Joey McIntyre Opens Up About Rhys’ Hearing Loss

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Joey McIntyre Opens Up About Rhys’ Hearing Loss
Joey McIntyre Opens Up About Rhys’ HearingLoss – Moms & Babies – Moms & Babies - People.com

When Dad’s a pop star, every minute of the day comes with a soundtrack.

“There’s always music in the house,” says New Kids on the Block’s Joey McIntyre, who lives in L.A. with his wife, Barrett, and their sons Griffin Thomas, 2, and Rhys Edward, 3 months.

But from the day he came home, the youngest McIntyre has heard little of it.

Rhys failed a routine hearing test at the hospital after he was born Dec. 13th, the couple tell PEOPLE, and extensive follow-up tests at UCLA showed that he had severe hearing loss.

Says Barrett, “What’s wild is we will never really know how [anything] sounds for him.”

When the McIntyres got the diagnosis two days before Christmas, “We went through a full range of emotions,” says Barrett, 31. “As a mother you want to protect your kids. I thought, ‘How could I let this happen?’ I felt responsible.”

But as with most cases, there is no known cause of Rhys’ hearing problems.

“You’re just shocked, and your stomach gets in knots,” says Joey, 37.

“It feels like you’re holding your breath. And that feeling lasted for a few days, until you get educated. You go from, ‘Oh my God’ — fearing that someday my son might be walking into the street and I’m calling after him and he’s not going to hear me — to ‘It’s going to be okay’ to ‘It’s going to be amazing.’ Rhys’ hearing loss is part of who he is. His life is going to be as special as Griffin’s. There’s just work involved.”

Doctors says Rhys’ condition will not get better over time, but how he processes sounds can be improved.

“We’re being totally proactive about the situation,” says Joey. That meant signing up for speech therapy and getting Rhys fitted for hearing aids in both ears when he was just a month old.

“You put his hearing aids in, and his little eyes just widen,” says Rhys’ auditory verbal therapist Sylvia Rotfleisch. “He’s so tuned in.”

The weekly therapy sessions with Rotfleisch have become family bonding time, as Rhys’ parents hold him and make particular sounds to elicit coos and other noises from him.

“It does enrich your life,” says Joey. The first time he responded to those sounds, Mom and Dad had tears in their eyes.

“He knows our voices now,” says Barrett. “He’s a sweet, responsive baby. He’s doing all the things he should be for a baby his age, and that’s beautiful. It’s all of the things you take for granted.”

“His hearing aids make a huge difference,” Joey adds. “Griffin goes, ‘Cool hearing aids, Rhys-y.’”

They won’t know for at least another nine months whether Rhys will need cochlear implants (electronic devices surgically inserted behind the ear), but no matter what happens, they’re optimistic.

“A family friend has a 5-year-old girl with hearing loss, and she goes to the same school as her sister,” says Joey. “Just to learn that was like a burst of sunlight. Will Rhys hear as finely as we do? I’m not sure. But he’ll be able to come to one of my shows and take it in [in his own way].”

While they were thrilled to learn that they will be able to “do everything together as a family,” says Barrett, the McIntyres do think about how other kids will treat Rhys when he’s older. Barrett feels his temperament will only help.

“He’s really easy-going; he has that chill vibe,” she says. “Rhys’ hearing loss won’t stop him from doing anything. That’s not to say his first day of school or when he goes to high school, I won’t be sick; It’s hard enough to go to school with curly hair and a zit. But he’ll be so cool that hopefully he won’t have a problem with it.”

For now, the couple revel in family moments like 6 a.m. breakfasts, when Gene Kelly’s “Singin’ In the Rain” is on, Griffin and Mom are dusty with flour from making waffles, and Dad skims the newspaper and talks to baby Rhys.

“It gets better and better,” says Joey, who recently released his fifth solo album, Here We Go Again, and hits the road with the New Kids in May.

“This is the fabric of life. And I can’t imagine mine without this, because Rhys is awesome and perfect and great.”
 
Of course not, Frisky. Just like PFH's said in his other thread..it is all about speech and getting the child to talk.
 
The parents are hearing. My guess is they know nothing of ASL. And the baby can hear sounds with a HA, so it's not totally deaf.

If deaf parents have a hearing baby, and the parents can't talk, how are they going to talk to the baby? Same as for hearing parents having a deaf baby, they don't know ASL.

Some hearing children of deaf parents who can't speak, are behind on their own speech, since they were taught ASL and not speech.

If I had a deaf baby, I would expose him/her to both worlds. ASL, and talking. But I would not expect the baby to talk normally, that would take years of schooling.

It's a "new world" for hearing parents that have a deaf child. I'm sure, in time, they will learn more of the deaf culture as their child gets older...and I'm just as sure that when a deaf parent, who has no speech, has a hearing baby, they will want to expose the baby to sounds and speech and also ASL.
 
Most deaf people are happy to exposure their hearing children to the hearing world (afterall, how else they know how to interpret for them). I do it. It's too bad that some hearing parents don't do the same for their children.
 
If deaf parents have a hearing baby, and the parents can't talk, how are they going to talk to the baby? Same as for hearing parents having a deaf baby, they don't know ASL.

Some hearing children of deaf parents who can't speak, are behind on their own speech, since they were taught ASL and not speech.

Yeah... I can tell you haven't spent a lot of time in the Deaf culture.

Many CODAs (children of the Deaf) become interpreters. In fact, it used to be that interpreting field were seemingly almost exclusive to CODAs according to a few of my 'terps.
 
When I was a huge fan of NKOTB, I knew there was something special about them. Who knew that one of would end up with a deaf child like me.

Did I mention that I got to hug Danny when they came to my town on their bike. It was awesome.
 
The parents are hearing. My guess is they know nothing of ASL. And the baby can hear sounds with a HA, so it's not totally deaf.

If deaf parents have a hearing baby, and the parents can't talk, how are they going to talk to the baby? Same as for hearing parents having a deaf baby, they don't know ASL.

Some hearing children of deaf parents who can't speak, are behind on their own speech, since they were taught ASL and not speech.


If I had a deaf baby, I would expose him/her to both worlds. ASL, and talking. But I would not expect the baby to talk normally, that would take years of schooling.

It's a "new world" for hearing parents that have a deaf child. I'm sure, in time, they will learn more of the deaf culture as their child gets older...and I'm just as sure that when a deaf parent, who has no speech, has a hearing baby, they will want to expose the baby to sounds and speech and also ASL.

In my whole life, I met so many deaf parents of hearing kids do speak. I have never met anyone who can't speak because of deaf parents what in your bold. Have you met them before? I even met deaf single mom who don't speak of hearing down syndrome can sign and speak both.
 
In my case, I feel like my speaking and listening ability is hindering our son's speech. He can say it correctly but when he is talking, he goes back to his old habit. and I feel I might be responsible because I've gotten used to his way of speaking that when he was speaking correctly, I couldn't understand him so he goes back to his old habit of speaking. Also, he depend on me to teach him how to talk and I think I confuse him too much with my own speaking ability. I feel it is less confusing if I just leave it to the hearing people to correct him.
 
Yeah... I can tell you haven't spent a lot of time in the Deaf culture.

Many CODAs (children of the Deaf) become interpreters. In fact, it used to be that interpreting field were seemingly almost exclusive to CODAs according to a few of my 'terps.

You guessed right...only 2 yrs. at a deaf school, and my small town had no deafies there....but I've met lots of deafies here in Fla.....As for CODA children, it's great they can sign/intrepret. I have 3 boys, (adopted, hearing) and very seldom do I have them intrepret for me! The principal at one of my boys school, when I met him (to enroll one of my sons in advanced classes), when he found out I was deaf, he immediately went to my son to talk....that made me angry! I told him, "my son and my other 2 boys are not CODA children!....If you feel my deafness makes you uncomfortable, then pls. write down what you have to say". That basically shut him up....I feel I was in "the right", as I'm the Parent, deaf or not....I don't feel children should be subjected to adult business or even having to intrepret for the parents, only in certain cases.....My boys can sign, but they are not fluent, and neither am I.
 
In my case, I feel like my speaking and listening ability is hindering our son's speech. He can say it correctly but when he is talking, he goes back to his old habit. and I feel I might be responsible because I've gotten used to his way of speaking that when he was speaking correctly, I couldn't understand him so he goes back to his old habit of speaking. Also, he depend on me to teach him how to talk and I think I confuse him too much with my own speaking ability. I feel it is less confusing if I just leave it to the hearing people to correct him.

I have had the same problem (when my boys were younger)....they pronounced words the way they heard me pronounce. Some of them were wrong, and they corrected me! :giggle: We've had some hilarious moments! But all in all, the more they interact with other hearies, in school/friends, it all straightens out well.
 
In my whole life, I met so many deaf parents of hearing kids do speak. I have never met anyone who can't speak because of deaf parents what in your bold. Have you met them before? I even met deaf single mom who don't speak of hearing down syndrome can sign and speak both.

The closest I've come to hearing anything like this is that CODA's will often use "deaf voice" with their parents until they are exposed to the larger hearing world (usually when they start going to school). No personal experience here though, so I can't say for sure how much of this is fact.
 
In my whole life, I met so many deaf parents of hearing kids do speak. I have never met anyone who can't speak because of deaf parents what in your bold. Have you met them before? I even met deaf single mom who don't speak of hearing down syndrome can sign and speak both.

What I meant was:...it's not that the hearing child of a deaf parent will never speak....it's just that in a lot of cases, the hearing child's speech is somewhat "delayed". Hearing children with deaf parents/siblings are more prone to "sign" than speak, if no speech is used in the home. I believe that early intervention is necessary in those cases....day care, early Pre-K, intereaction with other hearing children, etc......The same for deaf children in an all-hearing family! So, it goes both ways.
 
Hearing children are very exposed to hearing world. It is very rare for them to live in a sheltered life. I don't think deaf people can keep them from hearing when they go out shopping, watch tv, visit friends or family or church, etc. Children can pick up language easily that way. But it is the opposite for deaf children. they can not pick up language easily unless someone show them.

My grandma's sister have two CODA (one of them was married to a hearing son of a deaf teacher) They grew up in ASL and I haven't noticed any problems. She is very adaptable to the hearing world without early intervention. speaking of that, I should ask my grandma for her email.
 
RR, yeah. some cases what you just said are true. I am just curious, Have you met them who speak with somewhat delayed before? I know some hearing parents of hearing kids do have somewhat delayed too. In my opinion, it depends on kids and their learning abilitiy of learning how to speak or read itself, or by bringing up being exposing in a setting environment in both ways.
 
RR, yeah. some cases what you just said are true. I am just curious, Have you met them who speak with somewhat delayed before? I know some hearing parents of hearing kids do have somewhat delayed too. In my opinion, it depends on kids and their learning abilitiy of learning how to speak or read itself, or by bringing up being exposing in a setting environment in both ways.

Yes, I have. A friend had 2 deaf little girls and 1 hearing son (he was the youngest). She had no speech at all, taught the girls ASL and the little hearing boy knew some ASL also. He very rarely, if ever, "talked"...altho' he could hear.....she did enroll him in daycare with other hearing children, so his speech got better and better. He's a teenager now and is doing fine.
 
I thought this sentence was interesting: "They won’t know for at least another nine months whether Rhys will need cochlear implants."

Need? :hmm:
 
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