzilla Newbie

Thank you both for the info. The gluten-free diet is definitely a great improvement! I don't have copies of his labs but I remember my pediatrician saying the levels were slightly elevated and his gastro saying that it was insignificant, so who knows! I feel way more informed and confident in that I knew there was a problem that wasn't being addressed. Thank you both again for your help!

Archived

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

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

    • Total Members
      133,318
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
    • xxnonamexx
      Thanks for the info. I have been taking the ones you recommended but when I saw this I was curious if it was something else to add to the journey Thank  
    • Jane07
      I used to be able to get the Rivera yougut i havent been able to get it lately. I like getting it did say it did say gluten free. I just looking for a good yogurt that gluten free that i can add some fruit and nuts to any suggestion would be helpful  thanks
×
×
  • 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.