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/Inflammation/Stiffness?


DrubNonie

Recommended Posts

DrubNonie Rookie

Hey Everyone,

 

A few months ago I was diagnosed with "celiac" disease by my GI(my antibody showed a 25 at labcorp with a normal range of 1-9, while my biopsy was negative). I had taken a gluten free diet at the start of August and seen an improvement in my symptoms and general well being(Mainly the constipation, bod aches, and severe brain fog). i was diagnosed shortly after going gluten free that I was also Vitamin D deficient and B12 was "low-normal". I started to supplement both respectively and also saw an improvement in my general being. While there were definitive health issues along the way, I had started to feel better until a few weeks ago. I had gone home for thanksgiving break(being that I am a college student). My relatives, as loving as they are, had made a pudding. being that I had assumed for whatever reason that I could eat the damn pudding without asking, I had consumed it. i had later learned it had quite a bit of wafers infused into it(crushed), which I had also assumed, for whatever reason, was safe(never asked, dumb ol me). A day or two after consumption, I had noticed twitching in my right knee. Then it went to my left knee. Then both knees were hurting like crazy. Then it felt like the inside of my knee were in pain. 2 weeks later, they still are. Every morning waking up since then had been quite difficult since my joints are so stiff, and stay stiff throughout the day. Exercise had helped this condition, and helps reduce stiffness and pain for about a day, but if i do not continue to exercise the pain returns reallll fast.

 

The real scary thing is that my hands have also become quite painful. There are red rashes all over my knuckles and I am experiencing pain all in my fingers and wrist and hand. Along with knee pain(and big toe pain here and there as well, but that not as much). Its already been a little over 2 weeks since "reconsuming" a heavy amount of gluten. Is this normal for a gluten reaction to last this long? My pain is symmetrical and sounds an awful lot like Rheumatoid Arthritis. However, I tested negative for all rheumatoid tests back in June. I am seeing a doctor tommorow, but I am wondering from the forum, is it normal for a gluten reaction to last this long? 

 

Thank you all and best Regards, I appreciate any words of advice


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

It can take a bit of time for the antibody reaction to go away.  I get joint pain and stiffness also when glutened and find hot showers, gentle stretching and an anti-inflammatory help a great deal.  I am so sorry you are in so much discomfort and hope it is over soon. Please be careful and ask questions before consuming any foods you haven't prepared yourself. In addition make sure that your family knows they should all be tested for celiac even if they don't have any symptoms or don't think they do.

cyclinglady Grand Master

Well, it could be RA or celiac disease as celiac disease affects the joints as well.  But since your symptoms appeared suddenly after a gluten exposure, it is most likely celiac disease.   My glutenings last for months.  Really severe symptoms last a month or more.  Then I gauge my healing based on recovering from lactose intolerance (I hate losing my dairy!),  ceasing to lose weight or the final elimination of daily hives (that lasts about six months).  I am not sure the hives are celiac-related or just autoimmune triggered by glutenings.  I do have Hashimoto’s thyroiditis too.   None of my doctors (GI, PCP or Allergist) can say either as my antibodies for both Hashimoto’s and celiac disease are usually really elevated.  

I hope your recovery is much shorter than mine!   Since it hurts for me to eat anything, I usually make a big pot of stew or soup and eat that at every meal.  I find that eating anything after a glutening can hurt.  It is probably why I lose weight fast.  

DrubNonie Rookie

Thanks for the replies! yeah, the doctor was also betting that it was likely a gluten reaction. Im currently on week 3 with legs improving a lot but hands getting much worse, so not sure where I stand haha. The doctor said if there isn't an improvement in 3 weeks to seek a rheumatologistt, so heres hoping xmas season ends well...

 

Thanks for all the replies!  

ravenwoodglass Mentor
11 hours ago, DrubNonie said:

Thanks for the replies! yeah, the doctor was also betting that it was likely a gluten reaction. Im currently on week 3 with legs improving a lot but hands getting much worse, so not sure where I stand haha. The doctor said if there isn't an improvement in 3 weeks to seek a rheumatologistt, so heres hoping xmas season ends well...

 

Thanks for all the replies!  

There are a couple things that I find helpful for hand pain and stiffness. One is doing hot and cold hand soaks. 2 bowls one with water as warm as you can stand and the other with cold water with an ice cube or two. Dunk hands in each going from hot to cold every two minutes or so for a bit and finish with the hot. I also use a parrafin bath. With both I do gentle stretching afterwards.  I found this helpful when I was having issues with hands so stiff I couldn't close them and fingers that were triggering. maybe check with your doctor to see if he/she thinks it might help. 

Ennis-TX Grand Master
15 minutes ago, ravenwoodglass said:

There are a couple things that I find helpful for hand pain and stiffness. One is doing hot and cold hand soaks. 2 bowls one with water as warm as you can stand and the other with cold water with an ice cube or two. Dunk hands in each going from hot to cold every two minutes or so for a bit and finish with the hot. I also use a parrafin bath. With both I do gentle stretching afterwards.  I found this helpful when I was having issues with hands so stiff I couldn't close them and fingers that were triggering. maybe check with your doctor to see if he/she thinks it might help. 

My recent exposure left my joints swollen and stiff, the hot and cold is helping...did not think alternating like would work but it did.  >.< I will admit what happened once I confirm the culprit. >.> my paranoid self is a bit ashamed about it but a bit of a learning experience I guess.

DrubNonie Rookie

Hey guys...on like week 3 or 4 now I guess.

 

Hand redness has gotten much worse and so has hand pain. No swelling, just constant redness and pain in finger joints. Knees have very little pain now, and only kick in after LONG periods of inactivity (up to a few hours). The finals arent really helping either in this case. It kinda hurts to even hold a coffee or tea now. And type too. is this still typical this many weeks out of a gluten reaction? 

 

obviouslly a slightly stressed post, but was jw... 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master
13 minutes ago, DrubNonie said:

Hey guys...on like week 3 or 4 now I guess.

 

Hand redness has gotten much worse and so has hand pain. No swelling, just constant redness and pain in finger joints. Knees have very little pain now, and only kick in after LONG periods of inactivity (up to a few hours). The finals arent really helping either in this case. It kinda hurts to even hold a coffee or tea now. And type too. is this still typical this many weeks out of a gluten reaction? 

 

obviouslly a slightly stressed post, but was jw... 

I am on constant stuff for my joints, I take Joint support by jarrow for years now, to the point I just take them in my handful of pills twice a day. I also been using collagen supplement powder in my smoothies twice a day. I think my magnesium also helps. I will admit after a recent knee injury I had to take some extra turmeric daily to get the swelling down. Seems to have healed from grapefruit sized to normal and movable in 3 days.
Some foods, partially if I consume excessive sodium without something to flush me seems to cause a edema issue and joint swelling.
PS when it gets really cold I have to put on gloves around my house or my fingers all go trigger locky style when it gets too cold. (no heater so during the winter my inside sometimes hits 35-40F ish.)

DrubNonie Rookie

Woah, sounds like a rollercoaster for sure. Am i to assume this to be permanent then? 

Ennis-TX Grand Master
1 hour ago, DrubNonie said:

Woah, sounds like a rollercoaster for sure. Am i to assume this to be permanent then? 

Might be a food trigger, keep a food diary and try rotating up your diet. Remove common inflammatory foods, like dairy, and see if you notice a improvement. With only 3-4 weeks in your probably have a bit of leaky gut and some other food is triggering your extra inflammation. >.< I am a bit special with my joints i walk like 14miles a day average, and am trying to body build. SO I need a bit extra, I gave examples of what I use to keep my joints lubricated and working great to see if they might help you.

ravenwoodglass Mentor
9 hours ago, DrubNonie said:

 Am i to assume this to be permanent then? 

As Ennis mentioned do check for other intolerances. For myself soy protein or flours cause joint pain in addition to gluten. A food and symptom diary can be very helpful as can be the elimination and challenge.  Sometimes when we eliminate a food the reaction when added back in can be delayed for up to a week. So if you, for example, drop soy for a couple weeks to a month be sure to eat it in some form at least once a day for a week before you decide it is safe. Do make sure when adding back in that you are only eating stuff you know you tolerate so the reaction to the 'new' food is clearest.

I hope you get some relief soon.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.