Content by young people with disability. Talking about policy, advocacy and lived experience.
“In my first job, I, unfortunately, experienced a lack of support as a disabled person. I believe that this came from their lack of awareness, not necessarily a place of malice.” Emily Unity reflects on their first experience of employment, what they’ve learned, and what they would do differently now.
Bethany Cody talks about her first job, and the value of diversity in the workplace.
“I couldn’t help but laugh that such a tiny airport was willing to take the time to train their staff in this program, but the big airports couldn’t be bothered.” – Ashleigh Keating writes about her experiences using the Hidden Disabilities Sunflower lanyard in North America.
Xander Wroblewski talks about the need for more balanced media coverage on the NDIS, and aspects of the scheme that can be confronting and stressful.
As a disabled young person, it’s heartbreaking to be bombarded by media that perpetuates ableist attitudes and myths. Especially with the recent federal budget, it’s awful to see headlines that paint people like me as a burden to society or a drain on the economy. I am writing this reflection to disrupt the normalised ableist narrative and bust the media myths that perpetuate it.
I’m still stuck in limbo, waiting to hear whether I’ve been accepted or rejected for the second time. They’ve taken two weeks to acknowledge the receipt of my identity documents, only to say they need more evidence that I do in fact exist and am who I say I am.
I was at school, and there was an expectation that I get on with my studies and put aside any internal struggles related to my disability. So, in a sense, I kind of skipped past the grief stage and was forced to accept it without having time to comprehend what was happening to me.
I got myself surrounded with a network of support. Friends that I could trust, support groups that I could talk to without feeling ashamed. These were the people that motivated me to care for myself and reminded me that I was not alone on this personal journey.
I used to think I hated learning. I remember being confused about why there were always “right” and “wrong” ways to communicate, sit, listen, and learn. However, it turned out that I didn’t hate learning – I hated the way school forced me to learn.
I can not do some typical self-care activities that others who aren’t deafblind might do. I can’t go to the movies and see a film, or watch Netflix while curled up on the couch …
One thing that brings me great joy and allows me to truly switch off, is reading, but the National Disability Insurance Agency (NDIA) are of the belief that funding braille translation of books is not “reasonable” or “necessary”.
Pre-service Teachers are still not required to learn about disability in their four years of study, and if they are taught about disability in education, it is usually only a very small portion of what should actually be taught.
I love self-care. I will gladly indulge in anything that gives me the happy brain stuff (also known as Serotonin and Dopamine), but my enjoyment of reading uninterrupted for days, or cleaning, or rewatching something I’ve seen a million times before isn’t generally perceived as “self-care”, despite its positive impact.
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© Children and Young People With Disability Australia 2023.
