When I was first diagnosed with IT,
the first emotion I felt was shock followed by lots of crying and obviously the
‘why me?’ question. I know it’s a cliché, but I did think that IT
was definitely something that happened to other people, but when the
unbelievable occurred and I found myself in that situation, lots of phrases
like ‘that’s unfair’, ‘what have I done to deserve this?’, ‘I shouldn’t have
drunk all that wine’, ‘there are far more unhealthy people out there who don’t
get IT!’ and other negative thoughts arose.
After the shock, came the rollercoaster of
appointments, tests, biopsies and scans which actually did help as there was no
time to dwell on IT. I’m sure most people
who are diagnosed with IT would agree that the months
of treatment following are actually a blur and it’s only when you reflect on
that time that you realise the extent of what you have been through.
I’m now at that stage where I don’t think about IT all
the time, only when I have an appointment, when it suddenly pops into my mind
for no apparent reason or when I am conscious of the aches and pains caused by
my medication. Even now, I still can’t believe that I had IT.
I feel very lucky in that my body hasn’t changed much at all as I didn’t need a
mastectomy so when I look in the mirror, it’s physically still me. The
only difference is my hair which is now white/grey and very short, but
apparently that is very on trend at the moment so I don’t mind that at all!
The ‘why me?’ question has now faded and has been
replaced with extreme gratitude for the superb medical treatment and care I
received and for all the support and love I have had from my fantastic family
and friends.
This piece was originally posted on Jackie’s own
blog here: http://lifeafterbreastcancer.co.uk/
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