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 Celiac.com!
    eNewsletter
    Donate

Joint Inflammation


MarkR555

Recommended Posts

MarkR555 Rookie

Hi guys, I am a newly diagnosed celiac (gluten free for 3 weeks). I have mostly had GI symptoms which seem to be getting better slowly which is great.

However right now I am suffering from a very painful bout of inflammation in my sacroilliac joint, making it very painful to walk. It's happened 3-4 times before in the last few years mostly as a result of hard impacts - I climbed a mountain two weeks ago which has brought this on. I saw a rheumatologist and had mri's etc last time this happened but to no avail. I was wondering if this could be caused by my celiac disease.

I was wondering if any other people get inflammation in their joints as a result of celiac? I know some people say they get stiff wrists etc when they get gluttened.

Thanks,

Mark

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Yes some of us do get joint inflammation. Mine was so bad that at one time I was thought to have RA. I have been in pretty much total remission from my arthritis since about 6 months after I went gluten free. If I get CC'd somehow simple asprin takes care of the inflammation and the pain.

Could you have gotten glutened on your trip? Not everything is gluten related but if you got glutened that may have brought this back on. Or could you have strained some muscles climbing? Perhaps cold packs alternating with heat might help if your doctor says that is okay.

Link to comment
Share on other sites
bluebonnet Explorer

yes, i struggle with bone and joint inflammation and pain. it's s.l.o.w.l.y. on the mend. it seems to be noticably aggravated if i get cc'd. have you had your vit. d levels checked? you might be as surprised as i was to find them depleted (even if you take supplements or are regularly outside in the sunshine). you will find many people on here that struggle with bone and joint issues.

mountain climbing sounds FUN! :)

Link to comment
Share on other sites
dilettantesteph Collaborator

I also had bad joint pain pre diagnosis which went away after gluten free. My back used to go out regularly before diagnosis. I've had it so bad I couldn't walk without pain pills. Now it only happens when I get a long term glutening and get lazy about my stretches. What helped me a lot to keep it from going out even pre diagnosis was daily stretching and strengthening exercises. I do leg stretches and sit-ups etc. I combined what the physiotherapist recommended with other things that seemed to help from various exercise classes. If I do them every day, my back doesn't go out even if I do get glutened.

Link to comment
Share on other sites
SaraKat Contributor

Yes, that was my main symptom and that is why I was shocked about the celiac diagnosis. My left lower ribcage/joint was so painful I ended up going to a rheumatologist in mid August and she is the one that discovered the celiac.

I've been on the diet for 1.5 weeks and there is a noticeable difference in the pain. I still feel it, but it is not disabling like it was the last couple months. I was even able to run on the treadmill for a while last week.

Link to comment
Share on other sites
MarkR555 Rookie

Encouraging replies, thanks guys.

The inflammation is always brought on by hard impacts / jumping from anything. I got it really bad last year rock climbing on a bouldering wall and jumping down from that. I am only 3 weeks gluten free though and i've had this inflammation problem for years, longer than my GI symptoms so I assume it might take a while to go away if it is the celiac. I am probably being cc'ed occasionally - I live in a shared house and am sharing pots/pans/plates (they are always clean, but still). I am going to buy my own kitchen stuff soon.

Once or twice since I went gluten free i've have bad liquid D in the morning, this never happened to me before. I'm thinking it's a sign i've had some gluten.

Link to comment
Share on other sites
ravenwoodglass Mentor

Once or twice since I went gluten free i've have bad liquid D in the morning, this never happened to me before. I'm thinking it's a sign i've had some gluten.

I agree that at those times you have likely been glutened. It is not unusual for our reactions to become a bit more severe after we have been gluten free for a while. It will take some time for the inflammation to go down, that often takes longer to go away than the GI issues. Hopefully you will heal quickly.

Make sure none of your roommates is using your nut butters, butter, jelly or anything that can be 'double dipped'. Even a crumb will cause a reaction.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



srall Contributor

Yes to the joint pain. I think it's my worst symptom. Or maybe I should say most aggravating. It is getting better on a gluten/soy/dairy free diet. I think I need to be stricter with the soy and dairy though. It's tough going. I'm sure you'll see a vast improvement as you remain gluten free.

Link to comment
Share on other sites
Chakra2 Contributor

Some people (like me!) find that nightshades cause joint pain, in addition to gluten. Pain that I had for years and that I always thought was running-related vanished on a gluten-free, nightshade-free diet. I do avoid soy, corn, and dairy too but with accidental experimentation I've found out that gluten and nightshades are the big problems for me in terms of joint pain. And this is pretty unlikely but you might want to read about ankylosing spondilitis too and the other autoimmune arthritises just to be aware of those symptoms. Hope your pain goes away!

Chakra2

Link to comment
Share on other sites
MelindaLee Contributor

Hi guys, I am a newly diagnosed celiac (gluten free for 3 weeks). I have mostly had GI symptoms which seem to be getting better slowly which is great.

However right now I am suffering from a very painful bout of inflammation in my sacroilliac joint, making it very painful to walk. It's happened 3-4 times before in the last few years mostly as a result of hard impacts - I climbed a mountain two weeks ago which has brought this on. I saw a rheumatologist and had mri's etc last time this happened but to no avail. I was wondering if this could be caused by my celiac disease.

I was wondering if any other people get inflammation in their joints as a result of celiac? I know some people say they get stiff wrists etc when they get gluttened.

Thanks,

Mark

Welcome to the club!!! :D

I was diagnosed 4 weeks ago. Since then, I have went off my arthritis meds. I thought my pain was due to aging...but have found a great releaf since I have been gluten free. I was glutened (my fault) last week, and noticed the joint pain worse than any GI issues. It took longer for that to resolve for me than the GI issues, which were gone within a day.

Hope you are feeling better soon.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,093
    • Most Online (within 30 mins)
      7,748

    Eva Ann
    Newest Member
    Eva Ann
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Oh, okay. The lower case "b" in boots in your first post didn't lead me in the direction of a proper name. I thought maybe it was a specialty apothecary for people with pedal diseases or something.
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! There are other things that may cause elevated tTg-IgA levels, but in general a reaction to gluten is the culprit:    
    • cristiana
      Hi @trents Just seen this - Boot's is a chain of pharmacies in the UK, originally founded in the 19th Century by a chap with the surname, Boot.  It's a household name here in the UK and if you say you are going to Boot's everyone knows you are off to the pharmacist! Cristiana
    • Denise I
      I am looking to find a Celiac Dietician who is affiliated with the Celiac Disease Foundation who I can set up an appointment with.  Can you possibly give some guidance on this?  Thank you!
    • Posterboy
      Nacina, Knitty Kitty has given you good advice. But I would say/add find a Fat Soluble B-1 like Benfotiamine for best results.  The kind found in most Multivitamins have a very low absorption rate. This article shows how taking a Fat Soluble B-1 can effectively help absorption by 6x to7x times. https://www.naturalmedicinejournal.com/journal/thiamine-deficiency-and-diabetic-polyneuropathy quoting from the article.... "The group ingesting benfotiamine had maximum plasma thiamine levels that were 6.7 times higher than the group ingesting thiamine mononitrate.32" Also, frequency is much more important than amount when it comes to B-Vitamin. These are best taken with meals because they provide the fat for better absorption. You will know your B-Vitamin is working properly when your urine becomes bright yellow all the time. This may take two or three months to achieve this.......maybe even longer depending on how low he/you are. The Yellow color is from excess Riboflavin bypassing the Kidneys....... Don't stop them until when 2x a day with meals they start producing a bright yellow urine with in 2 or 3 hours after the ingesting the B-Complex...... You will be able to see the color of your urine change as the hours go by and bounce back up after you take them in the evening. When this happens quickly......you are now bypassing all the Riboflavin that is in the supplement. The body won't absorb more than it needs! This can be taken as a "proxy" for your other B-Vitamin levels (if taken a B-Complex) ...... at least at a quick and dirty level......this will only be so for the B-1 Thiamine levels if you are taking the Fat Soluble forms with the Magnesium as Knitty Kitty mentioned. Magnesium is a Co-Factor is a Co-factor for both Thiamine and Vitamin D and your sons levels won't improve unless he also takes Magnesium with his Thiamine and B-Complex. You will notice his energy levels really pick up.  His sleeping will improve and his muscle cramps will get better from the Magnesium! Here is nice blog post that can help you Thiamine and it's many benefits. I hope this is helpful but it is not medical advice God speed on your son's continued journey I used to be him. There is hope! 2 Tim 2:7 “Consider what I say; and the Lord give thee understanding in all things” this included. Posterboy by the grace of God,  
×
×
  • Create New...