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Payday Loan Companies ‘Legalised Scam’ Targets Benefit Claimants

October 29, 2014

With many thanks to Benefits And Work.

The Guardian is reporting that payday loan comparison sites are hiding £75 charges for their services in their small print and are specifically targeting benefits claimants. Visitors, who often do not even get a loan, are having the money taken from their account and their bank details passed on to up to 200 other payday loan brokers, who may also try to take money from the same accounts.

In August alone, Nat West says that there were a million attempts by payday loan brokers to take money from customers’ accounts.

Astonishingly, the scammers are usually authorised by the Financial Conduct Authority, who have given over 5,000 licences to payday loan brokers before actually beginning to check up on them.

According to the Guardian:

“NatWest said it is seeing as many as 640 complaints a day from customers who say that sums, usually in the range of £50 to £75, have been taken from their accounts by companies they do not recognise but are in fact payday loan brokers.”

The banks also claim that scammers:

“. . .push their charges through bank payment processing systems between midnight and 3am, knowing that state benefit payments are added to accounts just after midnight. When the person living on unemployment or disability benefit wakes in the morning, they find their money has already vanished.”

Read the full story in the Guardian

UK Injured Military Veterans: Government ‘Failling Covenant’

October 29, 2014

The government is failing to abide by its military covenant, medical experts who treat injured soldiers have said.

Leading professors in psychology and orthopaedics say the healthcare system is not providing veterans with the service they have been promised.

The Armed Forces Covenant, described as a duty of care to the armed forces, states veterans should be “sustained and rewarded” .

A Ministry of Defence spokesman said it was “fully committed” to the covenant.

‘Do better’

But Professor Neil Greenberg, from the Royal College of Psychiatrists, said he believed ministers were failing to honour the military covenant promise.

“In my view the government needs to be a bit more honest about what it is delivering and just what it says it’s delivering, because the two are definitely not the same,” he said.

Freedom of information figures obtained by the military charity Help for Heroes show almost 13,000 service personnel have been medically discharged for musculoskeletal disorders since 2001 – those who have lost limbs or have problems with ligaments and joints – with many requiring constant care throughout their lives.

Prof Tim Briggs, a leading orthopaedic surgeon, recently wrote the Chavasse report which outlined the problems former personnel face on the NHS.

He said he was “moved” by the sacrifice made by veterans who attended his clinics, and he believed “we can do better and we should do better”.

He said that “finding access to specialist care was sometimes proving difficult and as a result some veterans were falling through the net and we had to improve things”.

Labour’s shadow minister for veterans, Gemma Doyle, said the medical experts’ comments were a “damning indictment”, and proof the government had failed to meet its obligations.

Shot in the face

Simon Brown, a corporal in the Army for more than 10 years, was shot in the face by a sniper in 2006 and was medically discharged four years later.

“The bullet hit my left cheek between the eye and the nose and exited my right cheek between the nose and the ear,” he said.

“My cheek bones were obliterated, my jaw was broken in four places, I’d lost my left eye totally and there was very little hope of any sight returning to my right eye.”

Almost a decade on, he says he has still not had all the surgery and treatment he requires and insists it is not the fault of staff, rather the system is flawed.

‘Good investment’

“It has been long processes – there’s been a lot of jumping through hoops you know. I actually had to see a committee to see whether or not I was entitled to free plastic surgery,” he said.

If veterans got the treatment they are entitled to they could remain “productive members of society”, he said.

Injured troops receive treatment at Headley Court Defence Medical Rehabilitation Centre in Leatherhead, Surrey

“I see it as it’s actually a good investment to look after these people and give them the support and help they need.”

More than 200,000 men and women have been deployed to Iraq and Afghanistan since 2001.

The military covenant states that soldiers could be called upon to make the “ultimate sacrifice” but in return they and their families will be “sustained and rewarded by commensurate terms and conditions of service”.

The moral obligation to treat veterans should not stop when service ends, the covenant states, saying veterans should receive priority healthcare from the NHS when they are being treated for a condition dating from their time in the armed forces.

Once a veteran leaves the forces, their healthcare is the responsibility of the NHS.

The main principles of the military covenant were enshrined in law in the Armed Forces Act 2011.

The government says the defence secretary must report annually on the progress made by ministers in honouring the covenant.

Help For Heroes has estimated that 75,000 service personnel could suffer mentally and physically as a result of operations in Afghanistan.

With some NHS staff unaware of the covenant – and veterans not always keen to tell their doctors about their past – the charity has said a government database would help to make sure they receive the care they are entitled to.

Earlier this year, the Conservative MP James Arbothnot told the Defence Select Committee he was disappointed the government kept detailed records of sheep and cows, but couldn’t do the same for veterans.

Labour MP Madeleine Moon, who also sits on the committee, said that the government had promised things but not followed through.

She said a renewed focus needed to be on “the long term”, and making sure that veterans did not get “lost in the system”.

But health minister Dan Poulter said the government had invested more than £22m in mental health and prosthetic services, “specifically for those most in need”.

The investment included 10 regional veteran mental health teams and nine veteran-focused prosthetic centres providing support and care for ex-servicemen and women.

He told the BBC Radio 4’s Today programme that care for veterans had been vastly improved, and as a result “it had raised the game” in terms of dealing with complex cases for the wider population generally.

“Where there is an equal clinical need between two patients, under the covenant it is the veteran who will receive priority,” he said.

An MoD spokesman said the government had “worked hard to ensure our serving personnel, veterans and families have the support they need and are treated with the dignity they deserve”.

“That is why we enshrined the covenant in law in 2011. Since then all local councils have signed up to the Community Covenant, and more than 300 companies have signed up to the Corporate Covenant – including Tesco just this week.

“We are very proud and grateful of the commitment that all those that have signed the Covenants have made and it demonstrates the immense amount of respect and gratitude there is for our armed forces,” the spokesman added.

Conventional police interview techniques are not effective for people with autism

October 29, 2014

A press release:

Police find interviewing and interacting with witnesses and suspects with autism a real challenge, a study has revealed – highlighting that the ways officers have been taught to interview are at odds with what is needed in these situations. Existing interview techniques tend to focus on open questions, only later narrowing down to closed questions, but research shows that people with autism may need focused questions from the outset.

The Economic and Social Research Council (ESRC)-funded research studied what does, and does not, work when police interview people with autism. The researchers – Dr Katie Maras, University of Bath, and Dr Laura Crane, City University London – are calling for better training of police and criminal justice professionals as, at present in the UK, these groups currently have no standard compulsory training about autism.

“Laura Crane and I have heard of many cases where problems have arisen because police and other criminal justice professionals know very little about autism,” says Dr Maras. “Research in this area is still in its infancy, but it’s steadily accumulating. There’s a crucial need to get findings to practitioners to help them obtain the best evidence possible from people with autism.”

More than 400 UK frontline and investigative police officers holding a variety of ranks provided information for the study. They spoke of the difficulties and challenges they encounter when obtaining written, oral and identification evidence. Officers reported, for example, finding it hard to build rapport with people with autism, which usually plays an important part in interviews. They also described difficulties in arranging a suitable environment for interviews.

“Police stations tend to be noisy with bright or flickering lighting and strange smells,” says Dr Maras. ‘But people with autism are often sensitive to sensory input and as a result they can struggle to maintain concentration in interviews.’

Over 600,000 people in the UK have autism, many of whom will come into contact with the police at some point in their lives. Poor social-communication skills can make them vulnerable when involved with the Criminal Justice System as a victim, witness or suspect. Individuals with autism process memories in a different way from other people, which can lead to misunderstandings.

During the study, officers also answered questions about existing interview practices that they considered worked well, and were asked what could be done to develop understanding and skills. The researchers found examples of excellent practice, especially among police officers who were able to draw on their personal experience of the disorder through familiarity with a family member or colleague with autism.

On a further positive note, related research shows that there are simple and effective strategies that can enhance the evidence that people with autism give and improve their credibility as witnesses. For example, providing information about a witness’s diagnosis can improve his or her perceived credibility; unusual and stereotyped behaviours can be attributed to autism – rather than a lack of credibility.

At an event for police officers entitled ‘Experiences of autism and policing’, Drs Maras and Crane will lead a research-based training workshop that aims to improve practices. It takes place on 4 November as part of the ESRC’s flagship annual Festival of Social Science.

 

 

New Pitch For Blind Football Opens At St George’s Park

October 29, 2014

On 8 September 2012, Dave Clarke scored for England’s blind football team against Turkey in the play-off for seventh and eighth at the London Paralympics. England won 2-0 and the goal, in no small way, brought about the end of an era.

It was Clarke’s 128th in 144 international appearances, made across 17 years, and doubled up as virtually his last competitive kick of a football. He retired afterwards; eight months later his status in the wider game was underlined in front of 90,000 at Wembley when he handed the FA Cup over to Wigan Athletic, but as an active role model for blind football he seemed a huge and remarkable act to follow.

On Tuesday, at St George’s Park, Clarke donned his boots for the first time in two years and on this occasion it meant that an era had very much begun. This was no playing comeback for the 43-year-old – not officially, anyway. Clarke was lining up for an England Legends team against the current national side in a match arranged to officially open a new purpose-built blind football pitch at the FA’s national football centre, whose second birthday fell this month.

It is the second such pitch to have been opened in England – the other is in Hereford at the Royal National College for the Blind – and will be used as the team’s training base in the build-up to the 2015 European Championship which will be held in England, and beyond.

“It’s absolutely brilliant that the pitch has been built and that the requirements of the blind football squad have been incorporated into St George’s Park,” Clarke tells the Guardian. “The fact that the team can now train there at a first-class facility that replicates what it will experience in championships will be a huge help.”

Replication of the tournament environment – or, at least, its pitch specifications – is a running theme at St George’s Park: Roy Hodgson’s squad play on a pitch designed to Wembley’s parameters, for instance. For the blind team, fine-tuning the length and width is only one of several requirements. The pitch, built over a five-week period in the summer, measures 40m by 20m – the same as a typical futsal pitch – but is flanked by barriers, 2.4m in height, that keep the ball in play and also facilitate players’ echo location.

The surface is hard enough to allow the ball, heavier than a normal futsal ball, to run truly. It is situated in the quietest area of the complex, in a corner surrounded by trees, to shelter it from the wind and other extraneous influences that might hamper a player’s ability to navigate his or her way around the pitch using their hearing. There is space behind the goals for the guides who instruct footballers during play; referees and spectators have also been thought of, although Hereford can hold more of the latter and matches at the European Championship will be held there.

“We have been lucky to have the pitch in Hereford,” says Clarke, “although that didn’t come until around 2008. Before that we were generally playing on normal five-a-side courts.

“There are lots of things that we’ve all had to work very hard to achieve, that I wish I’d had when I was growing up. This is one of them. When I was born it wasn’t possible to play for your school, let along your county or your country, so the pathways through to elite sport are outstanding now and developments like this can only help. The FA have done a phenomenal job of driving blind football forward in England and across the world. We now have a professional squad training full-time at St George’s Park with world-class facilities, and it’s going to stand us in excellent stead for the Euros.”

In addition to the new pitch, the FA has granted the national team £1m of funding over the next two years. It marks a significant, decisive turn from what were times of uncertainty this year when UK Sport announced a decision to pull funding from the blind team following a disappointing eighth-placed finish at last year’s European Championship in Italy. That prompted an urgent brainstorming session among the FA board, which pledged to plug the gap with resources of its own. As well as the competitive element – and this has not been a remotely unsuccessful side, qualifying for every major tournament since 1996 – there was the fundamental and more pressing need to boost take-up nationally.

“There is an issue right across the country in terms of the availability of quality facilities for kids and adults to play blind football,” says Clarke. “The more we have, the more sessions we can run and the more coaches we can train.

“Disabled sport is a very challenging field to try and grow because you’re often trying to reach people who aren’t aware of the opportunity, and aren’t aware that not only would they quite like football but they’d be pretty good at it as well. It’s about trying to get to those who are not conscious that the opportunity exists.”

Jeff Davis, head of disability football at the FA, agrees that while the new pitch at St George’s Park is a huge step forward it needs to be the start of a concerted drive to increase the number of state-of-the-art facilities.

“I think we need to place another one or two pitches across the country so that people don’t have to travel so far for access to a bespoke blind pitch,” he says. “Our regional centres have movable barriers, but there is nothing of such high quality. We’ll work with our facilities team at the FA to see if we can get them in place.

“But this investment is a real example of how the FA has got behind disability football and a real beacon of good practice for all governing bodies in England. What it says is: ‘You should be including disabled people in your sports provision.’”

England need to reach the final of the European Championship in order to reach the 2016 Paralympics. Davis says that the players have told him it is “the best training facility they have ever used, and the best surface”, while Clarke points to the level of impact it could conceivably have in the longer term.

“At London 2012, six of the eight teams competing were full-time professionals,” he says. “We weren’t at that stage, but we still drew with Argentina, Spain and China, who all were.

“It’s no surprise that since we went full-time we’ve beaten the European champions [Spain] three times and drawn with Brazil, the world and Paralympic champions. We’re already seeing the benefits of that and the new pitch at St George’s Park will only help our capability to challenge for honours. The team has some great players and a superb coach, John Pugh, who is a master tactician – so I’m sure they can make it happen.”

WW!’s Forgotten Heroes: Secret History

October 28, 2014

I’ll be watching this on Channel 4, Sunday, 7pm.

Former Royal Marines commando Arthur Williams embarks on an emotional journey to explore the experiences of nearly two million British soldiers who suffered life-changing injuries and disabilities during the First World War.

When the conflict ended an unprecedented number of amputees and disfigured servicemen returned home to face a new set of challenges.

Largely forgotten or ignored after the war, they fought for recognition, respect and equality and many became pioneers who helped to transform the nation’s attitude towards disability.

In 2007, Arthur was involved in a car accident that left him paralysed from the waist down. In the course of his journey, Arthur draws closer to the experiences of those wounded and disabled men by confronting the hard challenges he faced while learning to live with his own disability.

He returns to the military rehabilitation centre at Headley Court for the first time since his accident and speaks openly about the difficult months of his early rehabilitation.

The programme features extraordinary and rarely seen footage and a never-before-seen cache of medical photographs of World War I amputee patients from Queen Mary’s Hospital Roehampton.

Bring Tianze Home To Scotland For Christmas

October 28, 2014

I’ve just signed this at Change.org:

My 16 years old son Tianze has autism, a learning disability and sometimes behaviour issues.

We live in Fife, Scotland but in May Tianze was moved to a hospital in Middlesbrough, England. It was only supposed to be for a 12 week assessment but he is still there which is over 25 weeks currently. Now he has been placed on the mental health register and we’ve been told there is no place in Scotland that would care for my son.

Every week I have to travel more than 200 miles to see my son in England. It is 12-14 hours journey for a two hour supervised visit. It is not only exhausting but also financially difficult. We are a British Chinese family in Scotland, family life is central to our culture. My son misses home so much. He loves music, so he has written a song called “Back Home” that he sings everyday. Every time, when we finsih this two hours visit , we have to good bye, it is always heart broke for both of us.

When Tianze is stressed, his behaviour can deteriorate and since he has been away from home his self-harming has gotten worse. I am really worried for him.

My son’s assessment has been finished in earlier August in that hospital in Middlesbrough, however because there is no specialist care ready for him , the doctor there still holds him. He is locked in the hospital  without education and  activities . Only sleep and drugs which made him so frustrated .It is  hurting him  now by putting him such long time in an  improper  environment and limits his freedom. He is suffering daily,our whole family are suffering daily .

 Charities say that children with learning disabilities like Tianze should whenever possible be cared for in their communities, with the support of their families. This is what we want for our son. To get him the care he needs, where he knows he is close to the people that love him. As parents ,we feel so powerless toward our son’s placement options.We feel we don’t have our rights toward our son in our modern civilized country!

Thousands of people signed a petition for Josh Wills, a 13 year-old living with autism, to be brought home and cared for near his family in Cornwall. And it worked.

We want the same for Tianze. Please help bring my son home.

Please see Tianze’s back home song which he created by himself as following:

 

Miss home, back home song

 BY Tianze in xx hospital

 Back home,

 Back home,

Back home,

 

I miss home,

 I dream home,

 I miss mum,

 I miss Dad,

My home is in Scotland…..

 

 I miss home

I dream home.

 I miss home food ,

 I miss home family together,

 I count days to back home …..

 

 Back home ,

Back home,

Back home.

Nesta Inclusive Technology Prize

October 28, 2014

A press release:

£50,000 prize for enterprises and individuals to create new technologies, products and services that will enable disabled people equal access to life’s opportunities

Designers, makers and entrepreneurs are being challenged to apply for the chance to gain a contract worth £50,000 and to develop the next generation of products, services and technologies that will make a real difference to the 1 in 5 of us living with limiting long term illness or disability in the UK.

The UK’s innovation foundation, Nesta, is working with the Office for Disability Issues, Innovate UK, The Department for Business Innovation and Skills and Irwin Mitchell to champion the issue of assistive technology through the Inclusive Technology Prize. The challenge will encourage innovation through co-creation with disabled people, meeting needs as defined by the users themselves and challenging people to use lived experiences of disability to develop life changing technology.

The competition will be judged by an expert panel, including leading comedians Jess Thom, who has Tourette’s syndrome, and Laurence Clark, who has cerebral palsy. The panel will be looking for ideas that enhance independence by building, inventing, developing and co-creating a more equal and accessible society. The full judging panel is available at www.inclusivetechprize.org.

David Constantine, co-founder of mobile disability charity Motivation and Inclusive Technology Prize judge, said: “Motivation designs, builds and provides low cost wheelchairs for developing countries. The designs are innovative in that they are low cost, and suitable for the environment people are living in. The wheelchairs are reparable and replicable in country.

“I agreed to be a judge because I think the Inclusive Technology Prize is really important. It’s a substantial amount of prize money for the winner that will interest companies to really get behind the design of a product or service for the future.

“I’m looking for innovation, aesthetics are very important for me too. I want to see products that people not only feel they need, but feel like they really want to use as well.”

Jess Thom, comedian and Inclusive Technology Prize judge, said: “The Inclusive Technology prize is looking for people to apply with products that are beautifully designed, systems that are turned on their heads, and technologies that harness the best of computing and mobile technology to kick start new ideas that will have a long lasting impact for the 12.2 million disabled people in the UK.”

The judges are looking for ideas that will fulfill their vision for a more equal society. Products could be functional objects like a watch that tells the time through touch, systems and technologies might include text to voice apps for computers and mobiles that make voting systems accessible by reading and recording the vote by voice.

Constance Agyeman, Programme Manager for the prize, said: “We are excited by the potential of the Inclusive Technology Prize to generate a whole new wave of product design and to encourage people to innovate for independence.

“Together with partners, Nesta is looking for entries that are co-produced with disabled people and will improve the lives of the everyday person experiencing day-to-day challenges.

“Assistive technology, aids products and technologies should be readily available for anyone looking for the solutions that will make their life easier and simpler.  The Inclusive Technology Prize is about making that vision a reality.”

Submissions must have the potential to make a difference in education, home, work, leisure, or transport, and can have cross over in any or all of these areas.

The Inclusive Technology Prize, which is designed to be accessible to all, is open to individuals, groups or organisations. The competition has several stages and entrants will be whittled down to 25 semi-finalists who will each receive mentoring and support, and then a final 10 who will develop prototypes ready for impact testing. The winner of the £50,000 contract will be announced in March 2016.

Interested organisations and individuals should visit www.inclusivetechprize.org to apply.

Deadline for applications is 16 January 2015.

 

Is This It For Lord Freud?

October 28, 2014

Main Parliamentary business for today. Listen live online here. I will be!

 

Poster seen on Facebook- many thanks to Adrian Wait.

Fears For Scope Care Home Residents

October 28, 2014

Nearly 150 disabled care home residents face being moved over the next few months as the charity Scope closes a number of its properties.

Scope say the eight homes are outdated, and no longer meet the aspirations of people with learning disabilities.

But some of the residents have been in the homes for decades and there is concern among families about the distress the move could cause.

Michael Buchanan reports.

An Update On Eddie- Who Is Now Hoping For A Merciful JobCentre Advisor

October 28, 2014

Right. This one goes out to anyone who still believes that there’s a safety net in place. It’s also for anyone who believes that the jobcentre system is still vaguely functional, or that there are checks and balances in it to keep things fair.

This post is an update on a story I’ve been writing about a man with learning difficulties who is signing on for JSA. He sometimes struggles with his jobsearch, because he isn’t able to use a computer to apply for work. He hasn’t been sanctioned so far, because his jobcentre adviser has been reasonable. The problem is that she’s suddenly no longer his adviser. Now, he’s in a precarious position. It is unlikely that he’s the only one.

Full story at Kate Belgrave.

Margot Martini, Toddler Behind #SwabForMargot Campain, Died This Morning

October 27, 2014

Some very sad news this evening, readers.

Inspirational toddler Margot Martini who touched hearts around the world as she courageously battled cancer, died this morning surrounded by her loving family.

A heartbreaking statement issued by parents Vicki and Yaser said the two-year-old “died peacefully and was surrounded by those who love her.”

The toddler underwent a bone marrow transplant in February after a match was found but the cancer returned, reports the Birmingham Mail .

The poignant statement said: “At 10:24 this morning, our dear little daughter, Margot passed away at home.

“She died peacefully and was surrounded by those who love her. Thank you for all your love and support. Vicki, Yaser, Oscar & Rufus.”

Margot had been diagnosed with both acute lymphoblastic leukaemia and acute myeloid leukaemia last year.

Yesterday her parents, originally from Essington, near Wolverhampton, had posted on their Team Margot site on Facebook that they were taking the situation “hour-by-hour” as their little girl’s condition worsened.

The statement said: “Margot’s condition has deteriorated significantly over the past couple of days and in particular since yesterday (Saturday) afternoon; she’s now in a very poor and fragile state.

“A syringe driver has been introduced to combat the increased & more intensive need for pain relief. This is a pump that runs 24 hours a day, continuously administering a slow infusion comprising morphine & ketamine and latterly midazolam and anti sickness meds as well.

“To compound matters, Margot has picked up a line infection in her port and consequently today, the port has been de accessed and the syringe driver is now working via sub cutaneous access in her right leg.

“It’s an extremely difficult time for Margot and for all the family. The only thing we can now do is continue to monitor her constantly changing condition and try and keep her comfortable.

“Margot has been asleep all day and she continues to sleep peacefully. Mercifully, for now at least the drugs appear to be working.”

Celebrities including Stephen Hawking, Omid Djalili, Catherine Tate, Boris Becker and Bill Bryson had all given their support for Margot.

And a special video was previously recorded by her favourite TV character Peppa Pig.

The message from Peppa – voiced by 12-year-old Harley Bird – ends with the touching words “Goodnight Margot, sleep tight.”

Brave Margot inspired hundreds to become life-saving bone marrow donors as part of the Delete Blood Cancer awareness campaign.

SA Prosecutors To Appeal Pistorius’ Sentence And Conviction

October 27, 2014

South African prosecutors say they are going to appeal against the conviction and sentence given to athlete Oscar Pistorius for killing his girlfriend.

Last week, Pistorius began serving a five year prison sentence for the culpable homicide of Reeva Steenkamp, although he could be out in 10 months.

The double-amputee Olympic sprinter was cleared of murder.

“The appeal on conviction is based on the question of law,” the national prosecuting spokesman said.

Pistorius’ family have said that he will not appeal.

The athlete was also given a three-year suspended sentence for firing a gun in a restaurant.

Jobcentre Whistleblower Tells Dispatches Of UC Memo Titled ‘Ideas Please. Sinking’

October 27, 2014

From today’s Guardian:

A leaked staff memo at the Department for Work and Pensions (DWP) appears to show the government is still struggling to roll out its flagship welfare programme, Universal Credit (UC), across the UK.

The memo, seen by the Guardian and titled: “Ideas please: Sinking”, appears to be a plea from a jobcentre manager to her staff for solutions to tackle an ever-growing workload brought about by the new system for delivering social security to more than 7 million people.

The internal email, sent in late September and uncovered by Channel 4’s Dispatches as part of an investigation into UC to air on Monday evening, appears to show that one of the 60 centres where the scheme has been rolled out is generating such a substantial backlog of claims, centre staff will have to work three times more than their limit to clear it.

UC, which is projected to generate £7bn in economic growth to the UK, will combine six major benefits, including jobseeker’s allowance and housing benefit, into a single payment which will rise and fall more smoothly with people’s circumstances.

The DWP had promised to have 1 million people on the scheme by April 2014 but, dogged by delays and tens of millions of pounds of IT write-downs and write-offs, the original timetable has been scrapped. Just 15,000 people are on the system.

Last week, the work and pensions secretary, Iain Duncan Smith, declared that the project would not be tied to a final delivery date. “Arbitrary dates and deadlines are the enemy of secure delivery,” he said.

A jobcentre employee has alleged that the UC claims process, which is meant to save the government hundreds of millions in staff costs by being highly computerised, is unable to handle complicated cases. The whistleblower told Dispatches:“The IT works for single claimants, the straightforward cases. More complex claims have to be done manually. That’s slow and easy to get wrong.”

He added that UC’s IT for staff on the ground is “completely unworkable, badly designed”, and already “out of date”.

The DWP minister, Mark Harper, has denied there were problems. He said he had spoken to frontline staff at the 100 service centres rolling out UC and received “nothing but positive feedback”.

A DWP spokesperson added: “There is no evidence that more complex cases cannot be dealt with successfully.”

The Guardian has previously reported on how leaked Whitehall documents warned of a failing IT system, more than £1m in wasted expenditure, and how only 25,000 claimants would likely be served by the system by the time of the general election next year.

The government has written off or written down £130m on the project, which is designed to revolutionise the culture around claiming benefits. It now expects 100,000 people to be on the system by May and for 100 centres to be involved in its delivery by the end of this year.

The Dispatches investigation will also allege that UC’s failures are leaving claimants in desperate circumstances. One couple told the programme it took three months to register their change-in-life circumstances, leaving them struggling to feed themselves and their child.

Jay Montrose had previously been living on his own and claiming UC as a single person. In June he moved in with his partner, Nikki Colton, who is pregnant, and their four-year-old son, Ethan.

After being informed they would be treated as joint claimants under the scheme, Montrose and Colton told Dispatches their claim took so long to process, they were unable to pay for food, rent and other bills, built up debts of £2,500 and an eventually received eviction notice from their landlord. The couple said they received the correct money only after staff told them their claim was being processed manually.

“I was worried because I’m pregnant at the moment and I should be eating at least enough to get me through. I shouldn’t be living off a packet of crisps in the day because that was all that [we had] that could be spared and that Ethan didn’t need,” Colton told Dispatches.

The DWP said the couple’s claim had been delayed because the pair had failed to complete the correct forms. Responding to Dispatches’ findings, a spokesman told the Guardian: “Universal credit’s IT system is robust and effective, and we have trained 26,300 work coaches who are successfully providing new support to claimants to help them better prepare for work.

“We are rolling UC out in a safe and controlled way to ensure we can make changes to the system if necessary. But there is absolutely no evidence that cases cannot be dealt with. When fully rolled out, UC will make 3 million families better off by £177 a month and lift up to 300,000 children out of poverty.”

• Dispatches: Benefits Britain is on Channel 4 at 8pm GMT on Monday 27 October.

JobCentres Go Digital

October 27, 2014

Any thoughts on this press release, readers?

Old-fashioned ‘signing-on’, job cards in windows and Full Monty-style dole queues have been consigned to the past as Jobcentres across Britain undergo a digital revolution.

High-tech equipment, including specially-designed computers that bring all Jobcentre services into one device, will be installed at more than 700 sites to make it easier for people to find work.

Around 23,000 electronic signing pads will also become a new fixture at Jobcentres around the country – signalling an end to the old-fashioned paper booklets that jobseekers carry around and sign every time they visit and saving more than £1 million a year.

Minister for Employment, Esther McVey, said:

Every day, Jobcentres across the country are helping people into work, contributing to record falls in unemployment.

But as the economy grows and the jobs market changes, so are Jobcentres. Long gone are the Full Monty days of job cards in the windows and queuing for your dole.

We’re seeing record employment levels – and with this digital revolution, the government is doing even more to help people into work.

Claimants will soon be signing on using electronic pads in a move that will help to improve security, reduce fraud in the welfare system and make the jobseeking process paperless.

At the same time, free wi-fi and 6,000 digital jobsearch computers will be installed at Jobcentre Plus sites across Britain to give claimants a new opportunity to search and apply for jobs online, using the equipment on site or their own devices.

They will also be able to use the computers to keep on top on their claims, calculate benefits and update their CVs.

Removing the standalone jobpoints, which have been a fixture of Jobcentres for 2 decades, and installing the new computers, will save more than £2 million a year.

The new equipment has already been installed in a number of Jobcentres across the country.

The electronic pads will be appearing in Jobcentres from this month – with rollout set to be completed by spring next year.

New tech coaches will also be on hand to help jobseekers get the most out of the new technology.

Seven Day Benefit Wait Brings Hope To Wonga

October 27, 2014

With many thanks to Benefits And Work.

In a move that will bring new hope to struggling payday lenders, the DWP have extended the waiting days for employment and support allowance (ESA) and jobseeker’s allowance (JSA) from 3 days to 7 days from today.

The new rules mean that claimants applying for ESA or JSA will not be entitled for any payments during the first 7 days that they would otherwise be eligible for benefits.

Claimants will not be affected if they have made a previous claim for ESA or JSA in the preceding three months, however, as they will be considered to have already served their waiting days. ESA claimants will also not be affected if they have claimed statutory sick pay immediately before claiming ESA.

Terminally ill claimants are exempt from serving waiting days.

The move has brought condemnation from trade unions and charities, but the chancellor George Osborne argues that: “Those first seven days should be spent looking for work and not looking to sign on.”

Last month Wonga was forced by the Financial Conduct Authority to write off £220 million in loans interest and charges to people who should never have been given loans in the first place. There have been calls for other payday lenders to suffer similar penalties.

But the decision by the Coalition to extend the waiting period for ESA and JSA to seven days means that there is likely to be an upsurge in applications for short-term loans by people with no other resources to fall back on.

Given that waiting times for a first payment of universal credit (UC) are likely to be around 6 weeks – and up to six months for people whose earnings were too high, according to new government proposals – and bearing in mind that UC also includes a housing costs element, the future for payday lenders is beginning to look rosy again.

Legal Review Launched Against PIP Delays

October 27, 2014

With many thanks to Welfare Weekly.

 

Lawyers have launched legal action against the government over “unnecessary and unacceptable” disability benefit delays, it has been revealed today (24 October 2014).

Irwin Mitchell is representing a disabled woman from Kent, who is thought to be among thousands of people left “financially and socially isolated” by delays in assessing claims for the new disability benefit Personal Independence Payment (PIP).

The disabled woman is said to be struggling to feed herself and heat her home, after being forced to wait more than six months for her PIP claim to be processed.

The public law experts will argue in a judicial review that delays of more than six months in assessing claimants for PIP is leading to financial hardship for thousands of disabled people.

Anne-Marie Irwin, from Irwin Mitchell Solicitors, said:

“PIP was created to ensure that the thousands of vulnerable people across the UK are able to get support for extra costs caused by long-term ill health or disability.

“Through our work, we have seen how people have been left in the lurch for a number of months as a result of these issues, with many contacting the Department of Work and Pensions disability helpline several times to check the status of their claims – only to be told they must wait in line.

“The delays that our client and potentially thousands of others have faced are simply unnecessary and unacceptable, as they need this support to be able to get the most from everyday life. This issue has left our client struggling to cope financially, with the strain and stress of these issues also having a significant impact on her health and wellbeing.

“We’ve been left with little choice to take this action to ensure that the voice of our client is heard.”

Of the 349,000 claims for PIP made between April 2013 and March 2014, final decisions have only been made on 84,000 by the end of February 2014, say Irwin Mitchell. Lawyers claim that this has potentially left several thousands struggling to get by day-by-day.

The National Audit Office reported in December last year that just 19% of new claims for PIP had been given a decision. The actual time for making a decision was 107 days for claims from people without a terminal illness and 28 days for claims by the terminally ill.

Anne-Marie Irwin said: The delays are putting people at a significant disadvantage and if their PIP claims are granted it would meet the additional financial costs which arise because of an illness or disability and so enable them to benefit from a greater quality of life.

“It is clear that urgent action is needed on this issue.”

At the launch of a Public Accounts Committee report into PIP in June this year, the committee’s chair Margaret Hodge described the scheme’s implementation as “nothing short of a fiasco”.

Irwin Mitchell is representing Ms C, from Kent, who suffers with severe depression, ME and high blood pressure. Ms C experiences severe physical exhaustion and many other health problems. She applied for PIP in January 2014 after she was forced to give up her job when her condition worsened.

Ms C said: “The delay has had a massive impact on my life. I applied for PIPs so I could look after myself, but without it I can barely eat and only ever leave my house for a weekly trip to a supermarket.

“While PIP wouldn’t solve all of my problems, without it I just feel financially and socially isolated.”

Disability Minister Mark Harper said in September this year (2014): “We accept that the delays faced by some people are unacceptable, and we are committed to putting that right.

“Between May and July we have doubled the number of claims processed and we are working hard to continue to make further improvements.

“By the end of the year we expect that no-one will be waiting for an assessment for longer than 16 weeks.”

Mother Makes Legal History Winning Right To End Disabled Daughter’s Life

October 27, 2014

A mother has made legal history after she won a High Court case to end the life of her severely disabled 12-year-old daughter.

Nancy Fitzmaurice was born blind and suffering from hydrocphalus, meningitis and septicaemia, which left her unable to talk, walk, eat or drink.

Her quality of life was so poor she depended on round the clock hospital care and was fed, watered and medicated through a tube at London’s Great Ormond Street Hospital.

But when a routine operation left her screaming in agony her devoted mother, Charlotte Fitzmaurice, who had given up work to look after her daughter, made the heartbreaking decision to end Nancy’s life.

In a landmark case, Great Ormond Street fought on behalf of Charlotte, and dad David Wise, to give her the right to die.

In a statement given to a judge explaining why her daughter should no longer suffer Charlotte said her daughter longed for peace.

After reading the heartbreaking words Justice Eleanor King at the High Court of Justice granted the request and Nancy died in hospital.

The ruling sets a precedent as it is the first time a child breathing on their own, not on life support and not suffering from a terminal illness, has been allowed to die.

In her summing up the judge said Charlotte’s love for her daughter is apparent and she had “great admiration” for her devotion to Nancy.

“The last day was the hardest of my life. It was absolutely horrifying. I miss my beautiful girl every day and although I know it was the right thing to do, I will never forgive myself. It shouldn’t have to be a mother’s decision to end their child’s life, doctors should be able to take that away from you.”

– Charlotte Fitzmaurice

Ian Mulholland- Sanctioned, Starved, Jailed

October 24, 2014

The story of Ian Mulholland, who is now in jail for stealing food, is a sad indictment of Tory Britain.

Yesterday’s news that Ian Mulholland, a 47 year old recovering drug addict, received a custodial sentence for stealing food after he had been sanctioned by the DWP should have been front-page news throughout the nation.  The sad fact that it isn’t tells us how far the media has been normalised to the harshess of Westminster, neo-liberal politics.

Mr Mulholland, who is facing leg amputation, was sanctioned for 9-weeks by his local jobcentre for missing an appointment.  Mr Mulholland missed this appointment after his ulcerated legs left him unable to get to the jobcentre.

Hunger, lack of funds and his inability to get to a local foodbank forced Mr Mulholland to take drastic action. He stole three packets of casserole steak, worth £12.50, from his local Sainsbury’s store.

This is a prime example of folk being forced into crime due to the draconian benefit sanctions that are used by the DWP. Maybe it is too much to ask for empathy in this day and age but, sadly instead of empathy, Mr Mulholland faced the full wrath of the English judiciary system and was sentenced to a 6 week jail-term for theft but due to previous convictions Mr Mulholland will face 14 weeks behind bars.

Full article at A Working Class Man.

Could Amputees Regrow Lost Limbs?

October 24, 2014

Amputees could one day re-grow their missing limbs, according to researchers at Imperial College London.

The 25-year, £60m programme, aims to explore the possibility of regenerating human tissue and eventually remove the need for prosthetic arms and legs.

Former England footballer Sir Bobby Charlton is the key fundraiser behind the project, as Tim Muffett reports.

Mum Shoplifted To Feed Family After ESA Stopped

October 24, 2014

BENEFIT sanctions have been dubbed as “pure evil” after a woman had to steal food and groceries to feed her family when her money was stopped.

Lucy Hill, of Westcott Road, Kidderminster, was caught taking chicken and washing powder from a Spar store on October 1, after first stealing more meat two days earlier.

The 35-year-old’s Employment Support Allowance had been sanctioned after she missed an appointment at the Job Centre and her defence solicitor, John Rogers, said it was “necessary that she committed this offence” for the good of her partner and their 18-month-old baby.

And now the public have rallied behind her agreeing they would have to steal as well in her position, with Kate Bennett from the Wyre Forest Citizen’s Advice Bureau saying sanctions are doing more harm than good.

“The whole idea of sanctions is to stop people from taking the Mickey, and that’s fine, but this is starting to get too much now and to be a punishment,” she said. “You can get a four-week sanction for a silly mistake or for being late and it might not be your fault, and they are sometimes counter productive, as you can see that some people shoplift as they haven’t got enough money to live on.”

ESA claimants in the work-related activity group, where an adviser assists them with training and skills, like Hill who was convicted of two counts of theft which she said was a result of the suspended payment at Kidderminster Magistrates’ Court on Thursday, October 16, are subject to sanctions. These are handed out for failing to attend a mandatory interview or failing to take part in a work-related activity.

In the district in the last 12 months, there has been a 30 per cent increase in the amount of people getting their benefits sanctioned.

“People who have tax payers’ money should do all they can and have to to get it but we should be helping people like this woman,” Ms Bennett said.

“It’s not just the job seekers that suffer from being sanctioned, it’s the families.”

On The Shuttle’s Facebook page, members of the public shared the same view.

Sue Longley said: “Sanctions are pure evil and should be outlawed completely.”

Sy Hawkes said he would do the same as Hill.

“I am in full support of anyone who needs to steal food because the Government has essentially taken away their right to live.

“How can they reasonably expect people to help themselves and be respected in society both by other people or employers when they are made to suffer. It’s no easy ride even when you do get benefits, but when they sanction those benefits it leaves people with no choice at all. You either have to beg, steal or borrow to stay alive or you commit crime after crime to put food in your belly.”

Another victim of a sanction was Bonnie Bullen who said she was sanctioned for two months after being five minutes late for an appointment, despite having to support three children.

The benefits sanctions system is set to be overhauled by the Department for Work and Pensions as it was revealed suspended payments have gone up 64 per cent across the country, and some claimants will be able to apply for hardship payments in place of sanctioned benefits.

Anyone experiencing sanctions should visit a local CAB or foodbank for help.

Business Disability Forum associates and members named on inaugural list of influential disabled people

October 24, 2014

A press release:

A number of Business Disability Forum (BDF) Associates and individuals from BDF Member and Partner organisations were recently named on the inaugural 2015 Power 100 List of Britain’s most influential people with a disability or impairment. The first of its kind to be published in Britain, the list includes 100 of the most powerful, influential and inspiring disabled people in Britain.

Phil Friend OBE, BDF Associate and CEO of Phil and Friends Ltd, was recognised for his work on disability and diversity projects across the globe, and his efforts in promoting disability awareness in the business sector.

Alice Maynard, Founding MD Future Inclusion Ltd and Chair of Scope, was mentioned for her work with major institutions to change society for the better. Her work within the rail industry contributed to making rail travel much easier for disabled people.

Dawn Milman-Hurst, CEO at Equal Approach, was recognised for using her HR background and expertise to set up the unique, inclusive recruitment agency Equal Approach.

Simon Minty, Director of Sminty, was ackowledged for establishing his disability and diversity training company through which he has consulted and trained numerous well-known and respected organisations.

Remploy CEO, Beth Carruthers, was commended for her work within the UK’s leading supplier of specialist recruitment services. Her work abroad was also mentioned, specifically her willingness to exchange disability employment knowledge through foreign visits.

Stephen Duckworth, Director of Disability Assessment Services at Capita, was recognised for his work in this role and as founder of research company Disability Matters.

Crossbench peer and disability rights campaigner, Baroness Jane Campbell, has gained recognition for her many years of parliamentary lobbying for disabled civil and human rights.

Under the Arts, Fashion & Design category, Dr David Bonnett is noted for pioneering many aspects of accessible design, advising on the implementation of Access standards and a design guide on the subject.

In the Media & Publishing sector, Geoff Adams-Spink is mentioned for his work as former Age and Disability Correspondent for the BBC. More recently Geoff’s own company, Adams-Spink Ltd, has been very active in the area of technological solutions for disabled people.

Vincent Neate, Partner at KPMG, was also acknowledged for his years of work with senior leaders in the private and public sector, where he has challenged thoughts around responsibility, resilience and longevity.

Mark Harper MP, Minister of State for Disabled People, commended the Power 100 List for acknowledging “an extraordinary range of disabled people and their achievements in all aspects of life, from education, politics and law through to sport and media”.

Susan Scott-Parker, Chief Executive and Founder of Business Disability Forum said:

“It’s wonderful to see so many Business Disability Forum associates and employees of member organisations represented on this list. This indicates the high level of thought leadership that can be found within our membership and among our associates and strategic alliances. Congratulations to all 100 people named on the list for their various contributions to business and society.”

 

Disability Hate Crime Convictions Drop, Finds CPS

October 23, 2014

Prosecutors have pledged to do more to tackle disability hate crime after a drop in the number of convictions.

The total number of hate crime convictions rose by over 1,000 in 2013/14, according a report by the Crown Prosecution Service (CPS).

But convictions for hate crimes against disabled people dropped, prompting the CPS to pledge fresh action.

Director of public prosecutions Alison Saunders acknowledged there was “more to do” to combat such crimes.

A hate crime is a crime committed against someone because of their disability, gender-identity, race, religion or belief, or their sexual orientation.

The overall hate crime conviction rate is part of an ongoing upward trend over the last six years, and almost 85% of hate crime prosecutions now result in a conviction.

Successful convictions for disability hate crime cases during 2013/14 increased from 77.2% to 81.9% – but the number of convictions fell over the year, from 494 to 470.

The report also found that:

  • There was an increase in the rate of decisions to charge for disability hate crime, from 72.4% to 80%
  • Of the 11,818 racially aggravated cases prosecuted last year, 85.2% resulted in convictions and 75.9% of those convictions led to guilty pleas
  • Some 550 cases involving religiously-aggravated hostility in 2013/14 were prosecuted and 84.2% resulted in a conviction
  • The conviction rate for homophobic and transphobic hate crime stood at 80.7% – the proportion of cases resulting in a guilty plea increased from 71.6% to 72.3% in 2013/2014, and there was an increase in the number of guilty pleas over the year from 785 to 819

This year, the Transgender Equality Management Guidance was issued to police along with specific guidance on flagging transphobic hate crime.

Ms Saunders said: “While I’m delighted to see a record high conviction rate and that the rate of cases we are charging is up to 80% from 72.4% last year, we will be working hard with the police to encourage more disability hate crime cases to be referred to us, and we will be really focusing on our handling of these cases through the court system.

“Hate crimes can be particularly devastating to victims who have been targeted simply because of their race, their religion, their sexuality, gender, disability or age.

“These crimes display an ugly element of our society and one which it is very important that police and prosecutors feel empowered to tackle so they can bring offenders to justice.”

‘Shocking’

Stephen Brookes, of the Disability Hate Crime Network, said action on the issue was “still miles away from where we should be” and that there had been a failure “at all levels” to give disabled people confidence in the judicial system.

“There is a new working party needed to look in some detail at aspects of reporting, charging and sentencing of disability hate crime, at a time when we have a wake up call to the whole criminal justice system to step up the need to increase the number of prosecutions to reflect the seriousness of attacking all disabled people.”

James Taylor, head of policy at charity Stonewall, said there was still “much work to do” on hate crimes.

“In the last three years alone 630,000 lesbian, gay and bisexual people have been the victim of a homophobic hate crime or incident.

“It’s shocking that in 2014, lesbian, gay and bisexual people still face violence and intimidation simply for who they are on our streets, in our communities and on our sports fields.”

Thousands With Degenerative Conditions Being Found Fit For Work

October 23, 2014

More than a third of people with degenerative conditions such as Parkinson’s and multiple sclerosis are having their benefits slashed because the Department for Work and Pensions deems they will recover enough to look for work.

Thousands of those with diseases that only worsen with time – and who have become too ill to work – are being denied full Employment Support Allowance. Instead they are assessed as suitable for work-related activity which is designed for people likely to recover to the point where they can seek employment.

People in The Work-Related Activity Group receive less money and the threat of sanctions if they do not attend regular sessions. Many also have this benefit removed after a year as an added “incentive” to find employment.

Steve Ford, Chief Executive at Parkinson’s UK, said: “These latest figures are an utter disgrace and serve to underline just how little the Government cares for those with progressive conditions like Parkinson’s. To set up a system which tells people who’ve had to give up work because of a debilitating, progressive condition that they’ll recover, is humiliating and nothing short of a farce.

“These nonsensical decisions are a prime example of how benefits assessors lack even the most basic levels of understanding of the conditions they are looking at.”

When people with illnesses and disabilities are assessed for ESA they are either paid full support, told they are fit to work or, if they are deemed likely to recover, put into a third Work-Related Activity Group to apply for jobs and prepare for the workplace.

Almost 8,000 people suffering from Multiple Sclerosis, Spinal Muscular Atrophy, Parkinson’s Disease, Cystic Fibrosis and Rheumatoid Arthritis have been put on this third, lesser benefit. Of these, 5,000 were put into the category despite assessors explicitly recognising on reports that their prospect of working is “unlikely in the longer term”.

The figures were released by the Government following a Freedom of Information request from a coalition of charities working with people with degenerative and progressive conditions.

Experts say the new data highlights just how poorly those living with progressive conditions are understood by benefits assessors. Atos healthcare has come under staunch criticism for the way it conducts the assessments and has pulled out early of a DWP contract to provide the service.

Over the last five years seven out of 10 new claimants with a progressive condition have been reassessed two or more times on the same claim, which health experts say causes unnecessary stress and anxiety for people who are already unwell.

Mr Ford said: “There can be no more excuses. Those who are severely unwell should not be subject to the ongoing indignity of repeated assessments. The Government must let common sense prevail and ensure that anyone living with a condition that can only get worse is automatically placed in the Support Group, and given the assistance they desperately need.”

The five charities behind the investigation – The MS Society, Parkinson’s UK, Motor Neurone Disease Association, the National Rheumatoid Arthritis Society and The Cystic Fibrosis Trust – are calling for people deemed unlikely to return to work in the longer term to be automatically placed in the support group.

Shadow Minister for Disabled People Kate Green said: “This worrying report suggests too many sick and disabled people aren’t being treated with the dignity and respect they deserve under the Tories. Labour has called for fundamental reform of Work Capability Assessment which isn’t working for thousands of sick and disabled people. We will look carefully at how the system of assessments works for people with degenerative conditions and ensure it treats them fairly.”

Between October 2008 and September last year, 7,800 people with degenerative conditions were put into the work-related activity group. Of these, 3,000 had multiple sclerosis, 800 had Parkinson’s, 3,800 had rheumatoid arthritis, 100 had motor neurone disease and 100 had cystic fibrosis.

Ailsa Bosworth, chief executive of the National Rheumatoid Arthritis Society, said: “To continue to regularly reassess claimants with progressive conditions, such as Rheumatoid Arthritis, is absurd and unnecessary. We know that most people with Rheumatoid Arthritis want to work for as long as they possibly can and will only claim ESA as a last resort.”

An Atos Healthcare spokeswoman said: “Our healthcare professionals are trained in the assessment of chronic and progressive conditions such as Parkinson’s and understand that, sadly, some people’s conditions will only get worse over time. In line with Employment and Support Allowance policy we are required to assess an individual’s level of function at the present time, rather than what may happen in the future.”

A DWP spokesman said: “It’s not fair to write someone off as unable to work if they are at the early stages of a progressive condition – and many people welcome support to prepare for work if they feel able to. If the effects of someone’s condition are considered severe enough based on their application and evidence, they will not be required to attend a face-to-face assessment. Our reforms support people into work where they are able, instead of writing them off.”

Case study

Chris Haigh, 57, from Southport, was diagnosed with Parkinson’s in 2005. His wife Karen, 54, says he was traumatised when he was told to look for work.

“We’d filled out a few forms and we were waiting for Chris to be called for a medical exam. But instead only two weeks after sending the forms off we got a call from DWP to say that Chris would be put in the Work Related Activity Group. I could physically see his whole body slump as the call went on. We were told his current benefit was going to stop in November and he would be reporting to the job centre to apply for work. How can you make a judgement about something that serious without seeing someone?

“Chris stopped working at the end of 2005 having been diagnosed with Parkinson’s earlier in the year. He had been self-employed repairing washing machines and tumble driers and had noticed the symptoms 18 months before he was diagnosed. The loss of dexterity made it impossible. I’ve watched his condition progress. He has mobility problems and can’t walk far and he suffers from a tremor internally as well as externally which makes him exhausted. He also has stiffness which means he sometimes can’t move at all and he’s on an awful lot of medication.”

“The person at Atos who did the assessment was a nurse, not even a doctor, and she claimed on the form to have met him before but she never had. We contacted our local MP and within 48 hours of him contacting DWP the decision was overturned. Someone from DWP even called to apologise for the two weeks he waited he was very unwell because anxiety and stress exacerbates the condition.

MPs To Launch Benefit Sanction Inquiry After 200000 Sign David Clapson Petition

October 23, 2014

MPs are set to hold an inquiry into benefit sanctions after 200,000 people signed a petition in the wake of an ex-soldier’s death.

More than 211,000 people signed a Change.org petition started by Gill Thompson calling for an inquiry into benefit sanctions after diabetic David Clapson, 59, was found dead in his home.

Gill’s three-month campaign called for an independent inquiry into benefit sanctions – which refers to occasions that money is withheld from claimants if they fail to meet the terms agreed.

The Work and Pensions cross-party select committee has now agreed and its inquiry into benefit sanctions is due to start early next year. It is expected to be completed shortly before the General Election in May.

Full story at Vox Political.

Lord Freud, Theresa, and the evil of workfare: The ‘fragile artifice’ of morality

October 22, 2014

Ann McGauran's avatarAnn McGauran

In a long essay in yesterday’s Guardian, John Gray notes that our leaders talk frequently about conquering the forces of evil – for example when Barak Obama vows to destroy ISIS’s ‘brand of evil’. But he believes that this rhetoric illuminates a failure to accept that cruelty and conflict are basic human traits.

John Gray’s essay – I urge you to read it here – refers us back to an ‘old-fashioned understanding’ that is ‘a central insight of western religion’, as well as Greek tragic drama and the work of the Roman historians  that ‘evil is a propensity to destructive and self-destructive behaviour that is humanly universal’.  He adds: ‘The restraints of morality exist to curb this innate human frailty; but morality is a fragile artifice that regularly breaks down. Dealing with evil requires an acceptance that it never goes away.’

His essay continues: ‘When large populations collude with repressive…

View original post 1,491 more words

Disabled Inmates At Oscar Pistorius’ Prison

October 22, 2014

Tell their stories of poor treatment.

UKIP’s new friends in Europe: “disabled shouldn’t be seen on television”

October 22, 2014

Tom Pride's avatarPride's Purge

(not satire – it’s the UKIP!)

Here are a few quotes from the Polish KNP party – UKIP’s new friends in Europe:

“Democracy is the stupidest form of government ever conceived.”

“Women are dumber than men and should not be allowed to vote”

“Evolution has ensured that women are not too intelligent”

“The general public should not see the disabled on television” (during the 2012 Summer Paralympics)

“The European Commission building should be turned into a brothel.”

“Gays are a gang of louts imported from abroad.”

And here you can see the leader of the KNP Party – Janusz Korwin-Mikke – clearly using the word ‘n*ggers‘ in the European parliament:

.

Well done Nigel. You’ve just confirmed once and for all every accusation there has ever been of racism, sexism and homophobia against UKIP.

But of course, Farage will get into bed with anyone if £1 million of European Parliament gravy train…

View original post 14 more words

Educating The East End: Final Episode Tomorrow On Autism Provision

October 22, 2014

Readers, I just thought I’d write a quick post to let you know that tomorrow’s final episode of Educating The East End will meet Christopher, a Year 10 student on the autistic spectrum, and explore the autism provision at Frederick Bremer School.

I’ll be watching it, at 9pm on Channel 4, with even more interest than usual.

Capita Equality Act Challenge

October 21, 2014

From Disability Rights UK.

Wolverhampton Welfare Rights are in the process of bringing a claim against Capita and the Department for work and Pension (DWP) for failures under the Equality Act regarding assessment centres

The challenge concerns cases where someone’s disability might suggest that they are unable to make the journey to a particular centre.

In one case someone with developmental and learning difficulties, first onset psychosis and resulting challenging behaviour was sent to an assessment centre which was 16 miles from their home. In this case a home visit should have been made.

Wolverhampton Welfare Rights is looking for examples of similar situations; where people are forced to travel long distances for assessment where their disability that might suggest a home visit was more appropriate, both in Capita and ATOS areas. You must say which area you are in – ATOS or Capita.

If you have an example of this happening elsewhere in the country please email Dan Manville; dan.manville@wolverhampton.gov.uk

– See more at: http://www.disabilityrightsuk.org/news/2014/october/capita-equality-act-challenge#sthash.jpuHVCRH.OKqfv2IL.dpuf

A Poster From The Government’s Benefit Fraud Campaign

October 21, 2014

I’ve just spotted one of the posters from the Government’s benefit fraud campaign on Facebook.

Photo: Are you committing benefit fraud? If your circumstances have changed and you haven’t updated your details then you need to let us know. It’s better to be safe than sorry. gov.uk/dotherightthing

Oscar Pistorius Sentencing: Twitter Reacts

October 21, 2014

https://twitter.com/JackofKent/status/524480442955608064

https://twitter.com/suzanne_moore/status/524480836083920898

Update: The BBC are reporting that the International Paralympic C ommittee will not allow Pistorius to compete again, even if he serves his full sentence. Personally, I’m pleased they’ve seen sense.

BREAKING NEWS: Oscar Pistorius Gets 5 Years Imprisonment

October 21, 2014

https://twitter.com/OscarTrial199/status/524477801970143233

 

https://twitter.com/OscarTrial199/status/524478401717886977

 

https://twitter.com/OscarTrial199/status/524478819718029313

 

https://twitter.com/OscarTrial199/status/524479244747804673

Cell Transplant Allows Paralysed Man To Walk Again

October 21, 2014

A paralysed man has been able to walk again after a pioneering therapy that involved transplanting cells from his nasal cavity into his spinal cord.

Darek Fidyka, who was paralysed from the chest down in a knife attack in 2010, can now walk using a frame.

The treatment, a world first, was carried out by surgeons in Poland in collaboration with scientists in London.

Details of the research are published in the journal Cell Transplantation.

BBC One’s Panorama programme had unique access to the project and spent a year charting the patient’s rehabilitation.

Darek Fidyka, 40, was paralysed after being stabbed repeatedly in the back in the 2010 attack.

He said walking again – with the support of a frame – was “an incredible feeling”, adding: “When you can’t feel almost half your body, you are helpless, but when it starts coming back it’s like you were born again.”

Prof Geoff Raisman, chair of neural regeneration at University College London’s Institute of Neurology, led the UK research team.

He said what had been achieved was “more impressive than man walking on the moon”.

The treatment used olfactory ensheathing cells (OECs) – specialist cells that form part of the sense of smell.

OECs act as pathway cells that enable nerve fibres in the olfactory system to be continually renewed.

In the first of two operations, surgeons removed one of the patient’s olfactory bulbs and grew the cells in culture.

Two weeks later they transplanted the OECs into the spinal cord, which had been cut through in the knife attack apart from a thin strip of scar tissue on the right. They had just a drop of material to work with – about 500,000 cells.

About 100 micro-injections of OECs were made above and below the injury.

Four thin strips of nerve tissue were taken from the patient’s ankle and placed across an 8mm (0.3in) gap on the left side of the cord.

The scientists believe the OECs provided a pathway to enable fibres above and below the injury to reconnect, using the nerve grafts to bridge the gap in the cord.

Before the treatment, Mr Fidyka had been paralysed for nearly two years and had shown no sign of recovery despite many months of intensive physiotherapy.

This programme of exercise – five hours per day, five days a week – has continued after the transplant at the Akron Neuro-Rehabilitation Center in Wroclaw.

Mr Fidyka first noticed that the treatment had been successful after about three months, when his left thigh began putting on muscle.

Six months after surgery, Mr Fidyka was able to take his first tentative steps along parallel bars, using leg braces and the support of a physiotherapist.

Two years after the treatment, he can now walk outside the rehabilitation centre using a frame.

He has also recovered some bladder and bowel sensation and sexual function.

Dr Pawel Tabakow, consultant neurosurgeon at Wroclaw University Hospital, who led the Polish research team, said: “It’s amazing to see how regeneration of the spinal cord, something that was thought impossible for many years, is becoming a reality.”

Mr Fidyka still tires quickly when walking, but said: “I think it’s realistic that one day I will become independent.

“What I have learned is that you must never give up but keep fighting, because some door will open in life.”

The groundbreaking research was supported by the Nicholls Spinal Injury Foundation (NSIF) and the UK Stem Cell Foundation.

NSIF was set up by chef David Nicholls after his son Daniel was paralysed from the arms down in a swimming accident in 2003.

To date the charity has given £1m to fund the research in London and a further £240,000 for the work in Poland.

The breakthrough

A key difference with Mr Fidyka was that the scientists were able use the patient’s olfactory bulb, which is the richest source of olfactory ensheathing cells.

This meant there was no danger of rejection, so no need for immunosuppressive drugs used in conventional transplants.

Most of the repair of Mr Fidyka’s spinal cord was done on the left side, where there was an 8mm gap.

He has since regained muscle mass and movement mostly on that side.

Scientists believe this is evidence that the recovery is due to regeneration, as signals from the brain controlling muscles in the left leg travel down the left side of the spinal cord.

MRI scans suggest that the gap in the cord has closed up following the treatment.

None of those involved in the research want to profit from it.

Prof Geoff Raisman said: “It would be my proudest boast if I could say that no patient had had to pay one penny for any of the information we have found.”

NSIF said if there were any patents arising, it would acquire them so as to make the technique freely available.

Mr Nicholls said: “When Dan had his accident I made him a promise that, one day, he would walk again. I set up the charity to raise funds purely for research into repairing the spinal cord. The results with Darek show we are making significant progress towards that goal.”

Prof Wagih El Masri said: “Although the clinical neurological recovery is to date modest, this intervention has resulted in findings of compelling scientific significance.”

The consultant spinal injuries surgeon, who has treated thousands of patients in the UK, added: “I have waited 40 years for something like this.”

All those involved in the research are keen not to raise false hopes in patients and stress that the success will need to be repeated to show definitively whether it can stimulate spinal cord regeneration.

The scientists hope to treat another 10 patients, in Poland and Britain over the coming years, although that will depend on the research receiving funding.

Dr Tabakow said: “Our team in Poland would be prepared to consider patients from anywhere in the world who are suitable for this therapy. They are likely to have had a knife wound injury where the spinal cord has been cleanly severed.

Sir Richard Sykes, chair of the UK Stem Cell Foundation, said: “The first patient is an inspirational and important step, which brings years of laboratory research towards the clinical testbed.”

“To fully develop future treatments that benefit the 3 million paralysed globally will need continued investment for wide scale clinical trials,”

Panorama’s To Walk Again is on Tuesday 21 October at 22:35 BST on BBC One.

Government Advertising Campaign To Target Benefit Fraud Across 50 Cities

October 21, 2014

A press release:

We’ve launched a major advertising campaign targeted at nearly 50 towns and cities across the country.

A range of television and radio adverts, posters, letters and Facebook ads will be used in each region to urge claimants to report changes in their circumstances or risk a jail sentence.

The advert displays a map pin icon landing on the region and tells claimants if their circumstances have changed to ‘call us to update your claim before we call you.’

Department for Work and Pensions Minister Mark Harper said:

We are giving benefit claimants every opportunity to tell us if their circumstances have changed, as the majority do. But those who cheat the system need to know we will use everything in our power to stop them stealing money from hardworking taxpayers, and that they could land themselves in jail when they’re caught.

Our fraud investigators have new and better methods of detecting benefit cheats so it’s becoming harder to hide and more difficult to escape punishment.

Area Fraud Investigator Jane Baker said:

What might seem like a white lie can quickly escalate into a serious case of fraud, with the claimant suddenly finding themselves owing thousands of pounds to the taxpayer and risking a prison sentence.

We’ve seen far too many people taking this road and regretting it later. So our message is to tell us about changes to your circumstances or be prepared for the consequences.

Ministers are highlighting the types of fraud that are hiking up the estimated £1.1 billion benefit fraud bill (2013/14), such as:

  • people who fail to tell us a partner has moved in
  • people who don’t notify us if there is more money coming in

The campaign also appeals to members of the public to call the benefit fraud hotline if they suspect someone is claiming benefits illegally. Calls to the hotline topped 150,000 in the last year, an average of more than 600 calls every working day.

Ministers have also announced that there is a new tool in the armoury for cracking down on benefit fraud, with the ability to now cross-check benefit claims against Real Time Information (RTI) on earnings and pension income from HMRC. Previously this data was submitted by employers annually, potentially resulting in thousands of pounds of overpayments before discovering fraud or an error.

In the last year the government recovered more than £1.3 billion in fraudulent payments. In addition to RTI, it has also introduced a raft of measures to counter benefit fraud, like:

  • introducing tough new rules so that 40% of individuals’ benefits can be taken to repay stolen cash – on top of any fine or custodial sentence handed out by the courts
  • increasing penalties that someone committing fraud can receive from £2,000 to £5,000, without taking them to court
  • using bailiffs to confiscate high-value possessions from convicted benefit fraudsters
  • continuing to roll out Universal Credit to more sites, which is expected to reduce fraud by £1 billion in 5 years when it is fully in place across the country
  • extending the loss of benefit for offences which result in a conviction of 13 weeks for a first offence, then 26 weeks for a second offence and 3 years for a third offence
  • issuing a new £50 civil penalty for claimants who negligently give incorrect information on their claim or fail to report a change in circumstances which results in an overpayment

Life After Uni For Three Disabled Graduates

October 21, 2014

BBC Ouch catches up with three disabled graduates to find out what they have been doing since leaving university.

Over the last decade, BBC Ouch has followed the progress of three disabled university students. They kept diaries on campus and we watched as they began a new stage in their education, and as they got to grips with living independently surrounded by new people.

So much sudden change can demand a lot of organisation and confidence, raising questions like: Will I be able to get around campus? Will other students include me? How will I employ and manage assistants or carers?

Below you can catch up with three of our students who have since graduated from university. How did it go? And, with almost 50% of disabled people unemployed, how are they doing in the jobs market several years later?

Do you have a story about life as a current or former disabled student you want to share? You can do it using #disabledstudents on social media, or get in contact using the details below.

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Darren Paskell

Darren Paskell is 29 and lives near Egham, Surrey. In 2004 he began at Keele University, where he was studying Computer Science and History. A bad virus in 2006 forced him to retake his second year and eventually he decided to move to a university in London to concentrate on computing. He went on to complete a further three years there and finished in 2010.

He says: “At the end I only came out with a diploma which still riles me.” He believes the course could have been made more accessible: “If you look at my marks they range from 7% to 79% and it’s clear which classes I had the best support in.” He praises one imaginative lecturer who created tactile maths graphs using metal chains that he could feel.

The proliferation of eBooks must now make studying easier for blind people, says Paskell, but back then he often found himself on the phone to publishers asking if they could send electronic versions from their office files. He can read them on his computer which has screen-reading software on it, but – often unable to get hold of any – he had no option but to make his own accessible versions. This meant he ended up spending 12 hours a week scanning books.

“It took two or three minutes per page on average,” he says and added that it proved unsustainable.

Paskell has spent a lot of time unemployed since his university days. Last year he became a part-time waiter at a London restaurant where diners eat in the dark and are served by blind staff.

“You’re more than a waiter there,” he says, “you’re their link with the outside world almost, people want to be reassured.”

However Paskell says he never would have chosen to become a waiter and still hopes for a job in IT. “I spent six years studying Information Technology and have been an expert user of PC systems for a decade and a half. But frankly I’d take anything.

“I probably wouldn’t make the best postman but I’d take absolutely anything.”

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Arunima Misra

Arunima Misra is 28 and lives in Islington, London. She’s a wheelchair user who also uses crutches due to paraparesis which makes her leg muscles weak. In 2004 she began a law degree at Cambridge University.

On her time there, she says: “I think my best years are yet to come but it was so much fun.”

She was at Peterhouse, the oldest college at the university, and was the first wheelchair-user in its 800-year history.

The university made adaptations on campus and and in Misra’s accommodation before she arrived.

She says her first year was hard as it took time to get used to living alone, and she didn’t venture out much. But she says she had no difficulties making friends who understood her disability.

“Once I made my needs known to those around me no one batted an eyelid,” she says. “Friends carried bags and did things like always holding parties in accessible venues.”

She now works for an investment bank after deciding that being a solicitor was not for her.

“I had Ally McBeal in mind when I entered the profession – endless banter and solving cases with the flick of my pen,” she laughs, admitting she didn’t appreciate the very long hours that those in commercial law have to work. Those hours were not easily compatible with managing her condition but she says the firms she worked for did well at trying to support her. Arunima says she would never want to put others off law.

“They can only do what they can do, and still meet the expectations of the customer,” she says.

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Charlotte Faragher

Charlotte Faragher is 23 and lives with her parents in Oldham, Greater Manchester. She has tetraplegia, meaning she is paralysed in her arms and legs. When BBC Ouch met her in 2009 she was beginning a Film Studies course at Lancaster.

Looking back, she says it was good being at a university of more than 12,000 people as the “odds were good” that she’d come across someone who didn’t see her “difference” as a problem.

But she says she still had to “size up” potential friends with care. Her limited mobility and “little” voice gets in the way of starting casual conversations, which means she has to make a real effort to approach and engage people.

“I would listen to what fellow students said in lectures, and work out if I’d be in tune with them before attempting to chat,” she says.

When she finished university she felt that there would be fewer job opportunities for her because of her disability. Not wanting to sit at home doing nothing she decided to do a masters, also at Lancaster.

Seeing friends move onto jobs at that time was difficult for her and she advises people should take a masters degree “only if you are completely out of other options.”

Since then she has completed a local course in mental health, become a youth rep on a local education committee, and is about to start befriending at an old people’s home nearby.

She says: “I want to be as effective a member of society as I can be in whatever form I can be. I don’t want to be looked at as a scrounger. I want to contribute and make something of myself, but how much I’ll be able to do remains to be seen, as it’s a new situation for everyone.

“I don’t know if at the end of it all I’ll end up getting a job because I think there might be too many barriers in the way, but I have self belief, I know I’ve got a lot to offer, and know I’d be a valuable employee.”

Deadline For Replacing ATOS For WCA Will Be Missed

October 20, 2014

Many thanks to Benefits And Work.

One of a collection of long overdue freedom of information requests received by Benefits and Work demonstrates that another of Iain Duncan Smith’s deadlines is unravelling before our eyes. The memo reveals that the new contractor delivering work capability assessments (WCAs) should already be in place and beginning to take over from Atos.

A memo headed ‘Atos Healthcare will no longer deliver Work Capability Assessments by 2015’ was sent out to DWP managers on 27 March 2014

The document explains that the Atos is to exit early from its contract to deliver WCAs, which was due to end in August 2015. The memo goes on to say that:

“The most effective way to stabilise and then increase delivery of Work Capability Assessments is to bring in one national provider to deliver the services. The plan is for the new contract to be awarded later this year. There will be a gradual transition from Atos to the new provider with a view to the new provider taking responsibility for delivery of Work Capability Assessments by 2015.”

However, that plan began to unravel as early as July of this year when the DWP realised that Atos owns all the hardware required to run the LiMA software used in WCAs.

As the Central Government Computing website revealed, the DWP were having to pay Atos an extra £10 million to carrying on running all the hardware for assessments for an additional year whilst a new IT provider is sought. The new contract runs into 2016 with options for it to continue right into 2020.

Meanwhile, however, there is still no sign of a company stepping in to carry out the actual face-to-face assessment. The possibility of Atos being fully replaced by the end of the year now seems very slim as another of IDS’ projects misses its deadline.

DPAC #SackFreud Protest- Watch Live

October 20, 2014

Four In Ten Disabled Children Living In Poverty, Finds Report

October 20, 2014

With many thanks to The Children’s Society.

Baroness Tanni Grey-Thompson recently led an inquiry – supported by us, Citizens Advice and Disability Rights UK – into the impact of the new Universal Credit benefit system on disabled people and their families.

The inquiry’s final report, Holes in the Safety Net: The impact of Universal Credit on disabled people and their families, summarises the findings from three research reports which are based on evidence from surveys of almost 3500 disabled people and a parliamentary evidence session. The report finds that several key groups of disabled people and their families will lose out financially under the new system.

The evidence from the inquiry suggests that reducing financial support could have a devastating impact on these groups. The report makes key policy recommendations to ensure that Universal Credit really supports all disabled people and their families.

The three research reports are:

The inquiry’s first report, Disability and Universal Credit, outlines a series of scenarios of the impact Universal Credit will have on disabled people and their families in different circumstances.

Four in every 10 disabled children are living in poverty

Our report 4 in Every 10: Disabled children living in poverty (summaryfull report), shows that 320,000 disabled children – far more than previously estimated – live in poverty in the UK than previously estimated. The Children’s Society warns that cuts in support for disabled children under the Universal Credit, as outlined in the Holes in the Safety Net inquiry report, threaten to push even more disabled children into poverty.

Labour To Call Commons Vote Over Freud Comments

October 20, 2014

Labour will force a Commons vote on Lord Freud’s future after David Cameron refused to dismiss him as welfare minister for his suggestion that some disabled workers are not worth the minimum wage.

The Conservative peer has been allowed to remain in his job after apologising for the comment, but Labour will table a motion of no confidence to be voted on later this month.

Separately, the Independent on Sunday reported that a second government minister had made contentious comments over the role of disabled people in the workplace. Andrew Selous, a justice minister, was said to have told a fringe meeting at the Tory party conference that “disabled people work harder because they’re grateful to have a job”.

Rachel Reeves, the shadow work and pensions secretary said the prime minister’s failure to act to remove Freud was astonishing. She said: “When the disgraceful and offensive views like this go unchallenged within the Conservative party it’s clear that mask has slipped and the nasty party is back. Labour will table a motion of no confidence in Lord Freud because we believe it’s completely unacceptable that David Cameron has failed to sack his minister for welfare reform.”

The shadow housing minister Emma Reynolds said it was “absolutely disgraceful” that Freud had not been removed from his post, and rejected the suggestion her party was playing politics with the saga. She told the BBC’s Sunday Politics: “I don’t think suggesting that disabled people, regardless of their disability, should be working for £2 an hour is acceptable.”

Andy Burnham, the shadow health secretary, said the implication of Freud’s comment was that “some people aren’t worth as much as others”. He disagreed with the suggestion that the peer had been talking about topping up wages with benefits as a way of getting more disabled people into the workplace.

He told Pienaar’s Politics on Radio 5: “This isn’t the first thing he has said … he is completely out of touch, this bloke.” He was referring to a comment last year that an increase in numbers of families using food banks was not necessarily linked to benefits sanctions or delays.

Last month Freud was recorded at a conference fringe meeting responding to a Tory councillor who suggested that people with mental health problems may be unable to work because employers were unwilling to pay them the statutory minimum.

He replied: “You make a really good point about the disabled … There is a group – and I know exactly who you mean – where actually, as you say, they’re not worth the full wage and actually I’m going to go and think about that particular issue, whether there is something we can do nationally, and without distorting the whole thing, which actually if someone wants to work for £2 an hour, and it’s working, can we actually …”

Cameron flatly disowned the peer’s remarks when questioned by the Labour leader, Ed Miliband, at prime minister’s questions, and later ordered Freud to apologise. Freud has since offered “a full and unreserved apology”, saying he was foolish to accept the premise of the question.

Freud said: “To be clear, all disabled people should be paid at least the minimum wage, without exception, and I accept that it is offensive to suggest anything else. I care passionately about disabled people. I am proud to have played a full part in a government that is fully committed to helping disabled people overcome the many barriers they face in finding employment.”

The vote on the motion of no confidence is expected to take place on 29 October during an opposition day debate.

Second Government Minister, Andrew Selous, Says ‘Disabled Work Harder Because They Are Grateful’

October 20, 2014

A second government minister made contentious comments over the disabled and their role in the workplace at the Conservative Party’s annual conference last month, The Independent on Sunday can reveal.

Andrew Selous, a Justice minister and former parliamentary aide to Work and Pensions Secretary Iain Duncan Smith, told a fringe meeting that “disabled people work harder because they’re grateful to have a job”.

His comments are revealed just days after David Cameron faced calls to sack Lord Freud as Welfare Reform minister after a recording emerged of him telling a separate fringe meeting that disabled people were “not worth” the full minimum wage. The IoS has learned that Labour will hold a vote of no confidence in Lord Freud, in the Commons. Labour will table the motion tomorrow and the vote will be on 29 October, the first available opportunity, when it has its opposition day debate. Labour sources said the pressure would be on the Lib Dems to back the motion after Nick Clegg said last week that Lord Freud’s comments were “deeply distressing and offensive”.

In a further development, David Blunkett, the blind former Cabinet minister, said people with his form of disability should be able to work on “equal terms”, after the journalist Tom Utley wrote that his father, the late Daily Telegraph journalist TE Utley, was happy to work for less money than his sighted colleagues.

Responding to Mr Utley’s article in the Daily Mail on the Lord Freud row, Mr Blunkett told The IoS: “I am very sorry that Tom Utley recalled his father’s situation in this particular dispute. He was always applauded for being able to work on equal terms and to use his remarkable memory… to do his job. It saddens me to have his memory diminished in this way.”

While Lord Freud apologised for his comments, supporters have insisted that he was discussing the idea, previously backed by Labour and some disability groups, for the Government to provide additional support to employers who take on disabled workers.

The emergence of a second minister’s comments risked adding fuel to the row. Mr Selous made the comments at a Centre for Social Justice fringe meeting, where he was speaking on the Government’s reforms to the criminal justice system. Tania Bassett and Dave Adams, two senior members of the Napo probation union, which opposes the reforms, were sitting in the front row.

Mr Adams said: “I was shocked. It was one of those moments where you think ‘did he really just say that?’.”

And Ms Bassett said: “There was a lot of muttering, like ‘I can’t believe he just said this’. He was talking about employment for offenders, suggesting that, like disabled people, they’ll work hard.”

Mr Selous defended his position last night. He said: “I was Iain Duncan Smith’s PPS [Parliamentary Private Secretary] for four years. My recollection is that the point I was making was the feedback I had… that employers are often very, very pleased with disabled employees; they work harder, they are loyal. These are good reasons to employ disabled people and offenders.”

Privately, disability rights campaigners are split over whether Mr Selous’ language was offensive or not, though most agreed that the word “grateful” was misjudged. A spokesman for Disability Rights UK said that case studies backed up Mr Selous’ views, pointing out that many disabled people are “pretty determined to do well”, but he added “it’s not necessarily about gratitude”.

But Kate Green, the shadow Disabilities minister, said: “These new comments about disabled people from another Tory minister show they just don’t get it… Many would love to work, but Tory policies are failing disabled people.”

On the Labour motion, shadow Work and Pensions Secretary Rachel Reeves said: “David Cameron’s failure to act after Lord Freud said that some disabled people are ‘not worth the full wage’ is astonishing… it’s clear the mask has slipped and the nasty party is back.

“Labour will table a motion of no confidence in Lord Freud because we believe it’s completely unacceptable that David Cameron has failed to sack his minister for Welfare Reform.”

Margarita, With A Straw: Review

October 18, 2014

What’s the first thing that comes into your mind when you hear the title Margarita, With A Straw? Alcohol? A cocktail? A bar?

So what would you say, readers, if I told you that this is the title of a Hindi movie about disability?

The lead character is a university student called Laila, who has severe Cerebral Palsy. Laila lives in Delhi with her loving family and attends Delhi University. This movie is the story of her life- but most importantly it is the story of her loves.

She has a close male friend who, just like her, is a wheelchair user. He is in love with her, but she breaks his heart when she meets a non-disabled musician- who later breaks her heart.

And this is the point when the movie really starts tackling sensitive subjects. It has several sensitive themes, each tackled as well as the last.

Heartbroken and embarrassed after making a fool of herself with a boy who doesn’t love her, Laila leaves Delhi University and enrols on a Creative Writing course at NYU. Here she meets a blind student activist, Khanum, who is half Pakistani, half Bangladeshi- but, surprisingly for a movie mostly set in India, that’s not the problem.

Khanum teaches Laila several things about herself. Early on, she encourages her to try alcohol for the first time. Her choice? Margarita, with a straw.

Later, Khanum reveals that she is gay, and the young women begin a very serious, special same-sex relationship. However, Laila remains bisexual, and once cheats on Khanum with a boy. Never afraid to say the wrong thing, at this point Laila says just about the most hurtful thing possible- when asked for a reason, she says it happened because he could see her.

A movie with a severely disabled main character can never completely ignore disability, and this one doesn’t ever try. So as well as facing all the same issues as any other young adult, Laila faces issues that I, as a person disabled since birth, recognised instantly. Although she loves her mother deeply, Laila longs for her own independence, and for some privacy. The mother and daughter have their first real fight when Laila’s secret stash of porn websites is accidentally discovered!

Towards the end of the movie, Laila has to face yet another challenge, when her mother is diagnosed with cancer. As many adult children would do, at the end of her mother’s life Laila takes on the role of carer.

The script, throughout, has a great sensitivity to disability. It never shows disabled people as perfect, but only as real people. For this, writer and director Shonali Bose must be thanked.

The only negative thing that could be said about this movie is that the two lead actresses do not share their characters’ disabilities. However, they both play their roles to perfection. Perhaps disabled actors for disabled roles is the next step that Indian cinema needs to take- but this movie is proof that when it comes to tackling disability issues well, that is the only step that Indian cinema has left.

Daily JSA Sign On: Part Of ‘Help To Work?’

October 17, 2014

This is a report about having to sign on every day for jobseekers’ allowance – an entirely pointless “process” that seems to be taking hold:

On Wednesday, the Kilburn Unemployed Workers’ Group and I went to talk with JSA claimants at the North Kensington jobcentre.

Almost as soon as we got there, people brought a significant fact to our attention: the North Kensington jobcentre appears to have instigated a daily JSA sign on regime for some people. Daily sign on does, or at least is, pretty much what it says on the tin – it means that people must present themselves at their local jobcentre every single day of the week and sit and wait until they see an adviser for a brief time. Their attendance is noted and there’s a (very) quick catchup about people’s jobsearches. And that’s it.

Daily sign on was one of the platforms government’s ironically-named Help To Work platforms. The Help To Work scheme was launched in April to much fanfare (by government) and consternation (by reasonable people). I wonder if we’re seeing evidence now that it is underway, after a fashion. We’re certainly seeing evidence that people were right to dread it. The daily sign on exercise is nasty and utterly pointless – certainly as far as helping people into work goes. The three people who I talk about in this article reported that absolutely nothing happens at their daily signon appointments. I think we’ll say that again – absolutely nothing happens. JSA claimants must turn up at their jobcentre and have their attendance noted. One person reported a quick chat and check with a jobcentre adviser about jobs applied for – “and that’s ridiculous, because they can check everything that I am doing online,” he said. “They forced us to use [Universal] Jobmatch, so they can check everything already.”

Full story at Kate Belgrave.

Accessibility in the City: How Does Delhi Compare to London?

October 17, 2014

This is a guest post by Pano Savvidis. Thanks to Pano.

Delhi is slowly becoming a more and more accessible place for those with mobility issues. Over the last few years, various steps have been taken to make Delhi barrier free and more accessible for the elderly and disabled. But how does it compare to other capital cities, namely London?

Transport

There is a range of different types of transport in both London and Delhi.

London’s transport includes the Tube, buses, overground trains, the DLR, taxis, trams and, now, the cable car. The Tube is supposed to make travelling around London easy, but if you have mobility problems it can be very difficult, especially when it’s very busy. There are only certain stations that are step free, and on top of this, there is generally a gap between the platform and the train. So, although you might imagine London to be more accessible, the Tube itself is probably not the best option for an individual in a wheelchair. London buses are much easier, as all 8,500 are low floor vehicles, and they also have a retractable ramp. For wheelchair users they are free to travel on too. All the back cabs in London are wheelchair accessible, and many more private cab companies offer wheelchair accessible cars too, so all in all, the accessibility of London for wheelchair users is relatively good. While the buses and taxis are good, the Tube has a lot of catching up to do.

Delhi’s public transport comprises of the Metro rail, buses and auto-rickshaws. Buses are the most popular means of transport in Delhi. The DTC buses, or the Delhi Transport Corporation, are low floor vehicles with a manual ramp, just as London’s buses are. And, like London buses, they can become crowded and therefore difficult for wheelchair users. The Metro Rail is very accessible to wheelchair users, with lifts, low height counters, level platform entry, wider doors and lots of space for wheelchair parking. Auto rickshaws are great for taking you to exactly where you want to be, unlike buses that only take you to designated places. So if you’re willing to be handled to transfer into the back of the rickshaw, and your wheelchair is foldable, then an auto rickshaw can often be one of the best ways to travel as an individual with mobility problems. In Bangalore, a local start up providing taxi services to the city’s physically disabled offers hope that there may be something similar in Delhi soon, so elderly citizens and wheelchair users can get around very easily.

Looking at this objectively, it seems that Delhi is on a par, if not more so, with London in terms of its transport’s accessibility. London and Delhi both have room for improvement, however.

Landmarks and Sightseeing

Both cities are hugely tourist driven, and as more and more wheelchair users are gaining confidence to travel, it’s hugely important that those with mobility issues are catered for.

Delhi has many incredible places to see, and with lots of paved streets and ramps instead of steps, they are mostly easily accessible by wheelchair.

The Dilli Haat is a traditional rural haat, or village market, selling crafts, food with cultural activity, but with no barriers. There are ramps with railings throughout the market and ticket counters have been lowered.

The National Zoological Park is a huge zoo spread over 214 acres and is regarded as one of the finest zoos in Asia, but it is only partly accessible. As the park strives to give its animals a habitat that very closely resembles their natural habitat, the park may not suitable for wheelchairs in some areas.

The Lotus Temple is one of the most incredible architectures of Bahai faith. Made of marble, cement, dolomite and sand, it looks like a huge lotus flower. However, despite the fact that there are no restrictions for visitors, it is only partly accessible for the disabled.

London’s attractions, however, are much more accessible. Buckingham Palace, for instance, offers level access, lifts, and free-of-charge wheelchairs. The Natural History Museum, too, has a whole range of accessible facilities so you can see most, if not all of the exhibits even if you have mobility problems.

So, in comparison, Delhi has a long way to come before it meets London in this respect.

If Delhi continues on the path it is on with regards to accessibility, it may yet be on a par with one of Europe’s most wheelchair accessible cities.

A Letter A Day To No 10: No 886- Jackie Doyle-Price

October 17, 2014

As Keith Ordinary Guy always says, shares are encouraged and welcomed.

London Tesco Refuses Blind Woman’s Guide Dog

October 17, 2014

This is not the first time Tesco have done something like this, readers.

A blind student was left in tears when she was refused service in a Tesco supermarket – for bringing her guide dog inside.

Maya Makri, a student at London’s Central School of Speech and Drama, was buying groceries at the supermarket in Belsize Road near Swiss Cottage on Monday.

But when she approached the checkout with her friend and her dog, a cashier shouted “pets are not allowed”.

Despite the obvious high-viz guide-dog jacket worn by the black Labrador, named Jemma, Ms Makri said staff would not acknowledge the animal was not a pet.

The other two cashiers apparently joined in and said there were “no exceptions”, before being told she could stay for the time being but could not return to the store in future.

Ms Makri, 39, said: “I pointed out that this was no pet, but a guide dog. This should have been immediately obvious from the dog’s high-viz harness and fluorescent guide dog label on the lead.

She added: “I repeatedly said that I was registered blind and that this was a trained assistance dog, to no avail.

 “Various customers tried to back me up, but we were shouted down. I burst into tears outside the store in sheer frustration.

“A woman followed me all the way to South Hampstead station, just to say how terribly upset she was about what she had just witnessed and that this had to be challenged.”

Ms Makri, who previously worked as a conference interpreter and at the University of Leeds, said it was the latest in a series of difficulties she has faced since moving to the capital to study 10 years ago.

She also struggled to join her local gym and has been refused access to restaurants because of the dog.

Ms Makri, of Queen’s Park, said Jemma, who has been in her care for six years, helps her become an “active member of society” and has been a lifeline since moving to London.

She added: “I went up to Leeds to do some teaching at the university yesterday and I truly dreaded coming back to London. This is not what I expected from our metropolis.”

A Tesco spokesman said: “This clearly should never have happened and we will contact Ms Makri directly to apologise. We do allow guide dogs in stores and have reminded colleagues of that. We also offer customers with guide dogs help with their shopping, if they would like assistance.”

Last year a report released by charity Guide Dogs found people with guide dogs were increasingly being refused access to shops, transport, cafes and other venues. The charity said they were receiving more complaints from blind people struggling to access venues.

 

Freud Row Councillor David Scott Rents Rooms To People With LD

October 16, 2014

Many thanks to Benefits And Work.

 

The councillor at the centre of the row over David Freud’s comments about disabled people and the minimum wage owns a property in Tunbridge Wells, which he rents to people with learning disabilities via a charity. He receives housing benefit payments from the local authority.

At the Conservative party conference, Councillor David Scott told Lord Freud:

“The other area I’m really concerned about is obviously the disabled. I have a number of mentally damaged individuals, who to be quite frank aren’t worth the minimum wage, but want to work. And we have been trying to support them in work, but you can’t find people who are willing to pay the minimum wage.

“We had a young man who was keen to do gardening; now the only way we managed to get him to work was actually setting up a company for him, because as a director in a company we didn’t have to pay the minimum wage, we could actually give him the earnings from that.”

Councillor Scott, along with his partner, is the director of or has an interest in several limited companies. They also own several properties in Tunbridge Wells.

One of these properties is a house in Cadogan Gardens, known as Scott Properties, of which Councillor Scott is both the joint owner and landlord.

According to Zoopla, the average value of a property in Cadogan Gardens is over half a million pounds.

Rooms in the house are ‘Rented to disabled persons directly or through Pepenbury, a registered charity.’

According to their website, Pepenbury:

“. . . provides high quality care and support for adults with a learning disability and complex needs, some of the most vulnerable people in society. We give them choice and control over how they live their lives and believe that every individual has the right to live an independent and rewarding life, whilst feeling safe and supported.”

Councillor Scott told Benefits and Work that the young man he told David Freud about has never lived at Cadogan Gardens, has never worked at any property owned by Councillor Scott and has also not worked at any property connected with Pepenbury.

Councillor Scott has also talked to his local newspaper about the issue, saying:

“If you have got some gardening work to be done you won’t pay someone for four hours when you could pay someone else for half an hour to do it. If you have a lawn in the garden and you employ a person who is doing it with support from somebody else there, you know you can employ them and it could cost you £10 to do it.

“If this person is going to take four hours to do that, would you be willing to pay £40? If you do not give them £40 you are not paying them minimum wage.”

When asked who the ‘we’ referred to in his discussion with Lord Freud was, Councillor Scott told us that it was:

“People working with my daughter when she was alive.”

Benefits and Work also contacted Pepenbury for a statement about whether the young man was one of their service users, but we have not yet received a response.

Jackie Doyle-Price Backs Lord Freud

October 16, 2014

People in power should not reveal outdated opinions in public places. Twitter has become a very public place. End of.

A Letter A Day To No 10- No 885: Lord Freud

October 16, 2014

As Keith Ordinary Guy always says, shares are encouraged and welcomed.

A Simple Question To David Cameron On Lord Freud

October 16, 2014

Readers, I’ve just Tweeted a simple question to David Cameron on Lord Freud.

There is no doubt in my mind of the answer to the question. None.

So why, at time of posting, is Lord Freud still a minister?

ESA Stats Rise For Fourth Quarter Running

October 15, 2014

With many thanks to Benefits And Work.

The number of people in receipt of employment and support allowance (ESA) and incapacity benefit (IB) has risen for the fourth quarter in a row, according to DWP statistics released today. At current rates of increase there will be more claimants in receipt of ESA and IB by the next election than there were when IDS took over. It also means that the enormous suffering caused by the massive IB to ESA transfer programme has so far reduced the clamant count by just 2.5%, a drop of only 70,000 out of over 2.5 million.

The latest ESA estimates by the DWP reveal that the number of people in receipt of ESA and IB rose to 2,515,000 in August 2014, the highest number of awards since August 2012.

In just the last three months, awards have increased by 35,000.

At current rates of increase this means that by May 2015 the number of claimants receiving ESA and IB will stand at 2.62 million, which is higher than the 2.61 million claimants when IDS took over the DWP in May 2010. The current trend reverses a long-term fall in the number of sickness benefits claimants.

It also means that in spite of the hundreds of millions of pounds spent on moving claimants off IB and onto ESA, the claimant count has dropped by just 2.5% since migration began.

A pilot involving 1,700 claimants being moved off IB and onto ESA began in October 2010, but migration proper did not begin until February 2011, when the claimant count was 2.58 million. It is now 2.51 million.

A massive amount of distress, hardship and worsening of health conditions has been caused by the IB to ESA transfer, which is far behind schedule and still not quite completed. It now looks as though all that suffering will have had absolutely no effect on the number of IB and ESA claimants, but will have enriched private sector companies by many tens of millions of pounds.  If his success in cutting the benefits bill and helping the sick and disabled back into work is what IDS wishes to be judged by, then it seems likely that he will be judged very harshly indeed.

The latest DWP monthly statistics can be downloaded from this link.

Salford Couple Must Pay Deaf ‘Cellar Slave’ £100K

October 15, 2014

A millionaire couple who kept a girl from Pakistan as a slave in their Salford home have been ordered to pay her £100,000 in compensation.

Ilyas and Tallat Ashar were jailed last October after the girl was found in their cellar in 2009.

Now in her 20s, the woman, who is deaf, was repeatedly raped and forced to work at the family’s many properties.

Manchester Crown Court ruled the couple must also repay more than £40,000 of benefits falsely claimed in her name.

It is believed to be the first time the Proceeds of Crime Act has been used in a case of modern slavery.

The Ashars must also pay £321,000 towards the cost of their court trials.

Money laundering

Now in her 20s, the victim, who cannot be named, is believed to have been as young as 10 when she was trafficked into the UK.

She was found sleeping in a cot bed in the Ashars’ cellar by trading standards staff, who were investigating allegations of money laundering.

Police said the victim’s details were used on bank accounts linked to the couple.

But when officers tried to speak to her at the house, they realised she was incapable of communication and moved her to a place of safety.

Police said she could not read or write and accepted the benefit fraud was carried out by the Ashars.

The victim had to learn a form of sign language to give evidence at the trial last year, when her progress was compared to “a butterfly coming out of a chrysalis”.

She is now living independently and has improved her sign language skills, said police.

Lord Freud Urged To Resign For Saying Disabled People ‘Not Worth’ Minimum Wage

October 15, 2014

Huffington Post reports on this shocking statement by Lord Freud, which was apparently made at the Tory Party Conference.

Readers, I wrote a long post here in 2011 when Tory MP Philip Davies made similar comments.

My views on suggestions that we don’t deserve the minimum wage are still, now, what they were then. I would not like to repeat myself at this site, so I’ve simply linked to the old post.

I have little else to add except that people in power should keep outdated, insulting opinions to themselves.

I would deeply love to see Lord Freud resign over these remarks. In fact, if David Cameron really wants to distance himself from the remarks, he should sack Freud as a minister.

Update: I am hearing that Freud has formally apologised for his comments. But readers, it’s not enough. He has too much power for an apology to be enough. He should resign or be sacked.

Update 7pm: There is a petition to David Cameron calling for Freud to be sacked.

 

400,000 ESA Claims Disappear From Stats

October 15, 2014

Dr Greg Wood posted this last Tuesday. I hope you’ll agree with me, readers, that this is one of those times when old is gold.

The old men of Caxton House might seem unworldly, but they know how to pull off a conjuring trick: they’ve made 400,000 claims vanish into thin air.

The Atos bottleneck has led to a huge number of jobless people getting stuck in welfare limbo (or “limboland” as IDS said in the House the other day). They wait…and wait…and wait for their ESA claims to be assessed.

In the meantime, how does the DWP classify them, in its official stats?

  • JSA claimants?
  • Unemployed?
  • ESA recipients?
  • Employees?

Answer: none of the above.
They aren’t recorded anywhere in the data fed to the press.

SHAZAM! The number of people claiming out-of-work benefits has fallen by 400,000!

As if by magic, job centre performance has improved too! Double bubble!
This legerdemain is actually a boon to JSA claimants being hassled to find jobs that don’t exist or they will never get. With a sick-note from their GP, they can disappear from the job centre roll faster than the staff there can wave a blank ESA50. These former JSA claimants will then be put on ‘assessment rate’ ESA – they’ll be paid at the same rate as JSA, but they won’t be expected to look for work and can’t be sanctioned until their fitness-for-work test comes around.

A blessing and a curse
Sadly, this hocus-pocus is not good news for everyone. The people who lose out are those who have a strong claim to sickness benefit. While they wait for a WCA, they will be forced to get by on less than their full entitlement.
Here’s the kicker: even when the claimant has a strong case, she might nevertheless wait so long that she has recovered from her illness or injury by the date of her WCA, at which point she will be assessed as being fully fit for work – and won’t get a single penny!

How’s that for smoke and mirrors?

Scheme Helps Disabled People Enter Local Politics

October 15, 2014

When prospective councillor Tom Garrod went door-to-door canvassing aged just 18, his first experience did nothing to calm his nerves. He asked to speak to the householder; “I was told they had passed away yesterday,” he says.

But it was only a minor setback for Garrod. Living with cerebral palsy, he also had to be creative to get his message across. As the condition alters his speech, he had to abandon telephone canvassing. “People thought it was a prank caller,” he laughs. But he made up for it by making good use of his digital savvy, spreading his ideas through social media – something he says older councillors weren’t able to do so easily.

The young Conservative was elected to Norfolk county council, in 2009. Now aged 25, Garrod’s experiences have helped shape a new scheme aimed at encouraging more people with disabilities to become councillors.

The scheme is part of the Local Government Association’s “be a councillor” campaign to widen the diversity and number of new councillors.

“We do struggle to get good quality councillors,” says Gary Porter, leader of South Holland district council and vice-chair of the Local Government Association (LGA), who mentored Garrod through his early years as a councillor.

“There are about 11 million people who are disabled in one way or another and we’re just not getting enough of those people coming forward. Most of them have to deal with challenges in their own personal lives that make them pretty strong characters.”

In 2010, a parliamentary report into political representation identified barriers to disabled people becoming elected representatives, including the cost of services, such as interpretation or mobility aids that would be required for candidates to do their job. In response, a central government scheme, Access to Elected Office, was set up in 2012 to provide grants to cover the additional costs for disabled candidates.

But the LGA saw there was still a gap: often potential candidates didn’t know where to turn or who to ask if they wanted to get involved in politics. So in February, it set up the pilot scheme, which provides mentoring for future candidates with disabilities and taps into Access to Elected Office funding to provide support grants of between £250 and £40,000to spend on anything that might help break down barriers to disabled people seeking local office.

Candidates are identified by the LGA’s political party groups, and go through a competitive process to secure their place. “We’re looking for people who have an interest in local government,” says Nan Sloane, a diversity expert hired by the LGA’s Labour group to search for its prospective councillors. In total, 20 will be selected before the 2015 local elections, split across the parties. They are then assigned a mentor from their party (or, in the case of smaller parties, from the LGA independent group).

One of the first to be signed up is 29-year-old social entrepreneur Susanne Rees, a prospective candidate for the Green party in Northampton. Diagnosed at 19 with a genetic condition that causes tumours to grow on her central nervous system, it is the 10 years she has spent being supported by the NHS that drives her political ambitions.

“I’m turning 30 next year so I’m still really young, but I’ve got a lot of life experience. Almost every single public service you can think of I’ve had experience of,” she says. “I’m very concerned about the future of the NHS. It’s being torn to pieces at the moment. I really owe my life 10 times over to the NHS.

“One of the biggest things for me was to see how out of touch the government is with those people who are on the grassroots side and I think that’s what fuels me the most. I see a lot in the power of localism and that’s really what drove me to go and explore politics at a community level,” she says.

Rees set up the social enterprise iDID Adventure to change the way physiotherapy is delivered to young people, using exciting sports such as rock climbing to rebuild muscle and improve movement. “It came from my experience of physiotherapy when I was younger. It was crap because I was 19 and everybody else was in their 60s and 70s. I felt too well to be there,” she explains.

A former Liberal Democrat, she became interested in the Green party last year as she looked for a new political home that aligned with her values. “A lot of my philosophy of life is about social equality. I was one of those who was really disillusioned by the coalition.”

Five years ago, Rees lost her hearing. She will spend her grant money on an interpreter. “I think the biggest barrier for me is to do with my confidence,” she says. “Whilst I am actually quite good at lip reading, after an hour lip reading someone you don’t know very well you need a kip. Communication support is absolutely vital. It makes me be the best I can be for the role.”

She adds: “If you have a disability, and there are barriers you’re going to face, [politics] looks volatile and it looks scary, so psychologically it’s not accessible – especially if you’re not somebody who has a family in politics.”

Her mentor is Ray Morgan, an independent councillor at the London borough of Havering, who has been in office for 12 years. “As with any role you come into, you need somebody to show you the ropes and give you a helping hand,” he says. “Hopefully I’ve got quite a lot of experience that I can impart. We need the diversity of different people so they can truly reflect the local community.”

Each candidate’s disability and their needs will be different, and Garrod, who advised the LGA on the mentoring scheme, stresses the need for flexibility about the size of the grant and what it is spent on, be it taxi transport, speech therapy or confidence training. “I said [to the LGA], I can tell you what I need, but let’s not design the whole scheme on that. The best person to ask is the candidate who’s applying.”

He also says it’s important that the candidates aren’t pigeonholed by their disabilities once they are elected.

“I came into politics because I care about the community, not because I’m disabled,” he says. As deputy cabinet member for children’s services, Garrod became involved in a project around special educational needs. “One of my fellow councillors said, ‘Tom, this is the perfect thing for you’. I said, ‘why is that? I don’t know what it’s like to be autistic or have Down’s syndrome’,” he explains. “I haven’t got a monopoly on knowledge about disability.”

Rees has no worries about facing a public who she admits can have unsavoury ideas about disabled people. “I’m quite confident to go out there and show people that this is me. I think that’s what’s great about schemes like this – it puts disability out there. Disability is still misunderstood and that’s why we still have these attitudes in society.”

ATOS And Capita Have Employed More Staff To Increase PIP Assessments

October 14, 2014

Welfare Weekly reports on the latest edition of the DWP staff magaine, Touchbase:

Touchbase also reveals that Atos and Capita have employed more staff to increase the number of assessments they do for the new disability benefit, Personal Independence Payment (PIP).

The reports used by assessors have also been improved, claim the DWP, and changes have been made to the PIP IT system. DWP say that PIP decision-makers have doubled their output since April 2014.

They also claim that disabled people will not have to wait more than 16 weeks for a PIP assessment by the end of 2014.

The news comes after charities and politicians raised concerns over a growing PIP assessment backlog.

Call The Midwife Actress Sarah Gordy Now Playing A Non Disabled Character

October 14, 2014

In a new play, Crocodiles, in Manchester. Guardian Professional have interviewed her today.

Wheelchair Accessibility in London: Present And Future

October 14, 2014

This is a guest post by Pano Savvidis. Thanks to Pano.

Although London is special for all manner of reasons, one of the most important ones is that it is one of the most widely accepting and forward thinking places on the planet. Although this might not mean much to many people in practical terms, for people in wheelchairs, it is a practical matter that holds a great significance.

So what’s it like trying to get from point A to point B in London on a wheelchair accessibility front? In this article, we’re going to look at the huge progress London is making in terms of wheelchair accessibility, and look at how future emerging technologies – some of which that are launched, nearly ready to launch or far off in the distant future – are making getting around in a wheelchair easier than you’d expect in England’s Capital.

The Forward Thinking Nature of London

Although it’s not quit there yet, London is on the verge of becoming a megacity. With 8 million residents, the city is by far and away the largest in the UK, and with more and more people moving there each year to get a slice of the action, it’s clear that the current levels of growth are only the start of things to come.

But what is life like for those with extra accessibility requirements in this large city? At the moment, London is one of the UK’s most accessibility friendly places to live, but it could be doing a lot more to make people feel welcome. For example, not all tube stations have step-free access, and this makes getting around on the underground a hassle for those in wheelchairs who desire to use the service.

Along similar lines (but not travel-related), housing in the capital – as we all know – is difficult at the moment. Prices for lets are high even for able-bodied people, but when you add on to the regular average letting price the prices for so-called accessible housing in the capital, the price becomes a huge barrier.

All in all though London does more than most other cities to try to make the lives of wheelchair users as easy as they can with the limited financial resources the government has.

The Future of Accessibility in the Capital

Going forward, the London is going to up its game with respect to the ease of which a wheelchair user can move from point A to point B around the capital, and there are several projects in the works which will help it to do so.

First, transportation methods that are already well-established and popular in the capital – such as taxis – will all move towards accessibility-friendly taxi models from firms such as this one. The same goes for the tubes, too, and with more and more rail and tube stations being built across London and the wider southeast, step-free access and full accessibility should be the norm.

Looking further ahead into the future, driverless cars are almost ready to go, and the British government has already announced that they will be legal on the roads from January 2015. These will make getting across the capital even easier than it is now.

Ultimately, London is a forward thinking place that tries to cater to those with accessibility needs, but more needs to be do to achieve full equality and easy accessibility. Hopefully, some of the emerging technologies of the future should resolve this.

Sir Walter Scott Celebrated In Braille

October 14, 2014

A press release:

Two great anniversaries are being marked in Edinburgh today (14 October) with the launch of a new book amidst a sea of words in Waverley Railway Station.

The Great Scott! campaign, developed by Edinburgh UNESCO City of Literature Trust, aims not only to celebrate the 200th anniversary of the publication of Waverley by Sir Walter Scott, but also marks the 10th anniversary of Edinburgh’s designation as the world’s first UNESCO City of Literature.

Quotes from Sir Walter’s books and his thoughts will be written across the floors, windows and walkways of Waverley railway station and collected in a free book called Great Scott!: Celebrating Sir Walter Scott.

As part of the campaign to bring alive the man and his words, 25,000 copies of ‘Great Scott!’ will be given away in the station and, thanks to the Scottish Braille Press, the book will also be available in Braille and audio formats.

Telling the story of Scott’s incredible life, the pocket-book includes a timeline, quotes and musings, and gives tips on things to see, read and do relating to Scott. It is available in Waverley Station in October, online in audio, and as an e-book at www.cityofliterature.com/waverley.

John Donaldson, Manager at the Scottish Braille Press, said: “The 6-dot Braille system was invented in 1824, just 10 years after Scott’s Waverley was published. It is a fitting part of its 200th anniversary that we can make ‘Great Scott!’ accessible to blind and partially sighted people.

“The Scottish Braille Press transcribes documents in Braille, large print and audio for businesses, the public sector, charities and individuals and we are delighted to have worked with City of Literature and Lothiansound to produce Great Scott! in Braille and audio formats.”

Ali Bowden, Director of the Edinburgh UNESCO City of Literature Trust, said: “As a City of Literature we want to see books, words and ideas celebrated as widely as possible. Most people know about Scott but they might not know his books and we hope this campaign helps people discover the man and his words.”

Janelle Scotland from Lothiansound said: “Lothiansound Talking Newspaper has been pleased to work with the Scottish Braille Press and Edinburgh City of Literature in the production of this informative and entertaining book.”

For more information please contact:

Frances Chisholm, Fundraising & Marketing Assistant, Royal Blind

Tel: 0131 229 1456 Email: frances.chisholm@royalblind.org

Video Games For Blind Players

October 14, 2014

From yesterday’s Guardian.

Super Mario 64 (Nintendo 64, 1996) is commonly held to be one of the best games of all time, but it has more than its then-innovative 3D worlds to recommend it – it can also be played by the blind.

“There were all these musical cues and cues in the sound design,” says Kevin Satizabal, a keen gamer who’s been blind since birth. “You could tell when you’d picked up a star, or when the player was jumping, or when you picked up coins.” When you can’t rely on visual cues, having a different audio cue for each event in the game is more than just a bonus.

“Fighting games are a perfect example,” says accessibility specialist Ian Hamilton. Through learning the audio cues for each move, vision-impaired players have been able to master them. One, Brice Mellen, even beat the creator of Mortal Kombat at his own game.

One genre takes this principle of great sound design to another level, reducing or removing the visual elements to create games playable only by ear. Audio games have been around for a while – Satizabal mentions GMA Tank Commander and Shades of Doom, both of which came out more than a decade ago – but they are gaining recognition thanks to the vision-impaired community’s latest console of choice.

“The idea of a blind person using a touchscreen may be a strange one at first,” says Hamilton, “but smartphone uptake was actually faster among people with impaired vision.” Thanks to Apple’s decision to include a screen reader called VoiceOver on every device since the iPhone 3GS, catering to vision-impaired players on iOS is easy. “So easy,” Hamilton adds, “that Zynga made Hanging with Friends blind- accessible entirely by accident, just by naming their buttons correctly.”

More intentionally blind-accessible games include audio games, such as the Papa Sangre series (iOS) and The Nightjar (iOS), both from developer Somethin’ Else, which are played using simple touch controls – or, as Satizabal prefers, the gyroscope – to navigate towards sounds that represent goals and away from those made by monsters. Many exploit our fear of being blind, which makes for an intense experience but could be problematic if overplayed.

“Horror has its place,” Satizabal says, “but it can be a little bit cliched. And also, visual impairment already has enough negative associations without it being brought out in the gaming world.”

Richard Harlow, who lost most of his sight to an optic nerve disease five years ago, agrees, saying these games can give the impression that blindness is “incredibly scary, and that you can’t be left by yourself”.

One studio taking a different tack is Incus Games, which is developing an audio-only adventure for PC and Mac. In Three Monkeys, players control a protagonist called Tobar who becomes a hero precisely because he was born blind and is thus best equipped when the world is cursed into darkness. “We wanted to create a world in which not being able to see was your biggest strength,” says Stephen Willey, producer and composer on the game.

“It’s more about empowering your sense of hearing,” says Satizabal, who met Willey while both attended Birmingham Conservatoire and is now a consultant on the game. He brings expertise from his experience both with audio games and “just getting around on a daily basis as a blind person using sound” to make suggestions such as adding more background noise to the forest in which the demo takes place, to make the game feel more real.

In that demo, a sprite called Yoska teaches the player how to use their hearing to hunt a bird and shoot it down with a bow and arrow and fight bandits and goblins with a sword. It sounds like something you’d expect to do in a modern big-budget RPG, which Willey says is intentional: “What we’re really aiming for is an audio game that has a kind of AAA [those with the highest development budgets and levels of promotion] feel about it.”

That should appeal to vision-impaired players such as Harlow, whose experience of “real video games” before he lost his sight has led him to consider many audio games “kind of bad, and just not entertaining”. But Willey and Satizabal both hope sighted players will enjoy the game too, so that they can have a shared experience with those who are vision-impaired.

“When there’s something that everyone has in common, that’s something that bridges people together,” Harlow says, “And that’s the awesome thing about video games.”

Shirebrook JobCentre: An Update

October 13, 2014

With many thanks to the WelFair Foundation.

We are pleased to bring you an update on the story of Shirebrook Jobcentre calling Support Group claimants in for Work-focused Interviews.

We wrote to Shirebrook Jobcentre and the local MP for that area, which handily is the brilliant Dennis Skinner, to try to resolve this matter and we can confirm today that Shirebrook Jobcentre have sheepishly back-tracked and blamed the whole thing on a ‘communication error’ between the Jobcentre and the DWP.

Apparently, claimants who were previously in the Work-related Activity Group but later moved into the Support Group by the DWP did not have their records updated by local Jobcentres. This means that local Jobcentre records are out-of-date and this is supposedly the reason Support Group claimants have been getting called in for Work-focused Interviews.

If you are currently in this position and your Jobcentre is refusing to back down then contact your MP for help.

An Update On Eddie- Who Must Do Jobsearch Online Even Though He Can’t

October 13, 2014

A couple of weeks ago, I posted an article about Eddie (name changed) and the problems that he was having with his online jobsearch. I’ve met twice with Eddie since then.

Eddie is a 51-year-old Kilburn man who has mild learning difficulties. He struggles to read and write. At the moment, he signs on for jobseeker’s allowance. He has worked for most of his life as a catering assistant in hotels, pubs and in kitchens, but was made redundant about four years ago. He has been unemployed ever since. He is very keen to get another job, but has not been able to find one. He wants someone to help liaise with potential employers on his behalf – to ring people who take staff on, put him forward as a candidate, promote him and his work history and to talk through any problems that employers may have with his literacy difficulties. Eddie has taken CVs into businesses all over Kilburn. He never gets called back.

The upshot of all of this is that Eddie must go to the jobcentre every fortnight to sign on and to show that he’s searched for at least 14 jobs. This post will show you how difficult and pointless this jobsearch exercise is for him. One of Eddie’s main problems is his struggle to read and write. He can write letters out if people tell him which ones to choose (for example, he asked me how to spell “Customer Service Advisor” when applying for one job, then wrote it as I spelled it out), but has trouble with more complex words. He also finds computers challenging. He doesn’t have a computer at home, which means that he rarely uses one. He wasn’t sure what a browser was when I took my laptop around to his flat to help him with his jobsearch (you’ll see some of this in the videos below).

Full story at Kate Belgrave.

Fashionable, Suitable Clothes For People With Downs Syndrome

October 13, 2014

What do you think about this, readers? Is there really a need for people with Downs to have specialist clothes?

Two US companies are designing clothes to better fit the body shapes of people with Down’s syndrome. But are different clothes really needed?

“Ashley has a typical Down’s syndrome body,” says Connie DeRamus. Talking about her 32-year-old daughter, she says: “At 5ft tall, Ashley is shorter than most women. She has a stocky, wide build, is short in the torso and is small in the top half.”

Indicators of Down’s syndrome includes smaller femurs and humerus bones, meaning arms and legs aren’t quite as long as average. Typically people with the syndrome are shorter and it’s reported that some can have stomachs which are a little larger, thought by many to be a medical consequence of the condition.

Ashley DeRamus began designing dresses for women of a similar shape to herself when she couldn’t find anything in High Street shops that fitted well. The company she founded with her mother, Ashley by Design, based in Alabama, sells dresses based on Ashley’s own measurements. Providing clothes for women, the outfits include features like ruffles and overlays “to cover up big stomachs” as Connie puts it.

In Ohio, Karen Bowersox runs Down’s Designs, a company which makes jeans and fashionable trousers for kids and adults with the syndrome. When she struggled to find clothes on line with arms and legs short enough to fit her granddaughter Maggie, she suspected that others might be having similar problems and investigated further.

Agreeing with DeRamus, she says that in most cases, her customers are larger round the middle – something she attributes to low muscle tone: “Holding in the tummy is challenging.” She says 60% of them have told her they don’t like trousers that sit on their stomach. Her solution is what she calls “dip-downs” which are of regular fit at the back but sit below the “tummy” at the front.

The knees of people with Down’s are much higher up, she says, so her company uses lots of stretchy fabrics to create “a more appropriate bend”.

But as well as look and feel, Bowersox says there are many practical matters when putting on clothes. Many with Down’s syndrome have fine motor skill problems which make buttons and zips hard to use. Some, she says, are “relegated to wearing sweat pants”.

Bowersox strongly believes that dressing independently instils confidence. She says: “Imagine school having to help you pull your pants down.”

Though the idea for accessible fashions which flatter the body might be new to people with Down’s syndrome, wheelchair-users are already able to purchase clothing designed for them to look good and feel comfortable while sitting – including trousers which are higher at the back so that they don’t slip down, with long legs that don’t ride up.

Tops for wheelchair-users are available with bigger-than-usual arm holes for more freedom when self-propelling, and for women, there’s a lot of detail high up on the garments to draw attention away from the legs and towards the bust line. Dresses and coats are cut to fit over the chair and drape elegantly.

So are specially adapted clothes welcomed by the Down’s syndrome community?

Writing on the Future of Down’s forum on Facebook, mum Linsey Tree Sim says: “[My daughter] has short, chubby arms and legs. It’s a struggle finding clothes to fit unless it’s t-shirt and leggings. She also has small feet so onesies that fit her torso flap around her legs and feet.

“I would definitely shop from a place that had specific designs as long as it wasn’t extortionately expensive.”

Another mum, Jane Gordy, whose daughter is Sarah Gordy, an actress with Down’s syndrome who has appeared in BBC TV’s Call the Midwife, dismisses the idea that people with Down’s have shapes which aren’t catered for. She says there’s no need to use special shops and, addressing the stomach size in particular, says: “I bet there’s no reason for the majority of people not to have good muscle tone.” She believes this could be more about parents’ expectations of their children and a “lack of ambition” for them. She says: “Sarah works out every day using three exercise tapes and she is a dancer so is pretty fit.”

Not everyone has the energy to put in lots of time towards staying in good shape and it is recognised by many that it is more of a challenge for people with learning difficulties.

The two specialist companies Ashley by Design and Down’s Designs are growing, however, and believe they’ve hit on something that people really want.

DeRamus says her clothes are sold before they even get listed online, and not just to people with Down’s. They are bought by non-disabled women of a similar shape, and by siblings of people with Down’s so that they can have matching outfits – helpful for occasions when people need to coordinate, such as bridesmaids at a wedding.

More than 72,000 people follow Bowersox’s Facebook page and she has shipped her jeans to eight countries. She raised more than $20,000 in a crowdfunding campaign this summer and won a $50,000 marketing bursary.

But neither of the companies is a money-making venture and Bowersox says that’s why more people aren’t designing for people with Down’s: “There are only 400,000 people with the syndrome in the US.” She deals with each order personally, which is time-consuming.

Ashley DeRamus says: “I feel good in my clothes and I feel great seeing other people wearing my clothes.” She and her mum feel so strongly that looking great means feeling great, they regularly give their dresses away to women with Down’s syndrome who can’t afford their designs.

Disabled Pensioner ‘Could Face’ £1500 Bill For Placing Blue Badge Upside Down

October 13, 2014

A disabled pensioner claims he is facing a parking bill of up to £1,500 – all because he failed to display his Blue Badge correctly.

John O’Callaghan, 66, parked in Liverpool city centre to visit a friend who was in hospital, reports the Liverpool Echo.

When he returned his Ford Focus car had been slapped with an £80 ticket because his disability badge was the wrong way up.

But he did not have enough money to pay the fine and now a bailiff company acting for Liverpool council is demanding he forks out a whopping £422 – or face having his possessions confiscated.

And the retired factory worker, claims he has been told over the phone the final bill could rise to an eye-watering £1,500.

Mr O’Callaghan, who suffers from a heart condition and uses a walking stick, said: “They are threatening to come round to my flat and clamp my car.

“I parked in Crown Street and left my badge the wrong way up, it was an honest mistake.

“I told them I couldn’t pay £80 in one go so asked if I could do it over two months but the council wanted it straight away.

“Now I’ve had a letter saying it’s gone up to £422 or they will send the bailiffs round. I think these are bully-boy tactics.

“And they are threatening it could go up to £1,500.

“The stress of all this has been really bad for my health – I’m not a well man, I’ve got a heart condition.”

He added: “They want me to pay an absolute fortune and it’s frightening the living daylights out of me.”

But Liverpool council has defended its position and said there will always be “additional charges” when bailiffs are called in.

A spokesman said: “Before bailiffs get involved there are opportunities to appeal against the notice, several reminder letters are sent out and we would ask people not to ignore these letters.

“If anybody has difficulty in paying the penalty charge notice, they should contact us to make arrangements about paying.

“We also require a county court order before the matter is sent to the bailiffs and there would have been further opportunities for people to state their case.

“If bailiffs do become involved there will be additional charges so it is important that they get in touch with us at an early stage.”

BREAKING: Tania Clarence Will Not Face Murder Charges

October 13, 2014

Her guilty plea to manslaughter on the grounds of diminished responsibility has been accepted by the CPS.

Disabled Man’s Search For Reader Goes Viral On Twitter

October 13, 2014

Dear readers, this is a serious question. Where can I contact this man? I love books and would love this job!

The advert tweeted

A blind man who put a note in a bookshop window seeking someone to read to him says he has been inundated with offers after the advert was tweeted.

Andrew Bailey, 34, from Nunhead, south-east London, has Friedreich’s ataxia – a degenerative disease which stopped him being able to read 15 years ago.

A picture of the ad was posted on Twitter on Saturday and has been retweeted more than 1,000 times.

Mr Bailey said the response made him “feel very good really”.

Andrew Bailey is looking forward to hearing Charles Dickens read to him, he says

His carer Bradley Baxter-Hassell wrote two adverts for Mr Bailey, placing one at Goldsmiths University and one at Foyles bookshop on the South Bank, about three weeks ago.

The message read: “There has been a huge empty space left in my life. I got much pleasure from reading.”

Mr Bailey, who read American Studies at Northampton University, has about 100 books he would like to read and says audio books can tend to sound “too robotic”.

His favourite author is John Grisham and among the books he wants to be read are My Sister’s Keeper by Jodi Picoult and The Growing Pains of Adrian Mole by Sue Townsend. He also wants to hear books by Charles Dickens.

He first showed signs of his inherited condition when he was four and began using a wheelchair at the age of 11. Five years ago he was registered blind. He needs 24-hour care and has difficulty hearing and speaking.

Corrie’s David Platt Has A Real Life Disabled Son He’s Never Met

October 12, 2014

I’ve never liked Dwight Yorke. Now I’ve just found out there’s another male celebrity ignoring his disabled child. I’m suddenly very glad I’ve never seen Coronation Street in my life.

The mum of Coronation Street star Jack P Shepherd’s ­disabled lovechild has warned the actor he may regret not meeting him.

Sammy Milewski, 29, had son Greyson James after a one-night stand with Jack, 26, in 2010 – behind the back of Lauren Shippey, now his fiancée.

The three-year-old suffers from the incurable one-in-a-million genetic disorder called alternating hemiplegia, which paralyses parts of his body and leaves him in intense pain.

Speaking exclusively to the Sunday People, Sammy revealed Jack, who has a son and a daughter with Lauren, 25, has never met Greyson – but has known for two years he is battling illness.

She said: “To Greyson, his biological father is just another man on TV.

“His father has not been in his life. I don’t know why because we don’t speak but I imagine it’s that he’s not wanted to.

“Nobody knows what the future holds for any child, disabled or not.

“Anything could happen and one day he might regret not meeting him. But only one person can answer that.

“I would like my son to have a father in his life but how can you feel sad for something he’s never had? I guess it’s sad in itself to say that.”

Softly spoken Sammy finds it hard to speak about Jack, visibly shrinking into herself when his name is ­mentioned. She won’t even say it and uses the words “the baby’s father”.

Her pain is easy to ­understand. Jack, who pays maintenance for his son, refused to ­acknowledge Greyson, forcing Sammy to ­demand a DNA test.

Speaking at the time, Sammy, who said Jack claimed he was single when she met him in a Leeds nightclub, said: “Jack obviously isn’t rushing to acknowledge his son so it will mean I need a DNA test to prove it.

“Without that I can’t have Jack’s name on the birth certificate and my child will be illegitimate.

“I don’t want that. My baby has done nothing wrong.”

 

Ever since the birth – after which Greyson battled for his life in intensive care in Rotherham General Hospital, South Yorks – Sammy has been a single mum. The former model now leads a quiet life with her son as its focus.

“I don’t want to criticise the baby’s father because Greyson and I do fine,” she said. “I’m speaking out to raise awareness of ­alternating hemiplegia.

“I don’t see his father in ­celebrity magazines and start screaming with rage. Sometimes I do feel ­that I go through quite a lot on my own, because nobody really ­understands but the parents, do they?

“Our situation is very tough and having a dad in Greyson’s life would be a help.”

Cuddling Greyson on the sofa of her apartment, Sammy describes her son’s illness matter-of-factly, sounding professional as she uses medical ­jargon.

But she breaks down as she describes watching her boy suffer. He spent his first two birthdays in ­hospital.

“It is terrifying and ­heartbreaking,” she said, tears rolling down her face. “I’ve seen him struggle to breathe with seven doctors round him and felt ­completely helpless.

“I have my down days when I just cry. I worry so much about Greyson.

“Parents worry about the slightest cold or cough their kids get but when your child is having doctors check his pulse it’s a different level of upset.

“No parent should have to watch their child go through that.”

Greyson has been in and out of hospital since he was born in January 2011. He had his first attack, in which his eyes flickered, when he was four months and had testing for all sorts of conditions, including epilepsy.

He was diagnosed with alternating hemiplegia on the eve of his second birthday. Only 25 people in the UK are thought to have the condition.

Sammy said Jack was informed his son was ­battling illness a couple of years ago but until last week, when she tweeted an appeal to raise money for ­alternating ­hemiplegia, he was unaware of his son’s exact condition.

“It sounds horrible but I don’t think it’s important he’s aware of it,” Sammy said. “Greyson and I don’t even know him. It would be like telling someone off the street.”

Jack quit Twitter on Monday – the day after news of Greyson’s disorder broke.

“It is nothing to do with me,” said Sammy. “I genuinely tweeted what I did to raise awareness for charity.

“I don’t care what anyone else thinks, my little boy comes first. He has a ­disorder which can put him in hospital, struggling to breathe, and is so rare many people haven’t heard of it.

“We need to fund more research to find a cure.”

Greyson suffers two kinds of attacks regularly. In one, part of his body, ­typically an arm and a leg on one side, goes limp for up to three weeks.

In the other his limbs tense up and Sammy can give him medication to relax his muscles – but this makes him scream in pain. The boy’s genetic condition could have come from his mother or father, or a mutation in his own genes.

Sammy has had tests and is waiting for results. If she is found not to carry the gene, Jack could be contacted for testing. This is not ­something Sammy wants to discuss. The dignified mum also dismissed talk of Jack’s fiancée, Lauren, as “irrelevant”.

When asked about Greyson’s half-brother and sister – Reuben, ten months, and Nyla, five – she said: “It’s a very ­difficult situation but I don’t want to talk about Jack’s children because I wouldn’t want them talking about my child.”

Greyson is a happy lad who is clutching his Postman Pat toy and eating Weetabix with medication crushed into it when we visit Sammy’s home in Rotherham.

And although his condition means Sammy can rarely make plans for fear of an attack, it is clear her son, who is a year behind in his development, brings her joy.

She said: “He started walking earlier this year, which was an ­absolutely ­fantastic moment. I was bursting with pride. And he can say a few words now.

“I have an amazing, brave little boy and I’m lucky to be his mum. As soon as an attack finishes, he starts smiling.”

 

Sammy left her modelling career to care for Greyson and now works locally in field sales. Greyson is attending nursery, where he is exceeding expectations, and discussions are under way to see if he will be able to attend a regular primary school.

“Through the charity for the condition, I know children who will never walk and talk,” Sammy said. “That’s why I’m ­speaking out – for them.”

Sammy said Jack has never tried to see his son. In fact, no family members from Jack’s side have ever made contact.

Although Sammy is fiercely proud of her family unit and describes the actor as “just another absent father” she admits life hasn’t turned out how she imagined.

She sighed as she recalled: “When I was younger I wanted the fairytale ending. I never thought I’d be doing it on my own. I grew up with a mum and a dad around and I would like that for Greyson.”

As for the future, Sammy looks ­protective when asked if she would like any contact between her son and the soap star

“I’m not impressed by celebrity and I don’t want to be associated with Jack just because he’s famous,” she said.

“I was making a cuppa one day when I saw him being interviewed on Lorraine.

“Greyson was playing in front of the TV and I turned it over quickly.

“If I saw Jack in the street I would carry on walking.”

She added: “I’ve not thought about Greyson asking about his dad but I would never lie to my child and I’m not going to do that whenever the time comes.

“I don’t want to criticise Jack because I don’t want my son growing up ­blaming me for his father not being around. That’s nothing to do with me.

“When he’s gone to nursery and the other kids say ‘dad’ Greyson says ‘mummy’.

“If the baby’s father did want to meet him I would have to think long and hard about it and decide what was the right thing for Greyson.”

Hate Crime Awareness Week 2014

October 12, 2014

Readers, I’ve just found out that yesterday was the start of  National Hate Crime Awareness Week 2014.

Political leaders have issued statements to support the Week, which are linked above, but few of them have mentioned disability hate crime. And when disability hate crime is mentioned, it is just in passing.

Readers, this Hate Crime Awareness Week, Same Difference officially calls for the Week to receive deserved publicity and recognition.

Because of course, readers, no hate crime is acceptable, for any reason, ever.

Readers, this Hate Crime Awareness Week, Same Difference also calls for the mainstream to recognise disability hate crime and give it equal importance to homophobic hate crime, race hate crime and gender-based hate crime.

What can the mainstream do to recognise disability hate crime equally?

Well, first of all, we need to improve and increase disability awareness in the general public. The biggest problem disabled people face is that the general non-disabled public see disability as a significant and negative difference. Disability is, of course, a significant difference- because unlike race, sexuality or gender, disability makes it extremely difficult, and sometimes impossible, for people to do things that non-disabled people take for granted.

But, disability does not have to be a negative thing. With the right support, there are many things that disabled people can do. We need to improve and increase awareness of this fact within the general public. We need to improve and increase awareness of the fact that disabled people are intelligent. We need to improve and increase awareness of the fact that disabled people have feelings and that hate crimes hurt our feelings.

The second thing that we need to do to recognise disability hate crime equally and give it equal importance to other hate crimes is to raise disability awareness within the police. The police need to be fully trained in how to interact with and react to people with all disabilities. We need to make it easier for disabled people to feel comfortable reporting disability hate crimes to the police.

Work needs to be put in to explaining to people with all disabilities that disability hate crimes need to be reported to the police. Work needs to be put in to explaining to people with all disabilities at levels, and in ways, that they can understand, how to report disability hate crimes to the police. Whether this means Braille, large print, Sign Language or Easy Read.

The media are not helping, either, with their negative coverage of disabled people as ‘benefit cheats’ and ‘scroungers.’ They need to realise that negative coverage of a group of people already viewed negatively by the general public will only add to disability hate crime rates.

Readers, there is a long way to go and of course, what needs to be done will not come cheap. You may even say it will be much more expensive to work on raising awareness of disability hate crime than it would be to raise awareness of hate crime against any other group. You may even say that is why there is still so little awareness of disability hate crime.

And readers you would not be wrong. But what needs to be done needs to be done, because no hate crime is acceptable, ever, and it is about time disability hate crime was firmly on the list- not just as a word in a sentence but as a topic being considered by everyone with the power to consider it.

 

 

 

 

 

Letter To JC Staff On Recording Of Interviews/Phone Calls

October 12, 2014

Spotted here.

General
Claimants may seek to record a telephone conversation or an interview with DWP either openly or covertly using digital recording devices such as cameras, microphones and mobile phones. There are a number of reasons why the Department should stop this happening in open plan public spaces. Jobcentre Plus has particular guidance on this here.
A key concern is that if the claimant is visiting DWP premises such as a Jobcentre, and is using, or intends to use, their recording equipment, in an open plan area they could record other claimants’ personal information. This is not acceptable.
If the claimant insists on recording their interview, a private interview room must be used. Where such a facility is not available on site and no other solution is possible, arrangements to use an alternative Jobcentre Plus office will need to be considered.
Staff should also be aware that interviews can be recorded where it is a “reasonable adjustment” requirement under the Equality Act 2010. If necessary speak to your local Disability Equality Adviser who can facilitate this.
If a claimant indicates that they intend to make a recording of a conversation or interview and staff involved are uncomfortable about being recorded, the matter should be raised with local management. Another member of staff who is less concerned about being recorded can take the call or conduct the interview. This may take time and a future appointment may be necessary.
A claimant may resort to threatening to record, or actually record, telephone calls or interviews as a last resort if they are unhappy about the way they have been dealt with by DWP. It may be more appropriate to resolve the underlying service issue in which case they may not feel the need to record their dealings with DWP.
Letter to be issued to a claimant before a recording takes place (bear in mind the possible need for alternative formats (where available) for disabled claimants).
You should alert the claimant that recording a conversation, may mean that they take on legal obligations they are not aware of. A letter [here] should be issued to the claimant before the interview begins. (Or in the case of already recorded telephone conversations as soon as possible afterwards).
Claimant publishes recording on internet
In spite of guidance and warning notices about claimants not making recordings in open plan public spaces, some may well do so without permission and they may occasionally publish videos, photographs, voice recordings etc of interviews or conversations with DWP staff on the internet.
If so they are exceeding the private and domestic use of such information permissible under the Data Protection Act 1998. In this event, you should write to the claimant adapting the letter below (for example, change the first sentence to read; It has come to the attention of the Department that you intend to/have published on the internet recordings of your business with DWP.)
Consider contacting the relevant Internet Service Provider (ISP) and ask them to remove any such recording. Often the ISP will comply and remove the content, though the claimant may still post the recording on a different website.
The benefits of contacting the ISP(s) may be outweighed by the lack of impact the content will have and so may not be proportionate or justifiable. However, this will depend on the nature of the material and each case must be judged on its merits. The Complex Case Advisory Service can advise in individual cases where material has been published without consent and members of staff have concerns about their own personal privacy or health and safety.
For guidance about the Department’s own routine recording of telephone calls with claimants please click here.
Text to include in letter to a claimant intending to publish, or who has published telephone/video recordings on the internet:
You have asked to have your interview with Departmental officials recorded. It is your right to do so.
However, you should know that you are entitled to record your business with DWP if the recordings are to be used by you for domestic purposes only, that is your personal, family, or household affairs (including recreational purposes),
Publishing the recordings on the internet, or in any other way, may not be treated as a domestic purpose and may indicate that you are acting in law as a data controller under the Data Protection Act. If you intend to make the
contents of your recording publicly available you need to notify the Information Commissioner of your actions.
The Information Commissioner is Parliament’s independent regulator of the Data Protection Act and he may take formal enforcement action to ensure your compliance with the Act. It is a criminal offence for a data controller to process personal information if they have not registered this with the Information Commissioner.
*[Please confirm to me that you have understood this letter and that no [further] use of the material will be made on the internet. If not we intend to alert the Information Commissioner to your unacceptable behaviour].
*[If you are not satisfied with the service that you have experienced from Jobcentre Plus/ PDCS* then arrangements can be made for you to discuss your concerns with a senior manager. Please let me know if you wish to arrange such a meeting.]
* delete as appropriate

World Arthiritis Day 2014

October 12, 2014

Today is World Arthiritis Day 2014. This video marks the occasion and explains why Seconds Matter for people with arthiritis.

Margarita, With A Straw: Trailer

October 11, 2014

This is previewing next Friday and Saturday at the London Film Festival.

Now LJ Duut’s DLA For Care Has Been Stopped

October 10, 2014

 

To make things even worse, it looks like she owes them three years of payments.

I have no words.

A Question From The People Vs The Government, DWP And ATOS

October 10, 2014

The Facebook group are asking for this question to be shared:

Please share, even if you don’t want to answer.

We don’t know if this is going to be as easy as we think it should be, but lets have a go.

Who has felt suicidal after their benefits money has been affected negatively by a decision by the DWP, Jobcenter or Atos? This can be delays, sanctions, withdrawals or being told you’re fit for work, JSA, ESA, IB, IS, DLA, PIP (any DWP benefit).

Please answer “I have” or “I have not” (and any further information you’d like to add.

If you have tried to commit suicide or have had a family member die because of the DWP, please, if you don’t mind, could you indicate thusly. We hope to copy the whole thread into a letter or email to the appropriate MPs.

Thank you for your time.

DWP Manager’s Carer’s Allowance Fraud

October 9, 2014

Readers, next time someone at the JobCentre annoys you, show them this!

A manager with the Department of Work and Pensions(DWP) defrauded her own employers by claiming she needed a constant carer to help her get through the day and night.

Gina Duane, 34, said she even needed the companion to advise her how to dress, and accompany her to and from work and to watch over her as she slept

As a result she was paid the highest possible rate carers allowance for what a court heard was a bi-polar condition.

But the communications manager with the DWP has now been exposed as a cheat.

Sentencing her, a magistrate said: “You are an experienced officer with the DWP and knew the rules, but you chose not to follow them.”

When her £28,000-a-year job required her to travel to meetings around the UK, she would use the trains, taxis and London Underground alone.

She would also stay alone at hotels. One of her line managers became suspicious of what she was doing and Duane, of Caxton Avenue, Bispham, was investigated by the DWP fraud unit.

Magistrates at Blackpool heard how she had never told the department how much her condition had improved, even though she was sent reminder letters.

As a result, she was overpaid £7,415 over an 18-month period.

Duane had been found guilty at a previous hearing, and returned to court to be sentenced.

Pam Smith, prosecuting, said that when she was interviewed about what she had done, Duane said her mother had filled in her original claim form, but the information in it was correct.

She admitted her condition had improved, but had forgotten to tell the very 
department she worked for.

She said that when she went on work trips, she had kept in touch with her carer by phone.

Sentencing Duane, chairman of the bench Barry Birch told her: “We accept you have medical issues, but you went very, very close close to going to prison today.

“You are an experienced officer with the DWP, and would have known exactly what you were doing every day.You knew the rules and you have left the public purse out of pocket,because you knew that should have notified changes in your circumstances, but you chose not to.”

Ashley Fisher, defending, said that Duane had been on a £25,000 spending spree, and as a result was in mortgage arrears and made bankrupt.

He said: “Since proceedings started against her she has been suspended from work. She is now concerned that following this hearing she will be dismissed.”

Duane was put on 18 months’ supervision by the Probation Service, and ordered to pay £1,000 costs.

In a letter written before the hearing, Duane wrote: “I have embarrassed myself, my friends and family. I have spent crazy amounts of money on things I did not need.”

Michael Hilton Jailed For 10 Months

October 9, 2014

I’ve just read some bad news, readers.

Michael Hilton, whose case Same Difference has followed closely, has been jailed for 10 months for ‘booby trapping’ his home to stop bailiffs evicting him.

Readers, maybe he didn’t behave in the right way. But, readers, to take such extreme actions, he must have found himself in a very difficult situation. He must have felt he had no other choice.

I have to wonder whether a jail sentence was really appropriate for him.

 

 

Carers Could Lose CA Over £3

October 9, 2014

A new minimum wage has come into force this month, with the hourly rate going from £6.31 to £6.50.

It might sound like good news, but the reality is more complicated.

If you care for a friend or relative and also work part-time, the increase could cost you more than £60 per week.

Moneybox presenter Paul Lewis explained the catch to BBC Breakfast presenters Naga Munchetty and Charlie Stayt.

Bionic Hand Restrores Touch To Two Patients

October 9, 2014

Advances in bionic hands have restored a sense of touch to two patients for more than a year, report US scientists.

The men can now delicately pluck the stalks out of cherries.

Sensors on the artificial hand are used to send signals directly to the nerves, the study, published in Science Translational Medicine, said.

Meanwhile, a Swedish team has made a separate breakthrough in artificial limbs – anchoring bionic arms directly on to the bone to improve control.

One of the beneficiaries of the American work was Igor Spetic, who lost his right hand in an accident four years ago.

He was fitted with a bionic replacement, but it was incapable of feeling the world around him.

He had to carefully watch what he was doing and judge by eye whether he was squeezing too hard.

A team at Case Western Reserve University attached sensors to the bionic hand and in surgery fitted “cuffs” around the remaining nerves, which were capable of delivering electronic stimulation.

The team could send different patterns of electronic stimulation to the nerves using a computer. These were interpreted in the brain as different sensations.

The team “mapped” these sensations to 19 different locations on the hand, from the palm to the tip of the thumb, and matched the sensors to the different electronic patterns of stimulation.

They then moved on to pressure and textures. Mr Spetic can tell, while blindfolded, whether he is handling different materials such as Velcro or sandpaper.

He has been using the sensing hand for two-and-a-half years. Another patient has been using the system for one and a half years.

Lead researcher Prof Dustin Tyler told the BBC: “They can do really fine delicate tasks now.

“We believe within five to 10 years we will have a system completely implanted so we would see a person in the morning, they would have the procedure to put electrodes on each nerve and a device for their pocket, so that when they turn it on they can feel their hands.”

Mr Spetic said: “I would love to feel my wife’s hand, just to hold hands would be the ultimate.”

In both patients the modified hand had the added bonus of eliminating “phantom limb pain”, in which patients still feel pain from the hand that is no longer there.

Meanwhile, scientists at Chalmers University of Technology in Sweden say they have implanted the first bone-anchored bionic arm.

The technique known as “osseointegration” involved connecting the arm directly to the bone, nerves and muscles in the residual stump of the patient’s arm.

It gave the patient better control.

Dr Max Ortiz Catalan said: “We have used osseointegration to create a long-term stable fusion between man and machine, where we have integrated them at different levels.

“The artificial arm is directly attached to the skeleton, thus providing mechanical stability.

“Then the human’s biological control system, that is nerves and muscles, is also interfaced to the machine’s control system.

“Reliable communication between the prosthesis and the body has been the missing link for clinical implementation of neural control and sensory feedback, and this is now in place.”

CP Woman, 35, ‘Humiliated’ After Wetting Herself When Mitcham JobCentre Refused Her Use Of Toilet

October 8, 2014

A woman with cerebral palsy who suffers from a weak bladder has told of her humiliation after she wet herself in front of a room full of people when she said Jobcentre staff refused to let her use the toilet.

The incident took place when Rebecca Weston, 35, was called to the Jobcentre in London Road, Mitcham, to review her benefits.

A Jobcentre spokeswoman said it did not have public toilets and an alternative was offered to Ms Weston at the time.

Ms Weston, from the Pollards Hill Estate, said: “When I went in there I requested to use the toilet and explained to him, ‘please let me because if you don’t I’m going to wet myself.’

“‘Well, that’s not my problem.’ he said to me. I’m standing in the middle of the job centre, 35 years-old, and I wet myself in front of a room full of people. I have never been so frustrated and humiliated.”

The Jobcentre does not have a public toilet, but Ms Weston wants to see the centre make exceptions for disabled people after the incident on September 29.

A staff member advised her to use the toilet in a cafe down the road, but she warned them it might be too late and wet herself as she headed towards the exit.

A spokeswoman for the Department for Work and Pensions, which manages the Jobcentre Plus offices, said: “Jobcentres don’t have public toilets, but our staff will always try to accommodate people’s individual needs where possible.

“However people should also be aware that we do not tolerate abusive behaviour towards our staff.”

Ms Weston, who receives employment and support allowance, said she only used an expletive after the incident when the staff member continued to be unsympathetic.

She said: “I think it’s totally disgusting to humiliate disabled people in that way. I don’t claim benefits because I want to. I think people need to know about this.”

Letter From LJ Duut’s Housing Association

October 8, 2014

LJ Duut has been waiting for post from the DWP about whether she can keep her Survivors’ Benefit. There’s no sign of that but she has recently had this instead.

Claimant Assaulted By G4S Guards At Southampton JobCentre

October 8, 2014

Readers, this should go viral.

Annette Brooke MP Describes Case Of Disabled ‘Bedroom Tax’ Victim

October 7, 2014

THE death of a severely disabled Dorset resident who took her own life while battling the bedroom tax left her MP “absolutely distraught”.

Annette Brooke, MP for Mid-Dorset and North Poole said that she felt compelled to stand up and speak in a House of Commons debate after supporting one of her constituents, who she did not want to name, during a 10-year battle over disability and housing benefits.

Mrs Brooke said the woman who was an accident victim and was left severely disabled after an operation went wrong, killed herself after being turned down for discretionary housing benefit.

“Every bit of the way she had to fight. There’s no way that you could say that the bedroom tax was the sole factor of her death but just to get the message that they are being turned down for housing and she did need the extra room because of all the equipment she needed.

“She was so disabled that she needed a taxi to get anywhere and going out even once a week was quite expensive for her.

“The housing association was fantastic, so we were working together and I think we would have won but it’s not surprising that she got depressed from it all.”

She was speaking during the Second Reading of the Affordable Homes private members bill, submitted by fellow Liberal Democrat MP Andrew George.

This aims to introduce three new significant exemptions to the spare room subsidy, excluding all claimants who have not been offered reasonable alternative accommodation, certain disabled people living in adapted accommodation and some in receipt of Disability Living Allowance or Personal Independence Payment who are unable to share a bedroom.

“I wanted to really make the point that this is the human side of it, that this is somebody who was fighting every day to cope, and it was just the last straw,” said Mrs Brooke.

Men Set ‘Pit Bull’ On Girl, 12, In Wheelchair

October 7, 2014

A girl in a wheelchair was bitten by a dog which was set on her by two men, police have said.

The 12-year-old was out with her father when she was attacked in Lings Wood, Northampton, on 3 October.

She became upset about the men and the “pit bull-type” dog passing too close, so one of them commanded it to “get her”.

Police said the girl’s arm guards, which she wears due to her disability, prevented her from being injured.

Insp Kev Byrne from Northamptonshire Police described it as “an absolutely disgraceful incident”.

“It is not a case of a dog being out of control, but being used as a weapon in an assault on a very vulnerable girl,” he said.

‘Appalled by incident’

“Had it not been for the victim’s arm guards, she could have been seriously injured,” Insp Byrne said.

“I know local residents will be appalled by this incident and I would urge anybody with any information to contact us immediately.”

The two men are described as black and in their 30s.

One was about 6ft (1.8m), clean-shaven with short black hair and wore a blue T-shirt and jeans. The other was 5ft 10in (1.78m) and had “medium length Afro-style hair”, police said.

The dog is described as a black and white pit bull-type breed.

Updated 8/10: I’m very pleased to see this being covered in the Mirror.

Scottish Author Says It With Braille

October 7, 2014

A press release:

Trailblazing author Sue Reid Sexton – whose latest work was published in Braille at the same time as general release – will join Royal Blind pupils today (Monday) to celebrate the start of National Braille Week 2014.

Sue will read from her first novel Mavis’s Shoe – about a child’s experiences of the Clydebank Blitz – to a class of English and History students at the school. Wartime-themed snacks will be provided by the Home Economics team. The event is part of a mini literacy festival at the school this autumn, the ‘Falling Words Festival’.

Sue will also visit the Scottish Braille Press, who produce the Braille versions of her work. A member of staff with visual impairment will read from a Braille embossed copy of Rue End Street.

Speaking before the event, Sue said:

“I am delighted to be involved with National Braille Week.

“Royal Blind organise this week to celebrate the life-changing impact of Braille. If you can imagine a world without books, then that is the reality for many – or would be, without Braille and other accessible formats. Braille is a code that helps over 120 million people worldwide.

“I’m looking forward to a tour of the Scottish Braille Press and the Royal Blind School and to meeting the staff and pupils there. I’m going to read from my novels Rue End Street and Mavis’s Shoe – I’m very pleased that both books are available in Braille and thank you to the Scottish Braille Press for their hard, excellent work.”

Davina Shiell, Marketing Manager at Royal Blind said:

“Sue has been a huge supporter of Braille and other accessible formats so we are delighted that she’s here to help us celebrate National Braille Week. This is an important way to raise awareness of the difference Braille has made to so many lives.

“We hope that many people will be able to join us in celebrating National Braille Week this year by organising their own activities, taking part in our social media campaigns or viewing our exhibitions online.”

National Braille Week is organised by Royal Blind and runs from 6 – 12 October this year.

It aims to raise awareness of the importance of Braille and other accessible formats, and their many uses across the UK.

To find out more visit www.nationalbrailleweek.org

Curious Incident Opened On Broadway Yesterday

October 6, 2014

A stage version of The Curious Incident of the Dog in the Night-Time has opened on Broadway, to stellar reviews.

Believe the buzz,” Variety’s critic said of the acclaimed National Theatre production, calling it “spectacular, like Cirque du Soleil with brains”.

The New York Times’ man agreed, saying it “one of the most fully immersive works ever to wallop Broadway”.

The play tells of a teenage boy with Asperger’s syndrome who investigates the death of a neighbour’s dog.

Directed by Marianne Elliott, the Olivier-winning drama was adapted from Mark Haddon’s best-selling 2003 novel.

It opened at the National in 2012, transferred to the West End the following year and had its opening night on Broadway on Sunday.

Time Out New York was among several publications to be impressed by Elliott’s “dazzling and pulse-pounding” staging.

Others included the Hollywood Reporter, who said the show was “a tremendously exciting demonstration of the power of theatre”.

Writing in USA Today, critic Elysa Gardner called the play “highly original [and] deeply engaging” and praised Elliott’s “beautifully sensitive” direction.

Only Newsday’s Linda Winer expressed a degree of reservation, concluding she had been more “filled with admiration” than “enraptured”.

“The results brilliantly capture the sensory overload in the journey of a sweet, compulsive, instinctive and unpredictably violent child,” she wrote.

“What the adaptation does not do, at least until the very end, is transcend the spectacle to dig out the emotional life that coexists with [his] confusing perceptions.”

Alex Sharp plays the lead role of Christopher in the show, which continues at New York’s Ethel Barrymore Theatre.

Man With Tourettes Designs Identity Card

October 6, 2014

How do readers with Tourettes feel about this idea?

There are estimated to be around 300,000 people with Tourette’s Syndrome in the UK.

Paul Stevenson from Berwick, Northumberland, developed Tourette’s suddenly at the age of 46 after the death of his best friend.

Living with Tourette’s is a constant challenge for him because it involves uncontrollable body movements, tics and swearing.

Now he has come up with a novel plan to explain the condition and his behaviour to other people.

He has designed an identity card to reduce the stigma attached to Tourette’s.

Inside Out is broadcast on BBC One North East & Cumbria on Monday, 6 October at 19:30 BST and nationwide on the iPlayer for seven days thereafter.

IDS Considering Taxing Disability Benefits

October 6, 2014

The possibility of disability benefits being taxed was reported yesterday in the Independent.

Where’s The Benefit has a very good post on why it wouldn’t be a good idea.

The idea of disability benefits being taxed makes me shake with fear. Same Difference will do anything possible to make sure it is never anything more than an idea.

Meet Duncan Enright- The Man Taking On David Cameron In 2015

October 6, 2014

I spotted this on Reddit and I think he deserves our full support.

My name’s Duncan Enright and next year I will be standing for the Labour Party in Witney. The constituency is currently held by the UK’s Prime Minister, David Cameron.

A sitting Prime Minister has never lost his or her constituency before, so we are attempting to make history.

But the main reason we are doing this is because we think Mr Cameron’s policies have damaged the UK. He has cut funding to vital services and cut benefits to those most in need, while at the same time reducing taxes for the richest.

Mr Cameron has represented Witney for the last 13 years but achieved next-to-nothing in that time to benefit the area. We still have problems with congested roads, a lack of affordable housing and a lack of jobs in the area – most require a commute to Oxford. And nothing has changed during his 13-year tenure.

Yesterday we launched a crowdfunding campaign on Indiegogo.com. We think we may be the first Parliamentary campaign ever to try and raise money this way. Please visit: https://www.indiegogo.com/projects/help-us-to-kick-out-cameron-in-2015.

We also think I may be the first Parlimentary candidate from a major party ever to try an AMA on reddit.

For more information about me, visit duncanenright.com

So, without further ado, Ask Me Anything!

Edit: Proof it’s me: https://twitter.com/duncanenright/status/518775742067654656

Edit: Thanks everyone for your questions. I hope I got to yours, but apologies if I didn’t. I was delighted to get so many questions, and by their range. Mostly polite too! I will be doing more work on internet policies and censorship! Oh and chorizo, brie and beer. I was at this for four hours, but it felt less – went really quickly! I hope you’ll follow the campaign and do get in touch if you can help (particularly our fundraiser on Indiegogo!)

Intel Intern Invents ‘Smart Wheelchair’

October 5, 2014

A 20-year-old summer intern at chip giant Intel has created an internet-connected wheelchair.

The wheelchair collects data to gather information to flag emergencies – for example when a user has slumped forward.

It can also monitor that the chair itself is functioning properly.

The robotics student, Tim Balz, actually secured a patent for a similar idea while he was in high school.

Developers can also use the information to make apps which will enhance a wheelchair user’s experience.

He says one application would be to feed in the location information to crowdsource accessibility around cities.

Tim showed the BBC’s North America technology correspondent Richard Taylor how the wheelchair works.

Cancer Patient Sacked- For Taking Too Much Time Off Sick

October 4, 2014

From the Mirror:

Lorraine started working for adult care provider SEQOL in Swindon, Wiltshire, in August 2009 on a full-time permanent contract.

It was her dream job as a re-enablement officer, supporting patients leaving hospital and assessing if they are capable of living at home.

In early 2012, she was signed off work for four months after she was diagnosed non-alcohol liver disease and needed regular hospital trips to see a specialist.

She returned to work after four months as planned, until she began to experience headaches in early 2013, which was initially put down to stress.

Following six months of headaches and nosebleeds she was told she had nasal septum cancer and signed off work in July 2013 and began undergoing biopsies.

The cancer was found to have spread, but following four operations on her nose she returned to work in October 2013.

In April this year, the cancer was found to have accelerated again and she was signed off work for six months while she underwent intensive radiotherapy and an operation.

Despite the fact her body is still fighting cancer, Lorraine was due to return to work on October 20, but she has now been told by a panel that her contract has been terminated.

Full story here.

Pay the rent or we take the kids – yes KHT are at it again

October 4, 2014

ESA SG – Invited to JobCentre Interview? DWP States – You Can Say NO

October 3, 2014

jaynel62's avatarjaynelinney

Last month I wrote DWP Breaks its Own Rules when threatening Support Group Members, today I can confirm that despite how the letter below, suggesting “your benefit could be affected” if you do not attend, the DWP state attendance is totally voluntary;

shirebrook-job-centre-scan-1

a FOI request to WhatdotheyKnow  states

It is not mandatory for claimants in the Support Group to attend a WFI when requested
to do so by their local Job Centre. All engagement for claimants in the Support Group is
voluntary.

Clearly the regulations show Disabled people in the Support Group can not be enforced to attend a Work Focussed Interview, despite how the invitations read.

If you receive such a request and don’t want to attend – file the letter in B1N

Don’t let the DWP bully you !

Fight Back – Join #Truth Campaign – New Project coming SOON

#ImpeachDWP #NOWPetition 

View original post

Kestna’s #WCA and other reasons not to be cheerful

October 3, 2014

Ann McGauran's avatarAnn McGauran

Kestna Marsh is disabled. He was forced to the foodbank after a tribunal upheld a  DWP decision to stop his benefit. Kestna Marsh is disabled. He was forced to the foodbank after a tribunal upheld a DWP decision to stop his benefit.

Kestna Marsh was 62 this week. At the moment he probably feels he has little cause for celebration.

This former construction worker struggles to walk  as he has arthritis in his right knee,  left leg and left shoulder.  He can’t lift anything with his left arm. On the day he came into this London food bank with his voucher, his mobility was obviously restricted and he struggled with his walking stick  to move from room to room. Because of his mobility issues I felt hesitant about asking him to move even a few steps into a quieter room. Kestna walked that distance because he wanted to share his experience of Work Capability Assessment (WCA).

He was left without the money to buy adequate food after a tribunal hearing at…

View original post 627 more words

Work Programme Shamelessness

October 3, 2014

The wonderful Kate Belgrave says she shared this story because she loved it.

I don’t love it. I’m sharing it because sharing it allows me, and you, dear readers, to laugh at the DWP.

 

Angela Smith is a woman with a Master’s degree and a long history of working in policy and disability support. She also has cerebral palsy and uses an electric wheelchair to get around. I’ve been accompanying Angela to her compulsory fortnightly Wembley jobcentre signons and meetings with the Reed Partnership, her work programme provider in Harrow. We’ve shown how difficult London buses can be for disabled people to use. We’ve also shown how pointless those fortnightly meetings at the jobcentre and the work programme really are when it comes to finding work.

Anyway. Angela has a new job. She got it without any help whatsoever from the jobcentre or the Reed Parntership. She found the job advertisement, filled in the application form, went to the interview and got through.

She did the whole thing entirely by herself. But that hasn’t stopped the work programme provider from trying to claim the result for itself. I went with Angela to her final meeting there a couple of weeks ago and saw this in all its glory. Her work programme adviser – a pleasant enough woman – congratulated Angela on finding a job. Then she said something along the lines of: “look, I know we haven’t helped you get this job at all – but would you be prepared to be featured in our Success Stories poster campaign? We could get your photo done and get a poster made. That would be really good.” There were posters on the office walls of people working at various jobs and saying things like: “I’m now running a successful business.” Angela and I decided that they must have been a bit short on successful-placements-of-disabled-people-in-work stories so they’d figured they’d have hers. Pity they had nothing to do with it.

Everybody’s Somebody’s Child

October 2, 2014

A brilliant point brilliantly made by the brilliant Vox Political.

zcameronson1

Hayley Fraser, 5, Is First Child To Have A 3D Hand

October 2, 2014

A Scots girl is thought to be the first child in the UK to have a prosthetic hand made with 3D printing technology.

Hayley Fraser, 5, from Inverness, was born without fully-formed fingers on her left hand.

Jackie O’Brien reports.

Nick Griffin Expelled By BNP

October 2, 2014

So readers, it’s official. Even the BNP don’t like him!

A Brilliant Summary Of Cameron’s Speech And Disability

October 1, 2014

From the brilliant Political Scrapbook. Linked with thanks.

Students Using Food Banks: A Disabled Student’s Experience

October 1, 2014

Following this shocking article about York University students using food banks to eat, Same Difference spoke to disabled former student LJ Duut who used a food bank while studying Law at  Cambridge   in 2011.

Here LJ shares her experience:

My GP referred me to foodbank when I was studying. The problem was that you have no choice- for example I have never ever eaten weetabix and neither had hubby and we were not used to biscuits so they were a waste. It came with a booklet of recipes – me being a vegge I was told that I had chicken soup to mix with pasta. I was told there was not much chicken in it? . Hubby tried to eat it but by that point his pallet couldn’t tolerate lumps of pasta as he was too ill. Tea- we both never drank tea and that also went to waste. There was no way my dog could survive on 1 tin of dog food eternally but the toilet roll did prove useful especially when mopping up sick from the chicken soup hubby tried to eat. There was a tin of tuna- I will never forget it- it had a sticky substance on it with what looked like thick hairs stuck to it- now tuna was about the only thing I could eat and that made me want to puke. My worst complaint was the telling me that I needed to attend church part. Having a critically ill husband, studying and attending church since you were given a box of food didn’t appeal at the time. It certainly did not help hubby – his body was not used to processed food – all of the food has to be processed and not fresh. If your body is used to fresh food stuff then it does take a toll on you. Also , a simple ticking questionnaire about diets of different people would be useful? Or if people drink tea or coffee? that way tea could be saved for tea drinkers. The thing about it that what was in the box you could hardly make a meal out of. It was as if things were just randomly thrown into the box without a thought. Thats my personal view on foodbanks.

LJ adds that she could not complete her studies “due to my husband starving as he could not eat the food from food bank.”

Readers, I did not set out to find a Law student from Cambridge- however the fact that I did only proves the point of this post. No matter whether you study, no matter what you study or where you study, no matter whether you work- food banks are needed, desperately, by anyone and everyone at any time.

 

Employer Changes Job, DWP Sanctions Employee For Refusing Job

October 1, 2014

Mike Sivier carries the story of his friend who applied for a job in a hotel kitchen in Wales.

The job was offered to a younger applicant because this meant paying lower wages. But the younger applicant soon proved unsuitable. So Sivier’s friend was offered the job, working 22 hours per week. So far so good.

But then, before he started,  he was told that the job is now for 40 hours a week. The man can’t work those hours, for personal reasons. So he had to refuse the job.

The hotel contacted the Job Centre, who told the man he may be sanctioned for refusing an offer of work.

It looks like employers are refusing benefit claimants. It looks like employers are helping the DWP keep benefit claimants out of work.

If this carries on, dear readers, how will benefit claimants ever get paid jobs?

Have you had a imilar experience? Please let us know.

Plymouth Man With ‘Mild Autism’ Killed Himself When He Faced Eviction

October 1, 2014

A GARDENER who was unable to pay his housing association rent may have taken his own life on the day he was to be evicted, an inquest heard.

The body of Peter Kelleher was found on June 25 by police after a neighbour alerted them to a build up of post, an abundance of flies and a strange smell coming from his ground floor flat in Diamond Avenue, Greenbank

Officers forced their way into the property and found the 44-year-old kneeling behind the flat door, a ligature round his neck attached to the door handle.

Police reported that Mr Kelleher’s body was in a state of decomposition and that all windows and doors were closed and locked.

 Det Con Matt Wood, who investigated the circumstances of Mr Kelleher’s death told the inquest the deceased was one of four siblings.

He had been born in Ealing, London and brought up by his mother. After his parent’s divorce he had initially went to live with his father in Fulham but seven years ago his mother and he both moved to Plymouth.

When his mum became ill, Mr Kelleher gave up his job as a gardener for SERCO and became her carer.

His mother passed away in September last year and in February this year his brother, Michael Kellerher, helped him moved out of her home into a flat of his own. When their father then fell ill, Michael returned to care for him in London.

Det Con Wood said during his investigation, Michael – who attended his brother’s inquest – explained how Peter was a shy person, who he felt had a “type of mild autism but never diagnosed”.

His inquiries found that Peter had been prescribed Fluoxetine, but had not taken the anti-depressant.

Michael Kellerher told Plymouth coroner Ian Arrow that he had found a series of letters from a housing association addressed to his brother in the pile at the front door demanding rent payments, highlighting the bills went from “£200” to “£700”.

He said had also found a notice of eviction set for June 17 – the date he believes his brother took his own life.

Coroner Ian Arrow said a post mortem report found that Mr Kelleher’s bladder and stomach was empty.

Michael told the coroner he had learned that from the day his brother moved into the address: “He wasn’t receiving any benefit whatsoever.”

Sadly, he said his brother had given his family no indication that his financial situation was “so severe”.

He said: “These letters were saying ‘you owe us £200’ and ‘you owe us £700’.

“But for him not to have told us this is just unknown to us. I’m having major trouble with that part of it.

“He must’ve gone hungry for more than a day. Why didn’t he tell me?”

Michael Kellerher revealed his brother had left a note bearing two names and two phone numbers.

Mr Arrow recorded a verdict that Mr Kellerher had taken his own life.

The Herald later learned the property was managed by DCH, formerly Devon & Cornwall Housing.

Asked what efforts they made to assist Mr Kellerher with his finances, a spokesperson from DCH said: “Our thoughts are with Mr Kelleher’s family at this time and we will continue to offer our support to them.

“We are unable to discuss the circumstances of individual residents however we are committed to ensuring each and every one of our residents has access to the relevant support and advice they need and our teams work hard to deliver this, working closely where possible with each individual resident.”

Osborne’s ‘Hidden Blow’ To Disabled People

September 30, 2014

As usual, says Ekklesia in this very useful article, the myth that ‘disabled people won’t be affected’ is just that- a myth.