Thursday, 31 January 2013
Tuesday, 29 January 2013
Let’s be totally, brutally honest, Governments don’t want to tackle social care.
Let’s be
totally, brutally honest, Governments don’t want to tackle social care.
They may
want to be seen as dealing with social care but the reality is to tackle it
properly will cost money and Ministers would rather spend that money on things
that get them re-elected than on an area which, frankly, does little to ignite
the public imagination.
There are,
of course, many individual MPs who are intensely passionate about social care
as the recent debate on dementia showed, many have personal experiences of
dementia, ageing and social care and they bring at least some balance to the
lack of real debate on tackling largely unanswered questions on the future of
social care.
While
social care may fail to ignite public imagination it does, frequently spark
public indignation. Widely publicised cases of abuse or of people having to
sell homes to pay for social care lead
the social care debate and, while the majority of those who receive social care
services are satisfied with their care, it is the negatives that drive
Government reaction to social care and influence policy making decisions.
This,
unfortunately and detrimentally to social care, means that the reality of today’s
society is ignored completely in favour of short term reaction.
The
reality is people are living longer and because of that there are an increasing
number of people who need or will need social care services as the get older.
Ageing increases to probability of age related conditions in turn increasing
the need for people needing support in their everyday lives. Whilst, rightly,
people are encouraged and supported to remain at home as they age there also
has to be a recognition this will not always be possible nor will it always be
in the best interest of the person. So we also need to recognise and
acknowledge the place of care homes in the social care system.
The
perception of care homes is, perhaps, outdated. The image of a home for retired
genteel folk is outdated and the reality is that those who do go into
residential or nursing care do so at a much later age and those care providers
are having to become increasingly specialised in dealing with age related
conditions, such as dementia, incontinence and osteoporosis. Yet the need for
such specialism, and the cost of it, goes largely unrecognised in Government
policy.
Naturally
not all care providers are perfect and there are certainly those who do not
provide the necessary training in the specialisms required and those whose sole
aim is profitability rather than care provision yet they can only exist in a
culture that doesn’t focus on the reality of social care and policy that fails
to meet this reality.
The ageing
society also provides other challenges to social policy that Governments have
failed to tackle. People with disabilities are also living longer and need services
to meet the challenges of ageing. Many people with learning disabilities are
unknown to social services and support during their life by their parents, but
as they age, and their parents age or pass away, they are increasingly in need
of social care services yet social policy has yet to recognise this demographic
and appropriate services are in woefully short supply.
Not
everyone who needs social care services is over the age of 65 and that needs to
be equally recognised. For these individuals the issue of who pays for social
care is unimportant and many of the health related ideas of integration are
minimal compared with the need for integrated services in housing and
employment.
If society
is to provide the best possible social care to those who need it we need to
recognise the changes to society and the increasing importance of social care
to our society. We need to change how we think about social care and recognise
that ageing comes to all of us and our own future is equally tied into social
care policy as that of those who need social care services now.
Government,
of whatever colour, must lead the change in thinking about social care, it must
raise the debate for all who need social care services, no matter what age and
it must find the money to meet the demands of social care now.
Thursday, 24 January 2013
Front Line Social Care Health & Well-Being
Ergonomics, occupational health, employee well-being.
Probably familiar phrases if you are employed in a large organisation, in fact
those larger organisations will usually have people employed specifically for
occupational health to ensure the well-being of their employees. This is often
supplemented, particularly in public sector organisations, by union
representatives with specific roles in promoting workplace well-being.
Smaller organisations, generally, do not have any of this
and 80% of social care is provided by smaller organisations.
Naturally the principle focus of social care is on those
who use services yet in order to deliver those services we have to rely on
front line workers and, unfortunately, little attention is paid to ensuring
their health and well-being in performing such a vitally important role.
We need a wider focus on those who actually provide care
in order to improve the quality of care as well as the quality of life for the
workers the nation depends on.
For example, much is made of the 15 minute visit rightly
maligned by many as inadequate for those who need care and support services.
Yet how often is the effect it has on care workers? Simply imagine the stress
of having to complete a visit in such a limited time, or, maybe, think about
the pressure of travelling between visits. I am sure everyone has been in a
situation where traffic delays get us frustrated as we try to get to an
appointment, what impact would that frustration have to a person who then has
to rush through a 15 minute visit before heading out onto the road again to get
to the next?
What is the impact on the health and well-being on those
who daily support those who have challenging behaviours? What is the impact on the health and
well-being on those who daily support those at the end of their lives? What is
the impact on the health and well-being of those who daily support those need intense
physical support? And, importantly, how does this affect the quality of care
delivery?
It is not rocket science to know that how we feel, both
physically and mentally, impacts on the way we work, no matter what our job is
yet for front line social care it will also impact on those who receive care
services.
It is not unusual to hear about the work-place stress on
social workers who are becoming increasingly over-loaded in their work. We hear
about it because the majority of social workers work for public sector
organisations where such things are monitored both by the organisation and
unions. What hear little about is the workload and stress of front line care
workers because most are employed by small employers with little union
representation across the sector.
Whenever those who set policy for social care, national
Government or Local Authority, speak there always seems to be an assumption
that social care is a public sector service and that it operates in the same
way as public sector bodies and that those who work in social care are the same
as any other public sector workers. The truth is that the vast majority of
social care workers are employed by small, private sector companies who do not
have the same ability as larger companies to employ people to manage
occupational health.
If we are to ensure the health and well-being of those
who need social care services then we have to also ensure the health and
well-being of those who deliver those care services. To do so we need
Government to recognise that the thousands of small companies that provide care
services need support to be able to do this.
Wednesday, 23 January 2013
Dilnot or Not Dilnot - The think tank question
At the start of the month there was a call from the think
tank, Centre Forum, for Winter Fuel payments to be concentrated on those who
receive pension credits in order to fund the reforms proposed by the Dilnot
Commission, particularly those focused on capping the cost of care for
individuals who have to contribute to their care costs.
This week another think tank, the Centre for Social
Justice, have called for the Dilnot Commission proposals to be ignored stating,
“Whilst the CSJ is not against the Dilnot proposals in principle, it insists
this measure must come further down the Government’s priority list. Any new
funding, says the CSJ, should be targeted at the poorest people in the current
means tested system who have few or no assets. It adds that the Dilnot plans
are the wrong priority at the wrong time.”
Naturally the question many will ask is who is right yet,
perhaps, it would pay to look a little deeper.
Both think tanks describe themselves as independent
organisations. The Centre Forum describes itself as liberal and there can be no
doubt of its Lib Dem leanings, just a quick glimpse at its advisory board will
tell you that. The Centre for Social Justice has a distinctly Conservative
flavour, founded by Iain Duncan Smith and currently chaired by Mark Florman, a
former senior deputy treasurer of the Conservative Party.
Obviously it could be entirely coincidental that the Centre
for Social Justice raise the issue of the Dilnot proposals in the same month as
Centre Forum, in which case we are faced with the equally daunting case of
bewilderingly mixed messages being sent out by organisations with very close
links to senior coalition Ministers.
So is Dilnot the solution for social care or not?
Perhaps surprisingly of the two messages it is the Centre
for Social Justice who stress the current care crisis calling it a broken
system stating “People delivering care services can think of much better ways
to spend the £3.5billion that is about to be invested in the Dilnot proposals.”
The CSJ focus on the elements of the care crisis that will not be settled with
the capping of care cost, such as 15 minute home care visits and “Tackling the
destructive underpayment from Councils to care homes which forces many providers
to cut corners”.
Centre Forum on the other hand focused on paying for the
Dilnot proposals and the particularly controversial idea of withdrawing the
Winter Fuel Allowance as a universal benefit and calling for “ the "appropriate legislative levers" to be inserted into the
draft care and support bill so that the Dilnot Commission's proposals on care
financing can be delivered in full by the end of this parliament.”
Certainly, as I
have argued before, the Dilnot Commission was limited in its scope, focusing
almost entirely on who pays for care and bypassing the crucial question of how
much does quality care actually cost. It also has some short comings in terms
of the reality of imposing a cap (see The
Social Care Capping Debate MUST be Wider) and is unclear on how some of the
proposals will impact on younger adults who need care and support services (Isolated
and Underfunded). Yet it remains an important part of the debate.
The danger is that with two think
tanks with close connections to the coalition partners calling for different
approaches to social care that the debate with Government will become
protracted to the extent we see nothing happening in this Parliament and social
care left in the wilderness for another few years until the next Government
either acts or, as previous Governments have done, prevaricates over social
care to the detriment of the millions who need or provide care services.
Thursday, 17 January 2013
Isolated and Under Funded
How would you feel if you were unable to
wash, dress and feed yourself without support yet that support was denied to
you, you would be outraged, wouldn’t you, and certainly agree there was a
crisis in the care system.
Talk of a crisis in care often evokes imagery
of older people who need care and support as they age, of coping with life as
the rigours of life take their toll on the body and mind. Yet new research,
published today by five major charities, shows the crisis in care is much wider
and that the needs of younger, disabled people are not being met.
The report, ‘The Other Care Crisis’
highlights the fact that nearly 40% of disabled people do not get sufficient
support in their daily lives with such things as washing, dressing and eating.
Also highlighted is the £1.2 million funding gap in social care support for the
disabled under the age of 64 with services being withdrawn because of a lack of
funding and the criteria for being entitled for support becoming ever tighter.
It does not stop there, the report estimates
that more than 100,000 people will be affected by proposed Government reforms.
It is not just about the clinical financial practicalities
of providing care and support, it is about individuals. Being unable to wash
without support is bad enough yet the impact on self-esteem is immeasurable,
ask yourself now, how do you feel when you are dirty? Being unable to feed
yourself without support has much greater impact on health and well-being and
while Ministers talk of ‘prevention’ to reduce hospital admissions etc it
seems, from this report, that the rhetoric remains more important the any real
action.
The most shocking revelation in the report
was nearly half of those who were interviewed in the study said the lack of
support they receive meant they were unable to take part in community life in a
way they wanted to. Once again imagine yourself in that situation, how would it
feel to be socially isolated and unable to take part in the activities you
enjoyed, the opportunities to talk and engage with friends. Picture the impact
such social isolation would have on your mental well-being and the general
frustration with life that would start to eat away at you.
In fact just over half of those interviewed
for the report stated they felt anxious, isolated or experienced declining
mental health as a result of services being cut.
It is time Government, and the wider
discourse of social care, changed. When there is talk of integrated services it
often basically means integration between health and social care yet the needs
of younger disabled peoples goes far beyond that. There needs to be integration
with housing services, integration with employment services and integration
with benefit services. The debate on social care must encompass all those who need help and support, including those
under the age of 64.
There are many great schemes that have been
developed over recent years, such as direct payments, but these depend on
individuals actually meeting eligibility criteria and as this becomes tighter
less and less people will actually be entitled (although Governments will claim
success as the percentages will be higher because less people are entitled!).
Today’s report has to be commended for
highlighting the care crisis does not just apply to older people nor does its
solution solely rest on whether or not property needs to be sold to pay for
care. For those under the age of 64 who have life-long conditions the current
system is failing many of them.
Yes we live in austere times and economic
sacrifices have to be made but that does not mean we should penalise those in
society who need societies support to live their lives in a way most of us take
for granted.
The
report “The Other Care Crisis” has been produced by Scope, Mencap, National Autistic
Society, Sense & Leonard Cheshire Disability and is available at
Monday, 14 January 2013
Let's Not Forget Physical Decline
There is some fantastic work and developments focusing on
the needs of those who suffer with Dementia. We have had the ‘Christmas to Remember
Campaign’, the Department of Health announcing £22 million being made available
for dementia research projects and the work of the Dementia Challengers has
been outstanding in raising the awareness of the disease which impacts on the
lives of millions.
Yet while dementia is the most prevalent of the age
related conditions that could impact on the life of an older person there is,
perhaps, a danger that the discourse of elderly care becomes one where adult
social care for the over 65’s is solely equated to dementia . Whereas there are
many other age-related conditions which are debilitating for individuals and
which also need to be fully addressed.
Parkinson’s disease affects around 127,000 people, the
majority of whom are over the age of 65. It is a disease which leads to
physical, rather than cognitive, decline as the disease progresses but can also
include other problems such as depression, pain and constipation. As the
physical deterioration progresses it becomes harder and harder for the
individual to make the tasks of daily living and increases the need for help
and support.
Naturally it does not take a huge leap in imagination to
think about how you would feel if your body no longer functioned properly, yet
you retained you cognitive awareness, imagine the frustration and potential effect
on your mental health. Being unable to undertake the simplest daily tasks
without help can be frustrating, I know, from personal experience how
embarrassed my Nan feels when she cannot even make a cup of tea for guests when
they call.
Other physical deterioration may also affect an
individual. Sight, in particular, is subject to deterioration through many
different conditions such as macular degeneration, glaucoma and cataracts. As
people lose their sight they may need social care support to help them in their
everyday lives to make adjustments in how the undertake daily tasks and to
reduce the risks of physical injury.
Sight, obviously, is not the only physical deterioration
that can come with age and we need to ensure that anyone who needs physical
help receives the support they need.
Naturally all of these physical conditions can also
affect those who have dementia. There is always a danger that those who provide
care and support only see the dementia rather than the range of issues
affecting an individual. It is easy to focus on the one condition of cognitive
decline yet ignore the other issues that a person needs to be supported with.
Yet we also need to ensure that those who do not have
dementia but have other age related conditions of physical decline also receive
the correct level of support. Physical decline can lead to other issues, such
as being prone to falls, which then further impact on a person’s life.
Social care services must focus on all needs and it is
important to ensure that alongside the excellent initiatives for dementia
people with other conditions and diseases are recognised and supported.
Wednesday, 9 January 2013
Social Care: A Simple Philosophy
Social care exists because people need care
and support in their everyday lives. The type of care and support may vary,
those with learning disabilities will have differing needs from those with
physical disabilities and older peoples care and support will vary depending on
the age related conditions affecting them but the bottom line is social care is
about supporting those individuals who need some form of help in their everyday
lives.
Policy, bureaucracy, regulations etc. have no
real meaning in social care unless the directly benefit those individuals who
need care services.
So a simple philosophy should begin with a
simple question, “how is what I am doing benefitting those I am providing care
and support for?”
This simple question can be applied at all
levels of social care provision.
At the front line of social care the question
is more simplistic and, perhaps, applied more easily. So, for example, maintaining effective
infection control routines benefits the individual from reduced risk of infection
or supporting an individual to attend community events benefits their social
well-being. There are, of course, examples of where the question is not
applied. I am sure we have all heard of tales were care staff take those they
are supporting out to places that are of more interest to the staff than the
people they are supporting and, at the extreme end of the scale, the behaviours
of staff at Winterbourne View were abhorrent and bear no reality to providing
care.
Yet at the point of care delivery the
philosophy has to be “how is what I am doing benefitting those I am providing
care and support for?” the question should also be the basis of care
inspections by the Care Quality Commission, or other inspectorates. Not every
care provider works in the same way and they should be able to show that their
care and support works in a way that benefits those they are delivering a
service too.
As we move up through the levels things
become a little more complex but the same simple question should apply. The Care
Quality Commission should base their work on the same principle. How does their
inspection system benefit the individuals who receive care services. After all social
care inspectors exist only because social care exists and social care is about
those individuals.
At local authority level there is a multitude
of bureaucratic levels but each must apply the question to their work. The most
obvious level of local authority work is done by social workers and social work
assistants (or whatever the preferred term is in a particular authority!).
Social workers/assistants have direct contact with social care users but they
are subject to systems and procedure and it is those that need to be looked to
see if they are designed to benefit those who need care services or if they are
designed to benefit the local authority. There is a need for a certain amount
of red tape, reporting and recording are essential but each part of that red
tape needs to be challenged to find out who it benefits and whether or not it
enhances the life of the individual who needs support.
The back office functions, commissioner’s,
funding panels, payments etc. must all exist only to improve the lives of those
who need care services and their functions must be a benefit to the rather than
the local authority itself. Elected councillors should learn to challenge the
social care departments and asking how working practices, policies, procedures
etc. actually benefit those who need care services.
Even at the highest level of Westminster
ministers and civil servants who deal with social care should ask themselves
how their work benefits the needs of social care users. As with local
authorities the multiple levels of bureaucracy must have the question in mind
as they prepare policies and reports, in the edicts they send out to local
authorities.
Naturally there are many thousands of people
and organisations involved in social care but each should ask themselves how
what they do benefits the lives of the individuals who need care services and
apply this question to every aspect of their work. How does this process benefit, how does this
terminology benefit, how does this job role benefit etc.
People do, unfortunately, often justify
themselves in ways that satisfies their own actions therefore it is important
that, at all levels of social care that we challenge people by asking “how is
what you are doing benefitting those who need social care service.” David
Cameron should be asking Jeremy Hunt who should be challenging the Permanent
Secretary right the way through the Department of Health. The Department of
Health should be challenging local authorities and national social care
organisations who receive Government funding. It should a question that
commissioners ask providers, and vice versa, it should be a standard question
in every supervision of a person employed, in whatever capacity, in social
care. It is a question that should be asked in every meeting and every time
procedures are reviewed. It is a question that should be at the heart of everything
to do with social care.
Social care does not exist to create jobs,
those jobs exist because people need care and support. Social care does not
exist to satisfy bureaucracy those systems are in place because people need
care and support. Social care exists because people need care and support in
their everyday lives and everything we do must be centred around those people.
Ask yourself now – “how is what I am doing
benefitting those I am providing care and support for?”
Monday, 7 January 2013
The Social Care Capping Debate MUST be Wider
Whilst the social care debate on funding has once again
been raised by Paul Burstow and Centre Forum, calling for the implementation of
the Dilnot proposals with funding from means tested winter fuel allowances the
fact remains that this is only one side of the debate and, arguably,
unanswerable without tackling how much social care actually costs and who is
eligible for funded social care.
One issue largely glossed over is who will be eligible
for social care services and state funding under any new scheme.
Over the last few years those entitled to funded support
have been needing to meet ever tightening criteria meaning many thousands have
not been entitled to support even when they have high (but not critical) needs.
This naturally has led to a fall in the numbers of older people receiving supported
care services and increased the numbers either paying for themselves or relying
on family and friends for support in everyday life.
The debate on the Dilnot proposals must include the level of need at which people are entitled to
state support. For those not quite meeting the criteria but with little other
option may well still need to sell their homes in order to pay for necessary care
services and it is essential that this element of the proposals is equally
publicised before many thousands are led into a false sense of security
believing that their care needs will be met by the state after the cap.
Local Authorities have, over recent years, continued the
practice of increasing fees to providers at less than the rate of inflation and
over the last two years many have given no increases at all. The shortfall is
often made up by care service providers by charging top up payments which
individuals pay themselves or by the level of fees they charge private paying
users.
While the Dilnot proposals state that no one should pay
more than £50000 for their care costs it does not mention the level of fees in
the equation. So once an individual has
reached that cap will the Government/Local Authorities pay the higher rate
normally charged by providers or will they only pay the reduced fee associated
with the current system.
Additionally Dilnot proposed a rise in the means testing
threshold to £100,000 if introduced this will immediately move many of those
who currently pay private fees to being on local authority fees, dramatically
reducing the income of care service providers
If there is a dramatically big drop in what providers are
receiving then how will care providers survive with radically reduced income
and what impact will that have on the quality of care services.
Of course that debate is somewhat mitigated by the fact
that the Dilnot proposed cap only applies
to care services not to accommodation or food. On this issue the
recommendation is that individuals be charged between £7000 & £10000 a year
to cover such costs.
The debate needs to be wider than the proposed cap and
include exactly who will be eligible, how the cap will impact on the quality of
care provision and the impact it will have on the lives of those not eligible for state funded care
services.
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