i've had tinnitus for awhile now, in both ears, since maybe 2010 at earliest. not sure how it started but i remember one day hearing ringing in both ears.
over time (5ish years) its subdued to a low rumbling in both ears and that was good, i was feeling happy about being free from the ringing.
the concerning part is a few months ago, i woke up one morning with random new 'morse code/singing/bird chirping/fluttering' low frequency (1450hz) tinnitus in my RIGHT ear only!!!! and it's loud, i hear it pretty much everywhere I go. it's like the volume is constantly going up and down per SECOND. very annoying and debilitating
this, accompanied with 'ear fullness' that i've been experiencing in my right ear for atleast a year now, as well as noticing that my right ear has been slightly less clear and hears less than my left ear, noticed that symptom about a year and a half ago. i've had a handful of hearing tests trying to figure out my tinnitus, and it's been shown that my right ear has a slight dip (not sure, they said it was very subtle)
It seems like it has only gotten worse, since then, though. the area around my right ear feels 'hot' and 'full' also there is a slight sensation of facial numbness when i compare touching my right cheek and left cheek...
Since this new ringing sound in my right ear only, and the fullness, i've been wondering why this would randomly happen, and my research has led me to acoustic neuroma,...
let me also say my dentist has suspected TMJ issues in the past, and I wear a mouth guard at night to help with biting/grinding of my jaw. (they suspected I have tinnitus because of TMJ issues ,but i don't know anymore)
Since all of this new information, and comparing my symptoms with acoustic neuroma, i'm desperately afraid and scared that I could have a tumor... music is my life and I cannot afford to lose ANY hearing, as i'm an already depressed and anxious person, I can't imagine life after finding this out...
anyway I went to my GP and she ordered a CT scan, and I recently had that done complete with contrast dye. I am waiting for the results..
If CT scan shows nothing, should I be worried, and want an MRI? I've read CT scan can sometimes not show AN's.
Any advice is appreciated.
over time (5ish years) its subdued to a low rumbling in both ears and that was good, i was feeling happy about being free from the ringing.
the concerning part is a few months ago, i woke up one morning with random new 'morse code/singing/bird chirping/fluttering' low frequency (1450hz) tinnitus in my RIGHT ear only!!!! and it's loud, i hear it pretty much everywhere I go. it's like the volume is constantly going up and down per SECOND. very annoying and debilitating
this, accompanied with 'ear fullness' that i've been experiencing in my right ear for atleast a year now, as well as noticing that my right ear has been slightly less clear and hears less than my left ear, noticed that symptom about a year and a half ago. i've had a handful of hearing tests trying to figure out my tinnitus, and it's been shown that my right ear has a slight dip (not sure, they said it was very subtle)
It seems like it has only gotten worse, since then, though. the area around my right ear feels 'hot' and 'full' also there is a slight sensation of facial numbness when i compare touching my right cheek and left cheek...
Since this new ringing sound in my right ear only, and the fullness, i've been wondering why this would randomly happen, and my research has led me to acoustic neuroma,...
let me also say my dentist has suspected TMJ issues in the past, and I wear a mouth guard at night to help with biting/grinding of my jaw. (they suspected I have tinnitus because of TMJ issues ,but i don't know anymore)
Since all of this new information, and comparing my symptoms with acoustic neuroma, i'm desperately afraid and scared that I could have a tumor... music is my life and I cannot afford to lose ANY hearing, as i'm an already depressed and anxious person, I can't imagine life after finding this out...
anyway I went to my GP and she ordered a CT scan, and I recently had that done complete with contrast dye. I am waiting for the results..
If CT scan shows nothing, should I be worried, and want an MRI? I've read CT scan can sometimes not show AN's.
Any advice is appreciated.