I’ve spent Christmas trying not to think about
whether I’m going to die soon, and have been quite successful, on the whole.
Just over a year ago, I was diagnosed with invasive breast cancer, since when I
have undergone a lumpectomy, 5 months of chemotherapy, 3 weeks of daily
radiotherapy, and am now taking the anti-oestrogen drug Tamoxifen every day. My
body – and mind - have taken quite a battering, but the cancer has been attacked
with all the current state of the art oncological weaponry: I have been
mutilated, poisoned and burned, and now the ‘wonder drug’ Tamoxifen is playing
havoc with my hormones. The cancer should have been beaten into submission, and
my prognosis is excellent, but…
Two weeks ago I found another lump in my
theoretically now cancer-free breast: a small, hard, irregularly-shaped lump
very close to the scar where they removed the sentinel lymph node near my
armpit during the surgery. Blue dye is injected into your breast beforehand,
and the first lymph node in which the dye appears is called the sentinel lymph node. If the
cancer has spread beyond the breast this is where it will go first – so they cut
it out, and check. My sentinel lymph node contained a tiny clump of cancer
cells – what they call a micro-metastasis – which is why I had to have systemic
chemotherapy treatment as well as local radiotherapy on the affected breast:
the cancer had just begun to spread beyond my breast into the lymph nodes.
It’s hard to describe what happened in my brain in
the seconds after my fingertips found the new lump; something like a car engine
flooding, I imagine.
‘THECANCER’SBACKANDI’MGOINGTODIE,THECANCER’SBACKANDI’MGOINGTODIEANDALLTHISTORTUREWILLHAVEBNEENFORNOTHING’
I had always thought that if the cancer came back,
it would be by metastasising to my bones or my brain, which are generally the
places where breast cancer likes to go next once it has escaped from the
confines of the breast; it never for a moment occurred to me that it might
return in the same breast, what they call a ‘local recurrence’. My big fear was
of ‘circulating tumour cells’ managing to escape into my blood stream, dodge
the chemo, and then swim off to colonise pastures new.
Lumps were no longer on
the agenda, until two weeks ago.
Once I stopped panicking, I emailed the news about
the new lump to my Breast Cancer Care Nurse, Vanessa, saying that although I
knew it was probably just scar tissue, I was a little alarmed, and asking what
she advised. She emailed straight back saying that of course it was probably scar tissue, but that the lump should be
investigated; she had booked me an appointment at the Breast Clinic for
Saturday 28th December. I would see a surgeon and, if necessary,
have a mammogram, ultrasound and biopsy.
Again.
Naturally, I googled.
It is overwhelmingly likely that the lump is either just scar tissue that I simply
hadn’t noticed before, as I have left the sentinel node scar alone, for the
most part, or the charmingly titled ‘fat necrosis’, i.e. a random little lump
of fat. It's too hard to be a cyst, I think. Sometimes, however, new tumours do
appear near scar tissue, and that lymph node did have some cancer cells in it.
The consequences, should it turn out to be a recurrence of the cancer, don’t
really bear thinking about: probably a mastectomy, a complete lymph node
clearance with attendant risk of lymphoedema and loss of arm movement, and last
but not least more chemotherapy.
I repeat, MORE CHEMOTHERAPY.
Imagine that.
I can’t imagine more chemotherapy, actually. The
horror of the FEC chemotherapy remains with me still, and whenever I see that
photograph of me in the pink helmet, or even just think about it, I shudder, my stomach contracts and I want to
vomit. My mind just can’t encompass the idea of more chemotherapy, but the terrible
thing is that if this is a recurrence,
it would still count as being part of the same early stage cancer, and the
prognosis would be good – so long as I had the treatment. Again.
It would be stupid not to, right?
But after a year of feeling like a tortured lab rat,
it’s almost impossible to contemplate the idea of going through all that again, including being properly
mutilated this time.
You may be wondering what all this has got to do
with Jennifer Saunders. A couple of months ago, in an interview with The Times
to publicise her autobiography, Saunders took it upon herself to criticise
fellow breast cancer sufferers for saying that you can never put the disease
completely behind you. These women liked
the attention they got from having breast cancer, she said, wore the disease ‘like
a badge’, and were probably sorry when their hair grew back; she herself always
got lots of attention because of her career, and did not feel the need to hang
on to her breast cancer as a way of getting attention. The doctors had told her
she was not going to die of it, and she believed them; she had no more chance
of getting breast cancer again than the average person.
Well, good luck with that, Jennifer.
Perhaps you have superhuman mental self-discipline,
and never think about what might happen if the disease comes back, as it all
too frequently does; cancer treatment is still not very effective. My
chemotherapy treatment theoretically increased my chances of survival by about
six per cent, but they still can’t distinguish in advance who will be helped by
chemo and who won’t; similarly, Tamoxifen theoretically increases my survival
chances by 8 or 9%, but there are some people who can’t metabolise Tamoxifen.
Again, there is no way of telling if it is actually working.
My cancer is not’ cured’, and the chance of it
coming back is very real. The treatments may have mopped up all the cancer
cells, or they may not; you can never know, unless and until the cancer comes
back. That’s why you are never free of breast cancer, Jennifer, and if you
think you are, then you’re living in a fool’s paradise.
You don’t think about it all the time, though: just
as all humans, even healthy ones, know they’re going to die sometime, but get
through life by not thinking about it. During the last couple of months I was
getting on with my life again, treatment over, and hardly thought about cancer
at all, until two weeks ago.
Tomorrow I will find out if I have anything to worry
about – or rather, anything out of the ordinary to worry about. If the surgeon deems there is something to worry
about, and they give me a biopsy, then the results will take another ten days.
Happy New Year.
Anonymous here, wishing you the very best of luck. I know in a small way how it is waiting for a diagnosis, and can't really imagine how it would be facing the prospect of chemo all over again. Hoping very hard that it is nothing.
ReplyDeleteI know what you are going through. I've had some very bad scares recently. It is horrific. I really hope you get the all clear. Keeping everything crossed.
ReplyDeleteMaire
There are no words. If support and hope and good wishes were a cure, you'd have banked enough for a hundred lifetimes. Sharing your life with strangers is difficult and selfless and even though most of your readers probably don't know you in real life, we couldn't be more on your side.
ReplyDeleteOUTRAGE. I HATE Jennifer Saunders. What a belittling little bitch!
ReplyDeleteThinking of you my dear Hocam. Missing you and hurting for you. Every possible limb and digit crossed and waiting for news... xxx
Caroline. Just reading this gave me cold chills, am imagining what's going on in your head... Even with your description of how you're feeling I can imagine it's even worse because no way do I believe sufficient words exist...
ReplyDeleteI followed you through chemo...shared the experience, in fact, and, dear God, I cannot imagine going through it again. I guess if that was the only way to have any chance of staying alive, I'd have to agree to it - but could I stay sane? That's the question that hovers round me like some kind of bat-like creature, swooping in from time-to-time to remind me IT COULD HAPPEN.
I still have my port. I have to go in periodically to have it flushed, so no blood clots form and polish me off on the spot. So far, my tests have been good, but that port imbedded in my shoulder continues to be part of my reality.
My faith and trust have been challenged since last we communicated: My mother went into hospital and there contracted something called C-Diff. Have you heard of it? Thousands die of it every year, but I had never heard of it. And it's contagious. And I was in the room with my mother when she was diagnosed and placed in quarantine...me, with my chemo-compromised immune system.
My mother died. In my arms. I did not catch the C-Diff - tho for some time I didn't care a whole lot.
But I do.
I cried reading your post. Am still crying. But now I'm going to do for you what I've been doing for myself: I'm going to hang onto every positive thought with a fierce grip, and pray with the earnestness of a child that this is not what you fear. And I am not about to tell you not to worry...of course you're going to - I just want to remind you you are not alone.
And btw, a big, fat NY raspberry to Jennifer Saunders - tho in the deep south we just call a ridiculous woman like that a right heiffer!
Love from Jen
Oh bummer! Keeping my fingers crossed for you and sending positive thoughts. X
ReplyDelete