“Cancer will be sorry it ever met me”
“I was shocked mostly because this was so out of the blue. I had no…
In the early 80s, in a mainstream school, my younger brother was often in time-out spaces as early as kindergarten.
Throughout his childhood he was labelled as a problem child. Often excluded socially and wanting so desperately to belong, he gravitated towards the wrong crowd. It wasn’t until after he left school, and after brushes with the law, that he was assessed as having a borderline intellectual disability and mental health issues.
My brother is so very important to me and has shaped my life. He speaks my language of fairness. He is the reason I know what inequality, unfairness and exclusion looks like. If not for him I wouldn’t of chosen my job at Disability ACT, my uni degree or my friends or come to know the community, academic, government and business leaders who are as passionate as I am about creating a more inclusive community. He is my drive. My purpose in life that is bigger than me.
I have thought long and hard about the systemic reasons that contribute to my brother’s experience of life, poverty and how this interacts with disability. His disabilities affects how he weighs up risk, how he judges people’s character – often seeing the dangling carrot and not the costs or consequences that sit behind. He is often ripped off by others.
I now understand my brother’s life in the context of the bigger picture. The research shows that people with intellectual disability and mental health issues are over-represented in the criminal justice system and are at relatively higher risk of homelessness. The unemployment rate for people with intellectual disability or psychological disability (regardless of severity) is high in comparison with other disability groups.
To create more inclusive future communities for our kids, we need to look in our own backyards, our homes, our workplaces, services and schools for practices, interactions and spaces that might be contributing to the bigger picture of exclusion and subsequent negative life outcomes.
This involves asking ourselves uncomfortable questions about how we might have personally contributed to exclusion of others as adults, or when we were kids through our words or actions. I often ask myself how did my early teasing of my brother affect him for the rest of his life. Asking this question requires moral courage as our protective ego and external reward and punishment systems are good at blocking uncomfortable thoughts and it is easy to give up looking for solutions because the questions are too hard.
We need to find better practices, interactions and spaces so that kids with disability are not seen by their peers as the ‘others’. Being perceived as an other is fertile ground for bullying, reactions to bullying and facing the consequences (like major disruption to learning, conflict at home), negative feedback circles about your potential and low expectations that can negatively impacts the rest of life. The international research shows a strong link between parents and educators about expectations and academic achievement, for both kids with and without disability.
As a parent who cares deeply about the kind of community my daughter will grow up in and contribute to, here are my suggestions on practical things that parents can do to help all kids thrive and reach their full potential.
I strongly believe if we can see people, including ourselves, beyond our limitations we will live a truly rich and diverse life. Our differences unite us.
Some Great Talks on Disability
Disability, Resilience and Achieving the Supposedly Impossible: Jeanette Purkis at TEDxCanberra
Creating a meaningful life for Jackson: Sally Richards at TEDxCanberra
Stella Young : I’m not your inspiration, thank you very much
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