Stigma remains one of the most enduring and complex barriers in hearing healthcare—shaping public perceptions of hearing loss, delaying help-seeking behaviors, and limiting the adoption of hearing technology across all age groups. Despite advances in treatment and expanded access through over-the-counter (OTC) devices, many people still hesitate to pursue care due to fears of looking old, feeling different, or being misunderstood.
In this insightful panel discussion, consumers, clinicians, and industry leaders come together to explore how stigma shows up in clinical settings, family conversations, and broader societal messaging. Drawing on personal experience and professional expertise, the panel examines the subtle ways that language, product design, and even well-intentioned advice can reinforce stigma—and what can be done to replace those barriers with messages of confidence, connection, and empowerment.
From the role of primary care physicians and educators to the impact of emerging technologies like hearable glasses and invisible hearing aids, the panel explores practical ways each stakeholder can contribute to reshaping the narrative. The discussion also highlights the importance of consumer storytelling, inclusive terminology, and consistent messaging across sectors to create a more accepting, proactive, and person-centered hearing care experience.
Whether you’re a provider, policymaker, advocate, or someone navigating hearing loss yourself, this session offers meaningful insights into what progress looks like—and how we can all be part of it.
Full Episode Transcript
Well,
here we are at the Future of Hearing
Health Care meeting and our
task as a panel today,
a panel of industry people,
clinicians and consumers.
We’re our task today is to discuss
the hearing loss and stigma issue and
try to break down some
barriers to care.
And
first thing I’d like to do is to have
my colleagues on the panel
introduce themselves.
And so Bill,
would you introduce yourself?
Absolutely. Hello everybody.
I am Bill Schiffmiller, founder of Akoio.
Akoio is a consultancy on
accessibility and auditory
health manager.
I am a lifelong hearing aid user and
I am former lead of Accessibility
initiative at Apple.
Great.
Tony, would you introduce yourself?
Thanks, Bob. Hello everyone,
my name is Tony Sulsona.
I am the director of the audiology
channel for Nuance Audio.
In other words,
the Nuance Audio OTC hearing classes.
And
Michelle?
Hey there, I’m Michelle Wiebke.
I’m an audiologist and I’m joining
today as the senior Lyric Audiology
and Education manager at Phonak.
Great Andy.
Thanks Bob.
Andy Bellavia and I was formally
responsible for marketing and business
development at the hearing health
tech company Knowles.
And then three years ago I split off
to form my own consultancy and I guess
I cover two out of three because I’ve
been now seven years a hearing
aid wearer as well.
Shari.
Hi everyone,
I’m Shari Eberts and I am the founder
of livingwithhearingloss.com as well
as the co author of Hear and Beyond
Lives Skillfully with Hearing Loss.
And I have been wearing hearing
devices since my mid-20s.
Second, Michelle.
My name is Michelle Hu.
I have been a pediatric audiologist
for over 16 years now.
I’m a bilateral cochlear implant user
and I’m founder of mamahuhears.com or
also on Instagram where I help support
hearing parents of deaf children
navigate the journey.
Fabulous.
As you can see,
we have a great group of colleagues
here that are going to help
us navigate through
the issue of stigma.
And it remains one of the most
persistent barriers to
hearing health care.
Shaping how people interpret
hearing loss
delays help seeking and limits
adoption of hearing technology.
Hopefully this panel now can begin
to address those issues. And,
and I think I’ll just start
a little bit with,
you know,
when I had my practice back
in the 70s as we early on
people would have to be about 95 years
old and have about 60 decibel hearing
loss before they would even consider
walking in the door.
Just in general,
how do you see as a group,
how do you see that maybe that
has changed somewhat.
In.
The new century,
and particularly in 2025
relative to say 1975.
I’ll take this one.
I think definitely Covid played a
good part in this. Maybe not.
It was very difficult in the beginning
with the introduction of masks.
It became very difficult for us deaf
and hard of hearing people to
communicate, to feel comfortable.
Especially in doctor’s appointments
when our healthcare providers were
covering up their mouth
and their facial,
their half of their face so that we
couldn’t get those visual
cues to communicate.
That was our superpower and that was
stolen out from under the rug,
from the stigma,
I think is very much an external
societal type of pressure or
creation of story where
you know you were.
Denial is something very
much more internal.
What kind of stories are we making
about either ourselves or what
society is thinking about us?
And stigma just fuels this,
adds fuel to that fire.
I think that because we are much more
expressive and emotionally intelligent
or like we built upon that realization
and opening our awareness.
It’s become less and less because
we’re communicating with each other.
We’re building a deaf and hard
of hearing community
so that we can support each other.
And I don’t think we had that before.
It was very much behind closed doors.
Your business is your business.
And now it’s like, you know what,
let’s share, let’s grow together,
let’s grow stronger.
I think that’s part of melting it.
Away a little bit.
Great.
Some other comments on that,
on that one statement about how maybe
things have evolved to some
degree over the years.
I think that’s probably the
key benefit for OTC.
Even though we all know right now OTC
has not really fulfilled its promise.
It’s barely making a dentist in a
number of people seeking hearing
care of one kind or another.
But on the other hand,
there were a tremendous number of
positive messages in the popular press
surrounding the release of otc.
And then subsequently,
like Apple’s entry and Luxottica’s
entries for example,
but really mainstream.
A ton of mainstream press coverage on
the importance of hearing care and
what OTC is meant to address,
which even if people didn’t go for an
otc, they were hearing those messages.
And I have to believe that that caused
the dent in the Stig slash
denial problem.
Some other comments.
So I have a profound healing loss.
So I use prescriptive hearing
aid that’s non negotiable.
I do not have any other choice.
I need it.
And in the years of building
our consultancy on auditory matters,
no matter how you reframe hearing
loss, no matter how Much.
You put a name in term,
people won’t address it.
What did change to Michelle’s point
with the pandemic where
you had the mask?
There was a startup called Listen
Lively and Listen Lively suddenly was
going after tech Savi people in their
40s saying I got power in my hand,
I like technology,
I like the Internet,
what can I do to take care of myself?
And I think as we were waiting
for FDA approval on occ,
this enlivening which was acquired by
GN that became Jobbering Hands
started something.
They started to recognize
younger COHORTS,
not the 95 year old that you
mentioned, Bob, from the 70s,
but now for years where the uni
manufacturers have been trying to get
those outside of the baby
boomer generation.
Like how are we looking at human loss?
How can we approach it differently?
And I think we started to do that.
It’s not taking off as
much as we’d like,
but we’re starting onto something.
I think a lot of audiologists
split into two,
like anti OTC and supportive of OTC
because they thought the ones anti
thought that OTC would threaten their
jobs. I’m in this camp over here.
It’s another stepping stone to get to
if they need prescriptive hearing aids
or custom programmed hearing aids.
It’s a step of, oh, you know,
like the reader at CVS by the
register, maybe these will help me,
they help me a little bit,
but I think I need some more and
that’s a stepping stone to get there.
And companies like Apple who are
bringing in their AirPods as an and
marketing them as OTC hearing aids
with a hearing test is a very
good step in that direction.
Part of the issue with otc,
at least initially,
was that the first wave of products,
I don’t know,
missed the boat a little bit, right?
They looked like typical devices.
There wasn’t always Bluetooth
streaming.
It didn’t give the consumers
necessarily what they were looking
for from a device of that type.
And I think the media
coverage was great,
but a lot of it contained some of
this outdated imagery, right?
So we weren’t seeing that modern look,
that new look that people with mild to
moderate hearing loss were really
going to be attracted to and that
perpetuated the stigma a little bit.
But like we’ve all said,
I think some of these recent new
products with different form factors
from big names are going
to start to help.
But really what I think is going to
get these mild to moderate people who
are the target obviously for
the over the counter,
over that hump of trying to use that
device is that the devices
need to work well,
they need to meet their needs in the
situations that they’re looking for
them to use that. And so when we show,
I think when these devices
show the benefit,
that’s when the stigma is
going to be fading.
Because if people can talk about,
you know,
I actually use this kind of cool thing
and it actually helped me
in this restaurant,
that’s when that stigma is really
going to start to come down because
people will understand the benefit
that they’re getting from it.
Sherry,
I love the fact that you said cool,
because for many, many years,
and I’ve been in the traditional
hearing aid space for many,
many years as well,
and over 22 years in the industry,
and I used to always say to
colleagues, consumers, et cetera,
you know, when will hearing solutions,
especially as we approach otc,
before it was approved,
what will it take?
And I used to say the same word.
When hearing aids become cool,
they become attractive.
When they become attractive,
become viral, more adoption there.
Then you can branch out into
innovation, etc. And thank goodness,
like other wearables,
hearing aids are,
or in that early stage of looking at
different modalities
and shapes and etc.
That create a sense of attraction or
at the very minimum, intrigue,
not only from the consumer, but,
but certainly from hearing
care professionals.
So while we’re at this,
let’s throw another thing out there.
Do you think
that there’s a real difference between
stigma and denial or does one
kind of feed on the other?
Well, I think like Michelle said,
they’re interrelated.
But, you know,
stigma sometimes comes more externally
and denial, I think,
sometimes comes little
bit more internally.
Denial also is, I think,
part of the nature of the beast,
because hearing loss a lot of times
comes on grass. Gradually. Not always,
but a lot of times it
comes on gradually.
And so we may not really know how much
we’re missing until there’s sort of
an event or. Or something happens,
like the masking in Covid,
or like the TV gets to
a certain level,
or everyone just starts
complaining about it.
So we’re kind of in denial because
we don’t experience,
you know,
the actual external impact of that
hearing loss. But the stigma comes,
I think, from the outside.
But where it really hurts is when
we take that inside ourselves.
And I think a lot of people do.
And part of that is because of the way
it’s portrayed still in
mainstream media.
You wouldn’t make fun of somebody on
a television show who was blind
for bumping into something,
but you can make fun of somebody
for mishearing something.
And until we’re really
not seeing that,
where people with hearing
loss don’t look foolish,
that external stigma is, you know,
we’re at risk of internalizing that.
Yeah, I agree.
And there’s a dimension to that, too,
which is harder to overcome,
and that’s ageism.
In many Western countries,
ageism is pretty prevalent or
perceived ageism, if not real ageism.
I’ll give you one example.
The job site Indeed.com they actually
published an article.
They were forced to pull
it by the outcry,
but they published the article which
showed stages of one’s career
and at 50 or 55,
were in decline.
And so I’ve got.
I’ve actually got the graphic because
people published it before
they pulled it off.
The airline a long time ago.
Andy,
you and me both, right?
I mean, by now, so.
But. But that sort of thing,
those messages are prevalent.
And so if you’re, say,
in your 50s and you’re worried about
your future career prospects or
feeling like you’re being left behind
in favor of younger people,
it may be that the last thing you want
to do is show up with hearing aids
because of that perception.
And so that’s a hard barrier
to overcome.
Go back to your 1970s haircut, guys,
and. Because that’ll help a lot.
Sorry, Shari.
Oh, that’s okay.
I was just saying it is
a perfect example.
That just happened to me the
other day, actually, Andy,
that speaks to that point exactly,
is that a cousin of mine called
and said, you know,
I’m a little bit worried I’m not
hearing so well at work,
and I’m not hearing so well at these
cocktail parties. But, like,
I can’t be that guy with hearing aids.
So, like, what do you got for me?
But I can’t because I’m worried how
that’s going to impact my appearance
and my performance at work.
So it’s a perfect example of what
you were just talking about.
Absolutely.
And I know I’m jumping issues here,
but that’s why I really like the
alternative form factors like
the nuance glasses,
because they don’t,
they won’t combat stigma,
they hide the stigma.
But on the other hand,
if you’re taking say a 50 year old
person and getting them
hearing care today,
that’s the most important thing of all
because especially in the workplace,
if you don’t treat your hearing care,
you look like that out of touch old
guy, because you’re missing things,
hearing things improperly and so on.
And so that’s an important
part of the equation.
Even though it doesn’t address stigma,
it hides it.
It does get people’s care earlier.
And then as a stepping stone,
which was said before by
a couple of people,
once they’re in that sort of thing
and they get comfortable,
if they need to go beyond what they
can get out of the glasses or AirPods,
then they may be more
amenable to getting
a better prescriptive solution.
I think that’s a really.
All at once.
I think it’s a really great
point you just made there,
especially with that it doesn’t
combat the stigma. I mean,
we definitely have a lot of patients
who wear Lyric who really want it for
its invisibility and that’s
why they come to Lyric.
But they end up telling a lot of
people about it after they’re fit
because they love how they’re hearing.
And so I think if we look at it as
these form factors aren’t helping
push the stigma forward.
I think we have to reshape that
ourselves because it is pushing it
forward because they are getting help,
maybe earlier or maybe they,
whether it’s the stigma or denial,
whatever it is, if,
if we don’t have a solution that
fits whatever they want,
then maybe they go without a solution,
which is not helping any of us.
So it does move everything forward,
I think by having these other options
and certainly giving these interesting
ways to treat something.
And especially as I think the entire
field even advances in looking at
hidden hearing losses and some of the
things that are happening even in the
lower spectrum of the hearing
loss scale as well.
In everything you said.
Yeah.
Go ahead.
Yeah.
For Andrew Michelle,
to your point on that,
two things.
One is whether it’s masking
it or hiding it,
the fact that you can put on or wear a
solution that you have confidence in,
to the extent that you’re even willing
to showcase it to someone,
means that you are sort of promoting
the solution and not necessarily
hiding it,
which is a good thing to be
able to get to that point.
And the second point is just one
for a little comic relief.
There’s not too many hearing solutions
out there right now that you can have
a dramatic effect of putting them
on and taking them off.
Voila.
To Tony’s point,
what he just showed is something
glamorous. It’s a lifestyle choice.
And are you putting on yours too,
Andy? Oh, yeah.
I like what I have with the hearing.
But one of the things that’s
happening now is
there’s a generational distinction
between what we are accustomed to
hearing related to stigma with older
folk to the younger cohort today.
Now you have all kinds of earbuds with
nice features built in
that would discreetly
enhance your hearing,
maybe for communication,
for noise management
or sound wellness.
Now you’re starting to see I am taking
care of my hearing without being told.
Traditionally, we were told,
you need to get a hearing aid.
You can’t hear.
That doesn’t feel good.
That’s why you have this resistance.
But now you have these cool consumer
as well as prescriptive solutions that
have a cool factor to what Tony
was saying. And you know what?
I don’t know why, why it was,
but there’s something in it that’s
making me feel and even hear better.
I think there’s also something
to say about ableism.
I think that more and more people
are starting to spotlight it,
starting to cheer for that
underdog and say, oh,
everybody that is misrepresented
or underrepresented,
do you see how significant they are or
how much value they can
contribute to society?
And I tell parents all of the time,
it’s much harder to acquire a hearing
loss than it is to grow up with one.
Because when I was learning
my life and social skills,
that’s the challenge that I had
presented to me versus going through
life having normal hearing.
And all of a sudden I have to learn
these new skills that I’ve never had
to use. I don’t have that muscle to.
So growing up, Bill, Shari,
you and I, like,
we grew up having to use those skills
little bit by little bit in our
everyday life versus, oh,
I’m a CEO of a company,
and now I suddenly realize
I can’t hear something.
What do I do? Give me a device.
Give me a magic pill.
Give me something.
So I think that we’re shifting
that view of ableism,
the underdog and being much more
adaptive and open minded about it.
I think to further your point,
Michelle,
and what Bill and Tony just said,
I think there’s something about the
psychological impact of treating the
hearing loss and we definitely see it
in the lyric space because patients
aren’t reminded every day
about the hearing loss.
So that tends to add to this
confidence and just an increase in
their overall well being because
they don’t wake up thinking,
I have a hearing loss,
I need to put something on and
multiple times to remember to put
it on. But I think that overall,
as Tony said,
that confidence that the hearing care
can provide in any solution really
speaks to their overall well being as
well as that psychological
benefit too.
And I think confidence in a way is the
exact opposite of stigma, right?
Because confidence is when you feel
good about yourself and your ability
to walk into a situation and be able
to participate in a confident way
versus that stigma of worrying that
you’re not going to be able
to walk into a situation.
So I feel like any type of device
that’s going to give people confidence
is going to break down stigma.
I don’t think it’s really
hiding the stigma.
I think it’s actually building that
confidence which is in turn going
to break down that stigma.
And when you feel that for yourself,
when you feel that confidence,
you feel less stigmatized.
And I think then you’re willing to
sort of talk about it, say, hey, cool,
look at my cool new devices,
or look at this cool, cool thing,
or wow, have you tried this?
This helped me so much at the theater.
And that’s really going to be what I
think over time accelerates and breaks
down that societal stigma which
hopefully becomes that, you know,
virtuous circle. You get more inside.
But it really starts, I think, with,
with that building confidence that
breaks down that stigma you’re
feeling. I think it’s interesting.
Go ahead.
I was just going to say that the,
the, one of the,
one of the most strange things I’d
heard in a long time when we were
doing clinical trials on Lyric and,
and then with patients thereafter,
they would always say, you know,
I wear a hearing gauge,
but you can’t see them.
You know, if you just wait,
look way down in my ear.
You can see it down in
there somewhere.
But so people who were,
who would be very self conscious about
amplification in general if they’re
wearing something else,
walking around,
showing people just exactly where it
is, that way down in their ear.
In fact,
I’m surprised he didn’t have an
otoscope so they could show
them where it was.
But anyway, I do that sometimes.
I definitely do that.
Oh, I bet. So, yeah, I mean,
but, but the bottom line is that,
that I think that those
kinds of products,
the form of the products is,
is making somewhat of a difference to
many people, people who, you know,
were high level executives and didn’t
want to look like they
were losing anything.
Those were,
were big candidates for Lyric and some
products like that. But, you know,
you’ll,
you’ll see the people about the same
age on the other side who,
who will actually be an individual
who doesn’t care,
and it doesn’t make any difference.
And so you’ve got one side
and the other side.
And I think the form is helping.
Helping a lot. Because even,
even instruments that do a lot and
hook up to a lot of things,
they’re getting smaller and smaller
and smaller over time. So,
so if we were,
how can the different stakeholders,
like clinicians and
companies and consumers,
how could each of you guys contribute,
not you guys,
but each of those classifications
contribute to reshaping the narrative?
We’ve been talking about
it a little bit,
but maybe we want to kind of hit that,
that issue just a little bit.
What can we do as clinicians,
consumers and industry to facilitate
the reduction of this,
this issue?
And I will jump in and just say that
there’s many answers to this and we’ll
hear from this distinguished panel.
You would,
because you got the glasses, man.
But there are a lot of other cool
solutions that we all can relate
to that we’re all part of.
It’s not just one,
but part of it is whether you’re a
clinician or you’re in a
storytelling capacity,
it is really the ability to keep,
also from a professional perspective,
not only consistent messaging,
but it’s got to be positive messaging.
Often we talk about hearing loss,
all the things we cannot do,
as opposed to changing the script
and talking about lifestyle and
improvements and enhancements and
empowering and confidence.
This is the kind of language that we
have to move sometimes. You know,
the baseline of clinical audiology and
solution based conversation
is critical.
It adds
validation to what is being prescribed
or being provided.
But there has to be a certain level
of enthusiasm that starts
from the clinician.
And that’s where influencers and
companies and those that
have great messaging,
that are positive and open the eyes to
hearables, makes a huge difference.
And I think also it’s about
setting expectations.
Born with a hearing loss or late
in life with the hearing.
Two very different approaches. I mean,
you,
you know,
we all know about Richard Einhorn,
who was a composer and who late in
life sudden had a sudden hearing loss.
So he’s on a mission
to find a solution.
But we need to be setting the right
expectation to whomever,
wherever they’re at and
what’s out there.
The key thing is
listen to what they have to say to go
in and get a hearing test and
use your audiogram results.
Now,
I’ve been wearing hearing AIDS
since I’m 6 years old,
and it wasn’t until my 50s that I knew
that there was a distinction between
consonant and vowel.
No one ever told me that.
But the important thing is,
what are you experiencing? Talk to me.
What are you going through?
Let’s find a solution for you maybe
prescriptive or OTC or some kind
of awesome assistive device.
And that’s what we need to do is to be
able to have a dialogue
with that individual.
What’s going on in your world?
Let’s talk about it.
I talk a lot about access,
inclusivity.
It’s not that something
changed about you,
like you as your personality
or your being.
It’s.
It’s you don’t have access to certain
sounds that can add to your
quality of life now.
So when I’m counseling patients,
I will say,
what is it that’s important to you?
When Shari mentioned theater,
is that something that really
gives you life,
that really invigorates your soul?
Is it hearing your grandchildren?
Is it just hearing, you know,
the Price is Right on tv?
What is it that gives you so much
excitement to get you through the day?
How can we get you access to that?
It might be a device.
It might be some more visual cues
or practice from your family.
How do we raise that awareness?
We’re also changing the language
around hearing loss. I think, Bill,
you mentioned that I grew up using the
words hearing impaired and now I
shifted over to some people.
I say I have hearing loss.
It depends on my audience.
I say I’m deaf to people who are
hearing and then I’ll say I’m hard of
hearing to people who are
deaf and use asl.
It’s very different in the wording
that you choosing because how you
relate to other people also is a huge
reflection on how do you relate to
yourself and your own deaf identity.
And we need to keep working
on that language too.
Matthew Alsop brought this up.
Why are we calling it age
related hearing loss?
Why don’t we just say that your
ears wear out over time?
And I really like that.
I think about I’m a distance runner
and I can tell you my race times now
are a lot slower than they
were 20 years ago.
And nobody says that I have
age related speed loss.
Why do we have to make that aging tie
in when we have an ageism problem?
Why don’t we just talk about the fact
that our ears get a little
bit worn out over time?
And then with those positive
descriptors you mentioned, Michelle,
I can get you access to the theater or
better access to the theater or better
access to the television and stay away
from the labels that feed
into the stigma.
And Andrew, you know what.
I was going to just say
when it comes to the
to like the terminology,
I think there’s generally a
misunderstanding in the spectrum
that is hearing loss.
I’ve had plenty of patients that show
up with minimal hearing loss,
but they say they’re deaf.
But also when it comes to,
like the common terminology that
we used to your point, Andrew,
how we talk about it.
But you’ll even get patients who’ve
had someone say you have a certain
percentage of hearing loss to the
patients who are told they have
a mild or a minimal or.
And so it’s really difficult, I think,
for the population to know how to
break that down or to understand
what they need to do about it.
Obviously,
if I’m told I have a
mild hearing loss,
is that something I should
do something about?
Maybe, maybe not.
But if I’m the person that’s really
struggling to your point, Bill,
and just listening to them,
maybe that person with the minimal
hearing loss does need help because
they are struggling significantly in
those environments that they’re in.
But it seems as though we do lack some
of this common terminology that helps
the general population maybe approach
hearing help with a less stigmatic
way or with less denial.
That’s really important about just
this overall messaging is
expectations, right.
And that it has to be about
more than the device,
because hearing aids,
cochlear implants,
we all know they’re not going to take
our hearing back to normal.
Right?
It’s not going to fix the entirety
of our communication issue.
And I think it’s really important for
people to understand that because if
they don’t and they start using any
type of device, a professional device,
an OTC device,
and it doesn’t solve their problem,
they are going to be disappointed and
throw the thing in the drawer and
not continue to work at it.
But what I think a very important
change and messaging from everyone in
the industry needs to be that
it’s technology plus. Right.
It’s all about the attitudes that we
hold about hearing our hearing loss.
And then also behavioral changes,
visual cues,
other things that combine with the
technology to help us to communicate
better. We have to sort of shift that,
I guess,
focus from hearing better
to communicating better,
because that’s really what we’re all
looking for from our devices.
Plus,
you know, Sherry,
there’s always a point where I walk
down to the bookshelf over
there and get your book.
Don’t make me do it now.
Sorry, I witnessed that before, Andy.
I have. So I’ve seen you go over.
One of the things I would like
to add to that, Shari,
is taking a moment when you
really listen to somebody.
I am shocked to learn I
have a hearing issue.
I have a noise issue.
And now Part of what you were asking,
Robert, where’s the stigma?
What is the stigma?
I think the problem is, okay,
I think I have a noise issue and you
want me to buy a $4,000 hearing aid.
Whoa. Something not right here.
Give me more.
Let’s talk about it a little further.
So,
and like Michelle,
what you were saying,
what is the lifestyle thing
you want to do?
That’s what we need to be finding.
We need to unravel what’s going on
there to get you on the
right direction.
That hearing devices,
the most common misconception about
them is that they level the playing
field. We still have issues in noise.
We still benefit from visual
communications.
Just like closed caption on the TV
were created for deaf and hard
of hearing individuals,
not for the hearing people who just
want to be able to know
the score at the bar.
And I’ll just piggyback on what some
of you have said regarding
expectations.
And that is one thing that OTC does
bring to the table is a reset on
expectations in that early patient
journey to open the door for them to
recognize that they can use this for
situational solutions on the OTC side,
which is hardly ever talked about on
the prescriptive side
for obvious reasons.
Right.
It’s a constant matter of fact
of hearing improvement there.
But I think that opens the door for
early adoption and acceptance when you
look at the possibility of looking at
this as an entryway for situational
opportunities.
The other thing I would say,
and this might be bias from
my position, was,
but the integration of the optical
world and the hearing world
opens up the narrative,
opens up the discussion,
because now you have got another huge
group of professionals in optical
that are saying, look, you know,
now that hearing aids are available,
of course we’re on the glasses side of
it, but they’re populating the story,
the early education of go see a
hearing care professional and
understanding that because we all
know that as we do get older,
as a matter of fact,
both our vision and our
hearing decline.
So being able to just look at
that from a greater scope.
A greater scope and cross referencing
with other healthcare professionals,
even GPs,
at some point is going to be great for
everyone at every part of
the patient journey.
That kind of brings us to our next
kind of stimulation question here,
guys.
That has to do with the role of
primary care physicians
and other gatekeepers,
and I might just say about the
optometry people or the
optical people,
that
early on,
when a lot of optical shops decided to
add hearing aids into their shop,
a substantial amount of those went
bankrupt because they really did not
understand the hearing impaired
individual walking. In the front door.
They kind of worked with them more
like they did on the optical side
rather than on the other side.
Now I see with our entrance more
into some of the optical stuff,
it’s going to make a difference.
So you might mention something about
that. But the big thing now in this,
in this discussion would deal with
more with what do we do with the,
with the physicians and the nurse
practitioners and the,
and the optical people as well as
dentists and everybody else that seem
to be semi gatekeepers to maybe change
their focus toward some
of the things that,
that perplex people that are
considering amplification.
And by the way,
those gatekeepers really should
be defined as door openers.
Oh. Oh, well, that’s good.
That’s a sales way to say it, Tony.
I understand that. So I love that.
Been talking to a lot of pediatricians
and geriatricians as well,
and pediatricians do a lot more
screenings for the development
of things. How are we doing?
How are we growing? How are we,
you know,
at what rate are we doing this?
And they don’t do similar types
of surveys in geriatrics,
which is such a bummer because
as Michelle was saying,
somebody could have an audiogram
mild hearing loss.
But what she didn’t mention is another
person could have the exact same
threshold but be completely different
in their cognitive ability to process
and hear and understand speech.
So they need to figure out,
and work together, I think,
with audiologists to figure out where
are they in that decline?
Is it processing, is it noise induced,
what kind of hearing loss do
they have and identify.
Go to an audiologist who can do speech
perception testing on them.
Not just threshold testing because the
threshold really don’t
tell you that much.
I could probably hear more with a
moderate to severe hearing loss
because I grew up wearing hearing aids
and processing it that way versus
somebody who’s newly diagnosed with
mild to moderate and can’t process as
surely or confidently.
I have a question for
Bob and Michelle.
Since you are experienced
practitioners,
how many referrals have you gotten
over the years from a general
practitioner saying, hey,
we believe this person has a hearing
challenge and would refer
by the physician?
I’ve been educating with people.
I used to get a lot of referrals
from physicians,
Bill. You know,
in fact,
I had a,
a huge referral source in my city and,
and they would actually,
they wouldn’t really write a letter,
but I’d get a lot of little
prescription pads
and, and, and, and phone calls from,
and, and when I, when you first start,
and you start at a time when
audiology isn’t well known
back in the 70s,
what happens is that they don’t
even let audiologists,
when you have a hospital appointment,
park in the physician’s parking lot.
But as it turns out, and you.
And you get to know those guys and you
take care of some of
them in the clinic,
as well as take their referrals,
and their patients come
back and tell them,
then you not only get
the parking spot,
but you get a lot of their referrals
back from those individuals.
So I had a lot of referrals.
So now, Michelle,
you can maybe speak to that.
Some of the other colleagues here
can speak to that as well.
Obviously,
I get more pediatric referrals just
because of my patient population.
But I think that there are more things
set in place to catch hearing
loss in kids.
Preschool teachers are trained
and developmental.
Regular teachers,
pediatricians, optometrists,
all of them are kind of interrelated.
But when they’re talking about adults,
it’s harder because it is
an invisible disability.
Someone who has a spouse can
lean on their spouse. Hey,
can you do this phone call for me?
Can you make this appointment for me?
But now we have new devices and apps
such as Innocaption that closed
captions their app,
but they still have that default, oh,
someone else can do that for me.
My daughter, my son,
my wife will be able to make
that appointment for me.
I think it
has a higher significance of falling
through the cracks when we’re older.
And also a certain amount of people
perceiving hearing loss as cognitive
decline in older populations, too,
they automatically assume it’s
cognitive decline and never
even think about.
Hearing or isolation or depression
or something like that.
Michelle,
I love those points you make,
Michelle, because obviously,
even after preschool or
the younger ages,
you still get hearing tests regularly
throughout schooling until you
graduate at times, right? So, like,
there’s this regularity of
that that does fall off.
And I know there’s been advancements
even in ways to do hearing screenings.
And it would be great if people could
just start setting their own reminders
to just check in and do that once a
year in that interim population,
if you will.
But coming back to the other
caregivers as gatekeepers,
I think
I’m happy that, Bob,
you got referrals, and obviously,
Michelle,
you’re getting them from some
of the pediatric side,
but I don’t think it’s as
common as it should be.
Kind of probably where you
were thinking, Bill,
I think we can absolutely
get more referrals.
We just have to do a lot more
education, which is a challenge.
It’s hard to get time with
some of these physicians,
maybe even how do you change the
narrative in schooling for them when
they’re trying to take on so much
information that seems much more
life and death, if you will.
Even so, it’s a challenge, I think,
but I think their perception
really impacts it.
We know patients trust what
their physicians say.
So if they brought up anything about
ringing or tinnitus in their ears and
they’re like, yeah, everybody has it,
Nothing you can do for it,
that’s a huge disservice to the
patient when there is something you
could do for it just the
same for hearing loss.
So we need to have a way to help those
caregivers build their confidence to
pass that knowledge on to
the patient that, yes,
there’s something you can do for this
and you need to go see this person,
but it,
it just doesn’t exist as broadly as I
think we would all like for it to.
I mean, I agree with that.
I, I have hearing loss, right?
My doctors theoretically know this.
They have never,
other than my audiologist obviously
has never asked me,
how are you doing with your hearing?
It was never something that was
brought up by a doctor ever in
my whole entire life, right,
Unless I brought it up.
So I think what we really need to hope
to do is have physicians make that
just a normal part of the
conversation. They ask you about,
what are you eating? They ask about,
you know,
are you regular in the bathroom?
You know,
there’s a whole host of questions,
but they’re not asking,
how are you doing? Communication wise.
Steve.
And they, and they won’t until the,
in this country,
until the US Presented Preventive
Services Services Task Force
agrees that that’s an important
part of the protocol, right?
Doctors are very overstretched.
And the conclusion when they
reviewed a few years ago,
the USP FDS was that
it’s not efficacious to address
hearing with a peer screen test,
a pure tone screening test
in older populations,
because it’s not an adequate screen
and too many people aren’t
taking action afterwards.
And therefore they are not
recommending that doctors address
hearing loss as part of their
normal health checks.
And that has to change before
overstretched doctors will take it on.
Andrew. To that point,
one of the things that even though
hearing may not be the headline,
more and more news and education that
we hear about, for example,
in dementia takes the lead that allows
us to dovetail hearing loss.
And so when we start talking in terms
of integrated impact on overall
health and societal good,
that’s what we have to utilize and
promote even more so because
that helps everyone.
Education and self care.
Yeah,
a very good reason to drive
that change. I agree.
And hopefully that will start
to take place as a result.
The relationship between
hearing and dementia.
I think it was an interesting point
you made though, Andrew.
It’s a little unfortunate if it’s
being pushed that those physicians
need to do the screening.
Right.
Because I think that’s adding to their
overstretchedness, if you will,
where really it’s just them being able
to refer them on even if they don’t
know if they truly have a problem.
But if the patient says that
they are having an issue,
that’s when the hearing care
professionals need to be treated
as the professionals,
just as equals to these physicians to
say that’s where you need to go.
They’re going to be able to assess
you just as the patient.
That may come to a hearing care
professional that may have
some cognitive decline.
I’m not going to treat it.
I know I need to refer.
Right.
So like there’s that back and forth
versus needing to do
the full screening.
I don’t know that that
has to live there.
As long as they’re open to having that
conversation of you can have someone
help you with this and this
is where you should go.
Yeah, Right.
If the patient is proactive
and brings it up. Right.
Then I know cases where local hearing
care professionals have forged links
with the local doctors to get
that sort of referral.
So it’s not a proactive
check of hearing,
but if the patient brings it up,
they do refer.
Right.
It takes seven years for typically
seven years for somebody to realize,
oh,
I can’t hear something and
get into the office.
I think it’s more like 10 to 14 years.
But how would you know if you’re
missing something if
you don’t hear it?
The words are not hanging in midair.
Like if I can’t read something,
I need to go to an optometrist
or ophthalmologist.
The words are not hanging in there in
midair for me to reread or rewind to
go back to. How would we know, Bill?
Change of mindset,
I think for these physicians is that,
you know,
that hearing is actually an important
part of overall health.
It’s not an afterthought.
It’s not something that,
you know,
it should be recommended against.
And they don’t have to,
like Michelle said,
they don’t have to do the
screening themselves.
They just have to ask about it as a
normal part of somebody’s life.
Are you having any issues
with communication?
It doesn’t even have to be about
hearing specifically.
It can be an open ended question
that addresses hearing.
It addresses vision, it,
it addresses isolation.
It addresses so many things with
just one open ended question.
And it really puts that piece of
health at the forefront rather than
as something over to the side.
And Sherry, to your point,
as part of the routine checkup,
what do they do?
They check in your ear while they’re
checking your rest of your sinuses.
And what a great moment to say,
so how are your ears?
And if the person doesn’t respond
that’s an indication of something.
And repeat it.
Lets talk about that.
And I think if you.
Such a natural way to begin
that discussion,
not just, oh,
do I have impact wax or whatever.
And the other thing that also needs to
take place is my pediatrician once saw
I had something horrible on my eardrum
and it turned out to be a piece of
tissue pressing against the eardrum.
And the pain was
beyond exclusive. So what did he do?
He unravel a paper clip from his
files to take it out?
Now,
I was all better and all that.
I was grateful for the pain.
But there needs to be some kind of
medically responsible approach as to
how you address the hearing issue.
As much as people bash OTC hearing
aids or maybe Apple AirPods,
they have screenings in there.
So I applaud the that they have a
hearing screening built into the
software Apple AirPods
and OTC hearing aids,
they can take a hearing test in
the comfort of their own home.
Now,
I would not put my license on that
audiogram or threshold
test that they take,
but at least it’s a step
in the right direction.
Agreed.
So now one of the things that wasn’t
on our list of topics that
we should talk about,
but I think I’ll bring this up
because we have consumers,
industry and clinicians all here.
Do you think that as audiology moves
into a provider status that things may
change somewhat because we’d
be seen more as colleagues
with our other
providers and so on?
So anybody have some thoughts on what
happens when we become providers?
Will that modify this stigma thing
just a little more or less or not?
I hope so.
That’s what I’m doing online.
I’m trying to erase that stigma.
I’m trying to show people all of the
things and all of the different hats
that I wear as an audiologist.
I’m a counselor, I’m a mentor,
I’m a diagnostician.
Like I am a hearing aid fitter,
a cochlear implant like programmer.
But at the very bottom of it, I am.
I like what Tony says,
I’m a door opener.
I am here to provide information and
resources so that you can make the
best decision for your life or your
family dynamic because you
actually do know it best.
I think there’s a shift in physician
or provider dynamic that, you know,
my parents just heard the physician
and they did what the physician said.
Now there’s more of a shift of, okay,
they’re giving me some information,
but I’m going to be empowered and feel
confident in making the choices.
Now is the choice I don’t have to
do just what the doctor said.
I’m going to get a second opinion or
I’m going to sit on this information
for a little bit. I hope it changes.
I’m trying to do that for
anybody who’s got kids.
I mean I’ve got a daughter who’s 26.
I mean I didn’t come from a point in
my life where I could go onto the
Internet and self learn everything
from how to build a cabinet to how to
really get a self diagnosis of what
might be going on with me.
I think that opens up the door for
addressing stigma as well too and from
a clinical perspective because now I
think that the consumer is much more
empowered and self learned and can
work with professionals and that only
populates or stimulates you
as you were earlier, Bob,
the ability for people to have this
and open that discussion and see the
appropriateness of different
types of solutions.
I think it also raises quality of care
when our community is more empowered
and learning on their own because it’s
like well, I heard about, you know,
a verifit machine.
Do you have that in your clinic?
I would like for you to do that so I
can have a little bit more data
and feel better about myself.
I agree.
I really like when you’re talking way
at the beginning of this Michelle,
about the hearing loss community and I
think that’s one of the changes that
has happened too is just how much more
information is more readily out there,
even whether it’s always correct but
just the engagement with
social media as well.
But I think because of that educating
that patients are doing on their own,
it also puts the onus on us as
clinicians for those of us who
are to be well educated.
And if the patient for instance is
coming in asking for an
invisible solution,
convincing them that a Rick is
invincible actually isn’t
meeting their needs.
So are you actually sending them out
the door because they knew what they
wanted but you couldn’t help them meet
that or can you help them find
really what they want?
I always feel like the best solution
for any patient is the one that
they’ll wear and it may not be the one
that’s in your book or my book or any
book as the most technological
advanced or, or something like that.
But if they’re, they won’t wear it,
it’s not the best solution for them.
So I think hearing truly kind of to
some of Sherry and Bill’s
points earlier too,
hearing truly what the patient’s
saying or what they’re looking for,
whether it may totally fit their
audiogram or what we think
is going to work,
may not matter because if they won’t
use it. What good is it?
And if they walk out the door with
nothing, we haven’t achieved anything.
Bill, real quick,
the interesting thing too,
obviously I would never call anyone
out and this could be a little
controversial and maybe grate
some people. And that is,
I had a really wonderful conversation
about a year and a half ago when OTC
was, you know, trying to take off.
And in a conversation with two very,
very phenomenal hearing care
professionals, the debate that we had,
a playful debate, was are you,
is your scope of practice practice a
prescriptive dispensing practice,
or is your scope of practice hearing
health care, which brings early,
early onset OTC all the way through
implant, et cetera?
Because I think that we also have to
look at how are our clinicians
positioning themselves.
And there’s nothing wrong if your
expertise is solely on prescriptive.
But if you back up and look at the
entire journey and we look
at that mentality,
that’s where you’ll be able to draw
in more patients as far as
their understanding,
their acceptance and getting
going on that journey.
That really starts with,
I think the way we’re educating the
students, audiology students,
the way they’re coming up through
their educational system,
is that there’s so much focus on the
device and the programming and the
measurement and not enough focus on
the oral rehab and the counseling and
asking open ended questions of your
clients so that you can determine what
their needs are so that you
can better meet those.
And I think part of the solution,
I think,
is really including advocates and
other people with hearing loss who are
willing to share their experiences and
their stories and their expertise
as part of these curriculums,
whether it’s in the classroom or
at annual conferences. I mean,
there’s just so much room for the
person with hearing loss to share
their expertise with the industry.
And it’s nice that it’s
becoming more typical,
but I think that there’s a lot of room
for additional sharing in that regard.
I precept audiology graduate students,
and if so, I don’t know, is that me?
I precept audiology graduate
students and I tell them,
you know what your appointment starts
the second that your name comes out of
their name comes out of your mouth and
you are starting a potential lifelong
relationship with them.
So you get to know them as a person,
get to know what ticks, what talks,
what bothers them,
what is it that fulfills them.
Get to know them as a person,
not as a number,
not as their audiogram.
And I’m trying to Shift that over to
hearing healthcare provider
versus somebody.
Like maybe you’ll see them one time
because that most of the
time is not the case.
Yeah.
And I do want to add that back in the
day when MFI made for iPhone
hearing aid was introduced,
I was shocked by the stubbornness
of audiologists saying, well,
it’s not my job to be connecting
hearing aid to your iPhone.
I don’t go near iPhone type.
Whoa.
This is a great enhancement.
This is the best thing since sliced
white bread. Come on.
This is a lifestyle thing that
you’re providing. Come on.
You’re in the hearing health care
business. Don’t be stubborn.
You’re almost like a horseshoe.
You’re hard to bend.
I’m trying to get you to
bend and see otherwise.
And each time we introduce a new
technology or a different concept.
Oh, that was just. No, we don’t know.
No,
we come from this old school of
disease. How we do things.
We don’t like change.
Let’s hope most of those old school
people are, are moving on.
Bill.
Now we, we really.
It’s kind of time for us to close up
our discussion as we’ve had a very
lively discussion on this topic and,
and listen to a lot of points of view.
We’ve had a whole lot of orientation
right before we, as we close,
you know, does anybody have some.
Just a short comment about the future
and then we’ll begin to
wind down our session?
I do, Bob.
Okay.
No more excuses when
it comes to stigma.
Hearing technology today and what’s
available to us has never been
greater than ever before.
Okay,
I’ll go, I’ll.
I’ll keep it short as well.
I’m going to continue that thought.
Just a general concept.
As we look at the future
through the perspective of, let’s say,
otc, that early onset,
not only does the consumer need to
have access to cool innovation
and confidence,
but the same applies to those
professionals that are working it.
So moving away from, well,
just try this to this is
a solution for you.
And that enthusiasm and confidence
behind it is critically important for
a patient as well to hear
and experience.
So
with that,
I think we will wrap up our session
and I want to thank
our panel for being with us today.
Michelle Wiebke, Bill Schiffmiller,
Michelle Hu, Shari Eberts,
Andrew Bellavia and Tony Sulsona,
thanks so much for being with us today
here at the Future of
Hearing Health Care.
And yeah,
you had to just put your glasses on
right there, Right there, Tony.
Anyway,
so thanks for being with us at Future
of Hearing Healthcare Today and we’ll
see you around the conference.
Thank you, Bob. Thanks, everyone.
Thanks, Bob and everyone.
Thank you.
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About the Panel
Robert M. Traynor, Ed.D is a hearing industry consultant, educator, and author with decades of experience in audiology, specializing in hearing and tinnitus rehabilitation. He serves as adjunct faculty at multiple institutions, including the University of Florida, University of Northern Colorado, University of Colorado, and University of Arkansas for Medical Sciences.
Bill Schiffmiller is the founder of Akoio, a consultancy focused on accessibility and auditory health management. He is a lifelong hearing aid user and previously led the Accessibility initiative at Apple
Tony Sulsona is the Director of the Audiology Channel for Nuance Audio, where he oversees their over-the-counter (OTC) hearing glasses. His work focuses on broadening access to hearing technology through consumer-friendly innovation.
Michelle Wiebke, AuD, currently serves as the Senior Lyric Audiology and Education Manager at Phonak. She brings extensive clinical and educational experience to the field of hearing care.
Michelle Hu, AuD, is a pediatric audiologist with over 16 years of experience and the founder of Mama Hu Hears. She is a bilateral cochlear implant user and supports hearing parents of deaf children through education and advocacy.
Andrew Bellavia is the Founder of AuraFuturity. He has experience in international sales, marketing, product management, and general management. Audio has been both of abiding interest and a market he served professionally in these roles. Andrew has been deeply embedded in the hearables space since the beginning and is recognized as a thought leader in the convergence of hearables and hearing health. He has been a strong advocate for hearing care innovation and accessibility, work made more personal when he faced his own hearing loss and sought treatment.
Shari Eberts is a passionate hearing health advocate and internationally recognized author and speaker on hearing loss issues. She is the founder of Living with Hearing Loss, a popular blog and online community for people with hearing loss, and an executive producer of We Hear You, an award-winning documentary about the hearing loss experience. Her book, Hear & Beyond: Live Skillfully with Hearing Loss, (co-authored with Gael Hannan) is the ultimate survival guide to living well with hearing loss. Shari has an adult-onset genetic hearing loss and hopes that by sharing her story, she will help others to live more peacefully with their own hearing issues.








