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Day 3 - Day 9 - Day 13
- Day 24 Updates
This is the story
of Kirra Nareece Jade Doyle, her experiences after being diagnosed with
a brain Tumour (21 September 1998). This story is not to be taken as
Medical information or used as such. It is here as a record of the
events leading up to and after being diagnosed with the tumour as
remembered by her parents. (Paula & Myself.)
It's now 18 December 2012 and Kirra is very well.
Introduction.
Some time in May 98 Kirra's Mum
became concerned that she was constantly leaning her head to the left
and took her to see our Doctor. The Doctor found nothing wrong and
Paula was told to bring her back
in a week if she was still concerned. In a week Paula returned. The
Doctor still thought nothing was wrong, but made an appointment for
Kirra to see a Consultant at Swindon PM Hospital. The Consultant sent
her for a sight test, which showed
she had normal vision. Shortly after Kirra suffered with two ear
infections and her medication seemed to stop her leaning, When she
finished her medication her head tilt came back again. Kirra had
a second eye test which she also
passed. On the second visit to see the consultant Paula mentioned we
were going on holiday and Kirra would be flying.
The consultant wanted Kirra to have a Brain Scan before she flew.
(By this time Paula felt everyone thought she was just a paranoid
mother, but she felt something was not right.) An MRI scan was arranged
for the day before we were due to
fly out to the Canaries.
Day 0.
On Tuesday the 22nd of September
1998 we sent the two elder kids off to school, then Mum and I went to
Princess Margaret Hospital ( Swindon, England.) with Kirra. We didn't
mind waiting 3 hours before
Kirra's Scan, rightly or wrongly we did feel the staff thought it was a
waste of their time, Kirra was running around playing and chatting like
any 17 month girl would be. In fact the lack of concern was quite
reassuring, as we just wanted
the all clear so we could fly off to the Canaries in the morning. The
registrar's notes stated Kirra was to have a cannula fitted to
administer the sedative, this puzzled the doctor as he had always given
oral sedation, still he followed
the registrar's instructions and we took Kirra down to the MRI scanner.
After a while sitting next to this big noisy machine a nurse came in
and injected some contrast into Kirra's cannula, we thought nothing of
this, the nurse said it's
just to highlight the blood vessels. After another 20+ minutes the
nurse came back and said as she had a neck tilt they wanted to scan her
spine. (Good I thought nothing wrong so they're looking elsewhere.) Due
to Kirra waking up and a
second sedative not having any effect, it was decided not to do a spine
scan. We were taken to a little side area where the MRI Doctor told us
the scan was not normal, (a bit of a shock to say the least, as I also
thought Paula was being
paranoid and it was just an ear infection.)
Kirra had a lump in her brain just above her neck. We were taken to
another room and had to wait to find out our next step. When the
doctors came back they showed us the scan. The tumour showed up as a
white lump about the size of a hens
egg. We were told she would have to go to The Radcliffe Infirmary
in Oxford. We wanted to take her ourselves, and after going home,
arranging for friends and relatives to look after our other two girls,
we repacked our suitcases and
headed for the Radcliffe Infirmary.
We arrived at the Radcliffe Infirmary about
4.30pm and Kirra was admitted to the Children's Ward. Kirra was started
on Steroids to reduce an inflammation around her Brain Tumour.
Day 1. Blurrrrrr!!!!
In
The morning we had a meeting with Mr. Richards (Neurosurgeon), The
Senior Paediatric Registrar, the Hospital Registrar and
Kirra's nurse. Only Mr. Richards Spoke and no one else gave eye
contact. ( we didn't find out until weeks later they suspected the
worst.) Mr. Richards started by saying The next few weeks will be the
most stressful we would ever have.
Kirra has a Brain Tumour and if it is not removed she will die! The PMH
scans did not show as much detail as needed and Kirra will need to have
another scan tomorrow, they will also do a spine scan to see if the
Brain Tumour has spread. Out
of the three possible outcomes ( Benign, Mixed or Malignant ) prepare
for the worst and hope for the best.
We weren't told much more, as the Scans weren't as detailed as they
would have liked. Kirra spent the rest of the day either in the ward
play room with her sisters or around Oxford with us.
Day 2. Second MRI scan
Slept quite well. Kirra ended up
sleeping on the fold up mattresses with us. Took Kirra to Oxford
university Park for the morning. Back to Hospital for 12pm so Kirra
could have her pre-med. Paula
carried her down for her second MRI Scan about 1.30pm. We didn't
collect her until 3.45pm. Dr Mann (the Anaesthetist.) informed us Kirra
had stopped breathing under the anaesthetic, this was why she was so
long in recovery. Dr Mann also
said Kirra would have to be transferred to the John Radcliffe Hospital
Paediatric ICU after her operation tomorrow. This was a precaution as a
heavier anaesthetic was to be used and her oxygen will have to be
monitored for 48 hours after
the operation. The steroids Kirra was taking gave her a good appetite
and she demolished two large oranges before she finally went to sleep.
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