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.
Late last week, the Federal Government announced a new growth target for the NDIS of 8 per cent per year by 2026. This is significantly lower than previous projections.
With the dramatic rise in rents and basic costs of living, Children and Young People with Disability Australia (CYDA) supports recommendations in the Interim Economic Inclusion Advisory Committee Report to Government to raise JobSeeker and Rent Assistance payments as a matter of urgency.
Minister for Social Services, Amanda Rishworth MP, has announced an increase in funding for 17 Disability Representative Organisations – including Children and Young People with Disability Australia (CYDA).
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.
Diagnoses of invisible disabilities (for example, MS, ADHD, arthritis, brain injuries, diabetes, learning disabilities, chronic pain and fatigue etc.) are undeniably tricky to navigate, and can be especially difficult for parents with young children with little to no experience of the disability sector
