Subtle changes…mean a lot to me.
Still Changing and Learning for Better Hearing
Ten Years Ago
Silver Wings
While driving home from work today, I was listening to a CD that I put together a couple of years ago with a variety of songs on it. About ten minutes into my 40 minute commute, I heard what seemed like wind or a whistle in my car. I remember thinking, “Oh great, my car is making a new sound.” As I focused and tried to figure out what was making this new sound, I came to realize it was in the music! I muted the CD player and it went away, so I turned it back on and listened. I played the song again and really listened. Is it a piccolo or strings? I listened again – I think it is strings! It is a whole orchestra and I can hear the strings! I have been looking on YouTube trying to find the version of the song I was listening to, but I’m not finding it. The song is “The Ballad of the Green Beret.” I am hearing the soft start up of the strings when they begin the crescendo at the words “silver wings.”
I have had my implants 9 years on the left and 3 years on the right and I am still experiencing improvement! I have been procrastinating about scheduling a mapping thinking there hasn’t been enough change to warrant an appointment with my audiologist, but now I’m thinking otherwise.
One of my earliest memories of really knowing that there were things I could not hear was in 9th grade typing class. I never did hear a typewriter bell. How I ever got through that class with a B, I will never know. As I was enjoying hearing more of a song I have liked probably since I was in 9th grade, I was thinking that my cochlear implants give me such wonderful hearing it just might be possible to hear better than normal someday.
Getting off the Roller Coaster
Something wonderful happens to people after they have had their cochlear implants for a while. They get on with life!
As a late-deafened adult and cochlear implant recipient, I know the emotional roller coaster of losing one’s hearing; the life and relationship issues that go with that; and finally the high of getting sound back. Definitely “emotional roller coaster” is the right descriptive phrase.
Have you ever ridden a roller coaster? What can you do when you are riding one? About all you can do is ride. You might talk with the person next to you, laugh, or yell, or scream, but you won’t be composing a report or holding a meeting.
As my hearing loss progressed, I participated in life less and less. I quit going to movies, parties or anything that involved a large noisy group or a large room that might echo sound. I stopped using the phone and pretty much limited my communication to family and close friends. Anything beyond that was intimidating, like standing up in a roller coaster. If I had to be on this ride, then I was going to stay seated in my little box and hang on so I felt safe. I might look at the scenery once in a while, but it was easier not to.
I like the feeling of getting off a roller coaster. That first step of putting solid ground under your feet feels so reassuring. I love looking around and being able to walk away and put some distance between me and a ride that I don’t like.
With my cochlear implants, I can get off the ride. I’ve got the ground under my feet again. I can walk away and join the world for the day and I don’t have to get back on until the sun is down and the roller coaster sleeps.
It is fun though, especially when you don’t like a ride, to go on the ride with friends. I attended my first Hearing Loss Association of America (HLAA) convention this year in June. It was a wonderful experience and the first time I really enjoyed the ride, the hearing loss roller coaster. When we get on the roller coaster together, we hug, we smile, we share the ride and we laugh!
I have noticed that many of the friends I have made through my blog, the Bionic Ear Association, the HLAA and the online forum, Hearing Journey, are getting off the roller coaster and walking away. They have other things to do and lives to live. What a wonderful thing this is!
Jonathan’s Cochlear Implant Activation 8 mo., Rt Ear cont’d
I love watching this little guy’s reaction to his activation. It is so moving.
I Can’t Hear You
I am the oldest of five. For the most part, my siblings and I share similar political beliefs. Unfortunately, our parents seem to feel quite the opposite, so if we happen to end up talking politics at a family gathering, a heated discussion may escalate into a shouting match. We are learning to avoid certain subjects.
Last time I was visiting my parents, while my mother and I were preparing breakfast, the conversation started dancing around a sensitive subject. I don’t know what possessed me to do it, but I happened to announce where I stood on the issue. My dad didn’t agree and started on a tirade denouncing what I believe. Immediately I regretted having said anything but I was not going to back down. My mother was getting uncomfortable and wanted everyone to stop – which was fine with me, but dad was not getting the message. I was at the kitchen sink wiping a dish and dad had his back to me. I decided to give him the message visually. I put the dish down, wiped my hands, walked around to get in front of him and when he was looking at me, I reached up and with exaggeration I knocked my CI headpieces down to my shoulders. He got it. He looked at me and his mouth stopped moving. There I was in my silence feeling like a naughty child. I didn’t enjoy disrespecting my father, and I didn’t enjoy being disrespected.
I have shared the story of that incident with my girls and one of them said she finds herself wondering how many children with cochlear implants or hearing aids, have, or eventually will, take their hearing off in the face of being scolded or lectured. I suppose it is the equivalent of a hearing child plugging her ears with her fingers and taunting, “I can’t hear you.” With a CI it is much more dramatic and effective – but still naughty.
HLAA
I have been thinking about this for awhile and I finally decided to go to the HLAA Convention in Milwaukee in June. I have never been to one before and I’m really looking forward to it.
Last spring I attended a mentor training for the Bionic Ear Association. That was the first time I was part of a group with the commonality of hearing loss. I really enjoyed the feeling of kinship and continue to enjoy the friendships that developed. I’m really looking forward to this convention and hanging out with my friends.
