The chief side effect of this pain is numbness in the extremities, filling me with the not irrational fear that I shall lose the ability to write. Without that ability, I feel sure in advance, my “will to live” would be hugely attenuated. I often grandly say that writing is not just my living and my livelihood but my very life, and it’s true. Almost like the threatened loss of my voice, which is currently being alleviated by some temporary injections into my vocal folds, I feel my personality and identity dissolving as I contemplate dead hands and the loss of the transmission belts that connect me to writing and thinking.
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You answer as yourself. Nobody on FLAPSS answers as anybody else.
Rachel Cooke, The Observer, 1 December 2019 source ↗
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View all 19 →At first I - I felt that it was confined to my liver and that they had - the operation had completely removed it. And so I felt quite relieved. And then that same afternoon we had an MRI of my head and neck and it showed up that it was already in four places in my brain. So I would say that night and the next day, until I came back up to Emory, I just thought I had a few weeks left. But I was surprisingly at ease. You know, I've had a wonderful life. I've had thousands of friends and I've had an exciting and adventurous and gratifying existence. So I was surprisingly at ease, much more so than my wife was.
Somebody who won't go to the doctor for a normal checkup is fearful and nervous. ... But once you find out what it's like on the other side, you can go beyond fear.
We received death threats, yes, but you see when you are in a struggle, there are going to have to be casualties, and why should you be exempt? But I often said, “Look, here, God, if I’m doing your work, then you jolly well are going to have to look after me!” And God did God’s stuff.
More from Clive James
View profile →Yeah. These books are all around me and they'll be here when I go and I'm that sick. I just don't know when it ends. But in 2010, I got really ill and leukaemia was one of the things I was diagnosed with and eventually it will switch me off. So it raises the question: what do you do? Do you lie down and give up? Read the Bible? Or do you go on as you were reading and writing. And I've done the second and I've just done a little bit called Latest Readings which is about the books I've been reading lately and I could do another volume of that because I'm still reading.
One thing, it's too big a subject and I want to talk about it on paper if I talk about it at all. But I can say this much, because I thought the life that my father and mother would have had together was cut short and something of what they might have achieved I hope that I'm achieving in my work.
Yes, but I don’t think I have the energy. I’ve been hit in the face by a cricket bat at 1,000 miles an hour. I think the last round-up is here. But that’s OK. It would be bad manners to complain. I’ve had a lucky life, and I’m grateful for it.
It’s here. I’ve always thought that it was here. If you play to the gallery, that’s posterity. The best you can hope for is another gallery after you’ve gone, but you won’t see it. Statistically, it’s unlikely that much of what one does will be read for ever. It may just be one or two poems. For example, my Japanese Maple poem is famous among people who own a Japanese maple.
I think I actually wrote it in one of my poems is that my decline has been the making of me - I forget how I put it. Yeah, simply more reflective. I haven't got the excuse of moving forward just on impulse anymore, which I did, I think, for a long, long time.
What I’ve got doesn’t hurt. I’ve been lucky. The treatment has been benign. I don’t know if I could concentrate if I was in pain. I’ve never had to stop.
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