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

Neuropathy


Marie1976

Recommended Posts

Marie1976 Enthusiast

I am dealing with neuropathy (I guess that's what it is) in my hands and arms. It is sometimes really painful. I used to think it was caused by accidental "glutening" but I am getting it more frequently. Does anyone else have this problem? Is this celiac-related or ... not? Just wondering about other celiacs' opinions/experiences on this. 


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



Celiac.com Sponsor (A8-M):



1desperateladysaved Proficient

I don't know.....  I have neuropathy in the form of numbness pretty much everywhere.  There have been times it lessoned, and it isn't at its worse level of all times, but is pretty thickly numb now.  I have read it has to vitamin B, but vitamin B didn't seem to help me get rid of it.  I know time for healing is needed.  One person said their problem cleared after 3 years gluten free.  If I ever get to the bottom of the numbness, I will try to let you know.

 

Dee

LauraTX Rising Star

While neuropathy can be caused my a Celiac ingesting gluten/ untreated Celiac, it can be caused by other stuff, too.  So if you are getting it much more than usual, a trip to the doctor is in order to make sure there isn't another cause.

frieze Community Regular

perhaps benfotiamine would help?

Azenka Newbie

Too much B6 is also a known cause of neuropathy and nerve damage, (a source, but I've read other, better ones years ago) Open Original Shared Link

Other source I've read showed that even 50mg a day can be too much for some. Unfortunately every B vitamin complex seems to have a minimum of 50mg of it. 

B12 deficiency can cause neuropathy, as can folate (it's also a B vitamin) deficiency.

 

Personally, I cannot have coffee or chocolate anymore, neuropathy and mood changes (which is, really, just nerve issues in the center of my nervous system). I can abide chocolate chip cookies in moderate amounts, but that's it. (Yes, the chocolate is always gluten free.)

 

Tea and caffeinated things like red bull do not have anywhere near the severity of problems that having a cup of coffee give me, but if I've had more than a serving, my neuropathy gets noticeable. I would not be at all surprised for me if it's simply linked to reduced blood flow in my extremities in regards to caffeine. Caffeine constricts blood vessels, and poor circulation to, well, anywhere is linked to things like cell death, reduced healing of various other tissues (like in planar fasciitis), and all sorts of other issues. De-constriction of key blood vessels in Muscular Sclerosis, MS, which is *defined* as a nerve disease, is a fairly recent surgical option for sufferers. It's controversial because it's not -supposed- to work, but yet I know someone for whom it's worked nothing less than amazingly.

Anyways, I personally think that the neuropathy I do have (which is nowhere near as bad as the OP's is) is initially caused by nerve damage, and so gets exacerbated quite easily. I also figure I  must have issues with something else in coffee and chocolate besides caffeine.

cristiana Veteran

Hi Marie

 

I'm wondering if you might also have some nerve entrapment?  I read somewhere that celiacs are prone to carpal tunnel etc.  I was diagnosed with ulnar nerve entrapment earlier this year. I have had pins and needles and numbness but I admit it tends to be there mostly when I wake up and wears off.  I have buzzing in my left foot and up my calf: it was worse at diagnosis but still get it, particularly after excercise.  I noticed that as my B12 and iron levels improved, so too has the neuropathy.  Mind you having that said, I have also noticed that when I get pins and needles they last longer than before I was ill.  A doctor told me that when we celiacs have deficiences, our nerves start complaining!

 

Anyway, here's some info on ulnar entrapment.

 

Open Original Shared Link

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,112
    • Most Online (within 30 mins)
      7,748

    tomhaley
    Newest Member
    tomhaley
    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

    • trents
      Then it does not seem to me that a gluten-related disorder is at the heart of your problems, unless that is, you have refractory celiac disease. But you did not answer my question about how long you had been eating gluten free before you had the blood antibody test for celiac disease done.
    • Xravith
      My genetic test results have arrived - I’m homozygous for DQB1*02, meaning I have HLA-DQ2. I’ve read that this is one of the genes most strongly associated with celiac disease, and my symptoms are very clear. I’m relieved that the results finally arrived, as I was getting quite worried since my symptoms have been getting worse. Next step, blood test. What do these results imply? What should I tell my family? I’m concerned that this genetic predisposition might also affect other family members.
    • Roses8721
      Two months. In extreme situations like this where it’s clearly a smoking gun? I’m in LA so went to a very big hospital for pcp and gi and nutritionist 
    • rei.b
      So far 3 months in - worsening symptoms. I have had the worst constipation in my life and I am primarily eating naturally gluten-free foods like potatoes, eggs, salad with homemade dressing, corn tortillas, etc. I hate gluten-free bread and pasta so I don't eat it. Occasionally I eat gluten-free almond flour crackers. As stated in the post, I don't have any vitamin deficiency. I was already tested.
    • rei.b
      As I said, I do not have any vitamin deficiency. I was already tested.
×
×
  • 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.