Author Archives: Liz Flores

Advocacy leads Kim Russell to find the right hearing solution for her single-sided deafness

Kim Russell

At 10 years old, Kim Russell was diagnosed with a chronic ear infection that could not be helped with antibiotics. She underwent a mastoidectomy to remove the infection, resulting in permanent hearing loss in her left ear. Her mother, having had the same issue when she was younger, also lost her hearing and therefore single-sided deafness (SSD) was a normal part of life in her family.

“School, work and social situations were hard, and the options were not as robust as they are now,” Kim said.

Kim became accustomed to living life with one good ear and didn’t receive intervention or aid until she was 25. Her job had hearing aid coverage and she looked into what options were available for her hearing loss. She discovered BiCROS hearing aids and wore them for 30 years. Although the hearing aids helped, no solution is perfect. Crowds were still difficult and loud places like bowling alleys and restaurants made it impossible to hear people speaking and know where sound was coming from. Her audiologist had never mentioned any other options, so she believed BiCROS was the only type of hearing loss solution available to her.

A chance encounter with a bone anchored hearing system

Kim stumbled upon a bone-anchored hearing system (BAHS) on Facebook when a friend happened to post a video at the right time. “One day on Facebook, a friend of mine who is a nurse posted a video on her Facebook page and normally it wouldn’t be anything I would pay attention to. It was something about a surgeon performing a surgery for the first time in West Michigan. They were doing a MIPS procedure (Minimally Invasive Ponto Surgery). He’s the only MIPS surgeon in this part of Michigan and they mentioned single-sided deafness. I did some research and realized this was for people like me!”

Kim searched for the name of the doctor’s office online and learned it was located in the building next door to her dentist. She scheduled an appointment, and learned she was a great candidate for the Ponto System. After trialing a Ponto BAHS on a softband for a week she had the MIPS surgery in July of 2018 and received a Ponto 3 SuperPower. “It was easier than a dental procedure. I was in, out, dressed and drinking coffee in about 58 minutes,” she said.

A new world of sound emerges with the Ponto 3 SuperPower

After Kim’s MIPS procedure and Ponto 3 SuperPower activation a new world of friends, advocacy, and interaction opened up to her.

“For the first time since getting my Ponto, I went for a walk with a friend. I’ve always kept people on my good ear (right side) so we put her on my left to see what would happen. I about jumped out of my skin. Her voice was clear and crisp, even with the radio blaring in the background.

The sound quality from trying the Ponto on a softband vs. an abutment is so much better, so crisp. I call it ‘organic’,” she explained.

As Kim has learned more about Ponto and become more involved in the hearing loss community, she has learned just how important advocacy is. “How did I go so long being hearing impaired and not knowing there were other options? This BAHA World Hearing Facebook group was where I received most of my education. It’s important for people to look into all of their options, and do their research.”

Kim’s advocacy and education came full circle last year after she attended Oticon Medical’s yearly advocacy conference. She met fellow Ponto users and collaborated with Oticon Medical staff.

“Before, I had never told anyone I wore any kind of hearing aid. This time, as soon as I got my abutment I shared it on Facebook because it’s important to get the word out. Knowing what was available made a difference in my life. Every now and then I notice the crispness of something I haven’t heard before. I hope advocacy and sharing my story can do the same for someone else.”

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The Ponto 3 SuperPower spurs a 180 degree change for Amelia

Allison and Amelia

Allison Richardson’s three-year-old daughter, Amelia, was born with Auditory Neuropathy Spectrum Disorder and has severe-profound unilateral hearing loss. At the time of Amelia’s diagnosis, family members and doctors advised her not to worry. But with three of Amelia’s older brothers diagnosed with Apraxia, a speech sound disorder, Allison knew the importance speech and hearing was to development.

While pregnant in 2009 with one of her sons, Allison began joining groups on Facebook for parents. She found these to be supportive networks where she could turn to for help and develop friendships. Once Amelia was born, she set out to find a Facebook group for parents of children with hearing loss, which is where she found the “BAHA Kids Club” Facebook group.

After learning about bone-anchored hearing systems (BAHS) and doing her own research, Allison brought Amelia to her ENT’s office to inquire about a BAHS. After learning the pros and cons of different devices, the personal stories of parents online, and about feedback and Oticon Medical’s great customer service, they advocated for a year-and-a-half to secure a device for Amelia.

180 degree difference with Ponto

Life for Amelia changed after being fit with the Oticon Medical Ponto 3 SuperPower. “She went from being an unfocused child speaking no more than five words to a focused student and dancer who now talks more than anyone at home. Her five older brothers say that Amelia has a bionic ear,” Allison said.

Amelia currently attends preschool and sits in a classroom with special needs and non-special needs students. The mix, Allison noted, provides special needs kids with mentors, and teaches non-special needs kids acceptance.

Amelia Richardson

Advice for parents

Allison’s advice is simple when it comes to making a medical decision for your child: “Go with your gut and don’t compare kids”.

She continued, “Do what you think is best for your child, not what other people say is best, because you know your child.”

The journey to better hearing and finding the right hearing device for your child’s individual hearing loss can be long and sometimes feel like a never-ending waiting game. Continue to advocate for yourself and your child, reach out to online support groups, try all your options, and as Allison reminded us, “Don’t give up.”

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Determination and perseverance lead to better hearing for Elizabeth Collins

Elizabeth Collins

After a slow progression of hearing loss in her right ear, Elizabeth Collins became permanently deaf on her right side from a mastoidectomy surgery at the age of 14. She has lived with single-sided deafness (SSD) for most of her life, struggling to hear in school and at work.

“I had a fear of not wanting to raise my hand in school because I didn’t want to make a mistake. Growing up with single-sided deafness and not having the access or advocacy that we have now meant dealing with a lot of stigmas around being hearing impaired. I had to overcome a lot of insecurity, adversity, and bullying as I grew up,” Elizabeth explained.

The first hearing aids she used were BiCROS hearing aids, but the solution wasn’t enough for her hearing loss. It wasn’t until Elizabeth was 38 years old, when she decided to go back to college, that she began researching new hearing loss solutions for SSD. While completing her associates degree at Tidewater Community college she noticed a picture of someone wearing something behind their ear — a bone-anchored hearing system (BAHS). Audiologists hadn’t presented BAHS as an option, so Elizabeth did her own research, and found BAHS could be the right solution.

Obstacles and persistence

Elizabeth encountered her first obstacle while trying to get approval for BAHS surgery —insurance. After her insurer rejected the surgery multiple times,  she reached out to a BAHS advocate who educated her on insurance codes. After two years of fighting, she was finally approved and moved forward with her abutment surgery in 2012.

A year later, Elizabeth encountered another issue when she tried to upgrade her device because she was struggling with the type of BAHS she was using. The device wasn’t helping her in school and customer service was not supportive of her needs. She researched other brands of BAHS and found the Facebook group BAHA World Hearing where she first learned about Oticon Medical’s Ponto bone-anchored hearing system. Elizabeth was given a Ponto loaner to try. She shared her reaction for the first time in a heart-tugging video (see below).

Elizabeth Collins tries a Ponto bone-anchored hearing system for the first time

Elizabeth made the decision to switch to a Ponto BAHS and got ready for her next battle — a revision operation to have an Oticon Medical abutment implanted. Two years after she graduated college and began her career as a Contract Specialist at Norfolk Naval Shipyard, and despite confronting more insurance rejections for her re-implantation surgery, Elizabeth finally received her Oticon Medical abutment in October 2018.

Life with her Ponto 3 SuperPower

Elizabeth Collins with her Ponto 3 SuperPower

Since receiving her new abutment and Ponto 3 SuperPower, Elizabeth has been experiencing a new world of hearing. When in meetings for work she can hear sounds more clearly and doesn’t miss what her co-workers are saying, whereas before she would struggle to make sense of conversations. Last year she graduated magna cum laude from Strayer University with a Bachelor of Arts degree in Business Administration and is now pursuing a Master’s Degree.

“Now I get to discuss and elaborate on topics. I do presentations and trainings where before, never in my life would I have wanted to go up in front of people and present. I’m excelling at my job and advancing to leadership roles. The most important difference I’ve noticed is that my speech has improved, my family has started to respect me, and I feel more confident,” she said.

In the end Elizabeth feels the switch was worth it. “Oticon Medical has captured my heart and I’m not going back. When people see my Ponto and ask me what I’m wearing, I let them know that this is my ear.”

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SuperNOVA receives super hearing from her Ponto 3 SuperPowers

Nova Cox

Pfeiffer Syndrome is a craniofacial disorder that affects one in every 100,000 people and impacts the way bones grow. Nine-year-old Nova Cox was born with Pfeiffer Syndrome, and in her case her head, neck, and arms have been affected resulting in hearing loss in both ears.

Because hearing loss is common with Pfeiffer Syndrome, her parents Elizabeth (Liz) and Jason connected with other families, utilized Facebook groups for bone conduction wearers, researched online, and consulted their audiologist before Nova was fit with a bone-anchored hearing system (BAHS) on a softband.  

That’s a new sound

After wearing a bone-anchored hearing device on a softband for 7.5 years, Nova began advocating for abutment surgery. After doing research with her family, they consulted an audiologist and were able to try on different types of BAHS before her surgery.

“Nova made the decision to have the implant surgery and was able to ask her questions and be a part of the decision-making process. When she learned more about it she advocated for it and we moved forward when she was ready. When she tried on the Ponto, she didn’t want to take it off,” Liz explained.

Nova chose the Ponto bone-anchored hearing system because she experienced less feedback and better sound quality after trying different devices. She had bilateral abutment surgery and was fit with two Ponto 3 SuperPowers. On the day her Pontos were programmed it was raining and her mom recalls she asked, “Does the rain always sound like this?”. Nova’s parents knew they had made the right decision and for the first few weeks of having her Pontos on abutments they liked to play a game called That’s a new sound, where Nova shared new sounds she was experiencing.

Life with Ponto

It’s been a year since Nova’s bilateral abutment surgery. Today, she is a fierce and mighty force of nature advocating for herself, her health, and her life as an active kid.

She says she loves her Ponto BAHS and enjoys using the Oticon Medical Streamer in class and when she’s in the hospital so she can watch movies to pass the time. And like lots of kids her age she likes Legos, Star Wars and Pokemon and spends her free time playing music, soccer, Taekwondo, and watching movies with friends.

Nova hiking

Nova practicing Taekwondo

Empowered to tell her story

Inspired to share her story especially with young children, Nova created the video below as she was preparing to give a talk in Washington, DC advocating for high-quality accessible healthcare for children.

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Advice to others

Nova and her family have learned a lot in just nine years. A few important pieces of advice that they want to share with other families is to try multiple hearing devices in order to find the right solution and make decisions when the time is right for you or your child. As for Nova, she has the best advice — “Judge Less, Love More”.

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Benefits of the Ponto System: Learn Faster, Remember More, Less Effort using Direct Sound Transmission and Higher Maximum Output

Choosing a system and sound processor for you or your child’s individual hearing loss is an important decision that can impact everyday life in fundamental ways. Choosing the right system affects how quickly a child will learn as well as their ability to remember what they hear, while sound processor choice impacts the level of effort needed to understand speech.

Today, we’re excited to share three recent studies that measured the benefit of Direct Sound Transmission and maximum output on learning, remembering and listening effort with the Ponto Bone Anchored Hearing System.

Ponto Evidence #1: Learn Faster

In a recent study conducted by Dr. Andrea Pittman from The Pediatric Amplification Lab at Arizona State University, school-aged children (mean age 11) were fitted with the Power version of the Ponto Bone Anchored Hearing System on a softband and an abutment. These children were tasked with listening and learning six new words. The purpose of this study was to quantify the benefits that children receive from a surgically implanted device compared to wearing the device on a softband.

The results showed that on average, children learned new words 2.5 x faster using a system with Direct Sound Transmission compared to a solution with skin transmission. Direct Sound Transmission systems can provide an extra 10-20 dB of output in the mid to high-frequency range, which contains the most important sound information for speech understanding.

Ponto Evidence #2: Remember more

In a similar study conducted by Professor Thomas Lunner, a senior scientist and research manager at Eriksholm Research Centre in the Denmark, a memory and recall test was performed on participants (mean age 58) who wore the Power version of the Ponto on a softband and abutment. The participants were tasked with recalling specific words after listening to seven sentences.

The result was a 13% relative improvement in recall performance with Direct Sound Transmission vs. skin transmission. With Direct Sound Transmission fewer resources are needed to process sound, more resources and energy are focused remembering.

Ponto Evidence #3: Less effort

In order to measure listening effort objectively, participants were tasked with listening and repeating sentences while an eye-tracking camera monitored their pupil dilation, as a measure of listening effort. These participants (mean age 59) were given sound processors with different maximum outputs like the Ponto Pro, Ponto 3 and Ponto 3 SuperPower (P3SP).

The result was significantly less effort with the Ponto 3 SuperPower as indicated by reduced pupil dilation.

What this means for you, the user

Choosing a system and a sound processor has an impact beyond hearing and can affect everyday activities like learning, remembering and listening. With Direct Sound Transmission and a sound processor with higher maximum output more cognitive resources can be used for understanding, remembering and enjoying life.  

We believe in providing patients with the best possible sound quality which is why the Ponto Bone Anchored Hearing System uses Direct Sound Transmission with an abutment and the P3SP is the most powerful abutment-level bone anchored sound processor.

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Artist, Priscila Soares, uses imagery to advocate for the hearing loss community and adds new artwork to the Oticon Medical U.S. office

Priscila Soares creates works of art that tell the stories of real people behind hearing loss. After losing her hearing on both sides when she was young and advocating for her son, she began creating art that empowers and advocates for the hearing loss community.

Advocacy through art
Priscila is a hard of hearing artist and mother of three living in California whose hearing loss journey began when she was 17 years old. After undergoing surgery to remove a Cholesteatoma, a destructive skin growth that develops in the middle ear, problems with the surgery rendered her deaf in her right ear. At 24 years old, her left ear showed the same Cholesteatoma condition. She underwent surgery again which was successful, however, they discovered the bones had already been corroded resulting in hearing loss on her left side.

It wasn’t until her second son, Jason, was born with a moderate to severe hearing loss that Priscila began meeting other people within the hearing loss community at his preschool for deaf and hard of hearing children. It was within this environment that she met others with Bone Anchored Hearing Systems.

“I wanted to get the best quality of sound I could. It was hard to participate in group conversations. I couldn’t keep up with what everyone was saying, and I was trying to put together the missing words in between,” she explains. Priscila was bilaterally implanted with the Ponto Bone Anchored Hearing System four years ago.

“Ally Is Looking Out for Microtia”

Hearing loss portrayed through art
As Priscila became more involved in the hearing loss community, she was inspired by the people she encountered and the knowledge she was learning and sharing. This led her to combine her two passions, hearing loss and art. Primarily using acrylic paints, dry pastels, and homemade clay she began to document her own journey – My Luckyears.

“It was two years ago that I decided to take my art seriously and my Ponto was a part of that. As I’ve felt more confident in my hearing, I’ve had the courage to pursue things I didn’t think were possible.”

This year, in recognition of National Microtia Awareness Day, Priscila created an art piece called “Ally is Looking Out for Microtia” – inspired by Ear Community Founder Melissa Tumblin’s daughter, Ally.

“The piece ‘Ally is Looking out for Microtia’ is part of a series of pieces I’ve been creating based on real children with hearing loss. I first created the piece because I wanted to honor all children with microtia and atresia. I added the butterfly to land on the Ponto, for good luck.

Different from my more personal paintings and sculptures, these sculptures are not about me and my personal journey, rather I just become the catalyst of what connects the child’s journey to the rest of the world. I like to portray children because those are the foundational years of a person’s life and I want them to feel empowered!” she says.

A new addition to the Oticon Medical U.S. office
Priscila’s work revolves around acceptance and helping those with hearing loss overcome hardships which is why we are proud to now have “Ally is Looking Out for Microtia” displayed at our U.S. headquarters.

“My most powerful way of sharing what I have learned for those starting their journey is through art. I hope this piece at the Oticon Medical U.S. office will be a reminder and an inspiration to look out for each other, advocate, and not be afraid to be who you truly are.”

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Becky Zingale shares how her daughter navigates Treacher Collins Syndrome and conductive hearing loss with her Ponto 3 through her blog

You might be familiar with the blog “The BAHA Mama”, a well-known resource for parents and families who have children with hearing loss and Treacher Collins Syndrome (TCS). The blog, which was created by Becky Zingale, follows her family’s journey of navigating TCS, hearing loss, speech therapy, sign language, and parenting.

Becky began writing around 10 years ago to document her travel experiences. Later, when she and her husband learned that their second daughter, Ariasha, had TCS, Becky focused her blog on sharing knowledge and personal stories with other parents.

“My husband is a marketing consultant and has empowered me to be a thought leader. I’m a great success story for what happens when you follow the advice of your marketing consultant (husband),” she says.

Ariasha, also known as “Little Lioness” and “PipSqueak”, was born with Treacher Collins Syndrome and microtia and atresia, just like her father Duane. She underwent cleft palate surgery in 2016 when she was sixteen months old, which is when they discovered her conductive hearing loss. Thinking Ariasha would follow in her father’s footsteps and wear the same bone anchored hearing device as him, she trialed his device first but experienced issues with feedback.

Through online Facebook groups focused on hearing loss like this one and this one, Becky discovered the Oticon Medical Ponto Bone Anchored Hearing System. All the information they received convinced her that Ponto was the right choice for her daughter.

They trialed the Ponto and Ariasha now wears bilateral Ponto 3’s on a softband. During the first few weeks of her wearing her Ponto, Becky noticed just how much it was making a difference in her ability to communicate.

“She had her Ponto for two weeks and I tried dropping her off at childcare. I thought the noise might be overwhelming so I decided she shouldn’t wear the Ponto, and she was really upset. It turned out that she had become so used to being able to hear for those two weeks, that she preferred dealing with a loud environment than not knowing what was going on. She has also become more social since getting her Ponto. Beforehand, when people would come over, she wanted to go to bed. We thought she was really introverted. But with her Ponto, now she wants to interact with people since she can distinguish sound, hear different voices, and has an idea of what’s going around her.”

As Ariasha continues her hearing loss journey, Becky documents everything they learn and answers common questions from parents online through informative blog posts and personal stories. One such post discussed a common question posed by parents – how to show a child to place their BAHS (Bone Anchored Hearing System) in a safe place to avoid it getting lost or broken.

“Sometimes Ariasha decides to change her clothing randomly in the middle of the day and her Ponto will end up in a pile of clothes. So, we created “Ariasha’s BAHS Box”, a safe place to put her Ponto. The other day she went upstairs to play and then came downstairs wearing a new outfit. ‘Where is your BAHS?’ I asked. She responded, in a very sassy teenager-ish tone, ‘In my BAHS box’.”

Learning about Bone Anchored Hearing Systems and advocating for Ariasha has definitely become a family affair. Ariasha’s sister Chloe, also known as “Monkey” or “Big Sis” on the blog, helps to check whether her sister’s Ponto needs new batteries and event sports matching headbands with her.

To parents trying to figure things out, Becky’s advice is to find a community. She says the online community has been very helpful with discussing things like speech therapy and how to get your child to keep their BAHS on their head.

“Hope is what the name Asha means. It’s my hope to inspire and encourage mamas in their journey to raise healthy, thriving families in spite of whatever challenges life brings.”

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CardioThoracic nurse, Iris Leak, shares how her Ponto 3 SuperPower makes a difference at work and at home

Working as a CardioThoracic nurse for 27 years, Iris had become accustomed to noisy environments. However, after the removal of a glomus tumor and cholesteatoma, she found herself with conductive hearing loss and challenged to perform her work duties. She began searching for a solution and found the Ponto 3 SuperPower.

The effects of her hearing loss
Iris had been relying on her “good” left ear for some time, but as her hearing loss became more severe it also became increasingly difficult to hear and understand her co-workers and family.

“People at the hospital would have to throw things my way to get my attention because I couldn’t hear them anymore. It was getting more and more difficult to hear in my work environment,” she says.

In social situations, she struggled to keep up with conversations and found her hearing loss isolating her from family and friends. “I’m a talker naturally and I love being around people. But with my hearing loss, I found myself becoming more isolated because I couldn’t hear the conversations and couldn’t participate. I wasn’t myself.”

Finding the right solution
Iris started doing her research. She found support and resources through online Facebook groups like this one and worked with an audiologist who helped her understand her options. She demoed different bone anchored hearing devices and ultimately chose the Ponto.

In November of 2017, she had the Minimally Invasive Ponto Surgery (MIPS) and received her Ponto 3 SuperPower in January of 2018. To ensure her abutment was placed in the best position to accommodate her reading glasses and CPAP (Continuous Positive Airway Pressure) mask she brought her glasses and mask to her surgeon to mark the abutment site. When she received her Ponto on the abutment for the first time she immediately put it to the test. “I went out to eat afterward, and I picked the noisiest place I knew—the mall. It was amazing! I love hearing and I feel like myself again.”

As Iris has grown more accustomed to her new world of hearing, she’s started using Ponto’s accessories like her Oticon Medical Streamer, which she describes as “game-changing”. “I hadn’t listened to music in years, but now it’s possible with my Ponto 3 SuperPower and Oticon Medical Streamer.”

Iris’s advice for those looking at a hearing loss solution is to remember nothing is perfect. Do your research to find the solution that is best for you.

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Isabella’s Ponto Bone Anchored Hearing System helps her on and off the volleyball court

Despite being born with a bilateral conductive hearing loss, Isabella doesn’t let anything, especially her hearing loss, slow her down. She has microtia on her left side and bilateral atresia. When her parents realized she had a hearing loss at birth, they worked quickly to ensure she received early intervention.

“When I was little and I hadn’t had my reconstruction surgery yet for my microtia, I used to tell people that I was in an alligator fight and that an alligator bit my ear off. I was instantly the coolest kid.” – Isabella Rodriguez.

Her mother, Lupita, began advocating and researching this new world of hearing loss which led her to join Georgia PINES (Parent Infant Network for Educational Services). Through her work as an early interventionist for Georgia PINES and Georgia Hands and Voices, she learned first-hand about the latest hearing technology and spoke with local audiologists. This is how she came across Oticon Medical’s Ponto Bone Anchored Hearing System.

Starting high school off right
As Isabella entered high school, her parents knew she needed to upgrade to the newest technology to ensure she was set up for success. After trialing different brands, Isabella chose the Ponto and started her high school days with a Ponto Plus Power on a softband. “The Ponto was a lot clearer, had less feedback and had a sleek design, while the other options sounded robotic,” she explains.

And in a school of more than 3,000 kids, her Ponto made a difference. Whether she was taking part in group projects, communicating with classmates in the cafeteria, or socializing in the courtyard.

“In the classroom, the new lecture style of teaching where the teacher moves about the room would have normally been really difficult for me to hear, but my Oticon Medical Streamer helps. I wear my Streamer and the teachers use an FM system to send sound to my Streamer which sends sound to my Ponto.” – Isabella Rodriguez

Connecting with other Ponto users at local events
As Isabella now plans for college next year, she and her family have started researching abutment surgery. Surgery can come with a lot of questions and we know that conversation and discussion through the lens of experience is the most powerful tool in making the right decision for the best hearing care. After attending a bone anchored hearing meetup in Georgia, hosted by Ross Wiseman earlier this year, Isabella and Lupita were able to meet other Ponto users who wear their Pontos on abutments.

“We were able to connect with Ross and two other women who had the Ponto abutment surgery at the meetup. They explained their experience with the surgery and how their hearing had improved,” Lupita explained.

Wearing a Ponto Bone Anchored Hearing System in high school
Isabella currently plays competitive volleyball with her Ponto, which she says helps her hear coaches and teammates.

“I never play without my Ponto.” – Isabella Rodriguez

As she’s grown older, she has gained more confidence and become used to educating her teachers and fellow students on what it means to have a hearing loss. To other young people with hearing loss who may be struggling with self-confidence, she says, “Don’t be ashamed. Everyone is different and there is nothing wrong with you.”

 

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The Ponto 3 SuperPower ignites a love for music for Talia

Three-year-old Talia Jarvis was born with unilateral microtia and atresia, and bilateral moderate-severe hearing loss. When the Jarvis family adopted Talia in March of 2017, they took her to an ENT right away to begin her hearing journey.

“I wasn’t familiar with all the different devices. Our audiologist said they were all pretty much the same. They didn’t provide the Ponto so we took home a different bone anchored hearing device to trial and it didn’t reach our expectations.” – Laurie Jarvis

Talia’s mother, Laurie, began doing her own research because of the severe feedback issues Talia was experiencing. She began speaking to other users online in Facebook groups like this one and this one that helped her find the Ponto 3 SuperPower and halt her current bone anchored hearing system order until Talia trialed the Ponto. “I told my doctor that if they didn’t let us trial the Ponto device we would be switching to someone else, ” she explains.

Since receiving her Ponto 3 SuperPower Talia’s world has expanded and is happy to wear her device all day. She is now learning language and her mother says she can hear the differences in sounds. 

“With the Ponto, she cried the first time I took it off at night. The next morning she pointed to it on the dresser and every day since then it’s the very first thing she asks for in the morning.

Before it was hard to get her to sit still to read a story. Now she will ask for book after book after book. She wants to learn new vocabulary and is constantly asking me what this and that is. That interest was not there before.” – Laurie Jarvis

One of the greatest differences her family has witnessed is seeing her discover a love for music. At home, Talia now enjoys listening to her sister play the piano, a sound that until recently was something she had not heard.

 

“My oldest daughter was playing the piano one morning and Talia was sitting in her highchair eating breakfast and she looked at me and she pointed to my daughter who was playing and she signed ‘piano; It was obvious that she was hearing something different.” – Laurie Jarvis

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