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

Bones/joints Q


Mummyto3

Recommended Posts

Mummyto3 Contributor

Has anyone had problems with their joints/bones before they found out they were celiac? Test results not back til next week. Two years ago, my left hip started popping/clicking/grinding. A year later (last yr) I was diagnosed with an underactive thyroid. This year, my right hip started feeling like its grinding when I lift my leg and now my left shoulder is grinding and popping. There's no pain but it's just a horrible noise, and I'm starting to worry. I've always had probs with anemia, but luckily recent test is normal and so is thyroid, with help of meds.


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



Celiac.com Sponsor (A8-M):



Mummyto3 Contributor

PS My ankles are the same, noticed today. I also have persistant lower back pain too. My jaw also clicks, happened since being a teen. I have to 'unlock' it if I come to yawn otherwise it locks and it hurts. I'm falling apart!

zimmer Rookie

I had bad hip pain that has gone away since going gluten-free.

I have similar problems with my jaw locking, but I can't tell for sure if this is better since it doesn't happen often. I catch myself when yawning to be sure I don't open too wide, but it also happens in my sleep. I thought this was more related to a TMJ problem.

I have weak ankles, and have had shoulder trouble in the past. My shoulders don't hurt so much anymore. However it's hard to tell what's related to gluten except for my hips since that was an immediate improvement. Also I recently got glutened and the next day was really hurting in my hips.

Lower back pain - not so much a problem for me but I expect it to show up later. My mom has arthritis in her back so I think I may get it. But then, arthritis & celiac are connected somehow so I'm hoping a gluten-free diet may lessen my troubles if they should arise.

IrishHeart Veteran

I have horrid joint/bone/muscle pain and TMJ dysfunction. :blink: It's slightly better 6 months gluten-free, but I work at it with a PT, a chiropractor and an MT. I have arthritis, too. :( I was crippled by this pain and the nerves were affected as well. I have hope it will reduce. I never give up. I figure it happened because of the inflammation and if the inflammation goes down...then I should feel better. (the PT, MT and chiro think so too.)

Lots of people on here report a reduction in this pain after going gluten-free. Hang in there--you are young and may likely recover faster. :)

best wishes!!

Harpgirl Explorer

I won't get my test results back until the 7th of next month, but going gluten free has helped my cramping.

I too have trouble with my jaw. My dentist said it was TMJ and suggested that I not chew gum. I still (well, not anymore) have trouble with really chewy breads like Panara Bread's sourdough crust because of it. If I'm really tired and don't pay attention to how I yawn, it will catch very painfully.

I've never really had much trouble with the rest of my joints except one knee that I injured back in high school. To be honest though, perhaps gluten made it really weak or something because all I did was sit down wrong in my desk, and it caused me to have 2 arthroscopies (the last one they found a 1 inch chunk of cartilage floating around loose in there). Prior to that second surgery, I too had lots of popping and cracking. I still have a little trouble with it and try to stick to low impact cardio (when I ever exercise :P )

Anyway, that probably doesn't help you much except that I'm kind of in the same boat pre-results. ;)

txplowgirl Enthusiast

At one time I was at a point I couldn't stand for longer than an hour because my lower back and legs would go numb and get so weak they wouldn't support me.

Right side hip pain so bad, sometimes I couldn't walk without limping. I thought I would have to have a hip replacement. My shoulders, wrists, ankles, knees all would snap, crackle and pop from the time I was a kid. My dad would sometimes laughing say "Here comes the Rice Krispies Kid!" And yes my jaw has done the same thing too. It took a good year at least for all of that to go away but I not only had to get rid of the gluten but soy, dairy and the nightshade vegetables also.

Mummyto3 Contributor

Thanks so much for the replies. I yawned loads last night and my jaw clicked each time. Luckily it wasn't painful. Talking of chewing, if I have something chewy and I chew and chew my jaw will start aching really badly. This happened a few weeks ago, it was horrible. I'm so worried now.


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



Celiac.com Sponsor (A8-M):



Harpgirl Explorer

Thanks so much for the replies. I yawned loads last night and my jaw clicked each time. Luckily it wasn't painful. Talking of chewing, if I have something chewy and I chew and chew my jaw will start aching really badly. This happened a few weeks ago, it was horrible. I'm so worried now.

Yep, that happens to me too. I still chew gum, but there are softer ones that don't bother me as much. Trident is a good one, but even then I'll have to spit it out before the flavor dies all the way. Those sourdough bread bowls at Panera Bread use to be my favorite, but it was always disappointing to not be able to finish it just because my jaw was too sore. I wonder if there is a tasty gluten-free sourdough?

fairydust81 Rookie

I'm not yet officially diagnosed but it's likely that I have coeliac and DH. I was diagnosed with a form of rheumatoid arthritis earlier this year. When I eat food containing wheat/gluten my skin starts to burn/tingle. Within 12-24 hours the rash covers my arms. A further 24 hours later and I get a bad arthritis flare. The last bloods showed my inflammatory markers were high too.

Very painful and at present I'm waiting for my new meds to kick in (hydroxychloroquine).

Mummyto3 Contributor

The dr today was useless. Not only did she see me 20 mins late, but she said she didn't know what was wrong with me! I went to her about the fatigue, clicking joints and extremely painful lower back. Grrrrr :angry:

julandjo Explorer

The dr today was useless. Not only did she see me 20 mins late, but she said she didn't know what was wrong with me! I went to her about the fatigue, clicking joints and extremely painful lower back. Grrrrr :angry:

Joint pain, specifically in my spine/hips, is one of my first symptoms of a reaction. It's horrific and immediate with gluten; with other "bad for me" foods it can take a few days to set in. It takes anywhere from 3-5 days after an exposure to go away. I'm 32, and I never knew until recently what it felt like to live pain-free. I thought the way I felt was normal - life now is SO much better!

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. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,956
    • Most Online (within 30 mins)
      7,748

    Crismedin
    Newest Member
    Crismedin
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.