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Francis Andrews | | Person with diabetesBorn in Cheltenham in 1931. Diagnosed Type 1 in Cheltenham in 1939
Overview: Dr. the Rev. Francis Andrews was diagnosed with diabetes on the day that war was declared in September 1939. He was the son of a doctor who`d worked as a medical officer in Flanders during the First World War. Francis also trained to be a doctor, and eventually became a consultant physician in rheumatology, having been advised not to specialise in diabetes. He married and has 6 children, 15 grandchildren and 1 great-grandchild, none of whom have diabetes. He took early retirement to train as a Catholic priest, and was ordained in 1994. | [View Full Interview] |
| Transcript... |
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| (1) Can you tell me about your parents
| (1) Can
you tell me about your parents?
Yes, my father was born in 1893.
He was the son of a shipwright, who had moved out of being a shipwright because
they no longer made the warships of wood, and he became an undertaker, and
my father was his eldest son. They were not really terribly well off, they
lived in Portsmouth, they weren‘t
very well off, but my dad did very well at school and he got a scholarship
to study medicine. And he went up to study medicine at the Middlesex hospital,
and he qualified in 1914 just as the First World War started, and so he went
from being a medical student to being a medical officer in the RAMC, and he
spent the whole of the first world war in Flanders, where he had a fairly
horrific time, I think. My mother was born right at the end of 1893. Her
father was a cabinet maker and her mother was a court dressmaker, a very elegant
lady indeed. My mother trained as a teacher and she qualified, I‘m not quite
sure which year but I think it was in 1912, I‘m not absolutely sure of that
but I think that was the case, and she taught in various schools in and around
Portsmouth. She met my dad in 1913, they met on a tram in the centre of Portsmouth, and they were married in 1916. They
even told me what they did on their honeymoon, which was to go and see the
original production of Chu Chin Chow in London.
I‘m actually the youngest of three children. My sister, the eldest, was born
in 1920, and my brother in 1921, and I was born in ‘31.
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| | (2) After
the war, my dad first of all worked in various hospitals. He was very interested
in the psychological effects of war injuries, and what I suppose came to be
known as shell-shock, and he spent quite a lot of time in two separate hospitals
dealing with soldiers who had this sort of war injury, if that‘s the right
term. Those were in Leicester and later in Chepstow.
Which hospitals, do you know?
I don‘t think either of them
any longer exist. I‘m afraid I don‘t know precise details. The one at Chepstow
subsequently became a plastic surgery unit and might be traceable from that
point of view. Leicester, I think it was Leicester Frith, but again memory‘s a bit
vague on that, and dad was never too happy talking about his time there.
After that he went into general practice and he ended up being a general practitioner
in Cheltenham, and as was the custom in those days he had additional interests,
and he was a general practitioner anaesthetist and he used to do a lot of
anaesthetics at the Cheltenham General Hospital.
This was mostly before the creation
of the NHS?
Oh yes, I mean the NHS was started
in 1948 and my dad never became an NHS general practitioner, he continued
in private practice. This was partly because by that time he was really rather
an ill man. He had had a coronary thrombosis in, I think it was 1941 or 1942.
He had a difficult time because he was in a partnership of three, and the
senior partner died just immediately before the war started, and the third
partner had only joined a year or eighteen months before, and the junior partner
was in the Territorial Army and therefore, of course, went off
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immediately into the forces. And for many months my dad had to run that three
partner practice single-handed, and I think it was very largely as a result
of that enormous overwork that he was so ill. Subsequently he had a very
nice little Czechoslovak doctor came and helped in the practice, and there
was also a very elegant, I suppose you would have to call him a refugee.
He was a general practitioner in one of the wealthier bits of London,
and when the bombing of London started he came to Cheltenham
and again he spent several years as a kind of assistant to my dad. Anyway,
dad continued getting less and less able with worse and worse coronary artery
disease and he died in 1954, quite suddenly. He died a month or two after
I had qualified.
Is there any history of diabetes
in your family?
Well, many people have asked
me this, many hospital clinics have asked me this, and it‘s a bit odd. My
dad was injured in the First World War. The exact nature of his injuries
I don‘t know, but it wasn‘t that he got a bullet through him or anything of
that kind, but he was injured while working in one of the military hospitals,
I think it was the Nineteenth Field Hospital in Flanders.
It was said that he had glycosuria immediately after the accident, but subsequently
he didn‘t have glycosuria, and up to the time of his death he had no other
evidence of diabetes. But that‘s the only possible bit of diabetic history
that I know of in the family.
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How did your own diagnosis of diabetes come about?
Well again, obviously, the precise
details of this are a bit vague, but in early 1939, I suppose it must have
been in the summer of 1939, of course I‘m not sure, I got whooping cough and
I was clearly pretty bad. Even now I can remember the episodes of coughing.
I suspect that I collapsed a segment of lung at least, and certainly I can
remember being very unwell for quite a long time. When I got better, my parents
had obviously been tired like nobody‘s business by my coughing and the worry
they had had, and so I went to stay with my maternal grandparents who lived
in Portsmouth, and my parents went off to have, I think, a sort of week or
fortnight’s holiday; I suspect a very well deserved week or fortnight’s holiday.
I can remember while I was staying with grandpa and gran, I can remember being
extremely thirsty, and I can remember my grandfather, who tended to be a bit
of a worrier at the best of times, I can remember him being very, very worried
about this and being extremely glad when my parents arrived to take me back
home. They took me back home, and my memory is of them exclaiming how much
weight I’d lost in the week or ten days they had been away. I can also remember
feeling absolutely frightful, really, just, it was sort of... I don‘t think
I ever verbalised exactly what I felt, but I can just remember feeling awful,
and why it was I don‘t know, but I don‘t think that my dad could have clicked
as to what was happening because he and my mother took me away again.
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And we went to stay at Prestatyn in North Wales, and
I can remember walking on the beach there and just feeling I couldn‘t put
another step in front, couldn‘t put my legs up and put them down again, feeling
absolutely dreadful. And that was right at the beginning of September of
1939, and the news came of the German invasion into Poland, of which,
of course, I took no notice at the time, and my dad decided that we‘d better
get back home quick, and he drove back. My dad was a very rapid driver even
in those days, and he drove back from Prestatyn to Cheltenham.
I arrived back in Cheltenham and my brother exclaimed
when I arrived back, and I can remember him doing that, and I think at that
point my dad realised what had happened, or what was happening, and I can
remember being carried by my brother into the hospital. I can remember him
lifting me up, and it wasn‘t very far, it must have been quarter of a mile
or thereabouts, and I can remember him carrying me that distance, and I can
remember him putting me onto the bed.
Which hospital was this?
That was in Cheltenham, I think at that time the only going hospital was the Cheltenham
General. There was another hospital, St
Paul’s, but that was right down at the other end of the town, and so it must
have been the Cheltenham General. And I was under the care of a certain Dr
Haslett, who was always known as Ham, not quite sure why he was known as Ham,
but he did have rather a red face and he was a bit overweight, so maybe that
was why.
Was he a specialist in diabetes?
No, he was just one of the local
physicians. At that time there were only two consultant physicians in Cheltenham,
and he was one of them. He was a very nice man, he was very kind to me, but
of course the war was just breaking out at that time and things were beginning
to go a bit sort of haywire, with various doctors leaving to join the forces
and goodness knows what, and I think he too was very busy indeed, but he was
a very kind man. And I can remember him coming, I can remember him taking
blood from me and I can remember being given insulin, I‘ve no idea, it must
have been soluble insulin I imagine at that time, and I can remember feeling
quite dramatically better a few hours later. Previously, I think, I had probably
really been in pre-coma, because although I can remember my brother lifting
me and carrying me, I can‘t really remember anything about what happened when
I actually got into the hospital - a number of sort of vague impressions,
but nothing that I could really put a name to at all or describe.
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That day I was admitted to hospital was actually the day that Chamberlain
made his speech in parliament declaring war on Germany.
I have no recollection of that at all, obviously, but I can remember, it must
have been a day or two later, my dad coming in very distressed, because, of
course, he had all the memories of the trench warfare in the First World War.
And indeed the poor man, right up to the time of his death, used to get appalling
nightmares about the First World War and the state of the trenches and how
people were buried. And on one occasion, the hospital he was working in was
inadvertently shelled, and I can remember him telling me of the difficulty
they had trying to get wounded men and nurses and other members of the staff
out from under the rubble, under which they had been buried. And right up
to the time of his death, he used to get this nightmare of digging people
out from the rubble, even when he was severely ill with his coronary artery
disease. I can remember that very clearly. Anyway, I had my diabetes treated
and I got better. And I can remember having a second blood sugar done, and
I can remember the enormous size of the needle and the enormous amount of
blood that seemed to be being taken from me, but looking back on it, I can
only remember those two occasions of having blood taken in the course of my
initial diagnosis and initial treatment. I don‘t think that this sort of
investigation was, in fact, done quite as light-heartedly as it is now: we
did, after all, need 5ml of blood, and laboratories weren‘t as well geared
up. But I don‘t then remember having another blood sugar done until I was
in my teens and went up to medical school, so from the age of about eight
up to the age of about eighteen or thereabouts, I don‘t remember having any
other blood sugars done at all. I do remember having urinary glucose estimations
done very frequently, two or three times a day. I do remember a great deal
of fiddling about with insulin. Having been stabilised initially on a soluble
insulin, they changed me onto protamine zinc insulin. Again, that must have
been endish of September of 1939. I had a lot of trouble with that protamine
zinc insulin, because I kept on going hypoglycaemic in the early hours of
the morning and waking my parents up as a result. And they fiddled a lot
with the insulin arrangements, and I ended up on the combination of soluble
insulin with protamine zinc.
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Can you remember back at the hospital any training in doing injections?
No, I had no training in doing
injections then. My parents did all my injections up ‘til the time, I must
have been about thirteen or fourteen, can‘t remember for sure, but they did
it all. I didn‘t really get taught very much about my disease process. I
went back to school, and it was a school which had quite a hefty emphasis
on physical activity. I mean, I was playing rugby and all these sort of nasty
games, you know, and I can remember that they took precautions at school against
my going hypoglycaemic, and I think the poor unfortunate games masters must
have had a very difficult time with me. They were always very good and they
never complained, but I think they must have had a difficult time looking
back on it. But really, I got very little education in terms of the disease
and how to manage it. I don‘t think that at that time the importance of this
was realised at all.
What do you remember about the
urine testing?
Oh Benedict‘s solution, yes,
having to boil the urine specimen with Benedict‘s solution over a little spirit
lamp. My mother became very expert on this, but nobody ever taught me how
to do it up until very late, so my mother used to do it. And I can remember
that every now and then she used to shatter test tubes by heating them too
quickly, and this produced a lot of mess and tended to be a sort of rather
unpopular event in the household, but I myself didn‘t get taught anything
about this. Again, it must have been up to the age of about thirteen or thereabouts,
thirteen-fourteen, again I‘m not absolutely sure. Round about that time as
well, a decision was made to change me from that mixture of protamine zinc
insulin and soluble insulin onto globin insulin, which was fairly novel
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at the time. Now I fear I just can‘t remember the date of that, but I know
it was within a month or two of globin insulin becoming freely available in
this country, so the date could be checked that way.
Can you remember perceiving any
changes yourself?
No, not really. I think if there
was any change that impinged on my consciousness at all, it was that I didn‘t
have any night-time hypoglycaemic episodes, but whether that was related to
the globin insulin change or not, that I‘m not certain about, but I do know
that later in my teenage years, I was never bothered by night time hypoglycaemia.
When you talk about hypoglycaemic
episodes, did you pass out at any time?
Oh yes, on several occasions,
and again, obviously, I don‘t remember any of this in detail, I suppose I
wasn‘t conscious enough to remember it or to record it mentally. But I do
know that on a number of occasions my dad gave me intravenous glucose - I
can remember there being whacking great ampoules of the stuff. Dad was actually
rather good at intravenous injections. I suppose being an anaesthetist part-time,
he became rather more skilled in intravenous work than a lot of doctors, but
I also remember that he never seemed to think that it was important to have
sharp needles, which wasn‘t so pleasant, but there we are!
Can you remember at the age of
eight, any change in your diet?
I can‘t really, I mean there
must have been, but I don‘t really remember it. We had tended anyway to be
a family that, I suppose nowadays, would be thought of as eaters of healthy
food. We‘d always tended to be this way, so maybe from my point of view there
wasn‘t quite the dramatic change of diet that there might otherwise have been.
I do remember, of course, that during the war years, diabetics were allowed
to swap their sugar ration for various other things, and I can remember all
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But I remember it mainly in terms of having to go to the food office to get
the ration books countersigned and stamped, and little bits of extra paper
put in. I don‘t actually remember it as being a change of dietary habit or
anything.
Can you remember what you got
instead of sugar?
I can‘t remember exactly. I
know we got extra cheese, I think we got extra eggs, but again, in detail
I‘m afraid, I just don‘t remember. My mother tended to be a very sort of
‘I‘m in control of the kitchen‘ sort of person, and I don‘t remember any detail
at all about this.
Can you talk about life at school,
and how you managed your diabetes from diagnosis onwards?
I‘m not sure that it made an
enormous difference to my schooling. I think that the masters at school,
and it was a single sex school, I think that they were all aware, and I can
remember on one or two occasions masters saying to me things like "I
think you ought to go along and see matron", because matron had a little
office. It was a boarding school, although I was a day boy, and I can remember
traipsing along the fairly long passage to matron‘s office. And I can remember
matron, who was a very motherly lady indeed, cooing over me rather, and I
think she must have given me sweetened tea. I don‘t remember being given
anything like glucose drinks, because I can remember having been given glucose
drinks at one stage and they tended to make me feel very sick indeed, so I
think probably she gave me something like sweetened tea or sweetened coffee
or something like that, but I don‘t remember.
And how did you manage school
meals?
Oh we didn‘t have school meals
in those days, we didn‘t have school meals, no. I got on my bicycle and I
rode home for my midday meal, and I rode back again afterwards -
it was about a mile and a quarter. And then we finished school, we used to
finish school fairly late, in the prep school we used to finish at about four
o‘clock, and again I would ride home. When I went up to the senior school,
we started
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half past eight in the morning, and we broke off for our midday meal at one
o‘clock, and we started again at half past two, so I leapt on my bicycle at
one o‘clock and peddled home furiously, it was downhill all the way fortunately,
had something to eat, and then leapt on my bicycle and peddled uphill all
the way back. And in the senior school, we started half past two and we finished at just after five
o‘clock. It was fairly hectic as a school time, I remember.
And how well did you manage the
physical exercise aspect of your education?
I loathed it, but that was because
I‘m disinclined to take physical exercise anyway. I don‘t think the diabetes
made an awful lot of difference to that, frankly. As I think I said before,
the various games masters used to keep an eagle eye on me, and they had a
tendency to, when playing games, to put me into places where I wasn‘t going
to be quite so physically active. I can remember being padded up like the
Michelin man and put in goal playing hockey, and actually, I think I became
quite a good goalkeeper in hockey. And I remember also being plonked as full-back
in rugby, and I didn‘t like that much, I much preferred being a wing-forward.
And playing cricket, I got almost inevitably plonked down as wicket keeper,
and I can remember on one occasion a ball went up in the air came down on
my head and knocked me out. Very pleasing that must have been, because they
actually carried me off the field, but I don‘t actually remember any details
of that at all, but I can remember being told the tale afterwards.
What were the attitudes of your
fellow pupils to your diabetes?
I think that they were very accepting.
I don‘t remember anybody being nasty to me about it at all, I mean it‘s possible
that they were, but I don‘t remember that. And I can remember that on one
or two occasions, one or two of my close acquaintances actually sort of steering
me along to the matron, so my impression is that they really
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were very nice to me; certainly I wouldn‘t have any reason to complain of
my fellow pupils being difficult in any way in relation to my illness. There
were one or two other damaged pupils in the school at the time. There was
a boy, for example, who had been much damaged by polio and walked with sticks,
and people were very accepting of him, so I suspect that there was perhaps
an atmosphere in that school of acceptance, in a sort of sense of a duty of
care of one pupil for another.
Was there anyone else with diabetes?
There was. There was a chap
called Duckworth. He was very tall and very thin, but he only lasted a term
and a half, because his diabetes was so unstable that they just couldn‘t cope.
I don‘t know what happened to him. When I‘d been in the school, back from
my initial diagnosis, a couple of years, he came, and I think the idea was
that they had experience of looking after a diabetic in me, and they thought
they‘d be able to look after a diabetic in him. But I can well remember the
poor lad was keeling over right, left and centre. He clearly, either his
diabetes hadn‘t been as well managed, or perhaps he just wasn‘t being as careful,
I just don‘t know.
Did you get good warning when
you were going to have a hypo?
I got a bit, it was usually fairly
brief. I think that other people used to notice before I did. I know that
one of the masters, a man whom I subsequently got to know very well, and I
knew him very well when I was an undergraduate, I know he said to me later
on that he used to notice sometimes as I went very pale, and that he regarded
that as a warning sign. But I don‘t remember myself getting very much warning,
except fairly briefly feeling just a bit confused, a bit disorientated, not
quite with it.
You hadn‘t been given a deliberate
hypo when you were first diagnosed?
No, and anyway you see, with
changing from one insulin to another, that alters the nature of the onset
of hypoglycaemia very considerably, as I‘ve noticed since they changed me
to human insulin, so fiddling with the insulin may have made quite a bit of
difference to the individually felt symptoms of hypoglycaemia.
Can you remember any more detail
of that of the different symptoms when you changed?
Well, when I changed later on,
yes. I got changed off globin insulin when I went up to be a medical student
and Alan Kekwick took over the care of my diabetes at the Middlesex, and he
changed me from the soluble globin insulin to twice-daily soluble. And I
can remember when that happened I felt very much better in general, and I
think I coped much better. I found then that the first symptom I got of hypoglycaemia
was tingling of the tongue and of the lips, but again if I didn‘t do something
about it pretty quick I got into big trouble very quickly, and I‘d become
discoordinate, and I‘d become clumsy, and see double, and goodness knows what.
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Well let‘s move on then to leaving school, and can you talk about what happened
then?
Yeah, I did fairly well on examinations
when I left school, and I actually got a scholarship for the medical school.
Wasn‘t very much of a scholarship - it was forty pounds a year, but considering
that the medical school fees at that time were sixty pounds a year, and that
I lived in London on five pounds a week, that wasn‘t bad. It was quite useful.
Which medical school?
I went to the Middlesex Hospital Medical School
where my dad had trained, and indeed where an uncle of mine had trained as
well. I can remember being interviewed for that. I was interviewed by Sir
Harold Boldero, who was a paediatrician and was the Dean of the medical school,
and had actually been more or less a contemporary of my dad. And I can remember
being interviewed by him, and I think I got into medical school entirely on
the basis that Sir Harold Boldero felt very sorry for me being a diabetic.
I‘m not sure that academically I was really up to it. I don‘t know, maybe
I was, you can‘t judge your own academic abilities. But I can remember when
I was interviewed him looking very pathetically at me and saying "oh,
you poor lad", so I suspect that got me into medical school! But I went
up, I lived in digs in Camden
Town, I lived in digs with a very nice Swiss family, who clearly regarded
me as an additional son, and they looked after me with great care for all
the time I was there. And I enjoyed medical school enormously, and I actually
enjoyed playing rugby, not very distinguished rugby, but I played rugby for
the Middlesex Hospital B team. I used to play cricket for the Middlesex as
well, never for their first but occasionally for their A team. And I had
no major problems at the medical school, until I went and got glandular fever.
What year was that?
Now I‘m just trying to remember
the year. I think, I‘m not absolutely sure, but I think that
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must have been 1950, and I just felt awfully unwell, and I actually went to
the casualty department of my own teaching hospital and they got me admitted.
And my diabetes had become unstable, and I had lots of lymph nodes up in various
bits of my body, and I had the diagnosis of glandular fever made. And I was
off at the medical school for, I‘m not sure exactly how long, but it must
have been about a couple of months, and I know that when I went back I was
still feeling really rather tired, but okay, I coped, and it was okay. Yes,
I went to casualty, and I was admitted from casualty under the care again
of Professor Kekwick, but the person whom I remember most was a certain John
Friend, who was senior registrar in that department at the time, but he subsequently
went up to Keele or Stoke on Trent as a physician. And he was very kind indeed
to me, and was very helpful, both in educating me a bit more about my diabetes,
and indeed, I think, helping me towards realising what I could and couldn‘t
do, and trying to disabuse me of the idea that I had acquired in my earlier
teenage years, that my prognosis for life was really very poor.
Where had you acquired that idea
from?
I‘m not quite sure, but I think
from my parents. And I don‘t think that this was ever in a precise way articulated,
but they clearly had the expectation that I wouldn‘t make old bones, and clearly
had the expectation that they would be attending my funeral rather than that
I would be attending theirs.
Your father wasn‘t a diabetes
specialist, so where did he get his information about diabetes from?
Where did dad get his information
about diabetes? There was a very good book, or perhaps it was a series of
books, by the late RD Lawrence. They were entitled, I think, "The diabetic
life", and I think Dad got most of his knowledge from there. I subsequently,
after I‘d qualified when I was doing my first medical house job, I actually
met RD Lawrence, who came across to me as quite a different sort of person
from the one that my dad had thought he would be from reading his books.
I don‘t think dad got any other source. He may well have attended meetings,
he may well have chatted to various people, but I‘m afraid I just don‘t know,
I just don‘t know at all.
Just quickly on the subject of
RD Lawrence then, how did he come across as different from his books?
Oh, the book, I gather, gave
the impression that he was a bit rigid, and
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yes, he had his system of diet, his Line system of diet, and so on and so
on, and he clearly from the book had expected everybody to stick with great
rigidity to all this. He was, of course, himself a diabetic, and indeed was
one of the very first people ever treated with insulin in the early 1920s.
When I met him, he came across as being rather a jolly man with something
of a twinkle in his eye, and nothing like as rigid in his approach as his
books had suggested. I never got to know him very well, but I must admit
I rather liked him. I was introduced to him by a chap who was his assistant,
and for whom at that time I was house physician, and that was Wilfred Oakley,
very nice man. Yes, very nice man who tried to persuade me to leave clinical
medicine and go into pathology, which I didn‘t want to do at all!
Had your father kept you to the
Lawrence Line diet?
I think he had tried to, but
in fact it was almost impossible, given how the school times varied, and given
the fact too, I think, that my mother used to have great difficulty over coping
with all the assortment of rations. Our house was a big house, and as a result
of this we got used as a refuge for all sorts of people. And we used to have
grandparents arriving from Portsmouth
looking shattered after the bombings, and cousins arriving from London, again looking shattered after the bombings,
and they got even more shattered when a bomb landed next door to us and we
lost the chimneys to the house. They all went very quickly after that. But,
even so, after a little while they began to come back, and there were times
when we had twenty five people staying in that house, and it was very cramped
indeed. And I think my poor mum did her nut over the cooking!
How did she manage your quantities?
Well, she had a series of scales
around the place. The great trouble with mum and scales was that she was
always losing weights. If you had a half ounce weight, there was a fair chance
she‘d lose it. If you had a quarter ounce weight, it was absolutely certain
she would lose it. So she went in for spring loaded scales,
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and of course spring loaded scales need to be readjusted constantly. And
she used to have a set in the dining room and a set in the kitchen, and if
I remember rightly she also had a set in her sitting room as well, because
habitually we used to have afternoon tea in the sitting room. And these three
sets of scales never agreed with each other, so I suspect my lines got a bit
twisted from time to time!
Back then, where we left you,
with glandular fever. What happened next?
Oh, they admitted me to the ward
at the Middlesex. They treated my unstable diabetes, clearly there wasn‘t
very much to be done about my glandular fever, because there‘s no real treatment
of glandular fever. So I gradually got better, and my diabetes was stabilised
again and all was okay, apart from the fact that I felt very tired for a long
while. Oh, there‘s one other thing that I didn‘t mention. Before I got glandular
fever, and this was only very shortly after going up to medical school, I
got acute appendicitis, and again I was admitted to the Middlesex with my
acute appendicitis, and I had my appendix taken out. And I can remember being
very surprised at that time that it didn‘t seem to upset my diabetes at all,
and I suspect that was because the professor, Prof Kekwick, and his juniors
had kept a very close eye on me at the time of my admission. I was very surprised
that I had so little bother; I was in the Middlesex for only about five days,
which at that time for an appendicectomy was a very short stay indeed. I
did actually go home for about a fortnight afterwards, but no problems. It
was wonderful.
Now the classic image of a medical
student‘s life is rather sort of irregular, and full of drinking and so on.
How did that lifestyle combine with your diabetes?
I don‘t think I was ever very
well off to indulge in much in the way of drinking. There was a pub almost
opposite the Middlesex, the Cambridge Arms, and there were a group of three
of us who used to go over
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there occasionally. I can never remember drinking any vast quantities. I
suppose I must have had the occasional beer or whatever, but I don‘t remember
this as a sort of habitual thing at all. I did find, there was a funny little
restaurant just down the road from the Middlesex, it was called The Glory.
I suspect it was called The Glory because it was so obscure and so peculiar.
And rather than use the hospital canteen, which the medical school students
were entitled to use, I used to go to The Glory midday,
usually with a friend of mine, Ian Dawson. I‘m not sure that it was necessarily
a particularly wise choice, but certainly one used to get served a good deal
quicker than one got in the hospital canteen, and consequently you could at
least sort of gear yourself to finishing a session in the morning and starting
a session in the afternoon. If you went to the canteen, at times you had
to wait three quarters of an hour to get your meal from the sort of buffet
counter, cafeteria counter, and this was a bit disconcerting when you were
trying to get back to lectures and things.
Were you weighing food yourself
at this stage?
No, I mean it wasn‘t practical.
My very nice Swiss landlady used to get very worried that she wasn‘t weighing
food, but again it wasn‘t really practical, and you couldn‘t ask a little
body, who made her livelihood out of hiring rooms to students, to take that
degree of special care of an individual. They were very good and very kind
to me, and were very careful over what they gave me to eat, but I don‘t think
they ever weighed things, not that I can remember anyway.
Would you say, at the period
when you were a medical student, that you were keeping very strictly to a
diet and strictly to a regime of insulin, without doing any adjusting yourself?
I think I was keeping pretty
strictly to my insulin regimen. I was doing urine tests very frequently,
usually morning and evening, and I used to adjust insulin, usually adjust
the soluble insulin part of the regimen in the early days, later, of course,
it was only soluble insulin, according to the results of those urine tests.
I don’t think that my dietary intake could have been anything like as well
controlled; I don‘t see how it could have been quite honestly. I think I
did as well as I could, as well as was practical, but certainly, how should
I put it, I never became obsessive about it. Perhaps if you become obsessive
about these things, your disease takes over from you rather than you controlling
it, I‘m not sure.
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Can you talk now about when you qualified?
Yes, I qualified in 1954. I
got the London MBBS. It was at a time when there were a lot of people qualifying
who had been in the services during the war, and we were told, when we qualified,
that the house jobs, the house surgeon, house physician jobs at the teaching
hospital would go as first choice to people who had been in the services during
the war, which seemed reasonable - after all, they had given up a lot of their
lives to fighting for, basically, I suppose, for us. So that when I qualified,
I did in fact apply for jobs at my teaching hospital, but I wasn‘t at all
surprised that I didn’t get them. I then, my dad rang me up, and my dad said,
would I like to do a house job at the Cheltenham General Hospital, and so
I did. I went there as a house surgeon and I did my first six months there,
which was very busy, and I don‘t think it was as well supervised as it ought
to have been. I can remember, for example, being asked to give an anaesthetic
to a young man who had come into casualty after a plate glass window had fallen
on top of him when he was trying to install it in a shop in the centre of
Cheltenham. And he had a great dagger of glass going
into his neck, and the surgeon who was on duty said "oh, you can give
him an anaesthetic, it‘s easy". Well, I had been instructed on how to
give anaesthetics, and I had done one or two under supervision, but I‘d never
actually done one completely unsupported before. And I must admit, I was
exceedingly, exceedingly glad when that young man came round from the anaesthetic
he had given me and seemed to be perfectly well. And indeed, I think the
chap who took the glass out of his neck was quite heroic, and perhaps should
himself have had a gold medal, because that fragment of glass was actually
landed in between
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the carotid artery and the carotid vein, separating them without actually
puncturing either. Quite a horror that was, however.
What sort of hours did housemen
work in those days?
Well, the hospital had two house
surgeons and one surgical registrar, there was a casualty officer, there was
a gynae house physician and a paediatric house physician. But the paediatric
beds were three miles away and the gynae beds were three or four miles away,
so that the whole hospital was run with one house physician, two house surgeons,
a medical registrar, a surgical registrar and a casualty officer. And we
took all the emergency work from Cheltenham, from Stroud, from Nailsworth, from Winchcombe, from Tewkesbury,
and all the countryside round about. It was very busy indeed. I can remember
being up night after night when the winter was upon us - and that for two
reasons. One was that the ice on the Cotswold roads used to produce enormous
numbers of skids of lorries and cars, and people would come in with head injuries
and long bone fractures. And I can remember also the pressure there was on
casualty with people coming in with infections. There was a lot of poverty
in that area at the time. One tends to think of Cheltenham as being a sort
of town of middle class retired people, fairly well off, but there was in
fact a considerable area of that town where there was a great deal of poverty.
There was a notorious street called St Paul‘s Street North, and I can remember
going down there on one occasion to visit somebody who was ill. I went down
with my then consultant, George Dorling, and I can remember being absolutely
horrified by the blatant poverty of that house, and the way in which the little
lady, whose husband and herself and I think it was three children lived there,
how she laboured to keep that place clean and neat, and how blatant the poverty
was. Very distressing, as I‘d never come across real poverty before. But
there was a lot of that in Cheltenham, and consequently
there were a lot of people who used to roll up in casualty with chest infections,
other infections, very much precipitated by cold and lack of heating. And
as a casualty officer, because when the casualty officer himself was off duty
the two house surgeons took it in turn to run casualty, I can remember seeing
these people coming in, and very often having to sign the death certificates
a few hours later.
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So how many hours do you think you worked in an average week?
I find it very difficult to say
this. I think it would be very unacceptable now, the number of hours we worked.
But I can remember, we did come to an arrangement whereby alternate weekends
the house surgeons took off. The other house surgeon who was there with me
was a chap called Williamson, and he was a Scotsman, and he had a girlfriend
who lived, can‘t remember exactly where, somewhere in the Midlands, and I
had just got married, and so between the pair of us we came to this arrangement
that we would cover each other alternate weekends. It wasn‘t terribly popular
with our superiors, but the pair of us insisted on it. But other than that,
we worked, I suppose, about a twelve hour day, and we were on call, certainly
alternate nights, and if things were very busy, as they were sometimes, we
were, of course, we were working through the night as well. It was a very
busy job, it really was.
So how did you manage your diabetes?
I‘m not sure whether it was by
luck or by judgement, but I do remember that I didn‘t really have awful amount
of trouble with it. The other juniors there were again, they were very kind,
and I can remember on occasion the surgical registrar saying to me "look,
it‘s about time you went off and had some breakfast", or "it‘s about
time you went off and had something to eat". And they were very kind,
and I think, you know, they tried to be very helpful, and indeed they were.
They were a very nice group, very nice group.
Were there worries that you might
not have adequate warning of a hypo in a situation where you were responsible
for somebody else?
Well, I must admit that I myself
used to take precautions over this. I think I‘ve said before that I had great
difficulty if I had to drink glucose drinks, but I used to carry in my pocket
a tin of those funny little compressed glucose pastille things, I think they
contained five grams of glucose each, though my memory may be faulty on that.
And I used, if I thought I was going, as it were, to run over time, I used
to suck one of these before doing anything, before perhaps going to theatre
or whatever. I do know that I didn‘t in fact have any major troubles or difficulties,
and I suspect that it was the combination of the helpfulness of my colleagues
and that little square tin of compressed glucose.
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What happened after Cheltenham?
There was a shortage of house
physician jobs, and as you probably know at that time, this was shortly after
the changes in medical registration, and people had to do six months as a
house surgeon, six months as a house physician, with six months in obstetrics
and gynaecology as an alternative to one or the other of those. And there
was a great shortage of house physician jobs, but I‘d been somewhat fortunate.
We had got married and we‘d got a little house in Cricklewood, and we used
to go to church at the little church dedicated to St Andrew in Dollis Hill
Lane, and that was next to the Catholic Hospital of St Andrew‘s, Dollis Hill.
And it so happened that in that church, the chap who was the secretary, the
hospital secretary, and his wife also worshipped, and we got to know both
of them quite well. So when I was getting to the end of my time at Cheltenham
and I was beginning to look round for a house physician job, my wife mentioned
this to the hospital secretary, and the hospital secretary said to my wife
"well, we‘ve got a house physician job coming up", I don‘t know,
it must have been in six weeks time or something like that, "why doesn‘t
your husband apply?". So I did, and I got short-listed and I was interviewed
and I got the job, so that was very nice, because it was only about a mile
from where we were living. It was a job I needed, and indeed it was a job
in which I was working for good chiefs who went out of their way to teach
me, and I think I learnt a very great deal. I can even remember the salary
I was paid. I was paid a hundred and fifty pounds for the six months, and
we were living on that. It seems extraordinary, but we were living on a hundred
and fifty pounds over six months. Surprising really, but we did it.
Were you required to be a Catholic
for that job?
No, I think I was the only, I
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think I was the only Catholic on the junior staff there, and I suspect that
the nuns who ran it tried to pamper me as a result, but, I didn‘t like being
pampered very much. It seemed a bit sort of, a bit off beat really. But
it was a very happy hospital, not very big, it had about a hundred and forty
beds. I was the only house physician, there was no medical registrar, there
was a surgical registrar, an anaesthetic house officer and there was one,
and later two, house surgeons. There was no real casualty department there.
But it was a happy hospital.
Were you beginning to think about
what area you might specialise in?
Yes, I was actually. I‘d actually
wondered about specialising in diabetes, and one of the people I was working
for there was Wilfred Oakley, I‘ve mentioned him before. He was on the staff
at King‘s College, the diabetic unit at King‘s College Hospital in South London, and that was how I came
to meet RD Lawrence. Wilfred Oakley was very, very much against my trying
to specialise in the care of diabetics. He said, and I sometimes wondered
whether this was because of his close association with RD Lawrence, who was
himself a diabetic. He said that he thought it was a bad thing to specialise
in a disease which one had oneself, because one was too close to it to be
able to be objective. Looking back on it, he was probably right, though at
the time I didn‘t think so and I got a bit uptight about it all. But he tried
to persuade me to go into pathology, and he actually arranged an interview
for me with the professor of pathology, Professor Scarfe at the Middlesex Medical School.
Professor Scarfe was again very kind to me, and he said to me that he thought
my interest was an interest in people rather than in corpses, and he was quite
right, and consequently he advised very strongly against
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going into pathology as a sort of long term career prospect. One of the other
physicians at Dollis Hill, a chap called Alec Wingfield, he suggested to me
that I needed to get a higher qualification, and this I‘d really not thought
about at all. And he suggested that I applied for a job at another hospital
where he worked, which was the Seamen’s Hospital in Greenwich, and I applied for that house job and I got it. And that
too was a very interesting job. And later on, when I became a consultant,
I discovered that I was the only consultant in Reading who had actually treated
leprosy, and had actually had to cope with cerebral malaria, and actually
knew a bit about intestinal worms, not that that was the consultant post that
I attained, but it was quite interesting to find that that bit of experience
had brought me into an area of knowledge that wasn‘t commonplace. Anyway,
I did that job, and I then went to the Willesden
General Hospital as medical registrar. When I finished
my two years there, again I was working for Alec Wingfield, and he, I think
there‘s no doubt at all, he manoeuvred me into a registrar post at the Middlesex Hospital, at the Middlesex Hospital and at the Arthur Stanley
Institute, the Arthur Stanley Institute for Rheumatic Diseases. I hadn‘t
wanted to do rheumatism at all, but I found it absolutely incredibly intriguing,
and I found that the patients were the most long-suffering in many senses,
and people who were so rewarding to try and help that, within a very short
while, I had become completely converted to the idea of working as a rheumatologist
as my life‘s career, which indeed I did. And it was, from my point of view,
a very, very happy career choice. But I came into it entirely by chance,
entirely by chance.
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And clearly the Lord was pushing me rather than me directing myself, but it
was very good and very happy, and I loved it.
Had there been any changes in
your diabetes during this period we‘ve talking about?
I don‘t think there‘d been any
major changes. I had had one or two infections that I had sort of picked
up, usually picked up from people in casualty. ‘Cause again at the Seamen‘s
Hospital, the seamen used to come in at high tide into the port of London,
and you would see people with many, many, and very varied, acute illnesses,
and one used to have to go down to the casualty department there to cope with
these. And some of the illnesses they had were bizarre to say the least of
it. And I can remember I picked up a real good old fashioned pneumococcal
pneumonia from one of the seamen. It was picked up, of course, very quickly
by my colleagues and treated very quickly, and I don‘t think I was ill for
more than a day or two. I don‘t remember that, anyway, as being a prolonged
illness. It was a good place to work, the Seamen‘s Hospital. I‘m sorry it‘s
closed.
Did you have any regular check-ups
for diabetes?
At that time, no, not at all.
Life was too busy, life was much too busy. My boss, Alec Wingfield, he used
to run the diabetic clinic, both at the Seamen‘s Hospital and at Willesden.
The Seamen‘s Hospital diabetic clinic, of course, was pretty tiny, because
no diabetic seaman got kept on as a seaman very long. Sometimes you got people
like engineers who were diabetics, and I can remember on one occasion a sea
captain who was a diabetic. I‘m not sure, looking back on it, whether his
diabetes was newly diagnosed or not, but I can remember him coming in from
his ship, accompanied by his first officer, in pre-coma, but I don‘t for the
life of me remember whether he‘d been treated as a diabetic previously or
not. I can remember that the shipping federation people retired him with
great speed, and he was terribly distressed by that. However.
When you did treat people with
diabetes before you specialised in rheumatism, did your own diabetes have
any relevance?
I suppose it did, because I suppose
it helped me to have a little bit of insight into the difficulties people
were having. I know that I used to spend quite a lot of time talking to newly
diagnosed diabetics about their disease. I‘m not sure that at that time that
was very commonly done - I may be misjudging people by saying that, but people
I can remember being really rather grateful that one had taken time and trouble
to talk to them. But other than that, I don‘t think it made an enormous difference.
I did at that time become really rather skilled at doing blood sugars, because
you always had to do these yourself during the night, and of course you didn‘t
have any of the kits. You had to do it all in the laboratory with five mls
of blood and spinning it off and goodness knows what. But I got rather skilled
at that, I could do them very smartly indeed. However!
This is for yourself or for your
patients?
Mainly for the patients. I mean,
I occasionally did one for myself, though I‘ve never found it very easy to
take five mils of blood from myself - it‘s not the easiest of tasks, and I‘ve
never quite understood how heroin addicts manage to get needles into their
own veins so readily. I could never get needles into my own veins with ease!
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When did you go to the Arthur Stanley?
I‘m not absolutely sure, but
I think it was in 1960. I must admit I‘m a bit vague about this, time goes
by, but I think it was in 1960, and I was there for just about the two years.
I worked for Dr Oswald Savage, who was a great man, Oswald Savage - a very
good physician. And I worked for Tony Boyle, who was also very good, but
you didn‘t see a great deal of Tony Boyle. I think he had recently remarried,
his first wife had died, he‘d recently remarried and bought a house down near
the coast, and I think he was very interested in his new house and his new
wife, so he wasn‘t there quite as often as perhaps was desirable. But Oswald
Savage was very good. He used to teach a great deal, and I owe a great deal
to Oswald, very nice man. And there was a third person I worked for, a certain
Kenneth Stone, a very quiet little man. A very, very good example to a junior
doctor in the care he took for people, and the way he put himself out in caring
for people. He retired while I was there, and I was very sorry, very sorry
that he retired. I wrote him a thank you letter, and I‘ve still got the reply
he sent to me, which I treasure - one of the nicest and gentlest bits of fatherly
wisdom that I‘ve ever come across. A lovely man. When I finished at the
Arthur Stanley Institute, I went to the rheumatism research centre at Stoke
Mandeville under Alan Hill, and Alan Hill too I would regard as being a great
man - very gentle, very hardworking, very caring, a very good teacher. His
juniors used to always end up with superlative jobs all over the place. One
ended up as Professor of Medicine at Leeds, one ended up as Professor of Medicine in the Lebanon, one ended up at Manchester
in the teaching hospital there, one ended up at Sheffield
in the teaching hospital,
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one ended up at High Wycombe. I ended up in Reading.
It was a good place to work and the experience was very good indeed, and the
teaching superlative. I was there, first of all, as a registrar, then as
a research fellow, a research fellow with an honorary contract as senior registrar.
And in 1966, I went from Stoke Mandeville to the position of Consultant Physician
in Rheumatology to Reading, and to
the Reading group of hospitals.
And there I remained until I reached the age of sixty, or sixty and a bit,
and I retired early, at the end of 1991. I was one of the people who took
advantage of the offer by the Department of Health of early retirement for
people in whose speciality there was an excess of senior registrars, and therefore
a shortage of jobs for senior registrars. And so I took advantage of that.
And I took advantage of it, partly because I began to feel I was running out
of steam - I had been working very hard for a long time and I had been Tutor
in Medicine at Reading as well, and partly because my Bishop had written a
pastoral letter, in which he had said that he wanted men who were perhaps
reaching retiring age or who had taken early retirement to train for ordination
to the permanent diaconate. And the circumstances that I heard of this pastoral
letter were exceedingly odd. At that time, we had a parish priest here who
was suffering from Alzheimer’s disease and who never read the pastoral letter
out, indeed I‘m not sure that he even opened it. But by a curious series
of chances I got to hear of this pastoral letter, and I wrote to the archbishop
and he sent me a copy, and I read it. And two or three days later after reading
it, I had a letter on my desk at work from the regional medical officer saying
that I was entitled to claim early retirement under the health service scheme
for senior registrars, and I had a feeling that I was being kicked very firmly
in the bottom to do something. And that was reinforced a few days after that
by somebody else, who told me that there was a vacancy in the next training
scheme. So I took early retirement, the archbishop interviewed me and accepted
me, and I went off and did three years of training in Birmingham and got ordained
in 1994, almost ten years to the day from now.
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Before we get on to what you did after you were ordained, can you talk about
how large a part diabetes had played in your life, up until that point?
I must admit, I was always afraid
that it would rule my life, and I was always pretty determined that it shouldn‘t.
I mean, it‘s all very well to have a chronic disease, but you want to control
the chronic disease, you don‘t want the chronic disease to control you. So
I always did my best to, how shall I put it, be sensible in relation to the
diabetes - realise that it was there, realise that it was a disability with
which I had to cope, but on the other hand, to feel pretty strongly that life
had to be lived, and life had to be lived as normally as possible. I think,
in general, I managed that balance fairly well. A great deal of the ability
to manage that, I suspect, comes down to the goodness and tolerance and abilities
of my wife. She was a nurse, indeed she was a night sister, and she had worked
on the professorial medical unit at the Middlesex, and therefore perhaps had
rather more insight into the management of diabetes than a lot of nurses would
have had. But she has looked after me, and helped me to keep on the relatively
straight and relatively narrow.
Would you say that since marriage
it was she who had controlled your diet?
Shall I say that I‘m the world’s
worst cook. If I had any instruction in cooking, it probably came from one
of the Italian poisoning families. I‘m absolutely no good at cooking at all,
and now that I have to try and do the cooking for my wife, I really, I‘m very
sorry for her. So I think from the diet point of view, Mary has looked after
me with very great care, and I owe her an enormous amount, an enormous and
continuing debt I‘ve got to her. So I suppose yes, she did a great deal,
a great deal through the fifty odd years that we‘ve been married.
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about the time when you were training for ordination, the three years in Birmingham.
I started training for the diaconate
in September of ‘91. This entailed a great deal of reading, a great deal
of writing of essays, and I must admit I was out of the habit of writing essays.
We had to go up to Maryvale in Birmingham, which is up in Kingstanding, and it‘s
a bit of a traipse - it was a hundred and eight miles, door to door. The
arrangement was that we went up every weekend, and we had lectures and what
have you. We did a great deal of discussion, the group of trainees - there
were about twenty of them at the time, but there were only three in my year.
We had lectures and we got given enormous reading lists, and one of the great
problems was that the library at Maryvale was appalling, and you weren‘t allowed
to take books out of it, and it wasn‘t opened during mealtimes, and it wasn‘t
open after four o‘clock and our lectures didn‘t finish ‘til five o‘clock,
so the library was quite useless. Fortunately I could use the public library
here, and the librarians in the public library here were very helpful indeed
in getting books, so I didn‘t have to do that amount of travel. I did sometimes
have to go up to the library at St Benet’s Hall in Oxford, where again they
were very helpful, and sometimes I had to go to the library at Douai Abbey,
which is at Woolhampton, half way between Reading and Newbury, and sometimes
I had to go to the library at Downside, which is near Bath. But everybody
was very helpful, and I got a great deal of support from all sorts and conditions
of people. Anyway, I did the three year training. When I was getting towards
the end of the first year, something happened, and nobody has ever quite managed
to discover exactly what happened, but my diabetes went very suddenly and
very completely unstable.
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I mean, my thought was that I‘d picked up an infection. But I was admitted
to the Radcliffe in Oxford rather
urgently, and they did all the usual things; they put me on a drip and gave
me lots and lots of insulin and what have you.
You were in a coma, were you?
I was in pre-coma. I can actually
remember arriving at the Radcliffe, but I can‘t actually remember getting
to the ward. My wife tells me that I was very, very drowsy indeed by then,
but as I say I‘ve no recollection of that at all. I was only in there about
five, six days. They never discovered what had produced that sudden instability.
They never found any evidence of infection. They got all high powered and
took the ampule of insulin that I‘d been using and sent it off, to see if
by any chance there was something amiss with the insulin, but there wasn‘t.
And certainly I hadn‘t omitted a dose of insulin - neither my wife nor I had
any suspicion that that had happened, so goodness only knows how all that
occurred, I just don‘t know. Anyway, they re-stabilised me and all was okay.
They suggested that I changed onto human insulin, and that I did. I didn‘t
actually find, personally, that there was any enormous benefit from that change.
There was one enormous disadvantage, and that was I lost any forewarning of
going hypoglycaemic. I lost all the funny business of getting my lips and
tongue tingling, and that was a plague, but I had in fact developed cataracts.
Whether these were diabetic cataracts or not, I don‘t know, but it is certainly
true that my brother and sister, neither of whom are diabetics, have also
developed cataracts at about the same age, so maybe they are or maybe they‘re
not diabetic. Anyway, I had the cataracts extracted in Reading as a day case and under local anaesthetic, and it‘s quite an
interesting experience.
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And after I had the cataracts extracted, I found that every now and then I
got a curious scintillation in front of my right eye, very close to the fixation
point. The eye surgeons got very worked up about this, but they couldn‘t
find any evidence of my developing a retinopathy, and after a while I discovered
that this was actually a warning of hypoglycaemia. So I have, in fact, developed
a very unusual forewarning of hypoglycaemia, in that I get a sort of scintillation
in front of my eyes, close to fixation point. It‘s quite useful, because
it certainly draws itself to your attention - you can‘t miss it, and it responds
very quickly to quite minimum doses of glucose. I have also discovered that
at that time, my blood sugar is usually running around about 1.5 millimole
a litre.
Had you been having regular eye
checks before your cataract operations?
Oh yes, I had had regular eye
checks for a long time. I can‘t remember when it was, but it must have been
in, I suppose, the middle ‘80s, one of the registrars in the eye department
at the Royal Berks saw me, and he said something like, "well you‘ve had
diabetes for fifty five yeas now and you‘ve no evidence of retinopathy. I
doubt very much if you‘re going to get any retinopathy in the rest of your
life". I felt quite cheered up by that. Certainly they get a better
view now that I‘ve had my cataracts taken out, and certainly they still say
I have no evidence of retinopathy, so this is a good thing.
Up until this point, how much
contact had you had with medical checkups for eyes, feet, or whatever? And
what‘s meant by regular?
I‘d been seen by the eye people,
I suppose roughly at six monthly intervals, I couldn‘t be too sure but it
must have been about
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that length of time, and that‘s going back certainly to before the time when
I came to Reading as a consultant. I couldn‘t actually date
it any more accurately than that. So far as regular checks of my diabetes
went, when I came to Reading, I acquired as a General Practitioner Tom Stewart, who was
himself very interested in diabetes, and indeed set up one of the first diabetic
clinics in general practice in this part of the world, and he sort of took
me under his wing. He was a General Practitioner in Sonning Common and I
was living in Caversham, so, you know, it was a mutually very agreeable arrangement.
And Tom and I were anyway great friends from another occasion. He had been
a registrar at the Central Middlesex at the time when
I had been a registrar at Willesden, and we had got to know each other at
that time, so it was a mutually advantageous and mutually happy arrangement.
Unfortunately, Tom went and had a stroke and died in, just over ten years
ago now. A great loss, great man. Now, from the time I went up to the Radcliffe,
the Radcliffe people, who have now moved to the Churchill Hospital in Oxford,
have seen me with fair regularity. It runs out again between once in three
months and once in six months, more recently it‘s been once in six months,
and I‘ve been going up to Dr Levy‘s clinic. About, I can‘t remember the exact
timing, but a little while back, they suggested that I went on to using a
pen and having four times daily injections, and that I‘ve done. I‘ve found
that to be more convenient, because it means that your meal times are not
quite as fixed, but I haven‘t actually felt any better for it.
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I must admit, I‘m not too sure of the timing of that change, but it‘s been
suggested to me that it‘s 1996, and that sounds a very reasonable dating.
Very recently, they‘ve suggested a change of my night-time insulin to one
of the new insulins. That was suggested the last time I went up to the clinic,
which was just before the New Year. Their letter took more than a month to
get to my GP, but that‘s about par for letters from the diabetic clinic -
I don‘t think that they know what a first class post is. But it eventually
arrived with my GP, just at the time when my wife was taken ill, and he suggested
that I changed, and I said I didn‘t think I wanted to change while I was coping
with my wife‘s illness, and so I haven‘t. I‘m still using the long acting
Human Insulatard at night time and I haven‘t changed to the new insulin at
all, and I certainly have no intention of doing that while I‘m having to cope
with the very variable degree of disability that my wife is now showing.
It simply wouldn‘t be fair on her to have to cope with me fiddling about,
conceivably going hypoglycaemic and what have you, so it will have to wait,
it will just have to wait.
When you go for these six monthly
checkups, are your feet looked at, or other aspects of your health?
Yes, oh yes. My feet get looked
at anyway by the jolly chiropodists. I see the chiropodists over at Henley;
they‘re very good. They see me, they don‘t do it regularly, what they do
is they wait for me to ring them up, and I ring them up and I‘m usually seen
about a week later. And I go over there about once in three months, and they
provide me with nice insoles. They haven‘t been able to do it for the last
six months, because as an economy measure, the health service in Reading is not providing insoles. I can‘t quite
see how much money gets saved by insoles, if you then find that people develop
ulcers on their
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feet that take a long while to heal and take up a lot of in-patient time,
but then that‘s their choice, and if they‘re barmy in the crumpet, I can‘t
do anything about it. They do look at my feet very carefully, and I have
got a neuropathy which affects the feet, and the peripheral pulses in my feet
are not awfully good. When I go to the diabetic clinic, they also look at
my feet, they also assess the feeling in my feet. They don‘t usually look
at my eyes at the diabetic clinic, ‘cause the people in Reading do that anyway. And anyway, if I drive over to Oxford to the clinic, it makes it a bit difficult
if I have my pupils dilated and then have to drive back, so they‘re usually
rather kind and leave it to the people in Reading. And the people in Reading, a friend of mine takes me down to the clinic and brings me
back when they‘re going to make me filled with belladonna. And belladonna’s
supposed to make you a beautiful lady, I don‘t know that I‘m a lady at all,
I‘m certainly that I‘m not beautiful!
You mention this, what you consider
to be a bad decision about insoles, so this might be a good point to ask you
to reflect about your experience of the National Health Service and how it‘s
changed over the years.
How‘s the health service changed?
It‘s very difficult to say much about this because, of course, I‘ve been inside
it. My appointment as a consultant was, of course, part of the Oxford Regional
Health Authority‘s priority to try and develop service for the population
of rheumatics, and therefore, I suppose, I would have to say that at that
time I think that there were considerable improvements occurring. When I
came to Reading as a consultant, nobody had started doing
hip replacements, knee replacements, or indeed any joint replacement surgery,
but shortly after I came here, one of the newly appointed orthopaedic surgeons,
Pat Chesterman, and I got alongside each other, and we decided that we would
try and start a hip replacement programme.
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And the arrangement was that I would admit patients into one of the beds that
I had at Battle Hospital, and
he would operate on them, and they would then come back to my beds. This
meant that the orthopaedic department‘s overcrowded beds didn‘t get further
overcrowded, and that we would be able to get reasonable numbers of hip replacements
done. And that worked very well, but the trouble was it became too popular,
and after about a year or eighteen months, we found that we had a waiting
list that was itself likely to be a year or longer long. And this was really
very worrying, and we found it very difficult indeed to do anything about
it. But then another orthopaedic surgeon was appointed, a man who is as well
known for being a musician as for being an orthopaedic surgeon, Arthur Theman
- plays the saxophone and plays it beautifully - and he sort of joined the
team, as it were, and began doing not only hip replacements but knee replacements.
And this worked very well indeed, but, of course, again the waiting lists
increased, because people sent us people for needing hip replacements and
knee replacements from all over the place, all over the country, and we worked
like mad to keep that list down, but it was a quite impossible task.
And what are your impressions
of how changes in the National Health Service have affected the treatment
of diabetes?
Well, I suppose one great thing
of course, when I was a lad, and up ‘til 1948, my parents were having to spend
a lot of money buying insulin, and it cost a lot of money.
Can you remember how much?
I can‘t remember how much I‘m
afraid, but I do know that my mother was extremely relieved when the health
service came in in 1948, and this ceased to be a fairly considerable household
expense. I can‘t give you any figures at all. I‘m sure you could get those
figures, but I have no notion. So that, I think, was an enormous improvement.
And I can well remember meeting, for example, a very nice little
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doctor from Ceylon, who was in this country and subsequently went back to
Ceylon, and she, quite almost casually, said to me one day "did I realise
that in Ceylon, even the well off could only afford to have insulin injections
alternate days because of the cost?", and I began to wonder whether the
impoverished in this country, prior to the health service, had been in the
same sort of position. And I remembered Wilfred Oakley talking to me about
the incidence of the complications of diabetes, and saying to me that he had
a very strong impression that these were much commoner in people in social
class four and five than in social class one two and three. Now, I don‘t
know where he had that information and I‘ve never checked it, but if it‘s
the case, I would just wonder whether it‘s got something to do with people
earlier on not being able to afford to buy insulin for themselves, adequately
in quantity.
And what have been your experiences
of the NHS in recent years?
I must admit that I‘m not that
impressed by recent changes. Yes, recent changes in the orthopaedic department
in Reading have got the waiting list for hip replacements down from about
eighteen months to about five months, and that‘s jolly good, and the same
applies to knee replacements and shoulder replacements. Unfortunately it
doesn‘t apply to finger joint replacements. These seem to be hanging around
a year or longer. But there we are; you can‘t have everything. I am not
impressed by the way in which changes in the health service have affected
the rheumatic population locally.
What about the diabetic population?
I‘m not so sure about that either.
I‘ve never attended the diabetic clinic in Reading,
so I can‘t talk about the Reading
diabetic clinic. The diabetic clinic at Oxford
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runs very well, but the inpatient care I don‘t think is quite as good. I
think that the turnover has been speeded up a great deal, and in one sense
I suppose that‘s a good thing, but on the other hand the actual educative
business of being an inpatient, especially if you happen to be a new diabetic,
gets truncated, and I get the impression that people are not understanding
about the diabetes quite as well. And I have one very good reason for saying
this. I was at Dorchester, and I met an old lady and her husband at Dorchester,
and this old lady said to me "oh, I saw you the other day in the diabetic
clinic", and it turned out, of course, that we were both diabetics and
both attending the clinic in Oxford. And she said to me "I‘ve been a
diabetic for four or five years", she said, in other words shortly after
the health service changes began, "nobody seems to be able to tell me
anything about my disease. They keep on telling me to read things. I mean
it‘s all very well reading things, but what you need to do is to ask people
questions and to get them to talk to you, and that just doesn‘t seem to happen".
Now she may be an individual case, but I have actually since met one or two
other people who have had similar experiences, and this seems to me to be
a very bad thing. I am ill-impressed by the changes in nursing care in the
wards, and that isn‘t specifically in relation to diabetes. It‘s in relation
to the care that my wife has had over her recent illness in the Royal
Berkshire Hospital, though
I would say that the neurosurgical unit at Oxford the nursing care was exemplary and very good indeed. But I
was very ill-impressed by the nursing care at Reading, and I went so far as
to tick off the sister of one ward, who told me that she hadn‘t been able
to give my wife anything to eat for three days because she hadn‘t ordered
some tablets from the dispensary. And I‘m afraid I called her some very rude
names indeed, and I think they were justified.
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And how have you got on with the Oxford
clinic?
Oh, in general, very well indeed.
There was a phase, this seems to have passed, but there was a phase in which
I found that I was being seen by very inexperienced doctors, who clearly knew
nothing about diabetes. There was, for example, one young man who told me
that it was absolutely contra-indicated to mix different varieties of the
lente insulin, and I pointed out to him that the whole idea of the lente insulins
was that you could mix any variety of them in any proportion you cared to
mention. And he then went off and told me what a fool I was. I was not impressed.
And there were one or two incidents of that kind, with rather inexperienced
people trying to cope with disease processes in which they had no real insight,
and I think this wasn‘t helped by the fact that they didn‘t seem to have any
good system of problem-orientated record-keeping in the department. I did,
in fact, make my feelings known to Dr Levy, and I suggested that having some
kind of flowchart might actually make the running of the clinic easier, and
might make the relatively inexperienced pick up more quickly the things that
they needed to know. After all, junior doctors need to be trained, and you
have to have a sensible system for training them. I hope that was helpful.
Certainly since that time, I‘ve always been seen by a senior person, so maybe
I‘ve benefited. I hope other people have, ‘cause I wouldn‘t want to be just
a bloody-minded nuisance.
Your experience of the health
service is obviously not typical as you are medically qualified, but have
you observed any changes in attitudes of medical staff to patients?
I do find this difficult to answer.
I am a bit worried by the attitude of junior medical staff. They don‘t seem
to be interested any more in the
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continuity of care. I know that when I was newly qualified, one of the things
that I found most helpful was the fact that I was around in the wards all
the time, and therefore you could observe how a disease changed. How for
example somebody with a cerebral thrombosis, how their disease changed, or
the manifestations of their disease changed in quite a different way from
the way in which the manifestations of a cerebral bleed changed. I know it
was jolly hard, and I can remember how tired I got, and I wouldn‘t want anybody
to get as tired as I used to in those days, but if that is sort of excised
from the junior doctors‘ job, then they miss an enormously important bit of
experience. And when my wife was in the Royal Berks recently, I noticed that
she came in, and if I remember rightly she was admitted mid afternoon, she
was seen by a young doctor who went off duty at about five
o‘clock. And another doctor came on and wandered gently in at about half
past six, and didn‘t seem to know anything about what had been happening to
my wife, didn‘t realise that she‘d been having multiplicity of fits. Maybe
it was all down in the notes and he just didn‘t bother to look at the notes,
but I was ill-impressed. And then she was transferred to another ward, which
was on the sixth floor of another building, and the house physician never
came there because it took such a long time to get from the main acute ward
up to the sixth floor of the maternity unit where she then was, that had now
become a medical ward, and they just seemed to come occasionally. And the
patients felt that no doctor was taking any interest. And there was certainly
a little lady, who was in the next bed to my wife, who was in severe pain.
I don‘t know what the cause of her pain was, but I saw her and she was in
severe pain when I went in to see my wife at about seven
o‘clock one evening,
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and my wife was then very ill so I went back again at about eleven
o‘clock, and this old lady was still in severe pain and hadn‘t been seen.
I was in and around the ward until about six
o‘clock the next morning, and this old lady wasn‘t seen at any time during
that period. She wasn‘t in fact seen ‘til the consultant came round the next
morning at about ten o’clock, and
the consultant himself wrote her up for pethadine, and I thought it was absolutely
abominable. And if the health service will allow junior hospital doctors
to treat patients in that sort of casual fashion, then the sooner the health
service is blown up and replaced by something else the better, and the sooner
that hospital managers are dismissed and put onto social security to understand
the difficulties people actually have who are impoverished, the better.
Have you noticed any differences,
any changes in society‘s attitudes to diabetes?
Have I noticed any change? Do
you know, I don‘t think I have? Possibly, well I don‘t know, possibly it‘s
regarded as more normal, I‘m not sure about that! I can remember a little
while ago, there was a family that I was visiting. One member of the family
had died suddenly, and I was going in repeatedly to try and give a bit of
support to this chap‘s wife. And there was a son in the family living at
home, and the son was a chap in his late thirties and he wasn‘t working.
And one day I said to mum, "oh, why isn‘t John working?". "Oh",
she said, "he‘s a diabetic, didn‘t you know?". And I said "well,
I‘m a diabetic and I‘ve been a diabetic for umpteen years, it‘s never stopped
me working". "Oh", she said, "nobody would let him work".
Now I don‘t know whether that‘s a reflection of changed attitudes or that
I was an advanced cohort of changed attitudes, or whether it was that that
particular chap was just so petrified of his disease that he had never actually
managed to try getting back to work, I don‘t know. But apart from that, I
don‘t think I personally have really
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noticed any special change. I just don‘t know.
From your long experience of
diabetes, would you have any message for someone being diagnosed with diabetes
now?
Oh yes, my message would be a
straightforward one. You rule the disease; don‘t let the disease rule you.
I was very worried a little while ago. I got a handout from one of the firms
that are making blood sugar machines, you know these home kits, very nicely
presented, very nice, but this firm‘s handout was decrying the fact that doctors
were not allowing patients sufficient test strips to test their blood sugars
more than four times a day. And I thought to myself, if you‘re testing your
blood sugar four times a day as a diabetic, once you‘re stabilised, your disease
is ruling you, you‘re not controlling it, and that‘s a bad thing.
So how often do you test per
day?
Oh I test about three or four
times a week, well, unless obviously I‘ve got a cold or something else that
may upset it. But, I mean, the modern gadgets are very easy and you can do
it very quickly, much better than the old days, so yes, it‘s a relatively
easy thing to do, but I still feel very strongly that I mustn’t let myself
become obsessed by my disease.
So could you describe a typical
day then, your regime in terms of diet, exercise, and everything?
Well I‘m up pretty early, I get
up just after six o‘clock, and I dress
and I perhaps have a cup of coffee. In the ordinary way, I would take a cup
of coffee to my wife as well. She doesn‘t wake up quite as early as I do;
she‘s probably got an easier conscience or something. But I leave the house
about ten past seven to get down to church, where I will open up, and then
we will meet and we will say morning prayer together starting at about half
seven, usually about twenty five to eight actually, and then mass at eight
o’clock. I will finish at about half past eight, or a few minutes after, and since we‘ve had
so much vandalism in the church recently
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we now have to lock up, so I usually lock up at about quarter
to nine, or thereabouts. And I come home and have insulin, and I have some
breakfast, and then what I do the rest of the morning varies enormously.
In general terms I‘m visiting. On Tuesdays, for example, I visit an old people‘s
home, I visit a nursing home, and talk to the people there, talk to the staff.
On other days of the week, I tend to go and visit people in their homes.
I always have insisted on having one day a week in which I do not do any church
work, and that‘s Wednesday, and in the ordinary way, Mary and I go out together
on a Wednesday. We may do nothing more than shop or goodness knows, it will
depend on circumstances. Afternoons, well… oh, I usually eat when I get back
from my visiting. One of the advantages of the regimen of four times a daily
insulin, you‘re not too worried about timing. During the afternoons, well,
I do all sorts of things, it depends what‘s needed. I read, there‘s always
a lot of reading needing to be done, especially when you‘re preparing sermons,
I maybe will go and talk to people about the baptism of their new baby, or
I may visit somebody in hospital, or whatever. It‘s a very varied menu of
activities in the afternoon. I reckon to be home again by about six, something
like that, and we tend to eat at about half
past seven, and after that Mary and I try to spend the evening together.
Sometimes we watch the telly, sometimes we do crosswords, sometimes we discuss
things, sometimes we play scrabble, and there we are.
And when do you take your insulin?
My insulin, before breakfast,
before my "midday" meal,
before supper and the long acting insulin at retiring, which is, my time of
going to bed varies, but it‘s usually around half ten to eleven.
Do you take any exercise?
Well, I suppose I run about a
great deal, but it depends on the distance I‘ve got to go. This parish is
very wide flung, and if I go off to Hammond‘s
End or Nettlebed, or any of the outlying villages, I go by car, because otherwise
it takes too long. I walk about in the village here quite a lot, and that,
I think, is my main form of exercise. I used to ride a bicycle a great deal,
but recently I‘ve been getting angina and I‘ve therefore had to give up bicycling.
It is a pity because I like bicycling, but there we are.
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Now, during our break you‘ve mentioned insurance problems during your lifetime,
and I think it would be worth setting those down for the historical record.
Yeah, when Mary and I were first
married and we had our first child,
Which year?
Claire‘s now fifty, so, you know,
take fifty away from 2004 and it brings us to ‘54, doesn‘t it? She was born
just before Christmas, a couple of days before Christmas. I thought that
it would be sensible to have some sort of life cover, and I had very great
difficulty in getting life insurance at anything like a reasonable rate.
I went the rounds of insurance companies over this. Eventually, the medical
insurance company managed to get me a life insurance at reasonable terms,
but even then I was paying roughly one and a half times the normal premium.
So that really was a problem. I think that‘s probably much less of a problem
now.
What about travel insurance?
Travel insurance, well, I don‘t
remember when it was that I first had to ask for travel insurance. On many
occasions I‘ve been abroad, by way of medical trade as it were, to various
conferences and what have you, and on those occasions I‘ve never had any difficulty
over insurance cover for travelling and health and all that sort of thing,
but when I retired from the health service and needed travel cover, there
was immediate difficulty. Some of the companies concerned said things like
"well, we‘ll cover you for anything, except for anything going wrong
with your diabetes". Some of them said "well, we‘ll cover you for
everything including your diabetes, but of course that would push the premium
up by a factor of three or four". And this was exceedingly difficult.
I must admit that we
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heard about SAGA, and this is going to sound as if it‘s an advertising blurb
for SAGA, but we heard about them, and we approached them with a view to a
holiday in Croatia, and what did we do
about holiday insurance? And they said "oh, we do our own holiday insurance.
We‘ve got an arrangement with a particular firm", they didn‘t tell me
who the firm was, and I said "ah yes, but I‘ve had trouble with holiday
insurance", and I explained, and they said "oh, don‘t worry about
that, that will be no problem at all. You‘ll pay the ordinary premium. The
only thing we insist on is that you inform the company concerned, and that
you inform the rep who will be with you on the holiday". And so that‘s
worked very well, but apart from that it really was very difficult indeed.
And a final question, how has
diabetes fitted into your family life?
I don’t think it‘s made an enormous
amount of difference. Mary and I have got six children, five girls and a
boy - at one stage I thought I was another Mr Bennett, but five girls and
a boy, and they‘re all grown up, they‘re all well, they‘ve all married, and
we have fifteen grandchildren, and we‘ve recently acquired a first great grandchild.
There is one thing that‘s worried me a great deal. My wife‘s family, when
we married there was no story of diabetes in the family at all, but my father-in-law
developed type two diabetes, and indeed died from complications of that about
twelve years ago, and it‘s always worried me a bit that there is a sort of
two strand diabetic history here, of type one on my side and type two on my
wife‘s side. Up to the time, none of my children have shown any evidence
of any sort of diabetic problem, but clearly it‘s a worry.
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