General status update
Hair: see below
Nausea demon: this is the first day in 39 days of chemo that I haven’t had
to take anti-emetic drugs; it seems the Nausea Demon has clocked off until
FEC3, next Wednesday. He’s very anxious about whether flights from Heathrow
tomorrow are going to be affected by the snow, as he’s scheduled the
much-heralded mini-break to Bilbao for this weekend, some much-needed down-time
after having been continuously on duty, pretty much, for the last 6 weeks. He
pointed out that this is all very wearing on him, too; I am proving to be one
of his more demanding gigs, what with my ridiculously high propensity towards
nausea.
Chemo Muse: She’s pretty disappointed in me at the moment, as it’s 9.38 pm
and I’ve only just sat down at the computer to write my blog-post.
Despair Demon: Told her to b***er off back where she came from, and set about
doing useful domestic tasks to drive her away – there’s nothing a despair demon
likes less than the smell of extra-strong bleach.
Chemo Brian: yeah, OK, I admit it, we might have had a little nap together on
the sofa this afternoon – but it was a happy nap, not a what’s-the-point-of-it-all-I-might-as-well-lie-down-on-the-sofa-and-turn-my-face-to-the-wall
kind of nap. We are over despair. We have moved on.
Fatigue/weakness: Given my current state, it’s hard to believe that between May
and September of this year I was swimming 5 plus miles every week. But in April
I will be able to get back in the pool and build up my strength again. One
length at a time.
Sleep, lack of: the problem has entirely reversed itself – now the difficulty
is in staying awake. Next Wednesday, after FEC3, it will be all change.
Anxiety level (1-10): rising, but mainly about whether we’re going to be able to make it up
to north Yorkshire on the train on Saturday morning. It’s bound to be the wrong
sort of snow.
State of mind: I’m perfectly fine – I’m not the one with rats in the attic,
after all.
Nora Ephron famously said that that not having to
worry about your hair any more is the secret upside of death, and until
recently I would have agreed with her: I have always regarded my hair as a
tiresome nuisance.
I wanted it be
thick and wavy, perhaps falling into natural ringlets; it doggedly insisted on
being very fine and very straight, albeit soft and shiny, at least. That was OK
in my youth, when it was the thing to have a waist- length sheet of straight
hair, but it’s not a look you can maintain into middle age unless you either simply don’t care about looking
like a portrait that’s escaped from someone’s attic or are seriously deluded about the laws of ageing not applying to
you – talking of which, one of the most tragi-comic things I have read recently
was an interview with the artist Tracey Emin, who was bemoaning the fact that
at the age of 49 she was, quite unaccountably,
peri-menopausal, and suffering from a greatly diminished libido. I can’t quote
her exact words - because I don’t have time this evening to search for the
original article - but she said something along the lines of ‘I am not the kind of person that people associate
with the menopause’, as if celebrated, funky, in your face female artists like
herself (belonging, moreover, to a group known as the YBAs -Young British
Artists) should obviously be exempt from the normal ageing processes that apply
to ordinary, less talented women.
We’re all that kind of person, Tracey (although not all with a greatly diminished libido, by any means. You've been unlucky there).
I digress – the point I was trying to make is that
once past the first flush of youth, there’s not much you can do with very fine,
very straight hair except cut it into a bob, unless you want to spend an hour
every morning with various hair torture instruments and a lot of product,
creating some kind of faux shape that will inevitably have collapsed by the end
of the day.
I always wanted to have the kind of hair that….but no,
you really don’t want to hear this, or look at the photos of the women who were,
mysteriously, given the hair I ought to
have had. It would only take 5 minutes for me to find them on Google, but
that really isn’t the point.
The point is that during all the decades of moaning
about my hair, and the total impossibility of doing anything with it, it never
once occurred to me what a simply magnificent
job it was doing fulfilling its prime purpose: covering my head. It just got quietly on with the job and never
complained, not even after that truly disastrous perm in 1988 which I have
always subsequently regarded as an Act of War by the hairdresser involved, whom
I would still like to hunt down and kill, although I would imagine that by now
some other equally enraged client has got there first.
It’s only during the 39 days since I started
chemotherapy treatment, during which time my hair has been under severe threat
from the toxins now regularly being pumped into me, that I have come to appreciate
just how completely I have taken my hair for granted. All chemo regimens have
particular side effects for which they are notorious, and the FEC chemo regimen
is famous for debilitating nausea, and instant alopecia – almost all women with
breast cancer who take FEC lose all of their hair very rapidly, usually not
long after the first dose.
I fully expected to lose all my hair, and prepared for
this by collecting together enough scarves and snoods to cover the heads of a
regiment of bald women. Although the cold cap – the pink helmet which I am
wearing in the photo on the right hand side of this page – helps some women not
to lose their hair, or not all of it – I had no particular reason to suppose I
was going to be one of the lucky ones.
So far, I have
been one of that fortunate few – after 2 doses of FEC, and two sessions of
scalp-cooling, or rather head-freezing, in the cold cap, I have yet to lose any
hair, although this could change at any moment. But for now, it’s still there,
and every day I wake up and find it hasn’t
come out all over my pillow is one where I give thanks again to my hair, just
for being there and covering my head.
Breast cancer is a disease that strikes very hard at a
woman’s femininity, her sexual identity, and treatment starts with the
mutilation of your body, to a greater or less extent, as either the cancer is
removed from your breast, or your breast is removed altogether. Surgeons can do
amazing things these days, with lumpectomies and reconstructions - which I'm going to write about later - but the
process is still hugely traumatic. And then, when you’re still recovering from that, the
chemo comes along and takes away another of the visible signs of your
femininity, your hair.
So then you’re not only mutilated, but also bald, and
my chemo buddies who have lost their hair already have grieved bitterly over
this. My counsellor at the Haven, who has accompanied innumerable women through
chemo, says the loss of their hair is the factor which brings many women to
their lowest ebb. Your hair will grow back eventually, of course, but
that’s not a lot of comfort to a woman who has just had her head shaved,
because she can’t bear hoovering it all up off the carpet any more.
I have been struggling with my morale this week:
chemotherapy treatment is a long, painful process, and before that there was
the surgery and associated unpleasantnesses. Sometimes it’s very hard just to
keep putting one foot in front of the other, but 39 days in, I’m one of the very
few to have kept my hair so far, so that’s one less loss and source of grief to
deal with. It helps, enormously, and I’m praying that I won’t have to deal with
it at all, that my hair will stay put through the next 4 doses of chemo.
The fact that I haven’t yet gone bald seems to be
simply because of using the cold cap, something which is now offered to chemotherapy
patients in many hospitals in the UK, but is by no means universally available.
I have written about how it works, and shown what it looks like, in
an earlier post , but a new development is an on-line petition to the government
by the manufacturers, Paxman, calling for the cold cap to be more widely
available.
I have signed the petition, as have many of my
friends, and if you would like to do so you can find it here:
R was a little dubious about this, pointing out the
manufacturers do have a rather vested interest in the subject, but his own
private meta-review of the limited academic literature on the clinical efficacy
of the cold–cap – which indicates that it
is indeed effective in preventing hair-loss in some, but not all, cases – left
him feeling reassured enough to sign it, too.
Your hair isn’t the most important thing – staying alive
is the most important thing - but every
little helps.
And sometimes a little can help a lot.
Addendum, 18/1/13: I forgot to mention that it seems the cold cap works best for people with fine hair - I'm sorry, Hair, for ever doubting you.
I can only sympathize for you, Caroline. As a man, my hair isn't as closely linked to my sexual identity as a woman. It's a good thing too -- my bloody hair started abandoning ship when I was about 18 or 19. By the time I was 30, it was almost entirely gone on top. For some reason, it then started turning gray, or grey for my UK friends. My sister had chemo and she lost virtually all of her hair and it was quite traumatic for her. In the end, she beat the cancer and her hair came back thicker and wavier, so she felt some small measure of appreciation in the end.
ReplyDeleteHope you and R have a most excellent adventure in Yorkshire this weekend. Perhaps you will be Big Sister Fo's Pied Piper and lead her rats away from Yorkshire. ;-)