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can anyone give us some feedback on this?
the ad says TREATMENT
it does not use the word CURE

You see, nobody know exactly why it happens, but TMJ is caused by most
of the muscles in the head (including the throat, tongue, jaw and the
shoulders) to stiffen up. This causes the pain and dysfunctions in this
area.

I just liked to share my story here, and ask about something.
My first real ear injury came in 2003 in the army, when I accidentaly
fired a blank shot with a rifle near to my left ear. The ear became
sensitive, and hasn't really recovered yet. Over the time I got to

Are many proposed T treatments linked to cause and symtom? Or, maybe
just cause?
For example lets look at 2 people who have T.
We have Jane Doe. She is 33 years old, smokes, and drinks lots of decaf

I had an endolymphatic shunt put in my right ear some years ago. As it
turned out the original diagnosis of menieres disease was incoreect, it
turned out to be TMJ.  The shunt seems to be adding to the tinnitus and not
helping it.

A couple of weeks ago  I downloaded a sweep wav file (10 khz to 20 khz)
to test out my hearing on the computer. I could hear to about 16.5 -17
khz on a lowish volume, being curious if I could hear beyond that I
paused to the point where I couldn't hear any more and cranked the

I just liked to share my story here, and ask about something.
My first real ear injury came in 2003 in the army, when I accidentaly
fired a blank shot with a rifle near to my left ear. The ear became
sensitive, and hasn't really recovered yet. Over the time I got to

I've read that some folks habituate to tinnitus at different rates,
that most do after a period lasting from a few months to a few years.
And yet there are some that do not habituate -- that is, their tinnitus
continues to bother them even after many years.

Coffee keeps me awake and being awake without occasional naps seems to
have improved my T.

Tinnitus
I just heard a sound called tinnitus
And suddenly my life will never be the same again
Tinnitus

It appears to me that quite a few American patients here would rather
suffer than to visit doctors.  There can be only 2 explanations; either
the doctors in the US are too expensive or they are as IN-experienced
as the many ones I visited in Hong Kong and China.

My ENT says I have Ménière's, except I don't get the spins.  My
audiologist says my symptoms are tinnitus only.
Every now and again I will experience hearing loss in one ear, not
complete though.  It starts gradually and increases until I can't hear

I was reading about a new hearing system under development. I hope it will
have a place in the treatment of tinnitus.
http://www.oudaily.com/vnews/display.v/ART/2006/04/10/443b292917516?in_archive=1

I hit my head one week ago, and since then have had symptoms that lead
me to believe I've got Benign Paroxysmal Position Vertigo.  Dizziness
upon repositioning my head, especially lying down on my right side, and
then also when sitting back up.  Can anyone give me some GOOD news