I am aware the metaphors are being thrown around somewhat
indiscriminately in this blog thread. Some
days it’s all about a show in five acts; today I draw upon the marathon analogy
of ‘hitting the wall’. I haven’t run a marathon and probably never will
now. My last boyfriend was training for
a marathon when we got together; it added to his glamour. To be possessed of such resilience and
determination clearly singled him out as someone special; to tackle such a
difficult feat for the first time in his fifties also, so I told myself,
suggested someone ready to take on a new way, moving forwards into the
future. Fortunately, my then
psychotherapist warned me kindly that he was in a period of change and I was
probably a transition after the end of his marriage and when he had settled again,
I would be cast aside. At the time I
tried not to think of the warning, but it was prophetic.
Sunday, 10 March 2019
Tuesday, 22 January 2019
FEC! (as Father Jack might say)
Chemo has started again.
Having braved the procedures last year, was it easier to walk through
the doors of the chemo ward? The answer
to that is, unsurprisingly I’m sure, both yes and no. A friend who had not accompanied me before
was at my side for this first of three FEC chemotherapy treatments. Whilst FEC is a standard breast cancer
treatment, this day would be new to me and I felt something like a first former
having moved up a year, the walls of the classroom were the same but the books
were very different. To add to the
novelty, my appointment was for a Friday at 3pm rather than a Wednesday at
8.30am. I wasn’t one of the new patients
for the new day: the rhythms were well established, the comfy seats occupied
and the biscuit basket had made many laps of the ward already.
Thursday, 3 January 2019
Intermission
I’m in another ‘downtime’ phase
after the excitement of my histology results. They were almost as good as
they could have been, with no cancer in the lymph node, the tumour completely
removed, and evidence that the chemotherapy had killed more than 90% of the
cancer cells. I was genuinely surprised, because I had to have a
therapeutic mammoplasty rather than a lumpectomy, as the footprint of the
tumour appeared largely unchanged from MRI data. I was bracing myself for
more surgery, disappointing chemo results and spreading cancer, but none of
this has happened. It seems that the only reliable evidence is when you
get to see the tumour for real and the histopathologist can do his (it was a
‘his’ in this case, not my casual sexism) analysis. It felt like the
horizon was opening up in front of me, such was the relief that enveloped
me. Nevertheless, my mood has changed as I deal with the practicalities
of life now and what comes next.
Saturday, 24 November 2018
Act 2: Beginners Please
My
attitude approaching surgery has been different from preparing for my
chemotherapy, partly because surgery seems more comprehensible than the potions
of the physician. The surgeon is going to cut the cancer out. We
can all get our heads round that; no need for bewilderment at the
technicalities of the chemicals that make up those black covered bags, the contents of which have been pumped into me. Of course, the surgery is
anything but simple, but the concepts are easy to grasp, and therefore the
reactions post-surgery should be easier to deal with. Maybe.
Tuesday, 30 October 2018
Rollercoasters
Even in the midst of
treatment for cancer I have found something to admonish myself for. Part of my
soul is relieved as, since I found that lump at the end of June, I seem to be
reinventing myself as a wise and content woman of strength, dealing maturely
with the challenges that have been thrown up. I can now assure you that inside
all that dressing there still lurks a very frightened child screaming ‘why me?’
and ‘it’s all my fault; I deserve this’. Yes, very confusing I agree. So what
disappointment has simultaneously soothed and reprimanded? The fact that I
promised myself (and by extension my band of readers) a blog at each stage of
this process and yet weeks and events have passed with my fingers not reaching
for the keyboard. I have thought about writing a number of times and even,
unusually for me, thought of a title for the blog before setting finger to
keyboard; but it is only now, when I know I’ve ‘let myself down’ that I can get
to the job of writing. Why? What is happening now?
Monday, 17 September 2018
Seconds Out
Of the many tangled issues to deal with when living with
cancer (oh, doesn’t that sound like the start of an advert ridden click bait
you’ve just idly opened), the biggest issue is one of time. You either have too much or too little of
it. For me, before treatment started
there was the creeping anxiety that my grade 3 tumour was going to spread too
fast to catch it, and now, I want it all done and over with. I’ve had one cycle of chemotherapy, I’ve been
brave walking forwards into the unknown, now is the time to be told ‘it’s fine,
you’re ok’. It isn’t like that.
Wednesday, 5 September 2018
Patience
Last Monday I thought about writing this next blog and was
worried it might be a bit tedious for the reader used to the high drama of
diagnosis and first treatment. I had got
through the worst of the pain of the first chemo and only had my wig
appointment to look forward to last week.
Much as I am apprehensive about losing my hair, I’m not agonising about
it, not yet. It’s not something I relish, but equally it isn’t something can
really do anything about except be practical. I have written about 'being practical' before, I thought about these things before, this is not new territory for me, and there I was, pondering what might
appear in the next blog. There is a
lesson in that, one of those that could be converted into a syrupy meme with a
hazy picture of a sunset as background.
Never worry about tomorrow, enjoy today.
If only I had known.
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