Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Joint Pain


tbritt

Recommended Posts

tbritt Rookie

Last Friday, I suspect I ingested gluten some time that afternoon (although I'm not sure from what). I handled dog treats given to me by the bank and didn't wash my hands afterward. I think I had a snack just a bit later. I spent the dinner hour that night on the toilet (and had no appetite). The following day, I was dizzy and "hung over" feeling. On Sunday and Monday, I was also feeling extra tired. On Tuesday, my hand started hurting in the same place I had a tendon issue before Christmas. (I had taken an antibiotic that apparently can give folks tendonitis. Leave it to me to get tendonitis!)

I use my hands hours and hours a day for work. It's not uncommon for folks in my field to get tendon injuries. However, I feel like my issues resolve when I'm all the way gluten free. When I gave up gluten, I was battling joint pain in my shoulder and neck. It would come back when I got gluten. It seems to have completely resolved at this point.

I am diligently doing PT exercises to heal my hand again. I am taking vitamins. I am eating a very bland gluten free diet until I feel like I've shaken whatever got me.

Has anyone else had recurring tendon problems after gluten ingestion?

I am considering giving up dairy and soy, but I don't want to if I don't have to. (I find it hard to get enough calories otherwise.)

I have been gluten free for more than 18 months. I have never intentionally ingested gluten since I quit.


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



Celiac.com Sponsor (A8-M):



rosetapper23 Explorer

Yes, I can definitely affirm that I have had tendon problems as a result of eating gluten. Actually, I've experienced tendon and ligament problems since I was 11 years old, when my celiac was triggered. Most recently, when I was glutened (after seven years of eating gluten free) in April 2009, the tendons were so badly affected in my feet, I ended up with stress fractures in both feet within five weeks of the glutening occurrence. I was very disabled for more than a year. Six years ago, when I damaged the tendons in my left thumb during a fall (all the tendons detached from the base of my thumb), I met with an orthopedist who immediately asked me, "Oh, my God! What kind of muscular dystrophy do you have?!" I informed her that I didn't have MD; rather, I was born with celiac disease. My son and I used to have tendon pain in our wrists (similar to carpel tunnel pain), but that resolved after following a strict gluten-free diet. Slowly, the medical community is beginning to see a connection between celiac and musculoskeletal problems....but more studies need to be done.

mushroom Proficient

If you have been gluten free that long and still having problems, I would try getting rid of the soy first. Then try the dairy if that did not work. Soy is such a big problem for so many celiacs. I wish you pain-free strumming.

dilettantesteph Collaborator

I get terrible joint pain from low level gluten contamination. I finally figured out my latest and it is so nice to be able to bend my elbow without pain again!

UKGail Rookie

tbritt - my glutening symptoms are exactly like yours re dizzyness/hung over feeling, bathroom runs etc. Add in a migraine with neck pain too. In the 3 years before going gluten free I suffered from frozen shoulder (capsulitis and tendonitis) in both shoulders. The most recent one eventually led to my diagnosis. Although I have only been gluten free for 4 months, I have noticed that the migraine, neck and shoulder pain all flare up either slightly from what I assume may be low-level contamination, and majorly if I get a good dose of it. It's not much fun. I am now trying to be really strict on a basic meat and veggies diet and avoiding places where there may be significant levels of gluten to see if that helps.

Aly1 Contributor

I do get tendinitis in my wrists really badly, it was one of my very first problems. Nowadays I also get stiff and sore finger joints when I eat corn, so I avoid that too...

tbritt Rookie

I am actually a violinist and violin teacher by trade, so the tendon issues are a problem. My shoulder pain kept me from playing for a year. Doctors kept blaming it on the violin. I don't think the violin was ever the problem. I think it was malnourishment.

I am hoping to shake it over the next few weeks. The exercises have been keeping it from getting worse. Thanks for all of the replies.


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



Celiac.com Sponsor (A8-M):



UKGail Rookie

I think it might be an autoimmune inflammatory response rather than malnourishment per se. My own pet theory for what it is worth is that systemic inflammation caused by gluten ingestion hurts our weak spots most. Where I suffered pain previously (and which seems to recur with gluten ingestion) is where I either have structual problems because of dodgy discs or where I have previously suffered an injury. I guess for you if you use your hands and shoulders a lot, this is where you are at highest risk of wear and tear problems. I hope you get better soon.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,060
    • Most Online (within 30 mins)
      7,748

    LaurieBTX
    Newest Member
    LaurieBTX
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Maybe celiac but maybe NCGS that was misdiagnosed as IBS morphing gradually into celiac. Is NCGS a new category to you? It shares many of the same GI symptoms with celiac disease but does not damage the small bowel lining like celiac.
    • knitty kitty
      Thiamine has antifungal properties.  The body uses thiamine to keep bacteria and yeasts from overgrowth in the digestive system.   Fluconazole use can cause thiamine deficiency.   Supplementing with thiamine in the form Benfotiamine would be beneficial as Benfotiamine promotes intestinal healing.   Thiamine and the other B vitamins tend to be low in Celiac due to malabsorption.  Talk to your doctor about supplementing vitamins and minerals.
    • Scott Adams
      Welcome @Natalia Revelo, your experience is profoundly difficult and, sadly, not entirely unique within the celiac community. It's the frustrating reality of "silent" or ongoing damage that isn't captured by the MARSH score alone, which only measures active villous atrophy. Your normal biopsy suggests your diet is preventing the classic autoimmune attack, but it doesn't mean your gut has fully healed or that other issues aren't at play. The inflammation from your newly discovered milk and egg allergies is a huge clue; this constant allergic response can create a low-grade inflammatory environment that severely hampers nutrient absorption, effectively creating a "leaky gut" scenario independent of celiac damage. This is likely why your iron stores deplete so rapidly—your body is both unable to absorb it efficiently and may be losing it through inflammation. While the functional medicine path is expensive, it's clearly providing answers and relief that traditional gastroenterology, focused solely on the gluten-free diet and biopsy results, is missing. To move forward, continue the gut-healing protocols your functional doctor recommends (perhaps exploring alternative options to glutamine that won't irritate your cystitis), maintain your strict avoidance of all allergens and irritants, and know that true healing is a multi-faceted process. You might seek a second opinion from a different gastroenterologist who is more knowledgeable about non-responsive celiac disease and the complex interplay of food allergies and micronutrient absorption, but your current path, while costly, seems to be leading you toward the steady health you need.
    • knitty kitty
      Have you had a DNA test to look for Celiac disease genes?  If she doesn't have any celiac specific genes, look for another explanation.  If she does have Celiac genes, assume they are turned on and active Celiac disease is progressing.  All first degree relatives (mother, father, siblings, children) should be genetically tested as well.   Sometimes blood tests are ambiguous or false negatives if one has anemia, diabetes or thiamine deficiency.  Certain medications like antihistamines and steroids can suppress the immune system and result in false negatives or ambiguous results on antibody tests.  
    • Heatherisle
      That was just the visual report, so need to wait for confirmation or otherwise from the results. They did take a biopsy from the upper end of the duodenum(D1). D2 looked unremarkable on the camera. Just wish we didn’t have to wait so long for the results as she’s naturally a very anxious person. But thanks so much for taking the time to answer me
×
×
  • Create New...