Putting The Pieces Together – Our Autism Journey

Screen shot 2013-12-11 at 10.32.21 PM

I remember holding my firstborn son, Samuel, in my arms all swaddled up in his blue blankie, pacifier in his mouth, and singing to him until he fell asleep for his daily nap.  Everything about him took my breath away.  Everything about him was samuel babyperfect.  Like many parents, I would look down at him and imagine his future:  What sports will he play?  probably Football since his daddy loves it so much.  When will he meet his wife?  He’s so handsome, all the girls will be following him around.  What career path will he choose? Something that can well support a family, I hope.  Web designer, or engineer, though a missionary would be awesome, too.  Samuel’s life according to mom, was looking pretty good.

Dec 28 2005 (47)The lack of hitting developmental milestones can be easy to overlook in the first year or so, especially if you don’t have enough experience with small children to be able to gauge “normal”.  It wasn’t until Samuel’s brother, Silas, just 13 months younger, began to progress as an infant and toddler should, that we began to suspect something may not be right with Samuel.  Little things, like lining up his cars by color, his delay of speech, his adversion to certain textures and water became highlighted by our younger son’s “normal” behavior.

Read our Autism journeyAt age two, with no sign of verbal communication and other behaviors growing worse, our pediatrician referred us to a speech and occupational therapist.  Within a year, Samuel was speaking in sentences and running through the sprinkler.  Washing his hair at bath time no longer required two adults and he had almost completely stopped banging his head on things.  Over the years the therapists used hopeful phrases like “closing the gap” to describe his progress, and we looked forward to a day when we would soon be “past all this stuff.” Just before Samuel turned 5, we moved away and had to stop his sessions.

Screen shot 2013-12-11 at 10.11.39 PMThen: Kindergarten.

That first parent-teacher conference brought us back down to earth.

“Samuel is having a hard time in his overall understanding and I am concerned about some of his behaviors.  He doesn’t seem to grasp anything being taught.  He also doesn’t understand what ‘No’ means, but he can take direction from visual Que-cards.  If I tell him ‘Don’t draw on yourself with the markers’, he looks at me blankly, then continues to draw on his arm. But If I make a sign with a stick-figure drawing  on himself, then put a circle with a line through it, and set that card in front of Samuel, he stops drawing on his arm.”

SAMSUNGFirst grade proved to be even more telling.  Samuel struggled socially.  Samuel struggled academically.  Samuel just struggled.  It was this teacher that got the ball rolling by saying what I imagine had to be very difficult for her.  “Samuel is not meeting the standards, and I really don’t know if he is able to.  I know this is hard, but it may help you to have him evaluated by a psychiatrist.”

It was so discouraging.  We didn’t want a “Label” on our son, but we wanted answers.  We wanted to know how to help him, teach him, and communicate with him, but we didn’t want to give him a crutch, which we thought saying the word, “Aspergers” might do.  Home life was growing more and more difficult.  Samuel was easily aggravated by his siblings, schedule changes, loud noises, and usually responded with aggression.  We needed help, but getting answers was no easy process.

First, we had to visit the Ped, who referred us to our local community mental health organization, who referred us to the Gonzaga Autism Program, who sent us to the school district’s psychiatrist, who said they don’t diagnose, and only SAMSUNGevaluate students for academic purposes, not social or sensory reasons….. and months later we were back to the ped again.  Our second referral, now into his second-grade year, was to the Northwest Neurobehavioral  Institute, where after a 12 hour evaluation and testimonials completed by teachers, our ped, and my husband and I, we finally received a diagnosis:  High Functioning Autism. 

I don’t think that anything could have prepared me for that moment.  It was a mixture of great relief for finally having an answer, and mourning for the loss of the life that I had projected for him in my mind.  Then the questions:  What will this look like going forward? Will he ever get married? What kind of a dad would he be? Will we need to support him forever? Will he go to college? What next?  What I remember feeling the most at that time was alone.  I needed someone to lean on emotionally while I processed this, and not someone with little knowledge and big answers.

first day of schoolSamuel is now in 4th grade, and I would say that we’re really starting to learn how to navigate these waters.  Each challenge that presents itself tugs at our heartstrings, bringing with it the “What-ifs”.  The worst of those are the days, or even weeks, when we go challenge-free and tend to forget about Autism until something happens and it shows up in full force, and a little bit of that mourning for the non-existent made-up son comes back again.  Getting a diagnosis like this for your child can be heartbreaking, but it can also be an opportunity to fall in love with your child in a way that is amazing and unique.  Here’s a few lessons we’ve learned along the way:

Love your child for exactly who they are.  This part comes after acceptance and letting go.  Your child will be better for it, and your heart will be better for it.  “In their hearts humans plan their course, but the Lord establishes their steps” – Proverbs 16:9

Pick and choose your battles.  And oooooooooooooh, do you have battles with an autistic child!  We basically take each situation as it comes and put it into one of three categories:

  1. This is a behavior issue needing correction.
  2. This is an Autism issue that can be accommodated.
  3. This is an Autism issue that we need to help him overcome so he can be successful in life.

For example, eye-rolling when told it’s time to start our homework would be number one and would need a discipline.  Changing his shirt 4 times in a day because he gets a raindrop on it and doesn’t like the way it feels is inconvenient for me as the laundry doer, sure, but it’s not hurting him or anyone else and is really OK.  Not wanting to wear his seat belt because it makes him claustrophobic, however,  falls into number 3 (or as we call it, the ‘too damn bad’ category).

Tell your child.  Don’t make it license for them to do whatever they want, but don’t hide it either for the sake of protecting them from the dreaded label.  If your child is very high-functioning like ours, he knows that he doesn’t fit in.  Hiding it from him will always make him wonder why.  There can be freedom in an answer.

Tell their siblings.  Samuel’s autism has forced some maturity on our other children.  They understand why Samuel has some different standards than they do (like not being required to make eye contact when talking to an adult), and it wouldn’t be fair to them to not explain why that is.  It gives them compassion for his meltdowns and, for us, has been a great opportunity to teach the kids how to pray for each other.

For God’s sake, laugh about it!  Yes!  It IS OK to find the humor in the quirky things they do.  Sometimes I will refer to Samuel as Mr. Spock, or have a good laugh over stories shared with other moms who have children on the spectrum.  It’s very therapeutic.

Praise their strengths!  Children, and adults, with Aspergers and High Functioning Autism often beat themselves up for their failures.  They’re usually extremely good at some things, and extremely bad at other things.  Praise them for the things they are very good at, and offer help to them for the things they aren’t so great at.

Be their advocate.  Go to any length to get them the help they need.  Early intervention and therapy can make a HUGE difference in the life of an autistic child.  Research.  Get a 504 plan or an IEP.  If you suspect your child needs to be evaluated, annoy the bajeezers out of your doctor until you get it.  Stand up for them.  Don’t be afraid to “educate” people who are treating them unfairly.  I am a pretty passive person, and I have had to grow some serious mama bear claws when it comes to dealing with others who interact with my son.  Lastly,

Love them some more.  Everything about him takes my breath away.  And everything about him is perfect.



Comment Here

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s