Where to Next?

My Pause - I feel like I need to explain my pause in posting.  I was posting daily when I started this blog up.  Then something unexpected happened.  I started feeling all those emotions I felt back then - when we got the news.  When we started processing it all.  I was suddenly overwhelmed with everyday life and was having a hard time coping.  If there's anything you learn in dealing with a lifelong illness for your child, it's how to cope.  So I took a break.  I apologize to my readers for not letting you know.  I had to recoup and focus on the progress we have made.  Focus on our wins.  Focus on our family.  Thanks for understanding. 

Back to 2013...

We were dealing with a lot and I was trying to spend as much time on my family and my son as I could.  A full time working mom, it was a lot to deal with and take in.  My posts became more scattered as I went to appointments, fought for treatment, set up private therapies and pushed forward through the labyrinth that is our medical system. 

My next post was 3 months later in January of 2014 and you can feel just how overwhelmed I was here. 

FRIDAY, JANUARY 17, 2014

 

Where to next?

I’m not sure where to go from here.  It’s a place I’ve never been before and there are no directions on where to go next.  “Take each day as they come” is the advice given to me, but I’m one that likes to prepare.  What will I need?  What tools should I make sure I’ve got?  How do I prepare for tomorrow or tomorrow’s tomorrow?  What are my coping mechanisms if everything falls apart?  How do I put it back together again?  Most importantly, how do I make sure things are WHOLE for my son.  My son.  My SON.  Who, truly is, the centre of my universe. 

Back in November of last year, we were given the news that Kiefer, our four year old bundle of joy and love, is autistic.  It wasn’t shocking news.  We weren’t blown out of our seats surprised at the news.  We had him assessed.  We obviously thought there could be something up when we signed him up for the ADOS testing.  But until you hear those words.  Until a doctor looks you in the face and says, “well, yes he has come back as being on the spectrum” you just have all these hopes and dreams as to what your child’s life will be like.  And for us, for me, the hardest part is not knowing what the future holds for Kiefer. 

“Well, we can’t really tell you what his future will look like.  He is clearly high functioning right now, but sometimes those kids degenerate and become worse off.  Sometimes they ‘outgrow it’, as much as you can outgrow autism”

I spent two months not talking about it.  The odd question would come up and I would answer, well, we just got back a diagnosis – but I couldn’t even bring myself to say the word.  Autism. 

My head fills with thoughts like will he be teased in school?  Will he be an outsider always wanting in with the other kids?  Will he know he’s different?  Will he be happy?  Will he learn everything he needs to know?  Will he go to high school?  Will he go to college or university?  Will he get married?  Will he always need to live with us?  Will that be a burden on us or will it be okay?  Will his brothers see him as a burden?  Will he be NORMAL? 

There are no answers.  The answers I get are ‘we don’t know’.  No one knows.  Just take each day as they come to you. 

So the original future wedding I had all played out in my mind, Kiefer wearing a tuxedo and a figure of a woman all dressed in white, are dashed away.  But there isn’t a scary image left in it’s place.  The canvas is blank.  Empty.  Dark. 

We fear the unknown.  I fear it.  I fear it for Kiefer.  I want to gather him up in my big Momma arms with his “squeezy hug?” requests and his favorite books on animals and stuffy’s and protect him from the world that I’m terrified will hurt him.  That I’m terrified will crush his easy go lucky, carefree happy spirit.  The spirit that everyone loves so much about him.  That I love about him. 

I don’t know where to go from here.  The only thing I do know is every journey begins with the first step.  Please be gentle with us as our footing on this journey isn’t quite stable yet.