So, where are we on the sensory relapse?
Hug - all gone. Thank fudge.
Wet clothes feeling - mostly gone. Huzzah.
Sandpaper hands - stubbornly remaining. Sigh.
But, as Meatloaf once wisely trilled, two out of three ain't bad, so probably a suitable time to celebrate.
And because I don't like making life easy for myself, I decided to mark the occasion with a bike ride.
Now this may not have seemed wise for a variety of reasons: crap balance, ropey grip, general tiredness, non-MS-related clumsyness.
But I felt the need to do something to recognise the almost-out-the-end of the relapse state, so a bike ride it was.
Off we trooped as a family to a nearby (and mostly flat) country park and saddled up.
My word, what a joy it was. I balanced, I whizzed through puddles, I didn't have to think about anything except peddling and smiling.
The absolute best part was trusting my legs to be able to get me up a (very) small hill and then freewheeling my way down the other side, laughing like a small child.
It was completely exhilarating and made me proud, post relapse, of what my body can do and how my mind has dealt with it.
:: Wheels on fire by Julie Driscoll, Brian Auger and The Trinity
A mixtape for multiple sclerosis
Showing posts with label bike. Show all posts
Showing posts with label bike. Show all posts
Wednesday, 21 August 2019
Wednesday, 26 July 2017
Dear Prudence
So
I thought I’d write a little bit about fear this week.
I
know, cheering.
It’s
been sparked by last week’s bike purchase and the things I
was thinking as I finally went out on said cycle. TWENTY FIVE years
after I’d last sat on one.
We
are lucky enough to live within easy reach of the countryside and
there’s a handy track behind our little estate,
just waiting for nervy cyclists wearing their brother’s old bike
helmet.*
So
filled with both trepidation and excitement – but mainly
trepidation – I clambered aboard and pushed off.
And
do you know what, it WAS wobbly and it WAS scary and I DID fall off
(distracted by a passing cat) but it was a complete and absolute utter joy.
I
was reminded of being a teenager and biking to school, skirt
hoiked up, whizzing happily in the traffic. I was suddenly
younger and free-er and far more smiley than I thought I would be.
It wasn’t without worry – my steering was questionable and the
brakes took me by surprise a few times. Also the seat really, really
needs more padding, but I was so proud of myself.
It
made me realise that I can, for the time being at least, do the thing
I wanted to do – not despite the fear, but alongside it.
And
I think this is quite a key part of living with MS.
There
will always be fear – fear of diagnosis, fear of the damage, fear of medication: the
side effects and the efficacy rates, fear of what others think, fear
of relapses, fear of progression, fear of the unknown and fear for the future.
And while I
don’t advocate not talking about your fears or refusing to
acknowledge that they are there, it cannot help to dwell too much upon them.
What can help is to find a way to
live with this ever
present companion and somehow accept it into your life.
Yes
fear has a voice, but it isn't the only voice.
There are other far more interesting, positive and wise speakers out
there that I would like to ride with.
*The
helmet might be kindly described as vintage, although my daughter
collapsed in fits of giggles when she saw it, so perhaps laughable is
a more accurate term. It belonged to my younger brother who last wore
it over his questionable mullet at the age of 14. When I mentioned to
my dad that I’d bought a bike but failed to buy a helmet, he went
immediately went to his magic hoarding shed and pulled the original
box out with helmet intact like some kind of head protecting wizard.
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