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

Help...neuro Symptoms & Other Food Intolerances


175comet

Recommended Posts

175comet Rookie

Hi!

After 2.5 years of numerous MRIs, bllod tests etc (you've heard it all before), I finally figured out my neurological symptoms (tingling, stiffness, arthrtic pain, twitching, myoclonus, vertigo) were related to gluten. 15 mths ago, I had a negative biopsy so figured it wasn't the problem. So I started eating wheat again. Then all the symptoms came back. My very good neurologist recommended going off wheat again. It's been 5 moths and I'm ab 95% better. I don't know if its celiac or gluten intolerance bc I never had the "full blood panel". According to the gasteroentologist. Sorry long story, but here is my question....

About 7 weeks ago I went on an elimination diet bc I know other food really bother me (bloating). So far I have determined: tomatoes, peppers, almond butter, red meat & dairy. I've accidentally eaten gluten 3x and I was soooooo sick. The tingling, myoclonus & vertigo came back and it felt like an alien was going to burst from my stomach. However sometimes I still get that tingly feeling on my face or vertigo even if i havnet eaten wheat (i toasted gluten free bread in our toaster and quckly learned that even crumbs really affect me). I'm wondering if this is just remnants or if other food could be causing it. It's soo hard if gutting out all the other food intolerances... And it sucks being so limited. However my energy level went from about a 3/10 to a 6/10 after going gluten free. Then I went from a 7 to a 9/10 on first 3 wks of the elimination diet!!!

Ahhhh! Thoughts??


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



Celiac.com Sponsor (A8-M):



Brandiwine Contributor

It takes awhile for the antibodies to die off from consuming gluten. Every time I'm glutened or get CC it's like mini replay of before starting on my GFD.

I am a vegan and I have some issues with soy and onions that I now know for sure and I'm allergic to Cinnamon. So there is alot that I can't eat, everything is made from scratch I spend hours in the kitchen and although I love to cook and create new dishes I get exhausted and sometimes just don't have the time to put in! When that happens or if it seems like I'm getting CC from some where or I suspect another food sensitivity I eat simply for every meal ithe day for a week like fruit for breakfast, salad or hummus for lunch, baked potato or stir fry for dinner when I'm not having those symptoms anymore I start adding things back in.

I have learned to steer clear of processed foods all together you never know what your reacting to there is just too many ingredients. If I pick up a package and there are ingredients I can't pronounce I don't buy it. gluten-free labeling doesn't mean it's safe for Celiacs, trace gluten makes me ill.

When I get vertigo its usually from CC, it's the first sign I get from gluten. My other food allergies doesn't effect my the same way gluten does so I just have to pay real close attention to how I feel.

175comet Rookie

Sorry but what is cc? Soy is definitely a prob for me too. Even strawberries gave me some bloating.

Brandiwine Contributor

CC stands for cross contamination.

Pegleg84 Collaborator

Cross contamination is a constant battle. In order to be 100% gluten-free, you should have our own toaster, cutting board, collander, anything that could be contaminated with gluten. Even a crumb can cause a reaction, and for some of us even tiny traces can be an issue. 

Of course, if your elimination diet is helping, then it's quite possible that you have sensitivities/intolerances to other foods. I'm intolerant to soy, and even trace amounts can bother me.

 

What foods are you "eliminating"? Have you figured out anything that's definitely bothering you? Dairy, soy, grains, and nightshades are common culprits.

 

Glad you're starting to feel better. Good luck!

175comet Rookie

Funny you say that as I'm so sick today. Not sure if its peanut butter or cross contamination. But im thinking cross contamination bc of how i feel (& i used the family PB jar). I know for sure all my neurological symptoms are related to gluten. I also have issues with dairy, soy, night shades, strawberries and almond butter so far. Eggs and white wine are ok. But mostly I just get bloated & have heartburn w these foods.

It's such a challenge. I also wondered if there is something in the chai tea I've been drinking. It's gluten free but maybe there is a spice in it that I'm sensitive to.

I worked w a dietician to set up this diet. But we didn't talk ab spices. I've also been ok with Bob's gluten free oats. But I've been eating them every morning so maybe that's not such a good idea either.

kareng Grand Master

If you are eating foods with gluten in them - like the family PB jar full of gluten bread crumbs, you won't feel good. Maybe you shouldn't be looking for more foods to cut out until you have managed to cut out alll the gluten for a few months?


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



Celiac.com Sponsor (A8-M):



175comet Rookie

Well I have been pretty good. But damn I keep forgetting the little things. Really I think it's only been 5x in 5 months that I've accidentally eaten gluten (2x at a restaurant so no more eating out).

The problem is that after going off gluten I've become so sensitive to other foods (like soy and dairy). I was really surprised about tomatoes as I had no idea they were a culprit. But after having acid reflux and heartburn so often over the last 5 yrs I just figured it was my body and not the food.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - CatS commented on Scott Adams's article in Winter 2026 Issue
      5

      Are Gluten-Free Processed Foods Making You Sick? (+Video)

    2. - Samanthaeileen1 replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

    3. - Wheatwacked replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

    4. - RMJ replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

    5. - Samanthaeileen1 replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,802
    • Most Online (within 30 mins)
      7,748

    BoroMike
    Newest Member
    BoroMike
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Samanthaeileen1
      thank you RMJ! That is very helpful advice. Good to know we aren’t crazy if we don’t do the endoscopy. We are going to try the gluten free and see how symptoms and levels improve.    thank you Wheatwacked (love the username lol) that is also reassuring. Thankfully she has an amazing and experienced pediatrician. And yesss I forgot to mention the poop! She has the weirdest poop issues.    How long did it take y'all to start seeing improvement in symptoms? 
    • Wheatwacked
      My son was diagnosed when he was weaned in 1976 after several endoscopies.  Given your two year old's symptoms and your family history and your pediatrition advocating for the dx, I would agree.  Whether an endoscopy is positive or negative is irrelevant.   That may happen even with endoscopy.  Pick your doctors with that in mind. In the end you save the potential trauma of the endoscopy for your baby.   Mine also had really nasty poop.  His doctor started him on Nutramigen Infant because at the time it was the only product that was hypo allergenic and had complete nutrition. The improvement was immediate.
    • RMJ
      So her tissue transglutaminase antibody is almost 4x the upper end of the normal range - likely a real result. The other things you can do besides an endoscopy would be: 1.  Genetic testing.  Unfortunately a large proportion of the population has genes permissive for celiac disease, but only a small proportion of those with the genes have it. With family history it is likely she has the genes. 2.  Try a gluten free diet and see if the symptoms go away AND the antibody levels return to normal. (This is what I would do). Endoscopies aren’t always accurate in patients as young as your daughter. Unfortunately, without an endoscopy, some doctor later in her life may question whether she really has celiac disease or not, and you’ll need to be a fierce mama bear to defend the diagnosis! Be sure you have a good written record of her current pediatrician’s diagnosis. Doing a gluten challenge for an endoscopy later in life could cause a very uncomfortable level of symptoms.   Having yourself, your husband and your son tested would be a great idea.  
    • Samanthaeileen1
      here are the lab ranges.  Normal ranges for tissue transglutaminase are: <15.0 Antibody not detected > or = 15.0 Antibody detected normal for endomysial antibody is < 1.5. So she is barely positive but still positive. 
    • JoJo0611
      I have been diagnosed with coeliacs disease today after endoscopy, bloods and CT scan. I have also been diagnosed with Mesenteric Panniculitis today. Both of which I believe are autoimmune diseases. I have been told I will need a dexa scan and a repeat CT scan in 6 months. I had not even heard of Mesenteric Panniculitis till today. I don’t know much about it? Has anyone else got both of these. 
×
×
  • 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.