
Debility
Debility describes the condition of being rendered functionally diminished—not solely by illness or impairment, but by social, political, and institutional forces that withhold care, recognition, or access. Unlike disability, which can carry identity, rights, and collective belonging, debility often operates in silence: a slow erosion of capacity caused by austerity, punishment, burnout, exclusion, or trauma. This tag brings together writing on how schools, systems, and policies produce debility in both children and caregivers—through neglect, disbelief, denial of support, or forced containment. It offers a lens for understanding not only who is marked as impaired, but who is made unwell by institutional design.
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When pain gets too close: Affective economies and the emotional cost of advocacy
I have always been someone who made people uneasy unless I carefully managed my presence—someone whose attention lands too directly, whose knowing shows too quickly, whose intensity disrupts the emotional choreography expected of mothers who ask nicely, grieve quietly, and remain grateful for whatever scraps of support are handed down. I carry detail and radiate…
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Non-coercive, trauma-informed alternatives to PBS/ABA in BC schools
Positive Behaviour Support (PBS) and Applied Behaviour Analysis (ABA) are behaviourist approaches widely used in schools to manage student behaviour. However, a growing chorus of neurodivergent advocates, educators, and researchers highlight that these methods often prioritise compliance and “normalising” behaviour over student well-being rcpsych.ac.uk. By focusing on making neurodivergent children appear neurotypical (meeting neuronormative standards), traditional PBS/ABA can…
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Debility is not a diagnosis: What Jasbir Puar helps us see about invisible harm in BC schools
There is a category of harm that most institutions do not name, do not track, and do not treat—because doing so would require them to admit that they caused it. This kind of harm accumulates in the body slowly, like sediment, until what once looked like coping becomes collapse. It is the product of chronic…
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Debility versus disability: what the system cannot acknowledge
My son Robin took to bed two weeks before March break. He had been soldiering on through the aftermath of a school transfer the district assured us would help him, though his body told me otherwise from the first day he arrived. I’ve seen that kind of shutdown before—at camp, at birthday parties, in classrooms…
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There’s no such thing as unexpected behaviour
This piece was hard to write. It holds my grief. It documents not only what happened to my child, but how systems made it worse by pretending to be surprised. I share it because too many families are made to carry this alone. Every time I see the phrase unexpected behaviour in a school document, a safety…
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The cost of masking: What we lose when children perform wellness
This evening, I walked my son down the street toward the place where his father was waiting to pick him up. It was an ordinary hand-off on an ordinary day, except I carried that soft, watchful question I always carry now, held quietly in my chest until the timing feels right. I asked if he…






