What the Fidget Spinners Fad Reveals About Disability Discrimination

bisexualwolverine:

dr-archeville:

I’m angry about the sudden popularity of fidget spinners, but probably
not for the reasons you think.  I’m not mad that they’re disruptive in
class, or obnoxiously trendy.  I’m furious because of what they reveal
about societal power structures, and the pathologizing of disabled people by non-disabled persons.

Autistic people (and others with developmental disabilities) have been
fighting a war for decades.  It’s a war against being forcibly, often
brutally, conditioned to behave more like neurotypicals, no matter the
cost to our own comfort, safety, and sanity.  And those of us who need to
stim in order to concentrate (usually by performing small, repetitive
behaviors like, oh I don’t know, spinning something) have endured
decades of “Quiet Hands
protocols, of being sent to the principal’s office for fidgeting, of
being told “put that down/stop that and pay attention!,” when we are in
fact doing the very thing that allows us to pay attention instead
of being horribly distracted by a million other discomforts such as
buzzing lights and scratchy clothing.  We’ve had our hands slapped and
our comfort objects confiscated.  We’ve been made to sit on our hands.  
We’ve been tied down.  Yes, disabled children get restrained — physically
restrained — in classrooms and therapy sessions and many other settings,
for doing something that has now become a massive fad.

Think about this: Decades of emotional punishment, physical violence,
and other abuses.  And then some guy (who just happens to be in a
position with more social clout than most disabled people will ever
attain) writes an article about how having a fidget toy helps him
concentrate during meetings, and all of a sudden, every neurotypical
person in America is falling all over themselves to get a fidget toy of
their own.  The first time I heard about the fidget spinner craze on the
news, I wasn’t sure whether to laugh or cry.  But I was leaning toward
“cry,” for the reasons I just explained, and because the irony made me
feel ill.  Sometimes the universe has a cruel sense of humor.

This is important.  Really important, so read this next sentence twice: Something
that was considered entirely pathological and in dire need of
correction when done by disabled people is now perfectly acceptable
because it is being done by non-disabled people
.  This should make
you stop and think, especially if you are someone who works with,
educates, or researches people with diagnoses like autism.

What else might we de-pathologize overnight once the “right” people, the
“normal” people, the “healthy” people start doing it?  Will somebody
write a tweet that makes it socially acceptable to avoid eye contact? 
Will a Facebook meme make it suddenly trendy to have texture
sensitivities?  Will hand-flapping become cool after it shows up in a
music video?

Normality is an illusion.  It doesn’t exist.  Human culture is constantly
changing, and our everyday behaviors are changing with it, more than
ever in the fast-paced digital age (yeah, I’m old enough to remember
when phones couldn’t go everywhere with you, and believe me, social
norms were very different back then).  Even if “normal” did exist,
setting it as the goal towards which disabled people should strive is
unacceptable.

Because insisting that disabled people act more like non-disabled people
is not about improving functionality, it’s about who has the power to
set social standards.  It’s the same reason certain accents and dialects
are considered less “educated” and the people who speak that way
snubbed.  It’s the same reason people with one skin tone are portrayed as
less capable, or more dangerous, than people with the majority’s skin
tone.  It’s​ why “women’s work” is devalued and underpaid.  In short, it’s
oppression, plain and simple.

Perhaps I should be more hopeful.  Perhaps we’re moving towards an era of
acceptance.  Even before the fidget spinner hit the spotlight, more and
more professionals have agreed that sensory needs are real, and should be acknowledged and met.  Many websites now sell chewy toys,
app stores abound with sensory relaxation apps, and plenty of autism
“treatment” programs (though certainly not all) have moved away from
their prior focus on sitting still with immobilized hands while
grudgingly accepted that stimming is actually a perfectly healthy thing
for autistic people to do.

But the power structure is still there.  There’s still a rigid hierarchy
of who gets to decide which behaviors are normal or pathological. 
There’s still a societal subtext that tells people who are different “be
less like yourself and more like us.“  We need to work on that. 

Ok so I wasn’t the only one feeling upset like this

What the Fidget Spinners Fad Reveals About Disability Discrimination

i think i have autism what do i do

soapoftheokapi100:

iicraft505:

soapoftheokapi100:

iicraft505:

soapoftheokapi100:

iicraft505:

Talk to a professional, or a trusted adult.

which professional

A professional who is certified to give proper advice on the matter.

How

Or an adult.

As to how I couldn’t fucking tell you, but there’s probably someone in your school or area that could be more help than me.

counsellor?

It sounds stupid in hindsight but yes that is what I meant.
Or, again, some other adult who could find you someone else.

I don’t know what sort of resources you have available to actually figure out.

If not, try to get a few friends to tell you what they think, and then find some resources that could help you, like on the internet.