My Kids, Myself, Special Needs, Uncategorized
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At Five, Considering “Normal”

Lucy bday crown

Today is Lucy’s 5th birthday.  Every year when one of my kids has a birthday, several times throughout the day I think of what I was doing that very moment on the day of my child’s birth.  I may remember when I was laboring in the shower with Eden, or when my water broke in the bedroom with Lucy.  So I’m having those moments today, and they are made all the sweeter by the fact that this is the first year Lucy really understands birthdays.

We have been to a couple of birthday parties recently and she’s seen the fuss made over the birthday kid, and that there’s cake and presents and having a birthday means that you are the center of attention.  We are doing Lucy’s birthday at a place with a bouncy house this year, so for a couple of weeks she’s been doing her Lucy thing of going over what the routine will be, exactly.

L:  Me!

M: You, what?

L:  Hop!

M:  Oh, you mean you’re going to hop in a bouncy house for your birthday?

L:  Uh-huh!

L: Help me!

M:  Who’s going to help you?

L:  Pop!  Op! (open)

M:  Pop’s going to help you and open the bouncy house?

L:  Uh-huh!

And this goes on.  We cover what we’re eating, who will be there, opening presents, and even transportation because apparently she really wants to ride in her dad’s car.  Anyway, the routine is the same every time.  Last year, it was all still kind of mystifying.  This year, it is ON.  And that is glorious to watch.

When you have a kid with special needs and you go through the long list of different doctors and health professionals, the first thing they want to know is if you had a healthy pregnancy.  With Eden, who has been a typically developing child, my pregnancy definitely would have been cause for concern.  I spent the first four months miscarrying her twin.  She was truly a miracle baby.  On the opposite end of the spectrum, Lucy’s pregnancy was a piece of cake.  I had virtually no morning sickness, a beautiful diet, a totally supportive partner and very little stress.  She even surprised us by coming ten days early, instead of making me wait until I’d made peace with being pregnant forever, like her big sister.

So here we had this perfect pregnancy, a perfect delivery, and a lovely, perfect baby.  And then after that year point, we began to see that she is wired differently.  We began the long diagnostic process.

In the early days, I cried.  I searched for every little thing that might have caused Lucy’s challenges.  I was devastated and angry, and sad and scared.  I’d lie in bed at night fighting hot tears and the knot in my stomach, just praying that everything would be alright.  I felt like something had been stolen from her, and from us.  “Normal” had been stolen.

We weren’t having “normal” birthdays and Christmases.  Playdates?  Definitely not “normal”.  Pre-school?  Not “normal”.  And I wanted all of those things for us, and for her.  I wanted her to get attached to characters on television and develop obsessions that I could indulge.  I wanted her to be able to eat the damn chili con queso and flour tortillas.  I wanted her to be able to tell someone her name, and how old she was.  But we didn’t get that.

In this last round of clinical assessment and diagnostic “stuff”, we sat in front of a pediatric psychologist, asking if she thought Lucy would one day be “normal”.  She just looked at us and said, “What’s ‘normal’?”

And that changed something for me.  Lucy is five today, and she is excited that it’s her birthday.  If you ask her whose birthday it is, she will yell, “ME!”  If you ask her how old she is, she will hold up all of the fingers on one hand.  If you ask her her name, she still can’t tell you, it’s still locked inside of her,  but she’s such a tenacious kid and hard worker that I believe it will come

If I could go back in time to when we got our first diagnosis, and tell myself anything, it would be that we would have all of the joy and sweetness and proud moments that we might have if Lucy’s brain was neuro-typical.  Because we have had all of that and then some.  I would tell myself that it wasn’t going to be alright.  Actually, it was going to be wonderful.  And I would tell myself not to worry; that we would have “normal”.  Because we do.  It’s just OUR “normal”.  It may not look like my friends’ “normal”, or the “normal” I’d envisioned during my perfect pregnancy, but that is okay.  After all, what is “normal” anyway?

Lucy bday crown

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5 Comments

  1. Carmen says

    Oh wow…this are my thoughts and feelings! I had this same conversation with my daughter’s first Special Ed teacher and have pretty much deleted the word “normal” from my vocabulary. Thank you so much for writing this.

    • Meredith says

      Thank you so much for reading, and sharing your experience with me, Carmen! It’s nice to hear another mom say the same thing.

  2. I agree, who in the family is normal? We all have “special needs.” In Lucy’s case we drop the word “needs” and add “very.” Lucy is Very Special to me.

  3. Sharon Stuart says

    I so enjoy following the writings of such a loving mother, asking questions we’ve all asked about what is normal…. referring to both our children & ourselves. Your ponderings, musings..so honest & loving.. are an inspiration. Plez continue to reveal yourself to us, Meridith, so that we may see ourselves.

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