For all of
my working life in nursing – over twenty years now – I’ve been involved, in one
way or another, with the basic limits, the boundaries of life. Either in
geriatric care (accompanying people who are coming to the end of their life’s
journey), or with people suffering from such serious, complex, debilitating and
restricting illness that their continued survival would rapidly be impossible
without the comprehensive, continuous support of professional health workers
(in my case, people in Persistent Vegetative States). Even in the little group of five children with whom I currently work, three
are in a PVS.
It is an
area where some very fundamental questions arise. What’s the basic point of
life? What is tolerable, intolerable? Where do we draw the line, or can we draw
any lines at all? When is a life not worth living any longer? What does “basic
human dignity” mean?
Hard
questions, questions for which I am ever more unwilling to offer comprehensive
answers, or even any answer whatsoever. There are those who find such things in
faith, or dogmas derived from faith (though most believers who actually work in this area – in my experience –
aren’t big into dogmas), but many of us are not believers, or don’t find our
motivation to continue actually doing this
work in any kind of religious faith.
I suppose
one of the basic things which keeps us at it (apart from the fact that we know how to do it and we need to earn a
living) is the very practical experience that this is work which has to be done; done now, done
immediately, done continuously. I think it is this daily experience which leads
most of those of us who do this kind of thing to a reaction of genuine
bewilderment when others praise us for it, you know, “I really admire you for
the work you do…” that kind of thing. There is, I suppose, a kind of deep
satisfaction in doing the kind of work which you know (at some level) makes a
literal life-or-death difference every day, every hour you’re doing it. It
certainly beats processing piles of paper or data (something I once did for a
year, and which nearly drove me batshit crazy), even if the ultimate results of
being a part of such a complex process actually means that practical things
happen somewhere.
Nonetheless,
we do often find these deeper questions coming up in the course of our daily
work. It’s inevitable in this kind of job. And, as I’ve already mentioned,
there aren’t any easy answers. Sometimes, faced with someone who seems to be
suffering a lot and, at the same time, doesn’t seem to be able to just die, there are no good answers at all.
You learn to cultivate a kind of staid attitude of compassionate resignation;
you do the best you can, the best possible for the person you’re looking after
and try to leave the questions aside. Because, honestly, they don’t help.
No, I often
don’t know any answers. What I do know are some stories, one of which I’d like
to tell now.
Jimmy was
the son of immigrants to Germany
from a Mediterranean country. They had left their homeland as young adults over
forty years ago, with little education or training, no knowledge of the German
language, and very limited concrete knowledge of the kind of life they were
going to lead. All they had – like millions of other migrants – was the hope
that life elsewhere would offer them and their children more possibilities than
a continued existence in the place of their birth.
They
quickly found somewhere to live, and jobs to do. There was plenty of work
available, even for people without high levels of training and very rudimentary
language skills. And, though the work was hard and often monotonous, the money
was good and the standard of living (material things like electricity and
washing machines and motor cars, and other stuff like health care) almost
immediately available to them was far beyond what they could have attained in
the old country. Certainly they were homesick, and getting by in a foreign
country was often stressful, but they felt sure that their decision had been
the right one. If nothing else, their children would have opportunities which
would have been impossible at home. And they themselves could dream of moving
back home when they retired, the modest amount necessary to build a really
comfortable house in their home village saved and a good German pension to give
them security in their old age.
They soon
had a daughter, but she died shortly after childbirth. And then Jimmy came along.
It was a difficult birth and the doctors told the mother that there would be no
further children. But Jimmy was a healthy and happy baby and grew up to be a
healthy and happy boy.
He became
the repository of all his parents’ love, and all of their hopes and
expectations. And he lived up to all of these splendidly. He was a lively,
fun-loving kid, bright as a button at school, helpful at home, popular in the
neighbourhood. He became an altar-boy and learned to play the piano. After
finishing secondary school with very good grades, he went back to his home
country for a year to do the mandatory military service demanded of all young
citizens, even those born and living abroad. When he came back to Germany, he
could have gone to university, but elected instead to train as a bank-official.
It meant he could continue living at home and it offered him the kind of career
his parents could never have hoped for. While Jimmy could have aimed higher, he
was quite content with the choice he had made and the life which was unfolding
for him.
He had
saved some extra money from summer-jobs he had done during his last years at
school, and his parents topped up those savings and bought him a car for his
twenty-first birthday. And, a few months later, driving to a placement in a
branch of the bank which was training him, a few miles from his home town, on a
cold January morning, Jimmy hit a patch of ice in a curve on the road and
collided with a tree.
The tree
won.
The car
wasn’t the newest, which meant in January 1997 that it wasn’t equipped with
airbags. And, if truth be told, Jimmy was probably travelling a bit faster than
was wise when he hit that ice – he was, after all, young and didn’t have all
that much driving experience. At any rate, when they pulled him from the wreck
he had broken fourteen different bones and had a very serious skull fracture.
For months
he wasn’t expected to survive. But his condition slowly stabilised, he came off
most of the machines and started to heal. The problem was that skull fracture;
Jimmy had very serious brain damage which was irreversible. But he had regained
consciousness, and that was both the wonder and the tragedy.
Apart from
leaving him almost completely paralysed, the brain damage had wiped out large
parts of his rational capacities. It’s hard to really describe his situation to
those who do not know him. In a vastly simplified sense, he is frozen at a
mental age around equivalent to that of a six-month-old baby. Speech is beyond
him, though he is able to understand some of what is said to him. He has a
generally friendly disposition, though he is inclined to be a bit reserved with
strangers – for he is able to recognise people he knows well. He can shout, or
rather, howl, which is something he does continually when he is in discomfort or
pain, a situation in which he becomes quite agitated. This happens regularly
when he is being washed, cleaned up, or dressed, for all of these operations
are both stressful and painful for him. Jimmy’s paralysis is that of the
spastic variety, one with an enormously increased muscle tone. This means, for
example, that his left forearm has – in the course of the years – completely
pulled up flush with his upper arm, so that it takes all the strength of an
adult to pull it far enough back to wash it, and check for irritation in the
crook of the arm, something which frequently occurs as a result of skin chafing
on skin and which then has to be treated. Something Jimmy does not enjoy. Or that his fingers are
hopelessly twisted around each other.
As I
mentioned, describing his mental state as that of a baby is only a first
approximation, for it is no more accurate to describe people with traumatic
brain injury as children, than it is to use the same comparison for people
suffering from Alzheimer’s. There are superficial, almost coincidental similarities
with babies (such as incontinence or linguistic inability), but the basic
situation is quite different. And Jimmy has retained some capabilities which
are far beyond those of a six-month-old.
Chief among
these is a sense of humour. In one sense it has become a little cruder than it
used to be – or it may be that some adult limiting conventions
have just been burned away. At any rate, Jimmy loves slapstick, the broader the
better. Somebody stubbing their toe and then cursing loudly in annoyance will
send him into peals of laughter. Abbott and Costello or Laurel and Hardy would
be right up his street, but – for some strange reason – Jimmy doesn’t seem able
to process TV pictures. The sound alone of somebody cussing is something he
finds amusing and the fouler the language the better, as far as he’s concerned.
I’ve often driven him into paroxysms of laughter (and distracted him from the
most uncomfortable aspects of what I was doing) while caring for him just by
making farting noises.
The
marvellous thing about Jimmy’s sense of humour is that it’s completely honest,
and absolutely total. And it is a gift which he is capable of putting to work
in a delightfully mischievous manner. Imagine a group of people sitting around
a table, engaged in a serious discussion. Then imagine that Jimmy is there too.
This can happen, for he is often sitting in the day-room of the ward where he
lives during a staff meeting. Sometimes he simply appears thoughtful, lost in
his own special world. But sometimes he feels like establishing communication
and he starts looking around at the group, trying to catch someone’s eye. Beware
– for if you look at him you’re lost!
When he
gains eye-contact with you, he grins. Almost instinctively, you smile back.
That’s all the encouragement he needs, indeed, even if you don’t respond,
catching your gaze is usually all he needs. He starts to chuckle and this
chuckling quickly develops into hearty laughter. Trying to hush him only makes
it worse, as he finds such attempts hilarious.
It really
doesn’t matter what you do anyway, because Jimmy’s laughter has another killer
characteristic. It is irresistibly infectious. There is something so honest, so
complete, so true about his laugh that it conquers all attempts to gainsay it. Before
you know it, you are laughing too, in the way that you found yourself
uncontrollably laughing at something you found funny when you were a child. And,
just like it used to happen when you were a child, you soon find everyone in
the group trying unsuccessfully to control that urge to laugh, to laugh until
your belly hurts and tears are running down your cheeks.
Jimmy has
done it again. Wrecking all the pretentions of serious adults at a meeting, he
has given them – us – all the priceless gift of joy, taking us beyond the
mundane concerns of our reality into a realm of simply revelling in the sheer
inexplicable fun of just being alive.
When I hear
people discussing situations in which they imagine it would no longer be worth
living, in which they feel they would rather be dead, I often find myself
thinking of my friend (for this is the best word I can use to describe how I
feel about my relationship to him), Jimmy. He is confined to a wheelchair, is incapable
of almost every voluntary movement, drools and dribbles, has to be fed through
a tube, would lie in his own piss and shit if he were not cleaned up regularly.
Is his human dignity worth any less than mine – or yours – because of all this,
and because he has been so severely mentally damaged? Is his joy worth less
than that of a physicist discovering a new sub-atomic particle, or of a
musician in that moment of performance when everything gels, or that of lovers during a shared orgasm?
Despite the
conventional tragedy of his story, Jimmy is possibly the happiest person I
know. The price he has paid for it in his life is, seen in a conventional way,
unacceptably high – one none of us would willingly pay. The loss of the Jimmy
who was, all that potential, the life destroyed the moment his car hit that
tree, is, of course, heartbreaking. Yet does that detract in any way from the
value of his happiness as he is today; make it somehow worth less than those
all too seldom and fleeting moments of unalloyed joy the rest of us have to get
by with?
I don’t
have any answers to questions like that. But then, when I see Jimmy, I don’t
need them.
Pictures
retrieved from:
Very beautifully and thoughtfully written.
ReplyDeleteTo experience joy and to pass it on to others are reasons enough for a life to be valued.
I couldn't help but chuckle at imagining you, Francis Hunt, making farting noises to entertain your friend. :-D
I loved reading the part about Jimmy's ability to make everyone laugh uncontrollably. Surely that means he benefits those of you who spend time in his company. It's impossible to know what makes life meaningful for anyone else, never mind someone who is chronically ill or who has suffered a life changing injury but the joy you've described makes me wish I too could share his laughter.
ReplyDeleteI’m glad you wrote this, Francis, in your characteristically excellent expository style. You’ve had exposure to extreme disability for 20 years, and I had only 2 days visiting the Mustardseed community in Kingston, Jamaica, as I’ve doubtless mentioned many times. But that was enough to concur 100% with what you’ve expressed here, and Jimmy reminds me of the girl I called Laughing Water.
ReplyDeleteIt’s really rather remarkable that Mustardseed is not publicly funded but has received voluntary donations to enable it to operate in a number of third-world countries, having been started by one man, Fr Gregory Ramkissoon, in 1978 when he was an academic at the University of the West Indies, Mona, Jamaica. He saw the need right outside the campus gates and the thing has grown ever since.
When I visited I got an insight into what makes it continue to grow and flourish.
I cannot deny the importance of Catholic belief as the rock on which it is built, in particular that sense of the sanctity of human life which sustains their opposition to abortion, contraception and homosexuality. (I suppose they believe that the bringing of souls to birth via procreation is the domain of God, whom we are to trust and assist, not frustrate.)
But there are two other factors: (1) the willingness of care workers to give their devoted love to the children in their care, for very low pay - easier to achieve in a third-world country with no social security and not enough jobs to go round;
(2) I think the most important thing in the Mustardseed operation is its openness. Visitors are welcome to come and help in simple ways, like spooning food into a child with no effective mobility, or giving a drink. There are many schools in the US which regularly, each year, send selected students to Mustardseed to play with or simply hug the brain-damaged children, as I describe in my piece.
For the children themselves, by the mysterious power of their presence, offer the best public relations to support their own cause! The students returning to the US tell what they have seen, funds pour in. They are raised locally in Jamaica too, with frequent publicity in the media.
Life, you may say, is its own ambassador, demonstrating even under extreme disability its own worthiness and viability in a largely utilitarian world. I don’t take the Catholic position on the policies I enumerated above, but I’m glad of Mustardseed and all similar enterprises for showing us more of what it is to be human than most ever see.
I suppose that in countries like Germany and UK, where there is a publicly funded health service, there’s no incentive to allow free access to visitors, and so the message doesn’t often get through. That’s sad.
I hope it’s needless to say that the message to which I refer has nothing to do with Catholicism or even the notion of God in a Christian sense.