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

5.5 Months gluten-free And Starting To See Issues Again


ryo

Recommended Posts

ryo Apprentice

hi,

my daughter was diagnosed with celiac in august.  our home is 99% gluten-free (my husband still keeps some beer in the house) and for the first 5 months she did great.  we had a few miss-steps where she was glutened and we were always able to pin point what had happened (eating out once, and another time i bought the wrong bread and gave it to her, not my best moment!).

 

for the last few weeks she has been showing symptoms again.  she is not eating, super moody/emotional, red rings around her eyes, always sleepy.  the symptoms are not as strong as they were before she was gluten-free or the same as the two times that we know she got glutened. i can not figure out anything that is causing the issues and honestly i don't know if i am just going crazy ;)  we are set to go back for her 6 month check-up towards the end of feb. and i am wondering if i should try to have her seen sooner.

 

my question for all of you is...

did you ever see the issues return and not be able to pin point the issue?

do you think maybe she is having reactions to another food?

 

thank you for any insight you may have!


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



Celiac.com Sponsor (A8-M):



frieze Community Regular

how old is this child? remember, not everything is gluten related.

ryo Apprentice

she is 5 years old and we have been trying to figure out if it is something else going on with her.  it is the level of being worn out connected with the not eating that really has me worried.  it could just be a normal development stage and it has gotten so hard for us to separate the two issues.  

StephanieL Enthusiast

Any possibility it may be art supplies or something else in school if she's in school?

Sorry you're dealing with this.

GretaJane Newbie

Playdoh?

Could it be medicines, vitamins or supplements? They can contain gluten as a filler.

Could she be anemic?

Maybe try going grain free for a whileto see if that helps. Most grains that are naturally gluten-free often contain cc gluten that can affect people.

A naturopath could help get a blood test to look for food intolerances.

Good luck!

StephanieL Enthusiast

Maybe try going grain free for a whileto see if that helps. Most grains that are naturally gluten-free often contain cc gluten that can affect people.

A naturopath could help get a blood test to look for food intolerances.

 

Can you site your source of your statement "naturally gluten free are often CC'ed"?  I've been reading and dealing with this for my child for  4+ years now and haven't found this to be so. Oats are often an issue but things like rice and other grains are most often fine.

snowmom Rookie

I feel for you! It's so hard to see your kid with no energy and no appetite. Have you called the pediatrician or GI? I'm so very new to celiac that I really don't know how long it takes to clear gluten, but after 6 months, maybe  you are right that it is worth investigating other food issues, other autoimmune issues that run with celiac, and other totally unrelated medical issues (even while you continue to ferret out possible cc as mentioned above). Or, like you said, it could just be a developmental phase.

 

I'm such a celiac newbie that I don't have useful advice to offer, but it seems like it is worth running your concerns past a doctor. I think your instincts about bumping up the late February appointment are sound.


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



Celiac.com Sponsor (A8-M):



greenbeanie Enthusiast

I would also try to bump up the appointment. If they're booked solid, maybe they could at least give you the lab slip to get the follow-up bloodwork done sooner, which might help sort out whether it's a cc issue or something else. They could call with the results even if you can't get in to see the doctor until late February. If this is the first bloodwork since diagnosis they'd need to run more than just the tTG, though, since you'd probably only have one previous test to compare it to. (I discovered this the hard way - my daughter's GI only orders tTG for follow-up, but not the DGP tests, which may have helped us distinguish between ongoing gluten exposure and just taking more than six months to decrease to a normal tTG level.)

My daughter was diagnosed 7 months ago, and I've also noticed a return of some of her symptoms lately, for no apparent reason. I can't be sure whether there's a real difference or I'm just imagining it. I'm hoping it's something simple, like perhaps low vitamin D, since we've been forced indoors by extreme cold for most of the last three weeks! (She was low on D at diagnosis despite lots of time outdoors, so even with supplements now it may still be low - doctors haven't retested it yet.) I hope your daughter feels better soon.

bartfull Rising Star

Have you tried eliminating dairy? That would be the first place to start.

ryo Apprentice

thank you all for your thoughts.  i did call her GI doctor a few days ago.  today we had all of her blood work done and are now waiting results.  over the past 6 months she has gained 1 pound and grown 1 inch.  based on the growth chart she has actually fallen further off her curve.  i know i need to keep this all in perspective but with the way she feels right now it was a hard fact to hear.

 

we have gone through everything in our kitchen and evaluated all sources of contamination.  right now the only thing we can really see as any option is her vitamins. please know i am not saying this is the cause of her getting gluten it just the only place we can really see room for error.  the brand she takes recently changed labels.  with this label change they removed "gluten free". i called the company when the change happened and they assured me they were still gluten free and it was just a design change.  i bought it at the time (about three weeks ago). but the last few days i went back to them and did some more research.  it turns out it was a change to how they are made but they still insist they are gluten free.  what doesn't sit well with us is why in the world would you remove gluten free from a kids vitamin based on design.  it seems fishy and that is enough of a reason for us to stop using them.  again i am not saying with any proof that this is the cause but it's all i can really try eliminating right now.

 

today we tested for food allergies, vit. d, iron levels, along with the other test she already had planned for next month.  now we wait and do our very best to get her back on track.

 

thank you again for all your thoughts!  very, very helpful. 

StephanieL Enthusiast

Many companies are taking the "gluten free" label off things because of the new government standard they are implementing. Companies aren't suppose to make the claim if they can't back it up even if there are no gluten ingredients in it. It may be worth getting test strips to see about the Vits. but they are very pricy.  That is how we found out a brand of mustard was an issue for us.

 

Have you seen an endocrinologist?  Tested for thyroid issues and nutritional levels and vits? I think I would start there. Between the way she's feeling and the growth issues that would be where I would start really.  DS is still very small but he did sprout a bit after we figured out he had a thyroid issue after his Celiac tests were coming back all over the place.  

Allergy testing is HIGHLY inaccurate.  Nothing you have said yells allergy to me so I'm not sure why that is even being tested for.  I would be highly suspicious of any allergy testing baed on what you have said.  

ryo Apprentice

the test strips are a great idea!  at this point i would love to have the help identifying if we have a gluten issue.

 

we are working closely with an endocrinologist.  when this all started she also had a low hormone level that was cause for further investigation.  at the same time her thyroid was tested and it appears to be in good shape.  i asked about retesting this time and we decided to wait to look into that at this point.  what i am having a hard time accepting is that she was doing so great for 5 months then all of the sudden it went down hill again (and quickly).  her growth has been very slow so that could be enough of an indication that something over then celiac is going on.  at this point so hard to know!  really looking forward to the blood test coming back next week so we can start to sort through the info.

 

yes, allergy testing is a crazy road to go down.  my doctor spent a bunch of time talking about how inaccurate the testing can be and how you really have to dig much deeper to evaluate if you are having a food allergy.  i guess it is like all the rest of this… testing, playing with food, waiting ;)  i am hoping it is not a another food allergy but we need to keep our eyes open for all possibilities. 

ryo Apprentice

i am thrilled about this...

 

"Many companies are taking the "gluten free" label off things because of the new government standard they are implementing. Companies aren't suppose to make the claim if they can't back it up even if there are no gluten ingredients in it."

 

if they can't back it up i don't want to feed it to my daughter! i know it will make it harder for companies to offer us gluten-free options but at least we will be able to trust the label more.

  • 2 weeks later...
Heather-707 Newbie

I second the oat comment.   10% of Celiacs can't handle oats, my LO included.   The reaction certainly isn't as obvious, but is definitely a problem. 

w8in4dave Community Regular

I just hate it when kids have to go thru stuff! I hope you find the problem. Hopefully you find it soon.

GFinDC Veteran

Hi Ryo,

 

Have you made a list of anything that may have changed in her diet since before the problems started?  I imagine you have done that, but it is easy to miss something in my experience.  So another review might be helpful.  The most likely source of a gluten ingredient slipping in is in processed foods or products like vitamins, meds, drinks.  Those are the first things to look at as the potential source.

mommida Enthusiast

YES We had improvement on a gluten free diet and then had "gluten symptoms" flare up again.

 

My daughter was diagnosed with Celiac when she was 15 months old.  Things went great on a gluten free diet until 5 1/2 years old she was diagnosed with Eosinophilic Esophagitis when she turned 6.  There is now a known link between Celiac and EE.  (an important note about EE and testing for EE ~ 1. the doctor must order the pathologist to test the sample for eosinophils.(red dye and counts) 2. Once the immune system activates eosinophils, they can keep harming healthy tissue for 12 days. 3. There is strong evidence that proves seasonal airborne allergens "trigger" eosinophil production ((this is important to remember for scoping for the eosinophil damage.  My daughter has been scoped in December~ the damage was there from late summer early fall allergens.  She was scoped in January ~ no damage present or eosinophils present.  She was on an elimination diet that removed all top 8 allergens and peas; and the deep freeze and deep snow covered any ragweed or plant pollens.  YOU MAY NOT GET A PROPER DIAGNOSES DEPENDING ON THE SEASON.

 

When we brought her back in for testing there is a list of disorders/diseases that present with "celiac like" symptoms that can be ruled in or out with an endoscopy with biopsy.  So you might have to consider having another scope done.

such as...

H. Ployri

parasites

congenital defect

eosinophilic disorders (eosinophil damage can be in any part of gastro tract)

Celiac disease that does get better on a gluten free diet/ Celiac sprue

another food intolerance

even the belly distention can be hiding a hernia

the list goes on and on......

 

Keep a journal of diet, activities, symptoms until your appointment.  It will help track down other food intolerances and help you become more knowledgable should you have to avoid any other foods.

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. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Son's legs shaking

    2. - Scott Adams replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Bob red mill gluten free oats

    3. - knitty kitty replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    4. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    5. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

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

    • Total Members
      132,868
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      @lizzie42, You're being a good mom, seeking answers for your son.  Cheers! Subclinical thiamine deficiency commonly occurs with anemia.  An outright Thiamine deficiency can be precipitated by the consumption of a high carbohydrate meal.   Symptoms of Thiamine deficiency include feeling shakey or wobbly in the legs, muscle weakness or cramps, as well as aggression and irritability, confusion, mood swings and behavior changes.  Thiamine is essential to the production of neurotransmitters like serotonin and dopamine which keep us calm and rational.   @Jsingh, histamine intolerance is also a symptom of Thiamine deficiency.  Thiamine is needed to prevent mast cells from releasing histamine at the slightest provocation as is seen in histamine intolerance.  Thiamine and the other B vitamins and Vitamin C are needed to clear histamine from the body.  Without sufficient thiamine and other B vitamins to clear it, the histamine builds up.  High histamine levels can change behavior, too.  High histamine levels are found in the brains of patients with schizophrenia.  Thiamine deficiency can also cause extreme hunger or conversely anorexia.   High carbohydrate meals can precipitate thiamine deficiency because additional thiamine is required to process carbohydrates for the body to use as fuel.  The more carbohydrates one eats daily, the more one needs additional thiamine above the RDA.  Thiamine is water soluble, safe and nontoxic even in high doses. Keep in mind that gluten-free processed foods like cookies and such are not required to be fortified and enriched with vitamins and minerals like their gluten containing counterparts are.  Limit processed gluten-free foods.  They are often full of empty calories and unhealthy saturated fats and additives, and are high in histamine or histamine release triggers.  It's time you bought your own vitamins to supplement what is not being absorbed due to malabsorption of Celiac disease.  Benfotiamine is a form of Thiamine that has been shown to improve intestinal health as well as brain function. Do talk to your doctors and dieticians about supplementing with the essential vitamins and minerals while your children are growing up gluten free.  Serve nutritionally dense foods.  Meats and liver are great sources of B vitamins and minerals. Hope this helps!  Keep us posted on your progress!
    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
      @SamAlvi, It's common with anemia to have a lower tTg IgA antibodies than DGP IgG ones, but your high DGP IgG scores still point to Celiac disease.   Since a gluten challenge would pose further health damage, you may want to ask for a DNA test to see if you have any of the commonly known genes for Celiac disease.  Though having the genes for Celiac is not diagnostic in and of itself, taken with the antibody tests, the anemia and your reaction to gluten, it may be a confirmation you have Celiac disease.   Do discuss Gastrointestinal Beriberi with your doctors.  In Celiac disease, Gastrointestinal Beriberi is frequently overlooked by doctors.  The digestive system can be affected by localized Thiamine deficiency which causes symptoms consistent with yours.  Correction of nutritional deficiencies quickly is beneficial.  Benfotiamine, a form of thiamine, helps improve intestinal health.  All eight B vitamins, including Thiamine (Benfotiamine), should be supplemented because they all work together.   The B vitamins are needed in addition to iron to correct anemia.   Hope this helps!  Keep us posted on your progress!
    • trents
      Currently, there are no tests for NCGS. Celiac disease must first be ruled out and we do have testing for celiac disease. There are two primary test modalities for diagnosing celiac disease. One involves checking for antibodies in the blood. For the person with celiac disease, when gluten is ingested, it produces an autoimmune response in the lining of the small bowel which generates specific kinds of antibodies. Some people are IGA deficient and such that the IGA antibody tests done for celiac disease will have skewed results and cannot be trusted. In that case, there are IGG tests that can be ordered though, they aren't quite as specific for celiac disease as the IGA tests. But the possibility of IGA deficiency is why a "total IGA" test should always be ordered along with the TTG-IGA. The other modality is an endoscopy (scoping of the upper GI track) with a biopsy of the small bowel lining. The aforementioned autoimmune response produces inflammation in the small bowel lining which, over time, damages the structure of the lining. The biopsy is sent to a lab and microscopically analyzed for signs of this damage. If the damage is severe enough, it can often be spotted during the scoping itself. The endoscopy/biopsy is used as confirmation when the antibody results are positive, since there is a small chance that elevated antibody test scores can be caused by things other than celiac disease, particularly when the antibody test numbers are not particularly high. If the antibody test numbers are 10x normal or higher, physicians will sometimes declare an official diagnosis of celiac disease without an endoscopy/biopsy, particularly in the U.K. Some practitioners use stool tests to detect celiac disease but this modality is not widely recognized in the medical community as valid. Both celiac testing modalities outlined above require that you have been consuming generous amounts of gluten for weeks/months ahead of time. Many people make the mistake of experimenting with the gluten free diet or even reducing their gluten intake prior to testing. By doing so, they invalidate the testing because antibodies stop being produced, disappear from the blood and the lining of the small bowel begins to heal. So, then they are stuck in no man's land, wondering if they have celiac disease or NCGS. To resume gluten consumption, i.e., to undertake a "gluten challenge" is out of the question because their reaction to gluten is so strong that it would endanger their health. The lining of the small bowel is the place where all of the nutrition in the food we consume is absorbed. This lining is made up of billions of microscopically tiny fingerlike projections that create a tremendous nutrient absorption surface area. The inflammation caused by celiac disease wears down these fingers and greatly reduces the surface area needed for nutrient absorption. Thus, people with celiac disease often develop iron deficiency anemia and a host of other vitamin and mineral deficiencies. It is likely that many more people who have issues with gluten suffer from NCGS than from celiac disease. We actually know much more about the mechanism of celiac disease than we do about NCGS but some experts believe NCGS can transition into celiac disease.
    • SamAlvi
      Thank you for the clarification and for taking the time to explain the terminology so clearly. I really appreciate your insight, especially the distinction between celiac disease and NCGS and how anemia can point more toward celiac. This was very helpful for me.
×
×
  • 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.