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

Gluten Intolerance Without Your "typical" Stomach Symptoms


not4sakn

Recommended Posts

not4sakn Newbie

I'm new to the forum and had a few questions regarding your own personal experience with gluten sensitivity/celiac and the symptoms surrounding it.

 

Is it possible to have gluten sensitivity without the typical stomach symptoms such as bloating, pain, gas, vomiting, diarrhea etc...?

 

I've read numerous articles on gluten and the whole host of symptoms surrounding it. I'm just curious how many actually suffered from neurological issues with very minimal to no stomach issues what so ever.

 

Over the past 5 years I've been suffering with symptoms that no doctor can seem to put their finger on. I've had countless tests and even a celiac biopsy which came back negative. 

 

My symptoms began with brain fog, pressure like head feeling, and visual floaters. Over the years its progress to constant neck pain, random facial tingling, mild dizziness, difficulty concentrating, memory issues, insomnia, anxiety, pounding heartbeat in my head and with all the many tests I've had done, the doctors say I'm healthy! lol

 

While that's great news my symptoms aren't normal and I recall a period in my life that I enjoyed life, things were great and my outlook positive. That's been quite a while since I can honestly say that but I haven't given up hope.

 

Many doctors brush off the likelyhood of celiac/gluten intolerance because I have no stomach issues. Sure I have mild reflux from time to time but nothing major. Could all these neurological symptoms be a direct result of gluten while my stomach remains "unharmed/untouched" by it? 

 

Thanks for your replies!


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Welcome to the board. 

 

Is it possible to have gluten sensitivity without the typical stomach symptoms such as bloating, pain, gas, vomiting, diarrhea etc...?

 

I've read numerous articles on gluten and the whole host of symptoms surrounding it. I'm just curious how many actually suffered from neurological issues with very minimal to no stomach issues what so ever.

 

 

Stomach issues aren't always the main problem for people. I did have some stomach issues (bloating and pain) that were getting harder to ignore but for the first 30 years of my life, they were merely an inconvenience. I never had vomiting or "d". Migraines were a major symptom for me and I developed a lot of arthralgias that affected my life. It had an effect on my cognitive function too. And then there were minor irritating symptoms like hair loss and such. I believe there are around 300 symptoms of celiac disease, only a few are GI related.

 

That all being said, a celiac's stomach is not left unharmed even if you aren't feeling it (not many nerves in there). Damage would happen to the villi.  If no damage is occurring, you would be classified as non-celiac gluten intolerant (NCGI) which means you would have the possibility of experiencing all the same symptoms that a celiac does, but would not have intestinal damage (so all celiac blood tests would be negative).

 

Sounds like you should be tested....

not4sakn Newbie

Welcome to the board. 

 

 

Stomach issues aren't always the main problem for people. I did have some stomach issues (bloating and pain) that were getting harder to ignore but for the first 30 years of my life, they were merely an inconvenience. I never had vomiting or "d". Migraines were a major symptom for me and I developed a lot of arthralgias that affected my life. It had an effect on my cognitive function too. And then there were minor irritating symptoms like hair loss and such. I believe there are around 300 symptoms of celiac disease, only a few are GI related.

 

That all being said, a celiac's stomach is not left unharmed even if you aren't feeling it (not many nerves in there). Damage would happen to the villi.  If no damage is occurring, you would be classified as non-celiac gluten intolerant (NCGI) which means you would have the possibility of experiencing all the same symptoms that a celiac does, but would not have intestinal damage (so all celiac blood tests would be negative).

 

Sounds like you should be tested....

Thanks for the reply! I was tested via biopsy which was negative for intestinal damage. Like you said, that doesn't mean I'm not gluten intolerant which from my understanding there is no test for. 

 

The only way to actually confirm this is to eliminate all gluten from your diet for atleast 2 months. I've read testimonies were some noticed positive changes within days. While others went through a detox period where symptoms worsened for weeks before they ever got better. "The storm before the calm" as some put it. This period took some close to 2 months to start noticing relief but everyday showed new signs of hope.

nvsmom Community Regular

Some doctors think the anti-gliadin antibodies tests (AGA IgA and AGA IgG) can be used for gliadin (gluten) sensitivity tests in both celiacs and those with NCGI BUT this is not a widely accepted idea and those tests are not the most reliable.  This report discusses it a bit on pages 10-12:  Open Original Shared Link

 

I'm glad you knew that it can take months to see improvemnets! Many expect improvements within a day or so, which can be true for some symptoms but not all, or even most.

WinterSong Community Regular

What's scary about Celiac is that most any symptom you can think of can be Celiac-related - even having no symptoms! I have a Celiac friend whose only symptom is joint pain. And another friend who has neurological symptoms (she wasn't tested, so we don't know if she has Celiac or a gluten intolerance).

 

Don't rule out Celiac just because you aren't having the traditional symptoms. I personally believe that Celiac should be a routine test for everyone that is done during yearly physicals. 

not4sakn Newbie

Thanks for replying.

I'm not ruling out Celiac. I'm saying I had a biopsy done which was negative. Doesn't mean I'm not highly intolerant.

I've also noticed a skin rash in my groin area. This comes and goes intermittently. My dermatologist gave me a steroid cream which helps but it always comes back. He says it's from sweat. I'm extremely clean, shower at least once a day and do not sweat much at all. This with all my other symptoms leads me to think it's gluten related.

GottaSki Mentor

Thanks for replying.

I'm not ruling out Celiac. I'm saying I had a biopsy done which was negative. Doesn't mean I'm not highly intolerant.

I've also noticed a skin rash in my groin area. This comes and goes intermittently. My dermatologist gave me a steroid cream which helps but it always comes back. He says it's from sweat. I'm extremely clean, shower at least once a day and do not sweat much at all. This with all my other symptoms leads me to think it's gluten related.

Have you had a recent complete celiac antibody panel or nutrient blood tests?

If not, IMO it would be wise to have them run and then remove all gluten for at least three months...longer is better...especially with non-digestive symptoms as the digestive symptoms are often the first to improve while other symptoms can take a very long time to improve.

Good luck to you :)


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



Celiac.com Sponsor (A8-M):



not4sakn Newbie

Would someone who's only gluten intolerant take as long to get well compared to a celiac with intestinal damage? 

 

When I had an intestinal biopsy the tests was negative for celiac. If there's no damage why would someone that's only gluten intolerant take as long to show signs of improvement if gluten is the culprit? I'm talking 6-8 weeks or more to see change?

frieze Community Regular

Open Original Shared Link   and check out anything else by Dr hadjivassliou.  good luck

Would someone who's only gluten intolerant take as long to get well compared to a celiac with intestinal damage? 

 

When I had an intestinal biopsy the tests was negative for celiac. If there's no damage why would someone that's only gluten intolerant take as long to show signs of improvement if gluten is the culprit? I'm talking 6-8 weeks or more to see change?

  • 2 weeks later...
not4sakn Newbie

So after more research I discovered that while the foods I'm eating are gluten free there could be cross contamination issues. 

 

I make home-made pico de gallo and guacamole which I love! I eat Tostitos multi-grain scoops which on Frito's website it's listed as a gluten free food. However, it goes on to mention that while it doesn't contain gluten it could be manufactured on the same equipment that has gluten in them.

 

This is very disheartening. It seems all my good efforts could possibly be in vain. I'm trying so hard to see if this diet helps and all the while I'm still possibly eating food with the very thing in it thats making me feel bad.

 

I read every label carefully and it seems this is all we have to go off of and yet that isn't enough. 

 

If I have been cross contaminated does this mean everything starts over since I truly havent been gluten free? Could it still take 2-4 months to see real huge differences if gluten is the culprit for me?

notme Experienced

i eat tostitos all the time and they are gluten-free :)  are you maybe having a reaction to corn?  sometimes when we take out the (obvious) gluten, we have a reaction to something else.  i have a secondary sensitivity to soy, which i didn;t figure out until i removed the gluten and my system started to settle down.  use a food journal, maybe.  also, have you replaced your 'old' (possibly with embedded gluten) cutting board(s), wooden spoons, etc ? 

not4sakn Newbie

On their website it says its manufactured on the same equipment containing gluten foods. That's what caught my attention.

 

My cutting boards are the thick plastic ones. Most of my spatulas, spoons, etc.. are also plastic. I do have a few bamboo ones that are hardly used. 

 

I haven't cut dairy out completely but I don't eat it often anyways. Every now and then I'll have cheese on a sandwich or a taco but that's it. 

 

The thing is, I don't know if gluten is causing all this or not. I was tested for celiac via biopsy and it was negative which doens't mean anything really just that I don't have celiacs disease. I don't know what to cutout to see what makes a difference. At this point I'm willing to try anything. 

GFinDC Veteran

Hi Not,

 

Welcome to the forum! ;)

 

Did you get a copy of the pathology report for your endoscopy?  Some members might be able to interpret that for you.  I think the  current recommendation is to take 4 to 6 biopsy samples but maybe it is 6 to 8, not sure really.  Anyway, the reason for multiple samples is the damage in celiac might not be universally present.  So it could be missed with a single sample, which is what some GI's do it seems.  You'll probably need to ask your GI how many biopsy samples he took to find out for sure.

 

You might want to read up gluten ataxia.  Gluten ataxia is when the brain is affected by eating gluten.  I think it was Dr. H. referenced earlier that did a study showing that patients with gluten ataxia may not show any damage to the gut.  Nerve cells grow slowly, so healing nerve related issues can take months to years.

 

You could try mission brand corn chips and corn tortillas if you are concerned about the Tostito''s brand.  Mission brand corn tortillas are made on dedicated lines.  I am not sure their chips are on dedicated lines but I've never had a problem with them.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,025
    • Most Online (within 30 mins)
      7,748

    Amari Love
    Newest Member
    Amari Love
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.