In June of 2011 I wrote “Reflections
on Going Deaf,” where I described how my hearing was progressively fading. I had seen a specialist (ear, nose, throat –
an Otolaryngologist ) who
sent me to see “the guy” at Ohio State Medical Center (who only does ears – an Otologist). His professional opinion was that there was
no discernable cause other than “sometimes this just happens.” He suggested that I just make the best of
things with hearing aids and expect that sometime in the future I would need to
have a cochlear implant.
Since then, I got more powerful hearing aids, our family
moved to the Massillon/Canton area and I changed audiologists (the guys that
program my hearing aids). Like everyone
always is, Walt, my new audiologist, was surprised at how quickly my hearing
was being lost. He suggested that given
the importance of hearing, I ought to get a second opinion regardless of how
good the OSU guy was. He recommended
that I see specialist that is “the guy” in this area and I did. Last August I drove over to Dr. Lippy’s
office in Warren, Ohio had a bunch of testing done and saw Dr. Berenholz (Dr.
Lippy is retired, I think). There I got
just about the same news that I had at Ohio State. No real reason for my progressive hearing
loss could be identified but some people, like me, are “just lucky.” Yippee.
What’s more, their evaluation determined that I had already lost
so much of my hearing that I probably qualified for a cochlear implant and insurance
would likely pay for it. At that time,
there were still a few tweaks left that we could do to make my hearing aids
last a little longer so we agreed to meet again in six months. We met again last month and did the testing
all over again. Not surprisingly, my
hearing has continued to get worse. With
my hearing aids on, sitting in a soundproof room, they read random sentences to
me (through a speaker) and I was supposed to repeat as much as I could
understand back to them. I got 40
percent. It was time to see if our
insurance would cover the implant.
For those of you who have never had hearing loss I want to
try to express what my loss might “sound” like to you. I have no hearing in the high frequencies at
all so even hearing aids don’t help because it doesn’t matter how loud you make
it. I can’t hear mosquitos or flies or
bees. I can’t hear the microwave beep or
the smoke alarm or my alarm clock. I can’t
hear a lot of bells or the warning beep that tells you that you forgot to turn
your headlights off. I can hardly hear
sopranos at all and pianos sound strange.
At my kids’ band concerts I can hear the percussion and the low brass,
trumpets sometimes, and woodwinds almost never.
Music doesn’t sound musical, and even familiar songs sound uncomfortably
strange and out of tune. My car radio is
rarely used because I can’t listen to music and while I can generally hear talk
radio when the car is sitting still, the ambient noise when in motion makes
everything unintelligible regardless of how much I turn up the volume. A lot of times what I hear sounds like my
head is inside a cardboard box.
Last week Dr. Lippy’s office called and said that our insurance
would cover 100 percent of a cochlear implant minus a sizable deductible. I have an appointment at the end of the month
to get a CT scan of my head and more tests.
After that I have to see my family doctor, have a physical and get his
permission, and then we can schedule the surgery.
After the surgery, there are four weeks of recovery before I
return to the office and they turn the implant on for the first time. Then, there are six months (or more) of
physical therapy as my brain (re)learns how to hear. I admit that I am a little excited and also a
little afraid. I look forward to being
able to hear again, especially to the possibility of hearing music again but I also
worry. What if there are side
effects? What if it doesn’t work?
In any case, the process has started. I am, gradually, going deaf and so I will
need the implant to function in a hearing world.
In the immortal words of Buckwheat from the “Our Gang”
television show… “I don’t know where we’re going, but we’re on our way.”
God be with you on your journey, John. I have a friend who went deaf in a way similar to yours, and her cochlear implants revolutionized her life. May it be so with you as well!
ReplyDeleteThank you so much for your kind words Cynthia.
ReplyDelete