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

Where Do I Start?


djmom

Recommended Posts

djmom Newbie

Hi-

I have a strong suspicion that my daughter(s) and I may have celiac disease. My mother has it.

One of my daughters and I were tested about 4 years ago and we were both negative. (antibody test)

She has a defect in the enamel of her permanent teeth which I know is very rare and often linked to celiac disease.

Here are my symptoms that "match" what I have read (I guess atypical in that I do not have the GI symptoms my mother has)

depression, extreme fatigue, frequent migraines, edema in legs, tingling in hands, gas, there may have been more that matched too, that is all I remember off the top of my head.

My question. Does it sound like I might have it? My mom thinks I do, but she thinks everyone does ;)

Do I go back and go thru the antibody testing or just bite the bullet and pay for genetic out of pocket? And if so, who would I test first?

If I test my daughter and she is positive, then I am positive, right? (pretty much sure since my mom is and my husband probably isn't). So then that is only having to pay out of pocket for one test.

But if she is negative, I have to test me.

If I test me first, if I am negative, do I need to test her?

Or is this one of these things where I will probably have at least some degree of a genetic possibility and I will need to test her anyways?

Which lab is the cheapest?

Or do I just go back to the primary care with my complaints and ask about celiac disease (again?) It is a new doctor now as my insurance has changed.

I do have two daughters so if this all starts coming out positive I guess she will need it too.

Any help in getting started would be appreciated. My mom is helpful, but I kind of want to deal with this on my own because I don't want her to know how crappy I feel.

Thanks so much in advance. Sorry this is so long, answers to all or part of the message are appreciated!


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



Celiac.com Sponsor (A8-M):



happygirl Collaborator

Go to your doctor, explain your concerns (i.e., the things you told us here), and ask for all to be tested using the Celiac panel.

AGA IgA

AGA IgG

EMA IgA

tTG IgA

total IgA

Your doctor can also order the genetic testing through their office as well.

Mtndog Collaborator

Uh...where to start. Well, if your mom has it then there is a 50/50 chance that you do. The genetic testing (I did mine through Prometheus) is about $400 but all that will tell you is if you have the genes.

You could go back and have the antibody tests again or ask for the biopsy (for you) or you could both go gluten-free, see how you respond and have the genetic test. I basically accepted I had it with a positive response to the diet and having one of the genes.

Since my doctor ordered it, my insurance covered the gene testing.

Either way, welcome to the board!

ShayFL Enthusiast

happygirl is right! Go to this new doctor. Might as well get as much as you can paid for through insurance. You pay your premiums so dont pay out of pocket unless you have to.

Just tell this new doctor your symptoms, your daughter's symptoms and your family history. Ask for complete Celiac panels for you and your two daughters. Also ask for genetic tests for everyone. All the doctor can say is no. You have nothing to lose by asking for EVERYTHING.

djmom Newbie

Great idea to ask for everything. Isn't it funny how managed care has beaten me down so much that I pretty much give up before even trying!!!

Thanks so much. I hope I don't become a permanent member by necessity, but if so, seems like I have found the right place!

For genetic testing, is it just a standard test, or is there something specific I ask for also? (certain gene testing)

Again, thanks.

ShayFL Enthusiast

Just Celiac gene testing.

imagine22 Contributor

I have celiac disease (no gastro symptoms either) so for testing my daughters (baby & 3yrs) I went with the saliva gene test first as its less invasive and then if they didnt have the genes I could not worry about testing ever again.

unfortunately they had the genes (but no surprise!) so now i will have them do a blood test each year to check, even if they are asymptomatic (as they have a higher than 1 in 10 chance of it developing at some point); but if they were sympomatic I would consider endoscopy even if bloods were negative.

You may be gluten sensitive or intollerant rather than actual celiac though. My mother is gluten sensitive but not celiac (bloating, reflux, depression, fatigue) but she wont give up the gluten permanently - just long enough to feel better then she gradually starts again and feels awful again!


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,061
    • Most Online (within 30 mins)
      7,748

    Sandra mc Donagh
    Newest Member
    Sandra mc Donagh
    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.