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. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

    2. - TheDHhurts posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      need help understanding testing result for Naked Nutrition Creatine please

    3. - cristiana replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

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

    • Total Members
      133,107
    • Most Online (within 30 mins)
      7,748

    Maggie1349
    Newest Member
    Maggie1349
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • knitty kitty
      @cristiana,  I react the same way.  Dairy consumption flushes out my digestive system within an hour, too! As casein is digested, it forms casomorphins that bind to opioid receptors in our bodies.  This is similar to digested gluten peptides being able to attach to opioid receptors in our bodies.   We have opioid receptors throughout our bodies including lots in the digestive tract. Casein raises tTg IgA antibodies just like gluten consumption does, which leads to further intestinal damage and continuing inflammation.  No wonder our bodies react to it by pushing the "emergency evacuation" ejection seat button! The mother of my childhood friend was British and introduced me to drinking tea properly with milk or cream.  I miss it so much.  And chocolate ice cream.  Not worth the after effects, though.  I've found taking Omega Three supplements (flaxseed oil, sunflower seed oil, evening primrose oil) helps shake those dairy cravings.   Green leafy veggies like broccoli, kale, and greens (mustard, turnip, collards) are great sources of calcium.  Avoid spinach as it is high in oxalates that block calcium absorption and may cause kidney stones.  Yes, more leafy greens are needed to reach the same amount of calcium in a glass of milk, but the greens have other benefits, like increased dietary fiber and polyphenols that act as antioxidants, reduce inflammation, and promote health.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards.  The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.   Some people in remission report being able to consume gluten again without consequence.  Another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.  
    • TheDHhurts
      Hi, I bought Naked Nutrition Creatine. It lists itself as gluten free but is not certified. (It used to be, but they dropped it in the past year or two apparently.) I wrote the company and asked them what testing results they had for creatine and they sent me the attached, which says the test result for gluten is <0.025MCG. I'm used to seeing test results as ppm, so I'm not sure what <0.025MCG means. Can it be converted to ppm easily? I want to confirm that it is safe to use.
    • cristiana
      When I was still recovering my gastroenterologist suggested I bought lactofree product as I was very bloated.  So I bought some from the supermarket and from memory, I drank a nice big glass of milk - and it went right through me literally within an hour or so, if my memory serves correctly.  I came off dairy completely next and it worked like a charm, but started to reintroduce quite gradually it as I missed it! To this day, if I overdo dairy products, they work like a mild laxative.  I've never wanted to give up milk completely as I like it so much, and my mum had osteoporosis and it's an easy way of getting calcium.  But it doesn't really 'sit' well with me.   You may need to experiment a bit as when I was healing certain dairy products were worse than others - I could cope with one brand of Greek yoghurt, but I got extremely and painfully bloated with another brand of live British yoghurt.  
    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for you.  
×
×
  • 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.