Miss Sherlock Figures Out the Sounds

We’re driving through Oregon, returning home to Canada after two months of touring southwestern United States in Flag, our fifth wheel.

Rain starts to plop on the windshield. I’ve always heard rain, but on a highway at high speeds, the sound mixed with other road noises and wasn’t always distinguishable. But today I heard the distinctive ‘plops’ and then I noticed another, higher, tinkly sound. My hearing aid (left ear) and my sound cochlear implant sound processor (right side) were delivering the raindrops in two different frequencies – lower on the left, higher on the right. Once I figured out it out, the sensation was delicious, different, tinkly. I felt proud – I heard this!

This is the bimodal life – one sound has two different profiles when delivered through different technologies; I hear acoustically with a hearing aid and electronically with a cochlear implant.

But as a new bimodal babe, I have to play detective to figure out the origin of some sounds which I may have heard all my life, but now they’ve changed in shape, frequency and volume. People who have had hearing loss for any length of time understand this reality: we have to readjust to new ‘hearing’ on a regular basis.

Obviously, when our hearing becomes worse, sounds lose clarity, become quieter or disappear completely. Understanding speech becomes especially challenging. Hearing also changes when we get new technology – sound is crisper, definitely LOUDER, and there are sounds that we’d forgotten or have never heard. Clocks ticking, water dripping, people breathing through their nose – the fun stuff.

Hearing perks up when we change our wax guards or our sound processor’s microphone protectors. It changes when we’re tired or when we are in a noisy place. And it certainly changes when our tinnitus flares up or is particularly bad.

We have to do some deductive reasoning to identify sounds. Driving the car, I see raindrops. I hear a sound at the same time of each raindrop. Eureka – that’s the rain I hear!

For the first few months after receiving my implant last year, things were tickety-boo, as we say in our family. But then I had a setback when tinnitus and hyperacusis set in, more debilitating than I had ever experienced. At first I thought my cochlear implant wasn’t working well, but that wasn’t the problem. My tinnitus was now compromising the quality of my hearing. When I’m listening in noise, the tinnitus gets roaringly worse, whereas noisy situations used to mask my head sounds.

My hearing professionals say my case is ‘complicated’, and the audiologists decided to dial things back a bit to give my brain some time to readjust. I’m only now getting back to where I was four months post-implantation, with mappings slowly increasing my “dynamic range”.  My audiologist suggested that I stop doing auditory practice for a while and I’m just now starting up again. The tinnitus still interferes, but it may never go away, so I need to adapt. That’s the human condition – always adapting to changes, however small, in our lives.

I’ve gone back to the beginning of figuring out some CI-delivered sounds.

With the really high frequency sounds – the songs of the smallest birds, keys tinkling, and rain on the windshield, I hear them perfectly with my cochlear implant. But the wing movement of birds as they move about in the bushes – where I can’t see them – is less high frequency and it’s a fuzzy, hissy sound that could be anything: slippers on a carpet, the air conditioner spewing out air, water rushing in the sink. I’m still trying to differentiate those sounds. I hear them, they don’t immediately register as a specific sound.

With low sounds that my left ear says is car traffic, my CI side hears a hum. But a leaf blower outside also hums. I’m supposing that hearing people can tell the difference between a car motor and a leaf blower.  And – is it really that important?  What is important, is the unidentified beeping somewhere in the house, making me run from room to room checking out possible culprits. Sometimes, I heard a beeping with such a high frequency that I could hear it only through my sound processor. Turns out it was the warning sound that my CI batteries were about to die. I’m slow, sometimes.

And while I do try to keep up my detective work, I have the patience of a flea. It’s much easier to ask the Hearing Husband, “what’s that sound”?


Note to Readers:  Our website has a fresh new look. The links to my previous articles, which previously appeared at the top, can be found below this blog. Scroll down just a bit and you will be able to navigate to previous posts. Thank you for reading the Better Hearing Consumer – I’m always happy to hear from you!

About Gael Hannan

The Better HearingConsumer addresses the personal experience of living with hearing loss. Editor Gael Hannan and her occasional guest bloggers explore every corner of the hearing loss life with humor and poignancy. Comment Policy   Gael Hannan, Editor Gael Hannan is an author, speaker and advocate on hearing loss issues. In addition to her weekly blog at the Better Hearing Consumer, which has a passionate international following,Gael has written two acclaimed books, “The Way I Hear It: A Life with Hearing Loss”and “Hear & Beyond: Live Skillfully with Hearing Loss”, written with Shari Eberts. She is regularly invited to present her uniquely humorous and insightful work to appreciative audiences around the world. Gael has received many awards for her work that advocates for individuals to become more knowledgeable and successful at dealing with their hearing loss and a more inclusive society for them to live in. She lives with her husband on Vancouver Island, Canada. Books and other media Hear & Beyond: Live Skillfully with Hearing Loss. Written with Shari Eberts and available anywhere books are sold. The Way I Hear It: A Life With Hearing Loss. Available through online bookstores. Unheard Voices, DVD, vignettes from the hearing loss life. Contact Gael Hannan to order.


  1. I also appreciated your descriptions of different hearing sounds (vs what others without hearing aids might say they are like), Gael. Thank you! But, I have a question which my audiologist can not verify for me. It has to do with my tinnitus and I’ve done lots of research.

    After living in my new suite for a few months, which I learned was above someone with a breathing apparatus, I started hearing the hum of that machine …even after she had moved from her apartment. While staying at someone else’s home, I was still awakened at night with the sound of the the subtle beating even though it was not my heart-beat!

    Do you know if our hearing (in this case my tinnitus) takes on other types of sounds?
    I am learning to ignore it, yet am curious to know if others have had this experience.

    – caroline from Vancouver, BC

  2. Hi Gael,
    Thanks for sharing your new hearing experiences regarding the different sounds youcan hear and can now identify. I look forward to reading all your articles.

  3. Hi, Gael

    What a clear and illuminating description of what it is like to hear through both a hearing aid and a CI. Keep up the good work, and happy travels to both of you.

  4. Thanks for this post.

    I was shocked to find that my first hearing aid made everything sound radically different than it had ever sounded before. My audiologist insisted this was all MY fault, and that the aids made everything sound like they always had, but I just couldn’t remember what sounds used to sound like (the day before), because my hearing loss was very minimal when I first got my first aids.

    It’s nice to have someone finally acknowledge that hearing aids change your hearing, and you have to learn what sounds mean all over again.

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