What a Way to End one Year and Start a New One

01/03/2014

I ended 2013 by undergoing the neck surgery I discussed in my last post. It would be cruel to not tell you how everything turned out.

The collaboration worked. Surgery lasted longer than estimated, but apparently much of that time was spent positioning me so they could get my head immobilized in the proper position to do what they had planned. In that process my top cervical vertebrae snapped back into place, making the eventual surgery easier.

I come out of the recovery room at about 4:00PM, eight hours after I was put under with nerve monitoring wires attached to all my fingers, toes and various other points on my body.

Surgery Image 5

Surgery Image 5 (Photo credit: UCDMedicine)

Thanks to the excellent surgeons and the high level or care I received at Valley Hospital, I went hope less than 48 hours after that. The plan was to keep me in the hospital for up to four nights but after just two I progressed so well I was sent home. I have already ditched the narcotic pain medicine for Tylenol.

My head is back on straight, I can turn it and move it up and down and side to side. While the range of motion is still limited, it will improve over time. I’m still not allowed to do anything, and I still have to wear my Miami brace 24/7 for a few more weeks, but a return to normal activity is in sight.

I am extremely grateful for all the support I’ve received from friends near and, in some cases, very far.

I have never been one for new year’s resolutions. I reflect enough the rest of the year and don’t normally feel a need for year-end reflections. But 2013 has been a particularly rough year personally and professionally in ways I cannot talk about now. I’m just glad that it is over.

I start 2014 with a new outlook. I have a sliver of a cadaver’s hip in my neck to remind me that life is fleeting but our usefulness does not end with death if we don’t want it to. I already signed a donor consent form noted on my driver’s license, but I’m redoing my living will to also specify organ donation in any form useful.

I am growing a beard, just to see what it looks like. Its a safe risk, but I need to start small. The bug risks are too scary for now.

I have a new opportunity to grow and develop into the best school librarian I can be, and I’ve certainly learned the value of collaboration. Don’t be surprised to get a call, text, email or tweet from me proposing some joint project.

But most of all I have learned I need to take better care of myself, physically, emotionally and in every other way you can imagine.

I hope your 2014 will be all you want it to be. I will be working hard to make sure mine is.

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Opening Minds for More than One Day

05/01/2011
There are days and there are days.

There are days I like: Thanksgiving; Labor Day; the first day of spring.

This is a day I’d rather not see again; Bloging Against Disablism Day, the sixth in what I fear will be a rather long run.

For the uninitiated, disablism is how most of the world treats people who have disabilities, like parking in a space reserved for handicapped people “just for a minute” while you run into the store. If that isn’t clear, a detailed description is available.

I’ve come across an example of disablism in my school.

Using underarm crutches.

Image via Wikipedia

Yesterday there were two students in our library all day. They weren’t there to do research; they were there because they have injuries that require them to use crutches. Apparently our school does not allow students using crutches to go above the ground floor, but all our classrooms are on

the two higher floors. We have an elevator but students can’t use it.

While all of their classmates are getting instruction, they sit in the library. The teachers are supposed to send down work for them to do but they usually don’t. Even if they do, it is a textbook and a worksheet, not exactly inspired teaching.

While all their classmates are chatting, socializing and learning together, these two boys (last year it was girls) sit and talk to each other. Sometimes they get so desperate for conversation they talk to me!

These boys don’t really think of themselves as disabled but they are, at least for the next six to eight weeks. That is not the problem.

The problem, what makes this an example of disablism, is that despite kids repeatedly breaking ankles, legs and other things necessitating crutches, my school has not come up with a better plan for dealing with these mobility issues and the students who have them.

It is truly an issue of “out of sight, out of mind.”

People who have disabilities don’t hide like they used to, don’t make it as easy to keep them out of mind as it once was. They’re on the streets, in the stores and at work more and more all the time. That visibility is helping to create mindfullness.

I hope this blog post contributes to this growing awareness. With any luck I won’t have to write a post like this next year.

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Oops, there I go again…

08/25/2010
White Tiger Mouth wide open!
Image by kabils via Flickr

I need to learn to keep my mouth shut more often.

This is doubly so when my ‘mouth’ is my fingers typing here, on Facebook or, most important, on Twitter where  I am known as Spedteacher.

Here’s what happens when I don’t.

I hate when that happens. But it is completely my fault when it does.

So now I’ll be easy to find on most Tuesday evenings starting at 8:30PM NYC time.

#spedchat is for teachers (and not just special ed teachers, either), parents, administrators, students and everyone else with any connection or interest in special education issues.

Topics proposed for the first chat on August 31st are:

  • How can parent-teacher relations be improved?
  • What do grades mean in special education?
  • Is inclusion working for general and special education students?
  • How do we get general education teachers to understand? (the current leader in the voting)
  • How have school budget cuts affected special education?

You can participate in the decision about what the topic will be by voting here.

To participate in the chat just log onto Twitter ( if you don’t have an account you can get one free, here ), then search for the hashtag #spedchat.

For a better explanation of all of this please visit my co-conspirator and #spedchat moderator Damian Bariexca’s excellent blog.

I hope to see you Tuesday.

I’ll probably get myself into even more trouble.

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Academics or Life Skills? Yes! No! Maybe!

05/07/2010
Floor balance scales, foot lever and two dishe...
Image by Lichfield District Council via Flickr

Essential Questions are fun because there is no one right or wrong answer.

There are many answers, each with the ultimate potential to be right or wrong, or even change from right to wrong or back at any given time.

Our Essential Question today is: Academics or Life Skills? Should special education teachers emphasize one over the other, or is there a happy medium?

My answer: Yes.

My other answer: No.

My third answer: It depends.

I’m not trying to be difficult (there are those who will say I accomplish being difficult without any effort at all) but this is one of those questions of which the answer one gives depends entirely on one’s conception of the purpose of education.

My conception of the purpose of education is that it is essential that children be prepared to lead adult lives.

Vague?

You bet!

This is the problem with statements that need to apply to everyone.

Even if we narrow the statement to apply only to special education students;

It is essential that children be prepared to lead adult lives to the best of their individual abilities.

Not much clearer, is it?

The problem is that in stating the purpose of education, we are trying to answer an essential question.

Every student, whether or not in special education, needs an individually crafted answer to questions of whether academics or life skills should be stressed and to what extent one should be stressed more than the other.

It gets more basic than that: For each individual student the definition of what is appropriate to teach changes as each student develops.

When it comes to education, there are no easy answers.

It is time we stopped looking for them.

___________________

This is the third and final posting of a string of blogs for the Classroom Insiders series at We Are Teachers. I appreciate the opportunity I’ve had to reach their audience.

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Finally, Something BADD To Say

05/02/2010
spinal fusion model 2
Image by Dillon K. Hoops via Flickr

Yesterday, May 1, was Blog Against Disablism Day.

I wanted to write something good, something intelligent, perhaps something engaging as my contribution to the effort.

Nothing came to mind.

Then I picked up the New York Times this morning and read about Dayniah Manderson.

Ms. Manderson and I have a lot in common. We are both teachers. We both teach in the east side of the Bronx. We both teach 6th graders.

When the elevator in my school doesn’t work I haul my cart and carcass up the stairs.

When the elevator in Ms. Manderson’s school doesn’t work she can’t do that.

My cart, at its most full, weighs about twenty pounds.

Ms. Manderson’s weighs just under 300 pounds.

Ms. Manderson has spinal muscular atrophy and her “cart” is her electric wheelchair.

Spinal Muscular Atrophy is something one is born with.

Children born with Type I usually die before they turn two. Ms. Manderson has Type II. People with that form of the disease rarely live past 30.

I don’t know how old Ms. Manderson is. It doesn’t matter so much because she is doing a lot with whatever time she has.

But this essay is not about Ms. Manderson.

It is also not about the principal who told Ms. Manderson that if she were hired as a teacher the students might “throw her down the stairs.”

No, this is about the other principal. The one who looked at Ms. Manderson and saw a teacher with potential, not just a person with paralysis.

I don’t know that principal’s name, but he or she got it and is one less person we have to convince not to engage in disablism.

Small victories need to be celebrated.

Next!

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Sticks and Stones… Yeah, Right

03/22/2010

It happened again.

I’m sure the person responsible for it didn’t mean to do it.

Why, I’m sure she didn’t even give it a second thought.

That is the crux of the problem.

We don’t give the words we use a second thought, at least not when we say them out loud.

When we write we choose our words carefully, aiming to get just the perfect nuance, the right shade of meaning.

When we write we recognize the power of words, how choosing one instead of another shifts meaning in subtle or overt ways. We use dictionaries and thesauri in tandem to aid us in our search for precision in language.

I do, and I am confident many other writers, cognizant of the complexity of our mutt-like English language, do as well.

While Professor Henry Higgins bemoans that “One common language I’m afraid we’ll never get,” the rest of us are free to revel in the diversity of words that Dutch, French, Turkish, Arabic, Spanish, Portuguese, Saxon, German, Greek, Latin, Sanskrit, Italian (itself a motley collection of distinct dialects), and more have contributed to what we commonly call English.

It is that very diversity that allows linguistic precision, and it is that capability for precision that makes it so very distressing when people who should know better use words carelessly.

It is one thing to use an imprecise word when speaking, but quite a different thing when one is writing and, perhaps, has the time to choose words more carefully then read and revise by picking a different word or phrase to better convey intended meaning.

Still, despite the opportunity to do better, I’m sure the person responsible for it didn’t mean to do it.

Perhaps I should say persons because the offending term appeared in a magazine article and this magazine has an editor who might have caught the offending term and suggested an alternative.

That this did not occur leaves me to presume dereliction of duty or, worse, intent.

I will not embarrass the writer, editor or magazine by identifying them, partially because that is not how I operate, but also because the offensive phrase is so commonly used.

Here’s what I’m going on about; just a few simple words:

“Regular education,” or in this specific instance, “regular classroom environment.”

I am known in many corners of the online world as Spedteacher. It’s a handle that takes SpEd, a common abbreviation of ‘special education’ and adds it to my job title.

Perhaps I should call myself ‘Irreguteacher ‘ instead.

The opposite of ‘regular education’ is irregular education. A classroom environment other than a regular one is an irregular one.

All people are different. We all come with a broad selection of abilities and things we’re not so good at doing. How can it be that only a very small group of that overwhelming selection of abilities is labeled ‘regular’ and the rest are implied to be irregular?

In the text for one of the many inclusion-themed t-shirts available from his Nth Degree Catalog (The Home of Wheelchair Boy Jeans) Dan Wilkins explains the problem with the phrase ‘regular education’ much better than I can:

“One of the problems I have with the Special” and “Regular” education dichotomy is that its very existence forces us to label every kid just so we know which box to put him/her in. It gets worse. Then we take all the kids in one of the boxes and we put each of them in their own box and slap another label on it…. perhaps two…or ten. After a while we forget about the kid in each box and just see the box (and all its labels). It gets worse. Inside the box, the kid, misjudges the edge of the box for the horizon and comes to believe ‘that’s all there is…’ In the eyes of everyone, including the child, the kid and the box become one. So much for dreams…the chase is over before it begins.”

There it is.

In general, it is better to call the classrooms most students are in “general education.”

Calling them anything else should be irregular.

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A New Perspective From the Old

02/22/2010
Hands
Image by dbz885 via Flickr

Today is the first day back at school after a week off and I’ve never been as eager to deal with children again.

I spent most of the past week tending to my 85-year-old aunt and uncle who live about an hour away.

He is in good shape and able to take care of himself, but she’s been in hospital or rehabilitation center since taking a nasty fall in late November.

At first the problem was a broken arm.

Now she is losing her mind.

It is odd how many of the same skills I use daily with my students I now use talking to my aunt and uncle.

He’s always been a deliberate person, considering options from every angle before making a decision, but now he processes slowly and remembers less easily, so waiting for him to make a decision requires every bit of patience and gentle prodding I can muster.

My aunt’s once focused mind is now lost in a world of its own creation. Her increasingly bizarre statements show she is no longer the person my uncle married 50 years ago this past Valentine’s Day.

Listening to my aunt is exhausting.

I’ve always said that I get energy from my students and that is so. Dealing with the elderly, I am discovering, has the exact opposite effect, rendering me  an old battery trying to start a car on a very cold winter morning.

Don’t get me wrong; I am happy to be able to help my childless relatives. I’m the oldest nephew and my uncle, a major figure in my childhood, has remained a reliable guidepost throughout my life.

Even so, dealing with my elderly relatives is far more difficult than dealing with the most difficult students.

I care deeply about my students, and not just their academics. I try to be for them what my uncle was for me; someone I could depend on when things got rough, someone who helped me learn that I did not have to be the person I often saw being modeled for me at home.

I tell my students that all experiences produce learning, but that we have to capture it and connect it to what we already know.

I enjoy working with my students, but I never thought of them as a relief before.

Being there for my relatives this past week has given me a valuable new perspective on what I do every day.

I will try to remain open to the lessons that new perspective offers.

.

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I’m Not In The Game

09/16/2009
flip_front
Image by Terry Freedman via Flickr

I’m not teaching this week and I may miss a few days next week.

I’m not happy about it.

I tore something in my knee and can’t walk until its repaired, probably sometime early next week.

One of my associates on twitter says I’m getting grumpy because I’m hurting.

I told him to deal with it.

Grumpy, indeed.

Now I know how baseball players on the disabled list feel. At least they get to go watch the games.

Another member of my twitter crowd says my students will miss me.

My students don’t know me, and I don’t know them.

I taught three days before becoming disabled. I’m just some large old guy in their eyes.

They may not even remember my name. But I’ll know theirs because of an idea I picked up on twitter.

On my first session with each class I took my Flip Video camera and had each student say their name, one or two things about themselves, and their name again. I’m spending my time watching the videos and connecting names with faces and interests. I even know how to pronounce all the names.

I wish I could credit the person who gave me this tip, but I don’t recall who it was. I’ve learned so much from my twitter PLN that its almost impossible to recall who taught me what even though I’m sure they’re all very memorable teachers.

While its great that I’ll know my students’ names, I’ll have other fences to climb.

Right now my students are not learning the procedures I want them to follow, not taking the assessments I created to test their prior knowledge. They’re not tuned in to my plans for the year.

Neither am I. Even though I knew I’d be teaching general education students this year I did not plan well. If what I saw and heard in the discussions on the first day or two are indicative, I have seriously underestimated the thought processes and knowledge of my 6th grade class. I only had one session with my 8th grade class and we spent that doing the name video and a bit of paperwork, but I bet I made the same underestimation of them.

Teaching requires a constant series of evaluations of and adjustments to the needs and abilities of students.

Continuing my baseball analogy, teaching is like playing shortstop. You keep track of the game situation and generally plan what to do if the ball is his towards you. You plan for a ball on the ground and for one in the air (with tech and if the tech doesn’t work), but you still need to react to the specific speed, spin and placement of that hit that just left the bat.

Some teachers are as good as Derek Jeter and others are more like Heinie Sand, but we all have to deal with the balls hit to us or the students in front of us.

I’ll get back on my feet and back in the game. I’ll adjust, and my students might also.

So what if we start a few games behind.

It’s a long season.

We can still be champions.

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Incidental Learning

08/11/2009
Pair of forks made of sterling silver.
Image via Wikipedia

Nothing that follows should be interpreted as demeaning or diminishing the importance of education professionals. No teachers were harmed in the creation of this blog post or in any of the events described in it.

Teachers and education administrators sometimes fall victim to the conceit that learning only or mostly occurs in schools. The fact is, every one of us learns most of what we know and can do outside of schools

Some of that out-of-school learning is every bit as deliberate and curricular as any teaching unit, a mother teaching her son to do the laundry or a father teaching his daughter how to hit a curveball for example.

But much of the learning in and out of school is unplanned and unintentional. This is constructivism writ large because an individual assembles meaning from disparate and not necessarily related circumstances or events.

I call that incidental learning.

Eunice Kennedy Shriver died this morning. That news helped me recall some incidental learning I assembled from the first time I met her and her sister-in-law Ethel Kennedy, Robert Kennedy’s widow.

Thirty-five years ago I was a radio news reporter and wire service stringer working on Cape Cod. The Kennedy’s, particularly the Kennedy children, were often good for a story. That’s how a nice, nominally Jewish lad like me ended up attending Mass more often than most of my Roman Catholic friends. I always knew where I’d be December 24th at midnight.

One hot August day I got a phone call from a colleague at a radio station in Connecticut. A busload of men, women and children were on their way to one of the Hyannis beaches, from which they were going to march along the shore to the Kennedy compound to protest the lack of public beaches accessible to people who were not residents of the town the beach was in.

What any of that had to do with the Kennedys was puzzling, but I knew a story when I saw one. I was there when the bus arrived and watched as the men in jackets and ties, women in dresses and fully dressed children got off the bus and started walking south toward the Kennedy family’s property.

It was brutally hot and humid, but they marched without pause. As we walked I interviewed the leaders of the group and got the gist of their complaint against Connecticut. They were marching on the Kennedys because they figured it would get them publicity. They were correct.

Eventually we got to the Kennedy homestead. You cannot see any of the buildings from the water’s edge. They are hidden by substantial sand dunes that some say were erected by the Secret Service when JFK was President.

For about ten or fifteen minutes we all stood around admiring the sand dunes or looking at the waves on the water. I sweated profusely, and most of the men and women were mopping their brows with handkerchiefs, but not one loosened a tie or took off any item of clothing. Neither did the children.

We just stood there.

I’m not proud of this, but I was waiting for the police to arrive, almost hoping for a noisy, perhaps violent confrontation that I could report on, sell to one of the networks and earn an extra $20 or so to supplement my $160 weekly salary.

Then I saw what I thought was a mirage.

Two tall, thin women carrying silver trays with large pitchers on them were coming down the dune followed by a half-dozen children, each carrying a silver tray.

As they neared I could see that the women were Eunice Kennedy Shriver and Ethel Kennedy

When they reached us, they  started pouring and serving cold lemonade to the protesters while their children circulated carrying sterling silver trays and offering sugar cookies.  Then the the various Kennedys and Shrivers stood around chatting with the protesters as if they were guests at a party.

It was almost surreal, but as I watched I realized I was seeing something special.

I was seeing class. and I was seeing a lot of it.

Class wasn’t something I had come to expect from the Kennedy family, but as the lemonade poured from their silver pitchers, class poured from Eunice Shriver and Ethel Kennedy

I didn’t figure out what it all meant until a few years later.

I was out of radio and working in a bar. One guy felt that another guy got in his space and comments led to shoving. I separated the jerks before they could fight, and threw one out. Later that night, as I reflected over a scotch and water, I recalled how those protesters got in the Kennedy’s space and how different their reaction was.

It occurred to me that people react to provocations many different ways. Everyone gets provoked, but we control how we respond.

And one more thing…

When you respond with class, things generally work out better.

Thank you Mrs. Shriver, for the Special Olympics and everything else you did for people with mental retardation.

And thank you for simple acts of kindness and class.

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Disabled? Who? Me?

07/26/2009
450 mm by 450 mm (18 in by 18 in) Handicapped ...
Image via Wikipedia

People are always asking me silly questions. Well, they’re silly to me and I doubt the questions, or any answers I might give, have any real import to the inquisitor. Perhaps they are just trying to make idle conversation. I don’t know. I’ve never been good at that sort of thing.

I’m talking about questions like,

“What is your favorite song?”

“What’s your favorite fruit?”

“What single malt whisky do you like best.”

I answer questions like that by saying it is a matter of context. When selecting a whisky to sip during an evening of conversation with friends (defined as people who have never asked me anything like one of the questions above) I sometimes enjoy the peppery flavor of Talisker, but on a damp foggy night in late autumn when I am sitting in my chair reading and listening to the muffled sounds outside, the iodine-laced Laphroaig appeals to me. Or when looking for a light refreshment….

By this time I’m looking at a slack-jawed head nodding slowly up and down with “uh huh” emanating from it. You’d think that would slow me down, but I’m just getting going.

At some point I’ll really hit my stride and say something like, “you see, context determines everything, even what we call disabilities.”

A long time ago I was involved in the disability rights movement on Cape Cod. This was long before the American with Disabilities Act. I belonged to an organization whose main activities involved teaching what I then considered to be “normal” people (I know, but I was young and foolish and this story is about how I learned better) about disabilities. We’d set up obstacle courses at malls with steps, doors too narrow, with handles too high or opening the wrong way), and other situations people see every day. We would give people the chance to maneuver through these obstacles in a wheelchair, using crutches, or wearing a blindfold and using a cane. Then we’d give them our spiel about architectural barriers.

One evening following one of our mall appearances all of us went out for drinks. The group included a married couple who both used wheelchairs because of polio, a woman with muscular dystrophy who would go on to be named Miss Disabled America, and a young woman, named Brenda, who had a spastic form of cerebral palsy and who may be the funniest person I’ve known other than my wife.

It was summer and we were on a deck over Hyannis Harbor chatting about how people react to people who have visible disabilities. One person said that people would speak very loudly to him.

“I tell them my legs don’t work but my ears do.”

Then Brenda spoke.

“You know what I hate. I hate those well-meaning people who look at me and ask what happened to make me the way I am, like there’s something wrong with me.

“Well, I fixed a couple of them the other day. I was standing by myself in the mall waiting for my ride to the eye doctor. These two little blue-haired old biddies kept eying me. Finally they came up to me and said, ‘Oh, you poor dear. Are you all right? What happened to you?’

“I got really pissed off. I looked them in the eye (at this point we all start laughing because Brenda cannot hold her head still at all). Well, I looked them in the eye as best as I could, smiled sweetly and said,

‘Ladies, what you see here is the result of ten years of hard sex!’

“I thought they were going to faint.”

Later on that evening I asked Brenda what she meant when she said, “…like there’s something wrong with me.” The answer I got was one of those simple statements that change your life.

“What I am, HOW I am, is normal. It is normal to me. It’s the only frame of reference I have. I’m normal to me, it’s the world that’s different.”

‘Tis.