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“If My Son Lived At Home, I Wouldn’t Be Here Now”

April 28, 2014

Jane Raca on her son, James, and the New Malden case.

In the summer of 1999, I was sitting on Whitby beach with my husband, Andrew, and our two-year-old toddler, Tom. There was a strong breeze that kept blowing sand into our ice creams, but the sky was bright blue, and the sun danced on the surface of the sea.

I didn’t know that the next day would bring a tsunami with it, one that would destroy the life I knew and leave me to rebuild a completely different one. I was only 24 weeks pregnant and my waters broke. Three days later, James was born weighing just 1lb 12oz, with extensive brain damage.

Until then, Andrew and I had lived in a state of comfortable ignorance, as affluent professionals. We had a nanny for Tom, and a nice house. James’s birth catapulted us into a different world, of life-and-death decisions, social workers, and the isolation caused by society’s lack of understanding about disability.

James is now 15, and has cerebral palsy, epilepsy, severe learning disabilities, and is severely autistic. He is doubly incontinent, can’t walk or talk, and can’t use his left hand.

Most people go silent when I recite this list. I like to add, then, that James is blond, blue-eyed and handsome, has a great sense of humour and will swipe the apple out of your lunch box before you can blink. It’s taken me 15 years, though, to be able to speak about him with equanimity, and I nearly didn’t make it at all beyond the first five years.

The seismic shock of his early birth, followed by the grinding reality of 24-hour caring with no support, led me ultimately into a state of suicidal depression. I escaped because I had a complete breakdown. Recognising that I couldn’t carry on, I used my skills as a former lawyer to take the council to court to get James into a residential school.

When the news broke last week that Tania Clarence, a nice, middle-class mother in New Malden, south London, appeared to have killed her three disabled children, I heard interviews with shocked neighbours saying how she had seemed so nice, she had seemed to be so happy and in control. We do not know what has happened in Mrs Clarence’s case – that is for the courts to decide – but the comments from the neighbours did make me think about my situation. There was a disparity between the coping face I had presented to the world and the awful reality I was living with at home.

It had probably been more insidious because at first we could cope. When James was discharged after four months in the neonatal unit, we were just grateful that he was alive. He was easily portable and particularly cute, with a ready smile and no obvious movement difficulties.

Then he became bigger and heavier, and my back began to ache from carrying him up the stairs. He grew out of the nappies I could get at the supermarket and we had to have special incontinence pads. The pushchair was replaced with a wheelchair, and a lift-hoist and ramps were installed in our house.

Knowing James may never walk was one thing. Getting his first blue badge in the post gave me the first of many days of searing emotional pain. James started to have seizures; always at night, and mostly silently. I would find him in the morning, sometimes blue-tinged and staring vacantly, having been sick. My sleep became restless with anxiety. I woke at every murmur, and would get up each time to check he was OK. Once his stiff arm got stuck in the bars of his cot and I raced in to find him in agony.

Then the nights took on a sinister new turn, as his autistic behaviour became more pronounced. He would often move his bowels in the night and play with the result, creating what we came to call “poo-fests”. It took hours to shower him from head to foot; to change the bed and disinfect the walls.

By the time James was five, I had given up all idea of work and was a full-time carer. In order for Andrew to function at his job, I had taken over most of the night duty.

Andrew and I were living in parallel universes. I was juggling several hospital appointments a week along with medication charts and a cohort of visiting therapists. The therapists gave me jobs to do such as standing James in a special frame, or stretching his stiff arm.

All the time I was stupefied by a lack of sleep. Meanwhile, Andrew was trying to come to terms with days that started with him calling an ambulance because James had stopped breathing, then continued with him putting on a suit and advising clients.

Tom, our other son, had become silent and withdrawn, until one day he burst out that he must be the loneliest boy in the world. We realised that we had been so busy caring for James that we hadn’t even had time to teach Tom to ride a bike. After that we took turns to take Tom out for a pizza or a film. We couldn’t take James because he was, by then, so terrified of change that he would attack us if we took him out of the house. The family was split and I, in particular, was under house arrest.

When James was five, Andrew and I attended an appointment with James’s community consultant, who made the mistake of asking how we were. We both broke down and wept. She asked us if we had any respite and we didn’t know what she meant. We discovered, then, that James was a “child in need” under legislation and that the local authority had been under a statutory duty to support him from birth. Five years too late, we were appointed our first social worker. It was then that we discovered the world of cash-strapped councils, and inefficient social-services departments.

It took a year – and an appeal – to get two nights of respite a month, when James would stay at a specialist centre. At first, to have even these little breaks was akin to a survivor in a desert being given a few drops of water. It saved our lives, and despite the tiny quantity, was intoxicating. We now had a baby daughter, Elizabeth, and we managed to give her and Tom trips out of the house, like normal families.

It wasn’t enough, though, and the inexorable downward spiral continued. I stopped being able to cope but, when asked how I was, I would still give a smile and say “fine”. The sense of unreality between the self I was presenting outside and the way I was feeling inside intensified.

I didn’t dare lose control, because my outward composure was the only thing that made sense to me and enabled me to deal with other people. What would we all do if I let out the feelings of panic and hopelessness that had taken over my life and just disintegrated?

But then I began to have images flash into my mind of drowning myself in our local reservoir. I didn’t plan the thoughts, they just popped up. I would suddenly be dreaming that I was at the edge of the water, with a ball and chain around my ankle. I would be about to wade in to the cool water until it closed over my head and shut out the chaos above. I never thought of hurting James or the other children, and the suicidal thoughts remained just that: thoughts.

I watched Rosa Monckton’s documentary, When a Mother’s Love is Not Enough, about mothers in my situation who had contemplated killing themselves and their children (Monckton herself has a daughter with Down’s syndrome). I understood their logic that if they couldn’t carry on, they would take their children with them in order to protect them. They didn’t want to leave them behind, being so vulnerable.

I have never wished James had died as a baby. Loving him has enriched my life immeasurably and he is the bravest, funniest person I know. He has an iPad now for evenings, which is locked in a safe outside his bedroom at school. After watching the staff open it a few times, he cracked the code, crawled over and fetched it out himself.

He now lives a full and happy life at Dame Hannah Rogers’ Trust in Devon, where he is checked every 15 minutes at night for his epilepsy, by nurses who work shifts, not 24 hours a day. We visit him every school holiday, and because of the expert psychological input he has had, we can take him out on trips. We have a wheelchair-adapted van, and he will come out with us to places such as the beach, which we couldn’t have contemplated when he lived at home.

Some people have still found it difficult to accept how I could “let go” of the care of my son if I really loved him. The answer is that I haven’t really let him go. I am still in charge of his life, and deal with his carers, doctors, social workers and teachers. We Skype him on his iPad and I send him letters and chocolate buttons every week. To the extent that he can’t live with us any more, the answer is simple. If he were still at home, I wouldn’t be here now.

Help To Work Scheme Launches

April 28, 2014

A new government scheme to help the long-term unemployed get jobs comes into effect on Monday.

Those who have not found work after two years on the existing Work Programme, will have to enrol on the Help to Work scheme or face reduced benefits.

Participants will have to go to the job centre every day, some will be offered community work placements and others will receive intensive coaching.

Those who fail to take part could lose jobless benefits for four weeks.

‘Huge waste’

Work and Pensions Secretary Iain Duncan Smith said: “Everyone with the ability to work should be given the support and opportunity to do so.

“The previous system wrote too many people off, which was a huge waste of potential for those individuals as well as for their families and the country as a whole.”

The programme was first outlined by Chancellor George Osborne at last year’s Conservative Party conference.

Labour says that the government has mis-diagnosed the problem.

Stephen Timms, shadow employment minister, said: “Under David Cameron’s government nearly one in 10 people claiming Job Seeker’s Allowance lack basic literacy skills and many more are unable to do simple maths or send an email.

“A Labour government will introduce a basic skills test to assess all new claimants for Job Seeker’s Allowance within six weeks of claiming benefits.”

BBC social affairs correspondent Michael Buchanan said the government had signed up more than 70 organisations to provide work experience under the scheme.

However, our correspondent added that the Salvation Army is not taking part, because it believes if someone has not found a job after two years of intensive support, their lack of work experience is not their only barrier to employment.

Benefits changes

Also on Monday, those wanting to claim Jobseeker’s Allowance will have to prove they are ready for work, before they can apply.

The government has said the changes will help to put an end to the “one-way street in benefits”.

But the TUC says the rules could discourage more people from claiming it.

“Making the JSA rules tougher and tougher will put people off claiming the benefits they need without doing much to help them get jobs,” said Frances O’Grady, the TUC’s general secretary.

But the Department for Work and Pensions (DWP) said there was no evidence that people would be put off claiming.

Stephen Sutton’s Story: When Life Gives You Cancer

April 28, 2014

London is no city for young women: Will Sarah return to escort work to pay for her debts?

April 25, 2014

Ann McGauran's avatarAnn McGauran

Down at the food bank, the volunteers hope that clients can over time move on from their challenging situations to something better. Sarah, who has featured here before, is struggling to get the proper support she needs to build a better life. She came here with a voucher a few weeks ago, worried that she was about to get evicted from her hostel. Some calls to the housing association were made, and the threat of eviction was withdrawn after her case was looked at again.

So she had a roof over her head for a while longer. But Sarah (not her real name), a 28-year-old law graduate who has battled for many years with a serious mental illness – Borderline Personality Disorder – came in again today and what she told me made my heart sink. This very intelligent, thoughtful and sensitive young woman has had to deal not…

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A TED Talk By Jess Thom

April 25, 2014

This is from October, but I’ve only just found it, and thought I would share it because she is one of my favourite disabled people.

 

Cllr Les Ford In Disabled Children ‘Burden’ Comment

April 25, 2014

Deputy council leader Les Ford has apologised for offending parents of special needs children by calling their loved ones ‘a burden’.

Parents, Mencap and the National Autistic Society have complained about Cllr Ford’s remarks during meetings where Cheshire West and Chester Council decided to bill parents of special educational needs (SEN) children £880 a year towards the £5,200 school transport costs.

Pupils up to four-years-old or between 16 and 19 years or with medical needs are eligible for the charge from September, which is reduced to £660 for the first year only. Low income families pay half.

Cllr Ford (Con, Helsby), who has since apologised for any offence, told the April executive meeting: “We have a burden, as everybody does, when you have a person like this in one’s family.”

Parents were also offended by the phrase ‘the state of that child’, when he told the March executive meeting: “Every parent has a duty to get their children to school, irrespective of the state of that child, whether it be SEN, autism or whatever.”

Explaining why he used the term ‘burden’, Cllr Ford told The Chronicle : “It’s our burden, not theirs, because we have to pay for these people.

“I was trying to be as careful as I could but obviously I didn’t quite succeed in their terms. They are very sensitive about it and I understand why.

“I am making no reflection whatever on their children. It’s nothing to do with that. It’s all to do with money, isn’t it?”

The deputy leader added: “They have misinterpreted what’s been said. I had my officers listen to the tape recording and they didn’t think there was anything untoward but at the same time there’s no reason not to say sorry.

“Why would I want to offend anybody? I would have no intention of doing so.

“My nephew is in the same boat. He is looked after permanently by Wandsworth Borough Council.

“He needs 24-hours-a-day care because my brother died some time ago so I know what it’s about.”

Michelle Jones, from Saughall, whose 17-year-old autistic son attends Greenbank School in Northwich, said in her official complaint: “I am not taken to being emotional in public but this man has reduced me to tears at both meetings by his clear lack of compassion and understanding of our children, despite our efforts to educate him during our speeches.

“This is not what I expect from any councillor, let alone one that has a very important position on the council.

“It is made even worse by the very fact that this is a public meeting, broadcast live on the internet and now available for viewing on the council’s website.

“This is clear prejudice towards people with disability and it has clearly influenced his decisions on the 16-19 SEN transport issue, seeking to blame people with disabilities for the pressures that his budget is under.

“I do not consider my son to be a burden, he makes our family life more challenging but we have all learnt from him and his sense of humour.

“I am still very upset and shocked that a high profile figure can be allowed to get away with such blatant prejudice.”

Emma Shepherd, from the National Autistic Society, said: “We’ve been contacted by many local families affected by autism who have been offended by Cllr Les Ford’s descriptions of disabled people as a “burden”.

“People with disabilities, including autism, can and do make huge contributions to society.

“But they are too often let down by outdated and damaging attitudes and perceptions about what they can achieve.

“The mark of a good society is how it supports its most vulnerable members. Rather than stigmatising disabled people, we should be supporting them to reach their full potential.”

Stephen John, Mencap campaign officer for the North of England, was given an apology after emailing Cllr Ford “with reference to a number of complaints”.

He said: “On April 2 at another meeting broadcast over the internet, you referred to disabled children, on more than one occasion, as a burden.

“This derogatory and misinformed language is certainly not a reflection of the love, affection and happiness that disabled children bring to their families.

“It is particularly worrying if you, in a position of trust and influence, have such a view of disabled people and I would certainly hope that it was a poor choice of words rather than the misguided view it portrays.”

Baroness Jane Campbell Tells Channel 4 News About SMA

April 24, 2014

Told she wouldn’t live beyond 2, Baroness Jane Campbell, now 55, speaks about the disability from a disabled person’s point of view.

 

Housing Association In Wales Offers Free Creme Egg To Bedroom Tax Tenants

April 24, 2014

Readers, you couldn’t make this letter up.

 

Full details here.

 

I don’t know whether to be patronised, or let out the laughter I’m struggling to hold back.

 

So I’ll ask you to help me send this viral and give me a sweet treat!

 

Carmichaels Win #Bedroomtax Case

April 24, 2014

Jobcentre Adviser: Sanctions are “generating the impression that unemployment is falling.”

April 24, 2014

Spinal Muscular Atrophy Explained

April 24, 2014

A woman believed to be the mother of three children found dead at a south-west London home has been arrested on suspicion of murder.

The children are believed to have had a serious genetic condition, thought to be Spinal Muscular Atrophy (SMA). The circumstances of the deaths are unknown, but police have focused attention on this little known disease.

Kelly Fletcher, whose daughter Lily Mae was diagnosed with SMA, and died shortly before her second birthday, explains the condition to the Today programme’s Mishal Husain.

First broadcast on BBC Radio 4’s Today programme on Thursday 24 April.

New Malden: Disabled Children Deaths

April 24, 2014

 

Yesterday morning, a story broke that affected me deeply. Twin boys, aged 3, and their sister, 4, were found dead in their home in South London. It was revealed early on that all three children had ‘life limiting’ genetic disabilities.

A woman, 42, was arrested in connection with the incident, on suspicion of murder. Her relationship to the children was not revealed immediately. What was revealed early on was that the family were wealthy- the father is a City banker and the family had help in the house from a nanny and a maid.

The instant emotional reaction of disabled people told us that the woman under arrest was the children’s mother. However, the revelation that the family had house help made some of us wonder whether one of the two house helpers may, just may, have been responsible for the tragedy. And I admit, I personally hoped that the mother was not responsible. Because I have been disabled since birth- and I am lucky enough to have parents who would never do any such thing. So cases like these always affect me deeply.

However, late last night, it was revealed that the woman under arrest was, in fact, the mother of the children.

A reader of Same Difference wrote online that parents killing their disabled children is a ‘common occurrence.’

Sadly, this is not a lie. There have been several cases over the last seven years, since Same Difference started, in both America and England, of parents who have killed their disabled children.

Three particular cases stick in my mind from England. The case of Naomi Hill, whose mother, Joanne, drowned her in a bathtub. Naomi, 4, had mild Cerebral Palsy. Joanne Hill said at the time that she was unable to cope with this disability.

The case of Ajit Singh, a 12 year old autistic boy who was forced to drink bleach because his mother feared he was about to be taken into care. She was reported to have had a personality disorder.

The case of Tom Inglis, whose mother, Frances, injected him with heroin as he slept, because she thought he was suffering after becoming disabled.

Each of these cases affected me deeply, for different reasons. However, in each of these cases, motives for the killings were revealed and, somehow, somewhere, made sense- if it can ever make sense for a parent to kill their own child.

We do not yet know a great deal about the New Malden case. However, on first impressions, it is simply very, very sad. And very little about it appears to make sense.

As I said earlier, the family were wealthy. News reports have revealed that they spent several months, and a fair amount of money, adapting their house to fully meet the needs of the three disabled children.

Neighbours described them as a lovely family and expressed their shock. The family had the support of the two women working in their home, and the mother was a full time carer for the three children.

Saddest of all, although the children’s disability has not been revealed, we know that it was already ‘life limiting.’ This makes it even more difficult to understand why anyone would have killed them too soon.

So, why are these three disabled children dead? Did their mother have mental health problems that no one could have seen coming, like Ajit Singh’s mother, Satpal, was reported to have had?

Did she, like Joanne Hill, feel shame, secretly, that she was afraid to reveal to her family, perhaps because they did not share these feelings? News reports have revealed that the father and the couple’s non-disabled daughter are currently on a holiday. Did she wait to act on her shame until they were out of the way?

Did she think she was ending their suffering, as Frances Inglis did with her son, Tom?

Or is she simply not responsible at all? Could the family simply have been the victims of a break-in or attempted robbery gone tragically wrong? Did she manage to save herself, but not her children?

Unlikely? Far fetched? Yes, readers, I know. But as the disabled child of loving parent carers, a part of me still hopes this is the case. Because, readers, I find the idea of any parent killing their own child simply too painful to think about. And the idea of a parent killing their disabled children is worse still for me- because I believe that real parents should love their children unconditionally.

I know how difficult disability is to handle, especially for non-disabled parents, who know what their disabled children are missing out on. But if, for any reason, this mother was unable to care for her children at home, I have to wonder if she considered putting them into care- or simply separating from the family while she dealt with her own pain, if their father was supportive.

I am sure full details will be revealed in the coming days and weeks. In the meantime, readers, I have one final thought to share with you: if many more cases like these are revealed in England, could we go back to a time when all disabled people are taken away from their parents, because Social Services are worried for their safety at home?

I, for one, sincerely hope not. Because the thought makes me shiver in fear and sadness, for what such a policy would do to the lives of the many disabled people who are safe, and deeply loved, at home with their families.

Update: Matthew Smith says the children had Spinal Muscular Atrophy.

Update 9am 24/4: Life With Hollywood, who has SMA, expresses many of my feelings on lifelong disability and death beautifully, in relation to this case, here.

UPDATE ON THE MHRN COURT CASE FOR THOSE WITH MHP’s

April 24, 2014

leonc1963's avatarDiary of an SAH Stroke Survivor

WCA JUDICIAL REVIEW UPDATE.

wcaThere will be a three day hearing in the Royal Courts of Justice in London on 22, 23 & 24 July 2014 in an attempt to establish what the DWP is going to do to remedy the substantial disadvantage that people with mental health problems suffer when being put through the Work Capability Assessment. This will follow a directions hearing that will take place in May.

Everyone knows that the only real remedy to our plight will be when these mock assessments are abandoned but, until then, we will continue the fight to try to improve them.

The case centres around the importance of further medical evidence for a person with mental health problems and on who is responsible for obtaining this evidence. Both the MHRN and the judges believe that such evidence is vital and that the DWP should be responsible and proactive in obtaining…

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Nikki Fox Appointed As BBC News Disability Correspondent

April 24, 2014

BBC News has created the role of disability correspondent, appointing Sony award-winning journalist and broadcaster Nikki Fox to the post.

 

Fox has reported on disability issues for The One Show and Rip Off Britain and has made documentaries for Radio 4 and Radio 5 Live, including Beyond Disability: The Adventures of a Blue Badger and Disabled and Desperate to Work.

 

She also regularly contributes to Richard Bacon’s Moan-In on Radio 5 Live.

 

From June, Fox will work as part of a team of three broadcast journalists based in Salford dedicated to reporting on disability issues, including producer Ruth Clegg and a cameraperson who is yet to be appointed.

 

Fox said: “I am beyond excited to be joining BBC News and am thrilled to be able to work as part of a specialist team of journalists, dedicated to the reporting of disability issues for a national audience, in a new and fresh way.”

 

Fran Unsworth, deputy director of BBC News, said: “Nikki’s appointment demonstrates BBC News’ commitment to providing the best disability news reporting across the country.”

 

Gary Smith, UK news editor for BBC News, said: “She is a talented broadcaster with an in-depth understanding of disability issues and her appointment is an important addition to our specialist journalism, allowing us to report disability stories with new expertise and commitment.”

Disabled Children Found Dead In London

April 23, 2014

 

Updated 2pm: News reports now suggest all three children who died were disabled. A woman has been arrested but her relationship to the children has not yet been revealed as far as I know.

 

Updated 12am 24/4: News reports are now revealing that the woman who has been arrested was the mother of the children. A bigger post follows on the case and the issues it raises.

 

Freedom of Information tribunal on benefit deaths – April 23

April 23, 2014

Mike Sivier's avatarMike Sivier's blog

Vox Political may seem a little quiet over the next 30 hours or so. This is because the site’s owner, Mike Sivier (that’s me), will be travelling to Cardiff to take the Information Commissioner and the Department for Work and Pensions to a tribunal.

The aim is to secure the release of mortality figures – death statistics – covering people who were claiming Incapacity Benefit or Employment and Support Allowance during 2012.

Figures for later dates were not part of the Freedom of Information request that forms the basis of this action (submitted back in June 2013, nearly a year ago), so it is unlikely that these will be forthcoming. The hope is that the tribunal will judge in favour of the information being released, ensuring that further requests cannot be blocked by the DWP.

The government’s claim is that a single-sentence, off-the-cuff line at the end of a Vox…

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No Triumph, No Tragedy: Sophie Christiansen

April 23, 2014

In this programme Peter meets Sophie Christiansen, who became a triple gold Paralympic medallist at the London 2012 Games and talks about her cerebral palsy how she is using her fame to help challenge attitudes around disability:

“We should use the Games as a platform to speak about disability as the public love the Paralympics and sport but don’t always understand what life as a disabled person can be like. Whenever anyone tells me I’m doing a good job at that, it means I’m doing the right thing.”

Sophie was introduced to horse riding on a school trip when she was just six years old – eventually discovering a love of speed riding which frequently saw her Dad running alongside her ready to catch her should she fall. Her first major international competition came ten years later – the 2004 Athens Paralympic Games, where, riding Hotstuff, she won an individual bronze medal. That same year, she was also voted BBC London Disabled Athlete of the Year.

Sophie was awarded an MBE in the 2009 New Year Honours list for services to disabled sport and an OBE in the 2012 New Year Honours list.As well as becoming a triple gold Paralympic medallist at the London 2012 Paralympic Games, 2012 also saw Sophie achieve her Masters degree in Maths from Royal Holloway University

Peter White explores her motivation, experiences and even her love life as the two chat about life after the Paralympics and the impact the Games have had.

Make Mail On Sunday Apologise For Food Bank Coverage

April 23, 2014

I’ve just signed this. Would you join me in signing?

Dear Mail on Sunday,

On Easter Sunday 2014, your newspaper printed a story

http://www.dailymail.co.uk/news/article-2608606/No-ID-no-checks-vouchers-sob-stories-The-truth-shock-food-bank-claims.html

which grossly misrepresents the noble and necessary role of food banks. As a result, the Mail on Sunday should apologise to all British food banks and their users and donate money to the institutions it has defamed.

Why is this important?

Rather than discussing the horrendous economic situation that has forced many people to use food banks, the article focused on the warped idea that food banks are merely an easy means of obtaining free food. This is not true, and suggesting this is an insult to the thousands of decent people who are living in poverty because of the cavalier attitude to unemployment and enormous welfare cuts that have been imposed by the government, which is supported by the Mail on Sunday. While we need a strong media to bring the ills in society to our attention, it is also important that the media should be honest and should not misrepresent issues for political gain or out of mere hatred. When the media uses inaccurate reporting to mislead the public, we must take action to stop them.

What Labour Said Then, What Labour Say Now And Why They Can’t Be Trusted On The Work Capability Assessment

April 22, 2014

johnny void's avatarthe void

atos_david_milibandWhat they said then …

Labour will: “increase support for claimants to return to work, replacing the old one-size-fits-all model, which writes people off as completely incapable of work, with a tailored, active system that addresses each individual’s capacity”

A new deal for welfare: Empowering people to work (PDF) – The Green Paper which proposed the Work Capability Assessment in 2006

What they say now (2014)

“We want the assessment to be part of the process of ensuring disabled people who can work get the support they need to do so, not to threaten or punish them. The test should be a gateway to identifying and assembling that support.”

How Labour would reform the Work Capability Assessment – Labour Shadow Secretary for Work and Pensions Rachel Reeves and Shadow Minister for Disabled People Kate Green

Then (2006)

“We will work with health professionals, personal advisers and disability groups (including the…

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Cameron’s office calls police on Bishop trying to deliver letter on poverty (not satire!)

April 22, 2014

Tom Pride's avatarPride's Purge

(not satire – it’s David Cameron)

Amazingly, David Cameron’s constituency office in Witney called the police when the Bishop of Oxford tried to hand in a letter about food poverty signed by church figures.

Anglican priest the Reverend Keith Hebden – who accompanied the Bishop on his visit to Cameron’s office – had this to say about the encounter:

“Summoning the police like that illustrates the sense of panic in this government about rising food poverty levels because they are in such denial about this problem.”

Here’s the full story from Al Jazeera:

UK row over Christian values and food poverty

This happened last week. So why has this not been reported in the UK media, I wonder?

.

Big thanks to Richard Bowyer for the heads up on this.

.

Related articles by Tom Pride:

Cameron’s morality resigns after being declared bankrupt

Scientists Claim Tiny Sub-Atomic Traces of Ethics Discovered in Barclays

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Cripple Of Irishmaan Gets Rave Reviews In New York

April 22, 2014

Daniel Radcliffe has won five-star reviews from US critics for his “warm, sensitive” performance as a disabled orphan in The Cripple of Inishmaan.

Originally staged in London last year, the play is the actor’s third Broadway outing, after Equus and How to Succeed in Business Without Really Trying.

Writing in The New York Times, Ben Brantley called it “his most satisfying stage work to date”.

Other reviews praised his “sympathetic” and “convincing” take on the lead role.

Set in 1934, the story follows disabled teenager Billy Claven, who lives with his “aunties” on the isle of Inishmaan off the west coast of Ireland.

Constantly mocked by the islanders, who call him Cripple Billy, he survives the tedium of daily life by reading books and staring at cows.

But the arrival of a Hollywood film-maker on a neighbouring island offers him a chance of escape to a glamorous new life.

“Daniel Radcliffe isn’t here just to flex his charisma for fans,” wrote Ben Brantley in the New York Times.

The former Harry Potter star “is entirely convincing as the boy who is regarded as least likely to succeed at pretty much anything in his God-forsaken rural Irish town,” he added.

Radcliffe “plays Billy with a crafty mix of guile and vulnerability,” wrote Thom Geier in Entertainment Weekly.

“His Irish accent is more than passable and while he doesn’t stint from the role’s physicality – curling his left hand and stiffening his left leg throughout the show – he refrains from milking the disability for easy sympathy.”

Johnnypateenmike
last summer

Writing in the Chicago Tribune, Chris Jones also noted the 24-year-old’s sympathetic portrayal of physical disability.

He “delivers a Billy with one heck of a limp, a body-twisting contortion that, when in motion, is quite the theatrical thing to behold,” he wrote.

“Radcliffe, a man of slight build, not only grabs onto this role physically, he understands that what interests us most about Billy is how he reacts when people add that ‘crippled’ to his name.

“Show too much pain and you’re off base. Show no pain at all and everything is a wash of black farce.

“Radcliffe rightly lands slap in the middle – his Billy has learned to go along to get along, but he still winces with quiet pain, mostly inside.”

“Radcliffe gives Billy a physical frailty and inner toughness combined with yearning that makes him a very sympathetic figure,” agreed Associated Press critic Jennifer Farrar.

Written by Martin McDonagh (In Bruges, Seven Psychopaths) in 1996, The Cripple of Inishmaan had never been staged on Broadway before now.

Directed by former Donmar Warehouse director Michael Grandage, it retains the (mainly Irish) cast from last year’s production at London’s Noel Coward theatre.

The supporting players also won favourable reviews, with Sarah Greene singled out for her “blissfully fiery” portrayal of Helen McCormick, the object of Billy’s affections.

“Walking dynamite,” said the New York Daily News of her performance, while the Associated Press noted she played the role “with gleeful meanness and a perfect touch of insecurity”.

“She also provides brittle, anti-Catholic comedy,” wrote their critic, “with her casual references to the clergy, whose groping she’s been violently fending off since childhood, at one point boasting, ‘I ruptured a curate at age 6.'”

“Ingrid Craigie and Gillian Hanna are blissfully dim as Billy’s loving maiden aunties,” said Linda Warner in Newsday. “Pat Shortt is perfectly irritating as the town snoop [and] Sarah Greene captures both the terror of the town hellion and her appeal.”

McDonagh “seems here to be both satirizing and celebrating the cliches about primitive Ireland and primal Hollywood, sending up the cruelties and seductions of the parallel universes as mutually exploitable pleasures,” she added.

“How right to have a real movie star as its heart.”

The Cripple of Inishmaan runs until 20 July, 2014 at the Cort Theater in New York.

An open letter to the Daily Mail…

April 21, 2014

squidgetsmum's avatarsquidgetsmum

The Daily Mail chose today to celebrate the resurrection of Jesus, champion of the oppressed, by publishing this article today.  Here’s my response.

 

Dear Daily Mail,

I’ve got a little boy.  His name is Isaac, and he’s nearly three.  Like any little boy, he loves cars, balls, and running around.  He’s barely ever still.

A few days ago though, he was.  I took him to the supermarket to spend his pocket money, and we passed the donation basket for our local food bank.  It was about half full – nothing spectacular, in fact, mostly prunes and pasta – and he asked what it was.  As simply as possible, I tried to explain that it was for people to give food for other people who couldn’t afford it.

This affected his two year old brain fairly deeply.  After a lot of thought, he decided to spend a little bit of…

View original post 715 more words

Sex Education And Disability

April 21, 2014

Danny Jarvis is a football coach with a degree in leisure management. He is funny, has an independent mind and loves his job. He also suffers from cerebral palsy and relies on a full-time carer to wash and feed him. At 32 he was still a virgin until his friend, Jennie Williams, took him to a brothel in Amsterdam.

For Jarvis it was a sexual awakening; for Williams, it was a wake-up call. Speaking to Jarvis after his first sexual experience, he told her he was worried it had gone badly because he didn’t climax immediately. This surprised Williams, who is also managing director of the disability charity Enhance the UK. “In every other way, Danny is sociable and knowledgeable,” she says. “But when it came to sex he didn’t know anything because he’d never experienced it and no one had ever told him about it.”

Williams began researching sex and relationships education (SRE) for disabled people. She found that very little was available. Despite recent TV programmes and films such as Sex on Wheels and The Sessions having brought the sexuality of disabled people into the open, many are still being neglected when it comes to receiving a proper sex education. This has worrying implications for their safety, self-esteem and sexual health.

According to a 2010 report by the disability charity Leonard Cheshire, almost 50% of disabled people surveyed said that they received no SRE at school. At the same time, people with severe physical disabilities are not exposed to the same everyday situations in which other young people learn about sex. They often also lack the ability and privacy to experiment with their own bodies.

Jarvis’s condition means that he occasionally ejaculates involuntarily. The first time this happened, he had no idea what was going on, simply because no one had taken the time to explain sex to him. His mother found it difficult to discuss the subject and it was not addressed at his school, either. This began to have a serious impact on Jarvis’s self-esteem. “At school I was under the impression that no one would want to have sex with someone in a wheelchair,” he says. By the time he was in his 20s he decided to take counselling.

People with disabilities – especially those requiring round-the-clock care – can often feel desexualised, Williams says. “If you have to have your bottom and face wiped for you, these are things that are associated with being a child. It is then assumed that you do not have adult sexual needs and, in the eyes of others, you become completely asexual, even if you’re not.”

Teresa Doyle, from the sex education charity Brook, agrees. She says that schools and parents often display “an utter blindness” to the sexual needs of disabled pupils.

In one instance, Doyle was called to a school to help a girl with a learning disability who required a pregnancy test. The girl’s teachers were convinced that she was lying because they did not believe that someone like her would be sexually active. The girl’s pregnancy test proved positive. Doyle explains that the girl had “ended up having sex because she didn’t know what it was”.

Doyle’s experience shows that SRE is vital for people with learning disabilities. A 2008 paper on teenage pregnancy in Wolverhampton states that around 28% of teenage mothers have some form of learning disability. The paper also includes figures from a special school in the same area that 40% of its female pupils had become teenage mothers within 18 months of leaving. Meanwhile, research in the Netherlands has shown that men with a learning disability are eight times more likely to contract sexually transmitted infections than those without.

In the UK, Ruth Garbutt – a research fellow at Leeds University’s centre for disability studies – has produced the report Talking About Sex and Relationships: The Views of Young People with Learning Disabilities. It shows that sex education provision for people living with disabilities is inconsistent, both at mainstream and special schools – and that teenagers are left vulnerable because of these shortcomings.

One parent told Garbutt that her son had pulled out all his pubic hair because he was ashamed of it. Another reported that their son was caught having sex with men in public toilets. “If he’d known more about what was safe and unsafe, and what was public and private then he might not have got into that situation,” Garbutt says.

Garbutt also heard that some doctors and teachers were advising parents not to talk about sex to their disabled children. Williams believes this sweep-it-under-the-carpet approach must change. “The truth is that disabled people have sex and disabled people like sex. But they don’t have access to the same advice and support as their peers.”

In an attempt to provide that support, Enhance the UK has launched the Undressing Disability campaign, which aims to create a comprehensive model of SRE for disabled people.

For Jarvis the message is simple. “I think if someone had talked to me about sex before, I wouldn’t have been so hung up about it,” he says. “In school they should tell people that just because you have a disability, it doesn’t mean you can’t fall in love, have kids and be happy.”

Food banks see donations surge after being criticised by Mail on Sunday

April 20, 2014

This is the best way to respond to the Fail and their scribbles.

Mike Sivier's avatarMike Sivier's blog

Daily Fail Logo

Britain’s biggest food bank provider has seen a surge in donations following a Mail on Sunday article criticised the charity for failing to run proper checks on people claiming food parcels, according to The Guardian.

“Before the article there had only been about 250 public donations since the Trussell Trust launched its JustGiving page in late January. But as of late yesterday afternoon, the number of donations had jumped to over 2,000, worth more than £19,000. Several donors cited the Mail article as the reason for making a donation,” the story states.

It continues: “‘The Mail story appalled me. This is the least I can do to apologise for their crime,’ said Anonymous after donating £10.

“Another, Spitting Feathers, said: ‘I am incensed by the disgraceful article. Call this journalism? I don’t. I’m not a Christian and admire the work being done by human beings for their fellow human…

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Victory- Cherry Groce Family Granted Legal Aid!

April 19, 2014

Some good news from Change.org:

After almost a thirty year battle to find justice for my mother Cherry Groce, we’ve finally been granted legal aid. This will allow us to have professional representation and actively participate fairly in her inquest.

Independent reports said that the events in 1985, when my innocent mother was shot by a police officer, sparking the Brixton riots, were a significant factor in her death in 2011. Despite numerous calls for legal aid to represent us at the inquest and unlock the truth surrounding her death our appeals were denied by The Legal Aid Agency.

But following our campaign, with over 133,000 of you supporting our family, national media coverage and help from Brixton MP Chuka Umunna, the Ministry of Justice were forced to intervene.

On Friday 11 April 2014 they said;

 

 

“Legal aid funding for lawyers to represent the family of Ms Groce at the forthcoming inquest into her death has now been granted. Having considered the request of the Legal Aid Agency, ministers have decided to authorise funding for this case. We hope that this legal representation will help her family and those who knew Ms Groce find out more  about the circumstances leading to her death.”

 

 

Please share this news — click here to tweet — it will come as a beacon of hope to others in my shoes who feel they are not being heard. When we come together, we can’t be ignored.

This is not the end, we need to make sure that the inquest brings us justice. The inquest is due to start on 30 June. In the meantime you can follow me on Twitter for updates: @mrleelawrence

Thank you for all that you’ve done for our campaign.

Lee Lawrence,
Son of Cherry Groce

PS We have set up a charity to honour our mother’s legacy dedicated to supporting those who have become disabled through tragedy, illness or accident. Please visit and support at: www.cherrytreetrust.org

You Can Complain When The JobCentre Fails

April 19, 2014

I’ve just spotted this on Facebook… thought it might be useful to some of you.

 

Anon
Hi I’ve not seen any posts relating to this but as the dwp love to upset so many people I thought I would share….. You are able to claim compensation when the jobcentres failings negatively impacts you, you fill in a standard complaints form but start it “I would like to request a special payment on the basis of…..” mark the complaint F.A.O Government Parliamentary Buildings. I received £655 from them when they misinformed me regarding carers allowance and stopped my mums money. Complain away people

Information tribunal on deaths of IB/ESA claimants – next week

April 18, 2014

Mike Sivier's avatarMike Sivier's blog

I have just sent out a ‘diary marker’ to press organisations, notifying them of the Information Tribunal that will be held in Cardiff next week.

Inevitably, there will be organisations I have missed – and I also want as much of the social media as possible to be aware of this and to be spreading the word. For that reason, I’m publishing the text of the press release below.

If you have a Facebook page, blog site, Twitter account or whatever, please feel free to use what follows and make sure people know that this is going on.

Diary marker

Tribunal – Law Courts, Cathays Park, Cardiff, April 23, 2014 at 10am

Incapacity benefits – deaths of claimants

A tribunal will decide whether the Department for Work and Pensions should be ordered to release its statistics on the number of people who have died while claiming Incapacity Benefit or Employment…

View original post 511 more words

Second British Woman, 99, Ended Life In Switzerland Because She Was ‘Tired’

April 18, 2014

Scary stuff, readers. How many more are there that we don’t know about yet?

 

A second British woman who grew ‘tired of life’ has been helped to die at a Swiss suicide clinic.

The woman, who was 99 and from London, was not ill or disabled and simply chose to end her life.

It comes after a retired art teacher committed suicide at the Dignitas clinic in Switzerland after she grew weary of the pace of modern life and how technology was changing society.

The 89-year-old felt that her failing health, as well as her belief that people were becoming ‘robots’ attached to their gadgets, gave her little reason to live.

The woman, who wanted to be known only as Anne, had suffered from worsening health in recent years, but was not ill or infirm.

The deaths have stoked the ongoing debate over balancing a right to die against the dangers that vulnerable people could be exploited.

Retired doctor Michael Irwin has helped a number of Britons end their life at Swiss suicide clinics. He told the Sunday Express that 3,000 ­patients are helped to die every year.

He said: ‘Doctors do not wish to stand by and watch their patients suffer needlessly. It has always gone on.’

He said that the second woman had not used Dignitas, but instead a smaller clinic.

He said: ‘She was not terminally ill, nor was she particularly severely disabled, yet she could not find much enjoyment in living any more and felt the time was right to say goodbye.

Mr Irwin, who founded the Society for Old Age Rational Suicide and helped with Anne’s application to Dignitas, said: ‘She was a feisty individual and a very independent person all her life.

When she became elderly and her daily activities became increasingly restricted, she decided to go to Dignitas.

‘If you are mentally competent you can rationalise whether or not you want to end your life, after you take a look around and decide you don’t like what you see.’

He said there were at least three people in similar circumstances to Anne who ended their lives in Switzerland in recent years.

There is to be a free vote in Parliament on the Assisted Dying Bill, under which two doctors could prescribe a lethal dose of drugs to a terminally ill patient with less than six months to live.

Man Amputates Own Hand ‘For A Reaction’

April 17, 2014

A man who suffered with chronic hand pain chopped the limb off so people “would listen” to him.

Mark Goddard, 44, had constant pain following a motorbike accident and became frustrated with doctors who could not relieve his symptoms.

The former mechanic decided to amputate the hand with a home-made guillotine in his back garden, but his pains have not stopped.

Mr Goddard told BBC Radio 5 live’s Chris Warburton: “I don’t like pain but it was something that I was prepared to do to try and get some form of reaction or get something done.”

Sainsbury’s Easter TV Advert Features Ben, 8, Who Has Downs Syndrome

April 17, 2014

Thanks to Sainsbury’s!

 

DWP Block Report To Cover Up Work Programme Shambles

April 17, 2014

johnny void's avatarthe void

IDS-slug The DWP are refusing to release an evaluation of the floundering £6 billion pound Work Programme despite the report having recently featured on Channel 4 news.

The evaluation is believed to be critical of the Work Programme and in particular benefit sanctions, warning that they found: “no conclusive evidence that sanctions were changing job search behaviour or increasing job entry rates.”

A Freedom of Information request asking to see the report has today been refused by the DWP on the grounds that they plan to publish it at an unspecified later date (PDF).  The evaluation was scheduled to be released in the Summer of last year.

This is not the first time the DWP have treated Freedom of Information (FOI) rules with contempt in a shoddy effort to conceal what’s really going on, and wrong, with the department.  A ruling by the Information Commissioner;s Office (ICO) ordering the release…

View original post 276 more words

“We Could Chop In Half The Cases We Needed To Help With If DWP Sorted Things Out.”

April 16, 2014

It was a muddle with a form that first made Craig, 31, lose his benefits. He had been looking for work in Coventry for nearly a year, diligently going to the jobcentre and trawling through adverts. Then he made a mistake that would leave him hungry for a month.

“I filled out a form saying I was searching for work from Monday to Friday and I was meant to put from Thursday to Thursday. It was just a mistake but I had my benefits sanctioned for four weeks. It was just before Christmas last year and I was panicking about presents for my kids, but the job supervisor said ‘you’re not paid to get presents, you’re paid to look for work’.”

Too proud to go to a food bank, the divorced father of two made it through the month surviving on the last few tins in his cupboard and limiting himself to one meal a day.

Craig suffers from severe depression and lost his job working nights as a courier a year ago because he had missed too many days to the illness. Last month he found out his mother had terminal cancer and his depression worsened. He went to the doctor, who said he was too ill to work and registered him as eligible for the sickness benefit employment support allowance (ESA).

That should have been the start of a time of respite, but bureaucratic delays meant the new benefit never came. Last Friday marked three weeks since he last received any money and Craig finally cracked.

His four- and seven-year-old sons were due for their monthly visit at the weekend and he had nothing to feed them, so he came to his local food bank in Hebron church.

“All I’ve got is a tin of peas in my cupboard and a bit of milk in the fridge,” he says, too embarrassed to make eye contact.

“I last ate yesterday morning and that was a bowl of cornflakes. In the last week I’ve had maybe six meals. I went to a benefit advice centre this morning and they sent me here. I’ve had to swallow my pride because I wanted to have food for my boys.”

Sitting in a cafe behind the church, he is handed five bursting carrier bags of food, including fresh vegetables, tins, pasta and bread. His hands shake as he packs the heavy tins into his rucksack and prepares for a wobbly cycle home with the plastic bags on his handlebars.

Coventry is now the busiest Trussell Trust outpost in the country. In the past year its network of food banks gave 17,658 people emergency food, up 41 per cent on the year before. The city has just opened their 14th distribution centre and a further two will open this year.

Food bank manager Hugh McNeil is a softly spoken churchgoer, and doesn’t look the tubthumping political type. But, when asked about the impact of the Government’s welfare reforms, he struggles to contain his fury. “Compassion has disappeared out of the welfare state,” he says. “There’s none any more. The way these benefits are being administered is just so punitive and nobody seems to be thinking about the children affected either.”

Hebron, an evangelical church in a converted bowling alley in the east of the city, is one of the trust’s newer branches. A mile or so closer to the city centre is The Hope Centre, the busiest of Coventry’s distribution points, which frequently gives food to dozens of families a day.

Louise Duffin, 35, has come to make sure she has enough food to make it through the school holidays with her children Nicholas, 12, and Natasha, 10. She has “practically nothing” left in her cupboards, beyond a couple of tins of beans and the dregs of a milk bottle.

“Being on benefits means that the kids get free school meals so in the holidays that means finding an extra meal a day,” she says. “I dread the holidays because of it. Not being able to afford to do stuff is a problem too.”

Ms Duffin has epilepsy and recently transferred on to ESA after having to appeal against a medical assessment that she was fit to work. “I’ve only just won, and while I was fighting it my income went from £165 a week to £71. I have child benefit and tax credit on top of that but it was still tough.”

After filling out a form and picking up dried and tinned food, she goes to a shipping container in the car park, where fresh produce and hot cross buns are added to five overflowing bags.

In the centre’s cafe, a  distraught mother with a  five-day-old baby waits, hoping for food and nappies. She has five children and the new arrival combined with the start of the Easter holidays has crippled the family’s precarious budget.

Makadi Mulambela, 28, is one of the last to arrive. He has been struggling to feed himself after being hit with a month’s benefit sanction. “They sanctioned me because I made a mistake on the job search form,” he explains.

“The website I’d been using was direct.gov and I wrote that I’d been on direct.jobs, which was wrong. I had been looking on it, I just wrote it down wrong. It’s difficult because when they catch you on something like that you don’t get  a chance to explain, that’s  just it.”

Gavin Kibble, the food bank’s operations director, is adamant that welfare reforms are responsible for much of the rise in need. “We’re seeing a lot of people coming through the food bank because of benefit sanctions. Around 43 per cent of our cases relate to a DWP issue, whether that’s a benefit change or sanctions. We could chop in half the cases we needed to help with if DWP sorted things out.”

Main Causes Of Referral To Trussell Trust Foodbanks, 2013-14

April 16, 2014

This bar chart, which I’m publishing with many thanks to the Trussell Trust, says it all about the reasons people are needing to turn to food banks.

 

Primary referral causes in 2013-14

 

DETERIORATING FINANCIAL SITUATION FOR LOW INCOME WORKING HOUSEHOLDS – NEW RESEARCH REVEALS #BeAware2014

April 16, 2014

A press release from Turn2us.

A new survey commissioned by the national charity Turn2us has found that almost three fifths (57%) of low income working households feel their financial situation has worsened in the last year. Despite signs of an improving economy, half of all people surveyed are worried about their financial situation as they struggle with a combination of falling wages, shorter working hours and rising living costs.

The survey, released to coincide with Turn2us‟ annual Benefits Awareness Month, has found that on average, working households are forced to spend half of their monthly income on utility bills and food. Worryingly, nearly two-fifths (39%) say their outgoings now outweigh their earnings. Households are also facing barriers as they try to improve their situation. With 1.4 million in part-time jobs nationally – 46,000 higher than a year ago* – over half (57%) say they want to work more hours but they cannot get the work. While a quarter of those surveyed (25%) have seen a fall in their income in the last year.

Over half of the 13 million people living in poverty in the UK are now from working households**. Turn2us‟ research found that over three-fifths (62%) are not claiming the benefits and tax credits they may be entitled to. Even more alarming, a huge 60% had not even checked their eligibility for this support, or did not know how to check what help may exist.

The toll this is taking on lives is severe. Over two-fifths (43%) have had no choice but to cut back on food and other essentials. Health is also being put at risk with almost a third (30%) unable to sleep and over a quarter (27%) experiencing depression.

In response to these ongoing problems, Turn2us Benefits Awareness Month is focusing on the huge numbers of people who are in work yet struggling to make ends meet. The campaign, „Be Aware‟, is encouraging everyone to check what financial support could be available by using Turn2us‟ free, online Benefits Calculator at http://www.turn2us.org.uk/BeAware. The website also features information on support for different employment groups, so that people can access further help, whether they are employed full-time or part-time, self- employed, on zero contracts, or on leave.

Alison Taylor, Director of Turn2us said: “Today, Turn2us launches Benefits Awareness Month and reveals the extent to which working households are struggling in poverty. Our research shows that the stranglehold on pay, underemployment and the climbing cost of living all show no signs of easing and any economic improvements are failing to reach the UK‟s poorest people. It’s clear that more needs to be done to combat poverty, especially for those people in work.

“Help is available in the form of Working Tax Credit and other welfare benefits and it can make a huge difference. We found that 85% of current claimants in work said benefits have had a positive impact on their lives and helped with housing costs, bills and even avoiding debt.

The Turn2us “Be Aware” campaign brings together our free Benefits Calculator and information so others can access this vital support.

“Our message is clear. Being in work does not mean the end of help. We want everyone to know they are not alone and to “Be Aware” of the support that is available.”

The “Be Aware” campaign is being supported by charities and organisations across the UK to help increase awareness of the support available for people struggling in work on low incomes.

For more information about the campaign, please visit http://www.turn2us.org.uk/BeAware or http://www.turn2us.org.uk.

Easter Play Schemes For Disabled Children Axed Due To Cuts

April 16, 2014

This Easter, children with disabilities are struggling to gain access to play services as funding for short breaks continues to be cut. Short breaks provide respite care for families and carers of children with disabilities, but since 2010 the money allocated for them by local authorities has been greatly reduced.

Lastest government figures show that funding fell by 6% in the last financial year across England. In 2011-12, 63% of English local authorities reduced their expenditure, a Mencap report found.

“Since our 2013 report, we have seen even more councils cut short breaks services locally,” says Dan Scorer, the head of policy and public affairs at Mencap. “Despite the government recognising the need for these vital services, family carers are still being left isolated, exhausted and at breaking point. This is because they care – sometimes 24 hours a day, seven days a week – without a break.”

“The government has invested in short breaks, but this money has not been ringfenced and Mencap has found it is not being spent on the services it was meant for,” he adds.

Councils assign families an annual allocation of hours of support, which they are able to use at a local short-break provider of their choice; providers range from play services to youth clubs, babysitters, overnight care and residentials.

Single mother Elizabeth Shapland (not her real name) has long relied on short break services to provide much needed respite from caring for her highly autistic son, Aaron. But, this Easter, she has been unable to get any support for him because she has fewer paid-for hours that she can use for short breaks. As a result, Aaron, 13, has had to miss the Easter play scheme at Hackney adventure playground, a specialist playground for children with disabilities run by the Kids charity, in east London, which he has eagerly attended for the last seven years.

Since 2013, Shapland says her allocation of short breaks from Hackney council has been reduced from 150 to 120 hours – this equates to two hours a week. Aaron is now only able to attend one weekly after-school session at Kids Hackney adventure playground, with nothing left for holiday provision.

“This has been the most terrible year yet. Because of the cuts, I have been unable to access holiday cover at Christmas or Easter,” says Shapland. “It’s like wartime rationing, if I eat all my rations now, I won’t have any hours left for the rest of the year.”

The borough has five short-break providers for children with disabilities. One will not be running any services this Easter. Cassandra Delisser, the project manager of the Huddleston Centre, says this is the first time the charity hasn’t run an Easter programme in the 15 years she has worked there. “We do not have enough funding, and the young people do not have enough days to run an Easter session so we have decided to prioritise summer,” she explains.

Una Summerson, the head of campaigns at Contact a Family, a charity that supports the families and carers of children with disabilities, says: “Cuts to short breaks services have further limited disabled children’s chances to take part and enjoy the things other children and families take for granted. We urge councils to think again – the knock-on effects on isolation and health could cost councils more in the long run.”

Shapland says her son’s autism means he has poor communication skills and becomes easily frustrated. “Without the support of the Hackney adventure playground, the number of exclusions and detentions Aaron receives goes up and he is more likely to come to blows with his sister, because he has no outlet for his frustrations.”

Hackney council maintains that since 2010-11 its expenditure on short breaks provision has been £950,000 a year. A council spokeswoman says: “We realise what a lifeline short breaks are for families, so we ensure funding is protected.”

The UK’s Shocking Food Statistic

April 16, 2014

Man With CP Refused Train Access

April 16, 2014

A train company is holding an investigation after a disabled man claimed he was not allowed to board a crowded carriage.

Colin Williams, from Welshpool, claimed a guard refused to let him board a train to Shrewsbury saying it was full.

But Mr Williams, 41, said several other passengers were allowed to the board the train, while the guard did not lower the ramp for his wheelchair.

Arriva Trains Wales said it was investigating the matter.

Mr Williams, who has cerebral palsy, and uses a wheelchair, was travelling alone to Shrewsbury to watch a friend perform at a music festival when he was left at Welshpool railway station on Saturday 5 April.

“I was one of about 20 passengers waiting to go on the train but the guard made no effort to get the ramp to get me on, even though people told him they would help me to the disabled area,” said Mr Williams.

‘Humiliating’

The ramp for disabled passengers is kept on the train, but the guard refused to lower it.

Mr Williams said: “I asked for the ramp to help me get on the train but the guard told me there was no room on the train for me.

“I told him I was willing to go anywhere on the train but he refused to let me on.

“I would have been quite happy to travel in the aisle with other people because the journey to Shrewsbury only takes about 20 minutes.

“As far as I am aware I was the only passenger that didn’t get on that train.

“It was a humiliating experience and I felt discriminated against because of my condition.

“I have written a letter and an e-mail to Arriva Trains asking for an apology.”

Mr Williams was able to board the next train which was two hours later.

“By the time I got to the event my friend had already finished his performance,” said Mr Williams. “My day was ruined and I am upset at the way I was treated.”

‘Investigating’

Mr Williams has since talked to passengers who were boarding and alighting the same train.

He said: “One person who got on that train has told me there was plenty of room if people had moved down the aisle a little bit.”

A disability group has urged the train company to ensure its staff are made aware of its own policies regarding disabled people.

It said the 2010 Equality Act makes it unlawful for organisations which provide services to the public to discriminate against disabled people in the way they provide or do not provide those services.

Rhyan Berrigan, Disability Wales’ Transport Policy Officer, said: “It is very poor customer service and it is clear the guard was not following procedures properly.

“We urge Arriva Trains Wales to ensure that all staff are made aware of their own policies and procedures regarding disabled people.”

An Arriva Trains Wales spokesman said: “We are sorry to hear that the passenger was unable to board the Aberystwyth to Shrewsbury service at Welshpool station and we are currently investigating this matter.

“Arriva Trains Wales remains committed to reducing social exclusion through a positive policy of improved access to trains and stations and works closely with rail industry colleagues and stakeholders to achieve this through positive partnerships.”

People First England Politics For All Party Conference Competition

April 15, 2014

Kaliya Franklin has asked me to publicise a competition being run by People First England. The competition is open to learning disabled people interested in politics and the prize is the chance to go to the Labour or Conservative Party conference with People First England.

 

If this interests you, full details are here.

Crohn’s Patient Loses Egg Freeze Legal Case

April 15, 2014

Any thoughts, readers?

 

A woman with Crohn’s disease has lost a legal challenge against a decision to refuse NHS funding to freeze her eggs.

Lawyers for Elizabeth Rose, 25, from Margate, Kent, claimed in the High Court it was unlawful to refuse the treatment to preserve her fertility.

Miss Rose fears an imminent bone marrow transplant and chemotherapy treatment she faces will leave her infertile.

She took legal action over a refusal by Thanet Clinical Commissioning Group (CCG) to provide funding.

Early menopause

Mr Justice Jay, sitting in London, dismissed her application for a judicial review.

“Unfortunately, it is a probable outcome of this gonadotoxic therapy that the claimant will be rendered infertile and suffer early onset of the menopause,” he said.

“Understandably, the claimant wishes to secure the best chance of having her own genetic children, and she therefore seeks NHS funding for oocyte cryopreservation before the chemotherapy begins.”

He said her application for funding had been refused on more than one occasion but she had failed to demonstrate any unlawfulness.

Postcode lottery

Miss Rose has had a severe form of Crohn’s disease since she was 14.

Her condition has deteriorated and doctors at King’s College Hospital in south east London are recommending a bone marrow transplant and chemotherapy to bring the disease into remission.

The Central Saint Martins College of Art and Design fine art graduate believes she is the victim of a “postcode lottery” as the treatment is available to single women in some other parts of the country.

Clinicians at King’s College applied on her behalf for funding so her eggs could be frozen but the case was contested by Thanet CCG.

Swindon Mayor Resigns After ‘Mongols’ Comment

April 15, 2014

Some good news for a change.

 

Swindon’s mayor has resigned after making derogatory remarks about disabled people in a training meeting.

Conservative Nick Martin, 63, was found guilty of breaching the members’ code of conduct after Labour complained about comments he made last year.

Labour councillors said they heard him say: “Are we still letting Mongols have sex with each other?”

The standards committee ruled he must apologise but Mr Martin said it was a word he “was brought up with”.

In a letter to the council, Mr Martin said it was “with regret” that he submitted his resignation as mayor “with immediate effect”.

He added that, following the accusations against him, he had cooperated with the independent standards investigation.

“I have made new apologies and am abiding by the other recommendations from the Standards Assessment Panel,” he said.

“However, it is clear that this will not stop the attacks on the office and person of mayor.”

Mr Martin was reported to the standards committee by Labour councillors Ray Ballman and Junab Ali after the remarks were made during a training meeting for councillors last year.

Last Thursday, the committee ruled Mr Martin must make a public apology within seven days and attend further training within a fortnight.

‘Deep-seated ignorance’

Conservative leader of the council, David Renard, said the process had “proved to be a robust system”.

“It was right and proper that due process took its course,” he said.

“The mayor accepted the recommendations and has agreed to resign. I think he has made the best decision that he could, in the interests of the office of the mayor and all involved.”

Richard Hawkes, of disability charity Scope said Mr Martin’s “outdated comments” showed a “lack of acceptance that disabled people have sex lives”.

“The mayor insinuated that there is something wrong with disabled people having sex with each other,” he said.

“The outcry following the mayor’s comments show that the general public don’t condone this kind of deep-seated ignorance towards disabled people.”

Disabled People Pay ‘Penalty’ On Everyday Costs

April 15, 2014

Tell me something I don’t know…

Disabled people pay “a financial penalty” on everyday living costs, spending an average of £550 a month extra, according to a report by Scope.

They needed specialist equipment and had to pay out for things like taxis instead of public transport, it added.

Disabled people were, on average, £100,000 worse off when it came to pensions and savings, the charity said.

The report pulls together existing research including new analysis of a 2010 survey by think-tank Demos.

That research was funded by Scope.

‘Shocking stories’

The new Priced Out report also features data from the Department for Work and Pensions and organisations including the London School of Economics, Save the Children, and the National Housing Federation.

Scope said 17% of disabled people paid £800 a month more on everyday living costs than able-bodied people.

And 10% paid more than £1,000 extra a month, it said.

Other examples of extra everyday living costs included keeping the home warmer to help certain conditions, using more energy to run more regular baths and replacing clothes worn out because of wheelchair use.

Scope chief executive Richard Hawkes said: “Disabled people and their families already have to buy things, like specialist equipment, that most families don’t have to budget for.

“Sometimes their condition means they have no choice to use more of something, like heating.

“But this situation is being made worse because disabled people and their families also pay more for the everyday.”

The charity had heard “shocking stories” including disabled people being charged double the price for a taxi and £31 for a modified knife, fork and spoon set, he added.

Scope said many people were struggling to pay the bills and were three times more likely to take out doorstep loans.

The charity is calling on the government to protect the Personal Independence Payment (PIP) from an overall cap on benefits.

 

RNIB Wants Eye Clinics To Provide Sight Loss Advisors

April 15, 2014

Every eye clinic in the UK should provide access to a sight loss advisor, the Royal National Institute of Blind People (RNIB) has claimed.

The charity found that almost half of all eye hospitals in the UK did not offer any support for people after their diagnosis.

Stevie Johnson from the RNIB told BBC Radio 5 live’s Morning Reports: “For a long time, the emotional and practical needs of people have been overlooked.”

An NHS England spokesperson said they were aware that eye health care was “fragmented with variations in outcomes” and they were determined to address those issues to improve care.

‘Second Skin’ Sensor Developed For Amputees

April 15, 2014

Researchers have developed a new type of pressure sensor – dubbed a “second skin” – which they say could prevent dangerous sores.

The technology is being developed initially for amputees who suffer rubbing against their artificial limbs.

If the Southampton University work is successful the sensors may also be used for others at risk, such as wheelchair-users and those confined to bed.

The new technology could be available to NHS patients within three years.

Pressure sensors are already used, but this Medical Research Council-backed project – in partnership with the prosthetics firm Blatchford – differs in that it is able to detect rubbing as well as downward pressure.

This could make it better at detecting sores at an earlier stage.

Richard Bradbury, 26, who is a technician at Blatchford and had an amputation below his right knee soon after he was born and then above the knee in his teens, has long experience of discomfort caused by pressure and rubbing against his prosthetic limb.

“It can be very distressing.

“When I was younger and getting bigger and growing more I had up to four or five legs a year. And because you’re getting bigger you’re not going into the socket as much. And it can rub, it can create sores, blisters.”

Pain and discomfort

It is thought there are about 50,000 lower limb amputees in the UK. A report in 2000 by the Audit Commission said nearly one in four did not use their prosthetic limbs as much as they would like – often because of pain and discomfort.

Dr Andy Franklyn Miller, a sports medicine specialist who has worked extensively with military amputees, said it was still a serious problem.

“A limb that doesn’t fit because of pain means a limb that can’t be worn. And often that then accompanies an increase in weight which means the socket that the body fits into, no longer fits. And so it’s a real catch-22.”

The sensor is thin and flexible like a small golden postage stamp. It is taped to a liner – essentially a cushioned sock – which is then placed in the socket connecting the stump and the artificial limb.

It sends that information to researchers and clinicians who can monitor the pressure peaks and troughs as the patient walks, and see if any adjustments are needed to prevent discomfort or pain.

The researchers are planning to develop a system of traffic light alerts for smartphones, warning of potential problems. That may mean just putting on an extra sock for padding, because the stump can change shape during the course of the day. Or it may mean a visit to a clinic for further assessment.

“Really serious”

Dr Liudi Jiang from the University of Southampton, who is leading the project, says the sensors could act as what she calls a “second skin”.

“A large number of lower limb amputees may suffer from nerve damage and they have reduced skin sensation. That means they don’t feel the pain or the tissue injury as effectively as we do. And it may be too late, because once that soft tissue is compromised it could lead to infection and could be really serious.”

Joe McCarthy, who does prosthetic research and development at Blatchford, hopes in time the sensors will mean those wearing artificial limbs will not have to worry about keeping a good fit.

“The next stage will be to develop some sort of system to adjust the fit of the socket so we’ll have a system that can react as the person’s wearing the leg saying, ‘OK, you’re a little bit far into this socket,’ and it can literally pump up some pads or adjust the fit in some way so the person doesn’t have to go to the centre.”

The researchers say the sensors may be available to NHS patients in as little as three years. Dr Jiang believes this technology may have many more uses which could prevent pain, infections and even amputations.

“This is a platform technology and we envisage it could be applicable in many other healthcare sectors such as smart shoe insoles for people with diabetes, or wheelchairs or mattresses – wherever the body rubs.”

Eastenders’ Lisa Hammond: There Will Be A Humorous Side To Donna

April 15, 2014

I wanted to wait until after her first scenes had aired to share this. Her first scenes aired last night, so here we go.

 

EastEnders newcomer Lisa Hammond has revealed that there will be a humorous side to her character Donna Yates.

Despite being billed as “aggressive and difficult“, Hammond has insisted that her character won’t be completely unlikeable.

Speaking to Inside Soap, the actress said: “Initially, Donna is very opinionated. But there is a humorous side to her.

“I don’t want her to just be a hard-faced cow. There needs to be a glint in her eye, tinged with a bit of sarcasm as well.

“It was hard to launch into being such a fiery character. Once I settled in, I thought, ‘This is fun – people will hate me!'”

Donna will immediately get on the wrong side of stallholders Kat Moon and Bianca Butcher after they mistakenly assume she is someone from the council and confront her.

Hammond said: “Not only did I come in on my first day as someone who is difficult and a bit nosey, but I had to do it with Kat and Bianca!

“They are really strong women, so it was daunting. But Patsy (Bianca) and Jessie (Kat) have always been a good laugh in between scenes, so it was very easy to settle in.

“Patsy is my mentor. She told me to come straight to her with any questions.”

Deaf Broadway Actress Phyllis Frelich Dies At 70

April 14, 2014

Tony award-winning actress Phyllis Frelich has died at the age of 70.

Frelich, who was deaf, was best known for starring in the Broadway version of Children of a Lesser God.

In 1980 she won a Tony for her role as deaf character, Sarah Norman. Marlee Matlin won an Oscar for her portrayal of Norman in the 1986 film version.

Frelich’s husband Robert Steinberg said she had died at her Temple City home on Thursday from a rare degenerative neurological disease.

Deaf parents

He said there were no treatments available for her illness, progressive supranuclear palsy, otherwise known as PSP.

“She was extraordinary, the finest sign language actress there ever was,” he said.

“We were married for 46 years. I would have been happy with 46 more.”

Frelich was born in Devils Lake, North Dakota, the oldest of nine deaf children born to deaf parents.

Her interest in acting took off while she was studying at Gallaudet College – now called Gallaudet University – in Washington DC.

She then joined the National Theatre of the Deaf where she met Steinberg, who was a scenic and lighting designer on several plays by award-winning writer Mark Medoff.

The couple inspired Medoff to write Children of a Lesser God, which is about the relationship of a deaf woman and a teacher at a school for deaf students.

In a 1988 interview with the Associated Press, Frelich said: “I was the first deaf person he (Medoff) had known. I told him there were no roles for deaf actresses. He said: ‘Ok, I’ll write a play for you.’ He did. He went home and wrote Children of a Lesser God.

“He wanted to write a good play. He was interested in me as an actress and he wasn’t trying to write a message play.”

Medoff, now a professor at New Mexico State University, paid tribute to Frelich on Saturday.

‘Our leader’

“The play opened and I really thought, ‘I’m working with as good as an actor as I’ve ever worked with in my life. And I’ve got to take advantage of it,'” Medoff told the Associated Press.

Frelich also starred a as a deaf playwright opposite Richard Dreyfuss in another Medoff play, In the Hands of Its Enemy.

“She didn’t start out as a revolutionary individual, but she became an incredible advocate for deaf culture,” Medoff said.

John Rubinstein, who also won a Tony for the male lead role of John Reed in Children of a Lesser God, praised his co-star’s energy and acting ability.

“She was 70 years old, but that statistic means nothing. She looked like a 40-year-old woman ready to run 25 miles,” Rubinstein said.

He added that Frelich expressed “what she needed to express with only her arms and hands and face and body.”

Arrested Development star Jeffrey Tambor, who acted opposite Frelich and Dreyfuss in The Hands of Its Enemy, called her “a walking acting lesson.”

“I just remember her eyes just radiating all this warmth and power and love and courage in her performance,” Tambor said.

“It was just a wonderful play and a wonderful cast. Phyllis was our leader. She was something,” he added.

Frelich also starred in TV series including CSI, ER and LA Law.

Scope Rejects Swindon Mayor’s ‘Forced Apology’ For ‘Mongols’ Comment

April 14, 2014

 

Richard Hawkes, the chief executive of the disability charity Scope, said the mayor had “missed the point” after the council demanded he provide an “unreserved” apology.

“Of course he should apologise for using this offensive term. But this isn’t just about political correctness and using the wrong words.

“Disturbingly, he has insinuated that there is something wrong with disabled people having sex with each other.

“This is about deep-seated ignorance towards disabled people and a lack of acceptance that disabled people have sex lives, which can be just as fulfilling – or unfulfilling – as anyone else’s.

 “The mayor’s public apology needs to acknowledge that it is more than just his words that are at fault. And that with his office, comes a responsibility to represent all of his constituents.”

What Does The Suspension Of PPC Deborah Hopkins Say About Labour Policy Towards Sick And Disabled People?

April 14, 2014

 

Readers, Deborah Hopkins, who, as many of you may know, was until recently a Labour PPC for 2015 in a Cornwall constituency, has caused a storm online all weekend. Why? Because she wrote on Twitter, swearing at an opponent, describing the British Empire as ‘genocide’ and saying that the current Government are ‘killing the sick’ and ‘starving the disabled’ as well as saying that a Government department is using ‘starvation’ to control the population.

I just went looking for Hopkins’ relevant Tweets, but they appear to have been deleted.

Now let me make one thing clear. I can see why her use of a swear word to an opponent would have been a serious problem. And the Tweet about the British Empire would, most likely, be seen as more than a little inappropriate by many people.

However, all the Tweets were a result of Hopkins’ personal opinions. She may have been a Labour Party member, but when she Tweeted, she was not yet an MP. And while I am the first to say MPs should not swear in public, surely party members should not be treated as if they are in the same position of power and authority?

Yes, Hopkins should have been disciplined for swearing at her opponent, and for her comment about the British Empire. Even asking her to delete those Tweets was perfectly fair.

However, on her Tweets about the current Government’s treatment of sick and disabled people, Hopkins has my full support. I write that sentence as an adult who has been disabled since birth. I write that sentence as a  disability rights campaigner who has heard horror stories of how the current Government’s policies, in particular their spending cuts,  have directly affected sick and disabled people more than almost any other group in society. I write that sentence as a person interested in politics who has closely followed Parliament for most of my adulthood so far. Over that time, I am sad to say, I have seen very few politicians prepared to admit to having the slightest bit of interest in sick and  disabled people or in the issues affecting us.

It was not as if Hopkins was speaking against sick and disabled people in the Tweets. And let me make something else clear, with perfect honesty. Even if she had been speaking against sick and disabled people, I would not have supported her suspension from the Party. Why? Simply because when she expressed her personal opinions, on her personal Twitter account, she was not yet an MP or even a councillor. Yes, I admit that I  would not personally have voted for her had she been speaking against sick and disabled people in the Tweets, but that is my personal opinion. Just like Deborah Hopkins’ Tweets were her personal opinion. Had I, as a voter with every right to choose who I voted for, chosen not to vote for Deborah Hopkins because I disagreed with her opinions or policies on disability issues, who would have questioned my decision? No one who understood democracy even slightly, I am sure.

So why should Deborah Hopkins be disciplined so severely for expressing her personal opinions, in a personal capacity, when she had not yet been elected into a position of power at the time when those personal opinions were expressed? Should she not have been allowed to stand as a Parliamentary candidate, so that the people of Cornwall, her potential future constituents, could have been allowed to decide for themselves whether or not they wished to vote for her?

Readers, if the strength of the campaign for the resignation of Cornwall councillor Collin Brewer last year was anything to go by, I think it is safe to say that the people of Cornwall would not have disliked Deborah Hopkins for her views on policies relating to sick and disabled people.

One final point, readers, and this is perhaps the most important point. By suspending Deborah Hopkins, the Labour Party distances itself from her personal opinions on everything she Tweeted about. Readers, I don’t live in Cornwall, so I wouldn’t have been able to vote for Deborah Hopkins anyway.

However, I have to wonder what the suspension of Deborah Hopkins says about Labour policy towards sick and disabled people. Is there, hidden in her suspension, a suggestion that the Labour Party supports those current government policies which hit sick and disabled people harder than most?

I hope not, readers, because if that is the case, I know many, many sick and disabled people, and carers, who would be very unlikely to vote Labour in any constituency at the next General Election.

 

 

 

 

DWP forced to confirm if it holds info on exploitation of workfare conscripts

April 14, 2014

www.refuted.org.uk's avatarwww.refuted.org.uk

“The Commissioner requires the public authority to take the following steps to ensure compliance with the legislation: Confirm or deny whether the requested information is held.” https://docs.google.com/viewer?url=http://ico.org.uk/~/media/documents/decisionnotices/2014/fs_50517872.pdf

About an FOI request: Groundworks and work programme placements https://www.whatdotheyknow.com/request/groundworks_and_work_programme_p#outgoing-284978

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Case Of Possible Inherited EDS Mistaken For Child Abuse

April 14, 2014

It was the type of accident that could happen to any parent – in a split second, a young baby rolls off the bed and falls to the floor.

For most, the outcome is a few tears and some cuddles, but for one couple it was the start of a terrifying ordeal.

They were accused of child abuse and their little boy was taken away from them for almost a year.

His parents were only allowed to see him for two hours, three times a week at a council contact centre.

Last night the mother and father, finally reunited with their son, said they were treated like monsters by social workers and made to pay for previous failings in child protection.

‘In a flash we went from being proud first-time parents to being a part of this nightmare from which we could see no escape,’ said the child’s 30-year-old mother, who cannot be named for legal reasons.

The accident happened in June last year as the baby’s father was preparing him for bed at 6.30pm.

Having laid him on their double bed, he turned away momentarily when the nine-month-old went into a roll and fell on to the carpet. The boy’s reaction, however, was abnormal.

His cries quickly turned into something more serious, and by the time his mother had run upstairs, his eyes were rolling back into his head and he appeared to be having a fit.

 

An ambulance was called, but the paramedic became suspicious about the child’s injuries and by what he perceived as his mother’s lack of emotion. He made a safeguarding referral and the police were told.

‘At the hospital in Lincoln, we  were told social services would be informed but that hardly registered as we knew we’d done nothing wrong and were both frantic about our baby’s condition,’ said the mother.

‘It was only when, a couple of hours later, the doctors decided to transfer him to Nottingham for surgery and we popped home to get some belongings that the implications began to dawn on us.

‘There was a policeman on our doorstep telling us our home was a crime scene and we would not be allowed in until we had given a statement.’

By the next day their baby was in an induced coma in intensive care. Tests had revealed an earlier brain haemorrhage and multiple haemorrhages behind his eyes.

The implication was that he had suffered severe shaking on more than one occasion.

‘We didn’t know what to think,’ said the father. ‘We were struggling to take in the horror of it all when a social worker came into the room where we were both  in absolute pieces.

‘She looked us up and down like  we were child abusers and told us that we were no longer allowed access to our son without supervision. From that moment on, it was like he did not belong to us.’

The following day, they were asked to attend a police station where they were arrested on suspicion of causing GBH with intent, questioned separately and held for nine hours.

‘I was scared to death,’ said the father. ‘Neither of us has ever been  in trouble before.

It was clear that they thought someone had shaken our baby on more than one occasion in the previous two weeks.

The  only other person who had been with him was my widowed mother-in-law and a few days later she was also arrested. She will never get over the shock. Our whole world had fallen apart.’

After three weeks, the baby was well enough to leave hospital and Nottinghamshire County Council placed him with a foster family.

‘It was unbearable,’ said his mother.

‘One of the hardest times was his first birthday. We were given an extra hour and allowed to take him to a farm but a contact worker was with us at all times.

‘We were considered guilty and it just seemed inevitable that we would end up losing our treasured baby to adoption.

‘But knowing we were suspected of shaking him, I started researching it and found a lawyer, Rachel Carter, who writes a blog about  such cases.’

At a High Court hearing last month, the medical evidence against the couple collapsed as experts agreed that the baby’s earlier brain haemorrhage had been caused during his birth by emergency caesarean and that the fall had triggered a dramatic re-bleed.

It also emerged that he had probably inherited his father’s condition, Ehlers-Danlos Syndrome type 3, which makes sufferers prone to bleeding.

With none of the other common signs of abuse such as bruises or neck injuries present, Judge Jeremy Lea ruled that the boy should return home.

His mother added: ‘The council were convinced we had shaken him and they acted with a kind of hyper-vigilance.

‘We were made to pay the price of all the previous failings in child care and it ended up costing the tax payer a fortune in legal aid.’

Steve Edwards, Nottinghamshire County Council’s director for children’s social care, said: ‘Our overriding obligation as an authority is to protect children from harm. 

‘All the evidence in this case has now been fully tested by the court and we support the decision made by the judge.’

 

Work Capability Assessment faces replacement if Labour wins election

April 13, 2014

Mike Sivier's avatarMike Sivier's blog

'To see ourselves as others see us': It is hard to stand on a platform when you can't even stand - but the social media are giving disabled people a stronger voice and a chance to take the spotlight, rather than the sidelines. ‘To see ourselves as others see us’: It is hard to stand on a platform when you can’t even stand – but the social media are giving disabled people a stronger voice and a chance to take the spotlight, rather than the sidelines.

The Labour Party is likely to scrap the hated Work Capability Assessment for people claiming sickness and disability benefits, replacing it with “something that looks very different” – but you haven’t heard anything about it on the news, have you?

Labour’s shadow minister for disabled people, Kate Green, said she would be treating with “great seriousness” the Beyond the Barriers report by the Spartacus online campaigning network, which concluded that the WCA is “inaccurate, unreliable and invalid” – but you won’t have heard anything about that on the TV or radio, or read it in the papers either.

Vox Political found it on the Centre for Independent…

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Congratulations To The Winners Of The London Marathon Wheelchair Races

April 13, 2014

 

And many thanks to the BBC Sport website for the information.

 

 

  • Marcel Hug pips GB’s David Weir to victory in men’s wheelchair race
  •  Tatyana McFadden wins women’s race

 

Anne, 89, Needed Help, Not Dignitas

April 13, 2014

Readers, speaking as a disabled person who has never supported, and will never support, assisted suicide, this story scares me. Deeply.

IN a week of disturbing stories right across the news gauntlet – Peaches, Pistorius, the political car-crash of Maria Miller – one dark and troubling tale went almost unnoticed.

Published: Sat, April 12, 2014

The death of a retired art teacher, only identified as Anne, by assisted suicide at the infamous Dignitas clinic in Switzerland. 

The truly disturbing nature of Anne’s story is this: she was not suffering from any form of terminal disease. True, at 89, she had had her health problems – diseases of the lung and heart, requiring spells in hospital (which she hated). But she wasn’t dying of cancer, or one of the nasties such as Huntington’s Chorea, or multiple organ failure. 

Anne simply felt alienated from the modern world. Speaking days before she died – from a lethal dose of drugs provided by the clinic – she said she felt she faced a choice either to “adapt or die”, and announced she was not prepared to adapt to a world in which technology took precedence over humanity. She added that she had become frustrated with the trappings of modern life, such as fast-food, consumerism, and the amount of time people spend watching television. 

“They say ‘adapt or die,’” she said, having already made the decision to take the latter option by drinking a deadly dose of barbiturates. “I find myself swimming against the current, and you can’t do that. If you can’t join them, get off… all the old fashioned ways of doing things have gone.”

Now you may or may not agree with Anne’s world view, but judging by her comments (and there were more in the same vein) it sounds very much to me as if the poor woman was suffering from a classic case of clinical depression – feelings of hopelessness, alienation, despair and suicidal thoughts. 

Is that a condition Dignitas should be giving itself permission to treat with a lethal cocktail of drugs? I don’t think so. Its own rules state that it will only provide help in cases of “illness which will lead inevitably to death, unendurable pain or an unendurable disability”. 

Anne’s niece, Linda, 54, accompanied her aunt to Zurich and was by her side when she died. She has said she “cannot think of a better death”. 

Hmm. I don’t doubt her personal belief in that statement and I am sure she genuinely believes she did the right thing by her aunt. But Anne’s death raises disturbing questions. What if she’d been 10 years younger, say, 79, but held exactly the same bleak view of the world? Would she still have been offered assisted suicide? 

Or what about 69? Or 59? At exactly what point does the combination of (undiagnosed) depression plus advancing years get the thumbs-up from the Dignitas doctors? 

Personally I have always supported the principle of assisted suicide but Anne’s exit from this world has made me seriously wonder if it can ever be properly controlled. 

This disturbing story could be the thin end of a very unpleasant wedge.

DWP Can’t Understand Concept Of Disabled Woman Being Married

April 13, 2014

An email I received yesterday. Can I just make clear, for readers new to disability, that the headline comes from old ‘typically mainstream’ attitudes towards disability and marriage.

 

2012, 1st forms completed to move from IB to ESA.
Had to appeal initial decision as they totally ignored my mental health issues.  I had been placed in WRAG but as someone who is housebound and suffers severe panic attacks when going out, I was never going to manage to get to the JC on a regular basis.  I did actually get offered a home visit from my allocated JC advisor, (whilst I awaited the appeal outcome), but the appointment date fell just days after I got the appeal decision to go into support. 
I was, at that time, very fortunate to be assessed based on submitted paperwork and did not have to have any face to face assessments.
It turned out that the GP at my practice, who filled in the report, had never met me as a patient (my usual GP was on holiday the week the forms came in) and he made an assumption about my use of Duloxetine being for the Fibro, However, I had been taking that medication for my major depressive disorder for at least 3 years prior to the Fibro DX.
On appeal, I was placed in the support group. I have Nick @Mylegalforum from Twitter to thank for this as he helped me with the appeal process and letters.
On 1st of December 2013 I received the renewal pack from ATOS stating I had to return it by Dec 31st, (not easy taking xmas into account) but I managed it.
NOTE: At this point, despite being notified of my marriage during the appeal, including a copy of my marriage certificate, they were still addressing letters to me in my maiden name.  (I got married during the whole form filling / appeal process)
I returned the forms along with another clarification of my married name.   I heard nothing.
Today, 12/04/2014,  I received another standard letter and form asking me to complete and return before May 13th.  This time addressed to me using my married surname but still as MISS not Mrs. 
Not only do they seem incapable of getting something so simple as a name right, but I have to assume that the last lot of forms I returned have been lost, mislaid, destroyed or other.  As I cannot fill the forms in by hand, this means further expense to me as I now have to print off my answers again. Thankfully I have it all saved.
I am also slightly confused as I thought ATOS had now ceased having anything to do with ESA and yet the return address on the envelope still shows as ATOS Healthcare, Bootle office. (Letter is dated April 10th)
Leigh JamesFibrography@yahoo.co.uk
http://www.facebook.com/FidgityDigits

A Care Home Worker Blew A Whistle On Abuse. You Won’t Believe What Happened Next.

April 12, 2014

I’m shocked. Shocked. Shocked.

 

What happened to all the promises the Government made after Winterbourne View? At this moment, it seems they were all empty words.

 

Please share this as widely as you can.

 

Share it with David Cameron.

 

Share it with Nick Clegg.

 

Share it with Ed Miliband.

 

Heck, share it with Nigel Farage.

 

Tell them that they have to fix this, and fast.

 

Otherwise the storm created by Winterbourne View will have blown over forever.

 

Readers, I watched Winterbourne View unfold on my TV screen. Simon and Simone could so easily have been my best friends. I won’t let there be another Winterbourne View. I can’t.

 

Football Access For Disabled Fans Must Improve

April 12, 2014

Football clubs across Britain must urgently redress the “woeful” lack of facilities for disabled fans at many stadiums, says a government minister.

Mike Penning, the disabilities minister, has written to every professional club in the country to highlight their legal obligations.

“I’m blowing the whistle on discrimination against disabled people by football bosses,” said Mr Penning.

He wants to meet Football Association chairman Greg Dyke about the issue.

A BBC report last month revealed that only three Premier League stadiums provide the required number of wheelchair spaces.

Mr Penning said a complete overhaul of grounds was required, “starting at the very top”.

He added: “The situation is currently woefully inadequate and it is not only wheelchair access that falls short, but access for people with all kinds of impairments.”

Joyce Cook, chair of Level Playing Field,  formerly known as the National Association of Disabled Supporters, said: “The experience of disabled football fans varies across the country. That’s not acceptable and it’s time all football clubs took their legal obligations seriously.”

Guidelines on how football clubs in the UK should cater for disabled spectators have been in place since 2004.

The Accessible Stadia Guide  sets out minimum standards that all new grounds have to meet in the provision, location, and quality of facilities for disabled fans. The number of wheelchair spaces a stadium should provide is based on its capacity.

Since the implementation of the Equality Act in 2010, and legislation dating back to 1995, it has been illegal for service providers, including football clubs, to treat disabled people less favourably than other customers.

Clubs can be ordered to make reasonable adjustments, which can include providing induction loops for those with hearing impairments, audio-description facilities for those with sight impairments and free tickets for carers who accompany disabled fans at games.

DWP Admits It Is Helping Watchdog With ‘Cumulative Impact’ Project

April 12, 2014

With many thanks to the Disability News Service.

 

The Department for Work and Pensions (DWP) has admitted it is helping equality experts devise a way to assess the overall impact of spending cuts on disabled people, even though ministers have repeatedly claimed such a project is impossible.

Disability News Service (DNS) revealed last week that the Equality and Human Rights Commission (EHRC) was working with the Treasury and other “key” departments to develop a way of assessing the cumulative impact of spending decisions on different equality groups.

The commission believes its project will promote “equality and fair financial decision-making” in next year’s spending review, and try to ensure that the potential for spending decisions to widen or close equality gaps is “given proper consideration”.

The project is, in effect, devising a way of carrying out a cumulative impact assessment (CIA) of spending decisions on disabled people, something MPs and disabled activists – including the Pat’s Petition campaign and, later, the WOW petition campaign – have been demanding from DWP since at least 2011.

DWP has now confirmed to DNS that it is working on the project with EHRC, the Treasury and other government departments, even though a string of work and pensions ministers have previously ridiculed the idea.

Mark Hoban, at the time the Conservative minister for employment, said last July that a CIA would be “so complex and subject to so many variables that it would be meaningless”.

Esther McVey also dismissed the idea, telling DNS that the information gathered would be “incoherent and inconsistent”.

And Mike Penning, her successor as minister for disabled people, told MPs last week that a CIA was not possible because there were “no real results that can be broken down and are reliable enough to show the effect on disabled people”.

But this week, a DWP spokeswoman admitted that it was one of the departments working with EHRC and the Treasury on the CIA project, although its views about such assessments were “unchanged”.

She said: “DWP does know about EHRC’s work in this area – we and other government departments have representatives engaging with EHRC on their project.

“There is no contradiction between, on one hand, government departments being willing to engage with EHRC on their work to determine what they will want to recommend in this area and, on the other hand, our view (shared by the authoritative Institute for Fiscal Studies) that results cannot be reliably disaggregated for disabled people.”

She added: “We look forward to reading the final recommendations from EHRC after they complete their still on-going assessment of their evidence on this issue.”

But Dame Anne Begg, the Labour chair of the Commons work and pensions select committee, who has repeatedly called for DWP to carry out a CIA, said: “It sounds as though they are trying to find a way of doing what DWP said was impossible. It’s something that should have been done all along.”

But she said what would be crucial would be how any research was used by the government in making future spending decisions.

Dame Anne said she believed work and pensions ministers always knew that such research was possible.

She said: “They simply didn’t want to do it, so they were just looking for excuses not to do it.”

She added: “I think part of the reason DWP was resistant to having a CIA was that if they had found out that all their welfare reforms were having a disproportionate and negative effect on the income of disadvantaged groups, they would have had to do something about it.”

Pat Onions, the founder of Pat’s Petition, also welcomed the decision to carry out the CIA research.

She said: “We called for this in our petition launched in 2011 and the need for an impact study has grown ever more urgent as new reforms have come so thick and fast.

“As people and families affected by these cuts we knew right off how the impacts would cut deep. That’s why we campaigned as early as we did.

“Common sense tells you that fully assessing anything first is vital and a necessity for safety.”

But she said that even if a CIA was carried out now, it would be too late for many people.

She said: “Disabled people are now in crisis and urgently need immediate damage limitation.

“Real families are affected already by these changes, and they need action now. Real people with real lives, not statistics.”

Mayor Of Swindon Apologises For ‘Mongols’ Comment

April 12, 2014

A Tory town mayor has been ordered to apologise after he called disabled people “mongols” during a council meeting about abuse they might face.

Two colleagues claimed Nick Martin, 62, asked them: “They aren’t still letting those mongols have sex with each other are they?”

They reported the “distasteful” remark to investigators, who concluded he had breached the members’ code of conduct and must apologise.

The mayor of Swindon, who has always denied making the remark six months ago, apologised yesterday. The comments were made while a council officer was making a presentation about issues faced by disabled adults in the borough, at a safeguarding adults meeting. The mayor was referred to the authority’s standards board and an independent officer’s report was drawn up and passed to an assessment panel which this week told him to apologise.

A statement from Swindon Council said: “The panel was satisfied that in order to resolve the matter at the earliest opportunity, a local resolution should be sought on the following terms: That councillor Martin makes an unreserved apology within seven days, accepting that he has breached the Members’ Code, and that this apology be made public; accepts further training from the council’s monitoring officer within the next 14 days; and that the findings of fact of the Independent Investigating Officer are made public.”

Mr Martin said he accepted the outcome. “I have apologised for using a word I shouldn’t have,” he added.”I will publicly apologise as I have been asked to.”

DWP Appoints Paul Gray For PIP Review

April 11, 2014

From Fightback.

 

DWP appoints Paul Gray to carry out independent review of personal independence payment.
Review to look at the assessment process during the first two years of operations
11 April, 2014

The DWP has appointed Paul Gray CB, chair of the Social Security Advisory Committee (SSAC), to carry out the first independent review of PIP during its first two years of operations.

In a written statement, Minister for Disabled People Mike Penning said –

‘The review will provide valuable independent insight into the how the assessment process is operating in its early stages.’

Mr Penning confirmed that during the period of the review, which aims to report before the end of 2014, Paul Gray will stand aside from any consideration by SSAC of issues relating to PIP.

Mr Penning’s written statement is available from Hansard.

‘Social cleansing’ of London is well under way – BBC documentary

April 11, 2014

There were no disabled parents or children shown in the programme. However, I grew up in Brent and have many disabled friends who lived there. I have to wonder- how many disabled adults, or parents of disabled children, will be moved from their homes as a result of this policy? If a disabled person has to move council, they often lose vital services or have them cut. It would change, and negatively affect, their lives very significantly.

Mike Sivier's avatarMike Sivier's blog

Cartoon by Martin Shovel. Cartoon by Martin Shovel.

Leading Conservatives must be delighted with the success of their benefit cap in getting single mothers and people with large families out of London – as depicted in the BBC Panorama special, Don’t Cap My Benefits, yesterday evening. (Thursday)

The change means that nobody in the UK is allowed to receive more than £26,000 in benefits per year. The government has claimed this is the same as the average family income, but readers of Vox Political will know that this is a flimsy lie and average family income is in fact more than £5,000 per year higher, at £31K+. The reason benefits weren’t pegged at that level is that far fewer people would be affected by it. Make no mistake – this measure was enacted to shift people from the capital.

The film shows the effects of the change on a number of families in Brent…

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Mark: State welfare is failing our citizens and food banks aren’t the answer

April 11, 2014

Ann McGauran's avatarAnn McGauran

Mark Bothwell. Still in pain and waiting for the outcome of his employment and support allowance application. Mark Bothwell. Still in pain and waiting for the outcome of his employment and support allowance application.

A study presented earlier this week to the All-Party Parliamentary Group on Hunger and Food Poverty says the rise in food banks and charity food is a clear sign of the inadequate nature of social security provision and the way it is delivered. As reported in the Guardian, the report by Sheffield University researcher Hannah Lambie-Mumford warns of the danger of charity food becoming a fundamental part of, or even replacement for, formerly state-funded welfare.

As shown by Eoin Clarke here, by January this year the number of food banks in the UK had grown to more than 1,080. Give that number a bit more consideration. There are more food banks now in the UK than there are branches of Sainsbury’s. The experience of Mark Bothwell (pictured above), here at…

View original post 525 more words

Disabled Author, Adrian Mole Creator, Sue Townsend Dies Aged 68

April 11, 2014

The author Sue Townsend, whose most popular character Adrian Mole defined a generation, has died at the age of 68.

She was best known for the fictional diaries of Adrian Mole, who began confiding his deepest desires and ambitions in the Seceret Diary of Adrian Mole 13 3/4 in 1982. His teenage years were recounted in the Growing Pains of Adrian Mole and further novels dealt with married life and middle age.

Townsend died on Thursday evening after a stroke. As the news of Townsend’s death broke, tributes were paid to the writer on Twitter. Stephen Mangan, the actor who played Adrian Mole in a TV adaptation of the books, tweeted: “Greatly upset to hear that Sue Townsend has died. One of the warmest, funniest and wisest people I ever met.

The writer Caitlin Moran wrote: “One of the funniest women who ever lived.”

Danny Wallace, a comedy writer tweeted: “Farewell, brilliant Sue Townsend. Rest in peace, Adrian Mole” and playwright Simon Stephens wrote: “I met Sue Townsend. Very early in my career. She was much more inspiring than I thought she would be and I thought she would be amazing.”

Sarah Millican, stand-up comedian and TV panellist, wrote: “Such sad news about Sue Townsend. Just about to start reading ‘The Woman Who Went to Bed for a Year’. Will do so now with a heavier heart.”

The character of Mole – which made Townsend a bestselling novelist – is an average teenager but sees himself as am overlooked intellectual. He aspires to the love of the more middle-class Pandora Braithwaite, but ends up with having a child with Sharon Bott. He later becomes the middle-aged and better dressed man who runs a bookshop and survives prostate cancer in Adrian Mole: The Prostrate Years (2010).

Mole was set in the east Midlands and Townsend was herself born in Leicester, the eldest of five sisters. Her father worked in a jet engine factory and became a postman when it closed. Her mother was a housewife who worked in the factory canteen. She could not read until she was eight. It was her mother who taught her with Richmal Crompton’s Just William books – the inspiration behind Adrian.

After failing the 11-plus, she went to a secondary modern, South Wigston high school. She left at 15 but kept reading, devouring Woolworth’s Classics (Jane Eyre, Heidi and co) before moving onto Russian and American literature.

As a chain-smoking teenager, dressed in black, she was fired from a job in a clothes shop for reading Oscar Wilde’s The Ballad of Reading Gaol in the changing rooms. From the age of 14 she was also writing in secret.

By the time she was 18, she had married a sheet-metal worker and, by 22, had three children under five: Sean, Daniel and Victoria. When, after seven years, her marriage ended, she worked in assorted part-time jobs: at a petrol station, as a receptionist, for Bird’s Eye foods.

The toughness of that time is something she never underplayed. She remembered making pea soup for her children out of one Oxo cube and a tin of garden peas. Although her books later made her fortune, she said that no amount of “balsamic vinegar or Prada handbags” would make her forget what it was like to be poor.

Her first two books made her the best-selling novelist of the 1980s. They were followed by several more in the series including Adrian Mole: The Wilderness Years (1993), Adrian Mole and the Weapons of Mass Destruction (2004). The books were adapted for radio, TV and theatre.

In 2001, Townsend wrote The Public Confessions of a Middle-Aged Woman aged 55¾ (2001), a collection of monthly columns written for Sainsbury’s magazine from 1993-2001. Leicester University awarded her an Honorary MA in 1991. Sue’s most recent novel is The Woman Who Went to Bed For a Year, published by Penguin in March 2012.

For some years, in Who’s Who, Townsend listed her interests as “mooching about, reading, looking at pictures, canoeing”. But all these, apart from the mooching, were to be sabotaged by ill health. She had TB peritonitis at 23; a heart attack in her 30s; Charcot’s joint–degenerative arthritis, which meant she was in a wheelchair. She described herself as the “world’s worst diabetic” – finding the disease hard to manage.

In the 1990s, she started to lose her sight. In 2001, she was registered blind and although, characteristically, she made jokes about it, she also wrote about the sense of loss, the disappearance of detail, the misery of suddenly finding she could no longer distinguish between a daffodil and a tulip. She talked about what it felt like to “throw words into the dark”.

She dictated all her later books – usually to her eldest son, Sean. In 2007, she suffered kidney failure (also diabetes related) and was put on dialysis. In 2009, after a two-year wait for a donor, she had a transplant (Sean donated a kidney). In 2013, she suffered a stroke.

Pensioner, 83, Banned From Seeing Wife Of 60 Years- For Giving Her Painkillers

April 10, 2014

Police have arrested a grandfather of 83 on suspicion of poisoning his frail wife after he gave her a pain-killing patch to alleviate her aches and pains

Walter Crompton attached the prescription patch to the leg of wife of 60 years Eileen after she said she had been left in severe discomfort by a blood clot.

But staff at Allendale Care Home in Blackley, Manchester where 83-year old dementia suffer Mrs Crompton has been residing for the past two weeks, contacted police because the patch contains morphine.

Four days later officers detained Mr Crompton and kept him in custody for seven hours during which he was asked to give fingerprints and a DNA sample.

The retired British Aerospace worker was released on bail after being questioned on suspicion of administering a noxious substance under the Offences Against the Person Act 1861.

But under the terms of his bail conditions he is now banned from contacting his wife.

The pensioner, from Blackley, is due to answer his bail at the end of the month when it is thought he will be told whether he is to be charged.

The maximum sentence for a conviction on administering poison or noxious thing with intent to injure, aggrieve or annoy is five years in jail.

Walter Crompton, 83, has been arrested and banned from seeing his wife. The pair are pictured here on their wedding day in 1953

But Mr Crompton said the patches had been prescribed by a doctor and said care home staff did not tell him the pain relief patches were banned – just that his wife’s codeine prescription was not allowed on the premises.

He added: ‘It’s a patch, nobody ever killed anybody with a patch.

‘I don’t understand why they needed to arrest me. I was just trying to help my wife and I didn’t know it was against the rules.

‘We’ve spent 60 years of our life together. She mustn’t know what’s going on. She is a dear lady, and a quiet character. She never wants any trouble.’

Retired factory machinist Mrs Crompton moved into the care home two weeks ago after a number of falls at home. She has dementia, heart problems and chronic arthritis, for which her doctor had prescribed codeine.

Walter has been his wife’s only carer for two years when she became seriously ill. He supplied the patches after she developed a blood clot in her leg that was causing her a lot of pain.

The couple’s daughter Caron Hampson, 50, said: ‘I think it’s awful. He’s an 83-year-old man and they treated him like a thug.

‘He was concerned about her leg which they didn’t treat right away, and I can imagine he got quite angry about it, but there is no way they needed to call the police. He’s not physically intimidating or violent.’

Greater Manchester Police said: ‘On Tuesday, 2 April 2014, police in North Manchester received of report of concern over medicine administered to a resident at a Blackley care home.

‘Officers from the Public Protection Investigation Unit started an investigation and a multi-agency strategy meeting was held with partner agencies to discuss how to best to establish the facts.

‘Subsequently an 83-year-old man was arrested on suspicion of administering a noxious substance.

‘He has been released on bail pending further inquiries until 28 April 2014.

‘Officers are continuing to work with partner agencies, including the care home as part of this ongoing investigation.’

Det Supt Joanne Rawlinson, of the Public Protection Division, said: ‘This is a potentially serious offence in which a vulnerable elderly woman with significant health issues could have come to serious harm and, as such, the police will always conduct a thorough investigation.

‘As part of any inquiry like this our priority is always to protect vulnerable people and this may involve certain bail conditions being imposed.’

The Allendale Care Home declined to comment.

Bin British Gas: Put Power in Public Hands! Take Action On May 12th

April 10, 2014

johnny void's avatarthe void

british-gas-protest A mass demonstration outside the annual AGM of British Gas has been called by Fuel Poverty Action Group on May 12th. Whilst many people are unable to properly heat their homes, British Gas made £571m in profit  last year.

Just staying alive in the UK is becoming ever more expensive as rents, fuel and food prices soar.  A low paid job now barely covers even the most basics needed for survival, whilst the safety net of the benefits system is being ripped away.  None of this is necessary or unavoidable.  Tesco workers get shit wages, whilst we pay extortionate prices for food, so that share holders and directors can make huge profits.  Pensioners are freezing in their homes so that energy company bosses can enjoy lavish lifestyles.

Virtually every last scrap of cash that passes through our hands ends up lining the pockets of the same rich who smear us…

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Congratulations Francesca Martinez!!!

April 10, 2014

I’m very very very proud to see WOW Petition campaigner, actress, comedienne, and woman with CP, Francesca Martinez, on the Woman’s Hour Power List 2014 Game Changers Top 10.

 

She came 8th. Doreen Lawrence, as you may already know, came first.

 

However, in the world of disability, most of us believe that while winning is wonderful, it’s the taking part that really matters. Just by being on the list, Francesca Martinez has broken down a barrier for disabled women that few disabled women would ever have thought it would be possible to break.

 

So, Francesca Martinez, thank you, from a disabled woman, and many, many congratulations and the very best of wishes.

 

Comedian, actress and disability campaigner

Francesca Martinez is a comedian, actress and disability campaigner who has cerebral palsy.

She spent a year campaigning to get 100,000 signatures required to trigger a milestone parliamentary debate on welfare reform and its impact on disabled people. Earlier this year, Westminster saw what was described as the ‘first debate secured by disabled people, for disabled people’. The motion in parliament, set down by the War on Welfare (WOW) campaign group, called for an assessment of the cumulative impact of the government’s welfare reforms on sick and disabled people. It also demanded an immediate end to the work capability assessment (WCA), the test that determines fitness for work.

In an interview with The Guardian she said: “It seems we’re living in a country at the moment where if you do get sick or if you do become disabled, not only have you got to deal with those challenges but you have to deal with the fact that the vital safety net that society provided for many decades is being eroded away.”

Before becoming a comedian, she was a regular in the BBC children’s drama Grange Hill, becoming one of the first mainstream actors with a disability. With sell-out runs at the Edinburgh Festival, she completed a 68-date UK tour last year. She continued to act in television with roles in Holby City and Ricky Gervais’ comedy Extras. Francesca Martinez is currently writing her debut book, What The **** is Normal, due to be published later this year.

Stop The Eviction Of Vicky

April 10, 2014
 “When it comes to millionaires like Maria Miller who’s got two houses, it’s one law, but when it comes to people like Vicky and those who live in Salford it’s another law…”

City West Housing Trust is set to evict the first Bedroom Tax victim in Salford tomorrow at noon. Vicky, who lives in Walkden, has a second bedroom for when her 15 year old daughter stays and cannot pay rent arrears.

The Greater Manchester Anti Bedroom Tax Federation has called for people to assemble outside Vicky’s house tomorrow from 11am “to stop this cruel eviction”.

Full details here…


First Salford Bedroom Tax Eviction First Salford Bedroom Tax Eviction First Salford Bedroom Tax Eviction
First Salford Bedroom Tax Eviction First Salford Bedroom Tax Eviction First Salford Bedroom Tax Eviction
click image to enlarge
Vicky is a City West Housing Trust tenant who lives in Walkden and has a second bedroom for when her 15 year old daughter stays. She’s lived there for 14 years but had some outstanding rent arrears that were accrued when she shared her home with her former partner. Most of her current £3,375.83 arrears, we understand, is made up of Bedroom Tax debts.As a consequence of the bereavement of a child, Vicky has also been suffering from severe depression. She is what most would call a `vulnerable person’ – and the code of good practice for landlords and bailiffs states that vulnerable people like Vicky should not be evicted.

Apparently, City West did not inform Vicky that she could apply for Discretionary Housing Payments to cover the extra rent which is the result of the Bedroom Tax.

Indeed, as revealed in the Salford Star four days ago, Salford City Council is predicting a £650,000 underspend in its Discretionary Support Scheme (a separate fund from Discretionary Housing Payments) for financial emergencies such as this (see previous Salford Star article – click here).

Nevertheless, City West Housing is sending bailiffs around to Vicky’s house tomorrow (Thursday) at noon to evict her, following a court case today at which she had no legal representation…

“Everything they said in court just went over my head” Vicky said outside the Civil Justice Centre in Manchester “I could not make out what was going on in court.”

Greater Manchester Anti Bedroom Tax Federation has called a rally to Stop the Eviction of Vicky from her home in Salford!

“When it comes to millionaires like Maria Miller who’s got two houses, it’s one law, but when it comes to people like Vicky and those who live in Salford it’s another law – and that is to go straight to court to get you evicted just for a few thousand pounds arrears” Mark Krantz from the Greater Manchester Anti Bedroom Tax Federation told Salford Star this afternoon.

“The Bedroom Tax is a cruel evil tax” he added And we will be assembling outside Vicky’s house tomorrow to make that she is not evicted onto the street and into destitution.”

A statement on City West’s website reads: “Our aim is to help you live as independently and happily as possible. This is why we’re always happy to help and support you, whatever it is you need. City West are dedicated to developing and delivering services that support our most vulnerable customers to maintain their independence and sustain their tenancies.”

In a press release issued this afternoon, the Greater Manchester Anti Bedroom Tax Federation stated that “City West told Vicky that she should go to homeless families at Salford Council to get re housed after being evicted.”

Stop the Eviction of Vicky
Assemble 11am. Thursday 10th April
23 Grosvenor Drive, Walkden, M28 3RW

* The Salford Star has asked City West Housing Trust for a statement. As soon as the Trust responds it will be added to this article

See also Salford Star report on the United Nations in Geneva condemning Bedroom Tax – click here

City West Office Invaded by Anti Bedroom Tax Campaigners – click here

For further details see www.nobedroomtax.co.uk

 

Updated 1pm **GOOD NEWS JUST IN**
Colin Gong …at the courts this morning , a four week stay was granted.

Disabled Man On Scooter Robbed

April 10, 2014

Are Hospitals Letting Deaf People Down?

April 10, 2014

Deaf people have been going on record about difficult experiences they’ve had in hospitals due to lack of sign language interpreters. See Hear looks at three cases where this trauma could have been avoided had sign language interpreters, or other communication support, been provided.

Deaf couple Nadia and Hulusi Bati were in University College London Hospital for the birth of their child. It was all going fine until the sign language interpreter’s shift ended at 20:00 while Nadia was having contractions and 90 minutes before she went into the final stages of labour.

Despite efforts from the staff, no interpreter was present at the birth which turned out to be a difficult forceps delivery. Nadia only held her baby for a moment before it was whisked away for emergency treatment in another room – they were unable to tell her why.

The child was treated in hospital for several days afterwards though the parents didn’t know what was wrong because sign language support was not forthcoming here either.

Dr Pat O’Brian, Clinical Director, Women’s Health, says the hospital does not comment on individual patient matters but told See Hear they had provided interpreters on-site for 97% of cases. He says: “It’s probably fair to say that of those 3% that we found it difficult to provide a face-to-face interpreter, it is more common in emergency situations.”

If you have a potential life-threatening condition, the priority for medical staff is to assess you and treat you appropriately. Finding an interpreter isn’t always possible at short notice, as Matthew Gurney found when he was rushed to hospital with suspected appendicitis in the early hours of the morning.

On arrival he provided the number of an interpreter he knew. She wasn’t available; its unclear what further steps were taken by North Middlesex University Hospital to find another. Instead Gurney and a deaf friend communicated with hospital staff through pen and paper but important details weren’t communicated effectively. It’s understood widely in the deaf community that detail can easily go astray in all types of conversations.

Gurney signed a consent form for an operation. On waking briefly after the anaesthetic he saw three marks on his stomach which he had understood from the staff meant that he had only had exploratory surgery; he was relieved. ON waking fully later, he learnt that he’d misunderstood and that his appendix had been taken out after all.

He left hospital having had no interpreter support for the duration of the stay.

A spokesperson for the hospital says they attempted to find an interpreter but none were available. Gurney left the next day and the hospital were satisfied he knew how to look after the wound after having been given advice though agree it would have been good to have an interpreter at that discharge meeting.

The Equality Act of 2010 exists to protect people against unfair treatment on the grounds of deafness or disability but, under law, communicating via pen and paper could be considered a “reasonable adjustment”.

A recent report from Signhealth, a deaf charity focusing on the health and wellbeing of deaf people, finds that deaf people are falling behind their hearing counterparts in terms of general health. They’re reluctant to go to their local doctor or hospital, expecting communication to be difficult or impossible.

The report, Sick of It, finds that relatively minor health issues, as well as major ones, are going undiagnosed. The House of Lords discussed the findings last week.

But why is basic communication sometimes failing to materialise?

Dr Andrew Alexander, one of the key people behind SignHealth’s report, thinks it may be a question of perception: “Hospital staff tend to think the interpreter is for the deaf person. They fail to recognise that the interpreter is also for the hearing member of staff. It’s vital in a doctor-patient relationship to have good communication.”

Philip Dixon had “good communication” for an appointment at York Hospital to discuss the results of a scan though, in his case, it was provided by his hearing son Matt who can speak BSL. On discovering an interpreter had not been booked, the two had decided they’d go ahead with the appointment to avoid further delay.

Interpreting the doctor’s words, Matt was shocked that it had been left to him to tell his own father that he had terminal cancer. Not being trained in medical language as an interpreter would have been, the difficulty was further compounded by the fact that Matt didn’t know the signs for some of the medical terminology and had to muddle through.

It happened several years ago, and his father died soon after, but Matt says he relives the experience daily. Looking back he wishes they had pushed for an interpreter and says: “Being put in that situation for me meant, instead of me supporting him, he had to support me because I was so upset. And that’s wrong. If an interpreter had been there I could have sat next to my father and supported him through it and focus on consoling him.”

A spokesperson for York Hospital says they were sorry to hear of Matt’s experiences and says their protocol is to provide interpreters to patients who need them and they’ve been monitoring and improving interpretation services in the last year.

When deaf people feel they aren’t getting the right level of service, they can raise the issue via the Patient Advice and Liaison Service (PALS), their GP, or elsewhere. Change should happen as a result – and if it doesn’t, then The Equality Act gives deaf patients the right to take that complaint further.

On this week’s programme, See Hear raises these stories with Neil Churchill, the Director for Patient Experience for NHS England. He says: “where the NHS has got something wrong and that’s given somebody a poor experience of care, then we need to apologise and we need to learn from that. I think everybody is interested in making sure that if something has gone wrong, it doesn’t happen again.

“My goal really is to put patients in positions of real influence where they can assess the quality of care and identify what improvements Trusts need to make in order to routinely deliver consistently great experiences of care.”

Panorama: Don’t Cap My Benefits

April 9, 2014

I’ll be watching this edition of Panorama, 9pm tomorrow.

 

As the government’s benefits changes begin to bite, Panorama gains exclusive access over six months to Brent – one of London’s worst-hit boroughs – and follows the personal stories of some of the people most affected by the changes. As claimants struggle with the loss of hundreds of pounds of benefits and have to move to other parts of the UK where rents are cheaper, we follow people battling to stay in their homes and a local authority forced to ask to them to leave as their benefits are capped.

Jimmy Daly #bedroomtax

April 9, 2014

A father of a disabled boy who will have to pay money back under the “bedroom tax” has hit out at the “dreadful” scheme.

Jimmy Daly from Stoke told Daybreak he was moved into his current two-bedroom home to help him cope with his son’s disabilities, but because his son does not live with him full time, Jim has to pay some money back.

“I was moved in here because of his disabilities, and now they’re saying because your son is disabled you have to pay this dreadful tax. It’s wrong.”

UK government refuses to accept responsibility for crimes against humanity

April 9, 2014

Mike Sivier's avatarMike Sivier's blog

131109doublespeak

A guest report by Mo Stewart ©Mo Stewart April 2014

Following the bogus Work Capability Assessment (WCA) conducted by Atos Healthcare, as contracted by the Department for Work and Pensions (DWP), the United Kingdom (UK) Government admitted that it was wrong to cut the disability benefits of Mark Wood, the vulnerable disabled man who starved to death following the removal of his benefits, in the 21st century UK, when weighing only 5st 8lbs.

Regardless of this tragedy, the UK Conservative led Coalition Government still refuses to accept any responsibility.

Despite the fact that the WCA was introduced by the Labour Government in 2008, it was originally designed by previous Conservative Governments, in consultation with the notorious American corporate giant now known as Unum Insurance, identified in 2008 by the American Association for Justice as the second most discredited insurance company in America.

Without a welfare state, sick and disabled people in…

View original post 3,065 more words

Beyond The Barriers- Launch

April 9, 2014

I saw this a little late, for which sincere apologies to Sue Marsh, who wants it shared far and wide.

BEYOND THE BARRIERS – LAUNCH!!!!!

Good morning.

The Spartacus team have been working for three years on research into ESA, WCAs, the Work Programme and employment for sick and disabled people.

Today, we launch Beyond the Barriers, the most comprehensive report to date on how the system currently fails, but more importantly what we need to do to improve it.

 
You can read the report 
You can read the press release
 
Beyond the Barriers aims to start an enormous conversation about what should replace ESA. People will be taking part in it across the political spectrum, all around the internet.
 
As we launch, experts from the disability community will be giving evidence on the failures of ESA to the Work and Pensions Committee live on Parliament TV You can watch and share the link 
 

If you want to get involved, we’ve provided the following tools to help :

TWITTER


Starting from now you can follow the new Beyond the Barriers @spartacusreport on Twitter. The account will have news, updates and links throughout the day, so do keep an eye on it as a central info source
 
The hashtag is #BeyondBarriers 
 
Tweets start NOW!!!!

The next slot will be 12 noon, then 2pm, then 4 pm (Thats 1200 hrs, 1400hrs and 1600 hrs for those with a military strategy!)
 
Here are some tweets you might like to use : 
 
BREAKING: from #Spartacus : groundbreaking report into disability
benefit flaws – and how to fix them. #BeyondBarriers http://bit.ly/R2hD2k

BREAKING: Major new report by #Spartacus “important contribution” to
disability debate (Anne Begg) #BeyondBarriers http://bit.ly/R2hD2k
#Spartacus team shows a way ‘beyond the
barriers’ of current disability support #BeyondBarriers http://bit.ly/R2hD2k

“If you read one policy or political document this week it ought to be
#BeyondBarriers” @LabourList http://bit.ly/R2hD2k

Major new report by disabled ppl shows policymakers how to
fix failing disability benefit system #BeyondBarriers http://bit.ly/R2hD2k
WATCH! Parliament confirm #BeyondBarriers report findings LIVE!! http://www.parliamentlive.tv/Main/Player.aspx?meetingId=15297 http://bit.ly/R2hD2k
We hope to have staged links available, which will link to the case histories you wrote for us on the Beyond the Barriers blog at http://beyondthebarriersspartacus.blogspot.co.uk/,  explaining how benefits or support have helped you to cope, and even to move on. Please visit the blog and add comments


Facebook Follow the WeAre Spartacus page for updates and links https://www.facebook.com/weare.spartacus.1?fref=ts
 
Local Media

We have a template letter out that you can send to your local paper, or to a National if you wish. You can view, copy and paste the template from 
 
 
Contact your MP
 
We have a template that you can send to your MP – it can be found 
 
 
Please  feel free to amend it or write your own 🙂 Personal letters are better but any letter is better than none 😉
 
You can find your MP here; http://www.theyworkforyou.com/ or here; https://www.writetothem.com/
Internet Blogs

There will be articles and blogs all over the internet – we will try and tweet and Facebook the locations for you as soon as we are aware of them.
 
We also have our own blog site just for this report. On that site you can see the whole report and supporting work.
You can find it here; 
 

 

DWP Target Mental Health Claimants For ESA Sanctions

April 9, 2014

Thanks to the brilliant Benefits And Work.

 

A staggering six out of ten employment and support allowance (ESA) claimants hit with a sanction are vulnerable people with a mental health condition or learning difficulty, according DWP figures obtained under the Freedom of Information Act. The proportion has rocketed from 35% of sanctioned claimants in 2009 to a massive 58% in 2013. The statistics prove that sanctions are now overwhelmingly aimed at the most vulnerable individuals by a government department which relies on a policy of institutional discrimination to cut benefits costs.

Sanctions of £71.70 a week are handed out when ESA claimants in the work-related activity group are forced onto the work programme and then fail to meet mandatory conditions imposed on them by private sector companies.

However, for a claimant to get into the work-related activity group on mental health grounds, they need to score a minimum of 15 points for problems with issues such as:

  • planning new activities,
  • changes in routine,
  • going to new places,
  • talking to new people,
  • avoiding behaving aggressively or inappropriately when stressed.

So, almost by definition, many will struggle to cope with regular and punctual attendance at training courses and work-experience placements with strangers in unfamiliar places. Even if they manage to attend they may not succeed in participating to the satisfaction of those running the courses or placements.

A MIND spokesperson told Benefits and Work:

“Based on what we hear from people we represent, these sanctions are often the result of people not being able to engage in a mandated activity because of their mental health problems; people being asked by the DWP to engage in activities that they are not well enough to undertake; and a lack of understanding at the DWP about mental health problems meaning that it is not picked up when someone had ‘good cause’ to miss an appointment or activity.

“Most people with mental health problems want to work, and given the right support many could. We do not believe that an effective system of support for this group of people involves continually mandating them to undertake activities under the threat of being left with no money.”

Sanctions, particularly in relation to Jobseekers Allowance (JSA), have saved the government huge amounts of money and allowed them to claim that the number of people in receipt of benefits is falling because the economy is recovering.

The statistics above relate to ESA – where ‘only’ around 20,000 claimants a year are currently sanctioned – there are no similar ones for JSA where the numbers are much higher. But many people getting JSA are claimants with mental health conditions who scored just below the 15 point threshold – often because they were wrongly assessed by health professionals with no experience of mental health issues. And it seems exceedingly unlikely that decision making in relation to JSA sanctions is any less harsh than that for ESA.

The DWP, however, have fought hard to prevent any evidence about who is being sanctioned leaking out.

One member of the work and pensions select committee, Debbie Abrahams MP for Oldham East and Saddleworth, has been leading the calls for an inquiry into the issue of sanctions. She told Benefits and Work:

“As a member of the work and pensions select committee I’ve been very concerned about the growing evidence of inappropriate sanctioning and demanded that that a second independent inquiry into the issue is established.

“When I made my demands face-to-face with Esther McVey at a Committee session back in November she agreed to set up an independent investigation into the ‘appropriateness of sanctions’ and her offer was welcomed by the Committee in their following report. But, in a deliberate snub to the Committee, the Government have now said they won’t set one up.

“My question is this. If sanctions are currently being applied correctly, an independent review will testify to that, so just what are Ministers trying to hide?

“It’s just another example of how Iain Duncan Smith and Esther McVey are using smoke and mirrors to avoid any criticism about the mess and misery they are creating in the social security system.

“No-one is arguing with the fact that anyone who is on work related benefits should do all they can to find appropriate employment. But there is a growing body of evidence that the way the government is implementing sanctions means vulnerable people are being targeted disproportionately and suffering terribly as a result.

“The last thing Iain Duncan Smith and Esther McVey want is for that uncomfortable truth to be uncovered by a focussed and independent investigation.”

We asked the DWP Press Office to explain the dramatic rise in the proportion of vulnerable claimants who are subject to ESA sanctions.

After six days of claiming that they were “still looking into your query” and a very ill-tempered phone conversation due to our insistence that we wanted a reply in writing rather than the press office calling us at their convenience to ‘explain’ the issue, we finally got this response:

“It’s only right that people should do everything they can to move off benefits and into work if they are able. Sanctions are only used as a last resort and we have robust procedures in place to protect vulnerable people, with a number of safeguards built into the system.

“Everyone has the right to appeal a sanction decision if they disagree with it.”

So, no denial that the figures were correct and no explanation for this exponential rise in the targeting of claimants with mental health conditions, in spite of the ‘robust procedures’ in place.

Instead, just the same empty reassurances backed by no evidence whatsoever.

So, we’re asking Benefits and Work readers not to let them get away with it this time. The work and pensions committee and the public accounts committee have both expressed concern about sanctioning of benefits claimants.

If your MP is on one of those committees please draw their attention to this article or explain the issue yourself using Write To Them. A list of the committee members is given below, but please don’t contact them if they aren’t your MP – spamming MPs is not going to help at all.

However, even if your MP is not on one of this committees you can still contact them and ask them to ask a DWP minister why they are refusing to hold an inquiry into whether sanctions are being applied fairly in the face of strong evidence that the DWP is pursuing a policy of institutional discrimination.

You can download a copy of the freedom of information response from here.

 

You can use Write To them to contact your constituency MP.

WORK AND PENSIONS COMMITTEE MEMBERS (excluding Debbie Abrahams, who we’ve already contacted)

Dame Anne Begg Aberdeen South

Graham Evans Weaver Vale

Sheila Gilmore Edinburgh East

Glenda Jackson Hampstead and Kilburn

Kwasi Kwarteng Spelthorne

Nigel Mills Amber Valley

Anne Marie Morris Newton Abbot

Teresa Pearce Erith and Thamesmead

Mr Mike Thornton Eastleigh

Dame Angela Watkinson Hornchurch and Upminster
PUBLIC ACCOUNTS COMMITTEE MEMBERS

Margaret Hodge Barking

Mr Richard Bacon South Norfolk

Stephen Barclay North East Cambridgeshire

Guto Bebb Aberconwy

Jackie Doyle-Price Thurrock

Chris Heaton-Harris Daventry

Meg Hillier Hackney South and Shoreditch

Mr Stewart Jackson Peterborough

Mrs Anne McGuire Stirling

Austin Mitchell Great Grimsby

Nicky Morgan Loughborough

Nick Smith Blaenau Gwent

Ian Swales Redcar

Justin Tomlinson North Swindon

‘Bedroom Tax’ Birthday Card For IDS On 60th Birthday

April 9, 2014

On the first anniversary of the controversial bedroom tax – a 60th ‘birthday card’ will be delivered to the architect of the ‘tax’, work and pensions secretary Iain Duncan Smith

Wednesday will see Iain Duncan Smith celebrating his own 60th birthday – he was born on 9 April 1954.

DATE: Wednesday 9 April 2014
WHEN & WHERE: 10.30-11.00 MPs will pose with the ‘birthday card’ at Old Palace Yard, Westminster SW1P 3JY – and they will also sign it.
WHEN & WHERE: 11.00-11.15 Unite community members will march to the Department for Work and Pensions at Caxton House, Tothill Street, London, SW1H 9NA to hand in the birthday card.

Unite assistant general secretary Steve Turner said: “As Iain Duncan Smith enters his seventh decade, he may care to reflect on the misery his creation – the bedroom tax – has caused to 600,000 families. It has brought nothing, but hardship and suffering to the already vulnerable and should be scrapped immediately.”

At the weekend, Unite’s demonstrations in five major cities and towns highlighted the misery that the ‘tax’ has caused to over 600,000 families, increasing financial stress, debt and eviction of some of the most vulnerable within our communities.

The protests came as hard evidence demonstrated its abject failure with only six per cent able to downsize in a desperate social housing market, and the cross-party House of Commons Work and Pensions committee confirming disabled people are suffering “severe financial hardship and distress” as a result of the ‘tax’.

Need For Food Banks IS Caused By Welfare Cuts Finds Study

April 9, 2014

The government’s welfare reforms, including benefit sanctions and the bedroom tax, are a central factor in the explosion in the numbers of impoverished people turning to charity food banks, an academic study has said.

The study, part of a three-year investigation into emergency food provision, was carried out by Hannah Lambie-Mumford, a Sheffield University researcher who co-authored a recently published government report into the extent of food aid in the UK.

That report concluded there was insufficient evidence to demonstrate a clear causal link between welfare reform and food bank demand in the UK. But Lambie-Mumford’s new study, to be published on Wednesday, says the rise in demand for charity food is a clear signal “of the inadequacy of both social security provision and the processes by which it is delivered”.

The report warns that as social security safety nets become weaker, there is a danger that charity food could become an integral part of the state welfare provision, or even an replacement for formerly state-funded emergency welfare schemes.

Lambie-Mumford’s study was based on 25 in-depth interviews with a range of food bank staff and volunteers in 2012 and 2013 and found many food banks were adapting to demand by scaling up food collection and storage provision “to accommodate the future trajectory of need”.

Her paper will be presented to an all-party committee of MPs which meets on Wednesday to finalise the terms of an inquiry into hunger and food poverty. The inquiry will examine the rise of food banks, an issue that has become politically charged as ministers attempt to deflect criticism that austerity policies, including welfare cuts, have had the effect of compelling more people on low incomes to rely on food aid.

Lambie-Mumford said her research showed that food banks were expanding to meet rising demand caused in part by a squeeze on welfare entitlements which made already poor people even worse off. This was compounded by inadequate processing of social security claims, including payment delays and “arbitrary and unfair” sanctioning decisions that left claimants without any income at all. There were other factors which had contributed to the rise of food banks, such as low wages and the rise in the cost of food. But it was important that MPs did not duck or underplay the importance of welfare reform. “The tricky thing is that welfare reform is the most political aspect of a political issue. But we should not shy away from it for this reason,” she said.

The welfare minister Lord Freud notoriously claimed last year that more people were going to food banks because the food was free, thereby triggering “almost infinite demand”. Last month Freud admitted people did not turn up “willingly” at food banks but said it was “very hard to know why” they did go.

The Trussell trust, which oversees a network of more than 400 food banks in the UK, has insisted repeatedly that welfare reform is the biggest driver of demand for food parcels. Its third-quarter data, published in March, showed that it helped 614,000 people in the first nine months of this year. Its final-year figures, expected next week, are likely to show that demand has more than doubled in the past 12 months. More than eight out of 10 food bank managers interviewed for the study acknowledged the impact of welfare changes and welfare processes as a factor in driving demand.

A DWP spokesperson said: “This report, which is based on just 25 interviews, fails to consider how welfare reforms are helping people off benefits and into jobs. The truth is that we now have record numbers of people in work, the highest employment rate for five years, and falling unemployment.” A DWP spokesman later added that the report “gave a one-sided view”.

WIN A Copy Of The Autistic Brain

April 8, 2014

The Autistic Brain

 

 In The Autistic Brain Temple Grandin offers her own experience as an autistic person alongside remarkable new discoveries about the autistic brain, as well as genetic research. She also highlights long-ignored sensory problems as well as the need to treat autism symptom by symptom, rather than with an umbrella diagnosis. Most exciting of all, she argues that raising and educating children on the autistic spectrum needs to be less about focusing on their weaknesses, and more about fostering their unique contributions.

 

For your chance to win a copy of The Autistic Brain simply answer this question: What year did the word ‘autism’ enter the psychiatric lexicon?

NHS Doctors Banned From Using Insulting Language

April 8, 2014

This article titled NHS Doctors Banned From Labelling People With Learning Disabilities ‘Retarded’   and written by Steven Preece was first published by the Welfare News Service on 8 April 2014  and has been reproduced here with permission’.

 

NHS doctors are to banned from using offensive language when describing people with learning disabilities, the Welfare News Service can reveal.

Many people reading this article could be forgiven for thinking such discriminatory and insulting language would already be banned, or even that this report is a late and tasteless April fools joke – it isn’t!

Having received an email from Bradford and District Disabled People’s Forum, we were shocked to hear that such language is not only still being used, but it is also regarded as totally ‘acceptable’ by some NHS doctors.

Members from Bradford People First, a user-led advocacy group, attended a local Clinical Governance meeting, where during a presentation a doctor showed a number of slides which included the words ‘retarded’, ‘morons’ and ‘subnormal’ when describing people with learning disabilities.

Members from Bradford People First approached the doctor conducting the presentation, who informed them that the language was regarded as ‘acceptable’ because it was included in the definition of disability provided by the World Health Organisation’s (WHO) clarification of diseases.

Damian Marshall from Bradford People First said:

“If professionals are given permission to use such degrading words, this will encourage the public to also use those derogative words towards people with disabilities. This as I’m sure you are aware can be considered a hate crime, as those words can be found to be very upsetting and offensive for people with a learning disability”.

Mr Marshall wrote to MP Philip Davies who forwarded the letter to the conservative Minister for Care and Support, Norman Lamb MP.

Norman Lamb replied:

“I was very sorry to read that Damian Marshall was upset by the terms used to describe learning disabilities”.

He continues: “Generally, NHS clinicians use the tenth edition of the World Health Organisation’s International Clarification of Diseases (ICD-10) to clarify mental and behavioural disorders”.

“Public Health England has contacted the Health and Social Care Information Centre, which represents England with the World Health Organisation, to propose that the language should be altered to take account of the terms that are currently used to describe learning disabilities in English-speaking countries.

“This proposal has been accepted and in the eleventh edition of the Clarification (ICD-11), which will be published in 2017, terms such as ‘mental retardation’ will be removed.”

Mr Marshall said the definition of a disability used by the Department of Health (DoH) “is more appropriate” and using that definition “would be better for people with learning disabilities”.

Bradford and District Disabled People’s Forum (BDPF) described the response from minister Norman Lamb as a “big change for us all” and congratulated Bradford People First for their campaign.

Real issues with Welfare Reform

April 8, 2014

jaynel62's avatarjaynelinney

Wearing my DEAEP Company hat, last week I met with a lovely man, I’ll call him Adam; Adam is in his 60s and worked all his life until last year, when his health deteriorated to such a point he could no longer physically manage. At this time he completed his claim for ESA, he heard nothing and then, out of the blue last month, Adam was called for an appointment with ATOS. He initially asked about home visit as he loves 12 miles outside the City centre but was told he needed a letter from his Dr to support his request; as this was not possible, Adam informed them he was happy to attend but he wanted the assessment recorded, ATOS assured him this was fine and he arranged a date.

He contacted me wanting support for the assessment and, after Adam struggling to make his way into town for…

View original post 648 more words

Three Month Old Baby ‘Youngest In UK’ To Have Cochlear Implants

April 8, 2014

A baby has become the youngest in the UK to have cochlear implants – at the age of three months and three days.

Evie Smith had the first device implanted in her right ear, and then the second one seven weeks later.

Evie is now aged six months – and returned to St Thomas’ NHS Hospital in London last week to have the devices activated.

Staff there have emphasised her case is exceptional.

Evie became profoundly deaf after contracting pneumococcal meningitis when she was just three days old.

She spent six weeks in intensive care, and needed to be on a ventilator for a fortnight.

She was given cochlear implants at an exceptionally young age because the meningitis led to bony growth – or ossification – in her inner ear.

The damage to Evie’s ears was getting worse, which meant that waiting for implants at a later stage was not an option.

Cochlear implants cannot cure deafness – but they help Evie and children like her experience sound.

‘Bad outlook’

Audiological specialists fitted external processors to the outside of Evie’s ears – these pick up sound and connect with the internal implants, which help send electrical signals to the brain.

The staff at St Thomas’ banged a drum to monitor Evie’s responses, as they programmed the processor. Watching her stir as she absorbed the sound meant the world to her parents.

Her mother, Jenny Harvey, 33, from Kent, told me: “When we found out she was deaf, what affected me most was the thought of her speech being impaired.

“But hopefully her speech should be very good – with input from the speech and language therapists.

“We’re looking forward to hearing her say mummy and daddy.

“We didn’t think we’d get to this stage. The outlook wasn’t very good for Evie when she was very ill.

“It’s such a relief that she’s responding to the implants. It feels as though we’re getting some good news now.”

Many hospital appointments still lie ahead for Evie – but activating the implants has been a milestone for her parents.

Her father, Barrie Smith, 34, said: “We’re hoping that Evie will go to a mainstream school.

“There are some things we still don’t know about Evie’s longer-term development – she will tell us as she grows older.”

‘Rich sounds’

Evie is now among around 5,000 children in the UK who have cochlear implants.

Some deaf people are opposed to implants, and believe that deaf children should instead learn to sign and become members of the deaf community.

Katherine Wilson, the principal audiological scientist at St Thomas’ Hospital, stressed that Evie had the implants at an exceptionally young age because of the after-effects of her meningitis.

She said: “We had to move very quickly to treat her. The bony growth in the inner ears that she had after meningitis meant we wouldn’t have been able to get the implants in later. It just wouldn’t have been a possibility.

“The activation process went fabulously well. We never know how young children will react, but Evie showed typical behaviours you’d expect from a baby of her age.

“This will be a long and slow process, with her coming back to hospital many times to have the devices re-programmed.

“We’re not trying to cure deafness – this is a way of managing and treating it.

“Implants give these children a different dimension to their life – something they wouldn’t otherwise have.

“When Evie has the implants on, she’ll be able to pick up on sound and speech, and hear her mum and dad calling her. When the implants are off, she’s still a deaf child.

“But because of her young age, she has every chance to develop her speech and language, to be able to communicate with hearing people, and to hear the rich sounds of the world.”

A baby has become the youngest in the UK to have cochlear implants – at the age of three months and three days.

Evie Smith had the first device implanted in her right ear, and then the second one seven weeks later.

Evie is now aged six months – and returned to St Thomas’ NHS Hospital in London last week to have the devices activated.

Staff there have emphasised her case is exceptional.

Evie became profoundly deaf after contracting pneumococcal meningitis when she was just three days old.

She spent six weeks in intensive care, and needed to be on a ventilator for a fortnight.

She was given cochlear implants at an exceptionally young age because the meningitis led to bony growth – or ossification – in her inner ear.

The damage to Evie’s ears was getting worse, which meant that waiting for implants at a later stage was not an option.

Cochlear implants cannot cure deafness – but they help Evie and children like her experience sound.

‘Bad outlook’

Audiological specialists fitted external processors to the outside of Evie’s ears – these pick up sound and connect with the internal implants, which help send electrical signals to the brain.

The staff at St Thomas’ banged a drum to monitor Evie’s responses, as they programmed the processor. Watching her stir as she absorbed the sound meant the world to her parents.

Her mother, Jenny Harvey, 33, from Kent, told me: “When we found out she was deaf, what affected me most was the thought of her speech being impaired.

“But hopefully her speech should be very good – with input from the speech and language therapists.

“We’re looking forward to hearing her say mummy and daddy.

“We didn’t think we’d get to this stage. The outlook wasn’t very good for Evie when she was very ill.

“It’s such a relief that she’s responding to the implants. It feels as though we’re getting some good news now.”

Many hospital appointments still lie ahead for Evie – but activating the implants has been a milestone for her parents.

Her father, Barrie Smith, 34, said: “We’re hoping that Evie will go to a mainstream school.

“There are some things we still don’t know about Evie’s longer-term development – she will tell us as she grows older.”

‘Rich sounds’

Evie is now among around 5,000 children in the UK who have cochlear implants.

Some deaf people are opposed to implants, and believe that deaf children should instead learn to sign and become members of the deaf community.

Katherine Wilson, the principal audiological scientist at St Thomas’ Hospital, stressed that Evie had the implants at an exceptionally young age because of the after-effects of her meningitis.

She said: “We had to move very quickly to treat her. The bony growth in the inner ears that she had after meningitis meant we wouldn’t have been able to get the implants in later. It just wouldn’t have been a possibility.

“The activation process went fabulously well. We never know how young children will react, but Evie showed typical behaviours you’d expect from a baby of her age.

“This will be a long and slow process, with her coming back to hospital many times to have the devices re-programmed.

“We’re not trying to cure deafness – this is a way of managing and treating it.

“Implants give these children a different dimension to their life – something they wouldn’t otherwise have.

“When Evie has the implants on, she’ll be able to pick up on sound and speech, and hear her mum and dad calling her. When the implants are off, she’s still a deaf child.

“But because of her young age, she has every chance to develop her speech and language, to be able to communicate with hearing people, and to hear the rich sounds of the world.”

Four Paralysed Men Move Legs For First Time With Stimulation

April 8, 2014

Four paralysed men have been able to move their legs for the first time in years after electrical stimulation of their spinal cords, US doctors report.

They were able to flex their toes, ankles and knees – but could not walk independently.

A report, in the journal Brain, suggests the electricity makes the spinal cord more receptive to the few messages still arriving from the brain.

Experts said it could become a treatment for spinal injury.

The spinal cord acts like a high-speed rail line carrying electrical messages from the brain to the rest of the body. But if there is any damage to the track, then the message will not get through.

People with spinal cord injuries can lose all movement and sensation below the injury.

Zap

A team at the University of Louisville and the University of California have been pioneering electrical stimulation of the spinal cord below the injury.

Three years ago they reported that Rob Summers – a keen baseball player who was paralysed from the chest down in a hit-and-run car accident – was able to move his legs while supported on a treadmill.

Now three more patients, who had been paralysed for at least two years, have gone through the procedure and regained some movement.

They were able to control their legs at a precise pace and all but one of them were able to control the force of the movement.

It confirms that function can be restored after paralysis and that Mr Summers’ case was not a one-off.

One of the researchers, Dr Claudia Angeli from the University of Louisville, told the BBC: “They will tell you that the stimulation itself and being able to practise and move around makes them feel a lot better, some of them will just describe it as feeling alive again.”

“Muscle mass increases significantly and they’ve all shown changes in bowel and bladder [function] as well.”

It is not certain how the stimulation helps, however the researchers believe that some signals are still crossing the injury, but are not normally strong enough to trigger movement.

The electrical stimulation made the lower spinal cord more excitable so it was able to respond when the messages did arrive from the brain.

Dr Angeli described it as “making it ready to listen”.

Progress

Dr Roderic Pettigrew, director of the US National Institute of Biomedical Imaging and Bioengineering, said: “Now that spinal stimulation has been successful in four out of four patients, there is evidence to suggest that a large cohort of individuals, previously with little realistic hope of any meaningful recovery from spinal cord injury, may benefit from this.”

Susan Howley, from the Christopher and Dana Reeve Foundation which funds spinal cord injury research, said the study confirmed Mr Summers’ case was “not an anomaly”.

She added: “The implications of this study for the entire field are quite profound and we can now envision a day where epidural stimulation might be part of a cocktail of therapies used to treat paralysis.”

Sarah’s story: The housing trust and council response

April 8, 2014

Ann McGauran's avatarAnn McGauran

This week I wrote about Sarah. She told me that she was forced to flee her home some distance away in another borough because of her relative’s violent behaviour. A housing trust which runs a hostel for the homeless in Greenwich took her in after she was registered homeless, but it has handed her an eviction letter, telling her that she must vacate by April 11.

It says that if she fails to hand in her keys by 11am that day, it will be ‘forced to carry out an eviction with the Metropolitan Police present’. It adds that following a review, ‘it has been decided that the services and facilities that the accommodation provides are no longer suitable for your needs’. It does not say why that is the case. Sarah says she’s been told it’s because she’s made a number of complaints to the hostel.

Sarah (not her…

View original post 586 more words

WCAs ‘Set To Be Scrapped’

April 7, 2014

I can’t believe my eyes either, readers.

DEMEANING interviews designed to force sick and disabled people back to work are set to be scrapped after experts branded them a waste of time.

The unpopular face-to-face interviews will be sidelined in a shake-up of the Government’s ­controversial work capability assessment.

The move aims to streamline the application process, address a huge backlog of claims, reduce the number of appeals and cut taxpayers’ costs.

If the plan goes ahead, the system would mean less input from companies such as Atos, who last month pulled out of a £500million contract to carry out WCA tests. The new system would give a bigger role to civil servants who will gather written evidence from applicants and their doctors.

The plan follows recommendations made by Dr Paul Litchfield, chief medical officer at BT, who was asked by the Government to review the WCA process.

In his 100-page report, he blamed the face-to-face tests for delays in processing claims. The Department for Work and Pensions, said: “Expediting the process will reduce the uncertainty faced by claimants, improve outcomes for those not eligible for employment and support allowance and reduce the consequent burden on taxpayers.”

Four out of five applicants currently have to attend interviews in which they are asked intimate details in order to assess if they are fit to work.

Labour MP Tom Greatrex, a fierce critic of Atos, said he still has reservations about any new scheme.

He added: “The WCA process hasn’t worked for years and the Government have failed to address it.

“The experience is demeaning, causes anxiety and 40 per cent of the tests are overturned on appeal which demonstrates it’s not fair or accurate.”

Trimethylaminuria

April 7, 2014

A woman who suffers from a syndrome which causes her to smell of “rotten garbage” and “sewage” says she wants to educate people about the condition.

Ellie James, 44, has the rare condition known as Trimethylaminuria (TMAU), which prevents the body from breaking down materials found in certain foods.

She told BBC Radio 5 live’s Breakfast: “I have been verbally attacked on public transport… and I’ve left a couple of jobs because of it.”

“You can’t often smell yourself – you’re relying on other people’s reactions. You don’t know what on earth is going on.”

When Rail Travel For Disabled People Goes Wrong

April 7, 2014

Stranded on trains, denied an accessible loo and forced to be carried through step-filled stations. Disabled rail travellers have been telling a new documentary what happens when the system designed to help them doesn’t work.

“Does the other end know I’m coming?”

This is the line wheelchair-user Baroness Tanni Grey-Thompson repeats time and again to staff on every train journey.

It may sound overzealous but Grey-Thompson says that while it makes for a stressful trip, lots of people who write to her about travel experiences do the same. Many disabled travellers worry that they won’t be met with the help they need at the other end.

“I’ve been left on a train at 01:00, with no ramp to help me off,” she tells this weekend’s 5 live Investigates on BBC Radio 5 live.

The crossbench peer works in London and lives in the Northeast of England. She travels regularly between the two by train, arranging help in advance via Passenger Assist, a specialist booking system for disabled people to reserve seats and arrange extra help at stations.

When no ramp materialised for Grey-Thompson that night, she says, “I had to get out of my chair onto the floor near the toilet, crawl off and push my chair off.”

She goes public when things go wrong, tweeting and writing about her experiences, “to make it better for other people”.

Speaking again of the night she was left stranded, she says, “If I’d been in a situation where I wasn’t as mobile as I am, I’m not sure how long I would have been stuck on that train.”

A report critiquing the Passenger Assist service by the watchdog Passenger Focus says that despite booking help in advance, there was no assistance for their disabled mystery shoppers to help them get off the train in 21% of cases.

The report highlights issues that are only too real for some disabled travellers. Claire Jones from Leeds, who uses a mobility scooter, recently booked assistance but when no one turned up to help it meant that rather than alight at Birmingham as planned, she was forced to travel on to Cheltenham, 40 miles down the line.

“When you have a disability like mine, which affects your energy levels, there is only a certain amount of time you can sit in a scooter. It determines how much time you can travel.”

Another issue uncovered by the recent investigation into the Passenger Assist Scheme was that disabled travellers were not given all the information they needed about a journey. There were instances where the mystery shoppers who’d been testing the system found that stations were less accessible than they were led to believe.

Wheelchair user Paula Moulton says that on one occasion she’d been made aware that a station’s platforms weren’t accessible via ramp, but decided that she could manage this in her manual chair by careful manoeuvring.

However, a “bizarre surprise” awaited her on arrival. “What they didn’t tell us was that there were two flights of stairs and a bridge to get over to the other side. Some really nice guys picked me up and carried me, which I hate happening, but I hadn’t got an option.”

In the past, lack of information has left Grey-Thompson without an accessible toilet for up to five hours.

“Disabled people are used to making lots of decisions about how they travel,” she says. If given the right information about the loo situation, “you don’t drink for an hour and a half before you get on the train to make sure you don’t need to use the bathroom”.

But what Grey-Thompson says challenges her most is that these “aren’t decisions any non-disabled person has to make”.

Having to book help a day in advance to guarantee assistance is a particular gripe of hers. “Disabled people just want to make decisions to meet a friend for lunch, or to just do something different. We don’t always know 24 hours in advance what time we want to travel.”

A spokesperson for the Department for Transport says, “The Passenger Assist Scheme is a vital service and we expect train operating companies to ensure it is working well. That is why we helped to fund a study into the system, and we will look to the rail industry to take forward any recommendations.”

A spokesperson for the Rail Delivery Group, which speaks on behalf of the industry says:

“We apologise to anyone who hasn’t had the service they expect. The industry has worked hard to improve facilities for disabled passengers which are better now than they’ve ever been with record numbers choosing to travel by train.

“While the UK recently came top of Europe’s seven major railways for accessibility, the industry is always looking to improve and to provide the best experience possible to disabled passengers.”

Minister of State for Transport, Baroness Kramer, says that fining companies for failing to provide assistance is the wrong approach. She says that instead we have to “culturally embed, from the top of the company down to the humblest person that (they) have as much of a duty to serve a disabled person as anybody else.”

Grey-Thompson says that getting assistance right and making trains and stations more accessible is important because “changes to welfare support mean that people who might have had a motability car in the past won’t – so there will be more people taking public transport”.

FOI: The Number Of Deaths During Benefit Claims

April 7, 2014

From here.

Darren Marshall made this Freedom of Information request to Department for Work and Pensions

This request has an unknown status. We’re waiting for Darren Marshall to read a recent response and update the status.

From: Darren Marshall

6 April 2014

Dear Department for Work and Pensions,

Could you please enclose information on the number of deaths that
have occurred during the claim process for Employment and Support
Allowance and Disability Living Allowance.

Also the number of deaths that have occurred after claimants have
been placed into the Work Related Activity Group for Employment and
Support Allowance.

Yours faithfully,
Mr Marshall

Rules On Unemployment Benefits Tightening

April 7, 2014

The government is to hail the end of the “signing on” culture when it announces that unemployed people will have to take “basic steps” towards finding work before they can claim benefits.

Esther McVey, the employment minister, will launch a significant government push on welfare this week by saying that unemployed people must prepare for their first interview with a Jobcentre Plus adviser by preparing a CV. They must also set up an email address and register on the government’s jobs website.

Iain Duncan Smith, the work and pensions secretary, will make a speech on his welfare reforms on Monday; Mike Penning, the DWP minister, will highlight a new crackdown on fraudsters on Tuesday and McVey will focus on migrants and benefits on Wednesday.

The government’s plans were thrown into confusion on Sunday when Duncan Smith appeared to steer clear of any policy announcements during an appearance on BBC1’s Andrew Marr Show.

He had little to say about an authoritative Sunday Telegraph report that said the government would give bailiffs greater powers to seize assets from welfare cheats, and even force the sale of a house. There will also be higher fines for claimants who give inaccurate information on official forms.

Government sources denied that Duncan Smith had pulled his punches to avoid an embarrassing clash of headlines as Maria Miller, the culture secretary, faces questions over her parliamentary expenses.

McVey will highlight tough new rules for newly unemployed people. She will say: “With the economy growing, unemployment falling and record numbers of people in work, now is the time to start expecting more of people if they want to claim benefits. It’s only right that we should ask people to take the first basic steps to getting a job before they start claiming jobseeker’s allowance – it will show they are taking their search for work seriously.

“This is about treating people like adults and setting out clearly what is expected of them so they can hit the ground running. In return, we will give people as much help and support as possible to move off benefits and into work because we know from employers that it’s the people who are prepared and enthusiastic who are most likely to get the job.

“This change will mean people start their claim ready to look for work and will show they are serious about finding a job as quickly as possible.”

Civil Servants To Help Capita Cover PIP Assessment Backlog

April 6, 2014

Ministers have been forced to intervene and deploy civil servants to shore up a private company struggling to clear a backlog of medical assessments for payments to tens of thousands of terminally ill, sick and disabled people.

In a letter leaked to the Guardian, a senior civil servant says the “one-off” step will be taken because Capita is failing to process the recently introduced personal independence payment (PIP) claims in time.

The benefit, worth between £21 and £134 a week, is meant to cover transport, care and other costs associated with being seriously sick or disabled. Waiting times for assessment have been so long that in some cases people with terminal conditions have died before receiving a penny.

Speaking on the BBC’s Andrew Marr Show on Sunday, the work and pensions secretary, Iain Duncan Smith, said his new PIP system would be fairer than the old disability living allowance (DLA). Under DLA, he said, people went “years and years” without being able to get the right support for their condition. With PIP, Duncan Smith said, many more people would get face-to-face assessments and the right sort of help.

However, the demand for face-to-face evaluations has overwhelmed the company contracted to carry them out – so much so that the DWP may cut back on such assessments to reduce waiting times.

In a letter dated 20 March, DWP staff were told they would be drafted in for a “one-off exercise” to clear Capita’s backlog. Work to reduce “the current backlog to a normal level of work … was now moving at pace”, the letter said.

It added: “Ministers have also been very clear that they see the need to drive up PIP performance to an acceptable level as a key priority for the department.”

In one of three steps to be trialled, the department will cut down on face-to-face referrals by getting its own staff to determine whether people are eligible for PIP using paper-only evidence.

“We are also considering whether DWP case managers could make more decisions earlier in the journey before formal referral” to Capita, the letter said.

The DWP confirmed that a pilot of paper-based decisions was starting in Wales and Bootle, but said it had always stated that if the case laid out in paper submissions was straightforward, not everyone would need a face-to-face interview with a medical professional.

PIP has already been criticised by the National Audit Office, which said in February that a backlog of 92,000 claims had built up and that people were facing “distress and financial difficulties” because of mismanagement by civil servants as well as Atos and Capita.

Last year the Conservative disability minister Mike Pennington said those diagnosed with illnesses such as terminal cancer would not have to wait longer than seven days to receive extra state aid. Asked why he had not imposed formal targets on Capita and Atos, Pennington said he would use his “size 10 boots” to enforce the desired wait times.

Following sustained criticism of their work, last month Atos confirmed it was departing early from another contract similar to PIP. Duncan Smith told the Marr show that Atos would be paying reparations for their failures on the work capability assessment contract.

“We have now actually asked them [Atos] to go, to leave. They didn’t ask us to go, we have asked them. And we will not pay a penny for that. They will actually pay reparations for failure to achieve what they were meant to achieve. The taxpayer will not be out of pocket.”

Mark Serwotka, head of the Public and Commercial Services union (PCS), which represents frontline DWP staff, said such benefit assessments should not have been outsourced in the first place.

“We have consistently said these sorts of services should be in-house, private companies have no place in providing them and have failed time and again. The DWP needs to invest in staff and resources to ensure disabled people get the support they need and deserve,” he said.

Capita said it was dealing with the situation by “taking on extra staff, including healthcare professionals, and extending the hours for carrying out assessments”.

It said: “We continue to deliver the assessments in a fair and objective way, providing high-quality reports to allow the Department to make its decision, and giving people the time they need to tell us how their disability affects them.”

A DWP spokesperson said: “Ministers are committed to driving up PIP performance and we’re in regular contact with our providers to do this, as you would expect.

“We’ve always said that where claimants have enough evidence they won’t need to be seen in person. However, the majority of people will continue to have face-to-face assessments under the new benefit this government introduced, unlike the old system of disability living allowance where only around 6% were seen.”

Update On The Cherry Groce Legal Aid Campaign

April 6, 2014

From Change.org. I publicised the petition here earlier.

Thank you for signing our petition to get justice for our mother Cherry Groce. It has meant so much to our family to have such huge support from the public.

This week we presented your signature, along with 130,000 others, to 10 Downing Street. We were joined by our MP Chuka Umunna who has been supporting us throughout this campaign.

After the delivery we found out that the Legal Aid Agency is reviewing our case and has referred our case to Lord Chancellor and Justice Minister Chris Grayling to make a decision.

This is a huge step forward. The Legal Aid Agency twice refused us legal aid but this petition has forced them to review the decision. The Lord Chancellor will have the final say and will base his decision on whether there is public-wide interest in this case. So it is more important than ever that we keep the petition growing.

Thank you for your help. We have been fighting for justice for three decades and finally we are being heard. Let’s keep it up.

Thank you,

Lee Lawrence
Cherry’s son

P.S. If you are on Twitter you can also tweet a message of support to the Ministry of Justice. Click here.

Robert Barlow

April 6, 2014

A disabled man died penniless when he lost his benefits after being judged fit to work.

Robert Barlow died last November aged 47 while suffering from a heart defect and brain tumour.

He was deemed fit to work by benefits assessors Atos despite doctors at the time urging him to have a heart transplant – he passed away less than two years later.

Now his family and Labour MP Luciana Berger want the Government to learn lessons from this tragic case.

His aunt Joan Westland, 85, said: “I don’t know how they expected him to work. Nobody would have loved to work more than him but he simply couldn’t.”

University of Liverpool graduate Mr Barlow, from Wavertree , worked as a Government scientist but gave up his job nine years ago when diagnosed with severe cardiomyopathy, a weakness or failure of the heart muscle.

By the end of his life he could not walk, struggled to read due to poor eyesight and often fell over, smashing his teeth on one occasion.

Doctors eventually gave Mr Barlow a year and a half to live and recommended a heart transplant.

He was often in and out of hospital during his final months. He never married or had children.

Mrs Westland said: “Robert said he wouldn’t have the heart transplant. He had no commitments and thought it would be better if there was a heart for it to go to somebody else.

“We tried to talk him into having the operation but he wouldn’t do it.”

 Mr Barlow, born in Wallasey , was given a fitness-to-work test by Atos in January 2012 and his Employment and Support Allowance (ESA) was stopped three months later. He also lost the right to free NHS prescriptions.

Mrs Westland said: “Robert was dying and he accepted that. I feel he should have been left to enjoy what little time he had left.”

The Department for Work and Pensions (DWP) says Mr Barlow initially challenged the decision to stop his benefits but the appeal was withdrawn because, according to Mrs Westland, he felt too ill to fight the case.

“Robert had very little money on benefits and nothing at all when his money was stopped,” his aunt said. “I know there are scroungers but he was not one of them.”

 Paying tribute, Mrs Westland continued: “He was a trained classical pianist, he could cook and he had a beautiful sense of humour.

“He loved cricket and was very knowledgeable about lots of subjects. He loved Beethoven and had an extensive collection of records.

“But he got so ill that by the end he couldn’t play the piano any more. He had a bad left eye so reading became difficult.

“I want these fitness-to-work tests to stop because I don’t want other people going through the same trauma. Robert was very, very distressed after his Atos assessment.”

Mr Barlow died after never regaining consciousness following a fall at home – just seven months after his mother passed away.

Wavertree MP Ms Berger, a shadow health minister, raised his tragic story in the House of Commons last month.

Since then Atos has quit its £500m contract and ministers are looking for a new provider.

Ms Berger told the Sunday ECHO: “It’s not enough to change the provider. The whole process needs to be totally redesigned.

“My constituent is someone who lost his life at a time when his ESA was suspended.

“He was too sick to appeal the decision and died while he had no access to benefits.”

A DWP spokesman said: “We have followed the correct procedures in the processing of this benefit claim. People have the right to appeal a decision, but if the appeal is withdrawn we cannot continue with processing the claim.”

Wirral West Tory MP and Employment Minister Esther McVey previously defended the fit-to-work tests, saying: “Our reforms will make sure the billions we spend every year give more targeted support.”

New Spartacus Website!!!

April 5, 2014

Posting by request of Sue Marsh.

We’re all really excited to announce the launch of the new Spartacus website!

http://www.spartacusnetwork.org.uk

You can still find all of our past work there with a few new additions
 
Stef Benstead has taken over the running of the site. 2 years of campaigning is like 412 effort years so huge thanks to Jane Young, the previous site director who produced and guided so much important work. 
 
The old address, http://wearespartacus.org.uk is now defunct but bear with us while we set up a redirect to the new address.

Stef is one of our lead researchers on ESA and has produced some seminal work already such as ESASOS, a report into how successfully Harington recommendations had been implemented and the Spartacus submission on ESA to the Work and Pensions Committee. 

Next week, Spartacus is on the march, so please watch twitter and Facebook extra carefully and if you want to be involved, email me at suey2y@gmail.com before Wednesday

It will be a great chance to launch the re-designed, updated site and I would appreciate it so much if you could help me to let people know about the new address. 

 

Williams Syndrome- The Opposite Of Autism

April 5, 2014

“I get so anxious if I want to go out to things. I live with my Mum because I don’t want to live on my own. I can’t do money. I wish I could.”

Chris Steele is 40 years old. He is remarkably friendly and engaging, and is happiest when he is on stage acting in plays such as George Orwell’s Animal Farm.

As a child, his caring nature led him to take to the bedside of a victim of the Hillsborough disaster, with such compassion and diligence he was given an award by former UK Prime Minister Margaret Thatcher.

But he is unable to go out alone – once, when he did, his openness towards strangers and difficulty in understanding when he is in danger meant he lent his phone to a stranger, who stole it.

He suffers severe anxiety, and needs constant reassurance from the people around him.

‘Reeling people in’

Chris suffers from Williams Syndrome (WS), a rare genetic disorder affecting around one in 18,000 people in Britain. It has often been dubbed the ‘opposite of autism’.

People with WS are empathetic, social, friendly and endearing but they tend to have a low IQ, making tasks such as counting money difficult.

They can suffer extreme anxiety over stimuli such as the buzzing of a bee, or the texture of food.

The need for reassurance in some cases can leave children of loving households calling 999 and feigning an emergency, as they crave adult attention so much.

WS, first identified in 1961, can also cause heart problems, developmental delays, and learning disabilities.

For the psychological side of the disorder, acting can play to sufferers’ strengths. Chris says: “I am good at reeling people in and being a character in different things.”

He acts with a charity called Mind the Gap, based in Bradford, near his home town of Bingley in West Yorkshire, and cites the time he was a pirate in a play called Treasure Island as amongst his favourites.

Behavioural subtleties

When he was a child, and visiting his father in hospital, Chris met Tony Bland, who suffered severe brain damage when he was crushed in the Hillsborough stadium disaster in 1989.

Chris befriended Tony, and stayed, loyally, by his bedside for weeks. “Chris can talk to anyone and doesn’t need a response,” his mother Judy says.

Judy says he is also “great to take to parties” as he happily introduces himself to new people.

But there is a flip side of this social ease. Judy says Chris is “too trusting”, and has been taken advantage of.

She said he also needs people around him to be happy and guide him in what opinions he should have.

People with WS may make prolonged eye-contact, and be over-engaging, which can put them in danger.

Language ahead of mind

There are also further aspects of the disorder which can land them in hot water.

Lizzie Hurst, chief executive at the Williams Syndrome Foundation, says: “People [with the disorder] conduct themselves in a way that makes them extremely vulnerable.

“They don’t have the cognitive ability to match their linguistic age.

“There is a classic autistic profile to which Williams Syndrome is the polar opposite. People can gauge the mood of a crowd and adopt without understanding the nuances of the situation.”

Ms Hurst says there were “questions to be raised” over whether sufferers could be legally responsible for themselves. “I would say they cannot,” she adds.

She is working to raise the profile of the disorder amongst GPs, as she says only one in 40 GPs will encounter the disorder and babies with WS can be difficult to identify.

Facial features in young children include a small, upturned nose, long upper lip, wide mouth, full lips, small chin and a white lacy pattern on the eye’s iris.

Autism ‘tidal wave’

Anxiety can be made worse if the disorder is not diagnosed, she said, as people feel even more isolated.

Ms Hurst’s charity does not get any funding from the government, relying on fundraising and donations. She puts on barbecues, Christmas parties and holidays for WS sufferers and their families.

“I think the government should do more,” she says. “It can be difficult when you see the surge of funding for the tidal wave of autism.

“WS people are just as needing as other people with mental disorders and in many ways they are more needing of support and attention, and that all comes at a price.”

Sufferers of WS do not have a lower life expectancy than other people, and some may go on to get jobs, most often in a voluntary capacity, where their helpful nature can be useful.

Dr Debbie Riby, senior lecturer in the Department of Psychology at Durham University, has been working on the disorder for 12 years.

Genetic basis

She says WS occurs when part of chromosome seven is deleted, which happens sporadically.

“Anybody can have a child with Williams Syndrome,” she says.

Dr Riby says there is no pre-natal screening, but often doctors can pick up clues if a young child has heart murmurs, and problems putting on weight.

She has been running parent focus groups to understand the anxiety side of WS to come up with practical steps families can do to help them keep their child calm and happy.

Dr Riby says: “The work around Williams Syndrome used to focus on the theoretical side. I wanted to focus on the practical side. There is still an awful lot that we can do.

“The most important thing is for us to think about how we can use research to support families.”

Assisted Suicide Campaigner Margo MacDonald MSP Dies Aged 70

April 4, 2014

The independent MSP and former SNP politician Margo McDonald has died.

A member of the Scottish Parliament since 1999, the 70-year-old had been suffering from Parkinson’s disease.

Her husband Jim Sillars said: “Today the brightest light in the Scottish political firmament has gone out.”

Ms MacDonald, a hugely influential figure in the Scottish independence movement, rose to prominence after winning the Glasgow Govan Westminster by-election for the SNP in 1973.

She later served as an SNP MSP for the Lothian region, before going on to represent the area as an independent member of the Scottish Parliament.

Mr Sillars, a former SNP deputy leader, said: “My wife Margo MacDonald died peacefully at home surrounded by her family today at 1.10pm.

“She leaves a void in our lives which will be impossible to fill and her death robs the Scottish nation of one of its greatest talents.

“She was without question the most able politician of her generation.

“Today the brightest light in the Scottish political firmament has gone out.”

Tributes for Ms MacDonald, herself a former SNP deputy leader, poured in from across the political divide.

‘Wit and sparkle’

Green MSP Patrick Harvie, said: “I’ve always enjoyed the wit and sparkle she brought to debates in the chamber, but she could also offer a formidable challenge when it was needed, and showed long term dedication to the causes she chose to work for.

“Margo won’t now see the culmination of two debates she was deeply involved in; the referendum on Scotland’s independence, and the Assisted Suicide Bill which she introduced last year.

“But as both these debates continue, I am certain that campaigners on all sides will recognise Margo MacDonald’s contribution to Scottish public life, her vibrancy and her passion.

“I know I’ll miss her every time I walk into the chamber.”

Scottish Parliament Presiding Officer Tricia Marwick, added: “Margo MacDonald was brave, passionate and committed.

To be known and recognised by a first name is reserved to very few. But everyone knew Margo. She had a rare skill in being able to translate political speak into language we could all understand.

“She was a sparkling jewel in the Scottish Parliament, her contributions were incisive, intelligent and always got to the heart of the issue under discussion.

“Margo cared about people and, in return, they cared about her.”

‘Force of nature’

Scottish Labour leader Johann Lamont, said: “Margo’s passing sees a bright light, and one of the biggest personalities and characters of Scottish modern political life, go out.

“Her sense of humour, passion, integrity and unflinching desire to speak truth to power, meant she came as close to a political treasure in Scotland as I think it is possible to be.”

Willie Rennie, leader of the Scottish Liberal Democrats, added: “Margo was a force of nature in Scottish life.

“The affection for her transcends party politics and political parties. Her personal kindness and professional charm will be missed in the parliament, throughout the Lothians and far wider.”

Work And Pensions Committee- First Oral Evidence For WCA Enquiry: Wed 9 April

April 4, 2014

The Work and Pensions Committee will hold its first oral evidence session for its inquiry into Employment and Support Allowance and Work Capability Assessments on Wednesday 9 April.

 

Witnesses

9.30am, Wednesday 9 April, Grimond Room, Portcullis House, House of Commons

  • Rachael Holmes, Head of Policy Research, Families, Welfare and Work, Citizen’s Advice
  • Tom Pollard, Social Policy and Campaigns Manager, Mind
  • Donna O’Brien, Social Policy and Campaigns Advisor, Parkinson’s UK
  • Anna Bird, Head of Public Policy and Research, Scope
  • Joanna Kennedy, Chief Executive, Zacchaeus 2000 Trust

Purpose of the meeting

This session, with claimant and disability representative groups, will explore:

  • The effectiveness of the WCA in determining whether people are fit for work, including the findings of the Evidence Based Review and possible alternative assessment models
  • Key concerns about the delivery of the WCA by Atos, and how these issues may be resolved with the new provider
  • How eligibility for ESA is determined by the DWP decision maker
  • Outcomes for claimants following assessment
  • The process for appealing a decision and the available financial support during this period
  • The impact of time-limiting contributory ESA for those in the Work Related Activity Group (WRAG)
  • The interaction between ESA and Universal Credit

Salvation Army And Workfare

April 4, 2014

Spotted on Facebook. Quite shocking. Please share widely.

 

Did you know that as a company that is part of the governments work program, the Salvation Army have the right to dish out sanctions to your anyone who has been referred to them by JobCenterPlus who doesn't follow the strict rules. Benefit sanctions can be given out to people for being late, missing appointments, or not carrying out instructions to the letter. </p><br />
<p>The charity that is supposed to help people who have fallen on hard times is now forcing some of those same people in to poverty.

Did you know that as a company that is part of the governments work program, the Salvation Army have the right to dish out sanctions to your anyone who has been referred to them by JobCenterPlus who doesn’t follow the strict rules. Benefit sanctions can be given out to people for being late, missing appointments, or not carrying out instructions to the letter.

The charity that is supposed to help people who have fallen on hard times is now forcing some of those same people in to poverty.

An Interesting Post On Maria Miller’s Expenses

April 4, 2014

I did think about covering this, because she used to be Minister For Us Lot. But I couldn’t see how to link her past job with this story, until I read this very interesting post from Political Scrapbook.

I have to wonder- what would happen if a benefit claimant tried to do what she did? Jail, probably. Sanctioning, definitely. Starving, quite possibly.

A Letter From Ingeus To A Small Business: PLEASE Take Someone From Work Programme

April 4, 2014

Originally posted here by Kate Belgrave yesterday. Reposted with permission.

Here we go then – a letter sent by work programme provider Ingeus to someone I know who owns a (very) small business. The letter just turned up in that person’s post. Looks like Ingeus touting for action – trying to get anyone it can find to “employ” young people from the government’s rubbish Youth Contract programme. I suppose this is what companies do when a “concept” is tanking – they spam away in the hope that somebody somewhere will bite. And in the hope that the press coverge will improve, I guess.

The usual Youth Contract carrot is dangled: the letter makes clear, in nice bold numbers, that £2,275 is available to employers “for every unemployed young person they recruit who is currently on the work programme.” It appears that the company has some sort of catalogue of “enthusiastic young people” from which employers can choose. Wow. Pick your own. “It won’t cost you a penny,” the letter continues. Because, you know – why should employers pay money to recruit if they can get someone to actually pay them to do it? Why shouldn’t we keep forking out for useless work programmes? Why should young people expect real, meaningful well-paid jobs?

Jesus wept. Somebody shut these tossers down and do something sensible. Please.

 

Ingeus letter

Michael Meacher’s Speech on Benefit Sanctions

April 4, 2014

alittleecon's avataralittleecon

There was a backbench debate in the House of Commons today on the DWP’s use of benefit sanctions. The official line is that claimants are only ever sanctioned if they are not doing what is required of them to either find work or prepare for work. The strong suspicion however is that sanctions are being used primarily to get people off benefits. Labour MP Michael Meacher opened the debate with a speech in which he gave numerous examples of where claimants have been sanctioned through no fault of their own, and highlighted the impact this can have on people’s lives. Here is the text of the first part of his speech (from Hansard):

“I beg to move,

That this House notes that there have been many cases of sanctions being wrongfully applied to benefit recipients; and call on the Government to review the targeting, severity and impact of such sanctions…

View original post 509 more words

Parliament Misspells Lord’s Name

April 3, 2014

I have just spotted this image on Facebook.

Photo: Parliament misspells Lord Freud, L. Fraud (on purpose?)

 

I thought you might smile, readers. Apparently, it’s from Parliament.

Cherry Groce Family Take Legal Aid Campaign To Downing Street

April 3, 2014

The family of a woman shot by police, triggering the 1985 Brixton riots, are taking their battle for legal aid to Downing Street.

Cherry Groce was paralysed below the waist when she was shot and now her family are to present a petition of 129,000 signatures to the government.

They are demanding legal aid so they can be adequately represented at her inquest this summer.

Mrs Groce died in April 2011, having spent 26 years in a wheelchair.

She was accidentally shot by police, who were seeking her son Michael, during an early morning raid on her home.

Dozens of civilians and 10 police officers were injured in the unrest in Brixton, south London.

A police marksman, Insp Douglas Lovelock, shot Mrs Groce and stood trial in 1987 charged with inflicting unlawful and malicious grievous bodily harm but was acquitted.

Mrs Groce’s inquest is due to take place in June and documents obtained by Channel 4 News have revealed that pathologists for both the family and the police concluded there is a causal link between the shooting and her death.

But her family’s request to obtain legal aid for representation at the inquest has been denied, prompting them to launch an online petition.

‘Difficult decision’

Mrs Groce’s son Lee Lawrence, who was 11 years old when he saw his mother shot, said: “The prime minister has the power to say our call for legal aid is in the public interest.

“It will not bring our mother back but it will bring her justice. She waited her whole life for justice, we owe her that.”

A Legal Aid Agency spokeswoman said: “This was a difficult decision which was not taken lightly.

“An inquest is aimed at helping families find out the circumstances behind the death of their loved one.

“The coroner is there to investigate the death and can put questions on behalf of the family during proceedings.”

Disabled Woman’s Kent Police Pension Row

April 3, 2014

A mother who is in constant pain from a disease called Complex Regional Pain Syndrome been told that she will not get a pension by the police force who dismissed her in case she gets better before she reaches retirement age.

Maxine Difford, 40, worked for Kent Police for 11 years but had to leave because of the condition that has left her with a persistent burning pain in her leg.

She told BBC reporter Nafisa Sayani the loss of her wage had left the family financially stretched and she worried every day about whether they would be able to keep their house.

Kent Police said it had no discretion over regulations set out by the local government pension policy and could not overturn the decision.

WARNING: Job Site Scams

April 3, 2014

Spotted on Facebook.

 

Tasha Tyler-Harris
Can I get you to give the page members a warning about something they might come up against, as it’s happening on the major sites, not just little ones? One of my friends, who has been out of work for 4 years, was just nearly caught by it.

There’s’s a very cruel scam going on right now on some of the job sites (Gumtree, Indeed, and a few others), aimed at the unemployed. When you apply to the job advertised you get an offer and sent a list of hours, but asked to send £50 or £60 to cover the cost of a CRB check. Now these scams are clever. They use either hijacked ads from real companies, or false businesses using a minor variation on a big company’s name. There is no actual job, and this sort of thing is run by truly sick people picking on the desperate.