Showing posts with label learning disability. Show all posts
Showing posts with label learning disability. Show all posts

Friday, October 30, 2015

KID KOAN II

How do you get your child to successfully complete their homework with minimum damage to family life?


To ponder:
On the Mystery of Not-Knowing:
What do you do when your bright child can understand and is assigned advanced math and science but still doesn’t spell, punctuate, space words properly, write on lines, focus, care, keep track of work, or have any detectible executive function OR discipline? When, in addition, s/he gets increasingly angry or tearful when you merely try to get him/her to do homework?

To ponder:
On the Virtue of “Helping:”
My friend over at Runaway Mama cracked me up with this one: The Homework Hokey Pokey:
I read, relating, laughing, crying, and commented as follows:
Homework right now, it's fair to say, is almost ruining my relationship with my son. That dance [her “homework hokey pokey”] is entirely too familiar. The balance is so much harder and feels more crucial when your child has learning and neurological differences...He'd be failing without oversight (MAJOR oversight) and yet is highly intelligent. I try to make sure he DOES and HANDS IN his homework, without ever doing it FOR HIM. If that makes sense...That alone is practically a full time job...
Yuck.

To ponder:
On Validation, as a Sort of Loving-Kindness (Metta) Meditation, from the Asperger Experts (a duo of young gentlemen on the spectrum who tell it like it is {from their points of view} and advise families):
What we want is for our support systems to step in and actually support us by validating our struggles... INSTEAD of always trying to "fix" the situation.
How do you validate someone?
You listen to them.
You hear them.
You take them where they're at instead of asking them to be somewhere or something they're not.
You stop what you're doing and become available for them.
This does not mean offering advice. This means simply listening. 
Period. The end.
I LOOOVE me some Asperger Experts. But this homework situation unquestionably needs “fixing.” When they advise parents – AKA “support systems” -- to listen deeply, to validate, and we do so...Do we then get to do the “homework hokey pokey”? I will keep listening, but how will that get my son to begin to take some initiative with his homework and not fail eighth grade? Surely he is validated by now; in fact, I sometimes think an overabundance of self-esteem is part of the problem.

To ponder:
On the Universal Nature of Universal Design:
Is it possible that Universal Design is not as universal as it is intended to be? This question comes up in my own teaching: which “malfunctions” in the homework department stem from learning differences per se, which are a result of executive function challenges, and which arise from sheer triflingness? And how on earth do we distinguish between these, as students, as parents, as teachers????

To ponder:
On the Practice of Email:
When you are emailing about homework with your son’s case manager [Thank you, C, you are an angel!], at length, more than once, on a Saturday night, is it too much?

Deep, Responsive Thought:
Yes.


Was that scary enough for Halloween? If you’d prefer, you can read about and even justify holiday candy consumption here.

Love,
Full Spectrum Mama




Tuesday, June 9, 2015

A SENSORY PROCESSING/NEURODIVERSITY MANIFESTO

My challenges have always been social–neurological–ethical-familial, never academic. My first encounter with academic challenges came when I – in my third and final (and, finally, successful [after a year as a runaway in the East Village]) attempt at high school – landed in a struggling Quaker boarding school that accepted a lot of students with learning differences. The dean there, the man I now call “Dad,” shepherded his motley crew of misfits with infinite love and respect. Students like me who were fleeing troubled, if wealthy, families, were treated just the same as wealthy, healthy, happy-familied students, scholarship students, “learning-disabled” students, all combinations thereof...all students, period. That is to say, equality really happened under his watch.

Until I began raising my son, who happens to have some learning differences, I actually never knew that the official term for such differences is “learning disability.” You see, Dwight, our dean and my “Dad,” referred to students who learned differently from the "average" student as having...wait for it...”learning differences.” And I spent most of my life thinking that this was how everybody thought about the matter.

How much did that linguistic switch mean to those students, my friends, some of whom had felt “less-than” most of their lives because they didn’t process and/or express information in just the same way as everybody else? You can bet it meant a great deal.

G’s early life involved quite a lot of testing, always at the request of his teachers. I began early on to use different terms for many of the labels that were used by professionals for my son and, later, me. I’ve suggested -- whenever the online or in-person conversation comes up -- that we use the phrase “Sensory Processing Differences” in place of “Sensory Processing Disorder,” and people have generally agreed. I do understand that there are contexts in which a disability label may be more effective in managing our differences. However, for the sake of our selves, and our communities, and our children, I contend that the following labels need to be changed, for daily use, if not for services and adaptations (and this is by no means a comprehensive list, just getting this here manifesto going!):

Sensory Processing Disorder              to                     Sensory Processing Differences
Autism Spectrum Disorder                 to                     Autism Spectrum
Accommodations                                to                     Adaptations
Disability                                             to                     Diffability 
Disabled                                              to                     Differently-Abled

Yes, we are different. That doesn’t always make us fundamentally disordered or syndromed.

We are all different. All that difference is not the same. Some of it is MUCH harder, because this world was constructed primarily by people who are embodied and think in “normal” ways. The adaptations some of us may need are framed as “special” “services” because of the way this world is designed – and for whom – NOT BECAUSE THERE IS ANYTHING WRONG WITH US.

Here’s an example I see as very simple and non-loaded: because of my Sensory Processing Differences, when I go into a big box store the artificial scents used in cleaners and scented candles etc. give me an instant migraine. Does this make me defective? In my humble opinion, it makes me more of a canary in a coal mine: Nobody should be breathing those chemicals...and it’s not “disordered” to know so in a very visceral way. 

Another thing about language: it’s okay to ask! There’s been so much discussion, much of it rancorous, around whether or not to use person-first language. How about using the language that the person/people in question prefer/s? I, for one, aim to use language that is respectful and egalitarian. When I speak with others, I am willing to use the language they deem respectful and egalitarian, so long as it does not demean me.

Changing the ways we talk about difference are an important step toward healing this world so that we are all included in the spectrum of equality. Although there is some weight to having “differences,” the word itself also implies variety and, in some important ways, validity. We must continue striving to speak and write in ways that are increasingly fair, as language evolves to better fit reality..

You’ll note I’ve no cute rainbow graphic for this Full Spectrum manifesto. (Please see Figure I.)


                                                    Figure I – No Cute Rainbow Graphic

...because the way we talk about stuff is serious.

Love,
Full Spectrum Mama







Welcome to the Sensory Blog Hop -- a monthly gathering of posts from sensory bloggers hosted by The Sensory Spectrum and The Jenny Evolution. Click on the links below to read stories from other bloggers about what it's like to have Sensory Processing Disorder and to raise a sensory kiddo!Want to join in on next month's Sensory Blog Hop? Click here!