Some of these pieces were originally on the 'Red Squirrel Party" Blog, but I thought they might detract a little from the more political polemic there.

So I started this one.

The title, just in case the odd reader may not have fathomed it, is a deliberate mis-spelling. Because those of us who are disabled know very well how the non-disabled are all too prone to "diss" us about what we are (or or sometimes erroneously think we should be) able to do . . .

Monday, 25 November 2013

Things People Say. . .

There's an article about what non-disabled people say to disabled people in the Huffington Post, in that favoured format of 'Ten things not to. . .". It wouldn't be a surprise to anyone who's disabled, or especially, a wheelchair user, what they are.

The first  ("Don't tell someone in a wheelchair how attractive they are as though it's a surprise") sadly, is not one commonly heard by Crippled Squirrel here. Though maybe "You must have good muscles to do that" counts? That's something I heard a bit during the summer as I whizzed up the ramp onto a bus and did my sharp three-point turn to shoot backwards in to the wheelchair space.

I'm not quite sure what my response to that should be. "Fancy a quick feel?" Maybe not.

Moving on, we have "I broke my leg/ankle/got an ingrowing toenail and I used a wheelchair, so I know what it's like." Actually, no you don't.

"You're an inspiration". The equivalent of this to males is something about being 'brave'. There's nothing particularly inspiring about being in a wheelchair, really. Or brave. It's just something you have to do.

"It's fate, karma, god's will", whatever. No it wasn't. In my case, as in some others, it was an accident.

"Let me help you!" Now this is a tricky one. Nothing wrong with that, as long as people ask first.  "Helping" takes several forms, some people in wheelchairs need, some they don't. It's people who don't ask first that are the problem. Someone rushes up and puts their hand between your legs to pick up your dropped cigarette lighter . . .Well, would you do that to just anyone? It's a bit disconcerting.

But it's people who decide you need an extra push that are not just disconcerting but frightening. It really is a nasty shock to find yourself suddenly propelled forward a few metres unexpectedly. Especially as it's from behind, and you don't see it coming. You wouldn't suddenly grasp a stranger round the waist from behind and twirl them round on a public pavement, would you?

It's very scary, that sudden feeling you've totally lost control over where you're going. Wheelchair users aren't particularly paranoid, but just a few seconds of fright as you wonder if you're going to be pushed under a bus or something . . .well, you can imagine, can't you?

Happened to me quite a lot this last summer.

And there's the perennial sidebar to the 'god's will' thing. The idea that with all that cheerful determination and will power, there's bound to be some miraculous cure one way or another, and one day you can throw your wheelchair away. Well, no, again. If there was, we'd have done that already. That determined look is just because, if you're disabled, you just have to be determined to get a lot of things done. Like climbing a mountain or swimming ten lengths of an Olympic pool or something.

Nothing particularly new about all that. But it was some of the responses that took me aback. It rather looked as though even some people who thought they'd got the point still managed to miss it.

"If i see a woman in a wheelchair who dropped her keys, i probably would offer to help, not so much because of the wheelchair, but more because it's a "damsel in distress". and let's face it, if you're cute, it's only going to encourage guys more to want to be helpful. this may not be fair, but it is life."

"I gave to one of my very good friends confined in wheel chair due to multiple leg fractures(had a nasty fall in the house) one latest book of her favourite author and two cds made of all soothing popular cheerful instrumental music so that she can listen this keeps her busy& cheerful and less chance of self pity."

"I hope you realize that you are admirable to some people - because you are a living reminder of all that able-bodied people take for granted. Make peace with the fact that your life has more meaning than you could have anticipated."

"As an adult who is well over 21 I am becoming impatient with being told what to say and how to behave. I refuse to become hyper-vigilant about how someone may react when my words don't meet their standards."

"Something I would like to ask , does your back hurt from sitting so much, I know if I sit for too long my back hurts and so does my backside."


Ouch.

Wednesday, 31 July 2013

Oh, what's the bloody use?

What a difference a year makes. there on the right, today, there is a quote from our politicians that goes beyond irony.

'This house… acknowledges the government's collective determination to build upon the London 2012 Paralympic Games, and create a legacy that shines a light on the abilities and achievements of disabled people."
Hasn't it bloody well just shone a light on our 'abilities' and our 'achievements' this last year? As far as this government is concerned (and the Opposition is no better), whatever your 'abilities' are, your opportunities for making any us of them have been increasingly disabled; what 'achievements' that we might have once had in our sights are being ever further put out of our reach.

And, of course, cuts, cuts, everywhere. I'm having to wait longer and longer now for the only ameliorative treatment that makes life even vaguely resembling what's normal for non disabled people for just one month in three. Thanks to NHS cuts, that's now going to be one month in six.

I'm weary of it all. Why don't they just round us up and put us on the trains to the gas chambers and be done with us forever? At least it'd be a quicker death, and the pain of it would be short.

Sunday, 28 July 2013

Can you Climb Everest in a Wheelchair?

No; and you can't get up all the way to the top of the Eiffel Tower in Paris in one, either. . .As a 'crowd-funded' disabled American making a film about it has just discovered. You can't get up to the dome of St Paul's cathedral in London in one either.


“I was right,” said Reid Davenport to his friend on the London Tube, according to his article in the Washington Post. “Europe is not accessible.”
And how did he reach this conclusion? 
I sat in the underground train exhausted, wondering how long it would be before we got to our stop. There was no announcement coming from the overhead speakers, but a man’s voice saying “Mind the gap” rang in my ears. My friend Pat was sitting next to me, holding my collapsible wheelchair in place.

I was visiting Pat and two other American friends studying in England. As we made our way to downtown London, Pat had to carry my wheelchair up and down flights of stairs at various tube stations because most of the elevators were out of service. Because there were no ramps, I was constantly forced to get up from my chair at various points to mount a step or more. And the 18-inch gap between the train cars and the platform made me wonder how British residents in electric wheelchairs manage to get around.
Well, Mr Reid and Pat, the answer is by bus. Did no-one explain that every single bus in London has a ramp and a wheelchair space? And wheelchair users travel free? (Your 'free bus pass' is your wheelchair.) I travel on them all the time in mine.

He claims, by the way that the Paris Metro, in comparison to London is all wheelchair accessible; it isn't. And, unlike London, not all buses have ramps. And if you travel by TGV (as I do) there are steps up onto the trains from the platforms, which are lower on the continent than in Britain. You need to arrange help.

But Europe-bashing generally seems to have become an increasingly popular sport in the US media ever since that infamous outburst about 'Old Europe'. It's just a little surprising that we should be written off for disability access as well like this.

Heaven knows, I moan about the kind of advance planning you have to do even here in London if you use a wheelchair; but that is true of anywhere. I keep wanting to try the Tube myself, and there is a map online which tells you exactly where you have to 'mind the gap' and the still infuriatingly few stations that have lifts and level access to the trains and the street. (Which neither Reid nor his |London friends knew about?) I'll get around to it one day; it's just that I live in a bereft area ass far as wheelchair access to the Tube goes, and getting on the Tube in a wheelchair involves getting on buses to get onto the tube anyway. . .

Mr Davenport 'did' four countries in twenty days. Or was it four cities? Dublin, London, Paris, Brussels. And the latter two by air, apparently. That would have been easier by Eurostar and TGV. Then his wheelchair might not have been damaged in the hold of the plane, either.

He made a film about it. I don't think I'll look out for it. 

Tuesday, 28 May 2013

Independent Living

Declaring independence isn't quite as easy as I thought. Well, declaring you intend to be is one thing; achieving it, relying as little on others as you can if you're using a wheelchair, turns out to be rather harder. But I'm not the only one to discover that.

A few weeks ago (I was on crutches that day, not on wheels) I tried to get some people on a rather crowded bus to shift out of the wheelchair space (or do I mean 'buggy space'?) so a young woman in a powered wheelchair could get in.

Blank incomprehension. The driver's efforts to get people to move didn't come to anything either. So she ended up parked sideways on, instead of safely against the backrest the way you're supposed to. I've had the same problem a few times, and you can't seem to get the idea across that if the bus stops suddenly, it's their feet you'll be taking off at the ankles. . .

However, we got talking, and she said when she got her wheelchair she thought it would make her more independent. She'd be able to get around more, without having to rely on her husband to push all the time. I said I'd put a motor on mine for the same reason.

"But," she said, "it didn't make me as independent as I thought it would. If I want to go much of a distance, I've still got to get my husband to come with me, so he can push when the battery runs out . . ."

I've hit the same problem. Well, not with a husband, obviously. According to the specs, the motor on mine should do ten miles. I don't know how, though: perhaps only if most of it is downhill? So far, it looks as though it probably won't last much more than half that.  I got that motor second-hand, and had to get a new battery for it; I ran out of power after less than three on the old one. And, of course, just at the point where the rest of the journey home was all uphill.

I'm luckier than my fellow bus traveller, though. She has rheumatoid arthritis which has affected her arms, and she can't wheel herself. She said, actually that some times she can't grip the joystick that controls the motor either, and has to nudge it around with her fists.

Thought for designers, here: every laptop has a trackpad. Why hasn't someone come up with something similar for wheelchair users that they don't have to grip?

Anyway, like her, for the moment, my happy thoughts of trundling along on my own all around London and getting to places I haven't been to for years because I'd have to walk too much either to get there or once I got there, and walking gets painful after a couple of hundred metres, are on hold.

At least until I work out how far that damn battery will take me. A friend suggested I simply rode around the block until the battery died to find out, but I already know what the surrounding scenery looks like, and that sounds a very boring exercise indeed. So I'm pottering about locally in different directions, with a cautious eye on the hilly bits and bus routes, so if the battery runs out on me, I'm not faced with the wheelchair equivalent of climbing Ben Nevis to get home.

I really hadn't understood until last year how strong you need to be to wheel even a lightweight wheelchair (even with an equally lightweight 'Squirrel' in it) even a kilometre.

It's tough. A lot tougher than I thought before I had to start doing it myself. Unless you have the sort of biceps marathon wheelchair racers have. And developing those weightlifting in a gym ain't within the range of possibilities for someone with a damaged spine like mine. It's just going to have to be practice. And aching arms. And I used to think I was reasonably strong for someone rather slightly built.

I could, I suppose, somehow store a spare battery under the wheelchair somehow, but with the motor and battery fitted, I have a wheelchair that already weighs twice as much as it does without. Those lead-acid batteries are heavy, man.

But Boeing gave me an idea. No, not the one about carrying a small portable fire extinguisher in my cabin baggage if I ever fly on a Dreamliner. Just about lithium batteries. They're generally smaller and lighter, I argued to myself. So, one would be ideal to stuff in the little bag on the back of my wheelchair to use as a kind of reserve fuel supply. After all in the days when I drove a car, not a wheelchair, I had a car that had a little reserve petrol tank tucked away under the boot.

Independence, however, as Ben Franklin, or Thomas Paine, or maybe George III, probably said, has its price. In this case, a 12V 17AH lithium battery (nice and small and light) with charger, a mere £150. And that was a special offer . . .Not sure how far it would take me, either. Apparently they're meant for electric golf trolleys. (I thought they were powered by human beings called caddies?) And they will last for 18-26  holes. I have never played golf;  nor had any interest in it. Except for taking a short cut across a golf course every now and then at night to get home quicker at one time.

(I gave that up after falling into some kind of pond in the dark. I'd always thought golf courses had holes in the ground full of sand, not bloody water.)

So I wonder how far 'eighteen holes' is? Haven't golfers heard about metres and kilometres? How long is one hole? I thought it was only a couple of centimetres. At least that's what I remember from being a kid on a putting green. I'll need to get a bit further than 52 centimetres on one battery. That wouldn't even get my wheelchair up a bus ramp.

Could be good in winter, if these things get as hot in proportion as my laptop battery does, though. I'd have an inbuilt heater. But would I need to clip a fire extinguisher to my wheelchair just in case it did a Boeing on me?

Anyway, a hundred and fifty quid? I don't have that sort of money to chuck around. I'm not a golfer. And any more of this government's damned cuts, I'll need that. I'll be scrabbling around down the back of the settee looking for stray five pence coins, let alone a tenner.

Independence costs, doesn't it? More than I ever imagined when I had more of it.

Sunday, 12 May 2013

My Space? Or Your Space?


When I first saw the new 'advice' for buggy-pushers a few months ago, I thought it was rather nice us wheelchair users were being looked after. I was a bit ambivalent as to whether it was really necessary, though.

Yes, I've been stuck at bus stops having to watch two or three buses leave without me, either because there are already one or more buggies in the wheelchair space I need.  Frustrating for me; for a lot of non-disabled people, something, I guess, that would lead quickly to an outbreak of 'bus rage'.  But it's something we have to take phlegmatically. No bus-driver is going to chuck a mother with a baby in a buggy off a bus to let me and my wheelchair on.

I've shared my wheelchair space with them. Once I'm in and safely parked, that's OK by me. Just as long as they're willing to move out of it so I can maneouvre my wheelchair out and off the bus.

That, by the way, like getting into it, is a little trickier than people might think. If most drivers had to do that sort of to-ing and fro-ing into a parking space, while constantly risking running over four or five people's feet, they'd soon start complaining. You wheel yourself in forwards, you see; but you then have to turn and back into the space so your wheelchair back rests against that vertical backrest they put there that people lean against so they can have comfortable long conversations on their mobiles.

It is really annoying when you have to explain to people like that who won't move, that the bus driver can refuse to start until I'm safely stowed against it and got my brakes on. And it's no good looking at me resentfully for needing their cosy standing place; they'd be (and a few times this last few months have been) a damn sight more resentful if I delayed their bus journey any longer than I already have while they wait for the ramp to come down and retract again.

But they are, mostly, open to persuasion, and I tend to put down their sometimes initial obstructionism simply to not understanding that my wheelchair can't bend round corners. Even so, I've skinned my knuckles on the grab rails a couple of times when people won't even shift their legs and feet, let alone actually stand up for a minute to make it easier to get in.

But it's the buggy owners that really have become a nuisance. And it's sometimes not even buggy owners with babies in the things, only shopping. (And sometimes, it's real shopping trolleys in the way.) To have to ask. let alone occasionally actually beg) someone to move either of those out of the way when there's completely empty luggage space up front, is immensely irritating.  It even gets to look like and sound like a confrontation, sometimes. Why, I don't know. It ought to be simply a matter of common sense.

There was an example yesterday. But I'd better explain quickly why it happened to someone else in a wheelchair, and not me in mine. I had one of my regular epidural injections into my spine just over a week ago, so, for a few weeks, until it starts wearing off, if I only have to walk short distances between buses, I can use crutches.

That trip started well. The bus was full (except, of course, for the woman who was sitting in one of the 'priority seats' at the front with her shopping in the other staring blankly and deliberately ahead refusing to acknowledge that anyone else might need to be as comfy as her shopping). But, as I settled myself against the wheelchair backrest and got a good hold of the grab rail, another offered me her seat. So thus it was I was sitting in one of the seats facing the wheelchair space, as three other people crowded into it.

At which point, the driver let the wheelchair ramp down, to let in a young woman in her wheelchair along with her young daughter. Only, of course, for her to come to a halt with people crowded around her so she couldn't get in. I asked people to move; I explained  that a wheelchair had to go against the backrest. The three there did move, eventually; but they simply moved into the aisle and wouldn't budge enough so the wheelchair could turn round.

And then . . .a woman raced her buggy up the ramp and pushed it right up to the wheelchair, driving it over my feet and knocking my crutch awry as she went. The bus driver told her there wasn't room, wheelchairs had priority, and she'd have to take her buggy off. She shouted at him and glowered at both the young woman in the wheelchair and me. We were lucky, in a way, because the driver  had obviously had enough, had realised he had some damn stupid (or damn stubborn) passengers, and set off even though that wheelchair wasn't 'docked' properly.

Even with the brakes on and properly placed, if a bus stops suddenly you can still almost take someone's feet off at the ankles: it's happened to me and the only thing that stopped my chair breaking both a passenger's ankles was me being able to grab the rails with both hands and hold on hard as my chair slid towards them.

Which the young woman I'm writing about would not have been able to do. It turned out, as we got talking, she suffered from severe rheumatoid arthritis, and wouldn't have the kind of grip or strength in her arms I can employ. She was actually relieved; she told me that she's actually been told to get off a bus by the driver more than once in the same situation. There's something pretty wrong there, isn't there? To be blamed for the intransigence of other people because you are disabled.

I thought, once, we weren't going to see that kind of thing, that kind of implicit blame game—"Your problem being a cripple, sod all to do with me, why should I give a fuck?"—any more. But now qfter the last year or so since I had to start using a wheelchair much more often, that looks like just another illusion to be dispelled.

She had a motorised chair, she said, because, apart from her condition not allowing her to wheel herself about any more—and you wouldn't believe how much strength that needs, unless you remember those Paralympics wheelchair racers' arm muscles—she wanted to be independent and not have to rely in her husband to do the pushing all the time. "Except," she said, "when things like this happen, it turns out I can't be as independent as I thought."

I recognised the disappointment in her voice. I've motorised mine, very unofficially, really in the hope I can get further on my own than I would be able to just using muscle power. I got (like her) a bit fed up with having to arrange little trips in advance with a friend; and what do you do if you want to go somewhere on some day, and she doesn't?  We share, fortunately, a lot of interests; but some we don't. And she has to work when I don't want to have to stay at home, or don't want to do something or go somewhere else, just because it's closer to home or easier.

You see, I hope, what I'm getting at? OK, wheeling a small child around in a buggy might be a bit  restrictive for you. But in proportion, nowhere near as it is every day, every hour, for us. Is it really that much to ask someone with a buggy to put their child on a seat or on their lap and fold it up to give me my space? Or wait just for the next bus, when I might have to wait for the third or fourth?

After all, in proportion to the number of people with buggies you see travelling on buses, how many wheelchair users do you see needing 'their' space? We are, I've noticed, beginning to use buses more, but how many buses do you see with a wheelchair user in them? One in fifty? One in a hundred? We are not asking you to cause yourselves much inconvenience, are we? Or that often?

And we—even those who can stand or walk a little—would find it far, far harder to fold a wheelchair up and haul it up onto the luggage rack than someone would a buggy. If anyone wants to take me up on that on a bus and try it, good luck to them.

Wednesday, 20 March 2013

Roulette Wheel

Selected for the Design Museum 2013 awards, wheelchair wheels that fold flat (or oval, anyway) look like a good idea. Though I've not (yet) entrusted my own folding wheelchair to a airplane hold, after the experiences of some Paralympians last summer, I think I might just stick to trains.


Yet another idea from those very inventive London design students. And I salute the cleverness. But . . .you need to be a winner at the tables to be able to afford them. According to the Morph website (the company that's selling them) they come out at 950 US dollars each!

Somehow, I think, if I have to put my wheelchair on a plane, I'll see if I can borrow a drum case from a percussionist mate to keep my wheels from getting bent into an oval by accident rather than design.

Wednesday, 13 March 2013

Now That's What I (Don't) Call Style . . .


Supposedly, building this. . .device . . .took its designer 'all over the USA'. I can't think why. UK wheelchair users will, no doubt recognise a bog-standard hundred and fifty quid basic chassis to it.

Plus a bit extra for the hood off a buggy, of course.

Good god. All that money . . . when she could have got one of these.


Or got a bit more up to date, and maybe got one of these:


Not to mention my own fave carbon fibre one, of course:


The green chair I found on a 'designer' website which I damn well won't link to. That's because the article was titled: "Wheelchairs bringing a ray of hope in bleak lives of physically disabled"

Bloody hell. Once upon a time as a sub-editor I probably wrote thousands of headlines. I have to admire that one. It's beyond my skills to fathom out how it could be any more offensive. Well done.

Anyway, the wheels there are only design concepts, I suspect, and are probably all impracticable.

Sunday, 27 January 2013

Faith, Hope, and . . .What was the other one?

I had been congratulating myself. I happened to mention to a friend the other day that I hadn't been pestered by any evangelical Christians for a good while.

You know the kind. They accost you in the street explaining how your life will be so much better if you trot along with them and engage in a lot of joyous shouting and generally sublime cotton-woolly good feelings about each other. Or God. But mostly about God.

If you're disabled, though, they always have another tack. They have a cure for you. It doesn't matter that they (of course) haven't the faintest idea why you're disabled, what the disability is, how it affects you, or how you live with it. I used to wonder why they never asked, but of course, none of that matters. They're not interested; and they are not interested because that would mean actually engaging someone and stepping, just for a few moments, outside of the tiny individual-sized narcissistic bubble they inhabit.

They are utterly confident that a few words will fix all. Not just any words, mind you, not even your own, but theirs.

So there I was, limping along on my crutch, feeling quite happy that it was, at last, moderately warm, dry, and sunny, and on the whole life was pleasant. Until Ladbroke Grove Tube station.

"Hello, my name's Francois," he said, getting rather closer to me than I generally like: in London, or any city, I suppose, someone getting within inches of your shoulder is at the very least, about to beg money, a cigarette, or maybe try to pick your pocket. I was prepared for any, but I was actually expecting to have to refuse to give him a ciggy.

(Why do people beg from me so often? It's a kind of inverse charity, I've come to suspect, since it doesn't happen to my non-disabled friends with anything like the same frequency.  Because I'm obviously disabled, in a reverse of normal expectations, they seem to assume I will be more charitable to them than anyone else. And give them money for the bus fare, the tube fare, a parking meter, or cigarettes. And these days, the beggars usually look better able to afford any of the foregoing than I actually can. So I refuse. I don't like being taken advantage of like that.)

"I can help you," he says, getting in my way so I miss the green light at the Pelican crossing. I pause, a little taken aback. As you'll have gathered, I'm more prepared to hear why I should help someone else, not the other way around.

"I can pray for you," he goes on. "And that pain will go! Just like that!" (He waves his hand, and a startled bus driver slows at the lights.) I've heard this before. I used to hear it around here every couple of weeks when I stepped out of my flat. How he knew I was in pain, I can't tell. As it happens, I was, but generally it doesn't show, and I'd just called at a friend's flat who is well attuned to my ups and downs and usually mentions it if it does. Apart from that, I'd knocked back some morphia not long before, so it shouldn't have shown anyway.

I wondered, of course, what his approach would have been if I'd been in my wheelchair? He would, I've no doubt. have been even more confident that he could have helped me fold up my wheelchair and walk. Since, in fact, that is possible for me—but, of course, he wouldn't have known that, and wouldn't have asked—I could have provided him with a rather startling example of the power of prayer.  For a moment I rather wished I had come out in my wheelchair instead of relying on painkillers and crutches to walk instead.

It would have been interesting to see his face. And what the consequences would have been. Would he have yelled 'Hallelujah' and rounded up the other passers by to bear witness to the miracle? Would I have been dragged along to the evangelical church as an example?

I thought of explaining some medical facts of life; that I was an atheist, so I could hardly see how any prayerful intercession with a non-existent deity could be at all effectual. But I've learnt from experience that others' beliefs don't matter; only theirs, and their confidence in them. I thought also, of asking if he had, say, ever broken an arm, or leg, or had appendicitis, and found the pain disappearing through the intervention of nothing more than a short prayer. But I've learnt from experience also that someone like this would claim exactly that.

Or they would offer up the mantra that suffering is God's will and fortitude bears away all pain. And it ennobles you. The latter being something I've heard from other than Christians as well; and long experience, not just as someone who has, and does, suffer extreme pain, but who's watched people do so as a nurse,  has never convinced me there's any truth at al in it.

While all this sprung to mind, for all the reasons I've suggested, it would have been a waste of time and breath uttering it. So I said, rather sharply (and possibly thereby proving that pain—or no doubt from Francois's point of view, atheism—can in fact make you rather short-tempered and less than noble and forgiving) that he didn't know what he was talking about, and to get realistic about it.

I was going to say "Get real", but I do hate that phrase.

At least, as the lights changed and I scuttled across the road, he didn't follow me as I'd expected. "That," I thought, was a display of 'faith' alright; an example of forlorn hope, too; but where I wondered, since like all troubles these come in threes, was the charity?

'Charity' (in the sense of practical help) not something these people at much good at, I think. Even when they offer any, they so often expect their reward not to be in heaven, but in your acceptance of them and their ideas. That you should reward them, in fact. I can't forget one who started off offering to push me around Tate Modern in my wheelchair, who grabbed it, quite unnecessarily, and pestered me with the same spiel. I had  to flee to the loo, and if there hadn't ben a queue for the 'non-disabled' one next door who gave him some odd looks, he'd have followed me in.

Fortunately, that must have embarrassed him. even though these people seem to find that very little does, or I'd have had to hide there even longer than I did. There really aren't enough public loos, especially wheelchair-accessible ones, in this part of London to hide from these people in, I've just realised. And would they be charitable enough to give me the twenty pence to get in, I wonder?









Saturday, 12 January 2013

Full of the Chablis of Human Kindness


I'll explain that later.

First, after being practically smothered in kindness by the staff at the London Colisseum which I went to see Sleeping Beauty on Thursday, I've ben wondering if one can have too much kindness . . .

It all started when a friend got an offer for half-price seats a few days before, asked if I'd like to go, and I said yes. She's just—rather late—discovering ballet; I'm not actually all that keen on classical ballet, I always preferred contemporary dance. Not that I've seen much of that of late. I think it's because I've feared seeing all that athletic dancing about might bring back too many memories of what I could do before I got crippled.

I was (you can believe me or not) actually a very good dancer. Discos, though, not princes in palaces. Actually, sometimes, I suspect I might still be a much better dancer than a lot I see in discos these days. Either on crutches or even in my wheelchair. Actually, I did feel some regrets watching Sleeping Beauty. Though not as deeply as I feared. After all, I thought, I never could really leap a metre into he air and scissor my feet together at the top of the jump. Well, not consistently reliably, anyway.

I was a little more worried because the afternoon before the performance, I'd had an unexpected bout of pain that lasted off and on, and despite the painkillers, for a good eight hours and left me hopelessly lame and having to use two crutches to get even from my bedroom to the kitchen, and having to 'bum it'   up and down the stairs to my bathroom. I don't much fancy doing that in public, so I decided I'd take my wheels to ENO.

Not done that before, so I phoned and asked if I'd be able to park my wheelchair somewhere outside the auditorium. (Mercifully, our seats were on level ground, I didn't have any steps to get to them.) Answer, 'yes', no problem. First obstacle surmounted: most public venues are happy to either find you somewhere to park it, or have someone who will do the disability equivalent of 'valet parking'. Only they don't, neither at the Albert Hall nor the Barbican (and not at ENO either), ask for tips for doing it.

On the other hand, they don't give my wheelchair  a quick polish and empty the ash tray either, but you can't expect everything, can you?

Well, I got there, and everyone was kindness personified. Did I need to take the wheels right up to the seat row? If so someone would take it out and park it at the refuge point by the lift. Would I need the loo? If so, there was a disabled loo just to the right behind the lift on the floor I was going to. Which floor would I like the lift to go to? The cloakroom? No problem. Was I coming back to the bar or going straight up to my seat? Someone would radio up (or down) so they'd be ready if I needed help. The cloakroom (I'd forgotten) is actually tucked away up a short flight of steps. Would I like, an attendant, with radio in hand asked, him to take my coat to it? Thanks, but my friend would take mine along with hers. Oh, and did I know where the disabled loo was? Yes, thanks; my friend will take me in and hold it for me while . . .no, don't be unkind.

Back to the bar where we ordered interval drinks. Barman points to a table, says we'll reserve that and put your drinks there so your friend can get his wheelchair in easily. By this time, I should have been feeling thoroughly pampered, but actually I was beginning to feel slightly embarrassed. As I've said before, I really prefer people not to notice I'm disabled (though admittedly, that's a hard trick to pull off in a wheelchair) and all this kindness and the offers of help were getting a bit too much. I could get used to it. And imagine the outrage you'd feel if somewhere, later that night, or the next day, people weren't that kind and helpful. As sometimes, they aren't.

As we discovered at the interval. Our table didn't have our name on it; it didn't have our two glasses of Chablis on it either. It did have two people sitting there who ostentatiously failed to observe a somewhat upset Squirrel in his wheelchair trying to espy two lost full glasses of Chablis anywhere.

The barman came to our help—one of the advantages of being that night the only wheelchair user. (Do others have the same suspicion that all that energetic prancing about might bring back unwanted regrets, I wondered?) He said he thought someone must have stolen them, it having taken Squirrel, of course,  considerably longer to get even the relatively short distance from seat to wheelchair to bar than most of the eager drinkers. We were surprised. Well, shocked, really. It's never happened to us at Covent Garden. "You'd be surprised," he said darkly, pouring us two glasses of white wine. Well, yes, we were. "I'm really sorry," he said—and gave us our money back!

So that is why on Thursday night, the Squirrel cup overflowethed (is that really the past tense?) with the  Chablis of Human Kindness at the Colisseum in London.

That is, until I tried to park my wheelchair in its spot by the lift. And nearly missed the start of the third act. Because there was a rather peculiar woman, dressed mostly in red, using that corner like a bag lady.        She'd emptied half the contents of a large handbag and two shopping bags there, and didn't sem to grasp that it was my 'parking space'. Any more than your average SUV driver seeing a double yellow line or any plebeian vehicle within two metres of the door of the shop they want to flash their platinum credit cards in.

As I hopped into the auditorium, I looked back, and it dawned she wasn't there for the show.  She hadn't (as I'd thought at first) been hunting for her ticket. Though in fact, she would have known that they don't ask you for your ticket after the intervals. She'd settled, bag and baggage, into an armchair just outside the bar.

Was it her, I wondered, who'd hoovered up our Chablis unnoticed amongst the first rush and dimmed the warm glow of kindness Squirrel had been basking in? She had, I recalled, as I sat down, sounded less than sober. As well you might if you'd just gulped down two large glasses of white wine in a hurry less than fifteen minutes before.

It was a lesson, I thought. The wine of kindness might flow strongly in the veins of the front-of-house staff of ENO; but it still runs vinegary in some people.

Though not, mostly, that night.

Excepting the woman with an enormous two tier buggy full of shopping who didn't even thank Squirrel for folding in his footrest to let her get the damn thing in. It was a few minutes before I, my friend, and the Spanish girl next to her, after peering at it that became less and less surreptitious, that there were no children in it, on either tier quietly suffocating. Just shopping. What is it with these buggy drivers? I've noticed that TfL must be getting pissed off with them too. Some buses, I've noticed, now have big notices telling people with buggies to fold them up if the wheelchair space is being used. But some of them are so big, it'd probably be quicker for me to fold up my wheelchair. 

And while I'm at it, does a two-seater buggy really need cup-holders attached to it on each tier? Hmm . . .I wonder if I could fit one to my wheelchair? A cup-holder on one side, and a wine bottle holder on the other? I've seen vans in France fitted with both . . . Maybe I could fit a waterheater thingy like you plug into a cigar-lighter in a car? I could maybe plug it into the motor's 12V battery? Have a hot tea stop every now and then in the cold weather . . .

This government's plans for us being what they are, maybe I could even make a small mobile drinks business out if it? A holder on one side with a stack of disposable cups like they have for water coolers; sachets of sugar and milk in the little pouch on the back? Have to think where I'd keep the water, though. A plastic tank under the seat? Get one of those clip on trays and sell sandwiches as well, even? 'Squirrelbucksmobile' here we come. Just remember, I thought of it first.

But that aside, all the bus drivers seemed to have taken pride on Thursday in stopping very neatly right opposite my wheelchair at the bus stops to let the ramp down so I didn't even have to manoeuvre an inch. I was impressed. And a young black guy passed me on my way home from the bus stop, even pausing his phone call to smile and say "Goo'night, take care man". I got that nice warm feeling you get when human beings are kind to you without being asked and with nothing to gain from it. And I'm almost positive that wasn't just the Chablis.