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

Peripheral Neuropathy


jebby

Recommended Posts

jebby Enthusiast

I have just been diagnosed with a peripheral neuropathy related to celiac disease.

My symptoms started about 1 week after being accidentally "glutened" earlier this month. I began to get numb and tingling sensations in my hands and feet.

My neurologist told me that celiac disease is now the 3rd most common cause of neuropathy (behind alcoholism and diabetes) and the most common cause of ataxia. He told me that the pins and needles sensation in my extremities should resolve within 6 to 8 weeks, but to expect getting it whenever I am exposed to gluten from here on out.

I am wondering if any of you have been diagnosed with a peripheral neuropathy (and if so, what your experiences have been).

Thanks a bunch!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Wow a neurologist who is knowledgeable about celiac!!!!

I found that sublingual B12 helped resolve the neuropathy. If you are not already taking it you may want to see if it will help.

AVR1962 Collaborator

Wow, amazing to have any doc actually tell you this. I have had issues with neuropathy for 2 years now, had all kinds of tests done, have done lots of reading. Make sure you are taking a very good B complex as the B vits feed the nerves. B12 is very hard to get into the body so we have to take it in greater quantities but a complex has it in the proper purportions. Keep taking your vitamin C as well, as good for the nerves. Are you having actual pins and needles pain? I have had them in my feet. I used L-carnitine, 1000 mg daily for the first year and then was able to reduce it to 500 mg daily.

Just over 2 weeks ago I was able to go off the L-carntine. After repeated visits to various docs and lots of blood tests and you name it, a doc finally figured it was my back that was causing me issues. I ahve been doing yoga now almost daily for 2 weeks (this is after some treatments on my back) and now the left foot is good and only an occasional twing in the right foot.

I would hate to see you go down the road I went. I would make sure this is not coming from your back before you decide for sure it is gluten related. I have 2 bulging discs in my back. 2 different docs said my back was fine but I finally had an MRI and it showed the problem.

jebby Enthusiast

I am having pins and needles pains in my hands and feet, right more than left. I am on Vit B12 1000 mcg/day and just had my level checked and it is >1000, which I believe is good.

It's funny that you mention yoga, because I am signed up for my first class tomorrow (I last did yoga in college about 15 years ago). I am hoping to do it regularly.

My neurologist is great, he is planning on going to the huge celiac conference in Chicago in September 2013 and seems truly interested in the neuro effects of gluten. This is after meeting another neurologist first who did not know what celiac disease is!

AVR1962 Collaborator

Jebby, that is great! Here is a link to some more info on natural remedies for nueropathy Open Original Shared Link

  • 2 weeks later...
frieze Community Regular

I am having pins and needles pains in my hands and feet, right more than left. I am on Vit B12 1000 mc, g/day and just had my level checked and it is >1000, which I believe is good.

It's funny that you mention yoga, because I am signed up for my first class tomorrow (I last did yoga in college about 15 years ago). I am hoping to do it regularly.

My neurologist is great, he is planning on going to the huge celiac conference in Chicago in September 2013 and seems truly interested in the neuro effects of gluten. This is after meeting another neurologist first who did not know what celiac disease is!

That test for B12 wouldn't be accurate, assuming you were taking the supplement right up to the day the level was draw. Need to stop for several days before the blood is drawn. good luck

gatita Enthusiast

I haven't been diagnosed with PN, but the pins and needles numbness in my feet early this year scared the bejeebers out of me (many months before my doc told to try gluten-free). I was sure I had MS.

All I know is that symptom has completely disappeared since going gluten-free. It took about two months to go away. Also, my severe joint pain is mostly gone too.

I still wake up sometimes with that tingly feeling in my hands, but it seems to be connected to sleeping with my arms all twisted up in contorted postions lol.


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



Celiac.com Sponsor (A8-M):



Takala Enthusiast

It took me longer than 6 to 8 weeks to get rid of it, it was a long, hard slog, but I had had this damage for decades and it was getting blamed on something else.

Traveller Rookie

I have PN secondary to gluten sensitivity, or so says one of the leading celiac researchers. My symptoms arise shortly after being glutened, and start with pain in random parts of either foot, progressing to uncontrolled leg movements (leg "jumping"). Unsually the symptoms stop after a few weeks. I went to see the research doctor after the symptoms did not stop. He told me that I must have hidden gluten in my diet. That gluten was stripping myelin off the nerves, and allowing signals to short circuit. He also said that if I found and removed it the hidden gluten, in 6-8 months the myelin should build back up to the point where the symptoms should resolve. I found the hiddel gluten (a package of Hershey's miniatures, of which I was eating 2-3 a day over several weeks), and in 8 months they symptoms disappeared.

But they reappear with each glutening. At least I know why. Interestingly, the symptoms are worse when I fly.

  • 4 months later...
KerryLad Rookie

hi jebby i have the exact same issues with pins and needles i have had it for 3 weeks now. it started when i went out and drank carlberg and got them the monring after dont go out that much but then after i ate mcdonalds and alot of foods kept doing it pins and needles were kinda going but then the weekend ate a lot of taytos sausages etc and came back at me... are u free from this pins and needles now its def after i eat it i get them in my hands like freaked me out at start taught my heart all my bloods came back clear but waiting for celiac desiese like if u can let me know would be greatfull thanks alot 

jebby Enthusiast

Hi Kerrylad, My pins and needles/numbness has totally resolved since taking all gluten out of my home (no more accidental cross contamination). The last time I had it happen was in January after getting gluten cross contamination at a restaurant. Do you have celiac disease or non celiac gluten sensitivity? Have you seen a doctor?

If you are linking the pins and needles sensation to drinking beer and eating at McDonalds, then there's a good possibility that it may be related to gluten. But, you need to make sure that you do to have multiple sclerosis, diabetes, lupus, or Lyme Disease, as these can all cause peripheral neuropathy to begin.

KerryLad Rookie

Hi Kerrylad, My pins and needles/numbness has totally resolved since taking all gluten out of my home (no more accidental cross contamination). The last time I had it happen was in January after getting gluten cross contamination at a restaurant. Do you have celiac disease or non celiac gluten sensitivity? Have you seen a doctor?

If you are linking the pins and needles sensation to drinking beer and eating at McDonalds, then there's a good possibility that it may be related to gluten. But, you need to make sure that you do to have multiple sclerosis, diabetes, lupus, or Lyme Disease, as these can all cause peripheral neuropathy to begin.

thanks very much for reply.. had my full bloods done and they are all clear dibities tyroid etc like celiac came back clear in bloods like i know whats im eating this has being going on for months as in stinging in intestines used come and go away id take no notice but recently the last 3 weeks hit with a bang like,, i had salmon yesteday with pastry on it potatoes and veg and cause on top i took the pastry off it and wipped the sause away and after eating it 15 mins later i felt sick and needed to get sick its just the bloods came back negitive cracks me up and these pins and needles are head wrecken and all the doctorrs from my place never heard of pins and needles from it like how long did it take for u to get rid of them and did u feel good on the new diet?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,537
    • Most Online (within 30 mins)
      7,748

    annelizabeth
    Newest Member
    annelizabeth
    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

    • 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!
    • ElisaAllergiesgluten
      Hello good afternoon, I was wondering if anyone has ever brought their anti-allergy pills? I have been wanting to use their Cetirizine HCI 10mg. They are called HealthA2Z and distributed by Allegiant Health.I’m also Asthmatic and these allergies are terrible for me but I also want to be sure they don’t have any sort of gluten compound.    I have tried calling them but to no avail. Has anyone ever used them? If so, did you had any problems or no problems at all?    thank you
×
×
  • 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.