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This is Chris Sosa with the Becker's Healthcare

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podcast.

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I am thrilled to be joined by doctor

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Abby Meyer, medical director of ENT and facial

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plastic surgery at Children's Minnesota, and Chelsea Kimlinger,

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an audiologist at the health system. They're with

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us to discuss Children's Minnesota's pediatric cochlear implant

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program. Doctor Meyer and Chelsea, thank you for

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joining us today.

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Thank you for having us.

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Thank you.

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Wonderful. For those of us,

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for those of us in the audience rather

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who do not are not familiar with your

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work, could you please introduce yourselves and tell

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us a bit about your backgrounds?

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Happy to. So my name is Abby Meyer.

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I'm a pediatric otolaryngologist.

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I did my training at the University of

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Minnesota and at Seattle Children's Hospital, and I've

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been in practice for a little over 13

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years now.

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I am the medical director at Children's Minnesota

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for ENT for and I've done that for

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2 years. And then prior to that, I

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was the director of audiology services at Children's.

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And one of the main focuses of my

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practice is caring for children who are deaf

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or hard of hearing.

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I am Chelsea Kimlinger, pediatric audiologist at Children's

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Minnesota.

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I work with children of all ages

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and their families to help,

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reach individualized

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hearing and speech and language outcomes.

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I am one of 2 audiologists that helped

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to start the cochlear implant program here a

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little over 10 years ago.

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So I have a passion for working with

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children and their families

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entering the cochlear implant process.

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Fantastic. Thank you both so much for filling

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us in, and thank you for all the

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wonderful work that you do in this area.

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As you mentioned, Chelsea, Children of Minnesota is

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working on 10 years of this pediatric cochlear

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implant program. My question is, what do you

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see as the biggest changes in cochlear implants

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over the last 10 years?

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Yeah. I would say that one of the

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biggest changes we have seen in this first

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decade of our program

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is the expansion of who is a candidate

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for a cochlear implant, particularly

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for 2 populations of children,

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that first group being single sided deafness.

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So in this population a patient has typical

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hearing in one ear and no functional hearing

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in the other ear. And until recently we

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didn't really understand how the brain could combine

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the acoustic hearing in the typical ear and

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the electric hearing from the cochlear implant in

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the other ear,

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together in a meaningful, useful way.

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And we know that one of the many

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factors that contribute to successful outcomes with a

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cochlear implant is dedicated practice with the cochlear

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implant.

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But when you're listening with a cochlear implant

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in one ear and you have typical hearing

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in the other ear, your brain is gonna

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crutch onto that typically hearing ear because it

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obviously does so well.

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But in order to achieve maximum benefit from

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your cochlear implant, you really have to exercise

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the device by itself.

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In

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most recent years, we've seen technology advancements

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where cochlear implant processors are now incorporating Bluetooth

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technology

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into their processors,

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and this has really opened the door for

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successful hearing rehabilitation in this population.

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Streaming through Bluetooth allows our single sided deafness

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patients to strengthen the auditory pathways with their

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cochlear implant without crutching onto the other side.

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And this has led to greater acceptance and

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success with their cochlear implant

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and offers the ability for these patients to

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take advantage of binaural hearing.

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And some of those examples of binaural hearing

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include improved listening and noise, better localization,

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better sound quality, and reduced listening fatigue.

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The other population we are serving more of

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now is younger infants.

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In 2020, the FDA actually lowered the approved

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age for cochlear implantation in infants with bilateral

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profound hearing loss from 12 months to 9

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months of age.

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However, the literature actually overwhelmingly

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supports implantation

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in these children even earlier, as young as

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6 months old.

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And implanting at 6 months old is really

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becoming the gold standard here in the United

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States at pediatric,

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cochlear implant centers, and it has actually already

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been the gold standard in Europe and many

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places,

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in Australia as well.

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And this is wonderful because we know that

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early implantation leads to a more typical trajectory

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of spoken language development. So the earlier that

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we can get these patients started with this

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process, the better.

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Thank you, Chelsea. It sounds like there have

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been some huge strides made, and I do

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wanna touch about on the future of these

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implants a little bit later.

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But before we get to that, doctor Meyer,

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could you do us a favor and please

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describe the connection between the surgeon and audiologist

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when it comes to these cochlear implants?

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Absolutely. Well, I mean, I I hope the

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feeling is mutual, but I just, I can't

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stress enough just

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how valuable a strong relationship between a surgeon

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and an audiologist is.

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We have to be on the same page,

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and, you know, we need to make sure

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that what we're thinking also,

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aligns with what the family wants for their

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child, their goals for their child. So that

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communication,

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that open communication, frequent communication

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is just so critical to the success of,

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of any cochlear implant program, but especially for

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children.

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So we, we're very fortunate. I think we

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have just really strong relationships between our surgeons

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and our audiologists.

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I've been working with Chelsea and,

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Lisa, who was another one of the original

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audiologists who started the program

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for the entire 10 years,

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and

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it's just been a joy to to work

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with both of them and all of the

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other people that have been added to our

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team since that time. I think what was

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really great is I constantly learn from our

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audiologists, and I think that I'm hoping, anyway,

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that they learn some things from us as

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surgeons too. And, you know, we both bring

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different perspectives, different experiences, different expertise,

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to this kind of partnership, but I think

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that they're complementary and we really continue to

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grow and I think also push each other,

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to stay up to date on what's, you

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know, the newest in the literature and and

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push each other to say, well, how can

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we make our program better? How can we

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take better care of our patients? So

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having that just open dialogue,

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open relationship, and also open to feedback is

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just so critical, and I feel very lucky

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that our program has all of that.

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Thank you, doctor Meyer. I'm glad you mentioned,

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commune the communication

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aspects

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of making this program work. And, Chelsea, you've

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already touched a little bit on on some

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of the different types of patients that you're

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dealing with at Children's Minnesota.

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Building onto that, what strategies have been most

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effective in meeting each child and and families'

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individual hearing goals?

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Yeah. I find that one of the most

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important things that we can do as provide

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providers in the cochlear implant,

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specialty

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is counseling on realistic expectations.

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We know that each child has their own

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unique circumstances

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and that that is going to contribute not

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only to their candidacy for a cochlear implant,

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but also what their outcomes with the cochlear

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implant may be. So it's really important for

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us to have honest and open conversations with

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families

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about the outcomes we may expect for their

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child so that they can make an informed

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decision on if a cochlear implant is the

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right thing for this child and their family.

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So, again, making sure that we are being

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honest and open with families,

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from the very beginning

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about what their child could potentially get from

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a cochlear implant so that they can make

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the best decision.

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One of the reasons I really love working

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with cochlear implants in Audiology is that there

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are a lot of appointments,

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and you get to know patients and their

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families pretty well.

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And when we have a better idea of

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what a patient's day to day life is

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like, we are able to better help them.

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For example,

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who is spending time with the child during

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the day? If both parents are working outside

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of the home, you know, who is watching

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that child? Because they are spending a lot

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of time with that child and we are

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going to need their support,

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in helping achieve the goals that we are

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hoping to achieve with this child.

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So I like to encourage families to invite

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these family members

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to some of our appointments so that they

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can learn more about cochlear implants and ask

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questions

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so that they feel more empowered to help

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support these children in their when they're in

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their care.

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Another example of this is, you know, getting

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to know does the patient spend time between

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2 different households?

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This is actually really helpful for me to

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know because when I'm ordering equipment for the

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child, in these cases, I like to make

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sure I have, you know, 2 full sets

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of batteries, 2 full sets of chargers

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so that these can be split between the

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households and parents don't have to constantly be

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worrying about packing everything every time the child

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transitions from one home to the other.

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So yeah. Really getting to know the kids

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and the family dynamics so that we can

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best support them because, you know, no 2

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child no 2 children are exactly the same,

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and we really need to get to know

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them better to help support their best outcome.

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This is a question for either doctor Meyer

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or Chelsea, but what sort of feedback have

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you gotten,

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from parents and

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really the children who have been receiving these

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implants and how it's enhanced their lives?

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I I mean, I think it's incredible as

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you see, you know, now that we've have

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you know, some of the kids that we

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implanted in the early years of our program

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are now

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know, in late elementary and even, you know,

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thinking about middle school. And to see them

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grow into these just, you know, really lovely

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people and see how far they've come. You

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know, when you meet a family

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and they receive the news that their child

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has

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you know, that is deaf or hard of

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hearing, and especially if it's a very significant

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hearing difference that puts them,

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you know, on the path towards cochlear implantation,

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it can it it often comes out of

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nowhere for these families. So you see,

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where they start, you know, where they start

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this journey. And then when you see them

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on the other side of the journey where

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their their kids are, you know, out on

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the soccer field, they're having sleepovers with their

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friends, they're, you know, they're just living their

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best life. It

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I mean, it is pretty it is a

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very special and remarkable thing. And I think

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I mean, families,

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for the most part, are, I I think,

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just incredibly grateful and and but it's kind

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of their normal life. You know? It just

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becomes, like, well, this is what we do.

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And

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and that's another special part to see how

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they come so far

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and and, you know, saying how am I

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going to do this? How are we gonna

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do this as a family?

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To then being, like, well, this is just

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what we do is is is pretty remarkable.

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That's certainly very heartwarming, and hopefully, more children

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will have

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access to this technology as time goes on.

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Another question for you, doctor Meyer, and that

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simply is what are you excited about or

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focused on when it comes to the future

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of pediatric cochlear implants?

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Yeah. I mean, it's an an incredible time

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to be in our field. There's just so

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much that's changing all the time. Some of

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the things that Chelsea,

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you know, pointed out as far as where

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we've come in the past 10 years. I

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think a couple of the things, you know,

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and most of what we're working on is

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really maximizing the benefits, knowing

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who could best benefit from this amazing technology

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and when. When is the best time to

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do it? How can we,

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put the child in the best position to

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meet their potential,

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with this implant and this technology?

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So, one example that we have,

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is, you know, unfortunately we do see children

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that have meningitis and meningitis,

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is a very,

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significant risk factor for developing a significant hearing

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loss. So,

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and it's

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a cause of hearing loss that if it's

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not identified early and intervened for early, it

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can,

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it may not ever be able to, have

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a cochlear implant, for example, that's very time

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sensitive. So,

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there really wasn't a meningitis protocol to follow

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that was published, and it was the standard.

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So we had a very small,

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baby that came into our hospital with meningitis.

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And,

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we actually, she was the youngest patient to

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receive a cochlear implant. We did it here

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at Children's Minnesota, and that really

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helped us develop a meningitis protocol.

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Basically,

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a protocol to follow when a child is

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admitted to the hospital for meningitis, how to

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follow their hearing so you don't miss that

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critical window, and we've since published that protocol,

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for other centers to use. So that's, you

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know, an an exciting thing that we're very

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proud of. I think in Minnesota, you know,

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we're the only state that screens all infants

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for congenital cytomegalovirus,

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and that is a virus that can cause,

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hearing loss later in life or it can

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cause a child to be born deaf or

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hard of hearing.

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And so we're in in a very exciting

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position in the state of Minnesota

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to,

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be able to follow these children and understand

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because a lot of them, are not I

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shouldn't say a lot, but several of these

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children that are born of this end up

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being cochlear implant candidates and and determining, okay,

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when when is the best time to do

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it? What are the other things we should

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be watching for?

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We're in a really great position that we

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can,

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you know, share this knowledge that we're learning.

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I think even things like,

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like gene therapy. So there is,

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there is a specific

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genetic cause of hearing differences that actually causes

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something called auditory neuropathy that

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there are successful gene for gene therapy for

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this specific gene change.

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And I think this is probably just the

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start of

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other

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genetic causes of hearing differences to potentially have

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that option of, gene therapy. So it's really

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exciting. And then figuring out, well, how does

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the role of cochlear implantation,

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you know, how do we

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tie that into these advancements in in medicine?

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And and do we learn more about, you

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know, again, who should have a cochlear implant?

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When should we do it? And is the

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gene therapy, how does that play a role?

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So it's it's really kind of exciting. There's

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all of these new things. And and I

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think the other thing is that the implants

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themselves

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continue to just get better and better all

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of the time. The tech the advances in

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technology,

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you know, like Chelsea mentioned, just being able

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to stream to practice with the implant, which

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is really critical for some patients.

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It's just crazy to think how much things

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have changed in the 10 years that I've

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been doing this surgery or actually 13 years

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that I've been doing this surgery, but 10

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years here at Children's. And then to think,

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well, where are we gonna go over these

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next 10 years is is just is pretty

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amazing to to think about and to be

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a part of.

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Doctor Mein, Chelsea, thank you so much for

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being so generous with your time and insights

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on this program. We cannot wait to share

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them with our audience, and we look forward

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to connecting with you guys again soon.

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Thank you so much. Thank you for having

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us.