“Even nerves
of steel are subject to metal fatigue.”
–P.K.
Shaw
This is one
of my favourite quotes because it reminds me that even the strongest in the
world have moments of weakness.
Well, today
was my moment, as I burst into tears during a gruelling physiotherapy session.
It totally
stunned me because I consider myself a seasoned traveller through the medical ups
and downs. Even though today’s treatment was particularly rigorous and tough, I
have suffered worse fates than that and survived before very well, thank you,
without even a grimace.
My tolerance
for pain is generally very high and even though my physiotherapist is working
through some “nasty” effects of connective tissue disease, she is gentle, kind
and expert at her job. Although there is
discomfort and pain (and no, these words are not interchangeable–tell your
doctors who like to use ‘discomfort’ as a euphemism for ‘excruciating pain’),
it is a short-term pain for long-term gain. We have been able to regain
mobility and maintain much of it between sessions. (Yippee! I can move a bit
more freely again.) So it’s all good.
So far, I
have tolerated everything no worries, but today was my ‘metal fatigue’ moment.
It came at the end of a very busy time which pushed me further than I like to
be pushed; for example:
Two busy days at the end of the week with non-negotiable
commitments during the day, each one requiring a late night to attend end-of-term
school functions; i.e. two late nights
in a row with barely enough rest in between.
Day 3: bedrest to recover.
Day 4: woke up cheerfully with a clear
head, no ‘fatigue fog’ and a little bit of energy and motivation to get things
done; except every time I got up to do something, the pain was excruciating–so disappointing
and discouraging.
It meant that
I would need to leave my planned activities for another day and to spend the
day either in my chair (again!), in bed or on the couch. Pfffth! <big fat
raspberry!> Pfffth! I had just spent
two days in my chair to survive the increased activity and the third day in bed
so all I wanted to do was get up and move! <sings nursery rhyme: “Pain,
pain, go away, (don’t) come again another day!”>
Day 5: woke up early with good intentions
but body argued; muscles weak and aching; succumbed to the inevitable and spent
the morning in bed with the crochet hooks and catching up on blogs, an
agreeable outcome despite the body’s protests.
Thank goodness I didn’t have to go anywhere and could ‘go with the flow’. I gratefully reflected on how lucky I was,
relieved that I did not have the pressure of appeasing an employer.
Day 6 (today): My skin and eye symptoms were flaring
up; I was feeling noticeably tired and fragile,
as remarked upon by the physiotherapist as she greeted me.
We were
continuing a series of treatments to loosen up the muscles and connective
tissue in my neck, shoulders, spine and hips.
Recently, my physiotherapist was the first one ever to enlighten me that
this is a pattern “typical” of my condition and she was not surprised at my
clinical presentation as it all fitted into the “connective tissue” picture;
interesting.
One one hand,
it was reassuring to have a reason for the way I was feeling, but on the other
hand, it was another confirmation of my diagnosis and everything that entails.
Today the
body was presenting with particularly “nasty” problems and we were going
through the usual procedures to solve them when suddenly it became all too much. My crazy immune system must have reduced my tolerance.
The pain was
extending further than the usual places and enveloping me from head to toe. (I
had experienced ‘trigger points’ before but this was ridiculously severe.)
My oversensitive ‘lupey’ skin reacted as the heat cream which usually brings welcome relief became a burning, prickling fire on my neck, burning deeper and deeper.
My oversensitive ‘lupey’ skin reacted as the heat cream which usually brings welcome relief became a burning, prickling fire on my neck, burning deeper and deeper.
My legs went
numb and I pondered whether I would be able to walk enough to get home as I
only had my ‘wheelie walker’ with me and then all of the little ‘throwaway
lines’ uttered by my physiotherapist entered my head, reinforcing that this was
reality these days, a reality I didn’t want to contemplate.
Involuntarily,
the tears came. I couldn’t fathom the
intensity of this surge of emotion. I felt embarrassed and defeated too–the
body won this round for sure. Why this
reaction? Why now? Why here at the physio?
Sensory overload,
fatigue, grief, the expectation that this sort of pain is likely to be a
regular fixture on the treatment list because, although we had success with
some of the earlier treatments, some of it needed to be done again because the
connective tissues tightened up again in the interim, essentially “undoing” some
of our good work of previous weeks.
And then I remembered
“Even nerves of steel are subject to metal fatigue” and I realised that just
because I “had a moment” doesn’t mean that I am weak. I can still be strong even with tears rolling
down my face. My sweet physiotherapist
was non-judgmental and comforting : “this is a good place to let it all out”. I realised it can be a sign of courage to
reveal one’s inner vulnerabilities and weaknesses, to drop the shield and bare
one’s soul.
Don’t get me
wrong–I wasn’t a wailing mess; just lots of tears quietly escaping. My physiotherapist finished her part and made
me comfortable with a blanket, tissues and a soothing towel for my neck, allowing
me to quietly contemplate this unexpected turn of events until everything had
settled.
After a short
while, I regained my composure, polished
up my ‘nerves of steel’ and walked out to face the world again.
Ah, Jodie. Will remember this. Even though my ocular MG is currently symptom-free, I do get an attack of the nerves every now and then :-)
ReplyDeleteI hope you don't have any attacks anytime soon. What are your strategies for coping when they do occur? Keep up with the healthy lifestyle choices, taking care and being kind to yourself.
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