This is wonderful, the talented Shaye, the 15 year old progeny of journalist Sonia Poulton has written, performed and made the video for her song 'Broken Britain' all proceeds go to charity and she asks fans to sign the WOW petition.
Thank you Shaye, we love the song and LOL'd bigtime at the Pleb chorus! Get your copy here.
The WOW Petition - 100,000 signatures captured. Next #WOWdebate2014 to stop the War on Welfare
26/02/2013
WOW Campaign say: Colin Brewer must Resign or be Fired
A Cornish councillor who said “disabled children cost the council too much money and should be put down” is refusing to resign. Colin Brewer, the Independent for Wadebridge East in North Cornwall, made the comments to members of Hayle charity Disability Cornwall. The ardent disability campaigners and the angry former salesman clashed as he left a ‘difficult debate’ and walked into an equalities fayre at Town Hall in October 2011.As a disablist statements goes this one rather takes one's breath away doesn't it? "Disabled children cost the council too much money and should be put down." A horrifying statement by anyone's standards, but what makes it even more horrifying is the man who said it. This was not an ignorant comment by someone who didn't know any better. It was made by Colin Brewer, elected councillor for Cornwall Council. What makes it even worse is that he said it to Disability Cornwall, at an equalities event, that was intended to inform councillors of the issues faced by marginalised groups. Equally shocking is that the only sanction he has faced is to be asked to apologise for what he said.
Well that's not good enough. Elected councillors are there to carry out the work of the council, which includes a duty of care to people with disabilities. That a councillor would think this, let alone say it to a Disability organisation, is an absolute disgrace. Councillor Brewer should resign immediately. He is unfit for public office.
Disability Cornwall's web page, people might want to send them solidarity messages.
To fight this wave of hatred sign & support WOW petition Sign Here.
Update Thurs 28th: Colin Brewer resigned.
To fight this wave of hatred sign & support WOW petition Sign Here.
Update Thurs 28th: Colin Brewer resigned.
09/02/2013
20,000 People Have Signed The WOW Petition
*** 20,000 ***
The WOW Petition has over 20,000 signatures!
A huge thank you for signing and sharing this urgent and important petition. The good news is that we are on target to reach our goal of 100,000 signatures.
During a television interview for ITN, Margaret Hodge MP, chair of the Public Accounts Committee revealed that the Department for Work and Pensions have figures of the deaths of 1300 people who are known to have died after being found "fit to work". MPs have acknowledged that the department is causing "misery and hardship" to benefit claimants. Government ministers are trying to defend a broken system. They must accept and take responsibility for allowing harm to be inflicted on sick and disabled people by the work capability assessment which is not fit for purpose, and the suffering caused by the cuts to benefits and care services that target people when they are most vulnerable.
Support is growing from charities, organisations and individuals. It is essential that you please continue to tell as many people about this petition as you can and ask them to sign. Together we can make a difference!
30/01/2013
Open Letter to Liam Byrne - Will Labour Protect Disabled People?
Pat's Petition is going to Westminster on the 6th February to meet with Shadow Work and Pensions Liam Byrne to find out what Labour will do to support sick and disabled people. WOW Petition was created to ensure that the work done by Pat's Petition will continue into the future and we have some points and questions for Labour to answer too.
An Open Letter to the Shadow Work and Pensions Secretary
Dear Rt Hon Liam Byrne MP
The WOW Petition is a crowd-sourced grass roots campaign created and supported by disabled people, people with physical and mental health illness, care workers, carers and family members. We have come together because we are frightened. We have each been affected by the devastating consequences of the Welfare Reform Act and feel we are fighting for our lives.
We are determined to continue and build upon the achievements of Pat’s Petition. We are not satisfied that the government will understand or care about the consequences of the cuts and changes to benefits and services until a comprehensive impact assessment has been completed. We are aware of the Prime Minister’s intention to scrap impact and equality assessments. It is vital therefore, that a cumulative impact assessment is carried out with urgency.
Since the WOW Petition was launched on December 18th 2012, at the time of writing almost 18,000 people have supported us. We expect to reach the 100,000 target as we expand into new initiatives and the campaign grows.
Our petition has been championed by disabled actress and comedian Francesca Martinez. Francesca has spoken out publicly against the arbitrary cuts and the unfairness of disproportionately targeting the benefits sick and disabled people rely on. She has appeared on Newsnight and BBC This Week Programmes to voice her concerns. Baroness Grey-Thompson has also supported our campaign.
Sick and disabled people do not understand why the government wishes to wage a “war on welfare” against them. People who are genuinely too sick to work have been cruelly labelled as “feckless” and “scroungers” by government ministers. Welfare statistics have, we believe, been purposefully misrepresented, and the tabloid media has chosen to wage a campaign of misinformation and misleading stories about the level of welfare fraud. This in turn has altered public perceptions of disabled people and hardened attitudes towards benefit claimants.
Where is the sense in forcing people suffering with long-term and chronic conditions onto a depressed employment market where eight people on average are fighting for every job? People with mental health problems find it especially difficult to overcome employment discrimination and to establish themselves in work even when the economy is buoyant. The greater cruelty is that many of these people will not have access to treatment or therapy.
Sick and disabled people do want to work, but the Work Capability Assessment completely fails to recognise their limitations or how they can realistically function in the workplace. The consequences of forcing people to look for work and mandatory Work Related Activity under threat of losing income could cause illness to deteriorate and place a further burden on stretched NHS and mental health services. Sick and disabled people can and do make huge contributions to society. This does not have to be purely based on their ability to make money. Voluntary work and caring is vital for the economy but isn’t paid. For some “making work pay” will not improve their life chances, opportunities and finances. These people deserve to be better supported.
The third ‘Harrington Report’ revealed that just 9% of people expected to recover within twelve months had found work eighteen months later. The support to get people back to work isn’t working. Less than 1.5% of disabled people referred to the Work Programme had found employment.
We are certain that you are already aware of the failings of the fitness to work test, and the increasing numbers of recorded deaths resulting from the loss of income and stress. The fear of the Atos envelope landing on the doorstep is real. When people know that they are not going to have a fair and honest assessment that takes the opinions of their doctors and consultants into account they feel frustrated, helpless and terrified.
Over 330,000 people have been forced to appeal a decision they believe to be wrong. 40% of these are overturned, rising to 70-80% with specialist advice. The government is removing legal aid to make obtaining legal advice at the tribunal stage even more difficult, and we can only presume that it is a cynical attempt to deter people from appealing rather than fixing a broken system.
Under clause 99 of the Welfare Reform Act sick people could be forced onto Jobseekers Allowance whilst potentially waiting many months for the DWP to reconsider a challenge to a decision. These changes are going to have a huge impact on people’s lives. It is insufficient and dismissive of government ministers to blame Labour for introducing Employment and Support Allowance and to complain that they have inherited a flawed assessment process. This is an unacceptable defence for a serious failure.
We want a reassurance that the current fitness to work test will be scrapped and replaced with a credible medical assessment carried out by medical professionals who are allowed to apply their discretionary judgement based on their medical expertise. People feel they are being ‘tricked’ by confusing forms, tick box assessments and an impossibly narrow set of descriptors which excludes severe and enduring illness from the support group. Assessment recordings should be made available to all who request them to reassure people that the face to face tests are above-board.
People will and do work when they are well and able and appropriately supported. Battling illness and battling the current benefits system for some, unfortunately, is simply too much to cope with.
Universal Credit is yet an untested system of delivering benefits but the uncertainty surrounding it is causing a great deal of worry and confusion. Contributory ESA is excluded but the means tested component is not. Some people receive an element of both.
Hundreds of thousands of sick people have lost and will lose all of their Employment and Support Allowance after 365 days because they have a working partner, regardless of whether they are recovered or not. This arbitrary cut is penalising working families and proves that the government’s aim was to cut the budget and not to support sick people back to work. Without access to specialist employment advice they will be further excluded and isolated from the workplace.
We learn that in Merseyside alone the cost of the new “bedroom tax” to social tenants will be £16 million annually. What is most disturbing is that three-quarters of the households include a disabled person. Depending on the locality some people will be asked to pay council tax from their disability benefit incomes.
The government promised vulnerable people that “they had nothing to fear” and that “disability benefits are being protected” but Coalition MPs voted to cap the annual benefit rise of Employment and Support Allowance at 1%. This also includes the support group as only the disability premium is excluded from the cap. With food prices expected to rise above 5% this year sick and disabled people will struggle to buy the basic necessities. Many, including households with disabled children, are already having to cancel hospital appointments due to transport costs, take out loans to buy essentials and are choosing whether to heat their homes or buy groceries.
Local authorities are being forced to cut back massively on the care and support services they deliver to vulnerable people. The charity Scope report a funding gap of £1.2billion for adult social care. 40% of disabled people who require care are saying that their basic needs are not being met.
Disability living allowance is being replaced by the personal independence payment and the ‘goalposts’ are being moved so that by 2018, 600,000 fewer disabled people will be entitled to the benefit as would have received DLA. This is another arbitrary cut as changing the eligibility will not change the disability. Just because someone is ‘less disabled’ than another doesn’t mean that they don’t require the additional support to allow them to stay in work, maintain their dignity, be independent and have an equal chance in life as their peers. 100,000 disabled people are expecting to lose their mobility vehicles because they can move a mere 20 metres. Not even the length of the Commons floor. How is this “supporting disabled people”?
The cumulative impact of these cuts and changes, inadequate social care, along with many others such as the cuts to Children’s Disability Premiums under Universal Credit, the scrapping of Independent Living Fund for disabled adults who live alone, closure of day-care centres, degradation of mental health services, NHS services, amongst others, is too much to bear.
We would like to thank you for considering our concerns and we look forward to your response. Our hope is that we can co-operate together for a better and fairer future for all sick and disabled people in the UK.
The WOW petition team
email info@wowpetition.com
website www.wowpetition.com
The Petition
An Open Letter to the Shadow Work and Pensions Secretary
Dear Rt Hon Liam Byrne MP
The WOW Petition is a crowd-sourced grass roots campaign created and supported by disabled people, people with physical and mental health illness, care workers, carers and family members. We have come together because we are frightened. We have each been affected by the devastating consequences of the Welfare Reform Act and feel we are fighting for our lives.
We are determined to continue and build upon the achievements of Pat’s Petition. We are not satisfied that the government will understand or care about the consequences of the cuts and changes to benefits and services until a comprehensive impact assessment has been completed. We are aware of the Prime Minister’s intention to scrap impact and equality assessments. It is vital therefore, that a cumulative impact assessment is carried out with urgency.
Since the WOW Petition was launched on December 18th 2012, at the time of writing almost 18,000 people have supported us. We expect to reach the 100,000 target as we expand into new initiatives and the campaign grows.
Our petition has been championed by disabled actress and comedian Francesca Martinez. Francesca has spoken out publicly against the arbitrary cuts and the unfairness of disproportionately targeting the benefits sick and disabled people rely on. She has appeared on Newsnight and BBC This Week Programmes to voice her concerns. Baroness Grey-Thompson has also supported our campaign.
Sick and disabled people do not understand why the government wishes to wage a “war on welfare” against them. People who are genuinely too sick to work have been cruelly labelled as “feckless” and “scroungers” by government ministers. Welfare statistics have, we believe, been purposefully misrepresented, and the tabloid media has chosen to wage a campaign of misinformation and misleading stories about the level of welfare fraud. This in turn has altered public perceptions of disabled people and hardened attitudes towards benefit claimants.
Where is the sense in forcing people suffering with long-term and chronic conditions onto a depressed employment market where eight people on average are fighting for every job? People with mental health problems find it especially difficult to overcome employment discrimination and to establish themselves in work even when the economy is buoyant. The greater cruelty is that many of these people will not have access to treatment or therapy.
Sick and disabled people do want to work, but the Work Capability Assessment completely fails to recognise their limitations or how they can realistically function in the workplace. The consequences of forcing people to look for work and mandatory Work Related Activity under threat of losing income could cause illness to deteriorate and place a further burden on stretched NHS and mental health services. Sick and disabled people can and do make huge contributions to society. This does not have to be purely based on their ability to make money. Voluntary work and caring is vital for the economy but isn’t paid. For some “making work pay” will not improve their life chances, opportunities and finances. These people deserve to be better supported.
The third ‘Harrington Report’ revealed that just 9% of people expected to recover within twelve months had found work eighteen months later. The support to get people back to work isn’t working. Less than 1.5% of disabled people referred to the Work Programme had found employment.
We are certain that you are already aware of the failings of the fitness to work test, and the increasing numbers of recorded deaths resulting from the loss of income and stress. The fear of the Atos envelope landing on the doorstep is real. When people know that they are not going to have a fair and honest assessment that takes the opinions of their doctors and consultants into account they feel frustrated, helpless and terrified.
Over 330,000 people have been forced to appeal a decision they believe to be wrong. 40% of these are overturned, rising to 70-80% with specialist advice. The government is removing legal aid to make obtaining legal advice at the tribunal stage even more difficult, and we can only presume that it is a cynical attempt to deter people from appealing rather than fixing a broken system.
Under clause 99 of the Welfare Reform Act sick people could be forced onto Jobseekers Allowance whilst potentially waiting many months for the DWP to reconsider a challenge to a decision. These changes are going to have a huge impact on people’s lives. It is insufficient and dismissive of government ministers to blame Labour for introducing Employment and Support Allowance and to complain that they have inherited a flawed assessment process. This is an unacceptable defence for a serious failure.
We want a reassurance that the current fitness to work test will be scrapped and replaced with a credible medical assessment carried out by medical professionals who are allowed to apply their discretionary judgement based on their medical expertise. People feel they are being ‘tricked’ by confusing forms, tick box assessments and an impossibly narrow set of descriptors which excludes severe and enduring illness from the support group. Assessment recordings should be made available to all who request them to reassure people that the face to face tests are above-board.
People will and do work when they are well and able and appropriately supported. Battling illness and battling the current benefits system for some, unfortunately, is simply too much to cope with.
Universal Credit is yet an untested system of delivering benefits but the uncertainty surrounding it is causing a great deal of worry and confusion. Contributory ESA is excluded but the means tested component is not. Some people receive an element of both.
Hundreds of thousands of sick people have lost and will lose all of their Employment and Support Allowance after 365 days because they have a working partner, regardless of whether they are recovered or not. This arbitrary cut is penalising working families and proves that the government’s aim was to cut the budget and not to support sick people back to work. Without access to specialist employment advice they will be further excluded and isolated from the workplace.
We learn that in Merseyside alone the cost of the new “bedroom tax” to social tenants will be £16 million annually. What is most disturbing is that three-quarters of the households include a disabled person. Depending on the locality some people will be asked to pay council tax from their disability benefit incomes.
The government promised vulnerable people that “they had nothing to fear” and that “disability benefits are being protected” but Coalition MPs voted to cap the annual benefit rise of Employment and Support Allowance at 1%. This also includes the support group as only the disability premium is excluded from the cap. With food prices expected to rise above 5% this year sick and disabled people will struggle to buy the basic necessities. Many, including households with disabled children, are already having to cancel hospital appointments due to transport costs, take out loans to buy essentials and are choosing whether to heat their homes or buy groceries.
Local authorities are being forced to cut back massively on the care and support services they deliver to vulnerable people. The charity Scope report a funding gap of £1.2billion for adult social care. 40% of disabled people who require care are saying that their basic needs are not being met.
Disability living allowance is being replaced by the personal independence payment and the ‘goalposts’ are being moved so that by 2018, 600,000 fewer disabled people will be entitled to the benefit as would have received DLA. This is another arbitrary cut as changing the eligibility will not change the disability. Just because someone is ‘less disabled’ than another doesn’t mean that they don’t require the additional support to allow them to stay in work, maintain their dignity, be independent and have an equal chance in life as their peers. 100,000 disabled people are expecting to lose their mobility vehicles because they can move a mere 20 metres. Not even the length of the Commons floor. How is this “supporting disabled people”?
The cumulative impact of these cuts and changes, inadequate social care, along with many others such as the cuts to Children’s Disability Premiums under Universal Credit, the scrapping of Independent Living Fund for disabled adults who live alone, closure of day-care centres, degradation of mental health services, NHS services, amongst others, is too much to bear.
- We would like to know how Labour intends to correct the injustices sick and disabled people are currently having to cope with under the policies implemented by the Coalition government?
- What reforms to the welfare system does Labour have planned?
- Will Labour scrap and replace the Work Capability Assessment with an objective and trustworthy medical test?
- How do you plan to support those disabled people who have lost work through the Remploy closures?
We would like to thank you for considering our concerns and we look forward to your response. Our hope is that we can co-operate together for a better and fairer future for all sick and disabled people in the UK.
The WOW petition team
email info@wowpetition.com
website www.wowpetition.com
The Petition
We
call for a Cumulative Impact Assessment of Welfare Reform, and a New
Deal for sick & disabled people based on their needs, abilities and
ambitions
Responsible department: Department for Work and Pensions
We call for:
A
Cumulative Impact Assessment of all cuts and changes affecting sick
& disabled people, their families and carers, and a free vote on
repeal of the Welfare Reform Act.
An immediate end to the Work Capability Assessment, as voted for by the British Medical Association.
Consultation
between the Depts of Health & Education to improve support into
work for sick & disabled people, and an end to forced work under
threat of sanctions for people on disability benefits.
An
Independent, Committee-Based Inquiry into Welfare Reform, covering but
not limited to: (1) Care home admission rises, daycare centres, access
to education for people with learning difficulties, universal mental
health treatments, Remploy closures; (2) DWP media links, the ATOS
contract, IT implementation of Universal Credit; (3) Human rights abuses
against disabled people, excess claimant deaths & the disregard of
medical evidence in decision making by ATOS, DWP & the Tribunal
Service.
22/01/2013
Pat's Petition Goes to Westminster - How You Can Help
Will Labour Offer Any Protection to Disabled People?
Pat’s
Petition is going to Westminster to find out.
After weeks of waiting - sorting out the
logistics of travel to London - Pat's Petition finally has a date for meeting with Liam
Byrne MP, Labour's Shadow Work and
Pensions Secretary. Wednesday 6th February will see five of us at
Westminster.
This meeting could not be happening at a more
crucial moment in the long, sad history of this persecution. Because there is
so much visible distress and so much suffering is now happening in real time in
the public arena – before the eyes of the nation – people are beginning to see
through the spin and myths – and see the truth.
There were two very serious debates in
Parliament last week. In the debate called by Michael Meacher on WCA and ATOS - MP
after MP queued up to recite the litany of appalling cases that they had seen
in their surgeries. Thank you Michael.
In the debate in the House of Lords,
motion proposed by Baroness Hollis, Lord Freud showed once again that he does
not care.
The
Centre of Welfare reform also released a report this week, How the cuts affect disabled
people PDF.
So Pat’s Petition is going to Westminster to talk to
Labour. We are hopefully going to finalise arrangements for an Opposition Day
debate calling for a Cumulative Impact Assessment. Someone has to measure and
record this persecution. Looking the other way and saying it is all too
difficult is no longer an option.
This
night of a thousand cuts cannot carry on unchallenged. Disabled people, their
carers, families and friends cannot take any more. The financial stress is
overwhelming and the emotional stress is more than we can bear. The public are
on our side now that the myths are exploding and they can actually see what is
being done in their name.
So we are going to ask Liam what Labour will
do to help us.
What will Labour promise us to protect us?
How you can help
It is vital you lobby your contacts across
all Parties; stress how much you/your members need a Cumulative Impact
Assessment undertaken.
Send us a supporting statement a.s.a.p. no later than February 1st of why
you think so.
This will be shared across social media platforms so more people
can see your concerns.
We
will also print them to take with us when we meet with Liam.
We look forward to your response.
Pat
x
19/01/2013
15,000 People Have Now Supported the WOW Petition
Since it was launched just five weeks ago, the WOW Petition has now exceeded...
15,000 signatures!
Thank you so much for supporting this vitally important petition. Please sign and share widely with everyone you know.
We need to reach 100,000 signatures urgently to call for a cumulative impact assessment of all the cuts and changes affecting sick and disabled people, their families and carers.
18/01/2013
Pat's Petition Taking WOW Signatures To Meeting With Liam Byrne
From CarerWatch:-
Pat has also said she will be taking WOW petition's signatures with them to the meeting along with those of Pat's Petition. Showing how the strength of feeling is increasing.
Before Christmas we mentioned that Liam Byrne had suggested meeting with him to talk about an Opposition Day debate to request a cumulative impact assessment. Arranging diaries hasn’t been the easiest of tasks, especially with the christmas holidays in the way. But we now have a date.
Five of us will be heading for Westminster on 6th February to meet with Liam Byrne
We can feel the start of a change of mood as people awaken to the individual impacts of the changes. More groups are protesting, more people are using social media sites to air their fears and concerns. There has been an unanticipated emphasis on Welfare Reform as tbe Benefits Uprating Bill makes its way through Parliament.
The Bedroom Tax is beginning to worry tenants as their landlords get in touch with them.
People are more familiar with terms like ‘Personal Independence Payment’ and ‘Universal Credit’ if not with ‘Employment Support Allowance’ and its two groups. Their sponsorship of the Paralympics means that everyone has now heard of Atos. Local authorities are making public decisions and we are hearing about the difficult decisions to cut vital services.
We are seeing language change to include ‘strivers’ as well as ‘scroungers’ but we’re still not convinced that the media gets the full picture for disabled people, their carers and families. This is why we need a Cumulative Impact Assessment, and it is what we will take to our talk with Liam: issues that are important to you, the 62,703 people who signed Pat’s Petition and all the people who have since said they would have signed it if they’d understood.
Please keep contacting your MPs, details here. Send them details of how the changes are impacting on you now.
Sign the new WoW petition by Francesca Martinez. You can read more about the WoW group here
We must all keep on keeping on.
Pat
x
Pat has also said she will be taking WOW petition's signatures with them to the meeting along with those of Pat's Petition. Showing how the strength of feeling is increasing.
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