Best Short Essay Ever

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cochlear implants

Marc Marschark does it again.

This time he writes a brilliant response to a question about the value of getting a child a cochlear implant (CI) as young as possible and how this is not at all at odds with using American Sign Language (ASL) with the child. The gist is that waiting until the child is “old enough to decide for himself” is to deprive the child of a meaningful opportunity to make such a choice. The evidence in favor of early implantation is, at this point, no longer in dispute in terms of the efficacy of the implant.

However, since children with CI do tend to score lower than hearing peers, he is clear that just getting the CI is not enough on its own.

I believe all deaf children should also be taught ASL even if their CI is working great. ASL allows them to connect to the Deaf community and gives them a fully accessible way to communicate in circumstances where the CI will not do as well. And especially for younger children, I think it is critical not to put a child’s whole communication ability into the CI basket. That is quite a gamble.

NAD Promoting ASL at EHDI

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ASL

I think this National Association of the Deaf (NAD) blog post about the upcoming Early Hearing Detection and Intervention (EHDI) conference is the best position statement I’ve seen on the topic of promoting Deaf Culture and ASL in the EHDI process. I hope NAD’s message is well received in Chicago.

We were lucky that our state has a Deaf Mentor program, because it took us a long time to learn how to get appropriate ASL support through our Early Intervention program.

For us, getting a Deaf Mentor was not simple either. It was Laura’s tenacity in seeking out support that got us a lot of contacts with our state’s Deaf and Hard of Hearing Services office and Hands and Voices. And we still had to apply for a grant to get the Deaf Mentor. Pre-school level support for ASL otherwise seemed to be limited to referrals to what classes in ASL are offered in the area. But that doesn’t do much to help you learn to adapt to raising a deaf child with ASL. It doesn’t even necessarily teach you vocabulary you need to use ASL with an infant.

Hard to say why services for ASL are so much more limited than for those focused on spoken English. Is it that parents don’t care about ASL, so programs aren’t developed? Or is that programs aren’t available, so parents don’t feel ASL is a viable choice?

I do think parents who are interested in spoken English, who pursue hearing aids or cochlear implants, are discouraged from also pursuing ASL. We have actually had professionals involved in our son’s case outright tell us that signing will impede speech. Others have simply dismissed ASL as unimportant. Given our experience I think that hearing parents who do want to pursue ASL have an uphill battle. Maybe hearing parents who focus only on ASL will have less trouble with this because they won’t be as involved with professionals in the “hearing business”. But I still have to wonder, at least in our area, how much ASL support they will find.

Navigating these waters isn’t made easier by the more reactionary elements of the Deaf community who insist that hearing aids and cochlear implants are “audism” or worse. So I’m encouraged to see a Deaf organization like NAD advocating for ASL without resorting to this sort of rhetoric. The more hearing parents feel forced to choose one route or the other, I think the more those parents will not choose ASL at all. If support for ASL feels like it comes with some sort of commitment to avoid spoken language, I think hearing parents will tend to shy away from it.

In my mind, the least that should be done is to provide every family with a deaf child a Deaf Mentor for the first year and separate ASL tutoring for two years. Sending mom to classes at the local community college is not enough. Signing Time videos on loan are not enough. If the family wants to refuse any kind of ASL support, fine– that’s their decision. But they shouldn’t have to fight for support the way we did. We didn’t have to fight for hearing aids and cochlear implants at all, really. These were covered by our insurance. All the doctor and audiology and speech therapy appointments were a lot for our family (especially for Blake and Laura), but we were essentially steered down that path every step of the way once our son’s hearing loss was identified.

In the EHDI process, at least here in Minnesota, ASL was given “equal time” with a lot of other options in all the literature we received. But it is not really getting the level of support it needs to have an equal opportunity to succeed–at least in my opinion. The EHDI journey essentially begins in the audiologist’s office, and because hearings aids and cochlear implants are tied in with the medical establishment, it’s easy to follow that path. And ASL does need more and better exposure and support in this process, I think.

So: Good work, NAD! Thank you and keep it up!

What about Deaf Identity?

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ASL

Alan Watts has said:

Trying to define yourself is like trying to bite your own teeth.

Before my son got his cochlear implant (CI) I felt a lot of internal unrest about it.

I’m sure a least a couple of you are thinking, “You should feel conflict and unrest about that. Cochlear implants are oppressive to deaf people. You are taking away his Deaf identity.” I think maybe Don G. would. He has vlog that includes the phrase “hearing people decide to rob Deaf children of ASL and their Deaf identity!” Blogger RLM “joked” that deaf parents of hearing children should be allowed to “deafize” their kids.

I didn’t think the joke was funny. What is funny to me is this idea that giving a child the opportunity to experience more of the world can somehow take something away from him.

Like some (but, unfortunately, not many) parents who get their kids CIs, we are learning ASL and are not opposed to sending our son to a bilingual/bicultural school where ASL is the dominant “spoken” language. If that seems like the best thing for him when the time comes, then that’s what he’ll get. And when I say that, we aren’t going to wait for him to be an “oral failure” — years behind and missing out — rather we hope to pay attention to what works for him all along. We are really trying to keep an open mind at this point.

On the topic of “Identity”: how can I help him form a Deaf identity when the closest I get myself is a “hard of hearing” identity?

Being hard of hearing did impact my life quite a bit growing up and is part of my identity. The constant ear surgeries (for tubes), the visits to the audiologist, the middle ear infections (it’s really fun having stinky stuff ooze out of your ear all the time just because you went swimming and your earplug didn’t hold well)… As an adult I have a “good ear”, so I always make sure people are on that side of me when walking. I can only talk on the phone using that ear or it sounds like people are miles away…

But hard of hearing (for me) is still fundamentally hearing. I’m not going to deny it or pretend that I have any real clue what it’s like for him. But I also don’t think I can take away my son’s Deaf identity by getting him a cochlear implant. I also don’t think teaching him ASL will automatically give him a Deaf identity either. It’s just not up to me what his identity is.

What I can do is try to make sure that my son and I have as much the same relationship we would have had if he had normal hearing. This is why I think ASL is important. He is always going to have times where whatever hearing tools he uses are going to be inadequate. And it certainly remains to be seen whether his hearing aids or cochlear implant will help him enough that he can get by on spoken language at a level where that is what he’ll “prefer” for day-to-day life.

The good news is that my wife and I seem to be making progress learning ASL (or at least I think so until I try to watch an ASL vlog or actually sign with a Deaf person in ASL). We’ve struggled quite a bit to get our local schools to assist us in this endeavor. And I have to say: this idea that hearing parents can just learn ASL and that everything will be OK is just too magical. If anything is going to prevent parents from learning and using ASL with deaf kids, it’s not cochlear implants.

It took William Stokoe a long time just to get ASL recognized as an actual language! There is just a lot of history here to overcome and slowly, but surely, we will get past it. The more important problem, in my experience, is that there is very little support for families getting the training they need to become confident, full-time ASL speakers. And for kids who do get value from hearing aids or CIs, families who lack training and confidence with ASL are naturally going to let spoken language dominate.

I think, therefore, to continually make this issue one of ASL versus CI is to make the same mistake as doctors, audiologists, and educators who tell families that signing will impair speech development. Spoken language does not impair signing. There are so many obvious obstacles to ASL for the average hearing family that I don’t think I could actually list them all. I know it’s not impossible because so many have done it. But I do know that it’s not as simple as wanting to do it.

So… If a Deaf identity hinges on ASL and exposure to Deaf culture, then a CI can neither help nor hinder. Distracting and upsetting parents who choose both ASL and CIs seems to be the favorite sport of anti-CI advocates. But this does nothing to promote ASL and actually makes parents who have chosen ASL as part of their approach to raising a deaf child feel unwelcome in the Deaf community. How will our children feel whole and learn to celebrate all parts of their identities when their parents are pushed away, given guilt trips, and generally forced to consider the Deaf community at a distance?

How do you think you are helping our deaf children by alienating us and criticizing decisions we make? Does it really have to be all or nothing?

I don’t think the constant debate about CIs does much to improve my child’s well being. Most of the Deaf people I’ve met in the real world have actually made me and my family feel welcome and supported us. Many have CIs themselves or gotten their Deaf children CIs. The negative, either/or discussion around CI is happily a small part of our whole experience, so far, as hearing parents raising a deaf child.

Hand Waving

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Scientific American has a short article on how gesturing while talking may actually help with thinking: “With a wave of the hand“. From the article:

But might gesture also serve another purpose? Many scientists now think that gestures can help the person making them — that moving your hands can help you think. Researchers have become increasingly interested in the connection between the body and thought – in the ways that our physical body shapes abstract mental processes.

The article talks about using gesture to help students learn math, of all things.

OK. Just had to share this one. :)

What About Simultaneous Communication?

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ASL

Dr. DonG has a blog post opposing the use of Simultaneous Communication (SimCom). He referred to a study in the Spring 2009 edition of Sign Language Studies to support his opinion (thanks to Don for posting the article).

This study proves the fairly obvious: that using a half language conveys half the information. In the study, participants were shown a presentation given in SimCom and then asked to answer questions to rate their understanding of what they heard/saw. The results showed that hearing people, by far, got around 75% understanding, while Deaf and Hard of Hearing (HoH) got around 30% understanding.

Unfortunately the study is suspect. It lacks controls and doesn’t report some important information that would be helpful in understanding.

For example, the hearing group includes a PhD educated individual. The HoH group only includes students aged 19-23. Therefore, the scores need to be correlated with education, to determine whether that has an influence. For all we know being a 57 year-old PhD, as opposed to a 19 year-old freshman in college, whether hearing or Deaf, had more influence on understanding than hearing status.

We also have no idea how well the research participants comprehend presentations in their first language. Most of the participants list either ASL or English as their first language. With all due respect to those involved, it is possible that there was some factor influencing the ability of the Deaf/HoH in the study to understand any presentation, not just one given in SimCom.

Also necessary is some attempt to “turn the tables”, by making ASL the dominant language during SimCom and let the spoken English suffer. Then show the presentation to similar groups of Deaf, HoH, and hearing (who know some form of signing). This could help reinforce the notion that partial linguistic information is a primary cause of lack of understanding… and certainly to show that using two communication modes at once does nothing to ameliorate the problem, even when those watching a presentation are familiar with both.

So while I don’t really disagree with Don’s conclusion, this study doesn’t make a very solid case for avoiding SimCom beyond the obvious.

Clearly the hope for SimCom users is that using two modes at once will help the user “fill in the gaps” by getting more information than they would if they only had one language worth of information. But using SimCom in this way is clearly motivated by a desire to make spoken English a primary language, since English is generally the dominant language and the signed “language” is then left to suffer.

Probably the reason for that is that hearing folks have a strong bias in favor of spoken language. The other part of this decision to use SimCom (especially in special education programs) probably stems from differing abilities in the group. If profoundly deaf kids are mixed with those with mild/moderate hearing loss, there is probably some idea that SimCom will allow for the “best of both worlds”, even though it’s really only the best of one world– and for kids with poor access to spoken English, they are bound to suffer. The irony is that the signing may distract the HoH kids from listening well, and thereby also losing information they would have otherwise gained!

(As a side note: the study should probably also be expanded to study this idea as well, what if only the signed video were played? What if there were no video, just audio? Then how would the participants’ understanding be affected?)

That said, for babies and infants, especially when the parents are not yet remotely fluent ASL signers, I don’t see too much harm in SimCom as place to start. At some point though, I guess it makes sense to migrate to either doing some sort of “sandwich” approach (say it in ASL, then say it in English), or just to mode switch depending on context. This allows each language to be complete and accurate.

The biggest problem with starting out using SimCom is the potential for it to become a habit for parents, who– especially with an infant– feel like they give and receive better information if both modes are used at once. I know we often can’t tell what my son is saying or signing, but when he does a word in both modes at once, then we can figure it out. But I expect that as we get better with ASL and he gets access to more ASL-dominant environments, that we will migrate away from SimCom, choosing the appropriate language for a situation given on context.

There is a balance to be found here. Our ASL, so far, is not good enough that we’d really be modeling ASL grammar if we signed voice off, so our son doesn’t really lose anything by us signing and speaking at the same time. But from fluent signers, he needs a fluent ASL models. And as our own ASL improves we’ll need to go voice off more in order for us to get used to using grammatically correct ASL.

Online Fingerspelling Practice

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ASL

This online fingerspelling practice site is awesome. I love the speed levels: slow, medium, fast, and Deaf.

Will Signing Hinder Speech Development?

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ASL

I ran across this thread on AllDeaf: http://www.alldeaf.com/sign-language-oralism/62109-some-thoughts.html

After quoting a study:

In summary, higher speech intelligibility scores acquired in 8- to 9-year-old congenitally deafened cochlear implant recipients were associated with educational settings that emphasize oral communication development and placement with hearing peers. Less accurate speech intelligibility scores at 8 to 9 years of age were associated with educational programs that emphasize the development of language via signs and placement in special education classes. (Tobey,  Rekart, Buckley,  Geers, 2004)

The user Faire Jour starts the thread with, “I think this would be in direct opposition to the idea that signing has no effect on speech development.”

This is largely a straw man argument.  There are two problems here. The first problem is that the study is only about one aspect of speech development: intelligibility. However, the study’s introduction refers to other studies that show that intelligibility is a major factor in effective oral communication. The second problem, the more important issue, is that most advocates for ASL are not saying that signing has no effect on speech development.

In all of these discussions we really need to be clear about what we want to understand. If all we care about is whether children with cochlear implants can pronounce words intelligibly, this is the study for us. But the debate is rarely centered on this one specific topic.

Before the advent of cochlear implants, this same argument against signing was made– that signing with deaf children would prevent them from developing speech. There are some competing theories here. One theory states generally that signing with deaf children has a net negative impact and that the best approach is to use only spoken language with deaf children (“oralism”). The other theory states generally that signing with deaf children has a net positive impact and that in general deaf children should be exposed to as much ASL as possible as early as possible (“bicultural/bilingual”). These are the two main groups, really, and there are variations within each camp. But, ultimately it boils down to whether signing is good or bad.

So with that in mind, let’s look further at what the study says. From the summary:

In summary, higher speech intelligibility scores acquired in 8- to 9-year-old congenitally deafened cochlear implant recipients were associated with educational settings that emphasize oral communication development and placement with hearing peers. Less accurate speech intelligibility scores at 8 to 9 years of age were associated with educational programs that emphasize the development of language via signs and placement in special education classes.

So, as a way of summarizing their findings, the study’s own authors are careful not imply that the educational setting was the cause of the intelligibility, but rather that there was an association.

In fact, they discuss this point rather specifically.

One cannot conclude from these results that oral communication mode or mainstream class placement causes children with cochlear implants to develop high levels of speech intelligibility. Children with a propensity for spoken language may be guided toward oral and mainstream programs. Mainstream classroom placement before and immediately after cochlear implantation was not a significant predictor of later speech development. However, mainstreaming became a significant predictor of speech acquisition with increased cochlear implant use. This result suggests that as children became more intelligible, mainstream placement and greater interaction with normal-hearing peers was the result.

In spite of this care not to draw too strong a conclusion, they do still state that “Communication mode, on the other hand, was consistently predictive of speech outcome.” So they’re saying that if a child is in an environment where speech is the only communication mode that their eventual speech intelligibility will be higher. That’s good information actually. And it’s not counter-intuitive. For the children in oral only environments it’s sink or swim. They are under a lot of pressure to articulate correctly because they have no other way to communicate.

Here is how they did the test:

Intelligibility measures were obtained by having the children repeat 36 sentences varying in length from 3 to 5 syllables. Embedded in the sentences were key words selected from a corpus of words known to predict speech intelligibility in deaf children. The speech samples were recorded, edited under computer control, and played to judges who designated by questionnaire that they had had no exposure to deaf speech. All judges signed consent forms approved by the University of Texas at Dallas institutional review board. Judges were allowed to hear a child speak only once and a sentence only once to avoid familiarity effects. Judges wrote the entire sentence. Correct key words were determined and averaged across the 3 judges per sentence per child. Therefore, the average speech intelligibility scores reported were obtained from 108 judges (36 key words times 3 judges) per child.

So it’s an excellent test of pure articulation.

I think it’s significant that we don’t have any comparison data presented in this study. They did not include any similar data for kids with normal hearing. That’s critical to be able to understand what a “normal” distribution looks like. Without any attempt at a control group of any kind this study is not a scientific experiment, it’s a survey. Also, the larger debate includes deaf children who are not cochlear implant candidates for a variety of reasons.

I don’t want to attack the survey or its methods too much, because it’s a nice, tightly focused investigation which is very informative.

But there are many inputs which are not considered or controlled. Further, there is a wealth of ancillary data that was either not gathered or not included in the article. Just because the children can repeat sentences intelligibly, does that mean that they can express themselves well? This study refers to other studies regarding intelligibility and speech development, so we’ll need to look at those studies for answers to the following question: Does having intelligible speech mean that they are using language effectively to communicate with others?

And I still have other questions: Are they learning things other than how to talk? How are their grades? How are their friendships? How do they get along with their families? What happened to these 8 and 9 year-olds later in life? Those are important questions that are not answered by this survey.

The study supports the idea that expectations and environment are important. A child who is expected to speak and whose environment requires it apparently does speak more intelligibly. But does this mean it’s a good idea to avoid signing with all deaf children? Does this mean it’s harmful to sign with deaf children who will get cochlear implants and be expected to use spoken language well?

This study is informative, but it hardly bolsters the case of the oralists outside of a very limited situation. And even if this survey is conclusive on its own, it leaves a number of important questions unanswered. It doesn’t address any broader risks that the oralist approach might carry with it.

Finally, as a conclusion, I like to share a link to a short write-up from Marc Marschark in response to the question, “Is there any evidence that providing or exposure to sign language to cochlear implanted children could hinder speech development?” His answer?

Actually, the research is very clear that sign language does not hinder speech development in children with cochlear implants… in fact it may facilitate it.

What about the Bilingual Delay?

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Bilingualism

Recently I was involved in an argument over the appropriateness of denying deaf children the use of sign language. The dialog started with a teacher in an oral-only deaf education program stating that she had valiantly protected her students from the dangers of sign language by throwing away fliers about a sign language class she was given to send home with her students.

I told her in no uncertain terms that I was simply astounded, amazed, and angry. ASL is not dangerous and she did the exact opposite of what I hope teachers of deaf children would do. I hope all educators and professionals involved in deaf education would promote the use of sign language. If that’s not comfortable, fine, don’t do it. But at least don’t spread misinformation that sign language will prevent deaf children from learning English or other spoken languages. That is not true.

I said there was no evidence to support the idea that bilingualism will cause language development issues and was told, in reponse, that I was ignorant. At first I was not referred to any actual studies, but when pressed another participant in the discussion did quote one study that he said supported the idea that a bilingual language delay is real.

The study was “Use of the language development survey (LDS) in a national probability sample of children 18 to 35 months old” (Rescorla, Achenbach, 2002). Go read the abstract and notice that the keywords do not include the words “bilingual” or “deaf”. If you have a way to read the full article, I encourage you to do so. That way you can be sure that I am not misrepresenting the study myself.

The primary purpose of the study was to evaluate the accuracy of a specific test form to determine when children have a significant delay in language. As part of the study they did gather information about some bilingual families and they reported that the children in bilingual homes had lower than average vocabulary word counts. It is this one data point which the anti-bilingualists picked up on to support a larger case against using sign language with deaf children. However, the study as a whole simply does not support this.

First, the sample of bilinguals in the study was biased ethnically towards Hispanic families and included no deaf/ASL families. So the data are about hearing children learning two spoken languages which are equally easy for the child to access. Meaning: the study is largely irrelevant to a discussion about deaf kids who often lack full access to any spoken language. However, it might offer some information about bilingualism in general, so we should dig deeper.

Second, there is little detail provided about the bilingual data and because of the ethnic bias of the bilingual portion of the sample population, the data are confounded. Meaning: the summary reporting about smaller vocabulary scores for bilinguals is only marginally informative even if it is reliable.

Third, they point out reasons to suspect the accuracy of the reporting of bilingual parents regarding their children’s vocabulary. Meaning: this data is seeming less and less accurate for bilingual children all the time, isn’t it?

Fourth, the study states that phrase lengths for bilingual children are comparable to those of monolinguals, and points out that those phrases often use words from both languages. The authors explain that they have reason to believe phrase length reporting is more accurate for bilinguals than vocabulary word counts. Meaning: bilingual children are developing quite normally on the measure of language development which is considered by the study’s authors to be the more reliable indicator for these children.

Fifth, the study only considers children under three and the authors are not making any sort of predictive claim regarding the lower vocabulary word counts found in bilingual children. Remember, their primary goal was to analyze the ability of the LDS to identify serious language delays. Meaning: using this study to support an assertion that bilingualism hampers language delay is improper. The study was not designed to investigate such a hypothesis and is quite limited in scope. While the study may provide reasons to want to investigate further, this study in and of itself comes nowhere close to making a case against bilingualism.

So…

Many times I have seen this pattern of misinterpreting studies, inflating claims made in studies and generally overrating the accuracy and relevance of various studies related to language development and linguistic issues in raising and educating deaf children.

When it’s done by people selling “make your baby a genius” merchandise, I don’t worry about it so much. Most of that stuff isn’t going to cause any real harm to children, usually those folks are selling CDs of classical music, videos, books and toys and other stuff most kids are exposed to anyway.

But when the spreading of misinformation is done by professionals who are guiding parents through difficult decisions and times of  uncertainty, it gets my hackles up. Conversely, I’m not thrilled when cochlear implant opponents do the same type of thing.

There is no one way to raise a deaf child, but there are certainly some approaches that are more likely to “work” than others. And when we are offered advice about how to raise our children, clearly we need to take time to really understand how the results of studies are being represented to us… or in the case of this recent discussion I was involved in: misrepresented.

Is Bilingualism Harmful?

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Bilingualism

I knew people were concerned that using sign language with deaf children would interfere with the child’s ability to learn to use spoken language. There is a long history of denying deaf children the use of sign language and insisting that they attempt to speak a language they cannot hear. But before we can really discuss that history, let’s lay a base for the idea that bilingualism tends to work in a child’s favor.

What I did not know before my son was born deaf is that there are people who are actually concerned with hearing children being bilingual! I would have never even thought to worry about that. The idea just sounds absurd to me since so many children all over the world have been raised bilingually and are just fine. Before Blake was born I had been planning to expose him to Spanish in the hopes that he would be bilingual in the two most commonly used languages where we live. Now I’m not fluent in Spanish, but I figured I could stay ahead of him. I’ve studied many languages in my life and have a knack for it. It never even crossed my mind that bilingualism could be a problem. If asked I would have guessed that it was not harmful. Luckily I don’t have to guess about this. There is ample research on this topic. Bilingualism is not bad for kids and is probably good for them.

Laura-Ann Pettito is a professor at the University of Toronto and the Director of the University of Toronto Scarborough’s Genes, Mind & fNIRS Brain Imaging Laboratory for Language, Bilingualism, and Child Development. Her research has produced a lot of evidence to support bilingualism as a positive thing for children. And the earlier the better, it seems.

By contrast, my findings suggested that very young bilingual babies have highly distinct representations of their two native languages quite probably from birth. (Pettito)

An early age of first bilingual language exposure had a positive effect on reading, phonological awareness, and language competence in both languages: early bilinguals (age of first exposure 0–3 years) outperformed other bilingual groups (age of first exposure 3–6 years). Remarkably, schooling in two languages afforded children from MONOLINGUAL English homes an ADVANTAGE in phoneme awareness skills. (Pettito, 2008)

Pettito was involved in an extensive study of bilingual language acquisition that refutes the notion that bilingual children are delayed in language development. She concluded: “one resounding and tangible fact emerges from the studies summarized here: early simultaneous bilingual (and bicultural) language exposure does not cause language delay and confusion and is actually best for the developing child…” (Pettito, 2002)

Furthermore Pettito’s research supports the idea that using American Sign Language (ASL) with deaf infants can help them develop language, because any language recruits and develops the same areas of the brain, even those previously thought only to be involved with spoken language and speech. The National Institute on Deafness and Other Communication Disorders summarized her findings as follows:

Petitto contends that not only is the mechanism the same for hearing and deaf babies, but it arises from the same tissue in the brain. Using positron emission tomography, a brain imaging technique, her laboratory has found that regions of the brain previously thought to be reserved for the processing of speech and sound, such as the superior temporal gyrus, were still functional in deaf people. She proposes that brain tissue involved in acquiring language is not so much dedicated to the processing of speech and sound but to more abstract activities that help us pattern the language we use, be it spoken or signed. (NIDCD, 2002)

Based on Pettito’s research I have to say I am less credulous than ever of the idea that ASL would interfere with a deaf child learning to use spoken language.

But I don’t need to rely just on her research anymore. We’ve been signing with our son since he was four months old when we found out he was deaf. We’ve also been using spoken English with him. He started wearing hearing aids around four months of age and got a cochlear implant when he was about eighteen months old. He’s always been a bit of a chatterbox and he shows no signs of slowing down. If signing has interfered at all, we’re not seeing it.

His first language actually seems to be English, but he does use ASL to emphasize things at times. This is helpful because, like a lot of little kids, his diction isn’t always clear. He’ll also string eight or nine “words” together, only one or two of which are intelligible to me (and maybe to him as well). I won’t understand what he’s saying. But then he’ll throw some signing in and the meaning becomes clear. Also, there’s lots of times when his hearing technology is not on or hasn’t been fully functional. At such times we still have a way to communicate with him. Sign language has been a tremendous benefit to us in our adventure so far.

Preface

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Our son, Blake, is deaf. Here we will write about our experiences with the unexpected adventure he lead us on.