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

How Long Is This Supposed To Take? The Waiting Is Killing Me.


Cara in Boston

Recommended Posts

Cara in Boston Enthusiast

Sorry to be so dramatic.

Here's the story:

My 5 year old son was complaining of stomach aches pretty consistently for about 10 days - at the same time, his behavior took a shocking turn for the worse - tantrums, melt downs, super sensitive to absolutely everything, etc. Doctor tested for Celiac and 2 of the blood tests came back positive. This was back in December! It takes about two weeks to book an appointment. We went to GI specialist, all he did was more blood tests. Wait two weeks. Get results. He has the genetic marker. Wait more to schedule endoscopy. Dr. busy, Dr. out of town, got appointment in mid-March for procedure. All this time he is still eating gluten and still as grouchy and unhappy as ever.

In the meantime, having learned about it more, I realized I have many of the symptoms so I got tested too (and my older son.) Took two weeks to get results. Some positive, some not. Can't get follow up apt. until Feb 28th (and I'm sure there will be more tests and more waiting to schedule . . . )

I know I need to be patient - especially to get proper diagnosis for my 5 year old. We will need it to ensure the school will comply, etc.

But, do I really need all the tests? I'm thinking of just going gluten free and if it makes me feel better, GREAT. Not sure at my age if I really need a confirmation of Celiac.

My blood tests were:

IgA: 376 (69-309) above normal

TTG Ab, IgA: 50.83 (0-15) elevated

Gliadin Ab (s), IgG: 4.35 (0-15) Normal

Gliadin Ab, IgG 5.47 ((0-15) Normal

TTG Ab, IgG: 5.47 (0-15) Normal

Any advice?

Cara


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



Celiac.com Sponsor (A8-M):



Takala Enthusiast

Well, how completely frustrating to have to wait that long for the GI doctor to not be "busy." :huh:

The reason to try to stick with it while waiting for Godot, is that if you go off of gluten for any length of time, you may then screw up your test results. Then the Doctors will look at you and Not Be Pleased. Don't go for a biopsy after you've been off gluten for awhile.

Some people can tell very quickly when they eliminate gluten that This Is It. Others might be expecting a big reaction, and be surprised that it's more subtle or slow.

But then. What if your biopsy comes back negative, anyway ? Sometimes this happens. You should, with those half results, try going gluten free, since you said you have symptoms and the kid had to inherit it from somebody.

How are you on sticking with something once you make up your mind to try it ? Because this isn't one of those types of things that you can't really commit to, and then change your mind, if this really IS the problem. I see a lot of people on here who have, to put it mildly, trouble sticking with a gluten free diet and are coming up with every excuse in the book to go off of it, but they know it's sort of wrong so they come in here anyway and leave a trail of breadcrumbs so somebody will talk them out of it. One of the symptoms of being glutenned is wanting to keep being glutenned....

I went on it on my own after self diagnosing, but I was so sick and the doctor(s) so clueless back at that time, that I was both highly motivated and fairly sure I could not be doing anything further to screw up anybody's idea of co operating with a testing procedure. I gave it pretty much a good go begging over about a two + year period for somebody to take the neuro symptoms seriously AND my response to grain, and with positive brain scan in hand (oh, look, lesions! ) they're still insisting Nope, not that because I am not thin, not wasting away, don't have D, and apparently can't get the ol' blood to cough up anything exciting.

I think I went several years before I even TRIED to make something that was not made of nuts or rice for a wheat substitute, I didn't even do potatoes at first, meat, nuts, vegetables, fruit, and I remember being scared the first time I made a little quinoa thing, because of my starting to get rid of the brain fog and ataxia and I had NO desire to experience that again as self induced from messing up. It doesn't even bother me to see other people eating junk food, like it does a lot of others.

I realized that at some point I had to let the GP in on the secret (your patient is not eating what you think they are) in spite of the last blood test (blood tests... :blink: ha hah hah ! oh, sorry, wrong universe, this reincarnation ! ) and I told him hey, notice how all these symptoms have gotten better, and guess what just put down that I don't do wheat products anymore if I need a prescription or treatment because I haven't eaten it in 4 years since that (dumb doctor incident,) and I'm never touching it again. Really. Not A Fad. Totally. This was several years back and he humored me.

But a person who does not feel bad when they eat it, isn't officially diagnosed, and may not be highly motivated because I or somebody else hasn't done a good enough job letting them know what could happen if they really are gluten intolerant and/or celiac and don't stick to a diet for it, could have problems. You won't have an Expert Opinion To Cite. You may not have a laundry list of associated symptoms and conditions. It does require a fair amount of stubbornness as people will try to give you unsafe food and sometimes act oddly when you have to refuse them, you try to give them gluten-free food and they wrinkle their noses, or then you have problems with relatives and cross contamination, or they just get frustrated shopping.

And then with other family members, you must advocate for them. Kids are subject to peer pressure, which can be immense. Teachers may mean well but not quite get the whole cross contamination thing.

So, no, you don't really "need" the tests, but you may wish in retrospect that you had them after all, or maybe not, because not everybody leaps into these lifestyle changes in the same manner.

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. - MogwaiStripe posted a topic in Dermatitis Herpetiformis
      0

      Dermatitis Herpetiformis Cleared up With EpiPen, etc.

    2. - Dr. Gunn replied to MicG's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Test interpretations

    3. - trents replied to MicG's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Test interpretations

    4. - Dr. Gunn replied to MicG's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Test interpretations

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

    • Total Members
      133,664
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • MogwaiStripe
      I had to rush to the hospital last week due to anaphylactic shock from taking a dose of an antibiotic. Received EpiPen, steroids, antihistamines, zofran (all injected/IV). When I woke up the next day, ALL of the rashes I've had that started since going gluten free were cleared up. EVEN THE dermatitis herpetiformis was gone. Has anyone else experienced this or happen to know why that would happen? The meds they gave me were all meds that I've taken to try to resolve the rashes, but they never worked in pill form. I'm wondering if it the addition of the epi that helped, it if injected steroids and antihistamines were what did the job.
    • Dr. Gunn
      Exactly! Negative genetics can rule out celiac disease with close to 100% certainty. It takes tTg antibody testing and biopsy confirm the diagnosis in a genetically susceptible individual. 
    • trents
      What Dr. Gunn states is essentially true. It is a rule out measure. But be aware that to possess either of the two primary genes that have been identified with celiac disease (or both) doesn't necessarily mean that you have or will develop celiac disease. Almost 40% of the general population carries one or both but only about 1% of the general population will develop active celiac disease. It remains latent until triggered by some stress event which may or may not occur. So, there is a genetic component to celiac disease but there is also an epigenetic component. 
    • Dr. Gunn
      Have you had celiac genetic risk testing? A celiac genetic test is accurate with or without gluten in your diet. If you don't carry the celiac risk genes you can effectively rule out celiac disease for life. 
    • Scott Adams
      Based on those results alone, it’s not possible to say you have celiac disease. The test that is usually most specific for celiac, tTG-IgA, is negative in your results, and the endomysial antibody (EMA) is also negative, which generally argues against active celiac disease. However, your deamidated gliadin IgA is elevated, and your total IgA level is also high, which can sometimes affect how the other antibody tests behave. Another important factor is that you were reducing gluten before the test, which can lower antibody levels and make the results less reliable. Because of that, many doctors recommend a gluten challenge (eating gluten regularly for several weeks) before repeating blood tests or considering an endoscopy if symptoms and labs raise concern. It would be best to review these results with a gastroenterologist, who can interpret them in context and decide whether further testing is needed.
×
×
  • 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.