DPAC UNIVERSAL CREDIT CAMPAIGN
www.dpac.uk.net
Linda Burnip
01926 842253
0771 492 7533
linda_burnip@yahoo.co.uk
Debbie Jolly
01572 820546
079461 40765
mail@dpac.uk.net
Universal Credit: What it means
The coalition government and New Labour before them agreed
that a reform to the current benefits system was long overdue. In November 2010
the Coalition published a white paper on Universal Credit. It is claimed to be
the biggest overhaul of the benefits system since the 1940s when what was known
as the welfare state began.
The Government White Paper, ‘Universal Credit: welfare that
works’ was published on 11 November 2010 laying out the first steps of the
overhaul of the welfare process. The Welfare reform Bill through which this
will be introduced was forcibly passed through the Commons and Lords earlier
this year by the Coalition government.
This paper deals with Universal Credit. It examines what it
means, what it may mean for disabled people and what the key changes will be.
What is Universal Credit?
The coalition notes that there are over 30 different social
payments or benefit systems in place. They think this is confusing and too
complex for people to understand. They believe that by combining social
payments/benefits into one universal payment things will be easier and better
for people. Universal credit is intended to be a new benefit which will
replace:
Child tax credit
Housing benefit
Income related
employment and support allowance
Income based
jobseekers allowance
Income support
Social fund budgeting
loans
Working tax credit
Universal credit is a proposed system that will see many
social payments or benefits merged into one single payment. The coalition
claims that nobody will be worse off under this system. However, the rhetoric
of a fairer system is coached in terms of welfare dependency which suggests
that this strategy main aim is to reduce welfare spending.
The white paper
begins by saying:
The Government is committed to reforming the welfare system
to make it fairer, more affordable and to tackle poverty and welfare
dependency, whilst continuing to support the most vulnerable in society
The scheme is estimated to cost 2 million to set up. First
steps towards the coalition’s vision included strategies introduced in the
budget and spending review of 2010. These included:
capping household benefit payments so that families do not
receive more in welfare than median after-tax earnings for working households;
withdrawing Child Benefit from families with a higher rate
taxpayer;
measures to control the cost of Tax Credits, Housing Benefit
and Council Tax Benefit; and
time-limiting contributory Employment and Support Allowance
for those in the Work Related Activity Group.
The capping of housing benefit payments is likely to hit
disabled people particularly hard at a time of rent increases in social housing
and the private rented sector.
Whilst withdrawing child benefit from families with a higher
rate tax payer may suggest making things fairer, it actually undermines the
principle of universality in built into child benefit to ensure that it was not
means tested but a benefit to aid mothers bringing up children. The removal of
higher rate tax payers is in effect removing that safeguard and the first step
towards to means testing.
Employment and Support Allowance (ESA) replaces incapacity
benefit for all disabled people from 2014. Those in the work related activity
group are deemed to be ‘fit for work’ and will have their benefit limited to 12
months retrospectively from the date of the comprehensive spending review or
the award if the award was made after the 20 October 2010. There are other
categories of the Employment and Support Allowance such as the support group,
these will be unaffected by the time –limits. Those in the work related group
will be expected to sign up for job seekers allowance a lower amount compared
to ESA.
At the time of the
White paper Universal credit did not include:
Bereavement benefits
Contributory jobseeker’s allowance
Contributory employment and support allowance
Disability living allowance
Child benefit
Industrial injuries disablement benefit
Maternity allowance
Statutory maternity pay
Statutory sick pay
Pension credit
However, since this time clear proposals to abolish
Disability Living Allowance (DLA) and replace it with Personal Independence
Payment (PIP) have been put forward with the reasoning that 20% needs to be cut
from the case loads of DLA.
The paper says universal credit ‘will consist of a basic
personal amount’ with additional amounts for ‘disability, caring
responsibilities, housing costs, and children’.
When will Universal credit begin?
The white paper stated that universal credit would be rolled
out in October 2013. Pilots are due to begin in May 2013.
Claiming and
accessibility
Claims are set to be made online and on the basis of
households, rather than individuals
Claims will be made on the basis of households rather than
individuals and both members of a couple will be required to claim Universal
Credit. Claims for Universal Credit will normally be made through the internet
and we expect that most subsequent contact between recipients and the delivery
agency will also be conducted online. People will be able to obtain all
elements of Universal Credit through a single application, ending the excessive
form filling of the current system, reducing scope for error and reducing
administration costs p.25
Two issues arise for disabled people; the first is that
claims made on behalf of a household will exacerbate some disabled peoples’
feelings of dependence as opposed to independence and independent living. The
second is that access to computers and to the internet is known to be lower for
disabled people and those with lower incomes. Although the paper mentions ‘
These changes will enable the targeting of resources to support vulnerable
people with additional needs’ (p.25) which we assume is disabled people, no
further method of the method or how this will be achieved is given.
Payment Periods
The paper states that the coalition is considering both
payment and assessments on a monthly basis. This would seem to suggest that
entitlement will need to be re-registered and hence re- assessed on a monthly
basis.
Critiques of
universal credit
The coalition claim that nobody will be worse off under the
new universal credit, however current proposed changes suggest that this may
not be the case for disabled people or others on low incomes. Universal credit
appears to be focused on getting people into work and away from benefits. It is
laudable that the coalition accept that some people may be worse off in work
than on benefits and are attempting to adjust the discrepancy.
At the same time as assessment s for ESA have come under
constant and increasing criticism for being unfair[i] it is unlikely that
disabled people declared as ‘fit for work’ under the Work Capability Assessment
will benefit from this change. The WCA shows that ‘target driven’ simplified
tests do not work. It is likely to be the same with one single benefit system
–how will this be able to address the complexities of different impairments,
multiple impairments, and the multitude of disabling barriers that disabled people
face?
Sanctions
In addition, the universal credit and welfare reform will
bring in ‘a commitment’ for those who fail to ‘apply themselves’ to proper work
seeking activities to tougher sanctions. Once again this will not address the
complexity of employment related barriers that disabled people face, even if
they really are ‘fit for work’.
Page 21 of the white
paper states:
We will require every Income Support, Jobseeker’s Allowance
and Employment and Support Allowance recipient to have a claimant commitment.
The commitment will set out our general expectations of recipients, and the
requirements placed upon them; it will also be clear about the consequences for
the recipient of failing to meet these agreed standards. This will be carried
forward into Universal Credit.
DPAC say that Disabled People and Disabled Children should
not be penalised in this way when £25 billion in unclaimed taxes remains
uncollected, bankers continue to receive massive bonuses, and MPs spend £40,000
for trees in Portcullis House plus thousands more for their personal expenses.
Summary of key points
of the bill:
The introduction of a Universal Credit to replace existing
means-tested benefits and tax credits for people of working age from 2013.
The introduction of Personal Independence Payments to
replace Disability Living Allowance with a stated aim of reducing the number of
claimants by 20% and replacing the current 3 bands of the care component with
only 2. Half a million disabled people will lose their entitlement to DLA which
in many cases is what allows them to work.
At the moment anyone getting the mobility component of DLA
before the age of 65 continues to receive it once they reach 65 but with PIP
proposals they will not be able to continue to claim PIP once they reach 65 and
there is no mobility component of Attendance Allowance.
Limiting of contribution based Employment and Support
Allowance payments to 12 months for those in the Work Related Activity Group.
This is what people think they are paying National Insurance contributions to
be entitled to if they need it. 100,000
people will lose out at the beginning of April 2013 and another 100,000 will
lose out the following April after 12 months on the benefit.
Removal of ESA entitlement from young disabled people under
25 years of age. Non-disabled young adults are treated as such from the age of
18 yet you will no longer be treated as an individual adult if you are
disabled. At the same time Income Support is being abolished as well so it
remains unclear what if any money younger disabled people will be entitled to.
Caps on the total amount of benefit any claimant can get,
for both housing needs and living expenses. The suggested total amount is £350
for a single person and £500 per week regardless of family size, or costs of
housing. This will particularly affect those living in areas such as London
where rents are higher than average. Currently 7 out of 8 people who get
Housing Benefit are in low paid jobs, so having a living wage might well reduce
the overall benefit bill more effectively than demonising benefit claimants
further.
Much has been made of the figure of £26,000 as the maximum
annual cap but the vast majority of claimants will in fact get far less then
£26,000. Only 1% of claimants will be affected by this cap level but that will
still be 67,000 families. In Brent alone 3,300 families are due to lose
benefits because of the cap. Social cleansing of poor families has already
started in boroughs like Westminster.
Half of all household affected by the cap on benefits has a
disabled person living in them. Moving is often not an option as care packages
are not transportable across local authority boundaries, and continuity of
other services is often essential.
Social housing tenants with a spare bedroom will no longer
get funding for the extra room. Most will lose £12 a week. The National Housing
Federation estimate 180,000 social tenants are underoccupying 2 bedroom homes
but there were only 68,000 1 bed social homes to rent in 2009-2010. Even the
DWP EIA said there were not enough 1 bedroom properties.
This is unlikely to reduce housing costs as a couple with
one child having to move from a 3 bed social house in Crawley and rent a
smaller property in the private sector would be able to get £66 a week more in
Housing Benefit.
It will link Local Housing Allowance rates to CPI index,
which excludes housing costs.
The resulting increase in homelessness will lead to local
authorities paying out millions more in costs.
Not excluding child benefit from the cap levels will mean
anyone having a child will not get any extra money to care for them. This will
increase child poverty rates and child benefit for a first child is currently
about £1,000 per year.
With the scrapping of Income support single parents with a
child over 5 years of age must work or be available for work to receive Job
Seekers Allowance.
The Severe Disability Premium currently part of Income
Support will disappear and there are no details about what if anything will
replace this. This amount makes up one-third of some severely disabled people’s
incomes.
Claims will be made on the basis of households rather than
individuals and both members of a couple will be required to claim Universal
Credit. If couples have savings over £6,000 or one of them receives an income
then the other will not be able to claim anything else.
As income support is being abolished carers entitled to
benefits will be reduced to 40% of current claimants. Those carers who are also
disabled will lose about half of their income as they will only be able to
claim one Universal Credit premium either as a carer or a disabled person.
Removal of the Social Fund which has previously given grants
to enable people to buy essential items or to allow women fleeing domestic
violence to move. Some of this funding will now go to local authorities but
will not be ring-fenced in any way.
Withdrawing Child Benefit from families with a higher rate
taxpayer will affect many families adversely and takes women’s rights
backwards.
Many families with disabled children will face a cut to the
financial support they receive from tax credits. The new system will result in
these children losing up to £1,400 per year The Government estimates that
100,000 disabled children would lose out under this change.
Changes to Tax Credits will also affect families caring for
disabled children as claimants of these will need to work at least 24 hours
rather then 16 hours per week so many families will lose tax credits.
To access the Child support Agency single parents will have
to pay a fee reduced from a suggested £100 down to £20 plus 7-12% of any
maintenance collected for them.
All claims are to be processed via the internet which is not
accessible for many disabled people.
In addition, the universal credit and welfare reform will
bring in ‘a commitment’ for those who fail to ‘apply themselves’ to proper work
seeking activities to tougher sanctions. Once again this will not address the
complexity of employment related barriers that disabled people face, even if
they really are ‘fit for work’.
Sanctions proposed include:
- Failure to meet a requirement to prepare for work (applicable to jobseekers and those in the Employment and Support Allowance Work-Related Activity Group) will lead to 100 per cent of payments ceasing until the recipient re-complies with requirements and for a fixed period after re-compliance (fixed period sanctions start at one week, rising to two, then four weeks with each subsequent failure to comply).
- Failure to actively seek employment or be available for work will lead to payment ceasing for four weeks for a first failure and up to three months for a second.
- The most serious failures that apply only to jobseekers will lead to Jobseeker’s Allowance payment ceasing for a fixed period of at least three months (longer for repeat offences). Actions that could trigger this level of penalty include failure to accept a reasonable job offer, failure to apply for a job or failure to attend unpaid Mandatory Work Activity.
- Some types of recipient, such as lone parents with young children, are only required to attend work-focused interviews and their failure to attend is more often due to challenging circumstances than wilful evasion of the rules. However, financial sanctions where necessary will be applied.
DPAC
Briefing Notes: Housing and Housing Benefit
Posted: 13 May 2012 03:04 PM
PDT
DISABLED PEOPLE AGAINST CUTS
www.dpac.uk.net
HOUSING AND HOUSING BENEFITS- BRIEFING NOTES
Linda Burnip
01926 842253
0771 492 7533
linda_burnip@yahoo.co.uk
mail@dpac.uk.net
The future prognosis for disabled people’s housing is grim
Already 30% of
disabled people live below the poverty line and 1 in 4 families with disabled
children can’t afford heating.
The Chartered Institute of Housing has calculated that the
cumulative effects of the coalition’s proposals mean that by 2020 every tenant’s
Housing Benefit will be too low to cover their rent.
Changes to Housing Benefits from April 2011
The size criteria
will be adjusted to provide for an additional bedroom for a non-resident carer
( ie not a member of your family who shares your home) where a disabled
customer has an established need for overnight care. This must be claimed for
and will not be awarded automatically.
While this is a very
small positive change it still totally fails to address the lack of an extra
room for disabled children who need an extra bedroom, pensioner and other
couples who need an extra room due to their medical needs, and a wide range of
other disability related factors which mean disabled people need extra housing
space including the need for space for dialysis, room to store equipment, room
to use a wheelchair, ground-floor and level access accommodation. The recent
DWP Select committee into LHA said that these factors were posing considerable
barriers to independent living and should be addressed urgently but still have
not been. In essence the overall proposed changes to LHA will simply increase
these barriers.
From January 2012 – Under 35s
Any single person under 35 years of age renting in the
private rented sector who is disabled but not in receipt of middle or higher
rate DLA care component will not be able to claim for more than a shared room
rate. As DLA is now being scrapped we currently have no idea of the full impact
of these 2 changes together.
The difference
between the LHA for a one-bed property and single room rate is almost 50% and
in Edinburgh the one bed rate is £114.23 per week compared to £66.92 per week.
It is generally agreed that there are not enough houses in multiple occupancy
for everyone who needs to move to be able to do so. ssac’s own report estimated
this move alone to change Housing Benefit could lead to 11,000 people becoming
homeless.
Disabled people who
are most likely to be disproportionately affected by these changes are those
who most need to live in peaceful surroundings such as those with Mental Health
and Neuro-Diverse impairments.
From October
2011
The Local Housing
Allowance has been set at the 30th percentile rent in each Broad Market Rental
Area, rather then the 50th percentile as before. Disabled people will only be
able to afford to rent in the cheapest properties in an area, which are more
than likely to be inaccessible.
This will also
increase the difficulties disabled people face in finding suitable
accommodation to live independently , increase homelessness amongst disabled
people and push disabled people further into poverty especially if DLA
recipients are cut by half a million as planned by DWP.
The proposed changes
to the 30th percentile, rather then the median, rent being used to calculate
LHA from October 2011 will only make these matters worse than they already are
and will constitute serious breaches of UNCRPD particularly article 28, article
19,and article 7. New changes to our legislation should not be allowed to
contravene these convention rights.
Longer term
reforms
These required primary
legislation
From 2013-14 Local
Housing Allowance and Housing Benefit rates will be upgraded in line with CPI (Consumer
Price Index) rather than on the basis of
local rents. CPI does not include any account being taken of housing costs so
this will result in the amount of money people can get to help pay their rents
being even lower. At the same time this will apply to increases in other
benefit rates and an estimate I have seen is that disabled people will be £300
per year worse off because of this.
Social
Rented Sector
There are plans to remove any security of tenure from social
housing tenants and to increase rents to 80% of market values. Together with
the caps on Housing Benefits this will make renting in the social housing
sector unaffordable in many higher priced areas
of the country.
The
Bedroom Tax
From 2013 housing benefit for working age social rented
sector customers will be restricted for those who are occupying a larger
property than their household size would warrant. This is something that the
Labour government and DWP tried to introduce in Welfare Reform bill 2007 but
were forced to drop by pressure from Housing Associations. It means that if you
are living in an adapted property which may have cost thousands of pounds to
adapt then if you also have an extra bedroom you have no apparent need for you
will only get HB paid at the one bedroom rate.
Evicting disabled
people from adapted properties when there are few other accessible and adapted
ones available seems an act of lunacy and an unnecessary expense to taxpayers
as well as causing untold misery to disabled people who will be affected by all
of this.
Social housing
tenants who no longer get funding for an extra room will mostly lose £12 a
week. The National Housing Federation estimate 180,000 social tenants are under-occupying
2 bedroom homes but there were only 68,000 1 bed social homes to rent in
2009-2010. Even the DWP EIA said there were not enough 1 bedroom properties.
This is unlikely to
reduce housing costs as a couple with one child having to move from a 3 bed
social house in Crawley and rent a smaller property in the private sector would
be able to get £66 a week more in Housing Benefit.
Discretionary Housing Payments
Recognising the chaos
their HB reforms are going to make the sum allocated by government has
increased by £10 million in 2011 and by £40 million in 2012. This will
apparently give more flexibility to local authorities but DHPs are not supposed
to cover long term housing costs and have to be applied for every 13 weeks.
There is no right of appeal if they are refused although you can seek a
Judicial Review. Leicester for example has now introduced a policy where they
will only pay for a maximum of 13 weeks during which time disabled people
getting a DHP are harassed to move to a cheaper property, regardless of their
independent living needs.
Less important changes for disabled people who live outside
of London, but disastrous for anyone living in London or other high priced
areas of the country. Planned introduction postponed until 2012.
Local Housing Allowance levels have been restricted to the 4
bedroom rate. The 5 bedroom rate has been scrapped.
Caps have been
introduced which are
A new upper
limit will be introduced:
£250 a week for a one bedroom property
£290 a week for a 2 bedroom property
£340 a week for a 3 bedroom property
£420 a week for a 4 bedroom property
According to
government figures about 3-3,500 disabled people rent privately in central London.
DPO’s in London however have raised concerns that as the centre of London
becomes unaffordable to most disabled people then there will be additional
pressures on local councils for example in Brent where there is already a 10
year waiting list for re-housing as more people are forced to move.
Half of all household
affected by the cap on benefits has a disabled person living in them. Moving is
often not an option as care packages are not transportable across local
authority boundaries, and continuity of other services is often essential.
Universal credit will
introduce caps on the total amount of benefit any claimant can get, for both
housing needs and living expenses. The suggested total amount is £350 for a
single person and £500 per week regardless of family size, or costs of housing.
This will particularly affect those living in areas such as London where rents
are higher than average. Currently 7 out of 8 people who get Housing Benefit
are in low paid jobs, so having a living wage might well reduce the overall
benefit bill more effectively than demonising benefit claimants further.
Much has been made of
the figure of £26,000 as the maximum annual cap but the vast majority of
claimants will in fact get far less then £26,000. Only 1% of claimants will be
affected by this cap level but that will still be 67,000 families. In Brent
alone 3,300 families are due to lose benefits because of the cap. Social
cleansing of poor families has already started in boroughs like Westminster.
Mortgage Interest changes
Changes to the amounts paid to mortgage interest for
disabled claimants have been estimated to potentially lead to an additional
64,000 disabled people becoming homeless.
Cumulative Impact
The resulting increase in homelessness will lead to local
authorities paying out millions more in costs.
DPAC Briefing Notes: ESA
Posted: 13 May 2012 02:56 PM
PDT
Employment and Support Allowance (ESA) is the benefit which
is replacing Incapacity Benefit. ATOS healthcare are currently making £100
million a year processing both new claims and re-assessing those who are in
receipt of Incapacity Benefit.
There are 2 types of ESA, one contributory ESA which
disabled people are entitled to, based on having paid National Insurance
contributions and Income based ESA which is awarded to those on low incomes who
are not in a partnership.
People claiming IB plus new claimants have to undergo a WCA
(Work Capability Assessment) to claim ESA. There are 3 things that can happen
from WCA
People can be found fit for work and have to claim JSA and
register or work and meet lots of requirements about looking for work. If they
don’t or they are late for appointments etc they are likely to have their
benefits sanctioned i.e. stopped for 13-26 weeks. (This means that they only
get an emergency payment of £30 p.w. to live on plus Housing and Council Tax
benefit stop being paid automatically and if they don’t know that and don’t
make new claim can end up with rent and
CTB arrears.)
Second group of people get put in WRAG group ( Work Related
Activity Group) that is they get ESA( a lower rate) but this entitlement to
Contribution based ESA for those placed in the WRAG has now been limited to 12
months and 700,000 claimants will be affected by this cut.
Disabled people in the WRAG have to jump through lots of
hoops and make themselves work-ready. Again if they don’t sanctions/ reduction
of benefits will apply.
Third group is the support group - those disabled people who
are considered unable to work due to their level of functional impairments.
Overall the Coalition
plan to remove 1 million disabled people from being able to claim ESA and
declare them fit for work and force them to claim JSA (Job Seekers Allowance
instead) Financially this is a loss of about £30 a week, but as well as losing
entitlement to Incapacity Benefit many are also losing entitlement to DLA (
both components so in total people may lose a further minimum £34 a week from an income which is
there to meet the extra costs of being disabled).
WCA assessment has been criticised by CAB, many DPOs,
disabled people, Cancer support groups, a GP
Paul Gregg who originally devised it but now says it isn’t
working.
Basically measures physical functional ability so fails
massively anyone with non-physical or fluctuating impairments. New WCA
assessment is even worse then what was in place and eg someone with a visual
impairment is likely to be found fit for work unless they need an actual person
guiding them. Someone who has agoraphobia would be fit for work and the fact
that they physically can’t get to a place of work is ignored.
Totally ignores any of the barriers disabled people face in
the labour market i.e. attitudes, physical access, environmental access, the
reduction in Access to Work funding.
At the moment 70% of those who fail the WCA with
representation win at appeal and have benefit reinstated, 40% who don’t have
representation win. Waiting time often up to 12 months due to backlog in
Tribunal service.
Another problem is that if you win your appeal ATOS can just
start all over again re-testing you which is what happened to one of our
supporter’s uncles. When he got papers for 2nd tribunal hearing he killed
himself as he couldn’t face going through it all again. ( he won 1st appeal
then had to have a second WCA, and failed that again )
DPAC Briefing Notes: Effect of Cuts
Posted: 13 May 2012 02:23 PM
PDT
Disabled people feel their lives are under threat and many
of them are living in fear.
Data from Family Resources Survey and the National
Equalities Panel Research (2010) found that:
- 75% of disabled women and 70% of disabled men are already at the bottom end of Britain’s income distribution scale living in poverty.
- A tenth of disabled woman have disposable incomes below £31 per week and a tenth of disabled men have incomes below £59 per week including earned income and benefits.
- Already 30% of disabled people live below the poverty line and 1 in 4 families with disabled children cannot afford heating·
- The median level of total wealth for households headed by an employee is £217,500 compared to only £21,100 for households headed by someone who is sick or disabled.
- Under the coalition government’s austerity drive disabled people are set to lose at least £140 per month through direct cuts to disability benefits (initially devised to pay the extra costs of being disabled) alone.
Care and Support funding. Funding from the Independent
Living Fund for care and support has now ceased to all new claimants and any
additional needs cannot be met by them. From 2015 the ILF will cease to exist
cutting £330 million from funding for care and support. For the 20,000 of the
most severely disabled people this is a total betrayal by the coalition
government and will prevent independent living.
Social Services budgets are under extreme pressure and
nearly all Social Services departments have been told to reduce their budgets
by 25% which has an obvious knock-on effect to their provision of support and
the amount people need to pay towards this. Local authorities all over the
country are cutting the amount of care funding available, tightening
eligibility criteria, and increasing charges for those who are still eligible
for care. In Warwickshire it is anticipated that one-third of people who
currently receive free care will no longer be eligible. In Birmingham the
council are trying to remove care from over 4,000 people and move to providing
care to those deemed critical only.
In many local
authorities charging for care services has rocketed. One woman has told us that
although she has had free care for the last 7 years she is now paying over £50
a week for the same level of service. We also know that in Dudley and
Warwickshire charges have risen steeply. Are there any other local government
services that people have to pay for twice, once through council tax and again
through charging policies?
The Coalition are scrapping Disability Living Allowance and
replacing it with a new benefit Personal Independence Payments. An arbitrary
figure of removing 20% of claimants from entitlement to PIP has been decided
regardless of need. Many disabled people use this benefit to help make up the
shortfall they have in paying their rent or for care costs.
The mobility component of DLA may no longer be removed from
disabled people living in residential care homes who do not pay for their own
fees. However many people who live in residential homes still face losing
mobility funding due to the abolition of DLA.
This will leave many more residents with only £22 a week to pay for
clothes, travel costs, outings, and basics such as toothpaste, soap, etc.
Many disabled people use this mobility component to pay for
wheelchairs, mobility scooters and travel to meet friends and family. Losing
DLA will leave disabled residents effectively trapped in these homes, and
denied any right to a family life.
Other Benefits
Employment and Support Allowance (ESA)
and work capability assessments (WCAs) have been criticised by CAB,
disability charities and Disabled People’s Organisations. Even people with
terminal cancer have been declared fit for work and removed from Incapacity
Benefit. The government have now said that from October 2010 they will speed up
the re-assessment of everyone currently claiming Incapacity Benefit so that
10,000 claimants a week are ‘processed. Their overall aim in this is to remove
a 1 million disabled people from higher paying Incapacity Benefit onto lower
paying Job Seekers Allowance.
These assessments which ignore GP and consultant views are
earning Atos healthcare £100 million a year.
Contribution based ESA has now been time-limited to 12
months and this will remove 700,000 from receipt of this benefit for any longer
than that even though people may have paid National Insurance contributions for
years.
At the same time as the government claim they want to help
disabled people back into work they have slashed Access to Work funding which
meets the costs to employers of any reasonable adjustments needed in a workplace.
Yet only 20% of people with Autism and 25% of those with a mental health
condition are in employment. They are not workshy, but excluded by physical and
attitudinal barriers.
From Guardian letters page June 3rd 2011. Letter from Claire
Debenham, Brighton
The government says it is committed to a ‘fair and accurate’
work capability assessment. The distress and injustice caused by this new
system needs to be publicised far and wide.
My brother died last week of kidney cancer. He was diagnosed
a year ago and at Christmas was told he had about four months to live. In the
spring he was summoned for a work capability assessment (by this time he had
two brain tumours) and found fit for work. In addition to everything else, he became
anxious about losing the small amount of money he was living on. He was asked
to go in to the job centre for an interview but was too ill at the time. On May
19th he received a letter from Jobcentre plus telling him he was to be tested as
having limited capability for work. The medical officer overseeing his case had
advised that “death within six months is unlikely to occur due to the client’s
cancer” and there would be no “substantial risk to his mental or physical
wellbeing if he were found capable of work-related activity.”
He died six days later, having been unable to get out of bed
for four weeks. What work were they suggesting he was capable of? He asked:”What
have I paid tax and national insurance for if not help to pay the bills and
feed me at a time like this?”
Changes to Housing and Housing Benefits
These changes will affect everyone living on a low income
who rents either in the social housing or private rented sectors. The majority
of people who get Housing Benefit and Council Tax benefit are in work.
There are 1.8 million
households on social housing waiting lists. Last year in Birmingham there were
almost 19,000 applicants on the homeless person’s register. Last year in
Leicester 500 people needed an accessible property and only one was available.
Currently 1 million children live in overcrowded households, changes to social
housing tenure and housing benefits will only increase these numbers.
The Chartered
Institute of Housing has calculated that the cumulative effect of the
coalition’s proposals mean that by 2020 every tenant’s Housing Benefit will be
too low to cover their rent
There are plans to time limit people’s right to live in
their social rented homes and it has been suggested that they will have to
reapply every 2 years. If they have improved their lives by getting a higher
income they may then be forced to move out of their homes. This will apply to
new tenancies or if anyone moves to a smaller/ larger property. As well as
removing the right to life-time tenancies it is proposed that rents in the
social rented sector should rise to 80% of market value rents- a 30% increase
in rent for most tenants. Together with the caps on Housing Benefits this will
make renting in the social housing sector unaffordable in many higher priced
areas of the country.
Local Housing
Allowance, Housing Benefit for those renting in the private sector, will be
reduced for the 2 million disabled people living in private rented
accommodation. The Local Housing Allowance has now been set at the 30th
percentile rent in each Broad Market Rental Area, rather then the 50th
percentile as before. Disabled people will only be able to afford to rent in
the cheapest properties in any area, which are more than likely to be
inaccessible.
This change will also
increase the difficulties disabled people face in finding suitable
accommodation to live independently, and increase homelessness amongst disabled
people. The caring Condems have said people will have to move to cheaper areas
yet that may be impossible for disabled people as care packages are not
transportable from one local authority to another. As each local authority has
its own rules and regulations the care someone has in one area may not be the
same as the care they can have if they move. It also means that disabled people
will lose their trained Personal Assistants.
Disabled people with
learning difficulties or those with visual impairments often need several years
to be able to find their way around an area and need consistency in services
like GPs, nursing services and so forth to be able to survive.
Due to the size
criteria for LHA parents of disabled children are also unable to get an extra
bedroom for a disabled child regardless of their needs as the number of
bedrooms you can get benefit for is restricted simply by the age and gender of
your children.
Already one in four homes in the social rented sector are
inaccessible and often disabled people are unable to get into and out of their
own homes.
Housing Benefit
levels have now been capped and will be capped again under Universal Credit
plans.
For families renting in the private rented sector Local
Housing Allowance levels is now restricted to the 4 bedroom rate regardless of
the size of your family. New upper limits will be introduced which are scarcely
likely to cover rent levels in many parts of London and the South East.
According to government figures about 3-3,500 disabled people rent privately in
central London. DPOs in London however have raised concerns that as the centre
of London becomes unaffordable to most disabled people then there will be
additional pressures on local councils for example in Brent where there is
already a 10 year waiting list for re-housing as more people are forced to
move.
From 2013 housing
benefit for working age social rented sector tenants will be restricted for
those who are occupying a larger property than their household size would
warrant. This is something that the Labour government and DWP tried to
introduce in Welfare Reform bill 2007 but were forced to drop by pressure from
Housing Associations. It means that if you are living in an adapted property
which may have cost thousands of pounds to adapt then if you also have an extra
bedroom you have no apparent need for you will only get HB paid at the one
bedroom rate. I know 2 local disabled people who have 2 bedroom council flats –
one who is blind and who needs to be able to live in a location and property
that he knows well, and another who has had adaptations made to his flat who
from 2013 will only get Housing Benefit for a one bedroom property which will
either force them to move or push them into further poverty.
Under 35s
Anyone under 35 years of age who is disabled but not in
receipt of middle or higher rate DLA care component will not be able to claim
for more than a shared room rate if renting in the private rented sector. Yet
these are exactly the same people who cannot get onto waiting lists for social
housing so they have no choice other then to rent from private landlords. As
DLA is now being scrapped we currently have no idea of the full impact of these
2 changes together. However for anyone with Autism or a mental health condition
being forced to live in a multiple occupancy house can be very difficult. The
difference in benefit payable for a one bedroom and shared room rate is an
average of £47 per week and it has been estimated by housing charities that
there are 11,000 too few multiple occupancy properties so we had all better get
used to seeing increasing numbers of young, homeless disabled people on our
streets.
Discretionary Housing Payments
Recognising the chaos
their HB reforms are going to make the sum allocated by government has
increased by £10 million in 2011 and by £40 million in 2012. This will
apparently give more flexibility to local authorities but DHPs are not supposed
to cover long term housing costs and have to be applied for every 13 weeks.
There is no right of appeal if they are refused although you can seek a
Judicial Review. Leicester for example has now introduced a policy where they
will only pay for a maximum of 13 weeks during which time disabled people
getting a DHP are harassed to move to a cheaper property, regardless of their
independent living needs.
Benefits will be
linked to the Consumer Price Index (CPI) instead of the Retail Price Index, so
claimants will lose £300 a year as the CPI ignores any housing costs you might
have.
VAT increased to 20% will hit those on the lowest incomes
the hardest – it is estimated this rise will increase each household’s costs by
£500 per year
What disabled people say about these changes:
.“I am in receipt of DLA, without which I could not survive.
I have severe allergies, home bound, mostly bedridden. I have carers, and have
to pay for extra hours not subsidized by social services. My utility bills are
extremely high, and I have to contribute to the rent, which is not met by
housing benefits. I also suffer from malnutrition! Being chronically ill is
costly, being depending on carers for everything.
Cutting DLA would mean that I have to find housing within
the Housing Allowance which is much, much lower than rental market. There are
pockets of housing, in undesirable areas, with mould and cockroaches, and no
amenities, no lift, or if on the ground floor, simply not safe.
I could go on and on, about the misery it would cause, to
remove DLA.
It would lead to a slow death painful death. Worth adding
here, I have spoken to many in my situation, who are discussing mass suicide,
rather than suffer more health miseries, for which there are no cures! They are
not depressed, but pragmatic about what awaits all.”
DPAC Briefing Notes: DLA Abolition
Posted: 13 May 2012 01:37 PM
PDT
DISABLED PEOPLE AGAINST CUTS (DPAC)
www.dpac.uk.net
Contact –
Linda Burnip DPAC
co-founder
01926 842253
0771 492 7533
linda_burnip@yahoo.co.uk
Debbie Jolly, DPAC co-founder
01572 820546
079461 40765
mail@dpac.uk.net
Background to the Abolition of Disability Living
Allowance
Disability Living
Allowance was introduced in 1992 to provide support with the extra costs of
living that disabled people face.
In the Budget (June
2010) and Comprehensive Spending Review (October 2010) the new Condem
government announced its intention to arbitrarily cut spending on Disability
Living Allowance by 20 per cent or remove eligibility from half a million
disabled people.
In December 2010, government then published its detailed
plans to abolish Disability Living Allowance (DLA) and introduce Personal Independence
Payment (PIP), for those of working age from 2013-14. This is in spite of the
fact that the fraud rate is only 0.5%.
The government said that the changes to the assessment and
eligibility would be the means through which a 20 per cent cut in spend and
recipient numbers would be achieved. By 2016 this cut was intended to amount to
savings of £2.6bn annually.
The government has said that it wants a more ‘objective’
assessment a statement driven by the political goal of lowering the spend on DLA,
as there is little evidence of unnecessary payments: fraud rates for DLA are low at only 0.5%[1].
This indicates there is sufficient rigor and objectivity under the present DLA
assessment system. In addition only about 50% of DLA claimants are successful
and in 2008 49% of appeals were turned down, which also suggests that the
assessment is rigorous.
“The new benefit will
have two components, linked to a range of activities that will be considered in
the new assessment. One will be awarded on the basis of the individual’s
ability to get around (the mobility component), the other on their ability to
carry out other key activities necessary to be able to participate in daily
life (the daily living component).”
The government continue to echo the notion that support
should go to those “who face the greatest need”. However they do not justify
how they intend to equate ‘greatest need’ with enabling disabled people to
fully participate within society and DPAC has concerns that any such false
distinction will simply further the
notions of the ‘deserving’ and ‘undeserving’ disabled.
The policy goal which
frames the PIP assessment criteria DPAC
would argue is totally flawed. We believe that the proposal for PIP is
driven by a cost cutting agenda and a predetermined goal of cutting spend by 20
per cent, rather than any kind of objective assessment of need of support to
cover disabled people’s extra costs of living.
Maria Miller has once more stated that the cost of
supporting disabled people is unsustainable but that “The Coalition Government
is committed to helping disabled people to exercise choice and control over
their lives and ” “We have been absolutely clear that our welfare reform plans
are designed to protect people in the most vulnerable situations, including
disabled people.”
However in reality both the work capability assessment for
ESA and the proposed planned changes of replacing DLA with a Personal
Independence Payment are simply designed to reduce the number of people whose
disability is recognised by this government.
We further believe that government ministers have
continually created confusion over DLA by linking it to a goal of encouraging
people to be in work. DLA is not an out-of-work benefit and people can receive
it whether in or out of paid work. For many disabled people DLA is what allows
them to be able to work and without it they will no longer be able to continue
in employment.
Assessment development group
The government formed an ‘Assessment Development Group’ to
design the assessment, comprising The government’s ‘Assessment Development
Group’ which drew up the draft assessment has ten health and social care
professionals plus government officials, yet only one person representing
disabled people. Since the numbers of health professionals and officials
heavily outweighed the number of disabled people present, it is not surprising
that the group was able to come to a ‘broad agreement’ on the proposed
assessment.
If more disabled people had had been present it is doubtful
that such a medicalised/ functional ability type of assessment would have been
agreed on. Disabled people should have
been fully involved in this decision making process at the early stage of
discussion, i.e. as members of the Assessment Development Group in at least an
equal number of disabled people representing disabled people’s organisations as
government and other officials.
Article 4 of the UNCRPD states; the general obligation on
government to consult with disabled people, before not after decisions or
policies are changed.
This lack of early involvement is compounded by the
government ignoring the concerns raised
by disabled people and their organisations via consultation responses by
refusing to amend the Welfare Reform Bill sufficiently to address these
concerns.
PIP components and eligibility
assessment
PIP Components
Personal Independence Payment will have two components:
Daily living component
Mobility component
Each component has two rates rather than the existing three
rates:
Daily living component standard rate
Daily living component enhanced rate
Mobility component standard rate
Mobility component enhanced rate
PIP Eligibility
Assessment
Activities for daily living and mobility
The new assessment will cover activities for daily living
and mobility. To qualify for PIP disabled people will need to score enough
points in the following daily living and/or mobility activities:
Daily Living
Activities:
Planning and buying food and drink
Preparing and cooking
Taking nutrition
Managing medication and monitoring health conditions
Managing prescribed therapies other than medication
Washing, bathing and grooming
Managing toilet needs or incontinence
Dressing and undressing
Communicating with others
The mobility
activities:
Planning and following a journey
Moving around
The number of points scored will dictate whether a claimant
is assessed as having a ‘limited ability’ or ‘severely limited ability’ to
carry out daily living activities and/or mobility activities. The score will
also dictate whether a claimant will receive the standard or enhanced rate of
the Daily Living component.[2]
PROBLEMS WITH PIP
In order to receive PIP disabled people must be aged between
16 and 65 years and satisfy the daily living and/or mobility activities test
for 3 months prior to claiming and be likely to continue to satisfy this test
for a period of at least 6 months after claiming.
It remains very unclear what will happen to anyone who
becomes 65 and is in receipt of the mobility component of PIP as they would
have to claim Attendance Allowance which has no mobility component. (currently
anyone in receipt of DLA mobility component who becomes 65 continues to receive
this). DPAC is therefore concerned that any older disabled people will lose
their independence simply because they have reached the age of 65.
There is also no clarity about what will happen when someone
is admitted to hospital for any length of time but with the proposals for PIP
as they now stand it would seem that even a very short stay in hospital could
result in someone losing their mobility cars, plus any equipment such as
wheelchairs or hoists and other essential equipment they may be using PIP to
pay for.
Government guidance on DLA states that ‘Disability Living
Allowance (DLA) is not based on your disability but the needs arising from it’.
This is not reflected in PIP and the assessment involves a rigid and crude set
of questions which examines what a disabled person cannot or can do from a
prescribed list that only covers basic mobility activities and daily living
activities. This method of assessment
follows the medical model of disability.
The Work Capability Assessment was described by Professor
Harrington as ‘impersonal and mechanistic’ [3] and has resulted in many flawed
decisions, which have been over turned on appeal. It is deeply worrying that
the government appears be adopting a similar rigid assessment for PIP.
The estimate for ESA tribunal appeals for 2012-2013 is £50
million and the backlog of cases is so long that tribunals are sitting even on
Sundays so the logic behind also adopting a similarly flawed assessment process
for PIP remains unclear to DPAC.
The cost of changing from DLA to PIP has also been estimated
to be £65 million and on top of that there are plans to regularly re-assess
even claimants whose condition will never improve. Not only does this seem a
waste of money but it will add unfair additional stress to the lives of people
who are already struggling to overcome the disabling barriers put in their way
on a daily basis.
DLA acts as a passport to other welfare benefits and
concessions such as the Blue Badge, loss of which will increase the impact of
losing DLA. We feel the government have failed to consider how these passporting
functions will be replaced if PIP is introduced.
Higher rate care component of DLA has passported disabled
people to eligibility for funding for care and support from the Independent
Living Fund although this is also now closed to new applicants and due to close
completely by 2015.
Being in receipt of higher and middle rate care components
of DLA has also passported disabled people to additional disability premiums in
both Income Support and Housing Benefits. These premiums are now also planned to
be abolished with no clear guidance on what these additional amounts of funding
will be replaced by or how people will become eligible for any additional
amounts of basic benefits.
Many disabled people will live in increased poverty because
of the new assessment. The government
has not sufficiently tested what the impact on those losing DLA will be. In
particular the cumulative impact of benefit changes remains unknown.
By depriving disabled people of a much needed benefit we
believe the government is failing in their duty under the Equality Act and its
responsibilities under the UN Convention on the Rights of Persons with
Disabilities.
The assessment of mobility impairment is ridiculously crude
and neither allows for cumulative impact, fluctuation in factors such as
stiffness and pain, nor for factors such as steps. A person may be able to walk
50 or 200 metres on one day but none on another. They may be able to walk short
distances on a flat surface but be unable to walk up and down steps to access
buses and tube trains safely. An assessment of these factors is needed.
Many claimants with Neuro-diverse and Mental Health
conditions also say that while they can plan a journey the stress and anxiety
involved in making such a planned journey has simply been ignored and that they
can physically only carry out the planned journey if they have support from
another person to do so. This is another group of disabled people whose real
needs will be ignored by changes to PIP>
Claimants with conditions such as arthritis or osteoporosis
may be able to complete a one off physical task, but completing several tasks
over the course of a day can have a cumulative effect and increase pain and
immobility to totally debilitating levels.
Additional consideration of the impact of pain and fatigue is essential.
Again many claimants with Neuro-diverse and Mental Health
conditions can physically cook a meal but find that to do so is stressful and
exhausting for them so in reality they are not able to prepare and cook a meal.
Disabled people are already twice as likely to live in
poverty as non-disabled people. Far from the intention to ‘improve the support
for disabled people and better enable them to lead full, active and independent
lives’, these proposals will lead to an increase in disabled people’s poverty
and isolation. Therefore DPAC is
strongly opposed to the introduction of PIP and the eligibility
assessment.
The government’s work and pensions select committee
recognised that many more disabled people need to be lifted out of poverty and
recommended a DLA awareness campaign.
DLA supports disabled people to become more equal and
independent. Instead of attacking DLA,
which supports independence (including helping to overcome barriers that prevent
some people taking up employment), government should be doing more to stimulate
demand in the economy so that jobs are available and to tackle discrimination
by employers by vigorously enforcing the Equality Act 2010.
DPAC, Inclusion London & London Civic Forum are
offering a free skill sharing session in June.
Posted: 13 May 2012 12:22 PM
PDT
DPAC, Inclusion London & London Civic Forum are offering
a free skill sharing session in June. Full details below.
Places are limited, so please act fast.
NEW COMMUNITY LEARNING OPPORTUNITY:
Take Part Skills-Sharing Day for Disabled Activists
When? 10.30am – 4.30pm, Saturday 16th June 2012
Where? SCOPE offices, 6 Market Road, N7 9PW
Includes lunch
BSL interpreters available – please notify if required.
This learning workshop, led by a skilled Take Part
facilitator, is an opportunity for community activists who identify as disabled
to learn together by sharing skills and expertise, and reflecting on
experiences.
Participants will choose one or two topics for shared
learning. These could include:
- Direct action: what works, and how?
- Increasing involvement: how can we develop our support base?
- Organising a London-wide, volunteer-led network
- Communications for strong campaigning
- Any Other Topics of Interest
When you sign up, please let us know what topics you wish to
explore. We will notify all participants of shortlisted topics before the day,
and the final decision will be made by the learner group at the start of the
session.
To sign up, please email Kate Burls at
kateb@londoncivicforum.org.uk or phone her on020 8709 9773. Please give full
contact details, details of any access or dietary requirements, and specify
THREE topics you would be interested in covering at the skills-sharing day, in
order of preference.
A maximum of 15 places are available. These will be
allocated on a first come first served basis, so please book your place as soon
as possible.
Take Part is a community learning approach which builds
learners’ skills, knowledge and confidence for social action, by supporting
them to recognise and share their own expertise, skills and experiences with
others. For more information please visit www.londoncivicforum.org.uk/takepart.
This skills-sharing session is provided by London Civic
Forum, with support from London Disabled People Against the Cuts, Inclusion
London.
Kate Burls
No comments:
Post a Comment