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

Teenager Facing Celiac Panel After 5 Months gluten-free


Mattie's mom

Recommended Posts

Mattie's mom Newbie

Teenage son saw a gastroenterologist for the first time last week. AFter hearing our extensive family history of undiagnosed but likely celiac disease and my sons story, she offered to run a celiac panel after 2 weeks on a gluten diet. (Son was breastfed for 3+ years, a chubby healthy baby, then by 2nd grade was tall and very thin. Gained weight on a Gluten-free Casein-free diet, but then "cheated" his way back to a still-tall but skeletal build. Last year in middle school, he developed terrible constipation with belly pain and headaches and missed lots of school. After that he agreed to be gluten free again, and has felt better since.) So now after about 5 months gluten free, we finally get an appointment with a GI doc, and are trying to survive 2 weeks of a gluten diet. Headaches are back, with terrible irritability. Are we all suffering for nothing to get bloodwork done on only 2 weeks of gluten? Second question: Is anyone familiar with Great Plains Laboratory's testing? Thank you.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

After being gluten-free for five months, it is extremely unlikely that your son's tests will be positive. Five months should have been enough time for a kid to heal, and two weeks back on gluten will not be enough to destroy his villi again, and give him positive test results.

I am afraid he is suffering for nothing, and that GI is clueless about celiac disease. Even if he would go back on gluten for three months, he might not get accurate results, two weeks are way too short.

You know that gluten makes him sick, and he knows it as well. He should have had the testing done before going back on the gluten-free diet, it is too late now. The only test that will still be accurate is testing from Enterolab, as it will give accurate results up to a year after going on the gluten-free diet.

He might as well not make himself sicker and get back on the diet. I wished there weren't so many ignorant doctors out there who think they understand about celiac disease, when they haven't got a clue.

nannyb Rookie

I say you have your diagnosis. If going back on gluten makes him ill he is at least gluten intolerant. Personally I have no faith in the blood tests since I know so many people with false negative results. Doctors who must have an official diagnosis are idiots. I know, my GI told me to continue eating gluten and when my endoscopy showed damage then I should go off gluten for good. Hello.

Even if your son's test results are negative what will you do. If the answer is stay off the gluten then don't go through the pain. You know, he knows whether your doctor accepts it or not is their problem.

A gluten free diet is not like taking pills if someone doesn't need it it won't hurt them. We all know our bodies better than any doctor (and our children's as well)

I have two teenagers (oops one turned twenty) who had negative blood tests but maintain gluten free because they know they need it. There choice not mine. Maybe you should let your son decide.

ravenwoodglass Mentor

You son has had a positive dietary response and became ill after adding gluten back in. That IS diagnostic. The best diagnosis there is. As many as 30% of us in even in the end stages of the disease will show negative on testing. My repeated negative blood tests lead me into a celiac world that is not fully recoverable from. My doctors never told me what they were testing for, in other words I was never given the chance to even try the diet as no doctor ever even told me what celiac sprue was. I was so ill by the time I was diagnosed that one of my children told me the family would understand if I committed suicide. That child was 15 at the time.

2 weeks on gluten will most likely show a false negative because after being gluten free the antibodies we form may not have built up enough to show on the blood test. The gluten challenge has already given you the answer. Do make sure you tell the doctor all effects of the gluten challenge. Also many GI don't know that celiac is anything other than a gut disorder. Mine had no idea that it could cause the neuro problems that I have. He was also clueless that arthrits can be another 'side effect' of gluten.

You may want to consider Enterolab. They do fecal antibody testing that can be much more sensitive than blood testing.

I hope your son is back to the gluten free diet soon and feeling better.

  • 5 weeks later...
Mattie's mom Newbie

We went ahead with the two-week challenge, which was waste of time, because the results (I requested copies) are negative. So we see the pediatric GI doc tomorrow, and we'll see what she says. My son is still eating gluten and is at the five-week mark now.

The first week he complained of headaches, took a lot of Tylenol and missed a day of school. He soon became his old gassy, gassy and cranky self. But by the end of the first week the pain had subsided. And what was really weird was that his chronic dandruff disappeared. Hmmmm. Constipation continued, as always. So we'll see what the doc says tomorrow. In spite of the "two weeks is enough time" bit, I like her. She listened to everything I said about our family history -- including my mother's two miscarries and four preterm births and my partial placental eruption with this son and my seizure disorder and chronic gassiness, both of which are gone since I've been gluten free for several months myself, and, and, and --- and dictated every bit of it in her clinic note (have a copy of that too).

Do you think it's worth it, since we're at the five-week mark of the gluten challenge, to request another celiac panel? Or see if they'll allow HLA testing?

Anyway, THANK YOU, all for your replies. I have learned so much from this forum.

And, Ravenwoodglass, your comment about your teenager saying the family would understand if you committed suicide really touched a chord: My dear mother did commit suicide after decades of what I velieve to be undiagnosed celiac, with attendant osteoporosis, arthritis, asthma, neuralgia, depression -- I know I'm leaving something out, but you get the picture.

Anyway, thanks again, so much.

Ursa Major Collaborator

Unfortunately, it could take three to six months, maybe even a year for your son's villi to be in such bad shape again that the blood tests will be positive. Do you really want him to keep eating gluten that long? He could have irreparable damage by then, or develop diabetes or other autoimmune diseases. Once you have those, you have them for life.

Mattie's mom Newbie

Diabetes and systemic lupus - those are a couple more of my mom's issues, and the diabetes surfaced in her 70's.

I understand what you're saying, but the down side of going through with the two-week gluten challenge is that now my son says: "I'm fine, Mom. Look, I'm gaining weight. I don't want to go off gluten again." The good news is our gastroenterologist said we could run the panel again - yes, in about a year - and if his sister is diagnosed with celiac earlier that she will order HLA testing right away. Sister's serology came back at way, way high.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

Can you afford Enterolab testing? It is still accurate up to a year after going gluten-free. It convinced my youngest daughter to finally go gluten-free (she is 16).

nora-n Rookie

Here it says six weeks to six years:

Open Original Shared Link

and they only looked at vitous atrophy.

And, we know that in about 20% of villous atrophy the blood tests will be negative.

In patchy celiac, the blood tests will be even less postitive than in total atrophy.

Many will only have the patchy variant.

And , I read in the british meddical journal that in 30% of celiacs they are over-weight, literally obese, especially if the celiac only is patchy. teh body seems to over-compensate in patchy celiac and grab as much as possible out of the food and you get fat, even though you are malnourished....different things are absorbed by differnt parts of the small intestines, and you are dficient in those things even though you put on weight.

Thie diagnosis of celiac is almost medieval, by some blood tests which may be positive or not, and random biopsies that are done just at the beginningof the small intestine and are hit and miss.

nora

Mattie's mom Newbie

Thank you, Nora, for posting the link to that pubmed article.

I'm educating my son about the potential of developing diabetes, etc., in the future. He's listening. Still he chooses for now to wait on his older sister's biopsy results, assuming her new GI doc orders a biopsy. Also appealed to his teenage vanity: "You'll probably gain some weight and be able to build some muscle mass finally, when you're ready to go gluten free again." That was effective. ;)

Will keep you posted.

  • 1 month later...
Mattie's mom Newbie

We decided against the Enterolab testing. But everyone -- five people in two separate households -- is off gluten anyway.

Though son's 2nd celiac panel, after 8 weeks on gluten, also came back negative, his older sister's celiac is now biopsy-confirmed. Both are committed to staying gluten free and are helping each other navigate the diet.

THANK YOU all for your guidance and support!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Ibuprofen

    2. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      My only proof

    3. - Scott Adams replied to wellthatsfun's topic in Coping with Celiac Disease
      1

      still struggling with cravings

    4. - Scott Adams replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Oh my goodness medication causing pain !!!!

    5. - Scott Adams replied to Me,Sue's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Knowing what to do when feeling unwell.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,871
    • Most Online (within 30 mins)
      7,748

    GR82BNTX
    Newest Member
    GR82BNTX
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      Hi Colleen Are you supplementing B12/having injections? I have learned recently that sometimes when you start addressing a B12 deficiency, it can temporarily make your symptoms worse.  But it is important not to stop the treatment.  Regarding your problems with anxiety, again that is another symptom of a B12 deficiency.   I didn't know what anxiety was until it hit me like a train several months before gastrointestinal issues began, so I can certainly relate.   Two books which helped me hugely were At Last A Life by Paul David (there is a website you can look up) and The Depression Cure: The Six-Step Programme to Beat Depression Without Drugs by Dr Steve Llardi.  Although his book is aimed at people who have depression, following the principals he sets out was so helpful in lessening my anxiety.  Llardi suggests we need to focus on getting enough: - physical exercise - omega-3 fatty acids - natural sunlight exposure - restorative sleep - social connectedness - meaningful, engaging activity   ... and we should feel a lot better. That is not to stay you must stop taking medication for depression or anxiety if you have been prescribed it, but adopting the changes Dr Llardi sets out in the book should really help. Can I just ask two more questions:  1) you say that you are B12 deficient, did they test your iron levels too?  If not, you really ought to be checked for deficiency and, 2) did they check your thyroid function, as an overactive thyroid can be cause rapid heartbeat and a lot of coeliacs have thyroid issues? Cristiana        
    • Jmartes71
      Hello still dancing around my celiac disease and not getting medically backed up considering Ive been glutenfree since 1994.All my ailments are the core issue of my ghost disease aka celiac disease. Im angery because the "celiac specialist " basically lightly dismissed me.Im extremely angery and fighting for a new primary care physician which is hard to do in Northern Cali.So currently without and looking.Im angery that its lightly taken when its extremely serious to the one who has it.My only evidence is a brochure back in the days when I got news letters when I lived at my parents.It was published in 1998.I was diagnosed before any foods eliminated from my diet. Angery doctors don't take seriously when Im clearly speaking.I did write to the medicine of congress and have case number.
    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
×
×
  • 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.