Tips and tricks: How to wear and customise your Baha SoundArc

Tips and tricks: How to wear and customise your Baha SoundArc

SoundArc_colors2

The Baha SoundArc is the newest hearing solution for people who live with conductive hearing loss, mixed hearing loss or single-sided sensorineural deafness (SSD). It is the world’s first non-surgical, behind-the-head bone conduction hearing device, specially designed for children who are not ready for a bone conduction implant and adults who want to trial bone conduction in everyday situations.

Whether you’ve got a SoundArc already or you’re ready to learn more about it, these how-to videos give great tips on how you can get the most out of the SoundArc.

soundarc_topshot_all_colours3_PPTThe Baha SoundArc comes in a range of sizes and features your choice between a variety of coloured tips, where available. You can choose to match your clothing, your hair or your mood. Choose between black, grey or brown tips to discreetly match hair color — or opt instead for green, pink or turquoise tips to add style to an outfit. Watch the first video below to learn how to change the coloured tips.

Don’t worry, your hearing care professional will ensure your Baha SoundArc has the proper fit when you first try it on. Still, this next video is a useful reference for when you need to take it off and put it back on throughout your demo period, or if you or your child is wearing it for a longer term. Watch the video below to learn how to properly wear the SoundArc.

If you are wearing two sound processors on your SoundArc, your hearing care professional will set up your SoundArc for bilateral use. You can refer to this last video if you need to adjust or remove the connector discs for any reason during the period you will be wearing the device. Watch the video below to learn how to assemble the Baha SoundArc for bilateral use.


LEARN MORE: Click here to read more about the Baha SoundArc, ideal for use as a demo device, or for children not yet ready for an implant.


Want to share your story, hearing tips or Baha advice with The Baha Blog? Let us know! Find us on Twitter at @TheBahaBlog, on Facebook at our page The Baha Blog or via email at bahablog@cochlear.com.

Meet the team who helped create the new Baha SoundArc: videos

Meet the team who helped create the new Baha SoundArc: videos

Meet the team who helped to innovate the new Cochlear Baha SoundArc.

Meet the team who helped to innovate the new Cochlear Baha SoundArc.

Have you ever wondered what goes on behind the scenes as Cochlear develops the latest hearing tech? If you’re curious about the new Baha SoundArc, Cochlear’s newest non-surgical bone conduction solution, look no further. In the two videos below, the teams behind the SoundArc describe the challenges and successes of this totally new design.

In the first video, listen to Henrik Fyrlund (Senior Project Engineer Technology Development), Stefan Magnander (Senior Mechanical Engineer) and Fredrik Boivie (NPI Project Leader) describe the challenges of designing the SoundArc as well as key moments in its development.

 

In part two, watch Linnea Agostino (Product Manager) and Jenny Andersson (Clinical Research Audiologist) talk about some of the features that make the SoundArc special when compared to other non-surgical bone conduction solutions.


LEARN MORE: Click here to read more about the Baha SoundArc, ideal for use as a demo device, or for children not yet ready for an implant.


Want to share your story, hearing tips or Baha advice with The Baha Blog? Let us know! Find us on Twitter at @TheBahaBlog, on Facebook at our page The Baha Blog or via email at bahablog@cochlear.com.

How the Baha System helped Jamie pursue her love of music: guest blog

This blog was adapted from its original article on Hear and Now, a Cochlear Americas recipient blog. Read it here.


 

Jamie G. has conductive hearing loss, and the Baha System has helped her pursue her love of music.

Jamie G. has conductive hearing loss, and the Baha System has helped her pursue her love of music.

At the age of 14, I was asked by my otolaryngologist what I wanted to be when I grew up. Excitedly, I told him I wanted to be a singer. He then explained that music wouldn’t be a good choice for me.

I developed many ear infections and battled a cholesteatoma in my early years. I lost most of my hearing in my left ear even after numerous reconstruction surgeries. Because of this, my ability to sing should be out of the question. Shortly after that, I sent him a tape of my recordings. After a listen, my doctor wholeheartedly supported my decision to pursue music.

Hearing loss certainly didn’t make my life easy. It made me withdrawn, depressed and a shy girl in school. But music was one avenue that made me feel confident and secure. I loved feeling the sounds of the bass in my chest as I listened to my favorite artist, the drums vibrating in my feet, or the soprano’s high notes bringing my hearing to clarity. In order to perform, practicing music had to consume most of my time, but I didn’t mind. Reading music, counting rhythms and knowing chord progressions took time, but it was vital in order for me to be successful as a musician.

Thankfully, I outgrew the ugly battle with the cholesteatoma. Sadly, my hearing could never be restored. Hearing aids were not an option due to my ear’s inability to move any drainage or wax. So for 30 years I adjusted my life around my hearing loss.

In July 2015, I was referred to an ENT-otolaryngologist in Kansas City for a second opinion. That visit changed how I looked at my future. I was a strong candidate for the Baha® Implant System due to my conductive hearing loss. It didn’t take much thought to know that the Baha System was the right decision for me.

My switch-on date was December 2017. I slowly adjusted to this new, but amazing world. My world of quiet was replaced with new sounds. I could now hear that thumping bass line without having to just feel it in my chest. I could hear my voice not only when I sang those soprano notes, but I loved to hear the rich lower tones of my voice now. I didn’t have to make sure I performed in a certain spot on stage. I had the freedom to move wherever I needed to be. I still prefer to be near the drums, feeling the music in my feet and chest while I express my songs.

I chose Cochlear because of my musical lifestyle. I needed access to streaming without a separate device. But I also wanted to connect my device to any in-ear monitor system while performing. I knew I needed the best technology for my device to function in all areas of my life, so I choose the Baha 5 Sound Processor.

Jamie G. uses the Baha System to help explore her love of music.

Jamie G. uses the Baha System to help explore her love of music.

When I first got it, I made sure my settings were adjusted to my liking, and it took a few trips to the audiologist to get it just right. I love the ability to switch modes. When I listen or perform, I need my Baha 5 Sound Processor to adjust to the sound of the music. The tones I want when I sing or listen to music are certainly different that my daily mode.

I use my Cochlear True Wireless Mini Microphone every time I perform with my monitor system. Using a Y-adapter plugged into the monitor, I plug in my Mini Mic to one jack, my in-ear headphones to the other. Once I pair my Mini Mic to my Baha 5 Sound Processor, I hear every tone of the piano, the full sound of the acoustic guitar, the intricate bass line, my vocals moving in progression with the band…all in stereo – in both ears!

My musicianship has improved and excelled in a way I only could dream of a few years ago. I can now lead musically, knowing exactly what needs to be done to move the band to a more unified and excellent sound.

Because of my increased musical abilities with the Baha 5 Sound Processor, I got to hit the studio for my very first recording a year after my implant. While using my Baha System, I recorded a CD with a full live band. It was a beautiful experience to see and hear my own songs come alive and to be able to hear them fully and in true form.

Hearing loss made me appreciate my gift of music through expression. But the Baha System has given me the gift to hear that expression fully.

I look forward to more recording sessions and producing many more songs that have yet to be written! To hear a sample of my music or to purchase a download of my CD, you can visit jamiegroshart.com.

The opinions expressed in this blog are my own views and not those of Cochlear.


 

If you are dealing with constant ear infections or a cholesteatoma impacting your hearing, click here to find a solution to help you get better hearing.


Want to share your story, hearing tips or Baha advice with The Baha Blog? Let us know! Find us on Twitter at @TheBahaBlog, on Facebook at our page The Baha Blog or via email at bahablog@cochlear.com.

‘A whole world opened up to him’: Celebrating a new life of sounds this Autism Awareness Month

Parents of children with autism can have unique challenges in diagnosing and treating their children’s hearing loss. For Autism Awareness Month, blogger Jen B. from Oregon, U.S. has written about her 3-year-old son Xander’s hearing journey, from difficult diagnoses to helping him learn to wear his new sound processor.

You can follow Jen’s blog here on WordPress or here on Facebook.

 


“Xander!” “Xander!” “Xander!?”

But no response did I ever get from my son.

Xander, now 3, plays at school.

Xander, now 3, plays at school.

He will turn on a dime if he hears his favourite theme song start up. He’ll sing along in perfect pitch. And yet, dogs barking right next to him never make him flinch.

My son was born three weeks early with a collapsed lung and rapidly dropping sugars. Very soon he was transferred to a hospital with a Neonatal Intensive Care Unit (NICU). When I first saw him it was obvious that there was a slight deformity of his right ear. I assumed he had lain on it wrong in utero, and that it would work itself out.

The hospital gave Xander a hearing screening, as was standard procedure for all NICU babies. The nurse came in while he was asleep on me and checked his left ear first, because that’s always, even now, the ear he has to have facing out while snuggling.

Everything was fine.

The nurse tried twice to check his right ear and still seemed perplexed, because she couldn’t get the readings she was used to. Ultimately, she marked it as a pass.

It was only later we learned Xander’s hearing wasn’t normal.


My son has Autism Spectrum Disorder. He was diagnosed at only 18 months old. He is now 3 years old and considered non-verbal. He speaks, but not necessarily with what professionals would call, “purpose.”

Autism affects all forms of communication. Where a neurotypical child with a hearing loss might pull at their ear, say they can’t hear, or make some sort of gesture – something — we got nothing. It gradually became clear he needed to have his hearing assessed.

At about 2 years old Xander finally saw an audiologist. Autism can make a child both seek out stimulations (sensory seeking) and feel overwhelmed by them (sensory overload), so diagnosing hearing loss can be a challenge. In a room with all sorts of things making noise and lighting up, Xander wasn’t very cooperative. His tubes were clear, but the audiologist scheduled him for a sedated Auditory Brainstem Response (ABR) hearing screening. All the worst-case scenarios came into my mind during the scan, which felt agonisingly long.

Jen poses with 3-year-old Xander, wearing his Baha 5 Sound Processor on a Softband.

Jen poses with 3-year-old Xander, wearing his Baha 5 Sound Processor on a Softband.

The doctors learned Xander had conductive hearing loss in his right ear, and to learn more he would need a CT scan of his temporal bone. The doctors decided further diagnosis was not urgent and told me things like, “just speak to him on the left side” and, “in cars he probably won’t be able to hear you.”

About six months later Xander need an MRI for another issue, so we decided to have the CT scan done at the same time while he was sedated. We learned he is missing the third stapes, or stirrup – one of the bones of the ear – on his right side, a rare condition.

There is a surgery to implant a prosthetic stapes, but Xander’s major facial nerve runs where the bone should be, making the operation too risky. We decided instead to treat Xander’s hearing loss through bone conduction.


The sensory sensitivity caused by Xander’s autism made it hard for him to wear his first sound processor. The constant vibration against his head, the increase in noise and the strap around his head were difficult for him to tolerate. I would try bribing him, like I do with his glasses. “If you put it on, you can have a candy.” It didn’t help much.

When Xander’s trial was over, he received his Cochlear Baha 5 Sound Processor, and we both loved the way it looked. When I pointed out how cool he looked wearing it on his Softband, he beamed with pride and wore it for several days, for long stretches at a time – even to school!

Believe me when I tell you that I cried when I said, “Xander!” and he looked up at me.

He was able to hear the start of his favourite show in the whole world. He was mesmerized. He had never noticed all the nuances of it before he got his Baha processor. He could understand enunciations. He could hear his electronic toys, the ones that had never interested him before. A whole world opened up to him.

But for a child with autism, that can be really intimidating.

After an accident left him injured, Xander has become even more sensitive to stimulation, and sometimes getting him to wear his sound processor is nearly impossible.

Well, every day is a different day in the world of autism. While trying to take a photo of him wearing his sound processor, I was able to capture a whole video. He let it stay on while cruising around a department store today. I was so excited, and I hope tomorrow he’ll leave it on even longer.

For children with autism like Xander, treating hearing loss might not be a linear journey, but each day brings new opportunities for him to listen to his teacher at school, his toys, and even respond when I call him, “Xander.”

The opinions expressed in this blog are my own views and not those of Cochlear.


If your child is showing signs of hearing loss, use this tool to find a clinic near you.


Want to share your story, hearing tips or Baha advice with The Baha Blog? Let us know! Find us on Twitter at @TheBahaBlog, on Facebook at our page The Baha Blog or via email at bahablog@cochlear.com.

What is MPO? A simple analogy for a complicated audiological term

Learning about the science behind treating hearing loss can be daunting. There are so many terms, concepts and measurements – it’s often hard to understand what each of them really means for your hearing, and how these concepts influence the way you treat your hearing loss.

Here we will try to explain one of those concepts, a sound processor’s maximum power output (MPO),  or maximum output force level (the technical term for bone conduction devices), with a simple analogy: the ceiling of a house. Understanding MPO can give you insight on why your audiologist chooses or recommends a certain sound processor for your individual hearing needs, and this knowledge can empower you to ultimately make a choice that best suits you.

Different people have different levels of hearing loss, measured in an audiogram. Your level of hearing loss will determine your need for amplification. The fitting range is the most common measurement for any given sound processor. Fitting range is a guide to understand the level of hearing loss a device can address. When audiologists determine which sound processor would provide the most benefit to you, they compare your hearing loss to the sound processor’s fitting range. For example, the Cochlear Baha 5 Sound Processor has a fitting range that covers hearing loss to 45 decibels (dB) SNHL.1

All sound processors have limits on how much power they can provide, and this limit is the most important contributor to a device’s fitting range. A device’s power limit is known as the maximum power output, or MPO. In a chart measuring a device’s output (see illustration below), the MPO appears as a line graph showing the maximum power (in dB) it can provide across the hearing (frequency) range – from deeper sounds like the hum of traffic to higher-pitched sounds like a bird’s song. Now imagine the MPO line takes the shape of a house’s ceiling.

MPO-07The height of the ceiling is important: Just as a taller person needs a high ceiling to be comfortable, a person with a high level of hearing loss needs a high MPO level to hear sounds comfortably.

Cochlear and other manufacturers make sound processors with different levels of amplification to “fit” your individual hearing loss, as the person in this illustration “fits” into their house.

However, just as its peak height (the highest level of power provided) is important, the shape of the MPO line – the way it slopes or curves across the chart – is also important. This shows how the sound processor delivers power across a range of the most important lower to higher frequencies. The average MPO is calculated across a number of frequencies, which illustrates the shape of this line.

MPO-03The MPO on some devices delivers significantly more power to middle-range frequencies than the lower or higher frequencies important for speech. For these devices, the MPO chart looks more like a house with a very pointed ceiling and short walls. A tall person may stand comfortably in the centre, but they can’t walk over to the window without bumping their head on the ceiling. In these sound processors, at the lower and higher frequencies important for speech, sounds hit the “ceiling” of the sound processor’s power limits, distorting them.

MPO-01Ideally, a device with a high average MPO allows you to clearly hear sounds across the frequency range – in the same way that a house with a gently sloped ceiling allows you to move around freely inside, all the way to peer out each window without bumping your head.

As most people have hearing loss across a wide range of frequencies, a peaked MPO means the sound processor may not amplify sound along the whole frequency range where they need it. The person wearing this sound processor actually hears sounds less clearly across these important frequencies.

A chart shows the shape of the MPO of Cochlear sound processors (yellow) vs. competitor (orange). Circles on the chart show what sounds are represented at certain frequencies.

A chart compares the power in a device with a high average MPO (yellow) with a device with a peaked MPO (orange). Circles on the chart show what sounds are represented at certain frequencies.

Two devices may have a similar fitting range but can differ widely in average MPO. Ideally you should experience clear sounds, even moving across lower and higher frequencies, without hitting the “ceiling” distorting the sounds you hear. This is what a high average MPO delivers.

To find out whether you could benefit from a more powerful device, or to learn more about your treatment options, use this tool to find a clinic near you.

MPO is compared between Cochlear sound processors (yellow) and a competitor's (orange). The graph shows what sounds are represented at different frequencies.

The power is compared between  a device with a high average MPO (yellow) and a device with a peaked MPO (orange).


1 Flynn M. (2015) Smart and Small – innovative technologies behind the Cochlear Baha 5 Sound Processor. Cochlear Bone Anchored Solutions AB, 629761.

 

 

When losing something leads to something ‘wonderful’: Dwight’s experience upgrading to the Baha 5 Sound Processor

When losing something leads to something ‘wonderful’: Dwight’s experience upgrading to the Baha 5 Sound Processor

This blog was adapted from its original article on Hear and Now, a Cochlear Americas recipient blog. Read it here.


Dwight J. of Colorado streams a phone call directly into his Baha 5 Sound Processor.

Dwight J. of Colorado streams a phone call directly into his Baha 5 Sound Processor.

Sometimes losing something important to you turns out to be surprisingly “wonderful.” Just take it from Dwight J. in Colorado, U.S.

After a day of hiking, Dwight noticed he could not hear as well as he was used to. He reached up and discovered his BP100 Sound Processor was gone. He looked everywhere for it, but he realised he must have lost it while out on the hike.

Dwight acted quickly and called Cochlear to get a replacement. To his surprise, the representative told him Cochlear no longer offered the BP100. They introduced Dwight to the Baha 5 Sound Processor, and he knew he wanted an upgrade.

“It’s wonderful,” Dwight said after upgrading.

He said he especially likes being able to connect to his sound processor with Bluetooth, stream phone calls and stream radio directly to his sound processor while out on a walk.

Dwight also said he carries his Cochlear Wireless Mini Microphone with him wherever he goes. “I put it on whoever I’m talking to, if I’m in a loud situation, so that I’m able to hear them,” he said.

When it comes to continuing his journey as a part of the Baha family, Dwight seems thrilled.

“Cochlear culture oozes with a four-letter word: care,” he said. “They care about people.”

Dwight is a member of his local chapter of Cochlear Community, a Cochlear Americas program that connects Cochlear recipients in the U.S.


Want to share your story, hearing tips or Baha advice with The Baha Blog? Let us know! Find us on Twitter at @TheBahaBlog, on Facebook at our page The Baha Blog or via email at bahablog@cochlear.com.

 

World Down Syndrome Day and hearing loss: Celebrating children like Chloe

The following is a re-post of a guest blog from 2014 about Chloe, who was born with Down syndrome and lived with hearing loss until she was implanted with the Baha System at 10 years old in 2010. Chloe was 14 when her mother Jane wrote this guest blog to share with us the affect Chloe’s Baha implant had on her life. Join us in marking World Down Syndrome Day today (21 March) and celebrating children like Chloe.


It’s been a while since you last heard about Chloe. She is now 14, in year nine at senior school and even more of a little madam than when we last met four years ago.

Unfortunately Chloe’s health hasn’t been very good the past two years. She has had some major operations which have left her bed bound for weeks, and in and out of hospitals. Chloe has shown incredible strength and determination, both because that’s the type of girl she is and because she was able to communicate effectively with hospital staff and myself.

This is all thanks to her Baha sound processor. Chloe’s language skills and attention skills have flourished over the last four years; her vocabulary has grown, she is learning new words each day and she is definitely more attentive to those talking to her (apart from when she chooses not to!). This meant the hospital staff was able talk her through what was going to happen and she could indicate her pain levels and talk to the doctors.

I dread to think how she would have coped six or seven years ago, when her hearing levels were so low, and she hardly had any language. The world would have been a very lonely and scary place for her.

Chloe still loves drama and attends a very good secondary school that specialises in drama so she can devote more time to her passion. She is still my drama queen and a budding actress, dancer and musician. Obviously she is becoming a young lady and her life is changing. Developing language and communication skills has played a big part in this and will continue to do so.

My one aim for my daughter has been to become as independent as her disability would allow her. The Baha [System] has contributed to the success of this aim. She can order her food in restaurants. She can shop at the supermarket. She is also very good at being a typical teenage and slamming doors on me!

So am I pleased with the Baha [System]? Yes, my only regret is that I didn’t push for it sooner. I would recommend it for any parent or young person who needs it. Read the literature, speak to the professionals and if you feel it right go for it! It opens many doors and not once have we looked back.”

Jane lives in Birmingham, UK. In 2013 she won the Birmingham Parent of the Year Award for her tireless work with a special needs support group, as well as caring for her own two children who both have special needs.


Want to share your story, hearing tips or Baha advice with The Baha Blog? Let us know! Find us on Twitter at @TheBahaBlog, on Facebook at our page The Baha Blog or via email at bahablog@cochlear.com.

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