Thursday, April 15, 2010

The Cold Hard Truth

Okay...here it is. Let me just be blunt. I'm sure you've noticed that my sweet, 23 lb toddler is not walking. We've noticed. We won't pretend we haven't. As active participants in our school's Parents as Teachers program (wonderful, by the way!), our PAT lady has noticed, too. Her developmental checklists "prove" it. And when we had Natalee in for her 15 mo check-up a 1/2 a month late the doctor noticed as well. I'm not blind...I see other 16 month olds running and climbing...

We've struggled with not pushing her--with not forcing her to walk (for how can you force a child to walk?). We've showed her how to move her feet, we hold her hands, we cheer her on. And yet, she crawls. However, perhaps more worrisome than that is at 14 months her gross motor really stopped progressing much at all. She pulls up, cruises some, and recently will stand for about 1-2 seconds by herself without holding on to anything. But that's it.

So I got brave and asked the doctor 'what now?' I'm an Early Childhood Special Education teacher. My kid shouldn't be "delayed" right? But here we are...

And so the doctor tested Natalee's muscle tone--very weak on the right side. And we discussed her birth. And we've concluded that it is possible that because of her cord being wrapped at birth and our sweet girl being born momentarily blue that she could have minor brain damage. And I cried...
Of course I did. Because no matter whether you suspect it or not it still hurts to hear. Because what I heard was not "your child may be special needs" or "your child isn't typical". What I heard is "life may be a little harder for your child." And who wants life to be any harder for their baby than it is already? And words like "mild cerebral palsy" were mentioned...and I cried some more. But I also felt relief. Because deep inside I knew/know that something isn't clicking...and now we go forward. Relief to know that despite us doing our best as parents we might need a little outside help...and it's okay. Of course she's special...she's my baby and she's the most special child I've ever met.

And so...
  • we have an appointment with a pediatric neurologist in June to see if these suspicions are true or to see if our girl is just a late bloomer.
  • we are chugging along assured that she's perfect and in God's hands.
  • we know she will walk--it's just a matter of the right combination of things to make it happen.
  • we are content and proud of who she is...and realize with doubtless assurance that this is who she was designed to be--that these are the things that make Natalee Natalee.
  • we don't want you to be sorry...because we're not.
We've struggled with telling people what's happening...certainly not because we're ashamed but because there are so many unknowns...and what we don't want are rumors and half truths floating around. But we know you've noticed, too, that Natalee is a little delayed--some of you have asked (kindly, might I mention--thank you for being so kind) & some have hinted. However, to temper the gossip train, I ask that you wouldn't say she has CP until we know...and that you don't treat this update as your gossip story of the week. She's our baby, you see...pretend she was yours. What you can do--the reason I finally decided to blog about this--is pray.

Pray that we get a cancellation call and our neurology appointment is moved up. Pray that Natalee learns patience for whatever is to come--and us, too. Pray that we get answers from our doctors--answers and a plan that we understand and can follow through with. Pray for our peace. Pray for our 2nd born--that when he comes we can balance our time in a way that he never feels shadowed or 2nd best...and for Natalee for the same reasons. Pray for my body and mind--as both get weary of being 7 months pregnant and carrying a 23 pound toddler up and down the stairs. But most of all, pray that God's pleasing and perfect will is carried out in Natalee's life--and that we see our role as her parents in that plan. For in this leg of our journey I have felt certain peace--that He's never left me and will walk with us the whole way. Praises for never having to journey alone. Who wouldn't feel peace when you've been given this?...
we are most certainly blessed.

9 comments:

Anonymous said...

Natalee is so very blessed. Prayers for your family as you make you way down this path. ~ Laci

Navman64 said...

May God Bless, and you know that our prayers will be with your family, those here and those yet to come. From one of my favorite songs. "Jesus loves the little children. All the little children of the World." "They are precious in His sight."

Love you guys,

Dick & Bev

Anonymous said...

Jenn and Mike
I know you feel helpless at this moment but believe God does have a plan and you will follow it-you just don't know what it is at this point in time. The helpless feeling does go away with time and prayer, you both have a good family base that is always there to help you that is so very important at this time and in the future.
I will be praying for you and Natalee.
Please believe me that it does get easier and the benefits of loving Natalee WILL out weight all obstacles you will face.
Praying for you
Dianna K

Andrea Frederick said...

Who could not love this little sugar lump? She is most definitely sweet and made just how God had planned. I am always praying. Love you.

Shonya said...

I WILL pray, Jenn--guess I was just not too worried about it, but you are her mommy and God gives mommies that instinct, so trust your gut. I am especially praying that people (family, friends, even you--whoever) will see her the way God sees her--His creation, created for His pleasure and glory, and He calls her 'very good'.

Andrea Frederick said...

one more thing: I know your title says the Cold Hard Truth...but oh how differently this story could play out. This little girl could have parents that don't notice or care to notice. They could deny there is an issue, which is just as damaging, or be so wrapped up in their lives that they can't bring themselves to be bothered. Instead, she has parents that will do everything in their power to make her as successful as God has planned for her. She can be anything she wants to be and she already knows that. And right behind her parents are loving aunties, grandparents, and a whole crowd of family and friends waiting to catch either her or you and Mike if you stumble. We are all waiting with open hearts for whenever you should and will need us. Whew....to sum it up: love ya!

Bree Shaw said...

looking at that precious girl and her big beautiful smile just makes you happy:) jenn i am so glad that you are letting us know how we can help you and that you are not trying to go about this journey alone. andrea is right when she says that there are so many people there ready to help you, mike and natalee whenever they are needed. i think your outlook is great and with your faith and your dedication to miss natalee will make all the difference in the world. remember to ask for help when you need it and that no matter what God is right there beside you ready to help. Love ya!

Corin said...

Praying. Let me know if there is anything else I can do.
Andrea's comment made me cry, she a very smart lady your sister.

Courtney said...

jenn-

Again we have never met but I find great joy in reading your blog about your little gal who is Finnean's age. I love your outlook on this recent challenge that you are facing. I will keep you in my thoughts. Take Care-
Courtney Wagler