Online Seminar via Zoom
Towards a brighter #socialcarefuture; Care Act rhetoric v reality
Monday 25 January 2021 | 18:00-19:30
A gulf has grown between the rhetoric in the Care Act and people’s lived experience of social care: our panel will address the reasons for this and possible solutions, including reforms to the law, policy and practice of social care.
The Care Act 2014 marked a watershed in the law governing social care, heralding a person-centred future, with care and support focused on generating the conditions for human flourishing and wellbeing. Yet in the intervening years a gulf has grown between the fine rhetoric in the Act and people’s lived experience of social care.
A great deal of this can be put down to the inadequacy of resources available to local government, a consequence of years of under-investment, supercharged by a decade of austerity. Governments for the past quarter century have failed to honour commitments to find a way to sustainably fund social care. The Coronavirus Act 2020 permitted local authorities to enact ‘Care Act easements’, essentially suspending their legal duties under the Act save where these breached the Human Rights Act 1998. While very few did so explicitly, there is much evidence that many who draw on social care to live their lives have found their support disrupted, cut back or suspended.
But money isn’t the only issue. At the heart of the Act lies the principle that individuals should be able to exert choice and control over their lives and hence over where and with who they live, who supports them and how, and over day-to-day life, reflecting the right expressed in Article 19 of the Convention on the Rights of Persons with Disabilities – living independently and being included in the community. While resource-scarcity clearly impinges in the enjoyment of this right, it is also clear that the attitudes and practices of different local authorities play a significant role in determining whether this power-shift happens in practice. For example, during the first lockdown of 2020 some local authorities relaxed rules to enable flexibility in the use of direct payments, while others tightened them.
How might imaginative strategic litigation help close the Care Act rhetoric-reality gap? How can the law be used to secure the rights of individuals whilst also exerting pressure on local and national government to make good the aims of this important piece of legislation? And how might it expose inadequacies in the law that demand further reform?
This seminar will explore these questions with contributions from:
Jamie Burton (chair), Head of Community Care and Health Team, Doughty Street Chambers
Head of Chamber’s Community Care and Health Team, Jamie is a leading authority on health and social care, homelessness, the Care Act 2014 and the rights of disabled people, children and migrants. He is an expert in judicial review and regularly appears in the higher courts, including the Supreme Court.
Julie Stansfield, In Control
Julie is a founder member and chief executive of In Control Partnerships. In Control instigated self-directed support and the personalisation agenda in health and social care policy and practice. This enabled people with disabilities and their families to be more in control of their health and social care provision. Julie has over 30 years’ experience in the health and social care sectors and is rooted in her passion for inclusion and enabling people to have the support they need to lead an ordinary life. She is one of the convenors of #socialcarefuture and one of the founders of the Be Human movement.
Neil Crowther #socialcarefuture
Neil is a co-convener of #socialcarefuture, a movement pursuing a future in which we are all able to live in the place we call home, be with the people and things that we love, doing what matters to us in communities where we all look out for one another. He is also an independent consultant, leading research, policy, strategy & communications work to bring about social change. His primary focus is on the rights of disabled people. He is currently leading research into the impact of the Covid-19 pandemic on disabled people across Europe.
Mitch Woolf, solicitor Scott Moncrieff
Mitchell Woolf specialises in human rights law and, in particular, the rights of the child and people with disabilities. He brings community care and public law challenges against state bodies such as local authorities, health trusts and government departments. He brings challenges on behalf of vulnerable children and adults, including children with disabilities, children in care and in detention and adults with disabilities/learning disabilities. He also challenges breaches of the Human Rights Act.
To register your place, click here.