Showing posts with label emotions. Show all posts
Showing posts with label emotions. Show all posts

Friday, May 10, 2013

How He Feels and Why He Loves Me

Yes, kids with autism can feel. 

The Boy has been fascinated with feelings lately. He's always asking how I'm feeling. He recognizes when I'm happy, sad or angry. And when I'm sad or angry, he always tries to make me feel better. 

But feelings are still complex for Norrin to understand and he's been working on them in school. He put together this book at his wonderful school and it was so cute and sweet, I wanted to share.

Here's what makes me happy: I go on the bus to go home

Here's what makes me mad: When I knock over the blocksHere's what makes me sad: I cut dad's hair

Here's what makes me laugh (it really makes me glad): Splashing water
I feel confused when I am sad

And this is my beautiful Mother's Day gift - I love it!
I love mommy because:
She dances with me
She gives me presents
She loves me
She's funny
I like to hug and kiss her
She takes me to the park

Monday, May 6, 2013

10 Things I'm Going To Do Now That I'm Done with Graduate School

Today I handed in my thesis. And that means I am unofficially done. I graduate on May 30th. (YAY!!!!)



Me (posing as proof of) handing in my thesis: smiling, sleep deprived, hair a hot mess.


Dust. I hope no one comes over and looks up my ceiling fans because it's pretty bad. 

Work on my apt to-do list. There are so many unfinished projects around the apartment. So many things I want to do. Closets that need to be cleaned out and cabinets that need organizing. It's going to keep me busy. 

Set up my home office. I'm tired of writing sitting on the sofa. I don't have much space but I need a little desk and a chair. The Unknown Mami gave me a great idea

Get back to writing fiction. I'm good at it. I want to get better. 

Continue editing/polishing 2 short stories and start submitting for publication. I wrote three short stories I'm proud of. I want them published somewhere. I need to get my hustle on. 

Sleep. I need it. 

Enjoy my family & friends. I've missed them, especially these last few months. 

Get a manicure and pedicure. It's needed in the worst way.

Go back to the gym. It's also needed in the worst way.

Start my non-profit and work on building My Dream School. The Bronx needs it.







Monday, February 11, 2013

"How Are You?"

"How are you?"

It's a question we are conditioned to ask. Even when we could care less or are too busy to talk. Asked as a greeting and often in passing. By strangers, coworkers and friends.  

It's a heavy question with a rote answer.

Because more often than not, our answer is usually the same. "Fine."


And I think of all the times I'm asked "How are you?" and I answer "Fine."

Even on days when I'm not. 

On days when the pain is unbearable.

On days when I doubt and question every what if.




I think of how I ask the question of others and I hear the same answer.

We can't all be fine.

And sometimes people just need to be honest and own their feelings. Sometimes they real answer needs to be coaxed out. 

The next time you ask someone "how are you?" 

Stop.

Look.

Listen.  

And you will know whether or not they are really fine. 

And if think they are not fine, ask them "Are you sure?"

Monday, July 2, 2012

Letting Go of Mainstream Dreams

I've been up since 4 am.  Not by choice.  That's the time The Boy woke up. 

By 5 am, I was up and out of bed.  Threw a load of laundry in the washing machine.  Laced up my running sneakers and headed out the door.  (On Day 4 of excercising)

By 6 am, I was half dressed and packing up The Boy's bookbag for his first day at a new school.

And by 7 am, The Boy's school bus pulled up in front of our building.  I introduced myself to the new driver and matron.  The Boy jumped on the school without looking back or a goodbye kiss.  But The Husband and I called his name and we got the goodbye kisses we needed.  


Walking back up to our building, I started to cry.  I know, I know - I'm a cry baby.

Norrin has been taking the school bus since he was a baby - barely 3 years old.  He's been taking the bus since before he could even talk and while he was still in diapers.  

This is the 3rd school he's been bussed to in the last four 4 years.

You would think I'd be used to it by now.  But it doesn't get easier.  Handing your child over to a stranger for the first time.  And this new school is the farthest The Boy's ever been.  

Don't get me wrong - I LOVE the new school. I'm so happy he's there.  It's the right place for him to be.  

It was just never the place I expected him to be.

When The Boy was diagnosed with autism 4 years ago and we started the therapies - I remember The Husband telling me, "This is just to get him up to speed.  By the time kindergarten starts - he'll be able to go to a regular school."

Because for many parents that's the goal.  Mainstream education.  It's the dream.  

I think there was this tiny part of me that wanted to believe that.        

That's the thing about life down the autism rabbit hole.  You can make peace with it,  embrace it but accept it?  Acceptance is not a one shot deal, it's an on going process.  There will always be something new to accept.

The Boy's kindergarten year came and went.  And the fact is, he couldn't cope in a typical public school.  Even in a classroom of 6 kids.  Even with all the accommodations.  Even with the after school ABA therapists coming to the house 4 days a week.  Even with sensory gym on Saturdays.  The Boy still couldn't truly be successful in a 'regular' public school. Granted The  Boy was set up for failure but this last year was a huge eye opener for me.

So this morning as I waited next to a mother with her 13 year old son - who was also waiting for his yellow mini bus to appear - I realized that The Boy may never go to a school within walking distance. 

The Boy may be 13, 14, 15 years old and will still need me to wait with him for the mini bus to pick him up.  The Boys new school goes to 21 - he will probably be there until that age.  The Boy will probably never have a mainstream education. I have to just let that dream go.  I'm okay with it.  At the end of the day, all I want is for The Boy to be in a place where he can be happy and accepted for what he can do.  I know The Boy's education is about goals not grades. 


And I also know there are plenty of new dreams to be had.               

      

Tuesday, June 12, 2012

Sometimes You'll Get Knocked Down

Last week - completely knocked me out.  And I feel angry, frustrated, anxious, bitter, depressed, guilty, emotionally bruised and beaten down. 

Because how can any parent not get emotional when it comes to their kid? 

There is so much going on right on.  And I can't keep it together long enough to write a post.  Truth be told, it's been hard for me to write for the last few months. 

But this week, is especially hard.

I'm having a hard time recovering from last week's knock  down.


This week, I'm trying to catch my breath.  I'm trying to stand straight on shaky knees.  I'm trying to clear my head.

Because getting knocked down, doesn't mean giving up.  It means having another chance to get up and make things right.

Tuesday, April 17, 2012

To Have or Have Not


The Boy fresh out the womb - 2006
This is one of my very favorite pictures - it's the first one of me and The Boy. Maybe it's the fact that I was coming off the drugs, but there's a look on my face that I've never seen in any other picture. Holding The Boy in my arms for the first time after feeling him grow inside over 39 weeks, was a defining moment.  I felt content, at peace, a feeling of love that I had never experienced.  Instant gratification to the umpteenth degree!   

On the day that The Boy was diagnosed,  the doctor asked if we were planning to have more children.  And while we weren't trying at the time, we knew we wanted more.  Until the doctor said, "You should consider genetic testing, if you want more children because you're more likely to have another child on the spectrum."  And it was two dreams shattering at once.

Everyone suggested we have another child.  My parents, family, friends, therapists - The Husband.  Everyone was asking when the 2nd one was coming.  Honestly, the thought of having another child with autism scared me - it still does. How will a second child impact The Boy?  What if I have a "typical" child who resents the responsibility of caring for The Boy?  I know parents do it every day with multiple children on the spectrum.  But could we do it? Not only emotionally or physically.  But financially. 

Then last year, at around this time, I decided I was ready. To take my chances.  Because I thought - what if, I was depriving The Boy of a potentially amazing sibling relationship.  I wanted another baby - autism or not.  I didn't care.  I knew in that moment, two and half years after The Boy's initial diagnosis that I had accepted autism.  The next month, we were pregnant.  And while I was nervous, I was so excited.  The baby's due date was to be on The Boy's birthday.  And I thought to myself - it's a sign.

But when I went in for my 16 week visit, my doctor couldn't hear the heartbeat.  And when we did a sonogram - we were able to see my baby whose heart had stopped.  My baby had died and I didn't even know. I'll spare you the details, but it's a loss I am still mourning.

There are days when I really want another baby. Especially when I see a pregnant woman or a newborn baby. And I am surrounded by pregnant women - at work, at Norrin's school, among our friends and family. I have days when our lives feel unbalanced and I can't help but think a baby would even us out.  Because I think The Boy would really be a great big brother. And then I have days that I'm content with The Boy because the thought of second loss would be devastating. And for a few minutes every month for the last six months, I am hopeful, only to be disappointed by the glaring pink line of negative pregnancy test. 

So while I absolutely love my first picture with The Boy, it makes me a little sad.  Because I wonder if I'll ever have a moment like that again.

~~~~~~~~~~~~~~~~~~~~~~~~~
(originally posted on April 14, 2011)  

Thursday, March 22, 2012

"As a Parent"

Going into IEP meetings, I've noticed that some education professionals like to start sentences with, "As a parent..." blah blah blah blah.  Maybe it's their way of letting parents know that, they get it.

But every time I hear those three words, I realize that they don't get it all.  And I want to hold up my hand and ask "Are you a parent like me?"   


Because as a parent, I have had to put my child on a school bus before he could speak and while he was still in diapers.  

As a parent, I've wondered if my child will ever speak.

As a parent, I've stayed up nights worrying about what my child's life will be like when I'm gone.

As a parent, I've had to separate my child from his diagnosis.



As a parent, I have had strangers in and out of my home, helping my child learn the most basic tasks.

As a parent, I've had to rearrange my work schedule to accommodate all the strangers in and out of my home. 

As a parent, I've had to turn down invitations to birthday parties and gatherings because therapy always comes first. 

As a parent, I've had to turn down invitations to birthday parties and gatherings because I knew the invitation would be in a place my child could not handle.

As a parent, I've had to teach my child how to imagine, to play and pretend.

As a parent, I use the majority of my vacation days for doctors appointments and evaluations. 

As a parent, I cried, the first time my child said Mommy because I thought the words would never return.

As a parent, I marvel at every single accomplishment my child makes, because I know how hard my child had to work to achieve it.

As a parent, I wonder what his days are like because even though my child has speech, he cannot tell me what he had for lunch, what he did in school or about the best part of his day.

As a parent, I've learned to ignore strangers staring at my child.

As a parent, I've had to study special education laws and different teaching methodologies.

As a parent, I've had strangers, determine what is most appropriate for my child.

As a parent, I've had to fight for my child to get the appropriate services he needs.

As a parent, I've had to fight the people who start their sentences with "As a parent..."

Thursday, March 8, 2012

Sometimes Things Fall Apart...

"Sometimes things fall apart so better things can fall together."
(not sure if this is the exact quote or who even said it.)

The other day one of my FB friends posted this quote or something similar (I can't remember exactly) as their status update.  And well, I certainly hope this is the case.  Because lately things seem to be falling apart.

There is so much uncertainty lately.  Well, if I'm going to be completely honest - there's been uncertainty since The Boy's first day of kindergarten.  I remember this time last year, feeling tangled in red tape, overwhelmed and unsure as to what would happen in September.   

And so much has happened this school year.  Things I cannot write about.  But I will say this.  It's been incredibly disappointing.  And frustrating.


And while The Boy has come so far since September and I'm please with his progress.  I'm still at a complete loss. 

And I have raised questions and concerns that go ignored and unanswered.

And I have become cynical.  And I have lost both faith and respect in the New York Board of Special Education. 

And that's unfortunate because I wanted so hard to believe that ultimately - people will do right thing by a child with special needs. 

And bottom line.  More often than not.  They don't. 

Children are no longer children but a number in a broken system.         
 

And then last week - I stood in the rain for an hour.  Waiting for The Boy.  With The Boy's ABA therapist (that I pay for privately).  Needless to say, The Boy lost an hour of therapy. 

And when I called the school bus matrons, I was told that 2 more children were added to the route. 

And I could hear The Boy in the background - his high pitched perseverating speech.  And I knew he was confused.  Nervous.  Unsure of what was happening because The Boy memorizes routes.

The Boy is put on the bus at 2:20 pm (I think this is the time.  Though when I called The Boy's school to confirm, no one seemed to know.  But they did tell me, the bus is often late.  But that's for another post...)  And he didn't get home until 4:45 pm.  That means my 6 year old autistic child was on a school bus for 2 hours and 25 minutes.  And the matrons told me that 4:30 - 4:45 would be his new drop off time.

And I'm supposed to shut up and be okay with it?  Oh Hell Motha Effin NO! 

The school is less than 6 miles away.  He just turned 6.  He's autistic.  He has a 6 hour school day and over 4 hours in commuting each way.  I'm sorry, I don't want to be on a bus for more than an hour - let alone 2! 

So I wrote a letter to the person in charge of Office Pupil Transportation (OPT). 

And I may have cc'd the Borough President.  And um...The Chancellor.  (Because you know, me & Dennis are cool like that.)


They are working on it and The Boy has been getting home a few minutes earlier every day.

And you know what the OPT dude had the nerve to say that it wasn't necessary for me to cc those folks. 

Well...I beg to differ.  I will cc whoever it takes.  I will call and write whoever I need.  And I will do whatever it takes.  To make sure that The Boy's needs are being met.  That he has the appropriate services he needs.  That is my job.


And even when the NY Board of Ed & OPT don't do their jobs - that's fine.  I will continue to do mine.

So let things continue to fall apart.  Mama's putting it back together. 


(Yeah...um, this post is kind of all over the place.  But I have lots going on and my mind if sort of all over the place too.)         

         
 

Thursday, January 19, 2012

Working Mom Guilt

Maybe it was the postpartum.  Maybe it was the fact that I was on maternity leave during the cold months of winter.  Or maybe it was because I had no SAHM friends to keep me company.  But I couldn't wait to go back to work.  Lots of moms told me about how they cried on their first day leaving their child.   Not me.

I was so laid back.  Well, laid back for me.  (The Husband will say that I'm a tad neurotic, controlling and sometimes a worry wart.)


And then after the diagnosis, I was reading about the 'cold mother' theory and well...in those first few months, I kept thinking of new reasons why autism was my fault.


Fast forward a few years...


I know autism isn't my fault.  But that doesn't mean the guilt is gone.  


So yesterday, I had my first breakdown of 2012.  I came home from work, sat on the sofa and just cried. (The Boy wasn't home from school yet.  I try not to cry in front of him, it's too upsetting for him.) And after I cried, I still didn't feel right. I hate that feeling, when my nerves get the better of me.  When my thoughts are all over the place and it's hard to focus.  And I have to keep reminding myself to breathe in and out slowly because my heart is racing and my hands are shaking.  Too much uncertainty, lots of built up frustration and other stuff going on that I can't discuss here.  Not now, anyway.


Tomorrow is The Boy's 6th birthday.  I'm going to send cupcakes and other party stuff into school.  But I can't be there.  I'd like to be.  I always have in the past.  But this year I can't.  I have to conserve my vacation days. (Last year, the majority of my vacation days were used on sick days, appointments, school interviews and IEP meetings. By the time December came, I had only 1 day left.) And since I'm taking Monday as a "vacation day" because we going through the evaluation process all over again, I can't take off Friday to go to The Boy's school. 


I missed so much at The Boy's last school.  It's impossible to take off for everything, even though I'd love to be there for everything.   And even this year,  I've missed a lot.  Like PTA meetings, because they're in the mornings and that requires me taking a half day.  The Boy's school trip to the NY Botanical Garden.   

It sucks when you want to be there and can't.  I know I can't quit my job.  And I know that lots of other moms are dealing with this same kind of guilt.  And I know that The Boy doesn't feel slighted because I'm not there.  And (most days) I know I'm doing the best that I can.  But it still sucks just the same.

(And if this post is all over the place, I apologize.  I'm still trying to breathe slowly.)



Thursday, December 15, 2011

The Thing About Christmas

It's supposed to be the most wonderful time of the year.  Right?

But it seems like a lot of work and worry for something that's supposed to be fun.


As a little girl, I loved this time of year: putting up the Christmas tree, baking cookies, singing Christmas carols, walking down the neighborhood streets admiring the glow of lights.  Going to see the tree at Rockefeller Center.  Walking by store front window's fascinated by the decorations. 

I didn't even mind going to Church - especially midnight mass on Christmas Eve.  And even though I'm a faux Catholic now, I would love to be able to take The Boy to midnight mass.

(The Boy isn't quite ready for church.  So I know I couldn't handle it solo and The Husband will not go with me.)  


The Boy is at an age where the magic of Christmas should begin.

The Boy isn't really interested in singing. 

Or the Tree at Rock Center.

Or store front windows.

Somehow, autism and magic and Christmas don't really add up.


The other day someone asked me if The Boy was excited about Christmas.  I shook my head, "Not really."


Even  though The Boy knows what Santa looks like; he likes loves getting presents and watches Charlie Brown Christmas almost every night - The Boy does not understand the concept of Christmas.  (Forget about trying to explain the whole Jesus aspect.) 

Now, if you are the parent of "typical" child, you may say to yourself, "That's all kids." 


10/29/2011

No - it's not all kids.  It's different.  Trust me. 

Because when The Boy sees snow, he thinks it's Christmas.  Remember back in October when it snowed?  The Boy yelled "YAY - it's Christmas time."  

 For the last few months, when we've gone out  to the store and The Boy reaches for something he likes, I'll say, "Christmas is coming.  We'll ask Santa."  I've been trying to explain the "Dear Santa" letter.   The original plan was to have The Boy write to Santa and ask for the presents we've already purchased so that he makes the connection.  

But now I'm wondering if I should even bother with explaining Santa at all? 

12/10/2011

I mean, technically, Santa only brings gifts to boys and girls who have been good all year long.

The Boy is a literal thinker with a razor sharp memory.  What if he recalls every single time he did not listen?  The Boy (for the most part) knows the different between good and bad.   

So if I press this whole Santa Claus thing year after year - he'll eventually get it.  And he's getting close to getting it.  (I think) I mean look at the picture ---->

Doesn't The Boy look surprised?  After "Santa's" appearance, I believe that's when The Boy ran to the Christmas tree and opened a gift.  (And yes, that's an oil painting of RuPaul in the background.) 

And by the time The Boy really really gets Santa and this whole Christmas business - it will be around the same time, we'll have to tell him "There's no such thing as Santa Claus."     

And bursting that bubble will need to happen. 
I know, I know - it doesn't really need to happen.  But, do I want a 12, 13, 14 year old kid asking Santa for the impossible - things that I cannot possibly afford or deliver?  Not really.

I don't know.  I guess I'll have to take Christmas one year at a time.  And this Christmas will be like last years - with too many presents for The Boy to open.  Much more than what he wants or needs.  Because Christmas means so much more to me, than it does to The Boy.  And in some crazy way, I feel like I have to overcompensate for that.



       

Monday, November 28, 2011

#YouMightBeAnAutismParentIf

you've been on twitter lately and following these tweets - #youmightbeanautismparentif. 

If you haven't - you should.  It's been steadily growing.  The idea for the twitter party was started by Many Hats Mommy and the hashtag was created by @RaisingASDKids.   

Honestly up until a few days ago I wasn't one for twitter.  I didn't really get it, couldn't keep up - I didn't really understand the point of the hashtag.  But since I've been participating in the #youmightbeanautismparentif twitter party, I've been a tweet freak.  I think I've come out of the Twitter closet and now ready to embrace @LaliQuin (my twitter name). 

I'm throwing out hashtags and retweeting and replying to tweets. (Ok, still working on my response time.) 

And when @HollyRod4kids retweeted ME.  I yelled out - OMG!  Because that's the kind of Twitter dork I am. 



The absolute best part of this ongoing twitter party is that I've connected with so many people, I may not have met otherwise.  I'm laughing and crying and nodding my head because the things other parents are writing I totally get.  Because it's always nice to know I'm not alone in my thoughts. 

Here are just a few of my favorites:  


@ you find yourself celebrating and heartbroken - at the same time and for the exact same reason.

@  you have to live forever. No, I'm serious. This isn't optional.

@  one moment, you feel completely alone & the next, you're a part of a large, passionate & supportive community.

@ You see a child breaking down in public and don't pass judgment on the child... or the parents.

@ you always talk like you are in a social story....."And that's ok"

@ you've read enough books on that you could practically be a doctor yourself

 
@ you wanted to write your own book because the ones you have are useless in your world.

@ youve accepted that NORMAL in ur house is exactly opposite of "typical" in pediatricians office

 

@ once child knows no Santa u watch him so he doesn't tell every small child bc "they need to know the truth too"

@ And the companion guilt: you feel guilty that your child says "I love you" when so many others don't.

@thecoffeeklatch If you want to follow the most inspirational thread on Twitter - get a kleenex and be inspired #youmightbeanautismparentif #TCK.


And here are a few of mine -
  AutismWonderland

you look at pictures pre-diagnosis and wonder "Why didn't I see it?"
 
you have a hard time going to sleep at a reasonable hour.
 
#youmightbeanautismparentif you've slipped on, stepped on, rolled over on (yes, in bed) Legos
 
YOU know in the grand scheme of things isn't a big deal, but hate when others say, "it's no big deal"
 
 
potty training is taking years not weeks. And let's not discuss night-time potty training...
 
hate hearing "Oh but that's all kids" Because no...it's really not.
 
 
Goals are the priority


Go ahead join the #YouMightBeAnAutismParentIf conversation on twitter! 

#youmightbeanautismparentif _____________________.

Tuesday, November 22, 2011

The Moment I Forgot About Autism

It happened in Target of all places, on a Sunday afternoon.  The husband had wandered off while I pushed The Boy around in the cart; though at four years old, The Boy was well over the weight limit.  It was easier to shop, if he was contained. 
Through the corner of my eye, I saw a woman. Unlike my frantic sloppy ponytail and my smear of cherry chapstick, the woman had time to fix herself before facing the world.  Her hair was neatly combed back in a ponytail; she wore bright coral lipstick, boot cut jeans and brown boots with kitten heels. Her nails were filed square and painted ivory. My nails were bare and bitten down.
I realized she was a mother.  She had one manicured hand on the handle of the shopping cart.  Her son lagged behind.  Every so often, her son wandered off.  When the mother called out a name, her son instantly reappeared.  Her boy was probably a year older than mine. 
I could never shop like that.  High heels were impractical when out with The Boy.  I never knew when I needed to run.  And there was no letting go of his hand.  If I let go, he’d wander away; the warmth of my hand would go unnoticed.  If I called out his name, he would ignore me, stuck in stim.  If he ran off, The Boy would never tell a stranger his name.  Not because he didn’t know it or couldn’t say it, the question just needed to be asked several times before The Boy provided a response; if he provided a response.  And it was unlikely that The Boy would look a stranger in the eye.  A stranger would give up.  And The Boy lacked the cognitive ability to say that he needed me or missed me.  The Boy was a kidnapper’s dream. No, I could never let go.
I wondered what that mother’s life was like; I wondered about the dynamic of her relationship with her son.  I was certain that she never had a team of therapists in and out of her house.  When she asked her child a question, he looked her in the eye and answered back.  And when she kissed that child goodnight, he would automatically say the three words every mother longs to hear, without any prompting and with genuine feeling.  When she let go of his hand, she knew he would return. 
Her boy wanted to start writing his Christmas list.  He wanted a new scooter and some video games.  The mother smiled and she said something that I did not hear.  I stopped listening.  It was hard to listen to their exchange and not feel envious.
We approached the baby section and The Boy attempted to stand, reaching out for the infant toys, his hands flapped with both excitement and frustration, bird-like sounds coming from his mouth.  Sit down. Use your words.”  I said in a firm tone of voice used by therapists. 
The Boy had words, lots of words actually – hundreds, maybe thousands.  But he used them sparingly and hardly spontaneously.  Most of his speech was scripted, memorized from books or cartoons. 
Mommy.  I want the toys please,” he asked. 
The Boy’s words were stilted, his high-pitched voice void of emotion.  With each syllable his head bobbed like a marionette. 
Fix it.”  I said. 
The Boy repeated the request in his natural voice.  Though his tone was deeper, it still lacked affect.  Words can be taught, emotional tone is much harder. 
We moved slowly through the aisles.  The store was crowed with holiday shoppers; the toy shelves were filled to capacity, not an item of out of stock.  Women walked with circulars in their hands, looking for sales; searching for price check machines. 
The glitter and sparkle of the Christmas decorations reminded me that I needed to buy a tree and pull the decorations from storage.  
Oh my!  Look at all these decorations,” The Boy said in his high-pitched voice.  His words were crisp and clear.  His facial expression was appropriate: happy and wide-eyed.  He pointed.  And I was surprised that he knew the word “decorations.” 
I pushed the cart closer to the decorations.  There were Christmas trees and wreaths, stockings and snowmen, candy canes and bright bulbs.  I didn’t care if he flapped; he was excited. 
What are the decorations for?” I asked.
The Boy looked me right in the eye. “For Christmas! C is for Christmas.”
The Boy kicked his legs against the cart.  He smiled the smile that I loved; it belonged to a four year old boy who was neither typical nor atypical; with dimples in each cheek, his eyes squinted and his nose scrunched up. 
I laughed.  That’s right!  Who comes on Christmas?”
Santa Claus!”
And what does Santa Claus bring?”
Presents!”
I praised The Boy again and again.  Gave him a hug and kissed his cheeks.  I must have looked like an idiot, making such a big deal over such a little thing. 
It was the first real conversation we ever had.  In that moment I forgot The Boy had autism.  I forgot about the mother in her kitten heels and her son with his Christmas list and my seconds of envy.  I forgot that a doctor once said, The Boy might never utter a word.  I forgot about all the hours of speech therapy that were needed to get to that simple conversation. 
I was just a mother and he was just a little boy, excited about Christmas.  And maybe letting go of his hand was not so far away.
~~~~~~~~~
This essay was written November 2010 but was never posted.