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

Celiac And Ee


stanleymonkey

Recommended Posts

stanleymonkey Explorer

We had an appointment with an ENT on Wednesday and may have found the best doc ever. Our 26 month old was sent to see this doc due to snoring, suspicions of apnea, and regression in eating. We were talking about her other health issues and mentioned she was gluten free because she had issues when she ate it such as constipation, rashes, screaming, and anemia. Told him our ped said to assume it was celiac, and he said if our ped ( who is also his kids ped!) said celiac it's celiac! Finally an official diagnosis for 1 of my little monkeys.

On the negative side he suspects EE, which I knew more about than the resident who was with him as our eldest was supposed to be scoped for it a 2 as well. We were just expecting to be told she need her tonsils and adenoids out. They also suspect central sleep apnea.

Anyone have a child diagnosed with EE this young?


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



Celiac.com Sponsor (A8-M):



momma bee Rookie

Our little one was so similar. She had ENT surgery at 15 months for sleep apnea, chronic sinus issues etc... When we saw our ent they got GI surgeon involved so they could scope during the surgery since he also suspected EE. In our case the scope result was negative for EE and positive for celiac. We are still unsure however if perhaps the EE triggers weren't there though as she is so much better with gluten free but still chokes frequently, gags and has some issues with eating. So there is still some suspicion of it I think?

The ENT here was pretty certain would be EE as he said "something" had to be making her adenoids and tonsils so huge... is that what your ent has said? Are you able to get scoping with the surgery? It was nice having all done at once.

mommida Enthusiast

My daughter diagnosed as "probable" Celiac when she was 16 months old and then EE when she was 6.  She was too ill to be scoped for the Gold standard Celiac diagnoses.

 

Keep a food journal and also take note of airborn allergens.  Living with EE for 4 years has proven a seasonal allergen connection.  (Not allergy testing)  If there is an EE diagnoses you should be reffered to an allergist.  Please keep in mind EE is an auto-immune issue and not a true allergy.  "Triggers" (food or airborn) cause the immune system to produce eosinophils that, once activated are active for 12 days.  An endoscopy with biopsies needs to be done.  ("normal" looking tissue also needs to be biopsied as the eosinophils can be embedded and not visible to the scope.)

stanleymonkey Explorer

Our ENT was really clued up about EE so hopefully he sends us to a gastro who is. The intern who did our initial consultation had never heard of it.

Her tonsils are normal size and the ENT said he won't remove her adenoids until he knows for sure it's obstructive apnea.

We already have an allergist, and she knows a lot about EE and she wanted our eldest scoped for it, do I know she'll push to get things done right.

We've already started a food diary. Seasonal a allergies being a trigger wouldn't surprise mits sneeze city between my eldest, their dad, and grandmother!

momma bee Rookie

Are they doing a full sleep study then for the apnea? For our daughter they also suspect some central sleep apnea but they felt adenoids still had some contribution so did remove adenoids and then will repeat the sleep study in may and if some apnea remains will start clap. As a mom don't like the delay in cpap! Don't like thinking of her jot getting enough oxygen regularly! But for us to be honest the adenoid removal doesn't seem to have had much effect to the naked eye on snoring or apnea as it still seems quite evident. So maybe a blessing to not have to do it yet. Especially if allergist is in tune! Hope you can sort some if it out quickly. It is tough waiting and coordinating these opinions etc...

stanleymonkey Explorer

They want to do a sleep study before even thinking of surgery thankfully. Our ENT is firm on sleep study before surgery. She's lost weight so the allergist will definitely push for an EE investigation. Today she ate scrambled eggs and yogurt, everything else she was given she chewed and spat out.

mommida Enthusiast

OK The chewing food and spitting it out can be a symptom of PICA.  (*Usually* the desire to eat non-food items caused by anemia.  This is the best scenario if she is just doing this with real food and not chewing drywall, dirt, and ??)  Get her iron levels checked.


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



Celiac.com Sponsor (A8-M):



stanleymonkey Explorer

She was aneamic but her last iron levels were really good. The things she spits out 6 months ago she used to eat. After she spits things out she starts crying that she's hungry. pICA was discussed but last time she even licked walls, ate her shoes, her sister, anything was food to her and she ate it! There main reason for questioning EE is regression, everything she used to eat she no longer does, she wants to but she won't/can't. Yogurt and eggs disappear quickly, she had 2 scrambled eggs for lunch yesterday and a yogurt at bedtime. She was offered gluten free pizza, but all she did was pick everything off and lick of the tomato sauce.

mommida Enthusiast

I wouldn't wait a day longer without working with a ped. gastro. and getting the endoscopy appointment.  (it can be a 3 month wait for finding a ped. gastro., but once your in the office the endoscopy gets scheduled right away.)

 

To answer another one of your questions, the tonsils are very enlarged for my daughter too.  It usually looks like she has strep throat.  Enlarged irritated tonsils (you can see blood vessels), creamy spots, and her breath smells like nasty pus.

 

I know you want to see her eat and you can't change her diet yet.  You can add chilled soothing things.  Slurpees and popscicles can help during the "worst time of day/evening".

 

The ped. gastro. does not consider the instant skin prick test for iron levels to be accurate at all.  At least you know about PICA.

stanleymonkey Explorer

We are in canada so everything is done through referrals, so they are pushing things through as fast as they can. We know who we want to see. My eldest saw a gastro so the sibling connection helps speed things up as well. Also thankfully for kids they do a vial blood test for iron. It's just a waiting game waiting for departments to sort out things.

momma bee Rookie

Yes, my daughter did the spitting the food out too!  Wow!  They have many similarities so I have been following your thread!  Are they treating her for reflux at all?  My daughter had done the spitting it out, got better temporarily with going gluten free but then it emerged again, we went back to our pediatrician who is thinking it is reflux so she doesn't want to swallow because it hurts so he is treating her for reflux and she has stopped spitting the food out and appetite has improved again.  They also had her on the same meds for this prior to scoping for EE as the GI specialist wanted to make sure what he was seeing wasn't "just" reflux and she needed to be on it for a while, so if she is not being treated for that it might be worth asking the pediatrician about.

 

Hopefully your referrals go through quickly, and the same for the sleep study- that can be slow to arrange.  We had had ours done prior to seeing ENT through a pulmonologist- are you seeing one?  If they are thinking central sleep apnea it also is likely a specialist you should get started on a referral for if not.  I am in Canada too and the wait time for that specialist can wait at times...  

stanleymonkey Explorer

We are in Vancouver bc children's does all the leg work, we are going to see a respirologist the ENT said it would be quick....hopefully

  • 1 month later...
momma bee Rookie

Was hopeful you have made progress in your referrals and testing!

stanleymonkey Explorer

Still waiting! And the last few days she has been pretty bad, of course probably because it's. Holiday weekend! They never get sick during normal office hours! She's had my mother in law freaked out a few times as she thought she was choking, guess a few phone calls are needed on Tuesday to chase up doctors.

momma bee Rookie

Aw that sucks! The wait is hard for all of these things! My daughter has been worse the last few weeks and the pulmonologist thinks perhaps is seasonal allergies with EE that just didn't show. And we just repeated her sleep study poat-op now so that was reminding me of you! I hope the referals speed up for you!!! And as you said, always gets worse on the weekends! And especially the long ones. Hope the referrals speed up, the waiting is the worst!

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. - Roses8721 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      gluten-free Oatmeal

    2. - Roses8721 replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      GI DX celiac despite neg serology and no biopsy

    3. - Scott Adams replied to Ginger38's topic in Related Issues & Disorders
      5

      Shingles - Could It Be Related to Gluten/ Celiac

    4. - Scott Adams replied to Xravith's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Challenges eating gluten before biopsy

    5. - Ginger38 replied to Ginger38's topic in Related Issues & Disorders
      5

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,472
    • Most Online (within 30 mins)
      7,748

    kygirlsusan
    Newest Member
    kygirlsusan
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Roses8721
      Had Quaker gluten-free oatmeal last night and my stomach is a mess today. NO flu but def stomach stuff. Anyone else?
    • Roses8721
      So you would be good with the diagnosis and not worry to check genetics etc etc? Appreciate your words!
    • Scott Adams
      As recommended by @Flash1970, you may want to get this: https://www.amazon.com/Curist-Lidocaine-Maximum-Strength-Topical/dp/B09DN7GR14/
    • Scott Adams
      For those who will likely remain gluten-free for life anyway due to well-known symptoms they have when eating gluten, my general advice is to ignore any doctors who push to go through a gluten challenge to get a formal diagnosis--and this is especially true for those who have severe symptoms when they eat gluten. It can take months, or even years to recover from such a challenge, so why do this if you already know that gluten is the culprit and you won't be eating it anyway?  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS--but those in this group will usually have negative tests, or at best, elevated antibodies that don't reach the level of official positive. Unfortunately test results for celiac disease are not always definitive, and many errors can be made when doing an endoscopy for celiac disease, and they can happen in many ways, for example not collecting the samples in the right areas, not collecting enough samples, or not interpreting the results properly and giving a Marsh score.  Many biopsy results can also be borderline, where there may be certain damage that could be associated with celiac disease, but it just doesn't quite reach the level necessary to make a formal diagnosis. The same is true for blood test results. Over the last 10 years or so a new "Weak Positive" range has been created by many labs for antibody results, which can simply lead to confusion (some doctors apparently believe that this means the patient can decide if they want more testing or to go gluten-free). There is no "Weak Negative" category, for example. Many patients are not told to eat gluten daily, lots of it, for the 6-8 week period leading up to their blood test, nor asked whether or not they've been eating gluten. Some patients even report to their doctors that they've been gluten-free for weeks or months before their blood tests, yet their doctors incorrectly say nothing to them about how this can affect their test, and create false negative results. Many people are not routinely given a total IGA blood test when doing a blood screening, which can lead to false negative interpretations if the patient has low IGA. We've seen on this forum many times that some doctors who are not fully up on how interpret the blood test results can tell patients that the don't need to follow a gluten-free diet or get more testing because only 1 of the 2 or 3 tests done in their panel is positive (wrong!), and the other 1 or 2 tests are negative.  Dermatologists often don't know how to do a proper skin biopsy for dermatitis herpetiformis, and when they do it wrongly their patient will continue to suffer with terrible DH itching, and all the risks associated with celiac disease. For many, the DH rash is the only presentation of celiac disease. These patients may end up on strong prescriptions for life to control their itching which also may have many negative side effects, for example Dapsone. Unfortunately many people will continue to suffer needlessly and eat gluten due to these errors in performing or interpreting celiac disease tests, but luckily some will find out about non-celiac gluten sensitivity on their own and go gluten-free and recover from their symptoms. Consider yourself lucky if you've figured out that gluten is the source of your health issues, and you've gone gluten-free, because many people will never figure this out.    
    • Ginger38
      It has been the most terrible illness ever! Going on 3 weeks now… I had chicken pox as a kid… crazy how much havoc this dormant virus has caused after being reactivated! No idea what even caused it to fire back up. I’m scared this pain and sensitivity is just never going to improve or go away 
×
×
  • 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.