I was adamant about still having some control over my new home. I refused to listen to therapists’ recommendations that I purchase an electric scooter to replace the rusty manual silver car that I no longer could drive, or modify my bathroom and install rails around my new home. In my state of denial I continued to stubbornly believe that putting in ugly disabled equipment was a waste of money and unnecessary when I was on my way to a 100 per cent recovery. Accepting any modifications to my home symbolised permanency and disability confinement, and suppressed any chance of hope. Those around me would assume I was no longer improving. I don’t think my therapists understood my state of mind, and often took my refusals personally. Of course their suggestions were right and in fact did seed the ideas. For example, after a while of getting around in cabs and trams and depending on lifts, I decided that a funky- looking scooter would improve my independence.

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Keeping up appearances…

It’s hard enough to maintain your ‘looks’ for any person right? Add “disability” and “ageing” to the mix and I’m highly unlikely to win a beauty contest anytime soon! Initially, I felt that my efforts to keep up my...

When the Body Says “Really? Now?”

Right now, everything feels hard. I’m dealing with an extremely sore in left foot. As my podiatrist suspects a stress fracture they think. I’m wearing a moon boot on top of an already-existing physical disability where I already use a walking frame. The pain...

Trusting What My Body Already Knows

Some weeks the body really reminds you who’s in charge. A few weeks ago I injured my foot while rowing. The pain was significant enough that it was initially treated as a fracture and I was placed in a moon boot and told to rest. A CT scan later showed there was no...