Yeah, we had to do it.
We think our precious girl would be just perfect as a BOND(S) girl!
will you vote for her?
Jaime H | BONDS Baby Search 2013
Friday, 22 February 2013
BONDS Baby Search 2013
VOTING IS OPEN!
Yeah, we had to do it.
We think our precious girl would be just perfect as a BOND(S) girl!
will you vote for her?
Jaime H | BONDS Baby Search 2013
Yeah, we had to do it.
We think our precious girl would be just perfect as a BOND(S) girl!
will you vote for her?
Jaime H | BONDS Baby Search 2013
Quiet Beginnings
My story begins in February of 2012, after feeling under the weather at work I returned home via the chemist to pick up a pregnancy test, mothers intuition perhaps? I was pregnant!
Now expecting our first child my husband and I were elated!
The next 9months were filled with excited planning and dreams of the little being that was rapidly growing in my belly.
"Birth-day" arrived and we welcomed a beautiful healthy baby girl into the world. My little angel was absolutely perfect in every way!
At two days old the nurses arrived to check Jaime's health and hearing, my husband was out at the time and I was not bothered in the least as everything was going to be fine, or so I thought.
I still remember watching the nurse hunched over my tiny baby laying content in her cot, "she has been there a long while" I thought to myself, and then she looked up and told me, "Jaime is not responding as I would like, it might be fluid in her ears, I will come back tomorrow". I was shocked but confident that tomorrow all would be fine, tomorrow came and went and another failed hearing test, this time I cried. Was my perfect baby not so perfect? How could this be?
Guilt, bewilderment, heartache... What went wrong?
I felt silly, how could I think this way about my child, my beautiful baby, was there truly something 'wrong' with her?
It was another month before we had a diagnosis, a month of both coming to terms with the thought that my baby might be deaf, but also a month of denial, 'surely they will turn to me and say it was all a mistake!'
I have a medical background and I am still undecided if this has helped or not, I knew that deafness can be managed, technology exists that can help my baby hear and achieve, but how will I cope, how will I look after a baby with additional needs?
At four weeks of age Jaime was diagnosed with sensorineural hearing loss, she is profoundly deaf on her left and has a sever hearing loss on her right (this means she can only hear sounds 80db and above)
At seven weeks of age Jaime was fitted with her first pair of hearing aids. This was an exciting step forward- the thought that she may, for the first time, hear her mothers voice, I had never thought about how much this could mean. Jaime's 'purple pair' were fitted and we waited, Jaime paused, deep in thought, hearing... Something...? A clap.. A blink.. Success! We returned home with hope for Jaime's future.
As we progressed through multiple appointments and fortnightly fittings for new hearing aid moulds, it became clear that her 'purple pair' might not be enough, this sent us down the path of the cochlea implant.
Before you judge my feelings of disappointment at learning that my baby is deaf, please I urge you to read "welcome to holland" I was handed this story not long after being given Jaime's diagnosis, I felt like finally someone was reading my mind...
My child is still perfect, perhaps not what I had expected or planned, but she still lights up my world, this tiny being that I first lay eyes on and with whom I fell instantly in love.
This tiny being is still exactly the same, only my knowledge has changed.
Now expecting our first child my husband and I were elated!
The next 9months were filled with excited planning and dreams of the little being that was rapidly growing in my belly.
"Birth-day" arrived and we welcomed a beautiful healthy baby girl into the world. My little angel was absolutely perfect in every way!
At two days old the nurses arrived to check Jaime's health and hearing, my husband was out at the time and I was not bothered in the least as everything was going to be fine, or so I thought.
I still remember watching the nurse hunched over my tiny baby laying content in her cot, "she has been there a long while" I thought to myself, and then she looked up and told me, "Jaime is not responding as I would like, it might be fluid in her ears, I will come back tomorrow". I was shocked but confident that tomorrow all would be fine, tomorrow came and went and another failed hearing test, this time I cried. Was my perfect baby not so perfect? How could this be?
Guilt, bewilderment, heartache... What went wrong?
I felt silly, how could I think this way about my child, my beautiful baby, was there truly something 'wrong' with her?
It was another month before we had a diagnosis, a month of both coming to terms with the thought that my baby might be deaf, but also a month of denial, 'surely they will turn to me and say it was all a mistake!'
I have a medical background and I am still undecided if this has helped or not, I knew that deafness can be managed, technology exists that can help my baby hear and achieve, but how will I cope, how will I look after a baby with additional needs?
At four weeks of age Jaime was diagnosed with sensorineural hearing loss, she is profoundly deaf on her left and has a sever hearing loss on her right (this means she can only hear sounds 80db and above)
At seven weeks of age Jaime was fitted with her first pair of hearing aids. This was an exciting step forward- the thought that she may, for the first time, hear her mothers voice, I had never thought about how much this could mean. Jaime's 'purple pair' were fitted and we waited, Jaime paused, deep in thought, hearing... Something...? A clap.. A blink.. Success! We returned home with hope for Jaime's future.
As we progressed through multiple appointments and fortnightly fittings for new hearing aid moulds, it became clear that her 'purple pair' might not be enough, this sent us down the path of the cochlea implant.
Before you judge my feelings of disappointment at learning that my baby is deaf, please I urge you to read "welcome to holland" I was handed this story not long after being given Jaime's diagnosis, I felt like finally someone was reading my mind...
My child is still perfect, perhaps not what I had expected or planned, but she still lights up my world, this tiny being that I first lay eyes on and with whom I fell instantly in love.
This tiny being is still exactly the same, only my knowledge has changed.
Welcome
Welcome to Jaime's quiet world.
In this blog I will share our story of living with a deaf child from diagnosis to hearing aids and the journey to cochlea implantation as well as the day to day joys and challenges in between.
This is our story and follows the choices we have made as a family. I hope that this may provide support to those who too are entering the world of deafness, wether be it newly diagnosed or well on your journey, confident or bewildered.
Feel free to leave comments, ask questions and share your story too.
(Please do not judge our decision to implant, I know there are strong objectors out there, I am open to discussions and questions however this is not a debate and negative comments criticising or attacking those who choose to implant their child will be deleted, I support everyone's choice however if you choose to object please do it somewhere else)
My aim is to support and inspire other parents of deaf children so they may walk through their own quiet worlds with confidence.
Come join us on our journey through Jaime's Quiet World!
In this blog I will share our story of living with a deaf child from diagnosis to hearing aids and the journey to cochlea implantation as well as the day to day joys and challenges in between.
This is our story and follows the choices we have made as a family. I hope that this may provide support to those who too are entering the world of deafness, wether be it newly diagnosed or well on your journey, confident or bewildered.
Feel free to leave comments, ask questions and share your story too.
(Please do not judge our decision to implant, I know there are strong objectors out there, I am open to discussions and questions however this is not a debate and negative comments criticising or attacking those who choose to implant their child will be deleted, I support everyone's choice however if you choose to object please do it somewhere else)
My aim is to support and inspire other parents of deaf children so they may walk through their own quiet worlds with confidence.
Come join us on our journey through Jaime's Quiet World!
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