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 Five Months After Diagnosis


RoseL

Recommended Posts

RoseL Newbie

Hi, I'm new to this forum. My husband was diagnosed with Celiac in January of this year. He has felt so much better up until recently, but has started having terrible joint pain. He's also gained fifty pounds back (he was emaciated before).

Anybody had something like this happen? I wonder if his was just so skinny before that he didn't feel his joints, and we've also had cold, wet weather here...but it does seem odd that he would have that much pain now and didn't have joint pain before. He was up all night with it.

He's also much more active now, had just about given up on playing golf before because he was so weak from anemia.

Rose


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Welcome to the board!

Various symptoms after going gluten-free are common. One cause seems to be increased sensitivity to certain foods, such as dairy, soy, corn, etc. Another is nutrient deficiencies. In the case of sensitivities, try eliminating a suspect food for a week or two, and see how it goes. The top allergens are a good place to start.

Also, if new things have been added to the diet, or are now substantially increased, that might be a factor. For instance, relying heavily on potatoes may be going above the body's tolerance level of nightshades. I can personally attest to this fact. It got to the point, that one serving of potatoes was enough to disable me for two weeks. There was pain all over, in various joints and muscles. Quite a lot of fatigue and weakness too.

Deficiencies of B vitamins, vitamin D, and certain minerals including magnesium and calcium can also lead to such pains. All of these are common in celiac disease, especially during the healing stage. A good co-enzyme B-complex, along with vitamin D3, magnesium, and calcium would be a good place to start. I also found a sublingual methylcobalamin (active form of B12) to be very helpful. Not just for body pain, but for fatigue, sleep cycles, mood, cognitive functioning, and more. Fortunately, not only are vitamin/mineral supplements inexpensive, but you don't need a doctor to prescribe them, and they're usually very safe in normal dosages. Just be sure to check the label for gluten and other no-nos. Both NOW Foods and Source Naturals are generally good about labeling which are gluten-free.

HTH

RoseL Newbie

Sorry, responded to your post with another post of your response...still learning how to use this forum. My response is below.

Thank you so much for responding!

RoseL Newbie

Thank you so much for your response. We have been looking at everything he's eaten and all supplements since we read your post.

The only thing we can identify is that he has been eating TONS of red meat. He says he wanted to get his weight and iron up. I read online that it's possible that too much red meat could cause arthritis. We're going to try cooking more fish and chicken and see if that helps.

  • 2 months later...
Lynayah Enthusiast
Thank you so much for your response. We have been looking at everything he's eaten and all supplements since we read your post.

The only thing we can identify is that he has been eating TONS of red meat. He says he wanted to get his weight and iron up. I read online that it's possible that too much red meat could cause arthritis. We're going to try cooking more fish and chicken and see if that helps.

The weight gain alone could be causing it. Adjusting to carrying around more weight can put stress on joints, back, etc.

Vit. D deficiency -- he might want to ask to have this checked. I was seriously depleted of D and my joint pain was HORRIBLE. I also became very weak and tired. Note: Do not self-diagnose this one -- it is important to not take excessive D unless under the care of a health care provider.

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. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,978
    • Most Online (within 30 mins)
      7,748

    Beverley Blanchard
    Newest Member
    Beverley Blanchard
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.