Amanda’s cycling to Rio

I’m now on my way home after spending 6 days in Spain. We’ve just lifted off Bilbao for Munich then it’ll be two long haul flights back to NZ.
So what was I doing in Spain? To keep a long story short, my reserve pilot Kirstie James needed to race in a UCI para-cycling world cup to be eligible to race at Rio if she was to be called up (ie if my main pilot, Hannah van Kampen gets injured and can’t race with me or if she called up to be a reserve for our another stoker), and the cut-off date to get Kirstie qualified was when the last round of para-cycling world cup was to be on..Cochlear implant recipient, Amanda Cameron. Paralympics



So Stu (coach), Kirstie and I headed to Bilbao, an old city north of Spain near the border so there are mountains surrounding the area which was pretty. It was where the final UCI Para-cycling Road World Cup before Rio was to be held. Exciting!!
As the purpose of the trip was a simple one, it meant the trip would be short as we had a tight turnaround to get back home and focus on training on track (which is my target at Rio). Kirstie and I were due to race in three days after arrival but disaster struck and our luggage didn’t arrive with us! Lucky I always make sure to have everything for few days in my carry-on luggage… Including charged and disposable batteries!)


It was a nervous wait for us but my single bike and the tandem finally arrived the day before racing. Half our luggage was still missing and it meant we didn’t have wind-trainers, tools or disc wheels but at least we could race.
Despite me not having a lot of focus on road racing, we finished 6th in the 21km time trial and 7th in the 70km road race, both results I’m really pleased with. It was also Kirstie’s first two tandem races after having only taken up piloting little over a month ago.
In between racing, the three of us got to do a little sight seeing and relaxation. Even when you’re busy or anxious, it’s important to take some time out and enjoy the scenery around you. As I’m a nervous person, I often have to be reminded to breathe and be in the moment. This is a cool short clip with captions (only about a minute long) on meditation. This is something I do often, especially when nervous or stressed (like before a race!) but it’s great to do every moment you can.Meditation – The Huffington Post
Anyway, nearly at Munich! I will write another update soon.


From Amanda Cameron.

Megan’s inspiring story

Megan was born profoundly deaf, but that wasn’t going to hold her back from her swimming dreams. Megan swam in the 2000 Paralympics.

Five years ago, Megan received a Cochlear™ implant and now enjoys hearing lots of different types of birds. Megan is also using the True Wireless™ Accessories and is finding her life easier at work and in the pool.

Watch her story here.

Michael travels the world in sound

Your son, Michael, will never be able to hear, speak, or do the things a normal hearing person would do,” my parents were told. I was diagnosed as being profoundly deaf at the age of fifteen months. My world seemed as if it had come to a narrow passage with very limited opportunities. However, it was the beginning of something unforeseen and beyond normal. All future dreams and visions seemed shattered, but they were actually expanding to a whole new dimension a normal-hearing person would never experience.
I was the first child to receive the Cochlear™ Nucleus® 22 Implant in Dallas, Texas, USA at the age of two in 1991, and since then I have thrived in the hearing world thanks to a team of family members, audiologists, auditory-verbal therapists, and Cochlear. I have upgraded multiple times over the years. With each upgrade, I experienced new sounds and adventures. Cochlear technology enabled me to push myself to do more such as appreciate music, talk on the phone, make the high honor roll in school, graduate college, travel, kick start my career, and receive an MBA.
I will celebrate my 25 year anniversary with the Nucleus 22 Implant in June. It has been an incredible journey filled with many “a-ha” and “wow” moments. The very first sound processor I had was the Mini Speech Processor (MSP). It was considered “mini” because the previous generation sound processor (Wearable Speech Processor) was rather quite large by today’s standards. It had a bodyworn processor that rested on my hip and connected to a behind-the-ear microphone via a long cord that ran up from the waist to the ear. The behind-the-ear microphone was about the size of what the Nucleus 6 Sound Processor is today. Isn’t it amazing how far we have come? It took something as big as the size of today’s sound processor just for the microphone back in the day! I used this speech processor during my toddler years. It helped me discover the world of sound and begin my journey to listen and talk.
After the Mini Speech Processor, I upgraded to the Spectra 22 Speech Processor. It comprised of a bodyworn processor connecting to a behind-the-ear microphone via a long cord very much like the Mini Speech Processor. It was tough and withstood many of my crazy shenanigans as a young boy such as completely dropping my Spectra 22 Speech Processor in a Colorado mountain river, and it still worked! I had this speech processor the longest; it very much became a big part of my life. I depended on it, and it supported me like no other technological device. In a way, I grew up with this speech processor.
Right before I entered high school, I upgraded to one of my favorite sound processors, the ESPrit™ 3G Sound Processor. It was completely behind-the-ear, the first of its kind I got to experience. Long gone were the days of struggling to tuck in my shirt because the long cord that attached my behind-the-ear microphone to the bodyworn processor was placed underneath my shirt. This sound processor was much more discreet, which served me well as I was a bit more vain going into high school. I used this sound processor for seven years. It gave me so much more comfort and flexibility throughout my high school and college years. I could not have made it as well as I did without this high-performing sound processor.
Shortly after I started working for Cochlear in 2010, I was still using my ESPrit 3G Sound Processor. I loved this sound processor and felt no desire to upgrade. Plus, I was a bit nervous about the upgrade as I heard that it might be a challenging upgrade. Little did I know what I had in store. After much encouragement from my mentor and work leader, René, I tried the Freedom® Sound Processor upgrade. I couldn’t believe how well I could hear with this upgrade from the get-go and how many new sounds I could hear with it. It was like I had a hearing loss with my previous sound processor, and all of a sudden, I could hear so much more with the Freedom Sound Processor. The upgrade was nowhere near challenging to which to transition; I had absolutely nothing to worry about this upgrade. This sound processor was the first all digital sound processor with which I ever heard. My previous sound processors used analog processing technology. I could not believe the sounds I was picking up with this new sound processor. For example, I always could always subtly hear the fizzing out of a soda pop can with my previous sound processors. With the Freedom upgrade, I couldn’t believe how loud the fizzing was after opening the can. Not only that, the fizzing continued for many minutes afterwards–I had no idea! So I learned an important lesson here: Do not be afraid of upgrades as they bring about very exciting, new sounds and experiences.
Fast forward nearly five years, the Nucleus 6 for Nucleus 22 launched. Naturally, I had to upgrade to this sound processor immediately. One particular area that I struggled in was hearing in noisy environments. I got an all-new noise program with my Nucleus 6 Sound Processor, and I could not believe how well I could hear in noisy environments. Instantly, my confidence to join a lunch meeting or a dinner in a noisy café or restaurant skyrocketed. I no longer felt the sense of dread when I received an invitation.
Just recently, for the first time in my entire life, I heard in water with the Cochlear Nucleus Aqua+. Growing up, anytime I jumped into the pool, took swimming lessons, or vacationed at the beach, I always had to remove my external sound processor and returned to a silent world. Currently, I am doing a secondment at the global Cochlear headquarters in Sydney, Australia. One weekend, I took surfing lessons for the first time and used the Aqua+. I could hear the instructor who was behind me; this would have never happened had I not had the Aqua+. It was remarkable to hear the waves crashing and the birds chirping from above–all while in the water! This is something that I really wish I had growing up, but I am even more thankful to have it now.
One other thing that I treasure in my life is the gift of hearing music. There are very few things that I appreciate more than music. With the Nucleus 6 upgrade, I got the Cochlear Wireless Phone Clip and the Remote Assistant. The music is so clear through the Phone Clip. Best of all, there are no wires. I spend many hours cranking out reports and presentations at my desk. I simply place the Phone Clip next to my keyboard and jam to music all day long. It is pure bliss! When I am traveling, it can be awfully noisy on the plane. So I whip out my Remote Assistant, and I adjust the mixing ratio so that I can completely eliminate sound coming through the microphones and completely focus on the sounds streaming through the Phone Clip. It is like having the world’s best noise-cancelling headphones. Last but not least, the Nucleus 6 Sound Processor is the most comfortable and discreet sound processor I have ever owned. It is incredible.
After receiving the Cochlear Graeme Clark Scholarship, I worked as a summer marketing intern with Cochlear Americas based in Centennial, CO, USA, the very company responsible for enabling me to grow up in a world of sound. I am now a Marketing Manager where I have the honor and privilege to manage Nucleus Sound Processor upgrades, recipient communications and Cochlear Celebration events.

Hamish’s inspiring story

Hamish developed a significant hearing loss at just 15 months old, four month later he received his Cochlear™ implants, and life changed for Hamish and his family.

Upgraded to the Nucleus® 6 Sound Processor with access to Cochlear Wireless Accessories, Hamish has enjoyed using the wireless accessories in his active life. Especially playing soccer. Before his upgrade he struggled to hear his soccer coach over the other children on the field. Now with the Mini Microphone, Hamish says he is able to clearly hear instructions over everything else going on – and his skills are improving!


Amanda’s now on the fast track

Since my last blog post, the road season has closed and I’ve changed to track cycling. I tried it for the first time only a few days before we were due to race in a track event. My pilot, Hannah, was already experienced, but only on a single bike, so we were both really excited to give track tandem riding a go!

I pretty much fell in love with it straight away and managed to quickly pick up what to do or not to do. For example, as I can’t see out front I get a bit dizzy, so I learned to fix my focus on Hannah’s back. Listening and being able to hear in track cycling is quite important as you need to hear the start beeps and when the coaches give you your lap times and split laps. Hannah and I are strong starters but we realised there was a slight delay between the two of our starts as I would watch her and move when she did. So it was (and still is) critical for me to listen to the countdown myself. With some practice I was soon nailing it and starting on time.

There are two events that we race in, which is the kilo and 3km individual pursuit. In the pursuit, which is 12 laps, one coach tells us how many laps there is to go, and a second coach tells us how long our lap was as we have to aim for a specific time per lap otherwise we might go too fast too soon or too slow. I have had issues with hearing them clearly at times because the aero helmets that we wear covers the microphone of the processors. Wearing the Cochlear™ Wireless Mini Mic is useful – the only issue is distance and static but we will play around with it some more. In the meantime we are looking at the helmet to see if we can adjust the inner shell. No matter the barrier, there is always a way to overcome them.

Anyway back to that first track event! Considering we had not trained specifically for track and with only a few hours of track riding under my belt, we did really well and I loved every moment of it. Half of it was due to knowing I was overcoming challenges not just as a para-athlete but by also having a hearing loss on top of it and being able to do well made me proud of myself.


I then decided to train for the upcoming track Nationals less than two months later with the goal of PBs with the same pilot. It is never easy training over summer when you go away visiting family, or on holiday for Christmas and New Year, but I was determined to get really good at track cycling so I lugged my bike home to my parents and kept up my training. I had a couple of days off while my family and I went camping with friends at the lake. It was relaxing. I even got to try out paddle boarding which was really fun! I don’t have the Cochlear™ Aqua+ accessory covers so I had to take off my processors, which was a little frustrating but the Aqua+ is on my wish list now!


In February, the track Nationals rolled around and Hannah and I competed in the kilo representing Wellington. We were nervous but we shaved two seconds off our previous time and achieved our goal of getting a PB which we’re stoked with. We were going to compete in the pursuit together as well but there was a last minute change so I rode with a different pilot – also named Hannah! We did really well in the pursuit with more PBs.


Fast forward to less than a month later, I’m now at a training camp as I will be part of the team going to track world champs in Italy next week with Hannah #2 as my pilot. The training is going well and I’m really looking forward to racing at a world class level. There are challenges I’m learning to overcome every day and I love every moment of it – remember there is no such word as ‘can’t’.




G.Clark Scholarship winner: Changing the ‘old school’

Hi, my name is Philipp Heyn, I’m 22 years old and I am from Germany. I have two Cochlear™ Implants and am currently here in Australia studying for a year. Back home in Germany, I study Special Education in Dortmund. I attended a mainstream school, during which I spent my 11th year at high school in the United States. I started university when I was 19 years old.


I was born deaf, or as my doctors put it, hard of hearing in a degree close to deafness. I can hear stuff that is louder than 110 decibels, which basically means nothing. Apparently, the little hair cells in my cochlea are way too short to process sounds within the normal decibel range. Because my parents were worried that I wasn’t responding when they talked to me, my dad put me in front of the stereo and started turning the volume up, until he couldn’t stand the noise anymore. I was still giggling and not taking any notice at all. That was the point when my parents found out that I had a hearing problem, which lead to me getting my first hearing aid within three months. This was very early for “my” time. I did not have any problems learning speech and so I never had to use sign language. When I was five, my parents decided to have me implanted on my right side, which turned out to be a great success.

CI-Operation November 1999

Later, in 2008, I was implanted on my left side, the Cochlear ear had become so dominant that my left ear just kind of fell asleep over time.

I started studying Special Education because I felt my high school was unprepared when I attended it. Most teachers didn’t understand how to teach a deaf child and I wasn’t confident about my hearing so I didn’t tell anyone I had a hearing problem. I would not say that I had a bad time at school, but I want some things to change and I thought my best chance of doing this would be to work in the business that is closest to the issue – Special Education. At Uni, I started volunteering as part of a team that helps people with disabilities who are studying. This and much more voluntary work is probably what enabled me to win the Graeme Clark Scholarship from Cochlear, making it possible for me to leave Germany and study in Australia for a year. I have been in Australia for seven months now and there are seven more to go!

Cheers, Phil

‘Liam the Superhero’ creates worldwide interest

The Cochlear Kids: Liam the Superhero is a new children’s picture book from author (and mum to Cochlear recipient) Heidi Dredge. It is a fun, informative and inspirational story about a boy with Cochlear™ implants. Here, Heidi shares why she wrote the book and what she hopes it can achieve.

Liam the Superhero - front cover.jpg

Creating The Cochlear Kids series of books has been a labour of love, a work of joy, and a celebration of my own daughter, Zia, who received a Cochlear™ implant when she was just a baby. When I went searching for children’s books to teach Zia about her hearing loss, I found very few available. I felt there was so much that could be told about the incredible journey that children with hearing loss and their families travel from diagnosis, surgery, and switch-on (activation), to the importance and fun of speech therapy, to making hearing devices part of normal life, through to learning to advocate for oneself in the schoolyard. And so I set out to create a series of books featuring a range of different children (each one a “Cochlear Kid”) to tell these stories in an entertaining, uplifting and informative way.

Liam the Superhero - pg 16.JPG

As the first book in the series, Liam the Superhero explains to readers what a cochlear implant is and how it works. The story is set against the backdrop of four-year-old Liam’s favourite pastime – pretending he’s a superhero.

Liam’s story is written in fun, rhyming prose to appeal to children and adults.

The implant goes inside the ear

in a special operation.

It is put there by a doctor

after much investigation.

It is intended to be a way for young children with hearing loss to learn about their own special ears, and a clear and simple way for family and friends to learn about them too!

The processor has a battery

that needs charging every day.

It powers the cochlear implant

during work, rest and play.

It has proven to be a great resource for classrooms, with families and teachers giving feedback about how Liam the Superhero has raised awareness and understanding of hearing loss, while also providing the children in the class with the right vocabulary to discuss hearing devices.

What you see on the outside

is like a mini computer.

It is called a sound processor

and is pretty super-duper.

Liam’s story is underpinned by an uplifting message that we are all superheroes when we follow our hearts. Each book in the series will offer children and families a moment of inspiration, euphoria and pride that they can recognise in their own hearing loss journey.

 (Liam’s Mum speaking to Liam)

“Every day you are my hero.

You let your heart be your guide.

You let nothing hold you back

and you wear your ears with pride!”

Most importantly though, my aim for the books is to contribute in a positive way to a sense of identity and belonging for children with cochlear implants.

Liam is a Cochlear Kid.

He loves his super ears.

He is so happy and so thankful

for all the sounds he hears.

Zia has connected beautifully with this element of the story. Late last year we were leaving her kinder-ballet class and I told her how much I love to watch her dance, and that I could tell she was doing some really good listening to the teacher’s instructions. To this she replied, “But that wasn’t just me Mum. My Cochlear ear helped me … because I’m a Cochlear Kid, like Liam!”

Liam the Superhero - pg 4.JPG

My hope is for Liam the Superhero, and future books in The Cochlear Kids series, to reach far and wide to raise awareness and understanding of children with hearing loss and cochlear implants, and to have a positive influence on the lives of these amazing children!


The Cochlear Kids: Liam the Superhero is available for sale only from

The second book in the series Zara at the Zoo is due for release later this year.

Stay up to date with The Cochlear Kids at

Heidi Dredge can be contacted at