Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Brain-fog


Jayne2222

Recommended Posts

Jayne2222 Newbie

I was diagnosed with asymptomatic Celiac in the last couple months.  Being that it can be hereditary I had my three kids tested as well.

However, long before I was diagnosed I suspected my daughter might have Celiac b/c of skin issues she'd had her whole life.  Once I was diagnosed I did some reading and came across the symptom of brain fog and that sort of thing.  Immediately I thought of my oldest.  In some instances he has great concentration and other days it's like pulling teeth to have a normal conversation with him, b/c he can't verbilize what he's trying to communicate.  Almost like the words have just escaped his head (he's 13 so it's not like a toddler not knowing the words for things).

I got a call the other day to go in and review the Celiac panel with the dr. For my oldest AKA he's tested positive. (Of course they didn't have the results of the other two kids yet.)

My question is, has anyone experienced the brain fog thing with their children while in school.  I suspect that this has hampered his performance in school for some time. Smart kid, just not stellar report cards.  Which I assumed was lack of effort.  What if the lack of effort was really brain fog making it difficult to get things done, resulting in him giving up.

Has anyone experienced something similar with their kids.  How does one sort things out with school, in terms of support and understanding for at least the time being (until his gut has healed and get the gluten out of his system).


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Brain fog is real for those with celiac disease or even Non-celiac Gluten Intolerance.  He may also have another condition which can impact his learning.  If negative for celiac disease, consider getting him evaluated by the school psychologist.  The school should (and is required by law) to help develop a plan for him.   In the US, celiacs can file a 504 plan (American Disabilities Act).  Learn more here:

Open Original Shared Link

If the celiac tests are negative, make sure the complete celiac panel is given to completely rule out celiac disease.    Not all celiacs (like me) test positive to the standard screening TTG test.  Remember, celiac disease can develop at any time.  I test my kid every few years, even if symptom free.  

Keep researching celiac disease.  Being well informed is a great defense!  Take care and ask as many questions as you like.  We are here to help.  

Jayne2222 Newbie

Thanks @cyclinglady ?

They did run a full Celiac panel and I'll get to see the results in a couple weeks.

I think the difficult or complicated part is that he does ok in school.  By no means is he failing.  And does very well in Math and some other subjects.  So it may not be as apparent that this may be affecting him.

What I think may complicate matters is that he has days where things seems fine and other days where things just don't seem to click.

I'll check out that link and see what kind of help that is.  Although we are not in the US so it won't be totally applicable.

cyclinglady Grand Master

My brother was very smart.  Did not apply himself at school.  His verbal conversation responses were, "Yeah, Uh Ha, Nah, and Maybe".  It drove my mother nuts.   She thought he would be a bum.  He did not finish college and my Mom evicted him (family rule was to go to University or get out and earn a living).  He got a job and became computer savvy.  He has been married for over 25 years, has kids, and is a VP at Fortune 100 company.

Thirteen is a tough age.  You just never know how they will turn out!  ?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,175
    • Most Online (within 30 mins)
      7,748

    Chels22
    Newest Member
    Chels22
    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

    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
×
×
  • Create New...