Once again, a rough month in our lives. Remembering Marian, Georgia and Jen always
makes the end of June that bit harder than the rest of the year (that’s not say
the rest of the year is easy sometimes).
This year, we had the frightening experience of finding out Alissa had a
level 4 melanoma. We discovered that on
June 12th, just after our very pleasant kid free few days away in
Auckland. Here’s how the stats went. At that point, Alissa has a 25% chance of
recurrence within 5 years. 2 harrowing
sleepless days later, we meet the consultant who takes us through next
steps/options. Removal of more tissue
around where the melanoma was –‘ gold-plated procedure’ he called it. The optional surgery was to go through a
radiation type dye procedure to detect the lymph node the area drains to, and
take it out. If the biopsy results on
the lymph came back positive for melanoma cells, stats move to 40%, if negative,
10%. We chose to have that done to work
with the numbers.
The consultant (Mr Smithers – yes, really) didn’t dwell too
much on the surgery side of things, perhaps because of what was a much bigger
issue at stake – it was no small deal.
Alissa was knocked out and had an overnight in hospital – apparently if
it was only the tissue removal, would have been a day surgery. Big chunk all the same.Then the agonising wait. Surgery was on a Tuesday and we were told Friday we’d get the results. Friday came and went and of course the mind plays all sorts of games as to whether it is a good thing or bad thing not to hear. Midday Saturday we got the call and it was good news. Of course everything is relative but it was all we wanted at the time. 2 weeks of tension and stress building up to that moment. I knocked back a strong glass of rum having barely had a drop of alcohol for 2 weeks. We’d both lost 3 kilos in the process.
The kids were troopers – knew there was something going on with all the support and flowers arriving – and they had got quite clingy around operation time.
By the time the anniversaries came around, we were in a better position to think about our lost ones and reflect a bit. And rethink our own life plans. Bring a few things forward and live a little more now rather than waiting until this or that is done.
Though one of my small efforts to try help a bit by buying that robomaid (robot vacuum cleaner) was not a success. Money back guarantee utilised for the first time in my life. Emma is still disappointed that the 'toy robot' had to leave.
The new 55 inch smart TV however was and is a roaring success. Still looks small in that big room I think. Should have gone 65 inch.
Now over 1 year since we moved into the house. And so Max has turned 1. Still stomping around the place as he has done for almost 4 months now.
Concrete slabs. Order of the day. 3 of them. Little ones, but enough to be able to mount a decent sized mailbox and 2 light bollards for the driveway. I haven't connected the latter - concrete mixing is not that dangerous, underground electrical wiring a different matter.
August is upon us. Time for all of Brisbane to get sick. Time for me to head off to Ireland with Emma.
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