AshJagla
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- Joined
- Sep 15, 2012
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Hi everyone, my name is Ashley, I'm in my early 20's, I have 2 little girls that are 2 1/2 and 1 yr. They were both premature, with speech delays, but we've just recently realized that our 1yr old's delays are due to her hearing loss.
Not really sure what I'm doing, still waiting to go to my daughter's first audiologist apt this coming Thursday, where I know I'll just be told that she will need further testing by a better hospital. I'm just feeling lost and impatient, I want to know how severe it is, I want to know what her options are and I really need that dx so we can get early intervention over here to help teach us asl and wok with her on speech.
She's 13 months and has never passed a hearing test, but we were always told that those infant ones are so sensitive that if she's too loud or moving too much, they will come back failed, so we didn't worry about it until we noticed she still wasn't responding to her name and hasn't said any words yet... She does coo though, and it sounds as though she varies her pitch... so maybe there is something there still. We've done things like knocking on doors and dropping pans nearby with no interest from her, I hold her on my lap and call her name while she's facing the other direction, she has yet to turn around.
Anyway, I just wanted to come here and see if anyone has had a small child with hearing loss and wants to share their experience, or even an adult who just wants to chat about completely non related issues to pass the time. You can share your thoughts on HAs and CIs or any opinions that you have. I want to try and understand what the world is like to her... I know this isn't a tragedy, a tragedy would be something that would hold her back from living life to the fullest, I don't want to feel sorry for her, she deserves better than that, I just want to be the best mother to her that I can be.
Not really sure what I'm doing, still waiting to go to my daughter's first audiologist apt this coming Thursday, where I know I'll just be told that she will need further testing by a better hospital. I'm just feeling lost and impatient, I want to know how severe it is, I want to know what her options are and I really need that dx so we can get early intervention over here to help teach us asl and wok with her on speech.
She's 13 months and has never passed a hearing test, but we were always told that those infant ones are so sensitive that if she's too loud or moving too much, they will come back failed, so we didn't worry about it until we noticed she still wasn't responding to her name and hasn't said any words yet... She does coo though, and it sounds as though she varies her pitch... so maybe there is something there still. We've done things like knocking on doors and dropping pans nearby with no interest from her, I hold her on my lap and call her name while she's facing the other direction, she has yet to turn around.
Anyway, I just wanted to come here and see if anyone has had a small child with hearing loss and wants to share their experience, or even an adult who just wants to chat about completely non related issues to pass the time. You can share your thoughts on HAs and CIs or any opinions that you have. I want to try and understand what the world is like to her... I know this isn't a tragedy, a tragedy would be something that would hold her back from living life to the fullest, I don't want to feel sorry for her, she deserves better than that, I just want to be the best mother to her that I can be.

My loss, amazingly so, wasn't noticed until I was six years old. My mother worked as an RN for many years and she was pretty aggressive in making sure I had all the resources I needed growing up in public schools, namely speech therapy, and she wasn't shy about holding back if the felt the therapists weren't doing a good enough job. I would recommend not getting too far ahead of yourself until she's been tested. It could be a mild, moderate or severe loss, but all easily managed with hearing aids. You sound like you have a positive outlook so stay positive and take it one day at a time. 
. Just sayin'. Anyways, my youngest step-son was born profoundly deaf in both ears and so his bio parents decided at the time to give him CI's so that he would be bilingual. That was the choice that they made, and he's been mapped out 5 times but the audiologist says he has full hearing now as far as that goes. But then again, I don't know exactly how distorted or anything CI's can be as I am mostly hearing. He will be 3 in January, however his hearing age is 1.5 years as far as I know. If it were my decision, I don't think I would've given him the CI's because of all the recovery time he required, and because frankly deaf culture is so beautiful. Besides, think of it this way.... we are created as we were intended to be at birth, as near mirror images of a divine source; why should human kind try to change that which is perfect to begin with ? Perhaps a bit too religious/spiritual in nature but it's just how I feel. In the end really it's the parents decision, if I can be of any help or support just reach out. Take care!