Follow Me on Pinterest Instagram

Sunday, September 30, 2012

Quick Look from the Pumpkin Patch

Quickly, I had to post a few pics of our Pumpkin Patch trip yestersday.  It was sooooo fun, the best year so far.  Here you go for now, I'll post more later!
On the way back from picking out our pumpkins

Kaden Loved this little pumpkin

Mahala was our navigator thru thru corn maze....Kaden was her sidekick

Kaden enjoyed running in the corn maze

Hidding from the sun...or at least trying to

Rolling in the Hay......literally  HAHAHAHAHA

More Later!

Wednesday, September 26, 2012

A Little Music for the Soul

Kayden has really taken a liking to the new Beatles rockband thingy that we got the other day. If he's not singing to the kung fu fighting song he is drumming to every rose has it's thorns.  He is so adorable singing and playing on drums.  It's even more awesome when he can get his brother and sister to play along with him.  And they do, their good like that.
Yesterday was so stressful and busy.  Kaden had to be out of the house all day and every chance that he could get he would remind us that he would rather be at home then doing errands.  Even at the movies he was dragging his feet, wondering when we were going to go back home.
So, I decided to let him stay at the house today.  Which meant Mahala and Skylar had to take turns staying with him.  First Skylar stayed with him and I took Mahala to get her braces off.  YAY!  And then we came home had lunch real quick and then Skylar and I was off to the mall to get a rebate form for his new cellphone.
It was a busy day for everybody today once again.  Right now we are about to make some delicious enchiladas,  I pray Kaden will even entertain the idea of it being on his plate.  Hahaha  I'll post a picture tomorrow and let you know.



Sunday, September 23, 2012

Do You Want to Know What it's Like Having a Kid with Autism?

 So I sat down to read a Blog I Love to read and I had to share her post........  A lot of it I have to agree with, if not all of it. 
Earlier this summer, a well-meaning acquaintance I was chatting with at a birthday party asked me an honest question — “What’s it’s like to be a mom of an autistic child?”  She wasn’t being nosy.  I happen to like her and know that she was genuinely interested in my experience.  But what I saw in her eyes was pity.  She even teared up while we were talking.  Those of us with special needs children know that look.  I called it The Look of Tragedy.  Again, she meant no harm.  So, I got to thinking.  What is it like to have an autistic child?  After all, they come in all sorts of shapes and varieties.  I’m just starting out on this journey, yet many have seen their children through to adulthood.  Some of our children will be self-sufficient.  And some will live with us or in a group facility for the rest of their lives.  So, I admit that I cannot answer that question for everyone.  But I can answer for me.  And, in that answer, I will likely be speaking for other parents of other very special children.
So, here it is.  Here’s what it’s like:

1.  To begin with, it’s [a kind of]* death.  No matter how much you plan to allow your children their freedom to achieve their own dreams, quite naturally you have a few dreams for them as well.  You dream of birthdays and holidays.  Santa and presents.  Playing dress-up, doing arts and crafts, playing Candyland, dance classes, Boy Scouts, sleepovers, team sports, high school graduation, getting married, and having children of their own to love.  And, though many of our autistic kids will grow up and have and do just those things, more than half of them won’t.  At least not without a great deal of assistance and likely not in any resemblance of the typical joy of those things.  So, you mourn.  You mourn for what might not be.  You mourn for what you and they are missing now.  And, later, you may mourn for what will never be.  
*Later I decided to clarify this statement.  As it was, it may have implied to some that it was equal to the literal death of a child — which it is not.  I meant it more as another kind of death, similar to divorce, estrangement, foreclosure, prison, and other profoundly life-altering experiences for which one goes through the stages of grief. 

2.  Despite the death of the dream child you envisioned, you are deeply in love with the child you have.  He still does adorable things you want to share with others.  He loves you too, but the rest of world won’t always get to see it.  Because when he is away from home, he is not himself.  He is not the happy, affectionate child who holds your hand, snuggling, and gazes at you adoringly while pulling your hand to scratch and rub his back.  They won’t get to see him at his most charming and you will know they are so very glad they aren’t in your shoes.  You will see pity in people’s faces.  And they won’t ever understand the very real, profound joy this child gives into your life every day.  Part of being a parent is pride in your children.  People won’t see what you are so proud of.  And that can be a lonely feeling.

3.  Guilt assails you from all directions.  You want to throw a beautiful birthday party for your child.  But he may not notice.  He may not be the least bit interested in the presents, and you will dread any look of disappointment on the giver’s faces.  He may be struggling to get down out of your arms during the party, and there is an air of sadness just beneath friends’ and family’s smiles.  So you consider not having a party.  You consider not taking him to others’ parties.  You want more than anything to give your child the experiences typical children have and feel guilty when you don’t.  But sometimes it is simply too overwhelming for you both to undertake it.  Therapists want you to spend hours doing activities to help him, but you also have a job, perhaps other children who need you too, and you need some downtime on occasion or you’ll go insane.  So it seems you can’t ever do enough for him.  The guilt is a killer.

4.  You live in a constant state of uncertainty of the future.  Yes, of course none of us knows our future.  But, if you have a typical child, you can be reasonably confident he will have friends, self-sufficiency, and love.  You know who to leave things to when you die.  But if you have a child with autism, you won’t know how to plan your estate.  Do you set up a special needs trust?  Do you leave it all now to the one typical child who can use it?  Because lifetime care for your autistic child will just drain it.  And what if he grows to do well and is able to care for himself?  Because you can’t yet guess what will be, every option is insufficient.  Uncertainty can affect every part of your life.  Should I settle here in this city or plan to relocate to a city with more intensive care for his needs?  Will he ever talk?  Will he ever be toilet trained?  You just won’t know until it happens or it doesn’t.  And you live with the fear that one day your then-elderly, vulnerable child will lie sick or dying without the comfort of someone who truly loves him.  Anxiety runneth over.

5. Spontaneity is a thing of the past.  You can’t just get up and go.  You have to determine whether there is an escape route from any new activity or location.  You have to pack things to distract him if he becomes upset.  You have to determine if foods he will eat will be present or if you will need to pack his meal.  If he isn’t potty trained, you will worry about where you can take him to change him that will afford you both some dignity.  Everything - everything - must be planned and considered.

6.  You begin to grow thicker skin.  Because people will and do stare.  They will stare in disgust, thinking he is simply badly behaved.  They will stare in curiosity, because that is the nature of man.  They will stare in horror or pity, because “there but for the grace of God go I”.  People stare.  And the thing that will come back to haunt you are memories of when you, also, made a judgment about another person in public.  Righteous indignation mixes with humility and all you want to do is get out of wherever you are as soon as possible.  But you can’t escape everyday life.

7.  You grow weary of everyone else’s opinion.  Because there are so many of them.  There are those who are certain they know how “this” happened.  There are those who are certain they know how to “fix” him.  There are those who don’t think you do enough.  There are those who believe you to be a saint.  There are those who believe your child’s very visible difficulties allow them to have an opinion over your finances, his education, your marriage, and even your decision to bear another child or not.  Opinions abound, but your patience may not.

8. But mostly it’s like love.  A love that you, if you are a parent, can probably imagine.  And a love that, if you don’t have a child born with a bulls-eye in a big, bad world, you can’t.  Unconditional doesn’t begin to cover it.  Limitless.  Earth-moving.  Making you question everything you know to be true about God and man.  And that kind of love will haunt you every moment of every day.  You can see it just behind the eyes of every special needs parent on the planet.  We are filled with a love we never could have predicted.  We are filled with fears we never could have imagined.  We are, quite simply, at capacity most every day.  And, yet, when inevitably called for, we find that capacity expands.  We aren’t better parents than you.  We aren’t saints.  And our children aren’t lucky to have us.  We are lucky to have them.  Because, despite all of these very challenging aspects to having an autistic child, none of us will walk away from this life without having grown – merely from having loved them.  Having become more than we thought we could be.
No, this – like many challenges one never asks for – isn’t easy.
But, I assure you, these children are worth it.  :)

Friday, September 21, 2012

Triple D's of Autism

There was no Silence yesterday!  Oh my goodness.....if you were a fly on my wall yesterday you would have begged for a fly zapper.
Kaden had such a wonderful time at his social club and both ABA sessions ran smoothly.  All was well in the Manic house.  On the way home I had told Kaden he could play star craft, but when we got there Skylar was on the computer talking with a friend on skype.   He told Kaden he would be off soon, well Kaden was upset and wanted to rub on Skylar's face and smell him.  Which is what he does all the time.  He uses his sense of touching people's face and arms and smelling to calm himself or when new things happen unexpectedly.  Skylar was not feeling it, because he was on Skype with a friend and yeah it might not be the coolest thing in the world to have your 5 yr old brother rubbing your face and sniffing your hair.  He sent him downstairs screaming his head off about how we have ruined his life, he hates himself and wish he was not alive.  On a side note I really don't think he was upset over the video game it was the chin rubbing and smelling.  And I think not knowing how to transition his emotions and feelings about what was going on. 
I couldn't speak any sense into him he was not calming down so I thought I would change the subject a little so I showed him his plate of dinner I had made for him on the table.  I had given him two choices earlier, spaghetti or turkey sandwich and chips.  He said that he wanted noodles and chips.
When he looked over at the food he became even more angry and started screaming he didn't want sauce.  I forget how literal he is, he said noodles and that's what he wanted....just the darn noodles.  I think spaghetti.....because I gave him that as a choice.  Life with a child on the spectrum is anything but dull.
So then he begins breaking everything in sight......very important things I might add.  And then he stops and realizes what he just did and starts overly explaining how this should have been made with metal and that should have not been put together so poorly.  I gave him my stunned on my gosh look and then he storms upstairs after I tell him that this behavior is not acceptable and that he has lost his privilege to play any kind of video game the rest of the night and the next day.  For the next 2 hours he screams and thrashes around in his room.  His sister goes up and tries to redirect his attention.  It finally works and then it's bed time and I'm dreading it.
He acts like nothing has happened at all, he goes and showers quickly and gets his night clothes on.  He gets on the bed and rolls himself up into a burrito and puts the pillows over his head.  Lights out for him and I just stood there like well helloooooooo.  I'm over here....your Mom....remember her????
He was asleep in 5 minutes and I was left feeling Deflated, Defeated and Distressed.
Today is a new day, he woke up and acted like nothing ever happened.  When he asked to play video games I reminded him that he couldn't and his reply was," oh yeah, I forgot that....ok".  It's like he pressed a reset button.  Today is a normal Kaden day just like yesterday started out to be.  I pray it doesn't end like yesterday though.

Thursday, September 20, 2012

It Makes Me Smile

I had to post this picture, it makes me smile.  
Kaden was on the bike trail with his "flower holding" bag.  Typical collar popped up on his shirt and hand twirling in his hair.  
*SMILE*

Wednesday, September 19, 2012

Kaden's Loud Life of Silence

Playing a game on the tablet
I ask myself all the time if Kaden feels lonely, but just doesn't know how to describe it to us.  In my mind I wouldn't want to spend hours of solitude up in my room while the rest of my family is downstairs having dinner, watching a movie or just hanging out.
It's not uncommon to find him in his room playing monopoly by himself or reading a book under the table or in a corner.  (We are working on that by the way in ABA therapy)
There are many faces of Autism, it's not a one size fits all kind of deal.  Kind of like autoimmune diseases, which I have one....evilly called Lupus.  Kaden's brain is wired so that noises and certain smells or touches can cause him to be frightened even hurt him.  He also processes sensory different in a way that he is constantly rubbing his hair or blankets, people sometimes.  He constantly smells people or objects when something changes, like our plans, a show ends or didn't record right.  Maybe he didn't understand something or is confused at what is being asked of him.  If he gets overly upset then he can have a hard time with repetitive behaviors, screaming, hitting and just not being able to move forward.  Meltdowns can be atomic with Kaden if they last too long.  So, our job as the family goes is to put the fire out as soon as a spark is seen.  ;)
Socially he doesn't want to be around people, doesn't want to go new places or try new things at all.  That even includes his family sometimes.  Making friends or just communicating can be hard, because he talks off topic, makes little eye contact and prefers to only talk about things he is interested in.  And usually that's not what they want to talk about.  If a friend does seem to break into his friendship circle with himself they get turned off by the lack of personal space Kaden allows and I haven't meet a kid yet that likes to be sniffed and have their hair all messed up by Kaden's little hands.  HAHAHAHA
Playing Legos

Part of his communication gap is his lack of being relaxed and going with the flow.  He takes everything literal and has no problem correcting you if he thinks your wrong.  :)  Adults love this, especially if they really are wrong.  He's very ridged and has his own schedule that can't be broken.
He's not coordinated and runs or falls everywhere and on everything.  I worry when we go out because he flutters like a butterfly.  I worry I will lose him, because he goes here, tumbles there, jumps onto that, scoots there.....you get the picture.
Now on a good note, there are many Autism aspects of Kaden that cause him to be brilliant.  He started reading when he was 2yrs old.  I taught him letters, but he taught himself to read.  He started organizing objects and grouping things together as soon as he could sit up on his own.  He hasn't stopped since.  He had a broad vocabulary at a young age, he hates phonics but loves to learn new words.  He started adding and subtracting at 3yrs old.  He begged to learn more, so when he was almost 5yrs old I showed him multiplication.  He is 5yrs old now and can multiply, divide, complete 4 to 5 step equations..  He wants to learn fractions and decimals now and I'm trying to hold him off, because he is so young.
Organizing the Blokus pieces
So, academically he is above his typical peers.  But, in many ways he is not your average, typical boy.  I hear his silence, if that makes any sense at all.  I feel bad for him, because he is so precious and even though he is verbal he chooses to be silent.  He chooses solitude over time with family or friends.  I guess today was just an emotional day for me.  Even though we were very busy today around the house he was nowhere to be found.  or quietly sitting on the couch counting beads.  I've asked for hugs even tried to bribe with chocolate chip cookies.  All I got was a smile.  But, I am thankful for that smile.  I love that smile!!!!!  I hope he wears that smile for a long time.  And his family will be right there beside him with a Big HUG whenever he wants one!!

Saturday, September 15, 2012

The Changes of Autism, Asperger Style

There have been little changes here and there with Kaden.  I have started keeping a written journal.  Especially since I have been without a computer for about a week or so.  I need to write, I have to write.
ABA therapy is helping him so much, yet it also brings out other aspects of Autism we didn't notice before.  Also, some of his obsessions have worsen because of the amount of work he does every day.  It's stressful for him to do everyday.  Even though the therapy may not look like it should be so stressful to the typical person, for him it is.  It would be like having to do 30 hours a week of the one thing you just don't understand.  That would be Math for me.  :)  I would be soooooo stressed and overwhelmed if I had to do Math for 30 hours a week.
So, we are just trying to work the program and be consistent.  I'm thankful for Kaden everyday, I just have to remind myself sometimes that life is different for him.  And it doesn't matter if we take the long way around the park.  As long as we get there happy, healthy and together.... it will be just fine.

Thursday, September 6, 2012

Smear What on My Face

One day I will wake up and be fully rested with the linger of pleasant dreams.  While I effortlessly go down the stairs I will look over to the the table and see a bounty of delicious breakfast foods.  All the kids will be waiting patiently as I scoop up my favorite iced coffee from the counter and site down in the chair marked Best Mom in the World.  HAHAHA HEHEHE  Everyone says please and thank you with big adoring smiles and when I look over to my tiniest eater I see a nice clean face.  And he's using his fork and napkin........ A Mom can dream......right?  For the most part my lovely daydream is true.  Except my coffee is not always waiting for me and my tiniest eater has food smeared from one end of his face to the other.  He does know how to use a fork I just think he prefers a more hands on approach.  Will this ever change?????  Lord, help us!!!  HAHAHAHA  I laugh only because even though it is embarrassing when we have company or out at a restaurant he is our little guy.  And he is trying hard to fit in to a world that He thinks is doing things wrong.  I can't imagine what it must feel like for him everyday.   Every meal we go over the same rules, the same suggestions, the same pleading.  And every meal we all get the same look from Kaden the same responses and the same mess all over the place. This is a process and we are all willing to go thru it.
I love him so much and I'm thankful that he is able to eat with us, I know there are many parents that don't have that luxury.  I try and remember that every time I feel like I can't take any more.  I caught Mahala rubbing food all over her face a few weeks ago.  I was like what are you DOING!!!!  She smiled and said she wanted to understand what all the fuss was about.  She said it was actually pretty soothing.  HAHAHA  Go figure......maybe instead of getting aggravated when Kaden eats like that we should all do it with him.

Wednesday, September 5, 2012

Sensory Fun!!

Mahala was so Sweet the other day.  She made up these different bowls with sensory items for Kaden to play with.
She used pasta, flour and rice.  He had to smell, feel, taste and guess what it was.
She also did one with beads and small toys.
The favorite one was the slime she made in his favorite color....blue.

The whole playtime lasted for over an hour and I would say a good 45 minutes was him playing in the slime and flour.
He Loved mixing the flour and slime

We are very Lucky to have a Sister like Mahala!!!!