Meniere's Disease
- Thread starter Teri
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Seems we are the opposite! My T is nothing. My H was really really bad. Now it's not so bad. Still a little off today. But I also have a headache and my light sensitivity is up in my right eye. That's happening a lot more lately.
I was in a job interview today. The room was quiet and only 2 persons and me there. Amazing how loud my T is. I actually couldnt hear everything they said and i found myself thinking this noise in my head. It is so hard to concentrate these days. I managed to get through the interview somehow. What i wanted to say is: i hate tinnitus. I hate MD. Absolutely.
@SueR @MichaelM
My hearing dropped and sound is a bit distorted in my T ear. There was heavy rain and I think probably more air pressure....probably low pressure. Do you happen to know if that will cause problems for us folks with inner ear issues? No H to speak of...thank goodness.
@MichaelM
Good luck with your job interview...I hope you can find some work that will be a good fit for you.
My hearing dropped and sound is a bit distorted in my T ear. There was heavy rain and I think probably more air pressure....probably low pressure. Do you happen to know if that will cause problems for us folks with inner ear issues? No H to speak of...thank goodness.
@MichaelM
Good luck with your job interview...I hope you can find some work that will be a good fit for you.
I dont want to sound too negative so let´s order some t-shirts!
http://www.cafepress.com/mf/78702733/shayne-towns-menieres-designs_tshirt?productId=856903553
http://www.cafepress.com/mf/78702733/shayne-towns-menieres-designs_tshirt?productId=856903553
The Tshirt clearly states the mindset of most doctors. At my last ENT appt I was told that what I have can be very debilitating but I must just go on and live my life. Very pathetic and poor quality of medical advice IMHO.
Michael...the tshirt needs to become our official doctor's appt attire. LOL
Michael...the tshirt needs to become our official doctor's appt attire. LOL
Have you thought about TMJ? I know a lot of people on this site and the FB sites I watch talk about TMJ. I rarely find myself with the teeth touching, so I doubt I'm clenching (which is a problem for people with TMJ).
Hmm...that is an idea Sue, but my jaw doesn't click as if there is TMJ issues. It just has an ache. What is interesting about it, is that it is prevalent when my ear is bothering me.
My ear has pressure know and my hearing has dropped. I really do not like this because I am always worried about T spiking, possible vertigo, or any other fun symptom that comes along.
My ear has pressure know and my hearing has dropped. I really do not like this because I am always worried about T spiking, possible vertigo, or any other fun symptom that comes along.
TMJ has been one of my projects for the whole year. No progress.... i need to see the dentist next week. ENT said "nothing wrong with your jaw" but that´s what they always say, nothing wrong so try to cope with it. Next ENT appt next week. Cant wait to hear all the cliches again.
My jaw is sore sometimes and usually it feels like numbness after dental anesthesia on my MD side of the head and cheek.
My jaw is sore sometimes and usually it feels like numbness after dental anesthesia on my MD side of the head and cheek.
Michael, I know plenty of people whose doc says that TMJ is the cause of their hyperacusis. If you think about it, the TM joint is very close to the inner ear. I dislike that your ENT has dismissed it outright.
TJM can not be the cause for MD. i believe this is a fact. ENT i saw told so. Nothing but MD alone cannot cause vertigo that last for hours. and that´s Certain MD as we already know. Possible MD.... i guess everything related to TJM can be TMJ-based as long as there is no hours-long-vertigos and hearing loss. but this is just me.... we should ask a doctor.
"my doc" said: should you have no teeth or no jaw at all you still would have 100% hearing.
one thing that came to my mind yesterday. Back in 2009 my car was hit in the rear by another car. Not too fast, perhaps some 30mph. Anyhow i was a bit dizzy for an hour or so.... not a nice feeling. got so called whiplash injury.
the other side of my head was totally numb for many days, also my right hand was numb and didnt work normally. all this went away within some weeks.
but
after some 6 months from that, 2010, i started feeling these first symptoms of MD: a little hearing loss and especially the aural fullness on my very same right side those whiplash injuries were.
I havent really thought of this before, never even cross my mind. Now that i think of it i am really scared.
WAS that the moment and and cause for my MD with all these symptoms.
i have to tell this to ENT next week.
i hope and believe all this is just a not-so-nice coincidence.
"Following the trauma, vertigo disorders can be triggered immediately or they can take months or years to develop. The purpose of IUCCA upper cervical chiropractic care is to reverse the trauma-induced upper neck injury, thereby reducing irritation to the nerves that trigger vertigo. While many vertigo sufferers recall specific traumas such as head injuries, auto accidents or falls, some do not." link: http://www.erinelster.com/vertigo.html
"my doc" said: should you have no teeth or no jaw at all you still would have 100% hearing.
one thing that came to my mind yesterday. Back in 2009 my car was hit in the rear by another car. Not too fast, perhaps some 30mph. Anyhow i was a bit dizzy for an hour or so.... not a nice feeling. got so called whiplash injury.
the other side of my head was totally numb for many days, also my right hand was numb and didnt work normally. all this went away within some weeks.
but
after some 6 months from that, 2010, i started feeling these first symptoms of MD: a little hearing loss and especially the aural fullness on my very same right side those whiplash injuries were.
I havent really thought of this before, never even cross my mind. Now that i think of it i am really scared.
WAS that the moment and and cause for my MD with all these symptoms.
i have to tell this to ENT next week.
i hope and believe all this is just a not-so-nice coincidence.
"Following the trauma, vertigo disorders can be triggered immediately or they can take months or years to develop. The purpose of IUCCA upper cervical chiropractic care is to reverse the trauma-induced upper neck injury, thereby reducing irritation to the nerves that trigger vertigo. While many vertigo sufferers recall specific traumas such as head injuries, auto accidents or falls, some do not." link: http://www.erinelster.com/vertigo.html
Michael, I do believe it can affect T & H though. There are non Meniere's folks who have T and/or H attributed to their TMJ (so they say).
I don't think this is my case, since my jaw doesn't hurt, I don't clench, no clicking, etc.
I don't think this is my case, since my jaw doesn't hurt, I don't clench, no clicking, etc.
I believe TMJ can affect T and H, too. Actually, i believe these days that it is, with occlusion problems, far more common a reason for T than people actually think. I have started reading about it just recently.
the dentist i saw last winter took panoramic dental X-ray and the "X-ray doctor" said there is nothing wrong with my TMJ. I dont know who to believe anymore... one doctor can say different things and the next doctor another thing.
I have seen only 2 ENT´s here + 2 dentist. I keep on searching more opinions. I believe now i really have MD but there must be more to this than just MD. This has pretty much ruined my life. it is hard to believe MD can cause ALL this.
the dentist i saw last winter took panoramic dental X-ray and the "X-ray doctor" said there is nothing wrong with my TMJ. I dont know who to believe anymore... one doctor can say different things and the next doctor another thing.
I have seen only 2 ENT´s here + 2 dentist. I keep on searching more opinions. I believe now i really have MD but there must be more to this than just MD. This has pretty much ruined my life. it is hard to believe MD can cause ALL this.
http://www.dizziness-and-balance.com/disorders/central/unlocalized.htm
Here is something that I came across that I found to be interesting. I did not even know there were different definitions of vertigo. Very interesting indeed.
@MichaelM
Do you think that some of your vertigo could be classified as "Psychogenic Dizziness"?
The reason I ask is that it is said that panic and anxiety are two conditions that arise commonly with MD.
Here is something that I came across that I found to be interesting. I did not even know there were different definitions of vertigo. Very interesting indeed.
@MichaelM
Do you think that some of your vertigo could be classified as "Psychogenic Dizziness"?
The reason I ask is that it is said that panic and anxiety are two conditions that arise commonly with MD.
http://www.drhschaaf.de/endolye.html
I found this study to be interesting too....
@Sue....this is what I found most interesting is the term "psychogenic dizziness". I was wondering if some of our dizziness is also related to anxiety.
I found this study to be interesting too....
@Sue....this is what I found most interesting is the term "psychogenic dizziness". I was wondering if some of our dizziness is also related to anxiety.
@Teri, interesting links. I have to read them all again.
i dont think i have been predisposed to MD. Tinnitus i have had in some forms for more than 15 years or so. Didnt really bother me properly until this MD thing. First time i visited a doctor because of T was in 2001. T back then for me was that classic "i hear it in a quiet room when i try to sleep". i have to say i got habituated....
to this current T i cannot habituate anymore.
I did drink a lot when i was younger and i was depressed but there really is no way that MD is a mental or psychological problem or caused by them. Every doctor keep saying it isnt.
And isnt this crazy. We have an MD here, a disease virtually unknown to everybody and here i am thinking is this a mental thing. WTF.... yes i have thought of this before.
Last 4-5 years have been stressfull. i am not sure if i undestand that psychogenic dizziness fully but my vertigo attacks just come and go no matter how or what i feel. They hit with full force. It is not dizziness but paralyzing. I literally cannot move anymore, it lasts for hours during which i sweat like a (any good american sayings here?), every single sound i hear is amazingly loud. So bad an H it hurts.... there is no "up" or "down" anymore then. just fast spinning. I cannot move for an inch. If I need to go the toilet---- well. i cannot.
What i was thinking is should i take a video next time. i havent found videos of vertigo attacks.
That could rise awareness what this MD is like with those vertigos. Mine are, so i have read, the Worst Class Attacks. Some people get them on a weekly basis. I have had 2 this year.
Oh... i found an article in Finnish about vertigo. Psychogenic also mentioned. If you want to know what this language looks like. Here it is.
i dont think i have been predisposed to MD. Tinnitus i have had in some forms for more than 15 years or so. Didnt really bother me properly until this MD thing. First time i visited a doctor because of T was in 2001. T back then for me was that classic "i hear it in a quiet room when i try to sleep". i have to say i got habituated....
to this current T i cannot habituate anymore.
I did drink a lot when i was younger and i was depressed but there really is no way that MD is a mental or psychological problem or caused by them. Every doctor keep saying it isnt.
And isnt this crazy. We have an MD here, a disease virtually unknown to everybody and here i am thinking is this a mental thing. WTF.... yes i have thought of this before.
Last 4-5 years have been stressfull. i am not sure if i undestand that psychogenic dizziness fully but my vertigo attacks just come and go no matter how or what i feel. They hit with full force. It is not dizziness but paralyzing. I literally cannot move anymore, it lasts for hours during which i sweat like a (any good american sayings here?), every single sound i hear is amazingly loud. So bad an H it hurts.... there is no "up" or "down" anymore then. just fast spinning. I cannot move for an inch. If I need to go the toilet---- well. i cannot.
What i was thinking is should i take a video next time. i havent found videos of vertigo attacks.
That could rise awareness what this MD is like with those vertigos. Mine are, so i have read, the Worst Class Attacks. Some people get them on a weekly basis. I have had 2 this year.
Oh... i found an article in Finnish about vertigo. Psychogenic also mentioned. If you want to know what this language looks like. Here it is.
Dont mention it, mate. Great article. Just found it today myself. Lots of new info for myself, too.
this was new (sorry, in Finnish: kiertohuimaus on aina merkki sisäkorvan tai aivojen pohjaosan vauriosta eikä voi selittyä pelkästään esim. niskajännityksellä)
I dont know how to translate that completely but it seems that rotating/spinning vertigo is always a sing of damaged inner ear or damaged parts in the brain. Therefore tension in the neck cannot be the cause for rotating/spinning vertigo.
Which brings us to Certain Meniere´s. MD is in the iner ear/(brains?) no matter how one´s neck or jaw is.
this was new (sorry, in Finnish: kiertohuimaus on aina merkki sisäkorvan tai aivojen pohjaosan vauriosta eikä voi selittyä pelkästään esim. niskajännityksellä)
I dont know how to translate that completely but it seems that rotating/spinning vertigo is always a sing of damaged inner ear or damaged parts in the brain. Therefore tension in the neck cannot be the cause for rotating/spinning vertigo.
Which brings us to Certain Meniere´s. MD is in the iner ear/(brains?) no matter how one´s neck or jaw is.
Michael, as severe as you have MD, the upside, if it is one, would be that you are probably going to reach that "burn out" stage sooner than later. That means that MD would have run its course and be done!
Am I correct about that?
Am I correct about that?
if I understand you correctly that is one interesting theory, @Teri
Some people actually believe this disease has a start and middle phase and.... an end?
My MD evolved quickly. Doc´s have said it, too.
My question is: when the burn out really hits does one notice it? I believe not.
It is like depression. You realize how depressed you where after you are back to normal.
Some people actually believe this disease has a start and middle phase and.... an end?
My MD evolved quickly. Doc´s have said it, too.
My question is: when the burn out really hits does one notice it? I believe not.
It is like depression. You realize how depressed you where after you are back to normal.
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