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

Joint Pain Due To Celiac?


TardyTurtle

Recommended Posts

TardyTurtle Newbie

Hi Everyone,

I have been having problems with my joints for the past year. It started with my knees scraping (feeling like bone on bone) and cracking as I walked up stairs and now all my joints feel affected - especially knees and wrists. I have been mostly gluten free for the past 6 weeks and feel these symptoms have escalated in the past couple weeks. My knees now hurt and feel inflamed. My wrists also feel weak and crack with some pain.

I have read celiac can cause an autoimmune reaction in my joints. Does anyone else have this experience and/or suggestions? Thank you!

BTW, I am 31 yrs old, not overweaight, and with no previous injury to my joints - so likely shouldn't have osteoarthritis -here is my dx detail:

Last week, lab tests confirmed active dietary gluten sensitivity, autoimmune reaction to transglutaminase, elevated anti-casein (cow's milk) IgA antibody, and two copies of a gene that predisposes to gluten sensitivity (HLA-DQ 3,1 (Subtype 7,6)) However, do not possess the main HLA-DQB1 genes predisposing to celiac sprue.


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



Celiac.com Sponsor (A8-M):



YoloGx Rookie
Hi Everyone,

I have been having problems with my joints for the past year. It started with my knees scraping (feeling like bone on bone) and cracking as I walked up stairs and now all my joints feel affected - especially knees and wrists. I have been mostly gluten free for the past 6 weeks and feel these symptoms have escalated in the past couple weeks. My knees now hurt and feel inflamed. My wrists also feel weak and crack with some pain.

I have read celiac can cause an autoimmune reaction in my joints. Does anyone else have this experience and/or suggestions? Thank you!

BTW, I am 31 yrs old, not overweaight, and with no previous injury to my joints - so likely shouldn't have osteoarthritis -here is my dx detail:

Last week, lab tests confirmed active dietary gluten sensitivity, autoimmune reaction to transglutaminase, elevated anti-casein (cow's milk) IgA antibody, and two copies of a gene that predisposes to gluten sensitivity (HLA-DQ 3,1 (Subtype 7,6)) However, do not possess the main HLA-DQB1 genes predisposing to celiac sprue.

Yes the ravages of gluten intolerance definitely can cause such joint problems. It certainly has for me. I am very sensitive to any gluten at all--even as it turns out in soaps and lotions etc. that have (wheat germ) vitamin E in them! This of course includes cosmetics. I also can't have any grain made anything including alcohol and white (or wine or malted) vinegar.

I suggest in the meantime to make your life easier you invest in buying some bromelain/papain caps and pancreatin enzymes. It will help your intestines deal with food better and you will have less inflammation. If you have the money, invest also in either nattokinase or serrapeptidase to take down the scar tissue and inflammation in your intestines. Best taken on an empty stomach maybe with some extra bromelain/papain or other enzymes. Taken away from food they are called "systemic enzymes" and help take down inflammation.

I have also had success using liver cleansing herbs to take down the inflammation--such as alternating one week on and one week off with either milk thistle (silymarin caps) or dandelion root. And yes -- no tinctures!

If you don't have D you can also alternate Oregon Grape Root and Yellow Dock. They help the liver and intestines get rid of toxins and thus again inflammation. Many people with arthritic like symptoms are helped by these detox herbs.

Marshmallow root and/or slippery elm will also help heal and soothe the intestines which will also take down inflammation as a byproduct.

These and other remedies really do help. I have other more extensive posts here on natural remedies.

Of course eat lots of greens and at first a more caveman (or woman!) diet--avoiding grains altogether at first is best.

And no sugar! Use stevia as a sweetner instead.

And exercise, mud packs on hands and feet plus saunas really do help!

Plus of course extra vitamin D (cod liver oil is best if you can tolerate it since it has vit. A plus Omega 3's), minerals including calcium & magnesium and sea minerals, and some good B vitamins, pro-biotics, vitamin E, etc. -- all gluten free.

Hope this works for you! Eventually you won't have to do as much but for now all the above can speed up the process of healing.

Bea

Lisa16 Collaborator

Hi Tardyturtle!

I have the very same genes you do and the same joint pain. Mine is slowly getting better after 5 months gluten-free. I think/ hope it will continue to improve. It hit my knees and hips first, and then it got my arms, hands and feet.

BTW-- there is a thread about that gene type on the post-diagnosis forum that you might want to look at. People with those genes list their symptoms.

Yolo gives excellent advice. I am going to take some of it myself.

Good luck!

Lisa

Candy Contributor

Same here -I have joint pain /trouble too-stiffness. I'll try cutting out foods we shouldn't eat ,I'll return to papain tablets (I used them when I was a teen,before I knew I had celiac).I haven't heard of the Pancreatin pills, I'll look them up(there are so many enzymes and stuff for consideration) I haven't given it much thought. The advice and response to the joint question was very good-I'm glad someone brought up the issue of joint problems in Celiacs,as I've that prob. myself amongst other things,like white spotted teeth and runny blood(I was advised to ingest more vitamin K to promote clotting.I did, it's also found in Parsley fresh or 2tsp.dried,now my blood isn't so runny if I get a cut).Viatmin K is fat soluble so I take it with some oil.

ravenwoodglass Mentor

Yes, by the time I was diagnosed I had some pretty severe joint damage to go with the pain. By six months gluten-free my canes had moved into a corner to stay. My damaged joints still look a bit knobby but I have been in remission from my arthritis with no meds now for over 5 years. Something that the doctors thought would not happen.

Just as an info tidbit, one gene that in the US is a RA gene, DQ9, is considered a celiac in other parts of the world. That is the one I have double copies of.

bluejeangirl Contributor

I noticed also it helps to drink lots of water, it keeps the cartilage healthier and plumper. Don't drink to much coffee or alcohol because they'll dehydrate you. Sugar and a hgh carb diet causes alot of inflammation. There are some good books on inflammation. I've read alot of them but its been a few years since and I can't remember a single title. :(

Gail

tarnalberry Community Regular

you talk about a couple of things, including the knees, and I thought I would check and make sure that you had been thoroughly evaluated by a competent orthopaedist. some things may relate back to celiac, but some don't. there are problems that can lead to joint deterioration that have nothing to do with autoimmune conditions (I have one, chondromalacia patella, that is caused by a muscular imbalance, and - likely - the way my bones are angled, genetically; I also have a tendency to chronic tendinitis in the wrist as I work at a computer all day). it's worth determining if any of the pain/inflammation/damage is caused by this, so that you can work with an appropriate health professional (be it a physical therapist, chiropractor (yes, they work on knees too), or whatnot) to correct any postural misalignments or misuses than could be contributing to the problem.


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Besides magnesium, what has helped me with joints is glucosamine. The product I take also happens to have MSM, and I don't know if that has anything to do with the effectiveness. It has done wonders for my jaw, which is what I started taking it for in the first place.

Wonka Apprentice
Besides magnesium, what has helped me with joints is glucosamine. The product I take also happens to have MSM, and I don't know if that has anything to do with the effectiveness. It has done wonders for my jaw, which is what I started taking it for in the first place.

I can't take glucosamine, it gives me awful stomach aches.

TardyTurtle Newbie

Thank you everyone for your informative, helpful responses. I have a lot to look into!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    5. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,084
    • Most Online (within 30 mins)
      7,748

    bigwave
    Newest Member
    bigwave
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.