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

Extreme right abdominal pain... Did I get the right diagnosis?


beccs

Recommended Posts

beccs Newbie

Hi! So... this is sort of a long story. Props to you if you read it all and can actually help me. I'm 20, a college student. About 2 years ago, I started getting these sharp and achey abdominal pains  on my lower right side every once in a while; especially when I was walking around or being active. Sitting down and relaxing made the pain go away. About a year ago, I finally saw my doctor about it. She was so hell bent on it just being muscle pain and putting me on muscle relaxers. I went through an ultrasound for my ovaries to cross that out, a full abdominal ultrasound, and then finally an abdominal CT scan with dye.. had to drink the borium and all. Ick. Everything turned out normal and she continued to try and feed me medications that never helped. As the year went on... the pain got worse. I was finally referred out to a GI about 6 months ago. She blood tested me for Celiacs, Crohns, and lupus. Now, it's not the first time that lupus has ever occured to me. My eye doctor asked me about it when he diagnosed me with chronic dry eyes because I am so young, and then my skin doctor mentioned it once the butterfly rash began showing on my face. Just small things, no biggie. I was also administered a HIDA scan and she checked my gall bladder and liver again. Once again, everything came back normal. She mentioned that my lupus test was "borderline" but still negative, and celiacs came back 4 points over the average limit.. positive. I cant remember which one it was, though. So, I endured an endoscopy. Everything was normal, no polyps or inflammation, nothing. The biopsies even came back normal. I've been gluten free for almost 3 months now, and the pain has yet to go away. Actually, sometimes, the pain appears when I haven't eaten in 6+ hours. Other times, it occurs right after I eat. But now, nothing can stop the pain. Not even lying down. Multiple times, it has even woken me up in the middle of the night and has hurt so badly to the point where I feel like i'm going to puke. It doesnt have a set pattern.. sometimes it will happen every day for a couple weeks, other times, i'll be fine for a month straight. But Days like today, the pain can last for 8+ hours and never subsides. Other than that, I didn't possess any other symptoms when I ate gluten. No upset stomach. No Bloating. No constipation or diarrhea... absolutely nothing. 3 weeks ago, I had a really bad cold and I ended up cheating and eating a package of ramen because when you're in college and broke... you can't afford or have the time to go huntimg for a 5 dollar can of soup. But I had no issues. My side didn't hurt, my stomach again didn't seem bothered, i was completely unphased.  I'm just not sure about my body at this point and am beginning to lose hope. Any thoughts..? Is it normal for people with celiacs to only have low right abdominal pain and nothing else? 


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



Celiac.com Sponsor (A8-M):



SmilingPolitely Newbie
On 3/1/2016 at 2:48 PM, beccs said:

Hi! So... this is sort of a long story. Props to you if you read it all and can actually help me. I'm 20, a college student. About 2 years ago, I started getting these sharp and achey abdominal pains  on my lower right side every once in a while; especially when I was walking around or being active. Sitting down and relaxing made the pain go away. About a year ago, I finally saw my doctor about it. She was so hell bent on it just being muscle pain and putting me on muscle relaxers. I went through an ultrasound for my ovaries to cross that out, a full abdominal ultrasound, and then finally an abdominal CT scan with dye.. had to drink the borium and all. Ick. Everything turned out normal and she continued to try and feed me medications that never helped. As the year went on... the pain got worse. I was finally referred out to a GI about 6 months ago. She blood tested me for Celiacs, Crohns, and lupus. Now, it's not the first time that lupus has ever occured to me. My eye doctor asked me about it when he diagnosed me with chronic dry eyes because I am so young, and then my skin doctor mentioned it once the butterfly rash began showing on my face. Just small things, no biggie. I was also administered a HIDA scan and she checked my gall bladder and liver again. Once again, everything came back normal. She mentioned that my lupus test was "borderline" but still negative, and celiacs came back 4 points over the average limit.. positive. I cant remember which one it was, though. So, I endured an endoscopy. Everything was normal, no polyps or inflammation, nothing. The biopsies even came back normal. I've been gluten free for almost 3 months now, and the pain has yet to go away. Actually, sometimes, the pain appears when I haven't eaten in 6+ hours. Other times, it occurs right after I eat. But now, nothing can stop the pain. Not even lying down. Multiple times, it has even woken me up in the middle of the night and has hurt so badly to the point where I feel like i'm going to puke. It doesnt have a set pattern.. sometimes it will happen every day for a couple weeks, other times, i'll be fine for a month straight. But Days like today, the pain can last for 8+ hours and never subsides. Other than that, I didn't possess any other symptoms when I ate gluten. No upset stomach. No Bloating. No constipation or diarrhea... absolutely nothing. 3 weeks ago, I had a really bad cold and I ended up cheating and eating a package of ramen because when you're in college and broke... you can't afford or have the time to go huntimg for a 5 dollar can of soup. But I had no issues. My side didn't hurt, my stomach again didn't seem bothered, i was completely unphased.  I'm just not sure about my body at this point and am beginning to lose hope. Any thoughts..? Is it normal for people with celiacs to only have low right abdominal pain and nothing else? 

I just joined this site, so please forgive me if I don't have a clue what I'm doing. I had a similar pain, strongest on the right side of my abdomen, and sometimes I couldn't stand up straight. I was having other symptoms that I didn't know were symptoms at the same time and lost my job because I just couldn't think clearly, couldn't complete simple tasks.

Now, I don't know your insurance situation, but it sounds like you've been going to doctors who haven't listened to what you're telling them. Happens SO often, especially if you have less than traditional or seemingly random symptoms.

It might be obvious that I'm rooting for a new, better doctor(s) for you because three weeks ago I was diagnosed with celiac disease, and although the pain's still there (I was warned that it would take awhile), I have hope after 5 years of suffering. There ARE doctors out there who don't just shrug and say "I dunno".

Of course, you have to find one...

cristiana Veteran

Hello both.

Beccs - is there any chance that it could be a grumbling appendix, as we call it here in the UK?

Smiling Politely, can you be more specific as to which quadrant this pain is appearing in?

 Open Original Shared Link

As a sufferer of mystery chronic lower left quadrant pain I extend my sympathies to you.  It is very frustrating.

Irene Joanne Explorer

As a child I had a grumbling appendix- horrible stomach pain for months before doctors figured out it was my appendix. 

cristiana Veteran
1 hour ago, Irene Joanne said:

As a child I had a grumbling appendix- horrible stomach pain for months before doctors figured out it was my appendix. 

I think this is definitely worth looking into - have the doctors done this, Beccs?   

frieze Community Regular

lol, chronic appendicitis was my first thought.  doesn't mean you don't have celiac, as well.

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

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

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

    emoryprose
    Newest Member
    emoryprose
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.