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

Vitamin Deficiency Neuropathy


Guest Eagle

Recommended Posts

Guest Eagle

Hello, I was just diagnosed as celiac and casein intolerant after I had overdosed on some toxic food. I didn't realize that I had a B6 deficiency and the doctor didn't even check my B levels when I came in with neuropathy. It really did a number on me before I figured out what was wrong. Has anyone had this happen and recovered completely? I have alot of numbness and burning and a bit of short term memory loss.


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

I also have experienced quite a bit of numbness, along with muscle/joint pains, twitching, spasms, weakness, etc.

What I've found most helpful are both a sublingual methylcobalamin supplement, and a magnesium supplement. The improvements are thus far astounding to me. I wish I had started them a long time ago. Since my digestive system would never handle a solid pill, the magnesium I chose is a powder, which makes it easy to mix into meals, fruit juices, and smoothies. It also makes for quicker/better absorption, which I'm sure is a good idea in my case.

I'm sure others will have fine suggestions for you to try/look into as well.

darlindeb25 Collaborator

B6 is helpful with neuropathy, yet generally it is a B12 deficiency that causes neuropathy for celiac's. I take 2400mcg of B12 daily. Have your doctor do blood work up for B12. Some doctors say that a level of say--400 is good, but it's not, that is way too low.

I have never been told about magnesium, I will have to research that.

mamabear Explorer
I also have experienced quite a bit of numbness, along with muscle/joint pains, twitching, spasms, weakness, etc.

What I've found most helpful are both a sublingual methylcobalamin supplement, and a magnesium supplement. The improvements are thus far astounding to me. I wish I had started them a long time ago. Since my digestive system would never handle a solid pill, the magnesium I chose is a powder, which makes it easy to mix into meals, fruit juices, and smoothies. It also makes for quicker/better absorption, which I'm sure is a good idea in my case.

I'm sure others will have fine suggestions for you to try/look into as well.

I get similar symptoms( except weakness) and have also found calcium/magnesium/zinc tablets and a prescription vitamin called Metanx for being very helpful. Metanx has biologically active forms of B12,B6 and Folate and is very strong. I have backed off on that to every other day now after 4 months daily use. I also get better when I can exercise. Anyone else seen this?

darlindeb25 Collaborator

I have neverheard of Metanx, I do not think I have ever read about it in my neuropathy forums. Didn't know it existed. I may research that--thanks.

Nancym Enthusiast

I take a B complex, B12 sublingually AND folic acid. If you are low in B12 and supplement folic acid it can make cognitive functioning worse, so I get both together. My neurological symptoms are VASTLY better. I think supplementing vit. D3 also helped a lot too.

WakeupNurse Newbie
Hello, I was just diagnosed as celiac and casein intolerant after I had overdosed on some toxic food. I didn't realize that I had a B6 deficiency and the doctor didn't even check my B levels when I came in with neuropathy. It really did a number on me before I figured out what was wrong. Has anyone had this happen and recovered completely? I have alot of numbness and burning and a bit of short term memory loss.

I think this is pretty common among celiacs but also many people with other autoimmune diseases. It can be pretty scary when you quit feeling your feet and hands like you should and can't remember things like before! I have a lot of neuropathy issues also. Mine are mostly caused from malabsorption and pernicious anemia (low B12). A good fish oil omega three supplement can help with neuropathy, as well as B12 or Bcomplex supplementation. There is also a med called Cerefolin with NAC out there that is prescribed for neuropathy that is several vitamins (B6, folate, methylcobalamin, & NAC if I'm not mistaken) that is often prescribed to diabetics with neuropathy that might help. Making sure you're getting enough of your calcium, potassium, and magnesium will help also. I wound up taking my vitamins in shot form because my absorption is so poor we couldn't ever get my levels up. Good luck!


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



Celiac.com Sponsor (A8-M):



  • 1 year later...
jeremy24 Newbie
Hello, I was just diagnosed as celiac and casein intolerant after I had overdosed on some toxic food. I didn't realize that I had a B6 deficiency and the doctor didn't even check my B levels when I came in with neuropathy. It really did a number on me before I figured out what was wrong. Has anyone had this happen and recovered completely? I have alot of numbness and burning and a bit of short term memory loss.

I've been recently are going to be going through test based on burning and numbness throughout my legs and arms. I've also had a MRI that showed my disc in my back are degenerate and are moving to my spine. I've also had a colonoscopy because there was blood in my stool. The doctors don't think that there connected, I do. The one doctor thinks that it could be neuropathy and the other thinks that there could be a calcium deficiency. Did you also have burning in your spine or have any other of these symptoms

Lizz7711 Apprentice

Just be aware that taking too much B6 in the Hcl form can also cause neuropathy, this happened to me when taking about 150mg per day. It's safer to take in the P5P form, but it's hard to find. I'm currently taking Country Life's activated B6 with P5P. If you were deficient, this may not be an issue for you, i'm not sure...but i'd still advise the P5P form instead if you can get it.

I think most short term nerve damage is usually reversible, so just give it a few weeks :)

Hello, I was just diagnosed as celiac and casein intolerant after I had overdosed on some toxic food. I didn't realize that I had a B6 deficiency and the doctor didn't even check my B levels when I came in with neuropathy. It really did a number on me before I figured out what was wrong. Has anyone had this happen and recovered completely? I have alot of numbness and burning and a bit of short term memory loss.
Nancym Enthusiast

You might as well get started on supplements. I think your damage can probably be repaired, I've heard of other folks doing it.

ravenwoodglass Mentor

Yea I agree get started with the B12 as soon as you can. I started having celiac related nerve issues at about 5 and had progressed to some very serious issues by the time I was diagnosed decades later. I have been amazed at how much nerve recovery I have had. The tingling and such stopped within a couple months of starting the B12 for me. The other issues like loss of reflexes, dead leg etc did take much longer to repair.

NicoleAJ Enthusiast
I've been recently are going to be going through test based on burning and numbness throughout my legs and arms. I've also had a MRI that showed my disc in my back are degenerate and are moving to my spine. I've also had a colonoscopy because there was blood in my stool. The doctors don't think that there connected, I do. The one doctor thinks that it could be neuropathy and the other thinks that there could be a calcium deficiency. Did you also have burning in your spine or have any other of these symptoms

This is interesting. I've actually had the same symptoms. I didn't react very well to the sublingual B12, so I take injections of B12 every two weeks, and that has really helped the neuropathy symptoms. As far as the degenerated spinal disks--I've had that too, and my doctor told me that is a totally normal finding for a 29 year old because the disks do break down over time.

I've had blood in my stool and occult bleeding of the GI tract on and off for about 4 years now. I've had 4 colonoscopies, 2 capsule endoscopies, 2 endoscopies, 2 small bowel follow throughs. They always find chronic inflammation, but then do not find the exact source of the bleeding, which is very strange since the stool tests and my ferritin levels show that I'm losing a lot of blood. They keep thinking it's Crohn's and then they don't find it. Let me know if they find the source of your rectal bleeding.

sumichls Newbie
Hello, I was just diagnosed as celiac and casein intolerant after I had overdosed on some toxic food. I didn't realize that I had a B6 deficiency and the doctor didn't even check my B levels when I came in with neuropathy. It really did a number on me before I figured out what was wrong. Has anyone had this happen and recovered completely? I have alot of numbness and burning and a bit of short term memory loss.
Yes! I have peripheral neuropathy in my feet. I wholeheartedly believe it is a result of nutritional deficiencies. I was told that sometimes it is reversable, that only time will tell.
AndrewNYC Explorer

It is potentially reversible. There are two different causes but most doctors who are not in the know will chalk it up to only one. They cite nutritional deficiency which on its own can cause neuropathy, and can be reversible. Doctors who are more familiar with celiac and allergies know that there is also an immuno response that can cause neuropathy. This is separate from vitamin deficiency. You can have normal nutrition and have neuropathy from immuno-allerginic response. This too can be reversible. On the other hand, both could be non reversible if left uncorrected for too long. You will need to give it lots of time. Maybe 6 months or more. Stay on the most basic diet that you can. Avoid gluten foods that were manufactured with potential for cross contamination. Consider yourself to be super sensitive.

ShayFL Enthusiast

B vitamins have not helped my neuropathy. I take them everyday (not more than 100 B6), full spectrum and 10000 B12). Have been for a year. I have recently discovered (last 4 months) that I am severely deficient in Vitamin D and I have very low Ferritin (Iron). Both of these can contribute to neuropathy. So under my doctor's supervision, I am now taking 5000 IU Vit. D a day and 200 Iron.

I am hopeful that one of these will be the key. I was taking 1/2 the amount of Vit. D and no iron for the last 4 months. I only got my Vit. D a little. A long way to go to be optimal.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,947
    • Most Online (within 30 mins)
      7,748

    Sinch23
    Newest Member
    Sinch23
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.