“i’ve had cancer nine times” - lizzie...
TRANSCRIPT
S T Y L I S T . c o . u k 7 7
t was in the
bathtub that
I made the
decision not
to let cancer
kill me. I was six weeks
into a gruelling round of
chemotherapy and had taken
a bath to soothe the aching in
my limbs. I remember trying
to pull myself out of the tub
and realising my legs were
too weak. I sat in that bath,
watched the water flow away,
and felt like I was draining
away with it. But gradually,
as the bathwater spiralled
“I’ve Had
Cancer
Nine
Times”
Emma Hannigan, 42, is fighting a long-running war
with cancer. She tells Stylist her emotional story
Emma strugglEd
to makE doctors
bEliEvE shE was ill
C o n f r o n t i n g C a n c e r
I
7 8 S T Y L I S T . c o . u k
painful. I knew that something
was wrong but I spent the
next five months in and out
of hospital trying to get
answers. Eventually, I sought
a second opinion from a skin
specialist at The Blackrock
Clinic in Dublin. I told him
about my medical history
with the BRCA1 gene and
explained my surgery. When
I told him about the two lumps in
my neck, he did a visible double
take: I was admitted immediately.
i n t r e at m e n t
Within a week, I had been
diagnosed with dermatomyositis
[an auto-immune disease that
causes inflammation of the
muscles and the skin] and cancer
in my neck, shoulder and under
my arm (the pre-cancerous cells
in my breast had spread to the
lymph nodes). It was hard not
to be angry, livid even – this
was what I had gone through
hours of painful surgery to avoid.
But I was determined not to
let it eat me up. Instead, I got
lumps and was told the cancer
had returned for the third time.
And so began the relentless
cycle of diagnosis and treatment
– over the following two years
I was diagnosed with cancer five
more times, and each case was
treated with either intravenous
chemotherapy, chemotherapy
tablets or radiation.
Each time I have found lumps,
I’ve called my oncologist, he has
organised scans and we have met
at his office for the results. It has
almost become a routine. That’s
not to say it isn’t terrifying. Each
time I sit in his waiting room,
I imagine the cancer has spread
to every one of my organs. I can
the walls; paintings and
drawings by the children
who’d visited or been
treated at the hospital,
and I remember seeing
a page of tiny handprints
signed by a little girl called
Amy. On it, she had
written, “Please help me
to die, I’m suffering.”
I thought I was going to
be sick. That would finish me – if
one of my kids was going through
this instead of me. Any time I’ve
felt low over the past 10 years,
I think about those little handprints,
and remember that I’m OK.
Of course, life has changed.
I may not always have as much
energy as I used to, but my friends
and my children are understanding
about that. Otherwise, things are
great. I started writing from my
hospital bed out of boredom and
have been lucky enough to turn
that into a career. I’ve had eight
novels published now. I see that as
the silver lining behind all this pain.
Last year, I was diagnosed
with cancer for the ninth time,
and am currently undergoing
chemotherapy. I am also on
a long-term chemotherapy drug
that helps to protect my organs
from the spread of cancer. Until
I’m told that there is nothing more
that can be done and the cancer
has spread to a place they can’t
attack, I will always believe
I am going to be fine. I have
never wanted to give up – every
year I add to my life, every
Christmas I see feels like success.
My goal is to keep on fighting; to
see Sacha and Kim get married,
have children and do what they
want in life. I know the cancer
may return and spread. But my
doctors and I believe I can remain
one step ahead for many years to
come. For me, the illness is shifting
from a deadly disease to a chronic
one. The grass is not greener on
the other side. Everyone’s got
problems – you can roll over and
die, or you can decide to stamp
all over them. I am fighting a
raging battle with cancer and
I will never be complacent. If I give
up now, cancer will have won.
That’s not an option. It does
not deserve to win. I do.
The Heart Of Winter by Emma
Hannigan (Headline Review,
£13.99) is out now
almost feel it travelling like ink
around my body.
i n n e r s t r e n g t h
I am a positive person, but I’ve
had dark moments. Just before
Christmas last year I was
diagnosed with a large tumour
at the base of my skull, and had
to undergo 50 sessions of
radiotherapy, back-to-back.
Because of the location of the
tumour, I had to be strapped
down onto a table so I didn’t
move. The mask was so tight it
left deep marks on my face, and
the table was as hard as marble.
It was a claustrophobic and
painful experience. Having to go
into hospital and do that every
day is one of the hardest things
I’ve ever experienced.
But there are moments that
put things into perspective. The
night before I had my double
mastectomy, I couldn’t sleep.
So I went wandering around the
halls of the hospital. Eventually,
I happened upon the children’s
wards. There was artwork all over
a solicitor to help me draw
up a letter demanding that the
hospital would never tell another
patient that pre-cancerous cells
weren’t a danger. That was
enough for me.
I was given steroids for the
dermatomyositis and underwent
six months of chemotherapy and
surgery to remove tumours from
under my arms, which left me
exhausted. I also lost my hair.
But eventually, the cancer cleared
up and everything was great
for a couple of months. Then,
I discovered more lumps in my
neck. I will never forget that feeling
of dread. I knew that the cancer
was back. Soon after that, doctors
confirmed my suspicions. I was
reeling. I hadn’t even considered
getting cancer more than once.
But I still had my husband and
children (Sacha, 14, and Kim, 13)
to think about. I simply didn’t have
time to have cancer.
However, about a month after
my next round of chemotherapy
had finished and I’d been given the
all clear, I discovered yet more
down the plughole, I became
incensed. I wasn’t going to
let that happen to me. I was not
going to go down the plughole
with this cancer. So I used all my
energy to haul myself out of there,
looked in the mirror and said,
“That’s it, enough; you’re not
going to let this thing beat you.”
When I received my first
cancer diagnosis in 2007, I felt
overwhelming relief. I’d been in
and out of hospital for six months,
trying to convince specialists that
something wasn’t right. Having
someone finally look me in the eye
and say, “Yes, you’re sick,” felt,
strangely, like justification.
Two years earlier, at the age
of 33, I’d tested positive for the
faulty BRCA1 gene – a genetic
mutation that raises your
likelihood of developing breast
cancer to 60-90% and ovarian
cancer to 40%. The gene
mutation had only recently been
discovered, so the National Centre
for Medical Genetics in Dublin was
looking for volunteers to be tested.
My mum – who had three siblings
and an aunt who had all had
cancer – put herself forward
and tested positive for the gene,
meaning my likelihood of having
inherited it was 50%. I tested
positive soon after that.
At that point, I wasn’t scared.
It was an easy decision to have
surgery to reduce the risk. I felt like
a ticking time bomb. There was
no way I was going to sit around
waiting for this cancer to hit. I have
a husband and two children.
I had a double mastectomy,
oophorectomy [full removal of the
ovaries] and breast reconstruction
surgery over 12 months. It was
tough, but I reassured myself that
it was just one year of hospital
visits, with a little pain thrown in
and after that I could get on with
my life. The doctors had found
pre-cancerous cells in my left
breast when they were doing the
mastectomy, but were adamant it
was nothing to be concerned
about. So what happened four
months later was a huge shock.
One day, I found two lumps
in my neck, about the size of
peas. Around the same time,
I developed a red, itchy rash all
over my face, arms and upper
torso. The muscles in my arms
and legs also started to seize
up and became unbearably
“EvEryonE’s got problEms. you
can roll ovEr and diE or stamp
all ovEr thEm. i’m fighting
a raging battlE with cancEr”
Emma has rEfusEd to
givE in to cancEr
C o n f r o n t i n g C a n c e r
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