Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

pcooley4195

Recommended Posts

pcooley4195 Rookie

New to the celiac forum... After being diagnosed with celiac after a year of bouncing around from Doctor to Doctor wondering what was causing all my knee pain ( at one point I was told that I dislocated my knee by immediate care and went to PT for 2 months) then the pain was in my other knee... I finally talked to my doctor about celiac after researching for months and had the endoscopy done as well as blood work which confirmed I did indeed have Celiac, My main question is what can I do to get rid of this neuropathy in both legs and left arm it makes concentration almost impossible... And I only showed low in vitamin D. Appreciate any attempt at help.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Welcome!  

I am sure others will offer you excellent advice, but neurological issues unfortunately are the last to resolve.  Keep to a very strict gluten free diet at least until you see some symptom improvement.  This includes a Whole Foods, less-processed,  diet and avoid going out to eat.

  Were your B-12 levels checked too?  

pcooley4195 Rookie

Yes.. Also it's only been 2 months since my diagnosis, and from all my research I understand healing takes time. But I was told I wasn't low in any vitamins just a little low in vitamin D. However it was slightly strange because I had been taking b12/magnesium/ Vitamin D for my strange muscle pains that I now know are from the celiac.

icelandgirl Proficient

Hi Pcooley!

For my peripheral neuropathy I take magnesium.   My Dr recommended 200-400 mg a day.  I started with 100 and found 300 to be the magic number for me.  I take a chelated magnesium.   It has reduced my symptoms almost completely.  It was so bad at one point that I had a hard time sitting and reading.

Are you supplementing with a good D3 for your deficiency?  That will help things as well.

Hole that helps!

pcooley4195 Rookie
4 hours ago, icelandgirl said:

Hi Pcooley!

For my peripheral neuropathy I take magnesium.   My Dr recommended 200-400 mg a day.  I started with 100 and found 300 to be the magic number for me.  I take a chelated magnesium.   It has reduced my symptoms almost completely.  It was so bad at one point that I had a hard time sitting and reading.

Are you supplementing with a good D3 for your deficiency?  That will help things as well.

Hole that helps!

That's exactly what I mean when I say it makes concentrating difficult, when I'm working on my college assignments or in class it's extremely hard to stay focused. I've been supplementing with magnesium/B12/D3 for about 6 months even before I knew I had celiac I also take a multivitamin. How long did it take you to notice the benefits of the magnesium?

GFinDC Veteran

@PCooley,

Another thing that can cause joint pain is nightshades.  You could try cutting out nightshades for a month or so and see if it helps.

pcooley4195 Rookie
39 minutes ago, GFinDC said:

@PCooley,

Another thing that can cause joint pain is nightshades.  You could try cutting out nightshades for a month or so and see if it helps.

My joint pain has definitely decreased the main issue I have currently is lower back pain... It seems my lower back is inflamed and the neuropathy in the legs and arms.


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



Celiac.com Sponsor (A8-M):



cristiana Veteran
45 minutes ago, pcooley4195 said:

My joint pain has definitely decreased the main issue I have currently is lower back pain... It seems my lower back is inflamed and the neuropathy in the legs and arms.

I had inflammation of the sacroiliac joints which felt like lower back pain, and sometimese referred to my groin, abdomen and thigh.  It was a burning sensation which showed up a few months after going gluten free, hung around for a while, then left me.  I still get it midly from time to time, especially when I've been carrying heavy weights.  It is apparently quite common in coeliacs.  You might want to look it up.

As regards neuropathy, two other things to consider:

I recently tested low/borderline normal for folate.  I hadn't been supplementing it to the extent I have been taking B12 and I'm pretty sure it could be a contributing factor.

Also, how are your ferritin levels/hemoglobin.? Again, this can cause tingling. I'm borderline anemic again (perimenopause thing) and again I think its part of my problem.

 

pcooley4195 Rookie
1 hour ago, cristiana said:

I had inflammation of the sacroiliac joints which felt like lower back pain, and sometimese referred to my groin, abdomen and thigh.  It was a burning sensation which showed up a few months after going gluten free, hung around for a while, then left me.  I still get it midly from time to time, especially when I've been carrying heavy weights.  It is apparently quite common in coeliacs.  You might want to look it up.

As regards neuropathy, two other things to consider:

I recently tested low/borderline normal for folate.  I hadn't been supplementing it to the extent I have been taking B12 and I'm pretty sure it could be a contributing factor.

Also, how are your ferritin levels/hemoglobin.? Again, this can cause tingling. I'm borderline anemic again (perimenopause thing) and again I think its part of my problem.

 

I'll definitely check with my doctor this Thursday in terms of a more in depth look at my hemoglobin levels as well as Ferritin, much appreciated. And my back pain started when I went to Pt who thought my tingling in my legs was from a lower back issue and after doing excersizes that targeted the lower back it made everything feel aggravated.

Alwayssomething Contributor

Don't know if you are already doing this, but for me I had to stop wearing certain things to avoid the extensive pain in my legs, arms and even in my hip from neuropathy.    I still can't wear some of them without getting a flare.    Nothing with elastic in the arms or legs, socks were tough but I just wore the ones that were lower on the foot.  This helped a lot!   For me seams running up on my hip like in jeans were a huge pain trigger and I had to switch to Columbia hiking pants.    Cost me  fortune but it was well worth it and after years I can wear jeans again without an issue, although I don't push it and wear them every day.    I have been gluten free for 7 years and still have some neuropathy here and there but nothing like before.   For me nightshades cause joint issues but not neuropathy.  By the way my Vitamin D and B12 are just now in the middle of the normal range where my dr wants them, but I can't stop taking Vitamin D or doing the B12 shots or my numbers slowly drop back down, I don't think I will ever be able to go without.    

cristiana Veteran
58 minutes ago, Alwayssomething said:

Don't know if you are already doing this, but for me I had to stop wearing certain things to avoid the extensive pain in my legs, arms and even in my hip from neuropathy.    I still can't wear some of them without getting a flare.    Nothing with elastic in the arms or legs, socks were tough but I just wore the ones that were lower on the foot.  This helped a lot!   For me seams running up on my hip like in jeans were a huge pain trigger and I had to switch to Columbia hiking pants.    Cost me  fortune but it was well worth it and after years I can wear jeans again without an issue, although I don't push it and wear them every day.    I have been gluten free for 7 years and still have some neuropathy here and there but nothing like before.   For me nightshades cause joint issues but not neuropathy.  By the way my Vitamin D and B12 are just now in the middle of the normal range where my dr wants them, but I can't stop taking Vitamin D or doing the B12 shots or my numbers slowly drop back down, I don't think I will ever be able to go without.    

Wow Alwayssomething - so I'm not the only one!  I have had this problem with elasticated and tight waists too.  I had to stop wearing certain clothes too.  Any pressure on my waist or hips was a disaster.  I think it pressed against my SI joints, but also added the pressure of trapped wind to an already painful area.

 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,596
    • Most Online (within 30 mins)
      7,748

    Vicki teach
    Newest Member
    Vicki teach
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Alibu
      I was tested back in 2017 and my TTG-IGA was mildly elevated (an 11 with reference range <4) but my EMA was negative and biopsy was negative. Fast forward to 2 weeks ago where I was like y'know what, I still have so many symptoms and I'm always so sick, I should repeat this, thinking it was not going to be positive.  I also found out through 23 and me that I do have the HLA-DQ2.5 gene so I thought it would be good to repeat given my ongoing symptoms. Well my blood work came back with a ttg-iga level of 152.6 with a reference range of <15 and my EMA was positive and EMA titer was 1:10 with reference range of <1:5. I guess I'm nervous that I'm going to do the biopsy and it's going to be negative again, especially since I also had an endoscopy in 2020, not to look for celiac but just as a regular 5 year thing I do because of all my GI issues, and they didn't see anything then either. I have no idea how long the EMA has been positive but I'm wondering if it's very recent, if the biopsy will show damage and if so, if they'll say well the biopsy is the gold standard so it's not celiac? I of course am doing all the things to convince myself that it isn't real. Do a lot of people go through this? I think because back in 2017 my ttg-iga was elevated but not a huge amount and my EMA was negative and my biopsy was negative, I keep thinking this time it's going to be different. But this time my ttg-iga is 152.6 with reference range <15, and my EMA was positive. BUT, my titer is only 1:10 and I keep reading how most people here had a ttg-iga in the hundreds or thousands, and the EMA titer was much higher. So now I am convinced that it was a false positive and when they do the biopsy it'll be negative.
    • trents
      Welcome to the forum, @linnylou73! Are you claiming this based on a reaction or based upon actual testing?
    • linnylou73
      Sams club membermark columbian coffee is either cross contaminated or the pods contain gluten
    • KimMS
    • Scott Adams
      This varies a lot from person to person. I include foods that are not certified gluten-free but are labelled "gluten-free", while super sensitive people only use certified gluten-free. Both types of products have been found to contain gluten, so there are no guarantees either way: It you are in the super sensitive group, eating a whole foods based diet where you prepare everything is the safest bet, but it's also difficult. Eating out is the the most risky, even if a restaurant has a gluten-free menu. I also include items that are naturally gluten-free, for example refried beans, tuna, pasta sauces, salsas, etc., which have a low overall risk of contamination.
×
×
  • Create New...