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

Stomach Pain & Nausea


horsegirl

Recommended Posts

horsegirl Enthusiast

I've now been back on gluten for about 6 weeks, while undergoing blood tests, Enterolab tests,

& an EGD/biopsy (next week). As I continue to eat gluten, not only are my fibromyalgia symptoms getting worse (muscle/joint pain, fatigue, weakness), as well as the obvious intestinal distress (gas,

D, bloating, etc), but I've had several episodes of nausea, sharp stomach pains (not intestinal), lack of

appetite yet feeling like I'm starving, & dizziness.

Has anyone else had these? I thought it would be contained in the lower GI/intestinal area.

Any help is appreciated! Thanks!

P.S. I really hate gluten right now & can't wait to go off it again, permanently!


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



Celiac.com Sponsor (A8-M):



Guest kivmom3

Did the doctor make you go back on gluten items for blood tests and endoscopy? YIKES! I haven't had an endoscopy to confirm yet, if i have to gluten myself for it, i may tell the doctor, no thanks check me now while i've been gluten-free for 6 weeks and feeling slowly better.

Anyway, I get major muscle/joint pain, depression, cranky, nausea, and lack of appetite as well. There are times I feel so hungry yet can't eat since i'm too nauseated! Sometimes my symptoms last a few days or a few hours depending on how much I glutened myself I'm thinking. Of course need not to mention the major GI distress i have, just awful.

I hope you feel better soon and get those tests done ASAP so you can start feeling better!!!! :)

Gg

L.A. Contributor
I've now been back on gluten for about 6 weeks, while undergoing blood tests, Enterolab tests,

& an EGD/biopsy (next week). As I continue to eat gluten, not only are my fibromyalgia symptoms getting worse (muscle/joint pain, fatigue, weakness), as well as the obvious intestinal distress (gas,

D, bloating, etc), but I've had several episodes of nausea, sharp stomach pains (not intestinal), lack of

appetite yet feeling like I'm starving, & dizziness.

Has anyone else had these? I thought it would be contained in the lower GI/intestinal area.

Any help is appreciated! Thanks!

P.S. I really hate gluten right now & can't wait to go off it again, permanently!

When you go back to gluten free you should feel a lot better but it may take a while for your system to recover. I noticed the name "horsegirl"...do you have horses? I spend a lot of time at the barn and have to be careful around the feed etc for the horses to avoid being glutened there--just a thought. Hope you're better soon. L.A.

horsegirl Enthusiast

No horses at this time, but I love them! I hope to eventually live someplace where we can have some;

in the meantime I have to enjoy them when others' have them! (I recently fell in love with a 2 month old Friesian filly; she was like a lapdog she was so sweet! But, that doesn't work in a subdivision!)

Thanks for the info about needing to be careful around horse feed though; is that because of CC from oats etc being on the hands & then potentially making its way into your mouth?

Have a great day!

-M

horsegirl Enthusiast

Yes, the doctor suggested I go on a gluten "trial" while being tested for celiac. I had been off gluten for about 5 months, because I'd learned people with fibromyalgia & arthritis respond well with elimination diets, so I stumbled upon "gluten free" living by accident. After I did more research, I learned about celiac, which I'd never heard of before. I decided I had enough symptoms to warrant being tested, so saw my primary doc. The blood tests through Prometheus were all negative (including the gene tests), but not surprisingly since I'd only been back on gluten for 3 weeks then, so the antibodies would have been negative. I'm waiting on test results from Enterolab, since you can be gluten free for up to a year & still test positive for gluten intolerance. I'll be glad to get the biopsy & be done with gluten. I'll keep everyone posted as I learn more. Good luck with your testing too!

-M

L.A. Contributor
No horses at this time, but I love them! I hope to eventually live someplace where we can have some;

in the meantime I have to enjoy them when others' have them! (I recently fell in love with a 2 month old Friesian filly; she was like a lapdog she was so sweet! But, that doesn't work in a subdivision!)

Thanks for the info about needing to be careful around horse feed though; is that because of CC from oats etc being on the hands & then potentially making its way into your mouth?

Have a great day!

-M

Yes. I usually wear leather gloves at the barn mainly because I would never stick a gloved-finger in my mouth. Then I can remove my gloves and wash my hands before I eat anything. I live in a subdivision too and keep the bad ponies at a stable close by. Take care.

SUZ42 Explorer

Terrible stomach pains/cramps and incredible nausea were my most distressing physical symptoms. I would also litterally have to eat every 2 hours because of the intense hunger. Yet I lost weight. I had to tell the doc it is the actual stomach, not my intestines. When I would say stomach, the docs would automatically think I was talking about abdomen. I am glad to report that I am no longer having the stomach pain/nausea. And I am also no longer starving to death. If that, alone, was all that was "fixed" by my going gluten free it would be enough to keep me on this diet for life. Anyway, it has been 4 1/2 months gluten-free and when people ask how I am, I honestly answer them Great! I can't wait to have bloodwork drawn again to see how my thyroid and iron def anemia are doing. :D


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



Celiac.com Sponsor (A8-M):



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.