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Eyeborg: Rob Spence Has A Camera For An Eye

August 31, 2011

Rob Spence is a Canadian documentary film-maker who lost one eye in an accident when he was nine. In 2009, he had his prosthetic replaced with a camera. In 2011, he collaborated with the makers of science-fiction video game Deus Ex: Human Revolution to make The Eyeborg Documentary on the current state and future of cyborgs.

The past
“I was in Ireland visiting my grandfather. I was nine years old and was shooting a pile of cow dung with a 12-gauge shotgun, because I thought that would be a good idea. And I wasn’t holding it correctly. The accident did a lot of damage to my right eye. It was legally blind and traumatised but stuck around until six years ago.

“[By then] it had gone completely blind and I looked like Le Chiffre from Casino Royale. Cool, but it was starting to get painful and there was a potential to affect the other eye, because they’re so sympathetic.

“In the meantime I had become a documentary filmmaker so when it had to come out, I thought I would put a camera in there. It’s not unique, that if you lose an eye you want a camera. It’s like if you lose a hand you think about getting a hook. It’s an idea that’s prevalent in pop culture. I just went through it.

“Kosta Grammatis was 23 when he saw me on Wired [Spence was interviewed in 2008 saying he wanted to replace his eye with a camera]. He asked if I wanted any help. You get a lot of calls from people when you do articles like that, but he ended up moving into my spare bedroom. He built the first prototype on my coffee table.”

The present
“How did I end up trusting him to put explosive electronics into my face? I had been working with older guys. But young people have a lot more spare time, they want to get stuff done and they’re a bit too stupid to know if stuff is impossible.

“The older people were a bit more ‘I’m an expert so here’s why this can’t be done’. Kosta just said ‘let’s do it now’. We ordered stuff – there was never any budget. So the first prototype was really low-tech. But we did it. A proof of concept. From there, Kosta helped me find other people.

“Since then, there have been four significant iterations of the eye. It’s now quite a clear video image. The big technical problem was that, for a while, we had a great camera working but the minute you stuck it in my head, it’s like taking any transmitter and depositing it deep inside a ham and seeing if it works from there. It’s exactly the same RF tech as most wireless microphones but it carries just video.

“In my eye socket there is a pin that’s drilled into a ball of sea coral. The coral is porous, very compatible. The blood vessels in the muscles grow into the ball of sea coral. Then you’ve got a base that you can marry to the prosthetic eye. So the camera looks where I look.

“Professionally, I use the camera eye in conjunction with a regular video camera because people aren’t ready for a 100% eye film. My director of photography will use my head as a camera and tell me where to look. I can direct myself – wherever I look is what I’m getting.

“The guys behind Deus Ex: Human Revolution did a lot of research on cyborgs – it’s a realistic version of the way things might go. And during their research they found me – I’m one of the guys you find on the internet if you look up ‘cyborg’ or ‘camera eye’.

“They said ‘why don’t you join forces with us?’ I said ‘why don’t you let me do a documentary I’ve wanted to do for a while on where we are now with cyborg technology‘?”

The future
“[While making that], the guy I found most interesting was Miika in Finland. He was in a three-month trial to get a retinal chip in his eye. He has retinitis pigmentosa. This blind guy gets a tiny chip in his retina and he can read four-centimetre-high text, recognise bananas, trucks coming towards him! Take an iPhone, Miika’s retinal chip and my eyeball camera and crush those into one and you’ve got [lead Deus Ex character] Adam Jensen’s camera eye in 2027.

“What exactly the future looks like is up for grabs. One of the things that pushes technological development is science fiction and pop culture. Star Trek was an inspiration for engineers to figure out stuff.

“There’s also a demand there. Look at schoolkids – the technology is already undetachable from their bodies. People missing bits of their bodies are the pioneers for an option we will all have for biomechanical augmentation. The world is changing from prosthetic to augmentation. As opposed to a high-tech sticking plaster it’s going to turn into an improvement – better, faster, stronger.

“We’re becoming less sacred about our bodies and what we’re willing to do with them. Look at fake boobs or tanning or Botox. Those are just to look better. What are the possibilities that people will cut or change their bodies for better job performance?

“All the prosthetics now are external, kinetic. In the game, Adam Jensen has stuff jacked right into his nervous system. The guys I’ve spoken to have said that will become more possible when surgery is based more on artificial intelligence – robots.

“If I were to try and map my arm’s movements from my brain, that’s a completely different part of my brain from your brain.”

“Once we work out how to make a neural interface, the next big leap will be nanotechnology. Whatever happens, it looks very likely that either your children or grandchildren will live twice as long as you. At the very least – people living twice as long as you, that’s a very different human being. We lived twice as long as our cavemen ancestors, but that was on a slow curve. Things aren’t changing that much, they’re just changing more rapidly!

“And, of course, like in the game – there are military uses for all this technology too. The number one organisation in the world pushing this technology is the Pentagon. But it’s the same feeling you have when you get on a plane and fly to Hawaii.

“The military are the ones who pushed the development of jet engine technology. The military is always pushing technology it can use for war, but that’s not necessarily where it ends up. Somebody’s going to get blown up, but it also means you get to go to Hawaii!”

No Triumph, No Tragedy: Shannon Murray

August 30, 2011

 

http://twitter.com/#!/BendyGirl/status/108500688157409280

Emails Reveal How Cuts Led To Winterbourne View Scandal

August 30, 2011

I thought some of you might be interested in this post from Liberal Conspiracy.

Call For National Policy On DNR Orders

August 30, 2011

A patients’ rights group is demanding the Department of Health in England draw up national rules on the use of “do not resuscitate” orders following the Guardian’s revelation that the husband of a woman who died in Addenbrooke’s hospital, Cambridge, is suing the hospital and health secretary Andrew Lansley.

Patient Concern wants legally enforceable regulations to ensure the orders are added to patients’ medical notes only with their consent or, if they are not mentally competent, the permission of their family or lawyer. Guidance would not be enough.

Janet Tracey, 63, who had terminal lung cancer, broke her neck in a car accident in February and died the following month. Her husband, David Tracey, alleges the hospital deprived his wife and himself of their human rights. He claims doctors twice put do not resuscitate orders in his wife’s medical notes, cancelling the first after she objected to it, then putting in a second order three days later without her consent or any discussion with her. He is also trying to force the government to follow Scotland’s policy of having national guidance.

Both the hospital and the health department deny acting unlawfully, while Addenbrooke’s insists its clinicians acted in accordance with its own policy and the health department says existing professional guidance is more appropriate than national regulations set by the government. Lansley’s advisers have said he will not comment on the issue.

The General Medical Council (GMC), which regulates doctors, and the British Medical Association both insisted medical staff have the final say on how the orders are used.

However, Roger Goss, co-director of Patient Concern, said that though doctors argue that cardio-pulmonary resuscitation (CPR) offers patients a poor chance of survival, refusing it when patients want it “reduces it to zero”. He added: “The medical profession opposes this approach because it transfers power from the medic to the patient.”

The BMA said only 15-20% of patients who receive resuscitation ever go home and, on ethical grounds, doctors should not attempt treatments where patients would not benefit. Each case should be taken on its own merits, they said.

The position of doctors was also inconsistent, Goss said. “They think it is legitimate to put in ‘do not resuscitate’ notices, maybe with patient’s consent, but the medical profession almost universally opposes the idea that patients should be given any assistance to die. You cannot have it both ways.”

He also claimed doctors “had no problem ‘selling’ procedures to patients with similarly low chances of success and/or terrible risks, providing it is an interesting case”. Goss also warned that with the NHS in England expected to make savings of £20bn over the next four years, do not resuscitate orders “could become surreptitious standard practice for everyone over a specified age.”

Patient Concern was an interested party in the case which the GMC says settled the law on who should make the decision on whether or not patients are treated. In 2005 Leslie Burke, who had a degenerative brain condition, brought a case before the courts claiming the right to artificial nutrition and hydration, come what may, which gave him rather than doctors the ultimate say in treatment. The GMC, which opposed him, won the case on appeal.

The GMC said the ruling meant doctors had no legal or ethical obligation to agree to a patient’s request if they considered treatment was not in the patient’s best interests.

Under A Year Until The Paralympics

August 30, 2011

On Monday, it is exactly a year until the Paralympic Games begin in London.

The venues which will be used next summer are being adapted to ensure they are accessible to everyone who will be attending and competing.

London 2012 Paralympic director Chris Holmes said seating was being tailored so, for instance, those with hearing problems would have better views of scoreboards.

Tickets for the Games go on sale next month.

Expert Wants Assisted Suicide Law Reform In UK

August 29, 2011

Terminally ill patients should receive medical help to commit suicide if they want to die, a government adviser has said.

Martin Green, a social care expert for the Department of Health, said those who were physically unable to end their own lives were being deprived of “choice” and “autonomy” in Britain where assisted suicide remains illegal. He has now called for a change in the law.

In an interview with The Daily Telegraph, he said policy should be decided with either a referendum or a free vote in Parliament.

“If you’re going to give people ‘choice’, it should extend to whether or not they want to die,” he told the paper. “If people have got the capacity to make an informed choice then it is my view that they should be allowed to make the informed choice.”

Last year, the Director of Public Prosecutions published revised guidelines which stated that assisted suicide would remain a criminal offence in England and Wales but that individual decisions on prosecution would depend on the circumstances of each case.

The guidance made clear that someone acting out of compassion, to help a terminally ill patient with a “clear, settled and informed wish to die”, is unlikely to face the courts.

However, the offence is still punishable by up to 14 years in prison and there is no legal protection for doctors or other medical professionals who help someone to end their life.

Mr Green, the chief executive of the English Community Care Association, which represents nursing and care home groups, said the decision to commit suicide was therefore not an available choice.

“In terms of people who have cognitive function, it seems to me to be wholly consistent to say, if you’re going to give people choice and control and autonomy, it should extend to whether or not they want to die,” he told the paper.

A Ministry of Justice spokesman said: “The Government believes that any change to the law in this emotive and contentious area is an issue of individual conscience and a matter for Parliament to decide rather than Government policy.”

Derek Paravacini

August 29, 2011

An Update On Rania

August 28, 2011

I read this on Facebook last Thursday. Looks like Rania can stay for at least three years. This is fantastic news and the family have my best wishes.

High Court Orders Halt To Classroom Cuts After Children’s Charity Legal Challenge

August 27, 2011

The High Court has ordered Stoke-on-Trent City Council to halt plans to cut educational support for deaf children.

The court is considering a legal challenge by the National Deaf Children’s Society (NDCS) for the council to reverse its cuts plan.

The NDCS has applied for a judicial review of the authority’s proposals which will be decided on 12 September.

The city council was planning to cut some teachers who visit and support deaf children in classrooms.

It was also planning to change the criteria which determined the support children got.

‘Reckless decision’

A spokesman for the council said it would not comment on the ruling until next week.

The High Court has ruled the council is unable to make any changes until the court has considered the NDCS application.

The charity said the council wanted to reduce the number of teachers of the deaf by one next week, meaning a reduction from six to three in less than two years.

The NDCS has called the plans “reckless” and claimed it would leave three teachers to cover more than 200 children.

It said the council is in breach of the law by failing to properly assess the impact the cuts would have on deaf children and by bringing in changes that risk putting deaf children at an even greater disadvantage.

Jo Campion, NDCS deputy director of policy and campaigns, said: “The High Court’s decision will be a relief to parents of deaf children in Stoke who have been in a constant state of uncertainty about their children’s future for months.

“Deaf children across the country are being left behind in the classroom and particularly in this case the council’s decisions to make cuts have been reckless.

“It is great news that the High Court has recognised the need to urgently protect these deaf children whilst it considers whether the case should be granted a judicial review.”

Do Not Resuscitate Orders: Open Thread

August 27, 2011

Today’s Guardian leads with the case of a man who is suing Cambridge’s Addenbrookes hospital and the Department of Health after a Do Not Resuscitate order was followed for his wife. The order was in her file against her wishes and without her knowledge.

Another article, published on the Guardian website yesterday, says that according to General Medical Council guidelines, DNR orders are placed in files on decisions made by doctors. Patients and families have no say in this.

Here’s where I admit that I don’t know enough about this issue to write a detailed post on it myself. But I do know that this is an issue which is well worth discussing. I would be very interested to hear any views, thoughts or experiences you may have to share on the case or the issues it raises.

Please treat this as an open thread and share these in the comments section below.

Starbucks Pays £45,000 For Sacking Employee Because Of Dwarfism

August 26, 2011

This article is a week old, but it carries very good news about the case of Elsa Sallard, which I featured on Same Difference earlier this year.

London 2012 Paralympic Schedule Announced

August 26, 2011

For anyone who is interested, the schedule for the London 2012 Paralympics has been announced today.

Scope To Take Over Cornwall Centre From Vitalise

August 26, 2011

This update on the story featured earlier this month is very good news, particularly, of course, for the service users and their carers.

Disability charity Scope has stepped in to run a day centre in Cornwall after another charity announced it could no longer provide the service.

Vitalise said it was pulling out of Churchtown at Lanlivery, near Bodmin, because its lease was expiring and it wanted to refocus on core services.

Scope will take over as the provider of day services on 28 September.

About 70 people with learning and physical disabilities currently use the service.

Vitalise made the decision to transfer its operations at Churchtown to other providers because its 10-year lease on the site was due to expire in September.

The charity also said it wanted to refocus on its core service, the provision of short breaks with care for people with physical disabilities, at its three UK respite break centres.

Ruth Sutherland, director of services for the disability charity Scope, said: “Scope is delighted to be taking over the management of the day service based at Churchtown.

“We have a long history with the site and a commitment to developing excellent services for disabled people in Cornwall, so we were very pleased when Vitalise began to discuss the service’s future with us.”

The two organisations have worked with Cornwall Council who will pay Scope at the same level as it did Vitalise.

Vitalise chief executive Chris Simmonds said: “Vitalise has been supporting people with disabilities at Churchtown for nearly a decade and we’re proud of all we have achieved there, but now regrettably our time is up.

“I am confident that the Churchtown day service will be in safe hands with Scope.”

The Mid Cornwall Hub at Par Moor, which was announced earlier this month, will still open on 12 September.

Why I’m Glad Tulisa Is An X Factor Judge

August 26, 2011

My latest article for Suite 101 explains why I’m glad Tulisa Contostavlos from N Dubz has been chosen as one of the new judges of the X Factor in the UK.

Don’t worry, readers, this isn’t teenage fan scribble- the reason is disability-related.

Tania Bonello

August 25, 2011

Meanwhile, profoundly deaf teenager Tania Bonello, 16, from Colindale, north London, has gained seven GCSEs, moving a step closer to her dream of becoming a crime scene investigator.

Tania passed exams in Japanese, double science, British Sign Language level 2, English, performing arts, maths and religious education.

She has been supported by a special teacher who sits with her during lessons to make sure that she is understanding everything.

Tania, who goes to Hendon School, said: “I find it hard because I have to work harder and focus more than the other children just to be sure I get all the information and work done.”

Jo Campion from National Deaf Children’s Society said: “Although deafness is not a learning disability, government figures show that 65% of deaf children in England fail to get five grades A* to C at GCSE, including English and maths.”

Ellie Simmonds ‘Over The Moon’ With Her GCSE Results

August 25, 2011

There was also success for double Paralympic swimming champion Ellie Simmonds, 16, who won the 100m and 400m freestyle in Beijing in 2008.

She gained four B grades, four Cs and one D, despite sitting four exams while at a training camp in Spain.

Her agent said she was “over the moon”.

Well done Ellie! She has my best wishes in and out of the pool.

PC David Rathband Arrested

August 25, 2011

The policeman blinded by gunman Raoul Moat has been arrested on suspicion of an assault at his home.

PC David Rathband, 43, was held on suspicion of carrying out an attack at his home in Cramlington, Northumberland, on Tuesday night.

A police source told the BBC that he was later allowed home pending further inquiries because he had complained of feeling unwell.

Mr Rathband was shot by Moat as he sat in his patrol car on 3 July 2010.

Samantha Stobbart, Moat’s ex-girlfriend, was shot by the gunman, who killed her new boyfriend before shooting himself after a manhunt.

Last year Mr Rathband, who is married to Kath and has two teenage children, set up the Blue Lamp Foundation, a charity offering help to injured members of the emergency services.

Subtitle Glasses At The Cinema

August 25, 2011

It seems to be the week when every disability group is talking about trying to make cinemas more accessible! These subtitle glasses could be a real step forward for cinema audiences who can’t hear. Please click the second link above to see a subtitled video of Charlie Swinbourne trying them out.

People who are deaf or hard of hearing have long complained that going to watch a film can be an unsatisfactory experience, with subtitled films on at unsociable times and often suffering from technical problems.

But a solution could soon available in the form of special glasses which allow the wearer to see subtitles directly in front of their eyes, giving them the freedom of choice afforded to hearing people.

Graham Satchell reports.

Sailability Club Gets Lottery Grant

August 25, 2011

A Shropshire sailing club has been awarded a £10,000 Big Lottery Fund grant to give disabled people the chance to take part in the sport.

Telford Sailability, based at Priorslee Lake, said the money would pay for a new dinghy as well as a hoist and specialist safety equipment.

The club said it hoped to work with local groups, including young people and stroke victims.

Telford Sailability was founded last year by Paul and Celia Devey.

Mr Devey said: “Sailing is one of the few sports in which able-bodied and disabled people can participate side-by-side, and the emphasis is on what people can do, not what they can’t.”

Jody McIntyre ‘Wins’ Police Complaint

August 24, 2011

I’m pleased to read this:

The police complaints watchdog has partially upheld a complaint from a protester dragged along a road after being removed from his wheelchair.

The IPCC said Jody McIntyre might have been assaulted by an officer using excessive force, but said it was too late to prosecute.

Mr McIntyre was taking part in student fees protests in December 2010.

In May Scotland Yard cleared officers who had moved Mr McIntyre based on the “perceived risk” to him.

The Independent Police Complaints Commission said it had now recommended “management action”, rather than more serious disciplinary proceedings, against the officer who had dragged Mr McIntyre across the road.

Mr McIntyre was among thousands of people who protested in central London on 9 December against student tuition fees.

He was outside Parliament where he said he was hit by a baton, taken out of his wheelchair and dragged across the road. Footage of the incident was later distributed online.

In a statement, the IPCC said that it had accepted the Metropolitan Police’s own findings in relation to a number of Mr McIntyre’s complaints.

The watchdog agreed officers had acted appropriately when they removed him from his wheelchair because they believed that he was in danger.

However, the watchdog said one officer had used “excessive force” by dragging Mr McIntyre along the road.

“The IPCC believes there was an indication that a criminal offence of common assault may have been committed and the matter should therefore have been referred to the CPS,” said the watchdog.

“However, the six-month time limit in which such a prosecution could be commenced had already passed by the time this appeal was lodged.

“The IPCC has upheld this part of the appeal and believe that that officer’s behaviour has fallen below the standards of professional behaviour and should be subject to management action.”

The watchdog accepted the Met’s conclusion that it could not find a case to answer against any particular officer for the baton strike – but it added that Mr McIntyre should receive an apology because he had a genuine grievance.

Speaking to the BBC, Mr McIntyre said the IPCC report showed he had been mistreated – but he said he could not understand why the watchdog had not criticised his removal from his wheelchair.

“This is clearly a very strange interpretation on the part of the IPCC and certainly not an interpretation that I agree with,” he said.

“What they are essentially saying is that the police officer was right to push me out of my wheelchair but then wrong to drag me across the road. It doesn’t make any sense to any rationally minded person.

“I think an apology on behalf of the police would be necessary – but this apology is completely insufficient and it’s far too little, too late.

“I am currently in discussions with my solicitor about further legal action that we will be taking.”

New MS Research Approved

August 24, 2011

The go-ahead has been given for further research into a procedure which could relieve symptoms for some people who have multiple sclerosis.

The procedure, called percutaneous venoplasty, aims to improve blood flow from the brain by using a small inflatable balloon or stent to widen narrowed veins in the neck which carry oxygen-depleted blood.

Multiple sclerosis is the most common disabling neurological condition affecting young adults. Around 100,000 people in the UK have MS.

The National Institute for Health and Clinical Excellence (Nice) is proposing in its draft guidance that the procedure should be used in the context of research only, so further evidence on its safety and clinical efficacy can be developed.

It has been suggested that there could be a link between narrowed veins – called chronic cerebrospinal venous insufficiency, or CCSVI – and the progression of MS.

Professor Bruce Campbell, chairman of the independent committee that develops Nice’s interventional procedures guidance, said: “Multiple sclerosis can be a distressing and disabling condition with a lack of effective treatments.

“This means that it is really important to find out whether percutaneous venoplasty is clinically effective and safe for use in the NHS.

“Based on the existing evidence, we believe that clinicians should only consider offering percutaneous venoplasty as a treatment option for people with MS who fit the diagnostic criteria for CCSVI, as part of structured clinical trials.

“In particular, we would welcome controlled research comparing percutaneous venoplasty against ‘sham venoplasty’, in the same way that drug treatments are compared to a placebo.

“This is so that we can learn more about whether venoplasty works and for how long. Further research could also improve the understanding of the relationship between MS and CCSVI, as this is very unclear at present.”

A Sponsored Walk To Fundraise For A Wheelchair

August 24, 2011

The best part is that 20% of the profits are going towards Kaliya Franklin’s wheelchair. The online donation page is here.

I’m Back On Able Life!

August 24, 2011

Yes, readers, after a short summer break, I’m finally back on Able Life on Able Radio, starting tonight at 8pm. George Johnson and I will be discussing wheelchair access in cinemas. As usual, I have a sneak preview of what we said for my readers, which you can listen to right now by clicking here.

Amputee Soldier Criticises NHS Prosthetics

August 24, 2011

An amputee soldier from County Durham has criticised the quality of artificial limbs provided by the NHS.

Chris Parkes lost a leg in Helmand in Afghanistan in 2009 and has a prosthetic limb provided by the Army.

He described NHS prosthetics as “almost prehistoric” and said the leg a friend received from the health service was like a pirate’s “peg leg”.

A spokesman for the NHS said it was reviewing the “effectiveness of prosthetics services” for veterans.

Rifleman Parkes said he was worried when he left the Army any replacement limbs he needed would be inferior to the one he had now.

He said: “There’s no way… I would get the same level of technical prosthetics.

“I’ve got friends who are amputees who’ve received their prosthetics through the NHS and it’s almost prehistoric, looking at some of their prostheses and then looking at some of the ones you will receive through military care.

“The leg I’m wearing now is designed for stability. It has an adjustable heel so I can run. The feet will bend. It’s not the most advanced, but it’s quite advanced.”

‘A wooden stick’

Rifleman Parkes, no longer able to serve on the front line with The Rifles regiment, has decided to leave the Army.

His concern is that he might have to rely on help from charities to pay for anything more advanced than that offered by the NHS.

He said: “One of my friends on the NHS who has a prosthetic, it’s a wooden stick basically.

“If you imagine a pirate who has a peg leg it’s not too far from the truth. It’s half wood, half plastic.”

‘Personal objective’

General Sir Nick Parker, Commander-in-Chief of Land Forces, was also concerned.

His son lost his legs in an explosion in Afghanistan in 2009.

He said: “I have a particular interest in prosthetics and I think it’s terribly important that those who leave the Army have the confidence that they will get the same level of prosthetic care when they leave as when they’re in and I will certainly make it a personal objective to ensure that that happens.”

A spokesman for NHS North East said it was looking at veterans’ rights to have “the highest quality Ministry of Defence prosthesis”.

A statement said it was reviewing the “effectiveness of prosthetics services in the NHS in England for veterans who have lost a limb while serving their country”.

“No final decisions have been made yet – but the intention is to ensure that the standard of a prosthesis which a veteran might receive following rehabilitation is maintained when their care is transferred to the NHS.”

Remploy Closures: Good Or Bad?

August 23, 2011

About 2,300 disabled workers fear that they could lose their jobs if a proposal to close the remaining 54 Remploy factories goes ahead. But could such a move actually help more people into work?

Paul, a worker from Sheffield, has been with Remploy for 33 years and is typical of those who fear for their futures if it is wound down.

“I weld the little bits for coffee tables that screw on underneath and keep the top on. It’s not a bad little job.

“If I lose my work, I don’t want to be called a layabout. I’m going to try and find another one but I’ve been turned down before. I know for a fact it’s because they think I’m, you know, ‘unwell’. They don’t want my sort.”

Remploy factories were established 66 years ago as part of the creation of the welfare state. The organisation gave jobs to disabled ex-coal miners and injured servicemen coming home from World War II.

In recent years, the organisation has been changing from a “sheltered” employer to a service which assists people with disabilities into mainstream jobs.

James Stribley, a Remploy convener for the GMB union and a former factory floor worker, has similar feelings to Paul: “Remploy is my life. I don’t know what I’d do if it closed, I just don’t know.

“I wouldn’t be able to do a physical job, I have chronic pain in my arms. I was working a machine but you’d have somebody to help you at Remploy. Other employers aren’t as understanding towards people’s disabilities.”

‘Not meeting aspirations’

Remploy’s employment arm assisted 20,000 people with disabilities into mainstream work last year, and its factories now have 2,300 employees due to a voluntary redundancy programme – about half of the workforce it had in 2008.

The government and Remploy describe the commercial side of the business as loss making, and a recent report has put the future of the factories into sharp focus.

The report, commissioned by the Department for Work and Pensions (DWP) and carried out by Liz Sayce, chief executive at the disability rights charity Radar, was presented to Parliament last month.

Ms Sayce praised the government’s Access to Work scheme, which provides funding to make jobs accessible. But she said it served just 37,000 people per year and was the government’s “best kept secret”.

She suggests 35,000 extra people could be supported into work for the same price it costs to support the 2,300 people currently at Remploy factories.

She recommends the withdrawal of government money from Remploy to fund Access to Work instead.

The minister for disabled people, Maria Miller, later told the BBC a third of the specialist disability employment budget went towards supporting individuals in segregated work at Remploy.

She added: “That money could be used to support far more people to be in the sorts of mainstream jobs that really meet the aspirations of disabled people now, rather than perhaps the aspirations that they had in the Second World War when Remploy was first set up.”

An average person receives £2,600 via Access to Work, whereas one place at a Remploy factory costs £25,000, according to figures provided by the DWP.

These are not like-for-like figures, however. The GMB supports Access to Work, but is quick to say it is not the same as a job.

Access to Work provides money for taxis to and from work, taxis within work, sign language interpreters, support workers, equipment and workplace adaptions so that disabled people can work in a mainstream environment or continue to do a job they are beginning to find difficult. You need to have a job first, however.

It remains to be seen whether or not the extension of the scheme will result in more disabled people in mainstream employment, as barriers to work such as prejudice cannot easily be solved with money.

‘Stigma and mickey-taking’

Remploy union representative Steve Morris says that Remploy gives real meaningful work to its employees, and thinks Ms Sayce’s plan is idealistic.

“The workers have already worked in outside industry. We don’t live in a politically-correct rose-tinted spectacles world that some academics believe is out there. There is still stigma and mickey-taking on the ground, and they don’t want to go back to that if the factories close.

“The economic climate at the moment is dire.

“Those companies that have got good disability awareness are more likely to be in the public sector which is an environment of cuts at the moment, and there are few opportunities to be had.

“The other thing is they are fully aware that their colleagues who took redundancy three years ago went from the factory to benefits and are still unemployed.

“Most people like to contribute to society and part of doing that is to be at work.”

Worker buyouts?

Ms Sayce’s report has echoes of the last 40 years of the disability movement embodied in it.

Grassroots organisations have fought against segregation in work, and more generally in education and domestic living.

They believe that if disabled people mix with non-disabled people more often, it will nurture a greater understanding of disability and ultimately lead to acceptance and more accessible environments.

Charities such as Mencap, Mind and the Disability Alliance have lined up to support the recommendations.

Jaspal Dhani, CEO of grassroots organisation UK Disabled People’s Council, says: “I think we have to understand the history behind schemes like Remploy, which were set up originally when disabled people were institutionalised and government thought it would be therapeutic.

“It was a good thing then.

“For those disabled people that can work, the starting point, perhaps the only point, is they should be able to provide for themselves in open work.

“They should be able to work in a company, whether big or small, that’s operating in the wider community and should be included in that mainstream society without having to depend on an institutionalised working service.”

Though government funding could be taken away from Remploy factories, Ms Sayce suggests that co-operatives could carry them on.

But Mr Morris is sceptical that any new money will be forthcoming to help with worker buyouts, and says people with disabilities need more help gaining new commercial contracts, not less.

A spokesperson from the DWP said: “No decisions have been made about Remploy. We said we would consult on the recommendations put forward by Liz Sayce and that is what we are doing.”

It does, however, say that it is “attracted to” the idea.

The consultation process is under way and is due to end on 17 October.

Oscar Pistorius’ Involvement In Olympics Will Not Affect Paralympics

August 23, 2011

Oscar Pistorius’ likely involvement in the London 2012 Olympics will not detract from the Paralympic Games, according to International Paralympic Committee president Sir Philip Craven.

Pistorius recently ran the ‘A’ qualifying time for the Olympics and is in Daegu, South Korea with the South African squad awaiting competition in the World Athletics Championships, which begin on Saturday August 27.

The double amputee looks set to compete in both the Olympics and the Paralympics at London 2012, leading to some suggestions that Pistorius’ involvement may devalue the importance of the Paralympics.

But Craven, a five-times Paralympian in wheelchair basketball, insisted that Pistorius is a Paralympian to the core.

“I know Oscar well and I do not believe his involvement in the Olympics will detract from the Paralympics,” said Craven.

“I welcome the news that he wants to compete at the Olympics but I know that Oscar is a Paralympian through and through.

“He has shown he is committed to Paralympic sports. He competed in the BT Paralympic World Cup and will be with us on International Paralympic Day in Trafalgar Square on September 8.”

Tim Hollingsworth, the new chief executive of ParalympicsGB, also threw his weight behind Pistorius’ ambitions but said he knew where the sprinter’s true allegiance lay. “I know that the Paralympics matters most to Oscar,” said Hollingsworth.

Seven-times Paralympic gold medallist Sarah Storey is another athlete hoping to compete in both the Olympics and the Paralympics next year.

If the swimmer-turned-cyclist succeeds in her ambition she will become the first Briton to represent the country in both Games.

Storey won team pursuit gold with Wendy Houvenaghel and Joanna Rowsell at February’s Track World Cup in Manchester and Hollingsworth insisted this showcased the excellence of Paralympic sport in the country.

“She’s been absolutely clear that she’s a very proud Paralympian,” said Hollingsworth.

“The Paralympic Games is the pinnacle of her career. But I saw her win the team pursuit gold in the World Cup and it’s a fantastic way to demonstrate that these Paralympic athletes are truly world class.”

Surgeon Removed Brain Tissue Instead Of Tumour

August 23, 2011

A Warwickshire hospital trust has admitted liability after a man suffered permanent brain damage after he was subjected to unnecessary brain surgery.

John Tunney, 63, from Sutton Coldfield should have been given tablets to control a pituitary gland problem.

But instead he was subjected to an unnecessary biopsy by a surgeon who then wrongly removed part of his brain rather than the tumour.

The former paramedic is now partially sighted and needs full-time care.

University Hospitals Coventry and Warwickshire NHS Trust said the surgeon involved was no longer involved in such surgery.

Richard Kennedy, chief medical officer for the trust, said: “I very much regret the tragic outcome for Mr Tunney and his family and on behalf of the trust would like to apologise for this.”

Benign condition

He added they had reviewed their “governance process” and he was confident measures had been put in place “to prevent this type of incident reoccurring”.

Irwin Mitchell Solicitors, for Mr Tunney, said he underwent a number of tests and procedures, initially at Good Hope Hospital but, following an MRI scan which detected abnormalities around his pituitary gland, he was referred to Walsgrave Hospital.

Blood tests were taken to determine hormone levels which would have revealed Mr Tunney was suffering from a benign condition known as prolactinoma which could have been controlled with medication.

But the blood tests were not reviewed prior to the biopsy and in April 2008 Mr Tunney underwent a biopsy on the pituitary tumour at Coventry’s Walsgrave Hospital.

During the operation, he suffered a brain haemorrhage and serious neurological injuries when the surgeon wrongly removed normal brain tissue.

Timothy Deeming, a medical law expert with Irwin Mitchell in Birmingham, said: “The fact that the surgeon managed to remove perfectly healthy tissue rather than a sample of the tumour tissue is, in itself, an appalling error.

‘Devastating effects’

“To then find that the procedure was totally unnecessary because clinicians had failed to review a blood test, really does add insult to injury.”

He added that before a settlement could be reached the firm needed to evaluate the cost of the lifelong care and support that Mr Tunney would now require.

Mr Tunney’s wife Pamela said: “John’s brain injury has had devastating effects on him.

“Prior to the surgery he was a very easy going person who was always active and on the go. To see the change in him and to know that it was all entirely avoidable is extremely upsetting.

“This mistake is not something that the hospital can just take back. I pray that they don’t make this mistake again and no other family has to experience seeing their husband suffer the pain and loss that John has.”

 

Mother Spared Jail For Plotting Attack On Disabled Daughter’s Facebook Bully

August 23, 2011

A mother who joined a revenge attack on a man responsible for a vile campaign of internet abuse against her disabled daughter has been spared prison.

Sylvia Hooper, 52, was described as a ‘decent and law-abiding’ woman who dedicated her life to her seriously ill daughter Kim Arnold.

But she snapped after looking on helplessly as a cowardly bully sent her a series of appalling comments via Facebook.

She faced a jail sentence after identifying Christopher Berwick and confronting him outside his home in Chatham, Kent.

But a judge – who labelled the messages ‘disgraceful and shameful’ – took pity on Mrs Hooper after hearing they were part of a long-term campaign.

The case is the latest evidence of the growing impact of online bullying and abuse through social networking sites.

Known as ‘trolling’, it sees abusers, who often hide behind a veil of anonymity or false identities, deluging their victims with cruel taunts.

Campaigners have repeatedly called for websites to take swifter action against so-called ‘trolls’ responsible for pain and suffering.

Miss Arnold was sent a series of messages via a false Facebook account that left her deeply depressed, Maidstone Crown Court was told.

One labelled her a cripple and said the wheelchair user should be left to ‘roll down a hill.’

Another message read: ‘Your mother should have had an abortion. She only had you because she felt sorry for you.’

Mrs Hooper realised the culprit was Berwick, who lived nearby, and joined her son Robert and his friend Soloman Taylor outside his home.

Mr Hooper, 19, punched the bully after his mother said ‘hit him’ and Berwick was then taken back to the family home by car.

He was forced to crawl inside and make a ‘grovelling apology’ to his victim while on all fours. At one point he was hit on the chin with a rolled up newspaper.

Prosecutor Neil Sandys said Berwick originally tried to blame his then girlfriend but eventually admitted being responsible.

He said the Facebook exchange was ‘low, mean, base and shameful’ and added that Berwick admitted doing it before.

Mrs Hooper’s solicitor Catharine Donnelly said the comments were ‘beyond the pale’ and told the court ‘none of us would be here today’ without his actions.

Speaking about Mrs Hooper, she said: ‘She is a decent woman who has devoted herself to her daughter. She has led a decent and law-abiding life.

‘It is clear she is a woman who will never trouble these courts again. She was an encourager, rather than a hitter.’

Danny Moore, for Mr Hooper, said Berwick got a kick out of ‘playing mind games with a severely disabled young lady’.

He highlighted how police told the victims there was nothing they could do and the bully was not prosecuted for sending malicious messages.

All three admitted assault but denied false imprisonment and the judge ruled that not guilty verdicts should be entered.

Judge Richard Polden said it ‘troubled him’ that Mrs Hooper had said, ‘hit him’, but accepted that Mr Hooper was acting out of a ‘protective instinct’ to his sister.

He said: ‘I sentence you on the basis that Mr Berwick sent messages that were wholly disgraceful and shameful but then tried to put the blame on his girlfriend.’

Mrs Hooper was given a conditional discharge. The two men were given community orders which included voluntary work.

Caring Too Much

August 23, 2011

 

http://twitter.com/#!/scope/status/105919749631901698

Link Between Physical Or Terminal Illness And Suicide

August 23, 2011

At least 10% of suicides in Britain are linked to terminal or chronic illness and account for over 400 deaths every year, according to a Demos report.

Louise Bazalgette, who works for the Commission on Assisted Dying and is a researcher at Demos, and Professor Jonathan Waxman of Imperial College London debate why there appears to be a “frenzy of interest” about suicide.

DLA Fraud Woman Filmed On Water Slide

August 22, 2011

A Cardiff woman has admitted claiming £25,000 worth of benefits after pretending to be severely disabled.

Annunziatina Attanasio, 51, claimed the highest rate of mobility and care for five years before she was caught.

She was filmed walking normally, as well as going down a water slide.

She claimed an amount which, says the Department for Work and Pensions, is meant for “people who are barely able to walk and need round-the-clock care”. She will be sentenced on 16 September.

Donna James, DWP’s fraud manager for Cardiff and Newport, warned potential fraudsters: “You will be caught.”

She added: “We have a realm of investigative techniques that we are able to use and we put those to our best use to bring all these sort of cases before the court.”

Trailblazers New Campaign- Same Ticket, Second Class Service

August 22, 2011

I have just received the press release below from The Muscular Dystrophy Campaign.

 Disabled movie-lovers are receiving a second-class service at major cinema venues across the country, according to the results of an undercover investigation by young disabled cinema-goers, released today.

The Muscular Dystrophy Campaign’s Trailblazers, a group of 350 disabled campaigners aged 18-30 who tackle social injustices faced by young disabled people, visited 125 independent and chain venues to report on issues faced by disabled customers. The campaign was sparked after young disabled people told of struggling to enjoy a trip to see a film with friends and family – even at cinemas just a few years old.

The group describe how many of the worst access and service problems for disabled customers occurred at branches of the major UK cinema chains, while smaller chain and independent venues fared comparatively well. The 100 people who took part in investigations reported:

  • Poor or very poor views of the screen from wheelchair-accessible seating at one in three major cinema venues
  • Over half of major chain cinemas have uncomfortable accessible seating areas, causing discomfort or even pain while viewing
  • Staff with poor or very poor disability awareness at a third of major chain cinemas, often leading to rude or embarrassing treatment of disabled customers
  • Nearly half of all the cinemas in the study did not offer an online ticket service for disabled customers
  • Single accessible screens at multi-screen cinemas mean some films are never available to wheelchair-users locally

While many cinemas both chain-operated and independent, were praised by the Trailblazers, the group says that the physical access issues, poor staff training and poorly thought out support found at some venues is unacceptable for paying customers and must be tackled. A report and documentary on the investigation have been produced, in a bid to convince cinema operators to raise the bar on accessibility.

Visiting the cinema is a particularly popular social past time with many young disabled people – on average 12 per cent of cinema audiences will have a disability.

Trailblazers campaigner Fiona Anderson (22) from Bury has the muscle condition minicore myopathy. She said that the important social aspect of a visit to the cinema is compromised at many venues.

“I went to test out my local cinemas with a group – a trip to see a film is a great, not too physically demanding activity for me to do with friends. Or, at least, it’s supposed to be. I was very disappointed to find that at two of the cinemas I investigated, my friends and I were split up when seated, as there was only one other seat next to the wheelchair space. Separating us deprived me of that social aspect of a film that is so important. Elsewhere we had a fairly positive experience. At one cinema the staff were fantastic – very helpful and ready to quickly assist with buying tickets. This kind of attitude can make a big difference to disabled customers, and is an area that costs so little to improve.”

Trailblazer Jagdeep Sehmbi (28) has the muscle-wasting condition limb girdle muscular dystrophy and is a wheelchair-user. Jagdeep, who investigated seven cinemas across Birmingham, said that cinema design is still failing to fully consider disabled customers:

“What I think really needs to be addressed is the design of auditoriums and seating for disabled people. I even went to one well-known cinema where major recent refurbishments have actually made it less accessible to wheelchair-users. People are often being given a very uncomfortable view and are unable to sit with groups of friends and family.”

The Trailblazers have now produced a charter laying out the standards of access and service that disabled cinema-goers should be able to expect of cinema operators and are calling for cinema operators to commit to working towards this benchmark. A petition has been launched for cinema-goers and members of the wider public to support the campaign, which will be presented at Westminster later this year.

Trailblazer Tanvi Vyas (27) from London who has led the campaign, said:

“When people go to buy a ticket to see a film they have simple expectations. To be able to book a seat in advance, to be able to sit with their companions, to have a reasonable view of the screen and to be able to buy refreshments. At many venues, disabled customers find that these very basic standards do not extend to them – despite paying exactly the same price for a ticket as everyone else.

“We have seen that tight budgets, historic buildings and physical access issues needn’t be an obstacle to making disabled customers feel valued. Yet at many major venues “disabled access” is still about putting in a ramp or two and putting a couple of wheelchair–accessible seats in the unpopular area in front of the screen. It really is time we left this kind of thinking behind.

“We hope that this charter will help to raise the bar on accessibility standards at cinemas and encourage cinema operators to think more progressively about their disabled customers.”

Figures within the British film industry, including Nick Frost, Simon Pegg and Miranda Richardson have already expressed their support for the campaign. Giving her signature to the petition, actress Miranda Richardson said:

“It would be great to see the major cinemas really taking on board what they should be doing to bring cinema accessibility fully into the twenty-first century. Everybody should have the opportunity to enjoy a great film, and as this petition shows, it is often the small considerations that make a big difference to the whole cinema experience for disabled movie-lovers.”

The Muscular Dystrophy Campaign Trailblazers cinema petition can be signed through the Trailblazers website: www.mdctrailblazers.org.

Why Do Disabled People Take On Dangerous Physical Challenges?

August 22, 2011

A new documentary with Prince Harry follows four wounded servicemen on a trek to the North Pole. But why do so many disabled people embark on adventures that most “able” people wouldn’t even think of doing?

The foursome accompanying Prince Harry to the North Pole includes Steve, who had his back broken, and 26-year-old Jaco, who is missing part of an arm.

They are far from being the first injured ex-servicemen to test their new bodies when faced with a disability.

In 1947, Denny Denly, who became a wheelchair user after contracting polio while on active service, fancied a holiday in Switzerland. He rode 1,500 miles across the French Alps on a petrol-powered tricycle with a top speed of 30mph.

His journey, which involved climbing to 8,000 feet (2,440m) through mountain passes, was documented by the BBC Home Service. Public reaction to the trip was so positive it led to the launch of the Invalid Tricycle Association, a precursor to today’s Disabled Motoring UK.

Left blinded and with part of a leg missing by a landmine in WWII, climber Syd Scroggie refused to be daunted and completed 600 ascents.

“Whatever we call the hills, it has nothing to do with sight,” he once said. “It is an inner experience and can be as poignantly savoured with your eyes shut as open.”

It’s not just ex-servicemen. All flavours of disabled person seem drawn to pushing themselves way beyond what’s called for in their daily routine.

Dave Heely, who went blind at 18, has just completed 10 marathons in 10 days, while travelling between each one on the back of a tandem. That’s 750 miles of cycling and 250 miles of running, from John O’Groats to Lands End.

Myles Hilton-Barber, also blind, is arguably the best known disabled adventurer in the UK. He lost his sight at 21 but didn’t start his career in adventuring until he reached 50. He now travels the world making a living as a motivational speaker.

He has completed an 11-day ultra-marathon across China from the Gobi Desert to the Great Wall. He became the first blind pilot to undertake a 55-day, 13,000 mile (21,000km) microlight flight from London to Sydney, using a talking navigation device.


So far in 2011…

  • In April, paralysed adventurer Barry West reached the top of Ben Nevis. He was pulled and pushed up Britain’s highest mountain by 18 friends. It took eight hours
  • In May, ex-motorbike stunt man Eddie Kidd walked the London Marathon route in 55 days with the help of a special frame. Eddie received a brain injury in a motorbike accident in 1996
  • In July, soldier Joe Townsend, who lost both legs in Afghanistan, completed the Ironman UK challenge. The event, which took him 13 hours, involves a 2.4-mile swim, a 112-mile bike ride and a marathon

Hilton-Barber believes that conquering these incredible feats of human endurance has changed his perspective on what it means to have a disability.

“Before I started doing this, I thought I needed sight to be happy. Now I realise it isn’t about focusing on what you can’t do, it’s saying what you want to do and then figuring out what you can achieve. I always wanted to be a pilot.”

But not all disabled people feel the need to test their physical and mental limits, says disability activist and campaigner Barbara Lisicki.

“I will never be able to climb a mountain or trek across the jungle but I don’t care. In the disability arts and culture world we call this phenomenon ‘supercrip syndrome’.

“Disabled people doing things that non-disabled people struggle to do and that’s what makes them great. Most of us are actually fine the way we are and don’t feel the need to prove ourselves.”

The need to climb a huge mountain isn’t something that comedian Francesca Martinez, who has cerebral palsy, can relate to.


Find out more

  • Harry’s Arctic Heroes is on BBC One on Tuesday 23 August at 21:00 BST

“I’m too lazy to do something like that,” says Martinez, who was asked to take part in the BBC adventure programme, Beyond Boundaries, but declined.

“I told them, if you have a show called ‘lying on the beach in the Caribbean, call me’. My goal every day is to eat three big meals and to get at least 12 hours sleep.”

When Denly was driving his trike, disability unemployment was high and those who were in work often held posts in sheltered workshops or similar enterprises. Even today, 70% of blind people of working age are unemployed.


Pioneers

  • In 1998, Tom Whittaker became the first disabled person to reach the summit of Mount Everest. He lost a foot due to overexposure while climbing
  • In 2004, Michael McGrath became the first disabled person to lead expeditions to the North and South poles. He was diagnosed with muscular dystrophy aged 18
  • In 2007, Geoff Holt, who is paralysed from the chest down following a diving accident, became the first disabled person to sail solo around Britain. The 1,400-mile voyage took 109 days

So is taking on adventures a substitute for lack of success in life against ordinary measurements?

Heely believes that his adventures, and the media coverage they create, have helped prevent him becoming a statistic.

“I was made redundant from a sales role in the early 90s and being blind, I knew I wouldn’t have a chance of getting another similar job. It is thanks to my challenges that I’ve become a motivational speaker, working in schools.

“Each time I take on a new adventure and get some publicity off it, it gives me another couple of years employment.”

Newspapers regularly carry stories about disabled people pushing their broken bodies to the extreme.

Hilton-Barber believes that media attention is an important motivator for disabled adventurers. He says disabled people who see other people with disabilities pushing the limits are inspired to fight for a new sense of identity.

“It gives them status. Disability robs you of your confidence. I lost my dignity, my independence, but I can jump out of a plane and people will have respect for me.”

But Lisicki has her own theories on why the media relish these stories.

“The press is always happy to focus on the old tragic but brave stereotype. Earlier this year, 5,000 disabled people marched against government cuts. This got very little media coverage, because people find looking at a collective of disabled people uncomfortable.

“It’s much easier for them to focus on one individual and say ‘aren’t they marvellous?'”

But whether it’s for the love of adventure, to prove that disability is no barrier or, as Jaco from Harry’s Arctic Heroes says, “to bring back the feeling of being able to do something again”, the disabled adventurer phenomenon is bound to continue.

CP Girl’s Operation Raffle Donations Stolen During Manchester Rioting

August 22, 2011

Thieves have stolen raffle prizes which were donated to help raise money for a girl with cerebral palsy to have life-changing surgery in the US.

Canterbury Road Day Nursery in Davyhulme, Greater Manchester, was broken into between 18:00 BST on 9 August and 06:30 BST the following day.

They were due to be used in a raffle to help Ria Stonehouse, five, have surgery which would help her walk unaided.

Among the items were signed Manchester United and Manchester City shirts.

Other prizes included a Manchester United ground tour and a picture donated by the club, two chess sets and various smaller prizes.

‘Cynical opportunism’

Police said the prizes were worth more than £1,000 and the cost of damage to the ground-floor nursery was estimated at £500.

The thieves also ransacked an office before stealing the prizes.

One of the burglars also tried to start a fire with some cardboard but it did not ignite.

The first man was described as mixed race, in his late 20s or early 30s, and had dark stubble.

He was wearing a light coloured hooded jacket with reflective strips on the arms and body and dark toggles on the hood.

The other man wore a hooded jacket with a large reflective Armani logo on the back.

Det Con Ian Prescott, of Greater Manchester Police, said: “This is a particularly cynical bit of opportunism by these burglars because this was the night of violence and disorder in Manchester and Salford and they would have known this.

“We are absolutely determined to catch these men and we want the public to help – I am sure the community will be as shocked as we have been by the fact that such a worthwhile cause has been deprived of its contributions.

“The burglar we can see on camera is wearing a particularly distinctive Armani hooded top with an emblem on the back and we think someone will recognise it.

“We would also ask anyone to have a think about where the raffle prizes might be.”

He urged anyone with information to contact police.

Bionic Fingers For Chloe Holmes, 15

August 22, 2011

A schoolgirl from Swindon has become the youngest person in Europe to be fitted with bionic fingers.

Chloe Holmes, 15, lost her her fingers as a toddler when she suffered from septicaemia after contracting chickenpox.

She wore a prosthetic hand until her family paid £38,000 for the high-tech hand.

Her father Pete Holmes said: “We’d go out as a family and people would stare for the wrong reasons – they stare now in amazement.”

Underlying Cause Of ALS Found

August 22, 2011

A breakdown of a recycling system in cells appears to be the underlying cause of a fatal nerve disease.

Amyotrophic lateral sclerosis (ALS), the most common form of motor neuron disease, causes paralysis.

A US team, writing in Nature, found the flaw in the way nerve cells in the brain recycle protein building blocks, which means cells cannot repair themselves and become damaged.

Experts in the UK said that the findings were significant.

ALS affects an estimated 350,000 people around the world, including children and adults, with about half of people dying within three years of its onset.

The breakdown occurs in the recycling system in the nerve cells of the spinal cord and the brain.

In order to function properly, the protein building blocks in the cells need to be recycled.

But in ALS, that system is broken. The cell cannot repair or maintain itself and becomes severely damaged.

The scientists found a protein, ubiquilin2, which should be directing the recycling process, does not work in people with ALS.

This means the damaged proteins accumulate in nerve cells of the spinal cord and brain, causing their degeneration.

‘A big news story’

The researchers, from Northwestern University Feinberg School of Medicine, found this breakdown occurs in all three forms of ALS – hereditary (familial). ALS that is not hereditary (sporadic) and ALS that targets the brain (ALS/dementia).

Lead author Teepu Siddique said: “This opens up a whole new field for finding an effective treatment for ALS.

“We can now test for drugs that would regulate this protein pathway or optimise it, so it functions as it should in a normal state.”

They also say the finding could have a role to play in other neurodegenerative diseases, including dementia and Parkinson’s disease.

Dr Belinda Cupid, head of research development at the UK’s Motor Neurone Disease Association, said: “This is a big news story for motor neurone disease research.

“We’ve known for some time that the waste and recycling system in motor neurons is damaged, but this is the first time that there has been direct proof.

“This discovery provides researchers with an exciting new avenue to explore as they search for an effective treatment.”

ME Researchers Face Death Threats

August 21, 2011

The full extent of the campaign of intimidation, attacks and death threats made against scientists by activists who claim researchers are suppressing the real cause of chronic fatigue syndrome is revealed today by the Observer. According to the police, the militants are now considered to be as dangerous and uncompromising as animal rights extremists.

One researcher told the Observer that a woman protester who had turned up at one of his lectures was found to be carrying a knife. Another scientist had to abandon a collaboration with American doctors after being told she risked being shot, while another was punched in the street. All said they had received death threats and vitriolic abuse.

In addition, activists – who attack scientists who suggest the syndrome has any kind of psychological association – have bombarded researchers with freedom of information requests, made rounds of complaints to university ethical committees about scientists’ behaviour, and sent letters falsely alleging that individual scientists are in the pay of drug and insurance companies.

“I published a study which these extremists did not like and was subjected to a staggering volley of horrible abuse,” said Professor Myra McClure, head of infectious diseases at Imperial College London. “One man wrote he was having pleasure imagining that he was watching me drown. He sent that every day for months.”

Chronic fatigue syndrome – also known as myalgic encephalomyelitis (ME) – is common and debilitating. A recent BMJ (formerly the British Medical Journal) feature suggested that as many as one in 250 people in the UK suffers from it. Patients are sometimes unable to move and become bedridden, occasionally having to be fed through a tube. For more than 20 years, scientists have struggled to find the cause, with some pointing to physiological reasons, in particular viral infections, while others have argued that psychological problems are involved.

It is the latter group that has become the subject of extremists’ attacks. The antagonists hate any suggestion of a psychological component and insist it is due to external causes, in particular viruses. In the case of McClure, her “crime” was to publish a paper indicating that early studies linking the syndrome to the virus XMRV were wrong and the result of laboratory contamination. So furious was the reaction that she had to withdraw from a US collaboration because she was warned she might be shot.

A similar hate campaign was triggered by a study published in the Lancet earlier this year. It suggested that a psychological technique known as cognitive behavioural therapy could help some sufferers. This produced furious attacks on the scientists involved, including Michael Sharpe, professor of psychological medicine at Oxford University. He had already been stalked by one woman who was subsequently found to be carrying a knife at one of his lectures.

“The tragedy is that this tiny group of activists are driving young scientists from working in the field,” said Sharpe. “In the end, these campaigns are only going to harm patients.”

This point was backed by Fiona Fox, director of the Science Media Centre. “Using threats and intimidation to prevent scientists pursuing specific avenues of research or speaking out is damaging not just science. It harms society,” she said.

None of the scientists contacted by the Observer believed chronic fatigue syndrome was purely psychological. All thought external causes were involved. “There is an element that is heritable,” said Dr Esther Crawley, a consultant paediatrician at Bristol University. “We also know that in children it is often triggered by a virus infection, while in adults it is associated with social deprivation. Stress and adversity is involved. To call this yuppie flu – as people have done – is a complete misnomer.”

Crawley has spent years trying to unravel the causes, but her refusal to accept that the condition is a result only of organic external factors has resulted in her being deluged with hate mail from extremists. “You evil bastards … time is running out for you so you have [sic] better start denouncing your flawed inhumane therapy and pray to God for forgiveness,” said one.

“To those who are responsible for preventing us sick ME sufferers from getting the help we need … you will all pay,” stated another. “It is depressing to receive emails like that, but I make sure that it does not get me down,” said Crawley. “I do check packages that are sent to my office, however.”

Many of the extremists’ claims are bizarre, said Professor Simon Wessely, of the Institute of Psychiatry at King’s College London. “They say I am in league with pharmaceutical companies in order to suppress data that shows a link between viruses and the syndrome. But why on earth would drug companies do that? If they could link the condition to a virus they would be well on the way to developing lucrative treatments and vaccines. It is crazy.”

Wessely has installed speed dial phones and panic buttons at the police’s request and has his mail X-rayed. He gave up his research on chronic fatigue syndrome several years ago, though he still treats patients. “I have moved my research interests to studies of Gulf war syndrome and other conditions linked to war zones,” he said. “That has taken me to Iraq and Afghanistan where quite frankly I feel a lot safer – and I don’t mean that as a joke.”

Bernard Cribbins Launches New Wheelyboat For Disabled Anglers

August 20, 2011

A boat that will enable disabled anglers to use Farmoor Reservoir in Oxfordshire has been launched by actor Bernard Cribbins.

The £12,000 Wheelyboat will give access to wheelchair users wishing to go fishing on the reservoir’s waters.

Mr Cribbins, patron of the Wheelyboat Trust, said: “It is of huge importance to give disabled anglers the same opportunities as able-bodied anglers.”

Farmoor joins the Blenheim Estate as a Wheelyboat location in Oxfordshire.

Mr Cribbins, 82, added that the Wheelyboat would “provide hours of entertainment for many keen anglers.”

‘Cracking trout’

Matt Prior, conservation, access and recreation manager at Thames Water, said: “The facilities for fishing here at Farmoor are some of the best in the country so we want to make it accessible to everyone.

“We’ve already had a lot of interest from disabled anglers who want to go out on the Wheelyboat and we can’t wait to hear about their catches.”

Mr Cribbins also said when not in use the boats could be used by spectators watching the sailing.

“But they’ve got some cracking trout in there,” he added.

Mr Cribbins is no stranger to the county, having trained at Weston-on-the-Green when he was part of the the Parachute Regiment at RAF Upper Heyford in 1947.

He voiced The Wombles in the 1970s TV series and played Wilfred Mott alongside David Tennant’s Doctor Who.

He was appointed an OBE in June.

The Disabled Golf Open

August 20, 2011

Disabled golfers from around the world are gathering at the East Sussex National Golf Club in Uckfield for the Disabled Golf Open.

This year the Junior DBO is also taking place, for the first time.

Players from Sussex include Nick Champness and John Eakin from the Royal Ashdown Forest Golf Club, Brendon Slavin from the Seaford Golf Club and Roger Hurcombe who plays at the Boars Head Golf Club.

The Telegraph Interview Oscar Pistorius

August 19, 2011

You can read what he told them here.

Update On Simon Richardson

August 19, 2011

Double Paralympic champion Simon Richardson has sent a “huge thank you” to well-wishers after he was injured in an alleged hit-and-run.

The 44-year-old remains in a critical but stable condition after being in collision with a van while cycling on the A48 near Bridgend on Wednesday.

A 59-year-old driver has been released on police bail after being arrested.

Mr Richardson suffered multiple fractures but following a scan, surgeons have decided not to operate.

His sponsor, Phil Jones said on Friday that surgery to his back, pelvis and breastbone has not been ruled out but the breaks will be given a chance to heal naturally first.

He added: “The wounds to Simon’s left leg will be closed today in order to reduce infection risk.

“No trauma injury was received to his right leg [which he pedals with], so there is some relief that no injury has been sustained to it.

‘Overwhelming support’

“Simon sends a huge thank you for the many thousands of support messages he has received from all over the world.

“His wife Amanda and close family are drawing great strength from the overwhelming support they have received at this difficult time.”

Mr Jones confirmed that Mr Richardson, who won two gold medals and a silver at Beijing in 2008, is currently sedated.

UK governing body British Cycling has called for road safety to be highlighted at government level after a crash in which a Paralympian was seriously hurt.

Gareth Sheppard, the team’s performance manager, said: “All our thoughts are with Simon and his family”.

He called for increased awareness of cyclists by all road users: “You’ve got little protection as a cyclist because you are so exposed.

“We very much want to make sure racing and cycling in general on the road is safe and there does need to be a government-backed campaign on the issue.”

Paralympics GB chief executive Tim Hollingsworth added: “We’re deeply shocked by the news of Simon’s accident.

“He’s in our thoughts and, on behalf of everyone in the British Paralympic family, we wish him a speedy recovery.”

Mr Richardson was airlifted from the scene of the collision outside Crack Hill House, Bridgend, and flown to the University Hospital of Wales in Cardiff.

Rehabilitation

Mr Richardson had been involved in another serious crash in 2001, which left him permanently disabled.

He was hit by a car, which left him with serious leg and back injuries and no feeling down his left hand side.

Doctors recommended cycling would help his rehabilitation, so he continued, using a specially-adapted bike powered by his right leg.

It was during his five-year rehabilitation that he started competing and became a medal winner in Beijing 2008. He was later awarded the MBE.

South Wales Police have appealed for witnesses to the crash at about 09:45 on Wednesday, or anyone who may have been travelling between Cowbridge and Bridgend on the A48 and saw a white small van leaving the area, to come forward.

Anyone with information is asked to contact the South Wales Police roads policing unit on 02920 633438 or Crimestoppers on 0800 555111.

Children’s Charity Taking Legal Action Over Deaf Support Cuts

August 19, 2011

A deaf children’s charity has said it is taking legal action against Stoke-on-Trent City Council for “reckless” cuts to support services.

The National Deaf Children’s Society said the authority has halved the number of specialist teachers.

It claimed if further cuts went ahead three specialists would be left to cover more than 200 children.

The council said it would be inappropriate to comment on impending legal action.

The legal action calls on Stoke-on-Trent City Council to reverse its decision to cut educational support for deaf children.

Four of eight posts for specialist teachers of the deaf in the city have been cut over the past two years.

Another teaching post will be removed in September due to restructuring.

The charity said the council was in breach of the law on at least two fronts – by failing to properly assess the impact the cuts would have on deaf children and by bringing in changes that risk putting deaf children at a greater disadvantage.

‘Utterly reckless’

Suzanne Pitchford, mum of seven-year-old Sam, who is deaf, said: “The council is just not listening, so this is the only way forward now.

“Sam isn’t getting any support at school at all because of the cuts. They are not taking the needs of deaf children to heart and by taking away this support they are jeopardising our children’s futures.”

The charity’s deputy director of campaigns, Jo Campion, said: “The council has been utterly reckless in its decision to cut support that deaf children in Stoke-on-Trent need to achieve at school.

“They have rushed these cuts through with no regard for the impact on the future of these deaf children and have left parents to rely on rumour to find out what exactly has been going on.”

Teachers of the deaf provide support and advice for parents, help deaf children learn communication and language skills before they go to school and work with children and their classroom teachers throughout their education.

Assisted Suicide Could Be ‘Legalised’ After Case Of ‘Martin,’ 46

August 18, 2011

A 46-year-old-man who wants to die after a stroke that left him almost completely paralysed is bringing a groundbreaking legal action that could effectively lead to the legalisation of assisted suicide in the UK.

Martin, as he has agreed to be called to preserve his anonymity and that of his family, was a fit and active man who enjoyed rugby, cars and socialising with friends in the pub before suffering a brainstem stroke three years ago. Now requiring round-the-clock care, his mobility is limited to moving his eyes and small movements of his head. He communicates by staring at letters on a computer screen which the machine recognises and forms into words spoken by a digitised voice.

Martin has been asking to die since six months after the stroke but says he has no one willing to assist him and cannot on his own organise a trip to the Swiss clinic Dignitas, where he could end his life legally. His wife, who chooses to be known as Felicity, says she will be with him if he dies but will not help bring about his death.

Human rights lawyers at the firm Leigh Day in London have taken the first step in an action on Martin’s behalf that, if successful, could have massive implications. One possibility is that the case could lead to a court ruling that Martin has the right to help not only from a paid professional to assist him get to Switzerland, but also to the services of a palliative care doctor in the UK to ease his death, should he decide to end his life by refusing food and drink.

Such a ruling would dramatically alter the current options for seriously ill and severely disabled people who wish to end their own lives in the UK. “There would be no more planes to Switzerland,” said Richard Stein of Leigh Day. “Why would you bother?”

However, Stein added that beginning this legal action would potentially put the lawyers working on it in legal difficulty, since both they and any doctor or psychiatrist who came to examine Martin for the case could be considered to be assisting his suicide, thus exposing them to potential prosecution or disciplinary action from professional bodies.

The case of Debbie Purdy in 2009 established that friends and family could help someone who is terminally ill travel to Dignitas without fear of prosecution on their return. Purdy has multiple sclerosis and wanted assurances that her husband, musician Omar Puente, could take her to Switzerland when she was ready to die, without legal consequences. In the guidance issued with the judgement Keir Starmer, the director of public prosecutions (DPP), made clear that those without a close emotional commitment who assisted a suicide – including professionals – could face criminal proceedings.

Stein is seeking an interim declaration from the courts that lawyers and doctors will not be prosecuted or disciplined if they prepare Martin’s case. Even though many lawyers have worked on right-to-die cases before, neither the DPP, Solicitors Regulation Authority or the General Medical Council would give assurances that preparing the case was legally and professionally acceptable.

“The important thing is that lawyers and doctors will know that, providing they have assisted somebody to end their lives compassionately and in good faith, they won’t face criminal prosecution or disciplinary action that will affect their livelihoods,” Stein said.

If the interim declaration is granted Stein can take the next step on Martin’s behalf – asking the courts to rule that a doctor should be able to assist him with pain relief and palliative care if he decides he wants to stop eating and drinking in order to end his life.

Scope School Seeks An OT

August 18, 2011

 

http://twitter.com/#!/scope/status/104147781941338112

Man Places Online Advert To Find Replacement For Himself

August 18, 2011

This is such a sad story. I wish something could be done to help this family stay together.

Liu Li, 39, has been diagnosed with Ankylosing Spondylitis, a form of arthritis that can fuse the back’s vertebrae together.
Medics have told him that although the disease can be aided with drugs and painkillers, it cannot be reversed and the cost of the treatment is too high for Mr Li.

The former medical student from Shizhuang, Jiangsu province, eastern China has persuaded his wife Shi Zhihong, 37, to divorce him and find a new husband to take his place.

The advert, posted online in China, says: “Please, please help me find a good husband for my wife. I don’t want to be a burden to her anymore.

“I’m a seriously ill person and my days when I will not be confined to a wheelchair are limited. But my wife is still quite young, she should have some good days, otherwise, I will not be at rest even when I die.”

Mr Li hopes to be able to help chose the best applicant who will become stepfather to his son and daughter.

“I can’t bear to see the hardship I am putting my family through. I can’t work and what small money we have goes on my treatment.

“It breaks my heart to see my children turn down sweets because they think it will help me,” he said.

“I have done my best but I am frail and they deserves better. It would ease my heart to see them settled,” added Mr Li.

But the couple have one last chance of staying together after appealing to charity organisations for help with their medical bills.

“We are a good but poor family and we need some help,” explained Mrs Zhihong. “I will still be his wife in this life and the afterlife.”

Simon Richardson Is ‘Critical’ After Crash

August 18, 2011

Paralympian cyclist Simon Richardson is in a critical condition after suffering multiple injuries in an alleged hit-and-run incident.

The 44-year-old from Porthcawl, who won two golds and a silver at the 2008 Beijing games, was hit by a van while on his bike on the A48 near Bridgend.

A 59-year-old van driver from Cowbridge has been arrested.

Mr Richardson’s sponsor, Phil Jones, said the crash is likely to end his dreams of competing in London 2012.

The cyclist suffered fractures to the spine, a broken pelvis, a broken breast bone, cuts to his legs, and a “detached” lung, which means only one of his lungs is functioning.

He was airlifted from the scene and flown to the University Hospital of Wales in Cardiff.

The cyclist’s wife Amanda, who described his condition as “critical but stable”, said he is likely to have surgery on Thursday.

Mr Jones told BBC Wales: “Although Simon wasn’t currently within the GB Paralympics performance programme, the times and training that he had been putting in up untill now were certainly making him a very top contender to be considered for the London 2012 Paralympics.”

Mr Jones said the severity of Mr Richardson’s injuries was all the more distressing as he was involved in a serious crash in 2001, which left him permanently disabled.

He was hit by a car, which left him with serious leg and back injuries and no feeling down his left hand side.

Doctors recommended cycling would help his rehabilitation, so he continued, using a specially-adapted bike powered by his right leg.

It was during his five-year rehabilitation that he competed and won medals in Beijing 2008 and was awarded the MBE for his sheer “mettle”.

“He really is a brilliant guy, made of real Welsh nails, highly motivated, and with such a positive outlook on life,” Mr Jones added.

Gerwyn Owen, of Disability Sport Wales, said Mr Richardson had been training very hard and competing in his bid to get into the London 2012 team.

“He is still a full time athlete, supporting himself, and he gets great support from his wife, Amanda,” he added

“Long may it continue and we look forward to when he gets out of hospital and we can assess his condition.”

South Wales Police are still questioning the arrested man and inquires are continuing.

They have appealed for witnesses to the crash which happened 0940 BST on Wednesday outside Crack Hill House, Bridgend.

Insp Tony McAlinden said: “Simon Richardson was apparently struck by a small white van travelling in the same direction.

Police appeal

“The van did not stop and continued east along the A48 in the general direction of Cowbridge.

“Police would like to speak to any person who witnessed the collision, or may have been travelling between Cowbridge and Bridgend on the A48 and saw a white small van leaving the area.

“Also anyone who stopped to provide assistance and who have not yet given their details.”

Two cars were involved in a crash at the same location following the collision.

They were a black Toyota Avensis estate car, driven by a 43-year-old man, and a gold Rover 25 car driven by a 74-year-old woman.

The woman has been released from the Princess of Wales Hospital in Bridgend after being treated for chest injuries.

Anyone with information is asked to contact the South Wales Police roads policing unit on 02920 633438 or Crimestoppers on 0800 555111.

 

Paralympic Cyclist Simon Richardson Injured In Road Crash

August 18, 2011

This is very sad. I wish him well.

A gold medal-winning Paralympic cyclist has suffered multiple injuries after being involved in a hit-and-run crash with a van near Bridgend.

Simon Richardson, 44, was thrown from his machine to the side of the A48, while the van did not stop, said South Wales Police.

A 59-year-old man from the Cowbridge area has been arrested.

Richardson, awarded an MBE after two golds and a silver at the 2008 Beijing games, was flown to hospital.

Two cars were then involved in a crash at the same location, with an elderly motorist released after treatment in hospital.

Police have appealed for witnesses after the crash at 09:40 BST on Wednesday outside Crack Hill House, Bridgend.

Police said Richardson was apparently struck by a small white van travelling in the same direction, which did not stop and continued east towards Cowbridge.

A black Toyota Avensis estate, driven by a 43-year old man, and a gold Rover 25 driven by a 74-year-old woman were then also in collision at the same place.

The ambulance service treated both Richardson and the female driver.

He was flown by air ambulance to University of Wales Hospital, Cardiff where he is undergoing treatment for multiple injuries.

The female motorist was released after treatment for chest injuries.

South Wales Police would like to speak to any person who witnessed the collision, or may have been travelling between Cowbridge and Bridgend on the A48 and saw a white small van leaving the area.

They also want to speak to anyone who stopped to provide assistance and who has not yet given their details.

The road was closed for four hours while the police conducted initial investigations.

Richardson, from Porthcawl, had been seriously injured in a cycling incident with a car in 2001 while out with friends from a cycling club.

He received the MBE in 2009.

He won Britain’s first gold at Beijing in the LC3/4 1km time trial in world record time.

One of Richardson’s sponsors is Phil Jones, of Brother UK.

He said he spoke to Mrs Richardson shortly after the incident and she told him her husband was “critical but stable”.

Richardson had been diagnosed with multiple fractures of the spine, a broken pelvis and a broken breast bone and only one of his lungs was functioning, he said.

Mr Jones told BBC Wales: “There is quite a big community of people who know Simon and know of his achievement. There’s a real sense of support for Simon.”

He added that the full-time athlete was shortly due to test a new time-trial bike as part of his training to qualify for the London 2012 Paralympic Games.

Gerwyn Owen, of Disability Sport Wales, said the incident highlighted the need for everybody to look after cyclists on the road and for cyclists to take care themselves.

“This happens very often in cycling,” he said.

Third Castlebeck Care Home, Arden Vale, To Close

August 17, 2011

A third care home run by a company at the centre of allegations of abuse against vulnerable patients is to close, it has been announced.

The Care Quality Commission (CQC) said Castlebeck had agreed to close Arden Vale, in Meriden, near Coventry, by next Thursday.

Castlebeck said it was making other arrangements for the 19 residents.

The company owns Winterbourne View, in Bristol, where abuse was filmed by an undercover BBC Panorama journalist.

‘No evidence’

Since the BBC One programme was broadcast, the home for people with learning disabilities has been closed by the CQC.

And Castlebeck announced last week that it was to shut Rose Villa, also in Bristol, for “operational reasons”.

Arden Vale, which cares for people with mental health problems and learning disabilities, was the subject of legal action by the CQC after it inspected the facility in June.

The move would have prevented Castlebeck from operating at the site.

Andrea Gordon, CQC’s regional director for the West and East Midlands, said it had taken action after seeing “no evidence” of the improvements to care it had demanded.

She said: “Castlebeck has responded to our action by agreeing to close the service on a voluntary basis.

“When CQC published reports into all 23 Castlebeck locations at the end of last month, we identified four services where we had significant concerns.

“Arden Vale will be the second of these locations to close; Rose Villa in Bristol closed last week. A third service, Winterbourne View, was closed following CQC action in June.

“We continue to monitor all Castlebeck services very closely.”

Lee Reed, Castlebeck chief executive, said it agreed with the CQC’s report and would not appeal against the body’s decision.

‘Improved reporting systems’

He said: “We will be working with the people in our care at Arden Vale, as well as their families and care managers, to ensure that there is minimum disruption and that the right services are found for their needs.”

The chief executive said Castlebeck was already in the process of introducing improved training and “significantly improved reporting systems”.

“We remain deeply sorry and apologise for any incidences where our services have in the past not met the high standards that we, those we support and their families, expect and deserve.”

Thirteen members of staff were suspended from Winterbourne View before it closed, after Panorama filmed an undercover documentary there.

The footage showed residents being pinned down, slapped and taunted.

At Rose Villa, four people were suspended before last week’s closure announcement. Few details have so far emerged about why they were suspended.

Meanwhile, documents seen by BBC Social Affairs Correspondent Alison Holt reveal the extent of complaints to the regulator about Winterbourne View.

Last year the CQC received nine reports about the care home – compared to four in the two years before.

Most of the documents – obtained under a Freedom of Information request – are official notifications of incidents at the home.

One says: “It was alleged that the support worker had squeezed the patient’s neck during a restraint and that the patient had found it difficult to swallow following this incident. The patient also stated that the support worker gets rough when angry.”

‘What was concealed’

Another worker was reported for slapping a patient twice. Both of these staff were disciplined.

A man also rang the CQC directly raising concerns about staffing and restraint. It took three months for someone to call him back.

The CQC said the incidents were reported to local authorities and all of the incidents were appropriately reported and investigated locally.

In a statement it said: “It is the job of the local authority or the police to investigate these incidents and to hold the provider or staff to account if necessary.

“The issue at Winterbourne View was not what was known and reported, but what was concealed.”

The role played by all the organisations involved with Winterbourne View is currently being examined as part of a serious case review.

Reverse The Bias Towards Segregated Education

August 17, 2011

I’ve just read about a campaign to reverse the current Government’s bias against inclusive education, and towards segregated education in special schools.

I had an inclusive education myself and, as regular readers will know, have always been a passionate supporter of inclusive education. So I fully support this campaign. Can I ask anyone who shares my view to visit the site linked above and do what you can to help.

This post is part of the Inclusion Rules! Debate at Same Difference.

Accessible Beach Huts Open On Bournemouth Seafront

August 17, 2011

The competition to design these was featured on Same Difference in  2009. I’m thrilled to read this update.

Four new beach huts designed for disabled users have opened on Bournemouth beach.

The Seagull and Windbreak beach huts have replaced five standard beach huts west of Boscombe Pier.

A wooden access trackway enables visitors in wheelchairs to access the beach down to the waterline.

The design was picked by residents after a competition in 2009 and the beach huts can now be hired for use from Bournemouth Borough Council.

Each hut can accommodate up to four wheelchair users and are equipped with chairs, a table, split level work surface, gas stove, lockable cupboards and shared fresh drinking water tap.

They also have high colour contrast surfaces and tactile floor surfaces to assist the visually impaired.

The council is also providing beach-going wheelchairs fitted with large balloon tyres that users can borrow for a refundable deposit.

Peter Francis-Lewis from Brighton based A:B:I:R: architects created the winning design and the DOTS Disability group worked with residents and Push Studies to construct the huts.

 

NHS Trust Discriminated Against Disabled Man Seeking Job

August 17, 2011

A 28-year-old man with Asperger’s Syndrome has won £25,000 compensation for discrimination from Northamptonshire Primary Care Trust.

An employment tribunal found the trust was wrong to offer Dale Morgan from Northampton a permanent job and then withdraw it over his disability.

The trust said the temporary worker’s references were “unsatisfactory”.

Now the trust admits its diversity and equality policy was not followed but would be strictly enforced in future.

Mr Morgan applied for a job as an information analyst with the trust in January 2009 while he was already a temporary worker.

During his interview, Mr Morgan said he suffered with this disability, stress and anxiety.

He was offered the job subject to satisfactory references but received notice it had been withdrawn the day before he was due to see an occupational health specialist appointed by the trust.

Mr Morgan went to see the specialist regardless in a bid to ascertain why the job offer was withdrawn as no explanation had been given.

He had been working for the trust for about 10 months and had experience in this type of work.

The judge found that Dale raised the issue of disability discrimination with the primary care trust but its staff failed to take this into account falling back instead on its policy of requiring two satisfactory references.

Lessons were learnt

Members of the interview panel were encouraged to be aware of the possibility of discrimination as a factor within an unsatisfactory reference, the hearing was told.

The primary care trust deliberately gave the disability no further consideration, the tribunal heard.

After the case a spokesperson said: “NHS Northamptonshire is committed to equality and diversity. This commitment goes far beyond just meeting statutory obligations.

“We are committed to further developing this organisational culture, which continuously promotes equality and diversity, eliminates unlawful discrimination and reduces health inequalities.

“The lessons learned from this case have already been incorporated in the way we continue to deliver our equality and diversity commitment.”

Mr Morgan was represented by Stephensons Solicitors who said: “The trust should have given consideration to their own guidance on disability discrimination.

“They then could have considered a whole host of adjustments that were not likely to be expensive, time consuming or difficult to arrange.”

Father’s Computer Game Takes Daughter’s Mind Off Cystic Fibrosis Physio

August 17, 2011

David Day is clearly a very special parent, and I wish him luck with getting his range of games out there, but I wonder if he knows that he is not the first person to have an idea like this?

His daughter’s treatment for her cystic fibrosis was something David Day used to dread.

Like the 9,000 or so other people with cystic fibrosis in the UK, four-year-old Alicia has to breathe into a tube for up to 10 minutes each day to stop mucus gathering in her lungs and digestive system.

As he saw her undergoing the boring and painful daily exercises, the University of Derby lecturer realised he might be able to harness the expertise of his colleagues to ease her suffering.

Now they have developed a range of computer games to help Alicia endure her treatment, which he hopes could benefit other children with the condition.

The games involve a device which connects breathing tubes to the computer so children can control characters and shapes on screen by exhaling at a certain pressure.

‘Cry and scream’

Dr Day said, despite the importance of the treatment, sitting his daughter down for it had been getting increasingly difficult.

“There were a lot of tantrums. Every evening she would cry and scream and run off and it was getting progressively worse the older she got.

“It was no fun at all. It was something you knew was coming and you would have to get it done before you could relax. It was a nightmare.”

Struggling for a solution, Dr Day came up with the idea of using the expertise of his workmates at the University of Derby’s School of Mathematics and Computing.

He said: “We’d been watching what was happening with kinetic consoles like the Wii.

“I thought a game might be a good way of getting Alicia to interact and engage more with her physiotherapy.

“I mentioned it to the computer games team here and they said it was a good idea so we decided to proceed with it.”

‘Sense of wonder’

Dr Day and his team used university funding and European grants to develop a range of games which transformed the breathing exercises into something more fun.

He said the effect on his daughter was instant.

“She blew into the device, saw the flowers move on the screen and looked at me with this sense of wonder,” he said.

“She asked me how it was doing that so I told her it was magic.

“She loved it and since then it has taken all the pressure and worry out of trying to get her to do her physiotherapy.”

As well as Alicia’s favourite flower game, the team built games involving pirate ships and flying dragons.

Now Dr Day is hoping to secure further funding to test the game on more children and eventually make it available to other parents.

He said: “We’re hoping in the next 12 months we can have a version of this for sale to the public so that other children and parents can benefit from it.

“From feedback I’ve had, it seems all parents dread getting their children through the physiotherapy.

“It’s a battle all carers and parents of cystic fibrosis children are having, so what we’re doing is absolutely vital.”

Paralysis Made Me A Better Man, Says Rugby Player

August 17, 2011

Six years ago, aspiring England rugby player Matt Hampson was at the top of his game, training for an under-21s match against Scotland.

But his life changed forever when he was injured during a training session. He is paralysed from the neck down and needs a team of 10 carers to get him through each day.

He spoke to BBC Breakfast.

Social Workers Mistook Brittle Bone Disease For Child Abuse

August 16, 2011

Two children who were taken into care after social workers mistook a baby’s brittle bone disease for evidence of abuse have been reunited with their parents.

The team of social workers accused a mother of abusing her baby son, when in fact he was suffering from a rare bone disease.

Parents Paul Crummey and Amy Garland were horrified when doctors told them their baby son, Harrison, had eight fractures in his arms and legs just weeks after he was born.

But they were devastated when social workers accused them of shaking their son by the legs and took him and their daughter Bethany, now five, into care.

The terrified couple were arrested, and banned from seeing their two children without supervision.

It took 18 months for social workers and doctors to realise baby Harrison was suffering from a rare form of brittle bone disease meaning the slightest touch could snap his bones in two.

Now, the family, from Bristol, have been reunited, after prosecutors decided to drop the case when they realised Harrison was suffering from Osteogenesis imperfecta.

Their nightmare began when Harrison was just six-weeks-old.

Miss Gardland, 26, said: “For the first weeks he was bringing up blood with his milk and he was irritable.

“I knew something wasn’t right so I took him to the hospital. They did tests on him but everything came back absolutely normal.”

But when she got home she noticed his legs were swollen.

X-rays later showed Harrison had several fractures in his arm, feet and legs.

Miss Garland said: “We obviously had no idea that this condition was in our family so when they asked us how they happened we were left with the answer that we didn’t know.

“They said they needed to investigate it and we were happy for them to do that.”

Tests showed Harrison’s vitamin D levels were abnormally low so he was given injections.

As soon as the fractures were discovered, South Gloucestershire Social Services were called in to speak to the couple.

Police arrested Miss Garland while she was in hospital with Harrison and Mr Crummey, who was recovering from an operation at home, was also arrested.

They were questioned separately under caution by police. Neither of them had been in any sort of trouble before.

“The police and social services asked us a lot of questions. They asked me if there was any family history of violence,” said Miss Garland.

“We found out the police were speaking to all our neighbours asking them what we were like. They went through our house. I was in absolute shock. I was shaking. I felt like a criminal,” she said.

While Harrison was in hospital, Miss Garland was not allowed to be alone with her son.

“I wasn’t eating and I couldn’t sleep because I was worried they would take him from me,” she said.

“Paul and I weren’t allowed to be alone together. I never for one second questioned Paul. Neither of us needed to ask each other. We just knew.”

At the time, Bethany was just 20-months-old and was placed in the care of Miss Garland’s father.

The case was brought before Bristol County Court, where a judge ordered the family to live in a family placement centre.

“The judge didn’t want to separate me from Harrison because I was still breast feeding,” the mother said.

“We were watched 24 hours a day and there were cameras in every room. It was like a prison because even when we were allowed to go out we had to have staff with us.”

After three months, staff could find nothing wrong and recommended the family should stay together.

But social workers applied for an interim care order and the children were placed into foster care with their grandfather.

They were only allowed to see the children for six hours each day under supervision for over a year.

“It was horrible. When I went home at night and the kids weren’t there, I just broke down,” said Miss Garland. “There was so much going on in our lives. We were a mess. We took things out on each other.”

In January 2009, Miss Garland found a medical expert who believed Harrison had Osteogenesis imperfecta after looking into the family’s medical history.

Six months later, the two other doctors involved in the case agreed he could have the condition after reading the expert’s report.

South Gloucestershire Social Services then dropped their case.

Miss Garland, who has another daughter, Juliet, 18 months, with current fiance Kai Howell, 29, said: “When I heard the news, I couldn’t even speak. I was sat in my mum’s garden in tears.

“Straight away, we took them to the park. It felt so right to finally be together as a family.”

A month later, Harrison was diagnosed with Osteogenesis imperfecta. Doctors also tested Bethany, who was found to have a lesser type of the condition.

Harrison is still having vitamin D injections to help strengthen his bones and sees a physiotherapist to help build the muscle surrounding his bones.

Mr Crummey, 41, said: “All we wanted to do was help our sick child but we were treated like criminals. We had to sit and watch Harrison in pain.

“We’ve missed out on so much of our children’s lives. They’ve been through so much. It tore Amy and I apart because we didn’t know how to handle it.”

“We’ve never received an apology from social services. It makes me feel very angry.”

A spokesman for South Gloucestershire Council said: “While we cannot comment on individual cases, we do have a legal duty to protect children and young people living in South Gloucestershire and we always put the welfare of the child at the heart of how we deliver our services.”

Wheelchair User Agrees Out Of Court Settlement With Taxi Firm

August 16, 2011

A Belfast wheelchair user has agreed an out of court settlement after taking a disability discrimination case against Value Cabs.

Nicola Nesbit alleged she was charged more than a non-disabled person for using an accessible taxi. She said the firm charged her an £8 call-out fee in addition to a fare and a half.

Value Cabs paid Mrs Nesbit £2,000 without admission of liability.

Mrs Nesbit, who has cerebral palsy, said she was delighted by the outcome.

“I was outraged, as I felt that I was being treated differently because I am disabled,” she said.

“I think it is important that all disabled people are aware that it is not fair to charge a disabled person more than an able bodied person for the same journey in the same vehicle, and that is why I decided to take this to court.”

Mrs Nesbit, who usually travels by bus, needed to use taxis to travel to hospital appointments during her pregnancy.

She alleged that, because it was a wheelchair accessible vehicle, she was charged an £8 call-out charge on top of the fare and a half, bringing her fare to around £14 for the short, one-way trip.

‘Reasonable adjustments’

Her case was supported by the Equality Commission.

Director of legal services at the Equality Commission, Anne McKernan said: “The Disability Transport Regulations require transport providers to make reasonable adjustments so that disabled people can have access to a service as close as it is reasonably possible to get to the standard normally offered to the general public.

“The law does not allow a transport provider to charge its disabled customers a higher price for the same journey in the same vehicle,” she said.

“The fare for the larger vehicle should be the same for everyone.

“The costs of making reasonable adjustments are part of a transport provider’s general expenses, just the same as complying with any other legislation.

“It is essential for all transport providers to make sure their staff are fully informed and operating their policies.”

Value Cabs have agreed to liaise with the Equality Commission to review their policies and procedures, which they believe to be compliant with the law, and to implement any reasonable recommendations made by the commission.

The company has also agreed to communicate its policies and procedures to its staff at all grades through a training programme recommended by the commission.

Stones Thrown At Woman In Wheelchair

August 16, 2011

A woman in a wheelchair has suffered swelling to her head after being hit by stones thrown by a gang of youths.

Sam Rogers, from Sittingbourne in Kent, said the ordeal had left her terrified and afraid to go out.

She said a stone hit her in the back of the head as she headed home. She was then subjected to “terrible abuse” before being hit again.

“Nobody should feel this amount of terror,” Mrs Rogers said. Kent Police have appealed for witnesses.

Mrs Rogers, who is in her early 40s, had been making her way across the Rectory Road playing field in Sittingbourne at about 19:00 BST on Friday, 29 July when she was attacked.

She told police there were about five youths in the gang, aged between about eight and 13.

She has been using a wheelchair for the past 15 years after suffering a spinal injury, and said she had tried to remain as independent as possible, but the attack had put that in doubt.

“I’m having to force myself to go out as I know I’m going to end up a prisoner in my own home and I don’t want that, and I don’t want other people to feel the way I’m feeling about it.

“It’s just not fair. Nobody should feel this amount of terror. Nobody should feel that they’re unsafe,” she said.

Her husband, Graham Rogers, added: “I don’t quite understand the mentality of the kids that are doing this sort of thing – because they think it’s fun or are they that bored that all they can do is pick on somebody who can’t really defend themselves?

“It does seem completely ridiculous to me.”

Kent Police are investigating the incident and have urged people using the playing field to be vigilant.

A Prosthetic Arm With A Mercedes Logo For F1 Fan Matthew, 14

August 15, 2011

A TEENAGER has a new £35,000 bionic hand – thanks to an F1 team.

Motor-racing fan Matthew James, 14, wrote to Ross Brawn, boss of Mercedes GP Petronas, asking him to pay for the hi-tech artificial limb.

He offered to let the team put the Merc logo on the hand for publicity.

Mr Brawn was so impressed that he asked specialist firm Touch Bionics to fit Matthew with an i-LIMB Pulse, the world’s most advanced prosthetic limb.

Matthew, of Wokingham, Berks, was born without a left hand, and controls the fingers through electrodes that sense arm muscle signals.

He can hold a pen, draw pictures and catch a ball. The hand will have a tiny Merc badge on it.

Matthew said: “It’s so cool.” Mr Brawn, who persuaded fans and sponsors to contribute, said: “It was a pleasure.

IDS Caught Using Disabled Toilet

August 15, 2011

Haha! Good on the guy who wrote this guest post at The Broken Of Britain.

http://twitter.com/#!/BendyGirl/status/103033177362276352

Peter White Meets Jane Cordell

August 15, 2011

I wish I’d known about this earlier. For anyone else who missed it, it will be repeated at 9.30pm today, or it’s available now on BBC iPlayer.

Peter White returns with the highly-acclaimed series which poses the questions about disability which other programmes are too embarrassed, or too politically-correct, to ask.

In the first programme he interviews the Foreign Office high flyer Jane Cordell, who had a diplomatic posting to Kazakhstan, her second overseas posting, revoked when officials ruled that her deafness made it too expensive to send her abroad.

She tells Peter that her disability makes her particularly attuned to social situations, reading body language and picking up on everything, from the way people clench their toes to nervous movements which might signal suspicion: “When I walk into a room I pick up immediately a sense of what the atmosphere is – whether there’s going to be a rapport with the speakers and what’s going on. You read people’s faces, their gestures, you can pick up messages that possibly people who aren’t deaf couldn’t.

“I always went into it with an open mind, believing that the more straightforward barriers presented by not being able to hear can be fairly easily overcome. But then I’m an optimist.”

Jane talks about her musical childhood and how in her twenties she coped with the realisation that she was gradually losing her hearing. But this did not deter her from pursuing her goals, although it’s acted as a good filter when it came to prospective partners: “It was possible to tell a lot about people by how they reacted to my disability and I used this as a good way to test whether someone was worthy of my friendship.”

Drug Offers Hope For Childhood Arthritis

August 15, 2011

A rheumatoid arthritis drug has been relaunched in the UK as a treatment for children whose lives are devastated by a severe form of the disease.

Tocilizumab is the first drug to be specifically licensed for systemic juvenile idiopathic arthritis (sJIA) which affects around 2,500 British youngsters.

The drug was already licensed for the treatment of adults.

Until now sJIA has mostly been treated using anti-inflammatory painkillers and steroid drugs.

Symptoms of the disease include joint pain, fever, enlargement of internal organs and a distinctive salmon-coloured skin rash.

Up to two-thirds of patients develop persistent and chronic arthritis, and half of these suffer significant disability.

Professor Patricia Woo, a rheumatology expert from Great Ormond Street Hospital for Children, said: “Systemic juvenile arthritis can be a devastating disease. It strikes often very young children, causing chronic illness, pain and disability.

“It is hugely encouraging to have an effective medicine now available to alleviate symptoms, control disease activity and potentially hold back the worst long-term consequences of the disease.”

A Phase III trial showed that 71% of children treated with tocilizumab saw a 70% improvement after three months.

Ailsa Bosworth, chief executive of the National Rheumatoid Arthritis Society, said: “Children with sJIA and their families can now look to a future with hope.”

Siblings Of Autistic Children More Likely To Have Autism

August 15, 2011

The siblings of autistic children are nearly twice as likely to develop the disorder than was previously believed, research suggests.

A study published today tracked the development of 664 infants with an autistic older sibling until the age of three, at which point they were tested for the condition.

Almost 19 per cent of participants developed autism spectrum disorders, considerably higher than previous estimates which pegged the risk for siblings at between 3 and 10 per cent. “This is the largest study of the siblings of children with autism ever conducted,” said the lead author, Sally Ozonoff, a professor of psychiatry and behavioural sciences at the University of California. “There is no previous study that identified a risk of recurrence that is this high.” The risk was higher for boys, with 26 per cent of brothers of autistic children developing the disorder, and greater still for children with more than one autistic older sibling, 32 per cent of whom were diagnosed. Four-fifths of autistic children are male.

Estimates of the prevalence of autism have risen dramatically over time, from four or five in every 10,000 a generation ago to a generally accepted rate of one in 110 today. But the exact causes of the developmental disability remain a mystery.

The research, conducted at 12 sites across the US and Canada and published in the American journal Pediatrics, adds weight to the prevailing view that genetic factors play a critical role in the development of autism.

Professor Ozonoff said the findings highlighted the need for close monitoring of the infant siblings of autistic children. “This may require more than the normal surveillance that a paediatrician might typically do,” she said.

She added: “Parents often ask what is the risk of having another child with autism and, until now, we were really not sure of the answer.”

But she stressed that the estimates were averaged across all families, meaning that “for some families, the risk will be greater than 18 per cent, and for other families it would be less”.

Mark Lever, chief executive of the National Autistic Society, said he welcomed the study but that it did not mean all parents of autistic children had an 18 per cent chance of having another child with the condition.

“While genetics are thought to play a part in autism, the condition is not inherited in a straightforward way. Parents of multiple siblings with autism may, however, be at an increased risk of having subsequent children with the condition than those with just one child,” he said.

“If any families already have a second child who they suspect might have autism we would advise them to seek professional diagnosis as soon as possible.”

Twelve Atos Doctors Could Be Struck Off

August 14, 2011

Twelve doctors employed by the firm that is paid £100m a year to assess people claiming disability benefit are under investigation by the General Medical Council over allegations of improper conduct. The doctors, who work for Atos Healthcare, a French-owned company recently criticised by MPs for its practices, face being struck off if they are found not to have put the care of patients first.

The Observer has found that seven of the doctors have been under investigation for more than seven months. The other five were placed under investigation this year following complaints about their conduct.

It is understood that the majority of allegations concern the treatment of vulnerable people when the government’s controversial “work capability assessments” were carried out, but the GMC refused to comment on individual cases. The development will add to fears over the pace and radical agenda behind the government’s welfare-to-work policy, which led to protests in Westminster in May by thousands of disabled people. It will also raise concerns about ministers’ commitment to Atos Healthcare, which was recently granted a three-year extension on its contract.

The government has repeatedly publicised figures showing that the “vast majority” of claimants for employment support allowance (ESA), which has replaced incapacity benefit, are fit for work. But four out of 10 of those who appealed the decision by Atos – whose parent company is run by a former French finance minister, Thierry Breton – to deny them benefits are successful on appeal, a process that costs the taxpayer £50m a year.

Last month Atos, whose staff assess around 11,000 benefit claimants a week, was savaged by the cross-party work and pensions select committee after it found that many people had “not received the level of service from Atos which they can reasonably expect”.

MPs further claimed that a combination of the company’s conduct and the test itself had prompted “fear and anxiety among vulnerable people”.

One GP who attended an Atos recruitment fair told the Observer she feared doctors could become “agents of the state” who were deprofessionalised by involvement in a system that did not make patient care its first concern.

Campaigners for the disabled seized upon the development, claiming the government needed to go back to the drawing board. Richard Hawkes, chief executive of the charity Scope, said: “If the government wants to get disabled people off benefits and into work then it needs to get its assessment right. The test should be the first step on the road to employment. But disabled people’s confidence in the work capability assessment is extremely low – and today’s news will send it to rock bottom.

“The test is massively flawed. Now it appears that it is being carried out by a large number of doctors who are under serious investigation.”

Neil Bateman, a solicitor who handles ESA appeals, said on two occasions his clients had been successful because, among other reasons, the doctor assessing them had qualified in Romania and registered with the GMC but had not been licensed to practise in Britain.

Citizens Advice told the Observer it was compiling a dossier showing the problems being faced by those assessed by Atos staff, who can be nurses or physiotherapists in cases where there are no potential neurological disorders. It said it regularly found inaccuracies in many of the medical reports featured in ESA appeal papers that could affect people’s chances of receiving benefits. It also found a lack of consideration for those being assessed.

A spokesman said a barrister who was unable to practise because of cancer and lymphoma had described the assessment as being like an “interrogation” led by a computer. The assessor moved the client’s legs, which caused her great pain, even though the client had warned that this would happen. In another case a claimant with learning difficulties who went for an assessment was found fit for work because he had found his way to the assessment centre on his own.

When asked about this by Citizens Advice, he reluctantly explained that he had got up very early, taken the bus to the town centre, and then kept asking passersby for directions. He couldn’t follow their instructions, so he would show the letter, walk in the direction they pointed, then ask again until he arrived.

Two doctors employed by Atos have already been taken by the GMC to an independent panel for adjudication on their fitness to practise. Dr Alexandros Mallios, who it was claimed had not carried out a proper examination of his patient during an assessment, was cleared by the panel last October. Dr Usen Samuel Ikidde, who qualified in Nigeria, was given a formal warning in January, to lay on his records for five years, after he was found to have worked for Atos while on sick leave from an accident and emergency department.

An Atos spokesman said: “Atos Healthcare is committed to providing a high-quality, professional service and requires these standards of all its employees. While we cannot comment on individual cases, any complaint made about an employee is taken extremely seriously.

“In addition to our own rigorous internal investigations we will co-operate with any external investigation to ensure all facts are properly established and the appropriate action taken.”

The Labour government introduced work capability assessments in 2008 when it replaced incapacity benefit and income support for new claimants with employment and support allowance. The government has accelerated the changes and started retesting all 1.5 million incapacity benefit claimants to see whether they are eligible for the new benefit.

A GMC spokesman said: “We can and do take action to remove or restrict a doctor’s right to practise if there have been serious failures to meet our standards.”

Charity Vitalise To Close Cornwall Centre

August 13, 2011

A charity which helps disabled young people take part in outdoor pursuits is closing its Cornwall centre.

Vitalise said the lease on its centre at Churchtown, Lanlivery was due to end in September.

It had decided “with regret” to focus its services on its three other UK centres in Hampshire, Essex and Merseyside.

The charity said it was working with Cornwall Council to keep a day centre on the site open.

The day centre, activity centre and residential and self catering accommodation for families has been leased for the past 10 years from the disability charity Scope.

Chief executive Chris Simmonds said: “We’re proud of all we’ve achieved there, but now is the right time for us to refocus our resources on our other centres around the UK.

“However, we remain hopeful that some solution can be reached that will enable the day service to keep supporting disabled people from the region, even at this late stage.

“We’re working closely with the council to keep supporting the service users and their families during this difficult time.”

The Churchtown 12-acre site includes an adventure course, a small working farm, climbing tower, nature reserve and archery range.

Activities include canoeing, climbing, and abseiling.

Ruth Sutherland, executive director of services at Scope, said Vitalise had made a “big difference” to disabled people.

“As the freeholders, we must now consider what the best option is for the site,” she said.

“We realise this news will be extremely disappointing to the people that use the centre and we will be speaking to Cornwall Council to see whether we can offer any support.”

RAD Legal Services

August 12, 2011

You don’t have to look very far to find stories about deaf people who have been let down by lawyers and the legal system.

There’s Funmi, a deaf Nigerian who has lived in the UK since 1987 but whose solicitor did not make her citizenship application correctly; David, a self-employed man whose solicitor did not fight his corner over benefits he was entitled to for being wholly reliant on his hearing mother to communicate with clients; and John, whose union solicitor did a bad job of his disability discrimination case against a well-known financial institution.

All of these people eventually turned to RAD Legal Services, part of the Royal Association for Deaf People and the country’s only dedicated legal resource for the deaf. Why are there not more, especially because – with nearly 10 million people suffering some sort of hearing problem – it is potentially a huge market to serve?

Its head, solicitor Rob Wilks, is not certain. “It could be because deafness is a ‘hidden’ disability,” he says. There are small signs of this changing. Blackburn law firm Joseph Frasier will next week launch a campaign to provide legal services for deaf people under the headline: “Representing your right to be heard.” Claiming to be the first private law firm dedicated to deaf and hard of hearing people, founder Saimina Virmani says it is the culmination of 18 months of preparation; the campaign was inspired by deaf staff working in the building where the firm is situated (which belongs to the East Lancashire Deaf Society) and by her experience of acting for a deaf client.

She has also come across “terrible” stories of solicitors denying deaf people access to interpreters and simply not understanding the different ways they need to communicate with deaf people, such as in the way they write letters.

The firm’s fee-earners, none of whom are deaf, are being taught British Sign Language (BSL) and it is adapting its communication channels. “The last few months have been a journey for us and we have loved learning about deaf culture,” Virmani says. “The deaf community is very tightly knit and although we see people who are deaf as being on the outside of our world, the tables have now completely turned and we are on the outside. As legal professionals we are trained to use the power of our advocacy and voice but in working with deaf/hard of hearing clients, this has essentially been taken away from us.”

The legal system, it appears, is simply not geared to the needs of deaf people – Rob Wilks says deaf people who use BSL as a first language often have poor literacy levels (the average reading age for deaf school leavers is 8-9 years). “This means that they cannot understand information leaflets and correspondence, or access telephone helplines using a textphone,” he says.

A report in 2009 by the Equality and Human Rights Commission found that the advice system of CABs, law societies, union sources and private firms of solicitors “are often still inaccessible to profoundly deaf customers” though the Disability Discrimination Act has been on the statute books since 1995. Now the Equality Act 2010, it requires service providers to make adjustments to ensure that a disabled person can use a service as close as it is reasonably possible to the standard usually offered to non-disabled people.

This is not happening across the legal system, both in most law firms and in the courts. Part of the problem, Wilks says, is the “chronic shortage” of interpreters, but it is just plain neglect as well.

One of Virmani’s projects has been to build a network of law firms (now numbering nearly 50) around the country that have committed to become deaf-aware and will be able to help deaf people in their area if face-to-face help is required.

The association began an advice service in 2000, transforming into RAD Legal Services in July 2007, when Wilks, who has been deaf since birth, qualified as a solicitor and the £500,000 Big Lottery Fund deaf minority advice project commenced.

Over the past four years, RAD has handled nearly 1,500 cases, with employment, welfare benefits, discrimination and housing the most in-demand areas of law. It has a contract (until March 2012) from the Equality and Human Rights Commission to provide discrimination advice to deaf and hard of hearing people throughout England, Wales and Scotland. Plans for the first deaf law centre are also well underway.

And there is further hope that the legal needs of deaf people will be understood. The legal services consumer panel has confirmed that the first of a series of studies into how specific groups of consumers (particularly disadvantaged ones) experience legal services will be in partnership with Action on Hearing Loss (formerly RNID).

Emma Harrison, a member of the panel and head of public engagement at Action on Hearing Loss, says the study has come out of work the charity has been doing to improve access to the courts and hopes to highlight the pockets of best practice that exist in the legal profession.

But the prospect of the legal aid cuts could worsen the situation for the deaf community, Wilks says. Aside from simply not being able to afford legal advice, law firms or other legal advice providers that have legal aid franchises will no longer be able to rely on legal aid to claim the costs of interpreters as a disbursement. “This means the number of providers willing to provide legal advice to deaf people is likely to decline.”

Given the low base from which this is starting, it is a woeful prospect.

Bus Service Cuts Threaten Most Vulnerable, Say MPs

August 11, 2011

Cuts to bus services in England are a threat to the most vulnerable people in society, a report by MPs says.

Local authority budget cuts have affected subsidised services – such as rural routes – and pushed up fares, says the Transport Select Committee.

It says elderly and disabled people are being stopped from working, taking part in education or accessing healthcare.

The government called the funding situation “challenging” but said it was closely monitoring the situation.

Subsidies are used to provide services which are not commercially viable – typically in the evenings, at weekends and in rural areas.

However, “extensive” cuts mean old, young or disabled people are being disproportionately affected, argues the report – which covers bus services in England, excluding London.

Last year’s Spending Review – which cut local authority budgets – prompted 70% of councils to reduce funding for subsidised services or increase fares, according to the report.

It also found that some buses had been withdrawn with little or no public consultation – something it says must change.

‘Greatest challenge’

Launching the report, committee chairwoman and Labour MP Louise Ellman criticised the government’s approach to bus services.

“The government claims it wants to see better bus services with many more smartcard-enabled journeys”, said Ms Ellman.

“Yet, following the government’s spending review, we have seen a significant number of bus services withdrawn around the country and there is every indication that fares are set to rise well above the rate of inflation in some areas.”

The industry is up against “the greatest financial challenge it has faced for a generation”, adds the report, which warns that ministers “cannot wash their hands of all responsibility for local bus services”.

MPs want the Department for Transport to monitor the cuts and review the situation again next year.

They also recommend that the Local Government Association should advise authorities on how best to deliver cost-effective community transport.

Transport Minister Norman Baker said the government would respond formally to the report’s recommendations in the next few months.

He added: “The grant arrangements are under review to ensure they deliver our goals of cutting carbon and supporting the economy and continue to offer value for money.

“We are keeping a close eye on whether councils are approaching this imaginatively, finding savings in procurement and backroom staff, or just reaching for the axe and cutting frontline services.”

‘Unprecedented crisis’

General secretary of the Rail, Maritime and Transport union, Bob Crow, said the report underlined the scale of an “unprecedented crisis” threatening bus services in many parts of England.

“Lifeline services, particularly in rural areas, face total collapse with fares on whatever is left set to rocket as a direct result of government cuts,” he said.

The Chief executive of the Campaign for Better Transport, Stephen Joseph, said councils needed to re-consider what was a priority.

“This isn’t just a matter of buses not being there, these are lifelines for many people – people who can’t get access to healthcare who really need it, there are people who would like to take jobs, or get education training opportunities, and they can’t access those because the buses simply aren’t there. Or there may be a bus out there – but they can’t get one back.”

Mr Joseph called on the government to reverse its planned changes to the bus services operators’ grant.

Alex Hannard

August 11, 2011

The family of a Hampshire boy who has a life-threatening condition are appealing for bone marrow donors during Cowes Week on the Isle of Wight.

Alex Hannard, nine, from Stubbington, has chronic granulomatous disease (CGD), which affects his immune system, and needs a bone marrow transplant.

His family and the Anthony Nolan Trust are recruiting for the register at Shephards Wharf Marina, Cowes.

They want potential donors, especially young men, to give a sample of saliva.

Alex was diagnosed with CGD in 2007 when he was just five and had complete respiratory failure within a week of first becoming ill.

Since then he has only been able to go to school about half of the time and has had several spells in intensive care.

‘Science nerd’

His mother, Louise, said: “The only chance of a cure is a bone marrow transplant.

“We decided to go ahead with it last year. We had a donor lined up but some matching issues came up so we lost the donor three days before the transplant was due to happen.

“He really wants the transplant. He told us, ‘I don’t want to be different any more – I want to be the same as everybody else.’

“He’s a real science nerd so he understands all the science behind it. He wants to work in genetics.”

Potential donors will be able to join the bone marrow register at Shephards Wharf Marina between 13:00 and 20:00 BST on Wednesday and from 10:00 BST and 13:00 BST on Thursday, or by contacting the Anthony Nolan Trust.

The trust is particularly looking for male donors aged between 18 and 30.

Aberdeen Asset Management Cowes Week is an annual sailing event attracting more than 100,000 spectators.

#DisabledRiotHelp

August 11, 2011

Well, dear readers, I’m still watching the news in shock. Now, as London cleans up and slowly recovers from the riots of the last few days, the disorder has spread to several other parts of England.

I’ve just found out about the Twitter hashtag #disabledriothelp which disabled people in any affected area can use if they need help, or want to help other disabled people. This is yet another example of Twitter working it’s special magic- please do follow it, I know I will be.

Genetic Clues To Triggers Of MS

August 10, 2011

Around 30 genetic risk factors for developing multiple sclerosis have been discovered by a UK-led team.

It brings to more than 50 the total number of genetic clues to the disease.

The research, published in Nature, will help identify risk factors and perhaps future treatments or even a cure, said the MS Society.

Most of the genes are linked to immunity, backing the idea that the disease is triggered when the immune system turns against itself.

Genes are only part of the story, however, with other factors, such as vitamin D or a viral infection, thought to play an important role.

The study, carried out by a consortium of international researchers, led by the universities of Oxford and Cambridge, is the largest yet into genes and MS.

It looked at DNA from almost 10,000 MS patients, and more than 15,000 healthy controls.

Twenty three known genetic variations, common in the general population, that give a tiny increase in the risk of getting MS were confirmed, and 29 new ones identified.

Another five are strongly suspected as being involved, bringing the total number of genetic variations associated with MS to 57.

Professor Alistair Compston of the University of Cambridge told the BBC: “This is suddenly a big new number of genes to try to understand.

“80% of the genes that are implicated by the 57 ‘hits’ are immunological. This shouts out that this is an immunological disease at the beginning. This is a very important confirmation.”

Around 2.5 million people around the world have MS, 100,000 of them in the UK.

MS is not directly inherited and there is no single gene that causes it. However, research suggests a combination of genes common in the general population make some people more susceptible to developing the neurological disorder.

Other environmental factors are involved, possibly something in the environment, such as a virus or bacteria, or Vitamin D from exposure to sunlight.

Simon Gillespie, Chief Executive of the MS Society said: “By identifying which genes may trigger the development of MS, we can identify potential ‘risk factors’ and look at new ways of treating, or even preventing, the condition in the future.”

Some of the genes found to be important in MS are also implicated in other autoimmune disorders, such as Crohn’s disease and Type 1 diabetes, a separate research paper, published in PLoS Genetics, has reported.

Castlebeck To Close Second Care Home, Rose Villa

August 10, 2011

A second care home owned by the company at the centre of allegations of abuse of vulnerable patients is to close, it was announced on Wednesday.

Castlebeck, which owned the Winterbourne View care home in Bristol where abuse was filmed by an undercover BBC journalist for Panorama, has said it will close Rose Villa, also in Bristol.

Four members of Rose Villa’s staff were suspended last month following an inspection by regulator the Care Quality Commission (CQC) while allegations of misconduct were investigated. But Castlebeck today said it was closing the rehabilitation centre for adults with learning disabilities, which has five patients and 30 staff, for “operational reasons”.

Winterbourne View, which saw 13 staff members suspended over allegations of abuse, closed in June.

Castlebeck’s chief executive, Lee Reed, the company was closing the site “with regret”.

“The service is being closed purely for operational reasons,” he said. “Whilst we recognise the concerns raised in the recent CQC inspection report, our decision has resulted from the fact that in reviewing operational practicalities, Rose Villa would be left on its own in the South West – some distance from the support that could be provided by our services in the West Midlands.

“The decision is purely voluntary and not at the instigation of CQC.

“We very much appreciate the support given to Rose Villa by commissioners since the service opened. However, we also understand the scrutiny they are under in terms of continuing to commission from a service where CQC have identified concerns, albeit that these could, in our opinion, be relatively easily addressed.”

The CQC carried out an inspection of Rose Villa on 1 July, and two members of staff were suspended after concerns were raised about safeguarding.

According to the BBC, another member of staff was suspended in June after a whistleblower went public, and the fourth worker is accused of mishandling a patient.

The CQC, in a report released at the end of July, said Castlebeck must make “root and branch improvements” to its homes.

In addition to Rose Villa, the CQC said it had serious concerns about three other Castlebeck services, while another seven did not fully comply with essential standards of quality and safety.

Castlebeck has 23 sites – 11 independent mental health hospitals and 12 adult social care centres. The four which the CQC said raised serious concerns are: Arden Vale in Solihull, Cedar Vale in Nottingham, Croxton Lodge in Melton Mowbray, and Rose Villa.

The seven non-compliant sites are: Acrefield House in Wirral, Briar Court Nursing Home in Hartlepool, Chesterholme in Hexham, The East Midlands Centre for Neurobehavioural Rehabilitation in Melton Mowbray, Hollyhurst in Darlington, Oaklands in Hexham and Willow House in Edgbaston.

Staff at Rose Villa, which opened in the Brislington area of the city in December 2009, were told of the decision to close it this morning, the company said.

It said it was looking to transfer patients to other facilities with minimal disruption. All staff, it said, “will be able to apply for alternative employment within Castlebeck as appropriate”.

Winterbourne View, in the Bristol suburb of Hambrook, was closed in June after horrifying allegations of abuse were made.

The Panorama footage appeared to show vulnerable residents with learning disabilities being pinned down, slapped, doused in cold water and repeatedly taunted and teased.

Extraordinary People Star Stuart Wickison Dies

August 10, 2011

A disabled man who starred in an emotional TV documentary about his rare illness has been found dead after driving his electric wheelchair into a lake.

Brave Stuart Wickison, who was diagnosed with degenerative Duchenne muscular dystrophy aged three, was spotted by a child at Shinewater Park, Eastbourne, East Sussex.

The 23-year-old, who starred in the 2007 Channel Five documentary Extraordinary People: The Boy Who Will Never Grow Old, had an illness which meant his body’s muscles were slowly shutting down.

Mr Wickison had began using a wheelchair aged 14 and had starred in the programme which focussed on how he dealt with the condition which only affects males.

He needed 24-hour care at Shinewater Court in Eastbourne, and had told in the programme how he ‘knew he would die some time soon’.

In the programme, Stuart said: ‘Of course, I go through moments of great bleakness and darkness when I think about what lies ahead, but I try not to dwell on it for too long otherwise I would go mad.

‘I know that I will die some time soon, and that before I die I will be very ill – possibly paralysed and in pain.’

He added: ‘The issue of my death seems much more real and it is not a pleasant prospect.

‘Instead, I think about how I want to live in the time I have left. I want to make my mark, to have achieved something. I have my art, my music and have just started at university.

‘These are all things that I take great pride in and that make my quality of life so much better than if I just gave up, sat in a corner and waited to die.’

A spokesman for the Shinewater centre said: ‘Stuart was a highly intelligent and artistic young man who will sorely be missed by all.’

The Disabilities Trust, which runs the centre, added: ‘We are all devastated by Stuart’s death. Our hearts go out to his family and friends.’

A Sussex police spokesman said: Stuart Wickison, a 23-year-old man from Milfoil Drive, Eastbourne, was found in Shinewater Park, Eastbourne, last Tuesday.

‘Police are not treating the death as suspicious. An inquest will be opened and adjourned within the next week.’

Mr Wickison’s parents, David and Mandy Wickison, were unavailable for comment.

Government E-Petition To Scrap PIP And Save DLA

August 10, 2011

I’ve just found out about and signed this e-petition on the Government’s e-petition site. It calls for PIP to be scrapped and DLA saved.

Same Difference has always supported the scrapping of PIP and the saving of DLA, so can I ask all my UK readers to take a minute to sign this e-petition.

Autism Friendly Films

August 9, 2011

What a great idea, especially in the summer holidays.

London Riots: The Disability Link Behind The Headlines

August 9, 2011

Readers, I feel the time is right to tell you something about me that you may not know. I live in London. Thank goodness, I’m safe and far away from the riot areas. I’ve spent the last three days watching the news in shock. So far, I hadn’t spotted a disability link in the riots. But, dear readers, to borrow a phrase from BBC Ouch, Disability Is Everywhere. Yes, even in the middle of madness. I’ve just spottted this Tweet:

http://twitter.com/#!/CrippledWriter/status/100695134273933313

So now, I think the time is right to ask you- are you a disabled person, or a carer of a disabled person, living in London? How have the riots affected your daily life and/or your disability? Have you had to cancel a medical appointment, or been left without transport or carers? Or do you live in an affected area? Please do share your experiences in the comments below.

Dave Heeley’s New Challenge

August 8, 2011

I first heard of Dave Heeley three years ago, when he ran 7 marathons in 7 cities in 7 days. I hope he is as successful now as he was then!

A blind man who raised thousands of pounds for charity by running seven marathons in seven days on seven continents is planning a new challenge.

Dave Heeley, from West Bromwich, aims to run 10 marathons in 10 days travelling from John O’Groats to Land’s End and cycling between each stage.

The race covers about 1,000 miles (1609km) and is in aid of Macmillan Cancer Support to marks its centenary.

Mr Heeley, known as Blind Dave, said he had been doing intensive training.

He set off this weekend for the competition which starts on Wednesday, to coincide with the birthday of the charity’s founder, Douglas Macmillan.

He will start each day with a marathon run of 26.2 miles (42.16km), before cycling by tandem to the next destination.

Mr Heeley will travel about 750 miles by tandem within 10 days.

The fundraiser said: “We’re going to be on foot and in saddle up to 14, maybe 16, hours a day so it’s going to be a tall ask but it’s a fantastic charity so we’re going to give it our best shot.”

Can Disabled Muslims Break The Rules Of Ramadhan?

August 8, 2011

A very interesting post from the BBC Ouch! Blog, that some disabled Muslims might find useful.

Oscar Pistorius Selected For SA World Championships Team

August 8, 2011

Progress for Oscar Pistorius:

The double-amputee runner Oscar Pistorius has been selected by South Africa’s athletics federation to compete in this month’s world championships.

Pistorius is set to become the first amputee athlete to compete at the able-bodied worlds after being chosen to represent South Africa in Daegu, South Korea, as its only runner in the 400m. He was also chosen for the 4×400 relay.

The 24-year-old Pistorius was named in a group of 26 athletes by Athletics South Africa after he smashed his personal best last month at a meet in northern Italy to make the qualifying time for the worlds and next year’s London Olympics.

The women’s 800m world champion Caster Semenya was also included and will defend the title she won in 2009 amid a storm of controversy over gender tests.

Eleven of South Africa’s athletes will be going to their first-ever world championships, including Pistorius, who had to take his case to the Court of Arbitration for Sport to be allowed to compete in able-bodied events on his carbon fibre blades. The International Association of Athletics Federations had banned the multiple Paralympic gold medal winner from able-bodied competition, saying the blades gave him an unfair advantage.

Pistorius was cleared to compete in 2008, but failed to qualify for that year’s Beijing Olympics and the 2009 worlds in Berlin. But, needing to run 45.25sec to make this year’s world championships, Pistorius clocked 45.07 last month in Lignano, Italy, his final race before the qualifying cutoff – having never run faster than 45.61sec before.

“We selected all those athletes who fulfilled the qualification criteria,” the new ASA President James Evans said. “With 11 athletes competing for the first time at this level we are very clearly looking to 2012 and beyond.”

Pitt-Hopkins Syndrome

August 8, 2011

From feral child to “human pet” at court in Georgian England, Peter the Wild Boy caused a sensation. And new analysis of his portraits may have solved the mystery of his unusual characteristics.

No-one knows if his name was really Peter – he couldn’t talk. Nor did he walk, preferring to scamper on all fours, picking the pockets of courtiers and stealing kisses.

Peter had been found living alone and naked in a German forest in 1725, presumably abandoned by parents who struggled to cope.

The following year – aged about 12 – he was brought to London by George I where he became a “human pet” at Kensington Palace.

There was much fanciful speculation that he had been raised by wolves – or perhaps bears – and this was why he ate with his hands, disliked wearing clothes and could not be taught to speak, says Lucy Worsley, curator of Historic Royal Palaces.

“At the time, people assumed Peter acted the way he did because he was a wild child. They didn’t suspect that something else could have been afflicting him.”

She initially assumed autism, but found more clues in this portrait of Peter, by court painter William Kent, that hangs in Kensington Palace.

Peter the Wild Boy portrait by William Kent (image courtesy of Historic Royal Palaces)

New analysis of this portrait suggests Peter had a rare genetic condition known as Pitt-Hopkins Syndrome, indicated by:

  1. His short stature
  2. Lustrous mop of thick curly hair
  3. Hooded eyelids
  4. Cupid’s bow mouth, with a pronounced curve to the upper lip
  5. He disliked clothes, but was wrestled daily into a green suit
  6. Pictured holding acorns and oak leaves – symbolic of living wild in the woods – and some fingers on his left hand (not seen) were fused

At Worsley’s request, Professor Phillip Beales, of the Institute of Child Health, plugged these characteristics into his database of conditions caused by chromosome abnormalities.

The closest match is Pitt-Hopkins, a genetic condition only identified in 1978, has severe neurological effects, says Professor Beales. “It’s severe learning difficulties, developmental difficulties and the inability to develop speech.”

Contemporary accounts chime with his diagnosis, such as this description of Peter’s first appearance at court:

“The wild boy played with a glove of Caroline’s [the Princess of Wales], grew fascinated by a pocket watch that struck the hours and, as was usual with him, attempted some mild pickpocketing. Furthermore, rumour spread that he had, in breach of all civilised decorum, seized the Lord Chamberlain’s staff and put his hat on before the king.”

Tales of feral children always fascinate, but Peter caused a sensation. It was the Age of Enlightenment, and he became a symbol in the debate about what it meant to be human.

“People were beginning to question established authority and religion. And they were interested in what distinguishes us from the animals,” says Worsley.

“If he has no speech, does that mean he has no soul? Do human beings really have souls? He raised lots of philosophical questions.”

A waxwork figure was exhibited in the Strand, and noted authors – Jonathan Swift and Daniel Defoe among them – penned pamphlets about the wild boy.

But attempts to civilise him came to naught.

The king invited him to dine, but was horrified by his lack of table manners. The court doctor tried and failed to teach him to speak. Each day courtiers would wrestle him into a green velvet suit and each evening would try to persuade him into bed. Peter preferred to curl up on the floor in a corner of his room.

His novelty eventually waned, and the court paid for him to retire to a Hertfordshire farm.

“Many people like him in Georgian England would have been freaks in a circus, but he ended up in good hands. The farmers were fond of him, and had a collar made for him,” says Worsley.

“It looks like the collar of a dog or a slave. But it was made with a kind thought, as when the wind blew in a certain direction, he would wander off. The inscription read: ‘Peter the Wild Man of Hanover. Whoever will bring him to Mr Fenn at Berkhamsted shall be paid for their trouble.'”

When he died, the locals paid for a headstone. Even today, flowers are laid on his grave.

“He was a very gentle character and in some ways, more human than the rest of us,” says Worsley. “His very existence exposed the shallow artifice of Georgian society as a bit of a sham.”

National Treasures Live, which delves into Britain’s historical sites and stories, is a five-part BBC One series starting Wednesday 10 August at 19:30

Training For Cumbria Deafblind Guides

August 7, 2011

More direct help is to be offered to people living with dual sensory loss in Cumbria, after county council bosses approved a £40,000 funding programme.

The cash is being used to train guides for deafblind people in the county.

Twelve guides will aid people with both sight and hearing loss with a range of issues, including the use of computers, telephones and public transport.

The number of deafblind people in the county is estimated to rise from 3,200 to 4,000 by 2020.

James Airey, cabinet member for adult social care, said: “Many of the difficulties that people with dual sensory loss live with are what the rest of us take for granted without a moment’s thought.

“There is a need for people who are deafblind, and have profound communication difficulties, to have regular support to maintain their independence and help them continue to contribute to family and community life and deal with the considerable challenges of living with dual sensory loss.

“The guides will be a link between the person who is deafblind and the community, minimising isolation and teaching the skills required for ongoing independence.”

Blue Lamp Foundation Helps Injured Paramedic Return Home

August 6, 2011

A Staffordshire paramedic who nearly died in a crash has been helped by PC David Rathband’s charity the Blue Lamp Foundation so that he can go home.

John Eames was badly hurt in February when a Polish lorry crashed into the ambulance he was travelling in.

He spent 22 weeks in hospital and is the first recipient of a charity for emergency personnel set up by the officer shot in the face by Raoul Moat.

The charity paid for home improvements to enable Mr Eames to live at home.

The paramedic’s right leg has been shattered and his house in Burton-on-Trent was found to be unsuitable for wheelchair use.

‘Amazing feeling’

The Northumbrian charity gave him £2,500 to adapt the house so that he could move back in with his wife Sarah and recover in his own home.

“It was a strange but amazing feeling when PC Rathband himself rang me,” Mr Eames said.

The foreign lorry was driving on the wrong side of the road when it crashed into the ambulance.

Mr Eames said he hoped one day to be able to resume his career as a paramedic.

PC Rathband was blinded by fugitive gunman Raoul Moat in Northumbria in July 2010 and his charity offers financial help to injured firefighters, police officers and paramedics.

Lib Dems To Demand Changes To ESA

August 6, 2011

A bit of good news from yesterday’s Guardian:

The Liberal Democrats are to demand sweeping changes to the much-criticised employment support allowance (ESA), the chief benefit for Britain’s 2.5 million sick and disabled people, providing a potential breakthrough for disability campaigners.

The Lib Dems are expected to back a motion at their annual conference next month calling for fundamental changes to the system, including the work capability assessment (WCA), a test that sick and disabled people are required to take before being deemed eligible for the benefit.

The test, run by a French company, Atos Healthcare, has been described as impersonal and ill-equipped to deal with the subtleties of medical conditions.

Campaigners have argued that as many as 70% of claims initially turned down are subsequently upheld on appeal, although the Department for Work and Pensions says the true percentage is 40%.

The scheme went nationwide in April.

The Lib Dem motion, to be proposed by Liberal Youth, will make five key demands at conference:

• A clearer assessment criteria and descriptors, to make it more apparent under what circumstances ESA is paid.

• Greater accuracy in assessment, particularly for those with fluctuating conditions.

• A less stressful assessment process.

• People with disabilities getting the support they need.

• All ESA claimants on appeal to be given access to adequate representation.

Ministers have admitted that the test at the outset was poorly designed and, following a review by Professor Malcolm Harrington, made changes. Professor Harrington has now been asked to conduct a second review.

Tom Wood, chair of Liberal Youth, said any assessment process that gets so many decisions wrong at the first attempt is not a true public service. “If the Royal Mail put 40% or 70% of its letters into the wrong mail box, and then said it would get it right second time, you would not have any confidence in the Royal Mail. The difficulty is that Atos are being paid to reject people that distorts the meaning of a public service. It is also clear that unless you have legal representation, the chances of an appeal being successful are a lot smaller. The changes we are seeking are not on the edges, they are fundamental.

“If this motion is passed, as I fully expect, then the government will have to listen. We have already shown with the health service that the Liberal Democrats can force changes onto the government and that is what we want here.”

It is also likely that if the motion is passed, political cover will be given to Lib Dem peers to press for changes to the welfare reform bill still before the Lords. The motion also calls for an end to the planned one-year limit on the payment of contributory ESA that is paid to those claimants satisfying national insurance contributions. The change is expected to save the government £1.1bn by 2014-15 and will affect 700,000 people by 2014-15.

Wood said he recognised the need to bring the deficit down, but claimed the one-year limit was arbitrary.

The DWP said: “The number of people winning appeals for the WCA is much lower compared to the old test, but we are determined to get this right. That’s why we are working closely with Professor Harrington to make the medical test as fair and effective as possible, and help more people to take the first steps towards sustainable employment.”

Storme Toolis- And Her Wheelchair- Star In The Inbetweeners Movie

August 5, 2011

Her very special mother, the writer Dea Birkett, explains all in this article from today’s Telegraph.

Alton Towers Customer Asked To Show Doctor’s Letter For Special Ride Access

August 5, 2011

This is crazy. Her disability is physical and very visible. She shouldn’t have to prove it in any way, let alone a way that causes such inconvenience!

Britain’s biggest theme park is used to giving its customers a truly shocking experience on its rides.

But for Rosie Belhamza the shocks began before she got to Alton Towers.

When she rang to book Rosie was told that despite having only one leg, she had to prove her disability with a doctor’s letter to get special access to rides.

Rosie, 47, who suffers from diabetic neuropathy which led to her losing her right leg after an accident, said: “I took my nephew to Alton Towers last year and all that was needed was my Disability Living Allowance letter.

“But when I rang last week they insisted I produce a doctor’s letter explaining my condition.”

The admin officer, of Derby, added: “I’m angry. They told me to book an urgent doctor’s appointment but I think most GPs would find this unacceptable. Many also charge up to £50 for a letter.”

The park, in Alton, Staffs, visited by three million people a year, boasts in its disabled visitors’ guide: “Our policy has been updated to provide an even better service to those who need it.”

But Neil Coyle of campaign group Disability Alliance said: “Forcing people to get a doctor’s letter is not reasonable.

“The Mirror has exposed this when a third of disabled people are in poverty. Many will struggle to afford both a day out and a GP’s letter.”

Alton Towers said: “We are sorry a customer was asked to book an urgent doctor’s appointment and we apologise. We aim to ensure disabled guests are treated with respect.”

The park – owned by global leisure firm Merlin Entertainments Group – said its policy was “reviewed with the help of organisations including Scope”.

But charity chief Richard Hawkes said: “We’d encourage Merlin to work with disabled customers to make their theme parks easier to enjoy, rather than putting extra costly red tape in their way.”

A Song For Danny Alexander

August 5, 2011

Written by Sue Marsh. Based on one of my favourite songs. Posted with permission.

Oh Danny Boy!
The jags and jags are calling.
From No.10 and from the Treasury.
The passion’s gone and ESA forgotten.
T’was you t’was you, but now you’ve turned away.
So come ye back! Remember how we need you
Disabled, sick and vulnerable in need.
We’re all still here, forgotten in the shadows.
Oh Danny Boy! Oh Danny Boy, we need you so.
And if one day, you think again of ESA
And I am dead, as dead I may well be
Will you recall, the times you said you’d help us?
Or hide away? Pretend you cannot see?
We have no friends, no politicians caring
No-one to save our fragile dignity.
Will you come back and fight for what your heart knows?
Your time has come to be the man you ought to be.

Stephen Delaney Attackers Get 3 Years Custody

August 5, 2011

Two men who attacked a disabled man in his own home have each been given three years’ custody at Mold Crown Court.

James Toby Wilkinson, 27, of Prestatyn, Denbighshire, and Thomas McManus, 19, of Gronant, Flintshire, admitted unlawfully wounding Stephen Delaney.

The jury heard the assault happened after they were not shown a display plate which they thought valuable.

Wilkinson was jailed. McManus, who also admitted possessing a knife, received three years youth detention.

Emmalyne Downing, prosecuting, said the defendants asked to be let in after ringing the doorbell of Mr Delaney’s home in Gronant in the early hours one day in March this year but were at first refused.

After being told they would not be long, Mr Delaney let them in and poured them a glass of wine.

Wilkinson began asking about a particular display plate he thought valuable, the court heard.

When Mr Delaney told them he had sold it, he was accused of lying and was attacked.

Wilkinson said: “Let’s do it”. As McManus held a knife to Mr Delaney’s throat, Wilkinson said: “Go on, do him.”

The court heard Wilkinson then picked up a vase and struck Mr Delaney twice over the head with it. When the vase broke, he picked up a jug and then used that to continue the assault.

Ms Downing said: “The victim felt powerless, was stuck in his chair and he thought that he was going to be killed.”

Judge Philip Hughes said Mr Delaney had been badly affected by the trauma and required 11 stitches.

Health affected

He told the defendants: “The two of you were in this very much together – a joint attack on a vulnerable victim in his own home.”

He said if the pair had been convicted after a trial then they could have expected a sentence of four-and-a-half years.

In a victim impact statement, Mr Delaney told how he was disabled, suffered flash backs, was reluctant to go out, and he said that the attack had set his health back.

The court heard that after the attack, the pair allowed Mr Delaney to ring the police who found the two defendants still sitting in the victim’s living room.

Henry Hills, defending Wilkinson, said his client, who had been drinking vodka, was ashamed and remorseful and genuinely could not remember what had happened.

The court heard that in his police interview, McManus suggested Mr Delaney had fallen over but had limited recollection of the incident due to the amount of alcohol he had consumed.

Gwyn Jones, defending McManus, stressed that the knife had not been used.

He said his client was a most naïve and immature teenager who accepted that anyone who had a knife in such a situation had to go to custody.

Leo Whiten

August 5, 2011

A “very engaging” little boy left with profound disabilities as a result of medical negligence during his birth has been awarded a compensation package worth around £6.6 million.

Leo Whiten, now aged seven, suffered severe brain damage when he was delivered at London’s St George’s Hospital in June 2004, resulting in “catastrophic injuries”.

At the High Court, Mrs Justice Swift, who assessed the various sums to be paid to Leo, said: “Despite his profound disabilities, it is clear that he is a very engaging and generally happy child who is socially aware and thoroughly enjoys the company and attention of adults and other children.”

Leo, of Tooting, south-west London, claimed damages against the St George’s Healthcare NHS Trust for personal injury and financial losses sustained as a result of the negligent management of his mother’s labour and his birth.

Breach of duty was admitted in September 2005, said the judge, and in March 2006 “the defendant further admitted that its breach of duty had caused the claimant’s injury”.

Leo was the first child of Simon Whiten, now aged 42, and insurance data analyst Samantha Nowell, now 33. Mr Whiten was the group commercial manager for the trade newspaper The Publican and now runs a “dotcom” business from home.

Mrs Justice Swift, giving her ruling in London, said the experts agreed that Leo “will always be totally dependant on the care of others for all his daily activities”.

She added: “He will never be able to live independently, will not be capable of any form of employment and will never have the necessary mental capacity to be able to manage his own affairs.”

Leo has limited mobility and cannot stand or walk unaided. He can vocalise, but has no “functional speech”.

The award includes a lump sum of £2.7 million, while most of the damages will be in the form of annual payments to ensure care for Leo for the rest of his life.

Distinctions Must Be Made In Assisted Suicide Debate Says Frances Ryan

August 5, 2011

In this interesting post from the Guardian’s Joe Public blog today.

Pensioner Pulled To Safety As Mobility Scooter Explodes

August 5, 2011

A PENSIONER narrowly escaped being burned alive – when his mobility scooter turned into a fireball.

Aiden Cassidy, 77, was stuck helplessly on the vehicle as an electrical fault sent flames spurting out under his seat.

Moments before it exploded, his home help Anita Coombs drove past, spotted the danger and dragged Aiden to safety in Melton Mowbray, Leics.

Stroke victim Aiden, who is paralysed down his left side, said: “I could have been barbecued if it wasn’t for Anita. The scooter cut out and flames were coming over the back where the batteries were.”

Modest heroine Anita, who works for Help at Home, said: “It was very fortunate I was there.”

Aiden was setting off for a car boot sale when the scooter, which he bought second-hand for £1,500, sputtered to a halt.

He said insurers had refused to pay out because a “botched” repair job had caused a short-circuit.

The Health Department has warned mobility scooter users to get them regularly serviced by reputable mechanics after recent fires caused by electrical faults.

Campaigners Want MS Drug Rethink

August 5, 2011

Health campaigners have expressed disappointment after the medicines watchdog rejected the first pill to treat multiple sclerosis.

The MS Society urged the National Institute for Health and Clinical Excellence (Nice) and drug firm Novartis to work together so Gilenya (also called fingolimod) can be re-appraised.

In draft guidance, which is subject to consultation, Nice rejected the drug due to “uncertainties” over its effectiveness, a lack of appropriate data and concerns over cost-effectiveness.

It said it was unclear how much the drug would help the specific group of people for whom it was licensed – adults with relapsing-remitting multiple sclerosis (RRMS) who experienced at least one relapse a year despite being treated with beta interferon drugs.

Another group of patients suitable for the drug were those with rapidly evolving severe RRMS, who experience two or more disabling relapses regardless of their treatment.

Nice said Novartis had submitted data mainly looking at a subgroup of patients with the former type of MS. Novartis also only submitted data comparing Gilenya with a placebo and with a type of beta interferon not believed to be widely prescribed on the NHS, according to Nice.

Professor Carole Longson, director of the health technology evaluation centre at Nice, said: “While it’s important that people with multiple sclerosis have treatment options, Nice has to ensure that the NHS provides treatments that bring benefits that are value for money.

“Unfortunately our independent committee wasn’t given sufficient evidence to show that fingolimod could reduce relapses considerably better than the other treatments currently being used.

“Based on the available clinical evidence and economic analysis, our independent committee concluded that fingolimod would not be effective good use of NHS resources.”

Simon Gillespie, chief executive of the MS Society, said: “This is disappointing news for people with MS and it will leave some people with no effective treatment option. Access to MS treatments in the UK is very poor – in fact people with MS would be better off living almost anywhere else in Europe, and this decision will only deepen that inequality.”

Choices Care In Administration

August 5, 2011

A care group providing services to about 800 people with learning disabilities in Scotland and north-east England has gone into administration.

Administrators were called in after Choices Care suffered continuing cash flow difficulties.

The Livingston-based group employs 1,400 staff and provides supported living, home care and residential services.

Administrators at Zolfo Cooper said services were continuing uninterrupted.

The supported living division has already been sold to Mears Care Scotland Limited, with about 500 staff transferring to their new employer with immediate effect.

Continue reading the main story

“Start Quote

We will continue to ensure that service users experience no disruption to the quality care they are accustomed to”

Peter Holder Zolfo Cooper

Zolfo Cooper said the registered services and home care divisions would continue to trade as normal with a view to selling these as going concerns.

The administrators said they had already received inquiries “from a number of interested parties”.

All staff employed in the divisions would continue to be employed as normal.

Zolfo Cooper partner Peter Holder said: “The key aspect all along in this process has been to ensure that services continue to be provided to all users without interruption.

“We are extremely pleased therefore to have agreed a swift sale of the supported living business and wish all parties concerned well in their respective futures as they continue to provide services to users.”

Mr Holder said administrators were now focusing on securing a suitable buyer for the remaining businesses.

He added: “We have already received a number of inquiries from interested parties and would welcome further expressions of interest.

“In the meantime, we will continue to ensure that service users experience no disruption to the quality care they are accustomed to.”

David Smith

August 5, 2011

David Smith was born with a club foot but went on to represent Britain in bobsleigh, karate and rowing.

Then last year, doctors discovered a large tumour embedded in his spine and surgery to remove it led to temporary paralysis.

He has not only now taught himself to walk again but has just been selected to represent Britain in the upcoming World Rowing Championships in Bled, Slovenia.

Here he talks about how he was diagnosed, and how he recovered from life-threatening surgery to row again.

Kieran Forde-Thain

August 4, 2011

A five-year-old boy from Greater Manchester who made an appeal on You Tube to raise money for surgery in the US is recovering from his operation.

Kieran Forde-Thain, from Davyhulme in Trafford, has a form of cerebral palsy, known as periventricular leukomalacia.

His online appeal helped his family raise £55,000 for surgery at St Louis Children’s Hospital in Missouri, which is not available in the UK.

He had the operation, called a selective dorsal rhizotomy, on 26 July.

The specialist team have carried out the procedure – which involves cutting unresponsive nerves in the spine to increase muscle tone – on about 50 children from the UK.

‘Long way ahead’

Kieran is due to undergo another operation on 11 August and will also have to have intensive physiotherapy for months.

The surgeon, Dr T.S. Park, said: “He will be able to walk by himself without any support.”

“Obviously that will improve the quality of his life and also it will improve the quality of his family because he won’t need any special care.”

Kieran’s father, Jonathan Thain, said: “There is going to be a long way ahead but we couldn’t have done it without everyone’s help.”

Amanda Forde, Kieran’s mother, said she was looking forward to being able to tell him that they had done all they could for him.

“We have made it the best we possibly could for him,” she said.

Access To Work: Good News

August 4, 2011

I’ve just seen this Tweet:

http://twitter.com/#!/michelelataylor/status/99103338259415040

This is good news. I used the Access To Work scheme in my last job. It paid my transport costs.

On a much less personal note, I think the scheme is a great idea that should hopefully encourage disabled people to do as much work as possible. So I think as much money as possible should be allocated to the scheme and to raising awareness of it- there are many disabled people who don’t even know it exists.

There are, like everything else, disadvantages to AtW- the biggest one being that they don’t support you unless you’re doing paid work. So employers also need to be made aware of the scheme. We can only hope that knowing that some of the extra costs of hiring a disabled person may be met by the Government would make employers more willing to employ disabled people.

Benefit Cheat Caught Playing Golf

August 4, 2011

A benefit cheat who claimed he could not work because of arthritis in his hands was caught when secret footage captured him playing golf.

Peter David Crowder, 50, from Maghull, Merseyside, claimed Disability Living Allowance worth £20,217 between October 2006 and September 2010.

He admitted failing to declare a change of circumstances and making a false statement to obtain benefits.

His case was adjourned at Liverpool Magistrates’ Court until 25 August.

District Judge Miriam Shelvey warned him that the offences could carry a custodial sentence.

The court heard how Department for Work and Pensions (DWP) investigators carried out covert surveillance on Crowder, of Parkbourn Square, following an anonymous tip off.

He was seen driving, chipping and putting golf balls at Hurlston Hall Golf and Country Club, Lancashire, where it is understood he was a member since 2006.

Golf competitions

Club records showed the former psychiatric nurse at Ashworth Hospital attended the club 151 times between 4 April 2009 and 28 May 2010.

The court heard he retired from his job on medical grounds claiming that he was suffering from rheumatoid and osteo-arthritis and had “problems” with his hands and feet.

He was seen in the footage unpacking a golf trolley and pushing it around the 18-hole golf course.

The DWP investigations also showed that he played in 49 golf competitions between 1 January 2007 and 17 March 2010 with club score cards showing that he played with handicaps of 26, 25 and 23.

Young People With Learning Disabilities Feature In New Mencap Ad Campaign

August 4, 2011

I have just received the press release below from Mencap.

 
YOUNG PEOPLE WITH A LEARNING DISABILITY FEATURE IN NATIONAL ADVERTISING
CAMPAIGN
 
Young people with a learning disability will feature in a national TV,
radio and print advertising campaign which aims to raise £300,000 for
learning disability charity Mencap. 
 
Procter and Gamble products available at Co-operative Food and
Co-operative Pharmacy stores will help raise funds for Mencap and sister
charity ENABLE Scotland as part of The Co-operative’s Charity of the
Year Partnership. The promotion will run for six weeks from Wednesday 3
August in Co-operative Food and Pharmacy stores nationwide and Procter
and Gamble will donate 3 pence on each product sold from over 20 of
their brands, including Fairy, Herbal Essence and Pampers, to the
charity.  
 
Ellen Goodey, Ben Morse, Kirstie Andrews, Matthew McCarthy and Dharmesh
Ladd from Mencap were filmed carrying out everyday tasks like any other
young people.  A recent poll by Mencap revealed that a large percentage
of the public (41 per cent) believe that the number of people with a
disability who they have seen, heard or read about in the media does not
reflect that of society as a whole. Encouragingly, 44 per cent of the
public are keen to see, hear or read more about people with disabilities
in the media than there are at the moment 
 
Geraldine Huse, Sales General Manager for P&G in the UK & Ireland
believes this partnership is incredibly worthwhile: “Mencap do
outstanding work and P&G is delighted to partner again with The
Co-operative Food for their Charity of the year programme. We are proud
to bring the strength and reach of our brands and marketing capability
to help raise awareness and much needed funds for this great cause.”
 
Mark Goldring, Mencap’s chief executive, said: “This advert is an
exciting and bold step towards a more inclusive society. We need to see
more positive role models of people like Ellen, Ben, Kirstie, Matthew
and Dharmesh on our TVs and in public life to help remove the stigmas
associated with disability.”
 
Money raised through The Co-operative Charity of the Year partnership
will allow Mencap and ENABLE Scotland to launch a ground-breaking
programme called Inspire Me. Inspire Me will work with thousands of
young people with a learning disability aged 16 - 25, their parents and
carers, and local communities, to overcome the exclusion and prejudice
that many face in their lives. The project will do this by providing
activities and training, together with volunteering and employment
opportunities. 
 
Mencap has worked with Grey London and Smuggler to produce the advert.
 
To see the advert visit: http://www.youtube.com/watch?v=T9i9B2ZGbAQ

Mencap’s Snap! Competition- Previews Of Winning Images Released

August 4, 2011

I have just recieved the press release below from Mencap.

Mencap have today released six preview winning images from this year’s Snap!, their annual film and photography competition, following the judging last month.

 

The judging for the competition, which is sponsored by FUJIFILM UK Ltd and The Sorrell Foundation, took place in July at Somerset House in London’s West End. The panel of 11 judges included journalist Kate Spicer, Lady Frances Sorrell, creative director Gary Harvey, two members of Mencap’s learning disability panel; Lorainne Bellamy and Dean Meuleman, and former Snap! 2010 winners, John and Shauna Hogan.

 

Kate Spicer comments: “The quality of the photographs is improving every year, and the stories they tell have real depth and impact. I loved the opportunity to look at every single entrant’s story, not just the winner’s, it’s a privilege.”

 

The panel sifted through over 600 strong entries to pick 32 photographs and four films as this year’s winners. These will be awarded prizes ranging from gold down to highly commended in the different categories.

 

To give a tantalising glimpse of the standard of the winning entries, Mencap have today released six preview images. These range from one entry entitled ‘True friendship’, a moving photo in the My heroes category of two friends who both have a learning disability to an entry in the My achievements category called ‘My mum says I’m sociable now!’ The latter is an engaging image of six year old Sebastian who has autism, settling into his after school club after initial difficulties.

 

Stacey Foster’s entry of ‘True friendship’ reads: “This is my very special friend from the day centre we attend. Even though I can’t speak it doesn’t bother him and he makes me smile and he makes me laugh every time I see him.”

Mencap’s head of communications, Sarah Bernard, says: “We’ve had some incredible entries in this year’s Snap. I think the judges have done a great job in choosing a selection of images which show a range of styles and subject matters. The preview images give people a taste of the great standard they can expect to see at the awards ceremony in September. People with a learning disability often face barriers in communicating with others, these images show a fantastic and creative insight into their world.”

 

The remaining 30 winners will be revealed at the prestigious celebrity awards ceremony on 13 September 2011 at London’s Rich Mix arts centre in Shoreditch. After the ceremony there will be a winner’s exhibition firstly at Fuji’s headquarters in Bedford and later at the Rich Mix gallery.

 

To view the six preview images go to www.mencap.org.uk/node/12897

 

Snap! is sponsored by FUJIFILM UK Ltd and The Sorrell Foundation.

Kaliya Franklin And The Electric Wheelchair Search

August 4, 2011

Well, that title’s not completely accurate. You see, she found the chair- this Guardian blogpost includes a photo of it. The problem is, the NHS won’t pay for the chair, as they say she’s ‘not eligible.’ The rest makes a brilliant blogpost.

Cpl Tom Neathway

August 4, 2011

A paratrooper who lost both legs and an arm in an explosion in Afghanistan is so determined to drive again he is training to compete in the Dakar rally.

Cpl Tom Neathway, from Worcestershire, who is based at RAF Brize Norton in Oxfordshire, was injured when a booby trap bomb detonated, in 2008.

He has now recovered enough to compete with the Race2Recovery team, with other wounded soldiers.

Cpl Neathway said the challenge kept him “sane” and helped him physically.

In total, the team of injured soldiers aims to raise £2m for three forces charities, The Royal British Legion, Help for Heroes and Combat Stress.

In 2012, the Dakar Rally route will cover more than 9,000km (5592 miles) from Argentina-to-Peru.

But the route for the race in 2013, in which Cpl Neathway hopes to take part, is not yet known.

Whichever country it takes place in he will have to spend 20 hours a day speeding over difficult terrain at 80 to 90 miles an hour.

He said: “It’s really demanding stuff.”

On Sunday night, the Race2Recovery team was featured on BBC Two’s Top Gear programme after being trained by former “Stig”, Ben Collins.

During the rally Cpl Neathway will be co-driving for off-road racer, Dave Marsh.

Mr Marsh owns the company that build the Wildcat off-road vehicles that the team will be driving.

If Cpl Neathway completes the race he will be the first triple amputee to do so but no concessions have been made to cater for their disabilities.

“The cars are completely standard,” he said. “We just wanted to be able to do it without any adaptations.”

Mental Health Expert William Bingley Dies

August 4, 2011

Did any readers know him?

Tributes have been paid to a leading mental health expert who died when he slipped and fell while walking on a Cumbrian fell.

William Bingley, 61, of Caton, Lancaster, was on a narrow path above Rawthey Gill leading to Uldale Force when he fell on Sunday.

He was airlifted to hospital, where he was pronounced dead.

A family spokesperson said he had “inspired great respect and affection” in those who knew him.

Mr Bingley was walking with his wife, Helen, and a friend when he fell.

‘Positive impact’

He was the former chair of NHS North Lancashire and chief executive of the Abaseen Foundation, a charity developing healthcare and education in Khyber Pakhthunwa, North West Pakistan, which he set up with his wife.

He had also been legal director of Mind and wrote the Code of Practice for the 1983 Mental Health Act for the Department of Health.

Mr Bingley was a former chief executive of the Mental Health Act Commission and professor of mental health law and ethics at the University of Central Lancashire.

The spokesperson said: “William inspired great respect and affection in all who knew him.

“His work at home and overseas has made a positive impact on the lives of many.

“He leaves his wife, Helen, two daughters, Alexandra and Harriet, and step-daughter, Andrea.

Details of his funeral will be announced soon.

Kylie Grimes Loses Compensation Claim

August 3, 2011

A woman who hit her head on the bottom of a swimming pool during a late-night party in Surrey has lost her claim for £6m damages in the High Court.

Kylie Grimes, now 23, of Stephendale Road, Farnham, was left paralysed after she dived into the pool in August 2006.

The pool owner David Hawkins, of Compton Way, denied liability and said he considered the pool safe.

Ms Grimes was paralysed from the chest down when she broke a vertebra below the base of her neck.

She claimed her injury was caused by Mr Hawkins’s negligence or breach of his duties under the Occupiers’ Liability Act.

Invited friends

The court heard in May that Mr Hawkins and his wife were away on the night of the accident, but their daughter Katie had asked her father to let her have a few friends over.

She said she did not invite Ms Grimes and did not expect people to go swimming, but did not know how to stop them, so turned the lights on for their safety.

She also said no accident had ever happened in the 30ft (9m) pool which had a deep end of less than 6ft (1.8m).

Philip Mott QC, for Ms Grimes, said the pool house should have been locked or there should have been warning notices.

He said Ms Grimes was “clearly” invited back and was lent swimming kit by Ms Hawkins.

Manchester City Council Loses Care Cost Appeal

August 3, 2011

Manchester City Council has lost an appeal over costs after unlawfully removing an 18-year-old with learning difficulties from his long-term carer.

The teenager, with a mental age of two, was not returned to his carer after a respite period as false allegations had been made against the carer.

The decision to remove the teenager was described as “deplorable” by a High Court judge in March 2010.

The Court of Appeal has ruled that the payment order will stand.

The amount of the costs has not been disclosed.

The order, which includes amounts to be paid on an indemnity basis, was made by Mr Justice Baker last March in the Court of Protection.

On Tuesday, Lord Justice Mummery, sitting with Lord Justice Hooper and Mr Justice McFarlane, ruled the order was justified by the council’s failings.

‘Stand by decision’

Liz Bruce, the council’s director of adult services, said the authority noted the ruling of the court.

“As we said at the time of the original ruling, we strive to make good professional judgements and offer the best support to vulnerable adults and families we can, but this case illustrates how difficult a job that can be,” she said.

“We had to act after serious concerns were raised about this young man’s welfare. It wasn’t an easy decision to keep ‘E’ in the home where he was receiving respite care, but his welfare was our primary consideration.

“While we stand by our decision to keep ‘E’ where he was, the court made it clear in its ruling last year that we made serious mistakes in the way we went about it.

“We regret this and have now put in place measures so that in future similar cases we will follow the correct procedures.”