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

Coeliac And Body Pains


Captain CJ

Recommended Posts

Captain CJ Newbie

Hello from the otherside of the 'pond' hence the different spelling of Coeliac!

Does anybody else suffer from muscular and bone pain which seems to worsen if contaminated by gluten? I'm going back to my GP soon for more advise on a persitant neck, shoulder and arm pain (left only). I've had a steroid injection mid December 2011 to little effect.

Also I sometime get a pain in my shin bones. All I can aliken it to is it feels like my bones are too long for my skin!

I would love to hear back to see if my body pains are related to being a coeliac or just part of getting a little older


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



Celiac.com Sponsor (A8-M):



Jnkmp8 Newbie

Hi

Although I'm not diagnosed with coeliac but only an allergy although quite severe to gluten & IBS-- I have so many of the coeliac symptoms including join & muscular pain when I've been poisoned.

My join pain occures in my left hand, my other pains occur in my thighs & lower arms- although I wouldn't describe it as 'in the bones' I feel mine is in the muscles-- when I move it feels like they'll explode!

I maybe just getting old too but it seems worse when I've been glutened.

My Doctors don't seem to be concerned with those symptoms- mind you it seems to we are in someways lagging behind in treatment, diagnostics & understanding re:coeliacs in the uk compared to the USA.

I'm interested in what others say too!

Good luck with your healing.

Jx

Captain CJ Newbie

Thanks for the reply. I agree with you for sure on the UK versus USA understanding of Coeliac disease. We seems in the dark ages with our attitude to other possible side effects of the disease.

rosetapper23 Explorer

Ah, the familiar shin pains. Yes, I know them well. I started having them when I was seven years old, so I had to wrap my lower legs in heating pads each morning or take a long hot bath in order to be able to go to school. As an adult, the pain was especially bad after I drank beer. I rarely drank beer (preferred wine...and still do), but after parties where beer had been served, I'd be in horrible pain the next day. All of my bones would ache, but especially my shins. I supposed it was the barley gluten in the beer. Unfortunately, I didn't find out I had celiac until I was 47.

I also had joint pain my entire life until I went gluten free, but, like you, the smallest gluten contamination results in tremendous joint pain throughout my body for about 4-5 days. My muscles, tendons, and ligaments have always been super-tight and sore, too. However, I read a book several years ago called, "The Hidden Story of Cancer," which advised readers to take a certain ratio of Omega 6's to 3's to relieve muscle pain. Supposedly, it helps to supply oxygen to the muscles so that even vigorous exercise does not leave a person with lactic acid build-up. Well, I started taking that ratio (because I've had cancer, and that's the primary reason for taking it), and my muscles did indeed stop hurting. I can even do very strenuous exercises now with no after-effect whatsoever. I take 1/2 teaspoon of organic flaxseed oil combined with 3/4 teaspoon of organic safflower oil in either a small glass of juice or a smoothie once a day. That does the trick--and it also helps with any remaining joint aches and keeps my skin looking soft and younger.

Captain CJ Newbie

Oh my goodness! I am so relieved is not just me......I'm a 'don't worry it will be better tomorrow' sort of person and I hate feeling poorly or weak, so to hear somebody else speaking about my same symptoms does really help me. But it also makes me realise I need to push for my GP to take me seriously.

ravenwoodglass Mentor

Thanks for the reply. I agree with you for sure on the UK versus USA understanding of Coeliac disease. We seems in the dark ages with our attitude to other possible side effects of the disease.

US doctors are just as clueless. It took over 40 years for me to finally get a diagnosis.

As to the pain I am unfortunately all too familiar with it. Do make sure you are strict with the diet and do avoid the products that have Codex wheat starch. My pain did resolve once I had been gluten-free for a few months but it does return when I get glutened or when I injest soy.

UKGail Rookie

Hi, I'm also in the UK, and my GP was also not very alert to the non-classical symptoms. However there are many celiacs in my family which was a pretty strong clue.

I only had vague non-specific abdominal pains, but I was suffering from migraines, which had gradually spread to my neck and shoulders (I always thought this was due to having been injured in a car accident some years ago - Wrong!). 3 years ago I had a frozen shoulder which took a year, several steroid injections and physiotherapy to more or less resolve. Then a year ago the other shoulder froze up. I went back to the physio, and it just got worse rather than better. The physio suggested that there might be an underlying inflammatory disorder, which should be looked at. Basic blood tests showed an ESR of 100, which together with my symptoms was sufficient to generate a referral to a rheumatologist and lots of expensive blood tests for various things, including celiac. None of them came back positive, just the high ESR and a high total IgM antibody level.

A trial gluten free diet quickly resolved the high ESR, high IgM, migraines, neck and shoulder pain (the frozen shoulder released)and back pain, improved the abdominal pain and various other things too.

If I get glutened it all comes back quite quickly.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,542
    • Most Online (within 30 mins)
      7,748

    Jacqueline Dee
    Newest Member
    Jacqueline Dee
    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

    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
×
×
  • 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.