Jump to content
  • You are not alone. Join Celiac.com for trusted gluten-free answers and forum support.



  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):

Diverticulitis or Celiac Flare


ktyler44

Recommended Posts

ktyler44 Contributor

I am so confused and don't know which way to turn now. This is rather lengthy, but please bear with me to get to my dilemma. Several years ago when I was having flares of stomach pain, my doctor originally thought maybe it was diverticulitis but no test was run at that time. I didn't think the symptoms matched up to that and took myself off gluten for awhile. All of my symptoms seemed to improve (I had other symptoms)  but without a diagnosis, I wasn't sure. So I asked the doctor about doing a blood test for Celiac. I was told to go back on gluten for the test but I was only back on it for a week or two when he did the test. Of course it came back negative. He had wanted me to have a screening colonoscopy anyway, so I asked him to do an endoscopy and biopsy at the same time. He did, but I found out afterwards that he only took one specimen and checked for H. pylori, not Celiac. The colonoscopy did show a couple of diverticula. So I took myself back off gluten but cheated from time to time. Then I would hurt, so I finally stayed off gluten. I got better over time and even have stopped having migraines. I changed doctors and my new doctor offered to test me, but I didn't want to go back on it for the test. We did do the gene test, which was positive. She made the diagnosis of Celiac based on that along with my symptoms and improvement by removing gluten. Here's why I'm confused. I recently thought I would like to do the challenge to get a definite diagnosis. I ate real bread and other things for 3 days in a row with no reaction. But then I got to thinking that maybe it was just because I had healed and I was afraid of causing new damage. So I stopped the challenge. Now a couple of weeks later, I've had the same stomach pain I used to get but haven't knowingly had any gluten. So could my problem really have been diverticulitis all along rather than Celiac? Should I go ahead and do the gluten challenge to be sure? I don't currently have insurance but I could probably pay for a blood test, just not an endoscopy.


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

This is a bit of a personal choice, you have genes and react badly to it. Some people will have the reaction in hours some withing days...weeks might be pushing it if you did it then stopped but do not quote me. The Gluten Challenge for the blood test takes 12 weeks of eating gluten, not much maybe a 1/2 slice of bread, few crackers, or a tsp of vital wheat gluten a day, you can try it at night and sleeping it off. You have to build up the antibodies and let them go from the gut to the blood stream which can take UP to 12 weeks sometimes less and heard of others showing positive at 8 weeks. Open Original Shared Link

I have UC and Celaic, might be my double whammy and random reactions to forms and the amounts I eat and why my reactions change SO much each time.

ktyler44 Contributor

It's possible that I accidentally got glutened. We were traveling and ate out a couple of times, so that would have only been a couple of days which is pretty normal for me. But what really confused me is that I didn't react for those three days that I knowingly ate gluten but have reacted at other times when I have accidentally eaten gluten.

ravenwoodglass Mentor
6 hours ago, ktyler44 said:

It's possible that I accidentally got glutened. We were traveling and ate out a couple of times, so that would have only been a couple of days which is pretty normal for me. But what really confused me is that I didn't react for those three days that I knowingly ate gluten but have reacted at other times when I have accidentally eaten gluten.

Three days may not have beenlong enough to see a reaction. When I went through my doctor guided and prescribed elimination diet I had to add items back in for a week before I could consider them safe. He explained that it can take up to a week for an intolerance reaction to show up.  Even after diagnosis it takes 3 or 4 days for the GI reaction to show up in me after a glutening although other symptoms do appear more quickly (neuro related). I think that diverticuli can be associated with celiac, or at least they were in my case. A year before diagnosis I had a colonoscopy where the GI found 'the most extensive diverticuli he had ever seen'. He said the out pouching covered my entire large intestine where usually only a couple are found on the descending colon. Five years after I was finally diagnosed celiac a repeat scope found they were gone.  If you can tolerate a challenge you may want to do so for 2 to 3 months and then get tested. You don't have to eat a lot of gluten a serving a day should be enough.  Do be sure to let your doctor know if your reaction wakes you at night. That is a clear sign of celiac since according to my GI the 'IBS' diagnosis doesn't cause that to happen. Good luck with whatever you choose to do and if you do the challenge I hope you get clear answers. In the end though it is your reaction to cutting out gluten that matters the most.

ktyler44 Contributor
3 hours ago, ravenwoodglass said:

Three days may not have beenlong enough to see a reaction. When I went through my doctor guided and prescribed elimination diet I had to add items back in for a week before I could consider them safe. He explained that it can take up to a week for an intolerance reaction to show up.  Even after diagnosis it takes 3 or 4 days for the GI reaction to show up in me after a glutening although other symptoms do appear more quickly (neuro related).

What I don't understand, though, is that I never did react after those three days. Yet, other times when I've only eaten a little by accident, I'm in pain for days. Also, how can I tell the difference if this is a diverticulitis flare or celiac flare? I always assumed these were from gluten. Now I'm not sure.

ravenwoodglass Mentor
1 hour ago, ktyler44 said:

What I don't understand, though, is that I never did react after those three days. Yet, other times when I've only eaten a little by accident, I'm in pain for days. Also, how can I tell the difference if this is a diverticulitis flare or celiac flare? I always assumed these were from gluten. Now I'm not sure.

You should talk to your doctor to be sure but diverticulitis can be very serious and can require hospitalization and antibiotics.  Do you get any other reactions that you know for sure are gluten related? Some will get a headache, brain fog or mood issues that show up with a glutening that can help us tell the difference. Do you keep a food and symptom log? That can be helpful if seeing a pattern.  Since you had no symptoms after three days back on gluten maybe a challenge and testing might be wise so you can know for sure.

ktyler44 Contributor
39 minutes ago, ravenwoodglass said:

You should talk to your doctor to be sure but diverticulitis can be very serious and can require hospitalization and antibiotics.  Do you get any other reactions that you know for sure are gluten related? 

I've never required antibiotics with these flares. It's digestive only with abdominal pain and constipation. It usually lasts 3-4 days and the pain is over the whole abdominal area.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
On 3/8/2018 at 9:34 AM, ktyler44 said:

I've never required antibiotics with these flares. It's digestive only with abdominal pain and constipation. It usually lasts 3-4 days and the pain is over the whole abdominal area.

IMHO you are dealing with a glutening. Diverticulitis would leave you very ill and running a fever. Most with that end up in the ER or at their doctors office. You say you have eaten out a couple of times so chances are you were glutened. Hope you are feeling better by now but if not a trip to the GI may be in order.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    2. - cristiana replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    3. - trents replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    4. - knitty kitty replied to CC90's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      Coeliac or not coeliac

    5. - knitty kitty replied to kevert93's topic in Gluten-Free Foods, Products, Shopping & Medications
      4

      Having issues with chips

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

    • Total Members
      134,184
    • Most Online (within 30 mins)
      10,442

    Dennis E. Schertz
    Newest Member
    Dennis E. Schertz
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Cristiana asks a very relevant question. What looks normal to the naked eye may not look normal under the microscope.
    • cristiana
      Hello @CC90 Can I just ask a question: have you actually been told that your biopsy were normal, or just that your stomach, duodenum and small intestine looked normal? The reason I ask is that when I had my endoscopy, I was told everything looked normal.  My TTG score was completely through the roof at the time, greater than 100 which was then the cut off max. for my local lab.  Yet when my biopsy results came back, I was told I was stage 3 on the Marsh scale.  I've come across the same thing with at least one other person on this forum who was told everything looked normal, but the report was not talking about the actual biopsy samples, which had to be looked at through a microscope and came back abnormal.
    • trents
      My bad. I should have reread your first post as for some reason I was thinking your TTG was within normal range. While we are talking about celiac antibody blood work, you might not realize that there is not yet an industry standard rating scale in use for those blood tests so just having a raw number with out the reference scale can be less than helpful, especially when the test results are marginal. But a result of 87.4 is probably out of the normal range and into the positive range for any lab's scale. But back to the question of why your endoscopy/biopsy didn't show damage despite significantly positive TTG. Because they took the trouble to take seven samples, it is not likely they missed damage because of it being patchy. The other possibility is that there hasn't been time for the damage to show up. How long have you been experiencing the symptoms you describe in your first post? Having said all that, there are other medical conditions that can cause elevated TTG-IGA values and sometimes they are transient issues. I think it would be wise to ask for another TTG-IGA before the repeat endoscopy to see if it is still high.  Knitty kitty's suggestion of getting genetic testing done is also something to think about. About 35% of the general population will have one or both genes that are markers for the potential to develop active celiac disease but only about 1% of the population actually develop celiac disease. So, having a celiac potential gene cannot be used to definitively diagnose celiac disease but it can be realistically used to rule it out if you don't have either of the genes. If your symptoms persist, and all testing is complete and the follow-up endoscopy/biopsy still shows no damage, you should consider trialing a gluten free diet for a few months to see if symptoms improve. If not celiac disease, you could have NCGS (Non Celiac Gluten Sensitivity). 
    • knitty kitty
      @CC90, Your Lansoprazole is a proton pump inhibitor and has immunosuppressive effects!!!!  This is why your endoscopy didn't show much damage to the intestinal lining!!  The Lansolprazole is suppressing tTg IgA antibodies in the intestines, but those antibodies are getting into the blood stream and causing inflammation and damage in other organs.   Proton pump inhibitors cause intestinal damage in the long run.  If you get off the Lansoprazole for a few months so your immune system is not blocked, then do a gluten challenge, and an endoscopy, THEN they would see intestinal damage. Sheesh!  Doctors can be so ignorant.  I've seen this so many times it's frustrating! Take the B Complex and Benfotiamine.  Get off the Lansoprazole.  Go with the DNA test results.   Welcome to the tribe! P.S. B vitamins are needed to correct anemia!  Not just iron.  
    • knitty kitty
      Hi, @kevert93, Those Gluten Assist enzymes digest carbohydrates, not just gluten specifically.  Eating a high carbohydrate meal can deplete Thiamine Vitamin B 1 causing digestive symptoms like you describe.  You could also be having difficulty digesting the oils used in those chips.  Thiamine in the form Benfotiamine can help. We need the eight B vitamins to digest our food, carbs, fats and proteins.  Poor digestion can cause symptoms like vomiting and stomach pain, brain fog, headaches, exhaustion.  Try taking a B Complex with the activated forms of the B vitamins (Life Extension's Bioactive B Complex is great!) and additional Benfotiamine.  The B vitamins are used to make digestive enzymes and will allow your digestive system to function properly.  The B vitamins also will improve headaches, exhaustion, and brain function.  Taking Thiamine in the form Benfotiamine will improve digestive symptoms and lower inflammation, too.  Benfotiamine and the B vitamins are safe.  The B vitamins are chemical compounds found in whole foods, not in highly processed foods like chips.   The body cannot make the B vitamins, so supplementing is beneficial.  Benfotiamine is safe and nontoxic even in high doses.
×
×
  • Create New...