wake up

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I get this question at least once a week.

Usually from friends who have friends. Usually from friends that are trying to be good friends.

“I think there is something wrong with my friend’s child… what do I do?”

I always first ask the age of the child. If they say 2-4… I breathe and begin the spiel calmly.

If 5+, I cringe and get a bit rage-ish

EARLY INTERVENTION people.

Let me back up…

If you have a child with autism or any type of special needs and you are proactive… then you are ON.

You are ON all of the time. 24/7.

thinking, doing, investigating, pushing, crying, praising, persevering, nasty persistent. Yep, it is unrelenting… but you are ON and being ON is good.

It’s really good.

If you are in {pause} mode, you are doing none of the above. Nothing.

Pausing for a while to catch breath? Yes, fine.

I am talking about pausing for months that turn into years and chalking it up to be “nothing but a speech delay.”

Oh how people love to use this phrase.

Oh if I had a penny for every mother in {pause} mode that tells me “it’s just a speech delay.”

What a cop out!

I haven’t even gotten started… this is your wake up call.

This is for you. Give me the evil eye now and thank me later.

Okay, if your child is speech delayed, seldom exhibits eye contact, does not interact/engage with others and has many repetitive behaviors…. the list goes on… then it might be more than a “just a speech delay.”

How do you know? You don’t always. That is why you get an assessment.

Get one.

Who do I call???  Start with a licensed Neurodevelopmental Pediatrician.

Look it up. Google one in your area. They are the Gurus and can steer you straight.

“Oh, but I don’t want to talk about it and I don’t want others to talk about it.”

I promise you, people are already talking.  Tis true.

For the love…Do something.

I can say all of this because I know the {pause} button well.

We were once short-lived friends…. Hallelujah!

Get off the {pause} button because that button is debilitating. It is.

That button is preventing you from being proactive.

That button can be a form of child neglect.

Ouch, harsh.

Yep, tough love. You need it.

Make the call. Get on the list. Have a full assessment done.

Call me. I will talk to you. I will cry with you.

But I won’t say it’s okay to {Pause} for too long.

I will never say that.

To read more blogs from Melanie, Seth and TheFowler4Group, check out their Website (www.lookatmyeyes.com) and while you’re there, buy a copy of their book, “Look At My Eyes”.  Or find them on YouTube.  To contact TheFowler4 Group email: info@thefowler4group.com

Photography by the famous Callie Shepherd at www.callieshepherd.com

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One response to “wake up

  1. I had to start following you when you posted this! I’ve read your book, amazing!!! My daughter is 17 months and I know she is on the spectrum. Currently we are 3 weeks out from getting the genetic results back on Rett Syndrome. She has been in a early intervention program since 13 months and it is amazing the progress I have seen. Thank you for blogging 🙂 I look forward to reading all your posts!

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