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

Severe Abdominal Pain


Cstrong

Recommended Posts

Cstrong Newbie

Hi everyone, I am 12 weeks post-partum today. My baby was delivered by a C-section and ever since her birth I have been experience a number of health issues. I was finally admitted to the hospital two weeks ago for hydration and a multitude of (not so fun) tests performed by a GI doctor. They did a blood test for Celiac Sprue and my IgA was 44.8 and my IgG was 184.5. I go in for a biopsy next Tuesday to confirm whether or not I truly have Celiac.

My question is, has anyone had severe abdominal pain as a symptom? My pain started about 6 weeks ago and on a pain scale of 1-10 it was a definite 10. At one point I even begged my husband to put me out of my misery because the pain was so bad!!! The pain is like someone lit my stomach on fire starting at my belly button and going straight up about 4 inches. It then moves over to the left hand side right under my rigcage, but the pain is different there, kind of raw and tender.

The pain has been constant but not as severe even since going gluten-free. However, on Tuesday night our neighborhood had a national night out party and I must have eaten something I shouldn't have because I woke up in horrible pain on Wednesday. Is this severe pain a normal symptom of celiac sprue? I have seen abdominal pain listed as symptom, but is the severity I am experiencing normal or should my doctor and I be looking for other causes?

Any advice you can give is greatly appreciated, I can't handle the pain anymore!!!

Thanks,

Carrie Strong


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

Hi Carrie:

I had hoped someone else who had blood tests would respond to your post by now. I had Enterolab stool test analyses to diagnose my celiac sensitivities to gluten and casein, so I can't interpret your results. However, your results seem pretty high (positive) to me.

Yes, abdominal pain is right up there with diarrhea and constipation as a celiac symptom. See this website's "Site Index" for FAQs and the answer to "What are the symptoms?". I mainly had the third (steatorrhea), fourth (abdominal pain) and fifth (excessive gas) symptoms. Occasionally I had constipation but rarely diarrhea. YES, my abdominal pain was EXCRUCIATING. It went from slight to chronic to excruciating over a 10 year period when I was consuming more gluten (esp. wheat bran cereals and whole wheat recommended for 'IBS' symptoms). HOWEVER, my pains were more often in the intestinal area. The worst felt like bits of broken glass slowly moving through my intestines. Sometimes I felt like something was inside my intestines trying to tear its way out. I also experience what feels like severe menstrual cramps, but I finished menopause 7 years ago. :huh: I get those symptoms everytime I accidentally consume gluten, casein or soy (mostly the cramps with the last 2). After about a week of avoiding those, all the pain disappears (until my next 'accident' :o).

Nevertheless, everyone's experiences of celiac symptoms are different. So your area of pain may just be unique to you. When my pain is really bad, it sometimes radiates up into my stomach area and even up my back to my shoulder blades. I also feel the pain move (perhaps as the offending food moves through my intestines) from right to left side of my intestines. After an 'accident' or painful episode, my intestines feel raw and tender when any food passes through for about a day or two. However, avoiding any foods to which I'm sensitive right now (esp. acidic foods and soy) as well as those to which I have diagnosed intolerances (gluten and casein) helps make that pain disappear.

I'm not sure whether your doctor told you to consume gluten before the biopsy, but if avoiding gluten relieves the pain, that's a pretty good indicator (plus those blood test results) that you have celiac. Hopefully someone else with pain in a similar area and someone who can help you interpret those blood tests will also post comments here. :)

BURDEE

GEF Explorer

Carrie,

I'd see your doctor, to be on the safe side. Things like gallstones aren't uncommon after a pregnancy. Hope you feel better soon.

Gretchen

XoHeatherxO Rookie

Severe pain was one of my main symptoms off and on for about 2 years. There would be times I couldnt move or get out of bed....I had blood results similar to yours and your IGG is actually higher. Your doctor should run a ttg test which is the most sensitive and specific of all the celiac blood tests. Also, make sure they take a sufficient number of slides and that they are reviewed by someone who is familiar with celiacs.

hapi2bgf Contributor

Looking back on it, I think my celiac symptoms started when I first got pregnant. I think pregnancy is one of the triggers for celiacs. But after the birth everything just hit the fan. I couldn't keep weight on and I was always sick, etc. I had all of the symptoms and no doctor who would help. I was labeled with IBS, told it was all in my head, etc.

I had the lower abdominal pain for almost 10 years (from first hospitalization) and after two surgeries for it I know my pain is adhessions. The odd part is that since going gluten-free I have not had the adhession pain again. Adhessions are like gumbands that connect the wrong parts of your body together. The first surgery found adhessions connecting my colon to my hip and the pain nearly killed me. The second surgery, about 5 years later, found more adhessions. The adhessions start growing after a surgery or infection, and are common with endometriosis. (I was checked for that too). Recovering from the surgery involves the gas working its way out of your system, and that was the most terrible pain I have ever felt. It settled under my should blades. The only help is to more around even though it feels like you are going to die.

Another source of serious pain in my stomach area was "gastroparesis". (right between the ribs where the soft skin is) My stomach fails to empty. That causes pain too.

The final one was the gall bladder (just near/under you ribs) also failed to empty.

So after the removal of the gallbladder, and the adhessions, they found the celiacs. Now I feel much better on the gluten-free diet. Many people feel removal of the gallbladder is a bad idea. For me, everything has worked out great!

Be sure to check about your eating gluten-free when you have an endoscopy coming up. If your intestines have started to heal, they will not see anything wrong during the test.

FYI: If your child has colic, is always fussy, etc, and you are breast feeding you may be having a problem producing enough milk for the baby while your intestines are suffering through Celiacs. My daughter had sever colic for around 7 months. Years later when I found out I had celiacs I think a lot of her pain may have been from my body not working right. I was dropping massive amounts of weight when she was trying to breast feed. She gained weight, but was alwasy sickly. So if that is the case for you, you may want to consider suppliementing with formula and see if that helps that baby.

Good luck it gets better eventually!

Cstrong Newbie

Thank you to all who replied to me. I appreciate all your advice and insight. I go today for my endoscopy/biopsy. I have been gluten-free for two weeks so hopefully it will not affect the results too much, but I am really scared to eat anything with Gluten in it because of the pain.

hapi2bgf - Thanks for the advice on breastfeeding. I actually just had to give it up because of a new medication I am on, and I really miss it! :( I am keeping my fingers crossed that my daughter won't develop Celiac.

Thanks again to all who replied!

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. - cristiana replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

    2. - trents replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

    3. - Dizzyma posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

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

    • Total Members
      132,923
    • Most Online (within 30 mins)
      7,748

    cmckurtz
    Newest Member
    cmckurtz
    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

    • cristiana
      Hi @Dizzyma I note what @trents has commented about you possibly posting from the UK.  Just to let you know that am a coeliac based in the UK, so if that is the case, do let me know if can help you with any questions on the NHS provision for coeliacs.    If you are indeed based in the UK, and coeliac disease is confirmed, I would thoroughly recommend you join Coeliac UK, as they provide a printed food and drink guide and also a phone app which you can take shopping with you so you can find out if a product is gluten free or not. But one thing I would like to say to you, no matter where you live, is you mention that your daughter is anxious.  I was always a bit of a nervous, anxious child but before my diagnosis in mid-life my anxiety levels were through the roof.   My anxiety got steadily better when I followed the gluten-free diet and vitamin and mineral deficiencies were addressed.  Anxiety is very common at diagnosis, you may well find that her anxiety will improve once your daughter follows a strict gluten-free diet. Cristiana 
    • trents
      Welcome to the celic.com community @Dizzyma! I'm assuming you are in the U.K. since you speak of your daughter's celiac disease blood tests as "her bloods".  Has her physician officially diagnosed her has having celiac disease on the results of her blood tests alone? Normally, if the ttg-iga blood test results are positive, a follow-up endoscopy with biopsy of the small bowel lining to check for damage would be ordered to confirm the results of "the bloods". However if the ttg-iga test score is 10x normal or greater, some physicians, particularly in the U.K., will dispense with the endoscopy/biopsy. If there is to be an endoscopy/biopsy, your daughter should not yet begin the gluten free diet as doing so would allow healing of the small bowel lining to commence which may result in a biopsy finding having results that conflict with the blood work. Do you know if an endoscopy/biopsy is planned? Celiac disease can have onset at any stage of life, from infancy to old age. It has a genetic base but the genes remain dormant until and unless triggered by some stress event. The stress event can be many things but it is often a viral infection. About 40% of the general population have the genetic potential to develop celiac disease but only about 1% actually develop celiac disease. So, for most, the genes remain dormant.  Celiac disease is by nature an autoimmune disorder. That is to say, gluten ingestion triggers an immune response that causes the body to attack its own tissues. In this case, the attack happens in he lining of the small bowel, at least classically, though we now know there are other body systems that can sometimes be affected. So, for a person with celiac disease, when they ingest gluten, the body sends attacking cells to battle the gluten which causes inflammation as the gluten is being absorbed into the cells that make up the lining of the small bowel. This causes damage to the cells and over time, wears them down. This lining is composed of billions of tiny finger-like projections and which creates a tremendous surface area for absorbing nutrients from the food we eat. This area of the intestinal track is where all of our nutrition is absorbed. As these finger-like projections get worn down by the constant inflammation from continued gluten consumption before diagnosis (or after diagnosis in the case of those who are noncompliant) the efficiency of nutrient absorption from what we eat can be drastically reduced. This is why iron deficiency anemia and other nutrient deficiency related medical problems are so common in the celiac population. So, to answer your question about the wisdom of allowing your daughter to consume gluten on a limited basis to retain some tolerance to it, that would not be a sound approach because it would prevent healing of the lining of her small bowel. It would keep the fires of inflammation smoldering. The only wise course is strict adherence to a gluten free diet, once all tests to confirm celiac disease are complete.
    • Dizzyma
      Hi all, I have so many questions and feel like google is giving me very different information. Hoping I may get some more definite answers here. ok, my daughter has been diagnosed as a coeliac as her bloods show anti TTG antibodies are over 128. We have started her  on a full gluten free diet. my concerns are that she wasn’t actually physically sick on her regular diet, she had tummy issues and skin sores. My fear is that she will build up a complete intolerance to gluten and become physically sick if she has gluten. Is there anything to be said for keeping a small bit of gluten in the diet to stop her from developing a total intolerance?  also, she would be an anxious type of person, is it possible that stress is the reason she has become coeliac? I read that diagnosis later in childhood could be following a sickness or stress. How can she have been fine for the first 10 years and then become coeliac? sorry, I’m just very confused and really want to do right by her. I know a coeliac and she has a terrible time after she gets gluttened so just want to make sure going down a total gluten free road is the right choice. thank you for any help or advise xx 
    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
×
×
  • 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.