Meniere's Disease Symptoms

74

By ajparker

Introduction to Meniere's Disease

Meniere's Disease is commonly known as Meniere's Syndrome and was named for Prosper Meniere who first classified the series of symptoms that have become known as Meniere's Disease. Because of the tendency of this disease to affect those that do fine detailed work it was also referred to as Watchmakers Disease. It is generally accepted that the cause is increased fluid in the inner ear and this fluid in the endolymphatic sac causes the structure to expand and put pressure on the other inner ear structures that affect hearing and balance.

It is common for people suffering from the symptoms of Meniere's Disease to only have symptoms in one ear although some experience the symptoms in both ears. It has not been concluded the exact cause of the excess fluid in the ears. Many traditional treatments for Meniere's disease revolve around limiting salt intake and taking diuretics. Patients with Meniere's Disease may find that they have food based triggers that prompt symptoms, while others may find that environmental allergies and even stress can bring on the symptoms of an attack of Meniere's Disease.

I was diagnosed with Meniere's Disease in December of 2007 after a long running problem with balance including two attacks of vertigo. The office visit during which I was diagnosed included an audio test as well as several balance screenings. I have good stretches and bad stretches. The year prior to my diagnosis I was almost constantly having hearing problems and balance problems stemming from my right ear. Possibly connected is the fact that I had a severe inflammation and infection of the right ear in High School. (Some 15 years or so before the other symptoms have appeared.)

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(Photo credit:http://www.flickr.com/photos/crobj/ / CC BY 2.0)
(Photo credit:http://www.flickr.com/photos/crobj/ / CC BY 2.0)

What are the Classic Symptoms of Meniere's Disease

Meniere's Disease is classically diagnosed as comprising of four symptoms.


The first common symptom of Meniere's Disease is a feeling or sense of pressure or fullness in one (or both) ears. This is reminiscent of when traveling by plane and your ears need to pop, or if you are traveling by car in the mountains and the elevation changes quickly. Basically, it feels the same, however as I recall when I was diagnosed my symptoms were acting up, I felt a sense of pressure, but there were no visible indications that was the case. This sense of pressure is not necessarily constant, but can come and go. For me it has come for days (even a week or two) at a time before going away.

The second common symptom of Meniere's Disease is Tinnitus. This is a roaring or ringing sound in the ear and for me it usually accompanies the sense of pressure. Many times the tinnitis will follow the pressurized feeling. The type of tinnitus can vary in frequency and volume. It may get louder, or softer and for me is usually a roaring sound. Tinnitus associated with Meniere's Disease also comes and goes as the attacks of Meniere's come and go. From my experience, the pressurized feeling comes first, followed after a day with the tinnitus or roaring. If that continues for approximately three days I then experience vertigo.

The third common symptom of Meniere's Disease is hearing loss. It's typically characterized by low end hearing loss. This loss can come and go as the other symptoms but eventually will be permanent. This low end hearing loss is markedly different from the typical hearing loss associated with exposure to loud music. Loud noise exposure typically starts affecting the high end of the audio spectrum first. Many physicians use the hearing loss signature to verify a Meniere's Disease diagnosis.

The fourth common symptom of Meniere's Disease is attacks of rotational vertigo. For me this is the culmination of an attack that may cover several days starting with the sense of fullness in the ear, progressing to the roaring of the tinnitus. After the roaring subsides I have noticed my hearing is perhaps diminished and usually when I realize that the roaring has stopped it's usually the day I have an attack of rotational vertigo. This symptom as all others is intermittent or episodic and comes and goes.  If I understand correctly, this sense of the tinnitus and hearing improving temporarily at the time of an acute attack is referred to as Lermoyez syndrome.

These are all of the symptoms that are recognized as being caused by Meniere's Disease.

(Photo credit:http://www.flickr.com/photos/crobj/ / CC BY 2.0)

Secondary Effects of Meniere's Disease

Even though there are only four official symptoms of Meniere's Disease, there are other effects that I consider secondary symptoms of the disease.

The first of these secondary symptoms is fatigue. In the aftermath of a full attack with vertigo I am usually very tired for several days. It can take a week or two before I feel like my energy level is back to normal.

The second of these secondary symptoms is a feeling of being off balance after the attack is over. I suspect this is due to the brain needing to re-interpret the signals it receives from the inner ear after damage is done by the increased fluid in the ear. Pressure from the fluid pushes against other structures changing the balance information that your ear passes along to the brain and the brain simply has to relearn. That at least is my theory on the matter.

A third of the secondary symptoms is depression. Long term deprivation of one of your senses with the capriciousness of possibly not knowing when an attack will end or when the next might begin as well as the long term diagnosis of permanent hearing loss can certainly affect the mood of a patient with Meniere's Disease.

Other problems are nausea and vomiting (due to vertigo), sensitivity to sound (recruitment and hyperacusis), anxiety, headache and "brain fog". This last one I have always suspected because the brain is too busy trying to relearn about balance which it usually is able to do without effort. This is a high energy process and other things seem to get lost in the shuffle. I have spent weeks feeling like I was living in the fog.

Do you or someone you know have Meniere's Disease?

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Tell about your experiences with Meniere's Disease

pauline tattersall 2 years ago

having just had another attack of meniers,i was wondering if anyone with meniers actually pass out.apart from the usual symptoms described,i always pass out ,i know when i am going but can do nothing to stop it,i sweat profuselly and the last couple of times it takes a few hours to fully come round

ajparker profile image

ajparker Hub Author 2 years ago

I am sorry to hear that you're having an attack, I'm a bit off balance today hopefully I'm not heading for full blown vertigo. I have not personally passed out during a Meniere's attack, but I am usually exhausted after the vertigo and may sleep for several hours as it subsides.

I have heard of some people having drop attacks where they do lose consciousness. I'm sure that makes it an even scarier experience. I hope you get to feeling better soon!

connie 22 months ago

I have a boyfriend with meiners disease. It has effected our relationship immensly. I dont understand why he doesnt want to see me for weeks, months at a time. He says he just wants to be alone. I feel on the other hand I should be there to help him out. Does this disease really last for weeks and months at at time? Should I take this personal and move on or what?????

ajparker profile image

ajparker Hub Author 22 months ago

I can't speak specifically for your boyfriend because I do know that different people have differing frequency of symptoms. These days I'm not doing too badly... I may have an episode or two a month and then a couple days afterwards that I just feel completely fatigued. Backtrack a couple years though and I was having dizziness that would last for WEEKS - I still tend to avoid lots of car trips if I can just because it seems like my head is still buzzing/spinning after the ride. After vertigo episodes I feel wiped out for days.....

The bottom line is probably that you need to open up a discussion with your boyfriend about his symptoms and what is going on. I know sometimes it's a hard disease to deal with because "you don't look sick". Although my wife has developed a pretty good gauge of when I "look green".

I should also mention that the symptoms of tinnitus/pressure in the ears - to me the sensory deprivation can lead to bouts of depression. (Music/sound is a large part of my life and getting part of that cut off for large stretches of time (not knowing if it will come back....) can affect you deeply.)

Arlene Davis 20 months ago

I'm 85yrs old. Have had Meniere's since 2005. I woke up one morning with a severe rumbling noise in the left side of my head, and have had a loss of hearing in both ears. Now the tinnitus is pulsating in the rt side and roaring in the left. I have had several severe vertigo attacks , but none now for over a year. Found out that the cause the last time was caffeine. The most disturbing thing for me is not being able to enjoy music anymore. Everything is flat, and the low notes drowned out the high notes. I can't tell what the piece is. I'm using the widex hearing aid with Zen , which helps me tolerate the tinnitus, but still have trouble hearing people talk. It's so hard trying to explain to anyone the way I'm hearing music. I'm open to any suggestions.

Ringo 15 months ago

i am 45 years old,,,my first experience was in a truckstop sitting at a table as i was trying to eat,,,it was terrifying,total confussion to say the least actaully had a death grip on the table to stop my self from falling out of the chair i was sitting in ,and according to my buddy sitting opposite me,,i went very pale,,,after a while the worst of the symptoms seem to pass,,so i staggered back to the truck for some rest,sleep,i had figured by this point that it all because of lack of rest,,well after laying down,,and i think i was a sleep(not sure)i happen to get the spinning feeling the inside of truck was spinning nausea heart rate was racing,total confussion,i some how managed to get my self to the local ER,,i still am not sure hw i managed to drive there,,,but it was approx 230am in morning,,and of course they pulled me in and hooked me up to all the eletrical machines and was looking what they thought a heart attack victim,,so its been 18months later and many attacks later,,,from falling out of bed from a sound sleep and crawling to the bathroom,,to hugging a fence post out side,,or just sitting watching the room go around and around,,i can safely say my trucking days r over,,,

Pritham 14 months ago

I don't know if I have this syndrome... but the reactions are similar. My first attack was on December 2008. I was not able to stomach anything. I threw up even liquids. I only had my younger daughter along. when she saw I couldn't even put on my pants she took me to the closest clinic and called my elder daughter. It was sheer panic situation. For a normally low pressure person, 45 K.Gs, 5'.2" MY B/P was 160/120... This severe attack has come thrice since then. No doctor here has told me why it is happening. I do not take any milk based, or fried food.

electricsky profile image

electricsky 8 months ago

While formerly in older times doctors thought it was a disease of the brain Prosper Menniere proved it is a disease of the inner ear and compared it to glaucoma of the eye and the degenerative changes. However treatment is serious because of the inner ear's location to the brain.

I have symptoms of Menniere's disease and am thinking of some of the treatments. Do you know anything about the side effects of getting treated for this as it is BRAIN SURGERY. Will I experience nausea and vomiting and lots of headache pain if I succumb to antibiotic injections (touching the brain) or worse yet, sac surgery which is inside the brain?

The ringing is maddening but I have read a book on the subject and while I understand everything it doesn't mention the side effects of such serious surgery.

Maybe it would be better to try homeopathic vitamins first?

Mighty Joe Young profile image

Mighty Joe Young 3 months ago

I'm interested in where you found the reference to 'Watchmaker's Disease', oddly enough I have had Meniere's since childhood, but as an adult I took to repairing watches as a hobby, so I guess I did things backwards.

If you're interested I have a social network for people with meniere's disease, you'll find it at:

www.menieresworld.com

Everyone's welcome.

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