It’s coming up to Cerebral Palsy Awareness week in Australia.
Time to grab a brief media opportunity to educate people about what CP is and means to people who have it.
Most families of kids with CP look to government and privately funded CP organisations to spearhead public education campaigns.
We want these organisations to publicly reflect what we spend a big chunk of our lives fighting for. Which is for the world to treat our kids as kids, not a medical diagnosis or disability … not different from every other kid.
So how can a positive education campaign end up reducing people with CP to a diagnosis?
With one lazy headline:
Yep, diagnosis first, person last. What happened to people-first language? Like “Champions with CP”?
For a clear explanation of the power of language to value or devalue people, check out Kathy Snow’s words of wisdom.
Words count. Information is power. How can we families convince the world to accept – let alone welcome – diversity, when our kids and friends with CP are presented not as people but as a medical diagnosis?
This is not about political correctness. This is about inclusion, treating everyone with respect. As people first, not just diagnoses.
There were only good intentions behind this CP awareness campaign about an interesting bunch of talented, determined people. So how could a CP service provider and educator get this crucial first impression so wrong?
Sorry TSCNSW. We want to educate the world, not reinforce stereotypes. Please lead by example.