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Hi, I'm new here, my name is karen. I just wanted to let everyone

know about my son. His name is Jake. He is 22 months old, blond hair

blue eyes. He was born dec. 23 2002, profoundly death. He failed the

newborn screen at the hospital after he was born. The nurse said it

was just fluid in his ears from being born. We took him anyway to an

ent clinic 2 wks later, where, for some reason he " passed " his abr.

Weeks and months went by, and we just had a gut feeling that he was

not hearing. At every checkup with his pediatrition, we questioned

his hearing and were told his ears were fine. At his 9 month check up

we questioned again. The doc told us in a very non caring voice, if

he is deaf, there is nothing you can do right now anyway. That was

the last time we saw that dr. we took him to Ark childrens hospital(3

hrs. away from home) on march 17 2004. they diagnosed him that day

with profound hearing loss. From that day, we have made that trip

once a week for therapy. On july 21, he was implanted in the left

ear, and turned on mid august. He has done great. we still go once a

wk, and just to let you know, he was implanted in the right ear on

oct6, and will be turned on , on oct 29th. We are very blessed to

have this special boy in our lives. His doc in ark calls him his

bilateral baby.

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Hi ,

Welcome to CI Hear. What a beautiful testimony of the abilities of a cochlear

implant! I'm so thrilled for Jake and for you too. It was a brave decision to

have him implanted and it is paying off. I'm sorry that the pediatrician didn't

help you with this decision. I know that if it were me, I'd make sure he's

aware of Jake's ability to hear now. There could be other children with the

same issues and that pediatrician needs to be educated rather than squashing all

hope.

Jake sounds as if he's a beautiful little boy and his future is bright because

his parents had the courage to seek out help for him. He is blessed to have

you. Thank you so much for sharing and I hope you will continue to tell us

about his progress. Best of luck to you with his second activation. I'm sure

it will be a wonderful day.

Alice

>

> Hi, I'm new here, my name is karen. I just wanted to let everyone

> know about my son. His name is Jake.  He is 22 months old, blond hair

> blue eyes. He was born dec. 23 2002, profoundly death. We took him to Ark

childrens hospital(3 hrs. away from home) on march 17 2004. they diagnosed him

that day

> with profound hearing loss. From that day, we have made that trip

> once a week for therapy. On july 21, he was implanted in the left

> ear, and turned on mid august. He has done great. we still go once a

> wk, and just to let you know, he was implanted in the right ear on

> oct6, and will be turned on , on oct 29th. We are very blessed to

> have this special boy in our lives. His doc in ark calls him his

> bilateral baby. Jake

>

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>

>

>

>

>

>

>

>

>

>

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, I just want to say that I applaud your determination. I hear these

stories and it just makes me want to cry. But these are the kids that will do

just great because their parents never give up on the dream. Congrats on going

bilateral. For us I don't know any other way but it was the best decision I

have ever made for my daughter.

Welcome to the group.

Mom of 4

Marcus 14

12

Jon 10

Annika 2.5

bilaterally implanted 3/1/04

hookup 3/25/04

spastic diaplegic CP

my son JAKE

Hi, I'm new here, my name is karen. I just wanted to let everyone

know about my son. His name is Jake. He is 22 months old, blond hair

blue eyes. He was born dec. 23 2002, profoundly death. He failed the

newborn screen at the hospital after he was born. The nurse said it

was just fluid in his ears from being born. We took him anyway to an

ent clinic 2 wks later, where, for some reason he " passed " his abr.

Weeks and months went by, and we just had a gut feeling that he was

not hearing. At every checkup with his pediatrition, we questioned

his hearing and were told his ears were fine. At his 9 month check up

we questioned again. The doc told us in a very non caring voice, if

he is deaf, there is nothing you can do right now anyway. That was

the last time we saw that dr. we took him to Ark childrens hospital(3

hrs. away from home) on march 17 2004. they diagnosed him that day

with profound hearing loss. From that day, we have made that trip

once a week for therapy. On july 21, he was implanted in the left

ear, and turned on mid august. He has done great. we still go once a

wk, and just to let you know, he was implanted in the right ear on

oct6, and will be turned on , on oct 29th. We are very blessed to

have this special boy in our lives. His doc in ark calls him his

bilateral baby.

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Hi -- what a special mom you are to have Jake bilaterally implanted at a

very young age. He will benefit from the bilateral implants. I am glad that you

persevered until you got the answers you needed for Jake and started him off on

the right path to hearing again.

Snoopy

bilateral CIer

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