New here and I am getting CI.

I was also able to tell that Devon was female based on her writing. It's interesting how you can tell a person's gender by their writing style.

Devon can be a male or female name. (I didn't know that until I saw a character named Devon on the Young and the Restless) The female name is generally pronounced DEVon while the male name is pronounced deVON.

Sorry. Back on topic...
 
I was also able to tell that Devon was female based on her writing. It's interesting how you can tell a person's gender by their writing style.

Devon can be a male or female name. (I didn't know that until I saw a character named Devon on the Young and the Restless) The female name is generally pronounced DEVon while the male name is pronounced deVON.

Sorry. Back on topic...
 
Well I have a little brother named Devon. Always associated it as a guy name.
Hear Again........I know some prelingal profounders can hear really well with CI. But don't those people tend to have had some residual hearing with hearing aids? Like they may have heard some speech and sounds with hearing aids, so with CI it's more "turning up the volume?" (metaphoricly of course.....I know that a CI isn't a traditional amplification device) After all, with the new qualifications, you can be able to hear 60% with hearing aids to qualify for CI. It's no longer total loss.
Also, I mean I thought that research had firmly established that those who may have heard normally at one time, even as infants, tend to be better CI users. I wonder if there's been any research on how well an always hoh person hears with CI/other amplification devices, vs. how well someone who heard for a month or so processes sound......would be interesting to know.
 
Dont blame u. Before, I was against CIs but after reading so many ADers experiences with CIs and their reasons for getting them, I had to ask myself this. If HAs stop working for me, would I enjoy being completely deaf? The answer is no so if this happens to me, then I will get a CI or CIs. :)

This forum has helped me to open my mind about CIs better.

Shel, I WAS in your shoes almost 10 months ago until our son Fragmenter and his wife VP'd us and told us they're seriously considering getting their 5-year old son Marshall implanted! I joined AD specifically for the HA/CI forum and tried keeping my mind open as I love our son unconditionally and was not going to turn him off if I railed against his son getting implanted.

I am SO glad to see you turning around. Like I had said somewhere on here I believe everyone is different and they all have different expectations of their CIs. :rockon:
 
Shel, I WAS in your shoes almost 10 months ago until our son Fragmenter and his wife VP'd us and told us they're seriously considering getting their 5-year old son Marshall implanted! I joined AD specifically for the HA/CI forum and tried keeping my mind open as I love our son unconditionally and was not going to turn him off if I railed against his son getting implanted.

I am SO glad to see you turning around. Like I had said somewhere on here I believe everyone is different and they all have different expectations of their CIs. :rockon:

Thanks! I am still against the false beliefs that specialists and parents have about CIs being the answer to all of their deaf child's problems and that it will make the child "hearing". Also, I still do not like the oral-only approach if it is not working for the deaf child with the CI cuz I see tooo many cases like that.
 
Hello Devon and welcome to AD! I'm also a CI Candidate as well. When I got tested at UNC in Chapel Hill, my audiologist said she'd recommend that my left ear get implanted instead of my right ear as it's the better ear and I'll have better chance of success. I was like :eek3: but since CIs aren't experimental anymore, I've decided to get my left ear implanted on Feb. 20th.

She thinks a CI would help me more than any HA on the market. I sure hope so as I have very little ability to understand speech without lipreading. I can hear a lot of environmental noises with my HA but I'm told a CI would help me more than a HA would.

GL with your implant!
 
DD,

The CI users I know were not able to benefit from hearing aids. Even for people (prelingual, perilingual or postlingual) who were able to benefit from HAs, I don't think it's a matter of simply "turning up the volume." I've been able to use my hearing for 27 years and yet it took me 2 weeks to understand speech with my CI and 6 months for speech to sound "normalized." Aside from learning how to interpret speech, I also had to learn how to identify environmental sounds. Some environmental sounds did not sound at all like I remember prior to losing my hearing. For example, traffic outside my window sounded like static with my CI and it took a few weeks before it started to sound like it should. I can still remember sitting at my computer desk hearing constant static and wondering what the heck it was. :) I finally made the association after walking over to the living room window and hearing the static sound become louder the closer I got to the window. I've read plenty of research studies which conclude that people who once had useable hearing generally tend to be better CI users. However, there are always exceptions. For instance, I know one CI user who is late-deafened who is unable to understand speech with his CI even after being activated for a year. Conversely (as I mentioned in a previous post), I know a prelingually deaf CI user who was able to understand speech on the day her CI was activated. Research findings may apply to the majority of CI users, but they do not apply to all.
 
Oh it was just a hypothesis...like they had a base on which to build their hearing experiances. Like doing it with a clean slate is very hard b/c you don't know what sound sounds like.

I've read plenty of research studies which conclude that people who once had useable hearing generally tend to be better CI users. However, there are always exceptions.
Yeah, even as babies. Doesn't that make sense that if you heard normally for at least a month or so, you could draw on that as a base? I wonder if that could explain how come the "CI hearing" comes in such a wide spectrum.

Shel, and everyone..........I have seen opposition to CIs in the Deaf culture go down drasticly over the years. I think it's great.....maybe then more hearing parents will be open to the Deaf culture. I know one reason cited by oral only parents, is that Deaf people don't accept CI or look down on oral kids.
 
There are some people called me DE-VON.. Im like no it is DEV-IN.
Sometimes when im on the relay.. they called me *Sir* I am like ugh.
i wish it was Jan 25th!! HURRY!!
 
Devon, the 25th is only 17 days away, just a bit more than 2 weeks and it'll be here before you know it! Keep on trucking, girl!!! :rockon: (you all probably think I'm obsessed with this icon but it fits my personality! LOL)
 
Welcome Dev! FYI, I always thought Devon was a female name anyway. It just sounds better rolling off the tounge when referring to a female. It sounds more like DevIn for female, and Devaan for a male. Anyway, Congrats on yoour decision for CI. Apparently you have done your research, and made your decision. It is your life and your ears, dont let people try to sway your decision. They dont live with the oputcome of those decisions, you do.
I am a hearing father of a deaf 2 year old. She had CI surgery in sept of 2005. Now she is getting her other ear implanted next week. Based only on my experiences, and Lillys progress, The risks of surgery are there. They are abour the same risks as any other surgery. The risks are mostly associated with anesthesia.
As Cloggy said, go ahead and ask away with any questions you may have. While I do not have a CI, I have done the research, and I get reminded daily of the incredible effect it has.
 
Thanks =)

Tomorrow i am getting my Vaccine shot! I already got my blood test done like a week ago or so. I guess that prob turn out just fine.

There is only 15 days left for my surgery! :eek3: I never had any type of surgery b4.. so this gonna be my first surgery!
 
Thanks =)

Tomorrow i am getting my Vaccine shot! I already got my blood test done like a week ago or so. I guess that prob turn out just fine.

There is only 15 days left for my surgery! :eek3: I never had any type of surgery b4.. so this gonna be my first surgery!

DevBaby:

Congratulations and best success on your implantation! Just 14 more days now! :)
 
I am kinda scare! :ugh3:
And i am also nervous about the IV! :eek3: Maybe I will end up running away from the doc, lol. I did that a lot when i was young cuz i hated the IV!
 
I am kinda scare! :ugh3:
And i am also nervous about the IV! :eek3: Maybe I will end up running away from the doc, lol. I did that a lot when i was young cuz i hated the IV!

The IV is not pleasant is it? Maybe you could mention to the nurse that you feel very jittery about that and they might be able to give you a sedative beforehand to relax you? I find that communicating with the medical staff about your fears really helps because they are now trained these days to be more sensitive about peoples' anxieties. Even if it only results in a soothing nurse sitting next to you and talking to you while the IV is being done it will help.
 
Dev, they have a cream that numbs the skin, and you don't even feel it go in!
 
Oh really? I never knew that. I will have to explain the nurse about it then. Thanks for letting me know.
 
IV and Surgery

Devon, Sorry this is so long but I hope it is useful information for you.

I'm a little ahead of you on getting a CI. About 5 weeks. My surgery was on December 16th and it was my first surgery as well. Actually, I didn't feel nervous but my blood pressure told the truth but I was OK. I have and still look at it as "what have I got to loose". If the CI does not give me any benefit, I'm back where I started from. If it helps, I have absolutely everything to gain and look forward to.

My Dr/Surgeon was very confident in that he told me he has performed many CI surgeries in the past and as he said, "he knows what he is doing." He also had the CT scans so he knew where everything was before he made the first move. I had and still have 100% confidence in his ability to perform the surgery if I choose to get bilateral CI's when my better ear totally stops working. I really hope you feel the same way with your Dr/surgeon.

As far as the IV, my wife has had several recently and said she really does not like it and thought I would have the same feeling. Initially when I was in pre-op, I thought I would not like the feeling at all but when the nurse stuck me, I thought, not that bad and that was really quick and easy. What she stuck me with was some numbing agent like what is used when you go to the dentist and it numbs your mouth and tongue for fillings. A couple minutes later, she inserted the IV and I did NOT feel a thing. My wife was so jealous that I had such a different experience. I guess she was only slightly hoping I could understand why she did not like it so much. You may want to ask for this before the IV goes in.

The anesthesiologist was cool. One thing he told me is I could call him anything if I had any problems but everyone else had to call him by name. He also told me about some of his "interesting" patients. I guess he did not want me to get on his interesting patient list. I can say I had no problems at all, they never told me to count backwards or anything. I remember a little about the ride to the operating room and only about 5 seconds of looking around the room before it was lights out for about 5 hours. Don't remember a thing from 12:00 until about 4:30.

They brought my wife back to recovery around 4:15 when I started waking up and can say I talked about being in quite a bit of pain but given what the operation consisted of, was to be expected. My Dr. told me what to expect so it was OK. Shortly before 5:00, they took me to my room where I ended up staying the night which was very good since I really did not feel up to traveling. They kept the IV in all night and I grabbed the railing of the bed with that hand and slept really well with the pain subsiding very quickly all through the night. By the next morning, I basically had just bad earache type pain which was totally tolerable. The Dr. came by to remove the bandage and look at the incision which he remarked that it looked good and nothing was out of the ordinary. Then began the waiting game until this coming Monday which I get the CI turned on.

I wish you luck but wanted to let you know of my experience since I too had the CI surgery as my first ever and since it was so recent.

Additionally, I just came off medical restriction where I can lift what ever I want and blow my nose. Lifting is fine. My ear/head tells me when I try to lift to much like 80-100 lbs but blowing my nose, NOT a good idea. I'm going to hold off for another 3-4 weeks before I do that. Causes immediate ringing and extreme earache type pain which is I think just the tender skin where the electrode goes into the middle ear and into the cochlea. The pain goes away within seconds and the ringing stops shortly after and I feel fine but again, something I'm personally going to avoid.

If you have any questions, please let me know.
Steve in Michigan
 
Maybe you could mention to the nurse that you feel very jittery about that and they might be able to give you a sedative beforehand to relax you? I find that communicating with the medical staff about your fears really helps because they are now trained these days to be more sensitive about peoples' anxieties. Even if it only results in a soothing nurse sitting next to you and talking to you while the IV is being done it will help.

This is definitely a good idea. Actually, sometimes they'll give you an anxiolytic - Xanax, Versed, and Valium are all common ones - which not only sedates you, but also makes you less anxious (hence the name) and might make you less likely to remember the hour or two after you take it. At least, not as clearly.

I was offered an anxiolytic multiple times before my last surgery; I declined (I wanted to remember the pre- and post- surgery - I'm weird that way), but my anaesthesiologist really encouraged me to take it!
 
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