Showing posts with label discrimination. Show all posts
Showing posts with label discrimination. Show all posts

Thursday, August 21, 2014

The T21 Blog Hop - August 2014

August, as they say, has been interesting thus far.

So much has been happening... It has gotten me thinking of Acceptance vs Awareness again, the question of what is normal and not, what is health and what is considered illness and when the change from one to another actually happens, if at all.

I guess what really hit it home today is the following quote from the agency who is monitoring and aiding in my son's development:

"-Wyatt has Down's Syndrome [sic].
 -Wyatt is Twin 'A'.  Twin 'B' is a healthy female."

Ow.

With this in mind, it's time for a little more acceptance, methinks.  Time for a little more slice of life, time for a little more "... is natural".  Down syndrome is a part of life.  Autism is a part of life. Disability, in any shape or form, is natural and not sickness.  They are not to be feared, extinguished, beaten.  They do not need a cure.

I'm going to extend it a little further this time too.  Depression is natural, as is anxiety and many other things.  They happen, they exist.  They can be quite disabling.  They are not to be feared either. 

I really look forward to a time when this isn't a discussion. 

Grab some ice for a nice cold drink, and read some great Acceptance blogging.



Sunday, July 6, 2014

In The News - June 2014

A collection of news articles, blogs, stories and information about Down syndrome, disability and special needs, from Down Wit Dat's Facebook page.  These are from June 2014.


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
IMAGE indicates a graphic, image or comic
LAWS indicates a new piece of legislation
LINKS indicates links or resource materials
PHOTOS indicates photos
POLL indicates an online survey
POST indicates an advocacy statement made through social media
PRESS indicates a press release
QUOTE indicates a meaningful quote
STUDY indicates a study or discovery
THREAD indicates an online discussion thread
TWEETS **NEW** indicates a Twitter Hashtag
VIDEO indicates a video or movie clip
VLOG indicates a video blog post


IMAGE"ac•tiv•ism \ˈak-ti-ˌvi-zəm\ Intentional actions to bring about societal change. Often used..."

A Point of View: Happiness and disability

Court throws out 'mental retardation'
IMAGE"Parody of the PETA "got autism" ad. A bowl of milk with a smiley face made out of cheerios..."

Why my daughter's birthday shames those who think people with Down's are not fit to live

Finnish Education Chief: 'We Created a School System Based on Equality'
BLOG
#yesallwomen Includes Women with Disabilities.
POSTMDC Class Action Law Suit in Store?

CA cop fatally shoots 18-year-old special needs girl after family calls for medical help

Mother charged in death of daughter, 22, with cerebral palsy who weighed just 40lbs
IMAGE"There can be no "cure" for Autism, because Autism is not an entity. There are only Autistic..."

IMAGE"the diversity of human brains and human minds. The enormous diversity among individual..."
BLOGTTC driver refuses to let riders in wheelchairs exit bus
TWEETS#‎StopAbleismBecause‬

IMAGE"help·er /ˈhelpər/Well intentioned person who wishes to assist those they perceive to be.."
POST"In a thoughtful act of generosity, an officer aboard a private chartered flight that we had..."

BLOG
The Ashley Treatment Rears its Ugly Head
BLOG
What Is Autism?


'Subminimum wage' for disabled workers called exploitative
BLOG
Five Steps Toward Autism Acceptance
BLOG
An Argument Against Pathologizing Autism – What Others Had to Say
BLOG
(Not So) Idle Hands

'Mommy blogger' accused of killing her 5-year-old son for Internet fame
BLOG"It's not easy being green, and it's not easy being Autistic when Autism Speaks treats..."
BLOG
A friend of mine.


Her Body Type Is So Ignored In The Magazines That We Don’t Even Notice It’s Missing?
EVENT
The T21 Blog Hop - June 2014
VIDEO
BLOG
S.R. Salas post: “Advocacy In Others’ Words” for T-21 Blog Hop @Down_Wit_Dat
BLOG
Mommy is Mad @SesameWorkshop
BLOG
Don't be a Dick*
BLOGThe Joy of Acceptance
BLOGWhy I Will Never Be an Autistic "Warrior Mom"
IMAGE"Autism is not what Autism Speaks wants you to believe. They have spread many lies..."
BLOG
Deconstruction by Design: A visual history of the Liberal attack on education
BLOG
The Room
BLOG
GUEST POST - Keep Abortion Politics Out of the Pro-Information Movement
BLOGDisability: My Connection
BLOG
BLOG
Why My Dad Isn’t a Hero or a Saint: A Father’s Day Tribute
BLOG
Camp Goodwill

BLOGThe Downside of Assumptions
BLOGAdult Autism and Program Leadership: Yes, It’s a Big Deal.
APPEALPlease let Amazon know how offensive this merchandise and the like are

A Mighty Girl
IMAGE

June also saw another edition of the T-21 Blog Hop...


Thanks to all who participated.

The T-21 Blog Hop will take place every month on the 21st, for three days and will continue to feature advocacy posts from across the disability community.  See you July 21st!


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

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)

Saturday, January 11, 2014

In the News - December 2013

A collection of news articles, blogs, stories and information about Down syndrome, disability and special needs, from Down Wit Dat's Facebook page. These are the last from 2013.

This month, in order to capture as much of the information as possible, I've included a "PRESS" category to showcase press releases.


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
IMAGE indicates a graphic or image
LAWS indicates a new piece of legislation
LINKS indicates links or resource materials
PHOTOS indicates photos
POLL indicates an online survey
POST indicates an advocacy statement made through social media
PRESS ***NEW!  indicates a press release
STUDY indicates a study or discovery
THREAD indicates an online discussion thread
VIDEO indicates a video or movie


BLOG
Hoist the Colours!
VIDEO
Disability Politics and Policy
POST
"What would a truly inclusive society look like?..."
EVENT
International Day of Persons with Disabilities - Blog Symposium
BLOG
"Today is the UN International Day of Persons with Disabilities..."
BLOG
Her place in the struggle
BLOG
Kick That Door Down
International Day of Persons with Disabilities
BLOG
Boycott Autism Speaks
Settlement Reached in Huronia Class Action Lawsuit
BLOG
'Disabled' Mannequins Ponder the Notion of Perfection
IMAGE
If physical diseases were treated like mental illness
POST
"You've just got to smile when Australia's Discrimination Commissioner..."
BLOG
Why? Why? Why?
APPEAL
Corporate Partners & Supporters of Autism Speaks: Terminate your financial support of Autism Speaks.
POST
"Only 50 years ago persons with intellectual disabilities..."
POST
"It is not a question of patronizing philanthropy towards disabled people..."
POST
"Many are saying and showing how Nelson Mandela changed the world..."
POST
"B. is the 14 year old autistic son of an online friend of mine..."
LINKS
In the News - November 2013
BLOG
Why I Don't Like Functioning Labels
EVENT
Boycott Autism Speaks Twitter Bomb
POST
"For whom does the bogus "autism charity" Autism $peaks actually speak?..."
BLOG
Lovely Video and the Disabled Body
The Forgotten Minority
BLOG
Inclusion and Autism... leaning in
BLOG
Safe
BLOG
Ritual Humiliation in the Hospital
BLOG
Autism Speaks and Signal Boosting
IMAGE
Depression Infographic (autism spectrum disorder and depression series)
VIDEO
Free our people.
IMAGE
Gender and Autism: A Preliminary Survey Post
BLOG
#BoycottAutismSpeaks: @HomeDepot
POST
"Please don't support Autism Speaks..."
POST
"Here is a plain list of the twitter handles..."
BLOG
Freeze mob fights ‘R-word’ stigma
BLOG
Why I stand with #BoycottAutismSpeaks
When Josie Webster and the disabled kids weren't invited to the school dance, her mother made a revenge video
BLOG
Real Consequences
BLOG
Wright vs Right: Autism $peaks is Completely Wrong
APPEAL
Stand up and fight for the society we want to live in- WOW Petition
MUM STANDS UP FOR DISABLED SON
BLOG
Be Gentle
BLOG
Mali Asked Me What "Retard" Means
BLOG
Inspiration Porn
Interview with Jay Dolmage, Author of Disability Rhetoric
BLOG
Telling Finn He Has Down Syndrome
BLOG
The Mermaid and the Smoo
Talk:Autism Speaks/Controversy links
VIDEO
Watch This Kindergartener Sign Her Class Holiday Concert As A Surprise For Her Deaf Parents
Dispatches: Will False Signs Bring Change?
BLOG
The Lobotomy Files: Forgotten Documents Reveal Government Lobotomy of U.S. Troops
PRESS
Disability Advocacy Group Condemns Legislation by Representative Tim Murphy That Will Harm Individuals with Mental Illness, Their Families and Society
BLOG
Hands
EVENT
Boycott Autism Speaks: Virtual March
BLOG
Want to know more about autism? Ask someone who is autistic
BLOG
Environments Like Pollock Taken Literally (A Poem)
BLOG
Out of the Goodness of Your Heart
POST
"Please share far and wide this plea from a desperate parent..."
BLOG
Normalcy Speaks: public service announcement
Belgian Senate votes to extend euthanasia to children
BLOG
Supporting a Loved One Through PTSD or Panic Attacks
Laws calls parent a 'retard'
TF uses rogue tactics in storefront stings across nation
The Arc Calls on Department of Justice to End Tactics and Thoroughly Investigate Allegations that People with Disabilities Were Exploited in Sting Operations
VIDEO
"Facebook's new changes are going to receive A LOT of backlash from users..."
“The Third Glance”
Facebook post lands Torrance special-education teacher in hot water
BLOG
Ho Ho Hum
IMAGE
"Presume competence rather than seek pity..."
VIDEO
P4A 2013 | Autistic Self Advocacy Network
BLOG
Red Dress
IMAGE
"When we can say we're a society that's not merely aware, but that's actually in acceptance..."
PRESS
Grassroots protesters condemn Autism Speaks as hateful and call for boycott
POST
Virtual March on Autism Speaks Information
BLOG
#SolidarityIsForTheAbleBodied, and Feminism’s Ableism Problem
EVENT
The T-21 Blog Hop - December 2013
IMAGE
"When Autistic people consistently tell you that something is wrong with an autism org..."
BLOG
ALLY
BLOG
Anger
BLOG
Reclaiming Our Autistic Children #BoycottAutismSpeaks
BLOG
Advocating, Why it’s Important
BLOG
Celebrating Difference
BLOG
Doctor How
BLOG
I Will Not Remain Silent
BLOG
Oh Come, Oh Come
BLOG
The Great Chicago TASH Adventure
BLOG
Merry Christmas!
BLOG
Iowa View: Harkin's antiquated stand on disabled wages
POST
"When police defend themselves with the following after killing someone with an intellectual disability..."
BLOG
This Is What Disability Binarism Looks Like
IMAGE
"Autism Speaks' brand of "awareness" from the "I am Autism" video..."
BLOG
Autistic Regression and Fluid Adaptation
BLOG
The Best of Times, The Worst of Times...
BLOG
What actually matters…
BLOG
December Disability News and Blog Post Round-Up
VIDEO
Shit academics say about access
BLOG
Talking is Hard
POST
"Let's work towards a world in which a father murdering his intellectually disabled son does not lead to reporting of an "act of love", but of a murder..."
PHOTOS
A Catalog That Believes Reality Can Sell Clothes Better Than Photoshop
BLOG
How to Be an Ally in Two Easy Steps
Netflix Will Caption All Streaming Videos by 2014, Per Settlement
Quit Using The "R-Word" In Three Easy Steps
AUDIO
Autism Spectrum and Social Media: fun times with misinformation.
BLOG
Autism Speaks…You Are #4
APPEAL
Walmart: Don't Target Autstic Children: Remove Autism Speaks "school supplies" from your stores
BLOG
Protesting Autism Speaks

December also saw another edition of the T-21 Blog Hop...


The T-21 Blog Hop will take place every month on the 21st, for three days and will continue to feature advocacy posts from across the disability community.

We look forward to January's entries!

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

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.

Thursday, November 7, 2013

In the News - October 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



VIDEO
15 Year Old Becomes The Youngest Astrophysicist in the World
BLOG
Don’t Mix Up Empathy and Civil Rights
PHOTOS

TBINAA Leadership Circle NEEDS YOU!Fall/ Winter 2013/14 Positions. APPLY TODAY!
Class-action settlement amounts to ‘hush money,’ says family of Huronia survivor
Too many people with disabilities live in poverty
BLOG
Guest Contribution from Alana: emotions are hard
BLOG
When we Slip and Slide - A Lament

BLOG
The Problem with “Use Your Words”
BLOG
“Look At Me”
BLOG
Look
BLOG
Who We Are

Actors With Disabilities In Big Roles? 'We Don't Have A Chance'

Huronia institution documents to be shielded by privacy laws

Identities of unnamed dead at Huronia Regional Centre emerge
BLOG
The Space Between
BLOG
BLOG
Feeling the Weight: Some Beginning Notes on Disability, Access and Love


BLOG
Why Curing Disability Should Not Outweigh Equality

We're not here for your inspiration
BLOG
Drawing as Non-Compliance
BLOG
Where Do You See Yourself…
BLOG
Epilepsy: Vulnerability Stays
BLOG
Internalizing What Others Believe

'Breaking Bad's' R.J. Mitte talks disability, bullying and hope

VIDEO
Police: school principal dragged child with Down Syndrome across concrete floor
BLOG
Ollibean Creed
BLOG
The Blurring of Diagnoses
EVENT
BLOG
That Mythical, Magical Chromosome
BLOG
Beyond Down Syndrome
BLOG
Awareness, Acceptance, Advocacy, Action

Exposing quotes that reinforce Down’s syndrome myths: The Truth
VIDEO
BLOG
I Will Not Model Compliance For My Child

Voice surgery sparks ethical debate
BLOG
Why I'm Outraged
BLOG
Feminist disability studies scholar attends the NSGC
BLOG
You Don’t Have to Make Retard Jokes to be Funny! (Why doesn’t everybody know this?)
BLOG
Feminism and Disability Collide
BLOG
Why the Dissies?
BLOG
Disability History Gets Forgotten Each Halloween
BLOG
Passing and Disability: Why Coming Out as Disabled Can Be So Difficult

Coming Out As...Disabled
VIDEO
That’s Not My Name – an anti hate crime anthem
BLOG
You are Not Alone
BLOG
Coming of Age in the Shadow of "Rain Man"
BLOG
Keeping it Real
BLOG
Having to Prove Competence
BLOG
Blogging
AUDIO
New Laws Give More Choice to the Developmentally Disabled
BLOG
Sincere Support

BLOG
Did You Know Cripples Can Do Things?: Inspiration Porn and the Ableist Commodification of Disabled Bodies

How the iPad can turn teaching special ed ‘on its head’
POLL
Disability and Abuse Project
BLOG
About DWD
BLOG
For New Parents...
BLOG
T-21 Blog Hop
BLOG
Cracked Article is Unusual Type of Inspiration Porn
BLOG
The Trouble with Treating “Behaviors”

Canadians with Intellectual Disabilities Ready, Willing & Able to Create an Inclusive and Effective Labour Market


I was diagnosed with autism at 40
BLOG
Shunning, Shaming, Renaming
BLOG
What Fuels the Helicopter?
BLOG
It's the Night of the Living Stim #LvngStm #FF
BLOG
Announcing the Turn: a blog for parents of kids with disabilities
BLOG
Cartographies
VIDEO
BLOG
Not the Lie Most Expect
VIDEO
VIDEO
VIDEO
Bainbridge school district loses bullying lawsuit
EVENT
Welcome (Back) to the T-21 Blog Hop!
BLOG
T21 Blog Hop:  Disability Acceptance
BLOG
Making a difference… and in good company
BLOG
Top Tips for Parents of a Child with a Learning Disability
BLOG
Guest Post: The Sum of One
BLOG
Humanity
BLOG
31 4 21 A Sonnet
BLOG
Hang on, I’m different
BLOG
BLOG
Down Syndrome Acceptance
BLOG
Myth: All Autistics are Emotionless
BLOG
AUTISM ACCEPTANCE…(But don’t tell anyone).
BLOG
Unacceptable
BLOG
I Am a Human Being
BLOG
Falling Inbetween
BLOG
Freedom
BLOG
Awareness and Advocating to the Reasonable
BLOG
BLOG
If You’ve Met One Parent With Asperger’s…
BLOG
Autistic Warriors
BLOG
Bridging The Gap Between Autism Parents and Autistic People
BLOG
The Joy of Being Wrong
BLOG
I am so OK with being wrong…
LINKS
Intersected

BLOG
The Next Right Thing
BLOG
We Disabled Folk Have Everything to Offer the World — Except Normalcy
BLOG
Loving My Challenging Life with Down syndrome
BLOG
The Myth of Passing
BLOG
My Sisters. My Allies.
BLOG
November is Autistic History Month
BLOG
To Educators, Therapists & Doctors
APPEAL
Ratify the Disability Treaty
VIDEO
Something Sickening Is Happening To Some Of Our Schoolchildren, And You Probably Have No Idea

People with a disability deserve the same rights as everyone
VIDEO

BLOG
November: Autistic History Month
BLOG
Advocacy
BLOG
How We Discuss Our Children
BLOG
Virtuous Strength
BLOG
A unique stink
BLOG
A Brief History of Down Syndrome, Part 1: How Down syndrome Got its Name
BLOG
A Brief History of Down Syndrome, Part 2: Before John Langdon Down
BLOG
A Brief History of Down Syndrome, Part 3: All In the Family
BLOG
Autistic Hands
BLOG
A Brief History of Down syndrome, Part 4: The Roots of Institutionalization and Eugenics
BLOG
A Brief History of Down syndrome, Part 5: From Education to Eugenics
BLOG
A Brief History of Down syndrome, Part 6: From Eugenics to Extermination
BLOG
A Brief History of Down syndrome - Part 7: Abused, Neglected, Forgotten
BLOG
Outing The Prejudice: Making The Least Dangerous Assumption

The 5 Scariest Autism 'Treatments'
VIDEO
BLOG
We Are Not Your Token Humans

Is boasting about less SEN pupils appropriate for a job advert?
BLOG
Autism is Not Like Cancer

Stevenage Down’s syndrome pupil left behind on school trip
VIDEO

October was Down syndrome Awareness Acceptance month...






25 Bloggers participated and made it the best one yet.  The T-21 Blog Hop will take place every month on the 21st, for three days and will continue to feature advocacy posts from across the disability community.

We look forward to November's entries for Autistic History Month.

...And that's the news.  Keep the stories and information coming!
Related Posts Plugin for WordPress, Blogger...