Chemo
Chemo sucks!
I don’t care for those who say they ‘breezed
through’ chemo. They couldn’t have had my cocktail.
Wednesday
Nov 29th, Chemo 1.
As they administer the liquid benefit, they
take you through a long list of possible side effects. It’s daunting but you
know that it’s the only way to kill off this thing, so you know you have to
just do it.
I had three steroid tablets and a large
anti-nausea tablet and had to wait for an hour for them to take effect. They found
a line in my forearm and hooked me up. Two different bags. It’s called ‘A/C’
and kills off the hormones that my cancer is feeding from.
It took about two and a half hours for the
chemo to drip into my body and I was sent on my way with a collection of
information and gifts from various groups.
Since then I’ve experienced a range of side
effects including; dizziness, metal-taste, headache, a near fainting moment
(followed by a drenching – maybe a huge hot flush?), tremors, and oh my, the
constipation. No one could have prepared me for that.
There’s once again a curiosity and need to
hear how others coped. I feel like I haven’t really done very well but how is
that measured? Most seem to say day 1-5 are the worst so I’m expecting to feel
a heck of a lot better tomorrow, just in time for surgery to have a port put
in.
Every message and card, of love and
encouragement fills me with joy. Thank you.
Monday
Dec 4
I rang the Cancer Council yesterday and got
some perspective. They have people ready to listen and I needed a good chat and
cry with someone who could understand. I think it’s partly the speed of
everything; less than three weeks ago I thought I was fit and well. I feel
refocused and better.
Tuesday
Dec 5 –surgery for the chemo port
I’d done the research and knew this was the
right thing to do. My veins are hopeless at the best of times and chemo also shuts
them down. It could get difficult for doctors and nurses to access my system
and this also allows them to take blood if necessary. This little thing sits
just under the right collarbone and feeds the drugs to near my heart.
However, it was a general anesthetic, another thing.
I fasted from 6.30am but knowing I’d feel
unwell, decided to take a ‘Maxalon’ before breakfast. I think this drug will be
my new best friend. I couldn’t believe the difference and will start my day
with it for a while.
The team at Modbury day surgery unit were
so lovely. It’s a weird thing… sit here, come here, change into these, sit
here, pee into this (just to absolutely make sure I’m not preggas! hahaha), wait
here with these other nervous people about to go under for various things… walk
into the operating theatre, see Dr Bev. And there she was. My surgeon. She is
just the loveliest woman. Smile, warmth and hugs. She held my hand as I went to
sleep.
Recovery. Done.
Another visit from Dr Bev while in
recovery. All went well. More hugs and, ‘You’re doing really well’.
I’m not sure what they put in that anesthetic
but I did not sleep one blink until 5.30am.
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