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Activated Today

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Steve,

Congratulations on your activation! The world is a noisy place, isn't it?

<smile>

I hope you'll let us know what happens at your mapping tomorrow. Good luck!

Implanted: 12/22/04 Activated: 1/18/05

Deafblind/Postlingual

BTE hearing aid user 20 years

Severe-profound hearing loss 10 years

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Steve,

Congratulations!

Great news. Enjoy your adventure!

Dale

--- steve stevens <bbb1340@...> wrote:

> Hello, ALL,

>

> My FREEDOM was activated today at 1:45.

>

> By 2:00, I could make out what my audie was saying

> with head turned away so NO lip reading!!!!! It was

> more emotional that I would have imagined. I was

> overwhelmed when I walked outside. I go back in

> tomorrow for more tuning.

>

> I can hear the keys on my laptop click as I type

> this.

>

> Thanks for all the info.

>

> Steve

>

>

>

> ____________________________________________________

> Start your day with - make it your home page

> http://www./r/hs

>

>

>

>

__________________________________________________

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How exciting! I have heard so many people talk about how emotional

their activations were. I am scheduled to have mine done around 3pm

on Monday August 22nd.

When you hear the new sounds, is it overwhelming?

Kathi Sampson

> Hello, ALL,

>

> My FREEDOM was activated today at 1:45.

>

> By 2:00, I could make out what my audie was saying

> with head turned away so NO lip reading!!!!! It was

> more emotional that I would have imagined. I was

> overwhelmed when I walked outside. I go back in

> tomorrow for more tuning.

>

> I can hear the keys on my laptop click as I type this.

>

> Thanks for all the info.

>

> Steve

>

>

>

> ____________________________________________________

> Start your day with - make it your home page

> http://www./r/hs

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Hi Kathi!

Everyone reacts in their own way on hook up day. For me, I was

not a crier on my hook up day. I was stunned speechless during my

activation and my youngest sister, who got the honor of taking me to

my hook up day, did the crying. All throughout my CI Candidacy, I

thought the implant motto was high hopes, no expectations. It's

actually high hopes, low expectations. Anyway, I had no expectations

on my hook up day. My sister had all she could handle with me, in

the waiting room, because I was still convinced that it was not going

to work for me. I was thrilled when I heard that first beep and all

the beeps when my audie set my T's and C's levels. I shot out of my

chair with the first beep. It had been years since I actually heard

a beep! Yes, I was overwhelmed! My sister said she never saw my

eyes so wide. When my processor was turned on, I heard my audie say

say a 3 syllable sentence. I turned to him and asked if he just

said, " Can you hear me now? " He had! I didn't hear it clearly; but

I knew this was going to be workable! It was then I let out a big

whoop and hugged my sister who was still crying. It took 3 more

months before speech discrimination started kicking in for me; but it

was AWESOME to be able to hear the environmental sounds and my

family's voices as they spoke even though I could not understand

what they were saying without lipreading.

Good luck to you with the rest of you recovery and your hook up

day! It's not far away now!

Patti

Surgery Day 11/25/02 (What A Day!)

Hook Up Day BWP 1/2/03 (A Happy Day!)

3G 1/31/03 (An Even Happier Day!)

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Steve,

You are in for a great ride now. Start a journal if you have not

already.

congrats and keep us all posted on your journey back to sound :-)

Cheers,

Evel

Nucleus Advocate

n24c 05/05/04

> Hello, ALL,

>

> My FREEDOM was activated today at 1:45.

>

> By 2:00, I could make out what my audie was saying

> with head turned away so NO lip reading!!!!! It was

> more emotional that I would have imagined. I was

> overwhelmed when I walked outside. I go back in

> tomorrow for more tuning.

>

> I can hear the keys on my laptop click as I type this.

>

> Thanks for all the info.

>

> Steve

>

>

>

> ____________________________________________________

> Start your day with - make it your home page

> http://www./r/hs

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  • 1 year later...
Guest guest

Hi:

This forum has been so helpful to me in just accepting my hearing loss. So,

a huge thank you!

And now my news......I am finally activated. And everything sounds like a

staticky male computer voice! I know it'll take some time to get used to.

It's strange to me how some sounds are so loud, and some sounds are so soft.

I know - have patience! I can even tell that I've made some progress in

just the 5 hours I've had my CI.

Rhona

4/3/07 Surgery

5/8/07 Activated

Univ of Miami

Dr. Balkany

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Guest guest

Wow Rhona, I'm so excited for you!!! This must be such an

overwhelming day for you, I'm sure! Every time someone posts about

their activation day, my heart starts beating faster and I get so

excited for them, just knowing that my surgery should be coming up

pretty soon and imagining how I would feel myself on that day!

I'm pretty new here, so sorry for this question, but how did you lose

your hearing? Or have you been hearing-impaired your whole life? I

had perfect hearing my whole life, but as a result of Autoimmune

Inner Ear Disease, which I was diagnosed with at the end of November,

I am now completely deaf! I've been deaf now since about the middle

of January, and let me tell you, what a nightmare this has been!!

But every time I come here and hear people share their stories about

how great their CI's are, I am filled with so much hope that this

might work for me too!

I really hope you do well with your CI, and I will be following your

story closely to hear how things go for you. Please keep sharing as

much as you can because I would really like to know what to expect

after my surgery.

Good luck, Rhona, and I wish you all the best!

>

> Hi:

>

> This forum has been so helpful to me in just accepting my hearing

loss. So,

> a huge thank you!

>

> And now my news......I am finally activated. And everything sounds

like a

> staticky male computer voice! I know it'll take some time to get

used to.

> It's strange to me how some sounds are so loud, and some sounds are

so soft.

>

> I know - have patience! I can even tell that I've made some

progress in

> just the 5 hours I've had my CI.

>

> Rhona

> 4/3/07 Surgery

> 5/8/07 Activated

> Univ of Miami

> Dr. Balkany

>

>

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Guest guest

Hi :

I'm so sorry to hear about your hearing loss with Autoimmune Inner Ear Disease.

I can somewhat understand what a difficult time it must be for you!

My hearing loss was gradual, starting with tinnitus in my early 20's and then

getting progressively worse in my 30's with hearing loss and tinnitus. (I'm

43.) I used HA (hearing aid) for both ears since 2004 though I only heard

sounds in my left ear and could not understand the words. The hearing in my

right ear would vary and go up and down, ranging from (in my own description)

" ok " to practically deaf " .

Today, I have severe to profound hearing loss in both ears, but no diagnosis as

to why I had the loss. As far as I know, my hearing loss is not genetic.

My CI surgery was not bad at all. I even had a small complication and had to

stay overnight as a precaution. Dr. Balkany (my surgeon and head of the dept

at Univ of Miami) were: " the first month will not be very different " (I had the

surgery but they wait about one month for activation), " the second month will be

frustrating and you'll question why you ever did this " (he is exactly right!)

but by the third month, maybe a little longer, you'll be through the roof

because you have more hearing than most people that have this surgery and your

brain remembers how to hear. Because of this, you should do very well. " SO, I

know Dr. Balkany is an expert in his field and trust that he absolutely knows

what is going on. I'm just trying to be patient with the process, which will be

a good learning experience for me as I am not a patient person.

I hope this answers some questions for you. I did not even know about this

group prior to surgery and it has been so helpful to me. Not only do I feel

more knowledgeable about understanding my CI, but I also feel SO much more

accepting about my hearing loss. Email me privately if you need.

Rhona

4/3/07 Surgery

5/8/07 Activated

Univ of Miami

Dr. Balkany

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