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

Need Advice! Lower Right Abdominal Pain.


MichelleBell

Recommended Posts

MichelleBell Newbie

Hey All!

Just a background - I'm 26 and a runner, and eat very clean. Three years ago I started experiencing sharp cramp like, stabbing pains when I ate certain foods. My family doctor thought it was my gallbladder not processing fatty foods, but the thing was, I really didn't eat that much fatty food. If I did eat a pizza or something, it would for sure happen, but other times it would just be because of a sauce (no BBQ sauce, no alfredo, no Chinese food, etc.). He did some tests and told me I should get my gallbladder out, despite my young age (I was the 10th one he recommended that week, after all). Well (thankfully) I took the advice of a co-worker and went to a specialist who said I absolutely should not get my gallbladder taken out. She gave me Sucralfate, which is actually a med for ulcers, and it seemed to help. I also tried to limit things in my diet that were giving me acid reflux like symptoms (not sure if they were both related or not). I went a little while and life was back to normal, but a short while later I started having pains again. This time, it didn't seem to be linked to fatty/greasy foods, but to milk products. I switched to soy, and for awhile, life was good again. About 1/2 a year ago, I started having very severe pains again. This time, I thought it was the dairy again, but it started happening when no dairy was consumed. It wasn't my gallbladder, because the pain was on my left, not my right. I usually have pain every day, and upon researching, I thought maybe all of the whole grain foods I was eating was doing it to me. The pain is always, always accompanied by bloating, gas, and immediate and frequent trips to the rest room (so not fun, especially in training for my 1/2 marathon... please please let me get better before my race in June!!). I have also tracked problem foods to things such as Jimmy Johns subs, because of the bread, but upon even more research, I learned that there are two components to milk: the lactose part and the casein part. Even though I had switched to a lactose free diet, I had unknowingly still been consuming foods with milk derivatives. Processed meat has a high amount of a casein type protein in it. So now I feel like I am back to square one. Is it the wheat, or the milk? Sometimes I'll have a piece of wheat/pb toast, and no problems at all (so maybe wheat is OK). Other times, I'll try to sneak in some ice cream, and I'll actually be fine (so sometimes dairy is OK). I'm just so confused. Maybe my key is a food journal. Does anyone have any idea or suggestions? I am desperate for anything at this point!! I'm scared to go back to my doctor for fear he'll want to yank out some other organ, or just jump to conclusions. Thanks a ton!! Michelle

*Correction - Can't edit topic title now, but the pain is in my lower left abdominal, not right. Typically gall bladder pain is in the lower right.


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



Celiac.com Sponsor (A8-M):



debmidge Rising Star

I have had gallbladder issues and had to have mine removed. But this information on link is

interesting :

Open Original Shared Link

This doctor (gastro) concluded in JAMA that the gallbladder doesn't work properly in

some people and it doesn't mean that the gallbladder has to be removed at once. This doctor is in NJ and is published. If the link doesn't work then google habbasyndrome.com.

I have post gallbladder removal gas and diarrhea and I still have mild discomfort on my

right side near ribcage. I had gallbladder removed 8/07. I am severely lactose intolerant and have IBS. In my case, my gallbladder was "calcified" and was no longer working and bile was

entering into my bowel at irregular intervals - bile digests fats and is acidic and irritating to the stomach and bowels. Bile triggered worsening of my IBS symtoms so I was having diarrea

almost 24/7 BEFORE I had my gallbladder removed and lost 20 lbs. in a month. As my

gallbladder disease progressed, I had pain, tenderness in upper abdomen and in right back near "wing", and I was losing my appetite to the point of not eating and finding the smell of

food disgusting (a first for me in my life). I knew I had to get the gallbladder out asap.

After surgery the gallbladder was biopsied and it did not have cancer.

Generic Apprentice

I had to have my gall bladder taken out a year ago. I never had pain on the right side. My pain was always in the center of my chest just below my ribs, on the right side and on my back between my shoulder blades.

I also had a kidney stone on the left side, so that is a possibility for you too.

Ahorsesoul Enthusiast

About a year ago I was scheduled to have my gall bladder removed. Before doing the surgery I asked for a second opinion at the Mayo Clinic. I saw a specialist in gall bladder surgery for less than 15 minutes. He kept looking at me and said you sure don't look sick. lol

He looked at my x-rays which showed two stones. Both of which were small enough to pass and not to be a problem He told to if I had pain after eating a very fatty meal that lasted about 6 hours, it could be gall bladder pain. Then I should come in again. But he said he didn't think my pain had anything to do with my gall bladder. (Turns out the pain is from a hiatal hernia.)

It's easy to test if it's gall bladder pain. Eat a very fatty meal that does not contain gluten or dairy. Try lots of bacon. If it's gall badder you should be in pain within 30 minutes that will last for up to 6 hours.

Remember to if you ask a surgeon what should be done about a problem he's most likely going to suggest surgery. Always get a second opinion from someone who isn't going to be making money from your surgery.

Co-Pay at my local clinic: $30

Total Cost for 15 minutes with a specialist who wanted to do surgery: $235

Insurance covered: $48

I had to pay the rest out of my pocket for bad advice.

Co-Pay at Mayo: $30

Total Cost for 15 minutes with a specialist: $36

Insurance covered the $6

Saved from surgery: Priceless

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    5. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,084
    • Most Online (within 30 mins)
      7,748

    bigwave
    Newest Member
    bigwave
    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

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.