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

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:
    Join eNewsletter
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

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

      My journey is it gluten or fiber?

    2. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    3. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    4. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    5. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

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

    • Total Members
      132,696
    • Most Online (within 30 mins)
      7,748

    Knotalota
    Newest Member
    Knotalota
    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

    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
×
×
  • 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.