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Smog: Health Advice

April 3, 2014

This health advice comes in relation to the smog/high pollution levels in the UK at the moment. These are expected to clear by Friday.

Dr Keith Prowse, honorary medical adviser to the British Lung Foundation, warned higher pollution levels could have a “significant impact” on people with respiratory conditions.

“People who use a reliever inhaler should make sure that they carry it with them. If they feel that their conditions are worsening then they should contact their GPs,” he said.

Kay Boycott, chief executive of Asthma UK, said the two-thirds of people with asthma who find that air pollution makes their condition worse “will be at an increased risk of an attack”.

Advice on the Defra website states that for high levels of pollution “adults and children with lung problems, and adults with heart problems, should reduce strenuous physical exertion, particularly outdoors, and particularly if they experience symptoms.

“People with asthma may find they need to use their reliever inhaler more often. Older people should also reduce physical exertion.”

It adds that “anyone experiencing discomfort such as sore eyes, cough or sore throat should consider reducing activity, particularly outdoors”.

The Undateables To Return For Fourth Series

April 3, 2014

 

With pleasure.

Did YOU Submit Evidence To The Work And Pensions Select Committee?

April 2, 2014
Did YOU submit evidence to the Commons Work and Pensions committee for its inquiry into ESA and the Work Capability Assessment? If so, I’d like to hear from you.

According to Dame Anne Begg, who chairs the committee, only 190 submissions of evidence were received. That seems an extremely low amount, considering the widespread publicity given to the call for evidence.

So I’ve been asked to do a ‘straw poll’.

If you submitted evidence, please send me a PM (personal message) on Facebook – either to Mike Sivier OR Vox Political, saying that you did so. The information will be treated in the strictest confidence – it’s numbers I want, not personal information.

Could readers please share this on any pages where people who submitted evidence are likely to read it? Thanks.

Fashion Industry Letting Down Disabled People

April 2, 2014

I thought this might be of interest to some of you.

Ban Ki-Moon’s World Autism Awareness Day Message

April 2, 2014

Five Hundred Legs For Gambia

April 2, 2014

Five-hundred redundant prosthetic limbs will travel from Leicester to Gambia next week to help amputees in Africa.

Tom Williams, from the Legs for Africa project, said the used prosthetic legs have been collected from hospitals and charities around the UK.

Mr Williams added that the artificial limbs would be “customised” for amputees 4,000 miles away.

Chris Mawby, who is transporting the precious cargo, hopes the first trip on 8 April will be one of many as there are “thousands of legs wasted every year in the UK and we aim to reuse all of them”.

Unemployed Single Parents To Be Forced Into Unpaid Work Placements

April 2, 2014

This article titled Unemployed Lone Parents To Be Forced Into Unpaid Work Placements and written by Steven Preece was first published by the Welfare News Service on 1 April 2014 and has been reproduced here with permission.

 

Unemployed lone parents could to be forced into mandatory unpaid work placements as part of fresh changes to benefits coming into force from the 28th April 2014.

Lone parents in receipt of Income Support who have a child between the age of 3-4 will be required to undertake ‘mandatory work related activity’ “to better prepare them for the full work-related requirements they will face when their child turns 5”.

The changes will also apply to lone parents in the ‘Work Related Activity Group’ (WRAG) of the sickness benefit Employment and Support Allowance (ESA).

It does not apply to those in the ESA Support Group: which is for sick and disabled benefit claimants who the Department for Work and Pensions (DWP) feel will not be able to begin looking for work in the foreseeable future.

Local authority childcare schemes will be made available to allow the changes to come into effect and help free up lone parents to partake in the new requirements. Up to fifteen hours of free childcare will be available for those affected.

Income Support claimants with a child between the age of 1-4 will also be required to take part in work focused interviews at their nearest Jobcentre. The time and duration ‘will be tailored to the needs of the lone parent’.

Failure to comply with the changes – without good cause – could result in lone parents having their benefits cut or stopped completely (sanctioned). The level of the cut will begin at 20% but could increase to 100% for ‘further failures’. However, only one Income Support cut will be permitted in a two-week period.

It has also been announced this week that jobseeker’s who have been out of work for over three years, and who have already taken part in the government’s controversial Work Programme, will be required to undertake ‘community work placements for up to 30 hours per week. They will also be expected to spend 10 hours per week looking for work.

The DWP has given the example of “clearing up litter and graffiti in local areas” which has previously been reserved for community volunteers and criminal offenders.

In this instance, failure to comply will result in jobseeker’s having their benefits cut for four weeks which could extend to several months for repeat offenders.

New Jobseeker’s Allowance (JSA) claimants will also have to wait 7 days before they become entitled for the unemployment benefit.

Opening the doors: Debt, domestic violence, power relations and an eviction notice

April 1, 2014

Ann McGauran's avatarAnn McGauran

Sarah, a single woman of 28 and a law graduate, came in on Friday and kindly shared her account of why she needed help. Before I pass on her story I’d like to remind readers that I don’t speak for those who run this London food bank, although they’ve allowed me to interview their clients. Any opinions expressed on this site from time to time are my own. I don’t represent the food banks in the borough of Greenwich. Neither do I represent the views of the Trussell Trust, which partners with churches in this area to run the food banks.

Sarah (not her real name) must have thought her life was on a more even keel when she finally worked up the courage to escape the violence in her family home. She had moved back in again in 2008 when she struggled to find a job after leaving…

View original post 1,505 more words

Constant Flux

April 1, 2014

Punk, with its raging, mad-eyed, opiate-guzzling musicians, might be a far cry from the patronised, victimised stereotype of people with learning disabilities. But in the burgeoning live music scene for people with learning disabilities it is punk and heavy metal that predominate. Lyrics, stripped of opacity, punch with the fury of the sidelined: “Why don’t you understand me?/You always torture me/Force me to clean toilets/Force me to eat/I don’t understand why you don’t let me outside”.

Other songs by Finland’s Pertti Kurikan Nimipäivät, one of the more established groups on the British scene, convey the disempowerment of living with autism, Asperger’s, Down’s syndrome or other learning-affected conditions: “I don’t want to live [in a] group home/I don’t want institution/I want respect.”

Now a new organisation, Constant Flux, hopes to bring the band’s music – and that of other learning disabled groups – to a wider audience. Launched last year by Richard Phoenix, a musician and music facilitator for learning disabled people, Constant Flux’s goals are simple but groundbreaking.

“The idea is to provide opportunities to perform live to integrated audiences in environments that aren’t necessarily so safe, where it’s not just a learning disability event,” he says. “We want musicians to be part of the wider community and part of the wider music scene.”

The concept builds on a gig night called The Rock House, which Phoenix set up in Brighton in 2010 while working for Carousel, a local arts charity for people with learning disabilities. “We put out an open call for musicians and bands with at least one learning disabled member to come along and either perform their material or improvise alongside a house band – The Rock House Band,” he says.

It proved a success with up to 100 tickets being sold each month, and now boasts seven different acts at each gig. It prompted some of the bands to consider touring, in turn triggering the need for Constant Flux. “I used to encounter so many musicians who were really passionate but frustrated about the lack of opportunities for playing with other bands, getting records out, or getting people to hear their music,” says Phoenix. “So it’s incredible to now be able to find ways to make that happen.” 

While help is already provided by other organisations for learning instruments, reading music, remembering the music and writing words, Constant Flux, funded by the Arts Council England’s Grants for the Arts scheme, steps in chiefly around the organisation and communication essential for keeping a band together and staging a tour. “Some of the musicians are truly exceptional, particularly some on the autistic or Asperger’s spectrum,” says Phoenix. “But they can need support with things like booking rehearsals and setting up gigs. Much of my job is like that of a tour manager. We also, for example, look after a band called The Express who play and write all their own songs but it’s difficult for them to communicate so a lot of the support we offer is helping them engage with each other.”

It is not always apparent which musicians have learning disabilities or what the diagnosis might be. This challenges audiences to think about how often people with learning disabilities’ needs go unnoticed simply because they are not obviously disabled. But it also shows people what can be achieved with the right support, says Phoenix. So far, the reaction has been overwhelmingly positive – and informative. The first London gig Constant Flux staged last year for heavy metal sextet Zombie Crash‘s tour was sold out, with around 700 attending. “A lot of audience members said they didn’t know what to expect or how they were going to react to the musicians but in the end people were just into the music and forgot they were watching people with learning disabilities,” Phoenix says.

Following the success of Zombie Crash’s tour, Constant Flux is now organising gigs for the electronic pop act, The Fish Police. Together for five years, the band had previously been struggling to find gigs in a more mainstream setting, let alone go on tour. But this month, they will be performing in seven cities, each time alongside three local bands: one with learning disabled members and two without.

Performing sell-out gigs for mixed audiences as part of a wider national music scene has also had profound effects on the band members. “The lead singer of Zombie Crash, who has Asperger’s syndrome, says when he’s on stage he feels like his learning disability goes away,” says Phoenix.

“We are finally blending with learning disabled and non-learning disabled bands alike in environments that befit us,” says Ryan O’Donovan, the band’s lead guitarist. “The tour was our greatest moment to date.”

• For details and tickets for the Fish Police tour visit constantflux.co.uk

New #BedroomTax Human Rights Legal Case

April 1, 2014

Child poverty Action Group (CPAG) is acting for Paul and Susan Rutherford and their grandson Warren in a judicial review challenge to the bedroom tax.

The case concerns the housing benefit bedroom tax restrictions for social tenants, as they apply in the case of children who need an overnight carer.

The regulations currently allow an additional bedroom if a claimant or their partner “require overnight care” but there is no similar provision for children.

CPAG are arguing that this discriminates against disabled children contrary to Article 14 of the European Convention on Human Rights, and that there is no rational justification for the exclusion of children from the exemption for overnight carers.

For more information go to http://www.cpag.org.uk/content/bedroom-tax-Rutherford

 

Better living, higher standards: improving the lives of disabled people by 2020

April 1, 2014

Mind Controlled Exoskeleton To Make Debut At The 2014 World Cup

April 1, 2014

Shortly before 5pm local time on 12 June at Arena Corinthians in Sao Paulo, a young paraplegic Brazilian will stand up from their wheelchair, walk over to midfield, and take the first kick of the 2014 World Cup.

For those hoping for miracles at football’s greatest tournament, the scene may be the closest they get to witnessing one. For Miguel Nicolelis, a neuroengineer based at Duke University in North Carolina, the moment demands faith of another kind. As hundreds of millions tune in for the opening match, they will see the first public demonstration of technology he claims will turn wheelchairs into museum pieces.

The technology in question is a mind-controlled robotic exoskeleton. The complex and conspicuous robotic suit, built from lightweight alloys and powered by hydraulics, has a simple enough function. When a paraplegic person straps themselves in, the machine does the job that their leg muscles no longer can.

The exoskeleton is the culmination of years of work by an international team of scientists and engineers on the Walk Again project. It was built by Gordon Cheng at the Technical University in Munich. Nicolelis’s team focused on ways to read people’s brain waves, and use those signals to control robotic limbs.

On Tuesday, the team launches a Facebook page that will document the project in the days leading up to the World Cup. A dedicated website is due to go live later this week.

Nicolelis is training nine paraplegic men and women, aged 20 to 40, to use the exoskeleton at a neurorobotics rehabilitation lab in Sao Paulo. Three will be chosen to attend the opening game between Brazil and Croatia, with one volunteer heading on to the pitch to perform the demonstration.

To operate the exoskeleton, the person is helped into the suit and given a cap to wear that is fitted with electrodes to pick up their brain waves. These signals are passed to a computer worn in a backpack, where they are decoded and used to move hydraulic drivers on the suit.

The exoskeleton is powered by a battery – also carried in the backpack – that allows for two hours of continuous use.

“The movements are very smooth,” Nicolelis told the Guardian. “They are human movements, not robotic movements.”

Nicolelis says that in trials so far, his patients seem have taken to the exoskeleton. “This thing was made for me,” one patient told him after being strapped into the suit.

The operator’s feet rest on plates which have sensors to detect when contact is made with the ground. With each footfall, a signal shoots up to a vibrating device sewn into the forearm of the wearer’s shirt. The device seems to fool the brain into thinking that the sensation came from their foot. In virtual reality simulations, patients felt that their legs were moving and touching something. One patient, whose spinal injury meant he could not feel or move his legs, told Nicolelis: “I feel like I’m walking on the beach, that I’m touching the sand.”

Nicolelis likens the effect to the rubber hand illusion, where the mind is tricked into thinking that an inanimate object is part of the person. “It confirms our prediction that we are going to elicit a sensation that the exoskeleton is an extension of their body,” Nicolelis said.

In other trials, patients have used the mind-control system to walk on a treadmill.

Nicolelis said he believed the technology was ripe for turning into everyday devices to help paraplegics and could ultimately replace wheelchairs.

“All of the innovations we’re putting together for this exoskeleton have in mind the goal of transforming it into something that can be used by patients who suffer from a variety of diseases and injuries that cause paralysis,” he said.

The system has been through numerous safety tests. The exoskeleton is fitted with multiple gyros to stop it falling over during the balancing act of bipedal walking. As an extra safety measure, it was fitted with multiple airbags.

Last month, Nicolelis and his colleagues went to football matches in Sao Paulo to check whether mobile phone radiation from the crowds might interfere with the suit. Electromagnetic waves could make the exoskeleton misbehave, but the tests were encouraging. The chances of the exoskeleton malfunctioning, and stomping off into the distance, are apparently slim.

Sethu Vijayakkumar, a roboticist at Edinburgh University, said exoskeletons were a natural progression for rehabilitation and made the most of robotic and human abilities.

“This is something that will happen, and needs to happen. Humans are very good at high-level decisions and making sense of ambiguous situations, but robots are very good at very precise, repetitive, accurate movements,” he said. “Exoskeletons are the way to marry these two together.”

World Autism Day Celebrations In Full Swing!

April 1, 2014

A press release from Autism West Midlands:

 

 

Autism West Midlands has announced a full calendar of activities to mark World Autism Day next month with a series of fun and exciting events designed to engage the autism community, raise funds and increase much needed awareness for the condition.

The festivities kick off at 6.30pm on April 1 with the Spectrum Spectacular. Held at the The Nautical Club on Bishopgate Street, Birmingham, the night is a lively celebration of autistic talents that recognises creative gifts and offers rare insight into the exceptional minds of people living on the spectrum. Attendees can expect to enjoy a variety of music recitals, creative writing, arts and crafts presentations and other performances. Tickets are available for pre-purchase at a cost of £3 for general admission and £2 for people with autism. Attendees are reminded that The Nautical Club is an 18+venue so the night is reserved for adult enjoyment only.

World Autism Day itself will be celebrated with a Family Fun Evening held at the Autism West Midlands headquarters in Edgbaston. The event is completely free to attend and offers a wide range of entertaining activities including party games, a sensory room, lego, board games, arts and crafts and even a disco. The evening runs in two slots from 4pm-6pm and 6pm-8pm, making it a great event for kids of all ages!

The fun doesn’t end on April 2, Autism West Midlands planning a flash mob for the coming Saturday. April 5 will see the Library of Birmingham descended on by a mob of purple clad supporters, flaunting the eye-catching colour in support of the autism cause. The event has already gained the support of 100 attendees, a number that is expected to continually grow as the date draws closer.

In addition to the one-off celebratory events, World Autism Day will see the launch of several Autism West Midlands initiated projects that are set to have a hugely beneficial impact on the autism community.

Ultraviolet Voices, the non-fiction book exploring the struggles and day-to-day difficulties of living as a woman on the autism spectrum, will be published on the 2nd April as part of the awareness event. With contributions from 15 autistic women as well as autism expert, Dr Juli Crocombe and neuroscientist, Dr Elisabeth Hurley, Ultraviolet Voices is a resounding, insightful and touching publication that is a must read for anyone wanting to enhance their understanding of the autism experience.

World Autism Day will also see the launch of the UK’s first ever autism social networking site, Connect. Managed and monitored by Autism West Midlands, the site offers a unique chance for members of the autism community to interact, unite and receive the support of others. Anyone associated with the condition is encouraged to join, the site providing a wonderful social opportunity for people with autism as well as their family, friends and carers.

To learn more about the Spectrum Spectacular or to purchase a ticket visit: http://shop.autismwestmidlands.org.uk/products/spectrum-spectacular

To learn more about the Family Fun Evening and to make a free booking visit: http://www.autismwestmidlands.org.uk/events/index.php?page=event&event_id=925515 .

To learn more about the Flashmob or to register as an attendee visit: http://www.autismwestmidlands.org.uk/aware/content/935555/flashmob/

To find out more about Autism West Midlands and how they provide much needed help and support to the autism community visit: www.autismwestmidlands.org.uk.

Facebook: https://www.facebook.com/AutismWM

Twitter: https://twitter.com/autismwestmids

About Autism West Midlands: Autism West Midlands is a UK based charity dedicated to providing all people on the autism spectrum with the specialist care and support they need to lead fulfilling and rewarding lives.

About Autism Awareness Month: World Autism Awareness Day occurs on 2nd April. It has been held every year since 9 September 1989. It was designated by the United Nations General Assembly resolution “62/139. World Autism Awareness Day,” adopted on 18 December 2007, proposed by Qatar, and supported by all member states.

Press contact: Sarah Francis

Email: sarahf@autismwestmidlands.org.uk

Tel: 0121 4507582 / 07545461180

I’m Starting To Wish We Had ATOS Back…

April 1, 2014

There, dear readers, is something I thought I’d never see written on this site.

But with ATOS, it definitely seems to be a case of ‘better the devil you know.’ There is less doubt in my mind with every article I read on them that Capita are worse…

Be careful what you wish for, dear readers.

Spotted on Facebook.

This was messaged to one of the groups this morning (via Carl Green)

This was PM’ed to Atos Demo this morning

“I had a conversation with a friend who is an Ex RAF Nurse and a former Staff Nurse at QMC Nottingham. She was sacked for misconduct from her Job at the QMC Notts last year. She has been out of work since leaving. She told me that she has a New Job she is training for… CAPITA.. She basically bragged that the Job of Assessor she is training for is as a Disability Assessor for the DWP. (£30,000 per annum) which is more than the salary she was on at the QMC as a Staff Nurse for the NHS. She told me that they have been told ‘Under No Circunstances’ are they to make the Public aware of what is happening and who they work for! (Wonder why???). She says basically she is being tested in Brimingham and then she will be approved or rejected by the DWP as to wether she gets the Assessors Job.
Wonder how many disabled people will have to have their needs based benefits stopped just to fund one Assessor…and then make profit for the company (CAPITA) by carrying on with the ‘Quota method of Denial). She said Capita are recruiting like crazy! They are taking ex NHS Staff and don’t care what their employment/disciplinary records are, its just the name and a qualification they need to be ‘within the Law’.
Hope this is helpful..”

Well I guess that extinguishes any hope that Crapita/G4S/Serco wouldn’t want to pick up the toxic Atos contract… unhappy sigh……

Edward Rainey

April 1, 2014

A paralysed artist has been forced to fork out £180 a week for care after his benefits were cut.

Edward Rainey, who has no use of his body below his neck, is shelling out the cash despite being in an NHS hospital.

He needs round-the-clock care and was “strongly advised” by staff at South General Hospital, Glasgow, to hire a private carer.

Mr Rainey said: “It’s deplorable. I just want to go back home. I’m not too ill. I think I could be out of hospital in three to four weeks.”

His independent living allowance was cut because he was admitted to hospital in January, leaving him to pay for the shortfall.

Mr Rainey, who was paralysed in a holiday swimming pool accident 30 years ago, said: “I have to have my carer coming in every day. This is on the strong advice of the hospital.

“It costs me £180 a week. I’m having to pay even though my allowance has been stopped.”

 

His carer helps him to eat and wash as well as changing his dressings and checking the machines that keep him alive.

Staff at the hospital are also unhappy with the situation and privately told the family they should go to the Scottish Daily Record to highlight his case.

Mr Rainey, a former soldier, said: “If I don’t take the care package they have arranged to go into a home, then I’ll not get any finance at all.

“I’ve got my own house. I’ve been out in the community for 30 years. They are violating my human rights.

“I feel there have been meetings when I’ve not been present, with no one representing me.

“They are reluctant to go on with my benefit from the independent living fund because I keep going into hospital. I can’t help that. I have a problem with my lungs.”

His niece, Bianca, said: “He doesn’t want to go to a home. He paints, he gets up, he socialises with friends. He is just a normal 52-year-old guy with a spinal injury.”

She added: “They have just all agreed that it is easier for them for him to go into a home.

“They have no right at all to tell him they are taking his money off him until he does.”

A spokesman for Glasgow City Council said: “Edward has major social care needs and requires round-the-clock support and supervision.

“Recent developments with his health and care arrangements mean living at home now carries a significant risk to his wellbeing.

“Social work staff cannot ignore these changes to his circumstances.

“They have concluded that Edward’s care needs would now be most appropriately provided for in a residential care home.”

A hospital spokesman added: “At this patient’s request, Mr Rainey’s long-term carer attends to his personal needs while he is in hospital.”

News Headlines: Tuesday 1 April 2014

April 1, 2014

Traffic Lights That Bark Invented To Help Blind People Cross Roads Disability Now

In a recent study, ten blind people reported being unable to recognise the sound made by the buttons they press at traffic lights to cross the road. So a group of sensitive scientists at the University of Kent decided to create buttons which would make the sound most familiar to this target group. As a result of their hard work, from April 1st, 2014, you may hear your local traffic lights barking. Please don’t be surprised!

 

Chocolate Wheelchairs Enable Paralysed Patients To Walk Again Able Magazine

Have you recently become a wheelchair user? Do you want to walk again? If the answer to both these questions is ‘yes,’ you will love chocolate wheelchairs. Eating one of these sweet treats a day will reportedly enable paralysed patients to regain movement in their legs. Unfortunately, these do not work for anyone who has been unable to walk since birth.

 

Tea Cures Cerebral Palsy Bobath News

 

We write to inform you that we have discovered a simple, yet miraculous, cure for Cerebral Palsy. Tea. After over 30 years of research into what was previously considered a lifelong condition, we have recently discovered that one cup of tea a day permanently keeps Cerebral Palsy away. We invite all patients and their families to the Centre from 9am on Tuesday, April 1st, where we will be pleased to present each family with a year’s free supply of PG Tips before we close down and celebrate the retirement of all our staff.

 

Disability Friendly Baked Beans Created By Heinz Tesco Magazine

Ever wanted to eat a  baked bean shaped like a guide dog or a white stick? Well, now you can, as these new inclusive bean shapes will be available at your local Tesco store from midnight on Tuesday, April 1st. We hope that disabled people will enjoy being able to eat essential pieces of equipment for breakfast, and that the experience will prove educational for everyone else.

 

Disability Campaigner Cured! Same Difference

The UK’s number 1 disability blog, Same Difference, reports that it has closed down as of midnight on Tuesday, April 1st. Editor Samedifference1 finds her lifelong disability cured after drinking a million cups of tea in one day and reports that she has decided to spend the rest of her professional life as a paid journalist for the Daily Mail.

 

ESA/WCA inquiry chair: ‘Victims are NOT being sidelined’

March 31, 2014

Mike Sivier's avatarMike Sivier's blog

Dame Anne Begg. [Image: BBC] Dame Anne Begg. [Image: BBC] Dame Anne Begg has responded to concerns that people who submitted evidence to the Commons Work and Pensions Committee’s inquiry into Employment and Support Allowance and Work Capability Assessments were being sidelined – with a denial.

The committee’s chairperson said the call for evidence generated 190 submissions, and every single submission will be circulated to all committee members.

In addition, the committee clerk in charge of the inquiry, who will be writing the brief for committee members, has carefully read all the submissions as they have come in, she stated in an email yesterday. (March 30)

“However, in line with our practice in the past when we have received a large number of submissions describing personal experiences (such as our inquiries into the roll out of ESA and the Pensions Bill) we have taken the decision that not all of the personal submissions will be…

View original post 364 more words

Disability in Britain: Then and Now… in statistics

March 31, 2014

Formerly Known As The Spastics Society: Why Scope Changed Its Name

March 31, 2014

I was 8 when the name change happened. I knew that it happened at the time- my parents always explained that the CP charity changed its name because ‘spastic’ was an insult to us.

I still hate that word, and regularly thank goodness that the name change happened. I think it went a long way to helping us, the CP children of that day, be accepted as not having that word attached to our disability.

It’s 20 years since The Spastics Society renamed itself Scope. Other disability charities have changed their names since. But in disability, what is a good name for a charity?

In 1994 Blur and Oasis were slogging it out for the Britpop crown, Don’t Forget Your Toothbrush was the hot TV show, John Major was our prime minister and people with cerebral palsy were still referred to as spastics.

Valerie Lang was on the executive council of the Spastics Society at the time. She has cerebral palsy and had been passionate about a name change for years before it eventually happened. “I felt that we could not afford to stay with the name we had,” she says. “The name spastic was a playground term of abuse. Children would shout to each other ‘You big spastic’ every time someone was clumsy or even if they just disagreed with them.

“Mothers with young babies who had cerebral palsy weren’t seeking help from the society because they had heard the word used in playground parlance. I think it put the younger generation off.”

Lang, now 74, says that people ceased to think of those with cerebral palsy as individuals. “We might have a brain injury in common but we are all different and don’t want to be put in a box labelled ‘spastic’.”

The charity made the change at an extraordinary general meeting in March 1994. The chairman at that time, Anthony Hewson, noted the tension in the room and was worried some of the wheelchair users in the room might “wheel forward and lynch me” if the wrong decision was made.

“Scope” was one of several names considered. Others were reminiscent of the single-word abstract names popular with companies in the 1990s – Clipper, Clasp, Canopy, Patch, Ibex, Adepta, Tasq, Fulcrum, Cognosis, Capability. Other more traditional names under discussion included Action Cerebral Palsy and the Cerebral Palsy Society.

Perhaps sadly, one of the big factors in choosing Scope, a largely neutral name with no obvious link to disability or cerebral palsy, was that it could not be turned into a term of abuse.

Since that time, other disability charities have come onto the scene with positive names such as Enable or Ability. Arguably this approach has itself become somewhat cliched, and may eventually come back to haunt the charities because of their earnest positivity. It’s terribly difficult to get it right when it comes to disability which – despite undoubtedly improving attitudes – is still an uneasy subject matter.

Perhaps the most notable and dramatic of recent charity name changes is that of the Royal National Institute of Deaf People (RNID), which is now Action on Hearing Loss.

Chief Executive Paul Breckell says it was a strategic decision. The name is a better reflection of the charity’s work, he explains, as it doesn’t only work with deaf people. He says many people weren’t very aware of the charity with its four-letter brand: “The public confused us with similar names like RNIB, RNLI and RSPB.

“People don’t always know what acronyms mean, they’re clumsy and clunky and words like ‘National Institute’ have a tendency to date an organisation.”

Mencap chooses to hold onto its name despite it being a splicing together of “mentally handicapped”, a term now deemed inappropriate by many. Even the charity uses the phrase “learning disability” to describe the people it helps. (As a reminder of how far attitudes have changed, it’s interesting to note that Mencap was actually called the Association of Parents of Backward Children when it was founded in 1946).

The charity defends its present name, and says that a change is not going to make any difference to the problems faced by people with learning disabilities. It points out that the name has, as it were, brand recognition and is widely recognised by the public and by politicians. Certainly, although the name may have its detractors, Mencap is a modern-thinking organisation which involves people with learning disabilities in its decision-making.

Though seen as a model for changing brand name, Scope has never rebuilt its brand awareness. Whereas 90% used to know what the Spastics Society was, only 64% answer “yes” when asked: “have you heard of Scope?” However, the charity says that although awareness may have declined, charitable income has not been affected.

Richard Hawkes, Scope’s chief executive, says it was a real risk to drop one of the UK’s best-known charity brand names, but it was important to make a strong statement that attitudes towards disabled people needed to change. “It was an important moment in our transition from being a traditional charity that helped vulnerable beneficiaries to being an organisation that’s about working alongside disabled people to make change happen.

“Changing the name meant we could be side by side with all disabled people – who at that time were campaigning for important changes, like the introduction of the Disability Discrimination Act.”

An Update On Some JobCentre Madness

March 31, 2014

Readers, an update on an earlier post.

The bedroom tax is domestic violence and abuse

March 31, 2014

At first glance, this doesn’t look like a disability issue.
However I have to wonder- how many disabled women need these ‘sanctuary rooms?’ How many mothers of disabled children need these ‘sanctuary rooms?’ Of course there could also be disabled men, or fathers of disabled children, in need of such spaces. But the post below was written on Mother’s Day yesterday and so was written with women in mind.

Mike Penning Needs To Read This

March 30, 2014

From Sue Marsh.

 

So, on Thursday 27th March, the DWP Press Office announced that Atos were no more.
Today we are announcing we are seeking a new provider to replace Atos for the Work Capability Assessment

Let’s be very clear : This is cause for celebration. It’s reputation in absolute tatters, Atos was left with no choice but to slink off, tail between its legs to lick its wounds. They have administered a failing test badly and hundreds of thousands have suffered their incompetence.

But for nearly 3 years now we’ve been warning that this was the only possible outcome. Atos would always fall because the work capability assessments themselves are so badly designed. They were contracted to fall. They were always the scapegoat. It’s astonishing really that none of their board could see it, and as late as last year were bidding for yet more disability assessment contracts for the new PIP (personal independence payments, the replacement for DLA or disability living allowance). How do governments introduce appalling schemes designed to hurt and harm? Make sure there is a middle man, then when the inevitable collapse comes, you can deny all responsibility. 

But DWP ARE responsible and we must not let anyone forget it for a second. This is a very dangerous time for our campaigns. It is entirely possible that the DWP will simply replace Atos with Capita or G4S or Serco, the test will still be fundamentally flawed and nothing will change. We can’t let that happen. It would be unconscionable for the DWP to re-tender the WCA contract without first conducting root and branch reform of the processes that guide it.

 
Do the DWP show any signs of this? Their next tweet said
Aim is to drive up the number of WCA assessments and cut waiting times
 
So not to improve accuracy? Not to stop ludicrous decisions leading to suffering and even suicides? Not to right a wrong but to force through even more of the same!
Later in the day, they released an official statement
Here’s today’s written ministerial statement on the Work Capability Assessment
Did you spot the glaring omission? 
 
WHAT HAPPENS NOW MR PENNING??????
 
You’ve just released an official statement confirming that an existing supplier has walked away from an enormous and sensitive contract. Millions of sick and disabled people are already IN the system, waiting for assessments, appealing decisions or being reassessed.
 
WHAT HAPPENS TO THEM MR PENNING?????
 
Will assessments continue? How? Who will do them? When? People are already waiting up to a year for decisions, what happens to them??
ISN’T IT SHOCKING THAT A GOVERNMENT MINISTER SHOULD ANNOUNCE THE TERMINATION OF A CONTRACT IN THIS WAY WITHOUT REASSURING CLAIMANTS THAT ALL WILL BE WELL MR PENNING?????
 
This is continents away from a joke now.
 
We warned PIP had to be paused. 
We were ignored
In the end, they had no choice but to pause it
 
We warned the bedroom tax would cost more than it saved leading to soaring housing benefit
We were ignored. 
Now we know we were right
 
We warned that the Work Programme simply couldn’t cope with the complexities of sick and disabled people
We were ignored
Less than 1% have sustained work for more than 6 months
 
We warned that Atos simply couldn’t manage the volume of ESA assessments
We were ignored
Now, reassessments have been paused and decisions are taking up to  year 
 
We warned that Atos were simply the middle man
We were ignored
Now they’ve gone, seemingly leaving nothing in their place. 
 
WHEN WILL THIS GOVERNMENT START TO LISTEN? 
HAD THEY LISTENED FROM THE START, NONE OF THIS WOULD HAVE HAPPENED
 
Finally, what if no-one wants the job??? I find it almost impossible to believe that Serco or Capita or G4S would take this on. They’ve all seen the reputation of Atos utterly decimated by the ESA contract. Possibly irredeemably. Why on EARTH would they fill the gap? They must know that unless the tests changed significantly campaigners will fight them just as determinedly – possibly more so for having absolutely no excuse – I mean, one might argue Atos didn’t know how bad things would get, how badly the tests would fail. Crapico4S know.
COULD IT BE THAT ESA IS DEAD BY DEFAULT???

 

Guide Dogs Charity Call For Pavement Parking Ban

March 30, 2014

Motorists should be banned from parking on pavements because the practice forces vulnerable pedestrians to walk in the road, campaigners have said.

The charity Guide Dogs say blocking the pavement, especially for blind people, is “inconsiderate and dangerous”.

There is already a ban on parking on footways on most London streets.

A poll for the charity suggested seven out of 10 people want restrictions for the rest of the country – and eight out of 10 councillors would back a new law.

Susan Williamson, who is completely blind in one eye and partially sighted in the other, said: “Stepping out to get round vehicles is really intimidating.

“It’s a constant concern which me and my husband (who is in a wheelchair) face every day and it would be so easily solved by parking on pavements being prevented by law.”

‘Real danger’

Her concerns were echoed by James White, Guide Dogs’ campaigns manager.

“It can be frightening for anyone who is forced to step into a road because the pavement is blocked by a van, car or other badly parked vehicle,” he said.

“Now imagine you have to step into a road where you can’t see oncoming traffic.

“We want politicians to act, preventing this form of inconsiderate and dangerous parking.”

Opinion pollsters YouGov carried out the survey for the charity, questioning 2,352 people in England, Scotland and Wales.

Separately 407 councillors in England and Wales were polled to gauge the views of local government.

Peter Box, chairman of the Local Government Association’s economy and transport board, said: “Inconsiderate drivers parking on pavements cause huge inconvenience and pose real danger to blind or partially-sighted people and wheelchair users.

“That is why councils fully support the call for a new law to end the current confusion caused by different rules for motorists parking inside the capital and around the rest of the country.”

Mark Wood Benefit Cuts Were Wrong Admits DWP

March 29, 2014

A VULNERABLE man who starved to death months after his benefits were cut should not have been ruled fit to work, the Government has admitted.

Prime Minister David Cameron last night described the death of Mark Wood as “tragic” following the admission by the Department of Work and Pensions (DWP).

And the DWP has now launched an internal review of the case.

The 44-year-old from Bampton had his benefits cut to just £40 in March last year after Atos Healthcare assessed him as being fit to work.

An inquest into his death in February, which concluded with a narrative verdict, heard he weighed just 5st 8lb when he died of malnutrition in August last year.

Mr Wood had obsessive compulsive disorder, Asperger’s syndrome, phobias of food, pollution, paint fumes, and social situations, and cognitive behavioural problems.

His sister Cathie Wood said the announcement was a “hollow victory” because it would not bring him back.

The 48-year-old from North Oxford said: “We are pleased but sad.

“They have reversed the decision – that is huge, but they obviously had the information at their disposal to make the right decision and if they had done that last March Mark would not be dead.

“It is good because it hopefully means we can now get some answers.”

Ms Wood and her mum Jill Gant, from Abingdon, appealed against the decision in his name earlier this month, acting on advice from Oxfordshire Welfare Rights (OWR).

Now the DWP has written to the family saying it had “revised” its decision to cut Mr Wood’s benefits.

Last night a spokesman said: “The coroner attributed Mr Wood’s eating disorder and food phobia as the likely cause of his death, rather than his benefits being stopped.

“However, after receiving new evidence from Mark Wood’s GP which was not presented at the first assessment, we have revised our original decision.

“We have written to Mr Wood’s family about this decision and are carrying out an internal review.”

Mr Wood’s GP Nicolas Ward told February’s inquest he was an extremely vulnerable and fragile individual who was coping with life.

He said: “Something pushed him or affected him in the time before he died and the only thing I can put my finger on is the pressure he felt he was under when his benefits were removed.”

On Thursday it was announced Atos is to quit its contract early following Government criticisms.

Atos made £111.76m operating profits in 2013.

Ms Wood added: “I think it is good that Atos has withdrawn but it is only part of the story – the whole system needs to be looked at.”

Suzy Drohan, joint manager of OWR, said: “Mr Wood lived in Cameron’s constituency and this happened.

“We are very sorry this had had to come to light from his death.

“There could be other cases in which people have died too. We know there are hundreds of decisions which are not right.”

Between January 2012 and January this year OWR took 312 cases to appeals against DWP decisions, and 281 were successful.

Mr Cameron said: “This is a tragic case and my thoughts are with Mr Wood’s family at this difficult time.”

The decision means the family doesn’t have to take the appeal to court.

Nicola Blackwood, MP for Oxford West and Abingdon, said: “This has been a tragic case and while this decision will not bring Mark back at least it sets the record straight. I have been very clear with the DWP that, in my view, Mark’s case was badly mishandled by Atos and that the family’s appeal needed to be dealt with as a matter of urgency and I am pleased they agreed.

“I also welcome Thursday’s announcement that the Government’s contract with Atos to conduct these assessments has been terminated early.”

Atos refused to comment.

Capita Faces Revolt From Disabled Staff Over Discrimination

March 29, 2014

Anyone who thought things would improve after ATOS, by all reports, seems to have been dreaming, sadly.

 

The company responsible for carrying out disability benefit assessments across Wales and central England is facing a revolt by disabled staff over allegations of widespread discrimination.

 

They say that Capita – already under fire over its performance in assessing claimants of personal independence payment, the government’s new disability benefit – appears to have no proper policies in place to manage staff protected under the Equality Act.

The employees all work for Service Birmingham, a joint enterprise that is two-thirds owned by Capita and one-third by Birmingham City Council and aims to “transform” the council’s public services, including its IT services and call centre.

Capita was criticised last autumn after Service Birmingham’s pre-tax profits leapt by more than half to £21 million.

Disability News Service (DNS) has heard from four disabled members of Service Birmingham staff, who have all raised concerns about the way Capita treats its disabled employees, as well as other issues about the way the company is run.

At least one member of staff is taking the organisation to a tribunal, while there are said to have been “multiple” grievances brought internally by other disabled employees.

One whistleblower has now come forward to raise concerns with the Labour councillor who chairs Service Birmingham, Dr Barry Henley – copying his email to the council leader, Sir Albert Bore – after trying unsuccessfully to persuade the company to deal with the issues internally.

In his email reply, Henley says that another whistleblower has raised similar concerns.

Henley told DNS: “At the moment they are all being investigated. I have not seen a final report but all the whistleblower investigations are having an independent investigation and eventually there will be an outcome.”

Disabled employees say they have asked repeatedly for the support they need, but their requests have been turned down or equipment has taken months to arrive.

Staff who have been denied reasonable adjustments under the Equality Act have then been handed warnings for taking time off sick, or have been demoted.

One was even told to go home by a manager because the organisation did not have the correct workplace adjustment in place to support her, but when she returned to work she was given a warning by the company’s human resources department.

Another – when she raised concerns that new duties she was being asked to do were inaccessible to her – was told to sign a new contract that was identical to those given to her colleagues, but without the annual pay increment.

Service Birmingham even admitted to one member of staff that it had “no idea” how to manage someone protected by the Equality Act.

One disabled employee told DNS: “I felt I was having to push and push and push for any support. Even if something was put on the table by a manager, they would then forget about it.”

He has to attend regular hospital appointments because of his impairment, but Service Birmingham managers tried to stop him attending, with one telling him: “You have to fall in line with everyone else.”

He was told he would no longer be paid if he needed to attend a hospital appointment because “it needs to be the same for everybody”.

Another disabled staff member said: “They really don’t know what they are doing. Capita want to be seen as all-singing and all-dancing, but the way they treat their staff is appalling.”

A third employee, who has also spoken to DNS, said he had been given a formal warning for time taken off due to a health condition.

He said: “I want to speak up about what happened to me so that none of my colleagues with disabilities has to go through what I went through.

“Line managers are woefully trained when it comes to what the law actually is with regards to the Equality Act.”

DNS has also heard from a fourth disabled member of staff, who has provided details of how she was bullied by a manager, and told that she would either have to perform work that was inaccessible to her or take sick leave against her wishes, as well as facing other discrimination.

She said the bullying had affected her career, her health and her personal life.

Capita said in a statement: “No tribunals have been upheld in favour of our current or former Service Birmingham employees, including anything related to disability discrimination. 

“Capita is committed to providing all of its employees with equal opportunities and putting in place reasonable adjustments for employees with a disability.

“In some parts of the Capita PIP business, Capita has pledged that 40 per cent of the workforce is made up of people with a disability. We work closely with disability organisations and aim to create a culture where disability is embraced.

“Although we would not comment on individual cases, these allegations are vague and do not contain sufficient information for us to respond. If an employee raises a concern, we will investigate robustly and take the appropriate action.”

The statement did not make any reference to the ongoing independent investigations into the whistleblowers’ allegations.

If Your WCA Is Scheduled, It WILL Go Ahead

March 28, 2014

From Facebook.

 

De

Atos Healthcare: clarification for ESA claimants about today’s announcement

There has been an announcement today regarding Atos Healthcare’s contract to undertake Work Capability Assessments (WCA) on behalf of the Department for Work and Pensions.

We have seen that this has caused some confusion for Employment and Support Allowance (ESA) claimants, especially those who currently have appointments to attend a face to face assessment. To clarify, we are continuing to complete WCA for anyone already referred to us by the Department for Work and Pensions and those referred going forwards. If you have been asked to attend an assessment please do attend as planned.

The WCA process that you will go through has not been changed.

The announcement only relates to WCA and does not affect the contract that we have for Personal Independence Payment (PIP) assessments.

Moment Woman, 40, Hears For First Time With Cochlear Implants

March 28, 2014

The moment a 40-year-old woman heard for the first time, thanks to cochlear implants, has been captured on video.

Joanne Milne burst into tears when she heard a nurse reading out the days of the week.

Ms Milne, from Gateshead, was born deaf and during her 20s she also began to lose her sight, due to the rare medical condition Usher syndrome.

She said she was delighted by the results of the “life-changing” procedure to fit implants.

‘So happy’

Ms Milne said: “The switch-on was the most emotional and overwhelming experience of my life and I’m still in shock now.

“The first day everybody sounded robotic and I have to learn to recognise what these sounds are as I build a sound library in my brain.

“Hearing things for the first time is so, so emotional, from the ping of a light switch to running water. I can’t stop crying.

“I can already foresee how it’s going to be life-changing and the implants will get better and better over time. I’m so so happy.”

Ms Milne, who works for charity Sense, said she was now a lot more aware of things around her.

‘Studio in floods’

She thanked the team at the Midlands Implant Centre at the Queen Elizabeth Hospital, Birmingham, for the procedure, which was carried out last month.

As a result of the transformation, her friend Tremayne Crossley decided to make her a compilation of songs – selecting one track from each year of her life.

He then sent the compilation to BBC 6 Music radio presenter Lauren Laverne.

After the playlist was featured on the show this week, Ms Laverne tweeted: “Just watched a video of today’s #Memory Tape recipient having her cochlear implant turned on and hearing for the first time. Studio in floods.”

Guardian Cartoon On ATOS Quitting

March 28, 2014

A Friday smile.

Steve Bell 15.5.2013
Steve Bell 28.03.2014

Toni Pearce

March 27, 2014

She’s the first NUS president not to attend university– but what really matters to me is that she’s disabled. She has EDS.

I’m not sure if the NUS have ever had a disabled president before, but I have my doubts.

ATOS Have Quit!!!!!!!!!!!!!!!!!!!!!!!!!!

March 27, 2014

ATOS have quit their contract today. They’ve quit. Gone. Got lost. Buzzed off.

The BBC want your thoughts on ATOS and WCAs. So do I.

My personal thoughts? Good riddance.

atos demo

 

Paul Farmer’s Anger As Taser PC Keeps Job

March 27, 2014

PC Stuart Wright used the 50,000-volt device after mistaking Colin Farmer’s white stick for a Samurai sword.

But after a gross incompetency hearing, he has simply received a “written improvement notice” and been told to say sorry.

Mr Farmer, 64, a retired developer, condemned the decision as “too little too late” and said he didn’t want “crocodile tears”.

He said: “He has been treated like a naughty schoolboy.

“I almost died that day and my life has been ruined. But he gets to walk away from it all with his job intact.

“An apology might make him feel better and take away some of the guilt but it wouldn’t be good for my health.

“The incident has left me terrified. I believe it was total negligence.”

The incident happened in October 2012 as Mr Farmer, from Chorley, Lancs, was walking to meet friends at a restaurant.

Witnesses saw PC Wright jump out of a police van, shout: “Stop, police or I’ll use Taser – I’ve warned you.”

Mr Farmer – who went blind in 2008 after a stroke – then fell to the ground twitching as PC Wright handcuffed him.

The officer was acting on reports of a “skinhead in jeans in his 20s” roaming Chorley armed with a sword. He said later: “I think I’ve got the wrong person.”

Assistant Chief Constable Tim Jacques said: “The officer made a dreadful mistake but was acting on a reasonable belief that his actions were necessary to protect the public.”

The Fish Police

March 27, 2014

Next month, a band called the Fish Police will be getting in a van and embarking on an eight day UK tour. This, in itself is nothing new and it’s likely that you might be asking yourself, “why should I care?”

Well, there are two reasons why you should care. Firstly, the band create some of the catchiest and most uplifting left-field pop music you will hear. Their album, The Marzipan Transformations, is a good time captured in music, a journey through their own unique world with nods to everything from MF Doom, Kraftwerk, De La Soul, the Ramones to Grace Jones (in fact, bassist, Charles Stuart, and drummer, Andrew McLean, can sometimes be found in Grace Jones’ backing band). The musical world in which the Fish Police exist has been created by and informed by singer Dean Rodney and guitarist Matt Howe’s autism, and the way they see the world. Dean pictures the world as if it were a TV show, he takes things he observes in his own life and twists them into unique creations.

Which leads us on to the second reason you should pay attention to this band. Because even if you’re able to resist the chorus of Chicken Nuggets for Me (nigh on impossible, by the way), then you have to recognise the that the band are breaking barriers and pushing boundaries as musicians with learning disabilities. Through being a band at the forefront of a nascent music scene, they are helping to shift perceptions and attitudes towards the learning disabled community. Up until this point, the concept of these musicians being able to tour across the UK has sometimes felt impossible. For years there have been arts organisations who have helped support people with learning disabilities to make amazing music, which in turn has created pockets of creativity and scenes across the world. However, making the transition into the more traditional pastimes of bands – such as releasing records and going on tour – has been elusive.

When I first saw the Fish Police it was at The Beautiful Octopus Club, a night run for and by people with learning disabilities in Deptford organised by Heart n Soul. I was so impressed by their charisma, the standard of playing and above all their music that I dutifully told everyone I knew about them as much as I could, over and over again. This was many years ago, and since then they have only improved, and I’m very pleased that I can now play their songs at home on my turntable. I was convinced that they would have no problem getting more shows, playing to bigger audiences and playing to audiences outside of the learning disabled community. Sadly this hasn’t been the case due to many reasons, one of which being the massively increased costs of adequately supporting band members who are vulnerable adults.

Last year – after I had set up my organisation Constant Flux whose aim it is to create more opportunities for musicians with learning disabilities – I applied for a grant from the Arts Council to put the Fish Police on tour. This grant came through and on the 4 April the tour begins, travelling through Nottingham, Leeds, Sheffield, Sunderland, London, Brighton and Swansea. They’re playing with some of the best bands in the UK’s DIY, alternative and learning disabled scenes, bands as diverse as the music The Fish Police make, such as Fair Ohs, Cold Pumas, Raviloi Me Away, Daniel Wakeford, Ultimate Thunder, Cowtown and Beat Express. All the gigs are in accessible venues and will be fully integrated, meaning the stages and the audiences will contain people with and without learning disabilities.

There is, of course, a serious side to the tour – it combats social exclusion and perceptions of ability. But mainly it’s going to be about dancing, having a good time and bathing in the Fish water.

For more information on the Fish Police go to their website and for more information on the tour visit the Constant Flux site.

Autism Begins Before Birth Finds Study

March 27, 2014

Scientists say they have new evidence that autism begins in the womb.

Patchy changes in the developing brain long before birth may cause symptoms of autism spectrum disorder (ASD), research suggests.

The study, in the New England Journal of Medicine, raises hopes that better understanding of the brain may improve the lives of children with autism.

It reinforces the need for early identification and treatment, says a University of California team.

US scientists analysed post-mortem brain tissue of 22 children with and without autism, all between two and 15 years of age.

They used genetic markers to look at how the outermost part of the brain, the cortex, wired up and formed layers.

Abnormalities were found in 90% of the children with autism compared with only about 10% of children without.

The changes were dotted about in brain regions involved in social and emotional communication, and language, long before birth, they say.

The researchers, from the University of California, San Diego and the Allen Institute for Brain Science in Seattle, say their patchy nature may explain why some toddlers with autism show signs of improvement if treated early enough.

They think the plastic infant brain may have a chance of rewiring itself to compensate.

“The finding that these defects occur in patches rather than across the entirety of cortex gives hope as well as insight about the nature of autism,” said Prof Eric Courchesne, a neuroscientist at the University of California San Diego.

Dr Thomas Insel, director of the National Institute of Mental Health, said: “If this new report of disorganised architecture in the brains of some children with autism is replicated, we can presume this reflects a process occurring long before birth.

“This reinforces the importance of early identification and intervention.”

Devastating impact

Carol Povey, director of the National Autistic Society Centre for Autism, said the study shed light on a complex and often misunderstood disability.

“Better understanding of the early brain development of children with autism could help us find new and more effective ways to support the estimated 700,000 people living with the condition across the UK,” she said.

“Autism can have a profound and devastating impact but the right support can make a huge difference.”

Bring Josh Home

March 27, 2014

Recently signed on Change.org:

 

My 13 year-old son Josh is happy (sometimes sad), beautiful, cheeky, observant, well behaved (sometimes not so well behaved), loving, wanting and caring.

However, Josh’s natural, endearing personality struggles against an urge to self-harm and severe autism that can make his world a confusing and frightening place.

 

To get to know Josh better, please watch my video.   

 

In 2012, Josh was moved to an assessment and treatment unit in Birmingham.  This was meant to be for 6 months…he is still there.

Josh has now spent both his 12th and his 13th birthdays in the unit, 260 miles away from me and the rest of his family in Cornwall.  He has never met his little sister.

 

This whole experience is heartbreaking for our family.  We have been fighting to get Josh the care he needs, closer to home and his family but Kernow CCG will not provide this.  In the last few weeks they have told us he can’t come back to Cornwall and must go to another service, still over 170 miles from home.

Josh continually asks for us and when he can’t see us he becomes anxious and more likely to self injure.  Josh’s self-harming is so severe that it is life threatening.  Last year he bit his tongue so badly that a third of it then had to be removed.

 

We visit Josh every weekend. This is exhausting but it still never feels enough.  Whilst the staff caring for Josh do a great job, what we can’t understand is why Josh can’t receive that same level of care, closer to home, so we don’t have to travel for over 5 hours just to give him a hug.

 

Josh is not the only child stuck miles away from his family and loved ones. There are currently 185 children and young people with a learning disability or autism in similar situations to Josh.  I am sure every one of their parents feels just as helpless and frustrated as I do.

What is needed for Josh, and others like him, is good quality care, close to home. As we face another Summer without him, we are pleading with Kernow CCG to put the missing support and services in place allowing us to bring Josh back to Cornwall.

 

All I want is to have my son closer to home. 

Let’s #BringJoshHome

 

Thank you,

Phill

@JoshWillsWorld

In which I raise some awareness of epilepsy

March 26, 2014

stavvers's avatarAnother angry woman

Today is Purple Day, a day for awareness and fundraising for epilepsy. In the UK alone, there are about 600, 000 people living with epilepsy, myself included, and it’s still a disability which a lot of people don’t understand. This leads to general stigma, but also a fair few fuck-ups from people trying to help.

When someone is having a tonic-clonic seizure, it looks terrifying. I’d always wondered, upon waking up from one of my own seizures, why everyone was running around like headless chickens and practically snogging me in relief. One time, when I was stuck on an overnight stay in hospital, I saw someone else fitting, and I suddenly knew why. It really does look awful.

Fortunately, a lot of the time, it’s not as bad as it looks. Here’s some really useful advice for what to do, which I’m going to repost here because it’s so important…

View original post 853 more words

Lyn Ward- Breast Cancer, Forced To Return To Work Days After Radiotherapy, Still Waiting For PIP

March 26, 2014

There are other similarly terrible stories of unacceptable PIP delays here, but this is the worst of them.

 

Lyn Ward, a 56-year-old mother, has worked all her life, holding down jobs since she was 14.

Last April, she found out she had breast cancer and applied for Iain Duncan Smith’s new flagship Personal Independence Payment. Eleven months later, she is still waiting for help.

While Lyn has been waiting, she has gone through an operation to remove the tumour and her lymph nodes, a mastectomy, chemotherapy and radiotherapy.

This week, finances became so tight she was forced to go back to work, just days after finishing radiotherapy.

“We’ve got a mortgage to pay,” she says. “We’ve still got to pay the bills and we’ve had no help. I’ve not even had a letter or phone call from Atos, never mind an assessment. I’m wondering why I paid my taxes all those years.”

Trailer- A Job’s Worth

March 26, 2014

Sharing this because sick/disabled people face/discuss so many of the issues covered. It’s three minutes long and really worth a watch.

 

Going By This, Capita Aren’t Much Better Than ATOS

March 26, 2014

Spotted on Facebook.

 

If you wonder why I’m sharing, please see the headline.

 

this is the email i sent to capita today

i wish to bring to your attention the way my wife has been treated by capita, her first contact was to receive a letter dated 19 December 2013 stating a home visit had been arranged for between 11& 16 november 2013, this would have been highly impossible unless you have a time machine.

on contacting you reference this a home visit was arranged for 16 January 2014 at 10.00 am, but at 09.40 am on the said date my wife received a phone call telling her that the appointment had been cancelled, with no reason given.

on contacting you again an appointment was made for 24 February 2014 at Greyfriars Court which my wife duly attended, where we were informed that her results would be forwarded to DWP/PIP within a few day and that we would have the results in approx 6 weeks, but today (25 03 14) it was still held by capita.

today 25 march 2014 my wife receives a phone call offering her a home visit, upon telling the caller that she had attended an appointment at Greyfriars Court the caller said that it was not on the system.

i originally put in a complaint to which i was informed i would be contacted within 20 days, with still no contact.

how are we expected to have faith in a company that with the stroke of a pen can cause so much heartache to a family yet seams to be run in utter chaos.

yours totally unsatisfied

Care Workers At Private Hospital Abuse Disabled Boy

March 25, 2014

Isolated incident? Really? After Winterbourne View, how can we believe that?

Two despicable carers were secretly filmed slapping and humiliating a brain damaged patient at a £3,000-a-week private hospital.

Rita Page, 68, and Lynette Crook, 33, smacked the young man’s legs and swore at him as they changed his bedding.

Page told him: “You won’t beat us, b******. There’s this very fine line between abuse and neglect. Don’t you dare be sick on me, boy. Don’t you dare, you dirty, scummy boy.”

Crook added: “Better not think about being sick on me, lad. I don’t do sick so stop it, scummy lad.”

The cruel healthcare assistants have now pleaded guilty to various offences, and have been warned they are likely to be jailed. The footage was filmed in 2012 by the patient’s family who hid cameras in his room.

They hatched the plan after becoming worried about the care at the hospital, which specialises in treating brain injuries. Page and Crook were suspended from duty at the Priory Highbank Centre in Bury, Greater Manchester, and arrested after the footage was handed to police.

At Bolton crown court, Page admitted two charges relating to using abusive language and slapping the man’s leg in a struggle when she put a pillow between his legs. Crook admitted three charges relating to jabbing the patient in the torso and head with a pen while he was asleep, using abusive language, and slapping his leg while taking his blood pressure.

Page, of Bury, and Crook, of nearby Ramsbottom, have been bailed until sentencing in May. Seven other charges will lie on file. The victim, who suffered brain damage after an accident when he was a youngster, cannot be named for legal reasons.

After the court hearing, his uncle said: “We had been very concerned about the treatment our relative was getting and we made that many complaints that two family members got banned from the premises.”

Malcolm Bower-Brown, regional director for the Care Quality Commission, described the abuse as “dreadful”. But he said the Commission’s most recent inspection, last month, found the hospital to be meeting national standards.

A Priory Highbank spokesman said: “We deeply regret the unacceptable actions of these two members of staff both of whom had over 10 years’ service and previously unblemished records.”

He said the women were both sacked for gross misconduct, adding that the abuse was “an isolated incident”.

Are ATOS Assessing “Customers” With Next To No Notes On A Regular Basis?

March 25, 2014

Spotted on Facebook. Sharing because they are asking a very important question.

 

Someone asked me to post this for them.

“I have Asperger’s Syndrome, a form of autism, and I’m suspected bi-polar, I’ve been on ESA for a while now and I’ve been assessed by ATOS before, the first assessment went off without a hitch and I passed it, I recently had another appointment for an assessment which was cancelled due to doctors ironically “calling in sick” (oh the hypocrisy, if it was me I would’ve been sanctioned and technically speaking I have more of a right to miss an appointment than them), they made another appointment for me which I went to only to find that I was being assessed by a NURSE (who after my mother started talking about my situation, decided she couldn’t deal with this case, that it needed to be passed to a doctor), rather than a doctor, apparently they’re behind in appointments and short of doctors at the moment. Also she has next to NO information on me and my situation in her folder on me, all’s there was, was that I have Asperger’s, no notes from my GP, no notes from my last assessment, no nothing, she didn’t know what to expect AT ALL, she looked absolutely bewildered when my Mum started telling her everything. The lady herself was lovely, the situation however was appalling.
Are ATOS assessing “customers” with next to no notes on a regular basis? Is this why people are being found to be “fit for work” and having their much needed money away from them. Because there’s no paper trail surrounding their condition? Because legally speaking without legal proof, regardless of what’s seen or told in the assessment room, ATOS are not accountable for those deaths?”

Anonymous Donor Gives Hospital £7500 Towards Ben Baddeley’s SDR

March 25, 2014

An anonymous donor has given thousands of pounds towards a young boy’s potentially life-changing operation.

Ben Baddeley, nine, who has cerebral palsy, was due to have a procedure on his back in February but the NHS withdrew the funding.

His mother, Amy, 29, said a man paid nearly £7,500 directly to the hospital after seeing Ben’s story in the news.

The selective dorsal rhizotomy costs more than £11,000 and the youngster will need also need aftercare.

Ben’s parents have been trying to raise £20,000 in total to pay for the surgery, health insurance and continuing physiotherapy for their son, and said they would continue fundraising.

NHS England had said there was not enough evidence to show the surgery was clinically or cost-effective.

But the family, from Silverdale, Staffordshire, hope it will allow Ben to walk and play more easily, and possibly stop him needing a wheelchair in later life.

‘So lucky’

Ben will need regular physiotherapy and hydrotherapy sessions after the surgery to help develop muscles in his legs.

Mrs Baddeley said the donation meant they could now concentrate on fundraising for physiotherapy and hydrotherapy equipment, including a specialised running machine for Ben at home.

While the donor wishes to remain anonymous in public, he has made his identity known to the family, after initially contacting them by email.

Mrs Baddeley said he is a successful businessman and grandfather-of-five.

“It’s a massive weight off our shoulders. We’ve been so lucky,” she said.

“The donor doesn’t want to take the attention from Ben and his fundraising needs, but once Ben is up and walking we will definitely meet him – he’s definitely on the Christmas card list.”

Ben will undergo the first stage of the operation in Nottingham in April.

Kris: Dying To Live

March 25, 2014

Prorammes like this, my dear readers, are why Same Difference strongly believes BBC Three needs to stay on TV.

BBC Three, 9pm tomorrow.

When Kris Hallenga was diagnosed with aggressive, terminal breast cancer at the age of 23, she decided to channel her fear and anger into changing the way young women, the medical profession and the rest of the planet see and treat breast cancer in young women.

This film is about the sheer strength, passion and indomitable spirit of Kris Hallenga as she battles her illness and tirelessly promotes her charity CoppaFeel! – an energetic and fearless awareness-raising campaign dedicated to making sure other young women and their doctors are made more aware of the risks.

Kris Hallenga is an inspirational young woman on a very personal mission. This is the film of her life-enhancing fight against cancer and her life-saving campaign to battle public ignorance.

Chris Grayling MP: Grant Legal Aid To The Family Of Cherry Groce For Her Inquest

March 25, 2014

I’ve just signed this petition at Change.org. Please sign and share it, the cause is a big and important one.

We the family of Cherry Groce the innocent mother who was shot and paralysed by the police in 1985. The shooting sparked the Brixton riots. To this day no one has been held responsible for what happened to her.

Independent reports state that the events in 1985 were a significant contributory factor in our mothers death in 2011. An inquest is being held in June. But we’ve been denied legal aid, without it we can’t afford a lawyer to represent us at the inquest and ask questions of the police. That’s why we would like your support in the appeal for our fight for legal aid.  

Without legal aid we will be financially excluded from participating, which means we are not able to adequately and effectively take part in such a complex case and it is unfair to expect us to do so whilst the other three interested parties are being publicly funded!

Following the request of a revealing report we have received an apology from the police which comes 28 years after the shooting (and is still yet to be made in public). 

One minute of your time will bring us closer to the answers we have been waiting 29 years for. 

Please sign to show your support in the fight for legal aid which will allow us a fair inquest. 

Thank you

Wolverhampton ATOS Centre: Please Read And Share With Those This May Affect

March 25, 2014

I’ve just seen this information at Fightback on Facebook. I’m sharing it in the hope that it might reach, and help, someone who has to use the Wolverhampton centre for an assessment.

 

Just on the way back from Wolverhampton atos centre what a debacle that was I had to threaten them with anti discrimination case under equality act as they insist you agree you can climb 28 stairs if they have fire and lift out of order or fire drill or cancel appointment if you say you cant. When challenged if they may have a fire drill unexpectedly and why they weren’t using their downstairs assessment rooms they eventually backed down when I mentioned failure to make adequate provisions for disabled people, Fightback and the fact I’m a disability lawyer. Took a bit of a rant but then suddenly 3 assessment rooms were opened downstairs and they couldn’t do enough. I even charged my phone up. Be warned they seem to use upstairs to deter people. Michelle

Give ATOS

March 24, 2014

A moving video that should go viral.

Panorama: The Great NHS Robbery

March 24, 2014

I’ll be watching tonight’s Panorama.

Bolding mine.

Panorama investigates fraud in the National Health Service. With the NHS under financial pressure as never before, reporter Fiona Walker finds fraud in/against the NHS could be far greater than benefits fraud but with fewer resources to tackle it. The programme hears claims that the health service in the UK is losing billions every year to fraudsters – enough to employ 330,000 new nurses. In Britain’s 21st-century health service, where multimillion private contracts are up for grabs, Panorama goes in search of the fraudsters to reveal their crimes and highlights calls for tougher penalties for those who harm patients and steal NHS resources and money that should be used to care for the sick.

A Very Sweet Update On Louis Barnett

March 24, 2014

I first covered Louis Barnett when Same Difference was first starting out. He was 15 then and hadn’t been going that long himself in the chocolate business. He’s someone I’ve always remembered and had in the back of my mind.

Now the mainstream BBC is asking him about chocolate exports! That just shows how far he has come. He’s always been an inspiration to me, and now I’m more than a little proud to call him a success story.

I hope to see him on the Dragon’s Den panel one day!

BBC Breakfast has been hearing from a young entrepreneur who became a success after leaving school at the age of 11.

Chocolatier Louis Barnett described how his learning difficulties had not held him back and he started supplying major supermarket chains in his early teens and now sells around the world.

Chocolate exports have increased by 9% to a total of more than £5,000,000 – according to the Food and Drink Federation, with China the fastest growing market for UK food and drink.

Mr Barnett said food safety was a big issue to the Chinese: “On all of our products we’ve got the Union Jack featured in a big way. One of the largest selling points is about the fact we’re British.”

Advanced Prosthetic Limb Offers Amputees New Hope

March 24, 2014

For many amputees, adapting to life after losing a limb is challenging – and while technology has advanced in recent years, prosthetic limbs can be uncomfortable and even painful to use.

 

Now a clinical study is trialling a new prosthesis, which aims to ease that discomfort by attaching a metal implant in the bone.

Michael Lloyd is a part of that study and spoke to BBC Breakfast to explain why the implant had made a difference to his life.

He said: “It’s revolutionised my life. It really has made things so, so much easier.”

Will The New Council For Evidence Based Psychiatry Tackle Learning Disability Abuse?

March 24, 2014

This is a guest post by Matthew Smith. It was originally posted here yesterday. Thanks to Matthew.

This morning, I saw on the Facebook group for Invest in ME a link to an article on the Mad in America website announcing the launch of the Council for Evidence-based Psychiatry (CEP), which is to take place at the Houses of Parliament (they don’t say which house; perhaps that will be supplied to people who attend) on 30th April. Their website seems to concentrate largely on the use of drugs in psychiatry, and includes a number of stories of people’s recovery from dependency on benzodiazepines (benzos), antidepressants and other psychiatric medications. The CEP was founded by James Davies, PhD, a psychotherapist and lecturer in social anthropology and psychotherapy at Roehampton, and the author of Cracked: Why Psychiatry is Doing More Harm Than Good. The launch is to feature Dr Joanna Moncrieff, a UCL psychiatrist, and Prof Peter Gotzsche of the Cochrane Collaboration, which analyses the results of drug trials. (The organisation is on Facebook and Twitter.)

That the link was on the Invest in ME page is natural, because people with ME have suffered years of interference in their treatment, and in public perception of their condition, by the psychiatric profession, and this has resulted in horrific abuses over the years, including sufferers being held in noisy wards, being made to do exercises at a time when their condition dictates rest, and being treated only for symptoms that are misunderstood (e.g. not eating because of nausea interpreted as anorexia) rather than the condition itself. However, there is a less obvious aspect of psychiatry that they may wish to take an interest in, which is its involvement in the treatment of people with learning disabilities, particularly when in crisis. The law gives them considerable power to intefere in the affected people’s lives, including to transfer them away from home (or from near home), and to prescribe the same medications that are used on people who are mentally ill, which often have dreadful side effects. The units, known as assessment and treatment units (ATUs), are meant to provide short-term treatment in a crisis, but they often end up holding people for months or even years, and the results are sometimes lamentable, even tragic.

 

Last night I watched a video in which Mark Neary, whose son Steven is autistic and currently lives at home with him in west London, explained what happened when he put his son into a local respite home in 2009, for what was meant to be a few days while he was ill with flu. After just a couple of days, Steven was transferred to a so-called positive behaviour unit after the respite centre staff claimed that they could not cope with Steven’s behaviour (as his routine had been disrupted by being placed in the unit without notice, his distress showed in challenging behaviour). The social worker and management immediately formed the impression that if his behaviour was “this bad” in the unit, it could not possibly be safe to return him home. They appeared to implement a “transition home” plan while secretly looking for residential care, eventually settling on a hospital in Wales that Steven would have to be sectioned to be sent to. However, just in time, Mark found a solicitor who challenged the orders the council had been using to keep Steven in the home, and he was released home just before they could transfer him.

 

In short, they would have had to find a pretext to impose a section on him (a section is the relevant part of the Mental Health Act that allows the detention of a mentally ill person who requires treatment). This is not the only time this trick has been used. Last September an ATU in south Wales imposed a section on a young autistic woman, Claire Dyer, who had attempted to run away a number of times and was sometimes violent, although was calmer when her parents and family were around, and was allowed out with them regularly. A month or so later, the team at the ATU conveniently decided she needed to be transferred to a secure hospital unit in Northampton, some 185 miles away, which would separate her from her family and friends whose contact obviously made a positive difference to her state of mind and behaviour. The family have fought the decision, but a tribunal is not due to meet again until May, and the team has refused to rule out the transfer to Northampton (where there are currently no beds and an interview was thwarted by her and her family’s lack of co-operation), something which has caused the young woman a lot of stress for which they at one point prescribed diazepam rather than simply abandoning the idea.

 

There are laws in this country which allow residential units to manage challenging behaviour and prevent escape attempts by people with learning disabilities or dementia when they would, for example, get themselves lost or run into the road or do something else dangerous, in particular the Mental Capacity Act. The Mental Health Act is meant for ensuring that mentally ill people get treatment when their illnesses mean they would resist, or cause them to behave dangerously.

 

NHS England has given a commitment to get long-stay residents out of ATUs by June this year, but only a small number have currently got an exit date of before June. The units are commonly used when there is a crisis in a learning disabled person’s life rather than the onset of mental illness as such; it is often precipitated by the end of school life and a transition to an uncertain adult life and the departure of most of their friends. An example was Connor Sparrowhawk, an 18-year-old who was autistic and had epilepsy, who was admitted to such a unit in Oxford in March 2013 after a crisis that was exacerbated by lack of support from local health and social services. It was intended that he remain there only as long as it would take to get home support in place, and the senior staff at the unit believed that he was not mentally ill and should be discharged. However, he drowned in the unit’s bath in July; he had been left alone, observed only at 15-minute intervals despite the staff knowing he had epilepsy. This, of course, is not because it was a psychiatric unit but because it was negligently run, as demonstrated by a subsequent Care Quality Commission inspection report and by the independent investigation into Connor’s death, but that an NHS trust can let that unit and its neighbouring unit get into that state does show that there is a lack of aspiration for people with learning disabilities in this country, and a low expectation of what kind of care can or should be provided for them.

It is to be welcomed that someone is publicly challenging the science behind psychiatry and exposing the harms caused by some common psychiatric drugs. All this is happening to people with learning disabilities as well, and for some there is no accommodation available other than one of these psychiatric units. I hope that his organisation will join in the fight to free both people with diseases like ME, as well as people with autism and other learning disabilities, from the tyranny of psychiatry, from sedatives which cause debilitating side effects, from laws which enable to clinicians to rearrange lives for dubious benefit at the stroke of a pen. They should, at most, be on tap rather than on top in the care of people with learning disabilities. Will Dr Davies join us in fighting this abuse against some of society’s most vulnerable?

Japanese Fashion Brand Ha Ha Designs Wedding Dress For Women In Wheelchairs

March 24, 2014

With thanks to the brilliant Models Of Diversity for the photo.

In a bid to create “universal fashion,” Takafumi Tsuruta said he aimed to design a Ha Ha collection that everyone could wear. To that end, he delivered men’s, women’s and children’s looks and even a wedding dress designed for a woman confined to a wheelchair. “I did a lot of research, and there are very few stylish wedding dresses for wheelchairs,” he said. “The back is made of jersey without any adornments so that you can sit in it comfortably but the front is very pretty.”

Tsuruta also used a print that at first glance looked like placed polka dots but was actually a visual representation of braille dots.

It looks comfortable, and beautiful.

Dear Ed Miliband, We’re Looking To You To Defend Us From Deplorable Welfare Cuts

March 24, 2014

This article titled Dear Ed Miliband, We’re Looking To You To Defend Us From Deplorable Welfare Cuts and written by E Davis was first published by the Welfare News Service on 23 March 2014 and has been reproduced here with permission.

Dear Mr Miliband,

I do not profess to know an awful lot about politics. In fact I did not even really care about it much, as I always felt secure. I always knew that as a severely disabled person I would be protected and looked after. However, since 2010 this has changed.

I remember well the pledge made by David Cameron that, “those who need help the most would get it.” That was a lie. The present government has attacked those who “need help the most” constantly and ferociously.

They have given us the Bedroom Tax, cut back on the amount of support given (by depriving local councils of funds). They have changed the qualifying criteria for Personal Independence Payment, stopped the Independent living fund, closed down Remploy factories, as well as changing the way people go for fitness assessments.

They have made severely disabled people wait, (in some cases up to two years) for their benefit decisions. This has often resulted in their death. The official figures put the number of people who have died whilst waiting for the Work Compatibility Assessment process (or after, having gone through it), at around 12,000. However, the unofficial figure is more likely to be 44, 000, and growing.

They have dismantled (and effectively privatised), the National Health Service, which has already made it more difficult for disabled people to gain access to the help we need.

Now, to add insult to injury, they want to set a benefit (welfare) cap!

You say that you are the party of the people. You claim to be the party that cares, and yet Ed Balls says that the Labour party will vote with the government in favour of a cap on the most vulnerable people in our society.

Many, many of us are feeling let down and betrayed and we are looking to you for support. We are looking for you to defend us against these deplorable welfare reforms, that have left so many of us in dire poverty, housebound, alone, and without support. So far we have seen and heard nothing.

Your friend Tony Benn once said, “if we can find money to kill people, we can find money to help them.” Your party, and that of the government, have so far only found money to kill and harm people. I hope you can all live with your consciences.

If things do not change, the situation for many will become dire and many more people will die as a consequence. I am often told I am a good judge of character. I am hoping I am right about you, and that you are of good conscience.

I hope too, that if you and your party get to be government next year, then you will stop the suffering and needless deaths of thousands of vulnerable people.

After all, as another great leader once said, “Society is measured by how it treats its weakest members”

Ms. E. Davis

Please Note: The views and opinions expressed in this letter are those of the writer/author only and are not necessarily shared by the Welfare News Service or Same Difference.

letters@welfarenewsservice.com

Benefit Caps- Clarification

March 23, 2014

Sue Marsh has asked for this to be shared. What great campaigners want, great campaigners get.

Before I type another word, I’d like to make it clear that I think the idea of an overall benefit cap is ridiculous.

When times are hard, say during recessions, you actually want to spend MORE on social security. It boosts the economy and is the best way of making sure money is spent locally and directly. When times are better and jobs are plentiful you can reform and cut back.

So the very idea of an overall benefit cap is utterly counter-Keynesian and, well totally pointless really.

I’d also like to make it clear that I’m dripping with contempt that Labour are going to support an overall benefit cap, not because they believe it’s a good idea or because it fits in any way with a Labour concept of how to run economies. Let’s be very clear : The ONLY reason Labour are going to whip their MPs to support it is because they think it would be electoral suicide NOT to. I detest political decisions that abandon all conscience, sense and principle, heaving a few million people onto the scrapheap of life, just to placate the Daily Mail

However, I do think it’s important to allay a few fears over what is actually proposed. There are two benefit cap policies and I believe they are merging into one in the justifiable outrage. This might be frightening people unnecessarily, so I’ll try to clear it up here. 

The benefit cap that will be approved on Tuesday is an overall benefit cap.  It WILL include DLA (disability benefit) and ESA (sickness benefit) but WON’T include JSA (jobseekers allowance). Osborne announced that it would be set at £118 billion next year. It is a common myth that sickness benefits increase during recessions. They don’t and nor do disability benefits. So as long as the overall cap is realistic, then including them is not as horrific as it might sound. Jobseekers DOES increase during recessions (obviously) so excluding it makes sense. (Excluding pensions has no logic and is simply shameless vote maintenance by the Tories)

The second policy refers to a household benefit cap. The cap will be 26k which the coalition argue is equivalent to the average household income. Of course it isn’t, because families brining in 26k are likely to get a whole host of tax credits, child benefit and housing benefit too, but let’s not spoil a good bit of spin eh? This is also an utterly ludicrous idea, taking no account of regional variations or individual circumstances. But DLA and Support Group ESA ARE excluded from this. This also makes sense as those totally reliant on the state for all support are likely to exceed a 26k cap in almost all cases.

So to sum up, the policies are ridiculous and Labour supporting them is shameless and weak, but I don’t think sick and disabled people will be unduly hurt by them.

There is a caveat of course : Many people living with very significant impairments DON’T qualify for  DLA and DON’T get assessed as needing to be in the ESA Support Group. As the assessments get ever more stringent, this gets more and more common. These people WILL be affected by both policies as exemptions won’t apply to them. But it’s OK. Both Labour and the Conservatives seem happy to pretend they don’t exist.

UPDATE : This rather good post looks into my claim that 26k is not the average income further, making the point, that this is really ll about punishing children for the decisions of their parents. 

http://emsyblog.wordpress.com/2014/03/23/the-tories-making-children-pay/ …

Also, James Bolton (@JamesABolton on twitter) makes the point that with 2% leeway built in either way, and no penalties should governments exceed the cap, the whole policy is just designed to sound tough on “scroungers” whilst in effect, having no teeth at all. If the cap is exceeded and people still have valid claims, they must be paid by law.

 

Woman With Epilepsy Has Purse Stolen During Seizure

March 22, 2014

A woman with epilepsy had her purse stolen by a bogus Good Samaritan while she lay unconscious in a city centre street, West Midlands Police has said.

The force said two women went to the 25 year old’s aid after she “blacked out” and collapsed in Summer Row, Birmingham.

When she regained consciousness she found her purse was missing.

Police have released CCTV images of two women they want to speak to in relation to the incident, on February 22.

PC David Horton, from the Jewellery Quarter police team, said it was “not clear if the two women were together” and that one of them may have genuinely tried to help.

“This was a callous and terribly sad case where a lady was taken ill just yards from her place of work, only to then become a victim of crime when completely defenceless,” he said.

A Letter A Day To No 10 22 March 2014: I Am Spartacus

March 22, 2014

 

A letter a day to number 10. No 689.

Saturday 22 March 2014. I am Spartacus.

Shares are encouraged and welcomed. If this letter speaks for you and you wish to send your own copy please feel free to copy and paste, and alter for your own needs, the text for your own letter.

http://www.keithordinaryguy.org.uk/

Dear Mr Cameron,

I have received the ESA50 Limited Capacity for Work Questionnaire from the DWP. I can tell you, it strikes terror in my heart to have this form here knowing that I am in hostile territory and at the mercy of a system without mercy. It’s a lose/lose situation because as a disabled man, fill them in or not, my life and well being rests in the hands of a system designed to penalise me at the head of which is the most reviled and vicious man in the UK, Iain Duncan Smith.

I know that you cannot have the faintest idea what this means. You want people who want to get on, but only on your terms.

Despite my disabilities I work hard and I doubt a man like you could work harder because whilst I have to work with my disabilities I have never stopped working for people and to broaden the understanding of the human condition and to help others reach their potential.

I am grateful for the years I have received Disability Living Allowance as it has afforded me the space to continue my lifelong work and to continue to give into the world of humanity I care passionately about. So I do two tasks, I do disability, which is demanding, time consuming and tiring, and I do my life long vocational work for which I care deeply.

All of this means nothing to you as you and your government don’t do individual cases. You don’t even care if people live or die as revealed when you didn’t even attend, or act on, Michael Meacher’s debate where he informed parliament of the 10.600 people who had died within 6 weeks of an Atos assessment. Iain Duncan Smith’s response was to stop releasing the figures for Atos related deaths!

Here’s the thing, though, Mr Cameron. Society is made up of individuals, each defined with an entirely identifiable and provable self. There is no society or group without the unique individuals who comprise it. There is no such discrete living entity as a group, it is an abstraction, an idea, a term for the association of individuals. A group is made up of somethings and it is those somethings which have substance and being. Group behaviour is defined by the actions of the individuals who comprise it, so I can say your party is heartless only because of the heartless actions of the individual members who make it up.

I’ll leave you with an expression championed by Sue Marsh who works tirelessly for social justice and encourages others to do the same and which resounded across the social media in an incredible group response from thousands of people. I am Spartacus!

https://www.youtube.com/watch?v=igHmfZTU4RE

http://mikesivier.wordpress.com/2013/06/25/dwp-refuses-to-provide-information-on-esaib-deaths-what-is-it-hiding/

http://diaryofabenefitscrounger.blogspot.co.uk/2012/01/i-am-spartacus-and-i.html

http://diaryofabenefitscrounger.blogspot.co.uk/2012/07/my-esa50.html

 

Disabled Women & Domestic Abuse Posters

March 22, 2014

pseudodeviant's avatarpseudoliving

I stumbled upon two extremely poignant posters created by Women’s Aid to highlight some of the issues surrounding domestic abuse and disabled people. I’m going to try to get pictures of them to share, but so far I only have links to .pdf versions.
They are fantastic resources and free to anyone wishing to use them. You can find the originals here.

Disability & DV Poster 1

Disability & DV Poster 2

View original post

Sue Marsh Says: Ask What You Can Do For The UN

March 21, 2014

Cross posted from Sue Marsh, in the interests of viralness.
When we first heard that the UN would be reporting on the progress the UK has made at implementing the UN convention on the rights of people with disabilities, your response was overwhelming.

In a way I’ve rarely seen before, people saw UN involvement as a once in a lifetime opportunity. More, they saw it as a lifeboat, not waving but drowning, hoping the wider world will see.

At a time when sick and disabled people feel more attacked and less heard than they have for generations, we all seemed to cling to this opportunity. I think it had become clear that our own UK government would compromise on nothing. They seem the least able to see or hear that we exist at all.

I asked people to email me with their stories to submit as case studies and my inbox exploded with fear and misery. I only asked very specifically for stories from those affected by the 1 year time limit of ESA, as this was the area I was going to focus on. Yet I got so many replies, it took me three weeks to reply to each one individually.

The pain in those messages was palpable, urgent, frightened. Just reading their suffering drained me as story after story flooded in. I practically got Stendhal syndrome from all the gasps of shock. Weeks later I still felt very down and defeated.

A thousand inbox whispers became a mighty roar. Together they painted a picture of the UK in 2014 that is beyond the comprehension of most.

The day I posted the call for evidence, a friend from one of the major charities DMd me, suggesting it might be unfair to big the news up too much as the UN couldn’t actually change anything. They have no jurisdiction under UK law and she worried it might be cruel to give false hope where none exists.

Unless you’re a campaigner, her lovely advice and care for people might seem logical. Why put so much energy into something that can’t actually make our lives immediately better?

But I’ve learnt the power of hope. From the day I launched this blog, we’ve all had the most impact when we shout together. However, sick and disabled people have shouted and shouted, endlessly and urgently, yet no matter how we cry out, no-one could hear us. As we sank out of view, few even knew to wonder where we’d gone.

I think that even the most pragmatic of us had all learnt very clearly by then that this government were not willing to compromise or listen in any way at all.

Like any minority, if all you have is the hope that, one day, things might get better and this whole sorry mess will end, just being heard at all is incredibly cathartic.

Over and over, people begged me to tell their stories, begged me to amplify their individual voices into something that could be heard. I think this UN report might be the most important thing we’ve done so far. The number of people who asked me to keep their stories anonymous told me all I needed to know about the climate of fear sick and disabled people are currently living under.

The UN have been very specific about what they need :

The “shadow” report needs to be succinct. They only want 30-40 pages, which might sound like a lot, but in report terms it’s very tight indeed They need people to produce a 30-40 page report that is well referenced with any statement that makes any kind of claim has to be backed up with evidence.

They want one united response that disabled people in the UK can support and get behind. 
Several groups have started their own reports, but it might be that no one report can say everything. Clearly, groups could still submit their own work independently, but it’s vital that we also produce one overall submission as an official UK shadow report that we can all rally behind and support

All claims must be supported with evidence. The inspector has only got 10 days in the UK later this year to finalise his report. This means that the more groundwork we can do for him and the more evidence we provide in advance, the easier his job will be and the more impact his report can have. Sue – do you mean the examiner? Is he coming to the UK this year? You may be right; I might not have been listening!!

Of course the overwhelming problem is what to leave out, not what to include. With so little space and 50 articles to the convention, it’s imperative to make sure that as many issues as possible are included, hence prioritising a few of the most urgent ones. Agreeing what those issues will be is vital.

Often a collective endeavour is more valuable than the sum of its parts. Very occasionally, an opportunity comes along that is so important, so urgent, that we owe it to ourselves to come together and present the strongest presence we can. Sick and disabled people have an unprecedented record over many decades of being able to do just that at the really crucial times. Unlike other campaigners, we never quite allow our coalitions to fall apart when co-operation is vital.

I’m really excited about seeing the finished report that’s produced in the end. I know all of you will be too. I know how desperately you want every last word to be used carefully, that not a single one is wasted. We have a duty to do our best for all disabled people the UK, for everyone’s stories to be heard.

Kelly Killick Can See Again After Pioneering Surgery

March 21, 2014

A blind woman’s sight has been restored in pioneering surgery at the Luton and Dunstable Hospital.

It involved using a powerful laser to remove scars on the corneas.

Kelly Killick, from Dunstable, who was born with a rare eye disease, is only the second person in the UK with the condition to be treated using this technique.

The hospital believes about a dozen patients a year will benefit from the operation.

Dear Future Mom- A Video For World Down Syndrome Day

March 21, 2014

This is why the Tory bingo poster isn’t just funny – it’s downright creepy:

March 21, 2014

Tom Pride's avatarPride's Purge

(not satire – it’s the Tories!)

Here’s an extract from George Orwell’s novel, Nineteen Eighty-Four (my highlights):

“Heavy physical work, the care of home and children, petty quarrels with neighbours, films, football, beer, and above all, gambling filled up the horizon of their minds. To keep them in control was not difficult. All that was required of them was a primitive patriotism which could be appealed to whenever it was necessary to make them accept longer working hours or shorter rations. And when they become discontented, as they sometimes did, their discontentment led nowhere, because being without general ideas, they could only focus it on petty specific grievances.”

Remind you of anything?

tory bingo and beer

Don’t say we weren’t warned!

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Related articles by Tom Pride:

Best of #ToryBingo on Twitter

Oops! Tory Chair Grant Shapps admits Tories are not hardworking people

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Please feel free to comment.

 

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Care Home Rapist Colin Stokes Jailed For 14 Years

March 21, 2014

A care worker who raped three vulnerable women at the home he worked in has been jailed for 14 years.

Colin Stokes, 48, attacked the women – aged 32, 50 and 54 – between January 2012 and April 2013 in supported living accommodation in Gloucestershire.

One victim has a mental age of a child, another is registered blind and the third needs aid to communicate.

Stokes, of Dursley, was sentenced at Gloucester Crown Court, where in January he admitted three rape charges.

Each victim, who cannot be named for legal reasons, has severe learning disabilities and requires 24-hour care.

At the earlier plea hearing Stokes denied a further charge of rape and one of sexual assault and the court was told those charges would lie on file.

‘Cruel and depraved’

Stokes was employed to work the night shift at the home, which also cannot be identified, and help with day-to-day tasks. Due to staff cutbacks he worked alone.

“Start Quote

We are very concerned about what might have been known in 2007, what actions might have been taken at that point and whether the matter could have been prevented”

Chris Haynes Gloucestershire County Council

Police branded him a “sexual predator” who deliberately targeted his victims and said he had not shown any remorse for the damage he had inflicted on them.

The mother of Stoke’s 32-year-old victim v said her “world fell apart” the moment she discovered her daughter had been sexually assaulted by him.

The victim’s sister said “that monster has ruined my life”, adding she had felt “sick, angry, upset, drained and so guilty for not protecting [my sister] from him”.

Judge Jamie Tabor QC jailed Stokes for 14 years and told him he would serve another six years on licence. He also placed him on the Sex Offenders’ Register for life.

“These three ladies had the bodies of adults but the minds of children and little children at that,” the judge said.

“They were every bit as vulnerable as little children and in some ways they were more vulnerable.

“You had sex with each of them. Such behaviour was cruel and depraved. None of these ladies was capable of giving consent, as you well knew.

“It is difficult to imagine a greater breach of trust.”

‘Best possible evidence’

It has emerged Stokes was arrested in 2007 for “inciting sexual activity with a mentally ill female at a care home”.

He was questioned and bailed but that was cancelled following an investigation and referral to the Crown Prosecution Service (CPS). No further action was taken.

A second investigation began in April last year when one of his colleagues reported that a resident had told them they had been abused by him, the court was told.

Stokes, who had worked in the care industry for 13 years and in his current job since 2007, was immediately arrested on suspicion of rape and sexual assault and suspended.

Interviews were carried out by the force, which said an intermediary had been involved for the first time ever in one of their investigations.

A specialist with experience in learning disabilities helped “communicate better” with the victims “and therefore get the best evidence possible”, police said.

Gloucestershire County Council had been responsible for contracting the firm which employed Stokes as a care worker for the home’s residents.

The authority has now called for an independent review to study whether the attacks could have been prevented.

‘We don’t have answers’

Chris Haynes, who oversees learning disability services for the council, said: “We are very concerned about what might have been known in 2007, what actions might have been taken at that point and whether the matter could have been prevented.

“We don’t have answers to those questions which is why I have requested the safeguarding board conduct a serious case review to help us answer some of those questions and make sure we can understand what happened in 2007.”

Rachael Scott, head of the CPS South West rape and serious sexual offence unit, said that when the 2007 complaint was made Stokes was interviewed and denied the offence.

“This was one person’s word against another,” she said.

“In the absence of any corroboration the decision was made that there was insufficient evidence to provide a realistic prospect of conviction.

“In 2007 the statutory process of using intermediaries was not available to us. Furthermore the recognised benefits of using an intermediary were in their infancy and their effectiveness was not known.

“The stance the Crown Prosecution Service takes today is fundamentally different to that in 2007. We no longer see the lack of corroboration as a bar to bringing a case to court.”

ATOS Accused Of Misleading Government Over Claim Processing Speed

March 20, 2014

The outsourcing giant Atos, one of two firms tasked with rolling out a new benefit for sick and disabled people, has been accused by a committee of MPs of misleading the government over how quickly it could process claims that has led to the distress of thousands of claimants.

The chair of the public accounts committee, Margaret Hodge, said the firm had submitted a tendering document to administer personal independence payments (PIP) which claimed there were agreements in place to work with hospitals and physiotherapy centres.

However, evidence obtained by the committee showed the document had “deliberately misled” the Department for Work and Pensions (DWP), she said.

Hodge also accused the DWP of turning a blind eye to discrepancies in Atos’ submission as civil servants rushed to find a way of implementing one of Iain Duncan Smith‘s new benefits. The DWP permanent secretary, Robert Devereux, denied they had done so.

The meeting follows a damning report from the National Audit Office (NAO) which showed last month that sick and disabled people trying to claim the new benefit are facing “distress and financial difficulties” because of mismanagement by civil servants, Atos and Capita.

The NAO discovered the new payment, which will replace the disability living allowance, will cost almost three and a half times more to administer and take double the amount of time to process.

At the committee hearing, Hodge said the committee had seen tendering documents submitted by Atos for London and the south of England in which the company committed to working with 16 NHS and 25 private hospitals and 653 physiotherapy practices.

Hodge read from the document, which claimed there were “contractual agreements” in place, and said: “In fact, only four hospital trusts agreed. In the contract document, you misled the DWP over where you were, didn’t you?”

“You should not have said that you had contractual agreements with trusts. You have only managed to work with a quarter of the trusts you named in the document. Isn’t that a lie?”

The senior vice president for health at Atos, Lisa Coleman, said: “We did not lie in that tender document. We corresponded with the suppliers and they were happy for us to name them.”

Coleman added that one of the problems with assessments has been an underestimation of the length of time it will take for each one to take place. She said: “We needed to double the capacity expected because assessments are taking twice as long as we expected.”

The committee also condemned Atos for misleading the DWP over the time it should take for claimants to get to assessment centres set up by the firm from their homes. About 40% of claimants take longer than an hour to travel to the assessment centres, the firm disclosed. The tender document submitted by the firm said that the centres were spaced widely enough that nearly all claimants would arrive within an hour.

The information submitted by Atos was later used by Lord Freud, the benefits minister, in parliamentary answers he gave when questioned about the suitability of Atos for the contract, Hodge said.

Devereux, asked about how the department had checked the tendering document, conceded that civil servants had not checked Atos’s system “end to end”.

Hodge also questioned why Atos was even considered for the PIP contract given that it had faced damning criticism and had contracts cancelled over the implementation of employment support allowance.

“It is a very similar contract, on a very similar area. What on earth was going on there? Why give them another chance?” she said. “This is the worst advert for using private contractors to deliver private services. It is awful.”

Devereux replied: “We were making a decision on the bids in front of us.”

The DWP had budgeted to pay £200m to administer the new benefit but pays Atos and Capita £127m to conduct face-to-face consultations or paper-based assessments.

The NAO report shows that within six months of the introduction of PIPs in some areas of the north of England in April 2013, a backlog of 92,000 cases had built up, almost three times the number expected. The DWP had made decisions in only 16% of the expected number of cases, the report states.

Poor operational performance in the early stages of Duncan Smith’s flagship programme have forced his department to stagger the full national roll-out of PIPs and increased the risk that it will not deliver value for money in the long term, the NAO found.

Atos was singled out for criticism in the report. In October, the DWP postponed the rollout of the benefit because of fears that Atos could not reduce backlogs or manage higher volumes of cases.

Contractually, assessment providers should complete 97% of assessments within 30 days. By the end of October, Atos and Capita had completed 55 and 67% respectively, the report states.

Claimants were waiting an average 107 days – and terminally ill patients 28 days – for a decision on their cases, an NAO report has found, rather than the predicted processing times of 74 days and 10 days respectively.

Delays in assessments have cut by £140m expected savings over the course of this parliament, with the DWP now forecast to save £640m a year by 2015, rather than its prediction of £780m, said the NAO. However, the DWP still expects to achieve annual savings of £3bn by 2018-19, with 3.6m claims assessed by 2018.

Each new PIP claim – worth between £21 and £134 a week to disabled claimants – costs an average £182 to administer, compared with £49 under the disability living allowance, the report states.

Atos submitted a tender supply information form on May 2nd 2012 to the DWP, as the French firm bid for four PIP contracts worth £127m a year – it eventually won two.

The document shows that the firm had claimed to have established a network of 1,738 consultation centre sites across Britain which meant that claimants would be at the most one hour away from an assessment.

“Their location, in particular the NHS hospitals, is often at the centre of established transfer links, meaning that between 75% and 90% of claimants will be less than 30 minutes travel time from a consultation centre, with the remainder only 60 minutes away,” it said.

The document implies that Atos had already sought and been granted access to accomodation. “Each partner has contractually agreed to providing accommodation to the required specification,” the submission says. Hodge claims this was misleading.

The submission document claimed that across Lot 3, covering London and south east England, Atos could deliver assessment centres in 56 NHS, 25 private hospital and 653 physiotherapy practices. “This creates a network of nearly 750 sites across Lot 3 (as shown in the diagram below) within which claimants can attend a face-to-face consultation. In virtually all areas, there is coverage by more than one supply chain partner, creating additional capacity and contingency,” the report claimed.

This, Hodge said, was grossly misleading.

#Torybingo #Carers #Budget2014

March 20, 2014

An Interview With @JobCentreMole About DWP Corruption

March 20, 2014

Cross posted, with thanks, from Guerilla Policy.

In November 2013 I interviewed the DWP whistleblower known as the Jobcentre Mole, who used Twitter to expose corruption and advise DWP victims. In the interview the Mole revealed the existence of sanctions bonuses and competition between JobCentres to sanction the most people. Now another whistleblower who tweets from the @JobcentreMole account tells his story, revealing that job centres use sanctions to reduce the number of JSA claimants and make it look like unemployment is falling. (All emphases mine).

Your partner Mole revealed that advisors are given bonuses for sanctioning and there is a list system to force Job Centres to compete with each other to sanction the most people. Could you describe when you saw bonuses being given out or when you saw advisors being blamed for not sanctioning enough jobseekers?

“Staff were getting marked as ‘must improve’…because they had not [sanctioned enough jobseekers].”

Well, there is an annual bonus payment in place and it is supposed to be performance related. Basically staff have two reviews per year, an interim & then a final about every six months. Staff are “reviewed” on their performance over the previous 6 months by their line managers. The final reviews will be coming up shortly, btw. The reviews are basically conversations about what you have achieved over the period, evidence you supply of examples of good customer service, say. The line manager then makes an assessment and gives you a performance marking: Excellent, Good or Must Improve.

Excellent and Good means you will be paid a bonus. There are mainly 2 staff grades in a JCP office which deal with customers. Band B staff mainly do the signing part and administration support. Band C staff are mainly advisors or line managers to band B’s. Band C are generally thought of as being a junior manager grade, god help us as this is where most of the dead wood is, & the grade above! The bonus payments are approx £360 & £520 for B and C respectively, so we are really talking about a fortune here when the head of DWP Robert Deveraux allegedly was paid a £20K bonus.

6 months ago band B & C staff were getting marked as “must improve” and it is true to say that many band C staff admitted that it was because they had not done sufficient DMA action on jobseekers. (DMA is basically instigating the sanctions). Here though is the stupidity of this system, when staff were asking the line managers how many DMA referrals they had to do the answer was “there is no target”.

I must explain here that the grading system was being screwed with by senior managers as there were rumours that they were trying to cut the number of bonuses paid due to media focus. So the ordinary staff member got it in the neck again, a lower than inflation pay rise for 4 years, and now a bar raising exercise to attain a meagre bonus.

As you can imagine morale is very low in the offices, so much so that the managers are setting up work groups to try and find ways for staff to engage with the department. This is the truth, if you wrote it as part of a comedy script people would say you were mad.

At all staff meetings DMA is always mentioned, the number of actively seeking or the number of refusing employment, always mentioned along with being told that our off flow targets are going thru the roof. As though we can’t make the connection that it is DMA which is generating the false impression that unemployment is falling and employment is rising!

Anyone sanctioned still has to attend to sign as they have to sign for their National Insurance contributions. So each offices’ register will look on paper as though it is reducing, but the number of people attending each day isn’t dropping! Talk about Orwell’s ministry of truth!

I must say that in my office, we are not told about neighbouring offices sanction rates. I can see that it would go on as some managers have an agenda all their own. Civil Servants are supposed to be non political, but I have heard managers quoting popular political soundbites and this culture is obviously filtering down to the front line staff.

It was a project that led you and the other Mole to set up the @JobcentreMole Twitter account. Was the project something you felt was unfair to jobseekers?

“I have heard and read statements which senior management have issued which have mimicked the politicians’ statements.”

My self and the other staff member worked on an initiative together for about [Slutocrat has chosen to redact this information to protect the identity of the Moles] and became friends. He has a longer service record than I have, and he would deal with the questions regarding the conditionality and regulations. I am more for combing the Internet finding stories in the media which highlight the departments incompetence. Due to unforeseen circumstances my friend is unable to contribute to the account at this time.

We did not start the Jobcentremole account because we were disillusioned, the feeling we had was that there was a need for it. We were under the impression that there were no other whisleblower accounts, fortunately we have been proved incorrect. I just simply want people to realise that there are staff who work in jobcentres who do actually care about people. One of the biggest issues at the moment for me is that civil servants are supposed to be non political but, I have heard and read statements which senior management have issued which have mimicked the politicians statements. Phrases like “the end of something for nothing” & “a stricter benefit regime” are being used regularly by staff who should know better. Please, be under no illusions, JCP are solely wanting people to “sign off” the unemployment register and they are not interested in why they do it, I personally think there is a serious unmentioned campaign to frustrate people off benefits.

How do advisors and managers keep jobseekers in the dark about their rights to appeal, get travel funding, etc?

“There is a culture of almost secrecy within the department, the steer from managers being that we wouldn’t tell people directly about [funds to help them get into work]”

In the dark? More like deliberately withholding information about services specifically introduced to remove a barrier to a jobseeker getting back into work. You are quite right about the travel funding also, many districts have local arrangements with transport companies which were introduced to help people looking for work reduce travel costs. You are asking why isn’t this information displayed in a prominent position in all jobcentres? Well think about this …When was the last time you ever saw a media campaign or advertisement informing the public about what benefits they may be entitled to? It just isn’t done is it? The department never advertises any benefits. The closest we get at the moment is information about claiming Jobseekers Allowance online. This is being done to force people to claim online, to save money & to pave the way for digitalising our services.

So similarly, there is a culture of almost secrecy within the department, the steer from managers being that we wouldn’t tell people directly about ADF (advisor discretion fund) a fund of money which can be used to help remove a particular barrier to work. Then there is Flexible Support Fund (FSF) another source of cash which can help pay for things like training or travel costs, again with the intention of helping people back into a job. We would only inform about these if a jobseeker asked about them directly. So we don’t tell & they won’t know!

There used to be the return to work credit, which was a payment of £100 for a single person or £250 for a person with a family, which was paid to someone signing off into work. The intention being that the payment would help someone until they were paid their first wage. The coalition scrapped it, so now lots of people worry about accepting a job with a monthly salary as there is no support for them.

Also to anyone reading this who is or has to attend appointments which are not on their signing day, claim your travel expenses!

The appeals process is in place for people to use, again no information about it is ever displayed in an office. One thing I will say here, a lot of buildings aren’t owned by the DWP they are leased from organisations like Trillium. This is going to sound crazy but there are rules about what can and can’t be displayed on the walls, and what size and shape it can be!

It really is like working in a parallel universe at times, you have to leave your common sense at the door.

Have you seen anyone being sanctioned unfairly?

“A sanction can be imposed for…being referred to a vancancy…and hasn’t provided proff that they’ve applied for it”

I’m not an Advisor or a Work Coach as the role is being renamed. I’m therefore not privy to the circumstances behind a sanction. The commonest reason for a sanction is ASE or not Actively Seeking Employment. This is the jobseeker not providing enough evidence of active Jobseeking. Previously, people set out the steps they were going to take to find work in a contract between themselves and the Jobcentre called a JSAG (Jobseekers Agreement). The sanction for ASE is applied when a jobseeker hasn’t shown or taken enough steps to find a job.

A sanction can be imposed for RE which is refusing employment. Usually a jobseeker is referred to a vacancy, mainly on the horrible Universal Jobmatch and hasn’t provided proof that they have applied for it.

A sanction can also be applied for missing a mandatory appointment. The JC take the view that a person is not working so they will be able to attend an appointment at any time. When a jobseeker does not attend a doubt is raised about a persons availability to take up employment, this is usually not done to someone who misses just one appointment. It is generally jobseekers who persistently miss appointments who are sanctioned. A form has to be issued if someone misses one appointment and another is re booked, this form warns the jobseeker that they MUST attend, on time, or it will affect their benefit.

I think jobseekers have been given Directions to do an action, like create a CV, and this is beyond their capability. This often results in a sanction, and in some cases I think that this can be unfair. What you have to remember is that the Jobcentre deals with all the spectrum of society, and it is widely acknowledged that some people do not & will not ever work. This group have no health issues or mitigating circumstances so, is it right that they can stick two fingers up to society and say “I want benefit but I’m not prepared to meet the conditions to be eligible for it”?

Courtesy of Slutocrat and @JobcentreMole

What Grant Shapps SHOULD Have Tweeted After #Budget2014

March 20, 2014

The New £1 Coin

March 20, 2014

No, readers, I haven’t lost my marbles.

Disability is everywhere, don’t you know?! Even in the design of a new pound coin.

Damon Rose explains how the new design will go some way to helping him buy stuff without eyesight in this article for Ouch.

Old pound coin, new pound coin

Former Grange Hill Actress Lisa Hammond To Join Eastenders As Donna Yates

March 20, 2014

Thank you, Eastenders, thank you.

EastEnders is set to introduce a new disabled character portrayed by former Grange Hill actress Lisa Hammond.

The 31-year-old will play tough market trader Donna Yates on Bridge Street, who declares war on stall rivals Kat and Bianca.
Despite the character not originally intended to be in a wheelchair, Hammond succeeded in her audition for the role among able-bodied actors.

Hammond has a restricted growth condition and is the second regular disabled character to appear on Albert Square, after Adam Best (David Proud) from 2009 to 2010.

“I’m really excited to join the cast of EastEnders, the actress said. “It’s a great opportunity to be a part of such a big and popular show. Donna is a bit of a handful but they’re always the most fun characters to play! It feels good to be bad!”

EastEnders boss Dominic Treadwell-Collins described her character as “flinty, aggressive and difficult”.

“Donna’s not an easy character to like at first,” he admitted. “As we get to know her better however, we will discover a funny, loyal but also fragile woman underneath. Lisa is a brilliantly comic and sharp actress and we’ve been trying to get her into the EastEnders cast for a long time – so I’m delighted that it has finally happened.”

Hammond started her acting career in Grange Hill at the age of 13 and has also appeared in Psychoville, Bleak House and Max and Paddy’s Road to Nowhere.

Carer’s Allowance Earnings Threshold To Rise From May 2014

March 20, 2014

I have been campaigning for carers to be allowed to earn the minimum wage from paid work for years.

So when I read that the earnings threshold would rise from May, I was thrilled.

But, readers, that was until I saw the amount it will rise by.

£2 a week. £104 a year. A very, very small reward for carrying out a role they didn’t choose, 24/7, without complaining, for free apart from Carers Allowance and the earnings threshold- in total just over £150 a week.

If an employer paid that, they would be accused of expecting slave labour.

Why does the Government get away with it, then, readers?

Hard working people? Carers are the hardest working people on Earth. Hard working people, my left foot.

Don’t Wake Me: The Ballad Of Nihal Armstrong Heads For Off-Broadway

March 20, 2014

Don’t Wake Me: The Ballad Of Nihal Armstrong is a beautifully written story of a loving mother’s relationship with her severely disabled, but very intelligent, son.

In 2013, British star of stage and small screen, Jaye Griffiths, brought the moving script to life around the UK.

Now, the show’s first international performances will take place between April 1-20 as part of this year’s Brits Off Broadway festival.

flyernyc

Please, if theatre interests you and you’ll be in the area, consider going to see the show, or recommend it to your friends. You won’t regret a single minute.

Mentally ill man left penniless by DWP is arrested at job centre for cracking a joke.

March 19, 2014

argotina1's avatarBenefit tales

Many of us have had the experience of having no money arrive when it us due, or being sanctioned, when we are already barely surviving.

One of our members, Herbert, went in to the Job Centre last Wednesday to find out why his ESA had not been paid. He was promised it would be in his account that afternoon – that his allowance was being “amended”.

Between 2-5pm he checks and checks, and nothing. He goes in the next day, and has to make the call to Belfast again. This time, they decide they need to know his bank Sort Code which they have never asked for before, so he has to go and get it. During a heated argument on the phone where Herbert is told there is no emergency payment that can be made, security staff think it is their job to ask him to quiet down, Herbert…

View original post 652 more words

Budget 2014: Cap On Welfare Spending

March 19, 2014

The biggest way in which we will be affected by today’s Budget, readers, seems to be the announced cap on welfare spending.

For 205-16 welfare spending will be capped at £119.5bn.

The cap will affect:

  • Severe Disablement Allowance. Does this mean DLA/PIP or is this something different? Could someone please clarify as DLA and PIP are not mentioned.
  • Incapacity Benefits. As there is no longer a specific benefit called Incapacity Benefit I wonder whether this is a general term including PIP/DLA, if Severe Disablement Allowance is something else? Also does this include Carers Allowance, as this is not mentioned separately but is claimed as a result of the incapacity of the person being cared for?
  • Child Benefit.
  • Maternity/Paternity pay.
  • Universal Credit- if it ever comes in to use!
  • Housing Benefit, unless the housing benefit is linked to Jobseekers Allowance, which will not be affected.
  • ESA. So they’ll cap spending on an employment benefit specifically for sick/disabled people, but not on the non disabled version (jobseekers?) That’s just great. Have they forgotten that ESA claimants are far less likely to ever find a job, and so will need the money for longer? Or do they just not care about this crucial fact?
  • Pension credits, but not the basic state pension.

However, more worryingly, Osborne made some statements about welfare and work that I’m starting to be able to quote in my sleep:

“Britain should always be proud of having a welfare system that helps those most in need,”

“But never again should we allow its costs to spiral out of control and its incentives to become so distorted that it pays not to work.”

And most worryingly of all, a cap on welfare spending looks set to stay permanently, with the announcement that the limit on total welfare spending will be set by the chancellor at the beginning of each parliament.

If the limit is breached, the chancellor will have to explain why, and a vote would be held in Parliament.

I hope you’ve found this post useful. There are points we all still need to clarify, but one thing is very clear:

There’s scary stuff ahead for us, readers.

 

Statins May Help Treat MS Finds Study

March 19, 2014

Statins may be useful in treating advanced multiple sclerosis (MS), say UK researchers.

 

Early trial results in The Lancet show the cholesterol-lowering pills slow brain shrinkage in people with MS.

 

The University College London (UCL) scientists say large trials can now begin.

 

These will check whether statins benefit MS patients by slowing progression of the disease and easing their symptoms.

 

 

MS is a major cause of disability, affecting nerves in the brain and spinal cord, which causes problems with muscle movement, balance and vision.

 

Currently there is no cure, although there are treatments that can help in the early stages of the disease.

Advanced disease

Usually, after around 10 years, around half of people with MS will go on to develop more advanced disease – known as secondary progressive MS.

 

It is this later stage disease that Dr Jeremy Chataway and colleagues at UCL hope to treat with low cost statins.

 

To date, no licensed drugs have shown a convincing impact on this later stage of the disease.

 

 

For their phase two trial, which is published in the Lancet, Dr Chataway’s team randomly assigned 140 people with secondary progressive MS to receive either 80mg of a statin called simvastatin or a placebo for two years.

 

The high, daily dose of simvastatin was well tolerated and slowed brain shrinkage by 43% over two years compared with the placebo.

 

Dr Chataway said: “Caution should be taken regarding over-interpretation of our brain imaging findings, because these might not necessarily translate into clinical benefit. However, our promising results warrant further investigation in larger phase three disability-driven trials.”

 

The researchers believe statins may have anti-inflammatory and neuroprotective properties that can guard the nerves from damage.

 

In an accompanying editorial, Jacqueline Palace from the John Radcliffe Hospital, Oxford, and Neil Robertson from Cardiff University in Wales, said the trial represented a promising starting point in the quest to find a treatment for secondary progressive MS.

 

Dr Susan Kohlhaas, head of biomedical research at the MS Society, said: “There are no treatments that can stop the condition from worsening in people with progressive MS. Scientists have worked for years to find a potential treatment that could help people, and now, finally, one has been found that might. This is very exciting news.

 

“Further, larger clinical trials are now absolutely crucial to confirm the safety and effectiveness of this treatment.”

Gary Boulet Of People First Talks #JusticeForLB

March 19, 2014

And Winterbourne View, carers and community care.

Undercover Doctor: Cure Me, I’m Gay

March 19, 2014

In this one-off documentary Dr Christian Jessen goes undercover to both investigate and undertake controversial gay ‘cures’ in the UK and the USA.

Christian is shocked to find that not only are there people who believe that homosexuality is a disorder which should be cured, but that there is a growing number of therapists and self-styled healers who believe that they have the ‘cure’ for the ‘illness’.

He sets out to prove or disprove their claims by offering himself up as a suitable case for treatment.

As a doctor who also happens to be gay, Christian is keen to find out what’s on offer for people who are uncomfortable with their sexual orientation and desperate for change.

He wants to discover whether or not these ‘cures’ are effective by trying them on himself.

From old school ‘aversion therapy’, carried out by the NHS, which required gay patients to sit in their own urine, faeces and vomit for three days on end, to modern day techniques such as ‘gay rehabilitation’ and ‘colour therapy,’ Dr Christian boldly undergoes as many therapies as possible.

Can he be ‘cured’?

I am openly straight. However I have never, and will never, see being gay as a ‘problem,’ an ‘illness’ or anything that can be cured.

I don’t think you can ‘cure’ gay, any more than you can help being, or becoming, disabled.

I watched the documentary, and it shocked me that people think like that, in the West, in the 21st century. I think they need curing of their attitudes.

Left To Die In British Detention With Dementia: Who Was Alois Dvorzac?

March 18, 2014

 

 

He died in handcuffs while detained at Harmondsworth detention centre – an 84-year-old Canadian with Alzheimer’s. Until now we only knew a name: Alois Dvorzac. But who was the man behind the tragedy?

 

 

Until now, all we knew about Alois Dvorzac came compliments of a paragraph in a report by HM Inspector of Prisons in January.

The report, based on a spot check of Harmondsworth Immigration Removal Centre, said: “The 84 year old Canadian man had been refused entry to the UK at Gatwick airport on the 23 January 2013.”

It went on to explain that despite being declared unfit for detention he ended up dying, in handcuffs, while still in detention two weeks later.

Channel 4 News has spoken exclusively to the doctor who examined him when he first arrived in the detention centre. She immediately knew this was the wrong man in the wrong place.

“This person was extremely vulnerable, he was frail, he should not have been there in the first place, let alone to be detained for such a long while,” she said.

“He was the sort of person you see and immediately identify with as a sort of grandfather figure.”

So first the doctor, who wants to remain anonymous to protect her career, spoke to her line manager. She wanted to alert her manager, the person in charge of the health and welfare of detainees, to Alois’s condition.

When the doctor asked that official why Alois was here in the first place, she was told: “UK Border Agency (UKBA) are not giving us this information because it’s none of our business”. According to her notes, she asked: “What do I have to do to get him out of here?”

What do I have to do to get him out?

Eventually she was told to fill in a form and fax it to UKBA, which she did. But she decided to go further. She rang UKBA directly. The official she spoke to there assured her that she would try to get him a place in an appropriate care setting or hospital.

The doctor went further still. She rang the Canadian high commission emergency number around the end of January. She explained to an official that she was really concerned about one of their citizens and gave them all the details.

“At that point, there was not much more that I could do. I definitely think that I tried to act ethically, I always do. I tried extra hard in this case to do the right thing by this patient and I feel as if nothing I said or did made any difference,” she said.

But about a fortnight later his heart gave way while still in detention. He’d been in handcuffs for five hours and was still wearing them when he died.

This is what the Canadian Department of Foreign Affairs, Trade and Development told Channel 4 News about Alois’s case: “Our thoughts remain with the family of the deceased Canadian in the United Kingdom. Canadian Officials in the United Kingdom have maintained close contact with representatives of the Home Office to press on this tragic case and to receive developments.

“We take the well-being of our citizens very seriously and look forward to the outcome of the investigation of the prisons and probation ombudsman into the circumstances surrounding Mr Dvorzac’s death. To protect the privacy of the individual concerned, further comments on this case cannot be provided.”

 

So this was Alois Dvorzac. But why was this elderly Slovenian, living in Canada, travelling through the UK in the first place? Who was he? And why did he die in detention at a British immigration detention centre?

We travelled to Maribor, Slovenia to try to piece together the mystery surrounding this man. A distant relative gave us an address there that, we were told, was his family home. We rang the doorbell of the old apartment block in the centre of the city. It was answered by Zlatka Hoceevar, Alois Dvorzac’s niece. She invited us in. She’d emptied out a box of old photographs and letters on the kitchen table.

He was born in 1928. His dad died when he was two. He lived in this house with his mother and three sisters.

He was super clever. He went to school in occupied Slovenia and his niece showed us his school report, complete with Nazi stamp. Every subject – sehr gut. After school a big blot on his report card, as far as the Nazis were concerned. As the war was ending he joined the Slovenian partisans.

 

As the new Communist regime bedded in in Slovenia, the young ambitious Alois started to become disillusioned. According to his niece: “The political system crushed talented people. Those that stayed here, had their wings clipped.”

He taught himself English and became the first of his family to go to university in the capital Ljubljana – all with a view to getting out.

Before he left Slovenia for Canada, he met the great love of his life, Dana, and they were married.

He wasn’t allowed to leave Slovenia legally at the time. He first made it to Austria and then Canada. This was to be only time in his life he could ever have been classified as an illegal immigrant.

In Canada, he was naturalised and forged a successful career as an engineer. He and Dana didn’t have children, but if the photograph below is anything to go by, they did have very happy life together for many years.

 

News

Which all leads us to the following devastating question: how did this life, so full of historical resonance, affection and adventure, end up extinguished, in handcuffs, in a British asylum detention centre?

In January last year Alois Dvorzac got on a plane in Canada. His intention was to fly to Slovenia to reconnect with the life he had left behind. Dana had passed away, and Alzheimer’s was setting in.

He got as far as Gatwick. No-one will tell us why he was taken off the plane. Perhaps he had some sort of episode. Perhaps he didn’t have the right paperwork. Either way, for some reason he was put in restraints and brought to Harmondsworth. He complained of chest pains while there and was examined by a doctor.

End of the journey

A Home Office spokesman told Channel 4 News: “The independent Prisons and Probation Ombudsman is investigating the circumstances of Mr Dvorzac’s death and we will carefully consider his findings.

“The recent report by Her Majesty’s Chief Inspector of Prisons on Harmondsworth made it clear that performance by the contractor running the centre has been below the high standard expected.

“It made a number of recommendations that we are taking forward and we are scrutinising our contractor’s performance closely. Clear instructions have been issued to staff making clear that restraint should only happen where absolutely necessary.”

But for Alois Dvorzac, that was the end of his journey. Two weeks later, still in detention, in handcuffs and gasping for breath, he died.

Premier League Failing Disabled Football Fans Finds BBC

March 18, 2014

Premier League clubs are discriminating against their own fans, according to a leading disability charity.

 

Joyce Cook, chair of Level Playing Field,  was responding to a BBC study that found that only three top-flight stadiums currently provide the required number of wheelchair spaces.

 


 

Of the 20 clubs in the Premier League, eight fail to offer even half of what they should under national guidelines – a situation that has remained largely unchanged for more than five years.

 

She called for radical change, claiming football has become “stuck” on the subject of disability.

 

“The experience for a disabled football fan is very varied, but it’s nothing like that of a non-disabled fan,” she said.

 

“It’s hard to get tickets, specifically for away games and especially for wheelchair users. When you get there, the sight lines can be pretty grim and it can be quite a miserable experience.

 

 

“There are a few good examples… but I think some of it is based on trying to manage a poor situation – a complete lack of sufficient seats.”

 

Asked if she felt Premier League clubs are being discriminatory and letting down their fans, Cook said: “I would say so, yes.”

 

 

When BBC Sport took its findings to the Premier League, it insisted it was working hard to accommodate disabled supporters.

 

“The highest standards of access are generally at clubs with new grounds, but all clubs, even those working within the constraints of older stadiums, work hard to make sure that disabled fans can attend matches and enjoy their football,” read a statement.

 

“We will continue to work with our clubs, fans and their representative organisations to make sure that the views of disabled supporters are taken into account as we make improvements in this area.”

 

But Arsenal fan and wheelchair user Anthony Joy said guidelines on disabled facilities were not being adhered to “in any way, shape or form”.

 

“There are not enough spaces around the country,” he said. “Also in terms of where you’re put, it’s sometimes an afterthought.

 

 

“My worst experience was this season at Crystal Palace. Arsenal won 2-0, but I saw next to nothing of the game.

 

“If you put disabled supporters halfway up a stand, you need to raise them up so they can see above someone’s head if they do stand. The next time we play at Selhurst Park, I don’t know if I’ll go.”

 

 

Crystal Palace chairman Steve Parish says the club has taken steps to address the situation.

 

He said the club has already blocked off three rows in front of the disabled section to improve the viewing experience.

 

“We have an old ground which has been under invested for many years by previous owners,” said Parish.

 

“I can assure you we are committed to improving the experience of every fan coming to Selhurst, with particular attention to ensure disabled fans can enjoy the game equally with others.”

 

But Joy, who has been following Arsenal home and away for more than 20 years, says he often has a very different experience from the friends he travels with.

 

 

At three Premier League grounds – Upton Park, Villa Park and Anfield – a limited number of wheelchair spaces means he is forced to sit with the home fans.

 

“I don’t want special treatment,” he said. “I don’t think any person with a disability wants special treatment, they just want equality. They want a chance to go and see the game, and ideally sit with their friends.”

 

Liverpool say Anfield’s age limits what they can do and insist they have carried out a number of feasibility studies into moving the wheelchair section for away fans.

 

“Currently, it can’t be done as travelling distance to the accessible toilets are outside the permitted maximum,” read a statement.

 

“However, if we progress with a proposed stadium development, then we would look to significantly increase the number of wheelchair bays as part of any expansion.”

 

Current guidelines on how football clubs in the United Kingdom should cater for disabled spectators have been in place since 2004 in the form of the Accessible Stadia Guide.

 

The document sets out a minimum standard that all new grounds have to meet in the provision, location, and quality of facilities for disabled fans.

 

Who Performs Best?

Wheelchair spaces provided as a percentage of Accessible Stadia Guide recommendations

  • 1. Swansea 121%
  • 2. Southampton 104%
  • 3. Cardiff 102%
  • 4. Arsenal 96%
  • 5. West Brom 89%
  • 6. Hull 89%
  • 7. Manchester City 88%
  • 8. Newcastle 73%
  • 9. Sunderland 70%
  • 10. Stoke 68%
  • 11. West Ham 60%
  • 12. Everton 56%
  • 13. Norwich 49%
  • 14. Chelsea 47%
  • 15. Liverpool 45%
  • 16. Manchester United 43%
  • 17. Crystal Palace 40%
  • 18. Aston Villa 39%
  • 19. Tottenham 28%
  • 20. Fulham 24%

 

The number of wheelchair spaces a stadium should provide is based on its capacity.

 

Old stadia are not exempt and, just like the local shop or parish church, football clubs must continually make “reasonable adjustments” to ensure everyone can access their services.

 

When considering what is “reasonable”, financial resources are taken into account.

 

But even though the Premier League is richer than ever, Joy believes little has changed in the past 10 years.

 

“Of course it’s going to be an issue with older stadiums,” he said. “I can kind of make allowances for that. But with the amount of money in the game, I think there should be some level of redress.

 

“While there’s a lot of money being spent on the corporate and hospitality side of the game, general standards of grounds are poor. That’s not just for people in wheelchairs.”

 

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.

 

Barrister Catherine Casserley says clubs that do not adapt to the needs of their disabled fans could be breaking the law.

 

“One of the things that courts will do to establish what adjustments it is reasonable to make is to look at what other guidance is around,” said Casserley.

 

“If that says that clubs should have a certain number of wheelchair spaces and they don’t have that – and they don’t really have any rationale for not having that – then the court might well decide that they breach the Equality Act.”

 

Access to tickets is another issue facing disabled fans.

 

 

Several clubs in the league have different ticket policies for disabled supporters, with restrictions that do not apply to non-disabled fans.

 

Casserley, an expert in discrimination law, says the majority of the football-related cases she has worked on involve ticket policies, but that fans are often reluctant to take action.

 

“I think football clubs are in a privileged position in that they probably rely on the loyalty of their supporters in not bringing claims,” she said.

 

“I have to say that the people that I’ve seen really have come to me at the end of their tether because they really don’t want to bring claims against their clubs but they want the same experience as non-disabled fans. Why shouldn’t they have that?”

 

Cook, however, thinks more football fans are willing to act.

 

“Disabled fans got a real taste of what is possible during the London Paralympics and they realise they’re getting a really raw deal,” she said.

 

“There’s always an argument about new and and old stadiums, but, quite frankly, you can pretty much make any stadium accessible if you have the intention, some smart design and clear thinking.

 

“It’s time we all come together and really put this right once and for all.”

 

 

 

ATOS ‘Not Fit’ To Sponsor Commonwealth Games, MSPS Hear

March 18, 2014

Petitioner Sean Clerkin told MSPs he believed Atos were “contract killers” who were “not fit” to sponsor the 2014 Commonwealth Games, on 18 March 2014.

Mr Clerkin’s petition calls for the Scottish Parliament to urge the 2014 Commonwealth Games’ organising committee to drop IT company Atos as a sponsor.

He told the Public Petitions Committee the company, who assess whether benefits claimants are fit to work, were a “toxic brand”.

Last month Atos confirmed it was seeking to end its government contract.

Staff carrying out work capability assessments for Atos have received death threats online and in person, according to the Financial Times.

Disability campaigners have described the work tests as “ridiculously harsh and extremely unfair”.

Mr Clerkin said it was disappointing no MSPs, apart from the convener David Stewart, asked any questions about the petition.

Iain MacInnes from Glasgow against Atos also gave evidence.

The committee agreed to continue the petition and write to a number of organisations including the Department of Work and Pensions, Atos and the Scottish government.

Wendy Hoose

March 18, 2014

Amy Conachan is a rising young star of Scottish theatre, who’s starring in a new stage comedy about the sometimes awkward reality of sex and disability.

 

Forthright and very open, 23-year-old actor Amy Conachan says her legs are “really small” and “don’t work” because her spinal cord “doesn’t go all the way down”. She’s already making an impact on the Scottish theatre scene, even though she’s only in the second year of a BA in Acting and Performance at the Royal Conservatoire Scotland – the first disabled student on her course.

 

Conachan is also one of the first in her year group to be offered professional work – with some challenging material that is very close to home, as well as close to the knuckle. Wendy Hoose is a sex comedy, according to its publicity. Some reviews have preferred the phrase “comedy of manners”.

 

It’s about a one-night-stand between two twenty-somethings, Jake and Laura, for whom the course of true love (or sex) runs far from smoothly, after Jake realises his date has no legs. The play takes its title from Jake’s (Scottish-accented) reaction to Laura’s home, with its accessibly low kitchen worktops.

 

The pair have only met online, when Amy invites Jake to her flat. She is awaiting him in bed, covered up, when he first sees her. Having described herself as “legless” in texts, Jake thinks Amy means “drunk”. He only discovers she means it literally during the throes of passion. The play explores the situation as it unfolds.

 

Amy Conachan spoke to Ouch before the play went on the road.

 

Tell me about the play

 

There are some very sexy scenes in it… and it is very politically incorrect. It’s farcical and rather funny too.

 

Laura and Jake meet via a hook-up app which is a little like the much talked-about Tinder. Have you ever used an app like that?

 

I am on Tinder because absolutely everybody I know has it. It is a quick way to make a decision on someone. All you get is their Facebook profile photo, their age and their name. They appear (in your feed) if they have friends or interests in common with you. You swipe left if you don’t like them. If you think they are attractive then you swipe right. If they like you too, you get a match. Then you can talk to them and can arrange to meet up if you like. I get a lot of hellos but it doesn’t go any further, which is fine, because meeting people in that way freaks me out.

 

Is being disabled a problem for you when dating?

 

It is always on my mind to some extent, which is funny, because I don’t really think about disability in any other aspect of my life. You are very vulnerable and it is about what they think of you – and there’s still more to discover that they might think of as negative.

 

What is your character Laura like?

 

She is very sure of herself and knows what she wants from Jake. No matter how offensive or insulting he is to her, she’s always able to match it with something else, while still being likable to the audience.

 

 

And are you anything like your character?

 

A bit. Living with a disability, your whole life makes you strong and a good judge of character. I make decisions about people really quickly and she does that in the play.

 

What’s it like to act out scenes of a sexual nature in front of an audience?

 

The first couple of times were really uncomfortable but once you get through that, it becomes part of your job. I’ve had people ask me, “Have you had sex” or “Can you have sex?” I always think, “Oh for God’s sake. Would you ask a normal person that question?”

 

The point of these scenes is to show the audience that disabled people do have sex and that they do enjoy it. I don’t feel a great responsibility to show the world we’re normal but I do hope they learn from watching because I’m aware that the question is on their minds.

 

Do you prefer playing disabled roles?

 

I’m keen to go for parts that aren’t written as disabled. I feel I should be able to play those characters which, because I’m the actor, become disabled.

 

What’s next?

 

After Wendy Hoose, I’m in Gerda Stevenson’s new stage production Skeleton Wumman, which is all in Scots. I play a woman who was severely disabled when alive, unable to walk or talk. It is set in her afterlife. She’s now a skeleton living under the sea telling stories about what happened to her during life.

 

Are you becoming the go-to Scottish disabled actor?

 

I’m enjoying the work to be honest so I’ll take what I’m given. I’ve realised that at first, while my name and my face is getting out there, I am most likely to be cast in disabled roles. But hopefully, in the long run, it will fizzle out and I’ll just get parts for being an actor.

 

Wendy Hoose, a co-production between theatre companies Birds of Paradise and Random Accomplice, tours Scotland during March 2014.

PIP Claim Delays ‘Unacceptable’ Say MPs

March 18, 2014

MPs have said it is unacceptable that disabled and sick people have to wait six months or more to find out if they are eligible for benefits as a result of government changes.

 

The Commons Work and Pensions Committee said delays to decisions about the new personal independence payment (PIP) were causing stress and uncertainty.

 

They also questioned the language used by ministers and the use of statistics.

 

Ministers acknowledged the delays but said benefits were being backdated.

 

New claims for the personal independence payment (PIP), the replacement for the disability living allowance (DLA), began in April 2013. They are worth between £21 and £134 a week.

 

Most people applying for PIP have a face-to-face assessment to determine eligibility, which is carried out by the private contractors Atos Healthcare and Capita Business Services.

‘Financial difficulties’

In a report last month, the National Audit Office found claimants were waiting an average of 107 days, and terminally ill patients 28 days, for a decision on their cases – much longer than had been predicted.

 

Some of the claimants affected by these delays are people with terminal illnesses.

 

Labour MP Dame Anne Begg, who chairs the cross-party committee, said any delays were regrettable but the time that it was taking in such cases was “completely unacceptable”.

 

The MPs say the average time taken to process new cases should be reduced to the expected 74 days, and seven days for terminally ill people.

 

Dame Anne said basic failures – such as appointments being cancelled without notice or unsatisfactory responses to queries about claims – were happening too regularly and claimants had often been unable to get any information about when a decision would finally be made.

 

“This not only leaves people facing financial difficulties whilst they await a decision, but causes severe stress and uncertainty,” she said.

 

“It is vital that all disabled people, but especially the terminally ill, experience as little delay and stress as possible in making a claim.”

 

Ministers, the committee added, should consider invoking penalty clauses in their contracts with Atos and Capita if the “current dire situation” did not significantly improve.

 

“By the end of last year, decisions had been made in fewer than 20% of new claims submitted since April 2013,” Dame Anne added.

 

“It is essential that the backlog is cleared before the limited natural reassessment of existing DLA claims is extended any further.”

 

Macmillan Cancer Support said the time being taken in many cases was “appalling” and the government must agree to publish waiting times for decisions on a quarterly basis.

 

Scope said the benefit was a “financial lifeline” for disabled people to reflect the extra costs they incurred in performing basic tasks.

‘Fast-tracked’

 

The introduction of personal independence payments is one of a series of major welfare changes being pursued by the government aimed at reducing the benefits bill and encouraging greater self-reliance and incentives to work.

 

But the committee said ministers must “exercise care” in the language used in press releases about these benefit changes and how they present statistics about their impact so as not to “feed into negative public views about benefit recipients”.

 

“Statistics should be used to shed light on policy implementation, not to prop up established views or feed preconceptions,” the report added.

 

“The Department for Work and Pensions should set out the specific steps it is taking to ensure that statistics are released in a way which is accurate and fair to benefit claimants.”

 

In response, the Department for Work and Pensions said PIP was a new benefit, based on face-to-face assessments and regular reviews.

 

“In some cases this end-to-end claims process is taking longer than the old system of Disability Living Allowance, which relied on a self-assessment form,” a spokesman said.

 

“We are working with providers to ensure that all the steps in the process are as smooth as they can be and the benefit is backdated so no-one is left out of pocket.”

 

Claims by those with terminal illnesses were fast-tracked, the department added.

 

“Latest statistics show over 99% of people with terminal illnesses who have applied have been awarded the benefit, which means over 9,500 terminally ill claimants are now receiving PIP.”

Please Share Widely- ATOS And Mental Health

March 18, 2014

Spotted on Facebook.

My sister developed severe depression and what seems like to be bipolar disorder and personality disorder.

We are waiting for Atos to assess her claim.
I called atos every week putting pressure on them. We were given a number to book an assessment and my sister got a call back from a nurse from atos.
I had requested a home visit but the nurse spoke directly to my sister and told her that she will have to come in to be assessed and when my sister insisted on a home visit the nurse asked how do you get to the GP’s … my sister said by car as it’s a 2 minute drive. The nurse said well if you go to your GP’S then we will pay for a cab for you to come in for an assessment.
My sister said ok as she would say that but it doesn’t mean anything because come the day of the assessment she would refuse to go to the DRs.
I called atos today and informed them that under no circumstances will I her carer share a cab with my sister due to her violent aggressive behaviour and the fact that she self harms and she may even have sharps on her.

The man at atos infomed me that they waive assessments on people who have such disorders and he filled in an online form with me and said that the DRs at atos will use the information i’ve goven to assess the claim.

Please share this with others who may have severe mental health needs or are carers for people with mental health problems.

Thank you.

Autistic Man’s Stairlift Row

March 18, 2014

A Teesside woman has described as “barbaric and humiliating” a decision by health bosses to remove a stairlift used by her severely disabled son.

Marilyn Barker, from Billingham, says she is now forced to make a daily trip to a nearby leisure centre so her son Philip can have a shower.

Health bosses, who say they are trying to find a solution to the family’s needs, removed the stairlift amid concerns Mr Barber, who has autism and epilepsy, could injure himself.

But Mrs Barker says she is now considering selling her home because of the “unbearable” situation.

Look North’s Stuart Whincup reports.

Sophie’s Choice- Cervical Cancer Screening

March 17, 2014

I’ve just read the very sad story of Sophie Jones, 19.  Sophie sadly passed away on Saturday morning. She lost a year-long battle with cervical cancer.

But when she first had symptoms, she was refused a smear test- because her doctors said she was too young to get the disease.

Now, family friend Pamela Keelan has started this petition to get the minimum age for cervical cancer screening lowered to 16.

Please, join me in signing, in memory of Sophie and to help make sure there are no other Sophies.

Hospital Patient Confronts MP Over Clause 119

March 17, 2014

Reader Paula Peters has just posted this on Facebook. I thank her for making me smile, and hope you will smile too.

Sitting in the blood test department waiting to be seen when my MP walks in sits down. I get called in so does he, he sits in the chair next to me….nurse says to him you look familiar, he looks uncomfortable, he said his name, she said you are an MP arent you? One of them tory ones. The room goes deathly quiet.

A voice pipes up, yeah hes one of the bastards who signed clause 119 last week to shut this hospital down. An elderly lady walked up to him and hits him with her handbag and calls him a shit….and a few other choice words…..made the start of monday and the week a pretty lively one.

A Hundred Voices For Change

March 17, 2014

This is a guest post by Rachael Holmes, Head of Policy- Families, Welfare and Work at Citizen’s Advice.

100 voices for change

In February this year Citizens Advice launched a new campaign to make ESA fit for work. As part of the campaign we asked people to share stories of their experience of ESA and we have been overwhelmed with the response.  We have now had over a hundred responses giving over a hundred reasons why it is vital that major reforms are made to ESA.

It is clear that too many people are being failed by the system, suffering from poor quality Work Capability Assessments and being left without the support they feel they are entitled to.

One of the most common topics has been how people have had bad experiences with their Work Capability Assessment (WCA) carried out by Atos.   We have heard stories like Lesley’s, who was told that the medical evidence she supplied from her neurosurgeon was just ‘her opinion’.   And Adam a legal companion trained to support people through ESA claims who has had to argue with Atos staff just to be able to attend a WCA, and has seen assessments cancelled at short notice when the claimant is already on the way to the assessment centre.

DWP will soon have to tender new contracts for companies to run the WCA.  With evidence of these failings we are calling on the Government to significantly improve the new contracts so that they can hold the new providers to account for poor quality reports and bad customer service.

Another major concern has been highlighted by stories like John’s who has been left relying on food bank vouchers  while he  has been waiting over a month without any money for DWP to make a final decision on his ESA application.  Citizens Advice is campaigning for the Government to change the rules so that claimants continue to be paid ESA during the ‘mandatory reconsideration’ stage, when DWP gives a second opinion on a claim.

We have also heard stories like Michael’s who is scared that DWP is going to turn down his appeal simply because he could not afford to pay his GP to get the necessary medical evidence to support his claim.  We are campaigning to change the rules so that DWP pick up the bill for GPs to provide medical evidence to make sure they can get the decision right first time.

Websites like Same Difference and these voices for change show how important it is that the Government listens to sick and disabled people and makes significant changes to how ESA works. To read the #FitforWork blog and to find out more about our campaign please visit our website at http://blogs.citizensadvice.org.uk/blog/was-it-fit-for-work-for-you/

Adla- The Disabled 9-Year-Old Syrian Refugee Desperate To Get To Britain

March 17, 2014

Is there any way we can help her?

For what it’s worth please share this article. It may, somehow, reach someone, somewhere, who has the power to help this child and her family.

Outside nine-year-old Adla’s tent, a fragile stem rises from the mud next to an open drain. Her mum says the sapling is an olive tree she planted as a symbol of hope in this camp of desperation.

 

Adla, who has cerebral atrophy, a brain condition that means she can’t walk or talk, stares blankly towards the tree, and waits.

 

She waits in a nappy to be carried by her dad to the toilet across the mud here in Iraq at Qushtapa camp.

 

She waits for a place outside her prison-like tent where she can crawl freely and play. She waits for crucial physiotherapy, without which she risks curvature of the spine that may stop her lungs fully expanding and lead to potentially deadly chest infections.

 

Her parents wait too. Almost three weeks ago, no longer knowing how to care for Adla at the camp close to Erbil, the capital of Kurdistan in northern Iraq, her mum and dad emailed the British consulate begging for help for their daughter.

 

But all they received back was an automated reply.

 

The family feel her disability means she cannot survive in the camp where they have sought refuge like thousands of other Syrians after fleeing the conflict in their homeland which began three years ago.

 

Her dad Adham, 42, shows me his desperate email. It pitifully reads: “My nine year old does not speak, she crawls, she falls on the floor, she gets hurt, bruises, she fell and cut her tongue. She needs rehab, she needs help to improve. We ask for your help and for you to accept her.”

 

I look at Adla, who giggles when you stroke her hair, and wonder how anyone could not want to help and accept her.

 

 

 

 

In total 225,560 of the 2.5 million Syrian refugees have fled to Iraq since its borders started to open last August.

 

It has now been almost two months since David Cameron promised urgent action by offering the most vulnerable of these people, including the disabled, asylum in the UK.

 

Adla’s parents know this – although they are not aware the offer has only been extended to 500, a figure which would also include their families. This compares with Germany’s offer to take 11,000.

 

It also compares to the estimated 915,145 refugees that Syria’s neighbour Lebanon has already taken – even though that country is smaller than Yorkshire.

 

Adla rips at a colouring book. She lashes out at her 16-month-old sister, Nazi, with the worn Teletubbie toy she has brought from Syria.

 

Like the Teletubbie’s fur, Adla’s patience is wearing thin. Adham and his wife Silava, 39, show me Adla’s battered wheelchair, which is useless in the mud.

 

Her mother says: “She needs medical treatment. A camp like this is not right for someone with her needs.”

 

Yet there appears to be no news on when cases are to be considered by the UK, and how the few will be chosen. Even if the Home Office acts swiftly, only accepting 500 means Adla is likely to miss out.

 

 

 

Outside the family’s tent, other children run through the mud flying kites. These youngsters are struggling, but they find comfort in play.

 

Tears trickle from the dark eyes Silava tries so hard to keep dry. She says: “I want to help Adla get better and have a future. I see ­children playing and feel so sad for her.

 

“We can’t leave her alone with other ­children, she cries because she can’t join them. We want her to have a childhood.”

 

In Syria, Adla received speech therapy and physiotherapy. The family, which includes her brother Jawan, 12, lived in a flat in Al Hasaka with enough bedrooms for them all, and a safe area on the roof where Adla could play.

 

They had a car, so she could be taken to the park. She loved swimming, and would spend hours flexing her legs in a pool.

 

As her parents describe this, she begins to move her arms in a swimming motion.

 

“She felt so happy there. She does not speak, but she mimics swimming,” says Adham, who was a counsellor in Syria but now works in a school on the camp for £240 a month. The other thing Adla has been known to mimic is the sound of gunfire.

 

“At home we were stuck between different security forces. When the rebels launched an attack there were clashes near our home, so we had to get out,” recalls Adham.

 

The family, whose surname were are not using to protect them, was forced to flee last August. Adla last saw a doctor a year ago.

 

Adham says: “The government soldiers would shoot in the air indiscriminately. The sound was scaring the children.

 

“We had no electricity or water, it would come on for an hour every few days. We went 12 days without water. We had to dig wells.

 

“Neighbours were being conscripted, the whole neighbourhood was criss-crossed with checkpoints.”

 

The family got through the border but then had to sleep in a school with 700 others.

 

“We had spent nine hours on a bus, then we were there for 17 days. Adla was screaming,” says Adham.

 

Silava adds: “Adla gets angry and restless because she is confined. She is afraid at night and needs the electricity on. Here it cuts out in the night and she trembles and cries.

 

“Other children make fun of her. It is unsafe for her here. There’s no hope. I’m not sure I have the strength to raise her here.”

 

Save the Children wants the UK to accept thousands rather than hundreds of displaced Syrians. The charity, which is providing child protection, shelter, and clothing to refugees, fears that without enough support from Western countries, Syria’s neighbours will have to close their borders.

 

Save the Children chief executive Justin Forsyth said Britain’s Government deserves “enormous credit” for helping the region, and providing more than £600million in aid.

 

But he added: “Given the scale of the humanitarian crisis, the UK has a moral imperative to show solidarity with Syria’s neighbours by sharing the responsibility of protecting some of the people fleeing Syria.”

More Jobcentre Madness, Youtube Style

March 17, 2014

Government Plans To Ditch Universal Jobsmatch

March 17, 2014

The government has drawn up plans to scrap its official jobs website, Universal Jobmatch, after recognising it is too expensive and that its purpose is undermined by fake and repeat job entries, according to leaked internal communications from the Department of Work and Pensions (DWP).

A cache of documents seen by the Guardian details how the government’s main website for job hunters – which tens of thousands of unemployed people have been required by the DWP to sign up to – is likely to be jettisoned when the contract for the service comes up for renewal in two years.

A year and a half after its launch, Universal Jobmatch has been ridiculed for hosting numerous fake jobs, including one for an MI6 “target elimination specialist” and “international couriers” for CosaNostra Holdings, as well as listings for pornographic websites.

More recently very serious problems have emerged. Separate investigations by Channel 4 News and the Labour MP Frank Field have uncovered hundreds of thousands of fake, repeat or, in a minority of cases, fraudulent job postings that enticed jobseekers to spend money needlessly – for example on fake criminal records checks – or were a means of harvesting personal information for identity fraud.

At the start of March, the DWP removed more than 120,000, or one-fifth, of all job adverts from over 180 employer accounts, because the ads did not abide by the site’s terms and conditions.

Field is now pressing the National Audit Office to investigate the site which he described as “bedevilled with fraud“.

The DWP said it regularly monitors Universal Jobmatch to remove jobs that do not meet its rules and that of 524,640 employer accounts only a tiny minority have proven to be in breach of them. The leaked information about Universal Jobmatch became public after the chair of the public accounts committee said last week that the DWP was on the verge of a “meltdown” over its relationship with private companies and welfare reform.

The leaked documents say that some of the website’s problems have partly stemmed from the decision by ministers that the site – which is run by the international online recruitment company Monster – be as “open” as possible to all types of employers. Recruitment agencies have taken advantage of this openness by uploading repeat adverts on the site.

The effect, the documents go on to say, has been that civil servants have been unable to determine how many genuine employment vacancies are listed on the site. According to one email, the data simply is not “robust” and rectifying the issue will be expensive.

Other internal communications suggest that civil servants have asked for more than one hundred changes to the service. However senior managers have decided to pass on only a handful of them to Monster because they have given up on improving the current site and expect to start afresh after April 2016.

In light of the high possibility that Universal Jobmatch will be cancelled in its current form, a communique to project heads said that the relationship with Monster now had to be managed “very carefully”.

A paper detailing options for overhauling the site includes:

• Getting an outside company to create a new service that would “learn the lessons” from Universal Jobmatch.

• Designing a site that would only cater for small employers. Jobseekers would be expected to use other sites to find work that was with larger employers.

• Coming to some contractual agreement with other major jobs sites to cross-post adverts and merge them into one larger DWP-run database. It is understood that ministers have not been involved in discussions about the new options.

The project to digitise job-searching activity for millions of unemployed people has been beset with problems from its start. The DWP was forced to rerun the bidding process for the contract and previously leaked documents detail how the department had to pay compensation to one of the failed bidders.

The multimillion-pound contract was won by Monster but Iain Duncan Smith’s department has been struggling to justify its rapidly rising expenditure. Civil servants say that the US company, which pioneered online recruitment two decades ago, has demanded an extra £975,000 to clear Universal Jobmatch of fraudulent employment ads.

Stephen O’Donnell, who runs the National Online Recruitment Awards, said that Monster was “quite exercised”. He said that while the company had made “very good money” on the contract, the DWP was to blame for creating a “real mongrel of a website”. “Monster … have real expertise worldwide in building spectacular job boards. They more or less invented the industry. So you do think ‘how come it’s so bad’? The reason for that is the civil servants basically told Monster ‘forget everything you know about job boards, this is what we want’.”

O’Donnell said: job centres used to have good checks before the site was launched. It used to be, to put a job in a job centre, a recruitment agency had to call and identify themselves, go through various checks and identify the employer.” However without those checks he said many more anonymous postings were being hosted under the DWP’s logo. “Anonymous job adverts are terrible. [The job] may or may not exist. It might just be a fishing trip for other information.”

” I do not hold Monster at fault: they have been directed by the DWP to do what they are told.”

“I think it’s criminally unfair to sanction jobseekers for not using such a clumsily built website, rife with spammers … identity thieves and anonymous job ads.”

A spokesman for the DWP said that the search for work had become increasingly digital in the last decade and that over the next six months, wifi and 6,000 extra terminals would be installed into jobcentres across the country so jobseekers had access to the latest technology.

Responding to the leak the department said: “Universal Jobmatch revolutionises the way jobseekers find work and ithas already helped many jobseekers find the jobs they want since it was launched in 2012.

“How people find work has become increasingly digital so it’s right – and responsible – that DWP should continually look to ensure we are making the best offer to jobseekers.

“The current Universal Jobmatch contract comes to an end in 2016 so any speculation on what will happen after that is premature.”

Monster declined to comment.

There Is Another Bedroom Tax Loophole

March 16, 2014

I think this is worth sharing. Who knows, it might help someone, somewhere, somehow. The question is why wasn’t it revealed from the beginning?

Social housing tenants can avoid the hated Bedroom Tax by using their spare room to set up a business.

Then they won’t have to pay an extra £14 a week because they can prove they are using extra bedrooms, the Sunday People reports.

Amazingly the loophole was revealed by a Government spokesman in the House of Lords.

Earl Attlee, who is a Tory despite being grandson of Labour post-war PM Clem Attlee, said: “The spare room subsidy encourages people to make full use of their property and to ­consider running a small business. I think that is highly desirable.”

But Shadow Welfare minister Chris Bryant said: “Instead of dressing up this unfair Bedroom Tax as a business opportunity, they should be scrapping it.”

Tenants would first need to get permission from landlords – their council or housing association.

Experts Call For Adult Cochlear Implant Review

March 16, 2014

A nationwide study should be carried out into the devices that could help adults who are profoundly deaf in both ears to hear, according to experts.

Bilateral cochlear implants are prosthetic devices that make use of electrode arrays surgically implanted in the cochlea of the inner ear to provide a sense of sound to those with profound hearing loss.

Together with therapy, they allow children born without hearing to develop excellent speech and language and enable adults to overcome feelings of isolation. A single implant allows users to perceive speech and sounds. However, a second enables users to locate the sounds enhances speech perception in bustling environments and ensures that, should one device fail, the user is not thrown into a silent world.

But guidelines from the National Institute for Health and Care Excellence (Nice) allow bilateral implantation in adults only if they have a second disability, such as blindness, that makes them more reliant on hearing.

Many believe the guidelines need to be revised to allow adults, like children, access to two implants. Azhar Shaida, consultant otologist and cochlear implant surgeon at London’s Royal National Throat, Nose and Ear hospital, said: “The problem is down to money versus benefit.” A single implant costs the NHS around £38,000-£45,000. If a second is implanted simultaneously, only one hospital procedure is necessary, meaning the cost is not double. However, Nice concludes, the second implant does not offer enough benefits, compared to the life-changing effect of the first, to justify the cost for adults.

Labour MP Lilian Greenwood said: “The criteria are based on evidence from patients who were predominantly wearing technology from the late 1990s. Since then, there have been significant advances in technology. Many clinicians would argue that the criteria do not reflect real world listening, and that more realistic tests should be deployed.”

Stuart McNaughton, a lecturer at Westminster Business School who also works for cochlear implant firm Advanced Bionics, is one of the few adults to have a cochlear implant in each ear. He says a second device helps adults to realise their full potential. “I understand that children need more input because they are developing language and they are developing skills, but what about all the people over the age of 18, 19, 20, 21? They should be allowed bilateral implants as well. Society puts pressures on adults too – relationships, jobs – it’s a rat race out there.”

David Selvadurai, consultant otolaryngologist surgeon at St George’s Hospital, London, and founder of their cochlear implant programme, also believes adults should have access to two implants. But, he says, it is vital that enough evidence is gathered. “What we don’t have at the moment is good cost benefit data to show that there’s enough benefit to the individual to demonstrate cost effectiveness for the NHS,” he said.

But that could change.Together with colleagues at UCL’s Ear Institute, Shakeel Saeed, Professor at UCL and the RNTNEH, is assessing a national study on bilateral cochlear implantation in adults which is expected to take four to five years to complete. “This is to create high quality evidence that Nice can then use to make a considered decision,” he said. “If we complete that study, then we will be able to answer a very simple question: does the benefit of having two [implants] in adults justify the cost? We might find it doesn’t – but I suspect that we will find that it does.”

Can You Help Keep Luca In Drama School?

March 15, 2014

Luca is 14. He loves Drama so much that he did his Drama GCSE in year 9- a whole 2 years early. And he got an A.

Luca is also autistic. He has found his talent, and his passion, and he wants to take it as far, academically, as he possibly can. This makes Luca, in my eyes, truly DisAbled- one of my favourite kind of people.

But Luca is one of 4 siblings. Austerity and the cuts have hit his family hard. His parents want to help him achieve his dreams, but it is becoming financially very difficult.

So, Luca has written the following message, with some help from his mother, blogger Bernadette Horton.

Please help me fund my private Drama school tuition.

I am Luca’s Mum – Bernadette –  and am acting on his behalf on this account. He has typed out the appeal below. His dad and I are extremely proud of his achievements and do all we can to support him, but austerity is biting our family severely as we are both self employed working poor.

Hi
My name is Luca and I am 14 and I am autistic. I am currently in Year 10 at school. Last year, in Year 9 I gained an A grade in Drama GCSE and took a grade 4 in Acting with the London College of Music at my drama school Thesps which I go to on Saturdays.

My ambition is to become an actor. I would love to be the next Dr Who. However, as I took my Drama GCSE in Year 9, I have two years with no drama in school before I move to 6th form. That is why Thesps Drama School is so important to me. I performed as mr Brownloe in Oliver last Christmas.

I am going to take grade 6 in Acting and grade 6 in verse speaking with the London College of music but taking the exams and paying for private tuition is too expensive for my mum and dad as I am the youngest of 4 brothers. My elder brother Joe has played cricket for Wales which has cost my mum and dad loads of money with travel, accommodation and cricket kit. My mum and dad are struggling to afford my £80 per month Saturday Thesps tuition  fees and I need to know I can afford the next 6 months – 1 year =  £480 for 6 months minimum,and I have to buy 2 anthology books, display folders which are £40 and pay £200 for 10 weeks for hourly extra private tuition fees plus a total of £100 for the 2 exam fees. If I don’t find the money I may have to give up Thesps shortly.

I am going to go to university in a few years to study drama hopefully, but I really need this help as my parents are struggling with running the house and helping me out and my brothers too. My mum and dad are paying already to send me to France on a French GCSE trip and the drama fees are just too much.

I would be soooooooooo grateful for any help and I would like to share and update my progress when the exams are held in June/July 2014. Although I have autism I am determined it will not stand in my way! and I will work extremely hard to achieve my dream. Please help me if you can. Thank you very much.

To help Luca, even if you can’t donate money, please consider sharing this link with your friends on Facebook, Twitter, or any other social media.

 

Save The Children Syria Appeal Advert Featuring Stephen Hawking

March 15, 2014

I’ve just seen Save The Children UK’s Syria Appeal TV advert. It features Stephen Hawking.

 

Texts From The NHS

March 15, 2014

I’ve just seen this on Facebook. Thanks to reader Jane Lauppen.

Text arrives on mobile phone 10 past 10 at night from NHS England,threatening if there is no reply, to de-register the recipient from their GP’s surgery.
As usual corporate , profit led organisations behaving like total bullies who do not care about the affect their demands,late at night or randomly sent through the post by day have on the recipient.
This was discussed today on BBC Lunchtime with Laurence with callers anxious to discover more about these letters, presented in similar format to a scammer attempting to elicit data.

This is terrible. I do hope it’s a scam.

By the way, Lunchtime With Laurence on BBC Radio Cornwall is a programme I have liked for quite some time. It often discusses issues of interest on health and/or disability.

Updated: Jane Lauppen has just confirmed that this  has been established NOT to be a scam. I now think it should be covered widely and stopped from happening. It is awful and causes great stress to patients and carers.

Congratulations Jade Etherington!!!

March 14, 2014

And her guide Caroline Powell. The most successful British women in Winter Paralympic history. Three silvers and a bronze!!!!

 

Five medals overall for us. We’ve smashed the target of two!!!!!

Bailiffs To Get Access To Claimants’ Credit Records

March 14, 2014

Do we have any privacy left?

 

Bailiffs are to be given access to benefit claimants’ credit reference records in an effort to clamp down on bogus claims.

The move is aimed at making it easier to confiscate high-value possessions if claimants have failed to pay back fraudulently claimed benefits.

The latest sweeping power was given to the Department for Work and Pensions (DWP) late last year and follows the controversial decision to give HMRC access to all claimants’ credit reference records.

Until last year the DWP only had access to credit reference records on an ad hoc basis if there was reasonable suspicion of benefit fraud, but the DWP now has complete access to credit reference data.

No 10 predicted cars, luxury items and state-of-the-art TVs belonging to “those who have stolen money through dishonest claims” would be targeted.

It is estimated that £1.2bn was lost to benefit fraud last year and ministers are determined to do more to get that money back. Downing Street claims recent cases have found individuals claiming multiple benefits for years despite having full-time jobs, property portfolios and undeclared capital.

The new power means fraudulent claimants will see their benefits repaid through the sale of their assets.

Downing Street said the use of bailiffs would act as a strong deterrent and encourage more people to make arrangements to pay back what they owed without the knock on the door.

Benefits can be – and are already – docked to recover fraud debt.

This year has seen the launch of a publicity campaign to encourage more people to correct errors in their benefit claims early and to persuade members of the public to report suspected benefited cheats.

A No 10 spokesperson said: “Getting the welfare budget under control is a key part of our long-term plan for the economy. We want to end the something-for-nothing culture and deliver for people who want to work hard and play by the rules.”

In December 2011 the HMRC said it was to draw on the expertise of credit reference agencies to tackle fraud and error. The departments have signed a 12-month contract with Experian.

Margaret Hodge: “DWP Programmes On Verge Of Meltdown”

March 14, 2014

Iain Duncan Smith‘s Department for Work and Pensions is facing “meltdown” over three of its biggest projects, Margaret Hodge, chairman of the Commons public spending watchdog, has said.

Ahead of a damning report on government contracts with private firms, Hodge singled out the DWP as a department particularly struggling with the delivery of welfare changes, which involve managing a relationship with private IT contractors, back-to-work providers and benefit assessors.

The public accounts committee report turns up the pressure on ministers to allow all government contracts to be subject to freedom of information (FOI) laws and examined by the National Audit Office (NAO).

Given that half of all spending on public services now ends up in the hands of private providers, departments must stop hiding behind “commercial confidentiality” when people want to know more about how these contracts work, it said.

The committee said two examples of contracts that the public deserved to know more about were the scandal of G4S and Serco charging for the electronic tagging of offenders who were in prison or dead, and the “complete hash” that G4S made of supplying security guards for the Olympics.

Following a stretch of negative publicity, the major outsourcing companies – G4S, Serco, Atos and Capita – are now willing to be subject to FOI laws when it comes to public sector contracts, but the government is still resisting, it said.

“Time and again when we see failures … it’s a failure of government to manage contracts,” Hodge said, adding that departments “simply have to up their game and get a grip”.

The committee said the DWP is particularly bad when it comes to private firms’ involvement in public services, including Universal Credit, its new IT system that will deliver an overhaul of benefits, the Work Programme, its back-to-work scheme, and the personal independence payment (PIP), the replacement for disability living allowance.

“All their programmes are on the verge of meltdown,” she said at a briefing to launch the report.

On Monday, a leaked internal review from the DWP said the government’s ambitious welfare strategy is at risk because of the speed and depth of the cuts imposed on the department, while a recent NAO report said the new PIP payment will cost almost three and a half times more to administer than the existing scheme.

Hodge said it was deeply ironic that if the DWP had been more open about the Universal Credit scheme – which she said was a “good policy” – there would have been a far better chance of the programme being implemented. Instead, she said, it was being “appallingly handled”.

A spokesman for DWP said the department has a “track record of delivery”. “We’ve already successfully launched the benefit cap, Universal Credit and the new personal independence payment. The industry tells us that the work programme has got almost 500,000 of the hardest to help into jobs. We are bringing in our reforms safely and responsibly,” he said.

John Cridland, director-general of the CBI, a business lobby group, said the report notes that the the private sector “plays an increasingly important role in running public services”.

“The public has a right to know how its money is being spent and the industry has pledged to meet a higher bar on transparency,” he said. “Businesses running public services agree that open-book contracting should become the norm. The National Audit Office should also be able to audit government contracts as long as this is done in a systematic way with the triggers for inspection, like missed performance targets, agreed from the outset.

“Rather than relying on individual Freedom of Information requests, we think FOI should be built into contracts when they are agreed.

Yet another Bedroom Tax tale to make your blood boil

March 14, 2014

Mike Sivier's avatarMike Sivier's blog

compassionbypass

Vox Political just had this Bedroom Tax story from a commenter on Facebook who has asked not to be named. I don’t think it needs any commentary from me:

“A neighbour of mine couldnt bear to give up the family home so she struggled and paid £24 a week for two spare rooms.

“She was missing all her other payments and not eating for days.

“She then had to start selling things from her house…

“Then started asking us if we had any old clothes because she had found a place where they weigh old clothes and give you money for them…

“Then because we had given her all we had, another so-called friend told her how she does without food… She then started taking speed as you don’t feel hungry and what money was left she could at least use to feed her daughter.

“She came to mine and…

View original post 98 more words

Emails Saying ‘You’ve Got Cancer’ Are Spam/Scam Says NICE

March 13, 2014

And very sadly, I found this terrible response to the NICE Tweet.

https://twitter.com/Thordale/status/444063226561851393

Full details here.

IDS Tells Trussell Trust: “Stop Scare-Mongering”

March 13, 2014

When the organisers of a charity food bank in Coventry received their 10,000th client, they held a ceremony during which the city’s mayor handed a free bag of shopping to a man considered to be the most deserving recipient.

Amid a ripple of applause from the crowd of officials, a grinning Darren Harvey stepped forward to receive the emergency supply of food, which was enough to feed him and his family for about three days.

The event was intended to highlight the plight of poor people who cannot afford to buy basic foodstuffs, a situation the Left has blamed on welfare cuts and described as a ‘national crisis’. It was filmed by a BBC TV team as part of a documentary called Britain’s Hidden Hungry.

 

The fly-on-the-wall crew gave viewers a revealing insight into 44-year-old Mr Harvey, however. For far from being deserving, he was exposed as a ‘conman’ — the local  newspaper’s description — who was slyly taking jobs while claiming benefits, accusations he denies.

In addition it was claimed he had a string of petty criminal offences, had been accused of tricking two women out of thousands of pounds, and was alleged to have been evicited by his landlord after refusing to pay rent. Little wonder the BBC documentary described him as a man with a ‘sense of entitlement’.

Of course, Harvey is not typical of everyone who uses food banks — which provide a valuable service for many genuinely needy people. But there is widespread concern not only that they are being abused, but also that they are being used by the Left and anti-poverty campaigners as a political tool to attack the ‘uncaring’ government’s drive to reform the welfare system.

The Left have been controversially supported in their view that the popular use of food banks is down to cuts by high-ranking churchmen, who say that although Britain is the world’s seventh largest economy, ‘people are going hungry’.

A recent letter to the Left-wing Daily Mirror signed by 27 of the country’s 59 Anglican bishops argued that government ministers had ‘an acute moral imperative’ to take action.

Interestingly, the key charity behind the growth of emergency food banks is the Trussell Trust, which organises more than 400 such banks. Run by Chris Mould, a Labour Party member, it has waged an increasingly political campaign to try to show that welfare reforms are leaving people starving.

The trust says that between April last year and December, around 500,000 people were given three days’ worth of food at its banks. If true, that means more than 8 per cent of the population has been forced to use charity food hand-outs. 

 

Work and Pensions Secretary Iain Duncan Smith has angrily accused the trust of ‘political messaging’ and told it to ‘stop scare-mongering’, adding that the politically-motivated campaign linking welfare reform to food banks is not based on facts.

Mr Duncan Smith’s claim is supported by the co-founder of one of the country’s leading food banks, who says that the soaring demand for free hand-outs is not principally to do with benefit cuts.

Robin Aitken of the Oxford Food Bank, which is unconnected to the Trussell Trust, says: ‘The whole debate has become hopelessly politicised. Ten years ago there were no food banks, but if you provide a service, people will use it.’

 

 

It is undeniable that people are suffering hardship as Britain recovers slowly from recession, with rising food prices adding to the problem. Across the country, there are now an estimated 30,000 generous volunteers who give up time to collect food and man the banks.

Not everyone qualifies for food-bank handouts. If applicants are considered deserving, specified ‘agencies’ such as doctors’ surgeries, schools, churches, social services, Citizens’ Advice Bureaux and JobCentres are authorised to give them vouchers which can be swapped for food bank handouts.

 

 

Even so, a snapshot of food banks around the country shows that their popularity hardly equates to the Left’s picture of a ‘starving Britain’.

Nikki Sanders, a 39-year-old mother-of-five, was in genuine need when she used one in Wimbledon, South-West London, after getting a voucher from a government-backed ‘Sure Start’ nursery.

She had just divorced, was out of work and waiting for income support to come through.

‘I was given a huge box of food. I couldn’t believe how much there was. It lasted two or three weeks.’

However, she soon realised that others were routinely obtaining vouchers despite having enough money to squander on drink-fuelled nights out.

‘People I know told me they often use it if they have been out on benders over the weekend and spent all their benefits,’ she says.

‘Come Monday, they have no money left. Then they just ask the Sure Start nursery staff where they take their kids for vouchers. They just fill out a form and lie. It’s very easy and very cheeky.’

Miss Sanders says that such people felt no shame in taking food donated by kind-hearted volunteers: ‘Their attitude is to hell with them. It doesn’t worry them. Benefits cash isn’t for people to go out and get drunk on. But they seem to think that they’re entitled to it.’

 

I visited another food bank in Hastings in Sussex. It is based at a community centre where a steady stream of people arrived clutching vouchers entitling them to free food.

A couple in their 20s arrived in a taxi, which they’d paid to take them the four-mile round-trip between their home and the centre.

The driver parked discreetly round the corner, out of sight of the food bank volunteers. The couple had chosen not to use a bus service which covers the route.

Next, two Latvians pulled up in a battered car. One said he was unable to work because he’d injured his foot and had been referred there by the Citizens’ Advice Bureau. While there were undoubtedly many deserving poor who turned up, these cases did not seem to be heart-rending examples of a national hunger crisis.

Kevin O’Doherty, a 54-year-old antiques dealer from East Sussex, has kindly helped street-beggars by driving them to a food bank, but has concerns about whether the people who use them are all victims of welfare cuts

 

‘When I took some people from St Leonards-on-Sea, they complained about the food they had been given. A lot of them are heroin addicts — they are white and British, not immigrants — who use the food as a form of street currency. These people know how to abuse the system.’

Meanwhile, Staffordshire police have been criticised after giving food bank vouchers to shoplifters who claimed they were so poor they had no choice but to turn to crime. Inevitably, there were complaints that this simply encouraged criminal activity.

The Trussell Trust strives to prevent abuse of the system by assigning serial numbers to each voucher, making them difficult to copy and limiting recipients to three separate handouts to stop them becoming dependent on food banks.

However, there is nothing to prevent recipients touring different accredited voucher ‘agencies’, and using different aliases, addresses and sob stories to get free food.

Last year, Bradford East MP David Ward told the Commons of his concerns about food bank abuse by immigrants. He said that a ‘growing number of Roma’ were accessing the increasing number of food banks in the Yorkshire city.

The truth is that food banks didn’t begin life as a result of welfare cuts. The Trussell Trust was set up under a Labour government, and its services were meant to supplement the Welfare State. But now the trust has become highly critical of the Tory-led Government, arguing that welfare cuts mean much more pressure is put on the charity sector to help the poor.

The trust’s four-page ‘briefing note’ of ‘statistics’ has been avidly taken up by Labour MPs, even though the figures are questionable.

 

Maria Eagle, Labour’s shadow food minister, repeatedly quoted the ‘fact’ that 500,000 people had used food banks when, in fact, the figure refers to the number of requests for food — rather than individual recipients.

In any case, food policy experts at the University of Warwick say it’s impossible to give accurate figures of food bank usage.

The country’s bishops, meanwhile, are equally culpable of misleadingly quoting figures. They said that 5,500 people were admitted to hospital with malnutrition last year, implying that this occurred as a result of poverty.

 

 

However, while it is true that a number of people were treated in hospital for malnutrition, the vast majority were elderly and the reasons were complex.

Although poverty may have been one cause, others could have been that they forgot to eat because of inebriation or because they suffered acute depression or dementia.

Also, the clinical definition of malnutrition includes people who are obese, while the NHS officially states ‘malnutrition due to inadequate food intake in this country is rare’.

Consider again the views of Robin Aitken of the Oxford Food Bank, a former BBC journalist who now collects unsold fresh food from supermarkets and distributes them to charities in Oxford.

He says: ‘Some people like to believe that there has been this enormous upsurge in food poverty. My point is that there have always been poor people in this country. You could have gone back ten, 20, 50 years and there would be people who don’t get enough food.

‘The fact is that food banks are a new phenomenon. Now we have got up to 500. If you provide a service, people use it.’

Significantly, he believes that people suffered greater hardship in the recessions of the Seventies and Eighties than today, when food banks didn’t exist.

More to the point, back then, there was not a disingenuous debate — fuelled by questionable and inflammatory statistics about ‘half a million people’ on the breadline.

The SCAR Project

March 13, 2014

Photographer David Jay didn’t set out to document scars.

It all started with one photograph of a friend who underwent a mastectomy at the age of 28.

Soon he began to take pictures of other young women with different stages of breast cancer, and the SCAR Project was born.

These searing portraits – of both men and women – show the physical reality of a disease that most people never see.

His next project, the Unknown Soldier, is a similarly raw look at severely wounded veterans of the wars in Iraq and Afghanistan.

Jay told the BBC he hopes his portraits will make people think about their interactions with others and give some perspective on what defines beauty.

Report Reveals How Elderly Are ‘Prisoners’ In Care Homes

March 13, 2014

Tens of thousands of vulnerable pensioners are being forced into care homes against their will, an inquiry reveals today.

It says laws supposed to protect the elderly are instead being used to take away their rights.

The House of Lords inquiry suggests many are dumped in residential homes to make it easier to control them or simply to save money.

Peers blame the scandal on Labour’s botched Mental Capacity Act. They say the law, which was meant to help those unable to make decisions for themselves, should be rewritten.

Lord Hardie, who led the inquiry, said: ‘The evidence suggests that tens of thousands of people are being deprived of their liberty without the protection of the law, and without the protection that Parliament intended.’

The retired Scottish judge singled out for criticism the ‘deprivation of liberty safeguards’ added to the act after the intervention of the European Court of Human Rights.

‘In some cases the safeguards are being wilfully used to oppress individuals and to force decisions upon them, regardless of what actions may be in their best interests,’ Lord Hardie said. ‘We were told the provisions were poorly drafted, overly complex and bureaucratic.

‘A senior judge described the experience of trying to write a judgment on the safeguards as feeling “as if you have been in a washing machine and spin dryer”.’

 

The 2005 legislation set up the Court of Protection, which is only now being opened to public scrutiny after a series of scandals.

Under a veil of secrecy, it has ordered people to be kept in care homes. In other cases, social workers have acted without legal go-ahead.

It is thought many of the pensioners could have stayed at home or in sheltered accommodation.

My father, taken against our wishes

 

 

Cloak of secrecy over spinster, 94

 

 

 

Councils often find care homes cheaper than looking after complex cases in their own houses.

The report also pointed to the way the act was used by social workers as an excuse for not helping people – and thereby saving money.

A provision in the legislation says people must be presumed to be able to make their own decisions unless there is clear proof they are incapacitated.

The report said one academic thought this had led to ‘vulnerable adults being left at risk of harm, in some cases leading to their deaths’.

In one case, a brain-damaged girl was left to be sent out by her boyfriend to work as a prostitute for drug money because social workers considered the law made this a legitimate ‘lifestyle choice’.

 

 

The report quoted a law firm which said the act had become for councils ‘an excuse to do nothing’.

The British Association of Brain Injury Case Managers told the nine-month inquiry: ‘Assessment of capacity is used as an economic tool to justify lack of provision, leaving the disabled person unprotected.’

The Law Society said people were left without help because ‘the outcome is going to be that the state spends less on them’.

The peers concluded that the act’s rules are ‘used to justify non-intervention by health or social care services, either erroneously, or in some cases, deliberately’. Among 39 recommendations, the report called for the scrapping and rewriting of the clauses on deprivation of liberty.

It also said the code of practice, the semi-legal document that tells social workers, doctors and lawyers how the act should work, should be torn up and replaced with a series of simpler codes.

The report also supported the opening of the Court of Protection to scrutiny and repeated demands for more openness from the judge in overall charge of its workings, Sir James Munby.

It said: ‘We believe that the reputation of the Court will improve with greater transparency.’

A permanent ‘independent body’ – in other words a quango – should be set up to oversee and monitor the workings of the law, the report said.

Lord Hardie said: ‘The act is not working at all well. That is because people do not know about the act, or do not understand it, even though many professionals have legal obligations under it.

‘Those who may lack capacity have legal rights under the Act, but they are not being fulfilled.’

The 2005 act was passed by Prime Minister Tony Blair and his Lord Chancellor Lord Falconer only after a rebellion by backbench Labour MPs and in a rush in advance of the election.

The Daily Mail campaigned against it, particularly those sections which allowed people to draw up ‘advance directives’ which could instruct doctors to kill them if they became too ill to speak for themselves.

A separate report released yesterday found that town halls are penalising the elderly by slashing vital services such as home helps rather than saving money through improving efficiency.

Official auditors found that massive cuts of 12 per cent in the last three years are placing families and hospitals under ‘intolerable pressure’.

The National Audit Office said most of the ‘significant’ drop in spending came from cuts.

Famous, Rich And Hungry- A Review

March 13, 2014

I have just watched the first part of Famous, Rich and Hungry. This two part documentary, filmed for Sport Relief, saw four celebrities spend a week living with four families who are in food poverty. They set out to experience hunger and see what life is like for those who can’t afford food.

Before going to live with their host families, food, wallets and phones were taken away from the celebrities. They were left with £3 for three days for food.

Theo Paphitis  went to Barnet, North London,  to live with single mum Ada. Ada spends £11 a week on food. In a moving moment, her daughter, 8, says mother and daughter trick each other by ‘accidentally’ leaving leftovers so that they both have enough to eat. Ada works part time as a dinner lady at her daughter’s school, so they both get a free lunch on weekdays. We learn that Theo, too, got free school meals as a child, because his family were on benefits. At the end, Theo appears to have learnt the most from the programme, and wants to keep in touch with his host family and continue to offer advice to Ada.

Jamie from Made In Chelsea went to Croydon to live with single mum Carly and her family. Carly spends £30 a week on food. In another moving moment, Carly’s daughter says that she lies to hide her own hunger, because she sees her mother shrinking. Carly has had no heating for two weeks, and has to use a food bank. I was pleased to see the programme giving a lot of useful information about food banks- most importantly the fact that people can’t just walk in to them, but have to be referred or show that they really need emergency food. Carly applies for training because she doesn’t want her family to learn to live on benefits. However, in yet another moving moment, she breaks down when  told that her private landlord needs to sell the house she lives in, which will leave her and her family homeless in a couple of months.

Soap star Cheryl went to Grantham, Lincolnshire, to Paul. She had working class roots but now thinks the whole country should have left food poverty behind, like she has. Paul, who has a collapsed lung, wants to work but can’t. He spends just £8 a week on food. He has to heat his living room but has no money for hot running water. In the ‘heat or eat’ choice, he says, he has to choose to heat because of his health. At one point in the programme, with their food budget used up, Cheryl takes food from a supermarket bin for Paul.

Rachel Johnson, journalist, author and sister of Boris Johnson, Mayor of London, went to South East London to widow Dee, who had a stroke two years ago and spends £21 a week on food for herself and her two daughters. She started the programme with  what is becoming a familiar attitude towards people in poverty or on benefits- by asking the question ‘what if they can’t afford food but spend on alcohol, cigarettes and satellite TV.’ However, at one point, food budget just about used up, we see her on the street outside the supermarket, begging for 9p so that she can buy mince meat to cook for Dee’s family.

The programme as a whole was moving and educational for me. What I liked most about it was something I found surprising because it has not been done in any of the similar programmes I have seen recently. Paul’s and Dee’s health problems were revealed straight away, although they were not focused on. In the case of Paul, his wish to work was made very clear.

I must thank the BBC for showing so clearly in this way what I have been trying to say for so long- that sick and disabled people do want to work but they just genuinely can’t. I wish more programmes about poverty and benefit claimants would highlight this fact as clearly.

I’ll definitely be watching the second half tomorrow on BBC1 at 9pm.