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

Which Kind Of Arthritis Is Related To Celiac?

mythreesuns

By mythreesuns
in Coping with Celiac Disease

Recommended Posts

mythreesuns Contributor
mythreesuns
Posted

The arthritis in my foot is what finally sent me over the edge and prompted me to start the gluten free diet. The story is longer than that I assure you, but anyway...

The dr thought I originally thought I had gout, which is of course food-related, but is it related to celiac? I had thought only rheumatoid arthritis was related, but after a negative blood test for gout and looking at the x-ray, the dr it looked like mild osteoarthritis, which of course I am a little young for (33).

He said it could still be gout, but the question remains, are all types of arthritis related to celiac, or just some?

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

Celiac.com Sponsor (A8-M):


ravenwoodglass Mentor
ravenwoodglass
Posted
The arthritis in my foot is what finally sent me over the edge and prompted me to start the gluten free diet. The story is longer than that I assure you, but anyway...

The dr thought I originally thought I had gout, which is of course food-related, but is it related to celiac? I had thought only rheumatoid arthritis was related, but after a negative blood test for gout and looking at the x-ray, the dr it looked like mild osteoarthritis, which of course I am a little young for (33).

He said it could still be gout, but the question remains, are all types of arthritis related to celiac, or just some?

Although the symptoms of my arthritis were more like RA than osteo they also told me it was osteo. The joint damage never changed but my pain level has. I can use all joints freely with no discomfort and no continuation of the rapid joint destruction I had pre gluten free. I believe many forms of arthritis can be linked to celiac and the inflammatory process it creates in the tissues.

2kids4me Contributor
2kids4me
Posted

My son had joint/leg pain that disappeared after going gluten-free, he still has flare ups when he gets a cold or something like that. The endo explained it this way: any autoimmune process can cause inflammation ion the joints, the cells that line the joints to become inflammed in response to the systemic autoimmune reaction - causing pain. The endo said that if joint pain was symptom of celiac for my son then in the future - any illness could cause the same reaction. she did howver review the symptoms and signs to be alert for for RA (this is the form of arthritis associated with other immune mediated diseases).

Redness, swelling over a joint, unexplained fevers, leg pain in the morning (as opposed to aches after a busy day)

penguin Community Regular
penguin
Posted

My mom had osteo in her knees (SEVERE) before she got her knees replaced (she's really young, only in her early 50's) and she says that she avoided wheat because it made her arthritis worse. As far as we know, she doesn't have celiac (though she hasn't been tested yet).

Rheumatoid arthritis is the one associated with celiac because they're both autoimmune. Osteoarthritis is more of a mechanical problem, as I understand it.

mythreesuns Contributor
mythreesuns
Posted
  • Author

Ok, why can I see this on the forums page under "last post info" but I don't see it when I click on the Message Board???

Well, anyway, thanks for the replies! My dr of course isn't discussing celiac with me because I couldn't have because it's just too rare... :blink:

penguin Community Regular
penguin
Posted
Ok, why can I see this on the forums page under "last post info" but I don't see it when I click on the Message Board???

Well, anyway, thanks for the replies! My dr of course isn't discussing celiac with me because I couldn't have because it's just too rare... :blink:

:o

Geeze, doctors. Just because you go to medical school and graduate doesn't mean that the medical world stops spinning and all facts remain static :rolleyes: Bring him some of the latest research articles showing that celiac disease occurs in as many as 1 in 133 people...

ravenwoodglass Mentor
ravenwoodglass
Posted
Ok, why can I see this on the forums page under "last post info" but I don't see it when I click on the Message Board???

Well, anyway, thanks for the replies! My dr of course isn't discussing celiac with me because I couldn't have because it's just too rare... :blink:

It can take a while for the new topic to show up, but it will.

You should print out the NIH websites info on celiac and bring it into your doctor. It is not rare and he needs to politely educated.

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

Celiac.com Sponsor (A8-M):


Archived

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

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

  • Member Statistics

    • Total Members
      133,344
    • Most Online (within 30 mins)
      7,748
    Scottweath
    Newest Member
    Scottweath
    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

    • Churley
      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

      By Churley · Posted

      Have you tried Pure Encapsulations supplements? This is a brand my doctor recommends for me. I have no issues with this brand.
    • asaT
      Supplements for those Diagnosed with Celiac Disease

      By asaT · Posted

      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
      Supplements for those Diagnosed with Celiac Disease

      By asaT · Posted

      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
      Insomnia help

      By nanny marley · Posted

      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
      nothing has changed

      By nanny marley · Posted

      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 
×
×
  • 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.