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

Mri Scan Finding?


whattodo

Recommended Posts

whattodo Enthusiast

Is there a link between Celiac Disease and Cerebrospinal fluid?

I am seeing a neurosurgeon tomorrow night but dont have a clue what the problem is. My doctor didnt have a clue neither, he just said that an area in the brain is larger than it should be. Perhaps inflamed. he refered to this area as the place where the brain fluid is found and then used to filter it around the brain.

My doctor admitted to me that he didnt know what this meant but it could simply be something i have had all my life. It still made me slightly worried so i asked him to refer me to a specialist to put my mind at rest. He said it could be a result of my numb face i get on and off.

I thought i would post it just to see if anyone has had the same thing when they had a mri scan.


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



Celiac.com Sponsor (A8-M):



Chris E Rookie
Is there a link between Celiac Disease and Cerebrospinal fluid?

I am seeing a neurosurgeon tomorrow night but dont have a clue what the problem is. My doctor didnt have a clue neither, he just said that an area in the brain is larger than it should be. Perhaps inflamed. he refered to this area as the place where the brain fluid is found and then used to filter it around the brain.

My doctor admitted to me that he didnt know what this meant but it could simply be something i have had all my life. It still made me slightly worried so i asked him to refer me to a specialist to put my mind at rest. He said it could be a result of my numb face i get on and off.

I thought i would post it just to see if anyone has had the same thing when they had a mri scan.

Hi Jay,

I don't know what it would show to be honest, but i still think you could be celiac. I have started with a slightly numb face and brain fog again after a while without it. We both seem to have extremely similar symptoms.

I had a full MRI scan last october when i was getting leg tingling, numbess around the body and headaches all day everyday. My result was all clear and these symptoms went away after a couple of months. Last time i seen my neurologist he did suggest that if the symptoms return he would test my Cerebrospinal fluid. Don't know what such a test would highlight though.

I know you also live in the UK? Do you mind me asking---- are you paying privately for your treatment?? I paid to see my neurologist and for the MRI scan i had although seeing another GI later this month on the NHS!

Chris

Chris E Rookie
Is there a link between Celiac Disease and Cerebrospinal fluid?

I am seeing a neurosurgeon tomorrow night but dont have a clue what the problem is. My doctor didnt have a clue neither, he just said that an area in the brain is larger than it should be. Perhaps inflamed. he refered to this area as the place where the brain fluid is found and then used to filter it around the brain.

My doctor admitted to me that he didnt know what this meant but it could simply be something i have had all my life. It still made me slightly worried so i asked him to refer me to a specialist to put my mind at rest. He said it could be a result of my numb face i get on and off.

I thought i would post it just to see if anyone has had the same thing when they had a mri scan.

Hi Jay,

I don't know what it would show to be honest, but i still think you could be celiac. I have started with a slightly numb face and brain fog again after a while without it. We both seem to have extremely similar symptoms.

I had a full MRI scan last october when i was getting leg tingling, numbess around the body and headaches all day everyday. My result was all clear and these symptoms went away after a couple of months. Last time i seen my neurologist he did suggest that if the symptoms return he would test my Cerebrospinal fluid. Don't know what such a test would highlight though.

I know you also live in the UK? Do you mind me asking---- are you paying privately for your treatment?? I paid to see my neurologist and for the MRI scan i had although seeing another GI later this month on the NHS!

Chris

whattodo Enthusiast
Hi Jay,

I don't know what it would show to be honest, but i still think you could be celiac. I have started with a slightly numb face and brain fog again after a while without it. We both seem to have extremely similar symptoms.

I had a full MRI scan last october when i was getting leg tingling, numbess around the body and headaches all day everyday. My result was all clear and these symptoms went away after a couple of months. Last time i seen my neurologist he did suggest that if the symptoms return he would test my Cerebrospinal fluid. Don't know what such a test would highlight though.

I know you also live in the UK? Do you mind me asking---- are you paying privately for your treatment?? I paid to see my neurologist and for the MRI scan i had although seeing another GI later this month on the NHS!

Chris

Hi chris, thanks for the response. When i had the MRI scan done it was done on the nhs. The neurosurgeon i am seeing tomorrow is being done private. I dont mind things happening to me below the neck, but things above the neck i do not want to mess with.

Why did the neurologist suggest that he test your cerebrospinal fluid, did he mention if it was celiac related or something else?

Do you get the numb face all the time or is it on and off or has it gone now you are gluten free (how long did it take). Mine used to be on and off but noticing it more now, its not really numb, its more like someone hit me in the face. Is this the same for you. Is the neurosurgeon the best person to ask for this strange sensation when i see him? I just want to ask him everything, for

neesee Apprentice

Hi Jay...It sounds like you might be describing the arachnoid membrane. I don't know if there is a connection between celiac and something like that or not. I do know that my son has a posterior fossa subarachnoid cyst. It had to be shunted in 2001. I am a biopsy diagnosed celiac.

By the way, you are only 1 year older than him and have the same name.

ravenwoodglass Mentor
Hi Jay,

I don't know what it would show to be honest, but i still think you could be celiac. I have started with a slightly numb face and brain fog again after a while without it. We both seem to have extremely similar symptoms.

I had a full MRI scan last october when i was getting leg tingling, numbess around the body and headaches all day everyday. My result was all clear and these symptoms went away after a couple of months. Last time i seen my neurologist he did suggest that if the symptoms return he would test my Cerebrospinal fluid. Don't know what such a test would highlight though.

I know you also live in the UK? Do you mind me asking---- are you paying privately for your treatment?? I paid to see my neurologist and for the MRI scan i had although seeing another GI later this month on the NHS!

Chris

I can not answer the first posters query but I do know that the reason he would want to test the spinal fluid would most likely be to look for the demylination that occurs with MS. The process throws cells into the spinal fluid. I had this done after my MRI showed UBO's to rule out MS. This is most likely what he is looking for in this instance. In my case although many signs pointed to MS all the nerve damage I have was due to celiac. Most has resolved, slowly, with being gluten-free.

Chris E Rookie

Hi Jay!

I was just wondering how your meeting went with the Neurosurgeon? Would be good to know what he said as we both seem to be experiencing similar symptoms. I have my appointment with my new Gi tomorrow so hopefully will get somewhere now.

Keep us updated

Chris


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,685
    • Most Online (within 30 mins)
      7,748

    Janahawk
    Newest Member
    Janahawk
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Brook G
      People who are Celiac don't have a gluten response to Quinoa, but some people who are gluten intolerant do.  I react to quinoa just like I do to gluten.  Freddies/Kroger came out with their own gluten-free Bread and I didn't think to read the ingredients.  I couldn't figure out where I would have gotten gluten in my diet until I read the ingredients in their bread... QUINOA
    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
    • trents
      Welcome to the forum, @growlinhard1! If eliminating gluten from your diet makes significant improvement in your symptoms then there are two possibilities. Either you have celiac disease (aka, gluten intolerance) or NCGS (Non Celiac Gluten Sensitivity, aka, gluten sensitivity). The difference is that celiac disease is an autoimmune disorder that creates inflammation and, over time, damages the lining of the small bowel which inhibits nutrient absorption whereas NCGS does not damage the lining of the small bowel. They share many of the same symptoms. At the end of the day, the antidote for both is to abstain from foods that contain wheat, barley or rye, the three gluten-containing grains. Some countries supply stipends and healthcare benefits for those with an official celiac diagnosis. If you live in the USA that does not apply. The main reasons for seeking an official celiac diagnosis are psychological and social. Many people have a hard time not falling off the gluten free bandwagon without an official diagnosis. They find it easy to rationalize it all away as being temporary or due to something else. When you have an official diagnosis, you tend to take gluten-free eating more seriously. Socially, family and friends are more likely to respect and attempt to comply with your need to eat gluten free if you have an official diagnosis of celiac disease. Your physician is more likely to take you seriously as well if you have an official diagnosis because there are typically other health problems that are spinoffs which develop from celiac disease in time. One autoimmune disease invites others. There are no tests for NCGS. Celiac disease must first be ruled out. We do have specific tests for celiac disease. By the way, some experts believe that NCGS can transition into celiac disease. If your endoscopy/biopsy is only a month away, I would encourage you to stick it out and go back on gluten to get an official diagnosis. You still have time to get a valid test result if you start back on gluten now, 10g of gluten daily which is about the amount found in 4-6 slices of wheat bread.
×
×
  • Create New...