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

Hoping That Gluten Free Will Help Me!


Philly Girl

Recommended Posts

Philly Girl Newbie

Hello Everyone,

This is my first post on the Gluten Free Forum but I have been reading it for a couple of months. I think this forum is wonderful and it has been incredibly helpful! Thank you to all that participate!

I have been sick with GI symptoms for over 8 years and it has been a huge inconvenience with work, school, and life in general. I have seen numerous doctors (GI, primary care, alternative medicine, nutritionist, etc.) and no one can ever seem to figure out what is wrong with me. I am noticing that this is a trend with Celiac Disease. The GI docs were always quick to diagnosis IBS and I was always told to stick to a bland diet consisting of mostly bread, crackers and pretzels (all gluten filled). Every couple years I will have the GI tests done. This past fall my blood work came back with signs of Celiac. My doc went ahead and did the endoscopy but that came back negative. My doc said that b/c of the blood work, there may be a chance that it is Celiac and there just isn't significant damage in the intestine yet. Has anyone heard anything like this before? I thought that since I have been sick for so many years, there would be signs of damage if it is Celiac? I started the gluten free diet at the beginning of January and my symptoms have not improved at all yet. I understand that it can take time but I am curious as to how long since my doc said that there was no intestine damage?

I should also mention that I tested negative for lactose intolerence but I still avoid most dairy products because they seem to bother me. I know that giving the Gluten Free diet is worth the chance - I am just wondering if anyone had test results like this before? I apologize if this was already discussed! Any feedback is greatly appreciated! Thanks so much!


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



Celiac.com Sponsor (A8-M):



wowzer Community Regular

HI, If your bloodwork looks like sign of celiac then you have it. You can have a false negative, but not a false positive. I went gluten free even though my bloodwork was negative. Going gluten free for me cleared up symptoms that I had complained to my doctor for years about. Good luck and I hope that you feel better soon.

cruelshoes Enthusiast
This past fall my blood work came back with signs of Celiac. My doc went ahead and did the endoscopy but that came back negative. My doc said that b/c of the blood work, there may be a chance that it is Celiac and there just isn't significant damage in the intestine yet. Has anyone heard anything like this before? I thought that since I have been sick for so many years, there would be signs of damage if it is Celiac? I started the gluten free diet at the beginning of January and my symptoms have not improved at all yet. I understand that it can take time but I am curious as to how long since my doc said that there was no intestine damage?

This may be of help to you:

Open Original Shared Link

Positive serologic tests in the presence of a normal biopsy

This situation occasionally arises. The presence of a positive EMA with a normal biopsy indicates either the presence of celiac disease that was not detected in the biopsy, either because of too few pieces being taken or misinterpretation. The biopsy should be reviewed by an expert gastrointestinal pathologist. If it is considered to be truly a normal biopsy the patient may well have latent celiac disease and will probably develop the disease at a later date.

It is not at all uncommon for people with positive bloodwork to get a negative biopsy result. Damage can be patchy, and many doctors take very few samples. In the presence of positive bloodwork, I would be inclined to go gluten-free.

I hope you get a resolution to your symptoms soon.

Ursa Major Collaborator

It is possible that you aren't getting better because the dairy you eat is hindering healing (the same goes for soy, if you are consuming it). You may be intolerant to casein, rather than lactose. My youngest daughter is intolerant to all parts of dairy, except lactose! If you are casein intolerant you won't outgrow it any more than a gluten intolerance (unless those are caused by another underlying condition like Lyme disease).

Also, if you have switched right away to all those gluten-free goodies to replace gluten ones, that could be a problem as well, as they are very hard to digest.

Some people take up to six months on a strict gluten-free diet before they see improvement, so don't give up yet.

Also, you could be glutened by cross contamination. Did you buy a new toaster? The old one can't be cleaned well enough to be safe. What about things like colander, wooden cooking spoons and cutting boards? If you use a plastic colander for gluten-free pasta (this doesn't go for metal ones) that has been used for wheat pasta before, you are glutening yourself, as it isn't possible to get gluten out of cracks (it is one of the stickiest substances on earth, they make industrial strength glue from it).

Have you checked your medications (if you take any) and vitamins for gluten? Many are unsafe.

It might also be a good idea to replace personal care products for ones that don't contain things like wheat germ oil, barley extract and oat bran.

Biopsies are not a reliable way of diagnosing celiac disease (despite it being the 'gold standard', which is not a good thing). The small intestine has a huge surface area, and to actually manage to biopsy a damaged area is just hit and miss (and you can't usually see the damage without a microscope, so looking with a little camera to pick the right spots is not necessarily helpful).

Your doctor is right with what he is saying, one of the few doctors who won't just declare that 'it can't be celiac disease' if you have a negative biopsy. I wished there were more good doctors like him around.

Philly Girl Newbie

Thank you all so much for your responses! I appreciate all of your feedback!

I did replace my pots, pans, utensils, toaster and condiments. I also checked all of my toiletries and medications. I am worried about possibly being intolerant to other things though! Do you know if there is testing for casein or soy intolerances? Or is it best to just try eliminating them?

nikky Contributor

there are only false negatives not false positives.. if the tests are inconclusive then id say get rid of the gluten.. dont take any chances

Thank you all so much for your responses! I appreciate all of your feedback!

I did replace my pots, pans, utensils, toaster and condiments. I also checked all of my toiletries and medications. I am worried about possibly being intolerant to other things though! Do you know if there is testing for casein or soy intolerances? Or is it best to just try eliminating them?

as far as i know there are tests but the thing to bear in mind is tests can be negative.. so you could try getting tested then go on a trial diet. remeber if you do want to get tested dont take the food out of your diet until after the tests.

another intolerance to bear in mind is lactose intolerance its common among coeliacs so you may want to get tested.

KaitiUSA Enthusiast

Celiac can be very tricky to detect in some cases because you here of alot of false negatives with some of the tests (depending which ones they run) Some are just better than others. Do you know which tests you had done? Either way if they came back inconclusive I would most definitely ditch that gluten. It really is not something to mess with. There is alot of risk involved long term if it is not dealt with.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,397
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    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

    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.