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

For Celiacs With Joint Pain


spirit-walk

Recommended Posts

spirit-walk Contributor

Do you have swelling? I have had joint pain for almost two years now, but I've never had any swelling. My joint pain is severe at times and although they get warm, they never swell.


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

While I DO have arthritis in my spine, the joint pain in my fingers and shoulders and knees and hips was caused by nightshades. I was intolerant to potatoes for a long time (psoriasis flares), so when I finally got them back I went on a potato binge. After a couple of weeks the joint pain came on strong, and remembering that folks here have said that nightshades could cause that pain, I gave them up and within a couple of days the pain was gone.

 

I've been eating a few potato chips lately and so far so good. Nightshades are cumulative. If I go easy and take breaks of a few days, it looks like I can eat them without pain.

spirit-walk Contributor

While I DO have arthritis in my spine, the joint pain in my fingers and shoulders and knees and hips was caused by nightshades. I was intolerant to potatoes for a long time (psoriasis flares), so when I finally got them back I went on a potato binge. After a couple of weeks the joint pain came on strong, and remembering that folks here have said that nightshades could cause that pain, I gave them up and within a couple of days the pain was gone.

 

I've been eating a few potato chips lately and so far so good. Nightshades are cumulative. If I go easy and take breaks of a few days, it looks like I can eat them without pain.

 

So you do not have swelling with the pain?

bartfull Rising Star

Nope. No swelling, just pain and stiffness.

spirit-walk Contributor

Nope. No swelling, just pain and stiffness.

 

Thanks.

SkyBlue4 Apprentice

I have had severe joint pain over the years but I have never had swelling with it.

MGR Apprentice

I have had horrendous joint pain for years. During my gluten challenge I swelled up so much all over, I couldn't even wear my wedding rings! I'm improving a bit now that I have been gluten free.


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

The first time I experienced a joint pain flare-up I had swelling, heat and redness. It scared me to death. i went from normal to not being able to use scissors within a week. I remember the relief when it finally passed a month later...

 

Ever since then, I do not get swelling or redness, and if I do it's very very minor. The pain is often the same and usually symmetrical on both sides of my body. Fingers, hands, shoulders, hips and elbows are usually the parts affected.

 

Frequency of attacks has lessened since going gluten-free. I had my last big attack from 3-6 months gluten-free, and I seem to be finishing a mild attack now - I'm taking hydrocortisol now so perhaps that lessened the intensity? No swelling at allthis past time, nor the last 3 month attack (from what I remember).

IrishHeart Veteran

I believe I just told you this in a PM exchange, but I will restate it here for other readers who may have the same question:

 

I do not have red swollen joints like in RA.  I have OA and osteoarthtiris does not cause red swelling in joints like RA does, but my knees are pretty big and my hands have obvious knobs on them (much to my dismay) .

 

Inflammation does not have to be "obvious". We all have inflammation but we may not "swell up"

 

There are tests that indicate a level of inflammation in the body--Sed Rate, C-reactive protein, for example. .

kareng Grand Master

I had some terrible joint pain. Occasionally, I still do. I found that regular yoga helped sooooooo much.

spirit-walk Contributor

I believe I just told you this in a PM exchange, but I will restate it here for other readers who may have the same question:

 

I do not have red swollen joints like in RA.  I have OA and osteoarthtiris does not cause red swelling in joints like RA does, but my knees are pretty big and my hands have obvious knobs on them (much to my dismay) .

 

Inflammation does not have to be "obvious". We all have inflammation but we may not "swell up"

 

There are tests that indicate a level of inflammation in the body--Sed Rate, C-reactive protein, for example. .

 

Yeah Irish, I started this thread before I pm'd you. ;)

SkyBlue4 Apprentice

I had some terrible joint pain. Occasionally, I still do. I found that regular yoga helped sooooooo much.

 

This so good to hear. I just purchased a beginners yoga video and want to see if it helps. 

greenbeanie Enthusiast

I had awful SI joint paint for twenty years, with no swelling. My skin in the area felt hot to the touch. I had six cortisone shots over several years, and also tried physical therapy and yoga, and those things hardly helped at all. The worst pain seemed to correspond to when the lymph nodes in my groin were swollen (which happened often for unknown reasons). My CRP and Sed Rate were normal, but my monocytes were moderately elevated most of the time (also for unknown reasons). I do not have a celiac diagnosis but had dozens of symptoms for decades, and after six months gluten free the joint pain is much better, though not gone completely.

IrishHeart Veteran

I had some terrible joint pain. Occasionally, I still do. I found that regular yoga helped sooooooo much.

 

I agree.

Yoga, walking, weight-bearing exercise of any kind, lifting weights, swimming, riding a bike....any kind of movement...these all effectively keep the horrible pain I once had down  to "non-screaming level".  :D I also highly recommend massage. The muscles around those joints are all tighter than heck and have trigger points in them (hyper-irritable knots) and need to be worked out.

 

 

I had awful SI joint paint for twenty years, with no swelling. My skin in the area felt hot to the touch. I had six cortisone shots over several years, and also tried physical therapy and yoga, and those things hardly helped at all. The worst pain seemed to correspond to when the lymph nodes in my groin were swollen (which happened often for unknown reasons). My CRP and Sed Rate were normal, but my monocytes were moderately elevated most of the time (also for unknown reasons). I do not have a celiac diagnosis but had dozens of symptoms for decades, and after six months gluten free the joint pain is much better, though not gone completely.

 

The SI joint pain is quite possibly the worst. I also had this, with pelvic floor dysfunction. I had physical therapy....lots and lots, including

visiting a very special PT who works on the pelvic floor. 

I'll spare you all the gory details, but it was not fun.

 

Before I was gluten-free, I tried everything to stop that pain, including the shots. No help.

Wrecked my gut using NSAIDs prescribed by rheumatologists. Never helped the pain level.

I take nothing now.

 

The point is....off gluten, healing, moving, therapeutic measures...calcium/mag/D and some collagen supplements for bones and connective tissues repair and I move better than I did when I was 35 (which was 20 years ago)

 

Hang in there, everybody!

dilettantesteph Collaborator

I get joint pain with swelling.  On diagnosis the swelling was so bad that I had stopped wearing any rings.  I had to keep putting them on smaller fingers and I gave up.  After the gluten free diet my finger joints went back to regular size and I was able to wear the same rings on the correct fingers again.  When I get into a bad period of glutening they swell up again, and I actually had to cut one of the rings off one time as I couldn't get it off otherwise and it was cutting off my circulation.  I'm back to normal now.

eers03 Explorer

Do you have swelling? I have had joint pain for almost two years now, but I've never had any swelling. My joint pain is severe at times and although they get warm, they never swell.

I get pain in some joints and I get pain in non-joint areas.  I have no swelling.  I recently had a chest x-ray incidental to a cold virus I had and they looked clear.  My blood work is clean.  Calcium, BUN, Albumin are all fine.  I have no RA factor.  I don't think its a fibromyalgia.  Its just weird.  Its not normal for me but my tests say I'm normal.  Go figure.

GFinDC Veteran

I get joint pain from nightshades, soy and hypo-thyroidism.  No swelling so far, just sore joints.  Well, no joint swelling, but plenty of leg and feet swelling.  For me the joint pain stays away as long as I take care of the issues that cause it.  It does provide some motivation! :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,017
    • Most Online (within 30 mins)
      7,748

    Sjcucinotta
    Newest Member
    Sjcucinotta
    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)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
    • knitty kitty
      Please do more research before you settle on nicotine. Dr. Paul New house is a psychiatrist.  His latest study involves the effect of nicotine patches on Late Life Depression which has reached no long term conclusions about the benefits.   Effects of open-label transdermal nicotine antidepressant augmentation on affective symptoms and executive function in late-life depression https://pubmed.ncbi.nlm.nih.gov/39009312/   I'm approaching the subject from the Microbiologist's point of view which shows nicotine blocks Thiamine B1 uptake and usage:   Chronic Nicotine Exposure In Vivo and In Vitro Inhibits Vitamin B1 (Thiamin) Uptake by Pancreatic Acinar Cells https://pubmed.ncbi.nlm.nih.gov/26633299/   While supplementation with thiamine in the form Benfotiamine can protect from damage done by  nicotine: Benfotiamine attenuates nicotine and uric acid-induced vascular endothelial dysfunction in the rat https://pubmed.ncbi.nlm.nih.gov/18951979/   I suggest you study the beneficial effects of Thiamine (Benfotiamine and TTFD) on the body and mental health done by Dr. Derrick Lonsdale and Dr. Chandler Marrs.  Dr. Lonsdale had studied thiamine over fifty years.   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/ I suggest you read their book Thiamine Deficiency Disease, Dysautonomia, and High Calorie Malnutrition.     Celiac Disease is a disease of malabsorption causing malnutrition.  Thiamine and benfotiamine: Focus on their therapeutic potential https://pmc.ncbi.nlm.nih.gov/articles/PMC10682628/
    • sleuth
      Thanks for your response.  Everything you mentioned he is and has been doing.  Tobacco is not the same as nicotine.  Nicotine, in the form of a patch, does not cause gastrointestinal irritation.  Smoking does. He is not smoking.  Please do your research before stating false information. Dr. Paul Newhouse has been doing research on nicotine the last 40 years at Vanderbilt University Medical Center.  
    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
×
×
  • 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.