Video Post!

As promised a while ago, I have finally made the new video.

Here it is!

Let me know what you think!

Until next time,

Annie

Rereading

I know I said that I wasn't going to update that often, but randomly I had my boyfriend say that he watched the video of me a lot and thought it was adorable, but I didn't remember what the video he was talking about so I went back into my older posts and watched it again.

He was talking about the video from my second post on this blog. And I was honestly shocked when I watched myself talk again, now this is pre-surgery... I am shocked at how different I sound... Like I talked differently... here's the video once again.

if it works. if not, just go way back in my blog for it. I want to make another video talking soon to show the difference. But don't have the time for that tonight.

It's hard to tell myself how much change has happened since the surgery, and I don't remember what I used to sound like or talk like but the video and other videos helped me remember... and it's a surprising thing to remember. It's as if I got a new accent since the surgery!

My parents have told me that I am speaking better and noticing how certain things are said in different areas, and also noticing accents more and how people accent on words. I wish that more people had the guts to tell me these things or even ask me questions about my hearing loss.

The other day, my boyfriend told me that his friend started asking him questions about my hearing loss and seemed too afraid to ask me directly to learn more about my hearing loss and everything related. It was kind of surprising, but it makes sense due to how people do not want to offend anybody or feel stupid for asking about a disability sometimes. I worked at a job all summer, and it was not until the very end of the summer that one of my coworker finally had the guts to ask me questions. I love getting questions from people that don't know because I rather have people be fully informed about my specific disability and hearing loss rather than base it off a generality. Every person in the world is unique, and that just shows that nobody should be stereotyping even though there can be similar situations, but it still doesn't mean that it's the same situation. Once again, my favorite saying "don't judge a book by its cover" can be used here, where you just don't know what to expect with each and every person and taking the time to get to know each person as who they are instead of being afraid by some intimidation factor and missing out on that knowledge. I guess my intimidation factor is my disability, where people could be intimidated by not knowing what or how to communicate with me or figure out just what I am, afterall I am deaf but I speak pretty damn good for one.

Anyways, I would love to know what people think, leave feedback or anything. I love questions, I love reflections, anything. It all helps me grow as a person to hear these things.

Until next time, who knows when that is, after all I was struck with inspiration!

-Annie

Eek.

I really have lost track of this. But then again, it has been around 6 months since I had to go back to the hospital for a checkup with Mark.

I should have came on to update on my one year mark of the surgery which was june 22nd, then the one year mark of having the implant turned on which was like mid-july, do not actually remember the exact date of it though.

Anyways, I just went for my appointment last week with Mark. It was the usual testing that he does, nothing new to report there. We decided to do a hearing test on my left ear since the last test was december 2009... a super long time ago! and way overdue. Once again the most favorite word of Mark's is "stable" I am the most stable hearing person. No changes with my hearing aid side, no changes with my cochlear implant side. It's all quite dandy.

We did also go to a speech pathologist that day too to just chat and see how I am doing mentally with the implant. The process of getting an implant and learning how to use it requires good mental strength... I have to be strong in my mind of how I really am doing and need to take measures to remind myself of my hearing strengths. I often feel like I am not doing good with my implant and that it isn't making a huge difference in my life. There are times where I have to pull the magnet off my head to remember that it is on, so basically wearing an Implant is easy in how you do not even notice that you are wearing it, which is a good or bad thing sometimes. I like being able to know that I am hearing through vibrations or feeling the sounds in my ear like the hearing aid does. But the Implant is not through my physical ear at all, so it makes it difficult for me to even know that it is on and that I am truly hearing these sounds.

Anyways I was talking about this with this doctor, and she confirmed my thoughts and said that it is tough for a person of my age to pick up the use of the implant quickly, and also I do not have a real sound map in my head since I was born deaf. Most people have that critical period when they are young to hear and learn these sounds for a map in their brain which will help with hearing everything later on in life. I do not have it, so it makes it more difficult for me to even know what I am hearing and have to ask a lot of what i am hearing.

I was feeling a bit down about how my progress was going, so she decided that we should do some tests to see how well i am hearing things. she put these sheets with words on them in front of me and said those words to me without me looking at her and i had to say back what word she just said. I got all of them right... finally she gives me her hardest test which was no visual cues or anything at all, and she asked me these everyday kind of questions and I had to repeat back them. I also got almost all of those correct, just not "how old are you" i said "how are you" instead. but on the second try i managed to figure that out. So those tests helped me feel better and realize that I really am suceeding with the implant more than I thought. My dad was with me at the appointments and he said that he thought I was doing great since getting the implant and it was nice to hear that from him since he doesn't often tell me things like that.

Overall, the appointment wasn't any different.

I do not have much else to report, and I have decided that I have grown tired of updating my blog, so do not expect me to update much more after this unless there's something new. It was useful for when I was going through the process of getting the implant, now it's just about growing older with it and using it.

Until next time, probably not until wintertime which is my next appointment I believe.

-Annie

Appointment update

Wow I've lost track of this blog, and apparently people are still reading it! So I figure I should update...

My last appointment was March 11th, and at this point everything is just staying stable... no new drastic changes. The programs that I have on my remote are the same basic ones, where I have two noise, one focus, and one everyday. They are designed for different types of environments, but the one I use the most is my noise program, it is the most comfortable one for me. I feel like I have not even talked about the remote that I have with my implant ever! Here's a picture of what it looks like:

I pulled up the image that has the labeling of what everything is on it so you have an idea of what it does for me. It's really handy to know the status of the implant through the remote rather than trying to use the controls on the implant itself, which are just two buttons and beeping noises to indicate what program I am on... but anyways I just plugged it into the computer to charge, and checked my volume on all of the programs... I'm maxed out at 10 on all of them... So basically at this point now, I am just working on getting familiar with sounds and voices rather than improving my noise range and stuff like that which was what was being done at the previous appointments.

But if you look at the remote, you can see the different colors indicate different programs, and the one I currently like the best and is using pretty much all of the time is the orange one: noise. I prefer that because it is more focused down in my environment and eliminates a lot of environmental sounds that are annoying and not really necessary for me to hear all the time, it's still there usually but quietened down. The focus (green) program is the more focused program, ideal for one on one conversations in a noisy environment, and you would have the person in front of you's voice made louder by the program to be able to understand better.

The everyday (blue) is the everyday... haha its just everything, no adjustment of softening the environment sounds or amplifying the speaker's voices and stuff like that. It's the sounds just as they are in my head. Sometimes it's nice, sometimes I just get sick of it, and use the noise program.

Anyways, not much news to report on my implant progress... everything is really just stable now and probably will stay this way for the rest of my life. Everyone has hopes for me to get better at hearing what people are saying, and I hope so too. but my expectations are not high because I do not want to disappoint myself if I can never reach my goals of understanding people without the use of lipreading... However I do have some good news on my next appointment, which should be 4-6 months from now, I'll be seeing Mark for the usual stuff and he will also be running tests on my hearing aid side too, since he's now my official audiologist since i got the implant. The other thing I want to mention is that I will also be seeing a speech language pathologist to help with my listening skills at that appointment too! About time I say!

My mom came with me to the appointment, and of course she frustrates me because when Mark asks me questions, she doesn't believe my answers sometimes, but she isn't with me all the time, and has no idea really of my progress. I did realize something after my appointment on my way home that I am starting to feel more comfortable and familiar with sounds in my implant only, like turning off the hearing aid and just listening through the implant. I have noticed that having the hearing aid off does not throw me off anymore, there are times where I had the hearing aid in, but not realize that I forgot to turn it on in the morning and just seem to do fine without the hearing aid. The level of understanding for me is increasing in my opinion, but it does not seem to be reflected when I take those tests in the booth. I kind of feel like it depends on what time of the day I take those tests, if it's morning time, I feel sluggish and don't seem to catch it that good... midday seems to be best for me. So next appointment has to be midday =P

Actually in class on tuesday, we usually have people just calling out terms to be written on the board for review terms. I always sit in the front row and usually just write down what's on the board, but I noticed that I was hearing the terms from behind me and understanding them and writing them down before the writer put them on the board. It was a good moment to realize that I am managing okay to understand people in class, and this is a large class... about a hundred of us or so.

Um... that's all I feel like talking about right now. It would be helpful if people commented on the post with any kind of question or topic they would like me to touch upon in my blog. But other than that, until next time... who knows when that will be?!

-Annie

My job

I realized something today, while I was at work.

I work at the textbook annex on my campus, and I am a cashier, the first type of job I've ever had that involves interacting with customers constantly. I first started this job back in the fall, and was so nervous about my people skills. I remember that I would always get flustered when I actually need to listen to them when I was asking for their information such as phone number and name, etc. If I could not understand them, I started panicking sometimes and just resorting to having them write down their numbers and all that information. Most of the time, I hated being at work because I did not like how nervous I got and how flustered I was with customers. Sure I was new at this, but I still felt that way at the end of working there for two weeks. I kind of wish that I had been working there with both hearing aids, just to know how difficult it would be for me to do all that I do with customers.

But my point is, I realized today, that my cochlear implant has helped me tremendously when it comes to interacting with strangers and asking for their phone numbers and trying to help them when they need it. My confidence level has improved in how my skills are for dealing with customers, like the past two days of work has been good, where I am not having much difficulties with customers, I have not resorted to using pen and paper just to find out something simple like a phone number.

Also, it has been interesting being back at work because at my job, there's always new people every day, and it's fun to get to know a lot of people, even though i may not see them again. I've been talking to a few of them about my hearing loss, and I've been hearing about how other people know certain deaf people and how other deaf people function in the world. One coworker was telling me about how she was in a class, and there was a deaf person there who had an interpreter and she thought it was fascinating how fast the person could sign, and told me of one time where they went to a place, and it had a lot of machinery in the background, and nobody in the class could understand what the professor was saying, and yet the deaf person knew what the professor was saying because the interpreter was standing right next to the professor and could translate everything for him to understand while the rest of the class just stood there clueless of what the heck the professor was saying.

But anyways, I just felt like saying something random and telling everyone about my realization. The other thing I want to mention is that I found another book that is a memoir by a deaf person that seems like it would be interesting to read. I have tried reading "the unheard" by Josh Swiller which I never finished... maybe someday. But the other memoir that I found is called "What's that pig outdoors?" by Henry Kisor, who is a deaf journalist, and it looks like an interesting read, so I may pick it up soon and start reading at it.

That's all for now,

next appointment at the hospital isn't until March, so who knows when the next time I'll post on here,

until then-

-Annie

First post of 2011!

So it's been about 5 months since the implant was turned on. On Wednesday before Christmas I went for my 3 month check up appointment at the hospital with Mark. This visit wasn't any different than the rest, it's becoming more stable when it comes to the tests.

However, having a stable progress with my implant is good, it means I am not getting worse over time, and is moderately just improving my comfortably of using them and understanding people.

There were a few differences with this particular appointment due to how I brought along someone new to it, who did not really know anything about the process or the implant's progress beforehand besides what I had told him, and that person was my boyfriend. He has always been interested in my hearing loss and how I function with the implant and my hearing aid in my left ear, and I thought it would be a good experience for him to actually meet my audiologist Mark and see what it is that I go through every appointment.

I always always always forget how exhausting it is to go to my audiologist appointments. We do our tests in the booth, which is a sound proof room and I am isolated in there with a glass view of my audiologist in the other room doing the tests through the computers and all the equipments. Usually that portion of the appointment takes about 20 minutes to 40 minutes depending on how frustrated and tired I get from repeating back words and using my listening skills... It's obvious how weak my listening skills are when it is tiring to be doing it for a good amount of time. By listening skills, I mean without any visual cues at all... which I pretty much rely on all the time! Therefore, my seeing skills and lipreading skills are awesome. =P Anyways, in there, we did our usual whole routine of me repeating back a word from a tape player of a man's voice saying "ready" then "ball" all that jazz. I still loathe that test... but as I took it this time around, I felt like I did a better job where I did not have as much frustration of trying to figure out what was said and seemed to get more words correct this time around, and yet Mark tells me I'm still stable! He frustrates me! haha. But it is progress towards better due to how comfortable I am getting with the sounds I hear through my implant and seem to have a better ease with how my listening is with it.

I still think that I have a severe to profound hearing loss, but in reality, I don't anymore. I pretty much wear my implant at least 16 hours of the day, and only take it off when I am sleeping. In the majority of my life, I am functioning as a person with a mild hearing loss, and that's it. I hear all of the little sounds now, like the other day I noticed that I heard the timer in the kitchen go off when I was in the living room with the tv on loud and the fireplace blower going... I couldn't believe it when my mom was like, did you just hear that? Because I had heard it without even thinking about it and reacted to it, and I wasn't like focusing on trying to hear it when it went off. Usually when I am cooking something and walk off to another part of the house, I have to try to keep the fact that I am cooking in the front of my mind and not get distracted by anything, but I don't really have to do that much anymore due to how I can hear the little noises that will alert me to the fact I am still cooking. I make tea every day with a tea kettle, and the high pitched noise was always too high for me to hear through my hearing aids without really focusing onto the sound. This is a great benefit for me to have my implant now because now I have a little less to worry about as I embark onto towards a life on my own away from my supportive parents who always gets me out of trouble... I've already had an incident of nearly burning down the house a few times... the one time my parents wasn't there, I caught the tea kettle on fire... oops. And that was all happening pre-implant.

Anyways... I ramble. Back to the appointment, at least what I can remember of it since it happened quite a while ago, right before the holidays. OH! this is the first post of the year! =D happy new years to everyone by the way.

After the tests in the booth, we went into Mark's office and did the adjustments which seemed to take forever, Mark had another audiologist shadowing him showing him the equipments and how to run the programs... and seemed to prolong the process of everything. He had me do the beeping test, where I count out how many beeps I hear, from 1 to 5 in a row. Usually that process is quick, and the point of it is to see how high of a sound I can hear to the lowest sound I can hear and develop a range of sounds that I am able to hear and get an idea of what the programs should allow, where it allows as much possibility for me to hear all kinds of noises, from high to low. While Mark was showing the program to the other guy, my boyfriend was also inching over to see what he was doing too while I'm tired and cranky about doing more tests... haha. But I'm glad he came with me to the appointment and could see everything that I go through, and also it was the second deaf person he was meeting, Mark is also deaf with two cochlear implants which makes him a really awesome audiologist because he knows what it's like to be me going through all of this. And yes, I was the first deaf person my boyfriend has had the opportunity to meet and get to know. =)

Anyways, that was the highlight of the appointment, then of course I had to go see Dr. Smullen my surgeon since she likes to check in and see how my head and ears are. Takes about 5 minutes... getting a bit repetitive and pointless for me to see her every single time I'm there... So I'm quite unhappy about having to make an appointment with her in three months time. I don't see why I can't just see her the appointment after that, like 6 months from now. My mom is the one who is fighting with me over this, and we'll see what the heck happens with that doctor.

That's all for now I believe, next check up appointment is during my spring break, and it's back to school in two weeks, hopefully my stress won't be so bad this time around where my ears hurt from TMJ (it only comes about when i'm really stressed) or tinnitus (also from stress usually) or whatever life throws at me. I'm having a good life, and is not gonna let anything stop me from having a good life. So take that TMJ =P

Until next time, probably March or so if nothing else major happens to my implant in the time being...
-Annie

Update

There is not much to update on.

Life is busy with school and a boyfriend.

However, I do want to say that I absolutely hate the telecoil button on my implant. I by accident turned it on a few days ago, and was freaking out over the noise that started in my head. It basically was extremely uncomfortable to have such static interference from the number of electric products around me, specifically the tv and the laptop.

I should explain how the telecoil works though... and I have to look this information up after all i never realized how it even works.

Basically the telecoil is a coil of wire inside the hearing aid and my implant. It picks up the magnetic sounds that comes from electrical products such as the telephone and tv. They provide sound through magnets and this is pretty much another way for us deaf people to pick up sounds, instead of using a microphone we are using a telecoil to pick up the sounds that is being projected from the magnet found in the electronics. Cellphones do not have magnets in them, so most of them are not usable with the telecoil setting on our hearing aids and implants, however they have created a way for it to be usable with cellphones, and those phones have a rating of from t1 to t4 which is the best.

Anyways... I'm tired of writing about the telecoil, basically I was just not remembering what it's like to have the telecoil turned on and freaked out over that. It was unusual to be hearing things differently through the implant for once.

The other update that I have is that I'm pretty much reattempting at learning sign language again, my boyfriend asks a lot about it, and I realized that I do not remember a lot and it's useful to quickly just sign something from across the room or in a quiet place such as the library where we are often...

Anyways,

back to the grind.

-Annie