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 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


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.

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! :)

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.

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.

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.

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.


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.

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

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.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,189
    • Most Online (within 30 mins)
      7,748

    Eric bell
    Newest Member
    Eric bell
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...