I’m celebrating Valentine's Day with a faintly embarrassing outpouring of affection, and here it is: I love my
body.
There,
I’ve said it. I do.
Don’t misunderstand me: I don’t stand in front of the mirror every morning and
evening talking outloud to it and affirming its loveliness, I am
British for goodness sake.
I’m
also not saying it’s picture perfect even in the kindest of subdued lighting. But on the
whole, I think it’s great.
And
the reason I think it’s great, the reason I don’t hate it despite
all the limitations it has or has the potential to have, is this: my
body is not letting me down. A disease is letting me down.
In
my mind, they are two very, very different things.
I
see my body as an increasingly knackered team member that is still
managing to turn out for my side.
In
the words of those irritating Prescott botherers Chumbawumba, it’s
got knocked down, but it gets up again.
Because
even if, as the widely held theory suggests, MS is an auto-immune
disease and my body is attacking itself, then I still prefer to think
it’s simply a bit bewildered rather than just plain mean.
It
can’t help the random spasms, it can’t help the skewed
temperature sensations, it can’t help the stabbing face pain and it
can’t help the thoughts-in-a-spin-cycle.
It
is not my body’s fault.
And
while it fails and falters, it also tries its very, very hardest to
help.
So
far, it’s managed to heal claw its way back from a number of pretty hefty relapses. Alright, it may never have been a 100 per cent recovery and alright, it might hold part of the damage back and unleash it again when I’m
too tired/too cold/have a virus/sat in a hot bath for too long.
But
generally, it’s on my side and it’s fighting very hard to stay
there.
However,
I am fully aware that this state of affairs is subject to change and
at some point, my body is likely to stop healing quite as well as it has done to date.
There’s
only a certain amount of times myelin can repair to an acceptable level before the damage really starts to hit and more significant and permanent disability develops.
So far I have been lucky, I have repaired to a reasonable degree. Even if each relapse has left a lingering mucky footprint on my balance, pain, sensation, cognition or vision.
I don't know how much longer this ability to mostly repair will last. And honestly, it's best not to dwell.
So far I have been lucky, I have repaired to a reasonable degree. Even if each relapse has left a lingering mucky footprint on my balance, pain, sensation, cognition or vision.
I don't know how much longer this ability to mostly repair will last. And honestly, it's best not to dwell.
So while it’s sometimes been on the losing side in the skirmishes, while it
can’t always make me completely better, I would officially like to thank my
body for repeatedly lacing up its gloves and stepping into the ring.
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