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

Confused by the gluten challenge?


elliespal

Recommended Posts

elliespal Newbie

Hi all,

I received a positive blood test for coeliac around 3 weeks ago and am currently awaiting my endoscopy appointment. 

I've been trying to explain and emphasise the seriousness of coeliac and how important it will be for me to be completely gluten free after the endoscopy (assuming it is positive). One thing that keeps cropping up is the question of; if gluten is so damaging to a coeliac to the extent that upon going gluten free I would need to worry about cross contamination etc, why am I allowed to continue eating gluten for the gluten test, especially without any monitoring from my current doctor? I do understand that the gluten challenge is a necessity for the endoscopy to understand the amount of damage and to receive an accurate diagnosis, however I'm finding it difficult to emphasise how poisonous gluten is for my system when it doesn't matter how much I currently consume?

On the same note, can anyone offer advice on how best to explain coeliac disease to family and friends in a way that makes them realise that this is more than an intolerance or lifestyle choice?

Thankful for any guidance on this strange journey ahead!

 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

This is a backward disease to dia, you have to keep eating to to show the damage....the more damage to be seen the more "oh this is bad"....the whole challenge in my opinion is to make it look as bad as can be for a positive dia....yeah stupid I know.
Open Original Shared Link
Depends on how you want to explain it....I have youtube videos to explain the disease to kids ....You can can simply say gluten is like drinking bleach/eating rat poison for my intestines. Or the more normal approach "My body treats the protein which is smaller then a germ and harder to clean off the keeping a CSI tech from finding blood, like a germ. And in creating antibodies to attack it, it also attacks and damages my intestines, (some people like me it can attack their nervous system and brain, or in the skin with DH). So any tiny and your own immune system (IE this is a autoimmune disease) will turn on your own body. SO gluten is very much like a bioweapon/poison to you and needs to be kept away from anything you eat, touch, or could get into your food (airborne flour, shampoos, lotion, etc.) Perhaps have them read the newbie 101 sections?
https://www.celiac.com/forums/topic/91878-newbie-info-101/

OH they do know this is genetic and anyone of them could have...or develop it later in life. And left untreated the damage caused can lead to other diseases, cancer, lymphoma, allergies, food intolerance, and in some cases like me brain and nerve damage that leave you with life changing disabilities and quirks.
 

 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,904
    • Most Online (within 30 mins)
      7,748

    Lizsan
    Newest Member
    Lizsan
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Shining My Light
      @trents I’m pretty sure what I’m left with when separating celiac to other causes is my 10% being a virus. The one I had about 3 weeks before taking this TTG test. Everything I’ve read says type 1 diabetes, rheumatoid arthritis, hepatitis and some viruses are what could cause the elevation. The other blood tests I had I can compare things against.  I’m going to give your article a thorough read. My support in my circle is very small at the moment.  @knitty kitty I think before EGD I would like to do the DNA test. I’m going to start keeping a better journal also.  I’ve read a crazy amount of these “articles” - these two I’ve not seen. Some articles spell celiac differently. Thank you for sharing! I’m gonna dive into those.   I started seeing the functional medicine doctors from fluctuations in my hormones and major anxiety. Recently I realize it’s mostly health anxiety also so this is more challenging to depict real from imaginary thus all the research and the back and forth. I know anxiety to be a common symptom in perimenopause. I’ve fought it my whole life however. Likely due to lots of different trauma but seeing her was my last ditch effort to try something to avoid SSRIs, HRT, etc. She told me not to blame everything on my hormones when there could be an underlying problem, so she ran some tests to see if anything stood out. The TGG tests stood out.  I do find it very interesting now that I think about it that I don’t desire bread, pasta and pizza. Sometimes yes, but mostly no. I guess I didn’t give that much thought. Also didn’t realize that those foods do contain more gluten than the tortillas and cake/baked goods. About 3 months ago I started ordering meal kits to make dinner easier. I went back over the menus that I picked. I have probably had bread and pasta a hand full of times over the last couple months prior to having that blood test. We used to get pizza every Friday and stopped doing that also. I’m all fairness about 2 months leading up to these blood tests I had less gluten containing foods than I thought.    I’ve been praying for wisdom. Thankful to find some counsel from people who I believe have dove harder into this than most doctors have. Thanks for all the advice. It’s appreciated more than you know. 💕
    • Alibu
      @knitty kitty My whole family has migraines and I started getting them at age 19, so I'm not sure mine are related to gluten, although I do feel like obviously the more inflamed my whole system is, the more likely I am to suffer from more of these things.
    • knitty kitty
      @Alibu, Just wanted to add... Migraines can be caused by thiamine insufficiency.  I used to have them, regularly, but haven't since supplementing with thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) and Magnesium Threonate.  These forms get into the brain easily and really improve migraines.  I do still get Ophthalmic migraines which are triggered by computer screens.  It's permanent damage from nutritional deficiencies.  An Erythrocyte Transketolace test is a more accurate test for sufficient thiamine. Keep us posted on your progress!
    • Alibu
      @knitty kitty Thank you for those, I will definitely bring them up!  I did send a message to my doctor basically asking what they think so I'll go from there.  He may very well just decide that this was enough to diagnose celiac, but I have no clue what his thoughts are right now.  I also asked for a second opinion on the pathology.
    • knitty kitty
      @HilaryM, Are you eating a diet high in carbohydrates?  You might find a Paleo diet easier on your digestive system.  A Paleo diet can promote changes in  intestinal flora, effectively starving out SIBO bacteria.   Be wary of gluten free processed foods.  Many are not enriched or fortified with vitamins and minerals lost in processing like gluten containing foods are.  Talk to your doctor and nutritionist about supplementing with vitamins and minerals while healing.  Vitamins are organic compounds that the body cannot make and so must get from the diet.   Supplementing ensures our bodies get a fair chance to absorb the essential nutrients it needs.  
×
×
  • Create New...