Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Hi, I had implant 3-11' and have almost same hearing as everyone, I have progressed to where people sound like they are from England and have a bad head cold. How I have adjusted to telephone usage: 1. computer(laptop is best) is a telephone with MagicJack. Your bk cable connects to the processor and to computer speaker output. 2. Your processor cable connects to wireless telephone. Maybe one problem most phones have 2.5mm jack. processor plug is 3.5mm. need adapter cable from RadioShack or EBAY etc $3-5. You might have to switch mic speaker wires in adapter cable. Just speak into phone and hear 3. This also works vary good with TV and Radios that have earphone jacks. The processor has crystal like microphones about the size of a head on a pen. crystal mics detect sounds and pass them all on at the same volume level making hearing understanding difficult for us. A dynamic mic keeps low volumes low and high volumes high.but smallest 4 times size of our processor. the above procedures bypass the processor mics. I guess for safety reasons the processor mics are still on about 25%. Good health and happy hearing Wayne, retired El Eng Me,Tippy,Penny and We N.F.-Dukee From: carol@... Date: Thu, 26 May 2011 12:01:35 -0400 Subject: Re: hearing with CI Has the audiologist asked for a Cochlear Clinical Specialist to help out at a mapping? If not, please request this. They are available to help out with difficult cases. That is what they do. After all, not everyone is a text book case and the company acknowledges this. Many people have problems with high pitched sounds but that should be able to be mapped so you could hear more normally. So if your hearing is still not what it should be, please be an advocate for yourself and do request this. And.... if your audiologist will not go along with this request, it is time to move on to a different audiologist. Happy Hearing! Carol Boca Raton, FL Cochlear America Nucleus 24C - left ear - Sprint 12/11/01 then 3G then upgraded to Freedom on 2/19/08 Cochlear America Freedom right ear -implanted 3/01/06 - activated 4/06/06 From: Judy wilkins Sent: Thursday, May 26, 2011 11:52 AM Subject: RE: hearing with CI , I feel the same way you do. I only heard great successful stories about their cochlear implant but my experiences have not been a success story. I had implanted " Cochlear Freedom " about 3 years ago and I still cannot speak on the phone, hearing chipmunk voices, high pitch voices, and you can forget about me hearing even a small group. I can only hear when someone is speaking to me directly and there is no background noise. My biggest problem is back ground noise of any kind. It picks up those sounds so clearly but yet I still cannot hear a person talking unless it is in a quiet place and it's one-on-one. I have had many mappings and they all turn out the same, everyone sounds like Mickey Mouse down in a deep, deep well. I am very frustrated and seeking a new audiologist to try and help me. So, you are not the only one, and I became deaf overnight due to medication the hospital gave me 3 years ago. So I have heard all my life until the last 3 years and this is the most horrible thing that has happened to me. Judy > mailto:%40 > From: mailto:lisayuan3%40 > Date: Wed, 11 May 2011 15:34:30 -0700 > Subject: Re: hearing with CI > > Hello, > > I've been hesitant to post any messages here, because the last thing I want to > do is create any negativity relating to CIs. Obviously, from everyone's posts, > the CI process is highly successful and has greatly improved the lives of most > people. However, I am one of the few people that, after over a year of having my > implant, am still hearing chipmunk voices and constant high-pitched tones, even > after repeated mapping sessions. My comprehension is still poor too. The device > has been tested, and CT scans have been conducted, yet everything looks normal. > So audiologists are stumped. The last visit I had, my audiologist confided that > even if my comprehension improves, if the sound quality is still poor after all > this time, it's not likely to get much better. So I may be stuck hearing this > high-pitched squawking forever, unless I decide to just stop wearing the > implant. > > I do not want to discourage anyone from getting an implant, because I know from > the stats, from all the posts here, and from everyone I personally know that has > one, that the results are usually miraculous and wonderful. I fully believe in > the process. But part of me also wishes that I had heard more of the less > successful stories when I was doing all my initial research. I may be part of > the 1% or less who have had less than thrilling results, but I still think > people should be aware of the possibilities. > > - > > > > ________________________________ > From: Deborah Herczog <mailto:dherczog%40> > mailto:%40 > Sent: Wed, May 11, 2011 4:08:38 AM > Subject: hearing with CI (to Joe) > > > I highly recommend NOT listening to opinions about CI hearing results from those > > who do not have experience working with CIs (or using one). The brain has > incredible plasticity, and for those of us who were post lingually deafened, it > works to make sense of input and we convert mentally to what was once familiar > because this is what the brain wants to do. > > Indeed initially many of us " hear " chipmunk voices (or in the case of my 2nd CI, > > a less common low pitched accent), but this typically declines/vanishes over > time with practice/rehab. Best analogy I can think of is that the brain routes > the " new " sounds from CI into old comprehension pathways and learns to > reinterpret that input along those old channels or circuitry so that sounds > begin to register a lot like the old ones. This means that the voices of family > > and friends now sound just like they used to. > > Having said that, when my CI was turned on, I was so ecstatic to comprehend > anything, that I said I would happily take that and only that for the rest of my > > life if that was all I got. Another huge benefit is that hearing with a CI is > so relatively automatic compared to hearing with hearing aids (in quiet) that I > started to wonder if the qualification standards should be lowered, meaning > those with moderately severe loss might hear better and more easily with CI than > > with hearing aids. I only wish I had had the surgery years earlier as that would > > have saved me a lot of stress, exhaustion, emotional wreckage. It takes post-op > > work (practice) and some CI patients do not have miraculous outcomes, but as my > Mayo Clinic audiologist says, these days, essentially 100% of patients hear > better with CI than before. > > PS: an ENT from a large practice in Texas told me that CI sound was fake, I > couldn't use CI with hearing aid, that I didn't qualify for CI anyway, and that > I should just take disability. I am a health care provider myself, and in my > opinion that was malpractice (or at least definite negligence) and resulted in > my feeling increasing despondency which could have had a very negative outcome > because I was at rock bottom. BUT thanks to HLAA information I figured I should > > get a second opinion and I am now leading a wonderful hearing life thanks to the > > CI. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Wayne, So you have to set up the MagicJack to use the laptop sound card to hear, and the phone handset to speak...correct? Jim On 5/26/2011 3:36 PM, wayne stephens wrote: > Hi, I had implant 3-11' and have almost same hearing as everyone, I have progressed to where people sound like they are from England and have a bad head cold. > > How I have adjusted to telephone usage: > > 1. computer(laptop is best) is a telephone with MagicJack. Your bk cable connects to the processor and to computer speaker output. > > 2. Your processor cable connects to wireless telephone. Maybe one problem most phones have 2.5mm jack. processor > plug is 3.5mm. need adapter cable from RadioShack or EBAY etc $3-5. You might have to switch mic speaker wires in > adapter cable. Just speak into phone and hear > > 3. This also works vary good with TV and Radios that have earphone jacks. > > The processor has crystal like microphones about the size of a head on a pen. crystal mics detect sounds and pass them > all on at the same volume level making hearing understanding difficult for us. A dynamic mic keeps low volumes low and > high volumes high.but smallest 4 times size of our processor. the above procedures bypass the processor mics. I guess > for safety reasons the processor mics are still on about 25%. > > Good health and happy hearing > > Wayne, retired El Eng > > Me,Tippy,Penny and We N.F.-Dukee > > > > > > From: carol@... > Date: Thu, 26 May 2011 12:01:35 -0400 > Subject: Re: hearing with CI > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Has the audiologist asked for a Cochlear Clinical Specialist to help out at a mapping? If not, please request this. They are available to help out with difficult cases. That is what they do. After all, not everyone is a text book case and the company acknowledges this. Many people have problems with high pitched sounds but that should be able to be mapped so you could hear more normally. > > So if your hearing is still not what it should be, please be an advocate for yourself and do request this. And.... if your audiologist will not go along with this request, it is time to move on to a different audiologist. > > Happy Hearing! > > Carol > > Boca Raton, FL > > Cochlear America Nucleus 24C - left ear - Sprint 12/11/01 then 3G then upgraded to Freedom on 2/19/08 > > Cochlear America Freedom right ear -implanted 3/01/06 - activated 4/06/06 > > > > From: Judy wilkins > > Sent: Thursday, May 26, 2011 11:52 AM > > > > Subject: RE: hearing with CI > > > > , > > > > I feel the same way you do. I only heard great successful stories about their cochlear implant but my experiences have not been a success story. > > > > I had implanted " Cochlear Freedom " about 3 years ago and I still cannot speak on the phone, hearing chipmunk voices, high pitch voices, and you can forget about me hearing even a small group. I can only hear when someone is speaking to me directly and there is no background noise. My biggest problem is back ground noise of any kind. It picks up those sounds so clearly but yet I still cannot hear a person talking unless it is in a quiet place and it's one-on-one. I have had many mappings and they all turn out the same, everyone sounds like Mickey Mouse down in a deep, deep well. I am very frustrated and seeking a new audiologist to try and help me. So, you are not the only one, and I became deaf overnight due to medication the hospital gave me 3 years ago. So I have heard all my life until the last 3 years and this is the most horrible thing that has happened to me. > > > > Judy > > > >> mailto:%40 >> From: mailto:lisayuan3%40 >> Date: Wed, 11 May 2011 15:34:30 -0700 >> Subject: Re: hearing with CI >> Hello, >> I've been hesitant to post any messages here, because the last thing I want to >> do is create any negativity relating to CIs. Obviously, from everyone's posts, >> the CI process is highly successful and has greatly improved the lives of most >> people. However, I am one of the few people that, after over a year of having my >> implant, am still hearing chipmunk voices and constant high-pitched tones, even >> after repeated mapping sessions. My comprehension is still poor too. The device >> has been tested, and CT scans have been conducted, yet everything looks normal. >> So audiologists are stumped. The last visit I had, my audiologist confided that >> even if my comprehension improves, if the sound quality is still poor after all >> this time, it's not likely to get much better. So I may be stuck hearing this >> high-pitched squawking forever, unless I decide to just stop wearing the >> implant. >> I do not want to discourage anyone from getting an implant, because I know from >> the stats, from all the posts here, and from everyone I personally know that has >> one, that the results are usually miraculous and wonderful. I fully believe in >> the process. But part of me also wishes that I had heard more of the less >> successful stories when I was doing all my initial research. I may be part of >> the 1% or less who have had less than thrilling results, but I still think >> people should be aware of the possibilities. >> - >> ________________________________ >> From: Deborah Herczog<mailto:dherczog%40> >> mailto:%40 >> Sent: Wed, May 11, 2011 4:08:38 AM >> Subject: hearing with CI (to Joe) >> I highly recommend NOT listening to opinions about CI hearing results from those >> who do not have experience working with CIs (or using one). The brain has >> incredible plasticity, and for those of us who were post lingually deafened, it >> works to make sense of input and we convert mentally to what was once familiar >> because this is what the brain wants to do. >> Indeed initially many of us " hear " chipmunk voices (or in the case of my 2nd CI, >> a less common low pitched accent), but this typically declines/vanishes over >> time with practice/rehab. Best analogy I can think of is that the brain routes >> the " new " sounds from CI into old comprehension pathways and learns to >> reinterpret that input along those old channels or circuitry so that sounds >> begin to register a lot like the old ones. This means that the voices of family >> and friends now sound just like they used to. >> Having said that, when my CI was turned on, I was so ecstatic to comprehend >> anything, that I said I would happily take that and only that for the rest of my >> life if that was all I got. Another huge benefit is that hearing with a CI is >> so relatively automatic compared to hearing with hearing aids (in quiet) that I >> started to wonder if the qualification standards should be lowered, meaning >> those with moderately severe loss might hear better and more easily with CI than >> with hearing aids. I only wish I had had the surgery years earlier as that would >> have saved me a lot of stress, exhaustion, emotional wreckage. It takes post-op >> work (practice) and some CI patients do not have miraculous outcomes, but as my >> Mayo Clinic audiologist says, these days, essentially 100% of patients hear >> better with CI than before. >> PS: an ENT from a large practice in Texas told me that CI sound was fake, I >> couldn't use CI with hearing aid, that I didn't qualify for CI anyway, and that >> I should just take disability. I am a health care provider myself, and in my >> opinion that was malpractice (or at least definite negligence) and resulted in >> my feeling increasing despondency which could have had a very negative outcome >> because I was at rock bottom. BUT thanks to HLAA information I figured I should >> get a second opinion and I am now leading a wonderful hearing life thanks to the >> CI. >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Jim, Yes comprehension vary good. I forgot one thing with the laptop's mic there is a little eco like with conference calls so i use a lapel mic cliped to my collar pluged into mic jack on laptop. Me,Tippy,Penny and We N.F.-Dukee From: jimwms@... Date: Thu, 26 May 2011 15:47:36 -0400 Subject: Re: hearing with CI and Lil Bk Cable Wayne, So you have to set up the MagicJack to use the laptop sound card to hear, and the phone handset to speak...correct? Jim On 5/26/2011 3:36 PM, wayne stephens wrote: > Hi, I had implant 3-11' and have almost same hearing as everyone, I have progressed to where people sound like they are from England and have a bad head cold. > > How I have adjusted to telephone usage: > > 1. computer(laptop is best) is a telephone with MagicJack. Your bk cable connects to the processor and to computer speaker output. > > 2. Your processor cable connects to wireless telephone. Maybe one problem most phones have 2.5mm jack. processor > plug is 3.5mm. need adapter cable from RadioShack or EBAY etc $3-5. You might have to switch mic speaker wires in > adapter cable. Just speak into phone and hear > > 3. This also works vary good with TV and Radios that have earphone jacks. > > The processor has crystal like microphones about the size of a head on a pen. crystal mics detect sounds and pass them > all on at the same volume level making hearing understanding difficult for us. A dynamic mic keeps low volumes low and > high volumes high.but smallest 4 times size of our processor. the above procedures bypass the processor mics. I guess > for safety reasons the processor mics are still on about 25%. > > Good health and happy hearing > > Wayne, retired El Eng > > Me,Tippy,Penny and We N.F.-Dukee > > > > > > From: carol@... > Date: Thu, 26 May 2011 12:01:35 -0400 > Subject: Re: hearing with CI > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Has the audiologist asked for a Cochlear Clinical Specialist to help out at a mapping? If not, please request this. They are available to help out with difficult cases. That is what they do. After all, not everyone is a text book case and the company acknowledges this. Many people have problems with high pitched sounds but that should be able to be mapped so you could hear more normally. > > So if your hearing is still not what it should be, please be an advocate for yourself and do request this. And.... if your audiologist will not go along with this request, it is time to move on to a different audiologist. > > Happy Hearing! > > Carol > > Boca Raton, FL > > Cochlear America Nucleus 24C - left ear - Sprint 12/11/01 then 3G then upgraded to Freedom on 2/19/08 > > Cochlear America Freedom right ear -implanted 3/01/06 - activated 4/06/06 > > > > From: Judy wilkins > > Sent: Thursday, May 26, 2011 11:52 AM > > > > Subject: RE: hearing with CI > > > > , > > > > I feel the same way you do. I only heard great successful stories about their cochlear implant but my experiences have not been a success story. > > > > I had implanted " Cochlear Freedom " about 3 years ago and I still cannot speak on the phone, hearing chipmunk voices, high pitch voices, and you can forget about me hearing even a small group. I can only hear when someone is speaking to me directly and there is no background noise. My biggest problem is back ground noise of any kind. It picks up those sounds so clearly but yet I still cannot hear a person talking unless it is in a quiet place and it's one-on-one. I have had many mappings and they all turn out the same, everyone sounds like Mickey Mouse down in a deep, deep well. I am very frustrated and seeking a new audiologist to try and help me. So, you are not the only one, and I became deaf overnight due to medication the hospital gave me 3 years ago. So I have heard all my life until the last 3 years and this is the most horrible thing that has happened to me. > > > > Judy > > > >> mailto:%40 >> From: mailto:lisayuan3%40 >> Date: Wed, 11 May 2011 15:34:30 -0700 >> Subject: Re: hearing with CI >> Hello, >> I've been hesitant to post any messages here, because the last thing I want to >> do is create any negativity relating to CIs. Obviously, from everyone's posts, >> the CI process is highly successful and has greatly improved the lives of most >> people. However, I am one of the few people that, after over a year of having my >> implant, am still hearing chipmunk voices and constant high-pitched tones, even >> after repeated mapping sessions. My comprehension is still poor too. The device >> has been tested, and CT scans have been conducted, yet everything looks normal. >> So audiologists are stumped. The last visit I had, my audiologist confided that >> even if my comprehension improves, if the sound quality is still poor after all >> this time, it's not likely to get much better. So I may be stuck hearing this >> high-pitched squawking forever, unless I decide to just stop wearing the >> implant. >> I do not want to discourage anyone from getting an implant, because I know from >> the stats, from all the posts here, and from everyone I personally know that has >> one, that the results are usually miraculous and wonderful. I fully believe in >> the process. But part of me also wishes that I had heard more of the less >> successful stories when I was doing all my initial research. I may be part of >> the 1% or less who have had less than thrilling results, but I still think >> people should be aware of the possibilities. >> - >> ________________________________ >> From: Deborah Herczog<mailto:dherczog%40> >> mailto:%40 >> Sent: Wed, May 11, 2011 4:08:38 AM >> Subject: hearing with CI (to Joe) >> I highly recommend NOT listening to opinions about CI hearing results from those >> who do not have experience working with CIs (or using one). The brain has >> incredible plasticity, and for those of us who were post lingually deafened, it >> works to make sense of input and we convert mentally to what was once familiar >> because this is what the brain wants to do. >> Indeed initially many of us " hear " chipmunk voices (or in the case of my 2nd CI, >> a less common low pitched accent), but this typically declines/vanishes over >> time with practice/rehab. Best analogy I can think of is that the brain routes >> the " new " sounds from CI into old comprehension pathways and learns to >> reinterpret that input along those old channels or circuitry so that sounds >> begin to register a lot like the old ones. This means that the voices of family >> and friends now sound just like they used to. >> Having said that, when my CI was turned on, I was so ecstatic to comprehend >> anything, that I said I would happily take that and only that for the rest of my >> life if that was all I got. Another huge benefit is that hearing with a CI is >> so relatively automatic compared to hearing with hearing aids (in quiet) that I >> started to wonder if the qualification standards should be lowered, meaning >> those with moderately severe loss might hear better and more easily with CI than >> with hearing aids. I only wish I had had the surgery years earlier as that would >> have saved me a lot of stress, exhaustion, emotional wreckage. It takes post-op >> work (practice) and some CI patients do not have miraculous outcomes, but as my >> Mayo Clinic audiologist says, these days, essentially 100% of patients hear >> better with CI than before. >> PS: an ENT from a large practice in Texas told me that CI sound was fake, I >> couldn't use CI with hearing aid, that I didn't qualify for CI anyway, and that >> I should just take disability. I am a health care provider myself, and in my >> opinion that was malpractice (or at least definite negligence) and resulted in >> my feeling increasing despondency which could have had a very negative outcome >> because I was at rock bottom. BUT thanks to HLAA information I figured I should >> get a second opinion and I am now leading a wonderful hearing life thanks to the >> CI. >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Folks should be aware that, with one exception, all 3 CI manufacturers specifically advise against connection of the processor to any but battery-powered devices, due to the risk of damage secondary to AC line spikes/surges. The one exception: use of the " TV/HiFi Cable " from Cochlear for their processors. Bob ............... hearing with CI (to Joe) > > > I highly recommend NOT listening to opinions about CI hearing results from those > > who do not have experience working with CIs (or using one). The brain has > incredible plasticity, and for those of us who were post lingually deafened, it > works to make sense of input and we convert mentally to what was once familiar > because this is what the brain wants to do. > > Indeed initially many of us " hear " chipmunk voices (or in the case of my 2nd CI, > > a less common low pitched accent), but this typically declines/vanishes over > time with practice/rehab. Best analogy I can think of is that the brain routes > the " new " sounds from CI into old comprehension pathways and learns to > reinterpret that input along those old channels or circuitry so that sounds > begin to register a lot like the old ones. This means that the voices of family > > and friends now sound just like they used to. > > Having said that, when my CI was turned on, I was so ecstatic to comprehend > anything, that I said I would happily take that and only that for the rest of my > > life if that was all I got. Another huge benefit is that hearing with a CI is > so relatively automatic compared to hearing with hearing aids (in quiet) that I > started to wonder if the qualification standards should be lowered, meaning > those with moderately severe loss might hear better and more easily with CI than > > with hearing aids. I only wish I had had the surgery years earlier as that would > > have saved me a lot of stress, exhaustion, emotional wreckage. It takes post-op > > work (practice) and some CI patients do not have miraculous outcomes, but as my > Mayo Clinic audiologist says, these days, essentially 100% of patients hear > better with CI than before. > > PS: an ENT from a large practice in Texas told me that CI sound was fake, I > couldn't use CI with hearing aid, that I didn't qualify for CI anyway, and that > I should just take disability. I am a health care provider myself, and in my > opinion that was malpractice (or at least definite negligence) and resulted in > my feeling increasing despondency which could have had a very negative outcome > because I was at rock bottom. BUT thanks to HLAA information I figured I should > > get a second opinion and I am now leading a wonderful hearing life thanks to the > > CI. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Since I won't have the N5 until Wednesday, does the cable you mentioned have a built-in filter? Is it otherwise a standard audio cable with stereo mini-plugs? On 5/26/2011 4:24 PM, MacPherson wrote: > > Folks should be aware that, with one exception, all 3 CI manufacturers > specifically advise against connection of the processor to any but > battery-powered devices, due to the risk of damage secondary to AC line > spikes/surges. The one exception: use of the " TV/HiFi Cable " from Cochlear > for their processors. > > Bob > .............. > > hearing with CI (to Joe) > > > > > > > > > I highly recommend NOT listening to opinions about CI hearing > results from > those > > > > > > who do not have experience working with CIs (or using one). The > brain has > > > incredible plasticity, and for those of us who were post lingually > deafened, it > > > works to make sense of input and we convert mentally to what was once > familiar > > > because this is what the brain wants to do. > > > > > > Indeed initially many of us " hear " chipmunk voices (or in the case of my > 2nd CI, > > > > > > a less common low pitched accent), but this typically declines/vanishes > over > > > time with practice/rehab. Best analogy I can think of is that the brain > routes > > > the " new " sounds from CI into old comprehension pathways and learns to > > > reinterpret that input along those old channels or circuitry so that > sounds > > > begin to register a lot like the old ones. This means that the voices of > family > > > > > > and friends now sound just like they used to. > > > > > > Having said that, when my CI was turned on, I was so ecstatic to > comprehend > > > anything, that I said I would happily take that and only that for > the rest > of my > > > > > > life if that was all I got. Another huge benefit is that hearing > with a CI > is > > > so relatively automatic compared to hearing with hearing aids (in quiet) > that I > > > started to wonder if the qualification standards should be lowered, > meaning > > > those with moderately severe loss might hear better and more easily with > CI than > > > > > > with hearing aids. I only wish I had had the surgery years earlier > as that > would > > > > > > have saved me a lot of stress, exhaustion, emotional wreckage. It takes > post-op > > > > > > work (practice) and some CI patients do not have miraculous > outcomes, but > as my > > > Mayo Clinic audiologist says, these days, essentially 100% of patients > hear > > > better with CI than before. > > > > > > PS: an ENT from a large practice in Texas told me that CI sound was > fake, > I > > > couldn't use CI with hearing aid, that I didn't qualify for CI > anyway, and > that > > > I should just take disability. I am a health care provider myself, > and in > my > > > opinion that was malpractice (or at least definite negligence) and > resulted in > > > my feeling increasing despondency which could have had a very negative > outcome > > > because I was at rock bottom. BUT thanks to HLAA information I figured I > should > > > > > > get a second opinion and I am now leading a wonderful hearing life > thanks > to the > > > > > > CI. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Hi, you get 2 cables the long one has filter And using with battery power devices is vary good advice be vary cautious and use filter cable with other devices. Me,Tippy,Penny and We N.F.-Dukee From: jimwms@... Date: Thu, 26 May 2011 16:34:30 -0400 Subject: Re: hearing with CI and Lil Bk Cable Since I won't have the N5 until Wednesday, does the cable you mentioned have a built-in filter? Is it otherwise a standard audio cable with stereo mini-plugs? On 5/26/2011 4:24 PM, MacPherson wrote: > > Folks should be aware that, with one exception, all 3 CI manufacturers > specifically advise against connection of the processor to any but > battery-powered devices, due to the risk of damage secondary to AC line > spikes/surges. The one exception: use of the " TV/HiFi Cable " from Cochlear > for their processors. > > Bob > .............. > > hearing with CI (to Joe) > > > > > > > > > I highly recommend NOT listening to opinions about CI hearing > results from > those > > > > > > who do not have experience working with CIs (or using one). The > brain has > > > incredible plasticity, and for those of us who were post lingually > deafened, it > > > works to make sense of input and we convert mentally to what was once > familiar > > > because this is what the brain wants to do. > > > > > > Indeed initially many of us " hear " chipmunk voices (or in the case of my > 2nd CI, > > > > > > a less common low pitched accent), but this typically declines/vanishes > over > > > time with practice/rehab. Best analogy I can think of is that the brain > routes > > > the " new " sounds from CI into old comprehension pathways and learns to > > > reinterpret that input along those old channels or circuitry so that > sounds > > > begin to register a lot like the old ones. This means that the voices of > family > > > > > > and friends now sound just like they used to. > > > > > > Having said that, when my CI was turned on, I was so ecstatic to > comprehend > > > anything, that I said I would happily take that and only that for > the rest > of my > > > > > > life if that was all I got. Another huge benefit is that hearing > with a CI > is > > > so relatively automatic compared to hearing with hearing aids (in quiet) > that I > > > started to wonder if the qualification standards should be lowered, > meaning > > > those with moderately severe loss might hear better and more easily with > CI than > > > > > > with hearing aids. I only wish I had had the surgery years earlier > as that > would > > > > > > have saved me a lot of stress, exhaustion, emotional wreckage. It takes > post-op > > > > > > work (practice) and some CI patients do not have miraculous > outcomes, but > as my > > > Mayo Clinic audiologist says, these days, essentially 100% of patients > hear > > > better with CI than before. > > > > > > PS: an ENT from a large practice in Texas told me that CI sound was > fake, > I > > > couldn't use CI with hearing aid, that I didn't qualify for CI > anyway, and > that > > > I should just take disability. I am a health care provider myself, > and in > my > > > opinion that was malpractice (or at least definite negligence) and > resulted in > > > my feeling increasing despondency which could have had a very negative > outcome > > > because I was at rock bottom. BUT thanks to HLAA information I figured I > should > > > > > > get a second opinion and I am now leading a wonderful hearing life > thanks > to the > > > > > > CI. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 Prior to the CP810 (Nucleus 5) processor, there were 2 cables: the Personal Audio Cable - for battery operated devices and the TV/HiFi Cable for AC powered. With the CP810, Cochlear supplies a Personal Audio cable and a Mains Isolation Cable - to be connected between the Personal Audio Cable and the AC powered audio source. You can read more in the CP810 User Manual, pages 67-74, here: http://tinyurl.com/2982d22 Bob ...... From: [mailto: ] On Behalf Of JIM WILLIAMS Sent: Thursday, May 26, 2011 4:35 PM Subject: Re: hearing with CI and Lil Bk Cable Since I won't have the N5 until Wednesday, does the cable you mentioned have a built-in filter? Is it otherwise a standard audio cable with stereo mini-plugs? On 5/26/2011 4:24 PM, MacPherson wrote: > > Folks should be aware that, with one exception, all 3 CI manufacturers > specifically advise against connection of the processor to any but > battery-powered devices, due to the risk of damage secondary to AC line > spikes/surges. The one exception: use of the " TV/HiFi Cable " from Cochlear > for their processors. > > Bob Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 OK...thanks. Here I thought I would need to install my Phonak FM receiver and plug audio into my Smartlink FM transmitter. I guess I could still do that and be wire free (and I wouldn't need to worry about whether the source is battery or AC powered.) Jim Jim Dayton, OH ________________________________ From: wayne stephens <stephens_wayne@...> Sent: Thu, May 26, 2011 5:50:20 PM Subject: RE: hearing with CI and Lil Bk Cable Hi, you get 2 cables the long one has filter And using with battery power devices is vary good advice be vary cautious and use filter cable with other devices. Me,Tippy,Penny and We N.F.-Dukee From: jimwms@... Date: Thu, 26 May 2011 16:34:30 -0400 Subject: Re: hearing with CI and Lil Bk Cable Since I won't have the N5 until Wednesday, does the cable you mentioned have a built-in filter? Is it otherwise a standard audio cable with stereo mini-plugs? On 5/26/2011 4:24 PM, MacPherson wrote: > > Folks should be aware that, with one exception, all 3 CI manufacturers > specifically advise against connection of the processor to any but > battery-powered devices, due to the risk of damage secondary to AC line > spikes/surges. The one exception: use of the " TV/HiFi Cable " from Cochlear > for their processors. > > Bob > .............. > > hearing with CI (to Joe) > > > > > > > > > I highly recommend NOT listening to opinions about CI hearing > results from > those > > > > > > who do not have experience working with CIs (or using one). The > brain has > > > incredible plasticity, and for those of us who were post lingually > deafened, it > > > works to make sense of input and we convert mentally to what was once > familiar > > > because this is what the brain wants to do. > > > > > > Indeed initially many of us " hear " chipmunk voices (or in the case of my > 2nd CI, > > > > > > a less common low pitched accent), but this typically declines/vanishes > over > > > time with practice/rehab. Best analogy I can think of is that the brain > routes > > > the " new " sounds from CI into old comprehension pathways and learns to > > > reinterpret that input along those old channels or circuitry so that > sounds > > > begin to register a lot like the old ones. This means that the voices of > family > > > > > > and friends now sound just like they used to. > > > > > > Having said that, when my CI was turned on, I was so ecstatic to > comprehend > > > anything, that I said I would happily take that and only that for > the rest > of my > > > > > > life if that was all I got. Another huge benefit is that hearing > with a CI > is > > > so relatively automatic compared to hearing with hearing aids (in quiet) > that I > > > started to wonder if the qualification standards should be lowered, > meaning > > > those with moderately severe loss might hear better and more easily with > CI than > > > > > > with hearing aids. I only wish I had had the surgery years earlier > as that > would > > > > > > have saved me a lot of stress, exhaustion, emotional wreckage. It takes > post-op > > > > > > work (practice) and some CI patients do not have miraculous > outcomes, but > as my > > > Mayo Clinic audiologist says, these days, essentially 100% of patients > hear > > > better with CI than before. > > > > > > PS: an ENT from a large practice in Texas told me that CI sound was > fake, > I > > > couldn't use CI with hearing aid, that I didn't qualify for CI > anyway, and > that > > > I should just take disability. I am a health care provider myself, > and in > my > > > opinion that was malpractice (or at least definite negligence) and > resulted in > > > my feeling increasing despondency which could have had a very negative > outcome > > > because I was at rock bottom. BUT thanks to HLAA information I figured I > should > > > > > > get a second opinion and I am now leading a wonderful hearing life > thanks > to the > > > > > > CI. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 You can do the Phonak MicroLink receiver with the CP810 by using the Euro Adapter from Cochlear: http://tinyurl.com/24zdyxr Bob ...... From: [mailto: ] On Behalf Of JIM WILLIAMS Sent: Thursday, May 26, 2011 6:18 PM Subject: Re: hearing with CI and Lil Bk Cable OK...thanks. Here I thought I would need to install my Phonak FM receiver and plug audio into my Smartlink FM transmitter. I guess I could still do that and be wire free (and I wouldn't need to worry about whether the source is battery or AC powered.) Jim Jim Dayton, OH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2011 Report Share Posted May 26, 2011 I've already been there and done that. We discussed it and you said, " Be prepared " . Remember...a couple days ago? Jim Jim Dayton, OH ________________________________ From: MacPherson <hohbob@...> Sent: Thu, May 26, 2011 6:28:22 PM Subject: RE: hearing with CI and Lil Bk Cable You can do the Phonak MicroLink receiver with the CP810 by using the Euro Adapter from Cochlear: http://tinyurl.com/24zdyxr Bob ...... From: [mailto: ] On Behalf Of JIM WILLIAMS Sent: Thursday, May 26, 2011 6:18 PM Subject: Re: hearing with CI and Lil Bk Cable OK...thanks. Here I thought I would need to install my Phonak FM receiver and plug audio into my Smartlink FM transmitter. I guess I could still do that and be wire free (and I wouldn't need to worry about whether the source is battery or AC powered.) Jim Jim Dayton, OH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2011 Report Share Posted May 27, 2011 My DUH! Bob ..... From: [mailto: ] On Behalf Of JIM WILLIAMS Sent: Thursday, May 26, 2011 10:23 PM Subject: Re: hearing with CI and Lil Bk Cable I've already been there and done that. We discussed it and you said, " Be prepared " . Remember...a couple days ago? Jim Jim Dayton, OH ________________________________ From: MacPherson <hohbob@... <mailto:hohbob%40verizon.net> > <mailto:%40> Sent: Thu, May 26, 2011 6:28:22 PM Subject: RE: hearing with CI and Lil Bk Cable You can do the Phonak MicroLink receiver with the CP810 by using the Euro Adapter from Cochlear: http://tinyurl.com/24zdyxr Bob ...... From: <mailto:%40> [mailto: <mailto:%40> ] On Behalf Of JIM WILLIAMS Sent: Thursday, May 26, 2011 6:18 PM <mailto:%40> Subject: Re: hearing with CI and Lil Bk Cable OK...thanks. Here I thought I would need to install my Phonak FM receiver and plug audio into my Smartlink FM transmitter. I guess I could still do that and be wire free (and I wouldn't need to worry about whether the source is battery or AC powered.) Jim Jim Dayton, OH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2011 Report Share Posted May 27, 2011 Wait a minute! Are you dissing our Boy Scout? He has been doing good deeds for all of us. Thank you Bob! Neely in Dallas Texas > From: [mailto: ] On Behalf Of > JIM WILLIAMS > Sent: Thursday, May 26, 2011 10:23 PM > > Subject: Re: hearing with CI and Lil Bk Cable > > I've already been there and done that. We discussed it and you said, " Be repared " . Remember...a couple days ago? > > Jim > Jim > Dayton, OH > > ________________________________ > From: MacPherson <hohbob@... <mailto:hohbob%40verizon.net> > > <mailto:%40> > Sent: Thu, May 26, 2011 6:28:22 PM > Subject: RE: hearing with CI and Lil Bk Cable > > You can do the Phonak MicroLink receiver with the CP810 by using the Euro > Adapter from Cochlear: http://tinyurl.com/24zdyxr > > Bob > <<snipped>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 27, 2011 Report Share Posted May 27, 2011 No way...not dissing him at all. :-) Jim Dayton, OH ________________________________ From: rsneely <rsneely@...> Sent: Fri, May 27, 2011 10:34:32 AM Subject: Re: hearing with CI and Lil Bk Cable Wait a minute! Are you dissing our Boy Scout? He has been doing good deeds for all of us. Thank you Bob! Neely in Dallas Texas > From: [mailto: ] On Behalf Of > JIM WILLIAMS > Sent: Thursday, May 26, 2011 10:23 PM > > Subject: Re: hearing with CI and Lil Bk Cable > > I've already been there and done that. We discussed it and you said, " Be >repared " . Remember...a couple days ago? > > Jim > Jim > Dayton, OH > > ________________________________ > From: MacPherson <hohbob@... <mailto:hohbob%40verizon.net> > > <mailto:%40> > Sent: Thu, May 26, 2011 6:28:22 PM > Subject: RE: hearing with CI and Lil Bk Cable > > You can do the Phonak MicroLink receiver with the CP810 by using the Euro > Adapter from Cochlear: http://tinyurl.com/24zdyxr > > Bob > <<snipped>> Quote Link to comment Share on other sites More sharing options...
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