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Don,

I wanted to congratulate you on taking the first step! Making the choice to

be evaluated for a CI is one of the hardest decisions of all to make. In my

case, it took several years before I seriously considered getting a CI. My

CI application spent close to a month lying in a drawer because I kept

telling myself that " my hearing couldn't be severe enough to qualify as a

candidate. " However, after reading the experiences of others on this list

and sharing many of the same frustrations, I knew the time was right and

that I had nothing to lose. Super power HAs with an FM system no longer

allowed me to hear/understand speech even in quiet one-on-one situations. I

was tired of using interpreters/captionists to hear/understand people around

me or being left out completely when a captionist or interpreter wasn't

available. My CI evaluation revealed that I was a good candidate. I was

implanted a few days ago and if I had to do it all over again, I would!

Here's wishing you all the best on your journey!! Good luck!! If you have

any questions along the way, please do not hesitate to ask. :)

Implanted: 12/22/04

Activation date: 1/18/05

Deafblind/Postlingual

BTE hearing aid user 19 years

Severe-profound hearing loss 9 1/2 years

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Don,

I have a cousin (also named Don) who had his CI done at one of the

universities in St. Louis. He's very happy with them. You may want

to look into that possibility. I know I looked into both KUMC and

Wichita Ear Clinic before deciding on Wichita Ear Clinic for my CI.

It's just nice to have choices. =)

Beth

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Don,

I have a cousin (also named Don) who had his CI done at one of the

universities in St. Louis. He's very happy with them. You may want

to look into that possibility. I know I looked into both KUMC and

Wichita Ear Clinic before deciding on Wichita Ear Clinic for my CI.

It's just nice to have choices. =)

Beth

Unfortunately in our age of HMO's, " choice " is not always a " choice. " I will

be checking with my HMO tomorrow to see what my options are. I'm not entirely

confident that they will even consider a CI, let alone allow me to have a

choice.

You're probably thinking of Washington U in St. Louis. One of the finest Med

Schools in the country.

And . . . as an old duffer who has seen " little things lead to big wars " in a

lot of instances, I would suggest you steer clear of the stem cell research

issue. It is bound to bring up some very visceral feelings. For some, perhaps

many of us, (including me) it is grounded in a religious belief - and you KNOW

what religious disagreements lead to. (If not, do a google on " jihad " and

" crusades " and see what you find.) The stem cell issue could certainly

fracture this group right down the middle.

Don C.

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Don,

I think it was Washington U that he said he goes to for his CI

stuff. If your insurance won't cover the CI, check with vocational

rehabilitation. Kansas Voc. Rehab. covered my CI because insurance

wouldn't. That doesn't help with the cost of mappings after the

rehab. is finished, and doesn't cover cords, batteries, etc., but it

does cover the surgery, rehab., a certain number of the mappings (I

think mine were covered for the first year), and two processors

along with the initial batteries, cords, etc.

Good luck!

Beth

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Just wondering how you felt about the Wichita Ear Clinic as that's where I

was selected for a CI.

Randall

Re: Re: Thanks for replies

Don,

I have a cousin (also named Don) who had his CI done at one of the

universities in St. Louis. He's very happy with them. You may want

to look into that possibility. I know I looked into both KUMC and

Wichita Ear Clinic before deciding on Wichita Ear Clinic for my CI.

It's just nice to have choices. =)

Beth

Unfortunately in our age of HMO's, " choice " is not always a " choice. " I

will be checking with my HMO tomorrow to see what my options are. I'm not

entirely confident that they will even consider a CI, let alone allow me to

have a choice.

You're probably thinking of Washington U in St. Louis. One of the finest

Med Schools in the country.

And . . . as an old duffer who has seen " little things lead to big wars " in

a lot of instances, I would suggest you steer clear of the stem cell

research issue. It is bound to bring up some very visceral feelings. For

some, perhaps many of us, (including me) it is grounded in a religious

belief - and you KNOW what religious disagreements lead to. (If not, do a

google on " jihad " and " crusades " and see what you find.) The stem cell

issue could certainly fracture this group right down the middle.

Don C.

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Randall,

The people at the Wichita Ear Clinic are the greatest! I had Dr.

Kryzer as my surgeon, and Kim Bell does my mappings. Molly at St.

Francis did my rehab, but I think Kim does that now, too. I think

you'll be very happy with them. I just can't say enough good about

them.

Beth

>

> Just wondering how you felt about the Wichita Ear Clinic as that's

where I

> was selected for a CI.

>

> Randall

>

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I too had Dr. Kryzer for consultation and was/is to be my surgeon, and I

think it was Kim Bell who did my first hearing test during my first visit

there. And Jeff did the pre op test to establish a base line for my present

hearing ( or lack there of ).

Just a little nervous right now playing the waiting game.

Thanks for the reply.

Randall

Re: Thanks for replies

Randall,

The people at the Wichita Ear Clinic are the greatest! I had Dr.

Kryzer as my surgeon, and Kim Bell does my mappings. Molly at St.

Francis did my rehab, but I think Kim does that now, too. I think

you'll be very happy with them. I just can't say enough good about

them.

Beth

>

> Just wondering how you felt about the Wichita Ear Clinic as that's

where I

> was selected for a CI.

>

> Randall

>

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Randall,

I know it's easier said than done, but try not to be too nervous.

You're in very good hands. Jeff is from my hometown. =) I'm going

in for an appt. with Kim tomorrow afternoon. If you feel the need

for moral support, I'll be back in Goddard 5 days/week starting Jan.

3rd.

Beth

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  • 1 year later...
Guest guest

thanks jo and angie (?) for your replies. im gonna get started on researching

this right now. i appreciate you both pointing me in the right

directions...thanks! phil

Re: [ ] new to group/anti viral Qs

Hi Phil

Welcome! Simply go to the autism treatment list and enter the 'files' section,

and you will find a huge file on viral therapy which directs you to all the

relevant websites.

HTH

Jo

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