She's completely deaf.
Her deaf ed teacher, H and I had suspected it for awhile, but her other tests had come back normal. Her ENT blew us off, but we pushed for additional testing. She had a "behavioral" hearing test today. The goal was to get her to look toward the noise. Not only did she not do that, when they looked at her physical response (eyes widening, blinking, sucking faster or slower on her binky, startling, etc.), she didn't flinch at a single sound - not even the ones that had me wincing.
The audiologist said it has to be neurological. The next step is another sedated ABR just to see if there's something the first audiologist missed and an MRI. We've been doing some signs with her already, but I'm taking an intensive class at the end of the month and we'll be trying to incorporate more and more signing with our conversations.
I had a minor meltdown, but I'm still in a bit of shock. I mean, we suspected it, but knowing for sure that she hears nothing is a pretty big blow.
Re: Confirmation. :(
That is a big blow. And I'm not going to offer any 'but at least...' or anything else.
Take whatever help and support you can get for yourself right now. Do whatever feels right for yourself right now.
I'm really sorry to hear that. I know it seems tough now but you all will learn signs so fast and she'll probably catch on quick too.
I went to school with two deaf girls and we all took classes so that we could communicate with them. They went to all of our regular classes and had an interpreter with them at all times. They never missed out on anything
Oh honey...
I'm so glad that she has proactive parents like you.
I frequent on another board, but i hope you don't mind me commenting.
I'm sorry, it is so hard to hear that diagnosis. As an Audiologist I hope I can offer another insight.
Has no one mentioned a cochlear implant? Children that are implanted early (around age 1-2) can often develop speech and language and enter kindergarten in a regular classroom. The outcomes of children implanted with CIs is much impacted by implantation age. The younger the better, thus allowing them exposure to speech and language and with therapy, help them right on tract with language development. Signing is great for the meantime, but I would not view this as a long term solution. Sign language is fine if you live within a deaf community, but replying on this as her primary form of communication will limit her opportunities. Many parents struggle with letting their child have the choice to have a cochlear implant. Unfortunately the reality is is a child is born deaf, the success rate of the implant really is related to age of implantation. Waiting even until age 5+ can severely impact the success of language development. A cochlear implant is an great example of what technology can offer. It is amazing to think a child born with profound hearing impairment has the opportunity to hear and lead a life of hearing .
I'm sorry for her diagnosis, it is a lot to take in! Find a good audiologist who can go over all of her options. She has many, and it will all turn out fine. Good luck!
when i open this post i want to send my condolences to you.
but then i thought about it.
you are an amazing mom to an amazing daughter, period. she is so lucky to have you as her mom- it really is a blessing.
whether our babies are deaf, lost before birth, special needs...they are our babies. we love and adore them for who they ARE not what they were supposed to be.
( i do want to send you huge hugs. hearing that our babies aren't totally perfect i hard to hear. we're all here for you in all your successes and bumps in the road.)
~Lisa
Mum to Owen and Lucas
aw hun, I'm so sorry
Ryan 5/2010, Kyle 1/2007, Eric 3/2005
I'm so sorry. That had to be hard news to take.
(On a somewhat random note, every time I see the picture of her, it makes me smile. She's a beauty.)
Kelly Monaghan's 5K - 5/15/11 - 3rd Place in AG
Walk the Talk 5K - 5/18/11 - 31:12 PR
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Oh girl, I am sorry to hear that. But like I said before, I am so not worried about Ruby. She's gonna be just fine.
(((HUGS)))
You take my ovaries, I take your yarns.
Yup. This. But extra *hugs* since I know how shocking it can be to get a diagnosis about your child like that. If you ever want to talk or just vent, PM me.
Nora Judith 7/2/06 Miles Chauncey 4/20/09 born with Trisomy 21 - Down syndrome
(((hugs)))
You have a little diversion in your expected path, but everything is going to be alright.
Charlotte Ella 07.16.10
Emmeline Grace 03.27.13
Thanks everyone for all the responses. I'm so glad to have this place for support.
I don't feel sorry for myself. I don't even really feel sorry for Ruby. I just hate to think of other people making her feel different. The world is cruel and I hate that she'll have to deal with more than an average kid.
At nearly 6 months old, I can already tell she's destined for great things (I know that's so cliche', but I truly believe it). She's an amazing little girl with a huge personality. She so charming and sweet. I'm so proud to be her mama.
Really, right now, I just feel a bit helpless. I desperately want to learn sign language RIGHT NOW so I'm armed with the tools I need to communicate with her. I hate thinking that she might feel left out.
To the PP who mentioned the cochlear implants: yes, we've been informed about them. However, at this stage in the game, we aren't considering them. While we realize what amazing technology it is and how much it has helped deaf children, we're just not sure they're for our daughter/family. We don't think of her as needing to be "fixed" to be like everyone else. At this point, we feel like she can have just as wonderful and fulfilling of a life without CIs as she could with them. They don't always work, the long-term effects aren't know and they would damage her ear(s), which are currently perfect structurally. We're not completely ruling them out and we absolutely see the attraction to them, but they aren't our first line of defense. We don't want to rely on technology that may not even help her. I appreciate the info, though.
I'm so, so thankful for Ruby's deaf educator. She offered to join us at the test today and was a great support. She's been so amazing over the past few months and I feel really confident in her helping Ruby learn everything she needs to to reach her full potential. I don't know how we'd be getting through it without her.
Hugs to you, Mama. What a rough road - but you got this. You and R will rock this. And in your 'moments', we'll be here to listen.
Kiwi Fruit, 10.2.06 & Ellie Bug, 4.5.09
My blog: Bear With Us
Ideas on Teaching Your Toddler/Preschooler at Home
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Aiden 10.17.07 Emma 07.15.10