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

Villi Damage-could Severe Food Allergies Cause It Or Only Celiac?


kmps

Recommended Posts

kmps Newbie

My question: I got tested in Feb. - EGD and blood work and blood was normal, EGD showed "beginning stage" of celiac (got 2 opinions on slide to confirm). At that time I was gluten free - mostly- for years since I felt so much better off of wheat.

Then I found out that I should have been ON gluten and started eating it. Now I went to a new Doc, well about 2 months ago. He said he thought it was irritable bowel until he had the second opinion on the biopsy done. Now he is "intreagued" by me and my craziness. :) Knowing that I am now on gluten for some time he just had me redo the blood work for celiac, which I did today and am DYING to call the lab right now and ask about!

Also after the EGD I hade gotten allergy tested for lots of foods and I was told that I have severe allergies to wheat, gluten, sugar (cane), potatoes, and so many other things that sometimes I cry because I can't eat anything in my house! My thought is: can the allergies cause a celiac type of damage? This Dr. tells me he doesn't really believe in all the food allergy stuff and I will be sending him all my records from that. I know I am allergic to sugar cane because now that I cut it out I feel so much more 'evened out'. Actually, my fingernails are growing for the first time without breaking in years and years. COuld it have been the sugar that caused the malabsorbtion/damage?? I do feel better overall since avoiding it.

ANything will help, thanks!

kmps


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



Celiac.com Sponsor (A8-M):



darlindeb25 Collaborator

My celiac support group had a gastro doctor from the area (she is trying to open a celiac center at Stony Brook Hospital) who said many things I did not agree with. She said that if a patient has flattened villi, but a negative blood test, then they can not be celiac. Many celiac's have had false negatives! She did say though, she feels if the blood work is negative, yet there is flattened villi, then it is from another cause, such as allergies! So, I guess some doctors do believe this.

You do the testing, and decide from there. If you know you feel much better gluten free, then you should be gluten free. I too, have many intolerance's: nightshades, all grains (soy, corn, rice, oats, and gluten), cruciferous veggies, red meat, dyes. etc. I have double DQ1 genes, and read recently that many with double DQ1 genes suffer from several intolerance's, plus neuropathy.

Amyleigh0007 Enthusiast

My son has Celiac and several food allergies including wheat, egg whites, peanuts, corn, and soy. His GI told us that the villi damage can only be caused by Celiac (not food allergies). My son's food allergies cause rashes and hives to form on his esophagus and the GI told us only food allergies can cause that (not Celiac).

Tim-n-VA Contributor
Although villous atrophy is not exclusive of celiac disease, it is considered a crucial finding. Other causes of blunted villi include tropical sprue, malnutrition, intolerance to cow's milk, soy protein intolerance, and infectious gastroenteritis. However, most of these conditions can be readily excluded on the basis of clinical history and laboratory data.

Above is from Open Original Shared Link [medscape is part of WebMD]

ShayFL Enthusiast

This is interesting.....Based on Tim's post...Let's say...Your doctor tests blood for Celiac and it comes back NEG. But you get a biopsy anyway and it comes up POS. So your go on a gluten free diet.....maybe you have little improvement....maybe none at all. You find this forum and everyone says.....Give it time....Or you might need to cut out dairy or soy because a lot Celiacs cannot tolerate them either. So you cut the dairy and get better. Was it the gluten or the dairy? Or you cut out all three and get better. Was it the soy?

Which one caused the villi damage? NEG blood POS biopsy are you Celiac???

Or just intolerant to something else....The only way to know is a challenge. And that can be pretty scary.....

kmps Newbie

Thanks everyone for your posts!

I did go on line after my last post to try and find some evidence for villi damage caused by allergy- and I did. I also found that there aren't many people in the web world that believe you can have sugar cane allergy. I was surprised by this and I was too tired to read more about why, but maybe my GI doc was meaning that....no allergies to sugar????

The info I found on a couple of sites mentions that celiac has 5 stages of villi damage while allergy has only 3.

Well, I do have so many allergies to foods (including celery of all things) and maybe all of them combined were causing my damage. ?? I have cut out mostly everything but I do "cheat" on most of them at times.

I have stopped taking every suppliment but one multi vit. in isotonic form - this even means no co enzyme B complex- that I have depended on forever and I must say that I haven't felt this good in a very long time. I think I may have mentioned previously that my fingernails are growing without breaking for the first time in 20 years or more!

What does this mean? Something is working. The only thing I haven't cut back on is wheat! And this is , of course, because I will be getting another EGD if my blood shows no gluten.

I still feel pains when I eat certain forms of wheat- like pasta. I still have constipation alternating with loose stools.

My previous biopsy states, "Due to the slight increase in intraepithelial lymphocyte minimal change or early phase of celiac sprue cannot be ruled out."

ANy opinions on this??

To throw one more thing in the mix, I also had a test show that I had no binificial flora and to much 'bad' bacteria.

Thank you so much,

kmps

ginnym Newbie
My previous biopsy states, "Due to the slight increase in intraepithelial lymphocyte minimal change or early phase of celiac sprue cannot be ruled out."

ANy opinions on this??

I also had a raised lymphocyte count on biopsy (count was 40) but it also said there was "no convincing villous atrophy" and my blood tests were negative so my docs have said I don't have coeliac. Gluten free diet has relieved my abdo pain so I'm assuming I have a gluten intolerance, even if it's not coeliac. I haven't found anyone who can explain whether the raised IEL count is due to the intolerance or whether it's caused by something else (or if it means I actually do have early coeliac).


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



Celiac.com Sponsor (A8-M):



kmps Newbie

I could just give up gluten and let this all go, I guess.....

It will be to easy for me to cheat if I don't have a diagnosis, yes, I have no will power!

Plus! IF you are dx with celiac you can deduct on your taxes the cost difference of gluten free food and the shipping or gas/mileage to get it.

Hey, every bit helps and with all the special diets in my house we have a whopping food bill every month.

kmps

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,955
    • Most Online (within 30 mins)
      7,748

    AnnaLousGFBakery
    Newest Member
    AnnaLousGFBakery
    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

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.