Miller holds firm on DLA reform
While disabled campaigners may be proud of recent successes in
the battle over welfare reform, Maria Miller tells Sunil Peck that what
she’s doing is right
The minister for disabled people Maria Miller has said that a U-turn on
plans to abolish DLA [Disability Living Allowance] was always unlikely.
“There is widespread support for a fundamental reform of DLA," she told
Disability Now. "I don’t think there is any question that most
disability organisations think that reform is needed. The approach that
we’ve taken from the start with this reform has been that of
co-production.”
The Government wants to cut expenditure on DLA by 20 per cent. Its own
figure is that there is a 0.5 per cent fraud rate But it’s clear,
according to Maria Miller, that DLA is out of date and not fit to
support the needs of disabled people in the 21st century.
“DLA has been poorly managed over the last ten years. We’ve got a
situation where there is over £600 million going out in over-payments
and equally as worrying, around £190 million in under-payments, so we
can’t be convinced that the money that is there is getting to people who
need it most.
“The system needs an overhaul and we don’t have systematic checks in
place to make sure that this is picked up when people’s conditions
change.
“These are some of the fundamental problems with DLA. We want to make
sure that we have a benefit that’s there to support disabled people.”
Despite Miller’s insistence that there is widespread support for the
abolition of DLA, the Responsible Reform report, researched and written
by disabled people, and published as the Spartacus report in January,
has obtained evidence that its authors say justifies accusations that
the Government misled the public and parliament over the extent of
support for abolishing the benefit.
Unsurprisingly, Miller is dismissive of the report. “It’s important to
listen to any sensible arguments that are put forward. My concern is
that it was a selective analysis of 500 of the five and a half thousand
responses that we received for the DLA consultation.
“I was saddened to see that little regard had been paid to our approach
of co-production and the fact that we had worked closely with many
disability organisations.”
In recent weeks, while the Welfare Reform Bill has been going through
parliament, websites, radio phone-ins and news bulletins have featured
disabled people who say that the loss of DLA will thrust them further
into poverty. So is Miller disturbed by the prospect of disabled
people’s lives being devastated?
“People who need help with extra costs will continue to get that help
under the Personal Independence Payments (PIPs). DLA is about the extra
costs of being a disabled person; it’s not about topping up their loss
of income.
“There are many other ways the Government supports disabled people in
the benefits system. We spend £40 billion of public money every year
supporting disabled people, and through our reforms such as the
Universal Credit we will be making the situation much more
straightforward, particularly for disabled people who do want to get
into work but perhaps for a limited number of hours.”
Eligibility for the PIPs will be determined by medical assessments. That
method of determining disabled people’s eligibility for support with
the Work Capability Assessments has already led to chaos, with people
wrongly assessed and the high cost of the appeals system.
“It’s not possible to say that we’re not going to undertake a thorough
and proper assessment of an individual’s needs because it’s a difficult
process. We acknowledge it’s going to be a difficult process but we’ve
learnt a great deal from the work that has been done to make the Work
Capability Assessments work better for people who are looking to get
into employment.”
What about the long-held suspicions among disabled people that the
Department for Work and Pensions has been feeding stories about
disability benefit cheats to the media with the aim of winning public
support for harsh benefit cuts?
“I am very clear, that is not something that I would be involved in at
all. It’s the system that has trapped people in a spiral of welfare
dependency. I know that disabled people want to live independently.
That’s what I’m here to help make sure that the welfare system and other
parts of government is delivering. We have a system that, because it’s
long overdue for reform, is easily brought into disrepute by the media
reporting on cases where the system is being used in a way that it
shouldn’t be.”
Some activists have threatened to stay away from future government
consultations because they say that the Government ignored their views
in the DLA consultation. If Miller thinks she has a job on her hands to
win them over, she’s not saying so.
“What has been good about this process is that there’s clear
demonstrable evidence that the Government has listened to the thoughts
and concerns of disabled people. Whether it’s the fact that we’ve now
said that we’ll continue to have DLA and PIPs available for people in
residential care homes to apply for, whether it’s the fact that we’ve
changed the qualifying period from six months to three months, whether
it’s the fact that we’ve put in place two independent reviews and a
third if required, I think all of this is clear evidence that
consultation is important and that we are listening to disabled people
and their concerns.”
DLA
Access at work is Cut how could we access to work through interpreter etc.
Plus you can't see what all work place is trying to avoid Deaf and disabled people in work that what all Deaf people is here in UK is very hard to get Job but they won't accept us because we are Deaf due lack communicate.
I feel strong you should NOT cut Disabled living Allowance, Access at work and its Equal Act 2010.
We want you provide Access at work for all work place and new law for work place must accept deaf or disabled people in work because we can do communicate through email, mini com, Skype and many more.. They don't think about that.
DLA Reform
The Spartacus Report points out that well over 90% of disabled people do not want to move from DLA as PIP's is a cost cutting exercise. The DLA as it stands may need reform, but it needs to be reformed in such a way as to include more people not less.
I do not need a crystal ball to see many of us will lose out. The money is for the associated costs incurred by having a severe disability and if Atos is involved some of the most disabled will obviously lose out.
Perhaps Maria Miller would like to name the 'disabled people's organisations' who have given her all this support, so we will all know which parties have "sold us down the river". That way we can chastise them too, and kick them into touch.
DLA
Do not forget labour under Blair and Brown wanted to end DLA totally not having anything.
But yes DLA has now ended well ok not yet but Motability will end the money to have a car will end, which means all those disabled who have been to ill to walk will all of a sudden get up and walk, (sarcasm)
In the end somebody has to pay the money for the bankers.
Home Truths
* Transform Welfare... 99 percenters have to work till they die.
* Gut public education... Drones don't need schooling.
* End Poverty... If you're poor you should eat less
* Reform the NHS... Old people should just die quicker
Does This Ring Any Bells??? Its no coincidence that UNUM, the vast disability insurer in the USA who have been fined multi-million dollars for taking premiums and then refusing on any and all spurious grounds to pay out on claims...have SUDDENLY started showing adverts for private diability insurance recently on the UK TV channels..or that the Tory Government have REFUSED to say how many meetings they have had with UNUM as advisors to their Health and Welfare reforms. MAKE NO MISTAKE..IT WILL SOON BE PAY FOR YOUR HEALTHCARE..OR DIE!
Theres a word for this governments actions!
"EUGENICS"
DLA
There Deaf/Disable/Blind people who need help ans support, there alot of poeple as many you can thing out there in world who can't get a job and other
know why
Deaf > How can Hearing and Deaf communication with each other at work when hearing cannot do the British Sign Language there is 3/4 with out Sign Language and 1/4 who can...
Disable > most of them cannot fit into work cause not access for them to get to work can't travel to work or meet the need at work
Blind > we know the answer that one!!
Just remember there NO BUT OR IF out there cause there going to one of the HEll Coming along
Just do me favour, David Cameron have got it all Jinx big time..



DLA U-Turn
Most would agree that reform was needed and that financial support should be targeted to those who need it most. How can the Government cut the spend by 20% and ensure that those most in need receive the support without alienating 100,000's of people who rely on the already meagre support, in short they can't.
The personal independence payment assessment will undoubtedly help them some way towards the 20% figure by simply drawing a line through peoples awards, we can see this to some extent with the points allocated to certain descriptors indeed we can see it with the wording of the descriptors. What they seem to have failed to grasp is that this type of medical assessment is flawed. Disabilities are dynamic, most are unseen and often played down for fear of reprisal, a snapshot in an unnatural environment will not give an accurate indication of what it's like to live every single day with a disability.
There is talk of using and giving more weight to medical evidence, again in theory a step in the right direction but in practice why have an assessment if the evidence is so overwhelmingly strong, simple answer so it can be challenged and ignored.
Given the fear that this change in support is already creating it is impossible to quantify of justify the devastating effect PIP will have on so many. I am disturbed daily by the amount of forum posts where people have stated "if I lose my benefit I will simply end it" surely this cannot be allowed to happen. The holistic or social approach to disability assessment is not perfect but in my opinion gives a clearer indication of the daily battles people face, to dismiss it out of hand again in my opinion is negligent.
I guess "we are where we are" we have very little chance of forcing a u-turn,all we can do is collectively continue lobbying and try to shape PIP into a benefit that limits the inevitable heartache and suffering.