Skip to content

Benefit Claimants Should Be Banned From Buying Alcohol Or Cigarrettes Or Watching Sky TV Says Tory MP

December 18, 2012

Benefits claimants should be banned from spending their state handouts on cigarettes and booze, a Tory MP has controversially claimed.

Alec Shelbrooke told the Commons those receiving payments should be given a welfare card which would work like a chip and pin debit card. But crucially it would not work if claimants tried to use it buy alcohol and cigarettes, he said.

Mr Shelbrooke, the MP for Elmet and Rothwell, said the plan would end the “damaging perception” that those who claimed benefits were scroungers, sponging off the state.

Proposing his Welfare Cash Card Bill in the Commons, Mr Shelbrooke said the changes would “encourage responsible spending” among claimants, adding it would ensure taxpayers’ money was spent “wisely” and “for the purpose for which it was intended”.

He said: “This would alter the spending habits of a minority, who prefer to take advantage of the system, getting something for nothing.

“The something for nothing culture encouraged by the previous Labour government created a two-tier benefits system where striving low-paid workers have been penalised for the idleness of the shirkers.

“This Bill works alongside the Government’s welfare reforms to support those hard-working families who strive to be self-supporting by ending the something-for-nothing stigma of the welfare system.

“Introducing a welfare cash card on which benefits will be paid, claimants will only be able to make priority payments such as food, clothing, energy, travel and housing. The purchase of luxury goods such as cigarettes, alcohol, Sky television and gambling will be prohibited.

“When hard-working families up and down the country are forced to cut back on such non-essential, desirable, or neg items as I have called them, it is right that taxpayer benefits be only used for essential purposes.”

These political types do talk some rubbish, don’t they readers? I’d be lost without Sky TV! How would he feel if someone asked him to live the way he is proposing we should?

I’d like to remind him that some benefit claimants claim through absolutely no fault of their own. Benefit claimants are human, too, and every human being deserves some pleasure in their life. If that pleasure comes from Sky TV, then so be it.

When I told my mum about this moment of madness, she reminded me that carers are also benefit claimants. Carers work very hard 24/7. As I’ve said before, I think their benefit is too low, if anything. Why should they not use Carer’s Allowance for anything they wish?

Mencap Expresses Dismay At UKIP Council Candidate’s Downs Abortion Comments

December 18, 2012

I seem to have missed this. Let me use this post to express my dismay at these comments and to say that now I have a reason to strongly dislike UKIP.

A disability charity has expressed dismay after a Ukip candidate suggested forcing mothers carrying foetuses with Downs syndrome or spina bifida to have abortions to avoid the child being “a burden on the state as well as on the family”.

In a self-styled “personal manifesto” on his own website, Geoffrey Clarke – who is seeking seats on Kent county council and Gravesham council in a byelection later this month, as well as to Ukip’s national executive – said there should be a review into various drastic measures to reduce spending on the NHS, such as “giving free euthanasia advice to all folk over 80 years of age”.

Among the other ideas listed for discussion was “compulsory abortion when the foetus is detected as having Downs, spina bifida or similar syndrome which, if it is born, will render the child a burden on the state as well as on the family”.

In a “clarification to avoid confusion and misrepresentation” on the website Clarke, a 66-year-old chartered accountant, stressed that neither he nor Ukip specifically endorsed the ideas, adding: “They are suggestions of matters for the review body to properly consider, in light of the stated desire of all political parties to reduce the national debt.”

The manifesto was condemned by Mencap, which campaigns for people with learning disabilities. Mark Goldring, the charity’s chief executive, said Mencap was “disgusted and horrified”. He continued: “Much has been written about the Paralympics this summer changing attitudes towards disabled people for the better. Yet in the very same year, a council candidate has proposed forced eugenics against disabled people.

“It is abhorrent that Geoffrey Clarke sees disabled people solely as a burden, when people with a learning disability lead full lives, and make valuable contributions to their communities and families. We question if he is fit for public office.”

Clarke’s manifesto contains a number of other ideas that will raise eyebrows among Ukip hierarchy as the party attempts to enter the mainstream and shed its image as, in David Cameron’s now revoked words, “fruitcakes, loonies and closet racists”.

On immigration he calls for the immediate deportation of “riff raff” elements, demands the revision of passages of the Koran and quotes seven verses of a self-penned poem about defending British culture titled, We Must Turn The Tide, And Then Advance.

Clarke told the Guardian that he did not support the forced abortion idea but did want to create a debate on how the NHS could be financed in the future. He said: “Those are suggestions for a review body to consider when they look into whether the NHS is affordable in the future. I do tend to provoke thought by throwing out ideas. I do like to be provocative.

“But they’re not necessarily my views. I’m throwing out matters for the review body to consider. I’m not qualified to consider them. Therefore they are not my views, as I don’t have the qualification to hold those views.”

Clarke said he apologised for any offence. Asked if he regretted raising the idea he said: “I regret articulating it in the way I have, and I’m going to rewrite it.”

Clarke said he knew one person with Downs syndrome and thought he knew one person with Spina bifida. Neither were a burden on their families or the state, he said.

Updated 9pm: I’m very pleased to read he’s been suspended!

Alan Martin Of Mouse On The Move Dies

December 18, 2012

I’m very sad to read of the death of Alan Martin, the wheelchair dancer and disability awareness trainer who ran Mouse On The Move.

Alan had Cerebral Palsy and used a communication aid, describing himself in his CV  as “the only dance workshop leader in the world who uses an electronic speech aid.”

My thoughts are with all who knew him personally.

Cystic Fibrosis Woman Died After Getting Donor Lungs From Smoker

December 18, 2012

A 27-year-old woman with cystic fibrosis died of cancer after she was given the donor lungs of a smoker.

Jennifer Wederell, of Hawkwell, Essex, died at home in August – 16 months after the transplant at Harefield Hospital in London.

Colin Grannell said he believes his daughter would not have agreed to the transplant had she known the middle-aged donor was a heavy smoker.

The hospital has apologised for not giving her that choice.

Jennifer had been diagnosed with cystic fibrosis at the age of two and by her mid-20s was using oxygen 24 hours a day.

She had been on the waiting list for a lung transplant for 18 months when in April 2011, she was told there had been a match.

Mr Grannell said the family had “lived all for that moment” for years, and thought it would help Jennifer “cheat” her condition.

She married her fiance David Wederell in September last year, but by February 2012 a malignant mass was found in her lungs.

‘Should have choice’

“The shock immediately turned to anger in so far as all the risks were explained in the hour before her transplant and not once was the fact smoker’s lungs would be used mentioned,” said Mr Grannell.

“She was dying a death that was meant for someone else.”

He has set up a Facebook group, Jennifer’s Choice, to encourage non-smokers to sign up to the organ donor register.

The Royal Brompton and Harefield NHS Foundation Trust said: “It is very rare for patients to specify that they do not wish to be considered for clinically healthy lungs from smokers.

“This is because the risks are much higher if patients decline donor lungs from a former smoker, and decide to wait for another set of organs which are both a match for them and from a non-smoker, to become available.

“However, we recognise that Jennifer should have been given the opportunity to make this choice.

“We have apologised sincerely for this oversight.

“Regrettably, the number of lungs available for transplantation would fall by 40% if there was a policy of refusing those which have come from a smoker; waiting lists would increase and many more patients would die without a transplant.”

Artist Taxi Driver’s Take On #Savetheparents

December 17, 2012

Thanks to the Artist Taxi Driver for covering the very impirtant issue of #savetheparents for his latest video.

Bus Drivers Being Trained About Dementia

December 17, 2012

Thousands of bus drivers around Britain are being given special training so they can help passengers with dementia.

It’s part of an initiative by the Prime Minister which is trying to encourage everyone to be more aware of the needs of older people who have dementia, to help them in their daily lives.

I watched a training session at a First Group depot in an industrial part of north-west London. It is home to more than 100 buses, and a work base for 300 drivers.

Upstairs, 11 members of staff gather for what proves to be a hard-hitting couple of hours. It begins with a simple memory test.

The trainer, Keith Sheard, promises the drivers an easy exercise. He asks them to draw a picture of both sides of a 1p coin, with as much detail as they can remember.

He jokes: “Dead easy this – you handle these coins every day!”

There are groans as some of the drivers fail to recall the portcullis, or find they have written “one pence” rather than “one penny”.

Twelve points are up for grabs – but the drivers only manage between two and five.

Keith puts the exercise into the context of dementia, telling the participants: “Imagine if you forgot the detail in every aspect of your life – having breakfast, getting dressed – just imagine how frustrating that would be.”

Next the drivers are asked to write down on different pieces of paper their most prized possession, the name of their most loved person, a skill they are proud of and a treasured memory. Keith then comes round and takes away one bit of paper from each person.

He tells them: “I was your dementia for that moment in time. Just take a moment to think what your life would be like without what I’ve just taken from you.

“And if you thought it couldn’t get any worse, it does. Because over time, I’m going to come back and take everything else from you – so you’ll be left with absolutely nothing.”

The drivers admit they are finding this emotional and hard to think about. Inevitably stories emerge about family experiences.

Troublesome passengers

The briefing includes details about how different forms of dementia affect the brain. This leads into a discussion about how drivers can help confused passengers.

There are some barriers to good communication – such as the screen designed to protect inner city staff from assaults.

And the drivers admit that if someone seems troublesome on a busy bus, their first instinct is to try to remove that passenger. But now they have an extra awareness of what might be amiss, particularly if there is no smell of alcohol on the passenger’s breath.

Keith explains: “You need to be aware of the difficulty of grasping day, date and time that people with dementia have.

“You might be telling me that my pass is out of date or that I can’t use it until half past nine – but if time doesn’t have any real meaning to me, I don’t understand your point or why you’re getting so excited about it.”

The drivers are given advice which includes smiling and making eye contact, letting the passenger sit down so they have extra time to compose themselves, and not pulling away quickly if they seem unsteady on their feet.

All those in the session will now train other drivers in the First Group, and the hope is that other transport companies will follow suit.

One of the participants, Krystyna Ryan, 59, “Drivers need to be able to help their passengers who have any health issue – and dementia especially, because it’s not always recognised or spoken about.”

Nick Vane, the commercial growth director for the UK bus division of FirstGroup, sees the awareness course as a natural extension of other work in the company.

He said: “This industry has moved over a long period to improve accessibility, with innovations like low floor vehicles to help disabled people. It seems a natural progression to now look at more hidden disabilities.

“It was fascinating to watch the interaction in the session. The participants related it to personal circumstances in their families, but also to how they can help people in their work.”

Around 3,000 of FirstGroup’s drivers will have gone through the training by February.

Andrew Chidgey, director of external affairs at the Alzheimer’s Society, which helped guide the training, accepts the health service still needs to play its part in treating people with dementia – but says helping sufferers in this practical way is also vital.

He said: “What this identifies for the drivers is they have a really important role in helping people in their community to remain independent. That’s also true for people like newsagents and other workers.”

Graphic novel tells of one man’s journey through schizophrenia to recovery

December 17, 2012

 

A new graphic novel tells the true story of one man’s life with schizophrenia and his journey through psychotic episodes, asylums, medication and vagrancy.

 

Side Effects was written by Andrew Voyce who has a diagnosis of paranoid schizophrenia, and illustrated by professional graphic artist Øivind Hovland.  It was edited by Hannah Cordle and published by Recovery.

 

Andrew Voyce, from Bexhill, was born in 1951 in London. A serious road accident at age 17 left him with a disability which, combined with other life events, led him to develop schizophrenia. Over the course of 20 years, Andrew received multiple admissions and discharges to asylums in East Sussex and Kent. He was admitted eight times, three of theseunder the Mental Health Act, and ordered to receive antipsychotic medication.

 

Administered by injection, the medication caused a debilitating side effect called akathisia, or constant restlessness, which lasted for seven days afterwards. Upon discharge Andrew would cease to turn up for injections, psychotic episodes would follow, together with contact with the criminal justice system, and Andrew would be returned to an asylum.

 

Andrew credits Margaret Thatcher for changing his life when the asylums were closed down under the NHS and Community Acre Act 1990 and community care introduced. He now lives a stable life in the community and has not been an inpatient or reoffended.

 

He has revived his academic career by obtaining an MA in social and public policy, engaged with the mental health service user movement, and has seen a quality of life with personal relationships.

 

Andrew is a believer in the power of narrative to be a therapeutic and cathartic activity. As well as being a creative process, narrative can lead to catharsis and can enable moving on from difficult times. Andrew has produced narrative in text, and has published work with Chipmunka Press and in service user anthologies, such as Mental Health Recovery Heroes Past and Present.’ Andrew has also been encouraged to develop digital cartoons, http://www.slideshare.net/AndrewsAsylumLife.  Andrew speaks as an expert by experience at mental health awareness events.

 

Andrew says he is pleased to be where he is now, and to have a quality of life. He acknowledges the support and encouragement he has had from day care staff, from artists, and from local commissioners who have enabled the setting up of a social enterprise which Andrew is proud to say has now achieved two successful years.

 

About Øivind Hovland

 

Øivind spent his university years ‘living’ in the print room, experimenting with various printing techniques. Screenprinting emerged as his weapon of choice, and the technique continues to influence his digital and printed work. To Øivind, illustration is about storytelling. ‘Even if you only have one small image at your disposal, a story can still be told. And that, in a nutshell is my aim, to tell a story using whatever means I have’. He has been fortunate enough to tell stories for a long list of international clients, over a broad range of media. Øivind is also the author of two illustrated books, published by Tabella, and his work has been short listed for the Nationwide Mercury Prize Art Exhibition. He is represented by NB Illustration.

 

About Hannah Cordle

 

After graduating with a degree in English, Hannah trained as a reporter and spent ten years working as a journalist and in communications. She has a particular interest in psychology and mental health, obtaining a graduate diploma in psychology in 2010. In the same year she co-edited a collection of narratives by people with schizophrenia/psychosis, Psychosis: Stories of Recovery and Hope published by Quay Books.

 

Side Effects was funded by a £14,400 grant from the Maudsley Charity. For further information or to buy a copy of Side Effects please contact SideEffectsBook@yahoo.co.uk

Autism Community Reacts With Anger To Media’s Link Between Newtown Gunman And Autism Spectrum Disorder

December 17, 2012

BBC Ouch Gives Tips For An Autism Friendly Christmas

December 17, 2012

People with autism can find Christmas difficult. If that describes someone you love, BBC Ouch has some tips that might help.

Paralysed Woman Controls Robotic Arm With Thoughts

December 17, 2012

Unrivalled control of a robotic arm has been achieved using a paralysed woman’s thoughts, a US study says.

Jan, who is 53 and paralysed from the neck down, was able to deftly pick up, move and place a variety of objects in a manner similar to a normal arm.

Brain implants were used to control the robotic arm, in the study reported in the Lancet medical journal.

Experts in the field said it was an “unprecedented performance” and a “remarkable achievement”.

Jan was diagnosed with spinocerebellar degeneration 13 years ago and progressively lost control of her body. She is now unable to move her arms or legs.

Robo-arm

She was implanted with two sensors – each four millimetres by four millimetres – in the motor cortex of her brain.

A hundred tiny needles on each sensor pick up the electrical activity from about 200 individual brain cells.

“The way that neurons communicate with each other is by how fast they fire pulses, it’s a little bit akin to listening to a Geiger counter click, and it’s that property that we lock onto,” said Professor Andrew Schwartz from the University of Pittsburgh.

The pulses of electricity in the brain are then translated into commands to move the arm, which bends at the elbow, wrist and could grab an object.

Jan was able to control the arm after the second day of training and over a period of 14 weeks became increasing skilful.

The report said she gained “co-ordination, skill and speed almost similar to that of an able-bodied person” by the end of the study.

Prof Schwartz told the BBC that movements this good had not been achieved before.

“They’re fluid and they’re way better, I don’t know how to say it any other way, they’re way better than anything that’s been demonstrated before.

“I think it really is convincing evidence that this technology is going to be therapeutic for spinal cord injured people.

“They are doing tasks already that would be beneficial in their daily lives and I think that’s fairly conclusive at this point.”

Sense of touch

The field of harnessing a healthy brain to overcome a damaged body is advancing rapidly.

Earlier this year, Cathy Hutchinson used a robotic arm to serve herself a drink for the first time since her stroke 15 years before.

In both studies the results were achieved inside a laboratory so are of little help in the home.

Researchers are now trying to mount the arm on Jan’s wheelchair so she will be able to use it in her everyday life.

There are also attempts to give sensation to the prosthetic arms to restore a sense of touch.

In a review researchers Gregoire Courtine, Silvesto Micera, Jack DiGiovanna and Jose del Millan described the control of the arm as “highly intuitive and probably responsible for the unprecedented performance of the brain-machine interface”.

They added that the system was a “remarkable technological and biomedical achievement” and that such designs were getting closer to a point which “might soon become revolutionary treatment models” for paralysed patients.

Parent Carers Of Disabled Adults Will Face Benefit Caps

December 17, 2012

I am a disabled adult. I live with my wonderful parent carers- the best anyone could ask for. Many of my friends are in exactly the same situation. We haven’t stopped being very dependent, and we doubt we ever will. So I find this more than a little scary- as well as completely unbelievable and very unfair.

The government’s proposed benefit cap will apply to carers looking after their disabled offspring, forcing some parents to move out of their home or put their child into care, it has been confirmed.

Ministers have repeatedly said disabled people will be exempt from the £500-a-week benefit cap that is due to come into force in April.

But they have now accepted that if a parent is still looking after a disabled child after they reach adulthood, even if the child’s mental age is as low as eight, the parent and the child will be treated separately, and the parent will be subject to the benefits cap.

In the Commons last week the work and pensions minister Esther McVey said: “In practice most carers will be exempt [from the cap] because their partner or child is in receipt of disability living allowance.”

She was then pressed by the Labour MP Andrew Gwynne to look at the rules again. He said: “Close reading of the regulations indicates that a household comprising parents and a disabled adult dependant receiving disability living allowance will not be exempt from the cap, despite the minister’s promises that they would be.”

McVey then admitted: “Should there be another adult in the house, that is then a separate household, so both have to be assessed separately.”

The change in the rules is already starting to bite with letters being sent to carers with offspring aged over 20.

Jacqueline Smirl from Maida Vale in north-west London has been told she is to lose roughly £80 a week even though she looks after her 20-year-old son, who is in need of 24-hour care and has the mental age of an eight-year-old owing to autism.

She told the Guardian: “The ridiculous thing is that the cap came in to incentivise people to go to work, but I cannot go to work because I am looking after my son full-time, and I am, in the process, saving the government money.”

She said she had received a letter last week from the Department for Work and Pensions telling her she was subject to the cap. She claimed many other parents, especially in the south-east, would be in the same position.

After the admission in the Commons last week McVey was pressed again by Karen Buck, the MP for Westminster North, the constituency in which Smirl lives.

Buck said: “Ministers have repeatedly stressed that a household containing anyone in receipt of disability living allowance will not be affected by the benefit cap, but constituents of mine who have an adult disabled child are now being told they will be affected by the cap because the regulations appear to state that if a family has an adult severely disabled person living in the household, that person is not a member of the household.”

She asked: “Please will the minister clarify whether the benefit cap will apply to someone who is looking after a severely disabled adult child?”

McVey replied: “A household is a basic family unit, and for the purposes of paying out-of-work benefits that will be a single adult or a couple and children, so once another adult is in the house, that is a separate household.”

She said discretionary payments were available to prevent hardship, but these are temporary.

Smirl has lived in Maida Vale since 1984. She lives in a £400-a-week private rented property and says her son is willing to move to a council property but none are available, forcing her either to leave the area or to put her son into care.

She said the threat of disruption to her already difficult life was putting intense pressure on her and she was receiving counselling.

Smirl has also written to the work and pensions secretary, Iain Duncan Smith, to examine the anomaly. She writes: “If I’m displaced, my son is displaced. My son is likely to be dependent on myself for the rest of his life and I have accepted the full-time job of looking after him. I do not want to give him up to the state at an enormous increase to the public purse.”

She points out that if she were looking after a partner, spouse or “child” she would be exempt from the cap.

“The benefit cap is to motivate people into work. I already work more than full time. I do it all by myself, with very little support and now I am put in this terrible situation,” she writes.

Buck said: “Ministers have frequently stated that a household where someone is severely disabled and in receipt of disability living allowance will not be affected by the benefit cap. It is now absolutely clear that assurance is absolutely worthless.”

She added she would be tabling questions to ascertain the precise number affected, and predicted it would run into the thousands.

Sports Personality Of The Year: Paralympians Win Prizes And Announce Pregnancies

December 16, 2012

Same Difference sends sincere congratulations to:

  • Helen Rollason Award Winner- Martine Wright, the sitting volleyball player who became disabled when she lost both her legs in the 7/7 London bombings. In a tribute post to those involved in the bombings in 2010, I wished those who became disabled on that day well in a life in which I hoped they would one day be very happy. Martine Wright spoke on the programme today about how much she loves sitting volleyball and how she believes she was on that train so that she would particpate in the Paralympics. She has accepted her new challenges with true strength and has used them to find a new ability for herself through which she has achieved great things. She’s a true inspiration and is truly DisAbled in every possible sense of the word.
  •   Team Of The Year- Team GB’s Paralympians, (oh, and the Olympians too) Both Team GB squads unsurprisingly won Team of the Year. This shows how far Paralympic sport has come and how seriously Paralympians are taken by the British public. Even though the main prize went to Bradley Wiggins, who I also sincerely congratulate, it was very good  to see the achievements of every single British Paralympian recognised with this award, in this very special, very appropriate way.
  • Sarah Storey, who along with Ellie Simmonds and David Weir, was shortlisted for the main award. Just by being on the list, these three sporting stars broke down a barrier that few could have previously thought it would ever be possible to break. Hopefully, one day in the future, one of them may win the award. That was too much to hope for this year, realistically, but they came closer than any Paralympian has come before.

However, Sarah Storey deserves congratulations for another very special reason. Tonight, live on national television, she announced her first pregnancy. In this way she showed the entire British public that it is possible for disabled women to get pregnant, too. Sarah Storey and her husband and fellow Paralympian Barney Storey have the very best wishes of Same Difference for the very good health of both mother and baby throughout the pregnancy.

Gary McKinnon Will Not Face Charges!

December 14, 2012

I have just heard very good news!

Computer hacker Gary McKinnon, whose extradition to the US was blocked, will not face charges in the UK, bringing to an end a 10-year legal battle.

Director of Public Prosecutions Keir Starmer QC said the chances of a successful conviction were “not high”.

Janis Sharp, Mr McKinnon’s mother, said the news was “amazing” and she was grateful the case was “all over now”.

Mr McKinnon, 46, admits accessing US government computers but says he was looking for evidence of UFOs.

The US Department of Justice said it would continue to collaborate with the UK government on a “wide range of shared concerns”.

Mr Starmer announced the decision not to prosecute some three months after Home Secretary Theresa May stopped Mr McKinnon’s extradition.

Low ‘conviction prospects’

The US authorities tried to extradite Mr McKinnon to face charges of causing $800,000 (£487,000) worth of damage to military computer systems and he would have faced up to 60 years in prison if convicted.

Gary McKinnon’s mother: ”It’s been life destroying, it’s difficult to explain how bad it’s been, and to have this over is amazing”

Mr McKinnon, who had been fighting extradition since 2002, suffers from Asperger’s syndrome.

In October, the Briton was permitted to stay in the UK on human rights grounds after medical reports showed he was very likely to try to kill himself if extradited.

In a statement, Mr Starmer said: “The potential difficulties in bringing a case in England and Wales now should not be underestimated, not least the passage of time, the logistics of transferring sensitive evidence prepared for a court in the US to London for trial, the participation of US government witnesses in the trial and the need fully to comply with the duties of disclosure imposed on the CPS.

“The prospects of a conviction against Mr McKinnon which reflects the full extent of his alleged criminality are not high.”

He concluded: “Against this background, the joint CPS/police panel recommended to the Assistant Commissioner of the Metropolitan Police that he should not commence a new criminal investigation into Mr McKinnon. The Assistant Commissioner of the Metropolitan Police has accepted that advice.”

Following the decision not to bring charges in the UK, Mr McKinnon’s mother said: “I’m very pleased and glad Gary’s not going to have to go through another long term of trauma.

“I would love more than anything now for Mr Obama to give Gary a Christmas pardon.”

She told BBC News: “Gary admitted to the intrusion, he always denied the damage. I feel the 10 years have been gruelling, it’s been life-destroying. It’s difficult to explain how bad it’s been.

“To have this over is amazing. Gary’s gone through enough. Other people have been accused of more serious hacking in this country and they’ve been given a £1,000 fine and a very short community sentence.

“Gary regrets what he’s done. He wishes he hadn’t done it. He wishes he hadn’t upset the Americans. We all regret it. But I’m grateful to Theresa May that this is all over now.”

Mr McKinnon’s lawyer Karen Todner said she had “mixed feelings” about the decision.

She said: “I am pleased he is not going to be prosecuted because I wouldn’t want to think he would ever spend any time in prison given his mental situation.

“But I am disappointed because the extradition warrant is still outstanding because he can’t travel anywhere outside of the UK and will have this hanging over him until it’s resolved.

“We have discussed approaching president Obama and asking for a pardon.”

The US Department of Justice said its “law enforcement relationship between the United States and the United Kingdom has always been predicated on trust, respect, and the common goals of protecting our nations and eliminating safe havens for criminals”.

It added: “Notwithstanding the home secretary’s decision in the McKinnon case, our extradition treaty serves the interests of both our nations, and the United States values our continuing collaboration with the CPS and British law enforcement authorities on a wide range of shared concerns.”

Risk of suicide

US authorities have described Glasgow-born Mr McKinnon’s actions as the “biggest military computer hack of all time” that was “calculated to influence and affect the US government by intimidation and coercion”.

Mr McKinnon lost appeals in the High Court and the House of Lords against his extradition, but two years ago a High Court judge ruled Mr McKinnon would be at risk of suicide if sent away.

Earlier this year Mrs May put the decision on hold, in order that Home Office appointed psychiatrists could conduct an assessment of Mr McKinnon’s mental state.

The psychiatrists concluded Mr McKinnon would be likely to take his own life if he was sent to face trial in the US.

Mr McKinnon was arrested in 2002 and again in 2005 before an order for his extradition was made in July 2006 under the 2003 Extradition Act.

 

PLEASE NOTE: Well over 100,000 to lose Motability vehicles under draconian new rules published yesterday (Thursday 13 December)‏

December 14, 2012

Reposted by request of Jane Young from here.

When I blogged on this topic back in January, I predicted thousands of disabled people would lose their Motability vehicles under the Government’s draft criteria for Personal Independence Payment (PIP), set to replace Disability Living Allowance (DLA) under the Welfare Reform Act. Yesterday, the Government published the final version of the criteria and the reality is far, far worse than we could have imagined.

Many consultation responses on the draft criteria complained that the descriptors for Activity 12 (Activity 11 in the draft), addressing physical difficulties in moving around, were unclear and confusing. We hoped they would be clarified; in particular, we expected clarification that being unable to walk more than 50 metres would qualify claimants for the enhanced mobility component and the Motability scheme. But we’re stunned by the decision that to qualify for Motability, a claimant needs to be unable to walk more than 20 metres – a far shorter distance*.

This has massive repercussions for the majority of Motability customers who, whilst they might be able to walk 20 metres, do nonetheless have very significant difficulties getting around. Under the second draft criteria, published in January, DWP predicted that 27% fewer working age people would be eligible for the scheme once PIP was fully rolled out. It is now clear from the Government’s own figures that 42% fewer disabled people of working age will be eligible for the Motability scheme once PIP is fully rolled out than would have been eligible had DLA continued unchanged (see Personal Independence Payment: Reassessment and Impacts, published 13 December 2012).

So what will this mean for disabled people? Only those with the greatest difficulty getting around, mainly those who use a wheelchair most of the time, will qualify for the Motability scheme on grounds of physical impairment. Huge numbers of disabled people with serious musculo-skeletal conditions, serious heart conditions or respiratory difficulties, cerebral palsy, neurological conditions such as MS and ME and many, many more will no longer benefit from the scheme. Their car will simply be taken away before they have a chance to appeal.

Those who no longer qualify for Motability are likely to be unable to get to work, attend medical appointments, visit friends, go shopping or, indeed, have much of a life at all. More than a hundred thousand people, who were previously able to get out and about independently, will find themselves staring at four walls; they will need more support for essential journeys, such as medical appointments, and their quality of life will be decimated. When visiting a small supermarket, 20 metres doesn’t even get you from the parking space to the entrance, never mind around the supermarket. In fact, lots of people have to walk more than 20 metres from their car to their front door when they get home again!

Disabled people who live in rural areas will be hurt the most. What little public transport is available is less likely to be accessible. There may be no local shops, no GP or pharmacy nearby; asking for a lift to the GP means asking someone to commit a considerable part of their day to drive a considerable distance.

Then there’s the knock-on effect on the UK car industry and the wider economy. In our report, Reversing from Recovery, published in June this year, the Spartacus network used the DWP’s own projections under the draft criteria to demonstrate the knock-on effect on the car industry and wider economy once all DLA claimants of working age had been migrated to PIP. However, under the DWP’s revised projections of the number of claimants eligible for Motability, under the final PIP criteria, the effect on the car industry and economy will be much more serious:

  • the car industry could lose nearly 50,000 new car sales a year (we predicted a loss of 31,450 sales under earlier projections),
  • more than 5,500 jobs could be lost from the economy (we predicted a loss of just over 3,500 jobs under earlier projections)
  • the Treasury could lose £126 million in tax receipts from motor-related industries (we predicted a loss of £79 million under earlier projections),

as a result of fewer claimants using the Motability scheme by the time PIP has been fully rolled out. And of course, if disabled people lose their jobs because they can no longer get to work, they will claim more in benefits and pay less tax. All in all, the original estimate of the effect on the economy was bad enough, but these figures are far worse.

For some, there is one slight cause for encouragement: the Government has listened to concerns about the speed of implementation and the necessity for evaluation and revised its timetable. DLA claimants with indefinite awards will only start to be reassessed from October 2015 – but newer claimants are more likely to have been given time-limited awards and therefore won’t benefit. And without extra assurances from either side of the political divide, we have to assume that the criteria published today will eventually affect all DLA claimants, albeit with implementation taking place over a longer timetable.

Hundreds of thousands of disabled people whose cars are vital to their life and health stand to lose virtually everything. No car = no independence, no job, no salary (with a consequent risk of homelessness), no social life plus increased dependence on family members, health and social care services and other benefits to survive. This begs the question: how does this cut help disabled people to fulfill the social contract of being part of society and contributing by work, volunteering or being part of their community? Even those held up by the Minister for Disabled People, Esther McVey, as inspirational role models will have their lives cruelly and unnecessarily restricted.

 

The Government has clearly paid little heed to the impact of this ‘reform’ on disabled people’s human rights. There is no doubt that the PIP criteria for people with a physical difficulty in getting around is retrogressive under the United Nations Convention on the Rights of Persons with Disabilities, ratified by the UK in 2009. The proposals seriously compromise disabled people’s human rights under several Articles of the Convention, including, among others, the right to live independently and to be included in the community (Article 19), and the right to personal mobility, specifically to….’ personal mobility with the greatest possible independence’ (Article 20).

This attack on the lives of disabled people who have difficulty getting around is NOT a price worth paying. MP’s on both sides of the House of Commons should vote these regulations down. The Government can, and must, do much better than this, if it really wants to build on the legacy of the Paralympics.

*************************************

* To get the enhanced mobility component of PIP, you need to accrue 12 points from either the first or second mobility activity in Part 3 of Schedule 1 of the PIP regulations. The first activity (Activity 11 in other DWP documents) covers non-physical difficulties with planning or following a journey and the second activity (Activity 12 in other DWP documents) covers physical difficulties in getting around. To get 12 points from the second activity alone, you have to be unable to stand then move more than 20 metres. If you have no difficulties with planning or following a journey and you can walk more than 20 metres, you will not be awarded the enhanced mobility component and you will not be eligible for the Motability scheme.

 

The Blind Busker

December 14, 2012

If you’ve travelled on the London Underground, you may have come across a whistling blind busker and wondered why he does it.

When Mark Campbell found himself unemployed in 1992, he didn’t know in which direction to turn as opportunities are very limited if you can’t see.

The 52-year-old has been blind since birth and had been comfortably in employment as a telephonist for West Mercia Police – then a common profession for blind people, but now superseded by technology.

“The trade of telephonist was dying. I was wondering what am I going to do. I was on the dole, time was going by and it was pretty soul destroying.”

 Other classic blind professions were suggested, but Campbell turned them down.

“There were lots of things I didn’t want to do, like a typist or word processor operator. I tried to become a piano tuner, but they wanted me to learn things like theorem of beats a second and Pythagoras.”

After being jobless for more than a year, Campbell serendipitously found his calling.

“I was on the way home from Shrewsbury and we saw a man busking, playing music on the street. I turned to my mate and said ‘I’m gonna have a go at that’. He said ‘what are you going to do?’ I thought about it for a second and said ‘I can whistle’.”

Amid laughter from friends, he borrowed a straw hat and set about whistling outside a branch of Boots on Shrewsbury’s Pride Hill.

When they returned, his friends took the hat to a nearby pub and counted the money inside. After just 90 minutes, he had earned £36.80. They couldn’t believe it.

“The weekly giro I’d been getting was something like £38. so in an hour and a half I did a couple of quid less than the cheque that was meant to last me the whole week.

“The next day I went to the same spot, this time for three and a half hours. I got £90. That was it, I didn’t look back – you could earn proper money.”

Campbell has developed a repertoire of tunes and has thematic cycles, as he calls them.

“I do a cross through the Beatles, Frank Sinatra, through to lots of hymns and things like that – people love hymns. I’m not a particularly religious man myself but they’re very popular. I do Bach to roots, reggae and old soul too.

“You have to compromise your own music tastes because you’re not there to please yourself, you’re there for what the public will want to hear and, touch wood, it works.”

Nineteen years later, Campbell is still whistling for a living and is now a regular performer on London’s Underground network. A ban on busking on the Tube system was lifted in 2003 and a regulated system put in place.

Performers have to be of a certain standard to get a licence from Transport For London and Campbell successfully passed the audition.

“I did a couple of tunes for them. They held the auditions on the disused Jubilee line platform at Charing Cross station. There were three or four on the panel and you set yourself up in the way you’d appear on your pitch.”

So, how much does he earn now? Campbell avoids a direct answer. “All you need to know is that I live in Wolverhampton, travel down to London four days a week, employ a helper and I make a good living.”

The helper gets Campbell to his pitch, brings him drinks of water, banks his takings and other administrative functions. He checks back in with Campbell every 20 minutes but doesn’t stay while he whistles because it puts people off giving.

When you think of a busker, you might conjure an image of someone performing with a violin case or a hat to collect tips but Campbell’s years of practice have led him to use a washing-up bowl.

There’s psychology at work here, he explains. “The thing that has to happen between punter and busker is that they have to like what you do but, in terms of them giving you money, it has to be a very minimal interaction.

“I experimented over the years using wider receptacles but a washing-up bowl is perfect for people because it’s big and it’s easy.”

Smaller receptacles, he says, mean punters have to step out of a crowd and physically engage with what he’s doing rather than just casually tossing an appreciative coin in his direction.

The streets of Campbell’s home town Wolverhampton are not as safe an environment for busking as in the public passageways below London with its official scheme, he says.

But personal safety aside, even though Campbell stands with his white cane in his collection bowl to try and detect unusual movement, he thinks that people do steal from him – though he can’t be entirely sure.

He judges it by the average number of £2 coins he expects to find in the bowl but which are sometimes conspicuously absent.

“You have a bowl with money and a blind man marshalling it, it’s an ideal opportunity for thieving. When I first started on the streets, I don’t think it happened hardly at all. Come the millennium it had increased 25%. Now I have thieving every single day.”

But, these difficulties aside, does being blind help in a profession where people volunteer a donation?

“It’s got to be faced that probably 25% of my money comes as a result of the sympathy card. I really do believe that is a factor. It’d be stupid to say it’s not. Fortunately I don’t believe it’s the main factor any more.

“I probably do earn more money than other buskers but I don’t believe all other buskers know the psychological hooks like bowl size. Playing the stuff you like is a nice luxury, but if you want to make proper money out of busking, you’ve got to do the stuff the public like.”

Mark Campbell can be heard on the latest episode of the BBC’s Ouch! talkshow

Patrick Lynch- The First Person Suing The Government And ATOS Over The WCA

December 14, 2012

Disabled people and carers have a long list of serious problems with the Work Capability Assessment and Atos Healthcare, the company contracted by the Government to carry these out.

The feeling against Atos is so strong that it could perhaps come as a surprise to anyone who follows these issues that no one has yet thought of suing the company over the WCA process.

No one, that is, until now.

Patrick Lynch, a former social care worker who was forced to stop work because of a brain condition for which he reportedly had surgery, was, like many other disabled and seriously ill people, incorrectly found fit for work after a WCA.

He is now launching legal action seeking a review of the assessments. He is claiming that   the government and Atos failed to record an interview despite assurances from ministers that all could be taped.

Before his first interview in September 2010, Mr Lynch had spent five months undergoing brain surgery. Yet he was found fit for work at this interview. Mr Lynch disputed this.

An examination by Atos found that Mr Lynch had “no abnormalities or tenderness to the neck or spine” despite the major surgery he had recently experienced.  The report of the examination did not consider his medical history.

Mr Lynch said: “I had been in hospital and lost 54kg (8.5 stone) in weight. The doctors told me I was on death’s door. I mean I came in on crutches and could not pick things up because I was afraid of falling over. But they did not say that. I even photocopied my medical notes and handed them over but because there was no recording it was my word against theirs.”

The DWP’s decision was eventually reversed, and Mr Lynch was given £100 in compensation for the stress he suffered.

He was reassessed this year, and asked for the process to be recorded. However, he was told “no recording equipment was available, that much of it was broken or being used outside of London and that it would take too long to obtain.”

Atos has just 11 recording machines to be shared between 123 assessment centres. Yet former employment minister Chris Grayling told MPs in February this year that the Government would offer everyone who wanted this the chance to have their session recorded.

Mr Lynch is arguing in his lawsuit that ministers and Atos acted unlawfully by failing to provide enough equipment to record sessions. He said: “That’s why I am launching my legal action. You cannot have Atos and the government carrying on like this.”

Hehas the backing of the TUC-funded anti-cuts campaign, False Economy.  A spokesperson for the group said its investigations had shown that “too many people feel vulnerable in this process. People feel that their final assessment reports inaccurately reflect information exchanged during work capability assessments. We’ve found it hard to pin down the DWP on recording policy. Universal recording, and giving people the opportunity to see their WCA reports before final eligibility decisions are made, will go some way towards restoring fairness and accuracy while the WCA process continues.”

Mr Lynch’s solicitor, Tessa Gregory of Public Interest Lawyers, said that the “assessment process… constitutes an unacceptable risk of unfairness. We hope these safeguards will be instituted to help mitigate that risk.”

The TUC general secretary Brendan Barber said: “Assessments of disability must be fair and proportionate, treat people with respect and be part of a consistent system. There is overwhelming evidence that they have fallen far short of these basic standards. It is right that they should be challenged in court.”

A DWP spokesperson said it had until 24 December to respond to the lawyer’s letter from Mr Lynch. Its own most recent review found the “work capability assessment is not in need of fundamental reform. There is a long history of judicial reviews concerning welfare reform and as always we will robustly defend our policies. We have already made substantial improvements to the process.”

Many disabled people and carers will be pleased to hear of Mr Lynch’s decision to take this legal action. It will undoubtedly cause him a fair amount of stress. That is before taking into consideration any financial costs.

However, if the action is successful, it is to be hoped that Atos will dramatically improve their assessment process as a direct result, and that this will be the last case of its kind.

PROGRESS! PROGRESS! SERIOUS PIP PROGRESS!

December 13, 2012

My dear, valued readers, I am so so happy at this moment.

In a Commons Statement earlier today, our new Minister, Esther McVey MP, set out Government plans for PIP. A video of the full statement and Labour’s response is here. 

A written transcript is here.

But, I haven’t yet revealed the reason for my excitement. The reason for my excitement is this:

The Minister announced something that will directly very positively affect me, and many others I know. That was that:

unless they report a change in their condition, those with a lifetime or indefinite DLA award will not be reassessed until October 2015 at the earliest.

We get to keep DLA as it is for a whole two years longer than we previously thought!

‘The Paralympic Effect’

December 13, 2012

Three-quarters of Britons feel more positive about the role of disabled people following the Paralympics, according to a BBC survey.

Some 79% of 2,400 non-disabled people questioned also said they thought wider perceptions of disability had improved.

But the figure fell to 65% among the 600 people with disabilities surveyed, as Jenny Hill reports.

The BBC have also interviewed two of my favourite disabled people/campaigners about these results- Kaliya Franklin and Lisa Egan.

#EverydayDisablism

December 13, 2012

Readers, you might have heard of the Everyday Sexism project.

Well, yesterday I discovered the disability version- Everyday Disablism. 

For those who have no idea what I’m talking about, it’s a Twitter project collecting stories of disablism.

It has my full support so I wanted to share it with you.

Stephen Hopkins, A Signer Of American Declaration Of Independence, Had Cerebral Palsy

December 13, 2012

I came across this little fact by accident last night. It proved the point of the Old Is Gold campaign to me yet again.

In history lessons in England, I can’t see this being much more than a fact to be slipped in to conversation. Still, it is a very interesting fact for people with CP to know.

Stephen Hopkins, one of the signers of the American Declation of Independence, is listed as one of Wikipedia’s notable cases of people with Cerebral Palsy:

Stephen Hopkins, signer of USA Declaration of Independence, reputed to have stated, “My hand trembles, but my heart does not.”

In a nutshell, dear readers, it looks like they let one of us lot help create America. The most powerful country on the planet.

Teachers, when were you planning to tell me that?

 

BREAKING NEWS: Scope Pull Out Of Mandatory Work Experience Programme

December 12, 2012

Disabled Woman Ordered Out Of Post Office Because Wheelchair Took Up Too Much Room

December 12, 2012

Unbelievable!

A PARAPLEGIC woman was kicked out of a post office because her wheelchair was “taking up too much room”.

Sue Hitchings was ordered out of the branch in Knowle, Bristol on Saturday while she queued with her husband to pay bills and buy stamps.

Insisting her electric wheelchair was blocking aisle, staff demanded she wait outside in the cold

Sue said: “I was so shocked and embarrassed.

“There were lots of other people in the queue who were looking at me – I felt humiliated.

“I have a normal electric wheelchair and am able to go into other shops without a problem.”

Husband Robert added: “What about all the elderly people who use the post office, if they are alone and in a wheelchair do they just get booted out?”

 When approached for a comment, the sub-postmaster, who refused to give his name, defended his decision to ban electric wheelchairs, on “health and safety” grounds.

He said: “Large electric wheelchairs don’t fit down the narrow aisles because they are too wide and there’s no turning space for them.

“We go out of our way to help all our customers, especially those with disabilities.

“I have asked many people in electric or motorised wheelchairs to stay outside while we get them what they want, or a family member gets it for them from the post office.

“We have had people in motorised wheelchairs lose control in the past. One customer had his foot run over, another was hit by a wheelchair and once a wheelchair user collided with our lottery machine. It is a health and safety issue.”

Save Parkwood Farms Therapy Center For Autistic Kids

December 12, 2012

An email I’ve just recieved from Change.org:

I started a therapy center for children with special needs because of my son, Julian. Julian has autism. When he was a baby, Julian was so withdrawn that he wouldn’t even eat.

Horseback riding therapy changed Julian’s life, and mine too — so much so that I decided to sell my house and build a therapy center to help children who were struggling like Julian. More than 40 children with special needs come to Parkwood Farms Therapy Center to learn and grow by working with and riding horses — but I could be forced to shut down my home and the therapy center because the bank is threatening me with eviction.

I was making all my mortgage payments until my bank sold my loan and my bills skyrocketed. Every three months, the rates increased until my monthly payments were double what they used to be. 

I need to stop this now — not just for me, but for the kids who need this therapy center. I started a petition on Change.org asking HSBC Bank to stop my eviction and work with me to modify my loan. Will you sign?

I’m so glad I opened the horseback riding therapy center: every day I see kids opening up, connecting with the horses, learning to communicate, and so much more. I can’t tell you how rewarding it is to help parents like me, who wanted to help their children but didn’t know how. For some kids, working with animals is the key to helping them open up and relate to the world.

I’ve been trying to negotiate to get my payments back down, but after following the bank’s instructions for two years, my credit has been damaged and I’m facing eviction. 

I don’t want to shut this center down. People in my community need it. That’s why the mayor and the entire city council came out to the center this month and gave speeches in support of Parkwood Farms. But I need your help too to put more pressure on the bank to negotiate with me. I know that Change.org petitions have helped push banks to meet with other homeowners facing foreclosure, and if enough people sign my petition, I’m confident that HSBC will follow suit.

Please help me save Parkwood Farms Therapy Center: Sign my petition to HSBC Bank now.

Thank you so much for your help.

Dr. Marilyn Peterson

Frances Ryan On The M&S Christmas Ad

December 12, 2012

Frances Ryan hopes that the inclusion of Seb White in the M&S Christmas advert will mean that in future, disability on TV will be a ‘normal’ sight for life, not just for Christmas.

ATOS Christmas Carols

December 12, 2012

An ATOS twist on Christmas Carols at the ATOS Stories blog. These made me smile, so I thought I’d share them with you.

Census 2011: Stats On Carers

December 11, 2012

I’m looking for stats on disability. If I find anything, I’ll post it. If you find anything before I do, please do let me know.

House Of Commons Statements On Winterbourne View

December 11, 2012

You can see care and support minister Norman Lamb’s statement to the commons on and the response by shadow health minister Liz Kendall on Parliament TV.

Speech Dating: Finding Love With A Computer Voice

December 11, 2012

Saying: “I love you,” should sound quite different from saying: “I hate you,” but in Lee Ridley’s case they both sound exactly like anything else he would say.

Lee is Britain’s only stand-up comedian to use a solely computer-generated voice, as he is unable to speak.

His new film sketch, Voice by Choice, follows three people who use speech-synthesis technology as they meet at a speed-dating event.

The film was put together in collaboration with the Creative Speech Technology (Crest) Network to show how valuable speech synthesisers can be and to illustrate the difficulties of living with some of the current technology.

As the three romantic hopefuls make their introductions, they notice they all have the same voice – even though one is a woman and two are men.

There are some awkward pauses as they give each other time to get their words in order on their machines, and comic mishaps with predictive text – all based on real-life experiences.

The charity Communication Matters says at least 30,000 children and adults in the UK could benefit from speech-synthesis technology.

And it predicts this number will increase as the population ages and more people with complex needs survive.

People need these devices for a variety of reasons. Some are born without the ability to learn the process of speech, due to conditions affecting the brain and the muscles involved in speech, for example in some cases of cerebral palsy.

Other people develop conditions that lead to a deterioration in their speech in later years – for example motor neurone disease, in which the muscles used to speak may weaken, or strokes affecting certain areas of the brain.

“There is an urgent need for this type of technology to be more widely available and for it to be more reliable and personal,.” says Dr Alistair Edwards, co-principal investigator of the Crest Network, based at the University of York.

‘More identity’

Lee says he would be lost without his machine.

“I don’t need to rely on other people to get my message across any more,” he adds.

“It has made me a lot more independent and a lot more confident.”

But he says it is still really hard to show how he feels.

“It’s pretty disappointing when you want to express how you feel and it just doesn’t come out right.”

If Lee could choose any voice, he would like to try one with a Geordie accent, so he could have “a bit more of an identity”.

Nicola Bush, the actress in the sketch, received her first speech-synthesis device at the age of 15.

She says: “I felt dead, but when I got my first voice it opened important doors for me.”

Nicola says her device allows her to have a closer relationship with the people around her, but she hopes more children will be given these devices at a younger age.

‘Emotions are difficult’

David Niemeijer, founder of AssistiveWare, one of the companies involved in this technology, says there are a number of reasons the devices have been slow to change.

” It is a complex process. It is very costly and people just accepted there were no children’s voices, for example,” he says.

“As everyone accepted that, there was little incentive to change.”

His organisation has worked with the company Acapella to make Britain’s first speech synthesisers that use children’s voices.

Until their system was launched earlier this year, children – who are the most frequent users of this technology – had to use machines with adult voices or an adult voice processed to sound more like a child’s.

“To build the voice, we record a real person for 15-18 hours and the data gets cut up into little pieces and stitched back together so the voice can say anything – even things the person never said,” says Chris Pidcock, chief voice engineer at CereProc, a company that develops speech-synthesis technology.

CereProc has recently built a voice with a Brummie accent.

‘Designer voices’

“Because making these voices takes a lot of effort and expense, most people in the past focused on neutral sounding voices. People were quite cautions, but this is changing,” Mr Pidcock says.

“Emotions are more difficult because the voice does not know what your intentions are. It can’t know what emotion you want,” says Mr Niemeijer.

Another significant problem with current systems is the inability to chat in real-time says David Mason, of Toby Churchill, the company that makes Lee’s machine.

This means there can be lengthy pauses as people put their words together, but the company is working with academics to improve this and make the voices more natural.

“Text-to-speech is getting better. But it can never replace human speech. People are spectacular in terms of all the nuances they can offer,” says Mr Niemeijer.

Dr Chris Newell, co-principal investigator of the Crest Network, says as technology improves, there might even be an opportunity to go further.

“Perhaps we can create voices that are more special than regular human voices or even designer voices – maybe one day you could choose a voice so you sound sexy or sound like a film star”.

Christmas Gibbons- A Charity Single By Adam Bojelian

December 11, 2012

Adam Bojelian, 12, has severe Cerebral Palsy. He communicates by blinking.

He’s also a poet with a blog  whose writing has won him awards including a Brit Writers Award, a Gold Blue Peter Badge and this year’s Young Scot Arts Award.

As a writer with Cerebral Palsy myself, I’ve been more than a little impressed by Adam ever since I first heard of him.

He’s a Same Difference DisAbled Inspiration. So I’m thrilled to be publicising the Youtube video of his first charity Christmas single, Christmas Gibbons.

This is one of Adam’s original poems set to music. It’s available to buy on Itunes from here for 79p, with 50p from every download going to the Children’s Hospice Association Scotland (CHAS).

 

Winterbourne View: The Full Final Report And Reactions

December 10, 2012

The full final report into Winterbourne View, reactions and relevant links are here.

Orkney Islands Have Highest Rate Of MS In World

December 10, 2012

Scotland’s Orkney Islands have the highest rate of multiple sclerosis (MS) in the world, according to a major new study.

Researchers said that the rate for probable or definite MS was now 402 per 100,000 people, up from a previous 309 per 100,000 which was recorded in 1974.

Teams at the universities of Edinburgh and Aberdeen carried out the study.

They are now trying to work out why the figure in Orkney is so high, but believe genes could play a key role.

With MS, the protective layer around nerves, known as the myelin sheath, becomes damaged.

Messages from the brain to the rest of the body are disrupted, resulting in difficulty moving, muscle weakness and blurred vision.

There are many suspected risk factors, and the disease is known to be more common away from the equator.

MS affects about 100,000 people in the UK.

The new study found that one in 170 Orcadian women suffer from the condition.

The current figure for Orkney compares to 295 per 100,000 in Shetland and 229 per 100,000 in Aberdeen.

‘So high’

Dr Jim Wilson, of the University of Edinburgh’s Centre for Population Health Sciences, said: “Our study shows that Orkney has the highest prevalence rate of MS recorded worldwide.

“These findings may reflect improved diagnostic methods, improved survival or rising incidence.

“We are trying to work out why it is so high, but it is at least partly to do with genes.”

It has previously been noted that areas of high MS prevalence around the world have been settled in by Scottish immigrants.

Previous studies have shown high rates of MS in Canada and Scandinavia.

The new study is published in the Journal of Neurology, Neurosurgery and Psychiatry.

Findings Of Winterbourne View Report

December 10, 2012

Ministers will on Monday order a programme of action intended to remove up to 1,500 people with learning disabilities and autism from private hospitals such as the Winterbourne View unit where a regime of abuse and humiliation was exposed.

Health chiefs will be told to review urgently the cases of all people placed in so-called “assessment and treatment” units and to deliver a “rapid reduction” in their numbers by planning more appropriate care and support.

The move comes as a report warns that the care sector risks slipping back into an institutional culture typified by the Victorian asylum system. It says strict, custodial practices are making a return in some modern care homes that are struggling with the effects of spending cuts.

Lord Best, a leading housing and care expert and president of the Local Government Association, said: “Unless organisations are vigilant, the older institutional culture can re-emerge anywhere.”

The crackdown on use of assessment and treatment units will come in the government’s final report on the scandal at Winterbourne View, near Bristol, where secret filming revealed routine physical abuse of patients by staff. Six former care workers at the unit have been jailed and five others given suspended sentences.

Although Winterbourne View has been closed by its operator, Castlebeck, and checks on similar units have raised no comparable concerns, ministers have agreed that the model of care is probably unsuitable for most of the people placed in them.

Assessment and treatment units are supposed to offer short-term care for people whose behaviour is seen as “challenging” and difficult to manage in the community. But evidence suggests patients are being left in the units for years on end – in one case, 17 years – at costs revealed in the Winterbourne View affair to be £3,500 a week.

The action plan will give local care commissioners two years to move people out of the units, ideally to other forms of accommodation in their home areas, unless there is a demonstrable clinical and time-limited case for them to remain.

To keep faith with the government’s commitment to localism, the plan will fall short of instructing commissioners to stop using the units, as demanded by pressure groups, but most such groups have signed up to a concordat of support for the programme.

Other measures will include new guidance on use of physical restraint strictly as a last resort in care homes and hospitals; provision for planning from childhood of the care and support needs of people with challenging behaviour; and enhanced powers for regulators to intervene in cases like Winterbourne View and, potentially, to hold directors of private care companies personally to account.

The warning on a drift back to institutionalism in the care sector comes in a report commissioned by Family Mosaic, a leading London housing association and provider of care and support, after it found abuse and poor practice in what it says was a small minority of its own services.

In two shared housing schemes, there were strict times set for getting up, eating and going to bed. In one scheme, access to the toilets was controlled by staff. In another, a woman who kept taking off her clothes had been dressed back-to-front to stop her doing so.

The report warns that, elsewhere, staffing cuts caused by reduced fees paid to care providers are causing residents to be left alone for hours at a time and are fostering excessive reliance on use of drugs and on physical restraint, “often for minor perceived misdemeanours”.

Brendan Sarsfield, Family Mosaic’s chief executive, said: “We would argue that if providers don’t believe this has ever happened in their services, it just may be that they haven’t looked hard enough.”

Local Paper Raises £20000 In 3 Months For Girl’s SDR

December 10, 2012

Winterbourne View Report To Be Published

December 10, 2012

A report into the Winterbourne View scandal is to be published by the Department of Health (DH) just over a month after the Government promised to “deliver real change” in the provision of care for disabled people.

In October six members of staff – four support workers and two nurses – were jailed for between six months and two years for their roles in the abuse at the private hospital in Hambrook, South Gloucestershire.

Five others were given suspended prison sentences by a judge at Bristol Crown Court, who condemned the “culture of ill-treatment” and said it had “corrupted and debased”.

On Monday, Norman Lamb, minister of state for care services, publishes his department’s review of the scandal.

The BBC’s Panorama exposed the scandal in June last year when it broadcast undercover journalist Joseph Casey’s secret footage, recorded when he was employed at Winterbourne View as a care worker.

Support workers Wayne Rogers, Alison Dove, Graham Doyle, Gardiner, Michael Ezenagu, Danny Brake, Charlotte Cotterell, Holly Draper and Neil Ferguson were caught out in the sting. Nurses Sookalingum Appoo and Kelvin Fore were filmed condoning the abuse by failing to stop it.

The journalist Mr Casey had got a job at Winterbourne View after whistleblower Terry Bryan, a former nurse at the home, went to the BBC after his complaints to care home owners Castlebeck and care watchdogs were ignored.

His shocking footage showed residents being slapped, soaked in water, trapped under chairs, taunted, sworn at and having their hair pulled, eyes poked and being illegally restrained. On one occasion three support workers forcibly held down a resident while a nurse forced paracetamol into her mouth.

Barristers representing the 11 defendants apologised on behalf of their clients but blamed the culture of Castlebeck – calling it a “disease”, a “cancer” and a “fog” that had engulfed Winterbourne View.

A serious case review published in August criticised the firm for putting profits before humanity. The 26-bed hospital opened in 2006 and by 2010 had a turnover of £3.7 million. The average weekly fee for a patient was £3,500.

#Match4Martin Martin, 20, Needs A Stem Cell Transplant To Give Him A Chance At Life

December 9, 2012

Please read this message- a young man with a whole life ahead and a loving mother desperate to save her son’s life. Please share it everywhere possible.

https://twitter.com/Hip_Priest_/status/277572890621255680

The Hottest Classroom On Earth

December 9, 2012

Readers, you might be interested in this documentary that I have just seen. It’s on BBC iPlayer for a week.

Documentary following the inspirational journey of ten pupils with behavioural problems, who embark on a life-changing expedition to Tanzania and the ‘hottest classroom on Earth’.

#PatsDebate Pat’s Petition Progresses And Succeeds!

December 8, 2012

Same Difference offered full support to Pat’s Petition from the very beginning. So I’m very pleased to be cross posting this from CarerWatch. What a wonderful tribute this progress is to the member of the group who very sadly passed away last week.

After a year of very hard work and wonderful encouragement from all of our friends and supporters Pat’s Petition  closed with over 62,600 signatures. We then sent an open letter to Liam Byrne.

We are delighted to announce that all the effort succeeded

and we have a result.

Liam Byrne has been in touch and the Labour Party are giving us an Opposition Day Debate in the Commons based around Pat’s Petition. This means the debate will take place in the Chamber at the House of Commons with Ministers and front benchers as well as back benchers.

So fantastic news – Pat’s Petition is moving to Pat’s Debate. Tell everyone – shout, sing, tweet using hashtag #PatsDebate. Let’s shake this government into listening to us at last.

The debate will probably take place some time in January and we will only have a weeks notice so the important thing now is to get ready for the debate and make sure all the issues we have been campaigning on get attention.


The theme of the motion for the debate will be the Pat’s Petition demand that the government – Stop and review the cuts to benefits and services which are falling disproportionately on disabled people, their carers and families and a demand for a Cumulative Impact Assessment. It’s a very wide brief so if you want to focus on a particular issue that’s fine.

We will need lots of help from you all to make sure that after all your effort this debate gets real results.

We are hoping that many of you will put up blog posts in support of Pat’s Debate and that we can collect the links together here.

We will also need your help to ask MPs from all Parties to speak in this debate and if we can direct them to your blog posts it will show them the kind of messages we want to put across.

Contact your MP details via this link

Watch this space to see how the plans for the debate are progressing.

Time is running out.

Please get behind this debate and make it a game changer.

Pat x

for further details contact  –  patspetition@gmail.com

If you have any suggestions/comments, please add them below.

Meet The Gay Foster Carers Looking After Children With Disabilities

December 8, 2012

Any thoughts on this, readers?

Rosie Davies Has Spine Repaired With Leg Bone

December 7, 2012

A five-year old girl has had pioneering surgery to repair a large gap in her spine using bone taken from her legs.

Before the operation, Rosie Davies, from Walsall in the West Midlands, was “basically a timebomb”, her family said.

Missing bones in her spine meant her upper body weight was unsupported and her inner organs were being crushed.

The lifesaving surgery came at the cost of her lower legs, which she had always been unable to move.

Rosie was born with a very rare disorder called spinal segmental dysgenesis. Five bones which made up part of her spine were missing, leaving a 10cm gap in her backbone. Her legs were also contorted up against her belly and she had very little feeling in them.

She was slowly running out of space in her chest – and running out of time. Eventually the internal crush would have led to Rosie’s organs failing, which would have killed her.

In her last scan before the operation there was evidence of her kidneys being crushed.

Leg-to-spine

Rosie’s legs were amputated from the knee down and a section of bone was taken to bridge the gap in her spine.

Two metal rods were then bolted to the upper spine and the hips to provide extra support.

The operation at Birmingham Children’s Hospital took 13 hours.

Her dad Scott said: “Before she was basically a timebomb – we never knew how long it would take to go off, we never knew how long we actually had with her.

“Since having the op she’s now had her life expectancy increased to that of a normal child.”

Since the surgery there have been early signs of sensation returning to her legs, which means it may be possible for Rosie to one day walk with prosthetic legs.

Her mum Mandy said: “Rosie is such a strong character. You give her the equipment to use and she’ll do it, whether it’s sticks or artificial legs or her hands – she’ll make a way of walking.

“All she has ever wanted to do is be like her sister. All she’s wanted to do is ride her bike like her sister, run like her sister.”

Rosie’s parents said she now had more confidence.

An operation of this scale has never been attempted in Europe before. The only similar procedure took place 10 years ago in New Zealand.

Mr Guirish Solanki, one of the consultant neurosurgeons who operated on Rosie, said: “We are delighted with the results of this operation.

“This is only the second time in the world that a surgical team has attempted to fix the thoracic spine to the hip side bones for a condition as rare as Rosie’s.

“This case was very complicated as normally children with this condition do not have a working spinal cord or nerves but Rosie did. So in carrying out this procedure we had to be extremely careful not to damage her nerves.”

Wheelchair User Mistakenly Left On Bus Overnight

December 7, 2012

A disabled passenger was mistakenly left on a bus parked overnight in a Manchester depot, it has emerged.

The 60-year-old man, who was in a wheelchair, was discovered by a cleaner at about 02:50 BST on Saturday at the Stagecoach site on Hyde Road, Ardwick.

It is understood the man was asleep and the driver failed to check the vehicle was empty.

Stagecoach said it was an “individual oversight” and an internal disciplinary process was being carried out.

It is not known what time the man boarded the bus.

An ambulance crew took the man, who was in a confused state, to Manchester Royal Infirmary as a precaution.

‘Absolutely ridiculous’

In a statement, the company said: “We were very concerned to hear about this case when it was brought to our attention at the time.

“All of our drivers are given very clear instructions that part of their job is to check the bus at the end of their shift.

“This was an individual oversight and the driver has been subject to our internal disciplinary process.”

Richard Currie, from Greater Manchester Coalition for Disabled People, described the incident as “preposterous”.

“I think it’s absolutely ridiculous that someone should be left on a bus for that length of time.

“Bus companies must ensure that the disabled person has a safe and comfortable journey, something in this instance Stagecoach has failed to do.”

Greater Manchester Police said no criminal offences had occurred and it was dealt with as a medical matter.

Hospitals Charging For Blue Badge Parking May Be Unlawful

December 7, 2012

As a lifelong Blue Badge holder, I’ve thought this for years! I’m very pleased to see it finally being recognised and getting media coverage. I hope this can be proved unlawful and stopped.

Hospitals charging disabled drivers to park could be in breach of the law, a leading lawyer says.

Some 37 NHS trusts charge disabled drivers to park, with some saying all drivers should be treated equally.

But disability rights lawyer Chris Fry told BBC 5 live this was a misreading of UK equality law.

The Department of Health said patients who went to hospital often or for long periods had a right to fair and appropriate car-parking concessions.

Of the 116 hospital trusts in England that responded to a Freedom of Information (FOI) request submitted by the BBC’s 5 live Investigates programme, 37 said they currently charged disabled drivers to park.

For a two-hour appointment, the Royal Cornwall Hospital in Truro was the most expensive, charging £4.80 for two to four hours parking.

The cheapest was Dartford and Gravesham NHS Trust, which charges £1 per visit.

The FOI request also revealed some trusts were citing “fairness” as justification for the charges imposed on disabled drivers.

Southend University Hospital NHS Foundation Trust, which brought in charges four years ago, told the programme: “All blue badge holders pay the same rate as other patients, visitors and staff.”

“The hospital forum feedback is that disabled persons wish to be treated the same, where practicable, as able-bodied persons.”

Equality Act

However, critics say disabled people often have no other choice but to drive to hospital, as they may be unable travel by foot and public transport may not be suitable or available.

Furthermore, hospital visits may take longer to complete for disabled people – which could lead them to incur higher parking costs.

Managing partner at Unity Law Chris Fry told the BBC: “Inevitably it will cost someone more to park because of their disability, and that must be clearly wrong.”

“Treating somebody less favourably as a result of their disability amounts to a breach of the Equality Act.

“That gives the individual affected by that a right of action against the local authority – either by judicial review or by way of a civil claim for compensation.”

The public sector equality duty, set out in the Equality Act 2010, explicitly recognises that disabled people’s needs may be different from those of non-disabled people.

It says: “Public bodies should therefore take account of disabled people’s impairments when making decisions about policies or services.”

The act – which applies in England, Scotland and Wales – suggests that this might mean treating disabled people differently in order to meet their needs.

Medway NHS Foundation Trust introduced fees for blue badge holders in July 2012 – a two-hour stay currently costs £2.50.

Its website states their charges are to “create fairness around concessions”.

But one local resident has begun legal action against Medway NHS Foundation Trust, describing it as “another tax on the disabled”.

‘Fundamental right’

Sue Groves, from Chatham, told 5 live Investigates the hospital’s policy meant there were additional barriers in place for disabled people.

“It takes longer for disabled people to get from A to bee, so they’re likely to incur higher charges,” she said.

“The public transport links aren’t great to Medway Hospital. There’s a distinct lack of accessible taxis and if you’re a wheelchair user the buses are quite difficult at times. – they’re not all accessible – which means that disabled people and blue badge holders haven’t got the choice that other people have.

“They’re also likely to be attending the hospital more often and more frequently, so basically they’re going to be paying more than other visitors to the hospital.

“I think they’ve looked across the board and said ‘equality is about equal treatment, so we’re going to make it fairer by charging blue badge holders’.

“But they haven’t actually thought of the implications of that.”

A Medway NHS Foundation Trust representative told the BBC: “The decision to implement this change to concessions was not taken lightly. Its purpose is to create fairness around concessions, which are now based on affordability, rather than purely on entitlement to blue badges.

“Patients who are entitled to specific benefits will continue to receive free parking.”

A Department of Health representative said: “Patients who need to go to hospital often or for long periods of time have a fundamental right to fair and appropriate car parking concessions, and we expect hospital trusts to provide them.

“All NHS organisations should support equality and ensure that there is no unlawful discrimination.

“They must produce evidence that the relevant equality issues have been considered. This can be done through an equality impact assessment, but can also take other forms such as engagement with local groups, or data analysis.”

You can listen to the full report on 5 live Investigates on Sunday, 9 December, at 21:00 GMT on BBC 5 live.

Listen again via the 5 live website or by downloading the 5 live Investigates podcast.

 

 

Classical Composer Jonathan Harvey Dies At 73

December 6, 2012

Tributes have been paid to the British classical composer Jonathan Harvey, who has died in Lewes, east Sussex aged 73.

Harvey, who had motor neurone disease, worked on experimental pieces with electronics as well as writing for orchestras, soloists and choirs.

Radio 3 controller Roger Wright said the composer, who died on Tuesday, had been “a hugely important figure”.

“His was a powerfully original music which rightly received international acclaim,” the BBC Proms director added.

“His gentle spirit and inner strength impressed me greatly and he will be much missed.”

Harvey, a music scholar at St John’s College Cambridge, went on to gain doctorates from Glasgow and Cambridge and was professor of music at Sussex University for 16 years.

His large-scale commission Weltethos, premiered in Berlin in 2011, was performed at Birmingham’s Symphony Hall in June to mark the opening of the London 2012 festival.

The married father of two received a lifetime achievement award this year from the Incorporated Society of Musicians, an accolade he described as “one of the greatest honours of my life”.

The BBC recognised his international standing in January with a weekend dedicated to his music at the Barbican Centre in London.

On Radio 3’s In Tune programme on Wednesday, broadcaster Suzy Klein said Harvey was “a man with a deep spirituality” who had been heavily influenced by Buddhism, Eastern religions and mysticism.

David Hill, chief conductor of the BBC singers, said he was “a genuinely gentle man” who was “totally engaged in humanity” and “always true to himself”.

Despite suffering from serious illness, Harvey completed three pieces of music in the final year of his life.

They were Cirrus Light for solo clarinet, The Annunciation for the choir of St John’s College Cambridge and the choral work Plainsongs for Peace and Light.

More Remploy Factories To Close

December 6, 2012

Hundreds more disabled workers at Remploy factories are at risk of losing their jobs under fresh closure plans, the government has announced.

A further 875 employees, including 682 disabled people, have been told they face compulsory redundancy.

Ministers announced earlier this year that a number of Remploy factories would close, arguing that the budget for disabled employment services could be spent more effectively.

Thirty-four factories have ceased operations since then and are in the process of closing, but the future of a further 18 sites remained unclear.

Some of the factories have the potential to move out of government-funded support, but others are set to close, ministers said on Thursday.

A Department for Work and Pensions spokesman said: “From today, Remploy will invite expressions of interest to take over the running of the remaining factories.

“Our priority throughout this process is to safeguard jobs, which is why we are offering a wage subsidy of up to £6,400 per disabled employee to encourage interested parties to come forward.

“We have also been clear from the start that we have protected the £320m budget for disability employment services.

“But we are following the advice of disability expert Liz Sayce to use the money more effectively to get more disabled people into mainstream jobs – the same as everyone else.

“All disabled employees affected by the changes will be guaranteed tailored support from an £8m package, including a personal case worker, to help with the transition into mainstream employment.”

Phil Davies of the GMB union said: “This is devastating news for the disabled workers in Remploy and gives the lie to the chancellor’s claim in his autumn statement yesterday that the vulnerable would be taken care of by the government.”

Arthur MacMorrough Kavanagh

December 6, 2012

Born without arms or legs, Arthur MacMorrough Kavanagh was an adventurer who rose to become a successful politician. Widely revered as a prodigy, he was also part of a rich and powerful family, writes Nicholas Whyte.

He was the heir to the ancient kings of Leinster. He was a horseback messenger for the East India Company in the 1850s. He wrote a book about hunting and painting on the borderlands between Greece and Albania.

He was a member of parliament for 14 years and became the leader of the Unionist MPs from Ireland.

And he had no arms or legs.

Arthur MacMorrough Kavanagh was born to a wealthy landowning family in the south-east of Ireland in 1831, a younger son of a much older father who had converted to Protestantism from the family’s traditional Catholicism. “It was manifest that his upbringing must be different from that of other men, born, as he was, without limbs,” wrote his cousin in her biography.

Various painful surgeries had little effect, but in the end Kavanagh was able to use the fingers of his vestigial upper stumps to shoot, paint and write, and became a fearless horse rider, strapped into a special saddle.

His older brother had inherited the family estates, and in 1849 – having returned from an earlier trip to Egypt and Palestine – he and his other brother were sent off on a long voyage to the East.

This epic trip took them through Scandinavia, Russia and what are now Azerbaijan, Iran, Pakistan and India overland – it would be tough to repeat that journey overland even today.

When their money ran out, Kavanagh put his equestrian skills to good use as an East India Company messenger, while his brother headed east and died of a fever in Java. Soon after, he learned that his other brother had also died, and he returned home to become landlord of Borris-in-Ossory.

For those of his class who wanted it, a seat in the House of Commons could easily be arranged, and so Kavanagh was duly elected, first for Wexford and then for his home county of Carlow.

His manservant carried him into the Chamber and was, exceptionally, allowed to remain there to assist him during debates.

Kavanagh had to pre-arrange his parliamentary interventions with the Speaker, as there was obviously no question of waving order papers.

Perhaps for this reason, the Hansard record shows a politician who delivered speeches (from notes poised on the crown of his top hat, placed on the bench beside him) based on diligent research, who was sometimes able to persuade his colleagues of the merits of his case.

But the 1870s were a time of change. The rise of the Home Rule movement under Isaac Butt and then Charles Stewart Parnell, combined with a secret ballot and an increase in the number of voters, eroded support for Irish Unionists like Kavanagh.

As their numbers dwindled, he became their leader, leading negotiations on land reform, state funding for Catholic university education, and nationalising the railways, taking a consistently pragmatic, thoroughly Conservative position, until he in turn lost his seat in 1880.

As an occasional researcher on Irish history and politics, and indeed an erstwhile election candidate, and also as the father of two profoundly disabled children, I find myself devouring any information I can find about Kavanagh – the four published biographies, his speeches in Hansard, and the late Victorian novel based on his life.

But it’s very difficult for us in the 21st Century to get a picture of how Kavanagh was perceived by his contemporaries – and by himself. His cousin, Sarah Steele, published a passionate account of his life in 1891, which concentrates on the marvels of his travels and on his devotion to his family.

Some of his later biographers speculate wildly about his private life, on very little evidence. Charles Kingsley’s daughter Mary, writing as Lucas Malet, used him as the basis for her novel, The History of Richard Calmady.

What’s striking is that all those writers portray Kavanagh as a unique prodigy, a man whose unusual disabilities were compensated for, to an extent, by unusual gifts. He becomes a moral lesson in divine providence, or the virtues of bloody-mindedness, depending.

But for today’s reader, that isn’t good enough.

Kavanagh made many speeches on behalf of his country or his social class, but as far as I can tell never once referred in public to his disability.

The portrait which adorns Steele’s book discreetly fades out at the shoulders. His achievements came not as a result of support from society in general for those of its members who need help, but from the accident of his birth into a wealthy and powerful (if fading) ruling elite.

In an era when disabled people were generally kept out of sight and out of mind, Kavanagh’s story is indeed remarkable.

Politicians with visible disabilities remain rare today. Dame Anne Begg, MP for Aberdeen South, and Brian Crowley, an Irish MEP whose constituency borders those which Kavanagh represented, are both wheelchair users and MP Paul Maynard has cerebral palsy.

The disability rights movement has a long way to go, but is gathering strength.

Kavanagh, however, wanted his disabilities ignored, so that he could be treated just like any other rich man. In the story of disability politics, he is an outlier rather than a trailblazer.

Age UK Pulls Out Of Mandatory Work Scheme

December 6, 2012

A high street charity has stopped providing mandatory work placements because of concerns that jobseekers are forced to work in its stores as a condition of their benefits.

Age UK has become the third large charity in three weeks to pull out of the multimillion-pound Department for Work and Pensions (DWP) scheme.

It said it would also pull out of other government-run schemes in order to ensure its volunteers were making the “appropriate choice” to work for the organisation.

The charity said that although it did not have a policy to provide four-week mandatory work activity placements, some of its 450 nationally run stores had developed local links with private companies administering such schemes. It added that a further 169 independent Age UK stores would still make their own decisions on the policy.

Following last month’s decisions by the British Heart Foundation and Cancer Research to drop out of the scheme, Age UK said it was now advising its stores to wind up their association with government employment programmes.

The latest charity departure comes days after the DWP handed new powers to job centre managers and back-to-work providers to force sick and disabled benefit claimants into unpaid work placements.

Former Labour communications director Alistair Campbell said the new regulations, which mean the 340,000 people on employment support allowance who’d been placed into the work-related activity group (WRAG) could have 70% of their allowance withheld if they fail to work, were “beyond any sense of decency”.

Campbell, who has written about his own issues with depression, said, “It is frankly beyond belief, and beyond any sense of decency, that patients with severe mental health problems, and serious physical illnesses, are being told they can work and that their benefits will be affected if they don’t.”

“I am all in favour of people who are ill being given hope of getting back into the labour market, but this is not about work for those who can, it is about work for those who can’t so that the government can cut the costs and try to help Osborne’s sums add up.”

Paul Farmer, chief executive of mental health charity Mind, said that within the disability and mental health sector there was confusion as to why the government had introduced the policy of mandating sick and disabled people into work when there was “very little evidence” that it worked: “I think there is a growing sense of anger and frustration that across the disability sector that this is heading in the wrong direction and it does bemuse people because I think we all know that there are [other] ways of enabling people of getting into work.”

Farmer said people in the WRAG weren’t “scroungers”, adding, “These are people who have been through the work capability assessment and that’s clearly [found] these people aren’t fit for work.”

“That doesn’t mean you should be forgetting about them and leaving them on the scrapheap, but it doesn’t seem to make a lot of sense to be forcing people into activities when there’s very little evidence that it works.”

The DWP said only a small number of claimants were expected to be mandated into work placements. Where “appropriate”, most would be offered voluntary placements, it said, adding that such placements would be flexible, with full consideration given to a claimant’s health problem or disability.

A spokesperson from the DWP said: “For people on ESA who are expected to go back to work when they’re well enough, a period of work experience is an excellent way to increase skills and confidence. Work experience is completely voluntary. In some circumstances, only where people refuse to take reasonable steps to address a barrier to work, it may be that a short, appropriate mandatory work placement – which must take the claimant’s health into account – would be helpful.

“Mandatory work activity placements benefit local communities while giving jobseekers valuable skills. We are grateful for the continued support of the wider charitable sector in helping unemployed people re-engage with the system and move closer to work.

“Age UK’s decision is entirely a matter for them.”

One claimant, who only wanted to be named as Annie, said the thought she could be forced into work was “terrifying”.

The 34-year-old, who has a teenage daughter, said she had previously worked in administration but now suffered from fibromyalgia, attention deficit disorder, anxiety and depression.

“I was working until April 2010, but after getting increasingly ill and even after my employer reduced my hours, and simplified my role as much as possible, I just wasn’t well enough to keep going in, even just getting to work was exhausting and painful.”

“My main symptom of fibromyalgia is constant, severe fatigue and exhaustion. I am currently finding it hard to get out of the house to go to the supermarket and having a lot of trouble doing basic things like cooking, bathing etcetera.

“I am not well enough to do work that would actually pay me real money and potentially improve my situation; I’m certainly not well enough to do unpaid work,” she said.

Age UK’s director of people and performance, Caroline Bendelow, said it was a large organisation with 7,000 volunteers: “We are committed to giving all individuals who volunteer with us an enjoyable and fruitful experience, with some finding it a useful way to move closer to the labour market.,” she said.

Asked why Age UK was leaving the government scheme, Bendelow said: “Age UK strives to give all its volunteers the best experience possible and we want volunteering with us to be the appropriate choice for each individual’s circumstances.”

She said there was no head office involvement in government schemes and Age UK was now “working with our shops to end any local links that previously existed to such programmes in isolated areas”.

However, she added that this national policy would not apply to the 169 independently run stores using the Age UK name as they made their own decisions.

“There are also 169 local Age UKs across the country who are independent charities making their own decisions based on the needs of their local communities.”

Have You Seen Neon Roberts?

December 6, 2012

Neon Roberts, 7, has a brain tumour and is in urgent need of medical attention. He recently had surgery for this and is currently at the centre of a High Court case over whether he should have radiotherapy.

He was last seen on Sunday in Tiverton, Devon, with his mother, Sally Roberts, 37. Ms Roberts, also known as Sally Leese, is reportedly opposed to her son recieving further treatment. Police believe Ms Roberts may have run away with her son as a result of this.

The pair were believed to have been seen in Sussex or Kent on Wednesday, but their current whereabouts are unknown.

Devon and Cornwall Police are coordinating the search.

I cannot comment further on the open legal case, of course. However, the most important thing here is that there is a seriously ill young child missing.

I will spread this post across all social media today, for what that is worth, simply because I sincerely hope that he returns home safely very soon. I ask my UK readers to do the same.

Updated 8am: Very good news readers. He’s been found safe.

Ed Balls Mocked For Stutter During Autumn Statement Speech

December 5, 2012

https://twitter.com/PrimlyStable/status/276321374786703360

https://twitter.com/DrEoinC/status/276338937465802752

(Includes still photo)

Morgan Freeman Has Fibromyalgia

December 5, 2012

Well, he kept that quiet!

Lack Of Sex Education Puts Young Deaf People At Risk Says Charlie Swinbourne

December 5, 2012

This is interesting.

It’s really good to see this important issue being discussed. Of course sex education classes and resources should be available and accessible to all as soon as age allows.

This Autumn Statement, Disabled People And Carers Will Be Hardest Hit

December 5, 2012

UK readers, you probably know that this afternoon, our Chancellor, George Osborne, will deliver his annual Autumn Statement.

I was planning to listen to the whole thing and pick out the parts that will affect sick and disabled people and carers one by one.

Last time Mr Osborne delivered a Budget, I sadly found this process a bit like looking for a needle in a haystack. So this time, I was very pleased to find that at least two kind journalists much more famous than my little old self have done the hard work for me in advance. So I’m going to do a link round-up instead.

  • And at Comment Is Free yesterday Polly Toynbee wrote that 42,000 young carers will lose £58 a week Severe Disability Premium, 20% of their weekly household income.

If I spot any more related articles, I’ll add to the list.

A Death Within The Pat’s Petition Family

December 4, 2012

Readers, many of you will remember the Pat’s Petition campaign, whose Government e-petition recently closed.

Today, they have revealed the very sad news of the death of one of their core members.

https://twitter.com/MargoJMilne/status/276013065210834944

Those outside the ‘Pat’s Petition family’ don’t know very much about her. However, we do know that a disability activist, one of our own, has died.  This loss will be felt by the whole of our very special little community.

My thoughts are with all who knew this disability activist better than I did. Having lost dear friends far too soon myself, I know that their emotions will be running very high at this sad time.

Wheelchair Users Suing Arriva Bus Company

December 4, 2012

I covered this last year. It looks like the case has now gone to court.

Disabled people in north-east England are being denied access to public transport because of discrimination by a bus company, a court has heard.

Darlington Association on Disability (Dad) is suing Arriva North-East, claiming some drivers have failed to stop for wheelchair passengers.

The case, which opened at Teesside County Court in Middlesbrough, is due to last two weeks.

Arriva said its staff complied with Department for Transport guidelines.

Seven members of the association also claim wheelchair users have been refused access to some buses where there was already a pushchair on board.

Disability training

Chris Fury, of Unity Law, which is representing the association, said: “There have been a series of incidents going back a number of years, where it is alleged that bus drivers have not done enough to free up space for disabled passengers.

“They have essentially been dumped back on the pavement and been told to wait for the next bus.”

The company denied it discriminated against disabled passengers.

It said it complied with the Disability Discrimination Act and offered disability training to all its drivers.

The firm said it adhered to Department for Transport guidelines which state that if other passengers are occupying wheelchair spaces, staff are not obliged to move them or make them move.

It also said the opportunity for a wheelchair user to travel may depend on other passengers and how full the vehicle is.

The case continues.

Disabled Man Left Behind In Wheelchair When ATOS Assessment Centre Evacuated During A REAL FIRE

December 4, 2012

I couldn’t believe my eyes last night when I read about what happened to Geoff Meeghan, 32, during a fitness-to-work assessment by ATOS.

The lovely people at Independent Voices sent me the information and asked to publish the results of my disbelief.

I ask my UK readers to share this across all social media, because what happened to Mr Meeghan can never be allowed to happen again.

My Eye-Opening Experience With 5-A-Side Blind Football!

December 4, 2012

This is a guest post by Richard Willow.

Like most Sunday league footballers, I fancy myself as an elegant player. I like to regale uninterested family members with tales of glorious goals and breathtaking dribbles. “If it wasn’t for my dodgy knee, I could have gone professional,” I tell them (not strictly true, I admit, but I have repeated the statement so many times, I’ve almost convinced myself as to its accuracy!). When I watch Premier League footballers on the television, I like to enlighten my friends (or anyone who’d listen) as to where these professional prima donnas are going wrong and how they can improve their sub-standard skills. So when I was offered the chance to play 5-a-side blind football, I thought to myself “How hard can it be?”

Blind football is a relatively new event in the Paralympics. Played on a small 5-a-side pitch, each outfield player must wear blindfolds with the goalkeeper being the only person in the team who is not visually impaired. The balls used in 5-a-side blind football are heavier than normal and contain ball bearings. The sound made by the ball bearings informs the players as to where the ball is and it is therefore vital that the game be played in complete silence. In addition to the rattling of the ball-bearings, the only other sounds you hear are instructions from the sighted goalkeepers. Communication is key in 5-a-side blind football, and the effectiveness of the goalkeeper’s instructions can often mean the difference between victory and defeat.

As I first donned the blindfold and stepped out on to the pitch, the first sensation was one of complete disorientation. Leaving aside kicking the ball, my initial aim was to run without stumbling or falling over. Bereft of sight, I had absolutely no confidence in any movement. When the ball did come near me, it would often bounce of my shins and roll away. After ten minutes of staggering around the pitch like a drunk, I – for the first time in my amateur football career – volunteered to be taken off.

As I continued to watch the game, I grew increasingly amazed at the level of skill involved. I watched blind players fly around the pitch with speed and dexterity showing little sign of being hindered by their disability. Displaying deft touches and astonishing dribbling skills, the players showed fantastic close control and some surprisingly accurate and powerful shooting. For those who have tried blind football, the ability of the players is all the more impressive. Whereas the skill of professional players can be understood and identified with by many, the skill of blind footballers is truly hard to comprehend. How do they control the ball so neatly? How do they pick out accurate passes and shots? How do they run with the ball with perfect balance? Even professional footballers have complimented the skill and dedication of blind footballers. David Beckham – who participated in blind football with British Paralympics team – has also described his amazement at the level of skill and concentration on show.

In an ideal world, blind footballers would receive the same attention as regular footballers. The level of skill and dedication is no different from the regular game, in fact, it is a great deal more difficult. For those who get the chance, I would recommend giving it a go. It is only once you have experienced the game that you fully appreciate the surprising level of skill and talent on show. What isn’t quite as surprising is the nation which is currently the champion in the sport……..Brazil!

Author Bio: Richard Willow is the founder of Willow Mobility, a company that offers solutions for people who have difficulty with mobility and movement. Having worked with people with an array of disabilities, Richard often writes about his experiences and offers practical advice based on decades of experience.

 

Revealing Disability To A Potential Employer

December 4, 2012

This is a guest post by Steff Green.

Entering the workforce with a disability can be both a daunting, and extremely rewarding, experience. The leap into the workforce can be scary, especially if you’re worried about how you stack up against the other applicants. But working for a company with decent products/services and ethics that align with yours can be a great way to regain confidence and feel as though you’re contributing to society.

 

Although employment numbers for people with disabilities are shockingly low, research estimates that there are more than 1.3 million people with disabilities in the UK who are available for and want to work (Shaw Trust, 2012).  The reasons many have not been able to find employment are many and complex, but one of them is the fact that given a pool of equally-qualified candidates, many employers simply won’t take the “risk” of employing someone with a disability when they don’t need to.

 

This brings the issue of disclosure to the fore. At what stage in the recruitment process should you reveal your disability to a potential employer? Are you even required to reveal it at all? How do you disclose your disability in such a way that you avoid the experience of discrimination, but protect your rights to adaptive equipment and accommodations in the workplace?

When is the Best Time to Disclosure Your Disability?

 

Disclose is a complex decision, and there are many factors that have to be weighed up. For one thing, you’re always dealing with the inbuilt prejudices employers or colleagues have about people with disabilities – whatever these may be. You may have a disability that’s immediately apparent – such as being blind or using a wheelchair – and will be revealed at any face-to-face meeting anyway. You may have a disability that is invisible to the eyes of an employer, but couldn’t be kept secret in the workplace without some danger to yourself. You may have experienced discrimination or disappointment before, and this affects

 

There are different points at which a disability can be disclosed. First, there is the resume or covering letter when you first apply for a job. The pros of disclosing on your application are that it allows you to be upfront about your disability from the onset, and leaves it to the employer to decide if the disability is an issue. However, your disclosure may cause your application to be passed over in favour of equally qualified candidates without disabilities, and doesn’t give you an opportunity to discuss your situation with the recruiter before they make a decision.

 

When the employer calls you to arrange an interview, you could tell them about your disability if it is something they will notice at the interview. This means you won’t surprise them by showing up in a wheelchair or with a guide dog, and will start the interview off with a sense of honesty and integrity.

 

At the interview is probably the best time to disclose and discuss your disability, as it allows the employer to ask questions and understand your skills and limitations. Create a script that briefly explains your disability and any adaptations you’ll need, and focus on the positives. Use specific examples to show how your disability has not impacted your ability to perform specific tasks.

 

Bringing up your disability at any time after an interview, for instance, when the job offer comes in, after you start working at the company, or when a problem arises during your duties, can foster distrust between you and your employer. The longer you put off disclosure, the more difficult it becomes.

 

Of course, depending upon your disability and the type of job you do, there may be no need to disclose it at all. But, in general, honesty is the best policy, and being upfront about your skills and limitations allows you to work with your employer to find adaptations that make your work life easier and more enjoyable.

How to Prepare for Disclosure

 

Before applying for a position or disclosing your disability to a potential employer, it’s a good idea to do your own research and pre-empt any questions or concerns they might have.

 

Many people find it helpful to prepare a “script” explaining their disability, and practice it in front of a family member or the mirror before the interview. The employer doesn’t need every detail of your medical history (and they shouldn’t be asking!) but they do need to know that you’re reliable, valuable as a team member and that you can do the job just as well as anyone else. Try not to focus on your disability so much as your skills, qualifications and experience. Keep your script positive and upbeat.

 

Consider any potential adaptations that will need to be made to enable to you to do the job – and come up with cost-effective solutions. Instead of avoiding the challenges, demonstrate to your employer that you’re aware of them and have already found solutions. This shows you are a solutions-focused person who’ll be an asset to the workplace.

 

If you use any adaptive equipment, it may be helpful to bring this in to the interview and demonstrate it to the recruiter, for example: Braille-note, or hearing aid.

 

If you have a medical condition or disability that may require you to have assistance from other employees, your employer will need to train them. This is an added cost to them and may be a deterrent to hiring you. You can briefly explain some of the activities you require help with and how other employees can be educated. An employer may not realise that staff are already trained – for example, anyone with a first aid certificate has knowledge in dealing with seizures.

 

You can point the employer to other sources of information. Offer to email them links to a couple of websites or local support groups for your condition. (This also gives you an opportunity to follow up after the interview).

 

When the answer is NO

 

Despite your best efforts to show your disability in a positive light, it’s inevitable that you’ll meet resistance from some employers. People will dismiss you the minute they see that cane in your hand or the hearing aid on your ear.

 

I trained as an archaeologist and then a museum curator. I had been interning at a living history museum for six months when they asked for applications for a paid position. I put in my application, but was passed over. When I pressed for a reason, I was told it was because they thought I would be a health and safety issue, because of the amount. I was fuming – so it was OK to have me work for them for free, but when I wanted a job, suddenly I was “a health and safety issue”?

 

It hurts. It makes you upset and angry. But it’s something every person with a disability who enters the workforce will probably experience at sometime in his or her life. You have to remind yourself that anyone who is going to discriminate against you for your disability is not someone you want to work for, and an amazing job with a horrible boss will quickly turn into a horrible job. I was much better off not working for the museum, because they weren’t ready to accept that I could do the job as well as anyone else.

 

 

Most employers are willing to take a shot on an employee with a disability; as long as they’re satisfied you can do the job you’re employed for. Look at the job-hunting process as an opportunity to educate people about your disability. If you can demonstrate to an employer that, with adaptations, you can do the job as well as anyone, and that you’ve taken the time to think of ways around any issues your disability may present.

 

Bio: Although she’s had many jobs over the years, including archaeologist, builder’s labourer and art gallery docent, Steff Green is now a legally-blind writer and illustrator based in New Zealand. Steff writes for the Disabled Shop Blog on disability advice, products and issues in the UK, such as her recent piece on Caring for the Carers.

The Fear- Drama About Crime Boss With Dementia

December 3, 2012

Peter Mullan has taken on the role of a gangster suffering from an aggressive form of dementia in a new Channel 4 series, The Fear.

As ageing crime boss-turned-entrepreneur Richie Beckett, Mullan is forced to face-off with an aggressive foreign gang trying to muscle in on his Brighton territory while inside his head, another turf war ensues as he struggles to keep control of his own senses.

At a screening of the first episode of the four-part series, Mullan admitted he kept his research on the condition to a minimum, merely watching a half-hour documentary on the illness.

“I’d lost a lot of family to Alzheimer’s and I watched a DVD on people coping with Alzheimer’s.

“It really just confirmed what I knew on whether there were any physical manifestations of the disease, which there aren’t. It’s different for everybody.”

The Fear was written by Richard Cottan, who scripted Kenneth Branagh’s Bafta-winning English-language adaptation of the Swedish detective series Wallander.

“It wasn’t essentially my idea,” he said. “I was approached with the idea of a gangster-type person who got Alzheimer’s and it came to me as a very different story.

“I thought it was a joke at first but then I thought about it as a very different way of treating the disease rather than some quite earnest indictment of the NHS with old people shuffling around in slippers.”

Though his condition provides the audience with a degree of empathy for Richie, Mullan is adamant the audience should not confuse the former gangster, who has since assumed airs of respectability, for a sympathetic character.

“He’s a nasty guy that has made a living out of people’s poverty and addictions and his lovely children have taken the benefits of that so I don’t have much time for them either if I’m honest.

“What intrigues me about it, was throwing together an highly unsympathetic character with a disease that obviously one feels for someone suffering from it.”

The Alzheimer’s Society has praised The Fear, in a statement it said: “It is good to see dementia portrayed in mainstream drama. As is shown in the series, dementia can be very frightening and confusing when you don’t know what the cause is.

“The storyline will help us raise much needed awareness amongst new audiences and show that dementia can affect anyone. There are 800,000 people living with dementia in the UK. We would like to see more high profile programmes tackle this important subject.”

Rising star Harry Lloyd, seen in the film Iron Lady, the BBC’s recent adaptation of Great Expectations and the hit TV series Game of Thrones, plays Richie’s son Matty.

He said the darker aspects of the drama actually brought out the actors’ lighter sides between takes.

“I had a ball doing it, as dark and horrible as it is, it quite often makes for a jolly set because you have this nervous energy.

“You do an intense scene and afterwards, especially being British, you can laugh it off and stay close to the people around you rather than dive into your little hole of desperation.”

As perhaps the most perceptive of Richie’s two sons, Lloyd is the first to suspect that there is something wrong with his father, though Lloyd said he deals with the discovery with more pragmatic concerns for the family business.

“For Matty, the Alzheimer’s, if anything, is a distraction and a frustration and to begin with he’s very cold about it because he’s used to being in charge, he’s the brains behind the outfit.

“I think in a way, it’s important that I didn’t understand the Alzheimer’s too much as I tried to get that feeling of looking into my dad’s eyes and trying to work out what he’s feeling.”

Mullan, who has carved a niche playing some unpleasant, often violent characters joked that every criminal is a wannabe actor and the the same is probably true of most thespians.

Lloyd agreed: “I think its very attractive to play someone who has a very different life to your own, its not about the darkness or the light or he’s sympathetic or he’s funny, these are the first adjectives you throw at them but you need more than one word.

“Obviously me being a public schoolboy and running a massive crime business in Brighton, it’s a massive turn on, it’s very exciting – I could never do that and so you learn and you try and get away with it.”

Amongst the heavier dramatic scenes where Richie slowly begins to unravel before his family are moments of grim humour.

Advising his son Cal, played by the former EastEnders star Paul Nicholls, to temporarily store some human remains in the freezer at the family home, Richie adds: “Don’t tell your mother, she’s always been a fussy eater.”

“I was talking with the producer about that, when you see it with an audience for the first time and you hear people laughing and you realise it’s one of those shows that people are desperate to laugh,” said Lloyd.

“Even the lightest moments, just the little nuances of relationships within a family are something you recognise, and you say: ‘Oh yeah, they’re humans, I’m safe again’. But it is unsettling because you know it’s not a comedy.”

Mullan, who won best actor at the Cannes Film Festival in 1998 for his role as a recovering alcoholic in My Name Is Joe, and has been Bafta-nominated as a director, screen writer and an actor is one of the most respected figures working in the British film industry.

He must be, in short, an intimidating presence on the set, particularly for a young actor playing his son.

“Before I met him , I re-watched all his films and I told myself I need to not be intimidated by this guy because he’s my dad,” admitted Lloyd.

“But seeing him on screen, he’s always pretty intense and I was a bit scared, and then you meet him and straight away he’s just the most relaxing man. Its impossible to be nervous acting around him – it’s very personal and fun and honest and lively and anecdotal – it was a real pleasure.”

Part one of The Fear begins at 2200GMT on Channel 4.

David Weir Given Freedom Of City Of London

December 3, 2012

Does anyone know of any other Paralympians who have this honour? I don’t!

London 2012 gold medallist David Weir has been awarded the freedom of the City of London in recognition of his sporting achievements.

The wheelchair athlete, nicknamed “The Weirwolf of London”, won four gold medals in the 5,000m, 1500m, 800m and marathon at the 2012 Paralympics.

It comes as a new programme of grants to widen sporting opportunities for disabled people is launched.

The City of London Corporation said Weir was being honoured to mark it.

Weir, from Wallington in south London, won two gold medals at the Beijing Paralympic Games in 2008, and has also won six London marathons.

‘Golden sporting era’

The City Bridge Trust, the City of London Corporation’s charity, has launched the City Sporting Chance grants programme.

A spokesman from the authority said it was hoped it would help inspire a new generation of athletes.

Billy Dove, chairman of the City Bridge Trust, said: “As the UK cheered on athletes such as David Weir, thousands of disabled people were inspired to get involved with their local sports club.

“Our new ‘City Sporting Chance’ will provide organisations with the resources they need to widen access to sport for those who may not have had the opportunity to take part before.

“We hope this will create a lasting legacy for sports opportunities for disabled people that extends well beyond this golden sporting year.”

Eastenders’ Roxy Mitchell Shock At ‘Abuse’ Jibe For Wanting Operation For Deaf Daughter

December 3, 2012

EASTENDERS star Rita Simons says she has been accused of abusing her deaf daughter for deciding she should have an operation to enable her to hear.

Simons, who plays Roxy Mitchell in the BBC soap, and her husband Theo Silveston have decided Maiya, six, will have a cochlear implant to give her hearing in both ears.

But she has revealed in a new interview that the couple had encountered “extraordinary” hostility because of the decision. She said: “It comes mainly from people who firmly believe deafness should be embraced rather than treated as a physical deficiency that should be corrected.

“I totally respect their point of view. But when a 19-year-old girl told me I was an ‘abuser’ to let my child have a cochlear implant, I was horrified and deeply hurt.”

In the interview in the latest edition of Hello! magazine, she added: “I would throw myself in front of a bus for my girls – and yet I was being judged by someone who didn’t know me or understand my emotional stance at all.

“We know it’s not a miracle cure and her hearing won’t be perfect. But, in time, her brain will process what it is hearing and compensate, making sounds more familiar to her.”

The British Paraorchestra’s First Single- A Cover Of Phil Collins’ True Colours

December 3, 2012

Thanks for info Disability Horizons.

A music video to ‘brighten’ up your Monday morning:

If you like this version of the song, you can buy it on Itunes here for 79p.

Personally, I like it so much I’ve set up a Facebok page to try to get it to Christmas Number 1.

Disabled People In Spain Protest Against Cuts

December 3, 2012

Streets in the centre of the Spanish capital were closed off on Sunday as thousands marched in Madrid to protest against the effects of government cuts on people with disabilities.

Spain has seen regular protests and two general strikes this year, but this is the first mass protest against austerity measures by disabled people.

Pascale Harter reports from Spain.

International Day Of Disabled People

December 3, 2012

That’s right, readers, today is 3rd December. The one day of the year when across the world, the mainstream stop and think about us lot. So celebrate yourselves or the DisAbled people in your lives in some way today, please.

Victoria Webster- The Doctor With Cerebral Palsy

December 2, 2012

I found this story so inspiring. It’s so good for me to see that Victoria Webster was given enough encouragement to follow her dream.

 

First T20 Cricket Blind World Cup Starts Today

December 2, 2012

England’s visually impaired cricket team start their inaugral T20 Blind World Cup series in India this weekend.

The first ever Twenty20 Blind World Cup is scheduled to begin on 2 December and run until 13 December, in Bangalore, India.

The BBC’s Mike Bushell met the team while the players trained at Edgbaston ahead of the tournament.

Artist Taxi Driver’s Take On ESA Voluntary Work Plans

December 1, 2012

WARNING- Extremely NSFW.

ATOS Head Gets £1M Bonus

December 1, 2012

The fatcat boss of a firm hired to help slash the benefits bill has won a bonus of nearly £1million.

Thierry Breton’s bumper payout means he pocketed more than £1.9million last year.

Details of the obscene sum paid to the head of French firm Atos come as David Cameron draws up draconian new welfare cuts.

Atos was brought in to reassess 2.5 million people on ­incapacity benefit to help the ­Department for Work and Pensions decide whether they are fit to work.

Mr Breton received his massive pay out despite mounting numbers of successful appeals by people ordered to get a job after being tested by the firm.

Heart attack and lung disease victims are among those judged to be well enough to work.

Some 3,100 claimants had appeals upheld in May 2011, up from 900 in the same month in 2010, the latest figures show.

On average almost two in five, 38%, challenged decisions are overturned at tribunal, nearly one in 10 of all those made.

And the appeals system costs taxpayers tens of millions of pounds to administer.

Labour MP Tom Greatrex says Mr Breton’s bonus will “sicken” those put through the reassessment ordeal.

The Atos chief’s latest payment comes on top of wages and perks totalling £1.83million in 2010.

It was revealed in its recent annual report in which it boasts about its “excellent service”.

Mr Greatrex said: “People will find it hard to believe that he sees fit to reward himself with millions, while thousands here suffer.

“It will sicken those who have been through the Atos process to hear the company crow about its expertise.”

He called on the DWP to get a grip on Atos and make the firm improve its performance.

“Thousands suffered because time and again incorrect decisions have been made on the back of Atos assessments,” he said.

An Atos source said decisions on fitness to work were not based solely on its ­assessments but also on information from ­claimants and their doctors.

A spokesman for the company said the bonus was unrelated to the firm’s Government contract, insisting: “No bonus payments are made as part of the Department for Work and Pensions contract.”

At this time of austerity and spending cuts nationwide, any excessive bonus, which this certainly is, is just plain wrong.

Tom Greatrex MP is absolutely right. Disabled people and carers who have been through the assessment process are sickened by this bonus. Those disabled people who have not yet been through the process, but who have heard the stories of what it is like, are sickened by this bonus.

This bonus should be fairly divided among benefit claimants, who are currently suffering as a result of the cuts, as well as all those who have appealed wrong decisions made by ATOS about their benefits.

These people genuinely need this money to survive.

People On ESA To Be Offered Voluntary Work Experience From Monday

December 1, 2012

Guardian & Observer Christmas Appeal

November 30, 2012

The Guardian and Observer have just launched their Christmas appeal. This year, they’ve chosen to support no fewer than eight disability charities.

Former Paralympian Dame Tanni Grey Thompson To Be On Panel Investigating Lance Armstrong Affair

November 30, 2012

I whooped with joy when I heard about this. The barriers this amazing Baroness has broken down for disabled people are just unbelievably amazing. Her inclusion on this panel is a huge roll forward for all disabled people everywhere.

It’s also a huge roll forward for Paralympic sport. The panel could have had any sportsperson, any Olympian. The fact that they chose a Paralympian says a lot about how seriously Paralympians are being taken today. To a disabled person who, growing up, was given no idea that Paralympic sport existed, that’s massive progress.

British Paralympic great Baroness Tanni Grey-Thompson has been appointed to the three-person commission that has been set up by the International Cycling Union (UCI) to investigate the Lance Armstrong affair.

The chairman of the panel will be former Court of Appeal judge Sir Philip Otton, with Australian lawyer Malcolm Holmes being the third member of the independent body.

The UCI set up the commission in response to a damning report from the United States Anti-Doping Agency (Usada) into a decade of cheating by Armstrong and his team-mates.

That report, published in October, resulted in the American being stripped of his seven Tour de France titles, but it also seriously called into question the UCI’s actions over the period.

It is against this backdrop that John Coates, the president of the Court of Arbitration for Sport and the Australian Olympic Committee, was asked by UCI president Pat McQuaid to compile a shortlist of credible candidates for the commission.

McQuaid welcomed Friday’s announcement of the panel, and thanked Coates for “assembling such a high calibre and truly independent commission”.

“The commission’s report and recommendations are critical to restoring confidence in the sport of cycling and in the UCI as its governing body,” he added.

“We will co-operate fully with the commission and provide them with whatever they need to conduct their inquiry and we urge all other interested stakeholders to do the same.

“We will listen to and act on the commission’s recommendations.”

Otton retired from the Court of Appeal in 2001 but has since worked as an arbitrator in a number of high-profile sports cases in Formula 1, football and America’s Cup sailing.

Grey-Thompson won 16 Paralympic medals, including 11 golds, during her athletics career and is now a member of the House of Lords.

The commission will meet in London 9-26 April 2013, and aim to submit its report to cycling’s governing body by 1 June.

Carers’ Rights Day

November 30, 2012

Readers, apparently it’s Carers’ Rights Day today. The Guardian has an article full of useful information about carers’ rights to mark the occasion.

The Leveson Report: Excellent News For Disabled People

November 30, 2012

The Black Triangle Campaign say the Leveson report could be excellent news for disabled people- if the Government choose to let it.

British Airways Breaks Fencing Champion’s Wheelchair

November 29, 2012

A national wheelchair fencing champion from Cornwall has claimed he could lose funding for the next Paralympics after an airline broke his chair.

Matthew Campbell-Hill, from Truro, has travelled to Hungary to compete at the World Cup this week, but said he may now not be able to take part.

It is “crucial” that he does well at the event in Budapest, so that he can secure funding for the next four years.

British Airways (BA) said it was trying to “rectify the problem”.

Mr Campbell-Hill – recently crowned the British wheelchair fencing champion – has had to weld parts of his custom-built competition chair, as well as using heavy duty tape to hold it together.

“This will hopefully make it secure, but it does keep falling apart at the moment,” he said.

It is now “a race against time” to see if he can get a replacement, and he has claimed that missing out will have “knock-on effects on his career”.

In a statement, BA said it was “extremely sorry that Mr Campbell-Hill’s wheelchair was damaged while in our care”.

“We are talking to Mr Campbell-Hill to rectify the problem as soon as we can and will also reimburse him for any costs incurred due to the damage to his wheelchair.”

Life With Photosensitive Epilepsy

November 29, 2012

“Viewers are warned that the following programme contains flash photography.”

It’s a message we hear repeatedly, but these flashing images don’t just occur on TV – they are appearing in a growing number of video games, films, music videos and on YouTube. So what is it really like living with photosensitive epilepsy?

Photosensitive epilepsy itself is quite rare; only about three in every 100 people with epilepsy have this type.

Jane Williams, 24, from Glasgow, was diagnosed at the age of 12. She says she was mollycoddled growing up.

“Teachers treated me a bit like a china doll when I was at school. They were worried about me taking seizures so I wasn’t pushed that much. I could get out of PE quite easily but I think the teachers should have maybe made me do a bit more,” she said.

It was only when Jane turned 18 and headed off to university that she began to notice her epilepsy have more of an impact.

“When I got to university I wanted to go to bars and nightclubs.

“For me though, a night out can be a bit of an ordeal. I have to be very careful about strobe lights and it requires a lot of planning.”

She explained how she would have to phone nightclubs in advance to find out what type of lighting they used.

‘One-eyed dance’

“Some nightclub owners just don’t understand what it’s like trying to plan your night out. Bouncers are a particular bugbear of mine. In one bar in Glasgow, a bouncer told me if I had epilepsy I shouldn’t be allowed out.

“I was furious – there are so many misunderstandings.”

Jane has since worked out ways to manage her epilepsy when she is in a nightclub through the “one-eyed dance”.

“My neurologist told me that both eyes have to see the light for you to have a seizure so if a light comes on and I’m not expecting it, I cover one eye with the palm of my hand, look down and keep dancing. My friends now know what that means and they all do the same.”

Charity Epilepsy Action says this method can be used to hold off a seizure.

Jane, who is now working for a publishing house, said that even though she could manage her epilepsy, she constantly worried when she was in a bar.

“I’m in constant fear that strobe lights might come on. I’m constantly thinking about my escape route and have even had panic attacks when lights have come on.”

It’s not just nightclubs that can trigger photosensitive epilepsy seizures. Films and music videos can also act as a trigger for some.

In 1997, an episode of Pokémon shown on Japanese TV caused almost 600 people to have seizures. Three-quarters of those had no past history of epilepsy.

For Oliver Spicer, 23, from Portsmouth, it was an Xbox game that was one of his initial triggers. Oliver was diagnosed with photosensitive epilepsy after a night out while he was studying at the University of Sheffield.

“I had been out for the night, had been drinking, and was tired. When I came home I had a seizure. I was 19 when it was diagnosed and I found it really hard initially.

“I became a bit depressed and thought I would never be able to hold down a job. Sleep deprivation is one of the main triggers of a seizure and I was worried about that,” he said.

However, over time Oliver was able to control his epilepsy by monitoring his sleep patterns and medication. He has now graduated and is a consultant for a large accounting firm.

“Most people think epilepsy ruins your nightlife or stops you pursuing things you care about but it didn’t ruin mine. I played in a ska band with friends at university, I enjoy a great deal of support from my partner, family and friends and I am treated very well by my employer. In short, I live a normal and happy life regardless of having epilepsy.”

‘Physically attacked’

But Epilepsy Action believes many people living with epilepsy are still discriminated against.

Stephanie McMaster, 21, from Belfast was the victim of bullying when she was at school.

“I was physically attacked for being different. The other kids threw stuff at my head on the bus, thinking it would make me have a seizure and they thought it would be funny to see.

“The teachers turned a blind eye because they didn’t understand either. I was constantly called names and left out. It’s made me shy to this day.”

Stephanie has recently had a baby and is now discovering the pitfalls of being a mother and living with epilepsy.

“My daughter is 16 weeks old. It can be quite hard, I’m not allowed to bathe her on my own in case I have a seizure or be left on my own with her. If I want to go up to the shop I need to get someone to come with me.

“My message to those reading this is look at me now; I have my own life, my own house, my own family. I turned out to be a successful person. People need to understand what it’s like living with epilepsy and realise it’s not a death sentence.”

Quasimodo Musical To Premiere In 2013

November 28, 2012

A little-known Lionel Bart musical about the hunchback of Notre Dame is to be staged for the first time, some 50 years after it was written.

Quasimodo will have its world premiere at north London’s King’s Head Theatre in March 2013.

Bart, who died in 1999, wrote Quasimodo around 1963, but the musical was never staged in his lifetime.

The composer is best known for his stage musical Oliver! – the film version of which won several Oscars.

“Quasimodo is a very serous work,” Adam Spreadbury-Maher, artistic director of the King’s Head, told the BBC.

“Lionel referred to it as operatic in nature. It’s very dark and sexual. It’s very honest as well, as he had sometimes identified himself as a kind of Quasimodo character, an outsider.”

It is the first musical at the fringe venue since Spreadbury-Maher took over in 2010. The show will be directed by Robert Chevara, who approached the Bart Estate for the rights to perform the work.

“Quasimodo was never really in a book-ready form and there was no cast album,” explains Spreadbury-Maher. “What it needed was a group of producers and actors to look at it again and take it forward.”

Based on Victor Hugo’s 1831 novel Notre Dame de Paris, Bart’s musical is set in 15th Century Paris and tells the story of the love between the deformed bell ringer and the beautiful gypsy girl Esmeralda.

Continue reading the main story

“Start Quote

Brilliant, dear boy, but were you on drugs when you wrote it?”

Noel Coward assesses Lionel Bart’s Quasimodo

The tale was famously adapted by Disney for a 1996 animated film, voiced by US actor Tom Hulce.

The closest the Quasimodo show came to the West End was a workshop for industry insiders in the mid-1990s.

The 1995 performance featured Tony Award-winning Frances Ruffelle as Esmeralda and Ray Shell (who currently appears in new West End musical The Bodyguard) as Quasimodo. A recording exists with Bart playing the piano as part of the band.

But the project never progressed and Bart died from cancer aged 68 four years later.

In an interview with The Independent during rehearsals for the workshop, Bart said he’d been fascinated by the story since he saw Charles Laughton as the hunchback in the 1939 film version.

“I was inspired by the story of this marvellous soul within a monstrous body. The simple premise of the piece, when I wrote it, was the question, ‘What is ugly?’ I hoped that you could realise, when you left the theatre, that the guy at the end of the row wasn’t so ugly after all.”

He added: “It’s a tragic story, but about being free to change, free to renew oneself. In a way I became the hunchback. It’s a great release and a catharsis for me to put it all in this work.”

Bart also confided that he sent the script to English playwright and composer Noel Coward, who responded. “Brilliant, dear boy, but were you on drugs when you wrote it?”

Since 2008, Spreadbury-Maher has developed a reputation for staging world premieres and first time revivals of work by playwrights such as Edward Bond, Arnold Wesker and Tennessee Williams.

His company’s production of Puccini’s La Boheme, staged by OperaUpClose in a pub theatre in Kilburn, won the best new opera production prize at the 2011 Olivier Awards.

Thames Valley Free School Planned For Autistic Pupils

November 28, 2012

A free school for children with autism and Asperger syndrome is set to open in Berkshire.

The Thames Valley Free School, which is sponsored by the National Autistic Society (NAS), is scheduled to open in Reading in September 2013.

The school, which was approved by the Department of Education in July, will serve 50 pupils aged 5 to 16 from the Thames Valley region.

A six-week public consultation on the plans runs until 15 January 2013.

‘Community links’

Fiona Veitch, the school’s principal, said: “A key aspect of the new school will be that it will aim to work in partnership with mainstream schools and colleges in the areas where pupils are from.

“They will have the opportunity to attend classes, activities and events at those schools or colleges, if and when this is appropriate for them.”

Ms Veitch added the school wanted pupils to “maintain their links with their communities”.

The NAS and Reading Borough Council are finalising plans for the site of the school.

An open evening about the school will be held on 3 December 2012 in the Waterhouse Chamber of Reading Town Hall.

Free schools are set up by groups of parents, teachers, charities, businesses, universities, trusts, religious or voluntary groups, but funded directly by central government.

Luton ATOS Assessment Centre Not Accessible

November 28, 2012

Oh, not another one!

A disability assessment centre in Luton has been criticised for not being accessible to wheelchair users.

A lift which serves the sixth floor office in Cresta House would become unavailable in an emergency and visitors would have to use the stairs.

Wheelchair user Eileen Carroll said she was “stunned” when she was turned away because she was a “liability”.

The Department of Work and Pensions (DWP) said it was looking for an alternative building.

“Where an assessment centre isn’t on the ground floor, as is the case with Luton, we endeavour to make this clear to people before they arrive for their appointment,” a spokesperson said.

“If people have mobility problems, which may make evacuation in the event of a fire difficult, a home visit or an appointment at an alternative assessment centre is arranged.”

‘Alternative location’

Ms Carroll said she was not asked whether she was in a wheelchair ahead of her visit to the fitness-for-work assessment centre, nor was she warned that access would be an issue.

“I turned up at Cresta House and was told I couldn’t be assessed because I was a liability,” she said.

“In order to get to that appointment I had to make several arrangements including my husband taking time off work.”

She was told she would have to be assessed in Milton Keynes, but Ms Carroll said this was too much to ask.

Her benefits have now stopped, she said.

Atos Healthcare, which runs the assessments for the government, echoed the DWP’s comment that people are warned of access issues before appointments are scheduled and said home visits could also be arranged.

“Luton is a government building so we are working with the DWP to ensure we best meet the needs of those claiming benefits,” the spokesperson said.

Last week, employment minister Mark Hoban said 31 of 123 fitness-for-work assessments centres used by Atos lacked ground-floor access for wheelchairs.

Man Jailed For Mobility Aid Sales

November 28, 2012

A Nottinghamshire man has been jailed for six months after he ignored a warning over the mis-selling of goods to elderly and vulnerable people.

In 2010, John Cooney, 37, from Radcliffe-on-Trent, signed an order to trade fairly after a series of complaints about goods not arriving.

But he continued to target the elderly and vulnerable with mobility products.

At Nottingham County Court, Cooney admitted 49 breaches of the Enterprise Act and was jailed for contempt.

Cooney and business partner Carl Mould, 46, ran UK Mobility Plus, which closed in January 2011.

‘Misjudged leniency’

In 2010, Nottinghamshire Trading Standards received 120 complaints about the company from across England.

Both Cooney and Mould signed agreements under the Enterprise Act but continued to mis-sell mobility products.

At another hearing in January, a judge told both men if they traded unlawfully before December 2014 they would be jailed.

Mould, of River Crescent, Nottingham, received a four-month sentence in September.

On Monday, the court heard Cooney, trading from Old Dalby in Leicestershire, had breached a Contempt of Court order and had taken about £3,500 from five customers in their 70s and 80s since March.

Judge Richard Inglis said he had previously shown “misjudged leniency” towards Cooney.

Outside the court, Trading Standards Officer Paul Gretton said Cooney knew what he was doing was wrong.

“What he was doing was cold calling elderly people or somebody was cold calling for him, getting him an invite,” he said.

“The first thing he was doing wrong was letting them believe he might be from social services. If they thought that he didn’t put them right.

“He would then actually physically go along. He’d get in the house, then he’d sell them stuff, stuff they probably didn’t need, that wasn’t suitable.”

Government To Publish Final Winterbourne View Report This Week

November 27, 2012

Ever since the 1969 inquiry into Ely hospital in Cardiff, improvement in the care and support of people with learning disabilities has been spurred by scandals. The most recent progress came five years ago, following revelations of abuse and neglect in Cornwall and in Sutton and Merton, south London, and, separately, Mencap’s devastating Death By Indifference report on the deaths of six learning disabled people failed by NHS healthcare.

Another lurch forward will come next week, when the government is due to release its final response to the Winterbourne View affair, and hopes are high that the widespread disgust triggered by the case will prompt a historic change in the way we treat people with what is termed “challenging” behaviour.

The closure of NHS learning disability hospitals in the last decades of the 20th century did not, we now know, put an end to long-stay institutional care for this group. Slowly and subtly, the private sector moved in to open facilities where many unimaginative care commissioners were only too happy to park people who proved difficult to settle in the community. Charges of £3,500 a week, as at Winterbourne View, were no deterrent.

Research by the Tizard Centre at the University of Kent in 2007 found that these so-called “assessment and treatment units” were typically less than 10 years old, demonstrating that they had been developed just as the last of the NHS hospitals disappeared.

Quite how much assessment and treatment has been undertaken in the units is open to question. Although they are supposed to offer short-term interventions, such as stabilising difficult behaviour, a recent survey by the Care Quality Commission (CQC), found patient stays of five to seven years were not uncommon and that one individual had been in a unit for 17 years. The abuse filmed secretly for last year’s BBC Panorama programme on Winterbourne View, for which six former care workers at the unit near Bristol have been jailed and five others given suspended sentences, was in part the product of a regime where little organised activity, clinical or otherwise, took place.

It is estimated that 1,500 people in England may be in units like Winterbourne View, which was closed shortly after the scandal broke. Although the CQC has found no comparable levels of abuse elsewhere and some units no doubt do deliver effective, short-term care, the overwhelming opinion in the learning disability sector is that the “assessment and treatment” model has been perverted beyond remedy and that people with challenging behaviour should be supported in other ways, usually in the community.

Ministers are expected to endorse this next week, calling for a rapid reduction over the next two years in the number of people with learning disabilities or autism in hospital-type units, and the closure of large-scale in-patient services in favour of personalised and local provision.

Commissioners will be given six months to prepare individual care plans for people in the units and a further 12 months to bring back to their communities all those placed inappropriately. By 2014-15, all the new NHS commissioning groups and councils across England should have agreed strategic plans covering a variety of services for adults and children with challenging behaviour. A wide range of organisations involved in the care and support of people with learning disabilities will sign up to a concordat setting out this ambition. It will describe the Winterbourne View affair as “horrifying” and say that the placing of people in hospital units for prolonged periods must stop.

For a government committed to localism, the report will be as close to a central directive as you are likely to get. Winterbourne View was a truly shocking episode, and no one would want to see vulnerable people hurt and ridiculed in that way, but good may yet come of it.

Disabled Woman Labelled Scrounger- For Parking Car Outside Hospital

November 27, 2012

This says it all, really, doesn’t it, readers?

Work Programme Figures: The Disability Stats

November 27, 2012

There’s been a lot of talk today about the Government’s Work Programme and how unsuccessful it has been so far.

I’ve just seen a statistic, Tweeted by Jenny Jones of the Green Party, that shows what this means for disabled people.

 

Study Suggests Autism Linked To Traffic Pollution

November 27, 2012

The possibility that autism is linked to traffic pollution has been raised by researchers in California.

Their study of more than 500 children said those exposed to high levels of pollution were three times more likely to have autism than children who grew up with cleaner air.

However, other researchers said traffic was a “very unlikely” and unconvincing explanation for autism.

The findings were presented in the Archives of General Psychiatry journal.

Data from the US Environmental Protection Agency were used to work out levels of pollution for addresses in California.

This was used to compare exposure to pollution, in the womb and during the first year of life, in 279 children with autism and 245 without.

The researchers from the University of Southern California said children in homes exposed to the most pollution “were three times as likely to have autism compared with children residing in homes with the lowest levels of exposure”.

They have previously shown a link between autism and living close to major roads.

They warn that there could be “large” implications because air pollution is “common and may have lasting neurological effects”.

But how?

However, other researchers questioned how pollution could alter the brain’s development and lead to autism.

Uta Frith, a professor of cognitive development at University College London, said: “It seems to me very unlikely that the association is causal.”

She said the study did not “get us any further since it does not present a convincing mechanism by which pollutants could affect the developing brain to result in autism”.

One of the challenges with this style of study is that it is difficult to account for every aspect of life which might affect the probability of developing autism, such as family history.

It means the study cannot say that autism is caused by traffic pollution, merely that there could be a link between the two.

Sophia Xiang Sun, from the University of Cambridge’s autism research centre, argued that cutting pollution would be a good idea anyway.

“We know that traffic-related air pollution can contribute to many other diseases and conditions, and it is biologically plausible it also has a role in pathways of autism.

“However, whether or not the potential association between autism and traffic-related air pollution exists, reduction of traffic-related air pollution would be good for public health.”

Fourteen Die In Fire At Factory In Germany Staffed By Disabled Workers

November 27, 2012

I heard about this fire yesterday, but didn’t take much notice until I saw there was, as there usually is, a disability link in the story.

Fourteen people died and at least six were injured after a fire broke out on Monday at a workshop for disabled people in southwestern Germany.

Markus Straub, a fire brigade spokesman, said it was not yet known what started the fire at the building in Titisee-Neustadt, a town in the Black Forest near the city of Freiburg.

The workshop employs 120 people with either mental or physical disabilities in a variety of jobs including metalwork, woodwork and electrical installation. It is run by the Roman Catholic church’s Caritas organisation.

Up to 100 firefighters tackled the blaze at the modern, three-storey building and dozens of paramedics attended.

There were usually 100-120 people in the building on a workday, police spokesman Karl-Heinz Schmid told Suedwestrundfunk radio. “It will take days to investigate what caused the fire,” he said.

Titisee-Neustadt mayor Armin Hinterseh said the centre’s buildings were quite new. “It is devastating. We now have to find out how it happened,” he told the Badische Zeitung newspaper.

Winfried Kretschmann, the state governor of Baden-Wüerttemberg, rushed to the scene according to his office.

 

Paralympians On BBC SPOTY Shortlist

November 26, 2012

Readers, since I’ve been following Sports Personality Of The Year, I’ve seen  Ellie Simmonds win the Disabled Sports Personality Award and the Young Sports Personality Award. I’ve seen the amazing Tanni Grey Thompson presenting an award last year. Until now, however, I’ve never known a disabled sportsperson to be up for the mainstream award!

But in the world of disability, progress is like buses in the city of London. You wait ages for a real, significant piece of progress, and then three come along at once!

That’s right, readers, this year’s SPOTY shortlist includes no fewer than three Paralympians. In alphabetical order, they are: Ellie Simmonds, Sarah Storey, and David Weir.

Same Difference wishes all three of them the very best of luck on the night. Just by being on the list, they have broken down a barrier that few could have previously thought it would ever be possible to break.

BBC Coverage For ‘Scroungers’

November 26, 2012

It’s good to see the BBC carrying articles like this on benefit claimants.

Policeman Recovering From Brain Injury

November 26, 2012

A police officer who was knocked down by a hit and run driver and left for dead at the side of the road, has been making a remarkable recovery.

Dicky Coetzee was nicknamed robo-cop because of his high arrest rate.

Now, with the support of his family, he is working to recover from the brain injury he suffered a year ago.

John Maguire went to meet him.

Remember Amit Sodha?

November 26, 2012

Readers, remember my good friend Amit Sodha, who ran the London Marathon earlier this year to raise money for a young boy’s new wheelchair?

Well, I’m very pleased to say that yesterday at his personal blog, Amit posted a photo of the boy, Jamie, sitting in the chair!

Wheelchair Pool And Snooker

November 26, 2012

As I’ve written here once before, I’m a big fan of snooker.  Actually, a very big fan. I’d love to play, but I can’t lift a cue.

So, why don’t I write about this more often? Because I’ve always thought that disability and snooker don’t really mix.

That was until about five minutes ago, when I found out that wheelchair snooker was a Paralympic sport until the 1988 Games. (There’s loads of cool information about wheelchair pool at that link too.) But of the two, snooker’s my preference.

So, I wonder why the wheelchair version is no longer recognised as a Paralympic sport? It’s a beautiful game, and I, for one, think it certainly should be!

 

The Curious Case Of The Clark Brothers

November 26, 2012

It’s late afternoon in a terraced house in Hull, and the Clark brothers are battling it out at Monopoly at the dining room table. “They love board games – they’d play them all day,” says their mother, Christine. “The only problem,” adds Tony, their father, “is when one of them finds out he hasn’t won, Then you end up with a huge fight, with the board and the pieces on the floor.”

It sounds like the sort of thing that could happen in any home with a couple of primary school-aged kids. But the terrible reality is that the children in question are 42 and 39. An extremely rare medical condition means Michael and Matthew Clark aren’t in their first childhood, they’re going through their second – and for their parents, the agony is almost unendurable.

The Clarks don’t like the boys hearing the story – and they’d never sit still for long enough to allow us to talk – so we retreat to the sitting room while they continue their game with the carers who come in each afternoon to give Tony and Christine a break. On the mantelpiece, there’s a picture of the boys aged around 13 and 10. But the reality, says Christine, 62, is that in many ways they were more mature then than they are now.

Looking back, Tony and Christine can see there were warning signs, through the years, that all was not well – but the situation they were warning about was so bizarre and shocking that no one could possibly have heeded them. “I remember taking the boys to Spain for a holiday,” says Tony, 63. “They were both in their thirties, and I remember, as the plane took off, they were shouting out ‘Yippee’ like a pair of kids.”

On the same holiday, Christine remembers having a nagging sense that something wasn’t right. “The boys kept squabbling, and they seemed really childish. I thought it was odd; by that stage Matthew was a dad himself.”

Both Michael and Matthew had done well at school. Matthew was offered places both in the Royal Navy and at agricultural college, though he ended up doing a variety of training schemes. Michael went into the RAF at the age of 20, and later qualified as a cabinet maker. Both men married: Matthew and his wife had a daughter, Lydia – now 19 – and Michael had stepchildren. “They left home, settled down, and all seemed to be going well,” says Christine.

By this stage, Tony was in his late  forties. He decided to take early retirement from his job as a prison officer. “And then we decided to move to Spain,” says Christine. So seven years ago, believing their years of heavy-duty childrearing were well behind them, they sold their home in Gloucestershire and moved to a village near Benidorm.

The plan was for Michael and Matthew to visit whenever they could, but from the outset things seemed strange. “They never answered their mobiles – I kept calling and calling,” says Tony. “And then, one day, Lydia phoned to say a worker from a hostel had called to say her dad was living there, and there were some problems he needed to discuss.”

Tragically, Tony and Christine’s departure had coincided with their sons’ downward spiral. “If we’d been in the UK, we’d have realised something was very wrong,” says Christine. Instead, Michael and Matthew, who were by this stage both divorced, ended up on benefits, sharing an increasingly squalid flat in Lincoln – and they became gradually unable to look after themselves. By the time their parents came back, the two were like a pair of toddlers unable to cope in an adult world. “The flat was an absolute tip, with the washing all piled up in one corner, and the kitchen took me hours and hours to clean up,” says Christine. “It was unbelievable.”

By this stage, the brothers had been squabbling so much that Michael had moved out of the flat and into a hostel. Workers there arranged for him to have medical checks: and when doctors realised he had a brother with similar problems, they ran a series of genetic tests. The results were devastating: both brothers were found to have terminal leukodystrophy. The boys’ brains were being destroyed: intellectually and emotionally, they were returning to their babyhood.

For Tony and Christine, there was only one possible course of action: earlier this year they left Spain for good (though because of the economic situation, they’ve been unable to sell their house) and came back to the UK to look after their children full-time. This summer, Hull Council gave them a specially adapted house, and they’re now living a back-to-the future existence as parents of two children who are, to all intents and purposes, getting younger by the day.

In almost every way, life for Tony and Christine is as it was three decades ago – the only difference being that the “toddlers” they’re caring for are six-feet-tall adults. “Michael is the most child-like: he’s moody, he can’t be left on his own. Matthew talks all the time, he says whatever comes into his head, and he tends to make big noises and to shout out a lot,” says Christine.

“They can be very affectionate, particularly with one another – they’ll often put their arms around one another, and Michael will say, ‘He’s my little brother’. Just like small children, they wake up a lot during the night – I was up seven times with them last night – and, also like children, they’ll deny and deny that they’re tired, even when you can see their eyelids drooping.”

At the moment, both boys eat normally but, says Christine, it’s only going to be a matter of time before that will be too difficult for them. “A few weeks ago, they could still manage with a knife and fork, but now that’s getting too difficult for them – they get the food on to their forks, but somehow it all falls off before it reaches their mouths.”

Walking, too, is becoming increasingly difficult: Matthew uses a wheelchair when he’s out, and Michael is finding walking more and more of a struggle. “I took him to the supermarket the other day, and I felt this big hand reaching out for mine,” says Tony sadly. “So we walked around hand in hand: we got a few stares, but if it’s what he needs to do, it’s what we’re doing.”

The boys have been called the “Benjamin Button brothers”, after the F Scott Fitzgerald character who is born as an old man and grows up to be a child. But Christine says the analogy is upsetting. “For one thing, they’re not getting smaller – there’s no return to them being cute little boys, they’re big strong men – and that presents a quite different set of problems,” she says.

Most tragically of all, there are occasions when her sons – especially Michael – are all too aware of their situation. “There are times when they know what they had, they know they were once normal adults with normal lives,” says Christine. “They’re aware of what it is they’re losing.” She and Tony, she says, are aware that both their sons might die before they do. “My biggest fear is that they’ll outlive us, because it would be terrible to think of them having to survive without us,” she says. “But I don’t know how we’ll begin to deal with losing them.”

One of the few things that make them happy, these days, is being around children – at a family event in the summer, says Christine, they enjoyed splashing around in the paddling pool and playing with a water gun. They don’t get much chance to mix with children – although, in a sad twist of fate, Matthew recently became a grandfather when Lydia gave birth to a son called Zachery. “She brought him over to meet us, but it was very hard all round,” says Christine. “Matthew loved him, and he knows he’s his grandson – but in some ways he seemed more like a slightly older brother. It all feels so wrong – this is so absolutely not how anyone’s life should ever be.”

‘The Curious Case of the Clark Brothers’ is broadcast tomorrow at 9pm on Channel 4

ME Professor Simon Wessely Should Be Stripped Of Award, Say Fellow Scientists

November 25, 2012

A British psychiatrist should be stripped of an award, fellow scientists said last night, as one of the most heated debates in medical science continued.

Professor Simon Wessely, one of Britain’s foremost experts on ME, won the John Maddox Standing up for Science honour earlier this month. The prize was created by the journal Nature and the charitable trust Sense about Science. It was given to Professor Wessely for “courage” in speaking out about his studies into ME in the face a prolonged hate campaign and death threats. The Chinese science writer Fang Shi-min shared the award.

But critics protested against the decision last night. They said the professor’s work perpetuates the idea that myalgic encephalomyelitis, also known as chronic fatigue syndrome (CFS), is a mental health problem, trivialising what they claim is a largely physical illness. Malcolm Hooper, emeritus professor of medicinal chemistry at Sunderland University, said: “He’s responsible for trying to make ME into a psychiatric condition when it’s not. He has done very poor science.”

Another opponent, the Countess of Mar, said: “I was absolutely horrified when I read he’d won the award and I would like to see it retracted.”

Dr William Weir, a retired consultant physician who says ME is caused by a chronic viral infection, called the decision “almost satirical”. “If the scientific data is properly examined it will be seen that Professor Wessely’s doctrine is wrong and it will be proved to be wrong in about five years’ time,” he said.

But Professor Wessely, head of psychological medicine at King’s College London’s Institute of Psychiatry, said: “I have published several hundred papers on this over the last 20 years. These have been published in world-class journals such as the BMJ and The Lancet, subject to rigorous peer review. I have never said that CFS is all in the mind. I do not believe that, and have never written that. I have said repeatedly the exact opposite. I have published many papers on possible infectious triggers to the illness.”

Sir Ralph Kohn FRS of the Kohn Foundation, which contributed to the prize said: “This is such a well-deserved recognition of John’s outstanding scientific work for many years and we are privileged to be associated with this initiative.”

Professor Wessely has previously come under fire for research he jointly conducted which concluded that cognitive behavioural therapy could be beneficial in treating ME. In August last year he told how he had been harassed, stalked and intimidated by fanatical lobby groups that disputed his the findings.

UKIP Foster Parents: Man ‘Works With Disabled People’

November 24, 2012

Dear readers and friends, disability is everywhere! There is a disability link, however small, behind every mainstream headline.

In the case of the foster parents who have had their foster children taken away because they reportedly belong to the UK Independence Party, the Telegraph reports that the man ‘works with disabled people.’

The case is being discussed on all sides of politics. Nigel Farage, leader of UKIP, is unsurprisingly upset. Perhaps more surprisingly, Michael Gove, Conservative Education Secretary, disagrees with the council’s decision to remove the children, and Labour leader Ed Miliband has called for an urgent investigation into it.

I, personally, certainly disagree with the council’s decision. The children, unlike the foster parents, are  “not indigenous white British.” The council had concerns because of UKIP’s immigration policy.

However, surely the foster parents knew from the start that the children were from an ethnic minority. I have heard arguments for children being placed with families of the same ethnic and religious origin. While these make perfect sense to me, sadly there are not enough ethnic minority foster carers or adoptive parents registered.

The couple are stable in life, experienced as foster parents. They even reportedly took steps to meet the children’s cultural needs, including finding a suitable faith school for them and allowing them to speak their own language.

I strongly agree with the many who are saying that political views have nothing to do with people’s ability to care for children. As long as parents allow children to develop their own political views, this should never be brought in to any parent/child relationship. Foster placements, as far as I know, are usually short term and these children appear to be too young to think about politics at the moment, anyway. This couple can provide everything the children are looking for in life right now. Surely that’s all that really matters?

The ‘Cure’ Debate- A Disabled Person Responds

November 23, 2012

US researchers have made a breakthrough in curing Downs Syndrome. This week at Independent Voices, Dominic Lawson, whose daughter has the disability, argued that he would not want her cured. His daughter, he said, is who she is- the person her parents and sister know and love. A cure, he added,  would give her the ability to count or read a clock, but those abilities don’t matter to her family.

A parent of a five-year-old girl with Rett Syndrome,  Catriona Moore, yesterday responded to Dominic Lawson’s column. She said that while she loves her daughter the way she is ‘unquestionably’ she also wants her to be cured ‘more than anything in the world.’

I can understand both views. I’ve been physically disabled since birth as a result of Cerebral Palsy, a condition for which there is, so far, no cure. There are, however, several treatments that lead to significant improvement.

When it comes to finding treatment for me, my parents have always shared the view of Catriona Moore. Perhaps because it is what I’ve always been taught, so have I. No doubt, Dominic Lawson’s daughter is very lucky to have parents who love and accept her for who she is.

I have never had any reason to doubt that my parents have accepted my disability. I have never questioned that they love me exactly as I am. Yet they have literally searched the world for treatments to improve my condition, and with it, my life. This search, to me, has always been a sign of their love.

Would I rather they had left me sitting on a floor, trying to crawl, stiff and twisted, and made no effort to get me walking? Of course I wouldn’t. To me, that would not have been acceptance. That would have been an effort to hide me, a result of shame because something was wrong.

So far, I have never read a piece by a disabled person about whether they would want to be cured. So, would I want to be cured?

Honestly, the answer is  that this is a very difficult question. I am proud to be disabled, because I’ve never known any different.  I’m proud of my parents and proud to be their child because they have accepted me, while doing everything possible to give me treatment.

My disability has allowed me to meet many people I love, who I think I would not have met if I was not disabled. I like to think my disability has made me more sensitive to all differences. It could well be the reason I don’t like racism, religious discrimination or homophobia. I understand that these differences can’t be helped. Would I understand this if I was not ‘different’ myself? Maybe not.

On the other hand, is there anything I would change about my disability? The honest answer is yes, there is. I would give anything to be able to drive a car- something my disability makes impossible.

My disability has also been the reason I have seen death from a young age, of people who were far too young to die. People I grew up with. People I consider my closest friends.  They were more severely affected by our disability than I am. Do I wish they had been able to walk? Of course. Do I wish they had been able to talk to me? Every single day.

What would I do if I was cured? I’d buy a pair of high heels, take a driving test, pass it and drive a fast car. Then I would cure those of my friends who are still alive today and have long, clear, verbal conversations with them on long walks around a lovely park.

That’s just a dream for me, though. Am I sad that it will never come true? Not really. If I put on high heels, I’d probably fall flat on my face, with or without a ‘normal’ ability to balance. If I drove a fast car, I’d probably crash it, with or without a disability. As for my friends, if we were all cured, I wonder if they would even want to know me. Since I would hate it if they didn’t, I’ll take my life exactly as it is, thank you very much.

UK Disability History Month 2012

November 23, 2012

UK Disability History Month 2012, which will run until 22 December, launched last night with an evening of speeches, videos and comedy. Now in its third year, this was easily the best attended launch event so far for the Month. As a supporter of the Month since it began in 2010, I was very pleased to see that this year, for the first time, it received national media coverage.

This year, the theme of the Month, which is once again Co-ordinated by disability activist Richard Rieser, is  Changing Lives, Changing Times; Challenging the ideas that lead to hate crime.

Speakers included Baroness Tanni Grey Thompson, who offered her support for the Month through a pre recorded video interview about her experiences as a disabled person and her hopes for the legacy of the Paralympics, and disability activist Lucia Bellini.

Rebecca Yeo from the UK Disabled People’s Council spoke about the Council’s Disability Mural project in Bristol with disabled asylum seekers. One woman who has been helped by the project, Manjeet Kaur, spoke about how disabled people’s organisations helped her to fight for her rights in this country. This was one part of the evening that will stay with me, as I had never given much thought to the experiences of disabled asylum seekers before.

Julie Jaye Charles from the Equalities Council spoke about the experiences of Black and ethnic minority disabled people. She said that this group of disabled people have, for a long time, not felt part of the disability movement, because many of them didn’t know there was a disability movement.

As a disabled person from an ethnic minority group myself, I have felt very much part of ‘the movement’ for the whole of my adult life, which I’ve spent campaigning for disability rights for disabled people of all ethnicities. So this idea stuck in my mind and made me smile to myself. However, I did understand the point, as my personal experience with people of ethnic minorities throughout my life has shown me that there is a long way to go before many of them understand disability, with or without rights.

The event, however, was well attended by disabled people and carers from ethnic minority groups. So hopefully, progress is being made in this area.

Katherine Quarmby, author of Scapegoat, a non-fictional book about disability hate crime, spoke about how the book began and what writing it taught her about the issue. She also spoke about her experiences of the Paralympics, making everyone smile as she recalled how the Games made her non disabled son want to participate in disability sport!

Entertainment at the end of the night came in the form of a comedy routine by Mat Fraser. I’ve known of Mat Fraser for several years as a radio presenter for the BBC and an actor, so I had been looking forward to seeing him as a comedian for the first time. I was disappointed not to find his jokes funny, although, of course, this was, as comedy always is, a matter of personal taste.

Overall, I hope the Month continues for many years to come, and that each year is bigger and better than the last.

ATOS Test Centres Lack Wheelchair Access

November 21, 2012

The firm carrying out fitness-for-work assessments for the government lacks disabled access at a quarter of its premises, MPs have heard.

Employment minister Mark Hoban said 31 of 123 centres run by Atos lacked ground-floor access for wheelchairs.

Six centres in particular had “terrible” problems, causing almost three-quarters of case backlogs by failing to inform applicants and arrange enough home visits instead.

One MP called the situation “potty”.

The Labour government replaced Incapacity Benefit with the Employment and Support Allowance four years ago.

The government is using French firm Atos to carry out the resulting face-to-face assessments of disability benefit claimants’ eligibility – known as the “limited capability for work assessment”.

‘Drive out’

Those judged able to work are taken off the benefit and given support to find jobs.

The Commons Work and Pensions Committee heard evidence from Mr Hoban, who said: “There’s a challenge in ensuring interview centres are accessible. What we don’t want to do is to get people to turn up to centres that they can’t effectively access.”

Mr Hoban said that, in cases where wheelchair access was not possible, home visits were offered as an alternative.

He revealed that 31 of Atos’s 123 sites did not have such access. Six centres – in Croydon, Ealing, Birmingham, Luton, Mansfield and Norwich – were responsible for 73% of the case backlog.

Mr Hoban said: “I think it’s terrible. I think it’s unacceptable that six centres account for 73%.”

He added: “I think it’s something that, over time, we should drive out.”

The committee’s chairwoman, Labour MP Dame Anne Begg, said it would be difficult for the Department for Work and Pensions to ask businesses to “put in access when the department cannot itself” guarantee it in buildings used for assessments.

Lib Dem MP Stephen Lloyd said: “Clearly, if we are getting 73% from six centres – that’s just potty.”

ATOS Doctor Found Dead Man Fit For Work

November 21, 2012

Updated: Thankfully, this is satire. However, sadly, I believed it. I think that says a lot about the true situation at ATOS assessments. That’s why I’m going to leave the article here. You can use this as an open thread to discuss ATOS.

In a shocking lapse of judgement last week, an assessor from ATOS Origin placed James Wright, 62, in the ‘fit for work’ group mere moments after he had suffered a fatal stroke.

“It was a nightmare,” Rosemary, Mr. Wright’s widow, stated. “The doctor assessing James asked him to stand up, so he did before slumping into a squatting position. The doctor took one look at him and said, ‘I’m placing you in the Work Program.’

Then he got up and shook James’s shoulder, and when he fell over, said that he’d be back when James had finished his ‘play-acting.’ It was quite obvious that he was dead.

What’s worse is that I received a letter from the DWP (Department of Work and Pensions) this morning informing me that James’s Job Seekers’ Allowance had been stopped because of his non-attendance at his work experience. I’d already informed them of his death the day after it happened!”

It seems to this reporter that ATOS assessors are so busy licking Tory boots that not only do they not notice when people are dying, they also don’t realize when people are actually dead. Of course, Mrs. Wright is a retired State Enrolled Nurse, whereas ATOS assessors receive no medical training whatsoever. Perhaps that’s why the man made such an egregious error.

Walk along the Wirral and raise funds for Motability

November 21, 2012

A press release I’ve just recieved:

Motability, the national disability charity, is organising an accessible fundraising walk to raise money for some of most disadvantaged and vulnerable disabled people in the UK. Walkability will take place along the Wirral Way in North West England on Saturday 2 March 2013.

 

Those wishing to take part can now sign up for the 12 mile walk, which starts in Hooton and finishes in West Kirby, on the coast of the Wirral Peninsula. For those wishing to walk a shorter distance, there will be a 5.5 mile route ending in the coastal resort of Parkgate Village.

 

The Wirral Way covers the route of the old Hooton to West Kirby railway line which closed in 1963. Having been recently renovated the paths are completely accessible which means that everyone can get involved, including wheelchair, scooter and powered wheelchair users.

 

“We are delighted be adding Walkability to our series of fundraising events at Motability,” said Aine Canavan, Corporate Accounts Executive at Motability. “This scenic route is accessible to everybody and offers wonderful views across the estuary to Wales.”

 

“All fundraising efforts will greatly benefit disabled people who cannot afford the right car or adaptations for their needs, or to help young disabled people with driving lessons.”

 

Each participant will be asked to raise sponsorship and pay a £20 registration fee. Children can take part in Walkability with a registration fee of £10 each. The registration fee covers the cost of experienced guides, first aiders and a fundraising and information pack, which includes a Motability T-shirt. For a registration form and more information call 0845 166 8786 or email fundraising@motability.co.uk.

 

Motability’s charitable work aims to raise around £2.5 million each year to help some of the most disadvantaged and vulnerable disabled members of our communities, some of whom without this support would not be mobile.

Blasphemy Charges Against Rimsha, 14, Dropped By Pakistan High Court

November 20, 2012

I covered this case with sadness and am now thrilled to see this Tweet:

Star Trek Schools

November 20, 2012

Independent Voices today carries a piece by Amol Rajan that has really got me thinking.

He writes about the possibility of a ‘radical future for education in the digital age,’ in which classrooms are abandoned in favour of online courses. He focuses on university education.

He makes a very good point about how online education would improve quality of life for students in countries where access to education is extremely limited. As a British Asian woman with ties to Pakistan, I know many people who would have benefitted a great deal from being able to study for free had online courses been available to them.  There may even be a chance that had Malala had this opportunity, she and her female classmates could have studied in safety from the comfort of their homes. She may never have experienced the attack that has, no doubt, changed her life forever.

As a disabled person, I can see several advantages to online education for disabled children of school age, particularly those who would be, as I was for most of my life, in mainstream education.

Online education would put an end to bullying, for all children, but particularly for disabled children whose differences, far more obvious than anyone else’s in today’s physical classroom, and far more difficult to understand, would  not be obvious over the internet. Instead, students and teachers would see that disabled children have skills and abilities, too.

In online ‘classrooms,’ all children could focus on doing their work, then logging off, without having to worry about bullying, or being bullied by, someone else.  Children could choose who to meet offline based on online chats through social media about interests and skills.

If all online lessons were stored in one place at a website or portal, all children could learn at their own pace and complete tasks at their own pace. This would mean that intelligent disabled children could be fully included. Disabled children often need much more time to answer questions and complete tasks. For many years teachers have feared that this would hold up mainstream lessons, so this has been a barrier to inclusion.

Online classrooms would put an end to PE lessons, but as a solution to this, if lessons were to be timetabled, breaks could be scheduled so that those who are able could do some physical activity. For those not able, the end of PE would, in my personal opinion, be a great advantage!

Online classrooms would put an end to handwriting. No doubt, with this, those able to write neatly by hand would lose something special and often beautiful. However, those disabled children able to hold and use a pen have struggled for years to make their handwriting understood. For such children, and for those unable to write by hand, the ability to type all their schoolwork would remove yet another barrier to having their thoughts and abilities understood by the mainstream world.

There is another point in Amol Rajan’s article that I must agree with. He says that ‘for those who care deeply for the combination of teacher, chalk and blackboard, Star Trek schools sound mildly scary.’ Yes, “teacher, chalk, and blackboard” have their advantages, as does going to school. I met my best friends at nursery school, and they are still stuck with me!

Also, I’ve always said that inclusion helps both sides, as it allows non disabled children to learn about disability. This would most probably be lost if classrooms went online.

There’s a long way to go before all classrooms go online, and there are strong arguments on all sides of the debate about whether they should. However, to me, personally, so far, the idea of Star Trek schools doesn’t sound scary at all.

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

Harrington’s Third Review Of #wca

November 20, 2012

Tumble Tapp Snap- Mr Tumble Touchscreen Game

November 20, 2012

From the BBC Ouch! Blog:

Tumble Tapp Snap is released today on the CBeebies website. Aimed at children with learning, developmental or motor function disabilities, it’s a matching game that you and a child can play on your tablet or mobile phone’s touch screen. It’s based on the popular Mr Tumble character, seen regularly on the pre-schoolers TV channel and created for a special needs audience.

The game presents a series of activities based on simple but important daily tasks such as getting dressed and going shopping. The aim is to hit the button when you spot a match.

This is the first web game from CBeebies designed especially for use on a smart phone or tablet. It’s widely appreciated that tablet devices are very accessible for this community.

Lucy Beckett, producer of the game at the BBC in Salford, says that for some disabled people, tablet devices like the iPad are taking over from the old specialist equipment you previously had to buy separately: “It’s really fascinating actually. Tablets only took off in 2010, and to me they always seemed like they were designed to bring entertainment to upwardly mobile people so they could watch The Killing on the train and things like that. But it appears by fluke that they happen to have created this amazing tool for special needs users who don’t usually get a look in and who aren’t normally at the top of the agenda.”

She describes them as being like “one big switch”. Switch is the name given to the big button mouse-like devices which some disabled people with poor motor function have traditionally attached to their computers to give them basic access at a level they can control.

Software producers know you can’t release a game without testing it on potential users. For special needs audiences, says Lucy, this is “incredibly” important: “One of the things not obvious to us was just how much we’d need to test with grown ups. We had to make sure they understood about changing the settings, swiping, what identical snap is, non-identical, and more.”

The testing helped them identify that not all children were able to perform the common swipe action on tablet devices and so weren’t able to move between pictures – an important part of the game. So now there is a setting where you can have those pictures move across the screen slowly like a shooting gallery and they can choose them as they appear: “The kids just need to bash the screen when they see the character they want to play with,” explains Lucy.

For added accessibility beyond the regular game of snap, Tumble Tapp Snap allows you to adjust the settings so that the gameplay can be geared towards the child depending on what his or her strenths are. For instance, some children with autism may see two pigs, one pink, one with patches, but may not be able to discern that they are both pigs because they look a little different. So, to build understanding in this area, you are given the ability to switch the game to an alternative mode that shows non-identical matches in order to stretch the child.

There are also advanced levels which use words that are outside of daily vocabulary, for instance you can help Fisherman Tumble identify a crab or sun cream. Everyday keywords, on the other hand, might include shoes, socks, trousers etc.

Mr Tumble, played by the irrepressible Justin Fletcher, appears in the series Something Special which airs every day on CBeebies at 9.45am. Since 2005 the programme has been teaching the simple Makaton sign language to children with learning difficulties and promoting important messages about inclusion whilst doing so.

On every episode, Mr Tumble pulls out a picture from his famous spotty bag and he and the children then go looking for the object in the picture. On the latest incarnation of the show Something Special: We’re All Friends, the modern day clown delves into the bag and pulls out a tablet device which he calls a Tumble Tapp. On it, he brings up a picture of what he’s looking for by ‘tapping’ buttons on the screen. In so doing, he’s reflecting the increased adoption of these devices by the community he’s broadcasting to.

Part of the testing of the game involved the team traveling to special schools in the north and south of England.

“I don’t know what it is about Mr Tumble, but the children love him,” says Lucy.

“We’d test on six kids each day and every kid was convinced Mr Tumble would be there due to a slight miscommunication. Quite a few were sign language users, we didn’t understand them but the teacher would say ‘he keeps asking where Mr Tumble is’.

“We must’ve been the biggest booby prize in the world.”

• You can find the Tumble Tapp Snap game at the the CBeebies website

Blue Badge Style- The Song Lyrics

November 19, 2012

Unless you’ve been living in the Australian jungle for the last three months, chances are you’ve heard Gangnam Style by Psy.

Well, I heard that, and then I heard of this app, called Blue Badge Style.

The little song below was inevitable after that…

Blue Badge Style

 

Drive the car?

Blue Badge Style!

We’re gonna do it Blue Badge Style!

We’re Blue Badge Style!

Woop, woop woop,

Blue Badge Style!

 

Park the car?

Close as we can, Blue Badge Style!

We’re gonna do it Blue Badge Style!

We’re Blue Badge Style!

Woop, woop woop,

Blue Badge Style!

 

Drive the wheelchair?

Blue Badge Style!

We’re gonna do it Blue Badge Style!

We’re Blue Badge Style!

Woop, woop woop

Blue Badge Style!

 

Live our lives?

Blue Badge Style!

We’re gonna do it Blue Badge Style!

We’re Blue Badge Style!

Woop, woop woop,

Blue Badge Style!

 

Domestic Violence And Disabled Women

November 19, 2012

I wrote about a study on this subject about two years ago. I’m very pleased to see it getting more coverage in today’s Guardian.

“My disabilitymeant I fainted a lot, though like a lot else it was made so much worse by the tension and the fact that my ex made me do so much around the house … I would pass out on the floor … and I would come round to him looming over me, shouting at me for being so stupid.”

Deborah, 31, met her ex-husband online when she was 17, two years after being diagnosed with a neurological condition. She had felt like a “freak” at the time, she remembers; self-conscious about using a wheelchair and isolated from friends getting on with their lives, away from illness. Ten months after meeting him, she moved in. For the next 10-and-a-half years he abused her at home.

According to research by Women’s Aid, one in four women experience domestic violence. For women with a disability, this figure doubles. Be it at the hands of their partner, family, or carer, almost one in two disabled women will be abused in their lifetime.

Some of their experiences fit within traditional definitions of domestic violence. Some do not. For a disabled woman, domestic violence can take on unique, complex forms, often specifically related to their disability such as having medicine withheld, being physically assaulted or deliberately not assisted to go to the toilet.

“A woman’s impairment can be used in the abuse,” says Dr Jackie Barron from Women’s Aid. “We’ve heard cases where a woman’s wheelchair was removed just as she was about to sit down, or a hearing aid thrown to the other side of the room leaving the victim unable to communicate.”

Common in other abusive relationships, there’s a disturbing ease with which power and control can be exerted – and the added opportunities. The abuser not only has a physical advantage, but is often the person being relied upon for care.

Deborah needed her husband to help meet her personal needs. It was help that was routinely withdrawn. “My ex constantly used my dependence on him against me,” she says. “When I was so ill I couldn’t fend for myself at all, he would threaten not to prepare food for me – and sometimes, he really wouldn’t, so I didn’t get a hot meal.”

Her husband cited various objections to a shower seat too. He would refuse to help her wash and then complain about “the state” she was in.

“There’s often humiliation and belittling as part of the abuse,” Barron says. “This can reinforce any existing feelings of low self-esteem.”

Deborah’s husband would describe her as a “psychological vampire”, whose needs sucked all his energy. “He would tell me what an inconvenience I was, not just to him, but to other people,” she says. “Sometimes he’d give me this lecture in front of friends and family.”

The combination of being told enough times that you’re a burden and the knowledge that, due to a disability, you do have additional needs, can make leaving an abusive home particularly difficult. Deborah’s husband often threatened to leave her or throw her out. “I was terrified of what would happen to me then,” she says. “But I really didn’t think I had any other options.”

“It can be harder for disabled women to get away, or to get support,” Barron says. Escaping an abuser can mean leaving a home adapted to meet their needs, or residential care. Refuges, already coping with cuts in funding, are not always accessible or able to meet needs. DeafHope UK, one of the only organisations designed to help disabled survivors of domestic violence, tells me of cases in which deaf women have returned to their abusive home after finding a refuge too difficult. “Some refuges have refused to accept a deaf woman due to ‘health and safety’ or insurance issues,” Lynn Shannon, DeafHope service manager says.

In 2010, Deborah left her husband. She had managed to arrange to stay with a friend because her disability made it difficult to physically organise the move, but she was forced to return. Unable to use public transport, Deborah had no way of getting to her new accommodation. At one point, this meant her ex was planning to drive her. “To be honest, I have my doubts I’d have ever got there,” she says. “That’s one thing that frightens me, with hindsight, that I could have imagined that would be a safe thing to do. But I couldn’t drive and I couldn’t take a coach or a train.”

The additional barriers to a disabled woman’s escape are particularly distressing because it’s often more difficult for them to speak out. The expectation that it’s normal for a disabled person to have someone with them during a GP visit, for instance, takes away a rare chance for privacy to disclose abuse.

Simply being believed – an obstacle for any abuse victim – can be especially hard for disabled women. “You often hear: ‘Oh, he seems such a nice man,'” Barron says. “This seems to be even more the case for disabled women. ‘This man is providing care. He’s giving up his life … ‘ It can mean they’re much less likely to be believed.”

For almost half of all disabled women, it’s abuse that is very real.

Thursday marks start of action to mark the UN Day for the Elimination of Violence Against Women and Girls. The Freephone 24 Hour National Domestic Violence Helpline is 0808 2000 247.