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The disability royal commission heard horrific stories of harm – now we must move towards repair

The Royal Commission into Violence, Abuse, Neglect and Exploitation of People with Disability has shared its final report. In this , we unpack what the commission’s 222 recommendations could mean for a more inclusive Australia.

Authors


  • Jack Francis Kelly

    Honorary Research Fellow, School of the Built Environment, University of Technology Sydney


  • Linda Steele

    Associate Professor, Faculty of Law, University of Technology Sydney


  • Phillippa Carnemolla

    Associate Professor, School of the Built Environment, University of Technology Sydney

The final report of the follows from the disability community. It gave voice to people with disability to tell their stories of violence, so policymakers and broader community would listen and take action. Segregation emerged as a key driver of violence.

The makes 222 recommendations to improve laws, policies and practices for a more just and inclusive society. They include a new disability rights act, including access to remedies when people experience human rights breaches.

The final report recommends disability service providers offer redress to people with disability who experience harm while receiving their services. This could include “apologies, compensation, reimbursement of fees, credits for services and other practical remedies or supports”.

However, there are no recommendations that governments should also offer apologies or redress. In addition, a call for governments and disability services to look back and repair the harm caused by century-long policies of segregation and institutionalisation is missing from the final report.

What do ‘institutionalisation’ and ‘segregation’ mean?

Institutionalisation involves grouping people with disability together – such as in residential, educational or work settings – and segregating them (keeping them separate) from people without disability.

All people with disability have the to live independently in the community regardless of how high their support needs are. This means providing access to services and support so people with disability can exercise choice and control over their lives and make all decisions concerning their lives.

In 20th century Australia, people with disability were institutionalised in many large residential settings. They were to

  • physical and sexual violence
  • medical neglect
  • use of (such as sedation, locking people in a room or restraining them in a bed or chair)
  • sterilisation (such as women having their tubes tied)
  • and unpaid work.

Eventually, Australian government policies prompted the gradual closure of many large residential settings.

Shutting down institutions has not put an end to injustices. Follow-up processes have not been established to of people who lived there.

This institutional history intersects with Australia’s violence towards and with (discriminatory “planned breeding”).

People with disability remain traumatised by their experiences, yet governments and charities have not been called to account.

Problems today

Today, many people – especially those with intellectual disability – live in where segregation, social isolation, violence and lack of choice in their daily lives are .

Harms such as , restrictive practices and below-minimum wages continue.

The disability royal commission heard how replicate the harm of large residential settings, with failing to prevent violence and avoiding accountability.

People with disability have called for an end to in housing and other aspects of their lives.

Recognising wrongs

are actions to recognise and respond to systemic wrongs. They might involve compensation, restitution (such as returning money or property) or rehabilitation (health or legal services). Reparations can seek satisfaction (with apologies and memorials) and guarantees something won’t happen again via law reform or human rights education.

In Australia, we’ve seen and apologies for .

We have also seen and an for members of the Stolen Generations.

People with disability are entitled to reparations as a , including for .

There are overseas examples of reparations for people with disability, including , , and .

What do people with disability want?

Co-author Jack Kelly describes the ongoing effects of institutionalisation:

People with disability were not seen as part of local communities when they lived in institutions. This has to change and still takes time. I think it is really important that we address the history of what has been going on and say; ‘Sorry that we didn’t look after your loved ones’ and ‘Sorry we didn’t value you as a person’. It is time to work with people with disability towards a national apology from the government.

Jack’s statement with broader calls by the disability community for reparations.

In 2021, the Council for Intellectual Disability demanded withdrawal of an of Peat Island (the site of a disability institution for 99 years) and for memorialisation and truth-telling.

There have been recent calls for in the mental health system and reparations for .

Our research explored what people with intellectual disability want the public to know about large residential settings.

We people with intellectual disability support the wider community learning more of what was experienced in these places. Sharing this history is an important step towards repairing past wrongs, ending institutionalisation, segregation and exclusion, and realising equality and inclusion.

A way forward

People with disability, those with intellectual disability, must lead reparation design and development.

The disability royal commission has highlighted systemic violence, abuse, neglect and exploitation in today’s Australia. These criminal practices reinforce a century-long history of injustice from institutionalisation.

Now is the time to act to ensure this does not continue. Reparations are one way to do this.

The Conversation

Jack Kelly has contributed to projects that have been funded by the ³Ô¹ÏÍøÕ¾ Disability Insurance Agency (NDIA).

Linda Steele has received funding from Women with Disabilities Australia, Council for Intellectual Disability, Dementia Australia Research Foundation, Australian Association of Gerontology, and Royal Commission into Violence, Abuse, Neglect and Exploitation. She is on the board of management of Intellectual Disability Rights Service.

Phillippa Carnemolla has received funding for previous projects from the ³Ô¹ÏÍøÕ¾ Disability Insurance Agency, ³Ô¹ÏÍøÕ¾ Disability Services and The Achieve Foundation. She is a Director for the Centre for Universal Design Australia.

/Courtesy of The Conversation. View in full .