WE MUST CREATE CHANGE

I was going to call this my “Hope For 2015”, but that is so passive and useless. Anybody can – and lots of people do – post warm, fuzzy notes with Hopes for the New Year, and others click and share. Lovely.

But this is NOT all warm & fuzzy. It’s literally dead serious (with many murdered throughout the year), and quite often blunt, because I am blunt at times. It’s also a call to a change of perspective for some of you.

Deal. Think about it. I’m not a lone voice. Click and share.

MY CALL TO ACTION IS FOR YOU TO READ THIS THROUGH, THINK, AND SPEAK UP. ALL YEAR LONG.

And the next year and the next.

This isn’t about some stranger, or Those Other People, or “That Kind”.

Children with disabilities or other differences are not diseased or broken. The same is true for adults. Yes, those “poor, little disabled children” grow up into disabled adults. Gee, so where’s the concern now? It sure isn’t at work; in the U.S. general unemployment is at 5.3%, but for disabled adults it’s twice that at 10.8%.

Nor are autistic or ADHD children some kind of modern mystery; millions of such adults have been around for decades, just unrecognized for lack of diagnostics. Most of us are profoundly relieved to find out Why. We still have to deal with the details, but that’s easier when you know that not all your difficulties are from some kind of moral failing, or from a lack of trying (and trying, and trying).

WHAT, YOU NEVER HAD KIDS LIKE “THAT KIND” IN YOUR CLASSES? YOU KNOW WHY?

Some were kept at home, because until passage of the IDEA in 1975, US law did not require public schools to teach everyone.

Some were warehoused in institutions, badly treated, undiagnosed or misdiagnosed, and oft uneducated.

But many of us were there; how we struggled through school and life, without accommodations or understanding, and often the target of bullying by peers and even school officials.

Untold numbers of women and men just knew themselves inexplicably “a bit odd”, and did best they could; some succeeding, others not so well.

At worst are those who not only lacked resources, but were shunned by society’s classism, ableism, racism and sexism, and (if still alive) are found among the imprisoned, derelicts, addicts, abused and enslaved populations.

YOUR CHILDREN AND EVEN COLLEGE STUDENTS WILL LEARN DIFFERENTLY, SO YOU MUST ADJUST

We are neither inherently stupid nor incapable of learning. Learning differently means teaching differently. Find what works. Everyone has limits, but a consistent lack of success means you should use another method, as well as more time. Sometimes the learning is highly irregular in pace. Tie learning to interests to motivate your children and students.

Also, be aware that sometimes the “simple basics” may be entirely bypassed by some students who leap to master higher concepts, albeit often forever struggling with those seemingly “simple basics”. People are humans, not robots. Learning is not always linear.

COMMUNICATION IS NOT JUST SPEAKING

Never assume that just because someone is nonverbal they cannot communicate. If you’re not getting their messages, then *you* are doing something wrong. Nor should you assume that because someone is nonverbal that they cannot understand what people say (though the processing may sometimes be delayed). Nor assume that because someone has been nonverbal for years that they’ll never speak. And damn, will you get an earful.

INCONSISTENCY IN DAY-TO-DAY ABILITIES IS FRUSTRATING FOR ALL, AND NOT A CHOICE

Importantly, just because someone is able to speak or do a task one day, that does not guarantee consistent results. It’s the nature of disabilities — regardless whether considered mental or physical – all involve the brain. Brains are funny things, and many of us have a few buggy Beta-version programs in our wetware. It’s frustrating as hell for all involved.

But don’t assume the “could-then-can’t-now” is intentional. “Oh, he can hear me when he wants.” “Well, you could solve those equations just fine yesterday.” I can guarantee that after a lifetime of such, ridiculing people and punishing them for things they cannot help only increases performance stress.

While that stress might increase focus from sheer terror, it often squelches overall functioning. (Do you want me to listen to you, or try to recall yesterday’s process, or slowly figure it out on my own? I can only do one — if my stomach will stay down.)

TRAMPLE THE TROPES

Ignore the media tropes and centuries of religious hype: disabled people are neither inherently amoral, soulless and evil, nor are they infinitely happy, friendly and angelic. People are people. A few will be nasty bits, some will be profoundly good sorts, and the rest are just ordinary folks who get mad, sad and glad, who screw things up sometimes, and who will also serve others selflessly despite bearing more abuse than anyone should.

We are definitely not incomprehensible, incomplete, little autism-puzzle-pieces, unloving, unlovable, or uncaring.

We are whole people with all the same cares, needs and wants as all humans. Beware — disability happens to anyone at any time. We aren’t a Them, and YOU can be among the world’s 15% in just one day. We are all Us.

STOP “TEACHING TOLERANCE”

Because tolerance means putting up with something one doesn’t really like, or that doesn’t really belong. We want full-fledged ACCEPTANCE.

Nor should we only be acceptable if we can somehow “overcome” our differences enough to pass for Normal Real People. Trying to “pass” all the time is exhausting, and invariably breaks down, oft resulting in the [supposed] Normal Real People assuming that one is lazy, stupid, crazy, all the above, or worse.

Training children for hours a day how to artificially perform “acting normal” does not serve to help them learn how to function best in the world. Yes, of course teach good manners, social and work skills. But suppressing every twitch of one’s natural being adds to stress, making everything else yet more difficult. This is especially when performing like a “normal person” means not doing the harmless things that reduce stresses.

STOP THE BLAME

I must call out the terrifying, unaddressed assumption which underlies so much daily trauma: “The reason the disabled [children] are targeted by bullies is because they are perceived as being weird”. Despite the pervasiveness of this social theme in society, most people are functionally unaware of it, all the while instilling in their Normal People children the same message. Normal People children need to act normal, and not act like That Kind. After all, that’s how the Normal People know the others are That Kind, who’s Us and who’s Them.

But it’s the disabled and different who are taught, over-and-over-and-over that not only is it their fault for behaving or looking weird, BUT ALSO if they weren’t so weird, well then they wouldn’t be bullied. “Quit being so weird! Just say No! Just say Stop.”

Just say BULLSHIT. Because this is blaming the victim. The problem is not that everyone isn’t the same, the problem is that there are bullies.

Even worse, blaming the targets actually empowers the bullies, because the social story says it’s the victim is the one who is acting wrong, so it’s not really the bully who is to blame.

Let’s just top off all that existing anxiety and depression with the trauma of trying to seek justice, but being told again that, “Well it’s your fault, you know. Attracting attention by being weird, and bugging people. You need to quit making trouble now. You already take up too much of our time with all of your “special” needs. Quit whining and go deal with it. — But no fighting, because we’ll know it was you who started it.”

By the way, it’s not “just a kids at school” thing that everyone will “grown out of”. It continues on through college, and happens at work, too.

YOU CAN’T WALK IN THE LITTLE BOY’S SHOES;

THEY’RE FLOATING DOWN-RIVER

It is NEVER acceptable to murder disabled children. Nor should these repeated, horrifying events be considered “understandable” or “excusable”, with the murderers being pardoned just because their son or daughter had a disability.

Increasingly more prevalent in social media, the crime becomes insidiously deemed more and more acceptable. Murderers re-cast themselves as martyrs, acquiring champions to their cause. Throughout repeated blog posts and news stories, they bemoan how taking care of disabled children is just too unbearable, they had to take care of them every day of the week, there was never any relief or help. (Even though there was.) Cue the groupies’ hand-wringing and protests upon the villains’ behalf: “Oh but won’t you walk in their shoes, how they’ve given up their lives, this wasn’t at all what they wanted.”

For in true sociopathic fashion, the poor, long-suffering parents revel in the attention, announcing to the world – sometimes ahead of time — what they have done, and all the while describing themselves as the victims. The dead children (young or adult) are unwanted, and deemed unwantable, less than human just because they couldn’t speak, or needed medical treatments, or used a power chair, or didn’t play with their toys the “right way”, or wore adult diapers … No one would want to live like that; the thing’s better off dead. And what of the groupies? Well, where do you think people get such terrible ideas that it’s okay to kill one’s own children?

ENOUGH WITH THE “DISABILITY INSPIRATION PORN”.

Quit using those heart-tugging videos, walk-a-thons, telethons, and other grand-society functions to win your supposed Cosmic Brownie Points for giving us your pity. Please stop dumping upon us the largesse of your unwanted rags (so Victorian, so passé), or creating useless functions requiring us to serve as targets of unwanted helpful-helper-helpiness for your ego-boo.

Get disabled people out of “sheltered workshops”. Yes, people need work they are suited to. But the segregation and token sweatshop “wages” are an embarrassment and humiliation to all.

YES, CHILDREN GROW UP.

YEP, STILL DISABLED, BUT NOW ADULTS

Do not assume your children will remain permanently childish and incapable — they mature on their own timelines. Allow adults to be adults. Support their needs and interests, but neither dress them like children, nor expect them to live their lives in naïve pre-puberty stasis, without adult desires for socializing with adult peers, life-long learning, mastering skills for some kind of job (even if that job is “just socially productive work” rather than traditional work), and yes, having a love life, however that may be expressed.

YES, PEOPLE ALSO NEED ACCOMMODATIONS;

THAT DOESN’T MEAN “CURE”

Most disabled or different people are not looking for cures to magically change them into someone else, some kind of fantasy Normal Real person that their families wanted instead. Our differences may result from physical events, by random mutation, and / or genetics. Your genetics. We are family. I’m Me, and I like being Me. If you somehow changed all the differences in my brain, I wouldn’t be Me anymore, with all my quirks and abilities.

Of course it will be great to find a means for preventing migraines, epilepsy, fatal medical conditions, et cetera. But it’s also a sad fact that some people have been so convinced of their undesirability as disabled human beings that they can only see “cure” as a means to being an acceptable Normal Real Person. (Worst of all, some people commit suicide because they’ve been taught to hate themselves, as useless and unwanted.)

But what’s really alarming is all the fund-raising, talk, research, and work going on today to eliminate entire kinds of peoples. I’m talking about the thousands of selfish individuals and sociopaths who believe that anyone with neurological or morphological differences should not exist at all, because That Kind takes up too much time, money, and resources.

That’s not “looking for a cure” – that’s eugenics and euthanasia, the same ideas that led to the Nazi Aktion T4 program and other horrors. (In my youth, the state hospital was still in the regular habit of sterilizing people. Had I been institutionalized, I might well not have had my lovely children and grandchildren.)

Yes, we want assistance, we want things that help us achieve what we want in life. Getting the things one needs to learn effectively, to move about, attend to their own needs, to work, to play, to be a part of the community, to have lovers or families. These things should not be seen as extraordinary, special, absurd, or a waste of money, just because they aren’t the same kinds of things used by other people. 15% of the people in the world have disabilities. That is a lot of humanity, and many are uneducated, abused, neglected, avoided, or shut away, depriving the world of incredible amounts of untapped abilities and talents.

CALL OUT BULLSHIT. REQUIRE ACCOMMODATIONS. DEMAND ACCEPTANCE.

MAKE IT SO.

Reasoning for a good cause

“Same thing,” she said, waving off the comment and walking off toward the time-clock to punch out.

“But– no, it’s not …” I protested, and then stopped talking as I saw her leaving not only the the doorway where I stood, but our conversation as well.

If you could call it a conversation; I’ve had longer dialogs with fellow elevator riders.

It was hard to stop my rebuttal. I so wanted to explain, and having to force myself to stop in mid-sentence (hell, mid-mini-monologue) is hardly my style. But I diligently keep practicing social skills, including noticing when others have quit a topic.

Having already clocked out, I gave up, left the building, and even waited to get into my car before expressing my complaints aloud to no one — except a fruit fly uselessly orbiting the fragrant-but-empty lunch bag I had just tossed onto the floor.

And a fruit fly doesn’t give a gnat’s ass about the seemingly subtle difference between reason and cause. No, it is not mere semantics, and they are not exact synonyms.

“So how was your trip?” she had asked as we met in the hallway. We had not yet crossed paths that day, delaying the obligatory Monday morning chit-chat.

“Oh it was lovely, except for missing a connecting flight, so I was only there two days,” I began. And I was proud that I had even mindfully planned ahead to next ask her if she’d ever been to Boston, thus fulfilling my offering volley in the chit-chat process — when she gave me that totally unexpected, inexplicable response:

“Well you know, ‘Everything happens for a Reason’ !” She chirped, nodding sagely.

“You mean a cause,” I began.

“Same thing,” she said, waving off the comment and walking off toward the time-clock to punch out.

“But– no, it’s not …” I protested.* Read the rest of this entry »

Writhe, Burn and Melt

My grandson, The Blur is beginning to start to get tired. I call him The Blur because he’s such an active lad, he can be hardly be photographed. He’s only 2 1/2, and little kids are generally bouncy, active beings, but he is especially so, and reminds his papa and I of when we were children*, which is alternately endearing, alarming, humorous, annoying, fun, and/or exhausting.

Especially the alarming and exhausting parts, because apparently he’s one of those kids who doesn’t need as much sleep. A few months ago he figured out how to pop off the child-proof doorknob cover to escape his room, and a few weeks later, had removed a couple of hinge pins to his bedroom door towards a similar escape attempt. (His parents just want to be sure of where he is when they are trying to sleep!)

Right now he’s squirming off and on and around his mum’s lap, and off and on the furniture, and off and on and around her lap again, and off and on and under me, and so on. His mum explained, “I call this the ‘Writhing’ stage.”

“Perfect term! He’s not ready for a siesta yet, is he?” I ask rhetorically. ‘Siesta’ = nap; we’re speaking in code over his head.

“No, next is the ‘Manic’ stage,” she sighed.

“Burnoff!” I confirmed, thinking of his evening hyperdrive mode, when he needs to burn off the last bit of energy.

“I know he’s ready when he gets to the ‘Melting’ stage.”

I’m imagining Dali’s watches flopped over tree limbs, and that’s pretty much what The Blur looks like when it’s time for reading books. And then after gathering a number of toys and bears and books, he “reads” to himself before possibly sleeping during naptime.

_______

* I’m not saying that he has ADHD like I do; he’s only 2 1/2. But we’re really conscious about channelling all that energy and nimble-fingered intelligence to positive stuff!

I meant to get around to this earlier…

Displacement behaviour: when suddenly you feel the need to shift a negative emotion or stressor to doing something else. Right now, that means sorting tax papers instead of finishing a class handout or sending out a query letter. (During Finals Week, my displacement behaviour was cleaning the bathrooms. My apartment was REALLY CLEAN after Finals Week.)

One rationalisation I have at the moment is that I am correcting for last year’s “planning fallacy” — organising and tracking down information and figuring out the electronic filing of my federal and state taxes took me longer than I had anticipated. (Folks with ADHD are terrible about planning fallacies, because of the weird fluidity of perceived time.)

Ooh, I just found some neat links on new research into the causes and coping strategies for procrastination … *

STOP!  

That’s just a rationalisation. Set aside those tax papers for this weekend, and get back to the correspondence. Damn. And, *sigh*.

Meanwhile, here are some of my mottos that you may like:

Fidget quietly.

Pile by file**.

Perseverate positively.

Obsess functionally.

_____________

* Go to the Wikipedia page on Procrastination; they’re at the bottom. Sorry; I can’t be an accomplice to all of us wasting too much time…

** Which of course, later turns into File by Pile. But if your piles are already rough-sorted, then they don’t need much more than sifting out unnecessary junk (credit card offers and candy wrappers and expired sticky-notes), and maybe some date-sorting.

I prefer the OHIO method for when I get the mail: Only Handle It Once. From the moment it goes from the mailbox to my hand, I don’t dare set it down until I have binned the junk, set the catalogs and magazines in the appropriate reading zone (e.g. the bathroom), and push-pinned the bills to my bulletin board with the due dates highlighted. Otherwise, if I put the stuff down, it gets lost and forgotten in the dèbris of my desk!

Singing teh Brain-Dead Workin-Hard Blues: Remodeling

Had a migraine this morning
Cancelled on my shrink.
Need to clean and organise
But I can’t even think.

Moved bedrooms three days ago
O where is my daily pill box?
Boxes and piles everywhere
O where are my clean socks?

I need to go out and garden
Weeds have eaten the side yard.
I need to finish planting
Heat’n’humidity too damn hard.

I need more hours at my job
Stocking groceries at the store;
717 pounds of charcoal
Added bruises to the score.

Need to hammer and hang things
But grandchildren are asleep.
Need to paint and put away stuff
Always more work and I just keep–

Charging for hardware I gotta buy
Like a frequent flier down at Lowe’s.
Wish everything was at the Restore*
Spending too much goodness knows.

Had a migraine this morning
Cancelled on my shrink.
Need to clean and organise
But I can’t even think.

Moved bedrooms three days ago
O where is my daily pill box?
Boxes and piles everywhere
O where are my clean socks?

* Restores are where Habitat for Humanity sells new/gently used building materials; they are a great way to reduce-reuse-recycle and save lots of money on building supplies!  The hitch of course is that the items vary daily at stores.

AD/HD Gaslight

Where is my grocery cart?

I’m pretty sure I left it down by the front end of the frozen aisles.

It’s not there.  Nor did someone move it out of the way behind the [rarely used] Register 1.

Huh.  Where is my cart?  Now I’m traipsing around for my trolley.

I’m not grocery shopping, when I stay in close proximity to my market merchandise.  This is my working wagon, a cart with my rubbish bag and duster, my list and notes, my repair tape and of course, the things I need to shelve.

With my ADHD brain set to Random and taxed by tiredness, yet trying to keep several tasks current on my mental “desktop”, it’s certainly not impossible for me to lose track of a thing to fetch or to put away, or the next task I’d set myself to do.  Generally my recursive tracks through the store are sufficient for me to come across either the item or the section of shelves that I need to “face” (straighten up).

Sometimes my mental perambulations cross back over a previous line of thought, and the same mental note will thus occur to me again.

It’s inefficient to be sure, but eventually everything gets done.  I try to streamline my process progress by keeping a running list of Things To Do. The list is also great at the end of my shift, for when I leave a note to my boss telling what usual things I’d done, and also what extra tasks I had tended. Plus, there is the external randomness that happens all night long: periodic calls to cashier during a sudden influx of customers*, and sporadic customer queries that result in my taking them to the item location.

And then — oh bother!  Where DID I park my cart?

Because of course, if it’s a Truck day, I’m stocking dozens of cases of candy or baby formula or soap, then the cart stays put in the aisle. I remove each case of new stock to set, and then return the flattened cardboard to the cart.

That’s fine.  But other days there is no Truck of new stock to set, and I am simply filling in various shelves with Back Stock (B/S, not to be confused with BS).

And right now I can’t find my cart. I try to “retrace my steps”, which more resembles surveying the aisles I usually frequent, because nothing this evening was particularly memorable to imprint itself on my memory.  All too often, my memory is topical, not sequential.

No, it’s not around anywhere; which discounts the “distracted by sequential customer queries” process that results in me being far from my original departure point.

Another hypothesis is that since it’s neither in the usual aisles, nor by Register 1, maybe someone decided to take it to the back stock room.

I pace to the back room, thankfully uninterrupted by a customer, whose query would have restarted this whole recursive process all over again.

Hmn … there’s my cart and equipment, but not the case I was going to stock.  I guess one of the managers decided to do something with it.  Maybe it was one of those new items for which we do not yet have a shelf tag, and they needed to enter the item into the inventory system. Thank goodness; mystery solved.

So I wheel down to the stock bay where the B/S bird seed and dog chews are kept, to fetch more cases.  After loading my cart again, I realize that it’s time to take my Break — some food and water would probably help the whole tired brain thing.  And if I leave a full cart, no one is likely to unintentionally “gaslight” me by changing my surroundings and leaving me to wonder if I’ve lost track of my stuff or my mind altogether.

* Why “everyone” wants to check out at once — no matter when they came in — is one of the mysteries of retail.

Stupid Irony!

Someone defined poetry as “life condensed”.  Sometimes I think that disability is life magnified.  Today’s lens is Irony:

  • I dropped my reaching tool behind the bed where I … struggled to reach it.
  • Forgot to take my ADHD meds.
  • Was too stiff to pull on my elastics:  the wrap for my elbow, the two pads for my knees, and the fingertip-less gloves.
  • Nearly in too much pain to remove the child-safe cap from the arthritis medicine.
  • Couldn’t see to find the wee screw that holds in the lens to my eyeglasses.
  • (Similarly,  when my ex-husband couldn’t hear his hearing aid squealing.)
  • Couldn’t understand the voice-mail reminding me of a follow-up visit with the audiologist.
  • Being unsure if that noise I heard in the audiologist’s testing booth was one of the test tones, or my tinnitus.
  • Asked a random store clerk to open the box and unpeel a bandage wrapper so I could stop the bleeding of yet another torn cuticle and pay for said bandages.
  • Sat on the grocery floor because I’d forgotten to wear my knee pads that day, and had to stock boxes of aspirin and arthritis meds.
  • When discussing my difficulties with social interactions with a counselor and mentioned that I thought I was missing things, I was unable to tell just what it was that I was not catching!

And so on, and so on.  Feel free to add some of your own!

Web buzzing

Just wanted to share some cool things I found recently!

INSECT-RELATED FUN

Amazonian ants apparently adore Tetris – ’tis a tee from Threadless Tees.

Cartoon with a green background, the upper half with five army ants on a branch, carrying pieces of leaves cut into various Tetris shapes. Below, the crowned queen ant awaits by a Tetris-shaped stack of pieces. (Unfortunately, she's about to get a square and won't have a place to set it!)

and,

NPR has a short episode with guest comments by the inimitable entolomogist and highly entertaining author, May Berenbaum,

There has been a worldwide proliferation of urinal flies, observed May Berenbaum, head of the department of entomology at the University of Illinois in her new book The Earwig’s Tail.

You can listen to the episode and/or read the transcript, “There’s A Fly In My Urinal”.

realistic black and white fly decal

and,

Jessica (the painter) and James (the author) of Project InSECT have a couple of books out, How Mildred Became Famous (book I and book II).  Mildred is a mantis, and one of the many gorgeous, large paintings that Jessica has done.

Detailed painting of Mildred, the praying mantis, plain chiaroscuro background

GARDENING / NATURE

A brief video:  One year in 40 seconds. Eirik Solheim’s gorgeous time-lapse of Norweigian woods.  Suitably short for the ADHD brain or a coffee break.  (Alas, I’ve tried several ways to get this URL embedded so it will display from this post, but WordPress is being funky.  So you’ll just have to copy-paste it to get to the YouTube page directly.)

youtube=http://www.youtube.com/watch?v=lmIFXIXQQ_E

and of course, a bit of geeky

ACCESSIBILITY


A dismotivational poster with the image of a Dalek (robot from Dr Who show) stuck in a concrete room with only stairs as a means of exit; its word balloon says, "FUCK". The poster caption is, "LIMITATIONS everyone has them"

Music to Bounce By

My five-month old grandson, AKA Tigger or Mr BoingBoing, has loved to bounce from the get-go.  Even when he was in utero, my daugher remembers how the sonography technician ended up sighing when she visited, because the baby was so mobile that it was hard to get a measurement.  Later on, the mom-to-be said that although the baby book bore the reminder to make sure that the baby moved each day, she never had to bother to check.

“I hope he learns how to sit for half an hour by the time school starts,” I mentioned, with ADHD concerns hanging unspoken in the air.

“He does have a great attention span.  I just hope he starts sleeping better soon,” added the proud but perennially tired mom.

“There are some children that never do sleep much.”

“But I don’t want one of those …”  The idea of spending the next decade or more taking turns sleeping was almost too much to contemplate.

“No one ever does!”

Thankfully, the lad loves his doorway bouncer.  Not only has his bouncy seat just been retired because he can he roll over and out of it, he’s even started getting on his hands and knees.

In my familial role as Bouncy Lady, I put together an iTunes playlist of “Music to Bounce By” for bouncing him on our knees, as babies love music, it’s generally more entertaining for all, and slightly less tiring for the adult if they don’t have to sing.  We want to expose him to a variety of music.  Right now, “Wipe Out” by the Ventures is a favorite.  (I’ve included links to a couple of pieces that are not well known, but are worth checking out.)

  • Good Vibrations    The Beach Boys
  • Ticket To Ride    The Beatles
  • Will It Go Round in Circles    Billy Preston
  • That’l Be The Day    Buddy Holly & The Crickets
  • Superstition  Stevie Wonder
  • Working In The Coal Mine    Devo
  • Satin Doll    Duke Ellington and His Orchestra
  • Crocodile Rock    Elton John
  • Think    Aretha Franklin
  • Sing, Sing, Sing    Benny Goodman
  • Mouse Jigs    Flook
  • Barracuda    Heart
  • Tijuana Taxi   Herb Alpert & The Tijuana Brass
  • Immigrant Song    Led Zeppelin
  • Dancing On The Ceiling   Lionel Richie
  • Another One Bites The Dust    Queen
  • Burning Down the House   Talking Heads
  • Shake Your Tailfeather    Ray Charles
  • Four Sticks    Sones de Mexico Ensemble
  • Pride And Joy   Stevie Ray Vaughan
  • Wipe Out     The Ventures
  • Hawaii Five-O    The Ventures
  • Linus And Lucy    Vince Guaraldi

Every few songs we have something a bit less frenetic, to keep from getting too fatigued.  And of course, we never get through the whole list in one pass; just a few songs at a time.

At least there’s one thing that he’ll sit still for:  watching Star Trek!  But that’s a story for another day …

What a great combo

ADHD + fussy baby:

“See?  There’s Bouncy Lady.  We call her Grandma.”

Hanging around the Web

Cruising the Web BW

A shiny robot spider hangs upside-down from a metal mesh

My son and I recently hauled a long dresser+mirror up two flights of stairs, and I cleaned up the master bedroom in preparation for the return of the new baby & parents from the hospital.  The downside of course is that after a day of labor, I must spend a couple-three days recuperating.  (In other words, I used up all my “spoons”, down to the last demitasse.)

I’m also on Day 2 of one of those low-grade-three-day migraines.  Right now it’s manifesting as misreads, which when I catch myself is kind of entertaining:

In light of all that, I thought I’d share some interesting reads/cool finds on the Web recently:

My sleep-deprived daughter would be envious of ant queens, who spend nine hours a day sleeping, while the workers must squeeze in micro-naps.

From the world of delightful architecture, an adult tree[less] house shaped like a bee skep, made of recycled lumber (wheelie adaptation not included).

The CitizenM hotels have the most amazing showers, which look like Star Trek transporter pads.  To start the shower, you simply shut the door.  I don’t know if they’re large enough for a wheelchair transfer to a shower seat, but with the zero-clearance there’s a chance of it (maybe Dave knows). Want!  (Or at least the trés geek LED shower head that changes from blue to red when your water’s hot.)

Reimer Reason posted It’s a Family Reunion! for the most recent Disability Blog Carnival.

In further hexapod news:  while I was distracted by our little geekling, Bug Girl has been faithfully covering Pollinator Week, including important information about CHOCOLATE. For more funs, Cheshire has teh latest Circus of the Spineless up.

And of course, what would a list of fun be without a LOLcat?

Six white kittens lined up and looking at the camera, while a seventh is distracted with a play ball

Six white kittens lined up and looking at the camera, while a seventh is distracted with a play ball. The photo caption reads, "PUZZLE PICTURE Find the kitten who has ADD."

What she said was, “Aquacise”

Random thought:

When my rheumatologist said to get more exercise,

I’m not sure she really meant

that I should be hauling meself up & down stairs

over and over because of my ADHD forgetfulness.

Cartfuls of Spoons

They’re out.  Or, Out.  We have the exquisite “Privilege of Being Clouted By Cabbage” and are navigating the hazards of the supermarket.  When things are done the way they’re supposed to be, going to pick up a few groceries is just as boring, or as Dave discovered, lonely, for disabled people as much as it is for everyone else.  But sometimes it isn’t, such as when Wheelchair Dancer finds herself navigating the hazards of anonymous donors that leave awkward brochures under her windshield wiper, and then dealing with the even more awkward social fallout with the clerk who’s assisting her.

People with a variety of disabilities come to the store to get groceries, movies, dry cleaning, take-out food, postage stamps, floral arrangements, and because it’s this time of year, garden plants, which is why I am working there.  I shouldn’t be surprised, but I am bemused to report that I realised that people with physical ailments are shopping at the store alla time!  After all, that is why we have some of those electric carts, in addition to automatic doors, ramped paving, lower check-writing stands, supposedly-accessible bathrooms*, et cetera.

Most of the time I just interact with the public as a “normal” garden center employee, but sometimes we are also interacting with that subtle overlay of disability, which entertains the social scientist part of my brain.

Being the token horticulturalist, I answer questions, help customers plan flower beds and suggest suitable plants for locations.  In addition to working the register, watering, deadheading and “facing” the stock (moving pots towards the fronts of the benches to fill in holes left by customers), I work with the others to come up with æsthetically-pleasing displays of the plants.  (Although there is no way of hiding the fact that the corporate HQ plagued us with a plethora of Pelargonium, a visual red tide of geraniums.)

I’ve seen plenty of plant displays at a variety of other stores, and have found their long lines of benches to be annoying.  It’s not just that endless tracts of pink & purple Petunias, orange & yellow Marigolds, and red Geraniums are mind-numbingly dull to the point of dampening any sort of inspiration for coming up with container or bedding combinations.  It’s that the long lines of “benches” block traffic flow.  You feel like you’re trudging up and down the maze of a ticket queue, unable to grab some pots of more-interesting Corkscrew Rush or Calibrachoa tha are hidden over there two aisles over.  It’s hard to break out of the march to exit stage left to the register (till), or even quit to go over to the entrance into the store.  The long lines of benches are especially boring for children, who have little more than a view of the edges of the benches and the pots, with little respite in sight.  (I’ve taken to offering children cups of the cold water from our water cooler barrel, as hot, thirsty children are cranky children.)

Worst, when at these other stores run out of available bench space, a lot of the pallets of potted plants just end up dropped by the pallet jack where-ever there’s room on the ground.  This means that the aisles are not really planned, so sometimes there are narrow dead-ends, or aisles blocked by broken bags of mulch, or the plants are simply hard to reach because they are way down on the ground or are way deep in the center of the pallet.  They are not accessible.

For a few days, we too of a dozen pallets lined up at the edge of our lot, albeit with sufficient aisle space.  It really “made my brain hurt”, because the plants had been shipped all higgedy-piggedy, with shrubs, grasses, annuals and perennials all mixed together.  There were Daylilies in four different places around our lot!  The flats of shade-loving Wax Begonias and Impatiens and sun-loving Verbena and Vinca were all jumbled by species and color!  (And OMG, still more Geraniums.  And Creeping Phlox, which only looks nice when it’s blooming, and now we have enough to landscape a highway interchange.)

But thankfully, I’m not the only one who has a strong interest in making the endless flats of plants look more interesting, and be more accessible. We’ve been stacking pallets or propping them up on cinderblocks to put the plants into easier view and reach.  (Plus, they’re also easier for us to clean and water — ergonomics, w00t!)  We’ve been making sure that the aisles are frequently broken up into side-paths, and we try to keep the aisles 3-4 feet wide so carts, strollers and wheelchairs can get through.  It seems to be working well; every day we get compliments about how good the plants look.

But what makes this place pleasant to work for is the concern for helping our customers.  Sure, it’s store policy to be helpful (doesn’t every business flog that slogan?), but we are glad to break from running the register or watering to carry things out to the car, or load up bags of mulch and rock, or show you where the Verbena is, or explain the differences between the four varieties of white Petunias.  When someone has their hands full, we grab some empty flats, and pull carts (buggies, trolleys) over to make things easier.

It’s this “serve everyone” approach that makes helping people with various disabilities so much easier.  One of the other clerks knows American Sign Language, so Deaf customers are sure to look for her (my ASL is rather limited).  When the gentleman in the power chair thanked a coworker for carrying stuff out to his van, I was tickled to overhear him say, “No problem!  We do that for everyone.”  Because we do.

Sometimes the “disabled community” moments are colored in large brush strokes.  An older man in a wheelchair came by in search of some herb seeds, accompanied by two women who were of the “care-taker” rather than “personal assistant” mentality.  Although neither said anything obviously untoward, there was still a patronizing aura, that his desire to go shopping was being honored but that they were still “humoring” him.  It made me uncomfortable, and I kept trying to scan the interactions in the triad to figure out what was going on.

But the women were intent on asking me questions of their own, even as they were simultaneously going through the motions of helping him.  “Here’s someone who can help you.  He’s looking for some seeds.  Tell her what you’re looking for.  Do you have any seeds?  Do you remember what it was he wanted?  Ooh, don’t you just love those pink flowers?  Isn’t that what you got on your desk?”

“Well I dunno, but it’s not flowering any more.  Was you looking for parsley?  He was wanting to grow some stuff from seed.  You sure gots a lot of plants out here.”

Trying to track all this verbiage flying by was making me dizzy, and I just wanted to focus on finding out what the man came to get.  The customer himself was having some expressive difficulties. (Who wouldn’t have, being around those two all day!)  I knelt down on a knee so I could speak with him face to face.  I had to.  I had to disengage myself from the chatty care-takers who were now trying to ask me random questions unrelated to the needs of my primary customer.  I had to be able to focus on what he was asking for, which meant watching him speak.  And I had to honor him personally as the customer, not as some second-class accessory.

My knees cracked noisily, and I knelt down on one knee, and we conversed, just the garden center clerk and the customer who wanted parsley seeds, and who considered and then decided against the Doubled-Curled or Flat Italian Parsley seedlings.

After that moment, I stood back up and we were sucked back into the vortex of the chatty care-givers, who asked me some confused questions about houseplants, and then led/followed him over to the main store entrance.  I hoped he would be getting the things that he wanted this evening.

Sometimes the community moments come by quietly.  I was checking out a couple flats of annuals and several perennials for a woman, cleaning off some old leaves and blossoms and chatting as the register processed her credit card in its own slow time.

“This is going to take me several days to get it all planted,” she offered.

“Well, that’s always a good thing to do anyway,” I offered, affirming her wisdom.  “It’s those marathon gardening sessions that break our backs.”  The register finally finished hiccoughing through the electronic transmission and spat out her receipt.  I picked up her potted rose bush, rested it on a hip, and then deftly tipped up the flat of annuals to balance them on my other hand.  (It only sounds tricky; in reality the flats are just boxy grates, and I can curl my fingers into them.)  “Here, I’ll carry these out for you,” I said, leaving her to handle her purse and a couple quart pots of perennials, then added,  “I can’t garden for ten hours solid since I got arthritis.”

“Thanks.  I have RA and can only do so much at a time.”

“Ah, yeah,” I commiserated.  “You have to make dinners ahead, because the next day you’re too exhausted from gardening.”  She nodded, already tired from just the idea of the ordeal ahead.  “It’s fun, but you just run out of ‘spoons’!”   And then I loaded things into her car and we swapped the mutual thanks.  My attention turned to the gardening work of my own, left uncompleted or never even started.  Oh, and errands.  Here I was at the market nearly every day, but I kept forgetting to get my arthritis medicationn refilled!

“Hey Andrea,”  piped up one of my coworkers, “it’s nearly time for you to go on break.”  This clerk is a good guy; he’ll remind me when something is coming up, he’ll remind me when it’s time to start, and even after I’ve forgotten it.  He asks me if I remembered to clock in, and reminds me (several times) to copy down the next week’s schedule before leaving.  It sure is wonderful to have garden center clerks who are so helpful, especially when you when you’re having seriously distracted & forgetful AD/HD days!

* I’ve never navigated the women’s restroom in a wheelchair, but there are still the stupid doors to wrangle …

ADD-ing new perspectives

My daughter is sailing rather gracefully through her pregnancy — well, as gracefully as one can when they have reached the “beached whale” stage that is the third trimester.

And yet, as with many pregnant women, she is experiencing some “third trimester brain rot”, that intermittent or semi-chronic reduction in frontal-lobe functioning.  Meaning:

  • forgetting important things you meant to do
  • not packing things you meant to take with you somewhere
  • getting sidetracked and forgetting what you were doing a few minutes ago
  • moments of being adrift when you lose track of what you were about to do
  • dysnomic moments of losing words or names you normally have on the tip of your tongue
  • being spectacular at some higher cognitive facitilities (“Look at this great post-colonialist literary critique I just wrote!”) and then realising that you suddenly can’t remember how to do something really simple (“Why are my pants pockets wrong? Oh, my pants are on backwards.”)

I’ve yet to read why this happens, aside from sleep issues or “It’s The Hormones”, that generic disclaimer for all things annoying during pregnancy (or indeed, between menarche and menopause).

The good news is that the brain fog isn’t permanent.  I reassured her that “third trimester brain rot” usually starts to go away after the baby sleeps through the night.  She looked at me suspiciously; surely “third trimester brain rot” should go away after the baby is born?  But then I reminded her about the chronic sleep deprivation that is nursing a baby every two hours.  (Were it not a normal part of human development, such sleep deprivation would surely be outlawed under the Geneva Convention.)

Of course, it doesn’t help that she’s finishing up her college senior capstone project, and it would really be useful to get a solid night’s sleep, or to wake up from a long night’s sleep feeling more rested, or to be able to schlep all those literary refs around campus more easily, or to not spend 33.3% of her life preoccupied with peeing. But, there it is.

On the other hand, we have had some bonding moments that go beyond shared maternity.  One day she was complaining about the general forgetfulness and fogginess, and I pointed out, “Hey, now you know what it’s like for someone with ADD.”

“Omigosh, I couldn’t stand it,” she replied, dismayed at the idea of being permanently stuck in such a state.

“But the thing is,” I explained (somewhat defensively) “when you have ADD or ADHD, that’s what it’s always been like.  That’s what you’re used to.”  The point being that one doesn’t feel the same sense of loss when it’s a life-long condition, compared to a late-onset disability.

And despite the obvious impairments, there are some positive aspects to AD/HD, due to the different functioning patterns of the brain.  There’s the hyperfocus, abilities to make different associative and intuitive leaps, and often a visual thinking style that lends to a variety of design strengths.

Having done through a few re-iterations of this conversation, there seems to be less of an “Oh noes!” reaction, and more of an appreciation of the chronic difficulties that I and other people with ADD or ADHD face.  Not only that, but I think the reasons for some of my demands for structure and routines that I developed as she and her brother were young, are becoming more apparent to her.

Maybe there are just some “mom-things” that one doesn’t appreciate in quite the same way until becoming a parent.

On the other hand, there are still a lot of things I do that bug her, and we must ever keep re-negotiating our relationship, especially as we continue to live in the same house, but with changing roles.

With a price tag like that, you know it’s what’s best

Would you pay more for name-brand headache medicine than the generic or store brand?  If your budget is like mine, probably not; after all, the tablets are the same, it’s just the packaging that’s different.

But on the flip side, what if your favorite practitioner recommends an expensive treatment that will help you or your loved one recover from a chronic condition? Not surprisingly, treatments with higher price tags make patients feel better, even when there are not any differences in the treatments, nor even when the treatments are just placebos!  Per research by Waber et al., (“Commercial Features of Placebo and Therapeutic Efficacy”)

These results are consistent with described phenomena of commercial variables affecting quality expectations and expectations influencing therapeutic efficacy. Placebo responses to commercial features have many potential clinical implications. For example, they may help explain the popularity of high-cost medical therapies (eg, cyclooxygenase 2 inhibitors) over inexpensive, widely available alternatives (eg, over-the-counter nonsteroidal anti-inflammatory drugs) and why patients switching from branded medications may report that their generic equivalents are less effective.

In other words, patients perceive more expensive treatment as being more effective.  This is in many parts “research as confirmation of what we already know”, also known as “A Duh! Study”.  (Which is why it was in the 2008 Ig Nobel Awards.)  However, this preference for expensive treatments can also be a post-purchase rationalization, where we have the unconscious tendency to rationalize why the things we have paid for were such good choices.

Human beings are subject to a large number of cognitive fallacies and biases of judgment.  We unconsciously deceive ourselves in a number of ways, which is why scientists must use randomized, double-blinded, and repeatable studies with falsifiable hypotheses. (The word “falsifiable” is somewhat confusing or misleading; it simply means that the hypotheses can be proven wrong, which is statistically safer than trying to prove them correct.)

Our brains love to find patterns — that’s how we make sense of all the sensory input we’re bombarded with — but we will also see patterns even when they don’t exist.  Even the most earnestly objective researcher can misinterpret incomplete data, or give more attention to data that supports their hypothesis than that which doesn’t.  This is why double-blinded studies are important, so neither the study subjects nor the data gatherers know who is in the treatment or the control groups.

Naturally, shysters will take advantage of people by Read the rest of this entry »

Comfort-able

For the first time in months and months — far longer than it should have been, but there we are with the insane busyness of life — a friend and I got together at her house for dinner.

“You look like you’re finally relaxing,” she said after I’d been there a little while, and we decided to not wait in conversational limbo for the third person (who never did show).  “You were so stiff when you came in,” and she made reference by some expression (that now escapes memory) of how I was indicating being relaxed by behaving more normally.

Not “normally” in the er, Normal (neurotypical) sense, but me-normal, where I felt comfortable enough to sit and rock slightly, to not worry about making eye contact, to get a bit flappy at funny events or when agitated, to shed the pent-up motor tics.  To just be me. To “let my hair down” and to set aside unnecessarily restrictive social norms.  To eat my chicken and rice with a fork, and the still-crisp cooked green beans neatly with my fingers (as one does with fries or asparagus), because her table was Nicely Set for our aesthetic enjoyment and yet we weren’t standing on formality.

We talked about typical stuff, like the foibles of spouses, the concerns for college-age kids, the drudgery of eternal home repairs, the quirks of cats, of temperamental computers and the thrills of new mobile phones, of career changes, and the vicissitudes of economic times.

We also talked about atypical stuff, like the difficulties of college education and employment when dealing with various educational/neurological disabilities, of managing arthritis pain and joint issues, of the wonders of TMJ bite blocks, of dealing with the profound cluelessness of the general public for the extreme pain of migraines and how hospital Emergency (A&E) is a horrid place to physically be when in the throes of gut-wrenching-head-splitting pain and the snarkiness of some medics therein.

Crip chicks like we don’t diss on our disabilities, we diss from our disabilities.  It’s not poor-pitiful-me whining but the healthy pitch-a-bitch whining from someone who understands, even when our respective glitches are not all issues shared in common.

I need more social life, but there’s so much of ordinary socialising that I find enervating.

I’m not antisocial; the interest in socialising is not a binary form, where one either does it or doesn’t do it.  But over the years I have learned what I actually enjoy (as opposed to what one is “supposed to” enjoy).  My intro/extroversion levels vary wildly because some kinds of social interaction are nothing but draining, while others leave me (if not physically) at least spiritually recharged.

I’m not fond of socialising by large quantities of people all chattering with each other in the same room, where the conversations get all blenderized from my Auditory Processing Disorder, to where I end up trying to tease apart sequential fragments of half a dozen unrelated conversations, fruitlessly trying to follow just one voice or two, and reasoning out from fractured context what some of the mis-heard words could possibly be.

I’m not fond of socialising where the content gets watered down to less-consequential subjects of chit-chat, by dint of less privacy and some unwritten code of how long one is “supposed” to entertain time with another guest before moving on, and by the other unwritten rules of conversational quid pro quo, where my monologuing to fully deliver a story complete with back-explanations and thesis statements delivered at the end is discouraged in favor of witty repartee.

I like the time to mutually share and analyse our respective news, and the real, content-laden answers to our mutual questions of, “How are you?”  The real “How are you?” question, not the fluff of “How-are-you?” or “How-was-your-day?” that is the social minefield trying to distinguish between polite interested query of acquaintances and polite disinterested query of associates (that latter social coin that is all form and no content), or the mental quagmire of trying to answer “How-was-your-day?” when the question is so vague and our answers are so experientially linear and tangential instead of whatever the hell others were expecting.

I was comfortable — we both were comfortable — because together we had created a social environment that enabled our mutual comfort.  It was an agreement that had been developed by long familiarity and by various conscious decisions over decades, to create a friendship that fulfilled our individual needs over the culturally-proscribed forms.  True friendship enables positive interactions, and supports needs and affirms and enriches our lives.

Here’s a toast to real friendships!

Wanted: Planet with longer rotational period

It’s not just me. A lot of people whom I know in person or via the internet have complained about near-futility of trying to get to sleep earlier at a “reasonable” time, meaning one that would give a person enough hours of sleep before having to rise for the next day.

My children and I can’t get to sleep before 11 p.m. unless we’ve been hit by dire viruses, or else have simply stayed up the entire night. In contrast, hubby can retire early and then go from laying down to snoring in less than five minutes, and we’re all mystified at how he manages this! Obviously, such a somnolent physiology was not something our children inherited from dad.

While our young adults have endeavoured to find college classes that start later in the morning (not unlike the majority of college students out there), I myself do not have the luxury of that option. I’m expected to be at the school at 7:30, which means leaving at 7:00. (In reality, I need to leave by 7:10, but I keep aiming for 7:00 to give me the necessary buffer in my nutz ADHD distractedness.)  Given the zombie-like staggering arthritic stiffness and mental sluggishness of my morning routine, I need to roll out of bed at 6. Now that really isn’t an unusual time for working folks to get up, but my problem is that for most of my life I’ve not been able to get to sleep until midnight, even when I’ve put myself to bed by 10 p.m.

Part of that delay was due to the fact that Read the rest of this entry »

shrinking

My Things To Do list has lain dormant in my purse all week. Not for having forgotten which Very Safe Place that I stuck it into. Not for having too few things to do to bother writing them down (as if).

Rather, because there is so little I can get done in a day. The effective list of Things To Do is reduced to:
dressing and eating breakfast,
working at job #1,
eating lunch and grading papers for job #2,
working at job #1,
eating dinner and preparing something like a lesson for job #2,
teaching job #2,
doing a bit more preparing something like a lesson,
and crashing in bed.

On Saturdays there are exciting departures from this plan: Read the rest of this entry »

“Mama said,

‘There’ll be days like this,’

‘There’ll be days like this,’ Mama said.”

The Shirelles, “Mama Said”

Coming down with some virus most likely, as the school nurse says it doesn’t look like strep throat (despite the sore throat that’s making it hard to lecture).  I can deal with that.

Headache, only ’bout a 4 out of 10, not so bad of itself. I can deal with that.

Ditto the tinnitus, which alas, seems to be making it more difficult to understand people, especially those students more than a few feet away from me, which is most of the time — why do the most soft-spoken students sit in the back corner?  The auditory processing glitches don’t help, either; I’m sure some of the students think I’m not paying attention, or am losing my hearing.  At least no one is going around yelling to me in the mistaken impression that volume = clarity.

Five hours sleep.  Definitely need to get to sleep sooner, and I would were it not for the class prep I have to do before and after classes.  Okay, now it’s getting really challenging.  I’m dropping words in the middle of my sentences once or twice an hour, and does that ever make me feel stupid.

I’m hungry because I didn’t eat much due to the sore throat & canker sore.

Two of the pieces of paper I really needed to have with me were not in my binder.  No, I’m sorry, I don’t remember the date of the next exam right off the top of my head.  No, I’m sorry, I haven’t memorized the ID labels to all of the slides (but I can tell you what’s important about the slide).

We were reviewing the results of the first exam.  This is the first college-level science class that many of the students have had, and some of them haven’t had a science class in years.  Bumpy ride.  It’s also the first full exam I have written, and every teacher knows the hidden hazards of writing such.

For some reason I decided to hand the graded exams out, rather than just letting the students pick their own test up.  I’m faceblind, and have not yet memorized the seating chart.  Definite planning error on my part.

My PowerPoint — that delightful gizmo that helps keep the tired, the distracted, the forgetful, the sick, and the first-time teacher from losing track of the game plan — the PowerPoint file on my flashdrive proved to be an older version that did not have the other half of the slides I needed to remind me what I was going to tell the class this evening. That too, of itself I could deal with, although the presentation was not at smooth as I would have liked, and we had to go back a few times and fill in something I had not mentioned earlier.

But all of these things together, oy vey!  I muddled through everything, but did not feel very brilliant or smooth.  I didn’t even have all of the lab equipment fully prepped because I had rushed in right before class.

And then shortly after class started, one of the professors came in to do a surprise Observation of me as a new instructor.

At least I didn’t have my trouser zip left undone, or have a strip of toilet paper (loo roll) stuck to my boot!

Mama said there’ll be days like this …

Depiling

That is, de-pile-ing*.

* Not to be confused with depilling, which is trimming off those annoying “pills” that form on knitted garments. Presumably those wee balls of fuzz form due to the blasted orneryness of the universe, especially with regards to the cosmos’ dreaded knack for providing supplemental stress to anyone with OCD tendencies.

Depiling means to systematically remove piles of clutter.  On my desk, that means not just the usual bills, statements and paperwork, but also:

  • documents to be scanned,
  • Copy Center requisition forms,
  • old appointment cards and unnecessary receipts unloaded from my pockets and other ephemera,
  • 35mm slides to be scanned,
  • an empty postage-stamp strip,
  • wire twist-ties,
  • caps to ball-point pens I don’t even use,
  • hort industry infomercials masquerading as press releases or “educational materials”,
  • spare tins of lip balm and cuticle salve,
  • important receipts to file,
  • a really cool concave rock to use as a water dish when I refresh Rosie’s habitat,
  • the booklet on Inservice courses for Job #2 that I cannot attend because of Job #1,
  • beads that are still surfacing from when the curtain tie-back snapped last month, Read the rest of this entry »

Backwards Symphonies

“It’s been a long week — I bet you’re ready to decompose.”

I stared at my husband, blinking through the mental fog of too-many-jobs-not-enough-sleep.

“I’m not ready for the compost pile yet,” I replied, trying to figure out what his latest malapropism was meant to be.

“Or whatever the term is,” he added.

My brain finally catches up. “Decompress,” I answered.

What an incredibly long week.  I can’t remember the last time I had one like this, and in my over-busy world that’s saying something.

Wednesday last week I had a pneumonia vaccination, which left my arm so sore I couldn’t take off my jogbra without assistance, nor even get my hand up to head level until the weekend.  Moreover, Read the rest of this entry »

The Crystal Ball Crack’d

The Kid recently took the ACT test, which like the SAT, is frequently used by colleges to determine scholastic abilities, and in his case helped place him for which college writing class he needed.  He had to ask his sister what the test was like, and her impressions about its difficulty level.  I could not personally provide any opinions, because I had never taken the ACT or SAT.

I never took them because no one thought I would go to college.

They made massive assumptions about my abilities and my future. So here’s what happened, and something to think about. I welcome you to please post comments, and more links to other positive blogs and sites.

My grades in secondary school grew worse over the years, and I had to re-take a semester in one class (English of all things, which in later years proved to be ironic when I became a freelance writer, with hundreds of items in print).

By this time in my life, my parents had divorced.  My dad lived in another state, and was even more of a non-player in my life.  Alas, my mother had spent years futilely trying to make me more “normal”, from requiring me to learn right-handed penmanship, enrolling me in a “charm school” at the local Sears & Roebucks to improve my feminine graces, and so on.  But as the years wore on, my faults (problems) became more and more apparent.  She no longer described me as “very bright”, but was quick to list all my failures and describe them in damning detail, until I was ready to vomit or pass out from the stress (though I never did, even though either would have been a relief).

By 9th grade it was apparent to all that I was not gifted scholastically, and the general consensus was that I was lazy, stupid at math, not trying hard enough, and acting up just to make her life difficult.  When she was drunk, my failures and interests and personality traits would be compared to her ex-husband’s, “you’re just like your father, the bastard”.  Even as much of a socially-clueless 14 year old that I was, I knew that these kinds of comments were untrue and inappropriate, and the problem was with her attitudes and her drinking.  But they still hurt, terribly.

I would not be diagnosed with ADHD, Auditory Processing Disorder, and Prosopagnosia until I was in my 40’s.  Such diagnosis hardly existed in those days; certainly my difficulties were not considered to be due to anything but my own personal failings.

No way, my family and school officials decided, could I be college material.  I could not keep track of my assignments, I still struggled to learn and remember my multiplication facts into 8th grade, and I flunked or barely passed classes.

Given my social difficulties and subsequent lack of dating, and even my utter lack of domestic abilities (mom warned me off taking a sewing class because doing so would “ruin my GPA” – grade point average), I was obviously not highly marriageable. This was the 1970s, and most people still thought along those lines — an astonishing number of girls went to college to “get their MRS”.

The goal then was to get me some kind of minimal trade training, so I would, as she fiercely reminded me many times, not be a burden on the family. It was made plain to me that once I graduated high school, and then later turned 18, I was to be out on my own.  I should not expect financial assistance from her.

So I was enrolled in typing, which was a miserable experience beyond the whole ordinary ordeal of learning to type on manual typewriters.  The room was a cacophony of noise.  The instructor was adamant about constant attention to task, proper posture, and graded with the intent on us producing perfection — as soon as a student produced a typographical error, then the score was made. (Additionally, the students’ pages were  held up to the light against her perfect copies to check centering and spacing). There were many days when I would produce an entire page that was otherwise perfect but for a typo in the second line, and my grade would be an F because I had such a low word-count.  Given my problems with developing manual speed, tracking text (near-point copying), attention, and transposing letters and numbers, I struggled to get a C grade.

But the clerical work that was deemed best for me also required taking bookkeeping.  Not surprisingly, this was also a very difficult class for me.  My aptitudes and interests were not really taken into consideration, because after all, even if writing and science and art were what I liked best, I had not done well in those classes, now had I?  Besides, clerical work was what my mother knew, so like many parents she expected me to follow occupational suit.

Unlike many such students, my story has a relatively happy ending.  I did manage to graduate high school, to everyone’s relief.  A year later, I even enrolled in an evening class at the local community college.  College classes were not easy, partly from my intrinsic difficulties, partly from not having the necessary study skills, and partly from not having a solid academic background.

But the glory of the American system is that such colleges provide opportunities for adults of all ages to acquire the these things, and to gain higher education. I worked hard, and slowly figuring out how I learned, which was not always in the ways that others thought I should study.  Sometimes I had to drop a class and re-try it later on, to finish it successfully. Later on in my 40’s I was to also get some of my issues diagnosed.

I now have a Master’s of Science. I teach college students.  No one would have expected this based upon my previous performance. (Employers who place near-complete trust in Behavioral-Based Interviewing, please note!)  And this point, amongst all the others about the perils of attribution errors, and learning disabilities, and dysfunctional families, this point is crucial:

A child’s future abilities cannot always be predicted,

when based upon their current abilities.

Many parents of children who have developmental disorders worry that their children will never be able to attend school, or finish school, or go on to college, or hold a job, or live on their own, or be loved by a partner, or have a family, or talk, or be potty-trained, or any number of milestones.  Just because the child cannot do the same things that their age peers can do, or are expected to do.

This is one of the biggest points of contention or discussion between the “autism community” (parents of autistic children) and the “autistic community” (children, teens and adults who are autistic, and many of whom are parents as well).  Even beyond the farcical assumptions that either community is monolithic with regards to attitudes and knowledge and politics et cetera, there are inherent issues that need to be mutually addressed.

One of the best resources for the autism communities are the autistic communities.  If parents go around just talking to other parents, especially those other parents who are consumed by the “Terrible Tragedy and Selfless Suffering Families” world-views, they may fall prey to this easy assumption:  If my child can’t do it now, he’ll never be able to do it, and our lives will be ruined.

Sure, not everyone takes it to that extreme.  Sure, there are a few children who do not achieve many of those life-goals.  But those lack of achievements does NOT automatically mean that their lives are ruined, or their families’ lives are ruined. They do NOT automatically mean that people cannot live relatively happy, healthy, and productive lives.

Please do NOT assume that not being able to use speech as a reliable means of communication is the same as not being able to think, or not being able to communicate, or not having anything to communicate.

Please do not assume that because a child does not learn in a traditional manner that they are learning “the wrong way”, or that they cannot learn at all, or that they must be taught “remedial learning lessons”.

Please do know that even when children have problems, and are slower to acquire skills, they are not doomed.

Please do not give up on them.

“Don’t talk to me like I’m an idiot.”

~First words (at age 35) of an autistic man [quote source]

I welcome you to please post comments, and more links to other positive blogs and sites. Kindly see the newly-updated “NOTES TO COMMENTERS” box in the top of the left sidebar for important information. Read the rest of this entry »

Prescription for Thought

This belated post is especially for Debora, who asked for my impressions about ADD/ADHD medications for children.  (Disclaimer: I am not a doctor, nor do I play one on television.)

Medicating kids or adults for ADHD is a sticky topic.  Everyone has opinions!  Like many topics of heated discussion, usually everyone has several good points to make, and there are always a few people who take things to absurd extremes.  So let’s look at these points individually.  (I’ve boldfaced the points, so if you’ve already reached a state of analysis on that point, you can skip to the next one.)

Does ADD/ADHD even exist?  Is it just some scam made up by drug companies to make money?

Some years ago I received an email from someone who had decided the latter. I replied back with the following, which I have updated to reflect new information: Read the rest of this entry »

A few updates

The 92nd Edition of the Skeptic’s Circle is up, and The Lay Scientist gives us the latest press conference news as given by the Team Skeptic Manager Martin, from the state-of-the-art Olympic training facility in Beijing!  Prepare to be amazed — but never bamboozled.

The July issue of the Pain-blog Carnival is now up at How to Cope With Pain blog.  Readers share a variety of subjective experiences and treatment information.

Speaking of things painful, I put up a couple of photographs I modified to demonstrate some of the visual disturbances I experience during migraines.  Due to the trigger potential, I put these on a special page.  (The images are described for those with impaired vision.)  Alas, the Kid was laid flat by a migraine today — the preventative meds certainly help reduce the numbers of attacks, but they don’t completely eliminate them.  However, he reports that the new medication is a definite improvement over the old one, wooziness notwithstanding. A quiet “Hooray” for this encouraging news.

And although the timing isn’t quite “news” anymore, it’s not so late for it to be “olds”, so do check out the 42nd Disability Blog Carnival over at Pitt Rehab, where Greg gives us a break from the usual busyness for some summery relaxation at the beach, and plenty of great links.

As for me, I have to blame day-long teacher training class all week for my dearth of posting.  It’s been really good, but so intense — having to sit and focus on attending, listening, and learning for hours on end is hard.  Every day I run an errand right after class, and then come home to crash for a 20-minute catnap for my brain to do some filing before I can even think about cooking dinner.  The fatigue is a good reminder of what it’s like for all our students!

(Now if only the tinnitus would Shut Up.)

P.S.  Time to play ADD hide-and-seek: if you were a $100 calculator left in some random location by a teenager, where would you be?

P.P.S.  We already checked the breadbox.

Remembering to Remember to Remember to …

I went and drew the bath. When the tub was full, I took off my pyjama top, and realised that I had forgotten my towel.

I fetched the towel and then realised that I meant to mow first before bathing.

Shut the bathroom door to keep the heat in, I went and changed into gardening clothes. Unplugged the mower from the charger, got one strip done, and then realised that I had forgotten to put on the bag — I wanted to bag the grass clippings to use them for mulching the vegetable garden.

Fetched the bag and put it on the mower. Mowed several strips, enough to have filled the bag, and then found out that I had forgotten to remove the chute block that lets the grass into the bag.

At this point, I realised there was a trend: I kept forgetting things, including the planning-ahead bits. Oh, yeah — I forgot to take my medicine this morning, including my ADHD med.

Usually I try to put my pillbox atop my MacBook when I go to bed, to remind myself the next morning to take my medicine promptly.

But that requires remembering.

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