Elizabeth is waiting for us in the conservatory. A tall,
powerfully-built woman in her seventies, she has the worn, slightly bewildered
demeanour of an athlete who threw a javelin so hard it never came back to
earth.
‘David’s in the bathroom,’ she says, pushing the silvery strands of
her hair back and showing us inside. ‘He didn’t fall with a terrible clatter or
anything, but he’s rather unsteady on his feet and a little reluctant to bend in
the middle. I tried to get him up myself, but I’m afraid I couldn’t quite
manage it. He’s had problems with his back for years. The other thing is a
touch of dementia, but we rub along, you know? So sorry to call you out like
this.’
The house is tastefully decorated, landscape watercolours on the
walls, silver photoframes on highly-polished furniture, the whole place as neat
and perfect as an illustration in a country catalogue. A chair lift snakes
round the balustrade up to a sunlit landing and the mosaic-tiled wet room where
David is lying on his back, surrounded by cushions. He’s as olympian as his
wife, except his health has taken more of a battering. His eyes are a pearlescent
gray, and his hands shake when they reach out to us, flailing around without
focus when we manipulate him into a better position.
We use our inflatable cushion to get David up from the floor. He can
weight bear, but paddles his feet in a dangerously unstable way. We fetch a
chair for him to sit on, and stand close in to keep him there whilst we
consider our options.
‘Is this shaking new?’
‘No. They think it’s benign, though. Not Parkinson’s. Look – before you
say anything – I just want you to know that hospital’s not an option. We’ve had
a rotten time of it these last few months. David simply cannot go back there. I
hope you understand. It may take some time to get him down the corridor and
back to bed, but if you wouldn’t mind bearing with us I’d be terribly grateful.’
In the end we have to wheel him there on a commode. Even alongside
the bed, David doesn’t seem able to make the transition. We help him to stand
as positively and simply as we can, but at the last minute he loses confidence,
relaxes his knees, and we have to sit him back down again. He’s easily
distracted, and struggles to understand our instructions.
‘Come on darling,’ says Elizabeth, stroking his silver hair flat and
kissing the top of his head. ‘There’s a good boy. We’ll get you to bed. You’ll
be comfortable there. You can watch Countryfile.
You know how much you enjoyed that last time.’
When she looks up at us she starts to cry.
‘He wasn’t always like this,’ she says. ‘He could do the Times
crossword in ten minutes flat. Couldn’t you, darling? Ten minutes?’
She kisses his head again. He turns his head from side to side, like
he’s struggling to pinpoint something he can hear in the distance.
‘Not the quick
crossword. The cryptic one, you know? The difficult one.’ Then ‘Come on, David.
You can do it. You’ve got to do it. One last try.’
7 comments:
So beautiful, so touching.
Kim
Thanks very much Kim.
It was so difficult for both of them. Such a painful situation - but at least they had each other, a lovely family & home.
Cheers for the comment! :)
At work, I sometimes have to check the statistics on dementia/Alz. and is look at my age group and that of my man and I have to stop myself from considering the possibilities.
I can still do the crossowrd, though.
Lovely couple Spence.Such a shame.
Sabine - It's a chastening thing to see how many people suffer from dementia of one sort or another. I think it's attracting more attention & resources in this country, but still underfunded. The social consequences are immense, of course. Such a hard thing to cope with.
Respect due re the crossword. I'm rubbish at the cryptic ones - the answers, that is. I could rattle off clues till the cows come home (e.g. cows come home? Eat consomme backwards and you'll approve) :/
Jack - It looked like they'd had a good long & strong marriage, and I suppose all things come to an end - but of course, none of that diminishes the tragedy of the situation.
Dementia is an awful weight to bear. I have worked in several EMI homes, and witnessed residents slide down the inevitable spiral from being highly articulate and having many lucid moments to being entirely dependent on others to do even the most intimate things for them. It's so sad, I dread my parents getting old.
It's such a tough illness to bear - maybe even more for the relatives, who have to find a way to cope with these profound changes in the person they know & love. I think EMI homes do a fantastic job in really difficult circumstances - so, respect for the work you did there, PH.
Post a Comment