New articles are published every month under the headings below.

Deaf Coast woman can't be stopped

Feb 2018 Sunshine Coast Daily

Doctors said Erin Turner would never walk or talk when she was born, but the Coast woman now prides herself on a healthy, active lifestyle and teaches sign language. The 28-year-old had to be resuscitated at birth and was born with several health problems. At 16 months old she was diagnosed as profoundly deaf. Ms Turner also suffers from ataxic cerebral palsy. Every day Ms Turner uses Auslan sign language to communicate with people, but had to teach herself to lip read for those who don't use it. "Group situations are particularly hard as it's impossible to follow who is actually talking,” Ms Turner said. "The worst and cruellest thing is when people say things like 'it's not important' or 'it doesn't matter'.

Erin TurnerErin Turner is deaf and suffers from cerebral palsy, but living with disability won't stop the 28-year-old from living her best life

"I received a cochlear implant in 2011, and many people think I can hear well because of it. I can't - it mainly gives me access to environmental sounds. I still have absolutely no idea of which direction sounds come from.” Despite this, Ms Turner keeps herself busy working three part-time jobs and staying active. "It's really important for me to maintain fitness and muscle tone because this helps control and minimise how my cerebral palsy affects me,” she said. "I've been a disability support worker for over seven years, and have just started a couple of other totally different jobs, including teaching Auslan to a community class. "Sometimes people try to stop me doing things or think that I can't do things, but I am pretty stubborn and won't let people put me down because of my disabilities.”

Backpacker's $15,000 hearing aids stolen

Feb 2018 Otago Daily Times

A deaf backpacker's cochlear implant and hearing aids, worth about $15,000, have been stolen from the Hot and Cold Pools near Rotorua. Julia Ofele, a 23-year-old German futsal player, took off her devices to go swimming but the bag they were in was stolen about 8.30pm on February 7.
She was left with nothing but the bikini she was wearing, her towel and her GoPro, which had fallen out of her bag. "We had no keys, no money, no passport. Nothing," she said. The AA was called so Ofele and her friend could gain access to their car and get their clothes. The police were called and have GoPro footage of the thief and the number plate of his getaway car.

Julia OfeleOfele was born deaf and has been travelling in New Zealand since August.

Since arriving in New Zealand she has helped at a futsal championships in Wellington, has met and stayed with other deaf people, made repeat visits to Rotorua, walked the Tongariro Crossing and visited Abel Tasman National Park. "The nature is very beautiful in New Zealand and most people are very friendly," she said. "New Zealanders are more accepting of people who are different."

But this is the second time her belongings have been taken. With her hearing devices stolen Ofele cannot hear. The friend she was travelling with is not deaf and does not know sign language, so the pair had to write notes. "It was hard to communicate," she said. "It was fine for me because I was born deaf and I use sign language. Sign language is a beautiful language.” After eight days without sound she visited the Hearing House in Auckland, a charity for deaf children and adults with cochlear implants and hearing aids. She was able to borrow a cochlear implant until replacement devices can be arranged. Ofele has health insurance and is waiting to learn whether it covers her cochlear implant. "If they pay that's good, but if not ..."

Rotorua police area prevention manager Brendon Keenan said police regularly got reports of thefts from Hot and Cold and other tourist locations, particularly ones that were isolated. "Tourists may not know the dangers of a popular hotspot.” Keenan said the tourists got clear images of the licence plates in their GoPro footage of Ofele's theft. "We are still making inquiries and following up leads with some strong suspects."

How an iPhone connection is helping deaf people stream music and videos straight to their brain

Feb 2018 Herald Sun

The Aussie invention that has brought the magic of sound to more than 10,000 deaf Australians can now connect to an iPhone and stream sound directly to the brain. The seventh version of the cochlear implant* connects directly to the Apple iPhone via Bluetooth allowing users to hear music and Youtube videos and other apps directly from the phone for the first time. The user can also use an app to adjust the hearing device to block out background noise in a restaurant and allow them to focus on the voices of people at their table.

Lily KingLily King has her cochlear implant adjusted by her mum Sandra

Associate Professor Robert Briggs, the clinical director of the Eye and Ear Hospital, said the latest upgrade would allow people with a hearing impairment to use their iPhone like a microphone. “You can put your phone directly in front of someone and stream their voice directly to your implant,” he said.

Jamie Lee Lewis, daughter of rugby league legend Wally Lewis, is just one of many excited customers waiting for the cochlear implant to be upgraded as she starts her new career as an apprentice carpenter. Ms Lewis was diagnosed as being deaf as a child and had her first cochlear implant at four and another when she turned 16. I found out about the new one — it would be awesome that you wouldn’t need a cord to connect it to the phone,” she said.Jamie Lewis

The seventh version of the cochlear sound processor Nucleus 7, which is smaller and lighter and with a battery that lasts 50 per cent longer, will be on sale in Australia next month.

Jamie Lee Lewis with her father Wally Lewis who is a Queensland Rugby League legend

Hearing loss surgery sounds great for 16 children from Yarrabah

Jan 2018 Cairns Post

The sounds of their tropical home will become much clearer for 16 children from Yarrabah who have gone under the knife to improve their hearing. Several health organisations united to assist the indigenous children with day surgery in Cairns under the federally funded Eye and Ear Surgical Support Services program. Children ranging from 2-15 years of age were treated for a series of hearing impairments, including perforated eardrums and middle-ear infections.

Aboriginal and Torres Strait Islander children experience some of the highest levels of ear disease and hearing loss in the world. Rates are up to 10 times more than those for non-indigenous Australians. Gurriny Yealamucka Health Service Aboriginal Corporation nurse Dannielle Gillespie said, due to Yarrabah’s relatively remote location, it was difficult for parents to get their children to doctors. She said an initial list of 200 children needing hearing loss surgery had to be whittled down to the list treated at Cairns Day Surgery.

Karen Leeman Registered Nurse Karen Leeman prepares 7 year old Dallas Sands for surgery on a perforated eardrum.

“Hearing loss in Yarrabah is right across all kids,” she said. “Basically, if the perforations in the ear are not fixed, then that has a future roll-on effect with their speech, their education, their learning abilities – even their social skills, it starts affecting that, too.” Yarrabah mum Zoe-Ann Sands’ daughter Dallas, 7, had surgery yesterday. Ms Sands said she was thankful her daughter would finally have better hearing. Funding for the surgery was provided to health advocacy group CheckUP by the Commonwealth Government.

Horsley boy Koby Butterfield ready for Kindy thanks to The Shepherd Centre

Jan 2018 Illawarra Mercury

Bedtime stories were once a struggle for Horsley mum Ashleigh Butterfield, with her little boy Koby seemingly unwilling to lie still and listen. It wasn’t until Koby was four, that she discovered that he had never been able to properly hear those stories due to bilateral hearing loss. Now fitted with a cochlear implant in his left ear – and a hearing aid in his right – he’s more than ready to listen and to learn when he starts ‘big school’.

The five-year-old is one of 43 deaf or hearing impaired children who will join their hearing peers in mainstream Kindergarten classrooms this year thanks to the support of The Shepherd Centre.
For Mrs. Butterfield, and husband Daniel, the Wollongong centre has been their “lifeline” since Koby’s diagnosis. “Without The Shepherd Centre, we would have no idea what to do next,” she says. “They have been an incredible help in understanding Koby’s diagnosis and how we help him grow and reach his full potential.”

Mrs. Butterfield said Koby’s diagnosis had come as a complete shock, with no family history of hearing impairment. ‘’Koby had had grommets inserted as it was thought he had middle ear problems, but we didn’t know the extent of his hearing loss until he was diagnosed last February,’’ Mrs. Butterfield said. “It had affected his behaviour and his willingness to learn – I couldn’t even read a book to him at night.

Koby Butterfield Now his interest in reading is growing and he’s so excited about starting school – he put on his uniform this week and wouldn’t even take it off when we went shopping.’’

Koby will continue to work hard on his growing speech and language skills with The Shepherd Centre, while attending mainstream classes at Hayes Park Public School with the assistance of an itinerant teacher.

Centre CEO Dr Jim Hungerford said the first day of school was a ‘’special milestone’’ for children who were deaf or hearing impaired. “For many of these families, they’ve really been preparing for the first day of school for almost their entire lives,’’ he said. “The majority were diagnosed with hearing loss shortly after birth, and they’ve since received regular speech and language therapy from us –  some with help from hearing devices such as cochlear implants –  since they were just a few months old.’’

How gaming is bringing new sounds to new ears

Jan 2018 Telstra Exchange

There’s a reason why the Remarkable Accelerator has such a bold name. In part it’s the remarkable ideas behind each of the program’s tech4good startups. But mostly, it’s the remarkable people making these ideas a reality. With applications closing soon for the 2018 program, we want to share these Remarkable Stories. This is Elliot’s - “I’ve never seen being deaf as a bad thing.”
Elliot Miller explains: “It really taught me to view, articulate and interact with the world in a different, open-minded and often unique way.” He’s right. The 30-year-old Brisbanite has unique view of the world. Growing up deaf in a hearing world, also meant he’s had a unique experience of it. It was one particular unique experience in 2013 that inspired an idea which would set his life in a new direction.

“I’ll always remember the day I first went running after I received a cochlear implant,” Elliot said. “I could hear a jingling noise. When I stopped running to focus on this unfamiliar sound, the jingling also stopped. I wasn’t sure what it was and kept wondering what it could be. It wasn’t until I got home that I realised the noise was coming from the coins in my pocket.”

At two, Elliot was diagnosed with severe hearing loss in his right ear and profound loss in his left. Twenty-four years later he received a life-changing cochlear implant. However this ‘fix’ wasn’t as simple as ‘switching on the sound’. In fact, learning to understand new sounds has been one of the biggest challenges Elliot has ever faced. But this experience led him to combine his skills in graphic design and game design to create Games 4 Hearoes, which uses gamification to help people with hearing impairments transform the way they hear.

Games 4 Hearoes“Games 4 Hearoes is a digital auditory training platform to help track, adapt and empower those with hearing loss, specifically those with a cochlear implant, learn new sounds,” Elliot said.

“When someone receives a cochlear implant it’s a common misconception that they will automatically gain normal hearing. However it’s quite a different experience for everyone who goes through the journey.” After someone receives a cochlear implant, what they mostly hear is almost like vibration feedback while the brain tries to identify the pitch and tone of the sound. Over time it steadies to ‘white noise’ until their brain is able to identify what the auditory feedback is and understand it. Recipients often need to relearn or learn how to hear – from environmental sounds through to understanding vocabulary. “I hadn’t been prepared for how much work was needed in the rehabilitation process,” Elliot explained. “In theory, the cochlear speech processor is a more powerful, sharper device compared to the hearing aid that I was used to. Although I am able to hear more of the world around me, especially the soft or high pitched sounds which I had never heard before, it took a lot of practice and stamina to make sense of it all.”

So he set himself on a new path to use technology to make this process quicker, easier – and even fun. And it’s through serious games – computer games with a purpose to train, rather than simply entertain us. But as Elliot explains, serious games can do both. “Games 4 Hearoes has a range of modules, starting with environmental sounds progressing to understanding sentences and dialogue,” Elliot said. “In each module, there is a library of gamified activities, which have been designed for everyone, from children to adults, to create an entertaining and immersive experience, rewarding participants as they progress.”

Games 4 HearoesIn developing Games 4 Hearoes, Elliot has drawn on his own experiences, as well as others.

“Even the small things in life, from the fridge alarm beeping to taps dripping – which had never been noticeable before a cochlear implant – can be easy to misunderstand in our noisy world,” Elliot said. “Using real life experiences and scenarios has helped the development of Games 4 Hearoes. Everyone we speak to brings new insights and ideas.”

Games 4 Hearoes was one of eight social change businesses using technology to change the lives people with disabilities, that took part in the 2017 Remarkable Accelerator. A partnership between the Telstra Foundation and Cerebral Palsy Alliance, the 16-week program has been tailored for early stage startups looking to build sustainable enterprises that have a big social impact. It does so by connecting them with the tools, skills and networks they need to succeed.
Elliot credits the program with helping him take the next step in making his niggling, ‘jiggling’ idea, a reality.

Elliot Miller“We’re continuing to develop Games 4 Hearoes and to date we’ve had incredible feedback, not only from those with hearing impairments, but also audiologists who have validated what we’re trying to do,” Elliot said. “We’re currently looking for people who have had cochlear implants, as well as audiologists to join us on our journey. Through the Remarkable program, I’ve gained the skills to now take the next step in launching this as a business.”

Elliot is passionate about the potential of technology to break down barriers for people with a whole range of disabilities – but especially for the hearing impaired. “As hearing aid hardware has moved from analogue to digital – the possibilities of new technology are almost endless,” he said. “Addressing an issue that is so close to my heart with something I experience every day, is essentially how this all started.”

Hearing loss didn't stop Kyle Cloete following his passion for making films

Dec 2017

Despite experiencing hearing loss a child, 16-year-old Kyle Cloete is a passionate film-maker, and has already won awards for his short films. He shares his story as part of Disability Pride week, to inspire other young people living with disability. I have two worlds – the hearing side and the deaf side. When I was born, my mum knew something was wrong but the doctor repeatedly assured her "Oh no, your baby is fine, don't worry about it”. I wasn't fine. After we moved to New Zealand, doctors found a tumour in my right ear. I needed surgery, and subsequently I was left with one completely deaf ear and moderate hearing loss in the other. I am forever in my parents' debt. They have always supported me and believed that I can achieve whatever I want to do.
Kyle Cloete says if you believe in yourself, you might end up doing what you love for the rest of your life.

Kyle CloeteAs a child, mum wanted to expose me to as many different languages as possible, both visual and oral. My mother is deaf herself so she communicated with me using sign language. My first signs at 6 months were mummy, moon and light. Sign language is so visual, which is why I also love comic books. I was also exposed to the oral world through music, and at seven I was fitted with a cochlear implant which gave me more access to the hearing world.

School was sometimes challenging, as I would miss out on the teacher's instructions, but otherwise I was much the same as other students. I feel lucky to live in New Zealand -compared with other countries in the world, it's very diverse and I have never felt that people judged me because of my disability. Sign language became an official language in New Zealand in 2006, and as more people learn it, our society becomes more inclusive, which is awesome. The deaf community is like a family. If you ever go to a deaf club, you'll be amazed at how quickly people can pick up signs because it is visual language.

I want to show people my world, and share other people's stories too. I think that's why I am so passionate about directing and screenwriting. I know it will be a long road, but I'll do whatever it takes to get there because that's all I want to do. My all-time favourite movie is an old film The Good, The Bad and The Ugly - I just love how Blondie is a silent character. I may be hard of hearing, but I never saw that as an excuse not to make films. You can't let your disability define who you are. You need to believe in yourself when nobody else believes in you. You need to imagine yourself in the future going "hey, I want that". The next thing you know, you might be doing what you love for the rest of your life too.

Queensland’s Senior of the Year Dr Dimity Dornan of Hear and Say helps improve deaf children’s lives

Dec 2017 Our Mail

Dr Dimity Dornan, has dedicated decades of her life to bringing sound to the lives of deaf children. If the senior years of life are supposed to be about doing nothing much except ticking off everything on your bucket list, Dr Dimity Dornan did not get the memo. There’ll be no lying back with a margarita on some exotic faraway beach for her. Instead, it’s business as usual for Queensland ­Senior of the Year 2018, the state’s entrant in Australian Senior of the Year, to be announced on January 25. Recognised worldwide for her groundbreaking work changing the lives of thousands of deaf children by helping them learn to listen and speak, Dornan was Queenslander of the Year in 2010, but admits to being slightly taken aback when approached to be Queensland’s Senior.

Pip Russell etc(left-right) Queensland Local Hero winner Pip Russell, Queensland Australian of the Year winner Johnathan Thurston, Queensland Senior Australian of the Year winner Dr Dimity Dornan, and Queensland Young Australian of the Year winner Phillip Thompson

“I suppose it’s really quite funny, I’ve now moved up to the senior section!” she says in our interview in one of the beautifully designed rooms at Hear and Say’s premises in Brisbane’s inner-west Ashgrove, which opened in 2015. “The Senior Australian of the Year people rang and asked if I’d like to accept it and I said, yes, I’d love to, but then I had second thoughts later on. (I told them) if I had to be Queensland’s ­Senior Australian of the Year, I’d really like it if you didn’t use my age if you can possibly do it.” But isn’t there a certain irony here? A person of senior years being feted for her achievements not wishing to mention her age? “I prefer to be treated as a professional, rather than have age define me,” she says. “I just feel that it’s such a competitive world, it’s much better to compete on your merits, rather than your age.”

Let’s just say then that Dimity Dornan, PhD, AO, ­author, speech pathologist of more than 50 years’ standing, inspirational promoter of the largest paediatric cochlear implant program in Queensland, which has used Auditory-Verbal Therapy (AVT) to empower some 10,000 children to fulfil their potential in life, is older than 60 but younger than 100.

Hear and Say – the private, not-for-profit organisation she ­established in 1992, treating six young ­patients from rooms she shared with her physiotherapist husband Peter Dornan in the inner-western Brisbane suburb of Toowong – has just celebrated its 25th birthday. A new book cele­brating the history of the centre, Sounds of Hope: The Hear and Say Story written by Brisbane author Madonna King and published by University of Queensland Press, was launched by Governor Paul de Jersey.

Hear and Say now has six centres around Queensland, treating children and their families here, as well as around the world, using new telecommunications technology that allows face-to-face interaction. The acclaimed facility ­offers its services to any deaf baby or child no matter where they live. Currently two in every 1000 babies are born deaf in Australia each year and it is the most common disability in newborns. Hear and Say ­relies largely on fundraising on top of ­government grants, and part of Dornan’s job as its executive director is being its tireless advocate, a lobbyist par ­excellence, a passionate and moving speaker whose eyes still fill with tears when she speaks of her life’s work, or the moment – which never ­becomes stale – a child first hears the sounds of the world. Dornan was born Dimity Crist (pronounced as in “crisp”), the eldest of four girls and a boy born to Richard “Dick” Crist, a Shell sales rep, and his wife Marjorie, a full-time mother. Dick Crist was a World War II veteran and, before their marriage, Marjorie worked in US General Douglas MacArthur’s mapping department.

The Crists were of German descent (the name was spelt “Christ” but along the way the “h” disappeared) and were pioneers of the Toowoomba region. Dick’s mother, Alice Guerin, was of Irish origin. Alice died before Dimity was born but she was always intrigued by the mystery of her grandmother’s portrait, and by the fact that she was a ­writer. But it was her grandmother’s work as a teacher that lit up her impressionable granddaughter. “She came from Ireland with her parents in the early vanguard of teachers who were meant to upgrade the quality of education in Queensland … she travelled with her father to different state schools, eventually became a pupil teacher and then a teacher herself at a very young age.”

Dornan’s parents believed in the value of education, too. The family lived on a large block at Corinda in Brisbane’s southwest, and Dornan and her sisters attended Our Lady of the Sacred Heart Convent there. From an early age, Dornan knew she wanted some kind of career that involved helping people. The family knew a professor of psychology from UQ who lived nearby, who told her about a new speech pathology course. Dornan would become one of the first graduates in speech therapy at UQ.

Dr Dimity DormanDr Dimity Dornan of the Hear and Say Centre with Edward Mewing (2)

Her first jobs involved working with patients with head injuries. “It was wonderful work, but then I got the opportunity to work with children with hearing loss. I said to my prospective employer, ‘but I don’t know anything about hearing loss!’ And she said something that changed my life, something I like to pass on to other people. She said: ‘No, but you have the ability to find out’. So I’ve been finding out ever since – I’ve become a lifelong learner and that’s what I’ve been up to. People think they’ve got their qualifications, and then they sit back, but I’ll tell you what, life’s not like that.”

Which is why, besides her work as Hear and Say’s executive director, the fundraising and the meet-and-greets she ceaselessly undertakes every day, Dornan is ­increasingly absorbed in the area of bionics, founding ­Bionics Queensland and the Human Bionics ­Interface, an Australian research collaboration project to grow the ­bionics ­industry. She has also ­secured a manufacturer for a cutting-edge invention, a hearing aid that allows people to hear in noisy restaurants.
This is a woman who is constantly learning.

As if her days aren’t busy enough, there are now four grandchildren she enjoys with her husband whom she married in 1967. The couple has two children – Brisbane-based Melissa, 49, who runs a business helping mothers get over traumatic births, and Melbourne-based Roderick, 47, known as Rod, who works in IT for IBM.

“I came late to my career,” Dornan says. “I was always a speech pathologist but I didn’t start doing Hear and Say until my own kids were in uni, so I’m sort of a late starter, if you like, in that area.” She began working with deaf children when she had to learn sign language to work with hearing-impaired children at Zillmere North Special Education Unit. She became frustrated that parents weren’t involved in reinforcing their children’s learning, and eventually found her way to the Shepherd Centre in Sydney, which in turn led to a Churchill Fellowship to Canada to study AVT.

Research shows that the critical brain period for learning to speak is within the first three years of life, therefore early diagnosis is essential. Once a baby or child has been fitted with a cochlear implant, AVT successfully develops the listening and spoken language of kids with hearing loss by stimulating auditory brain development. The input of parents is critical to reinforce learning.
When Dornan speaks of giving the gift of sound, her eyes fill. “I feel very strongly that I have a purpose in life,” she says.

Dornan mentions the Future Hear Project, which she is working on with Queensland University of Technology, which aims to build ears for children born without them. It involves the 3D printing of a prosthetic ear and a bio­degradable scaffold built from a child’s cartilage and skin cells that will allow an ear to grow. It’s nothing short of ­miraculous. It’s also nothing short of all the little miracles ­Dornan has guided along the way, from teaching a child to distinguish an “f” sound from an “s” sound, to getting ­citizens to part with their money to help a deaf child. Do we care if Dr Dimity Dornan is classified as a senior, junior or middle-aged Australian? My guess is we care more that people like her keep doing what they’re doing, while the rest of us keep being grateful.

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Here is a link to Deafblindness support and information. They are based in Western Australia and supported by Senses Australia.

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