ramblinwreck
New Member
- Joined
- Jun 29, 2011
- Messages
- 3
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Hey y'all,
I've had a CI for about 18 years (wow, has it really been that long?), and I got my second implantation two weeks ago. Why the long delay? Well, I was happy with unilateral hearing, but some electrodes failed on the internal part of the implant, so we don't exactly know how much longer it has before it completely fails. Could be a year, could be another ten or more. We decided to not risk going completely deaf by getting implanted in my second ear, for backup measures. I just got activated on Monday, and wow, what an awakening for my nerves, but the reason why I'm on here is because I have a couple of questions, since my audiologist is working part-time this summer and can't be reached all the time.
1) When I got activated on Monday, I put every electrode on the lowest setting possible because I wasn't sure how my brain was going to react to hearing stuff out of my cochlear for the first time in 22 years. Is it normal to be hearing just unintelligible noise right now? My audiologist did say it was normal, but I just want to confirm with actual users.
2) Whenever I put my cochlear implant on, my nerves on that side of the implant seem to flare up for a split second, but it goes away. Is that normal? Does that die down as time goes on? It makes it hard for me to want to put my cochlear implant on, but it would make it better knowing that it does go away with time. I would imagine so, since that it's the first time being "used" in 22 years (my current age).
Sorry, I know I'm asking a lot as a new user, but I first got implanted at the age of 4, and I don't remember going through any of this, so it is somewhat new (again) to me. I'm also a person who expects instant results and can be a little impatient, so this process is a bit tough for me.
Also, I might as well introduce myself, since I kind of bypassed that part, and it may help with answering one or both of my questions. I was born with profound hearing loss, currently a fourth year in college, and have been mainstreamed my entire life. My parents say that I used ASL before getting implanted at the age of 4, but I don't remember anything. Strictly oral only, and people can't tell that I was born deaf at all, so it's turned out very well for me, luckily.
Feel free to ask questions as well. I may not be on here for much longer, since I'm traveling for all of July and may not have time, but I'll definitely be around for the next day or so.
I really appreciate any feedback, and thanks in advance. Will try to respond as promptly as possible.
I've had a CI for about 18 years (wow, has it really been that long?), and I got my second implantation two weeks ago. Why the long delay? Well, I was happy with unilateral hearing, but some electrodes failed on the internal part of the implant, so we don't exactly know how much longer it has before it completely fails. Could be a year, could be another ten or more. We decided to not risk going completely deaf by getting implanted in my second ear, for backup measures. I just got activated on Monday, and wow, what an awakening for my nerves, but the reason why I'm on here is because I have a couple of questions, since my audiologist is working part-time this summer and can't be reached all the time.
1) When I got activated on Monday, I put every electrode on the lowest setting possible because I wasn't sure how my brain was going to react to hearing stuff out of my cochlear for the first time in 22 years. Is it normal to be hearing just unintelligible noise right now? My audiologist did say it was normal, but I just want to confirm with actual users.
2) Whenever I put my cochlear implant on, my nerves on that side of the implant seem to flare up for a split second, but it goes away. Is that normal? Does that die down as time goes on? It makes it hard for me to want to put my cochlear implant on, but it would make it better knowing that it does go away with time. I would imagine so, since that it's the first time being "used" in 22 years (my current age).
Sorry, I know I'm asking a lot as a new user, but I first got implanted at the age of 4, and I don't remember going through any of this, so it is somewhat new (again) to me. I'm also a person who expects instant results and can be a little impatient, so this process is a bit tough for me.
Also, I might as well introduce myself, since I kind of bypassed that part, and it may help with answering one or both of my questions. I was born with profound hearing loss, currently a fourth year in college, and have been mainstreamed my entire life. My parents say that I used ASL before getting implanted at the age of 4, but I don't remember anything. Strictly oral only, and people can't tell that I was born deaf at all, so it's turned out very well for me, luckily.
Feel free to ask questions as well. I may not be on here for much longer, since I'm traveling for all of July and may not have time, but I'll definitely be around for the next day or so.
I really appreciate any feedback, and thanks in advance. Will try to respond as promptly as possible.