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

My Son Has Celiac


mixxy231

Recommended Posts

mixxy231 Newbie

My 14 yr old son has had celiac for the past three years. I just found out I also have celiac (ate gluten for 3 months before test). My question is my 27 year old daughter has the signs of celiac but her blood test came back neg. Is this common for a mother and just child to have celiac and not the other children. I also have a 24 year old son and don't know if I should have him go get tested. My son that has celiac is also has type 1 diabetes. We found out he had celiac after his yearly blood test that the doctor does. Can you go years without Celiac showing in the blood test .....

melissa


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



Celiac.com Sponsor (A8-M):



gfp Enthusiast
My 14 yr old son has had celiac for the past three years. I just found out I also have celiac (ate gluten for 3 months before test). My question is my 27 year old daughter has the signs of celiac but her blood test came back neg. Is this common for a mother and just child to have celiac and not the other children. I also have a 24 year old son and don't know if I should have him go get tested. My son that has celiac is also has type 1 diabetes. We found out he had celiac after his yearly blood test that the doctor does. Can you go years without Celiac showing in the blood test .....

melissa

Difficult question... My mom and I are both diagnosed and my brother manages not to be. He chooses not to do a gluten-free diet but I honstly believe it would benefit him regardless of the test results since his 'symptoms' are very much like mine and my mothers when we are glutened.

cyberprof Enthusiast

Hi Melissa,

Celiac is genetic. If you have the gene, your children have a chance to have the gene or not (plus what they get from their dad- they could get two if he has it too). Having the gene doesn't mean that one will get celiac- something has to trigger the gene - illness, surgery, stress, car accident or Diabetes I are some possible triggers.

That being said, the blood tests are unreliable. Even the "gold standard" biopsy via endoscopy can be hit or miss, depending on how many samples are taken and how much or how little damage has been done.

I tested positive via a biopsy but negative on the blood test (I had very little damage in my small intestine - Marsh 0 or 1 with a high being a Marsh 4). My son, also 14, is negative on the blood test but we are trying gluten free for him to see if it gets rid of his symptoms and helps his growth get back on track.

Your daughter and older son may benefit from trying gluten free. They may feel better off gluten, which is the real test. A lot of people (like me) have symptoms that go away when gluten free. I feel so much better... I just didn't know how bad I felt. I just assumed "everyone" had stomach issues, brain fog etc.

Good luck!

blueeyedmanda Community Regular

Welcome! Sometimes, the tests come back negative but if the person goes gluten free they can see positive changes in their health. Hope that helps :)

SandraD1971 Newbie

I heard there is only a 30% chance of inheriting celiac so there is a good chance not everyone in the family would not have celiac.

I do believe you could have no antibodies for celiac in a blood screen if the disease is dormat. Sometimes it takes an illness or something which causes celiac to come out of "remission".

Hope this helps.

loraleena Contributor

The negative blood work is not always accurate. Given you and your son's diagnosis and the fact that she is having symptoms I would at least have her try a gluten free diet. You could have her checked for gluten intolerance by Entero labs. It is a stool test.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,038
    • Most Online (within 30 mins)
      7,748

    Briannas01
    Newest Member
    Briannas01
    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

    • Scott Adams
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
    • Beverage
      Exactly which blood tests were done? There are a few different ones and some docs don't do them all. Also, your results and reference ranges for each?
    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
×
×
  • 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.