Simone can’t hear.
I thought maybe typing that right at the beginning, getting it out of the way, would make this easier to write about, but guess what? No.
Yesterday was Simone’s big five-month developmental assessment at the NICU follow-up clinic. The appointment consists of visits with a neonatologist and nurse practitioner; a check-up; and a standardized test called the Bayley, administered by an occupational therapist. I might as well admit that I was feeling confident, going in. I knew Simone might have trouble with her fine motor skills, and maybe sitting, but I was wasn’t expecting anything but praise for how fine and fat she is growing, and what a strong, smart baby she has become. She is seen only once a month by Early Intervention, because after her evaluation in early September they decided she was doing too well to require more frequent visits. Though front-to-back still eludes her, she has started rolling back-to-front. Besides, each baby develops at her own pace: insert story about a friend-of-a-friend who didn’t talk until the eighth grade and is now a Rhodes Scholar, reminder that every child is a unique snowflake, et cetera, et cetera.
The evaluation started well. Simone is slightly above her adjusted age for cognitive skills, and a whole month above for expressive language. Her motor skills need some work, partly because I didn’t know she was supposed to be sitting at a tabletop to play with things (What does a baby need with a tabletop? A place to write? To hold tiny mock U.N. debates?), but her delay is relatively minor and not due to any physical limitation—she just needs practice.
I’m not sure exactly when it happened, but at some point the therapist began to look concerned. She asked whether Simone responds to her name. No, she doesn’t. Other words? Well…no. Does she turn toward noise? I hadn’t noticed, excellent and observant parent that I am.
Then, standing behind Simone, the therapist rang a metal handbell—LOUDLY. Loudly enough that my own ears were ringing. And Simone didn’t so much as flinch.
It was chilling, to watch Simone burbling obliviously in my face, while behind her gongs sounded and noisemakers shrilled. We tried rattles, crumpled paper, sudden clapping—nothing. I felt sick and panicked and unspeakably sad for my baby. And, I confess, weak with guilt. How did I miss this? How do you miss the fact that your baby can’t hear? Simone is very responsive to me, but it has now been demonstrated that she is responding to my facial expressions. She gets excited when Scott comes home from work, but not until she sees him. Her visual perception of her environment, it was noted, is especially keen, probably compensating for the fact that SHE CAN’T HEAR A DAMN THING.
After the Miracle Worker routine of bells and whistles and desperate cries of Helen!, the specialists conferred and then filed back in, looking grim. Because of what seems to be a hearing loss, Simone’s receptive language is at a two-month level. Examination of Simone’s ears reveals no wax or obvious fluid. She hasn’t had a fever or infection. She passed her newborn hearing exam, and because she learned a few months ago to mimic the intonation of “hello” (which, come to think of it, she hasn’t done in a long time), I am wondering whether she may have been able to hear at one point and now cannot. The neonatologist pulled some strings to get us a November 5th appointment with an ENT. November 5th seems terribly far away.
The best-case scenario, and the one I am fervently hoping for, is that there is fluid somewhere deep in Simone’s ears, and that all she will need is tubes put in to keep it draining and then therapy to make up the language acquisition skills lost by the months of deafness. The worst-case scenario is permanent, profound hearing loss. It can have a delayed onset, which I didn’t know, and Simone has several of the risk factors.
Believe me, I’m aware that as worst-case scenarios go this is a relatively cushy one; there are other, more devastating disabilities. But allow me to wallow for a moment. Simone has had PDA ligation surgery, multiple transfusions, severe jaundice, an infection, two bouts of acute renal failure, Retinopathy of prematurity, a small IVH, an aortic clot, osteopenia resulting in broken ribs, severe Bronchopulmonary dysplasia…the list goes on. She was doing so well, finally. And yet here we are, back in this place again.
This morning I was standing in the kitchen staring out the window when I remembered that the name Simone means “She who hears.”
You have to laugh, really. Well, I do, anyway, and I did, standing there with a bottle of formula in my hand. A possibly deaf baby named Simone. If I believed in god, I would think this was a slightly cruel divine joke. If my life were a short story I was editing, I would say this was a heavy-handed stylistic device and recommend the author stop trying to be so clever.
You have to laugh. People say that all the time, but I really do believe it. I think it is probably as close to a life’s philosophy as I get. Anyway, nothing is really any different than it was yesterday. I still love my Simone to distraction, she still needs to be fed and changed and nibbled on. We won’t know any more until her ENT appointment, and if the news is going to be bad, nothing we can do will stop it from coming. It’s business as usual around here. Except, I suppose, that we can now swear in front of the baby with impunity. I guess it’s true what they say about silver linings.


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I don’t know what to say except, here I am, a stranger, reading your words and…not mourning, precisely, but shaking my fist at the fates for throwing another curve ball your way. “You’re in my thoughts” sounds weak, but you are, you will be.
Yes, you do have to laugh! This is probably one of the most easily dealt with problems that Simone has ever faced even if it turns out that she is profoundly deaf. You can all live with this condition and early intervention gives the best results. Be positive whatever the ENT says. You have a live and happy daughter, deafness does not have to change that.
I have a friend who’s daughter became deaf following meningitis at age 2. She is now a qualified nursery nurse, drives a car, is married and has a son of her own. It’s all do-able :-)
Sending lots of love.
Oh, honey, I am so terribly sorry for this current setback. I am very much hoping for the best-case scenario for you all.
(Also, proof that I am a jackass: my first though was, “well, do babies that age really NEED to hear, anyway?” Clearly, they do, and clearly, I am stupid.)
Ah honey – and the hits just keep on coming, don’t they? What’s positive in this? Well, babies are routinely being taught sign language nowadays as a way of pre-verbal communication, and it works. I’ve seen children as young as 7 or 8 months old signing coherently and it’s happening all over the place. Chances are very good that there’s someone who can help you get started on that at your own neighborhood preschool or daycare center.
And she is happy, healthy, thriving and loved. You’ve gotten through so many things already, and you’ll get through this, whatever the outcome. Yes, you’re entitled to your wallow, but keep your head up – this is workable.
Guh. That hit me right in the solar plexus.
I am so sorry. I want to make you strong sidecars and have a good cry with you. And totally rig the vote for Simone for baby of the week. Not that she needs to cheat.
I’m searching for words, but nothing seems to be more appropriate than I’m so sorry you’ve been hit with another battle this quickly. I hope the appointment goes well for you and I’ll keep you all in my thoughts.
Coming out of lurking to say I am so sad. But…I am going to hope and pray that the problem is only fluid. I’ll keep Simone and you in my thoughts.
Unlike you, I am crap with the words. The irony, the unfairness, leave me speechless.
It is however, manageable, and I say this as one who has seen her children undergo countless hearing tests and endure various operations to combat the problems they had.
You are all in my thoughts.
Aw, shite. I’m sorry. Let’s assume it’s the best case scenario for now. Yes?
I’m sorry. Everything about it sucks. I suppose there might be a silver lining to this cloud, but the fact that there is a cloud in what should have been a bright blue sky, well, it sucks and it’s wrong.
I’m hoping that an easy answer comes your way at the ENT. And yes, Nov 5th seems horribly far off to have to be in wait mode. And yes, deafness (if it is indeed that) is not a death sentence, but that doesn’t mean you aren’t allowed to feel sad and startled by this possibility. Wallow away. And all your readers here will be pulling for the best case scenario. Please keep us posted and know we are thinking of you.
Alexa, i’m so sorry you’ve all been faced with yet another obstacle. I can imagine the mommy guilt and the confusion and the sadness that she wasn’t hearing all the love in your voice. But she surely felt it anyway. I hope the 11/5 appt brings good news.
I hope that November 5th finds that this is all a mistake :(
I will keep you both in my thoughts.
Ouch. I’m pretty sure the other meaning for Simone is “one who overcomes”. She has been so strong for longer than any baby should have to, but I just know she’s going to be ok. Thoughts (and prayers, I know you don’t, but I do, so I’m sending them) to you, Scott and your little overcomer. She’s still the cutest kid around.
Ok that just sucks!
In the meantime with a few weeks to wait why not start on some sign language? http://commtechlab.msu.edu/sites/aslweb/browser.htm
You can add it to some of the words that you would use for the ‘bigger’ moments during the day like ‘bath’ and ‘lunch’. Couldn’t hurt. I hope the news gets better for you all.
Jules
All the platitudes in the world won’t make you feel better right now, so I will just say that I am so sorry you, Scott and your sweet baby girl have another hurdle to face. I hope everything is cleared up Nov. 5. So, so sorry. But hopeful, just the same.
I’m at a loss. Your blog and fantastic writing has been opened up to so many wonderful well-wishers. I’ll be one too.
Aw hell, another battle? I was just showing Simone’s picture to Mr. Newt earlier this week, and we were both so ecstatic at how far she has come from that tiny winter preemie. And admiring her stylish loungewear.
I hate to think your family has another mountain to climb, however non-life-threatening. You are all, as ever, in my thoughts.
I am sorry that you have come to yet another hurdle. For me, these later obstacles are harder than the NICU days. At least then, I was always prepared that something “might” happen. Now, they hit me like a truck because they always come when I start to think all is going to be okay.
Laughing is the key to survival at our house, too, although I sure wish neither of us had so damn much to laugh about (said with much sarcasm, of course). It isn’t fair. It sucks. It hurts.
I wish that I had something more profound to say. All I can offer is my support if you would ever like to talk with someone who has been in the trenches.
I pray that the ENT brings answers and that Simone falls under the best-case scenario.
Hugs to you.
I’m sorry you have another obstacle to tackle. If anyone can rise above a little thing like not being able to hear it is surely Simone. Look at her rocking those pjs! So very cute standing on that chair… OMG she’s standing on that chair!
This made me so sad. I can only imagine how you must be feeling. Sure, there are worse things – it will be ok one way or the other – but still.
You will be in my thoughts, and I’ll be praying for good news.
STANDING???!!!! And since we’re swearing out loud, holy shit!?! We stand Asher up and he’s like “Wha…? Legs? What am I supposed to do with these?”
She is a beautiful, smart, perceptive girl. With you as her mama, she is going to have the beauty of words around her, whether spoken or written.
Maybe she won’t hear. But she strikes me as someone who will listen.
I am so sorry you have another battle to deal with. For all that this is a disability that Simone and you can learn to cope with, it does not make it any less devastating to adjust your vision of the future. I hope the time flies until Nov. 5th.
Lurker alert! Lurker alert!
Oh Alexa, I have been reading your blog since right after you lost Ames and Simone was born. I read your blog out loud to my husband (we were also new parents) and we both grieved for Ames and delighted in Simone’s progress.
Does it ever end for you? Of course I hope it is the best case scenario, and of course I wish you the best if it is the worst case scenario. But just as they are sometimes exactly what you need to get you through the day, sometimes wishful words are wearisome.
Irony is cruel. But Simone is beautiful.
Wow. What an awful shock. We’ll wallow with you awhile and then we’ll help you get up out of the mud, clean up and march towards the light.
I’m so sorry you have yet another hurdle. Stay strong and give Simone a kiss for me.
As if you haven’t been through enough!!!! All I really wanted to do was swear, but that’s not terribly helpful. I understand that, in theory, this is not the end of your world, but I bet it almost feels like that right now.
Thinking of you.
Another lurker coming out, a mom with a special needs kid. Our kids have had completely different paths, but the overwhelming and nearly debilitating worry (on the parent end) are pretty much the same. I have no particular calming words, only to say: it sucks, and lots of us parents with special needs/medical needs kids Sooo understand and know where you are right now (emotionally, not locationally).
And on with the Assvice! Get yourself some copies of the “Signing Times” immediately. (they are dvds). Whether or not Simone has hearing loss, you’ll both love the communication that Signing Times will enable. (Signing times was started by a mom whose first child was born without any (or much) hearing. The website is probably SigningTimes.com or the like.
So sorry. This lurker has her fingers crossed for all of you.
I have a feeling that it will turn out to be the absolutely most appropriate name she could possibly have – whatever the outcome of the tests.
Dear Alexa, I hope the appointment goes well, and you find an easy way to solve the problem. There are no words to make this lighter and brighter, I know, and it IS unfair that Simone has had to deal with so much already. Keep us updated, please.
I am sorry. I really pray that it is something that can be fixed relatively easily. She (and you) are such an amazing fighter – you will get through this!
Wow.. I don’t know what to say except I’m sorry.. What a punch in the gut.
I really pray they find something easily fixed at the ENT.
Well, shit. I’d give you the name of the amazing ENT who did my daughter’s tubes at Children’s Minneapolis, but I’m sure you’re already seeing the best person. We at least had the warning of chronic ear infections when we realized M couldn’t hear us, so we knew the likely cause.
I will say this, if they can resolve it, they catch up awfully quick to any time they may have lost not hearing. Resilient little things.
Oh, and the monkeys at the hearing test are scary as shit.
I am, like so many others, not sure what to say. I am of the “It could always be worse” school of thought, but that seems insulting coming from a stranger (or anybody, really). So I will just say that you will all be in my thoughts, and I will hope fervently for the best-case scenario.
Holding you in my thoughts, and hoping for the best of all possible outcomes.
I can feel the guilt about not noticing radiating out from the page (screen?)
My son needed speech therapy and it wasn’t me that noticed, it was his pre-school teacher. Once she pointed it out, how could I NOT have noticed he said k instead of t every time and his s were completely wrong and, and, and.
So I totally get the guilt for not noticing. No answers for you, just trying to let you know you’re not the only one who doesn’t spot everything.
I know what you mean. You do have to laugh, then you need to have a damn good bawl, then you get on with whatever you have to do. (((((hugs))))
Alexa, my thoughts are with you. Like so many of your other readers, my heart sank as I read your opening words. I read on, hoping for a punchline, something about Simone entering adolescence early or something.
But the thing I’ve admired about you right from the outset is your ability to accept and move on. You seem to have a magnificent ability to take whatever is thrown at you, and still manage to find the light and humour in the situation. This sucks for Simone, and I hope and pray that November will bring positive news for you. But I know that you’ve all come through so much worse, and that you are capable of getting the perspective on the situation which will enable you to deal with this also.
Hugs,
Jennie xx
As Mom to a 6 1/2 year old profoundly hearing impaired boy, please believe me when I tell you everything will be fine. This is not a quality of life issue — my son received a cochlear implant just shy of 3 and he is doing so well!! If Simone’s diagnosis TRULY is hearing impairment, you caught it VERY early (unlike the 2 years we spent trying to get an accurate diagnosis). I, too, hoped that it was fluid build up, a byproduct of my son’s serial ear infections . . . anything but hearing loss, but sedated ABRs don’t lie, and he really couldn’t hear anything. I would imagine that will be something they will schedule Simone for ASAP and you’ll go from there. There are so many resources and so much support for children experiencing hearing loss in this day and age, allowing them to be mainstreamed and part of the hearing world. I would be happy to hook you up with the professionals you’ll need . . . feel free to e-mail me (wed102499@aol.com) and we can take this offline. Please, please, please don’t despair . . . Simone is a fighter and if she’s challenged in this arena, she has a proven track record of success!! Hugs to you — Stacey
I was just thinking about Simone and Ames as I went to bed last night. So much to go through. I’ve worked with 2-3 families of children who are deaf as an early interventionist, and now I am a researcher in language acquisition.
When you see the ENT, and the early intervention specialist, ask lots of questions. Ask about what you should do NOW, and then stay with it and persevere. Simone is bright and doing well cognitively, and she needs to hear or see language going on around her. There are many things you can and should do regardless of whether this is a temporary loss or a permanent one, but the important thing to remember is that this is a critical time for her language learning.
My thoughts are with you! I have admired you from the time I first read your blog because you are able to take in so much information, understand it all so quickly, and then act. Hang in there, this is just another hurdle that you and Simone will get over.
The others are so much more knowledgeable than me – but I wanted to say I am so sorry you’ve been blindsided like this. Such a shock. Not knowing is always the worst, too. Hoping for best for you, as ever. x
I don’t know what to say. I could point out all the positives and present an ‘always look on the bright side’ approach.
But I know if it was me in your position, all I would want to do right about now is swear and laugh and cry.
So fuck it. Hasn’t she been through enough? And November 5th seems awfully far away right now.
My initial reaction to reading this is that I’m pissed off that you cannot just get on with things and not have to worry for 5 fucking minutes.
I’m going to send an email, as I have more I want to say but can’t put it into the right words at the moment. No for real, I’m sending an email!
Oh I’m sorry, it is never easy to find out your child has a problem, especially one that will affect the rest of her life. I feel for you.
I am involved in the deaf community, and let me tell you there is NOTHING they can’t do. I sign, my son started signing as a baby, your family can, and will get through this if it does turn out to be permanent. You are in my thoughts.
God, you’ve dealt with enough without this. I’m so sorry. I really am.
Oh Alexa. I’m so horribly sad and angry for you. Things were going so well! You were finally out of the woods. A happy ending! It was the way the story was supposed to go! And then your Tweet. And then this post.
I’m hoping with you that it’s fluid. Fixable. I know nothing about ears so that helps me to hope.
And of COURSE you didn’t notice! Who would have? She was hearing at first and her responses changed so gradually that unless you knew to look, you wouldn’t notice. It’s not like you bang a gong regularly before meals at your house. (Or do you?) You got used to your Simone as she is and she adapted to her environment seamlessly. You’d have noticed eventually but now? When she’s still so little? There’s no way you should be blaming yourself for that. You were looking for stuff that would outright kill her and there’s plently of that. No guilt, Alexa. That guilt is a lie.
And Simone? She hears you just fine. She hears all that love you are sending. Not with her ears right now. But with her heart. Which is perhaps the most important part of her that needs to hear.
xx
Wow. Talk about coincidences.
I’ve only just recently started following your blog, and I’m a deaf mom of a deaf daughter. We didn’t take our heads out of our asses and realize she was deaf until she was 15 months old. And we’re college-educated, proudly capital-D deaf people who’ve graduated from both hearing and deaf institutions. The self-kicking definitely took a while.
I have to admit feeling mixed emotions reading this post. One is the vicarious being knocked on my butt by the news effect. Another is my residual anger at parents who grieve, left over from years of seeing kids suffer from parents who think their kids are broken and mentoring parents who are still stuck in the world of looking for the mistaken diagnosis explanation. And yet I feel enormous admiration for the aplomb with which you’re taking the news.
Love to you. and yes, cussing in front of the kid? Definite bonus. The real struggle is convincing friends they can do it too.
Long term lurker, first time poster :) Also the mother of a 4 year old deaf boy, the light of my life…. Really hope that you get the best news possible from the ENT but wanting to let you know that regardless of the outcome you and Simone will be just fine.
Learning that your baby has/may have a hearing loss is certainly a roller coaster. I know so well that heartbreaking testing where a beloved child completely misses a clear and loud sound right there :( Everything you’re feeling is certainly normal. Please please don’t beat yourself up about missing it – kids are sooo smart and good at using all their senses. Even now so many people who know my DS well hardly believe he has a problem, it really is such an invisible thing. My little guy whispers to me and tells me how he loves me every day – all those things you wonder about ever hearing or doing when first diagnosed. Simone WILL have picked up on all your love and everything you have “said” to her in the past months, even if she hasn’t been able to hear all the words.
So much more I want to write but all a bit convoluted at the moment. Feel free to email me if you want info or support but here’s a couple of good links for starters:
http://www.babyhearing.org/index.asp
http://www.aussiedeafkids.com/Phidcoz/building_blocks.htm (Australian but still with lots relevant to you)
Loads of good thoughts to you and your whole family….
Well, Fu**. Sorry I’m not very eloquent, but you have been through so very much more than any person should have to stand. I agree with everyone that in the grand scheme of things it could be worse, but knowing that doesn’t make you feel any better I expect. It’s unfair, and scary, and you don’t deserve to continue to be kicked back down every time things start going well. But I know that you are fighters, and that you will deal with this, and move forward, and that it doesn’t change who Simone is.
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