Photo: Drs Larry Arnold, Damian Milton and Catriona Stewart
The National Autistic Taskforce
We work with autistic people, families and service providers, campaigning to give autistic adults a stronger voice in the decisions and directions of their lives – especially those with highest support needs and, often, least autonomy. We draw on deep knowledge of rights and obligations currently enshrined in Law but rarely respected in practice.”
As an autistic academic and father to an autistic son, the recommendations that come from such reports and how they are interpreted and acted upon are of great personal importance. The report highlights many of the issues faced by autistic people and their families, and offers some wise areas for investment, including in research. My involvement in the project was as part of the Autistic Advisory Panel. Through this opportunity, I and others could show through our passion and expertise, our worth to such projects. At the launch of the report, both Dinah Murray and I were fondly referred to as ‘productive irritants’. It was this recognition that our critique was always with good intentions, that enabled us to input into the report in the way we did, and I feel that the report benefitted greatly from it.
In the history of autism theory, policy and practice we are at an important crossroads. Whilst there have been improvements in general public awareness, in some areas of educational support, in autistic people supporting each other through community efforts, and so on, we also have the legacy of abuse scandals, preventable deaths, and mother blaming, for example that highlighted by the ‘Justice for LB’ campaign. There are many gaps in knowledge and service provision that adequately meets the needs of autistic people and their families. In many cases this can lead to horrendous consequences.
Earlier this year I wrote a blog piece for the project website where I suggested that:
Such work needs to have an impact on policy and practice however, in order to see real social and cultural change, and where instead of working against a person’s ‘autism’, practitioners can work with autistic people and their families with mutual respect.
It is for this reason, I am very proud to announce the launch of the National Autistic Taskforce (NAT), of which I will be taking up the role of Project Leader. The primary focus of the Taskforce will be to help empower autistic adults, including those with less autonomy and higher support needs, to have a stronger voice in the decisions and direction of their own lives. Unlike many other groups working in the autism and learning disability fields, the National Autistic Taskforce will be led by autistic people, and the group has been given complete freedom by the Shirley Foundation to set the direction and approach of their work.
Based on the principles of co-creation through a community of practice, the National Autistic Taskforce (NAT) will contain a series of working groups, each chaired by an autistic person and involving both autistic and non-autistic members and contributors. Each will be established to consider key topics, including care standards, family involvement, effective diagnosis and post-diagnostic support, psychiatry and research. The group is particularly interested in finding ways to help empower autistic people to exercise autonomy in the decisions taken about their lives. They will explore the protocols around how ‘choices’ are currently made, and work with autistic people, families and service providers to boost and call for more independent advocacy, for example through peer support.
Backing up this approach, we will look to set up a new, accessible website – AutNav – for autistic people and people with learning disabilities. It will provide information and links to a range of topics, including organisations working with autistic people, consultants and trainers as well as news, resources and advice on understanding the law.
The National Autistic Taskforce is a vital opportunity for the autistic community and its allies to work together to turn the core principles of the National Autism Project into reality. Namely: personalised actions, choice and control, addressing inequalities, and a life-long perspective. I would therefore like to thank in particular Dame Steve Shirley for her continuing support and for making this project possible. For too long autistic people have not had a strong enough voice in the decisions which directly affect their lives, this needs to change. From the outset we will be looking to make this project sustainable, and to that end I hope all of you here will lend your support to this new endeavour.
Dr Damian Milton