So, I am thinking this might be my last ever post on this blog.

I have reached the point where there is not really much new stuff to report.

I know it has only been 7 months since I got the implant (7 months! is that all???! Can you believe it?) But already, I think I have reached the peak, and plateaued. The implant will not get any better or different now in my right ear. It has reached its’ ‘zenith’.

And what a zenith that is.

I can hear on the phone now. Very well.

Normal pjhone and TTY phone now sit on my desk together.

It's goodbye TTY, hello normal phone since I had the implant. However, I keep the TTY on my desk just in case! Can't shake the feeling of needing it there.

So well in fact, that I have had a normal phone installed on my desk at work alongside my trusty TTY phone that I always used when totally deaf.

So, as you can see – the cochlear implant actually did what I dreamt it would do – it allowed me to reconnect with the world on the phone again.

I can also hear a lot better in group conversations and meetings. Where I used to strain to hear someone at the other end of a meeting table, now I can sit back and hear almost every word. That never ceases to amaze me.

The things I still can’t do all that well are:

  • hearing lyrics to music (I can hear them better than I could with the hearing aids, but they are still a bit unclear at times)
  • watching movies and TV – I still need captions if I am going to really relax and enjoy movies and TV – however, I have been to see Avatar and
    TV captions

    I still need to watch TV with captions. Which is why it's so frustrating when they don't have them!

    District 9 without captions, and understood most of it. I can also understand most TV news without captions.

  • I still tend to lip-read in noisy environments, but I can hear people a lot better in noise.

So, if I am going to leave anyone with a word of advice, or perhaps a message to the deaf community, or maybe parents considering an implant – having been through this all before, having met so many people who’ve had implants, having talked to ENT surgeons, doctors, audiologists and researched online – it would be this:

Kate’s Final View on Cochlear Implants

Disclaimer, this is only my view, no one elses. You might think it’s completely wrong, yo! If you do, then leave a comment, but make sure its a clever, well-thought out comment. I’ll delete stoopid ones!

  • A cochlear implant is not a cure for deafness. It is just like a hearing aid, except it is implanted in your head.
  • It does work wonders for some people, and not so well for others, just like hearing aids. To find out whether you are a good candidate, you need to see your cochlear implant specialist. A normal audiologist just won’t cut it – they just don’t know the real facts and figures.
  • It appears that people who go deaf later in life are probably going to benefit most. I was one of those, losing hearing over ages 11-19 years.
  • It appears that people who are deaf since birth, and get the implant after 5 years old seem to find it harder to adjust – maybe because of crucial years of language development have passed? Not sure.
  • From what I have seen, deaf people who get an implant before the age of 5 years old seem to find their cochlear implant more useful.
  • Even with an implant, you will always be deaf, and something like 20 per cent of the time you will not be using it (i.e. swimming, shower, in bed, when playing messy sports), so it pays to learn sign language and lip-reading to use with your family and friends.

I am glad I got the implant. I am also glad I waited because it was an emotional ride. But I would do it all again, definitely. If I had a deaf child tomorrow, I would give it a cochlear implant before the age of 4, teach it sign language and show it how to lip-read.

There, getting off my soap-box now.

Here are my final test results for the 6 month test at the Sydney Cochlear Implant Centre – please note the disclaimer my audi asked that I include on my hearing aid result!

These are the test results for my Phonak hearing aid in my right ear:

These are the test results for my Phonak hearing aid in my right ear: Note: These hearing aids use “Input Compression” or “AGCI” (Automatic Gain Control for inputs). This feature means that the hearing aids vary the amount of amplification according to the loudness of incoming sounds. Soft sounds are amplified more, while loud sounds are amplified less. The complexityof the aids means that they amplify warble sounds used in aided threshold testing differently to running spech. For this reason, aided thresholds measuired with a non-linear aid can only give a general impression about what is audible for complex sounds such as running speech.

Freedom Cochlear Implant hearing test result

This is the test result for my Freedom Cochlear Implant, in my left ear.

My final speech recognition tests were:


  • 100 per cent for both hearing aid and cochlear implant together
  • 100 per cent for just the cochlear implant
  • 66 per cent for just my old hearing aid


  • 84 per cent for just the cochlear implant (I was zero per cent when I used my hearing aid)
  • 20 per cent for just my hearing aid

So, I as you can imagine, I am contemplating getting a second cochlear implant.

But I am going to hold off for a few years, only because the hearing aid balances out the sound of the cochlear implant, and makes everything sound ‘normal’.

So I guess you could say ‘watch this space’ – I may come back with a new blog:

“Kate’s Second And Hopefully Final Cochlear Implant”!

Who knows!

Until then, bye, and thanks for reading!

Kate Locke, signing off!

Kate Locke, signing off! That's it from me - have a great 2010!

This is an important shout-out to all my Australian readers with a hearing loss.

The Australian Federal Government has launched a full Senate Inquiry into deafness!

Is there anything about having a hearing loss or being deaf that frustrates you?

  • Have you ever felt annoyed at the cost of buying – and maintaining – hearing aids and cochlear implants?
  • Have you ever been upset by the low standard of services of an audiologist?
  • Ever wished you could stay with Australian Hearing after you were 21 years old?

The Australian Federal Government want to hear from EVERYONE in Australia about what issues they face when they have to deal with a hearing loss.

They are planning on using your input to change the way hearing health is dealt with in Australia.

It is so important that you email them to let them know what it is like for YOU personally.

All you have to do is send a short email to by 9 October 2009, letting them know what frustrates you most about your hearing loss in Australia, and what you would like to change.

I have done one already. If you need help in knowing what to write, have a look here.

This is your chance to finally let your Government know how difficult it can be living with a hearing loss in a hearing world.

Don’t miss this chance.

30 September 2009

Re: Inquiry into Hearing Health in Australia

To the Community Affairs References Committee (

I would like to make a submission to the Hearing Health Inquiry.

I am a deaf young professional living and working in Australia.

The current Australian hearing health system is antiquated and not working well at all – it makes being deaf in Australia very difficult and expensive.

For example:

  • my hearing loss was first discovered at age 11, and I was given hearing aids without any sort of rehabilitation or support. it took me ages to get used to them and to wear them. It was a traumatising experience as a child. I didnt wear the ones I was given at 13 until I was 18, because I hadnt been given adequate support in understanding how to use them
  • When I did start wearing them, I received free hearing aids and batteries through Australian Hearing which was fantastic, and really helped.
  • then suddenly at the age of 21, just when I was unemployed and studying full time at university, I was told I could no longer get any services through Australian Hearing
  • I had to find a private audiologist, and many that I had didnt understand my hearing loss well enough, and I bought hearing aids from each of them, when one would have been enough. Each hearing aid is about $3,500 to $4,000. I was also convinced to buy expensive additional gadgets  for up to $1,500, which I have never used, because it was not correct for my hearing loss.
  • One of my hearing aids broke and I had to buy a new one, as it was not covered under private health insurance
  • I had to get a personal loan to pay for it, and then I had to go on Centrelink payments as well, because I had trouble paying my rent.
  • I have just received my first cochlear implant. I had to take out private health insurance in order to get this over 3 years at $90 per month. None of my hearing friends pay anywhere near this amount for private health insurance.
  • I had to take out special cochlear implant insurance at $300 per year to cover my cochlear implant, when someone who has an ipod can get that covered with their home and contents insurance. I have tried to get my cochlear implant covered under home and contents, and all the big insurers refuse to cover them.
  • I’ve had to buy a special TTY phone and special Telstra HipTop mobile phone in order to communicate with people, as these are the only two I can use being a deaf person.
  • Audiologists charge huge amounts for ear moulds when you don’t need them (up to $250), and for repairs (up to $500), and for batteries (they cost me $300 a year).
  • I have been to see the Minister for Ageing about these issues, but as hearing health is under Ageing, it’s not the main part of the portfolio. Hearing health gets lost in Ageing. It needs to be put over into Health.
  • Hearing health is not an ageing issue, I am only 29 years old, it is a health issue. Many of my deaf friends are under 30 years old.

There is an essential inequity as to how hearing health is perceived as compared to other health issues, even though hearing loss is one of the most prevalent health issues in Australia.

According to the Access Economics Report, one in six Australians has some form of hearing impairment, and this is projected to increase to one in four by 2050 (from Access Economics (2006) Listen Hear – The Economic Impact and Cost of hearing loss in Australia).

I would like to see the following changes made to the way hearing health is dealt with in Australia:

  1. Hearing health should be moved out from under the Federal government Ageing portfolio, and placed under the Federal Government Health portfolio, alongside eye health. It currently does not receive the attention it deserves under the Ageing portfolio.
  2. Subsidised government services should be offered via ‘Australian Hearing’ to people between the ages of 21 and 65 if they are on a low income, unemployed, full time students, or part time students. In Australia there is currently no help for these people in affording hearing aids, implants and other hearing health services.
  3. Insurance companies should cover hearing aids and cochlear implants if they are lost or broken. Currently most insurers will cover silly things like iPods, but not a cochlear implant processor, which is $8,000 to replace, and vital for many to be able to hear.
  4. Former child clients of Australian Hearing who are not unemployed, students, or on low incomes should not be suddenly cut off from services of Australian Hearing. They should be able to pay for services to stay on at Australian Hearing with their audiologist.
  5. All hearing aids, cochlear implants and other hearing health aides should be able to be claimed as a tax deduction once someone starts work. Currently you can’t claim expensive hearing aids as a tax deduction.

Thanks for accepting my submission.


Kate Locke

It has been three full days since I got the cochlear implant switched on, and boy, is it amazing.

Let me tell you things I have been hearing.

Ben and I decided to go to Kangaroo Valley for two days, to get away from it all, and give me a tranquil rural atmosphere in order to get used to the sound of the implant.

I realised that the drive up was going to be the first time I would be able to experience what music was going to sound like. We have quite a good stereo in the car, and we had a good two hours to go through all the archives.

What a drive.

I had mentally prepared myself for the horror of music. Blips and pings replacing beautiful harmonies that I remember from my childhood before I lost all my hearing.

But it was totally, mega, awesome, cool, futuristic, and the sounds in my head were like the feeling you get after drinking a big cold glass of water on a really hot day – like hearing those sounds was quenching this huge thirst in my ears – the thirst to hear the sounds I had been missing for so long.

It was electronic.

The best way to describe it is as if a synthesiser is playing all your favourite songs.

One of my favourite bands, Cut Copy, sounds GREAT. And of course, Daft Punk sounds flipping awesome too.

Then I listened to my favourite song of all time, kind of my ‘coming of age’ song, which I used to listen to at age 16: Portishead’s “Glory Box” …

And I could hear the voice of the lead singer, Beth Gibbons. Even though I couldn’t understand all of what she said, I could make out some of the words – and I would say to Ben “did she just sing ‘a thousand flowers’ something something????” And he cried “Yes!! She did!” These were words that I had never really heard before (this was the song I had to get my school friends to write out the lyrics for me, so I could sing along to it, even though I couldn’t hear what she was singing.)

I was just so happy. I couldn’t believe it.

So, as we drove I tried to focus entirely on the sound of the music in the implanted ear. The harmony and rhythm of all the different songs sounded like aliens playing electronic keyboards with two fingers at the speed of light.

Weird. But not when you think about how a sound is produced in the cochlear implant.

The implant  and the processor extracts noise and sounds from the environment around you, and then converts it into electrical digital signals, and transmits them to the electrodes in my inner ear. My nerve endings get stimulated electronically, and then send the signals to my brain, telling me its a sound.

Here is a perfect example:

Imagine the sound made by a flute, or maybe a violin. One long continuous note can be emitted, and you’ll hear it like that.

With the implant, sound is more like an individual piano key being played at an extremely fast rate in sequence – so fast, that it sounds like one long, smooth note, because they are played so rapidly.

This means that the sounds are different to me when I hear an old favourite song, but I can recognise it.

This is what makes it so amazing. As another song came on, I said to Ben: “I can hear that this is ‘Saturday’ by Cut Copy playing, but what is that whacky rhythm and melody playing in the background?”

I have never heard that melody of notes before! So even though it sounded very electronic, it was like my eyes were being opened to a tune I hadn’t been able to hear before. It was so worth it.

Then, huge moment … for two hours we’d been listening to music, and it was playing a song I didn’t recognise, but then suddenly, I definitely heard the words “1, 2, 3, 4”, and I turned to Ben, repeating what I thought I had heard: “Ben??? 1234????”

And he looked at me astounded, and yelped “Yes! But you don’t even know this song?”

Oh my god, we were just looking at each other so happy. Then I asked him what the song was. It was apparently ‘The Number Song’ by Cut Chemist. HAHAHAHAHA

The lyrics throughout the song are “1234” all the way through. hahaha!

But I had no idea … I HEARD IT!!!! I REALLY HEARD IT!

OK, so there were other lyrics in that same song that I hadn’t heard, but the fact that I could pick up those particular numbers that I would never normally have heard before just blew us away.

I just hope it will continue to improve… I wanted to include a very interesting analogy by Professor Jennie Brand-Miller, who has been mentoring me through this experience (she has TWO cochlear implants!), and she described the every day learning to hear with an implant below:

Think of your auditory pathways as like a gravel road at the moment … cars can’t go fast on them, electrical signals can’t whizz up them.

But everyday, the workmen are laying down the foundations of a super highway, smooth and capable of cars going 250 kms an hour.  It takes time to  do this … weeks, months and even a couple of years … but you’ll notice the difference … week by week, there’ll be a detectable difference.  You’ll enjoy the journey, no matter what the speed.

Amazingly well described. Thanks Jennie. 

And I believe it.

I am so excited!

I bet you are wondering what it’s like!

One word.


Totally. And. Utterly. Bizarre.

Triangle percussionists have taken over my ear.

Triangle percussionists have taken over my ear.

Remember playing the ‘triangle’ at school? Well, imagine everything I am hearing translated into that sound. That is the cochlear implant for me.

As I type on the computer right now, it’s as if the keys are either triangles dinging, or perhaps one of those old 80s electronic Casio Keyboards, and every computer key is making a dinging sound. I kid you not. I am really ‘playing’ my computer.


If I say that, it sounds like one long beep.

When I click the mouse, it is such a clear, nice, satisfying click! I bet that is going to annoy me later!!!

My new favourite words are “wheel” and “forces”. They sound TOTALLY MEGA AWESOME with a cochlear implant.

Actually, maybe another way of describing it is as if Kraftwerk had set up and was translating every sound for me.  

If you have ever heard Kraftwerk, then you will know what I am talking about when I say that it sounds like they've moved into my head.

If you have ever heard Kraftwerk, then you will know what I am talking about when I say that it sounds like they've moved into my head.

So I can hear pings and bips and bops and zings and more pings, some zoinks, robotic gings, paps, whizzes, swizzles, dongs and midges, wasps and bees.

Everything also sounds robotic. Very, very robotic.

So, should I start from the beginning?

We went to the Sydney Cochlear Implant Centre (SCIC) this morning, and it was all a bit out of the ordinary. The NSW State Minister for Health, John Della Bosca, had decided to use my switch on to launch some extra funding for the SCIC’s Adult Program.

Whoot! Extra funding! (They must have read my blog post “How much did my cochlear implant cost me?“.)

So, the Government has agreed to fund something like 15 extra implants for adults on top of the already existing 44. Might not sound like a lot to some, but when you realise that every implant will cost almost $30,000, you can see why it’s a big deal.

So, when we arrived, they had set up the ‘switch on room’ upstairs, with video cameras, so that it was beamed downstairs to the surgeons and ministerial staff, and journalists in the press conference area. Talk about pressure, man.

L-R: Rachel Stawski, John Della Bosca, journalists from the Daily Telegraph, Sharan Westcott, and my surgeon, Professor da Cruz.

L-R: Rachel Stawski, John Della Bosca, journalists from the Daily Telegraph, Sharan Westcott, and my surgeon, Professor da Cruz.

Luckily, Ben and mum were allowed upstairs to experience it with me. And I was REALLY happy that my surgeon, Professor da Cruz, was able to come. He apparently had a day full of surgeries – but managed to slip out for an hour or so in the middle (I am sure no one was left mid-surgery!) and be there for the switch on. How incredible is that? “Oh, just gotta pop back in a few minutes and finish that electrode array placement”. Nice! So was happy to see him there, because he was the one that ‘put it in’ so to speak. Nice that he was able to view it actually working.

So, we sat down and Rachel and Sharan plugged me in. Ben just watched bemused.

Getting plugged in is a bit fiddly. I was pretty nervous at this point. I mean what do you say to waiting media and a ministerial party if you can't hear anything! Gah!

Getting plugged in is a bit fiddly. I was pretty nervous at this point. I mean what do you say to waiting media and a ministerial party if you can't hear anything! Gah!

A switch on usually takes an hour or so. To set everything in the electrodes, they do a test to see if they are all working inside your ear (you can’t hear that test), and then each electrode is activated, and Rachel asked me to tell her whenever I heard three beeps in quick succession, for each tone. She said they would be really soft at first – but I wasn’t prepared for quite how soft. And it wasn’t really sound I was experiencing – more sensations!

So, she started – and I was thinking: “Hang on, what was that? Was that a sound? No?.. No. ..Yes! …No?.. I think? …Maybe? ….No….” it was really hard to tell.

Was that sound I could hear? It was so hard to tell - it just sounded so faint and strange - like nothing I have ever heard, so I wasn't even sure if I was actually hearing anything!

Mum and Professor da Cruz sit waiting to see if I can hear. I'm thinking to myself: "Was that sound I could hear?" It was so hard to tell - it just sounded so faint and strange - like nothing I have ever heard, so I wasn't even sure if I was actually hearing anything!

She turned it up and up and up, slowly slowly slowly. And by golly.

It was sound!

Holy crap, I heard that! It was a beep!

Holy crap, I heard that! It was a beep!

So then of course I started to giggle like a maniac, because I was hearing tones and sounds that I had not heard in a VERY LONG TIME.

Even though they were obviously electronic, it was like they were stimulating my deadened nerves, waking them from a very deep sleep.

So, this wasn’t even the official switch on! This was just mapping them. Once they had all the beeps and tones ‘set’, then they switched it on.

Feeling gleefully happy that I could actually hear tones and sounds that I hadn't heard in ages. Maybe I might be able to play the piano yet!

Feeling gleefully happy that I could actually hear tones and sounds that I hadn't heard in ages. Maybe I might be able to play the piano yet!


Noise! Noisy noise! No understanding! (‘Like normal?’ Ben might naughtily suggest?) 

Bells, pings, dings, all put together in one mish-mash so that it sounded like a high pitched static. And this was mainly sensations. I just do not know how to describe it any better. It is not like hearing normal sounds. It was like sensing a feeling in my head, imagine the sound that pins and needles would make if … they made a sound! Or it felt like I had eaten an ice-cream, and was getting an ice-cream headache. But it wasn’t unpleasant, even though it sounds bad.

If anything, I wanted it turned up louder.

It was great to hear those sounds. But totally and utterly weird.

Then came the test of speech.

OK, so I was hearing sounds … But the real question that I always had was … would I be able to understand what people are saying to me? I knew I would get lots of ‘noise’, but would I be able to decipher words and sentences? Would I actually be to ‘understand’ what someone was saying to me?

For the first few minutes, no. I couldn’t even work out a word someone was saying to me. But I could ‘hear’ them.

So when Rachel said, “ok, we’ll check you speech perception in that ear, switch your hearing aid off, and repeat back to me what you hear with just the implant”, I thought to myself – there is NO WAY I will be able to understand what anyone is saying to me. It is all garbled, all high pitched bells dinging. It doesn’t make any sense.

But then, as Rachel did the test, she covered her mouth and said some basic words.

The first word I ever heard in that ear, without lip-reading – was “August”.

To my UTTER amazement, I actually could also hear her saying “January”, and “October” without lip-reading, and some other months of the year.

I mean, I did confuse March with November (don’t ask me how that is possible – not even the syllables are the same!). But, still – I got most of them. Wow. That blew me away. It was hard, but even though I didn’t think I would be able to make out the words – suddenly, there they were. My brain was already going mad trying to process all this new stuff in my head.

But apart from those simple words, I couldn’t really understand what was being said to me. It was just too ‘ding-y’.

My head felt really ‘full’ of something. Nothing was very clear. It just felt full.

I really just wanted to sit down somewhere nice and quiet, and just listen to easy words, maybe just with Ben and me.

But you can’t do that when the world wants to talk.

The Daily Telegraph was there to film a video for their website, and write an article for the newspaper about John Della Bosca's increase in funding for the SCIC.

The Daily Telegraph was there to film a video for their website, and write an article for the newspaper about John Della Bosca's increase in funding for the SCIC.

After describing it to everyone, then I actually went back to Rachel and said “Do you reckon you could turn it up a bit more?? Right now?”

Already my brain had gotten used to it, and within an hour, my ears were wanting more sound.

So, she turned them up higher, and then that was it.

I got the run through of how to work it, how to look after it, all the extra bits and pieces I got in the cochlear pack, how to change the battery case.

And then everyone went home, and my family and I all went out to lunch!

So now I am at home, and I keep hearing something weird, and it is the talking on the TV.

I can hear paper crackling, but it is not very clear yet, just muffled. Of course, the computer keyboard is dinging and dinging like a percussionist, this is the coolest thing ever.

When we were in the car, I didn’t hear any indicator’s clicking like everyone says – but I did hear a strange alarm that went off when we parked the car, and Ben switched the engine off. He told me that it happens every time, it’s apparently to remind you to take the stereo with you! I had not really heard it until now.

So … as soon as I got home with Ben, he said “I’ll read to you!”, and asked me what book I wanted to read. I said “The Cheese Book”, which just lists cheese, HAHA. But he said “how about the Great Battles book?” and looked so hopeful, that I agreed.

So we sat together for about half an hour, with him just reading to me, and me following the words on the page.

It is truly amazing. I am having trouble hearing people’s voices, but that is because they sound like nothing on earth. It is like having to learn a new language. It just doesn’t sound like the english we know. I know that’s weird, and it’s hard to explain, but … you can see why you have to practice for months and months after this, just to be able to understand what people are saying.

Once I heard the bizarre cool way “wheels” and “forces” sound (terms taken and pronounced by Ben so nicely from his “Battles” book – they sound like a xylaphone sweeping up a scale, with robots harmonising in the background), I just realised how crazy cool this whole experience is going to be.

It will be hard.

I will have to totally re-train my brain.

But it’s going to be worth it.

Associate Professor Melville Da Cruz is my surgeon - lets hope he's had a good nights sleep, and isn't grumpy before my surgery!

Associate Professor Melville Da Cruz is my surgeon - lets hope he's had a good nights sleep, and isn't grumpy before my surgery!

Have you ever thought about what it must be like to be a surgeon? Do you ever compare it to what you do at work, and how you work? Call me weird, but I often do – even before I was booked in to get this implant, I often wondered how they do it.

I mean, think about it – how many times you get to work in the morning, and do things half-heartedly because you are just not in the mood? Or maybe your best friend is getting married so you celebrated “a la Hens Night”, and ended up waking up somewhere with beer bottle lids stuck to your forehead, and the knowledge you are going to be late for work?

I can’t exactly imagine a surgeon wiping the sleep and beer from their eyes, looking at their watch and saying “Oh shit!  Quadruple by-pass heart surgery in 30 minutes! God, I need a coffee. Will they be able to smell the Vodka Cruisers on my breath? Oh where’s the visine! My eyes!”

No. Well. You would hope not!

I have great faith in my surgeon. He seems like a good guy. He also plays a delicate instrument, the violin, which has gotta be a good thing if he’s performing cochlear implant surgery, huh? I can’t say I would feel the same way if he was a rugby player or sumo wrestler. That’s not to say Sumo Wrestlers wouldn’t make fantastic ENT surgeons. I know Rugby players wouldn’t.

And what about my audiologist?

Monica Bray, Senior Audiologist at the SCIC

Monica Bray, Senior Audiologist at the SCIC

Monica Bray is a Senior Audiologist at the Sydney Cochlear Implant Centre, and she is very reassuring because she has had so much experience with cochlear implants. She is my audiologist, and has been has been ‘mapping’ & fitting cochlear implants since 1989, and she was the one that suggested that I wait for a bit before I get my implant – and that was definitely a good move. You have to be so ‘mentally ready’ for an implant.

And finally, my cochlear implant hero – is Professor Jennie Brand-Miller. She is a bilateral cochlear implantee, which means she has TWO implants!

Professor Jennie Brand-Miller’s GI concept overturned our dietary ideas about carbohydrates, and she’s sold millions of books. So she is not just a pretty face, but a very clever woman.

She has a similar hearing loss to mine, and also had Monica as her audiologist – and now that she has had her implants, she can … (*gasp*)… talk on the phone!

Well, that would be awesome, but understandbly, they always say “don’t expect to be able to hear on the phone”, because many people are never able to hear on the phone after a cochlear implant.

But I know Jennie can, because I saw her!

I asked her once if I could come and talk to her about her implant, when I was thinking about getting one. I just really wanted to talk to someone, and see someone who had experienced this scary massive operation and rehabilitation, and had actually benefited.

Professor Jennie Brand-Miller

Professor Jennie Brand-Miller, bilateral cochlear implantee

So, I went to Sydney Uni to visit her in her office, and I arrived a bit early, and was standing outside the door to her office, and could see through her window. And there she was … SPEAKING ON THE PHONE. I couldn’t believe it. Like I said in an earlier post, I haven’t been able to hear on a phone for about 5 years.

So, to see that… I was taken aback, amazed, freaked out, happy, bewildered, hopeful. Couldnt wait to get in there and talk to her.

And so, Jennie would have to be my cochlear implant hero, because she started off with a very realistic, very intelligent view of the implants – that they would require work, and getting used to – but if she persevered and remained positive, she would ultimately benefit.

So – I salute you Jennie! And here’s hoping mine is as successful as yours. High five!

If you want to read about Jennie, check out her ABC Talking Heads interview about her career.