This morning at was at
Spire for my annual CT scan something that I will have to undertake annually
for 5 years….3 more to go and I am scheduled to see Professor Sebag Montefiore on the 20th for
my results.
My Bowel has been playing
games lately or should I perhaps say self induced. It was my birthday on
Tuesday and I went out with Gavin on both Friday and Sunday to celebrate.
Alcohol is one element that even today has its side affects and just a
hangover. My bowel reacts badly to it and since Christmas 11 I have had hardly
had a drop. So 2 days of indulgence resulted in 3 bad days. But now I know what
to expect I can manage it more effectively, with lots of wet wipes and Cavilon
at hand.
Diet plays a huge part of
my life and foods that I had previously enjoyed are no longer part of the menu.
Curry’s and anything spicy are no no’s and alcohol is also pretty much off
limits and when I do have one the next few days can mean frequent bathroom
trips. I deink more water than I ever did to maintain the right balance and to
help things I also take Fibogel daily.
Just before Christmas I hit
real low point. For the past 21 months since being diagnosed, medical
professionals surrounded me, however now I was all alone. I could not quite
work out what was happening so a visit to my GP put things into
perspective. I was struggling in the
main with emotions and after everything that had happened, this was not
unusual.
So back to research and bingo I find a course of
treatment that might just do the trick “Cognitive Behavioral Therapy
CBT)”. CBT is a psychotherapeutic approach that addresses
dysfunctional emotions, behaviors, and cognitions through a goal-oriented,
systematic process - Wiki’s definition. For me it was a way of talking through
what I had been through and putting meaning and a type of closure to the
events. Having had Cancer is something that one will never forget and something
that you can’t apply closure to. But to be able to park some of those
experiences away from my day to day
thoughts, will help me to move on.
David
Broadbent at Nuffield Leeds was to be my Consultant Psychologist and something
that I have just realized is that I was to be his last patient just before
retiring, just like I was for Mr Ambrose who retired back in March 2012 when
diagnosing me.
I had 6 eventful sessions
with David and I can’t thank enough for helping me with my issues. It was quite
ironic that for months I had been using the word stool or on occasion poo…..now
with David we went back to basics and we used the word crap….this light
heatedness helped me get through things and using methods such as discussion
and case studies put things into perspective. I still have a way to go but David’s
help, put me on the right path.
So its now 00:30 on Sat 9th
Jun 12 and Cold Case is on in the background and I can’t stop writing today,
having covered off the final 4 blogs and I am pleased with my efforts.
My approach to life has changed
however I do not treat each day as if it was my last as its not. My outlook is
that I have beaten this disease and I am positive that It will not return. But
if it does I will be prepared and will tackle it with all the enthusiasm as
previous. There are things though that I can’t do that perhaps previously I
could and I have to be mindful when I am out that I know where the toilets are
and that I choose places where I know that they are a standard that is
acceptable in terms of cleanness.
![]() |
| Mike Peters & me |
I now take an active role
in a number of projects such as being a Patients Voice for “Beating Bowel Cancer”
and I am also involved in several projects for Macmillian’s.
I am also extremely proud
to be a member of the “Stakeholder Involvement Group” for YCR. All of these
activities allow me to give something back to those that have helped and
hopefully using my experiences I can make a difference for others impacted by
Cancer.
As for the future who
knows were it will take me or even for how long….but one positive thing that
has come out from this experience, is that I met some wonderful people and have
made some new friends. During my illness for one reason or another some friends
have withered by the way side for one reason or another and those that have
been there for me, have been truly remarkable.
I look forward to perhaps
writing again in 12 months time to keep you all posted on events, but more
importantly I hope that my blogs have provided an insight into the journey of a
Bowel Cancer patient and I hope that my story may help others with their
journey…in that they are not alone and that there is light at the end of this
very long tunnel J
Alex Kuczera
Sat 9th June
2012

No comments:
Post a Comment