Jump to content
RemedySpot.com

RE: Cochlear Implants

Rate this topic


Guest guest

Recommended Posts

I have a friend that went through the process, but I don't know of any children.

If you like you might want to locate a cochlear implant support group. They may

help you or you might contact my friend. Let me know.

Patty

To: polymicrogyria

From: estherhutman@...

Date: Mon, 7 Feb 2011 01:22:17 +0000

Subject: Cochlear Implants

Hi everyone,

My 13 month old Sammy (PMG) failed the newborn hearing screening and has

been wearing hearing aids since he was 4 months old. We are seeing some

response to sound, but they are for the most part subtle and not

consistent. At our last visit to the audiologist, she recommended that

we start the process for cochlear implants, to determine if it is an

option for him.

Do any of you have experience with cochlear implants?

thanks,

Esther

Link to comment
Share on other sites

How much of a hearing loss does your child have?

________________________________

To: polymicrogyria

Sent: Sun, February 6, 2011 7:22:17 PM

Subject: Cochlear Implants

Hi everyone,

My 13 month old Sammy (PMG) failed the newborn hearing screening and has

been wearing hearing aids since he was 4 months old. We are seeing some

response to sound, but they are for the most part subtle  and not

consistent. At our last visit to the audiologist, she recommended that

we start the process for cochlear implants, to determine if it is an

option for him.

Do any of you have experience with cochlear implants?

thanks,

Esther

------------------------------------

Link to comment
Share on other sites

Our daughter was diagnosed with hearing loss at 6 weeks. She was fitted

with hearing aides and underwent numerous test to quantify her degree of loss.

At age 2 1/2 she had an ABR under GA and they determined she was profoundly deaf

in both ears.

She was put on the cochlear implant program and after a few months received an

implant in her right ear.

We then had to wait for 6 weeks for it all to heal. There is always a concern

that there will be no response when they finally turn it on, so we were stoked

when screamed. Meant she was finally " hearing " sounds.

That is the easy part. It takes a lot of time / commitment with the therapy.

It was a fair bit of learning for us and the audiologists / therapists. Kiddies

with other disabilities respond at much slower rates than kids with just hearing

loss. We found that we would sometimes have to wait 20-30 seconds for a

response to a sound.

We also changed her mappings much more slowly than normal as sometimes they

would bring on seizures.

is now five and can recognise >50 words and phrases. She does not speak

words herself, but has definitely started verbalising much more since being

implanted. Her mother is sure she says " mum " :-)

So in conclusion, a lot of hard work, but worthwhile so far.

Dad to , 5 yo with BFPPMG

Link to comment
Share on other sites

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.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...