First of all thank you too everyone for reading the first
part of the Blog. I had some great feedback and it was good to get everything
out via a Blog.
The last time I wrote anything was at school, I can remember
it vividly. We were asked to write a story about a man who was falling from a
building and we had to write about his life that flashed before him. It’s
ironic because that’s how I felt when I was told I had Bowel Cancer, the
feeling of dread is quite overwhelming once you hear that word. As the days went by though I quickly realized
the prognosis was good, and I have a 90% chance of making a full recovery all
because I caught it early(check your poo!!!).
So, back to the story on 21st of January Dawn and
I set off to the Hospital for a CT scan to see if the cancer had spread. I was called into a room where the nurse
prepped me by inserting a canula into my arm to administer the drug that goes
into my veins, this highlights the Lymph Nodes so they can see if the Cancer
has spread into them. The nurse informed me I would also need to drink a Barium
Meal. This shows up the stomach and bowel for the CT scan. It needs to be drunk
over the hour before the scan. I had noticed
a small plastic cup that I presumed was for the drink, easy I thought it’s only
a small cup east I thought I soon knock that back. Then she handed me a 1 liter
container of what turned out to be an orange flavored thick chalky milkshake
style goo, that did actually take a good hour to force down. Back in the waiting room the others waiting for
scans and drinking that drink winced with every sip as I did, there was
definitely no gulping going on. The scan was over in a few minutes and apart
from a feeling of nausea when what ever was in the drip was administered, but
that soon went.
We were told it would be three days before my tests came
back and it was going to be a long three days, luckily on the Monday, L(I’ll
call her) the Colorectal Nurse Specialist rang me to tell me that the
cancer hadn’t spread. To say it was a relief is an understatement of
the highest order. I rang Dawn straight away give her the good news, it was the
best news we had had over the last couple of weeks and we now knew there was a
light at the end of the tunnel.
The next appointment was to see Mr T(not that one) the
consultant. He was straight forward and professional as expected and explained
in full where the tumor was and what the operation involved. Apparently he’s
very well thought of and is at the top of this particular field, good to know
in in good hands. Actually the NHS have been fantastic so far letting me know what’s
going on as regards results and getting me quick appointments, keeping me in
the loop etc. Mr T also explained the op would be keyhole and I’d have 4 small incisions
as well as a larger one to remove the affected tissue.
The same day we were introduce to the Research Practitioner for the Oncology
Clinical Trials Team, also L so ill call her L2. I was asked If I would like to
take part in the Foxtrot trials, an international research study of drug
treatment for bowel cancer. I had already come across this on a web search for
my condition and thought if asked I would take part. On the trial you are put
into the computer and one of three courses of treatment are prescribed. I am
going to be having Chemotherapy (Oxaliplatin) intravenously for six weeks which consists of two courses
three weeks apart, alongside that a course of Chemo tablets (Capecitabine),
eight tablets a day for two weeks then a week off them before the second course
of treatment. The plans changed slightly when my Oncologist decided to put me
on a more intensive course of treatment as originally it was three courses of
chemo before the op. Anyway three weeks after the last chemo I go in for my op, and after that I’ll be on
another course of chemo for 18 weeks. So
hopefully that will be that, sounds easy and barring any complications I hope
it is, but as with everything so far we will have to take what comes, and we
are definitely not taking anything for granted.
Yesterday 14th January I went in for my first
course of Chemo, there were quite a lot of other people in the waiting room and
again I had one of those moments where it all becomes very real and quite
daunting on what’s in front of me. But saying that it seems everyone there is
just getting on and coping, it was quite a nice atmosphere really. Two lovely
ladies were constantly walking round offering tea anc]d coffee, biscuits,
toast, sandwiches etc. The nurses were great too all full of smiles, which is
always a good thing in a hospital situation.
The nurse plugged me in as it were and the drug took two
hours to go in. no real issues with it although it was very sensitive around
where the needle went in and I had bad pins and needles on and off throughout,
nothing major though. The worst thing about all of it was having the big
plaster near the needle taken off, IT WAS REALLY BAD, excruciating what with my
hairy arms. I am definitely shaving them next time, I might get some funny
looks but I am not going through that again. God knows why women get waxed they
must be mad.
So finally I’m at home and Dawn is looking after me. Not
feeling to bad at the moment either. I had trouble sleeping last night so
feeling tired today and a bit lethargic, but I’ll try and not have a nap today
as I did yesterday, I don’t think that helped. My arm is still a bit sore and
sensitive bit its nothing really. I’ve not had any side effects as yet, and no dashes to the loo for emergencies from
either end(sorry). I’ve had the first dose of the chemo tablets this morning
and am just waiting to see how I go with them.
I’ve rang work and informed them I’m available to work for
the next two weeks and hopefully that will be the case. So its onward to the
next treatment, I hope the the cancer is enjoying the Chemo HA!!!
Thanks again for reading .