Meniers Disease

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By Tom Beni

General Overview

Meniers Disease is a disorder of the inner ear that could be related to some abnormality of the inner ear fluids. Its main symptom is vertigo that comes in attacks that vary in length, intensity and frequency. Hearing loss is also a very common result of the disease. There is no officially known cause for Meniers Disease and no cure found.

What do you do when the medications don't work?


Symptoms

The following symptoms are associated with Meniers Disease:

  • Vertigo: attacks of spinning sensation that might lead to imbalance, nausea and vomiting.
  • Hearing Loss: although hearing may return to normal between attacks, there is a substantial hearing loss over time.
  • Tinnitus: A loud ringing sound in the ear.
  • A feeling of fullness in the affected ear.
  • In severe cases the person can suffer from sudden falls.

Attacks may vary in length, intensity and frequency and usually prevent the person for performing any normal daily activities.

It is crucial to remember that these symptoms are not unique to Meniers Disease, and might be cause by a different medical condition. Meniers Disease diagnosis is actually done by excluding all other testable options.

Causes

There is no officially known cause for Meniers Disease.

The main "suspect" for causing it is the labyrinth, an inner ear part. It is commonly believed that swelling or even a rapture in the labyrinth, causes a change in the ear's liquids volume and leads to Meniers symptoms. This swelling condition is called endolymphtic hydrops.

A healthy inner ear and labyrinth
A healthy inner ear and labyrinth
Dilated labyrinth in Meniers Disease
Dilated labyrinth in Meniers Disease

However, the connection between hydrops and Meniers Disease is questioned when reviewing the following statistics: not all of Meniers Disease patients are diagnosed with hydrops. And out of autopsies studies done on people who didn't suffer from Meniers Disease, 6% did have hydrops. And when you compared that with the estimate of only 0.2% of the population who suffer from Meniers Disease, it seems that hydrops might be connected to Meniers, but not necesserily a direct simple cause.

Some recent research suggests immune diseases may contribute to a substantial percentage of Meniers Disease, or even different types of viruses, but there is still not enough evidence to support that. Allergies are often associated with Meniers but it is also highly debatable.

A possible synthesis would be that Meniers Disease appears to be the final common pathway that the inner ear responds to nearly any injury, and that Meniers Disease has many separate causes.

Treatment

There is no known cure for Meniers Disease, so the treatment often tries to control the symptoms.

  • A rather successful way is a low-salt or salt-free and no caffeine or alcohol diet that would reduce the body's retention to fluids.
  • Changes in medications that either control allergies or improve blood circulation in the inner ear may help.
  • Reducing stress level is always a good way to ease the intensity or frequency of the attacks.
  • There is the possibility of a chemical labyrinthectomy, which destroys vestibular tissue and done by injections into the ear.
  • Labyrinthectomy surgery (removal of the inner ear sense organ) can help people with severe cases of sudden falls and effectively control vertigo, but sacrifices hearing and is reserved for patients with nonfunctional hearing in the affected ear.

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Comments

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Rachael  says:
9 months ago

If a person has this disease, are they considered "Disable"?

Tom Beni  says:
5 months ago

Well, I don't know about the offical laws, but I do believe that a person that suffers from dizziness and hear loss should be considered disabled.

sean  says:
4 months ago

i have miniers disease and im only 23, im currently doin thai boxing and my balance is not so good. will i be able to carry on?

Tom Beni  says:
4 months ago

I suggest you consult your doctor.
Hope you feel better.



todd  says:
3 months ago

i dont know if i have this but the symptoms are the same and im feel like im going crazy can they identify with test

Dan S.  says:
2 months ago

I have had this disease for 10yrs. I'm 41 now. I live in Tulsa,Ok and I am drawing S.S. Disability for this disease. Don't know about other states but, it took me 3 yrs. to get approved. So... its worth a shot!

laura  says:
2 months ago

I've been with the disease for years, the last 2 years i have 4 vertigo attacks and 3 the last month they are trying a new medication they say it seems to work. It is called Betahistine. Ask your doctor. I'll let you know in to weeks when I Finish my treatment.

Lisa  says:
2 months ago

my doctor has prescibed Serc and stemitl work good for me ive had meniers for 14 years, you can still do most thing but i have found as time goes on more things can trigger off an attack eg flickering lights some smells lack of sleep overa few days etc.

andy  says:
2 months ago

ive had meniers disease since i was 14 and was having regular attacks on a weekly basis, but then it grew less frequent and eventually i thought it burned itself out, until recently when it returned with a vegence. I'm 41 now and am having regualr bouts for the first time in over 20 years and i'm learnign to cope with it all over again.

guest  says:
2 months ago

are hearing aids able to help with the hearing loss?

Mariam   says:
2 months ago

I never knew why I would all of a sudden get dizzy, when i was in elementary school I would cry because I didn't understand what was happening to me. But it would only last a day or two, and now that I am 26 it comes maybe every 3 to 4 years but it comes hard. When it happens to me I feel like it takes my whole life over, I can't function I can't do anything and all I want to do is sleep. I recently had a MRI done of my head and inner ear to rule out anything super serious. Any suggestions on what type of medication or exercises I can do to help with this issue?

scott  says:
5 weeks ago

i was diagnosed with meniers disease after passing out. I had catscans, mris,heart work. the whole nine yards. I get these bouts moslty during allergy season, and during the dry winters here in Denver. I can feel an attack come on and get nausea and dizzy to the point of passing out. Have you ever experienced anyone passing out before? I had sinus surgery to relieve some of the pressure in my head, that seemed to work for a few years but now its back.

beverley healey  says:
4 weeks ago

I HAVE SUFFERED FOR THE LAST 4 YEARS , THE FIRST ATTACK I THOUGHT I WAS DYING I COULDNT EVEN GET OUT OF BED THE BED FELT LIKE IT WAS WHIZZING AROUND AS WAS THE FLOOR ME AND EVERY THING AROUND ME ,I SPENT 4 DAYS IN BED COULDNT LIFT MY HEAD WITH OUT VOMITING IT WAS AWFULL AFTER A WEEK FELT A BIT BETTER JUST LEFT WOBBLY AND WEAK AND SCARED IT WOULD HAPPEN AGAIN AND IT DID OVER 4 YEARS OVER AND OVER AGAIN HAD MRA SCAN THAT WAS CLEAR , HAD BALANCE TESTS DONE WHICH REVEAL THAT THE BALANCE ISNT WORKING IN ONE EAR ON BETEHISTINE WHICH LESSONS THE EFFECTS OF THE ATTACTS BUT DOSNT STOP THEM I TRYED TO GET DISSABILITY FOR IT BUT THEY SAID BECAUSE I CAN GET UP AND ANSWER THE DOOR AND COOK A MEAL I AM NOT REGARDED AS DISSABLED I APPEALED AND LOST BUT MY LIFE WILL NEVER BE THE SAME AGAIN IT STOPS ME DOING A LOT OF THINGS ,I CANT SLEEP ,AS I CANT TURN OVER THROUGH THE NIGHT AS THAT MAKES ME DIZZY AND THERE IS NO CURE YOU HAVE TO LEARN TO LIVE WITH IT WHICH IS EASY TO SAY WHEN YOU ARE NOT LIVING WITH IT EVERY DAY

BEVERLEY FROM BRIGHTON ENGLAND

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