Showing posts with label Don't be a dick. Show all posts
Showing posts with label Don't be a dick. Show all posts

Monday, January 13, 2014

Balls

I looked at the calendar on the way by this morning and realized it was January 13th.

Holy cats, we're almost midway through January.

How in the blue heck did that happen, I asked myself as I fumbled with the Tassimo.  Between the weather and work and the general carry on... well, it's been pretty much business as usual, hasn't it?

If by that you mean completely all over the place, then yeah.  Sure.

The week before Christmas hit us with an ice storm that downed many of the trees in my city, as well as leaving people without power for days.  In fact, there were places in Toronto that were out of power for up to nine days, making it a very cold and dark holiday for a lot of people.  Having several inches of ice everywhere ensured that I fell at least once a day.  During the middle of the ice storm, I had to walk (run!) through ice coated fallen trees for a block to make it to the next bus stop as my connection point was closed off by police.  I got my cardio in that night as heavy limbs cracked with the sudden violence of a gunshot before smashing to the ground like crystal chandeliers.  At one point it sounded like an enormous monster was after me.  Pop, crash... pop, crash... I was too busy moving to look back (and praying that there was no downed wires in the jungle I was climbing over).  That's an experience that I would not want to relieve anytime soon.  I don't scare easily, but I was still shaking an hour into my shift.

Looking down the connecting street Where is everything? Looking up our street
My 'hood.  Photos courtesy of L. Bonner. 

(Photo Description:  Three photographs depicting the destruction of trees by ice.  Thick limbs 
are broken and hanging, trees are bowed under the weight of several inches of ice)

We were fortunate to be traveling this Christmas and able to escape the destruction for a few days. While we were gone more ice came and brought some wind along.  As you can imagine, when we returned things looked much worse.  Many of these trees that you see above are no longer standing.  The branches have been moved off the sidewalk in *most* cases, but there are still places where the sidewalk is blocked with branches that are now frozen solid to the ground.  Again, we got off lucky as none of us in our area had a tree fall on their house, or car, or themselves.  We also have underground power in our area, so other than a few brief 20 minute spurts, we had light and heat.

Once the ice not-so-follies were over and the traces finally melted, the snow started to fly again.  We got several snow dumps, including one Boxing Day when we were traveling home.  We all started to get a little punchy about the weather and with everyone home, cabin fever set in really easy.  Then, we hit the deep freeze.
Winter is... here.
Winter is no longer coming.  Winter is here, yo.

(Photo Description:  Plastic Hallowe'en skeleton completely
 and creepily coated in ice)
After a few days of that,  I started to feel like I was desiccating, that slowly but surely my lips were pulling back from my teeth and soon I would look like one of those cave mummies that people find from time to time.  I felt like a dried out husk with a red mane of crispy clown hair as I put on my "Darth Mom" coat, Gore-Tex boots, thermal leather mittens and wound a scarf around my neck (and promptly buried my nose in it) before embarking out into Hoth in the hopes of making it to work on time.   I stood out for at least half an hour daily in temperatures and wind that would freeze bare skin in 5 minutes.  At one point it was minus forty Celsius, which is... minus forty Fahrenheit, oddly enough.  Everybody can agree then, it was ridiculously cold.  I danced in bus shelters to keep warm and one night had so much fun imitating Tauntauns while the Admiral and I waited for the Whaaambulance, that I actually hurt my throat.

 photo Tauntaun_zps479eaca8.jpg
Your Tauntaun will freeze before you hit the first marker.

(Photo Description:  scene from Star Wars:  The Empire strikes back depicting
characters Han Solo and Luke Skywalker on a tauntaun.  All are covered in snow.
 Image caption reads "Going to the store.  Need anything?")

Eldest did not return to school after Christmas break until Wednesday... until it warmed up into the minus twenties (!) and we weren't having a blizzard.  The younger two only went outside in a preheated van. Twice.  After several weeks of non-stop winter weather shenanigans, you can imagine that we were all more than a little wonky.  Work was not much better as the volumes and the acuity are astonishingly high.  Having left on our trip immediately after my shift before Christmas and returning to work immediately after our return, our schedule has not allowed for much down time. 

To make what is rapidly turning into a very long story, short:  I'm pooped.  With a capital "Poop".

I've done precious little over the last few days other than play a lot of video games, have the kids crawl over me and stare at one size screen or another. 

Without falling into self-pity, it is hard doing what I do... whether at work or home.  My kids are the easy part, the hard parts are the advocacy bits.  This blog always has and always will be a labour of love;  it's hardly a money making venture and I'm not in this for the book deal or to launch my "writing career".  I already have a career, one I love very much (even when it's trying to kill me), but I must confess, I enjoy doing this thing too.  Most of the time.

I'm just not feelin' it right now.  At.  All.

It could be the haters--there always seems to be a few of them lurking about, always ready to launch into a personal attack when my views/religion/political leanings/country of origin/general outlook on life clash with theirs.  It's hard to take sometimes when some of the worst other-ing comes from within your own "community". 

But, if you look at things objectively, this past year has been one of metamorphosis.  By comparison, in 2011 I wrote about choosing to surge forward through what seemed like a never ending sea of negativity.  In 2012 I encouraged compassion and hope. 2013, by contrast, was about change.  On a personal level, I managed to kick some lingering (and previously invisible to me) prejudices to the curb, realize the privileges I did have, and truly start moving forward into the land of acceptance. It sounds so easy and almost trite when I write that, but it is not easy to stop and recognize that even in your "do no harm" philosophy, you still manage to do just that, no matter how caring your intentions.  Those of us in patient care often think we know best... because we have to.  How else does one perform some of the things that we do without a heavy dose of self-assurance?  You can't.  The danger, however, lies in overconfidence and paternalism... where one decides they "know best" for an adult who is capable, both legally and in actuality, of making their own decisions.  Understanding how deep the rhetoric goes--how our very language is both shaped by our underlying fear and lack of knowledge--and how these states are perpetuated by it, was a big realization for me.  One I can't trivialize with an "Ah-ha".

There have been so many changes globally too.  We have learned how one voice can quickly become many as retailers, publishers and manufactures learned that language that disparages those with intellectual disabilities is not acceptable and will not be tolerated.  We saw a ground breaking case where a woman with Down syndrome, fought for, and won, the right to live where she chose to... a right that so many of us take for granted all the time.  At the same time however, it's been almost a year since the death of Ethan Saylor.  During that time, we have been reminded many times of the still pervasive view of people needing to be "controlled" and how little society still knows, or cares about those with intellectual disabilities.

As a family, we've seen some changes of our own.  In April, Wyatt underwent open heart surgery to repair his AVSD.   Since that time he has had to relearn many things.  He has added many new skills to his repertoire since then, including recently starting to walk with a push cart (or my computer chair), climbing up on everything in sight and a handful more signs that he is using consistently to engage us.  Like everything else, these were all discovered by accident:  I walked into the living room one evening to find him sitting in the middle of the coffee table watching TV.   At my gasp of surprise, he just looked over and gave me the chin lift, as if to say "Sup?" and went back to his show.  All righty, then...

I've had my own health problems this year, we've gone through some bullying with Quinn.  Money waxes and wanes, as do colds and bugs and shifts and mess.  Just like any other family.  That is how life goes.  Change is hard, as they say.  It is also exhausting and as messy as anything else. 

We were cleaning out eldest's backpack the other day, a task that included the discovery of what we can only assume was once half a sandwich, abandoned in the frenzy of the last day of school.  After having a brief discourse with this now rapidly evolving life form, we found a newsletter advising parents that kindergarten registration for children born in 2010 would commence in February.  Sean and I looked at each other in awe as that will be us, next year.  In one year we will be entering the IEP arena, my fears for our District School Board only bolstered by recent experiences by a few families that I know (and a lot of patient families that I have come into contact with).  My children are babies no longer.  In a short time they will all be going to school and a whole new level of advocacy will be added to our world.  There will be tears, sure.  There will be anticipation and angst and more watchful waiting.  There will also be new experience, joy and a whole lot of freedom for all of us. 

Life will continue to happen here, both good and bad.  The bad does not negate the good and the joyful does not erase what is horrible in the world.  In reality, I do not have the luxury to live in a climate where it is 72 degrees every day.  I, being me, do not have the exorbitance to do anything except being in the here and now.  Being present, bearing witness, to both very good and some very, very bad things (that some people wish I would not talk about) and challenging the way society views those that are "different" is who and what I am.  As a mother, as a nurse, as a human being, I wish I could, as one blogger put it, "stick my fingers in my ears and say "la la la la, I can't hear you", and pick and choose what I see.  I wish I could pretend that my kids were superheroes or that Wyatt's extra chromosome is made solely of "♥♥ love ♥♥♥" or that the only disability in this house is my "angry" attitude. But, I can't.  Further to that, I won't. 

Instead, I live where there are two distinct seasons:  winter and construction.  I live in a world where I've got three human kids, not just the one with the interesting condition or two if you count his neurotypical twin.  I don't get to bury my head in the sand or "cope" by churning out inspiration porn and succumbing to the grief narrative.  The society I live in is skewed against people like my kids, where our views of healthy and fit and appropriate don't deviate much from the eugenics dogma of yesteryear.  That has to change.  Disability is a natural state of being.  Neurodiversity and privilege are more than just theories. They are reality.

This year will bring it's own tastes and flavours.  There is, and will be, much joy.  And angst.  And potty training twins with different parts.  And itchy feet and boogers and period cramps and lack of sleep and worrying about the driveway and the lawn and so much coffee.  And love.  And coffee.   Once I rest up a bit, you can bet that there will be a lot of action here and in the other places that I hang out, regardless of what weather the skeleton happens to be wearing at the time.

Doing what I do, living the life that we lead... I think I finally have an answer to "I don't know how you do it."  The answer is the same as to how one lives through the Canadian winter. 

The answer is "well" and with a giant pair of these:



(Photo description:  two snowballs)

Tuesday, November 19, 2013

It's Never "Just A..."

It never ceases to amaze me how many feel that this is actually open for discussion.

I, and countless other advocates for the Intellectually Disabled (including self-advocates) hear "it's just a..." in regards to each new thing that crops up, each new use of the word "retarded".  It's just a word.  It's just a lipstick.  It's just a shirt.  It's just a cat.

"Political correctness", "my rights", "free speech", historical etymology... it's almost fascinating to watch the entitled defense of this word, except the posturing makes me sick each and every time.

Here is the thing:  it doesn't matter who you are or who you know.
It doesn't matter what context you felt you were using it in.
It doesn't matter what poorly fabricated rationale you or your PR team comes up with to explain the use of this word.

Truth be told, you wouldn't defend yourself so hard if you didn't already know what you are doing is wrong.

Ultimately though, it's not about you, or your rights at all. 

It's not even about the Ann Coulters or the Jennifer Anistons or the Kat Von Ds or some comedian or shock jock DJ or any other sheltered celebrity or athlete that thinks they know better than the rest of us. It's not how you feel about this word, whether you are currently engaged in a scholarly debate or describing your life's latest little inconvenience. 

It's about others.

It's about the hundreds of thousands of people with Intellectual Disabilities and Developmental Delays, whether acquired congenitally or otherwise.  It's about people with Down syndrome, Autistics and people that are brain injured.  It's for those with aphasia and disabilities that affect communication. It's about their families and those that love them.

It's about people that are different than you. 

This word, this "R word", whether used as "Mentally Retarded", "retard(e)", "tard", "celebutard", "fucktard" or any other mash up (portmanteau) word ending in "-tard", has been used to denigrate. 

People.

It has been used by those in authority, by those in society to condemn people to a life of poverty.  To segregate.  To ridicule.  To sterilize involuntarily and subject to horrific experiments.  To abuse sexually, physically and emotionally.  To deny health care that many of us take for granted.  To isolate and institutionalize, to deny the most basic of rights...  including "free speech".  To bury in nameless graves by the thousands.  To be determined "life not worthy of life", loaded onto buses and killed, the bodies burned after being subjected to experiments.  To have the stolen organs and tissue to still be laboratory curiosities decades later.

This word, the one that you insist on using, yet claim means nothing to you?

It means EVERYTHING to us.

I mean "us" on this too...  Advocates of all stripes stand together on this.  This word means enough to us to unite and motivate us all to action, to write, to call, to petition, to picket.

This word?  You can call it our Jim Crow.  It is our Holocaust, both in reality and in metaphor.  This resistance is our Stonewall riots,  if that comparison makes it easier for you to understand.  Whether you do finally or not however, understand this:

It is not about you. 

It is about people like my son and their right to live in society;  to have an education; to live their life like any other.

This word embodies the removal of some of the most basic physiological and safety needs.  When you use this word or any of its permutations, when you exercise and flex your privilege, you participate actively in the removal of the rights of another.  You perpetuate the scorn, the hurt, the marginalization.

Those with disabilities are flavours of humanity; this world needs to accept this once and for all.  What keeps people with disabilities from leading their lives is not their "conditions".  It is society and the able bodied people in it.  It goes beyond a ramp, beyond an accessible door or parking, past service animals and assistive devices, deep into the rhetoric of our own language

Those who continue to use and defend this word are party to the atrocities committed in its name.

So it's never just a cat or a lipstick or a word or a matter of being polite.  It's not about being "too sensitive" or "politically correct" or "thinking that way" or intent or even "toughening up".  It's not about your rights to free speech.  It's about people.  People who live in a society that is ever ready to abuse and discard it's own citizens.

This has to stop.

Please.

Tuesday, October 15, 2013

Keeping it Real

I'm not unhappy.  My life is pretty good.

I know this will cause many of you to say "duh!" rather loudly, but there are a lot of people out there that still can't wrap their heads around this.

We're not unhappy.  Life is not hard.

Oh sure, we have our fair share of poopy diapers and kitchens that don't clean themselves.  There is drama.  There are skinned noses, hurt feelings and juice spilled from one end of my house to the other.  There is life, sure.

But we're happy.

There are a lot of things we would like to change, of that I have no doubt.  My husband is a stay-at-home Dad and I'm pretty sure he'd be perfectly happy to be back at his old job on those weekends when I work nights.  Surrounded by the aforementioned poopy diapers, swimming lessons, yell-y kids, an utter lack of privacy, quiet, and a complete thought; he'd be bananas not to.  But, he's not miserable.  The little ones go down for a nap at some point and the big one is content to hang out playing video games or quietly watching a movie in the mean time.  In a related story, I'd give my (honorary) left nut to be able to stay home with the kids.  Ok, I'd probably work one day a week, but to not have the responsibility of everything fall directly on my shoulders is a nice dream too.  Something for "when we win the lottery".  I think there are times when we would both change this part of our lives.

But, we're not unhappy.  Not in the least. 

Back in the early days, the just post-potential-diagnosis-but-not-sure-but-there-is-an-AVSD days, I was pretty sad.  I had a right to be, having just lost an Aunt I cared about very much (and didn't call much in her final years) and almost losing a very dear colleague in a horrific car crash.  I was also super pregnant with twins, super heavy, slow, in pain almost constantly and had to wear "Batman" anti-embolism hose that took me no less than half an hour to sweat my way into each and every day (and a nerve wracking 5 minutes to gently fix every time I had to pee, which at that point was eleventy-zillion times a day).  I was very sad when I was told about my unborn baby's diagnosis.  As time went on, I was told I was sad as I was "grieving my perfect baby".  Once they were here, once we knew about Wyatt's karyotype, once the twins were being kept alive in the NICU, I was told by a social worker and every piece of literature that I was handed that I was grieving.  As I continued to write updates to my family, that is how I described it.  Grieving.  Down syndrome was making me grieve.

I learned more about DS when I  got the babies home.  I also learned all about them, their individual personalities and got really into the swing of being the parent of infant twins.  It was then that I started to figure out my emotions a little more.  Ok, so DS wasn't what I originally imagined for the ONE baby that I thought I was going to conceive, but really, is that one little chromosome the source of all my sadness?  How about postpartum blues, post-surgical pain, recovery, or multiple personal losses?  In relation to my son's very real cardiac condition and the two fragile lives for which I was terrified, how about simple fear?  In retrospect that sounds like the recipe for postpartum depression, not my son's T21.  My own husband, upon hearing the "grieving" bit, argued with me.  "It's not like anyone has actually died!"  he said to me, exasperated. His mother had passed away suddenly in 2001 and it was this very real loss that he referenced now.  However, as told to us by that social worker that came to see us while we held our tiny sparrow babies, we were grieving our son's Down syndrome diagnosis.  It was only natural, after all. 

It took me quite some time to sort out my thoughts and feelings, probably compounded by my early return to work and the challenges I faced because of that.  As the children grew and my son became more of a boy and less of a baby, it became more evident how he was just himself, not some list of potential or actual diagnosis, not some 'special' baby, not the source of any familial discontent.  You see, I was told that my husband would leave me, that having a disabled, a "retarded" baby would ruin our lives, our marriage.  I was told by many "well meaning" people that it was a good thing that "Down's children" were so loving as I would have a forever child.  I was told by every medical source, by every appointment, by every medical professional that his extra chromosome would be the cause of a life of sickness.  I was told by a nurse that it was a good thing he was a boy, imagine how tragic it would be if he was a girl?  I was consoled for his birth, often multiple times a day.

I wish I could wave the realization of what I had attributed exactly to his extra chromosome off as a "D'oh!" or "A-ha!" moment, but the reality is I was deeply ashamed at my participation in the "love the baby, hate the disorder" mentality.  How I would love him "despite" his Down syndrome.  How as a family we would "overcome this obstacle".  You can see that here in past posts, as my writing changes and as I became more of the advocate that I am today.  Of course, I still had to really start to check my ableism at the door and realize quite a few more things, but you can see where I actually started to get it.

This month, being Down syndrome Awareness month in the US, you would expect me to be all over this like in years past. But, I'm not.  There's a lot of reasons here, ranging from current personal illness to personal perspective.  I'm not so keen on the "awareness" any more;  the colours, the gew-gaws, the posters.  Instead I'm all about the education or the advocacy part.  Even the activism part.  One could argue that I always was more of an advocate than awareness raiser given the topics of most of my posts in Octobers past... I may partially agree with you too.  However, as I've stated before, I'm done with awareness.

Instead, I'm going to advocate.  Hard.  It may not be pretty, it will probably seem to some like I'm shouting.  It may seem to some that I am full of hate and anger and all the things that I am accused of because I don't write about unicorns and rainbows and flatly refuse to accept things as gospel as they have been "always done this way".  So be it.  I will continue to challenge the stereotypes and whatnot that many people maintain as "fact" about Down syndrome.  There will probably be swearing.  This is what I do. 

That particular social worker is no longer telling new parents of children with T21 about grieving the diagnosis.  In fact, I've helped develop resources for new parents.  This blog is routinely passed out as a reference and I have been personally thanked by a great many people.  I am no longer misplacing my emotions onto my son.   He is no more or no less stellar than any other child of mine.  My desire from day one was to ensure that nobody else would either, even if I couldn't process or understand it properly.  We are not unhappy.

We're us.  Full of emotions and drama and all the little things that make up Team Logan.  Sometimes we're happy, sometimes we're sad.  Sometimes we're silly and giddy sometimes we get frustrated with one another, hell, even argue.  Sean and I worry about the things that other couples do, like money and our health and whether or not we're getting enough sleep.  The kids romp around here together, spreading chaos and love in their wake... and occasionally whacking each other with toys.  Down syndrome is literally a microscopic part of that, if it is really a part of that at all.

We're not unhappy. We're real.

I long for the day when no one is surprised at that statement.


[A banner for Down Syndrome Uprising, depicting the text "Down Syndrome Awareness Month,
with the word acceptance stamped over the word awareness.]

Wednesday, October 2, 2013

In the News - September 2013

A collection of news articles, blogs, stories and information about Down syndrome, disability and special needs, from Down Wit Dat's Facebook page.

Legend:
AUDIOindicates an audio clip
APPEAL indicates an online petition or plea
BLOG indicates a blog post
CASE indicates a lawsuit or proceedings
EVENT indicates a scheduled event
LAWS indicates a new piece of legislation
LINKS indicates links or resource materials
PHOTOS indicates photos
POLL *NEW!* indicates an online survey
STUDY indicates a study or discovery
THREAD indicates an online discussion thread
VIDEO indicates a video or movie



Why People Have Such High Expectations of Parents of Children with Special Needs


VIDEO
“Don’t give up”: With family’s help, Latina with autism is in college, pursuing career

BLOG
Disabled People As A Test of Character: The Guinness Commercial
BLOG
Ode to the Stim: the printable sequel

'Of course we will help her at home, but I want to be Emer's mam, not her teacher'
LINKS
BLOG
Smoochie Paraplegic Cat: When Disability Tropes Take on a Life of Their Own
VIDEO

VIDEORobert "Ethan" Saylor's Family will deliver petition signatures to Governor
VIDEO



BLOG
Defending The R-Word
Bodies and Behaviors
POLLShould the governor open an independent investigation into the death of Robert Ethan Saylor?
BLOG

Action Alert: Contact Governor O’Malley of Maryland
to Demand an Independent Investigation Regarding the
Death of Ethan Saylor - See more at: http://www.ndss.org/About-NDSS/Newsroom/Recent-News/Action-Alert-Ethan-Saylor-Update/#sthash.2UoMhRDE.dpuf
Duncan wants to end test for disabled students that California overused
BLOG
Revolution!
BLOG
BLOG
BLOG
BLOG
BLOG
BLOG
BLOG
BLOG
Dirty Words: Autism Lingo
Like A Person
BLOG
BLOG
VIDEO

VIDEO

Toronto police pushed man out of wheelchair, rights complaint alleges
BLOG

VIDEO
BLOG
Aspergers unmasked
BLOG
Disability as Disaster
BLOG
Drawing No Lines
BLOG
BLOG
Beyond The Gift
BLOG
BLOG
LINKS
LINKS
Apps for Students With LD: Having Fun
LINKSCanadian Journal of Disability Studies
BLOG
On the Topic of Violence…

APPEAL
VIDEO

Silencing” the extra 21st chromosome
EVENT
VIDEO
B.C. woman with muscular dystrophy stuck in a care home due to government red tape
BLOG

BLOG
VIDEO


BLOG
Sincere Support
CASE
An update on the Huronia Regional Class Action Suit

BLOG
BLOG
Autistic Twins
AUDIO
Mother says autism intolerance more common than people think
BLOG
BLOG
BLOG


4 Countries With the Right Approach to Dementia Care

How To Help Sensory Sensitivity
Angela Bachiller, the World’s First Person with Down Syndrome to Hold Public Office


Older people with autism in Scotland 'invisible'

If A Parent Murders An Autistic Child, Who Is To Blame?

BLOG
Enforcing Shame Through Ableism

BLOG
bits and pieces
BLOG
Two Little Girls

The 2013 VATTA Committee

VIDEO
BLOG
I’m Not Here for Your Inspiration, and Neither is Michael J. Fox
BLOG
To the International Paralympic Committee: Let Victoria Arlen Compete

Intervention: Damaging for Autistic Children

Different

PAKISTAN: Focus on rat-children

A Code For Pirates


...And that's the news.  Keep the stories and information coming!

Monday, September 30, 2013

A Code For Pirates

Life is a little odd lately. Many of you noticed that I haven't been around much.  I've been battling a yet-to be diagnosed illness off and on for the greater part of September. Not only have I missed a week or two of blogging, but I've also missed work and landed in my own Emergency department twice.  Once overnight.  Once in the middle of a shift.  It's not pleasant.

Despite all the tests, I have no idea what this illness is.  I'm sure that stress plays a role here;  things have not let up on any front in that regard.  There are days, sadly, that I seemingly go from skirmish to skirmish as I deal with the issues in my path;  a forgotten appointment here, a malfunctioning appliance there.  The realization that we will soon need a new roof.  Life, all of it.  I've had many an hour to think about things since this has started...  It's true what they say, that ability is not forever.  It is indeed a fleeting thing:  accidents,   illness.  These things can easily change one's life in an instant.  As I wait for the next round of tests and the answers that they may or may not bring, I am dutifully taking my medication and appreciating what my life has given me thus far.

Time continues to march on with Team Logan.  The first week of September saw Quinn's somewhat anxious return to school.  On one hand he was eager to return to learning and structure, but on the other he was still a little nervous, given the bullying he had experienced at the end of last year and in day camp over the summer.  Maybe this year will be different, I thought as I walked back to the van the first day.

Flash forward to September 18, the night before "International Talk Like a Pirate Day".  It won't surprise you that this is a thing in our house.  Before bed, as we were watching some television, I was painting my nails black.  Quinn, who loves to watch me paint my nails and will wear it occasionally, asked if he could have his nails done.  "For pirate day" he said. 

I have to admit that I froze here for a second.  Not because he asked, not because he wanted to wear it, but because I thought of the bullying that he had already experienced.  The connection between nail polish and pirates didn't surprise me, as actors who have played pirates have sported painted nails from time to time (and lets face it, I have more than a few skull adornments lying around, including the ones I was about to stick on my fingers).  It was also Mommy time, a special little thing that he and I could do.  What came out of my mouth next surprised me, because it totally was geared towards damage control and had nothing to do with his desires for self expression.

"How about just the pinkies?", I asked, citing a bunch of stars, including Ozzy, Steven Tyler, Keith Richards who have rocked that look.  "Sure" he said, holding out his hands. 

The next morning, dressed in his pirate shirt, he went to school.  "Arrrrrr!" he said, flashing me the horns and showing off his nails.  "Hurry up!"  I countered, kissing his forehead "Love you, off with ye".

The boy who came home was not as exuberant.

His feet dragged, his face showed that sad weariness that I hoped to never see again.  What's worse, his polish had been scratched off, hurriedly, as his cuticles were red and there was black under his other nails. The ignorance from the other kids had started the moment he got on the bus and ended when he got off.  Some called him a liar, told him there was no such thing as "Pirate day" and could not understand that his nails were not a statement of gender or identification, but rather, one of art. 

He went off to play and I got angry.  Not the angry that I get accused of all the time for differentiating myself from a complacent door mat, or the "filled with hate" I'm supposed to be when I point out ableism, but an actual, all consuming, honest to goodness blind rage.  I swore like a pirate hooker into the phone at my BFF while furiously mashing apples into sauce over a hot stove.

I was at the canning stage and muttering to myself when Quinn came back into the kitchen to talk some more.  With a great deal of insight, he told me how not everyone had made fun of him but it did seem that way at times.  What was worse, he explained to me, were the people that were trying to help him take the polish off.  I knew what he was trying to say, that they were helping him "to be like everyone else".  How the people that claimed to accept him would still rather he be someone else.   It hurt me, that at seven years of age, my son was experiencing this.  He asked me "what do you want me to do?"

"Honey", I answered, "if you want to wear nail polish, wear nail polish.  If you don't, that's cool too."

I repainted his pinkies, by request, right then and there.  I added his index fingers and his thumbs... and painted the two middle fingers clear.  He flashed me an "I love you" sign as a way of thank you.  The next morning, also by request, we removed the polish as that was also his choice (and we made sure he was not doing it out of fear of more taunts).  I made sure that his teacher knew we were coming early for meet-the-teacher night so that we could discuss this.  To her credit, she made all the appropriate noises, but even she was a little taken aback when he told her that yes, he had told her... he had written about it in his journal and she had missed it.  I made sure she knew that we knew that Quinn is probably smarter than most of his classmates, that he is kind and artistic, that he is quirky... and all of these things make him a target.  I told her how the kids at camp physically assaulted and humiliated him.  I told her how one of the kids that bullied him at the end of last year is sitting directly across from him at his table in the classroom.  Patiently, kindly, firmly and without raising my voice I let her know that he is my son. That I love him, as is, dearly... and I will be damned if he is going to end up a statistic or one of the kids that come through my Mental Health ER. 

She agreed.

We drew up our plan, all of us at that time, Teacher, Mother, Father, Child.  We created a circle, a crew, one with a mission.  Everyone within is told if there is a problem, if Quinn encounters more of the same kind of treatment.  We all have a responsibility in this crew;  ours is listening to each other, including his teacher. His is telling us, especially if he can't manage it on his own.  We will act, ensuring that his needs are met emotionally and scholastically.  In nursing, it would be called a "circle of care".  In Team Logan's world, it is a code for pirates.  However you choose to look at it, the consequences of breaking the code are no less dire.

This is the first engagement of many, of this I have no doubt.  Then, in a few years, both Wyatt and Zoe will be going to school.  There will be IEP's.  There will be more circles, more crews and a lot more potential battles.  There will be high-falutin' adventure too.  But still, we must keep one eye out for changing winds as we sail these unknown waters.  We will continue to navigate this life as we always do, with the wind in our hair, the colours high, our crew at our back, giving and asking no quarter. 

Come what may.  We'll be ready.

"Every normal man must be tempted at times to spit on his hands, hoist the black flag, and begin to slit throats." - H. L. Mencken
The flag of Calico Jack Rackham, who sailed with his love Anne Bonney (and her love Mary Read)

Monday, August 26, 2013

Anger

"We need to call out the deaths of our people as hate crimes, not freeze-frame our bodies in sparkle-filled glamour shots that make us so super-humanly other."

I'm angry.

Not in an uncontrolled wildfire of rage that would consume my every waking moment kind of angry...   My real world life exists somewhere between a painful sleep deprived haze and caffeine fueled tangentiality.  I don't have the time (or the energy) for such wild abandon.

But I am angry.

And that is a good thing.

Our culture, ever ready with a label, likens anger to unproductivity.  It is the work of evil, it only causes harm.  Most people don't seem to consider anger as a tool, as a medium for change.  But it can be.  In my world, we call it constructive anger.  It has a large role in cognitive-behavioural therapy and treatment for things such as PTSD.  An event happens, you react with anger, a normal human emotion.  Instead of being consumed by it however, you calmly evaluate why the event angered you.  Then you use the energy of your anger to motivate you to change the situation that made you angry in the first place.

Or, in the words of Alyssa at Yes That Too:
"People talk about anger like it doesn't accomplish anything.  That's just not true.  Anger can be fuel to provide energy for activism.  Anger can be how people realize something is wrong, that something needs to be fixed."
Anger is a very powerful force.  There is a lot to be angry about these days.  There is an awful lot that needs fixing. 
 
This week saw this hateful letter delivered to a home that is just over an hour's drive from mine.  A letter, so full of ableist poison (and almost illiterate ignorance) that it made me physically sick to read.  Naturally, people reacted in disbelief.  How could this happen?  How could this happen here?  This is obviously a hoax, right? And so on...  Although technically "not a hate crime" (as no threats of physical harm were made), these things happen to those with special needs all the time.  This family in Colorado is fighting with their neighbours who want their wheelchair ramp removed from the front of their home for fear it will lower property values.  This flyer was put up in the Portland area, presumably to shame those with "fake" disabilities.  This veteran was kicked off the boardwalk in New Jersey and issued a summons for his service dog. While on the subject of service dogs alone,  this story was published in the New York Post, lamenting "fake" service dogs and as Stephen Kuusisto put it, is "...one of the most willfully underhanded pieces about disability I’ve ever seen in a newspaper."

These stories aren't random and isolated incidents.  They, and many more like them, have occurred this month

Ableism, whether you wish to acknowledge it or not, is running wild in the Western world.

I shouldn't have to mention how society views people like my son Wyatt and his extra chromosome.  Still disregarded out of hand, people with developmental disabilities like Down syndrome are still the butt of jokes in popular culture.  Children with intellectual disabilities are still denied access to education that is mandated by law;  in 2013 it is astounding that parents are still having to fight when research has shown over and over that performance of all students is improved in an inclusive setting. 

The stereotypes abound with DS, many of which are perpetuated by the medical community that we look to for advice and information.  Also sad is the fact that many stereotypes are perpetuated by those that call themselves advocates.  I've stated before, anything that describes my son as anything other than human is wrong.  Period.

A big bone of contention are the faddish inspirational memes/pictures (A.K.A. inspira-porn) which are pumped out at an alarming rate by many organizations.  I was told once, by a group that produce and condone many of those images that they were doing such to be positive.  That new parents (and --- let's get real here --- those considering pregnancy termination) needed oodles of positivity.  That the way to make life better for kids like my son, was to surround everyone in positivity because it all boils down to a matter of marketing.

I guess it's bad marketing that forces young people with disabilities to be housed in nursing homes in some places due to lack of community supports. It must be marketing that stands in the way of achieving inclusive schooling and accessible lives.  Marketing is what allows those that run social media sites such as Facebook and Twitter to not even bat an eye when new groups or events are created to mock those with special needs.  Even better was being told by some of the same people that the Down syndrome community didn't want to appear "divisive" much "like Afro-Americans [sic] or women".

People with Down syndrome come in all sizes, shapes, colours, cultures, abilities and ages.  Just like everybody else.  Many of the memes and slogans simply perpetuate the "otherness", by employing pedestal ableism and by alienating those with DS from the larger disability community.  In the words of Lawrence Carter-Long, Public Affairs Specialist at the National Council on Disability:
"Still think "the only disability in life is a bad attitude?" Try ordering from a menu with a blindfold on, smiling your way up inaccessible stairs or reading non-existent captions on a YouTube video. Don't like my "bad" attitude? Then provide equal access. You'll be amazed at how much my mood improves. Oh... and while you're at it, please check your unexamined privilege at the door. Thank you. Have a nice day!"
There is real danger with these memes.  In the act of creating this image of perfectly posed happiness, it doesn't allow for real life, for real emotions.  If happiness and docile complacency are the norm, it must have been a complete shock to many when Jenny, an adult with Down syndrome, fought and won the right to choose where she wanted to live.  Generalizations and stereotypes set up unrealistic scenarios and are damaging, no matter how well meaning.  Pedestal ableism is still ableism.  Those cute little children will grow up one day and want to have sex and get jobs and do all the things that all adults want to do.  Continuing to infantilize adults with DS, to pat people on the head and endow supernatural abilities to chromosomes will not assist with the completion of these goals.  Continuing to perpetuate the stereotypes that other disability advocates have been breaking down for decades is not surprisingly, making people angry.  From
"No, fucking no, we are not myths! We are not some mythical other! We are humans."
Essentially, to keep from being seen as "angry", or running the risk of challenging any actual ableism, real life civil rights are not on the menu with these organizations and their "inspirational" memes.  Instead, in the name of marketing, there are eleventy billion soft-focus pictures out there that are intended to make Down syndrome more palatable to people.  To be like Wonder bread;  soft,  not much to chew, devoid of any nutritional content and bleached very white.

I was also a little shocked to learn that I am not supposed to have a voice.  My son with Down syndrome is only two years old and I don't have the "experience" nor have I paid my dues.  My choosing to speak up regardless, makes me an "angry" person (which one could translate as "uppity", as I obviously don't know my place).   I too get patted on the head by some, told that in time "I'll understand" why the community chooses to operate this way.  I'm almost 42, have been a mother for 7 years, am the mother of twins and have been a nurse for over 17 years.  When exactly will that be?  How old does my son have to be before I can call shenanigans on the unjust practices directed at him?  I'm not arrogant enough to presume what my son thinks and perceives or know exactly the man that he will grow into.  I don't know that about my other two kids either.  I will do my damndest however to ensure that he gets the education he deserves and that he gets to make his own decisions, whether my CV has the "correct" amount of experience or not.

That will be done with constructive anger.  And humour... but anger will be the fire that stokes the boilers into action.  There is a lot of work to be done.  I don't think that it is too much to ask that September contains less stories of hate and ignorance.  Or that the stories that feature disability in every Lifestyle section of every mainstream publication not be written by the able-bodied or parents that haven't fully accepted their children with disabilities. I don't think that it is too much to ask that equal access and inclusive education be automatically available.  I don't think that it is too much to ask that you stop labelling my kid, stop putting him in a little box that says "happy moppet" on the outside and expecting him to act a certain way, just because you believe it makes it easier for people to accept him.  The reality is, he as a real, live human being with fully dimensional thoughts and feelings... who is just as full of shit as the rest of us.

I will leave you with the words of Cheryl Marie Wade, a lady that I only came across a few years ago when I started reading disability history for my A Brief History... series.  She passed away last week.  She was seen by some as "angry" too, which is probably why her death didn't make the papers.
"We ain't smilin' inspiration for the latest worthy cause
But generation after generation changing the laws
Parents fighting for their children.
Kids fighting for their dreams.
Maybe you've be deprived,
Maybe all you know is Jerry's kids--
Those doom drenched poster children hauled out
once each year to wring your charitable pockets dry.
The tragic--but brave, victim.
We are also Jerry's orphans,
Proud freedom fighters,
Takin' to the streets,
Takin' to the stages!
Raising speech-impaired voices in celebration of who we are--
Radical.  True.  Passing the word..."

The only way that any of this is going to get done is through action.  Through anger.  Through outrage. Through calling out the unjust and affecting change where needed.  It's going to take sweat, tears, rivers of determination and some serious balls.  Not five minutes in Photoshop.

I'm angry.

It's a damned good thing.

Sparks II
Fire, good.
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