MomToDeafChild
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- Mar 7, 2007
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If you or your child has been reimplanted (for whatever reasons), I would love to pick your brain!
My daughter was recently reimplanted after a soft failure, and while we've been told it can take a year for her to get back to where she was prior to the reimplantation, no one has said what it should be like NOW, and I really need to hear what other people experienced in the early days/months post reimplantation.
It is 3 weeks now, and I feel like Abby's ability to hear is right about the same as when she was first activated. We have a couple different programs to switch between, but it was difficult finding a map she could use without it causing an eye twitch (she has a malformed cochlea). With her old implant, if volume was too high she would get the eye twitch, and on all three of the programs she has now she gets it if I touch the volume.
I've noticed that when we practice listening with the Ling sounds, she misses different sounds with the different programs. On one program she misses the Ee and Oo. On the next program, she gets the Ee easily, sometimes gets the Oo, but Mm is difficult and Sh turned to Ss. I've been using open sets of 6 2-syllable word picture cards and she does ok on them, but doesn't get them right every time, which confuses me. Sometimes she can make out sentences, but most of the time she can't.
Hearing, though, is a different story. She was listening to the rain and thunder tonight, and she was easily able to hear her sister playing Connect 4. She is hearing right about the same levels as she was with her old implant, she just has no idea what anyone is saying!
I am just worried now that something wasn't done right and it is going to affect her ability to bounce back. The audi said the biggest hurtle she has is that she didn't hear for 5.5 months, followed by the newer technology (she went from a CII to the HiRes90K). BECAUSE the medical professionals did not believe she would get her hearing back (the reimplant was really just to confirm auditory nerve failure, and would help with the next step; they never expected it to work), I worry that maybe they didn't do as good as a job as they could have!
I'd appreciate any insight. Thanks!
My daughter was recently reimplanted after a soft failure, and while we've been told it can take a year for her to get back to where she was prior to the reimplantation, no one has said what it should be like NOW, and I really need to hear what other people experienced in the early days/months post reimplantation.
It is 3 weeks now, and I feel like Abby's ability to hear is right about the same as when she was first activated. We have a couple different programs to switch between, but it was difficult finding a map she could use without it causing an eye twitch (she has a malformed cochlea). With her old implant, if volume was too high she would get the eye twitch, and on all three of the programs she has now she gets it if I touch the volume.
I've noticed that when we practice listening with the Ling sounds, she misses different sounds with the different programs. On one program she misses the Ee and Oo. On the next program, she gets the Ee easily, sometimes gets the Oo, but Mm is difficult and Sh turned to Ss. I've been using open sets of 6 2-syllable word picture cards and she does ok on them, but doesn't get them right every time, which confuses me. Sometimes she can make out sentences, but most of the time she can't.
Hearing, though, is a different story. She was listening to the rain and thunder tonight, and she was easily able to hear her sister playing Connect 4. She is hearing right about the same levels as she was with her old implant, she just has no idea what anyone is saying!
I am just worried now that something wasn't done right and it is going to affect her ability to bounce back. The audi said the biggest hurtle she has is that she didn't hear for 5.5 months, followed by the newer technology (she went from a CII to the HiRes90K). BECAUSE the medical professionals did not believe she would get her hearing back (the reimplant was really just to confirm auditory nerve failure, and would help with the next step; they never expected it to work), I worry that maybe they didn't do as good as a job as they could have!
I'd appreciate any insight. Thanks!