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 Celiac.com!
    eNewsletter
    Donate

Gluten And Vertigo


Rick1254

Recommended Posts

Anne Newbie

Hi christiana

I have read that nerves in the neck/spine could effect hearing loss. If I am allowed to send a link <http://www.mayoclinic.org/diseases-conditions/menieres-disease/basics/symptoms/CON-20028251>

This and other links at a <www.bing.com>  search discuss the autoimmune possibility. There is a test for antibody presence perhaps in the wikipedia article.

I called the audiologist office today. I was disappointed to learn he does not screen for or treat Miniere's but the receptionist said he will be back in the office on Monday and will  call me back then. He has worked at a children's hospital and with a private practice for seniors and came recommended from two sources here. He is known as an expert for tintinus.

I researched and was surprised that I had never mentioned a lot of things to the Dr because I thought they were not about the hearing. The migraines, the salt connection, nausea recurring so I now have a prescription from the ER for something like orthodantrin, sublingual that shuts the symptoms down fast.  I had a scan in one of the bouts of that, as they wanted to rule out stroke. They found nothing (which is a requirement for considering Meniere's) and said it was a possible mild eschemic something. It has been a couple of years now.

But, my orthorpedic surgeon kidded me, "What's happening? Has your warranty run out?" with the fifth fall, in several years. A broken leg, a trip/swollen ankle, pinched fingers, double fracture of the forearm, and a rotator cuff tear. The last three since April 2014. I have avoided surgery. My primary doctor shook his head, "I will say it again, I don't see how you did not have to have surgery on that arm." My young physio therapist asked me to not drive in rain or bad weather. She has seen it happen too often that patients will get cut off in traffic thru someone else's error and raise the injured arm to defend themselves. She did not want me to re-injur. So, I am home more than ever in my life. But the rotator cuff was a fall at the bottom of my stairs at home. I just sort of spaced-out, a little dizzy and fell back onto my elbow.  But, good thing I was not driving. . .

The tear may be connected to an inflammed collar bone 'condritis-something' connected to inflammation in the chest cavity, trying to recover from a terrible thing from a supposed naturopath that was actually teaching a student, against my protests. I almost did not go that day. I was only supposed to get a prescription refill. I had a funny feeling not to go. I should have listened to that. Big time. God does His best, but what to do if I don't listen! That was before these last three bad things. I think that threw off my balance, also. Perhaps for another subject forum :)

So, as much as I do not like to go to doctors, and for me, often the less treatment the better, it is good to connect the dots for myself and be aware and informed / then I can say what I need to when/if the time comes. I don't want extreme measures or anything invasive or unneccessarily expensive. I need to learn all I can about management. And, thank Goodness,
 there is no pain or the swirling others are dealing with.

Do you like the actor that played Hercules? He wrote a book. He felt he should remind his chiropractor not to snap his neck. But ignored the thought, as he had told him not to do that before. He thought it again, but again dismissed the thought. Well, the book tells it better. You might want to look it up. He was in a good new movie last year. Kevin Sorbo.

Best wishes, all. Thank you, ;) 

 

 

 

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



cristiana Veteran
On 4/15/2016 at 7:59 AM, Anne said:

I have read that nerves in the neck/spine could effect hearing loss. If I am allowed to send a link <http://www.mayoclinic.org/diseases-conditions/menieres-disease/basics/symptoms/CON-20028251>

Hi Anne

I am sorry - I have only just read your post of nearly a week ago.

You certainly sound as if you have been through the wars.  A rotator cuff tear is supposed to be very painful.  I wonder if the doctor was referring to costochondritis.  

I think that is interesting what you are saying about nerves in the neck/spine.  I find when I am typing a lot, or have my shoulders hunched, I get a feeling of fullness in my right ear and it triggers off the rumbling noise (tinnitus) that I have.   My neck is in a bad way and the same actions can make the tingling in my cheek worse, so thanks for the tip.

Link to comment
Share on other sites
  • 2 weeks later...
Anne Newbie

Christiana,

I just felt to look at the site. I thought I had clicked to get email alerts. But, actually my email has been

'fritzing' sort of.  Thank you for your note. It is important for my diagnosis. I was diagnosed with chondritis

of the collar bone a few months before the fall that resulted in the immobile right arm. The osteo surgeon

gave me a cortosol shot that helped a lot. That MRI showed a rotator cuff tear nearly 2/3 thru the strip of tissue that connects the muscle tissue to the bone and makes the shoulder 'rotate' in place.  That was almost a year ago now. I have been learning to be very very mindful about how I use that arm, when I reach, carefully, how I rest it and sleep position. Interesting that I did see a search answer that said ' they are saying now that there could be a connection btn rotator cuff tear and inflammed collar bone. My primary doctor also said I could have an inflammed chest wall that resulted in the chondritis. I remembered that word from a child's diagnosis years ago. That was in his knees and was treated by this same osteo surgeon, by casting the legs over summer holiday, which ended in healed x-rays. That was osteo chondritis desicans. He said then, 'if it is horses, we would have to shoot them.'  I tried to get a blood test three weeks ago for the same antibody we were treating that child with thru his then pediatritian, for rheumatoid antibodies/ recurring strep throat. I had gotten a 'sort of' diagnosis, or agreement from that primary care doctor, allowing me to get the recommended antibiotics (one of the few treatments that it is allowed, because of the need to keep the hearing). But, his new nurse did not relay the request properly. I hate doctor office politics. I hope this newbie is not going to mess with this doctor's little family as well. Last month when researching Meniere's one of the things listed about it was that autoimmune disease is connected to it also. I was hurt before the falls and the inflammation and the collar bone chondritis and the rotator cuff tear. I was very very concerned about it setting off some kind of autoimmune inflammation reaction or worse that can happen when tissue cells are being repaired rapidly and it felt like lots of toxins were being cleansed and processed over a period of many months. The only similar feeling I have ever experienced was when I had a 'deep tissue massage' to release and cleanse a cortisol 'hump' I had after a prolonged period of high family stress situation. Right now, my primary (an O.D. , or osteopath) is working with me. There are two ENTs in this area he offered for Meniere's and has given me Physical Therapy at his complex for Balance Therapy.

It is great that that therapist has a MIL that is also dealing with Meniere's and getting exercises from a major hospital complex in the city. I was able to give her some celiac's diagnosis information. Sounded like her MIL and her son were likely to be candidates. 

I did not know what the definition was of the term 'vestibular' as in vestibular migraine, another connection to Meniere's. I just typed www.bing.com and then typed 'definition of vestibular.' That had information about the connections btn hearing and sitting positions.

I will look up costochondritis. Thank you, again.

Best wishes, Anne

Link to comment
Share on other sites
  • 9 months later...
LeeAnn10 Newbie

Before I found out I was celiac,  I was sent to many different doctors and went through a barrage of tests for allergies,  spinal issues,  brain issues, thyroid menieres, etc.  Everything came back normal and no one could tell me what was going on except the occasional scare from a doctor guessing it might be this or that.  I went to e.r several times for severe dizziness,  shaking,  chills, blurred vision, tinnitus,  joint swelling and heart palpitations.  I was told I was having anxiety and sent home.  I rooted top explain that the anxiety was occurring due to these other symptoms but no one listened. 

5 years ago by simple luck I was diagnosed by a gastroenterologist with celiac. Finally.  The gluten free diet made a huge difference.  I can tell immediately if I am poisoned because the first symptom is dizziness.  When I told a doctor that he told me I was crazy because that's not a textbook symptom of celiac.  But it clearly is.  In a glutened state,  the body reacts in many ways.  This is a type of allergic reaction and because your bodies defenses are down in regard to that it can cause any number of symptoms and some severe problems if left untreated.  

Celiac is also an autoimmune disorder. Autoimmune disorders affect the entire body and one can be linked to or cause another.  So celiac,  thyroid problems, arthritis,  lupus, ms, diabetes, and such are commonly linked together.  These are definitely systemic diseases. 

This group is a wonderful way too confirm that we are not crazy or imagining things and we certainly are not alone.  

Link to comment
Share on other sites
  • 2 years later...
Richard Gibson Newbie
On 3/29/2004 at 4:12 PM, Rick1254 said:

Has anyone here suffered from vertigo attacks triggered by gluten? I have had to go gluten free because gluten caused vertigo attacks.

thanks,

Rick

Yes. I have. About 3 years ago, I started suffering from vertigo attacks which would last two or three days. Mostly, I was just bed-bound, with the world spinning but once was worse, including vomiting. I read articles about gluten being a cause. I decided to try it. Over a period of about a month, my attacks got less and I've now been vertigo-free for more than 2 yrs. Interestingly, even before that I had become somewhat deaf;  gluten-free my deafness is still present but getting worse only very very slowly, at a 'normal' rate. It's weird but I dare not eat anything containing gluten now! I'd love more research to be done on this.

All the best,

Richard

Link to comment
Share on other sites
  • 2 weeks later...
OregonDonna Rookie

I suffered with unexplained vertigo for almost 3 years before being diagnosed with Celiac. They thought I had BPPV but PT did not help. They finally gave up and I was just suffering. I had anemia and low bone density. I decided to research on my own and found research done in Japan. Large study group with unexplained vertigo had one commonality~vitamin deficiencies in A and Folate. Both cheap to buy and the next day after taking them I was vertigo free. The study noted to take only the true form of Folate, 5-methyltetrahydrofolate (5-MTHF). If I forget to take them, the vertigo comes back so I know this is what works for me.

Link to comment
Share on other sites
  • 2 months later...
Zenith Explorer
On ‎3‎/‎29‎/‎2004 at 11:17 AM, tarnalberry said:

If you're just talking about dizziness... that's the first symptom I have if I've had something with gluten. A dizzy, disorientation in the head that makes things feel like they're moving (usually rotationally) when they're not. For me, it only lasts 15-30 minutes, and happens 15-30 minutes after I first ingest the offending substance, but it sure ain't fun. (I describe it to friends as something like the feeling of being drunk, without it being funny in any way whatsoever.)

Yes upon waken up in the morning it would be bad for like 1 hour.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



notme Experienced

this was one of my unexplained symptoms - gp said it was allergies, ent said it was because the tubes between my inner ear were too small to drain quickly enough to correct my balance?   when I quit gluten, this was another thing that went away.  celiac is systemic, which means it can affect any part of the body.  stopping the inflammation from ingesting gluten has solved many of my crazy symptoms!

Link to comment
Share on other sites
  • 8 months later...
sephorachick Newbie

I have been to over 24 doctors w/ no answers. I am dizzy 24/7. Anytime I eat gluten I just noticed recently my nose drains/drips A LOT. My ENY thought my tubes were too small so I had sinusplasty I've tried it all. I had allergy food test but NOTHING was abnormal. I think I'm going to give the gluten-free diet a go for 6 months to see. I did Whole30 before so hopefully this helps! Any blogs/recipe sites that you enjoy? I know I like nomnompaleo but am looking for more. Thank god I found this random search today. I have been dizzy 24/7 for almost 7 years I really hope that this is my answer!!!!

Link to comment
Share on other sites
Scott Adams Grand Master

Some describe this "dizzy" symptom as vertigo, and I had this symptom as well. It let to panic attacks at times. The good news is that a few months after going gluten-free this symptom went away.

Link to comment
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,091
    • Most Online (within 30 mins)
      7,748

    Nicole K
    Newest Member
    Nicole K
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Oh, okay. The lower case "b" in boots in your first post didn't lead me in the direction of a proper name.
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! There are other things that may cause elevated tTg-IgA levels, but in general a reaction to gluten is the culprit:    
    • cristiana
      Hi @trents Just seen this - Boot's is a chain of pharmacies in the UK, originally founded in the 19th Century by a chap with the surname, Boot.  It's a household name here in the UK and if you say you are going to Boot's everyone knows you are off to the pharmacist! Cristiana
    • Denise I
      I am looking to find a Celiac Dietician who is affiliated with the Celiac Disease Foundation who I can set up an appointment with.  Can you possibly give some guidance on this?  Thank you!
    • Posterboy
      Nacina, Knitty Kitty has given you good advice. But I would say/add find a Fat Soluble B-1 like Benfotiamine for best results.  The kind found in most Multivitamins have a very low absorption rate. This article shows how taking a Fat Soluble B-1 can effectively help absorption by 6x to7x times. https://www.naturalmedicinejournal.com/journal/thiamine-deficiency-and-diabetic-polyneuropathy quoting from the article.... "The group ingesting benfotiamine had maximum plasma thiamine levels that were 6.7 times higher than the group ingesting thiamine mononitrate.32" Also, frequency is much more important than amount when it comes to B-Vitamin. These are best taken with meals because they provide the fat for better absorption. You will know your B-Vitamin is working properly when your urine becomes bright yellow all the time. This may take two or three months to achieve this.......maybe even longer depending on how low he/you are. The Yellow color is from excess Riboflavin bypassing the Kidneys....... Don't stop them until when 2x a day with meals they start producing a bright yellow urine with in 2 or 3 hours after the ingesting the B-Complex...... You will be able to see the color of your urine change as the hours go by and bounce back up after you take them in the evening. When this happens quickly......you are now bypassing all the Riboflavin that is in the supplement. The body won't absorb more than it needs! This can be taken as a "proxy" for your other B-Vitamin levels (if taken a B-Complex) ...... at least at a quick and dirty level......this will only be so for the B-1 Thiamine levels if you are taking the Fat Soluble forms with the Magnesium as Knitty Kitty mentioned. Magnesium is a Co-Factor is a Co-factor for both Thiamine and Vitamin D and your sons levels won't improve unless he also takes Magnesium with his Thiamine and B-Complex. You will notice his energy levels really pick up.  His sleeping will improve and his muscle cramps will get better from the Magnesium! Here is nice blog post that can help you Thiamine and it's many benefits. I hope this is helpful but it is not medical advice God speed on your son's continued journey I used to be him. There is hope! 2 Tim 2:7 “Consider what I say; and the Lord give thee understanding in all things” this included. Posterboy by the grace of God,  
×
×
  • Create New...