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

Vertigo/imbalance


cristiana

Recommended Posts

cristiana Veteran

Hi Everyone

 

I am now having tests for my ongoing feelings of being on board a ship.  The ENT now thinks it isn't inner ear, so I just wondered, for any of you who actually have gluten ataxia, can you tell me, if you suffer from feelings of being imbalanced, vertigo issues etc, is it 24/7 or do certain actions set it off?

 

In my own case, I don't wake up with it - I usually find that bending down to pick something up, using the computer, carrying heavy objects sets it off.  The ENT thinks it is to do with the neck.   I did injure my neck and back shortly before this all started, so he may be onto something.  Sometimes I feel unsteady when I walk and that often coincides with lower back pain.

 

Many thanks.

 

 


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

I get it, occasionally.

I think bits associated with inflammation - for me, tmj from having my wisdom teeth removed ( one side was impacted and they messed up my jaw in that side).

I notice I'm more likely to get vertigo when allergies are bad (and tmj is bad).

I have luck with massage for my tmj, which relaxes the ligaments/tendons and relaxes everything.

cristiana Veteran

Thanks for your reply, pricklypear

 

That's interesting... do you get the spinning rooom vertigo .... or sort of swaying back and forth type, which is the type I get, along with feeling I'm on a ship's deck.

 

Also, do you feel your gait is slightly affected?

pricklypear1971 Community Regular

I get the Leaning Tower of Pisa /can't walk effect at its worst.

I get nausea, sort of slow-motion with a hint of spinning, most often with allergies. I can move around and do things but want to vomit on them, and get a terrible headache. Helps if I sit up/move around but not too much. I think I get fluid in my ear, and sitting up helps it drain.

cristiana Veteran

Thanks again pricklypear.  Glad I'm not the only one - although sorry you are going through it, if you know what I mean.

 

Just wondering, do you or does anyone else know if vertigo from gluten ataxia is a 24/7 feeling, rather than just lasting several hours every day?  I am not talking about the type which hangs around for a few days or even weeks as a response to recent glutening, but as a more chronic condition caused by sustained damage over a period of time, if that makes sense.   I mentioned the possibility of my having ataxia to one doctor and she dismissed it saying I wouldn't have got ataxia after my gastro symptoms stopped - the vertigo started about two months after adopting a gluten-free diet, when the gastro symptoms were a lot better.

 

Thanks.

pricklypear1971 Community Regular

I don't know....but I do know that gluten damage does not work the way your doctor is describing.

Ut uh. Different parts/systems recover at different rates...then that varies from person to person.

notme Experienced

i had vertigo, before i knew i had celiac.  they attributed it to an inner ear problem, maybe caused by inflammation from allergies.  it has since cleared up after i went gluten free :)


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



Celiac.com Sponsor (A8-M):



cristiana Veteran

Hi notme!

 

Did it take weeks or months?... for me, it hit two months after going gluten-free, that was July, and I still have it  :(

notme Experienced

it took a little while - i honestly didn't connect the dots and wasn't expecting it but suddenly i could carry TWO things down the stairs.  (not holding the railing for dear life)  and drive without feeling like i was falling off the road.  i think it's neurological, which is slower to heal.  hang in there!  mine was 'falling'  and  'leaning' - could not stand without feeling like i was falling.  sometimes trying to correct it, and falling anyway because it only FELT like i was off balance.  

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,769
    • Most Online (within 30 mins)
      7,748

    RedWolf8148
    Newest Member
    RedWolf8148
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      I seem to recall that my digestive issues actually started when I was taking NSAIDs c. February 2013 for some unrelated condition.  My stomach got so sore during that time I went to see my GP and she thought it might be an ulcer or gastritis so prescribed me Omeprazole.  That appeared to trigger diarrhea which, once I came off the Omeprazole, did not stop.  I went back to the doctors after a few weeks, and that finally led to my coeliac diagnosis, after months of unexplained neurological symptoms, low ferritin and anxiety,which did not seem to have a cause but of course we later realised was all down to coeliac disease. I occasionally take a very small aspirin for a sick migraine which sometimes only responds to aspirin, but it usually leaves me with sore stomach a few days later. I've been told co-codamol is another medication I could take with a sensitive stomach. I was once prescribed it, to use for just a few days. It is not an NSAID, but it contains codeine, which I understand can be addictive so should be used with care.  It can also cause constipation.        
    • Rogol72
      I also take Paracetamol. I haven't taken an NSAID in years since being diagnosed with UC. The can cause UC flares.
    • trents
      Welcome to the forum, @jessysgems! How does this affect you? What do you do to address it. Do you have to get up and consume something sweet?
    • Jmartes71
      Wow Im a tea drinker and didn't know, perhaps this is why im having issues with my ghost disease. 
    • stephaniekl
      She used to take supplements, but her abdominal pain is so debilitating that she hasn't been able to continue.  Her primary care team has been suggesting liquid supplements rather than pill form to help.  They just drew a lot of blood Friday and we are slowly getting all that work back.  I will definitely check into thiamine!  Thanks!
×
×
  • 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.