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17 Sep

We Don’t Need Another Hero, And Certainly Not One Who Cries All The Time

Here’s my worry about going to Africa to see the Born HIV Free project in action: that I’m going to start crying the moment that I arrive, and just not stop. And that I am then going to feel guilty about crying, and that I’ll then cry about that.

I fly to Lesotho on Saturday. I was supposed to go to Napa Valley, first, to hang out with some lovely women and discuss things like life lists and dreams and pixie dust and to drink wine and be light-hearted, and for some reason, some ironic reason or some absurd reason, that – that beautiful little oasis of self-indulgence – was grounding me, was helping me keep my emotional wits about me. I don’t know why, exactly. Maybe because they are opposing poles on the same fuzzy dreamscape, whereupon I live a life in which I get to do things like spend weekends in Napa and also go and support humanitarian projects in Africa and I wanted to see them reconciled.  Because these things, these actually very real things, are, however different, nonetheless connected, inasmuch as they both have everything to do with this, this thing that I do here, on this page that you are reading.

But things changed, and I’m not going to Napa Valley first, and it hit me this afternoon as I was pushing aside the pretty dresses in my closet to see what clothes might be appropriate for visiting orphanages in Lesotho – what does one wear to visit hospitals and orphanages in Lesotho? – that I had really been relying upon the whole idea of Napa Valley – the Mighty Summit – as a buffer against the soul-rattling hugeness of the journey to Africa. Or maybe not a buffer – a transitional zone.

27 Aug

Buffy Only Fought Vampires

I like to think that I’m the sort of person who doesn’t take things for granted. I know how fortunate I am to have the life that I have; I know, too, that the terms and conditions of that life include no guarantees against frustration and sadness and pain and loss. I know, even the most difficult moments, that I have much to be grateful for, that I lead a life that is, for the most part, what the old philosophers might have called choiceworthy. I know that it is choice, largely, that defines my fortune and privilege: I am fortunate enough and privileged enough to be able to choose, to some not insignificant degree, my path and all of its little detours, to choose my pace and my direction, to choose to linger over or to pass by the myriad distractions of life, to gaze into the gloom or to seek out the sunlight. I am lucky, I know this.

It is also a characteristic of this good fortune, this privilege, that I am vulnerable to frustration and sadness (and, possibly, to depression; I’ll reflect upon this further someday) when I am forced to confront my limitations, when I look down this path or the other and see no way around a certain obstacle – some figurative bog or rock or troll-ridden bridge – and have to stop, give up, go a different way. That’s the very definition of privilege, I think – the luxury of getting pissy about being thwarted. Not that those who are less privilege don’t get frustrated at the obstacles that they are forced to confront – it’s just that, I think, the fortunate are more likely to put their hands on their hips and stamp their feet and say that shouldn’t be there, how dare that be there? and collapse to the ground in a resentful huff.

Or something like that.

12 Aug

We Are The World

When all was finally said and done, it wasn’t appearing on CNN in a tutu – nor appearing on CBC in a tutu, or posing in Central Park in a tutu, or watching as a limo slowed down on Fifth Avenue and the passenger leaned out the window and hollered – at me – hey, I saw you on TV in that tutu! – that stood out as the most memorable moment of my week last week. Which, when you think about it, is memorable in itself: I had a week in which I appeared on CNN in a tutu and that particular experience will not be recounted here because, during that particular week, stranger things happened.

Stranger things, like the prayer circle.

4 Aug

What Is UP With All The Tutus?

tutus-for-tannerIf you have to ask that question, you should probably read this first – it’s the story of my nephew, Tanner, who is dying of Duchennes Muscular Dystrophy. It’s kind of a long story. But you should go read it, and maybe also my most recent posts about him, because the story matters. Take your time; I’ll wait.

Okay?

So, yeah, I’m trying to raise money to make his biggest wish – to live out what time he has left at home – come true, and I’m trying to raise awareness of DMD, and of the challenges facing terminally ill children and their families, and I’m trying to do something, anything, that will make everyone – myself included – slow down a little and really, really cherish the time that they have with their children. And, yeah, that’s all a big job, but Tanner’s worth it – every child who struggles through this kind of thing is worth it – so. But I’m not doing this on my own – far from it – a whole bunch of people have pulled on their tutus (you got to that part in your reading, right?) and designated themselves Fairy Godpersons and are doing stuff to support Tanner and dreams and wishes and the whole project of being real. Stuff like:

3 Aug

Black Flies And Dryer Lint And Dragons, Oh My

It took me a while to figure why I was crying, why I kept bursting into tears at silly, random things, like an excess of dryer lint, or a dearth of toilet paper. I had just figured it to be hormones, or a passing mood, you know, the kind that you fall into when you’ve gone too many nights with too little sleep and then you open the cupboard and there’s not enough coffee for a full pot and you slump against the counter and you cry.

It wasn’t that. I wasn’t crying about coffee.

27 Jul

A Real Boy

pinocchio_poster_92_500Every visit to the doctor, now, brings bad news. In the early days, there were reassurances and messages of hope – some boys make it out of their teens, there are ways to slow the deterioration of his muscles, he might stay mobile for a long time, he might still get to enjoy some of his boyhood in the ways that other boys take for granted – but now, there are only somber descriptions of what will happen next, of what needs to be done to make things easier, of what use can be made of his diminishing time.

They want to put rods in his spine, she tells me. So that he can stay upright for a bit longer.

Rods in his spine. He won’t be able to bend, I think, before remembering, he cannot bend now. Not in the real, active sense of bending, anyway: he slumps, he droops, he slides forward in his chair, unable to hold his own weight even while sitting, a Pinocchio without strings. His spine is collapsing under the weight of his body, his muscles having deteriorated beyond the point where they can provide any support. He’s like a doll now, a puppet. But he has no strings by which he might be pulled up. He has no Blue Fairy to wave a wand and make such strings unnecessary. He has only surgeons, and rods.