I've just come through another series of medical tests, examinations and reviews. These have ranged from the simple (various blood tests) to the more onerous (collecting all my urine for 24 hours in a large plastic container - to test my kidney function). At first I wondered why they had given me such a big bottle, but later I began to be concerned that I would fill it to overflowing. In the end it reached the brim, a whopping three litres.
I
have most of these medical tests every six months. They are all
mentally and emotionally troubling, especially when you are waiting
for the results: each test could signify that an important part
of you is not working properly (after all, I only have one kidney
now).
By
far the worst is the CT scan. This is to check whether there is any
evidence of the return of the disease.
The
scan itself is no real problem. You come to the hospital an hour
before the appointment and steadily drink a large jug of clear fluid.
It has an aniseed taste. The fluid is called contrast, it contains
metal particles and helps to clarify the images taken of your soft
tissues. Then you lie down with your arms above your head on a slim
bed in front of an enormous white ring doughnut. This is the scanner.
The radiologist goes to the control room. Suddenly the bed slides
into the centre of the scanner. It feels a bit claustrophobic. Then a
strange mechanical voice tells you to hold your breath. The scanner
spins and whirrs like an aero engine. A little panel at eye level
counts down in seconds and the voice tells you to breathe. You go
through this procedure several times and then the scan is over.
The
weeks leading up to your scan are filled with anxiety. And afterwards
it gets worse. The stress is intense, until you hear the results. For
you know that if the disease did return it would most likely be
fatal.
After
the scan is done the images are assessed by a consultant radiologist
and a report is written for the medic who requested the scan. The
report is usually done within 24 hours and uploaded to the hospital
information system. It is the responsibility of the medic requesting
the scan to relay the results to the patient.
The
result of my latest CT scan was all clear. A fantastic relief. And
all the other test results were normal too. That means I'm out of the
clutches of medics for the next six months.
But
I didn't receive this news from the medic who requested my scan, my
Urology consultant. Indeed, I still haven't been contacted by him.
And I had the scan almost four weeks ago.
By
chance I found out through a short-cut. One of my GP's has special
access to the hospital information system and he logged in and
downloaded the scan report for me a few days after it was posted.
Such access for GP's is under trial in Belfast, I believe it is
intended to become the norm.
If
I was still waiting to hear the result of my scan (by letter from my
consultant) I'm sure I would by now have become very ill due to
prolonged stress. And of course this would be highly detrimental to
my longer-term health.
Communicating
with out-patients is a big weakness of the NHS. Last year, when I was an
in-patient in the same hospital (Belfast City), I was given the
results of each of my scans within 24 hours.
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