ILF closure and the levels of care support disabled people with high support needs can expect
This blog by Jenny Morris gives an insight into the limits of council funding for care. It explains why the closure of the Independent Living Fund - a fund many people with severe disabilities use to top up council funding for care - puts the problems of council care funding into sharp focus:
Last year, I wrote about the history of the Independent Living Fund and why we need to defend it.
At that point, the Fund was closed to new applicants. In July last year, the government consulted on closing it entirely and transferring the over 19,000 current ILF grant holders to local authority funding.
In response to that consultation, the Minister for Disabled People announced that “In April 2015 the ILF will close and from that point local authorities in England, in line with their statutory responsibilities, will have sole responsibility for meeting the eligible care and support needs of current ILF users.”
A Judicial Review has been granted of the government’s consultation process and is due to be heard on March 13th. Disabled People Against the Cuts are organising a vigil outside the court in London.
Since it was set up in 1988, the ILF has enabled people with the highest levels of support needs to live in their own homes and to have choice and control over the support they need to go about their daily lives. Some people who receive ILF grants talk about what a difference it makes to their lives here.
The ILF is something of an anomaly in that it is a national system of allocating resources, whereas most other support to disabled people is delivered via local authorities, and this is a reason given by the government for abolishing the Fund. Nonetheless, since 1993 ILF users have had to qualify for a certain amount of support from their local authority before they can access an ILF grant so a more accurate representation is of the ILF as a way of providing a ‘top up’ to local authority resources so that those with the highest support needs can have access to opportunities for an ordinary life.
The overwhelming response to the consultation from disabled people currently receiving ILF funding was summed up by the government:
“ILF users tended to believe that local authority assessments of care needs were excessively budget driven and the ILF applied a more needs based approach. Users said they feared that the local authority may reduce the care package they currently receive or would not fund the type of activities that the ILF does.” In response, the government stated that “All disabled people, including those transferring from the ILF, will continue to be protected by a local authority safety net that guarantees disabled people get the support they need.”
The nightmare facing many people who are currently supported to live in their own homes is that they will, at best, be left with just ‘life and limb’ support (the ‘safety net’ that the government refers to) or, at worst, be forced into residential care.
That this is a realistic fear is evident from the local authority responses to the consultation.
The Association of Directors of Adult Social Services and the Local Government Association were in no doubt that most people would receive less support than they currently get: “As ILF recipients transfer into the LA system in 2015, and are subsequently reviewed against the FACS criteria, the value of the personal budget calculated through the Resource Allocation System (RAS) will generally be at a lower level than the initial ILF/LA budget.”
The government’s own Impact Assessment acknowledged that “some users may not receive the same level of support or be able to use their funding in the same way as they currently do”, while the National Association of Financial Assessment Officers (the people who carry out the means-test to determine whether disabled and older people should be charged for their care) told the government “some councils may determine that residential care would be a less expensive option than a high cost homecare package. “
There is a long history of local authorities operating informal ‘caps’ (linked to the cost of residential care) on how much they will pay to support someone living in their own home. This has primarily affected older people and there are fears that – with ever-tightening budgets – such a practice will also now increasingly be applied to people under the age of 65.
Local authorities are always very careful in the language they use to describe such policies as they would be acting unlawfully if they ‘fettered their discretion’ by applying a blanket limit on the amount of money to be spent on supporting people to live in their own home.
Thus we see the example of Worcestershire County Council consulting on a ‘Maximum Expenditure Policy’ while insisting that this does not mean they will impose a ‘cap’ on expenditure. George Orwell would have loved such an example of ‘doublethink’ (i.e. simultaneously accepting two mutually contradictory beliefs as correct).
The majority of people who receive funding from both the ILF and their local authority receive support costed at over £500 per week. These are people with the highest levels of support needs who, in previous generations, would have been consigned to institutions.
The ILF has been particularly effective at enabling people with ‘complex needs’ (a combination of physical and learning disabilities) to live in the community, supported by their families. Much of recent public debate about social care has been focused on older people but disabled people of working age in fact account for an increasing proportion of the total expenditure on social care.
Although they account for only a third of total service users, “there is evidence that there is a growing number of LAs where ..... expenditure for people aged under 65 is approaching the levels of expenditure for people aged over 65” (1). Currently, social care for disabled people of working age is under-funded and many people do not have their basic needs met.
Local authorities will experience a 28% cut in their overall budgets by 2015. Are we now going to see a reversal of the trend – experienced over the last 50 years – of a move away from institutional care for people with the most significant impairments? If local authorities cannot envisage being able to continue funding the levels of support needed by current recipients of ILF grants, what chance is there for people with high support needs in the future to receive help to enable them to live ‘ordinary’ lives in their communities?
(1) Blackmore, T. 2013. Local Authority Social Care Expenditure: A discussion paper, Disability Cornwall and Isles of Scilly.
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- Posted by: Jenny Morris at 10:22am on 5 March 2013
- Filed under: Disability, Health, Local government, Social care
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