Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×

  • 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 Celiac.com!
    eNewsletter
    Donate

Noisey Stomach

Guest jhmom

By Guest jhmom
in Related Issues & Disorders

Recommended Posts

Guest jhmom
Guest jhmom
Posted

I just wanted to know if anyone else experiences "audible bowel sounds"?

If so, do you know what causes it and should I be worried?

Thank you.

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


mg5676 Newbie
mg5676
Posted

I also have a noisy stomach, I think it's just digestion & nothing to worry about, but that's only a guess.

Link to comment
Share on other sites
tarnalberry Community Regular
tarnalberry
Posted

I did, before going gluten-free. (It took me a while to realize it was gone, since it's not painful, or for me, very loud.) (Note, mine was specifically noise from the intestines, not stomach. My stomach seems to be very shy... ;-) )

Link to comment
Share on other sites
Guest jhmom
Guest jhmom
Posted

I thought it could be digestion too but it started in August 02 when I believe I was in a celiac disease crisis. I thought after going gluten-free the noise would have gone away but it hasn't. I have been gluten-free since Sept 03.

Yes mine is in my intestines, not my stomach and it's pretty loud!

Link to comment
Share on other sites
MySuicidalTurtle Enthusiast
MySuicidalTurtle
Posted

I have rather noisey insides, too. LOL.

Link to comment
Share on other sites
celiac2 Newbie
celiac2
Posted

At about 4 every morning I wake up with noisy intestinal sounds. It almost sounds and feels like my food is dropping right through me. I'm new to this, Dec. of this year, so I don't know what it is, but I have it too. Don

Link to comment
Share on other sites
seeking-wholeness Explorer
seeking-wholeness
Posted

Audible bowel sounds are often my first clue that I've had a gluten accident, with diarrhea following the next morning. My intestines are no longer noisy unless I've eaten gluten, though they used to gurgle pretty frequently. My stomach only growls when I'm very hungry!

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


sophias-dad Newbie
sophias-dad
Posted

For me, a noisy stomach is the first sign that I've ingested gluten. It doesn't seem to happen to me under normal circumstances. It's usually followed by bloating and gas.

Link to comment
Share on other sites
gf4life Enthusiast
gf4life
Posted

My intestines are very noisy when I am on gluten. As well as very bloated and I am extremely gassy(and it is very painful). This is one of the first things to go away when I am gluten-free, and one of the first to return with a gluten accident. I would think that if you continue to have these noises in your intestines (or stomach) that you may want to consult your doctor about it. You may be getting into a regular source of gluten contamination and not realise it. But I don't think it is supposted to be normal...

Mariann

Link to comment
Share on other sites
Guest jhmom
Guest jhmom
Posted

My intestines ALWAYS make that noise at any time during the day but I notice more at night when I am laying in bed. I am pretty sure I am 100% gluten-free, if I wasn't I would feel it, with doubled over pain, diarrhea, etc....

I have talked to my GASTRO doc and he wants to see me on Feb 5th. The only thing is he is not accepting Dr. Fine's diagnosis. Which I really don't care I know his disgnosis is correct and I will stick to my gluten-free diet.

I don't know if any of you use www.webmd.com but I have in the past especially when checking Celiac Disease. In the search engine I typed Audible Bowel Sounds and it pulled up over 100 links regarding LUPUS! Talk about freaking me out, honestly it made me a little nervous.

This is why I want your opinions, to see if it is normal or worth checking out. Thanks for each reply, I really appreciate it (more than you know) :)

Link to comment
Share on other sites
SuJ Newbie
SuJ
Posted

My intestines rumble often also - my naturopath thinks I have a candida problem. Has anyone else had this suggestion made to them?

If you think the celiac disease diet can be rough you should try the B.E.Diet(Body Ecology Diet) This is a very strict diet designed to rid the body of harmful yeast. Most traditional doctors will find this idea laughable but ALL of my symptoms disappear when I am on the B.E.D. However, my will power fails after a few months and the rumbling returns when I add my dark chocolate and Apricot Biscuits back into my diet.

Feel Well and God Bless :D . Su

Link to comment
Share on other sites
MySuicidalTurtle Enthusiast
MySuicidalTurtle
Posted

I have the rumbeling no matter what I eat. . .I don't get sick or anything. If I eat a bigger meal it is louder. .. .I dunno. . .I think it is just the way I am.

-edit-Tonight, I had the rumbeling real bad and got so sick. Maybe I just never thought of being sick and the noise as coinsiding. . .hmmm. . .though, it does happen when I don't get sick, too. I think gf4life is on to something with the dairy. The cold medicene I am on has lactose in it and I took lactaid. . .I usually eat dairy in the day. . .this is all so interesting. . .hahahahaha-edit-

Link to comment
Share on other sites
gf4life Enthusiast
gf4life
Posted

Just curious, but how many of you with the rumbling, noisy tummies are still eating dairy products??

I was thinking about it, and I am casein sensitive as well as gluten intolerant, and I get the rumbling, gassy, bloating and noise when I eat dairy, even while 100% gluten-free.

Any of you still on dairy may want to just do a trial couple of days dairy free.

Mariann

Link to comment
Share on other sites
seeking-wholeness Explorer
seeking-wholeness
Posted

Mariann, excellent point! I am casein-free, but I forget to mention it anymore (can you believe that?!). That may very well be why tummy rumbling is so reliable a predictor of a gluten accident for me!

Link to comment
Share on other sites
  • 3 months later...
debmidge Rising Star
debmidge
Posted

My celiac husband always had intestinal sounds before going gluten-free; and still has them. My theory is that since he's been undiagnosed for 28 years, he probably has a good amount of villi damage and until that's cleared up he's going to get those rumbles. The rumbles do not result in loose bowel, just noise and some intestinal gas. As the "healthy" mate, I have to admit I get the "gubba-gubba's" as I calll them, every now and then and I am not celiac (as far as I know).

Link to comment
Share on other sites
  • 7 years later...
Bummed-out-Baker Newbie
Bummed-out-Baker
Posted

I thought it could be digestion too but it started in August 02 when I believe I was in a celiac disease crisis. I thought after going gluten-free the noise would have gone away but it hasn't. I have been gluten-free since Sept 03.

Yes mine is in my intestines, not my stomach and it's pretty loud!

I was my own walking slap stick comedy for five year olds--really lound, very gasey (but not gas) sounds. Very embarrassing. I"m just now getting diagnosed with Celiac, but in 2007 I cut out dairy and those sounds that plagued me since I was a kid, have almost disappeared. I only get them when I let myself have ice cream.

Link to comment
Share on other sites
  • 7 years later...
Mandie08 Newbie
Mandie08
Posted

I have hashimoto's thyroiditis and with all the symptoms of that have found that dropping milk helps the reflux. I have gone gluten free, started only 1 week ago, and although I feel slightly better I have a serious headache and my tummy makes these really loud noises like I'm hungry but I'm not!

Why? Is it my body getting used to gluten free?

Link to comment
Share on other sites
GFinDC Veteran
GFinDC
Posted
7 hours ago, Mandie08 said:

I have hashimoto's thyroiditis and with all the symptoms of that have found that dropping milk helps the reflux. I have gone gluten free, started only 1 week ago, and although I feel slightly better I have a serious headache and my tummy makes these really loud noises like I'm hungry but I'm not!

Why? Is it my body getting used to gluten free?

It sounds like you are starting the healing process from celiac damage.  It is not a quick thing and can take 6 months to 2 years or more.  Did you get tested for celiac disease?  You might still be able to get positive blood antibodies tests at this point, especially if you start eating a small bit of gluten each day.

It's really hard to go off gluten for a few months and then decide to get tested and have to go back on gluten for 12 weeks.  Some people don't make it through the gluten challenge because the symptoms are so bad.  Often they seem worse than before going gluten-free.

But if you have decided not to get tested then that's fine.   You can still go gluten-free for life.  The recovery process is more like 6 months to 2 years though.  And symptoms can come and go even if you aren't eating  gluten.

Link to comment
Share on other sites
  • 3 weeks later...
Kfw Newbie
Kfw
Posted
On 1/19/2004 at 11:24 PM, SuJ said:

My intestines rumble often also - my naturopath thinks I have a candida problem. Has anyone else had this suggestion made to them?

 

If you think the celiac disease diet can be rough you should try the B.E.Diet(Body Ecology Diet) This is a very strict diet designed to rid the body of harmful yeast. Most traditional doctors will find this idea laughable but ALL of my symptoms disappear when I am on the B.E.D. However, my will power fails after a few months and the rumbling returns when I add my dark chocolate and Apricot Biscuits back into my diet.

 

Feel Well and God Bless :D . Su

Are the biscuits gluten free they sound brilliant

Link to comment
Share on other sites

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      121,072
    • Most Online (within 30 mins)
      7,748
    SherryT
    Newest Member
    SherryT
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Fluka66
      Waiting for urgent referral.

      By Fluka66 · Posted

      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      14 year old with Celiac & EOE still suffering...

      By knitty kitty · Posted

      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      This forum might be the last hope I have in my life. Please I beg you

      By knitty kitty · Posted

      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      This forum might be the last hope I have in my life. Please I beg you

      By BluegrassCeliac · Posted

      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      14 year old with Celiac & EOE still suffering...

      By Scott Adams · Posted

      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
×
×
  • Create New...