Thursday, July 7, 2011

When Pigs Fly

It's that time of year again.

Counting down, getting close to my boys' birthday in late July.

Plans must be laid, preparations made.

Not the least of which is the cakes.

I make awesome birthday cakes, my one claim to domestic fame.

Think I'm exaggerating (as I have often proclaimed my complete disinterest and ineptitude at most things housewiverly)?

Nope:

Jake's "Very Hungry Caterpillar" cake, 2009
Ethan's "Lapras" Pokemon cake, 2010
(Want to see them all? See this post HERE)

In years past, I have pretty much known what Jacob's current favorite characters were, his obsessions up front and obvious. I have asked the rhetorical question: "Jake do you want a (insert favorite character here) cake this year?" And he has said "Yes." And that's it. Case closed.

Ethan's choice has been obvious and easy some years. Others have required research and negotiation, a delicate balancing between his desire for elaborateness and my ability to make 2 cakes in one day & evening while managing to still get enough sleep to function at the party.

One Pokemon of his choosing: yes! An elaborate battle scene with multiple Pokemon and trainers? Not in this lifetime, kid.

But Ethan will communicate with me, we'll hash it out together, sometime over the next week or so. If Wilton has ever made a cake pan shaped even vaguely like what he wants, I'll head to E-bay to acquire. If not, I'll hit up the internet coloring pages to create a pattern.

For Jacob, on the other hand, this year is a bit of a mystery; his cake, a puzzle that needs to be solved.

You see, this year, he is paying attention. He has been talking about "Birthday Cake" for about a week now. Constantly. He REALLY wants to help me make it, and is very specific that it MUST be round.

For some years now, I have been a bit smugly pleased that my son is "less rigid" than most other kids on the spectrum. I figured he was just innately more easygoing, thanked my lucky starts about it, thought it was his inborn "happy-go-lucky" personality shining through. (Can you see the smack-down coming?)

Turns out? It was because he was mostly just oblivious! As he has "woken up" into the world, is processing so much more, really understanding what is going on around him in a much more profound way... he is getting REALLY OPINIONATED, and well, rigid about things.

Le sigh.

So I can't just make a reasonable suggestion, have him go: "yes" and just carry on with whatever I make his cake to be. He wants it HIS WAY.

Now, if he were better at communicating what he wants, this would not be be MUCH easier. But he's not. Autism is a communication disorder, see. I know this seems like such a little thing, barely a blip in the big scheme of things,

But I know if I don't get it right he will be miserable. If his cake is "just right" what he really wants? Happiness will ensue.

No pressure here folks, really.

Well last night at bedtime I got him in an expansive, expressive mood. When he started up with the "I want my birthday cake, Mom!" routine,  I actually got him to answer some questions about it.

What he appears to be telling me is that he wants: a ROUND cake with layers "a tall cake, Mom."

Also? Chocolate. "Brown, darker brown chocolate cake!" No doubts about that. Damn!

As I make two cakes every year for the party (Twins!) and not everyone likes or can eat chocolate, I have always made one chocolate and one vanilla or flavored vanilla (lemon/orange/strawberry).

Since Ethan is a chocolate fiend and believes that non-chocolate cakes are a disgrace to desert-hood and have no reason to exist, well, you can see that Ethan's cake has always been the chocolate one.

So now? I am going to have to make two chocolate cakes (one gluten free for Jake) AND some lemon-vanilla cupcakes for the non chocolate crowd.

But all that aside, back to Jacob's elaborate plans. If I've got this straight (and this is for sure what he told me tonight, whether it changes tomorrow remains to be seen), he wants this cake to have:

"Yellow frosting, mom. Yellow AND orange frosting."

"OK. And what kind of picture do you want on it, Jake?"

"A pig!" No hesitation there.

Really? A pig?

"Jake, you want... a... pig?"

"Yes, Mommy! A white pig, Mommy! With green eyes, Mommy!"

"OK, a white pig with green eyes.  Jake, you got it." 

I kiss him a final goodnight, climb down the ladder from his top bunk, and then hear a little voice in the dark:

"With wings, Mommy, a white pig with wings."

So this year, in late July, be prepared to see a white pig with green eyes, flying across a TALL birthday cake. (And then coming to a blog post near you, soon.)

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Wednesday, July 6, 2011

Wordless Wednesday: Happiness

Happiness is: Three hours in a lake

 With a floating trampoline (Cannonball!)

Ice cream on a hot summer day

Unlimited ice cream

 Swinging

Really fast
 

Listening to Rock and Roll with Dad

Hours spent barefoot and the freedom to roam

Many thanks to our gracious, generous hosts for a wonderful family day, for the chance to blend in, be just another family amidst many families celebrating on this 4th of July weekend.

For once we weren't "that family." There were lots of little kids there, having way bigger meltdowns than Jacob. He was on best behavior. I told someone Jake was autistic and they were surprised, hadn't noticed he was different.

Three hours in a lake seems to be just the thing he needed. And live music. And fireflies.

At the end of the day? Two happy, exhausted kids. Perfect.

I’m linking up to Wordless / Wordful Wednesdays all OVER the place... at Angry Julie Monday... at 5 Minutes for Mom... at live and love...out loud... at Dagmar*s momsense... at Parenting by Dummies... at The Maven of Social Media        
 

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Tuesday, July 5, 2011

The Cube and I

I am sitting crosslegged on the sofa, ignoring the cat batting at me, attempting to wrest the Twinkie from my hand. She sprints to the living room’s windowed wall, fantasy-stalking the birds flitting about the feeder, newly filled by my mother.

Their hungry chirps an invitation to come outside and play before this winter afternoon’s blue light fades to black.

Though the huge nor’easter was two weeks past, there are still deep piles of snow out back, making odd, lumpen shapes out of our backyard’s buried furnishings: picnic table transformed into igloo palace.

But the pull of something else bears a stronger seduction: an ugly square box with golden antennae perched atop. Curved glass holding shifting ghosts of black and white.

It’s 4:30 PM. Sunday afternoon. I am watching TV.

And after today, February 23rd, 1969, my brain will never be the same again.

I am, as is common, alone; my parents busy, elsewhere…  Mom in the laundry room perhaps, Dad in the darkroom.

I turn on the TV set. Channel 4, NBC. OK, why not?

Something comes on. Something I have never seen before, and, for many years afterwards, am not sure I had actually seen then, not just hallucinated:

“The Cube.”  

I see this...

There is a man alone in a small white room.

Perfectly square.

A cube.

Each wall, floor, ceiling made up of a 4x4 grid of white squares, in turn.
 
The man is searching, questioning: What is going on? Why is he here?

People begin to enter the cube, interact with the man.

But no one gives him answers.

They only draw him into their own dramas.

The mystery deepens.

Existential angst engulfs.

People talk:

“None of us are real, he’s not real, we’re all projected.”

“Well, as I interpret what you’re doing here, this is all a very complex discussion of Reality versus Illusion. The perfect subject for the television medium!”

Reality shreds, hangs on by a thread, disappears completely, appears to return, and then? Poof, in a whiff of strawberry jam, it is gone…

What remains?

The Cube.

So yes, at age eight and a half, I had my already precocious mind completely blown by a bit of TV.

Produced for NBC Experiment in Television, directed & co-written by Jim Henson (yes, that one).

This will be hard for those born into the cable-TV-10,000-channels-that-must-be-filled-at-all-times years, but this aired exactly twice.

Once, the day I saw it, February 23, 1969, and once again in 1970.

Then it disappeared.

When I would describe it to friends, with a few rare exceptions, they would look at me as if I had three heads, shake their own heads and declare that nothing that strange had ever appeared on television; I must have made it up, so fantastic did it sound.

But oh, it was real. Very real.

If you have never seen it (and I am guessing this describes 99.9% of you) you must.

Here:


"The Cube" a tele-film by Jim Henson (& Jerry Juhl), 1969

Now imagine yourself a hyper-sensitive, highly intelligent not-yet-nine year old girl with an over-active imagination and a developing penchant for getting stuck in the revolving doors of her own mind, watching THAT alone on a long ago February afternoon...

Anybody have any questions as to when the seeds were planted for me to become a student of avant-garde filmmaking at an experimental college at 17? A hippie, lesbian, college-drop-out, bean-sprout farmer living in a primitive geodesic dome on a ridgetop in Northern California at age 20?

And then, at 33, a married, Manhattanite, globe-trotting corporate video producer with a closet full of suits?

I thought not.


This post was inspired by a prompt at The Red Dress Club. This week's RemembeRED assignment was to write a post about a TV show from your past. 
Please click on the button above, go to the link-up and read the other wonderful posts you'll find there.


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Monday, July 4, 2011

Firework

Katy Perry now takes up real estate in my brainspace. Whether this is for better or worse? Doesn't really matter, it just IS.

Every time I see, hear, think of fireworks - there's Katy belting out "Baby you're a firework..." Pretty much unavoidable this time of year, being the Fourth of July and all.

It's a damn catchy popsong. Plus there's that amazing, moving, meaningful video. It's old news certainly, out since last fall, but I catch on slow, being such an old lady. (You HAVE seen the video right? If not, head to the bottom of this post immediately.)

What really cemented it in my mind was hearing the graduating middle school kids singing the song at Jake's Special Ed school's end of year celebration. To hear these amazing kids, who have faced such deep learning challenges and persevered, singing this anthem of self-worth: "...it's always been inside of you, and now it's time to let it through..."?

Well, I fell in love with the song a little (and bawled my eyes out a lot, thanking the gods of waterproof mascara).

Sadly, we didn't get to see actual fireworks this Fourth of July.  I'm feeling kind of bad for depriving my almost 9 year old boys of this thrill, but it's just so hard to get to see them here in New York without spending insane amounts of time in insane crowds and for 2 out of 4 of our family members that would be sheer torture.

I was about to write "I have always loved fireworks" but then realized this is so NOT true. As a teenager and adult? Yes. Even as an older child, yes.

But as a little kid? Fireworks were a big problem for me. One of my earliest memories is watching them out the window of our Riverside Drive apartment and being shocked, baffled and TERRIFIED because I was in physical pain, and everyone else around me seemed unharmed; pleased, even.

And fire CRACKERS? Don't let me go there. As a child I was truly terrified of firecrackers to the point of being thoroughly phobic. They scared the everloving shit out of me.

One time, after we'd moved to the suburbs, my family had come into the city to go out to dinner with another family in Chinatown. No one quite realized it was Chinese New Year, or what that might mean for me.

When we went in to eat it was still daytime, and relatively quiet. But by the time we emerged in the evening, it was a full-blown firecracker inferno. I had to be carried, screaming and blubbering, down the stairs, through the exploding streets, to the car.

The memory is etched into my psyche. I thought I was going to die.

In hindsight? I can unequivocally diagnose my child-self with Sensory Processing Disorder (SPD), hyper-sensitive variety. Yes, as a child loud sounds were actually physically painful to me. Very.

And as I had outgrown it as I got older, I had just completely forgotten about my childhood sound/pain connection. Until I was reading up about SPD issues after Jacob's autism diagnosis. Then it all came flooding back.

Well, I've always said the apple doesn't fall far from the tree.

We know so much about this stuff now, how it is neurologically based. But back then I was just "weird" and often teased by my peers for being "sensitive." I was also hyperlexic.

But these are other stories for other days (and other posts).

Tonight? I leave you with fireworks. Thanks, Katy!




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Sunday, July 3, 2011

SOC Sunday: Thomas still visits my house

Exhausted after a full day fete at a lakeside house yesterday. We never get invited to anything, so are quite grateful for this now annual chance to party as a family with food, swimming (floating trampoline!), rides, live music and a firepit after dark for the last late stragglers (us, we always come late, stay late).

I am coming down with a nasty summer cold, so while Ethan is over at a friend's house (a deep thank you to every parent of a friend of Ethan's who has hosted more than your fair share of drop-off playdates due to Jacob's autism and my subsequent need to hand Ethan off for the day) Jake is home blissfully watching TV and playing on the computer while I try to drag my ill ass off the sofa to unpack from yesterday's excursion.

Maybe not happening (getting dizzy every time I try to stand up). While languishing on the sofa I am half taking in the TV, which led to this observation...

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One of the many gifts of Autism is that Jake takes a lot longer to outgrow his "babyish" loves and obsessions. Or seems to outgrow and move on and then (hopefully before I've given away all the toys & videos) circles back around and they are on his radar again.

Like Thomas the Tank engine, favorite of every 3 and 4 year old boy on the planet it seems...  Jake out grew it later than Ethan, but really seemed to be past it by 1st grade or so, watching all the horrible violent superhero shows that his brother liked on the Cartoon network or Disney XD.

Somehow or other, Jake is liking the superheros less these days, and is back in little-kid land when it comes to TV. Thomas, Curious George, Clifford and Arthur are all back in steady rotation in my house, at least when Ethan isn;t home and strong-arming control of the clicker. (I draw the line at Caillou, I WILL not watch that again no matter what!)

I was trying to figure out why this was, why Jake had seemed to move on & grow up & then slide back into little kid shows. But upon reflection, I think it is anything but a backslide, more of an upward spiral that looks like a circle back around, but isn't. He is revisiting the old shows but with much more understanding and insight.

It's all because of Jake's language processing issues (of course). for a while he loved the superhero and teenagery shows Ethan watched because there was a lot of visual excitement and movement in them (fights! Explosions!) and the scary aspects to them seemed to go right over ihs head.

But now Jake is understanding and processing more - and the scariness of those shows is actually starting to... scare him.

It seems a lot of stuff around which I thought Jake was fearless? Well, it turns out he was just clueless. Because you have to process and understand what is going on to be afraid. and he wasn't before. And now he is. So what looks like a step backwards is really progress.

So he is retreating to the "safe" little kid shows, but as he is processing more, he is getting more out of them -- understanding the situations more, getting the humor, getting more than just the basic story, the contexts of things that had just slid right by him before.

So, as I said it is a spiral, Old "friends" re-visited but with new, "higher" understandings, one turn up the spiral ladder of understanding.

So I guess my ticket off the Island of Sodor is going to have to wait a little longer. That's OK. Jake is happy and learning.

As long as I don't have to hang out with that damn whiny Canadian bald kid with the too-nice parents, who is clearly going to grow up to be a serial killer. (You knew that, right?)

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OK, back to bed now (Damn summer cold)!

New to SOCS?  It’s five minutes of your time and a brain dump.  Want to try it?  Here are the rules…
  • Set a timer and write for 5 minutes only.
  • Write an intro to the post if you want but don’t edit the post. No proofreading or spell-checking. This is writing in the raw.
You can do it, too!  Click on the picture link and let's hear your 5 minutes of brilliance...
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Saturday, July 2, 2011

SNSS: I am the Sister


Today brings a completely different voice to Special Needs Sibling Saturdays. Last week the stark. raving. mad. mommy. interviewed her children about their siblings…

Now, I bring you Luna, a young woman who is not a mother (yet) but who has a lot of experience with autism… as a sibling. Both of her brothers are on the autism spectrum.

She also has experience caring for children - other people’s - as she has worked as a nanny. She writes as ababynanny on her blog
Hand in Hand in Lala Land.

Obviously NOT a Mommy Blog, although she openly admits to “hanging around mommy blogs.” Most SN/Autism mombloggers don’t have paragraphs like this in their posts:  ”I wonder what would happen if I totally started dancing to this song down the aisle of the library?  The only trouble is, my skirt would definitely slip down and I’m not, as such, actually wearing underpants.”

(Oh, to be young, footloose, and fancy free again.)

If you go there, be prepared to hear the interesting, sometimes random thoughts of a bright, funny, unconventional young woman exploring the world and her place in it. 


But first, read this moving post about her experiences as the sister to two autistic brothers, here:

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I Am the Sister – by Luna (aka ababynanny)

I am a 21 year old girl, not yet a mother, but I think a lot about autistic kids because both of my brothers are autistic. Growing up watching my parents try to raise my brothers gave me a lot of huge, huge fears about motherhood.

But reading (some might say stalking) Autism Mom blogs – especially stark. raving. mad. mommy. – is helping me to see how mothers can be content with their special needs families, loving their kids and knowing they are awesome. Right now I'm really coming to terms with my future motherhood.

I am the youngest child in my family, with two older brothers and one older sister.  My oldest brother David (now 32) has Asperger’s syndrome and my brother Tyler (now 30) is mildly autistic with developmental and learning disabilities. Although these guys are my “big brothers,” my sibling relationship with them, growing up, has been far from typical.

When giving a definition of autism, a doctor might tell you about the impaired social interaction. Real life translation: I can’t remember ever receiving a hug from either of my two older brothers.

The doctor might tell you about low IQ.  Well, I can tell you that ever since I’ve learned to read, I have been reading aloud to my eight years older brother instead of the other way around, and we both love it.

The doctor might mention restricted and repetitive behavior, but I’ve experienced the variety of having a brother who can always tell me about the latest movies and Broadway plays, and can’t rest until he’s collected them all on DVD. (Don’t call it obsessive.)  There’s a whole lot about life with autism that a doctor can’t tell you.

In some ways, my brothers are a challenge.  Growing up, when I invited friends over, I had to educate them first. I'd take them to the stairs in the laundry room on their first visit, and clumsily but confidently talk about things like poor reading skills and special ed classes, while they always listened quietly and respectfully.

My brothers required more attention from my parents in many ways. And people with Asperger’s syndrome typically have an emotional maturity rate of about 2/3 their age, so for years I’ve had to deal with the frustration of a “younger” older brother in both David and Tyler.

And yet, overall, I love the experiences I have with my brothers.

As a little girl, it didn’t seem strange - in fact, I was lucky - that the person I played dolls with was my teenage brother, Tyler. David, always very smart, would teach me about interesting things that most people wouldn’t, from ancient history to modern medicine.

Whatever intellect or sociability he may lack, Tyler paints and draws and is one of the most creative people I know.  Despite Tyler’s supposed limited ability to relate to people, he has a streak of compassion that runs deep and that I admire.  

For some reason he has this adorable weak spot for vulnerable women.  He gets tender and nurturing around them. Tyler has a volunteer position (supervised by other adults) taking care of the toddlers at our church while their parents are in class.  We had a single, pregnant relative living with us, and every Sunday he would always bring her a Dixie cup full of animal crackers they had been feeding to the kids.

He's unusually high functioning for someone with his type of disabilities. He can't learn easily, but he wants to SO badly!  He has a voracious appetite for books. He is the favorite visitor of our librarians and the employees and Barnes and Noble, and he can take the bus there himself.

Tyler collects books he cannot read and his teacher used to report him copying from the pages of books for hours, which strikes me, as a lover of reading, as poignant and tragic. He is however quite well read through all the books he listens to on tape. When tested, his scholastic skills fall around kindergarten level, but his vocabulary is relatively off the charts at high school level.

My relationship with Tyler now breaks my heart.  I adore him, but in a very distant way. I used to spend hours playing dolls and writing stories with him when I was little. I brought the writing skills, but he brought the play and imagination.

As I got older, we both outgrew that, and he got... annoying. He could be a such a brat, and I could never work out our tiffs with him the way I could with a typical sibling.

Even being around him, today, as a young adult, makes me feel overwhelmed with frustration. I feel like gritting my teeth listening to him go on and on about some movie.  I think my guilt adds to my annoyance. Why can't I just be patient and accepting? I pray for help with that.

I feel a strong desire to enrich his life. This is because he's so limited by lack of socialization, lack of independence, and lack of, well, the ingenuity and opportunity and comes with intelligence.

I genuinely WANT him to come live with me and my future husband when we have a settled home someday. Nieces and nephews would enrich his life so much. He is pretty low maintenance as far as day to day stuff and needs lots of alone time, so it wouldn't be intrusive or a big deal. Then my parents could have a life.

I was a live-in nanny on Long Island recently. The family went on vacation, and said Tyler could come stay with me.  I excitedly emailed my mom - Tyler had been saving up for a trip to New York, (he loves Broadway) for FOREVER.

Well, I think he was expecting a wonderland, but Manhattan is OVERWHELMING for someone with autism! My mom ended up coming on the trip, and he ended up needing her for support, but also resenting her taking away from our freedom and fun with her stress.

His favorite part of the whole trip was when he and I were alone and I took him out for some "real New York pizza" in a boring Long Island strip-mall. He told everyone about it.

Then there’s my brother David. The way David affected me really messed me up.  I was afraid to have kids.  No kid could possibly have been harder to raise than David.  And ya know it's genetic.

He was hell. My parents did EVERYTHING THEY COULD THINK OF for him. AND NONE OF IT WORKED. They tried to shield me from it, but I could tell.

My poor parents just wanted a simple life.  They wanted to raise a few average Christian kids who would do things just right: go to college, get married, make them some grand kids.

Instead they got psychiatrists and doctors and government aid and social workers up their butt forever.  And my dad, a great provider, has worried constantly about paying all our mental health bills and, as moral support to David, attended a million and one support groups. 

My parents are, and weren't to begin with, the most emotionally healthy people, and I am unique in my family for the way I have addressed that as I became an adult and really worked hard to get better.  But one thing I do really admire my parents for is the way they tried and persevered and supported my brother.

I was supposed to be the good one. Quiet, eager to please, precocious, even "wise," I was their last and easiest kid. Until I hit my preteen years and the stress and lack of emotional support in my home became too much for my hyper-sensitive self and I slipped right into the pit of depression that genetics had ready and waiting for me.

But, too bad for me, my parents had completely been run out of steam for that sort of thing with David. They would angrily have "talks" with me about my slipping grades, and I would get the eerie realization they thought they were talking to HIM, not me. 

They would say, "We've tried everything and nothing works on you." David could not be motivated to change by any reward or punishment under the sun.

But I hadn't done anything...

The thing is, David doesn't just have Asperger's, he has severe depression (that started way too young when he was teased at school), OCD tendencies, severe ADD. He is completely negative and self defeating.  He made a lot of bad choices and brought a lot of darkness into our home.

He was sweet to me growing up.  I was his "favorite," the least obnoxious of his younger siblings, and I cried and ran out of the house the first time my parents had to kick him out for behavior they couldn't accept in their home.  I even watched him be escorted away by a police officer once.

I am PROUD that David REFUSES to think inside the box, I am PROUD that he is so very smart, and PROUD that he always maintained a goodness and sweetness even at his lowest point.  He is proud of his unique approach to the world and absolutely refuses to change it, even though I think it would make his life easier.

He wants to help people, and I'm sure what he's been through has made him empathetic.  He's a cat whisperer, full of faith, and knows everything about everything. He's amazing, really.

Having my brothers around has taught me a lot about open-mindedness, acceptance, and individualism. Through Tyler, I’ve had the opportunity to work with many people with disabilities, including assistant-directing a play for developmentally disabled adults, something I never would have chosen to do if it wasn’t for my experience with my brother.

And occasionally David's quirks can produce comedy that is the stuff of family legends.

Like the time he randomly got it into his head, to write a letter hoping to convince our grandfather that he should, like David, give medication a shot. Our grandfather is probably mentally ill, but is the kind of narcissistic jerk who makes everyone around him miserable, without being aware that he has faults.

From one dysfunctional man to another, David's letter (that never got sent) began with a tactful opening and then went: "It is my opinion that you are insane." The entire family laughed about that for months!

I do have a bottom line.  And it is that my brother's are freaking SPECIAL people.

If I could tell parents anything, it is that autism is not the end of the world. Try to still be happy. David has finally grown up a little, did great with lots of biofeedback, and is slowly taking college courses and wants to become a nurse. He's a good person, always was, and we always loved him.

He's perfect, really. Both my brothers are. That needs to be all that matters.

Oh, and LAUGH.

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I don't know about you, but this post made me laugh and cry. It made me think a lot about how my autistic son Jacob affects his brother Ethan, and what I ask of and expect from Ethan on a daily basis. 

That Luna has been through so much with her brothers and still clearly loves and values them gives me much hope for their future together. 

If you want to hear what Luna has to say about other things, go to her blog Hand in Hand in Lala Land.  

You might want to try this post about actually loving kids, or this one written to the fathers in her life on Fathers Day, or this funny one on keeping a sense of humor about kids tantrums. Also if you just want to get inside the head of a sweet, funny 21 year old? Try this post about, well, you'll see. 

Luna has also written a guest post on Scary Mommy about why it's hard to be a nanny. Well worth the read.

You can also follow her on Twitter, where she tweets as  

Thank you Luna, for sharing the story of your life with your autistic brothers with us here, today.


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Friday, July 1, 2011

Signs and Portents

I was cleaning up the living room today - don't snigger people, I do DO that (about twice a year or so) - trying to organize all the boys' papers from this past school year, when I came upon some wonderful drawings of Jacob's and a note sent home by his teachers that I want to share.

Here they are:

I asked Jake what this was. His answer: "I have veggie chips in my brain, Mom." They seem to be making him very happy in a serenely content sort of way. Works for me. Who needs brain cells when you can have yummy veggie chips filling up your head instead?

Jake wasn't able to tell me exactly who (or what) the figure in the middle of this somewhat disturbing image was. Though he did make it clear that he/it is a "bad guy" being tied up in a bathtub.  The significance of the numbers 56 & 48 in the circle on the lower left edge? Unknown. 

Ethan thinks it might be Jake's interpretation of a character from the Dragonball Z Kai TV show. I think it looks like an evil sunflower creature with a black hole in the middle of his head. The "X" marks on his face *might* be indicating that he is dead.

We will probably never know. Some of life's mysteries should remain just that, I suppose.


I have mentioned before my son's love of movies in general and Rango in specific. That his teachers "get" this and know exactly how to encourage & reward his hard work and good behavior (praise and a pic of a favorite character)? Thrills me to no end.

It was a wonderful school year for Jake, and so far three days into Summer Academy ("School Camp") he is happy as a clam - and they haven't even started swimming yet!

I feel that his fairy godparents must have been looking out for Jacob (FINALLY!) when we tumbled into this school, late last year at the very wee end of the placement process. It hadn't even been on my radar for the past few years (though I had toured it when Jake was a turning-5 tot and I was looking at SN Kindergartens).

And now, blink, blink, and it's been a whole year passed. And the school is a perfect fit for Jake. And I love each and every teacher, therapist, aide and administrator there, significantly more than words can tell.

Jacob's imaginative play and storytelling abilities are really growing by leaps and bounds right now. And while it seems to have just sprung out of the ether, I know it had to have been growing slowly, underground, like taproots for a long time before the wonderful comes bursting through into the sunshine.

Looking at these pictures from the late winter, I shouldn't be surprised at what's going on this summer. There is so much "story" in them. They really are signs of an active and engaged imagination. Portents of good things to come.

Now when Jacob takes my hand and asks "Can I tell you a story, Mom?" and then begins "Once upon a time..." I know it has grown from a happy Jakey with his head full of veggie chips.

Can't wait to see what pops out of his wonderful (and deliciously crunchy) brain next.



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