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

The Gene & Full-blown Celiac


celiac3270

Recommended Posts

celiac3270 Collaborator

I have celiac disease. Nobody else in my family does according to tests, although my mom, grandmother, and brother all have problems that would make you think they had it.

Grandmother -- EXTREMELY SEVERE osteoporosis

Mother -- Bloating, distended stomach after eating gluten

Brother -- Low weight (exact size/weight I was at his age...very thin).

The doc. thought it was likely that my brother had it and this question is concerning him. The GI tested him about 6 months ago, as soon as I was diagnosed, and then tested a month later in disbelief at negative bloodwork. He has the gene, I think, but not celiac disease.........I don't really know too much about this; does this make sense? Having the gene, I think, means that he could develop celiac disease at any time due to a number of factors that include high stress......I don't remember the others. If he has the gene, but not celiac disease, does he need to be on a gluten-free diet? We're gonna ask my new celiac doctor about this after we get my symptoms under control, but I was interested to hear what people here thought. Will he need to get tested many times in the future to make sure that it hasn't developed into celiac disease? I know that there is always the possiblity of inaccuracy on the bloodwork, but I was just wondering about this gene thing. Thanks.

-celiac3270


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



Celiac.com Sponsor (A8-M):



GEF Explorer

Hey celiac3270!

I was just reading something regarding this subject in the book, Dangerous Grains... good book, by the way. The author mentioned the need for repeat testing, as celiac can develop at any time. My symptoms started about 5 years ago, at a time of great stress but, seriously that's when it happend for me and I'm now 28.... nothing was unusual prior to that. It seems that more and more tests turn positive the longer I wait. I wish I could convice my family, esp my sister to get tested... so, I think it's great that your family is being pro-active. I'll see if I can find out where the author writes about this and give you some info. He really does stress genetic-predisposition and the need for anyone who has tested positive at all to go gluten-free... at least to see if their symptoms improve.

Gretchen

Guest ~wAvE WeT sAnD~

celiac3270--

At first I was going to say that your family members seem to be "carriers" of celiac disease--but obvious exhibition of the disease's most common symptoms leaves me as confused as you.

:ph34r: <---- I think the gene is hiding, just like this guy :P Has anyone else in your family had an endoscopy? If so, what were the results?

celiac3270 Collaborator

Thanks for the info.....that's what I thought, Gretchen, but I hadn't read anything about it, so I didn't know for sure. Jill, nobody in my family has had a biopsy. My dad tested negative in the bloodwork, which makes a lot of sense. Neither he, nor anyone else on his side of the family show any signs of celiac disease. My grandma has bloodwork done--negative. Mother had bloodwork--negative. Brother had bloodwork--twice--negative. Nobody has had a biopsy....and I know that there are relatively common cases of neg. bloodwork, pos. biopsy.........so he probably should've had a scope since we had such suspicions about him. Once we get my symptoms under control, we'll talk to the doctor about my brother......he seems to be really on top of things and knowledgable, so he'll probably know what to do about all this.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,071
    • Most Online (within 30 mins)
      7,748

    Gigic
    Newest Member
    Gigic
    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

    • Russ H
      This treatment looks promising. Its aim is to provoke immune tolerance of gluten, possibly curing the disease. It passed the phase 2 trial with flying colours, and I came across a post on Reddit by one of the study volunteers. Apparently, the results were good enough that the company is applying for fast track approval.  Anokion Announces Positive Symptom Data from its Phase 2 Trial Evaluating KAN-101 for the Treatment of Celiac Disease https://www.reddit.com/r/Celiac/comments/1krx2wh/kan_101_trial_put_on_hold/
    • Scott Adams
      BTW, we've done other articles on this topic that I wanted to share here (not to condone smoking!):    
    • Colleen H
      Hi everyone  This has been a crazy year so far... How many people actually get entire sensory overload from gluten or something similar ?  My jaw is going nuts ..and that nerve is affecting my upper back and so on ...  Bones even hurt.  Brain fog. Etc  I had eggs seemed fine.   Then my aid cooked a chicken stir fry in the microwave because my food order shorted a couple key items .   I was so hungry but I noticed light breading and some ingredients with SOY !!! Why are we suffering with soy ? This triggered a sensitivity to bananas and gluten-free yogurt it seems like it's a cycle that it goes on.  The tiniest amount of something gets me I'm guessing the tiny bit of breading that I took one tiny nibble of ...yikes ..im cringing from it .. Feels like my stomach is going to explode yet still very hungry 😔  How long does this last?! Thank you so much 
    • 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.
×
×
  • 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.