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

Recurring stomach pain?? Celiac or Ulcer?


Mermaid's Mom

Recommended Posts

Mermaid's Mom Enthusiast

I am trying to tease out what is going on with my daughter: 

We went Gluten/Dairy Free March 1 and she steadily got better but looking back through the journal tummy aches were still randomly occurring on a semi reg basis.  But she was improving so much that my focus was mainly on the improvements.

Then we brought back dairy and it all went down hill and she went right back to all her symptoms and tummy aches prob got lost in the fact that she now had so many other worse symptoms like headaches, fatigue etc.   The we went to the Naturopath and stripped her diet back to Paleo.  She is now NOT eating: Wheat, barley, rye, oats, corn, rice, quinoa, millet, etc.  Zero grains (though we do allow a trace amount of cornstarch that is in just a half dozen things she eats) and no dairy.  It is as hard as hell but it has really reduced the concerns about cross contamination.  She is not eating anything that could be problematic.  And again she is getting better.  But again the stomach aches keep hanging on.  They usually come at night.  They must be painful as she just shuts down and needs a heat pad etc.  She also has a lot of nausea about food.  Too nauseas too eat.  Or becomes nauseous WHILE eating.   

 It has only been 2 weeks of grain free so maybe I am just being impatient but I am worried that this is not just normal celiac healing??  She says it is stabbing pain and in the areas above the belly button below sternum.  Severe heartburn?   Anyone who is familiar with Ulcers doesn't think it is ulcers.  What are your thoughts?  Does this sound like the early stages of healing?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Have you contacted the GI who diagnosed her celiac? If not that would be a good idea so you can make sure nothing else is going on. In addition if she is taking a lot of different supplements you may want to stop all for a few days and see if the pain resolves. If it does then add them back in one at a time a week apart to see if she is adversly reacting to something in one of them. Hope she feels better soon.

Estes Contributor

I have ulcers in my stomach.  I get nausea but I have never needed a heating pad.  That sounds like cramps?

GFinDC Veteran

So, she is eating 6 foods with corn starch?  Try making that zero foods with corn starch and see if she improves.  The simpler her diet is the better.  Whole foods are the best way to go to start the gluten-free diet.  Maybe she can have hard boiled eggs for snacks?  Or deviled eggs?  Planter's nuts are labeled if they contain gluten.  So their plain cocktail peanuts are a good snack.  Jif natural peanut butter is good with celery sticks or baby carrots.  Bacon is handy too.

It really does take time to heal.  But healing also goes faster on a simple, basic diet with no or very little processed foods.

Victoria1234 Experienced

I totally forgot this, but I used to get these same symptoms! It's been since 2008 that I've been gluten-free! So personally those symptoms went away eventually with the gluten-free diet. I had these problems, especially the belly button area pain, since I was a child. I also have a hernia there that they say is not a problem. But I'd feel like an imaginary belt buckle was stabbing me! Hope this helps a little.

Mermaid's Mom Enthusiast

Thanks everyone!!

I think I have noticed a pattern...she is in pain and it is resolved as soon as she has a bowel movement.  I could be wrong but it appears to the be the case.  Will keep an eye on it.

The naturopath told us to "work towards" a grain free/Paleo diet and my daughter committed 100% and stripped away everything.  But after 7 days she asked if she could on occasion consume this handful of items that have scant amt of cornstarch.    We see the naturopath today so we will see what she says.  My daughter is kick ass so if she says to strip them away also I suspect she just will LOL!

As a mom I have to tread carefully.  Sometimes its better to have someone else suggest it! 

 

pikakegirl Enthusiast

I just spent a year with sharp pain to the right of my belly button. I have been diagnosed Celiac gluten free 10 years, no dairy, corn, gluten, on a 12 food elimination diet. I had dry stomach with gastritis and could barely eat. This was from ppi and antihistamine.?...from misdiagnosis other thyroid control problem confused with allergy. Anyway seems it is caused by foods I had added trying to increase variety. Culprits for now are  almonds, Turkey, sunflower seeds. Have gone back to brown rice, red and sweet potato, eggs, fish, green beans, peas, snap peas, apples, raisins, cantelope, dates, many sparingly. Also follow FODMAP. Also pain above belly button sounds like gallbladder. Before diagnosis Celiac I had billiard diskenisia not stones. Took a year of tests to finally get a had as an to show it was not emptying. I hurt no matter what I ate. Had it removed. If it is stomach I cured mine by drinking ginger tea after each Mel for years and really chewing my food down. My elimination diet keeps my vitamin panel up and I use a few supplements. Wish you answers soon.


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



Celiac.com Sponsor (A8-M):



pikakegirl Enthusiast

Sorry typos. Correction. Biliary Diskenisia and a Hidascan.

Mermaid's Mom Enthusiast

You're right that area is gallbladder!

Well we just saw the Naturopath - she was puzzled by the recurring stomach aches also but allows for the fact that it COULD just be healing - she did have that gluten exposure that I mentioned 2 weeks ago.  But she decided to start her on a digestive enzyme.  We shall see.

  • 2 weeks later...
Pocah Rookie

I used to get frequent intestinal pains due to gluten and the way it worked was always the same. The consumption of gluten eventually resulted in intestinal ulcers which can be in all sorts of strange places, but in my case they were very specific point pains. Twinges are a pre-cursor, a sharp stabbing pain is an ulcer. I gather that some people, though, report no pain at all, but for me the ulcer was very painful, and noticeable by how precisely located it was ~ I could point to exactly where it is within an inch. Peoples intestines ( large and small ) are everywhere (!) so damage from gluten can appear in the most odd places.  But also, the places that ulcerated or nearly ulcerated became somewhat sensitive to acids and spicy foods and so pain can continue, to a lesser extent, even after you have stopped eating gluten. In my case the pain is slow to build and slow to disappear, but normally will build through the day resulting in pain in the evenings that disappears overnight. This is simply as the food is passing through the intestines which starts five or so hours after you have eaten. Pain can also be activated by simple exercise because you are literally disturbing areas of the gut that are sensitive because they have been damaged. 

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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.