Blog - People with Disability Australia

[IMAGE Lisa Zammit and Gavin Moore in the 3CR radio studio.]

The Stolen Generation and the Disability Royal Commission

3CR’s Gavin Moore interviews Lisa Zammit, CEO of Connecting Home, about disability services for the stolen generation, and recommendations she would like to see from the Disability Royal Commission.

[IMAGE Photograph of Hannah Diviney, a smiling, young white woman with dark hair, wearing a red floral top. The handlebars of her wheelchair are visible behind her shoulders.]

They’re denying us a basic human right, and that will never be okay

I eventually won the fight to get the provisions I needed, but the road was convoluted and demeaning, writes Hannah Diviney.

[IMAGE Photograph of Issy Hay, a smiling young, white person with a purple fringe, leaf earrings, a nose ring and a plaid blazer.]

Accessible education should be the norm, not the alternative

I don’t think I will ever be able to describe what it meant to me, the first time a teacher asked “What can I do to make this easier for you, to support you?” That should be the norm, writes Issy Hay.

[IMAGE of the interior of a school classrooms with desks and chairs]

Adventures of the boy who was told he’d never speak

For year 7, I started at a little school in the NSW outback with an enrolment of 150 students from K-12. At first, there were no problems, then things started to go wrong, writes William McIntosh.

[IMAGE several open bottles of medication sit next to a Sunday to Saturday pill box]

Bad medication

A bad experience with medication can leave lasting trauma and close us off to truly helpful and positive use later, writes Ashley Waite.

[IMAGE a hospital corridor with a bed and hospital personnel at the very end of the corridor]

Visits to the hospital

As an autistic, mentally ill, transgender person with disability, Pippin Latham shares some experiences receiving medical care in hospital.

[IMAGE of Heidi Evereett wearing a red pullover. Photo by Therese Quinlan]

I used to know and love, my mind

Musician and writer, Heidi Everett, shares her experiences of psychotropic medications and hospital admission.

[IMAGE a tall black man wears a mask on the left handside of the photo. A woman wearing a mask is out of focus on the right hand side of the frame.]

Supporting our support workers

Interacting with people when a person has COVID-19 may become unavoidable if there’s no alternative arrangements. For many people with disability, isolation is not an option, writes Claudia Forsberg.

[IMAGE a dark brown mat with yellow letters spell out Welcome]

Welcome to my world

There is an aversion of gaze, amongst even the most socially aware able-bodied journalists, concerning the discrimination people with disability live with every day writes Kate Hood.

When the government asked people to wear masks

As a proud member of the deaf community, Charbel Zada shares his frustration with some government policies that negatively impact people with disability.

Category: Blog (page 7)

Categories

The Stolen Generation and the Disability Royal Commission

They’re denying us a basic human right, and that will never be okay

Accessible education should be the norm, not the alternative

Adventures of the boy who was told he’d never speak

Bad medication

Visits to the hospital

I used to know and love, my mind

Supporting our support workers

Welcome to my world

When the government asked people to wear masks