Sunday, March 10, 2013
I know it's been quite a long time since we wrote anything. So let me give you an update on Luke.
We met with the team of doctors at University Rainbow and Babies Children Hospital to discuss Luke's options and cochlear implant. Once the doctors were able to determine which type of cochlear implant Luke had, they contacted the manufacture to see if we could get an outside processor for it so we would know if it works and if he can hear.
A representative from the manufacture was very helpful and glad tocome to visit us at the office with the software. Once they hooked up the processor they were able to program it in order to give him sound. Now every month we visit the audiologist in order for her to program the implant. This is called mapping. We want to reach a level that is comfortable for Luke.
The only problem we discovered with his implant is that only 5 of the 12 electrodes are working. Now we have to determine if that will be enough for him to hear and discern speech sounds.
In December Luke received a hearing aid. The hearing aid is on loan from the manufacture. Just like the implant we need to decide if he is receiving enough sound in order for him to discern speech sounds in order to talk. Also, our insurance company requires a trial period of hearing aids before allowing implant surgery.
We have the hearing aid on loan to us until April 30. Then the doctors will need to make a decision if they should put an implant in the other ear. From what I have read about people who are profoundly deaf (which is Luke), they can not hear enough with a hearing aid in order to learn language. We're quite certain that we will need to put a cochlear implant in the other ear.
Luke is doing very well with bonding and attaching to us and the other children. It seems like he has always been part of our family. He fits right in with all the kids. He loves to play outside even when it's cold or gloomy. He is very good at letting us know what he wants.
He is also very smart and is learning his colors, shapes, and numbers. He is also learning how to write and recognize his name. We are teaching him new signs, but he sees a speech therapist who specializes in cochlear implant patients. We all want him to start learning to rely on his hearing and training his brain to recognize sounds.
We met with the team of doctors at University Rainbow and Babies Children Hospital to discuss Luke's options and cochlear implant. Once the doctors were able to determine which type of cochlear implant Luke had, they contacted the manufacture to see if we could get an outside processor for it so we would know if it works and if he can hear.
A representative from the manufacture was very helpful and glad tocome to visit us at the office with the software. Once they hooked up the processor they were able to program it in order to give him sound. Now every month we visit the audiologist in order for her to program the implant. This is called mapping. We want to reach a level that is comfortable for Luke.
The only problem we discovered with his implant is that only 5 of the 12 electrodes are working. Now we have to determine if that will be enough for him to hear and discern speech sounds.
In December Luke received a hearing aid. The hearing aid is on loan from the manufacture. Just like the implant we need to decide if he is receiving enough sound in order for him to discern speech sounds in order to talk. Also, our insurance company requires a trial period of hearing aids before allowing implant surgery.
We have the hearing aid on loan to us until April 30. Then the doctors will need to make a decision if they should put an implant in the other ear. From what I have read about people who are profoundly deaf (which is Luke), they can not hear enough with a hearing aid in order to learn language. We're quite certain that we will need to put a cochlear implant in the other ear.
Luke is doing very well with bonding and attaching to us and the other children. It seems like he has always been part of our family. He fits right in with all the kids. He loves to play outside even when it's cold or gloomy. He is very good at letting us know what he wants.
He is also very smart and is learning his colors, shapes, and numbers. He is also learning how to write and recognize his name. We are teaching him new signs, but he sees a speech therapist who specializes in cochlear implant patients. We all want him to start learning to rely on his hearing and training his brain to recognize sounds.
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