So in my final post, before I get on to some of my final
points about what this experience has meant to me, I want to talk about how
things have gone in my final week of chemotherapy, especially as my hair has
started to come out. It is quite
difficult to recognise your self in the mirror when you don’t recognise the new
person that you have become. Guess it will just take some getting used.
On Tuesday me and mum headed for what is likely and
hopefully my last trip to a hospital for the next three months. Thank fully the
cancer centre was not that busy was I was able to give a blood sample pretty
quickly, and then I got my blood results.
It’s quite weird to have no white blood cells and yet
actually feel physically fitter than you did the week before, but that’s one of
the many strange things about chemo.
One of the things which has been a bit of a frustration as
this process has gone on, is getting the
information that I need but normally about a week or two later than I wanted.
This appointment was no difference. Up until this point any conversation about
my hair had very much been answered ambiguously.
However frustratingly everyone seemed to be singer of the
same sing sheet today. Now why I was not told this two weeks ago I don’t
understand, but the approach of everyone I have dealt with seems to think it’s
best just to drop the reality on me, just as I am about to be hit with it. For
example being told that day that I was
expected to attend a follow up in two weeks, there had been no mention of this
ahead of time.
But thankfully, there was still some ambiguity just to stop
me from thinking I was actually getting talked to by people who has experiences
with similar case to mine. Now that I had, had my last injection of chemo
drugs, mine and my mum’s only quite simple question was when will I be fully recovered.
As I am going, to Belfast we both want to know when will we be able get
rid of
the chemo cards. The response from two different health professionals
was you guessed ambiguous. Any were between a week to two weeks from that
Tuesday. So yes my thermometer and my
temperature charts will be coming with me to Belfast.
Also I know have follow up appointments for the next five
years .That's my next 5 years planned out. Now I feel like that's
just the universe saying well you do like to plan long term.
Now to conclude as I come to the end of my treatment a
couple of points I want to close on.
Firstly I am very aware of how fortunate I am, despite what is written above, this blog would be going on a lot longer if I wasn’t so lucky with what kind of cancer I was diagnosed with and how my body has reached to the treatment.
Firstly I am very aware of how fortunate I am, despite what is written above, this blog would be going on a lot longer if I wasn’t so lucky with what kind of cancer I was diagnosed with and how my body has reached to the treatment.
Secondly I hope my story can help, but I am also very aware
and I hope you are to, my story only scratches the surface of a great many
stories of people of my age who's life really stops.
I have had to take a break from life and yes the next 5 years will be a constant what if, what if,
But many people have to suffer a lot longer to get the same result and that is a cruel injustice.
Hopefully in the future, those cases will decrease and hopefully I maybe in a small way can contribute to that.
I have had to take a break from life and yes the next 5 years will be a constant what if, what if,
But many people have to suffer a lot longer to get the same result and that is a cruel injustice.
Hopefully in the future, those cases will decrease and hopefully I maybe in a small way can contribute to that.
Thirdly massive thank you to friends and extended family who
have either supported me or any of my family/ gf at this time. I want to
thank my parents and brother for getting there 21 year old student back on a full
time basis. Just when they were looking forward to getting a last break before
I move back in to start at Birmingham.
Thank you to my gf, who despite third year nearly killing us
both off any way has been as much of a constant as she could be for me. It’s
rare in a relationship that both partners have near death experience in the
space of year. Its strange last year I was getting set to head of for camp and
3 months apart.
To then head on to Poland while she headed off to the Netherlands.Distance for those of you who have chosen to do it, is never
easy at the best of times and these past 6-8months have not been. No one
likes a bored boyfriend stuck at home trying to live vicariously through his
girlfriend in a different country. But we are still standing and exciting for what
our future will bring. Hopefully with less health scares.
Finally I think i want to conclude with one final statement. A common word associated with cancer is the concept of a battle. And if you survive you have beat it, if you die you have lost.
I have not beaten this. I was never in this fight.
Your body just becomes a vessel containing one side of the contest whilst the medical team tries to hopefully pock and prod your body in ways so they can control and minimise the diease. Let’s say they are successful you haven’t won anything. What you have gained is more time.
This disease has taken the next 5 years of my life, where I have to constantly plan my life around appointments. I have my life now but I don’t know this will be the case for ever because who really does know what tomorrow might bring. The treatment has reduced, not removed the possibility that this disease could come back. That is now my life time to get used to it.
Thank you and I hope to never write one of these again for obvious reasons I hope.
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