Love is in the air!
I am officially loved up!
One of my new ladies was Helen. She was living with Motor Neurone Disease and was in the very advanced stages; totally dependent and admitted due to a chest infection – it was believed that she had aspirated on fluids and had become quite poorly. Her daughter had been looking after her at home with a package of support, but at handover they said that she was waiting for an available place at the local hospice.
My dates (yes dates, plural) with Matt have been awesome and
so it was with a spring in my step that I returned to work last Monday after my
annual leave.
I must have looked a proper gorm, smiling from ear to ear
with that faraway look in my eyes. In fact, during handover one of the nurses
asked me if I’d been overdosing on Krispy Kremes for breakfast again!
I couldn’t wait to see my patients in Eden Bay. A couple of
my ladies had been discharged, but I had new ones to get to know and then there
was the die-hards – the ladies who seemed to have been there forever but who
never failed to keep me on my toes. It was lovely to see them again and even
more lovely when they told me that they’d missed me.
Jo wasn’t on duty my first day back so I was quite relaxed
and spent time catching up with my patients’ progress and finding out what I
could about my new admissions. I was regaling them with tales of my dates with
Matt and we were having a proper laugh.
I know there’s that misconception about hospitals being
miserable places where patients are pre-occupied with their illness, but that
morning, we chucked that theory out of the window and I really believed that my
ladies enjoyed hearing about my newly found love-life (to be honest, some of
the tales they told me about their own antics made me blush…!)
One of my new ladies was Helen. She was living with Motor Neurone Disease and was in the very advanced stages; totally dependent and admitted due to a chest infection – it was believed that she had aspirated on fluids and had become quite poorly. Her daughter had been looking after her at home with a package of support, but at handover they said that she was waiting for an available place at the local hospice.
I introduced myself to Helen. She could still speak but her
voice was soft and she soon became breathless. I needed to reassess her needs
in readiness for her move to the hospice and wanted to make sure that I
accurately recorded her wants and wishes as she approached the end of her life.
We talked about lots of things including making sure she was comfortable and
pain free and I scribbled it all down so that I could give a proper account to
the hospice team.
I don’t know what made me glance up at Helen, but when I
did, silent tears were streaming down her face. She wasn’t able to move her
arms to wipe them away, so I did it for her. I put my pad and pen on her
bedside cabinet and moved over so that I was sitting on the bed with her. Steve
the charge nurse would have throttled me if he’d seen me – perched like a fat
bird on Helen’s bed –but she seemed to need me close by and it seemed the
natural thing to do.
I didn’t ask her what was wrong, that was obvious, instead I
asked what I could do to make her feel better. She seemed to have a lot to get
off her chest and told me how worried she was about how her family would cope
after she had gone. She said that she knew that she only had a short time left
but that she was ready to go. She had lived with her condition for the last
twenty years and she was tired.
I don’t know who was more tearful – me or Helen. She was so
pragmatic about dying, so selfless as she worried about how her daughter (who
was also her best friend) would manage without her. Her daughter was married
with grown up children and from what I could gather Helen was still the
respected head of the family.
And then she shared her biggest wish – that she could live
for just one more Christmas. She told me tales about her childhood and how her
parents, with not two pennies to rub together, had always made it a magical
time for her and her brother. She had then tried to do the same for her
daughter and Christmas had always been her favourite time of the year.
I knew in my heart that Helen wasn’t well enough to see
another Christmas; her notes showed just how poorly she was and her transfer to
the hospice was being treated with a sense of urgency. How my heart ached when
Helen told me that she knew she only had a short time left on this earth – and
how it almost broke when she told me she couldn’t imagine how her daughter
would cope without her at Christmas.
And that’s when I had a cunning plan….
I sniffed out Steve in my break and shared my plan with him.
He looked at me with a kind of ‘ I despair of you Florence’ look before
agreeing, as long as it didn’t interfere with the care of my other patients.
I legged it down to the canteen and shared my plan with the
lovely ladies from the Royal Voluntary Service and they were chirping with
enthusiasm and ideas. I then rang Helen’s daughter and asked if she would have
any objections to the plot.
Having colluded with the other 5 ladies in Eden Bay, we then
came good with our plan.
On Thursday morning, we officially brought Christmas
forward.
The ladies from the Voluntary service were like ninjas as
they arrived on the ward before anyone was awake and decked out Eden Bay –
tinsel, lights and a 6 foot Christmas tree next to Helen’s bed. She awoke to
Christmas carols playing and a stocking at the end of her bed. Her face was an
absolute picture and she scoured the room until she found me and our eyes met.
I approached her bed tentatively, not quite sure whether I’d read this
completely wrong. I needn’t have worried – the tears she cried were not of
regret, or sadness but thanks. Thanks for listening to her and taking her
wishes seriously.
We had a really fun day. I’d bought Helen a present, and her
family visited throughout the day, bearing gifts and sharing memories. The
ladies in the bay would break into impromptu song and poor Helen had to suffer
every possible Christmas song from Jingle Bells to Rudolph the Red Nosed
Reindeer! Dinner was served complete with crackers, hats and a speech from
Queenie (Bed 2 – the closest we could get to the Queen!!) Even Steve joined in
the fun and came dressed as Santa.
At the end of the day, Helen called me over in her soft
voice. She looked absolutely exhausted but there was a look of contentment on
her face.
As I leaned over to hear what she was saying, Helen asked me
to lean in closer, and I felt her lips brush across my cheek. ‘Thank you’, she
said. ‘Thank you for bringing the meaning of Christmas to me one more time’. I
told Helen that it was the least I could do, to which she replied ‘The greatest
gift you can give anyone Florence is time – you gave your time to help make
memories for the people I have to leave behind – thank you.’
I cried that night when I got home. Cried for Helen and the
Christmas she wouldn’t see and wept with pride for the smile on her face.
Helen didn’t get to the hospice. She slipped quietly away
that night and the nurses told me they’d never seen such a beautiful and
peaceful face as they paid their final respects, with the soft tones of Nat
King Cole playing in the background.
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