With three chemotherapies down I now find
myself half way through the six cycles. How that happened I don’t exactly know.
It’s this weird experience of time having just flown by but yet knowing that
there’s still such a long way to go. In a way, I know that the next half will
fly by too but at the same time it still feels like a lot to get through.
The Plan C for the anti-sickness that I wrote
about it my last post went as well as could have been expected. The drugs
basically knocked me out so sickness was a whole lot better. Better asleep than
awake and having to deal with the nausea I reckon. Because my body didn’t take as
much of a whack in those first 24 hours as the last couple of times I was less
foggy for the proceeding days. The fog, however, lasted the same amount of time
that it did in the previous cycles. It then lifted right on cue on the 8th
day, in time for the arrival of my friend Zac, who’s joined the Little Keepers
Cottage crew from New Zealand… as have our 5 new friends in the photos. Well,
they haven’t joined the cottage crew
so much as forming the Little Keepers paddock crew. They’re very kindly
beginning to lay eggs for us, which is a real treat to have.
So the next chemotherapy is on July 30th
and I move onto a different chemotherapy now, docetaxul. Apparently, this one
is a much less aggressive chemo compared to the ‘FEC’ that I have been on.
They’re not expecting me to feel so nauseous and they wouldn’t expect the same
vein irritation that I’ve been experiencing so far either – both of which
sounds good to me. I think overall it’s a less taxing chemo on the body but at
the same time I’ve still got to deal with the cumulative effect of the chemotherapies
up until now. So it’s just a case of keeping putting one foot in front of the
other…as I am, and will continue to do.
So… just a short post for today, to update you
and introduce the new members of the family. I’m doing very well on the whole –
the first 8 days I do find very challenging but having the experience now and
knowing that there is light at the end of the tunnel of those 8 days, is enough
to get me through. And from then on, it’s such a treasure to be able to have a
nice time again. After such hard times, the good times are so good often they feel
so completely magical. It’s that pain and beauty is their full strength side by
side each other again. Lots of love to you all. xxxxxxx…
Words can’t describe how blessed I am to have so many incredible, loving, caring people in my life. I’ve created this blog so that I can share in some way my healing journey, so that whoever wants to, can keep up-to-date with how it’s unfolding, even if it’s not the preferred face-to-face sharing. The blogging idea came up in May 2014 so this is where my stories will begin. It has, however, been an incredible ride since diagnosis in December 2013, so when energy and relevancy allow, I'll post.
Monday, 21 July 2014
Sunday, 6 July 2014
Creativity as soul-food
In recent months I’ve
kept on coming into contact with the concepts of colour therapy and art
therapy. I haven’t yet investigated exactly how those with experience in these
areas define them but common sense tells me they are “disciplines” whereby
people use colour and art for therapeutic means, to assist with a healing
process in one way or another.
I remember back in school
days I did a lot of art and was really into it. I loved to paint, collage and
sculpt. The trouble was, as far as I see it now, I was always doing it to
impress; whether that be to get a good grade, or just to take home and be
praised by Mum and Dad. It was never used (for me) as a tool of
self-expression.
When I thought about
the concept of art therapy I wasn’t sure how I would even begin going about doing art as a process for expression and healing,
without worrying about the what the final product was, because I seem to be somewhat
conditioned for my art to look “good”…whatever that means. When I came to think
about it, I did wander how art can be good or bad, right or wrong? Art is art.
It’s an expression. As Clarissa Pinkola Estes argues in Women Who Run With the Wolves, the book I’m reading at the moment, it’s
soul-food. (This won’t be the last time I refer to this book – its one of my
sources of a huge amount of inspiration at the moment.) Creativity feeds, and
is an expression of, your deepest Self.
I’ve been meaning to
give this art therapy thing a go but for some reason I hadn’t got started with
it yet. It’s even available at the Olive Tree Cancer Support Centre where I go
to a young women’s breast cancer support group (they call it art counselling
there). I think it was that concept of not exactly knowing how to do art
without focusing on the final piece, and instead the process. Then I came
across this in Women Who Run With the
Wolves:
“Go ahead, struggle through it. Pick up the pen
already and put it to the page and stop whining. Write. Pick up the brush…and
paint. Dancers, put on the loose chemise, tie the ribbons in your hair, at your
waist, or on your ankles and tell the body to take it from there. Dance.
Actress, playwright, poet, musician, or any other. Generally, just stop
talking. Don’t say one more word unless you’re a singer. Shut yourself in a
room with a ceiling or in a clearing under the sky. Do your art. Generally, a
thing cannot freeze if it is moving. So move. Keep moving.”
It spoke to me…and so
I did.
I decided I wanted to
share this piece with you mainly because this was quite an experience for me
and this blog is, for me, about expression of my process, opening up my world,
and communicating some of that with those that want to be communicated with.
I’ve been feeling
rather nervous, and a whole lot of other emotions, about next week’s
chemotherapy, mainly because of my previous experiences so far. I simply don’t
want to go through it again. But who says this whole Life thing is about what
you want and don’t want, eh? It’s a process that I have to get through in my
own way, be present with and grow from in whatever way I can. There isn’t any
choice in it.
This afternoon I very
suddenly felt now was the time to use colour to express and channel those
feelings that were going on about next week’s chemo. I got out the pastels and
drew strokes of pink and black, for no particular reason that I knew of, side
by side each other on the paper, and before I knew it my eyes welled up and tears
started dripping from my face onto the paper. There was something about the
beauty and healing pink right next to the harshness of the black. So simple,
but that’s all I needed to express to release what was going on for me.
The piece went on.
Minimal thought into what it was turning into, just colours and shapes of
expression coming together.
A place of peace for
me is our bathroom. When I’m feeling rough in the mornings Kate often runs me a
bath and lights the candles in the bathroom. We have this gorgeous old
‘cottagey’ lilac-blue bathroom with a really calming feeling about it. I lie in
the bath as the morning sunlight shines through the wisteria-framed window. In
my fairly foggy state after chemo I like to look at the beautiful shapes and
colours that form as the sunlight falls on the water and the edge of the white bath.
Just looking at that in itself and being in that moment is enough to swallow me
up in a moment of raw beauty.
The colours that
started to come next onto my paper were those from the bathroom, that place of
tranquillity. And a teardrop shape emerged from the proceeding strokes around
where the tears had just fallen onto the paper. Despite the teardrop shape
though, and the contrast with the harsh black, the feelings of tranquillity and
beauty were the strongest, shining through and making their presence be known on
the paper. Then I realised that that’s my process in a nutshell…and I wanted to
share.
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