All posts by Peter

New Wheelchair–A Story about Bureaucracy

After about a year and a half of wrangling with the system, Jon has a new wheelchair.

His old wheelchair was never appropriate for his needs, and only really fit him in the last six months, although it was prescribed five years ago, with a rebuild three years ago. Given the cost of the rebuild, it should have just been replaced–in retrospect was a poor decision, but not ours to make. Though we authorized it. Let me elaborate.

To obtain a wheelchair that is funded (in whole or in part) by the public system, you enter a bureaucratic machine that is still a little overly complicated, to put it gently. I think that every individual involved is doing their best within the system, but I have a few bones to pick with the system itself.

To begin, you talk to a physiotherapist, or in our case (this time), the seating clinic of Bloorview MacMillan, the local hospital for disabled kids, who assigns you a PT. The first question our of their mouths is “Who will be the vendor?”, meaning the private company who will supply and service the wheelchair. The PTs are not allowed to recommend a vendor, which is understandable. Problem is, how are the parents supposed to know of a good one? We don’t even know how many suppliers there might be – wheelchair vendors aren’t exactly likely to be in the local mall! The only people who have a sense of the options out there – who work with all of the suppliers on a daily basis and who are most likely to have an idea of an appropriate vendor – are the physiotherapists, and they are not allowed to have an opinion.

Frustrating. At least in our case we have hooked onto some nice folks at HME Mobility , so off we go.

But as of last year Jon hadn’t grown out of his chair. And since we were asking for some government funding for the chair, the physiotherapists were extremely reluctant to authorize a new chair until he grew too big for the old, bad chair. (Without a compelling reason for a new chair there’s a chance that the government wouldn’t authorize the money. Of course, in my view the fact that Jon couldn’t wheel the old chair without slouching over is a damn good reason, but I guess that’s harder to put on a form than “grew too big”.)

Remember, these chairs are what the physiotherapists worry about in terms of
long-term posture–the kids are sitting in them for eight hours at school, and some of them at home as well. They are very touchy about how an incorrectly-prescribed chair could lead to permanent issues down the road.

But from what I see, if the chair is inappropriate but not too small, you are stuck. I’m sure this disconnect comes from the need to balance the expenditure of government cash with the needs of the child, but it does seem like everything is serving the system, and not the people in need.

As well, parents co-sign for the equipment along with the physioterapist who recommends it, but of course, we are going entirely on the recommendations of the PT. So in the long term it’s deemed as the parents’ fault if the equipment is inappropriate. We were led down the garden path by Jon’s first PT and vendor, and now we’re the ones that gets blamed for it by the current PTs. Grrrr.

As we delayed for growth, we dealt with some other bureaucratic issue on another front, so initial funding concerns for us were resolved and the hospital was told of this in late April, so were given an immediate appointment in… mid August.

This was the most productive meeting: We had a room of experts. The vendor, the therapist and the seating technicians, all taking measurements and discussing which bits and pieces will be the most beneficial for the wheelchairee. Sometimes we had a chance to offer an opinion, but more often it was a flurry of jargon. Occasionally we would interrupt to make sure we got a sense of things. Fair enough. HME was to provide the chair, the hospital would provide the seating. It would happen within 2-3 weeks of provincial approval.

Provincial approval took just over a month, and HME worked quickly, but it was early December before we were asked to come for the final touches. And that’s when we found out that though the vendor had supplied the parts correctly, all of the seat parts that the Bloorview Seating Clinic ordered were too small. They tried to brush it off by claiming that Jon had grown several inches since August. But since 1) they got other simple basics of the order wrong (like the type of seat belt latch we had all agreed on) and 2) WE’RE HIS PARENTS AND JUST NOT THAT STUPID (he had grown maybe one inch, if that) we just stared at them. They asked for another week, which turned into three. Just before Christmas, the new seat parts came in and we’re away to the races.

A chair that fits. Easy to push. Better for him to practise wheeling himself.

So onto the next challenge. In his new perfectly-fitting chair, Jon automatically slumps forward. What the ???

Well, we’ll see as the New Year progresses.

Happy Boxing Day!

Sorry for the quiet second half of December folks, it gets a little busy around here due to a self-created annual blitz. Every year, one of us (Laura this year) does up a New Year’s illustration and the two of us go into overdrive as we produce a New Year’s card, a fully designed Jon-themed calendar and DVD of Jon’s home movies for family, and we create a gifts for Jon’s teachers and Ed. Assistants– all of these based on that visual theme. So although we started into this when paying work had died down earlier this month, Laura and I were beavering away, up well past 2 am Christmas Eve working on the final design touches for the DVD and slipcase.

We go overboard.

So, in short, your card is on the way. And if you are family, you’ve got your calendar already, unless you live in the Yukon, in which case it’s on it’s way. DVD’s will be posted to the upper and lower West Coast in the next day or two.

Hey, maybe by New Year’s we’ll post a gallery of previous cards on Jon’s site. I’ve been meaning to do that… (Great, another deadline!)

Blog spam make Peter-Hulk angry

Grrr. A very odd event, but the second time it has happened: I was deleting a spam comment to this post, and when I rebuilt it had become the message!!

The original message is gone. Not that it was much of a message. The first time it happened we thought it was an accident (hence the title of this post), but now that it’s happened twice, I’ll assume that someone clever with no life has found a little bug that allows this malicious hack. It apparently requires the right conditions–I must have been sloppy in how I went about deleting…very odd.

Making Of Big Monkey

Just in case you don’t know already: Now that he’s finished with The Lord of the Rings, Peter Jackson is remaking King Kong (based on the 30’s version). He’s creating little five minute Production Diaries about various aspects of making it (some less serious than others). They are very well done and someone’s taking a lot of time to put these together. You’ll find them at kongisking.net. Now you know.

Shadows


Friend Andy linked me to this extremely cool picture taken by the Cassini probe that’s orbiting around Saturn. What you see is Saturn’s ring system (bottom) casting shadows across the planet’s clouds (with a cute lil moon flying past for good measure). The colours are as you would see them if you were there.
Click on the image to see a bigger version at NASA or here for the pic and a full description.

Book 50


It was just over 7 years ago that we took Jon to the opthamologist to hear her diagnosis that he was cortically blind–his eyes were fine, but something after the optic nerve, inside the visual cortex of the brain, wasn’t. And that he would likely see nothing beyond shadows for his entire life.

That night that Jon patiently posed for the cutest baby pictures we ever got from him. He seemed to know we needed a pick-me-up.

Meanwhile, visual therapist Mary Crow (or through Parentbooks ) had been waiting for this. She had visited us once, watched Jon, and said he’d have to be diagnosed before she’d be authorized to take us on. I’ll never forget Mary’s second visit declaration “He’s taking peeks.”

It’s a long story between there and where we are now. Like many kids with cortical visual impairment, Jon gained some function around 18 months, and it’s been a struggle to regain what we could from there. Jon’s vision is by no means normal–he percieves things visually in completely differently way from what we do, and always will–but we’re far ahead of what even some experts predicted.

This was with amazing support from a couple of great visual consultants, and a fabulous teacher who believed in Jon and started him on a bridge-reading course last year. It started with heavy repetition. We were all concerned with how well Jon could see the small words on the photocopied sheets, so for each book I made new booklets with the type heavily enlarged.

Last week, Jon hit the last of the series, Book 50.

It was a version of Goldilocks and the Three Bears, in simple sentences. The booklet I created for it was 27 pages long; most of the pages had four sentences of type (36 point size). We expected it to take Jon a few days, not for complexity, but for sheer length–you could see him get tired reading it. But he insisted on reading it through each time (and had a tantrum when I tried to introduce the concept of a “bookmark”).

He had it mastered in four days.

He’s moved onto the pre-primer of a new series. We decided to try him without type enlargement. He gets a little close to the page, but he’s able to read without enlarged type. And he’s already almost done the first book of the three-book series before moving on to the primer.

Book 50 feels like a milestone moment.