Dusty Wentworth

  The Public Loves Resilience Because It Costs Them Nothing Resilience is one of those words people like to use about disabled people. They say it with admiration. They say it with warmth. They say it as though it is always a compliment. But I have become wary of the word. Not because resilience is false. Disabled people are often resilient. Chronically ill people are often resilient. People living with pain, trauma, neurological conditions, fatigue, mobility loss, and bodies that no longer obey instruction often have to adapt in ways most people never see. The problem is not resilience itself. The problem is how easily society praises it while refusing to ask why so much of it is necessary in the first place. Resilience is praised most loudly by people who do not have to pay the cost of it. That is the uncomfortable truth. When a disabled person manages to leave the house, people see determination. They do not see the planning behind it. They do not see the medication, the pacing,...

  Why Disability Pride Month Isn't for Me July marks Disability Pride Month. For many disabled people, it is a time to celebrate identity, community and acceptance. I genuinely respect that. Everyone has the right to decide what disability means to them. Personally, however, it is not something I identify with. If I could wake up tomorrow free from Functional Neurological Disorder, Fibromyalgia, PTSD, the lasting effects of a ruptured brain aneurysm, and the limitations that made me a full-time wheelchair user, I would do so without hesitation. I do not feel pride in becoming disabled. I feel pride in adapting to it. There is an important difference. My disability has changed how I live my life, but it has never changed who I am. I am a husband, a father, a writer, a veteran and a friend. I happen to be disabled. It is part of my life, not the definition of my identity. That is why Disability Pride Month has never resonated with me. None of this is a criticism of those who find mea...

There is a quiet, painful irony in modern writing: the very mark of punctuation once used to capture the rhythm of human thought—the em dash—is now often treated as a tell-tale sign of artificial intelligence. It seems strange that a simple line could lead to an accusation of machine writing, yet in our rush for ‘content’, rhythm and expression are now met with suspicion. I remember when writing was taught with care. We learnt about structure, tone and the weight of a pause. Penmanship mattered. Words were crafted with intention, not mass-produced. Those of us who came before Google, before mobile phones and home computers, grew up with typewriters, pens and paper. We thought electric typewriters were cutting-edge. Writing meant thought and effort, not algorithms and templates—a distinction young writers now struggle to grasp. The em dash was once a writer’s most faithful ally. It carried a change of thought, a shift in emotion, a breath between words. It wasn’t decoration;...

Two years ago, my life changed in an instant. I had no idea that one ordinary morning would mark the beginning of a journey that would test every part of who I am. October 23rd, 2023 — a date that changed my life forever. It began like any other day, until suddenly it wasn’t. I collapsed without warning at home. When the ambulance arrived, stroke was ruled out, but that was only the beginning of what would become a long and life-altering journey. Doctors didn’t think I’d survive. Yet somehow, I did. ‎ The Eleven-Month Inpatient Battle What followed were eleven long months as an inpatient — three different hospitals, two stints at a Neurological Rehabilitation Centre, and countless challenges along the way. I was fighting battles not only for my health, but for my identity, my independence, and ultimately, my future. Those months were some of the hardest of my life. Every day brought new challenges: learning to move again, to speak clearly, to remember, to rebuild. The neuro...