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... Do I Need To Go To A Doctor?

Brrrandy

By Brrrandy
in Coping with Celiac Disease

Recommended Posts

Brrrandy Rookie
Brrrandy
Posted

I was glutened over a month ago, and ever since I have had symptoms that seem to be sticking around. Normally I feel off for a few weeks, but it's been a while now and I'm starting to get worried. I have had stomach pain that varies in its intensity in a very specific spot on the low right of my abdomen, GI upset, feeling really exhausted. It is almost always there though... either a mild dull pain or a more severe sharp or dull pain. Many other small things but those are the main issues. When I massage the area that is hurting, I can feel almost like a lump or blockage that goes away after I massage it. I've read some things about the ileocecal valve, could I just be experiencing problems with that?

I don't have health insurance right now, so I don't want to waste a trip to the doctor to be told nothing. At the same time, the stomach pain is worrying me. Is this just normal for some of you after being glutened, something that will get better on it's own eventually? Is there something I could be doing to help myself recover faster? Or should I be trying to find a way to get to a doctor?

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

Celiac.com Sponsor (A8-M):


shadowicewolf Proficient
shadowicewolf
Posted

Oh dear, low right is an interesting area. It could be your appindix thats acting up, or it could be the gallbladder (though it sits up higher).

I would go in just for peace of mind if nothing else. If it was a glutening, i'd think it would have started to ebb away by now.

Brrrandy Rookie
Brrrandy
Posted
  • Author

Thanks for the input... if it was appendicitis wouldn't it be more sudden then gradual over the course of a month, with no fever?

Oh dear, low right is an interesting area. It could be your appindix thats acting up, or it could be the gallbladder (though it sits up higher).

I would go in just for peace of mind if nothing else. If it was a glutening, i'd think it would have started to ebb away by now.

L.J. Rookie
L.J.
Posted

Hi Brrrandy! I looked up appendicitus...Open Original Shared Link Here is a link that tells you symptoms--The appendix is not something to "discount"--medical attention is needed if you fit these symptoms! :rolleyes:

As we know--we get worried when we have symptoms that are unusual--Have you had similar pain like this before? Do you have a low grade fever? Are you able to walk without pain? Keep us in the loop, OK? :)

shadowicewolf Proficient
shadowicewolf
Posted

Very possible for it to act up with no fever, just like its possible for it to be gradual.

L.J. Rookie
L.J.
Posted

Shadowicewolf you are soooo right! :D

I wish, Brrrandy, you had someone to check you out! To rule out the "biggies" regarding your stomach pain!!!

Brrrandy Rookie
Brrrandy
Posted
  • Author

Thanks guys. I am going to explore my options for visiting a doctor and I'll keep you updated!

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

Celiac.com Sponsor (A8-M):


ravenwoodglass Mentor
ravenwoodglass
Posted

Pain in that area could also be ovarian in nature. If you have a Planned Parenthood clinic in your area they have a sliding fee scale or possibly no fee. They might also be able to guide you to a clinic that could help if that is needed.

If the pain gets really severe go to the ER and contact the hospitals billing dept.afterward. Most can help folks without insurance either with a sliding fee scale or payment plan. If it should be your appendix you really don't want it to burst.

mamaupupup Contributor
mamaupupup
Posted

Hang in there! I also vote for going to a doctor. I had (and have) similar pain which I brought up numerous times (before and after I was diagnosed Celiac). Doctors palpated and didn't come up with anything. This went on for seven years. This summer I got diagnosed Celiac and had a colonoscopy which removed a pre-cancerous polyp. My brother died this year unexpectedly at 41 of a heart attack. Only after this truly horrible set of events did my primary care physician take my abdominal pain seriously and ordered an ultrasound. Turns out I have gall stones. My pain is rarely so bad that I feel I need to see a doctor, so I'm not planning to remove my gall bladder at this point (and will try to keep it!).

I do think seeing a doctor would be good to rule out all the ob/gyn stuff and anything life-threatening and may give you more peace of mind!

Wishing you well!

Lady Eowyn Apprentice
Lady Eowyn
Posted

Hi Brrrrandy

I had lower right pain a few years ago (pre- gluten-free) - it would not go away. Put up with it for several days until I became worried it wasn't going.

The doctor sent me straight to hospital as suspected appendicitis (had to go straight there). Pain could be felt by pressing the area. Appendicitis can be very dangerous if left untreated.

They tested me for everything (ultrasound, x-rays) but found nothing - pain worse laying around in hospital being given toast to eat!!

After 3 days went home - I think it was a version of constipation ( :ph34r: ) I'm ashamed to say and 2 days of laxatives cured me!

I would suggest a doctor visit to rule out anything.

Archived

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

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


  • Member Statistics

    • Total Members
      131,948
    • Most Online (within 30 mins)
      7,748
    Stephanie94
    Newest Member
    Stephanie94
    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

    • Jacki Espo
      Covid caused reoccurrence of DH without eating gluten

      By Jacki Espo · Posted

      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      New Celiac Mama in My 30s

      By Mari · Posted

      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      My only proof

      By Mari · Posted

      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
      Does anyone here also have Afib

      By knitty kitty · Posted

      Fascinating.
    • DebJ14
      Does anyone here also have Afib

      By DebJ14 · Posted

×
×
  • 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.