photograph ©Kristin Lord 2014 |
The dog days of late
August have been a memory for the past two years due to unseasonably cool and
wet weather in the northeastern provinces and states. As we headed into Labor Day weekend, I saw no
reason not to spend my last free morning taking down some overgrown foundation shrubs
from a four-foot painter’s ladder, especially when routine yard work usually
costs more to hire than I get paid.
“Let’s
just clip the tops to my height and then saw off the base,” I thought.
The first one went down quickly. No reason at all to
hesitate on the three others I had in my sights, at least not until I was three
feet in the air and heard a “snap” emanating from my right knee. After a few
minutes of excruciating pain, I was relieved to walking toward the shed, the
clippers in one hand and the ladder in the other.
Before five more
minutes had elapsed, I was on the ground twice more. The ladder had long since
spiraled off to the left, while the clippers narrowly missed my head. One of
the neighbors, hearing my torrent of Anglo-Saxon expletives, came running and
grabbed my cell phone for me from the car, while a second neighbor offered to
drive me to the hospital. I was down a third time before she could get me
there. On the proverbial pain scale of 1 to 10, these four falls were each at least
a 9. The only way to get through this was not to fall again.
The x-ray showed
nothing broken, which left me with a provisional diagnosis of a soft tissue
injury. “Can I drive?” I asked the attending ER physician. “I’d play that one
by ear, since you have hurt your right knee. Press down on the foot rest on the
wheelchair and see how you feel.” “The foot rest is broken.” “Then try the edge
of the foot rest.” “Thanks.” For once, there was no pain. I’d play it by ear, I
thought, literally and figuratively. If I could press down on that
malfunctioning wheelchair part, then I could probably use the piano pedal. If I
could manage the piano, then I could probably drive, and if I could drive, I
could work. It also followed that there was no reason to make more than minor
changes at the office. Indeed, I had already solved one problem while waiting
for the x-ray. I asked the ER physician for a physiotherapy requisition, got
fitted with crutches, and phoned our neighbor to come get me. Meanwhile, my
husband would pick up our daughter from her own work.
I got home, made my
way in through the small step at the back door, and sat down to work-related
paperwork. I even managed to get upstairs to bed and downstairs the next
morning.
I was going to be just
fine. See?! Left to my own devices, I went out the back door
on my crutches, checked my safety in the car, then drove to nearby Fergus and paid some bills.
Before I did that,
however, I whacked away at more of the paperwork that was sitting on my hard
drive. Little did I know that that would
be no more successful at that than attacking the sapling in the back yard the day
before. The Apple gurus in Waterloo, 30 minutes away, had told me a month
before that I was unlikely to need any more work on my computer, but if I did,
they would have to replace the memory board under warranty. Of course, the memory
board took that moment to go haywire. And of course, the .05 per cent of my
work that was not saved externally or emailed was the .05 per cent I needed for
a letter of recommendation and for the start of term after Labor Day.
The folks at Apple
were good at scheduling an appointment, once they had located my extended
warranty. They even understood why I no longer had my hard
drive hooked up to my Time Capsule (too many lightning strikes to the house
—that is apparently a common problem). Although the staffers made no
promises, they were optimistic that I could get the files onto my external hard
drive and memory sticks, which I could then install on an older machine, and
they even hopeful that I would have my “good” laptop back before I started
teaching the next week.
All I had to do was
drive to the Apple Store in Conestoga Mall by 7:30 that evening.
No, let me rewrite
that last sentence: all I had to do was to check my privilege. There is no
public transportation where I live. My ability to continue working while
temporarily disabled was entirely dependent upon being able to drive and having
access to a working vehicle. I also have a moderate amount of third-party
coverage for physiotherapy, thanks to the fact that the other adult in the family has a job with benefits. Single-payer medical care got me
through the hospital. My work is of the sort that can be managed by an employee
on crutches with insignificant adjustments (one of my departmental colleagues
worked from both crutches and a wheelchair at different times over many years).
This matters a lot, since I did not have to worry about losing my job. It also
matters because I might not have been eligible for workers’ compensation, given
that contract academics are not usually paid over the summer and that the
accident occurred at home in August. In sum, I was lucky that I did not have to
ask about the law but rather was able to turn up for work on schedule.
Along the way, I
discovered many other areas in which I could no longer take ordinary activities
for granted —not just the running or the sports that I had planned to take up
again but perhaps never can. (The jury is out on whether I will make a full
recovery, or even whether I should have an MRI, for which there is a waiting
list in Ontario.) Like most jurisdictions in O.E.C.D. countries, Ontario has legislation covering disabilities. Like most public
employees in these jurisdictions, I have been required to attend a briefing on
this legislation. Over the Labor Day weekend, I refreshed my memory about both
the law and its limitations in a hurry, grateful at every step of the way (so
to speak) that as these problems go, I was on the lower end of necessary
accommodations, and that at least some of them would likely be temporary.
Both the law and best
practices in many countries require “reasonable accommodation” to provide equal
access to the complete gamut of venues, services, and activities for anyone who
would otherwise be eligible if he or she did not have a disability. In many
cases, there is a difference between the minimum required and what is truly
equal access. For instance, the leader of our seminar at work gave the example
of a blind student taking a survey course that had one chapter on art and
architecture. “Reasonable accommodation” would at the minimum entail replacing
the unit on art and architecture with a mutually acceptable alternative, such
as having the student read a story or a play that made reference to art or
architecture in addition to the plays already assigned for everyone else. A
better approach would be to work with the student to make as much of the
section on art and architecture as possible available in a format which that
student could use, if necessary by getting expert assistance. The law, however,
recognizes that there are practical limitations to what may be feasible.
Despite generally
noble intentions, “reasonable accommodation” and universal access are easier
concepts to develop on paper than to put into practice. Most communities have a
large number of private houses that have been turned into businesses or
semi-formal public places, and not all meet standards of accessibility, whether
literally or in practical terms. Modern public facilities vary enormously in
accessibility. Some are superb. The new main entrance to the library at Wilfrid Laurier University, my employer for the last decade and a half, was designed with universal access in mind (photograph below). It is also carefully engineered to fit into the rather awkward slope between the library and the surrounding ground and buildings. The planter at the front will have a community garden (unfortunately, not edible at this point), and there will be more seating. Cannon Design, the architectural firm behind the project, did a splendid job actualizing the desires of the library staff. By coincidence, it was opened a day or two before my accident, and was almost immediately put to use by yours truly.
Conestoga Mall in Waterloo and Stone Road Mall in Guelph each have an ample supply of accessible parking. In fact, they appear to have more than the two major shopping malls in the Toronto area that we visited on consecutive weekends, despite the malls in Toronto being several times larger. On the whole, I have ended up with more problems in Toronto than that good city surely deserves. I had to cancel plans to attend a large public event held at the downtown convention center in Toronto because the nearest subway station was closed and there was no place to sit down at the function.
Conestoga Mall in Waterloo and Stone Road Mall in Guelph each have an ample supply of accessible parking. In fact, they appear to have more than the two major shopping malls in the Toronto area that we visited on consecutive weekends, despite the malls in Toronto being several times larger. On the whole, I have ended up with more problems in Toronto than that good city surely deserves. I had to cancel plans to attend a large public event held at the downtown convention center in Toronto because the nearest subway station was closed and there was no place to sit down at the function.
The most
egregious example of lack of access I have seen so far turned up when I phoned the Ministry of
Transportation of Ontario about my temporary accessible parking permit. The
staffer at the office of the MTO nearest my home, in a building that it had
occupied for no more than a decade,
rather apologetically informed me that either I or someone appointed by
me would have to retrieve the application from the Ministry in person, as it
was not available on line. In order to get the application processed in a
timely manner, I would then have to return the form with documentation, again
in person. (I am unclear as to whether I could have delegated that part of the
procedure, but in any case it was moot because of scheduling issues.) Doing so
locally would entail walking up and down twelve cement steps. Otherwise, I
could drive 30 minutes to the village of Arthur or use the outlet near my
office, 30 minutes away in a different direction but obviously more convenient
for me. Unfortunately, the MTO outlet near my office had a thirty-minute wait
at an off-peak time and no tag and number system allowing people to use one of
the few available chairs. A kindly woman let me cut ahead of her to retrieve
the form, which took a matter of seconds, but it would have been inappropriate
to do the same when finalizing the document, a much longer procedure. I drove
to Arthur, where I was the only client there.
What works for one
person may not for another. While the manager of the local supermarket was more
than happy to offer put me into a motorized cart, that may be overkill for
someone with crutches or a cane. (A friend who uses two canes to get around
mostly shops at smaller food stores.)
Disabilities are
expensive as well as time-consuming, a point seemingly lost on many of those who set the rates for people
who are on longer term disability pensions. There are noticeable increases in
living expenses even for someone in a short-term and relatively straightforward
situation, as shopping for groceries at the deli or on line usually costs more
than going to the supermarket. (Once again, I was lucky to have family members
able and willing to shop from my grocery list and to have a good and
reasonably-priced deli in the area.) Modifications to vehicles and housing are
unaffordable for many people who need them, even in wealthy countries, unless
they have access to public or private insurance. People who cannot drive often
have other impediments.
I have been fortunate
to have escaped the worst of what could have happened. Despite the issues of
parking and access to certain venues, I have experienced a great deal of
generosity from family, friends, colleagues, and medical professionals. In
particular, I racked up one of those debts that can never be repaid from a
friend with a more serious disability and one of longer duration. She had
invited me to join her at a restaurant for lunch before she knew of the
accident. On the day we met, I could not find her vehicle in the parking lot. I
must have arrived first, I thought, and so I left her the one accessible spot —
but in a scene reminiscent of O. Henry’s short story “The Gift of the Magi,”
she had placed her own car in such a way that the accessible spot would be left
for me. In the end, neither of us took it, and we each ensured that the other
made her way safely from the restaurant to her own vehicle. That same friend
urged me to do everything reasonable to ensure that I could walk safely without
a cane or crutches before the onset of ice and snow, lest some of my leg
muscles atrophy over the winter, leaving me with more permanent damage than
would otherwise be the case.
We never know when we
or another person will become disabled, whether physically or intellectually. Students
in one of my classes once wondered about the extra table and chairs located haphazardly
at the front of the room. I replied that they were probably there in case a
student came in with crutches or a wheelchair, although admittedly they should
be better arranged and labeled.
The spot was occupied
for its intended purpose before lunch the same day.
Some queries for Friends and Quaker
organizations:
In what ways do we
ensure that we are aware, both as individuals and as a Religious Society, of the range and types of
disabilities (of all degrees and likelihood of permanence, whether visible or
non-visible, including health and mobility-related, psychological, social,
learning, and developmental disabilities), the status of current legislation,
and our moral obligations as believers in equality? Do we get competent
professional advice when we are unsure what to do?
Do Quaker-related
facilities meet the highest standards of accessibility law and practice? If
buildings are grandfathered in under previous law, what is being done to bring
them up to code? If buildings are not accessible, do Friends’ business sessions
and other decision-making meetings take place in them? What about parking and
public transit routes?
What procedures do
your Meeting have to ensure that all members and attenders have, to the extent
possible, equal opportunities to participate in the spoken aspects of Meeting
for Worship and Meeting for Business? Large Meetings may have the money and the
justification to install a hearing loop, but what can be done in smaller
Meetings? At the very least, agendas and supporting documents can be posted and
the text of proposed minutes run by people who need a written summary.
Likewise, are Meetings able to ensure that those with visual impairments are
able to access minutes of Meetings for Worship for Business? Can we make it
possible for those with limited mobility to participate in discussions
electronically?
If Meetings for
Worship are held in private homes, to what extent are those homes universally
accessible (at least one entrance, toilet and sink, and suitable seating)? Do
the homeowners have adequate liability insurance? Do they tell people in
advance about any companion animals that may be part of their household?
Do Friends Meetings
take reasonable precautions concerning ice build-up (if relevant) and fall
prevention?
Is programming for
sessions such as Quarterly, Half-Yearly, Area, and Yearly Meetings designed to
be accessible to all?
Do Quaker children and
young people with exceptionalities (whether physical, psycho-social, or
intellectual) have access to the same range of Quaker-oriented programming and
facilities as their peers who are not so affected? If not, what can reasonably
be done to rectify the imbalance?
Do nominating
committees ensure that adult Friends and attenders, regardless of disabilities,
have suitable opportunities to serve the Meeting and/or larger Quaker bodies?
Can Friends “think outside the box” about what might constitute ideal
qualifications for a position?
Do Friends label foods
brought to potlucks and other gatherings, and do they try to provide a variety
of options so that everyone will have something to eat, regardless of food
restrictions? (Ann Arbor Meeting, in Ann Arbor, Michigan has an excellent form that can be filled in by
people contributing to potlucks.)
Are Friends aware that
others, both inside and outside of the Meeting, may have chemical allergies and
sensitivities that preclude being near people wearing perfume and cologne?