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

Tinglying In Feet And Face


bisja

Recommended Posts

bisja Apprentice

Does everyone here thats had any tinglying feelings neurologic symptoms always shown a vit or min

deficiency or have you had these feelings even though you show no deficiency? Had them leave after being gluten-free?


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Yes, others here have had symptoms such as yours. The neurological symptoms seem to be the last to subside.

jerseyangel Proficient

I had tingling in my face, lower legs, feet and left arm for about a year before being diagnosed. My left arm also had an "altered" feeling--somewhere between being asleep and tingling. The bottoms of my feet would have sudden, stabbing pain.

I didn't have any testing for deficiencies, but these symptoms did resolve after being on the gluten-free diet. The relief was gradual over months. I'll be gluten-free 3 years in June, and I still have a bit of numbness on the left side of my face at times, but that's it.

bisja Apprentice

Did any of you also suffer like chronic fatigue? I have one better day do some house cleaning and the next day feel terrible sometimes for days after feel terrible? Just wondering if the gluten can do alot of this. I also have alot of muscle pain.

jerseyangel Proficient
Did any of you also suffer like chronic fatigue? I have one better day do some house cleaning and the next day feel terrible sometimes for days after feel terrible? Just wondering if the gluten can do alot of this. I also have alot of muscle pain.

Yes--fatigue is a very common symptom, and it can persist for a long time even after taking gluten out of the diet. Muscle pain is also a symptom.

bisja Apprentice

This is all so crazy I am 54 years old and had stomach problems on and off all my life but the last 2 years have been the worst, I was very anemic was blamed on the change of life, then got mononucleosis, then said I had Lyme Disease on abx for 6 months now off that for a week and a half sent in tests to eneterolab and found out I have a celiac gene and a gluten sensetivity gene, still have these symptoms will go to my reg doc April 16th but do not want tunnel vision being put on Lyme as was already told to me the Lyme was causing my stomach problems and it deffinately wasn't the cause for me. I am hoping my immune system will get much stronger now that I get the gluten out and the dairy. This was the test results I got back then they explained each one.

A) Gluten Sensitivity Stool and Gene Panel Complete *Best test/best value

Fecal Antigliadin IgA 17 (Normal Range <10 Units)

Fecal Antitissue Transglutaminase IgA 10 Units (Normal Range <10 Units)

Quantitative Microscopic Fecal Fat Score <300 Units (Normal Range <300 Units)

Fecal anti-casein (cow's milk) IgA antibody 10 Units (Normal Range <10 Units)

HLA-DQB1 Molecular analysis, Allele 1 0201

HLA-DQB1 Molecular analysis, Allele 2 0202

Serologic equivalent: HLA-DQ 2,2 (Subtype 2,2)

They said no malabsorption problems guess thats why I was wondering if anyone had these problems from gluten even without vit min probs.

ravenwoodglass Mentor
This is all so crazy I am 54 years old and had stomach problems on and off all my life but the last 2 years have been the worst, I was very anemic was blamed on the change of life, then got mononucleosis, then said I had Lyme Disease on abx for 6 months now off that for a week and a half sent in tests to eneterolab and found out I have a celiac gene and a gluten sensetivity gene, still have these symptoms will go to my reg doc April 16th but do not want tunnel vision being put on Lyme as was already told to me the Lyme was causing my stomach problems and it deffinately wasn't the cause for me. I am hoping my immune system will get much stronger now that I get the gluten out and the dairy. This was the test results I got back then they explained each one.

A) Gluten Sensitivity Stool and Gene Panel Complete *Best test/best value

Fecal Antigliadin IgA 17 (Normal Range <10 Units)

Fecal Antitissue Transglutaminase IgA 10 Units (Normal Range <10 Units)

Quantitative Microscopic Fecal Fat Score <300 Units (Normal Range <300 Units)

Fecal anti-casein (cow's milk) IgA antibody 10 Units (Normal Range <10 Units)

HLA-DQB1 Molecular analysis, Allele 1 0201

HLA-DQB1 Molecular analysis, Allele 2 0202

Serologic equivalent: HLA-DQ 2,2 (Subtype 2,2)

They said no malabsorption problems guess thats why I was wondering if anyone had these problems from gluten even without vit min probs.

Although your malabsorption levels are good that doesn't always mean that there are not deficiencies as the fecal fat score measures the amount of fat that is in your stool not the vitamin and mineral levels. You may want to get a good sublingual B12, that will help resolve the nerve issues more quickly.


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



Celiac.com Sponsor (A8-M):



bisja Apprentice
Although your malabsorption levels are good that doesn't always mean that there are not deficiencies as the fecal fat score measures the amount of fat that is in your stool not the vitamin and mineral levels. You may want to get a good sublingual B12, that will help resolve the nerve issues more quickly.

thanks I was wondering about that fecal fat score as I eat very low fat meals as always get such bad heartburn from anything fatty would that make a difference in that test? Also what brand of sublingual B12 do you recommend? Plus how accurate do you feel the blood tests are they use to check for vit. min. deficiencies I have heard some people say that they are not that accurate.

ravenwoodglass Mentor
thanks I was wondering about that fecal fat score as I eat very low fat meals as always get such bad heartburn from anything fatty would that make a difference in that test? Also what brand of sublingual B12 do you recommend? Plus how accurate do you feel the blood tests are they use to check for vit. min. deficiencies I have heard some people say that they are not that accurate.

I take the Country Life vegetarian sub-lingual B12 with folic acid. There are other good brands also but I like the Country Life myself. I also use Royal Jelly (from bees) which has some B12 in it also and that seems to help my appetite quite a bit.

As far as the accuracy of the blood tests for levels folks are right about them not being a great tool, especially the B12 levels which can be bottoming out for quite a while before it shows up in the tests. However they can be useful when it comes to assessing how well we are healing if the tests are run when we first start the diet and then rerun at 6 months and a year postdiagnosis.

As to the fat and heartburn issue, your celiac could be impacting the function of your pancreas and or gallbladder. You may very well find after being gluten-free for a few months that high fat foods no longer cause the distress you are having now. I always thought I couldn't handle spicey foods, a spicey burrito or taco would lead to hours of pain, it turned out it wasn't the spice it was the poison it was wrapped in. I now enjoy a lot of foods that I couldn't eat prediagnosis, as long as they are gluten-free. I can't say for sure that will be the case for you as we are all different but you may be pleasently surprised after you have throughly healed.

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. - tiffanygosci posted a topic in Coping with Celiac Disease
      0

      New Celiac Mama in My 30s

    2. - knitty kitty replied to klmgarland's topic in Dermatitis Herpetiformis
      8

      Help I’m cross contaminating myself,

    3. - Yaya replied to Jhona's topic in Introduce Yourself / Share Stuff
      29

      Does anyone here also have Afib

    4. - larc replied to Jhona's topic in Introduce Yourself / Share Stuff
      29

      Does anyone here also have Afib

    5. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      8

      Help I’m cross contaminating myself,


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,919
    • Most Online (within 30 mins)
      7,748

    SB Willow
    Newest Member
    SB Willow
    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)

  • Upcoming Events

  • Posts

    • tiffanygosci
      Hello all! My life in the last five years has been crazy. I got married in 2020 at the age of 27, pregnant with our first child almost two months later, gave birth in 2021. We had another baby in April of 2023 and our last baby this March of 2025. I had some issues after my second but nothing ever made me think, "I should see a doctor about this." After having my last baby this year, my body has finally started to find its new rhythm and balance...but things started to feel out of sorts. A lot of symptoms were convoluted with postpartum symptoms, and, to top it all off, my cycle came back about 4m postpartum. I was having reoccurring migraines, nausea, joint pain, numbness in my right arm, hand and fingers, tummy problems, hives. I finally went to my PCP in August just for a wellness check and I brought up my ailments. I'm so thankful for a doctor that listens and is thorough. He ended up running a food allergy panel, an environmental respiratory panel, and a celiac panel. I found out I was allergic to wheat, allergic to about every plant and dust mites, and I did have celiac. I had an endoscopy done on October 3 and my results confirmed celiac in the early stages! I am truly blessed to have an answer to my issues. When I eat gluten, my brain feels like it's on fire and like someone is squeezing it. I can't think straight and I zone out easily. My eyes can't focus. I get a super bad migraine and nausea. I get so tired and irritable and anxious. My body hurts sometimes and my gut gets bloated, gassy, constipated, and ends with bowel movements. All this time I thought I was just having mom brain or feeling the effects of postpartum, sleep deprivation, and the like (which I probably was having and the celiac disease just ramped it up!) I have yet to see a dietician but I've already been eating and shopping gluten-free. My husband and I have been working on turning our kitchen 100% gluten-free (we didn't think this would be so expensive but he assured me that my health is worth all the money in the world). There are still a few things to replace and clean. I'm already getting tired of reading labels. I even replaced some of my personal hygiene care for myself and the kids because they were either made with oats or not labeled gluten-free. I have already started feeling better but have made some mistakes along the way or have gotten contamination thrown into the mix. It's been hard! Today I joked that I got diagnosed at the worst time of the year with all the holidays coming up. I will just need to bring my own food to have and to share. It will be okay but different after years of eating "normally". Today I ordered in person at Chipotle and was trying not to feel self-conscious as the line got long because they were following food-allergy protocols. It's all worth it to be the healthiest version of myself for me and my family. I would be lying if I said I wasn't a little overwhelmed and a little overloaded!  I am thankful for this community and I look forward to learning more from you all. I need the help, that's for sure!
    • knitty kitty
      On the AIP diet, all processed foods are eliminated.  This includes gluten-free bread.  You'll be eating meats and vegetables, mostly.  Meats that are processed, like sausages, sandwich meats, bacons, chicken nuggets, etc., are eliminated as well.  Veggies should be fresh, or frozen without other ingredients like sauces or seasonings.  Nightshade vegetables (eggplant, potatoes, tomatoes, peppers) are excluded.  They contain alkaloids that promote a leaky gut and inflammation.  Dairy and eggs are also eliminated.   I know it sounds really stark, but eating this way really improved my health.  The AIP diet can be low in nutrients, and, with malabsorption, it's important to supplement vitamins and minerals.  
    • Yaya
      Thank you for responding and for prayers.  So sorry for your struggles, I will keep you in mine.  You are so young to have so many struggles, mine are mild by comparison.  I didn't have Celiac Disease (celiac disease) until I had my gallbladder removed 13 years ago; at least nothing I was aware of.  Following surgery: multiple symptoms/oddities appeared including ridges on fingernails, eczema, hair falling out in patches, dry eyes, upset stomach constantly and other weird symptoms that I don't really remember.  Gastro did tests and endoscopy and verified celiac disease. Re heart: I was born with Mitral Valve Prolapse (MVP) and an irregular heartbeat, yet heart was extremely strong.  It was difficult to pick up the irregular heartbeat on the EKG per cardiologist.  I had Covid at 77, recovered in 10 days and 2 weeks later developed long Covid. What the doctors and nurses called the "kickoff to long Covid, was A-fib.  I didn't know what was going on with my heart and had ignored early symptoms as some kind of passing aftereffect stemming from Covid.  I was right about where it came from, but wrong on it being "passing".  I have A-fib as my permanent reminder of Covid and take Flecainide every morning and night and will for the rest of my life to stabilize my heartbeat.   
    • larc
      When I accidentally consume gluten it compromises the well-being of my heart and arteries. Last time I had a significant exposure, about six months ago, I had AFib for about ten days. It came on every day around dinner time. After the ten days or so it went away and hasn't come back.  My cardiologist offered me a collection of pharmaceuticals at the time.  But I passed on them. 
    • klmgarland
      So I should not eat my gluten free bread?  I will try the vitamins.  Thank you all so very much for your ideas and understanding.  I'm feeling better today and have gathered back my composure! Thank you kitty kitty   I am going to look this diet up right away.  And read the paleo diet and really see if I can make this a better situation then it currently is.  
×
×
  • 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.