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

What's The Main Difference Of Crohns And Celiac


faithforlife

Recommended Posts

faithforlife Apprentice

I know celiac usually improves on a gluten-free diet. Is Crohns related to celiac? Im reading that the intestinal damage looks similar. Just wondering if Crohns is something we should be tested for. I had my endoscopy late in the game 6 months after the gluten-free diet and the doc could see scalloping in duodenum. Will that heal in time? Makes me worry also that I'm accidentally buying cross contaminated groceries. Or could it be gluten-free oats? FYI I don't have celiac symptoms but was positive for antibodies and genetics. And still waiting on biopsy results.


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



Celiac.com Sponsor (A8-M):



Bubba's Mom Enthusiast

My sister has Crohn's and her main symptom is D. It's considered auto-immune too.

I guess they can tell by the biopsy if it's Crohn's or Celiac? They're both inflamatory but under the microscope they have different cells visable? There's some speculation that those with Crohn's would be wise to try gluten-free? My sister's Dr. told her diet didn't matter with Crohn's when she asked.

If I had to choose between one or the other, I'd choose Celiac. The treatment for it no gluten and that is much easier than having a disease with no known cause? My sister has to have IV treatmnts to knock out her immune system, and that's all they can do for her.

frieze Community Regular

....different ends of the digestive tract.

GFinDC Veteran

I think they can test for Crohn's by looking for antibodies to yeast. Some people do have both celiac and Crohn's. I guess that's different kind of CC. Some people with Crohn's follow the gluten-free diet also.

Gemini Experienced

My sister has Crohn's and her main symptom is D. It's considered auto-immune too.

I guess they can tell by the biopsy if it's Crohn's or Celiac? They're both inflamatory but under the microscope they have different cells visable? There's some speculation that those with Crohn's would be wise to try gluten-free? My sister's Dr. told her diet didn't matter with Crohn's when she asked.

If I had to choose between one or the other, I'd choose Celiac. The treatment for it no gluten and that is much easier than having a disease with no known cause? My sister has to have IV treatmnts to knock out her immune system, and that's all they can do for her.

As Frieze already mentioned, Crohn's is an inflammatory disease of the large intestine, while Celiac is the small intestine. Similar symptoms but each affects a different part of the bowel.

Crohn's has genetic components to it and that's why you see it run in families...like Celiac. However, you cannot knock it into remission by diet alone.

I think it much worse because many people with Crohn's have to have sections of the large intestine removed due to damage from poorly controlled inflammation. I have heard of Crohn's patients who follow the gluten-free diet and they claim it does help them a lot but I wonder if the 2 diseases are common together? I would bet they are.

The AMA has no real treatment for most autoimmune problems except to suppress the immune system but that can be dangerous to do for long periods of time.

I feel lucky as all hell to have Celiac and not something else that cannot be controlled by diet. I don't believe that diet is irrelevant with Crohn's.

That's just the misguided belief of the AMA.

Bubba's Mom Enthusiast

Crohn's can affect your digestive system anywhere from the mouth to the other end, and everything in between. My sister has had her Colon removed and it's now attacking her small intestine. It's brutal.

Celiac doesn't look as bad to me? At least it can be controlled?

ChristenDG Rookie

My best friend has Crohn's Disease (which runs in my family, but fortunately I do not have!). I very much agree that Celiacs is much better to deal with! Remove gluten and the damage can heal and you can have a fairly normal life! With Crohn's though, the way I understand it and from my experience, there's not much you can do. You can eat carefully and whatnot, but there doesn't really seem to be a way to control the symptoms. The symptoms are all very similar though and before I was diagnosed with Celiacs the doctors believed I might have Crohn's. Thank God it wasn't!


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



Celiac.com Sponsor (A8-M):



faithforlife Apprentice

Thanks everyone. I find it very interesting.

  • 2 weeks later...
49erlady Newbie

I was just dx with both Celiac Disease and Crohns on the same day. The dr told me they don't know of a def correlation but would not surprise him if the Celiac got so bad that it triggered the Crohns. However no way to tell. Balancing the two is going to be challenging but I will find a way. Long road ahead for me!

GlutenFreeAustinite Contributor

My grandmother was dx'ed with Crohn's when she was much, much older...when she was in her 70s. She was tested for celiac in the 1990s, but it came back negative. My family is convinced she had gluten-intolerance, and most likely celiac, even though she did have a negative test. The Crohn's was absolutely nasty--she eventually had to have a colostomy bag.

GFinDC Veteran

Hi 49er,

My younger brother had both celiac and Crohn's. It is not unheard of to have both. I wish you the best in your journey. I wish I understood more about celiac back then so I could have helped him. He didn't really follow the gluten-free diet. But we know a lot more about how to eat healthy these days. On some Crohn's forums they are people who say the gluten-free diet helps their symptoms. Some say it doesn't help them. So it is a variable thing. Maybe it will help you. :)

Open Original Shared Link

Open Original Shared Link

Links for info on IBD (Inflammatory bowel disease).

Open Original Shared Link

heidi g. Contributor

You will know if you have crohns because I've heard the pain from it be described as close to labor pains. Now I'll tell ya from experience those hurt! I had ulcerative colitis when I was younger and luckily it healed.by itself but (very similar pain as crohns) and id wake up sweaty. I know several people who have crohns disease and their Main symptoms are extreme pain and bloody diarrhea. It will only get worse too. You get sicker and sicker. Now depending on she. Your symptoms started but the doctors.most likely would of seen the extreme inflammation crohns causes. Hope that made you feel better. (I myself questioned if I had crohns at one point so I asked people who actually have it.)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    4. - Dizzyma replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,955
    • Most Online (within 30 mins)
      7,748

    JodyBledsoe
    Newest Member
    JodyBledsoe
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.