Update:
Just an update on this- I went to Little Rock last Tuesday and did the balance tests. The audiologist said I failed some tests. Ouch. Would you know that the tests made me sick to my stomach and vertigo did got worse that day and I had to take it easy by not overdo anything but rest and stay still. Whew!
Finally I got the letter from the doctor today. He did reviewed my vestibular testing's and said that some of tests that I did not performed well. My inner ear function is excellent but I don't have any useable hearing in my left ear and marked loss in my right ear.
My Ct scan is essentially normal, but it looks like I only have 2 turns of the cochlea. (a normal cochlea has 2 1/2 turns) The cochlea is shaped like a snail shell and your top turn appears to be overly open. This may well be the etiology of my progressive hearing loss. Interesting? I was surprised at this information? I wonder if anyone have this like me? I guess I am different, eh? ha ha
He said what I have is called Meniere's Disease. (In case you are not sure what this is. It is a fluid imbalance within the inner ear.) This periodically responds to diuretics (water pills). So he is putting me on medicine called Maxzide, 75 mg daily. Also another medicine amytriptyline, 10 mg at night to help with tinnitus and my balance. ( I am clumsy and will fall easily, yikes!) He also said walking 30 to 40 minutes a day will help with my balance and should improve the dizziness.
I have to come back in 6 weeks to see if there is a difference if I am responding to the treatment of the diuretics or not. If I have significant improvement and my hearing is up in my right ear then will continue the course of the treatment but If the hearing does not improve. We will then explore the pros and cons of doing a cochlear implant surgery due to the fact that I will lose my hearing over time.
My mom said it's impossible that I have this because I was born deaf. I told her I would look up the information online. Sure enough I did- It said deaf people do get this even stone deaf? They still have it no matter what.
I told her- See? She said ok. I guess it is new to her. Mom know best? Nope not this time. She know nothing, lol. I told her how do you explain that and why I can't hear at all in my left ear? I used to be able to? but not anymore? She said nothing more.
Sometimes I can't hear some days in my right ear but like today I can hear the modem ringing. For few weeks I couldn't? Sometimes it is frustrating as I can hear now but why not other times or especially every day? Sigh. I still wonder if it was from the accident? He didn't say so but I will ask if it can be caused by that or not?? Good question, hmm.
I guess I will lose my hearing over the time. Might as well get myself CI so I can and continue to enjoy hearing things like music anyway.
Any of you have this disease? I wonder? Let me know your treatments and what will work for you. I am curious.