Guest guest Posted February 8, 2005 Report Share Posted February 8, 2005 hello, everybody... i was going to take the time to put together a post specifically addressed to this lovely group, but am sooo POOPED after my 2nd day, i just can't do it. BUT! i figured i would copy-and-paste the " story " i e-mailed my friends and family. most of them are CI-illiterate, so most of the language is rather elementary. for this, i apologize, but am sure you all know what it's like. anyway, without further ado, here goes: well, yesterday was QUITE the day... to say the least. hubby and i showed up at my audiologist's office for my hook-up. one of the other women working there asked me if she could observe. i assume she's in training or whatever so i say i don't mind if she joins us. now it's hubby, my audiologist, Judy, and the other girl... the first thing Judy tells me is to take off my hearing aid (from my right ear) and then makes me promise not to wear it while i'm getting used to my CI. i was expecting this, but still ask how long i would have to go without it. Judy tells me maybe 2 weeks... it all depends. she says, 'if you don't wear your hearing aid and just practice hearing with your CI, you will make both our lives easier.' i get it... and am prepared (or so i think). the first thing Judy does is plug the speech processor into her computer so she can hook it up to the programming software. the magnet is attached to my head and the microphone is looped over my ear. then Judy starts programing the first map, which is determined by setting each of the 22 electrodes inside my cochlea. first she tests the T-levels (threshold) to be loud enough for me to be aware of a sound... and then she tests the C-levels (comfort) so the sound is not too loud as to cause discomfort. as Judy goes through the T-levels it takes a while b/c my tinnitus is acting up and i am having trouble distinguishing between the beeps from the computer and the beeping in my head. the mapping for the C-levels seems to go by much easier. it was even fun testing how loud i could handle the beeping! and even though the tinnitus is annoying, i think i manage just fine. i must mention that during this whole process, i can't hear a THING (except for all beeping), so being able to lip-read Judy is a relief! as soon as Judy is finished with the map, she says to me, 'okay, i'm going to turn you on now.' earlier, the girl that was observing us said that i looked really calm. i explained to her that 'i know what to expect because i ve done so much reading and research about it.' she was still surprised that i wasn't more nervous. maybe i thought i knew what to expect, but i definitely was NOT prepared for what i heard when Judy switched the processor on... it was SOOO squeaky and " squeal-ey " and uncomfortable! i was taken aback at how AWFUL everything sounded. i looked at Judy and simply said i didn't like it. she looked so heartbroken, IMO. i know she wasn't taking it personally, but my reaction was obviously not pleasant. i asked for a tissue and the tears started to fall. i was crying and crying because i just couldn't STAND the horrible noises i was hearing. it took me a second to realize that the ghastly squeaky sounds were VOICES! Judy and Kathleen (another audiologist who came to watch the hook-up) were talking to me... and it sounded TERRIBLE i honestly hated it. even though i *knew* that i shouldn't expect people's voices to sound natural, i definitely didn't expect them to be so DISTURBING! the best way to describe the way Judy and Kathleen sounded was like " Mickey Mouse on speed. " i can't think of anything worse than that... it really was NOT a fun sensation. i admit i didn't have my hopes up (or at least i didn't think i did), but then again... i didn't realize i would actually DISLIKE the sounds i was hearing. i even hated the sound of my OWN voice! granted, at least i *was* hearing things, even if i didn't necessarily enjoy them. what made the initial turn-on even more traumatic was the tinnitus. i told Judy that i kept hearing this constant squealing sound that would not go away. i heard this squealing *on top of* all the squeaky Mickey Mouse voices... it was just icky. well, when Judy turned off the processor to adjust the map, i STILL heard the squealing. Kathleen explained to me that it was my tinnitus and not any other noise from the outside. i was *not* happy about this at all. well, after i calmed down and let the sound wash over my " like a wave " (in Kathleen's words), i managed to stop crying. little by little i was starting to make out some words being said. i did not understand specific words, but could discern speech. THEN Kathleen stood behind me and started talking about the scab on my head from the incision (it hasn't fallen off yet and is really gross). i actually understood Kathleen saying, 'blah-blah-blah... scab fell off... blah blah blah' and i was SO surprised! even Judy's eyes popped out of her head. i guess that's a good thing, huh? as i write this, i am at the end of my 2nd day wearing the processor and things are MUCH better. i don't want to skip too far ahead by saying that other voices sound better and that my own voice isn't as awful, either. there is *so much* i am still absorbing... so much i'm still figuring out... so much i am still trying to make sense of... and the adventure has JUST started! at least sounds are making more sense to me today than they did yesterday, so i feel much better. i'll keep posting more 'CI moments' on my web page, but right now it's just TOO overwhelming to include it all. my ear is *very* tired - as it should be from a long day of listening - so i must go to sleep... g'night all! ~ Implanted: 1/4/05; Activated: 2/7/05 Implant: Nucleus® 24 Contour™ HOH Postlingual; bilateral HA user for 24 years Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.