Day 117
General status update
Anxiety level/insane euphoria (+/- 1-10,000): Yoo
Hoo! The Dexys are HERE!!! I am ruling the world this week and that Teletubby Infant
Despot in North Korea had better not start messing with me!
Fatigue/weakness: weird combo of artificial steroid
high and much enfeebled body –the spirit is up for pretty much anything, but
the flesh is very, very weak.
Nausea demon:
he woke me very early this morning and we had hot buttered toast and marmalade,
and big steaming mugs of tea, mine with a chaser of 3 different anti-emetic
drugs, a dose of Dexys, and some of the magic anti-Chemo Nano Rats elixir,
Omeprazole. I wonder what the calorie count of all those drugs is?
Despair Demon: has
cheered up a lot since his coffee date with the Chemo Muse yesterday – totally delusional,
of course. SHE’S USING YOU, YOU FOOL. Doesn’t the fact that her hair is made of
SNAKES give you a hint that she is not quite like other women?
Chemo Muse:
she’s inhaling the steroids and reverting to her full Dexy’d magnificence and
power – she‘s been filling my mind with ideas all day, non-stop.
Chemo Brian: we’ve
put in some quality time today, some of it in public, which was embarrassing
(see below).
PICC line (deceased): its
spectre appeared in the Chemo Ward yesterday, much to everyone’s surprise (see
below)
State of mind:
so happy – you cannot begin to imagine how happy I am – never mind the two weeks
of horrible side effects to come – I am HAPPY. No more FEC.
Hair:
in the snood, dude.
I won’t say that I actually skip down the Fulham Palace Road
towards my final dose of chemo, but there is definitely a spring in
my step, and a mood much lightened by an industrial-strength dose of
painkillers (pain from the Cold Cap, for
the alleviation of), some Lorazepam (dread
of FEC6, for the alleviation of), and the happy, happy thought that when
Matron Becky puts the needle in my arm this morning, it will be the last time
anyone comes after me with a sharp pointed instrument for some considerable
time.
But this is FEC, remember, and during the administration of
the first five doses things have gone consistently wrong, so why I am skipping blithely
towards the hospital assuming that nothing
can else bad can possibly happen now
is a mystery, the triumph of hope over experience, and perhaps the
influence of too many powerful drugs taken too early in the morning.
R is loaded down with one bag containing a Pret picnic,
fruit, and a variety of cold beverages, and the other containing my giant
knitted throw (cold from the Cold Cap,
for the alleviation of), my Smurf hat and snood, and lots of reading
material in various formats. You’d think we were going to Glyndebourne or
Glastonbury, not the Chemo Ward. By FEC6, we have now got this side of things
down to a fine art.
Since the removal of the late, unlamented PICC line from my
upper arm, I am now having the chemotherapy drugs injected directly into the
veins on my lower arm, and after Matron Becky did this for FEC5 she pointed to the
back of my hand and said ‘There – there’s one left we can use next time’, which
was very reassuring, given that my pathetic lack of veins was why they inserted
the PICC line into my arm before chemo started, after the unfortunate incident before
my lumpectomy operation when the anaesthetist couldn’t find a vein into which
to put the general anaesthetic.
So, I’m sitting in the Big Pink Chemo Chair for the last
time, and Matron Becky, resplendent in her maroon Matronal Frock, readies herself
to insert the Final Needle. She picks up my hand and looks at it doubtfully, as
do R and I. There are no veins to be seen. Not one. I’m just not a very
veiny person, but if you stare closely at the back of my hand you can usually
see a faint tracery of something pulsing deep under the skin.
Not today. The veins have run for cover and retracted deep
below the surface of my skin. There is nothing to be seen.
‘Hmmm’ says Matron Becky, and she puts a rubber strap round
my arm and tightens it to encourage the veins to come out of hiding. There is a
slight improvement, and Becky decides to go in…
I’ll spare you the gory details, but this is essentially the ‘Fo Veins Total Non-Cooperation Day’ and
all the time in the background, as my arm is plunged repeatedly into buckets of
hot water, and three different nurses stick a total of nine needles into my recalcitrant
veins, the spectre of my PICC line is standing to one side, laughing, and
saying ‘NOW do you regret throwing me on the scrapheap?’ Becky and I pretend not
to notice it; we don’t want to give it the satisfaction.
At one point during this one and a half hour needle ordeal,
Becky and I both find ourselves staring wistfully at the back of one of R’s
hands, which is not unlike a relief map of the Yangtze delta. There would be no
problems putting a needle in there.
‘You’ve got very good veins, R,’ says Becky.
R looks proud.
‘If you were in here as a patient, we could let the student nurses
practice inserting cannulas on you’ Becky continues.
R blanches visibly, and decides this might be a good time to
go and fetch more coffee.
After about the sixth painful, unsuccessful needle insertion,
I start to cry, which distresses both R and the nurses, who are doing their
best, and whose fault it most definitely isn’t; I just have the very worst type
of veins.
By the time we get to the ninth needle, and there aren’t
really other options left in terms of places for insertion, I am beginning to wonder
what will happen if they simply can’t get a needle to stay in – will they have
to postpone the chemo? Happily this question remains unuttered, as at last we
have lift off, and the cannula is put in place.
Now it’s time for the intravenous anti-emetics and steroids,
before we get to the main event, and the Cold Cap goes on for the very last
time, and I recite poetry and emit small squeaks of distress as the pain encircles
and penetrates my skull and my head freezes for the very last time. That pink
hat may look very jaunty, but I’m not going to miss it One Little Bit.
I don’t remember much about the chemo, except for the fact
that I have a nursing assistant sitting beside me for the whole time they were
infusing the bright red Epirubicin, most vicious of the FEC chemo drugs, to
make sure my vein didn’t explode. Seriously. She is under strict instructions
to pull out the cannula at the first sign of spontaneous vein combustion. This
stuff is NASTY.
R sits next to me reading and tweeting, a comforting
presence,
and at some point, exhausted by it all, I drift off to sleep under my big knitted throw. Then the nurse wakes me to say it is all over, and I can take the pink helmet off, and go home. I towel the ice off my hair, and don the Smurf hat and snood, while R packs up all our paraphernalia.
and at some point, exhausted by it all, I drift off to sleep under my big knitted throw. Then the nurse wakes me to say it is all over, and I can take the pink helmet off, and go home. I towel the ice off my hair, and don the Smurf hat and snood, while R packs up all our paraphernalia.
And that’s it: FEC6 is done - my chemotherapy treatment is
finally, finally over, after what seems like a lifetime. Two more weeks of side
effects to get through, two more weeks of trying to avoid infections which may
require more hospital treatment, and then I will be free, although it will take
me anywhere between 3 and 6 months to regain my full strength, by all accounts.
And there’s still the radiotherapy treatment to come in May
But the door to my chemical prison is now open, and I walk
out of it and up the Fulham Palace Road holding hands with R.
‘Your veins are amazing’ I say ‘You could give Madonna a run
for her money.’
‘Your veins are just non-existent’ he replies. ‘I begin to
understand why you claim to have been a trout in a former life. Has it ever
been formally confirmed that your body actually holds the full complement of
eight pints of blood?
‘Oh, bugger off, you’ I say.
We are so, so happy.
And to complement that mood, this video sent to me the other day by BigSisFo of a Beethoven's Ode To Joy flash mob in a Spanish square, is one of the most joyous, life-affirming things
I have seen in a long, long time...
So, so sorry you had such a ghastly time with 'the needles'. I have the same problem: no discernible veins. It's so bad my doctor insists my port stay in FOR A YEAR in case I have to have more chemo (please, God, let the pet scans, etc. come back clear)!!!
ReplyDeleteBut we aren't going to worry about down the road right now; we're going to be optimistic, right? We're going to relish life, grin at ourselves in the bathroom mirror, look at other people - those 'others'...you know the ones...the ones who have never been to ChemoWorld - and we're going to hope they never, ever have to visit that dastardly land...
We're going to savor chocolate, delight in the bubbly, feel the euphoria of floating in the water, enjoy the sun, the flowers, poetry - a good book, a painting that touches us; revel in loving and being loved: We're going to survive! And with any luck at all the memory of all that is chemo will fade from our consciousness...
I am more than two months past my last treatment now and although vacuuming the house today just about brought me to my knees, it was with me feeling victorious - I couldn't have done even that a month ago!
So don't let the side effects the next few days throw you (heck, you got through that needle ordeal, you can get through anything)!
And then, my friend, you will find 'Caroline' emerging. And you think you're happy right now? Just you wait - you ain't seen nothin' yet!
:))
xxx Jen
ps: Have just viewed/listened to Ode to Joy again - this time through good speakers.
DeleteGlorious!
Thank you for sharing. Have 'saved'.
thank you, Jen xxxx yes, we will get there. And your words are particular helpful right now as the side effects are pretty bad today, even with the steroids - FEC is not going to give me an easy ride on the last dose.
DeleteI keep watching and listening to the video again and again - it's wonderful, and wonderfully cheering..
So pleased for you. Enjoy the happy pills x
ReplyDeletethank you - and thank God for the Dexys.. xx
DeleteDear Caroline, I'm so, so pleased that you have come through FEC6 and out the other side. So pleased that even though you will have the ghastly side effects you will know, at the end of each day that you are getting closer and closer to full recovery. And that video was just perfect. I'm sitting here with tears rolling down my face, swept up by your writing and the sheer...well, joy (!) of Ode to Joy.
ReplyDeleteAs to the crappy veins, oh bugger, it's no fun. My last blood test came out of the top of my foot, with a butterfly needle. This caused much giggling by me and my unfortunate GP, in front of a very bemused medical student.
Watch that Chemo Muse, she's going to be all over you like the proverbial rash making the absolute most of the last batch of steroids...
Love from the frozen North,
C
xxx
Thank you , Christina xxx
DeleteGood grief - I didn't know they could take blood from your feet..
BTW, it was so lovely to see Pistachio's wedding photos on FB - she looks so beautiful, and so radiantly happy, as does her new husband, and it was clearly the most wonderful day..
Ode to Joy said it all. I am so, so happy and relieved for you. And looking forward to the future, beyond the inevitable side effects. Janet
ReplyDeleteThank you, Janet xx
DeleteAnd right now, what i'm most looking forward to is Ayvalik! Only a month away, now.
I can't really find the words, Hocam. You have emerged triumphant.
ReplyDeleteHappy for you ;-)
ReplyDelete