Perspective.
Comparisons. Sliding scales.
They’re
all interesting phrases when applied to the way you view things –
wealth, achievements, career, family, life. Illness.
Like
a number of chronic diseases, the perceived seriousness of MS sits on
shifting sands depending on who you speak to.
Perhaps
you’ve dealt with reactions from people at the oh-it’s-not-so-bad
end of the scale. They’ve seen someone being amazing on the
Paralympics with it. Or know a friend’s mum who has had it for 25
years and still doesn’t need a walking stick. Perhaps they know
someone who works fulltime and goes to the gym every other day?
On
the other hand, perhaps they’re at the other end of the scale and
they’ve got a pretty bleak outlook for you. Maybe they’ve cared
for someone with the primary progressive form? Watched someone
deteriorate before their eyes? Seen someone in the end stages of MS?
It’s
entirely possible you’ve dealt with these – and many opinions in
between – from the medical community.
During
the summer I saw a gp I don’t normally see. He asked how I was
generally and we had a general chat about MS and recent research.
He
concluded by saying it would be good for his newly-diagnosed patients
to see me still working and with a family.
“Because
really, for you, it’s just an inconvenience,” he finished. With a
reassuring smile, believing he’d said the right thing.
And,
if I take a deep breath to calm down and think about that
proclamation, then to some degree he was right. I’m currently not
hugely debilitated. I still work, drive and most of the time I appear
to function like everyone else.
To
a gp, who is bound to come across far more aggressive cases, he may
well believe he could describe my MS as ‘an inconvenience’ and
there’s a little bit of me that sort of accepts that.
But
to me an inconvenience means a flat tyre or the radiators needing
bleeding or running out of teabags.
It
does not mean slipping down the workforce ladder because I know I
couldn’t manage it or missing most of the things healthy people
take for granted or making the painful decision to not extend our
family.
None
of these things would I describe as ‘an inconvenience.’
So
while I do recognise that I am somewhere in the middle of the
health-death track bar, I think we would all like recognition of our
own personal scales and a bit more consideration of what might
actually count as our inconvenience.
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