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

Layman's Definition Of Celiac


Beth in NC

Recommended Posts

Beth in NC Contributor

I remember seeing somewhere on the board in the last few weeks where someone described what happens with Celiac in layman's terms. There were a few technical words, as you can't get away from it, but can anyone help me out? I can find tons of stuff on the small intesting damage, but my son isn't getting why this attacks other areas of the body and most "definitions" of celiac stick to the intestional issues. He's trying to explain it to the few friends he's willing to tell and he's getting most of his info from me, as he's in college and really too busy to spend the time I have spent researching this.

anyone?


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



Celiac.com Sponsor (A8-M):



elonwy Enthusiast

I describe it this way: When I eat gluten, my body identifies it as a poison which triggers an auto immune response. This creates antibodies that then attack my body, causing x symptoms. This also damages my villi, which then keeps me from absorbing vitamins and stuff, and causes secondary complications.

I use that or a variation thereof as a laymans cliffnotes. Not sure what the other one you saw was, but that's mine:P

Random funny story: I'm meeting a bunch of my bf's friends, and we go out to eat. He and I are discussing the menu, and he leans over to explain "she can't eat gluten". His friend pipes up "Oh are you a Celiac?" Turns out he's a biochemist at Stanford working with the Celiac Group. Sadly, they've lost their funding, but it was still cool to natter on about this stuff with someone who's been working on it.

ShayFL Enthusiast

He could just say. I have Celiac. It is kind of like an allergy. I cannot eat wheat, barley or rye and most oats. If I do, my whole body can be affected and I get sick. And even if I dont feel sick, my body can be damaged.

Beth in NC Contributor
He could just say. I have Celiac. It is kind of like an allergy. I cannot eat wheat, barley or rye and most oats. If I do, my whole body can be affected and I get sick. And even if I dont feel sick, my body can be damaged.

I think this is fine for him to say to others, but HE is still trying to understand it completely. He was in Alaska when I was doing all my initial research so he didn't learn any of that initial stuff. Me telling him what would happen to the rest of his body was part of what convinced him he needed to tackle this. He was ready to just ignore it.

Fiddle-Faddle Community Regular
I describe it this way: When I eat gluten, my body identifies it as a poison which triggers an auto immune response. This creates antibodies that then attack my body, causing x symptoms. This also damages my villi, which then keeps me from absorbing vitamins and stuff, and causes secondary complications.

Ooh, that's REALLY good. That's the best description I've seen yet!

Mango04 Enthusiast

The gluten protein causes the immune system to attack and destroy the intestines (or just "organs" would be fine).

I don't explain it to my friends though. Most of them just know I have some sort of mysterious and severe adverse reaction to certain common foods.

jerseyangel Proficient
The gluten protein causes the immune system to attack and destroy the intestines (or just "organs" would be fine).

This is pretty much what I say....it's short and to the point :)


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



Celiac.com Sponsor (A8-M):



Beth in NC Contributor

OK, for my OWN benefit....I used to be a nurse, so this stuff is important to me!! LOL! Doesn't something happen in the small intestine that allows the gluten to enter the bloodstream? So where ever that blood carries it, which is everywhere, the immune system will be attacking it right along, right?

elonwy Enthusiast

You're talking about Leaky Gut. Check out this web site. Its a lot of reading, but its well laid out.

Open Original Shared Link

jerseyangel Proficient
OK, for my OWN benefit....I used to be a nurse, so this stuff is important to me!! LOL! Doesn't something happen in the small intestine that allows the gluten to enter the bloodstream? So where ever that blood carries it, which is everywhere, the immune system will be attacking it right along, right?

You may be thinking of leaky gut, where the intestine--damaged from Celiac or something else--allows particles of undigested food out into the bloodstream where it is then attacked as an invader injuring other organs/systems in the body.

In Celiac, the autoimmune reaction happens in the small intestine. The damage done to other systems in the body by Celiac are generally secondary (vitamin deficiency, inflammation, autoimmune reaction, etc). For instance, I was glutened recently--repeatedly for a couple months-- from eating a product that used to be safe. (My own fault) It caused my liver enzymes to elevate--I had a workup (blood, ultrasound, endoscopy) and nothing else turned up to explain why they went up the way they did.

The latest round of bloodwork--after all this--revealed that they had all returned to normal :blink:

Celiac can affect us in lots of different ways.....

2kids4me Contributor

The way I told my kids is: the gut is inflammed and damaged. The good nutrients are not absorbed very well so the stuff your body needs to function well - just passes on through. Then because the lining is worn away from inflammation (I liken it to a skinned knee)...so bad stuff - bacteria, and proteins that normally shouldnt get past the "barrier" of normal tissue get into the body. Yes it does trigger an autoimmune response which is systemic, in addition - all this other stuff is going to the brain, nerves, muscles etc..which leads to a cellular response in various organs and this is why the symptoms are so varied among celiacs. My daughter had neurologic symptoms and my son had muscle aches and pains as well as bed wetting.

Back to the skinned knee - I use this analogy because they can visualize the scrape - they see it can get infected...and how the healthy intact skin is not red and oozing. Basically the difference between a heathy gut and a damaged one. Very simple and it gets the point across without a bunch of medical terminology.

So I told them, by eating gluten free the gut can heal and function as a normal barrier to bad stuff - just like normal skin does on the outside of our body.

Hope this helps.

Sandy

nora-n Rookie

When eating gluten, all people make zonulin, but celiacs make more and the effects last longer. so, noone really should have gluten. Zonulin opens the blood-gut barrier, and the blood-brain barrier at the same time.

Just type in zonulin in www.pubmed.com , and google it.

nora

Beth in NC Contributor

Open Original Shared Link

Really informative. That is what I was trying to figure out. So many Celiacs don't just have symptoms that are related to nutrient deficiencies, but things that go further than that...Hashimoto's, for example.

thanks everybody!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,137
    • Most Online (within 30 mins)
      7,748

    Jamy
    Newest Member
    Jamy
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Sarah Grace
      Dear Kitty Since March I have been following your recommendations regarding vitamins to assist with various issues that I have been experiencing.  To recap, I am aged 68 and was late diagnosed with Celiac about 12 years ago.  I had been experiencing terrible early morning headaches which I had self diagnosed as hypoglycaemia.  I also mentioned that I had issues with insomnia, vertigo and brain fog.   It's now one year since I started on the Benfotiamine 600 mg/day.  I am still experiencing the hypoglycaemia and it's not really possible to say for sure whether the Benfotiamine is helpful.  In March this year, I added B-Complex Thiamine Hydrochloride and Magnesium L-Threonate on a daily basis, and I am now confident to report that the insomnia and vertigo and brain fog have all improved!!  So, very many thanks for your very helpful advice. I am now less confident that the early morning headaches are caused by hypoglycaemia, as even foods with a zero a GI rating (cheese, nuts, etc) can cause really server headaches, which sometimes require migraine medication in order to get rid off.  If you are able to suggest any other treatment I would definitely give it a try, as these headaches are a terrible burden.  Doctors in the UK have very limited knowledge concerning dietary issues, and I do not know how to get reliable advice from them. Best regards,
    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
×
×
  • 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.