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

Pain And Spasms On Upper Left Side


SarahJimMarcy

Recommended Posts

SarahJimMarcy Apprentice

Hi everyone!

 

I went gluten free two years ago following a diagnosis of celiac.

 

The past six weeks, though, I have had pain and spasming in the upper abdominal area. I also have nausea. I have had the "flu" twice in September, once needing IV fluids.

 

I have had an x-ray, bone scan and CT - all normal findings. Blood counts are also normal.

Any ideas? My internist is suggesting an upper endoscopy.

 

I appreciate any suggestions. I know the vast amount of knowledge held within this forum!

 

Thank you!

 

 


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

Hi everyone!

 

I went gluten free two years ago following a diagnosis of celiac.

 

The past six weeks, though, I have had pain and spasming in the upper abdominal area. I also have nausea. I have had the "flu" twice in September, once needing IV fluids.

 

I have had an x-ray, bone scan and CT - all normal findings. Blood counts are also normal.

Any ideas? My internist is suggesting an upper endoscopy.

 

I appreciate any suggestions. I know the vast amount of knowledge held within this forum!

 

Thank you!

Hernia?

SarahJimMarcy Apprentice

I've got a partial answer, figured out by my chiropractor. I had a rib out of place. One treatment made a difference. If anyone in the Twin Cities needs a good chiropractor, who is gluten-free by the way, see Dr. Berg at Open Original Shared Link

 

Now, it is the nausea to figure out. I think I need to give up dairy and sugar. But Dr. Berg also suggested I be tested for Lyme.

 

I think having gone undiagnosed for so many years makes me immediately jump to the conclusion that it's more GI problems. Never occurred to me that it would be skeletal!

LauraTX Rising Star

You said the pain is in your upper left side of your abdomen, any pain on the right side?  That is where your gallbladder is, I have gallbladder polyps and they cause pain and nausea like the dickens when they decide to act up after I eat certain foods.  The pain is mostly in the upper right quadrant, but I get phantom pains in the upper left and lower right quadrant as well, and it will also cause crushing chest pains.  If your doctor is him-hawwing about what to do with you, maybe ask to get an abdominal ultrasound before they send you off for the more invasive and expensive endoscopy.  I also agree that seeing a chiropractor or D.O. (osteopathic doctor) for an adjustment check up may help as well, sometimes pain radiates to weird places.

 

Also, I had a CT done right before my ultrasound, and it did not detect the gallbladder polyps, only the US did.  Weird right?

Weeber47 Newbie

After I started having sharp pain, chest pain, and generally discomfort on my upper right side I had to have my gall bladder removed in May of this year. I agree that an ultrasound first to see what's going on underneath is a better idea than starting with the endoscopy. They are painful and very uncomfortable when results could be found with an ultrasound.

shadowicewolf Proficient

After I started having sharp pain, chest pain, and generally discomfort on my upper right side I had to have my gall bladder removed in May of this year. I agree that an ultrasound first to see what's going on underneath is a better idea than starting with the endoscopy. They are painful and very uncomfortable when results could be found with an ultrasound.

An ultrasound showed that my gallbladder was "normal", as did the blood tests. A HIDA scan showed it was working at 5%.

Weeber47 Newbie

An ultrasound showed that my gallbladder was "normal", as did the blood tests. A HIDA scan showed it was working at 5%.

 

Did they do an ultrasound of the affected area?


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

Did they do an ultrasound of the affected area?

Yes they did. Nothing was found and it looked "normal".

  • 5 weeks later...
SarahJimMarcy Apprentice

More answers, though partial. Shadowicewolf: You were right: it is a hiatal hernia.

 

I had my gall bladder out 16 years ago, so it can't be that. But I would like to have an ultrasound on the left side to see if anything's inflamed.Throwing up bile seems like more than a hernia? The endoscopy was not fun - glad that's over!

 

I am going to try Lactaid this week and see if that helps with the nausea. Also taking Prilosec. I'd rather do things naturally, but I don't want to feel bad any longer. 

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 commented on Scott Adams's article in Ataxia, Nerve Disease, Neuropathy, Brain Damage and Celiac Disease
      2

      Could Gluten and Alzheimer’s Be Linked? New Research Uncovers Surprising Protein Parallels (+Video)

    2. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    3. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    4. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    5. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

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

    • Total Members
      132,834
    • Most Online (within 30 mins)
      7,748

    SamAlvi
    Newest Member
    SamAlvi
    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)

  • Upcoming Events

  • Posts

    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
×
×
  • 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.