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Tony Nicklinson Meets Lord Falconer

April 17, 2012

A man from Wiltshire who has “locked-in syndrome” has asked for an explanation on why he should not be allowed to die.

Tony Nicklinson, 58, from Melksham, became paralysed from the neck down following a stroke in 2005, and is unable to take his own life.

A recent Commission on Assisted Dying report said the terminally ill should be able to end their lives voluntarily.

Mr Nicklinson met report author Lord Falconer earlier, saying he wants a doctor to be allowed to end his life.

The Commission on Assisted Dying (CAD) published a report in January which concluded there was a “strong case” for allowing assisted suicide for people who are terminally ill.

But the report said that to take someone else’s life would be a “step too far”.

Mr Nicklinson, who cannot speak or move anything except his head and eyes, met CAD chairman Lord Falconer for two hours at his home in Melksham earlier.

‘Not acceptable’

Communicating through a computer, he told him: “You say terminally ill people should have the right to die so they don’t end up like me, so why should I be forced to live like this?”

Lord Falconer said: “If somebody can’t take the final act themselves then somebody has to, in effect, kill them and I think, and the commission thought as well, that was a step too far.

“It was too risky to allow any situation to arise where one person could kill another that would be lawful.

“Allowing, in any circumstances, one person to kill another would be a massive moral and practical change in the view that the law takes about taking other people’s lives.

“That’s just not acceptable, I think.”

After the meeting Mr Nicklinson said he was “satisfied” that Lord Falconer had answered his questions.

“We must agree to differ on the question of someone killing another. He sees dangers where I do not.

“I believe the law has grey areas and needs clarification.”

NAIDEX Looks Ahead To 2012

April 17, 2012

A press release:

Naidex National takes place 1st-3rd May at the Birmingham NEC and is set to be an excellent show for healthcare professionals, trade, members of the public, and exhibitors alike. Registration for free tickets and more information on the event can be found at www.naidex.co.uk where you can also find details on all the products and services that will be on show along with details of the various features and activities available at Naidex 2012

 

Event Director Liz Logan commented: “2012 is going to be a fantastic year in the history of Naidex and the excitement of the Paralympic Games is certainly giving the show a fresh buzz. We aim to provide visitors with an experience that will inspire and engage them, and with enhanced features and innovative new products on display a visit to Naidex National this year is a must for anyone affected by disability or long term illness. ”

 

Visitors to the 2012 event can expect to see all of the Naidex favourites that make visiting so worthwhile, such as the Car Zone, KideQuip and Meet the Expert, not forgetting the 1000s of independent living solutions being showcased by the Naidex exhibitors. There will also be a wealth of free help and advice provided by OTs, counsellors, speech & language therapists, physiotherapists and paediatric experts on a wide range of topics and issues, so start preparing your questions for the experts now. Among these features, healthcare professionals will benefit from attending the new Naidex Conference that will offer free CPD knowledge building and career enhancing seminars and workshops.

 

You can count on the Naidex team to bring you exciting new features and zones each year, ensuring that the show provides something for everyone, and 2012 is no exception. New features of Naidex National 2012 include the Sports and Rehab Zone, an area of the show dedicated to sports products and the latest specialist exercise equipment for home rehabilitation to help improve quality of life and productivity of users, and a Sensory Room displaying the latest in sensory toys and equipment. The Independent Living Show Home will be inviting visitors to see how the latest products work realistically within the home to improve independence, and with new product trails marked through the show floor it will be easier than ever to find what you are looking for.

 

Mark Butterworth has a profoundly disabled son who needs highly specialist equipment. He says that by visiting Naidex he and his family get all the help and advice they need: “We can get these products on the internet, but you can’t really compare or touch them, so it’s great to see everything together under one roof and get advice there and then. Naidex has everything we need and more; it really opens your eyes to what’s out there and we just wouldn’t know what’s available without coming.”

 

So if like Mark you are looking for the latest equipment and advice on what products are best suited to your budget and needs, put 1st-3rd May in your diary and make the most of visiting the UK’s largest disability, homecare and rehabilitation exhibition. Make it a fun day out and visit www.naidex.co.uk to register you, your friends and family for free tickets by quoting priority code EGSR

Best Of Men

April 16, 2012

The history of the Paralympic Games is to be told in a BBC Two drama starring Rob Brydon and Eddie Marsan.

Best of Men will tell the story of a neurological doctor whose work with wounded soldiers led to the first official Paralympics in Rome in 1960.

Writer Lucy Gannon said Dr Ludwig Guttmann “revolutionised life for paralysed people”.

The first unofficial games for disabled people was at Stoke Mandeville Hospital.

‘Unsung hero’

German-born Dr Guttmann, who had been using sport as a therapy to rebuild strength on his patients, opened the games on the same day as the 1948 Olympics.

In the drama Brydon will play a paralysed soldier, who is admitted to Stoke Mandeville under the care of Dr Guttmann, who will be played by Marsan.

Now referred to as the 1948 International Wheelchair Games, it became an international event in 1952, when a team from Holland went to England to participate.

By 1960, the games were held in parallel with the Olympics in Rome.

Gannon said she found Dr Guttmann’s story “amazing”, calling him “an unsung hero”.

Ben Stephenson, controller BBC Drama Commissioning, said: “Lucy Gannon has written a moving human story that reveals the largely unknown history behind the birth of the Paralympic Games.”

Paul McCartney’s New Video Featuring Johnny Depp, Natalie Portman And Sign Language

April 16, 2012

Paul Harrison has been Tweeting about this new music video directed by Paul McCartney, because it features Johnny Depp and Natalie Portman using Sign Language.

Famous as they both are, they can also both hear. Paul’s question is:

https://twitter.com/#!/paulbharrison/status/191841246262726656

This has created a lot of discussion on both Twitter and Youtube. My personal view is that it is a very good idea for hearing people to learn, and speak, Sign Language if and when they wish to. I can hear and I wish I’d been taught it myself.

However, of course this should not take away any opportunities for Deaf actors and performers who are just as talented as anyone else. In videos like these, it would be great if Deaf actors could be signing along with the song. Unfortunately though, very few of them have the fame of Johnny Depp yet.

Another point to consider is that hearing celebrities may be trying to show that they understand the needs of Deaf fans by learning Sign Language, and that they would like to include this group in their music or performances. Lady GaGa revealed that she was learning American Sign Language last year so that she could communicate with Deaf fans, and this really impressed me and made me like her as a person as well as a musician.

So, readers, what do you think?

Legal Aid Bill Puts Thousands At Risk Warns CAB

April 16, 2012

A woman with learning difficulties, severe epilepsy, schizophrenia, cerebral palsy and asthma recently underwent an official assessment of her fitness for work, which concluded that there was nothing preventing her from taking up employment. She was told that her benefits were to be stopped and that she needed to start searching for a job.

Upset by the news, she visited the Walthamstow Citizens Advice bureau in east London, where welfare rights adviser Sarah Tabor mounted a legal appeal on her behalf, and managed to get the decision overturned.

“The decision was ridiculous. She has had problems since birth; any rational person would have looked at the range of her conditions and realised that it would be very difficult for her to work,” Tabor said. Without specialist welfare rights support, currently funded by legal aid, the woman would not have been able to contest the decision and would not have had her benefits reinstated, Tabor added.

The legal aid bill, which among other things aims to abolish legal aid for welfare and benefit cases, returns to the Commons on Tuesday and there is speculation that the government may use the controversial “financial privilege” rules to reject a Lords amendment that could mitigate some of its impact.

Campaigners warn that if the bill is passed in its original form it will leave some of the country’s most vulnerable people without recourse to advice if they face a problem claiming state support. The Citizens Advice bureau believes that tens of thousands of people will be put at greater risk of homelessness and poverty without funding for their advisers. The timing of the legislation is particularly unfortunate, they add, given that the ongoing reform of incapacity and disability benefits has thrown up so many difficulties, and given that the government will introduce a wholesale transformation of the benefits system next year when it launches universal credit.

Walthamstow CAB last year gave specialist legal support to 600 people who had been wrongly denied benefits and a further 500 people with severe debt problems. Around 70% of their clients contesting a benefits decision were people, like the woman with learning difficulties and schizophrenia, who had been classed as fit for work under the work capability assessment, which determines eligibility for the new incapacity benefit, employment and support allowance.

“The decision in her case was ludicrous, but it’s not particularly unusual,” Tabor said. Since the benefit was introduced more than 390,000 people have appealed against the decision that they were capable of working, and around 40% of these appeals have been successful; when claimants are given legal advice by organisations like CAB, that success rate rises to as much as 90%.

Tabor, who is not a lawyer but is highly specialised in the complex sector of benefits law, has also been advising the parents of children whose disability living allowance has been cut, as the government tries to reduce the size of the DLA bill by 20%. The rest of the advice centre’s legal aid clients were people in severe poverty trying to access crisis loans or people with housing benefit difficulties or complications with tax credits.

Andy Munton, manager of the Leytonstone CAB in east London, is trying to find alternative funding to save the advice service, in the event that the legal aid is cut off, but because local authority funding has already been cut, there are few alternative sources of money. If the bill is passed in its original form, he said the office will shrink and staff will be limited to handing out self-help letters to clients, explaining what they need to do to challenge decisions.

“Realistically they won’t be able to do it. Many of our clients have mental health problems, literacy difficulties, or they don’t speak English as a first language. They get into a bigger mess, and then it’s harder to pick them up. The stress makes them more ill, which puts more pressure on the NHS,” Munton said.

“The cynic would say that the government is doing this so that people can’t challenge the process effectively. From the government’s point of view, it’s a good policy because it will save them money. People will be less able to challenge the flawed decisions that are being made as a result of welfare reform, and the benefits bill will go down.”

A Ministry of Justice spokesman said in a statement: “At more than £2.1bn per year, we have one of the most expensive legal aid systems in the world, which in the current financial climate we just cannot continue to afford.

“The wide-ranging availability of legal aid can lead people to assume legal action is their only option, even where early practical advice could be of more help to them and avoid them needing a lawyer at all.” The statement added that the government had committed an extra £60m to support the provision of general advice by organisations like CAB over the next three years.

Gillian Guy, chief executive of CAB, said this money was not enough to preserve the services currently offered, and stressed that trained, paid specialists – who were able to digest the 9,000 pages of benefits guidance issued by the Department for Work and Pensions – were vital, if some of the country’s most vulnerable people were to get support in claiming the benefits to which they are entitled. She added that it was precisely this swift practical advice that the CAB and other legal aid-funded welfare rights centres were offering, adding that the charity’s research suggested that every pound spent on early advice saved around £9 later, partly by avoiding unnecessary and expensive tribunal hearings.

“People will suffer more and more hardship if they can’t get the payments they are entitled to,” she said.

A large consortium of disability charities has been campaigning against this aspect of the legal aid bill, and they still hope that the amendment successfully tabled in the Lords by the Lib Dem peer Baroness Doocey and others, which preserves legal aid for the most serious appeals against welfare benefits decisions, will be retained when the legislation returns to the Commons this week.

Richard Hawkes, chief executive of the disability charity Scope, said: “To cut legal aid at a time of unprecedented changes to welfare support would mean disabled people who fall foul of poor decision-making, red tape or administrative error being pushed even further into poverty as they struggle to manoeuvre the complicated legal system without the expert support they need.

“This could result in a ticking timebomb of poorly prepared and lengthy tribunals and appeals, choking the courts and not saving money, but actually costing the government far more in the long term.

Meet Simon Wheatcroft, DisAbled Challenger

April 16, 2012

He has retinitis pigmentosa and runs ultramarathons. Don’t worry, I hadn’t heard of them either.

Parkinson’s Study: ‘It’s With You For Life’

April 16, 2012

Researchers are to conduct the world’s biggest study into the causes of Parkinson’s disease, a brain condition that affects almost 130,000 people in the UK.

They are hoping to find better ways of both diagnosing and treating the disease.

Charity Parkinson’s UK is looking for 3,000 volunteers with the condition – and their siblings – to take part in the study.

Study director Dr Kieran Breen spoke to BBC Breakfast to explain more. He was joined by Paul Wilson, who was diagnosed with Parkinson’s in 2006.

Face Equality On Film- Changing Faces’ New Campaign

April 16, 2012

Some 750 cinemas across the UK will be running a short film to challenge movie attitudes to facial disfigurement.

The one-minute film, starring Downtown Abbey’s Michelle Dockery and Leo Gormley, will be shown ahead of feature films at Odeon cinemas for a fortnight.

“We are not suggesting that no villain has a scar, we’re just saying, let’s be more creative about this,” said Alison Rich, of charity Changing Faces.

“It’s just become a very lazy shorthand for film-makers,” she adds.

“Without saying or doing anything, an actor with a scar can walk on screen and audiences are attuned to thinking ‘there’s a baddie’,” Ms Rich, who is heading up the Face Equality on Film Campaign, told BBC News.

“And that portrayal sets up a moral judgement that extends to the wider world… to the playground, and to the job market.”

According to Changing Faces, one in every 111 people in the UK has a significant disfigurement to their face.

Yet a 2008 survey suggested that 90% of people find in difficult to attach positive qualities to people with disfigurements.

Ms Rich cites Pixar animation Finding Nemo as one of the few films where a physical disfigurement (a damaged fin) is “just one aspect of a character and doesn’t determine the storyline”.

“We don’t want to alienate the film industry, we want to work in partnership with them,” she adds.

The charity hopes their film will encourage audiences to think about the issue and plans to set up an advisory group to help film-makers include facial disfigurement in their work in a more positive manner.

“We’re so used to seeing people with disfigurements portrayed as the villain in films that it may be hard for people to imagine they could ever play someone’s friend, the Dad picking up his kids from school, the US President, or a lover,” says James Partridge, founder of Changing Faces.

“Freddy Krueger, Scarface and Two-Face are just some of the names that our clients get called at school, on the street and at work.

“Changing Faces hopes the film and campaign will encourage audiences and the wider film industry to think about how disfigurement can be portrayed in a more balanced way.”

There are notable exceptions in Hollywood of heroic characters with facial scarring including Harry Potter, comic book character Jonah Hex and Avengers star Nick Fury, played by Samuel L Jackson.

World’s Biggest Study Of Parkinson’s Disease Launches

April 16, 2012

A Glasgow-based doctor is to lead the world’s biggest research study into the cause of Parkinson’s disease.

The brain condition affects almost 130,000 people in the UK.

Dr Donald Grosset, a neurologist at Glasgow University, said he hoped to find better ways of both diagnosing and treating the disease.

Charity Parkinson’s UK is looking for 3,000 volunteers with the condition – and their siblings – to take part in the study.

Parkinson’s is a debilitating condition with symptoms which include tremors, mood changes, movement difficulties, loss of smell and speech problems.

The charity said it was investing more than £1.6m in the Tracking Parkinson’s study with the long-term aim of boosting the chances of finding a cure.

The study will follow 3,000 volunteers – people recently diagnosed with the disease, people diagnosed aged under 50 and their brothers and sisters.

The aim is to identify markers in the blood which could be used to create a simple diagnostic test for the disease, something which does not yet exist.

Parkinson’s UK said early diagnosis is crucial if doctors are to be able to prescribe the right drugs for people with the condition.

The responses to various treatments of those taking part in the study will be closely monitored for up to five years.

Eventually the project will link up to 40 research centres across the UK.

Dr Grosset said: “The cure for Parkinson’s is a global challenge and all the samples gathered from our thousands of volunteers will be available for analysis by researchers the world over.

“This, in itself, will speed up our ultimate goal – to develop a cure for Parkinson’s.

“I am very excited to be leading this cutting edge research collaborating with top researchers from Scotland, England, Wales and Northern Ireland.”

Dr Kieran Breen, director of research and innovation at Parkinson’s UK, added: “Finding a cure for Parkinson’s is like building a gigantic jigsaw, but we still have a number of the pieces missing.

“This vital new study will help us fill in some of the gaps in our knowledge.”

Hayley Okines’ Sister Completes Marathon Challenge For Progeria Charities

April 16, 2012

What a special sister she is too!

The sister of a 14-year-old girl with a rare ageing condition has completed her challenge to run the equivalent of 10 marathons in 10 days.

Hayley Okines, from Bexhill, East Sussex, has progeria, which means she ages eight times faster than normal and has the body of a 100-year-old woman.

Her sister Charlotte, 26, and friend Becky Reid, 39, started their journey in Yorkshire on 5 April.

They completed the 272 mile run to Cranbrook in Kent on Saturday.

The friends have raised more than £5,000 and set up the UK branch of the Progeria Family Circle so that children with the condition can all get together.

The pair set off from the Yorkshire home of Harry Crowther, another progeria sufferer, on 5 April.

Ms Okines said: “It’s one of the most incredible journeys I’ve ever done and to see my sister so proud of me, that’s what it was all about for me.

Pioneering treatment

“I wanted her to be proud of me in the way that I am proud of her.”

Ms Reid said: “We had a little bit of a tough time in the middle, and spirits were pretty low in day four and day five when the rain came.

“You just think what other people have to get up to every morning, and think: ‘Yes, you can do it’.”

Hayley is one of only 83 people in the world known to have progeria, which was diagnosed just before her second birthday.

The condition causes problems normally found in the elderly such as arthritis and heart disease.

Hayley was predicted a life expectancy of 13, but has been receiving pioneering treatment in Boston, USA, for four years.

Speaking as the friends crossed the finish line, she said: “I knew she’d be able to do it. I’m ridiculously proud. Words can’t even say how proud I am.”

England Manager Teaches New Skills To Blind Football Hopefuls

April 16, 2012

The manager of the England/GB blind football team has been in Berkshire to help train visually impaired players that want to get involved in the sport.

Tony Larkin held two sessions teaching skills to coaches and players at the FBC Centre in Finchampstead.

Mr Larkin said the participants had ranged from an eight-year-old to an ex-professional who had lost his sight.

He said: “It’s been a really worthwhile event and hopefully will encourage many more people to take up the sport.”

Podium place

Blind football is played on a five-a-side pitch, with the sighted goalkeeper, the coach and a guide behind each goal telling the players where the ball is.

Mr Larkin, who himself played football professionally for 15 years, said the skill of the blind players was remarkable.

“Their movement and spatial awareness is unbelievable,” he said.

The England/GB blind football side that he manages will be taking part in an international tournament in Madrid before the 2012 Paralympics in London.

Mr Larkin said it would be a great opportunity for his young side to get some experience against players from countries like Brazil, Argentina and France.

He said the week-long contest would give a good indication of how the England team would do in London where he was confident of a podium place.

He said: “I think with the Paralympics being held in this country, it’s a real chance to put the sport on the map.”

Strictly Wheels- Britain’s Got Talent 2012

April 15, 2012

I’ve been waiting for this year’s disabled Britain’s Got Talent contestant, and now I’ve finally found what I’ve been looking for. I’ve seen their audition, and they are wheely good (sorry!) I hope they get far in the competition.

It seems as if Alesha Dixon has been missing Strictly a little, with the judge gushing about how “inspired” she is by ballroom dancing pair Paula and Gary during tonight’s Britain’s Got Talent.

The singer was blown away by Strictly Wheels, who danced magnificently to Empire State of Mind by Alesha Keys for their audition.

Paula, 41, and Gary, 39, describe themselves as the “best of friends” and have been dancing seriously together for the last 18 months.

Paula, who admits that she would “never have put myself down to dance” before she started practicing with Gary, has been in a wheelchair for eight years after contracting MRSA during her 20s.

But the blonde says her condition hasn’t stopped her from doing anything she enjoys. She laughs: “I love dancing, I love going out – I just do things sitting down that’s all!”

 Paula and Gary, who won the UK dancing championships at debutante level, started their BGT performance with a slow routine, before thrilling the judges by speeding the music right up and jiving on the stage.

Afterwards, David Walliams says: “I thought that was amazing, you turned what might have been a negative, into a positive! You did things that two dancers wouldn’t normally do.”

Simon tells Strictly Wheels: “I thought it was going to be uncomfortable. But you were fun, I like you. Paula, you are much better than Gary by the way.”

Amanda adds: “Paula, your control of that chair and your muscle in your arms is unbelievable.”

But it was former Strictly star Alesha who had the most to say, telling the act how great they were with a big grin on her face.

She said: “Wow! You’ve got such a great connection.

“The guys have said it all – that was beautiful to watch. It was surprising, refreshing and unique. Wow.”


Lee Ridley- Lost Voice Guy

April 13, 2012

Sorry Laurence Clark- you’re hilarious, but I think you’ve got serious competition in this guy!

He is a stand-up comic, but he can not speak. Lee Ridley has Cerebral Palsy and uses a voice synthesizer to communicate.

Last year his friends encouraged him to take up comedy and two months ago he did his first show, calling himself Lost Voice Guy.

Entertainment correspondent Colin Paterson went to meet him.

Barry West- DisAbled Challenger And Torchbearer

April 13, 2012

A man from East Sussex who was paralysed from the neck down in a car accident is celebrating after being chosen as an Olympic torch bearer.

Barry West, from Framfield, will carry the Olympic flame through Rye.

He has undertaken a series of challenges since his accident, including paragliding and mountaineering, but said the torch relay will be one of his proudest moments.

Disabled People Tell London Mayoral Candidates About Transport Pain

April 12, 2012

I wonder what was said, and more importantly what will be done, about the Taxicard?

For many Londoners, travel is one of the main issues of this London mayoral election campaign.

Cost, overcrowding and punctuality are the prevalent concerns for able-bodied passengers however for disabled people, just being able to have access to public transport is top of their concerns.

At a hustings event held on the South Bank and organised by a coalition of disability charities, about 100 disabled people and those with learning difficulties challenged the four main candidates for election, with transport being the top topic for debate.

Guy Parckar, head of policy and campaigns for the Leonard Cheshire Disability charity, summed up this issue by saying: “It’s always one of those issues and the mayor has a lot of clout.

“Seventeen years after the Disability Act, people still can’t access buses and the Tube is a no go. There’s a long way to go.”

According to Green candidate Jenny Jones, there are 1.4m disabled people in London, while 20% of the total population has difficulty using public transport.

All of the candidates recognised that this was a problem and put forward their pledges to help improve public transport for those with disabilities.

Boris Johnson, the Conservative candidate and current mayor, said that during his term, 59% of bus stops were now accessible, up from 29% when he was elected. He added that there was also a 39% rise in step-free stations.

“We want to increase these projects to make London more accessible because they are important,” he said, adding that cost was an issue.

He said the stations people use often, such as Tottenham Court Road, Bond Street, Paddington and Victoria, would be upgraded soon.

‘Spontaneously travel’

Labour candidate and former mayor Ken Livingstone said his policy of cutting fares by 7% would save councils £22m as they would not have to pay out as much on freedom passes.

He would also make these passes uniform across all London boroughs, so “access shouldn’t depend on which borough you live in”.

Mr Livingstone also said all stations would be visibly manned, especially late at night.

Brian Paddick, the Liberal Democrat candidate, said he would ensure all councils support the freedom pass.

He would also choose carefully which Tube stations to make step free, so stations near museums for example would be upgraded first.

“Disabled people should be able to spontaneously travel,” he said, adding that accessibility should not be an issue.

Green candidate Jenny Jones pledged to make more stations accessible and said her party would extend the freedom pass to carers.

She said: “There’s a huge, wide gap. If you look at a map of stations that are accessible to disabled people, it’s almost blank… you can’t use the Central line. This is shameful.”

‘Fight for space’

On the issue of buses, Mr Johnson said the new buses were cheaper than hybrids and were wheelchair-friendly, however many people in the audience disagreed with this, saying the bendy buses were much better and that the current buses were not big enough for wheelchairs and for people with blind dogs.

Ramona Williams, 28, from Hammersmith, is visually impaired. She questioned the candidates on access to transport, as well as on the age limit to apprenticeships.

“Their answers were very brief,” she said, adding that the candidates needed to spend a day with them to see how difficult it was.

“The number 28 bus is nonsense. The new buses have less space and more seats.

“My guide dog was crumpled and I had to fight with other people so that he can have space. The bendy buses need to be brought back.”

Her friend Mohammed Mohfanali, 26, from Upton Park, who is also visually impaired, said: “Overall Boris hasn’t said anything, he hasn’t convinced anyone.

“With Boris, everything has been taken away.

“I’m still confused, I don’t know who to vote for.”

He added that he was beginning to have more confidence in Ms Jones, however he said she immediately lost his support when she said that shared parking spaces were a good idea – as many people in the audience expressed difficulties with them.

Josie Lombardo, from Sutton, has learning disabilities. She said she was worried about her bus pass being taken away because if that happened, she would not be able to afford travel costs, meaning she would not be able to go out.

Eric Martin, from Wembley, who has Asperger’s syndrome, echoed Ms Lombardo’s concerns about the bus pass as he would not be able to afford to get around if he lost the pass.

“I liked Ken. He had a good speech when he talked about investment in transport and more staff at stations. Overall I was impressed, but Ken will be back,” he said.

Had You Seen Carolyne From the Undateables On Dancing On Wheels?

April 12, 2012

Readers, did you know that Carolyne from The Undateables was a contestant in BBC Three’s Dancing On Wheels in 2010? I was on holiday when Dancing On Wheels was screened and have never seen it, so I didn’t know this until I read it on the BBC Ouch blog today.

Strangely, though, after watching The Undateables on Tuesday night, Carolyne’s was the story that stayed with me. She’s a blonde, beautiful wheelchair user whose childhood sweetheart left her four years ago after a ten year relationship because she became paralysed five years ago and, she thinks, “he found it difficult seeing me in my chair.”  As a disabled woman who would like to think she knows what love is, I strongly disliked him as soon as I heard this!

Ouch says Carolyne was eliminated in the first round of Dancing On Wheels– here’s hoping she has better luck this time with reality TV.

Dorset Police Shine Light On Blind Woman’s Writing After Pen Runs Out

April 12, 2012

Part of a novel lost when a blind woman’s pen ran out without her knowing has been salvaged with the help of a forensic police team in Dorset.

Trish Vickers, from Charmouth, had written 26 pages of her first novel.

But when she asked her son to read it back to her there was nothing but blank pages.

They called staff in the fingerprint bureau who volunteered their time and revealed the missing words by shining a crime light on the indentations.

Staff used the tool’s bright light on the pages as it enhanced the shadows left by the pen strokes.

Kerry Savage, from Dorset Police, said: “Fortunately apart from one line we managed to retrieve the whole lot.

“It was nice to do something good for somebody and it was nice to read the book as well.”

‘Over the moon’

Mrs Vickers, who lost her eyesight about seven years ago as a result of diabetes, said she was “over the moon” with the force’s work.

She said: “It’s not as though it’s a big blockbuster but as a hobby and something that is very important to me it was just wonderful that they put that time and effort in.”

Mrs Vickers now writes by following elastic bands stretched across her page rather than using lines on the paper.

She describes her book as a “simple” and “pleasant” story about a young girl.

Although she does not know when it will be finished, Mrs Vickers said Dorset Police would be first in the acknowledgements.

Woman Can Write For First Time In 15 Years After Gene Therapy

April 12, 2012

A British woman stricken with Parkinson’s disease can write for the first time in 15 years after receiving gene therapy.

Sheila Roy is one of only 15 people worldwide to undergo the radical treatment, which involves inserting corrective genes into the brain.

Diagnosed with Parkinson’s in her 40s, she has struggled with the disease for 17 years. The symptoms include severe tremors and loss of balance, making simple tasks such as writing impossible.

Doctors at Addenbrooke’s Hospital in Cambridge injected a modified virus carrying the genes directly into the motor centre of her brain. The genes provide the coded instructions for proteins needed to make dopamine, a brain chemical essential for proper control of movement.

Lack of dopamine leads to the symptoms of tremor, stiffness and poor balance associated with Parkinson’s.

Mrs Roy is taking part in an early-stage study of the ProSavin therapy developed by Oxford BioMedica focusing mainly on dosing and safety. Unlike conventional tablets, the therapy involves just one treatment that does not have to be repeated.

Mrs Roy, from Bedfordshire, says she is now starting to see “a glimmer” of the person she was before her illness.

Describing her experiences, she said: “Early in 2011 I was rapidly deteriorating. My medication was being less effective, there was increased involuntary movement, where I frequently hit myself but also other people, and had a four second switch from extreme movement to being ‘off’ and very still. This lasted for some time, up to two hours and more and I could do nothing.

“These unpredictable shifts were like a ‘Jekyll and Hyde’ transition, and outside of my control. At night there was no relief as I had terrible nightmares, and often woke my husband up with screaming or punching him.

“Parkinson’s disease changes the ability and capability of the individual affected. You lose confidence, dignity and hope. The ProSavin experience has restored my confidence, enabled better motor function and has given me hope. I can function more normally and, for the first time in 15 years, I can write.”

I’m Spazticus

April 12, 2012

Oh God. What on Planet Earth will Channel 4 do next?

Though after careful reading I have to admit- disabled people pranking non-disabled people certainly turns a stereotype on its head!

A sketch in a TV comedy show, which saw a blind man groping a life model, has been pulled after police were called.

Students at Southend Adult Community College were unaware they were being filmed by hidden cameras as part of a prank for Channel 4’s I’m Spazticus.

College principal Stephen Layman said they were “shocked” by the filming.

A Channel 4 spokesman said students “didn’t see the funny side, so as a gesture of goodwill we won’t be broadcasting the footage”.

Forthcoming sketch series I’m Spazticus – which has been commissioned to tie in with the London Paralympics this summer – features “disabled performers pranking able-bodied members of the public”.

Produced by Zeitgeist Television for Channel 4, it “uses the world of comedy to explore the world of disability”.

The prank, filmed three weeks ago at the college in Essex, showed a blind man groping a nude model during a life drawing class. Both the unnamed blind man and model were in on the joke.

However, the unwitting students were horrified, leading some in the class to call the police. Police did respond although no further action was taken.

“Southend Adult Community College agreed in good faith to participate in a project which we were informed was aimed at challenging people’s attitudes to disability,” said the principal, Mr Layman.

“We were shocked and surprised to discover the filming that took place within the class did not reflect the brief supplied.

“Since this incident took place three weeks ago we have received categorical assurance from both Zeitgeist Television and Channel 4 that none of this material will be used.”

An award-winning pilot of I’m Spazticus was first broadcast as part of Channel 4’s Comedy Lab in 2005.

Speaking this February, producer Jamie O’Leary said: “Whilst this is far from revenge TV, we hope it is both barrier and ground-breaking – it will never be worthy and box-ticking but hopefully funny.”

Three Sets Of Brothers Are Going To The Paralympics

April 12, 2012

Three sets of brothers have been named in the latest 20 athletes selected for the ParalympicsGB team for London 2012.

Beijing bronze medallist Sam Ingram and brother Joe join Dan and Marc Powell in the judo team, while Stephen and Peter McGuire make the boccia squad.

The powerlifting team includes world record holder Anthony Peddle, who will compete at his seventh Paralympics.

“I am delighted to welcome these athletes to ParalympicsGB,” said chef de mission Craig Hunter.

“It is the culmination of hard work and dedication on their part.

“From ParalympicsGB’s perspective the selection of many of these athletes is also testament to the success of BPA programmes such as our annual simulation preparation camp, our Paralympic Potential days and our Talent Transition Programme over the last four years.

“I am particularly excited because today’s selection of athletes means that we have now selected almost a third of ParalympicsGB for London, so it really feels like the team is starting to come together.”

Wednesday’s announcement takes the number of athletes selected for London 2012 to 80.

SQUADS

Judo: Sam Ingram, Joe Ingram, Dan Powell, Marc Powell, Ben Quilter.

Boccia: Dan Bentley, Jessica Hunter, Scott McCowan, Peter McGuire, Stephen McGuire, Nigel Murray, Zoe Robinson, David Smith, Jacob Thomas

Powerlifting: Natalie Blake, Paul Efayena, Jason Irving, Ali Jawad, Zoe Newson, Anthony Peddle.

Narcissa Robins- Beauty And The Unexpected

April 12, 2012

It seems the latest issue of Disability Now has a theme of disability and sexuality. They have interviewed Narcissa Robins, an artistic amputee who creates amputee erotica.

I feel the need to make it clear that the views expressed in this link are those of Narcissa Robins. If you don’t like it, don’t click it. Please comment, but please keep comments clean and polite.

 

People With Huntington’s Disease at Lower Risk Of Cancer Says Study

April 12, 2012

People with Huntington’s disease, a debilitating brain condition, appear have a “protection” from cancer, according to a study in Sweden.

Nearly 40 years of medical records showed patients with Huntington’s had half the normal expected risk of developing tumours.

Researchers, writing in The Lancet Oncology, said the reason was unclear.

Cancer Research UK said the findings presented another avenue to explore in tackling cancer.

Academics at Lund University analysed Swedish hospital data from 1969 to 2008. They found 1,510 patients with Huntington’s disease.

During the study period, 91 of those patients subsequently developed cancer. The authors said that was 53% lower than the levels expected for the general population.

Huntington’s is one of a group of illnesses called “polyglutamine diseases”. Data from other polyglutamine diseases also showed lower levels of cancer.

The authors said: “We found that the incidence of cancer was significantly lower among patients with polyglutamine diseases than in the general population.

“The mechanisms behind the protective effects against cancer are unclear and further research is warranted.”

Eleanor Barrie, senior science information officer at Cancer Research UK, said: “These are interesting results. It’s not clear how the genetic changes that cause Huntington’s and other similar diseases could protect against cancer, and research in the lab will help to find out more.

“Scientists at Cancer Research UK and around the world are probing the genetic faults that contribute to cancer in their quest to beat the disease, and this is another potential avenue to explore.”

The Prospect Of Mainstream Employment Scares Remploy Workers

April 11, 2012

Says this article from today’s Guardian.

Mother’s Horror Over Online Abuse Of Daughter, 16, With Down’s Syndrome

April 11, 2012

This is awful.

A mother says she is “horrified” photos of her daughter are again being used by “internet trolls” to insult people with Down’s Syndrome.

Liz Crowter, from Coventry, said she asked Facebook to remove photos of her daughter Heidi, 16, which she found on “derogatory and insulting pages” over the weekend, but they are still there.

She said the photos of her daughter as a toddler had been stolen from a website for a parents’ support group.

Facebook has yet to make a comment.

Mrs Crowter said Heidi had been the victim of internet trolls “lots of times”.

Heidi’s pictures were taken from a local support group website, which Mrs Crowter ran for about five years.

Mrs Crowter shared her experiences of being the mother of a child with Down’s Syndrome through the group and members also went on trips and holidays together.

‘Feel violated’

In October, she found her daughter’s picture on a Facebook page which insulted people with Down’s Syndrome and other learning difficulties.

Some of the comments left about her daughter and other people were of a sexual nature, she said.

The mother-of-four contacted Facebook and also West Midlands Police, who she said informed her it was not a matter for officers.

Heidi’s picture has been removed but the page remains, Mrs Crowter said.

Over the weekend Mrs Crowter was told by friends that Heidi’s picture had been put on a new page which insulted people with Down’s Syndrome.

Mrs Crowter said: “I feel violated and violated on Heidi’s behalf. I’m disgusted that people can be so sick.

“It’s not just Heidi, it’s photos of other people’s children as well.”

She said she and her friends had reported the latest incident on Monday using Facebook’s system to report abuse but the picture was still up.

Mrs Crowter said Heidi was a “very independent young lady” who was studying for her GCSEs at a mainstream school and doing a hairdressing course.

“She’s funny, stubborn and very kind,” she added.

“We’re all very upset and it and they [her other children] see her as a lovely sibling that they want to protect and support.”

Paralympic Swimmer Dave Roberts Could Retire

April 11, 2012

For 11-time gold medal winning Paralympic swimmer Dave Roberts missing out on London 2012 is a blow, but he feared it was coming.

Roberts, 31, failed to hit qualifying standards over the weekend ahead of the Team GB squad announcement on Tuesday.

He has now been left out of the squad, leaving him one gold short of becoming Britain’s most successful Paralympian.

After falling short of the qualifying time, he had already admitted he was thinking of retiring.

“I don’t really see much point in carrying on,” Roberts said before selectors confirmed that he would miss out on London.

“I’ve been doing this a long time and maybe my body is telling me it’s time to take stock of what I’ve done.

“I’ve won 11 golds, no-one can take that away from me. Swimmers here would kill to have the career I’ve had.”

Selectors could still have chosen him for the squad if they believed he could challenge for a medal, but his omission means he remains tied on 11 golds with Baroness Tanni-Grey Thompson.

The Pontypridd-born Paralympian was diagnosed with cerebral palsy at the age of 11.

A member of Caerphilly County Swim Squad, he was encouraged to start swimming as part of his physical therapy when diagnosed.

Nine years later, at the age of 20, he won seven medals at the 2000 Sydney games, including three gold.

A further eight golds were won in Athens in 2004 and at the Beijing games in 2008.

His success in 2008 saw him chosen to carry the Team GB flag during the closing ceremony.

Contracted pneumonia

Roberts, who also boasts eight World Championship medals, was awarded a CBE in 2009.

He had been hoping to go to his fourth games in London, but those dreams were dashed when he competed at the British Disability Swimming Championships in Sheffield last Saturday.

He failed to hit the 29.29s qualifying time in the men’s 50 metre freestyle, clocking 29.77.

His final attempt at qualification came in Saturday’s 100 metre freestyle, but a time of 1:05.38 left him over two seconds from the qualifying standard.

Roberts entered competition over the weekend after just three weeks of training as a result of illness and injury.

He tore a tricep muscle late last year and contracted pneumonia while on a training camp in South Africa earlier this year.

Huw Jones, chief executive of Sport Wales, the body that drives elite sporting performance, said: “I think it is a big disappointment, I think particularly for David.

“He’s been so successful winning 11 gold medals, the same number as Tanni Grey-Thompson over the years, and he’s not going to get an opportunity to break that record at the Paralympic Games in London.

“He has had enormous difficulties, both physical difficulties and things with injuries, and illness recently in terms of pneumonia, so it’s no surprise really that he’s struggled to make those times and qualify.”

Someone Else Who Thinks Ricky Gervais’ Character Derek Is Autistic

April 11, 2012

Is Tanya Gold at Comment Is Free.

Oxfordshire man to break new ground at London Marathon 2012

April 11, 2012

A press release from Leonard Cheshire Disability:

“Five years ago I struggled to getup the road, so it’s an enormous personal achievement to be taking on the London Marathon now.” Andy Gardiner

 

 

An Oxfordshire man will break new ground this year, as he completes the Virgin London Marathon in his wheelchair for Leonard Cheshire Disability.

 

The 35-year-old from Bicester took up sport following an accident in 2003, when his leg was amputated. He went on to become a squad member of the GB shooting team and twice winner of the Oxfordshire Disabled Sportsperson of the Year title.

 

The Bicester man will help break new ground at the Marathon, when he becomes one of five wheelchair users who will race alongside 35,000 other runners in the mass event this year. Previously, wheelchair entrants were restricted to the elite wheelchair races for professional athletes (1). Gardiner and his four fellow wheelchair users – as part of a two year scheme – will set off from theback of theGreenwich mass fieldwith the rest of the Marathon contestants.

 

Gardiner, who has been training for the event since April last year, aims to reach the finish line in The Mall within five hours and raise £1,800 for Leonard Cheshire Disability.

 

He said: “Five years ago I struggled to get up the road, so it’s an enormous personal achievement to be taking on the London Marathon. Sport is a huge part of my life, and if my participation in the marathon inspires more people to get involved then all the training will have paid off.”

 

Emma Barker, Events Officer at Leonard Cheshire Disability, adds: “We are delighted that Andy Gardiner is racing the London Marathon to raise funds for Leonard Cheshire Disability. We wish him lots of luck for his final preparations and look forward to seeing him at the finish line.”

 

If you would like to take part in a sporting event in support of Leonard Cheshire Disability, then the charity has a places for a number of events, including TriTogether – the unique short distance triathlon for people of all ages and abilities to swim, bike and run together in August  2012. Visit http://www.LCDisability/events, email events@LCDisability.org or call 0870 420 4301 to find out more.

 


How Do We Get Home?

April 10, 2012

Last Friday, I asked the London Taxicard service a simple question. A question I have asked them several times before. How many trips do I have left?

The answer? 52. The next question: When is that up to? Here comes the unpleasant surprise: That’s for the whole year.

Fifty-two trips a year? That’s one trip a week, I thought. That can’t be right.

That means that I can’t book a return journey using the Taxicard service- at least not unless I only use it once in two weeks.

Surely they can’t be expecting disabled people to only leave their houses once in two weeks? When I started on the scheme almost 5 years ago, I was told the trips could be used for social or medical reasons. At the time, I was given 104 trips per year.

For a start, I have weekly medical appointments. If I was to need to use the service to get to these under the current rules, how would I get home? And, only slightly less importantly, how would I ever have any sort of an independent social life if I used up all my trips on medical appointments?

Further research last night revealed that my London borough has halved Taxicard trips per year from 1st April 2012 for “members who also hold either or both a Freedom Pass or a Blue Badge.”

 

This discovery answered my questions. I have a Blue Badge.

 

However, the suggestion that a Blue Badge should entitle you to less Taxicard trips is madness. Blue Badges only entitle you to park within walking distance of wherever you want to go. I know there are other advantages but sadly, 24 hour access to a car is not one of them! I still can’t drive or use public transport without company. I carry my Blue Badge with me and use it in the car of whoever I happen to be with.

 

When I started using the Taxicard scheme it gave me a whole new and wonderful level of freedom. I could now get a cheap lift to the cinema or to a friend’s house. It significantly reduced the need for my parents to drive me around town- and for that reason it has become a valuable part of my life.

 

Now I am being told that just because I hold a Blue Badge I can either only leave my house independently once in two weeks or, if I choose to leave independently once a week, I still need to drag one of my parents out of the house to pick me up when the movie finishes or when my friends need me to leave their houses.

 

Where is the very independence that the Taxicard scheme was set up to allow? How is leaving the house once in two weeks a free, independent social life for any young person? And without these unreasonable restrictions, if we wish to keep our independence, how do we get home?

 

I am thinking of starting a campaign of this title and am looking for support- let me know if you would sign a petition on this topic, join a Facebook group or have any other suggestions about how we can get this very important issue noticed.

Disability And Sex Gets Studied (Shock Horror)

April 10, 2012

A lot has been said in recent weeks on this blog and many others about the fact that disabled people date. Still, the issue of disability and sex, and disabled people having sex, is not talked about enough. So when I opened Disability Now yesterday to find that a female sociologist with a disability has been studying this important issue, I was very pleased to see it getting some coverage.

For those who are interested, here is a link to the article by sociologist Kirsty Liddiard.

You are free to comment on anything concerning disability and sexuality below- but keep it clean and polite please.

Cleft Repairs Are Not The End

April 10, 2012

Jade is looking forward to her tenth operation in May. This time it’s a nose job.

“I want it really badly. I can’t wait,” say the 16-year-old from West Yorkshire.

“I think it will make me more confident, although I’m quite confident already.”

Jade was born prematurely with a unilateral cleft lip and palate. She weighed just two pounds at birth.

“We didn’t find out until she was born that she had a cleft,” says Andrea, her mum.

“But it never bothered us at all because we knew it could be operated on. Her size was more of a shock at the time.”

Jade had her first operation at seven months old, to close the opening in the upper lip between the mouth and nose.

There have been subsequent operations to fix the palate (the opening in the roof of the mouth), to remove teeth, to prepare for a bone graft, to strengthen the jaw and other orthodontics work.

Yet, despite all that, she is still bright and bubbly, her mum says.

But there have been difficult moments.

“The worst bit was in Year 9, when some people thought I was different and they used to tease me,” Jade says.

Failure to fuse

Cleft lips and palates affect around one in 700 babies born in the UK.

They are one of the most common birth defects in the UK, occurring when separate parts of the face do not join together properly when a baby is developing in the womb.

But, in many cases, the cause of this failure of the face to fuse is unknown.

It may be the result of a combination of genetic and environmental factors or just a ‘one off’ occurrence within a family.

In both situations, there is no way of predicting or preventing the condition in advance.

That’s why the world’s largest research databank for cleft lip and palate was set up in the UK recently to determine what causes these common conditions.

By asking parents of babies with these conditions to enrol in the five-year programme, the Cleft Collective team hope to gather and analyse the DNA of the children to see if they can pin down a cause.

The project aims to follow these 3,000 or more children throughout their childhood in the hope of working out the best course of treatment and the best surgery options for future generations.

‘Gappy smile’

This is good news for babies like Thomas Pennington, who has already had two operations to correct the bilateral cleft lip and palate he was born with ten months ago.

Two more operations are scheduled in the next year.

“We’ve been told it’s a big hole,” says his mum, Tamsin, who found out about his condition at the 20-week scan.

“It is massive, but it’s symmetrical. We got used to it quickly and don’t notice it at all now.”

After the first operation on his cleft lip, there was a big change to Thomas’s appearance.

“He still had a big smile, but it wasn’t the huge gappy smile we were used to.”

The second operation gave him a proper top lip and his nose has become more ‘nose-shaped’, changing his appearance yet again.

But the biggest challenge has been feeding Thomas, who is unable to suck.

Tamsin has used special bottles to squeeze milk into his mouth and only when his soft and hard palate are joined together will he be able to eat solid food.

She is acutely aware that there will be difficult times ahead for her son, at primary school and in his teenage years, when other problems connected to his cleft may arise.

Jonathan Sandy, professor of orthodontics at the University of Bristol who is in charge of the Cleft Collective project, says the information gathered by the database could help.

“Repairing a cleft is not the end of the problem. All children with repairs look good at two years old, but what about at 20?

“Sometimes the hearing is affected, or the bottom jaw grows too big or there are problems with speech or teeth. Even psychological problems. There are effects all the way through,” Prof Sandy says.

“Different genes are responsible for clefting and we want to find out how they interact so that we can make life better for youngsters with this condition.”

Classical Music Inspired Student With MS

April 10, 2012

A music student who was paralysed by a life-threatening medical condition has told how he has beaten the odds to continue playing the piano.

Aberdeen University student Paul Murray, 21, was diagnosed with a brain tumour and multiple sclerosis that left him unable to use his right hand, meaning he now only uses his left to play musical compositions originally intended for two hands.

After four brain surgeries, one lasting more than 14 hours, the undergraduate is using his musical talents to re-write pieces of classical piano music so that they can be played with only one hand.

Mr Murray found his talent for music at 15 while attending Bellshill Academy in North Lanarkshire, where he quickly progressed through the grades despite not having any formal teaching. After his brain tumour diagnosis and subsequent operations, it took four months in Glasgow’s Southern General Hospital learning how to walk and talk again, and he said that it was his family and love of music that got him through.

He said: “I had to go through a long period of rehabilitation which meant I spent my 18th birthday in hospital. I was told it would take two and a half years’ recovery time, but I’m always very positive with these things and I was determined to get back to university and continue my studies.”

Mr Murray continued to improve using only his left hand to play until he played at a concert and was giving a standing ovation.

However, the young student was hit with another blow when he discovered he was also suffering from multiple sclerosis (MS). MS affects the spine and brain, limiting the ability of the nervous system to communicate in the body.

The condition caused Mr Murray to lose the ability to play piano with his left hand for four months, meaning that he could only concentrate on his musical writing.

However, this latest revelation served as inspiration for Mr Murray to tackle a master’s degree after he graduates. “My passion for classical music has helped me overcome so much and I hope to be able to bring this music to those who, like me, did not grow up with it,” he said.

Dr David Smith, head of music at the University of Aberdeen, described Mr Murray as “a truly inspirational student, totally dedicated to his studies”. His story will be featured in a Channel 4 documentary, to be aired later this year, exploring the life of pianist Frederic Chopin.

Ricky Gervais Defends New Comedy Show Derek

April 9, 2012

Ricky Gervais has defended his new Channel 4 programme, Derek, following suggestions he was mocking people with learning difficulties.

The one-off comedy is billed as the story of “a simple, vulnerable man working in an old people’s home”.

Some people, including fellow comedian Stewart Lee, have said the show makes light of the “mentally handicapped”.

But Gervais, who plays the title role, said Derek was not intended to have a “specific and defined disablity”.

“Derek is a fictional character and is defined by his creator, me,” he told disability rights campaigner Nicky Clark.

“If I say I don’t mean him to be disabled then that’s it. A fictional doctor can’t come along and prove me wrong.”

“He’s different. But then so are a lot of people. He’s not the smartest tool in the box but he’s cleverer than Father Dougal [from Father Ted], and not as different as Mr Bean.

“He’s based on those people you meet who are on the margins of society. Nerds, loners, under achievers.”

‘Compassion’

Gervais was interviewed for Clark’s website ahead of the first screening of Derek on 12 April.

The campaigner has previously been a vocal critic of the comedian. Last October, she took him to task for repeatedly used the word “mong” on his Twitter feed.

She called on the 50-year-old to stop using the term, which can be used offensively in reference to people with Down’s Syndrome.

“If you find abuse of disabled people sickening, then please don’t use the terminology of bullies and thugs,” she wrote in The Guardian.

The pair eventually made contact, and Gervais asked Clark to watch a pilot episode of Derek.

She agreed with his assertions about the story, saying: “I’ve laughed and cried. I haven’t seen cruelty.”

“Instead of it being a mocking disintegration of a learning-disabled man -paraded for the amusement of comfortable unaffected people, it’s the story that really needs to be told at the moment,” she wrote on her website.

The character of Derek Noakes first appeared in 2001 as part of the Edinburgh show Rubberneckers, several years before the comedian achieved mainstream success with The Office.

Speaking to Clark, Gervais said his portrayal of Derek was sympathetic.

“It’s important to have compassion for the characters you are portraying because at some level comedy and drama relies on empathy”.

The Undateables Is Not Just Trash TV

April 8, 2012

There are beating hearts there too, and it has echoes of The Incredibles as well as untouchables, says today’s Observer’s review.

Alice Pyne Sets Up Children’s Holiday Charity

April 7, 2012

A very inspiring update about Alice Pyne.

 A teenager with cancer has set up a charity to provide free holidays in the Lake District for the families of seriously ill children.

Alice Pyne, who has Hodgkins Lymphoma, is raising funds for the charity with a line of mugs while continuing to campaign to get people on the bone marrow register.

Ellie Crisell reports.

The Rotary Young Citizen Awards will be presented on the BBC News Channel at 11.30am on Saturday 14 April.

Mirror Mirror And Its Dwarf Actors’ Frustration

April 6, 2012

In his hotel room in New Orleans, Mark Povinelli is reflecting upon the sort of scripts he receives. “They’re usually obnoxious. I flick through to what page I’m going to be on and … ‘Oh look! Biting someone on the ankle! Or punching someone in the balls!’ … The trick is to be one step ahead of them. You can’t just say, ‘I don’t like this’, you have to come up with an idea that is better. And that’s the real challenge – an extra added task that a lot of average actors don’t have to deal with. Not only do you have to be a good performer, but you have to come up with better material than you’re given a lot of times, to allow yourself to sleep at night.”

Povinelli has appeared in a string of TV shows and films, with his latest project being a main role in Snow White film adaptation, Mirror Mirror. He also happens to have dwarfism, a condition that means he stands 3ft 9in tall. It makes him a member of a specialist industry that is currently in a state of flux. While recognition for it increases, so do threats. It’s a livelihood which, in terms of screen work, is sporadic at best, and not always appealing.

The roles open to dwarf actors are, historically, of limited scope. Character-led parts have always been thin on the ground; what opportunities there are, tend largely to be confined to the fantastical — The Wizard of Oz, Star Wars, Willy Wonka and the Chocolate Factory.

There are exceptions, of course: Michael Dunn was Oscar-nominated as best supporting actor for the 1965 romance Ship of Fools, David Rappaport became a credible star on the back of Terry Gilliam’s Time Bandits in 1981 (“not even for a lot of money would I be a puppet or a robot,” he once said) and, more recently, Peter Dinklage won an Emmy for his portrayal of Tyrion in HBO’s Game of Thrones – a role soaked with humanity and depth. Even so, a limited range of roles is a frustration for any actor who wants to be taken seriously.

Yet dwarf actors also face a fight for their traditional roles on the most apt of battlefields: Snow White. Two separate adaptations are released this year: one of them (Mirror Mirror, in which Povinelli plays a character called Half Pint) uses a full cast of dwarf actors; while the other, Snow White and the Huntsman, replaces them with well-known names such as Ian McShane and Nick Frost shrunk using CGI.

Such a practice is hardly new, of course: Lord of the Rings famously used camera angles to resize its actors, as will dwarf-heavy prequel, The Hobbit, released later this year. Just as dwarf actors’ work is being threatened in pantomimes by child actors, such FX trickery is eradicating roles traditionally held by dwarves. It’s a novelty that isn’t going down well.

“What it ultimately comes down to is that this is a business,” Povinelli says. “And the driving force for making the [Snow White and the Huntsman] decision was to get names that would hopefully sell the film. I don’t agree with it, of course.”

“I mean, I’ve got no problem with Ian McShane playing a dwarf, if I’m allowed to play a lawyer or a doctor or all of the things we seem to be denied so often. I don’t want the market on the fantastical characters – that doesn’t interest me. I want the whole range. I don’t begrudge McShane taking on that role but the coin should be flipped as well and we should be allowed to play actual humans. Because … you know, it’s pretty obvious but that’s what we are. I’m not a leprechaun. I’m not an elf. I don’t live in a forest. I’m a dad, I’m a husband, I’m a sports fan, I’m a theatregoer … I’m everything everyone else is. And those are the things you want to portray.”

Danny Woodburn, an established TV and film actor best known for his roles in Seinfeld and Watchmen, also plays one of the seven dwarves in Mirror Mirror. He agrees with Povinelli. “To me, that’s still telling of the nonacceptance of dwarfism … You would never see this with any other minority — it isn’t acceptable. In today’s industry, you would never see someone seriously playing an African American who wasn’t an African American. Yet it is acceptable in the realm of actors portraying people with dwarfism, or disabilities in general.”

Woodburn is a member of the Screen Actors Guild for Performers with Disabilities Committee, and is outspoken when it comes to dwarfism issues – especially the sneery sense of schadenfreude and dehumanisation that they’re occasionally subjected to. “I have put it in my contract before that no one will pick me up in a scene, and I will not be required to bite anybody” he says. “Do you not see how humiliating it is to liken me to some kind of animal?”

It’s for this reason that Woodburn is surprised by the fuss surrounding Warwick Davis’s Life’s Too Short – the TV show that has triggered much debate about dwarf actors. “It’s amazing that people are so shocked and in uproar about this, when I’ve seen the exact same sort of treatment in a realistic way. No one goes crazy about that.”

The reactions to Life’s Too Short just go to show the variety of opinions on how dwarves should be seen on screen. Yet between the protection of traditional roles and the hunger for meatier ones, the consensus seems to be that what the dwarf acting industry needs is the chance for louder voices – something that was basically nonexistent in the days where Kenny Baker walked into the role of R2-D2.

Willow Management, a dwarf acting agency based in the UK, looks after almost 250 clients across the world. Their role, according to Peter Burroughs, who runs the agency with Warwick Davis, is to look after the interests of dwarf actors, put them forward for auditions and to “step in if our clients feel like they’re being exploited”.

Despite a relatively large number of actors on their books (although minuscule in the context of the acting industry as a whole), Burroughs says very few actually approach it as a serious, full-time career. He thinks it might be an issue of confidence, but is certain that’s changing.

“We put them forward for auditions and try to help them out so they’ll pass them,” he says. “We do acting lessons to give them confidence, and to be able to assert themselves as actors. We also try to make the industry aware that these people are capable of doing a good acting job. After all: as long as there’s good actors, the industry will survive.”

But what needs to change so that dwarf actors have the chance to showcase their talent? Woodburn singles out one of the biggest problems: a lack of understanding from writers. “A path writers go down is the pathos of smallness, where the person with dwarfism is pathetic because of their size … A writer will say, ‘Oh, you’re a sad little man’; but the reality is, ‘No, I’m not a sad little man, I’m just kinda pissed off because society won’t accept me as a man.’ If I’m going to be seen as a dwarf, then I want to be seen as the dwarf I know I am – not the one the writer has made up in their mind having no experience of people with dwarfism.”

Povinelli agrees; he is also optimistic for a future that is led by actors such as Dinklage. “The opportunity still needs to meet the talent level, but the glass ceiling is starting to shatter.”

“Hopefully we’re evolving as a society so that we’re coming to the realisation that people with a difference can actually offer something with a unique perspective rather than being something of wonder or something to be laughed at. And I think that’s coinciding with the fact that there’s a real pool of super-talented actors who are finally getting a chance to show what they can do – to finally be seen as actors first, and dwarves second.”

Mirror Mirror is out now. Snow White and the Huntsman is released 1 June.

Parry-Romberg Syndrome

April 6, 2012

A Manchester family are rallying support to save their daughter’s face with a pioneering US procedure.

A year ago, three-year-old Maha Asghar was diagnosed with Parry-Romberg syndrome, a rare facial disorder affecting one in a million people.

The disorder means her immune system is turning on itself and beginning to destroy her face.

The family have been fundraising to find the £70,000 needed to stop the toddler’s smile from sinking away.

‘Unbearable pain’

Her mother Shameem Asghar said: “At the moment it’s affecting her eyesight and that’s my main concern because it can leave her without vision.

“It’s just wasting the bones, it’s wasting away the tongue and the gum and it’s causing a lot of damage just behind her ear which can affect her hearing.

“She can have episodes of pain that can last two to three hours and it’s unbearable pain.

“It’s quite hard watching and knowing what could happen. It’s like we’re on an emotional rollercoaster.”

In the UK, the NHS only offers cosmetic surgery when she turns 16, but her family think that will be too late and want to send her to the US.

At the University of Wisconsin Hospital, Dr John Siebert, professor of surgery, is pioneering early intervention where microsurgical reconstruction repairs the deformity and is believed to slow or even stop the disease.

Parry-Romberg syndrome, also known as progressive hemifacial atrophy, is the progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face.

It can lead to loss of sight, severe pain and seizures and there is no known cure.

The family, from Oldham, set up the Maha Appeal two months ago and have already raised £50,000 through events and fundraisers in the hope of sending Maha for surgery by May.

Shameem Asghar said: “At the moment [the NHS] are offering to put her on the drug Methotrexate. The side effects can affect her kidneys, can even end [her] life.

“She is going to look abnormal, she’s probably going to have to go through the best years of her life feeling different to everyone else.

“As a mother I have to weigh up my options on what is best for my daughter, not what comes free for my daughter.

“My concerns are what tomorrow [will] bring and what she will go through, what she will deal with at such at young age.”

There are thought to be 750 sufferers of Parry-Romberg disorder in the UK.

More Information About Louis Barnett And Chokolit

April 6, 2012

A sweet Easter treat for you, my dear readers. Here is a full biography of Louis Barnett, DisAbled entrepreneur and chocolatier. He is truly amazing, and while I know the BBC found him first, I’d like to consider him a Same Difference success story, because he is one of the first disabled people I heard about and covered as a blogger.

And here is the official website of his business, Chokolit. This will also be added to the blogroll.

Usually, readers, I am passionate about the value of a mainstream education. But I also believe that every disabled person cannot handle the mainstream educational curriculum. Most of all, I believe that every child, DisAbled or not, should be given a chance to find their talent and use it.

Louis Barnett is living proof that everyone does not need a traditional mainstream education to succeed. He is a shining example of a young person who found his talent and used it to become very famous and make loads of money! And for that, he is about as DisAbled as they come.

I am truly inspired, and sincerely hope to see Chokolit flying high in the world of chocolate for a long time to come.

Paralympian Shelly Woods Tests Wind Tunnel

April 6, 2012

One of Team GB’s strongest gold medal hopes at London 2012 is Paralympic wheelchair racer Shelly Woods, who won silver and bronze in Beijing.

Through collaboration between UK Sport and BAE Systems she has had access to a wind-tunnel at Warton in Lancashire, normally reserved for testing the aerodynamics of fighter jets.

The aim is to help improve her racing position and performance.

Shelly Woods spoke to medical correspondent Fergus Walsh.

Louis Barnett Revisited

April 5, 2012

I first covered the amazing story of Louis Barnett almost 5 years ago in the very early days of Same Difference. Louis, now 20, has several learning difficulties, but this didn’t stop him starting his own chocolate factory aged 12.

The Ouch Talk Show interviewed him for their latest edition, Number 84, as an Easter treat. What a sweet update!

Disabled People May Be Exempt From The Hosepipe Ban

April 5, 2012

The BBC Ouch blog reports:

Because of water shortages following two very dry winters, from today seven water authorities across parts of southern and eastern England have introduced a hosepipe ban. Until the ban is lifted – which is unlikely to be before the end of summer – using a hosepipe to water your garden or your plants, to clean outdoor surfaces or to fill a pond are all prohibited.

There are a few exemptions – and you might be able to take advantage of one of them. If you’re a keen disabled gardener or just prefer your lawn to remain lush and green in dry summers, the good news is that you can go on watering your garden using a hosepipe. This is in recognition of the fact that many disabled people might not be able to handle or carry heavy watering cans. The bad news is that the rules aren’t entirely simple and straightforward.

First, there is no national policy on exemptions. It’s up to each individual water authority to decide their approach. In recent years, most water authorities have permitted disabled people to carry on using hosepipes, but if your provider introduces a ban you should always check first to make sure you’re exempt. Water authorities also reserve the right to impose the hosepipe ban on disabled people too if the drought becomes more severe.

Second, the exemption doesn’t include all disabled people – just those who, in the words of some of the water companies involved, have “severe mobility problems” and hold a Blue Badge. The Blue Badge requirement doesn’t, however, mean you can use a hosepipe to wash your car – it’s still only to be used on gardens, plants and the like. It’s also strictly limited to your own property, so if you were thinking of hiring yourself and your hosepipe out to the neighbours, think again.

Finally, if you don’t have a Blue Badge, but believe that the nature of your impairment will cause you severe difficulties watering your garden by hand, you can apply to your local water authority for an exemption from the hosepipe ban.

The question is, though: how many disabled people were previously aware of this exemption? It certainly seemed to be new information to some of Ouch’s followers on Facebook when we posted a link to the BBC News story earlier today, with the necessity to have a Blue Badge causing particular comment on both sides of the argument. Reader Louise Whittingham said: “Blue Badge holders are disabled and it’s generally used to park a car. Being disabled myself I’m not sure why if we had a ban where I live I shouldn’t abide by the ban too, Blue Badge or no Blue Badge”, while Bekkie Clarke echoed a popular view: “I think it’s great that it’s recognised that a lot of people enjoy their gardens but can’t carry around huge watering cans, but someone needs to spare a thought for those of us who don’t have a blue badge but face the same difficulties day to day”, and Angela Jane Shields suggested that the reason for using the Blue Badge as the reason for exemption is because it’s “a way of monitoring who is exempt from the ban at a council level”.

What do you think? When water is in such short supply, should disabled people be exempted from the hosepipe ban? And how could it be more easily applied so that it’s not just Blue Badge holders who qualify? Let us know your thoughts in the comments.

• For more information on the hosepipe ban, check out the BBC News Q&A. If you live in an affected area, then the following water authority web pages contain more information on the ban, including their policy on exemptions for disabled people: Anglian Water, Southern Water, South East Water, Sutton and East Surrey, Thames Water, Veolia Central, Veolia South East.

Hayley Okines’ Sister In Marathon Challenge For Progeria Charities

April 5, 2012

The sister of a 14-year-old girl with a rare ageing condition is setting out to run 10 marathons in 10 days.

Hayley Okines, from Bexhill, East Sussex has progeria, which means she ages eight times faster than normal and has the body of a 100-year-old woman.

Her sister Charlotte is running with her friend Becky Reid. The marathons, in aid of Progeria Family Circle, start in Yorkshire and finish in Kent.

“We are feeling good, but a little nervous,” said 26-year-old Ms Okines.

“We woke up to see the sun was out. Yesterday it was snowing.”

Ms Okines and Ms Reid are being joined for the first six miles (10km) by John Crowther, father of fellow progeria sufferer, 13-year-old Harry Crowther.

‘Determined to finish’

The runners set out from the Crowthers’ home in Mirfield, West Yorkshire, with Hayley and Harry there to cheer them on.

“Hayley is very excited,” said Ms Okines. “Harry didn’t know she was coming with us so it was a great surprise for him.”

Ms Okines and Ms Reid have been training for a year for the event, and have raised £3,000 so far.

“We are not really setting ourselves a time target for each day because we don’t know how we will feel by day three or four,” she said.

“So, if we end up taking six or seven hours we won’t really mind.

“We have been planning this for so long we are determined we will finish.”

Hayley is one of only 83 people in the world known to have progeria, which was diagnosed just before her second birthday.

The condition causes problems normally found in the elderly such as arthritis and heart disease.

Hayley was predicted a life expectancy of 13 but has been receiving pioneering treatment in Boston, USA for four years.

She has been unable to attend school since last year because of dislocated hips but hopes to return gradually.

Progeria Family Circle is a European patient network which supports children with progeria and their families.

Children’s Song- Teddy Bears In Wheelchairs

April 5, 2012

Does anyone remember the song Bananas In Pyjamas? I was bored, so I scribbled something disability-friendly to its tune. Parents and teachers, try using this version with the DisAbled young child in your life and see if you can get a smile or two!

Children’s Song- Teddy Bears In Wheelchairs

Teddy bears in wheelchairs
Come crashing down the stairs
Teddy bears in wheelchairs
Come down laughing in pairs
Teddy bears in wheelchairs
Get some funny stares
But they don’t care
‘Cause they try to
Catch people unawares!

Paralympians Don’t Want To Merge The Games

April 5, 2012

This is a little old, but interesting:

Double Paralympic champion Eleanor Simmonds  says she would not support any plan to combine the Olympic and Paralympic Games.

A survey in late 2011 suggested almost two-thirds of disabled people in the UK wanted an end to separate events. 

A recent BBC World poll revealed that, internationally, opinion is divided but Simmonds, who hopes to qualify for London 2012 this weekend, is clear.

“For me I prefer them being separate,” Simmonds told BBC Sport.

“The Paralympics is an amazing event, the second biggest event in the sporting field and having everyone in the team makes it really enjoyable.

“So I think it’s great the way it is and that it’s separate.”

Last year’s poll for the charity Scope  found that 42% of disabled people questioned did not believe the Paralympics had a positive impact on public perceptions of disability.

Speaking shortly after its release, Baroness Tanni Grey-Thompson said the Paralympics would “disappear off the face of the earth” if a merger took place.

“We wouldn’t have an opportunity to showcase the vast majority of sports like we do now,” she said.

Grey-Thompson, Britain’s most successful Paralympian with 11 gold medals, added: “There is not a city in the world that could host a Games the size of the two combined.”

Her view is backed by Britain’s two-time Paralympic champion swimmer Nyree Kindred. 

“Our Paralympic programme is nine days on its own, the Olympic programme is the same and you just wouldn’t be able to get athletes to peak over a two-week period,” said Kindred.

“We have our own identity and I’m proud to be a Paralympian.”

European Champion and Beijing Olympian Fran Halsall added: “I think it would make it very long and you don’t really want to make things too long.

“I get bored watching myself swim for eight days, so having more and more swimming I don’t think would work.”

Internationally, the idea of a merger was heavily backed in countries like Chile, France and Spain, but some of the most successful nations at the last Paralympic Games in Beijing, such as the US and China, showed the lowest support for the proposals.

Simmonds, who became Britain’s youngest ever individual Paralympic gold medallist in 2008 at the age of 13, will take part in the final London 2012 swimming trials this weekend.

The Swansea-based swimmer attained four qualification times, including a world record at the British Championships in March and can secure her place  at this summer’s Games with victories in each of her S6 races at the British International Disability Swimming Championships  in Sheffield.

“I want to qualify for the Paralympics in four events [50m, 100m and 400m freestyle and 200m individual medley] and hopefully there’s going to be some great racing and I’ll really enjoy it,” said the 17-year-old.

And she added she is hoping to at least match the 100m and 400m victories she attained in Beijing at the London Games.

“Hopefully I’ll regain my titles,” she said.

“I’m going to try and enjoy the experience, but in the back of my mind I would like a few medals.”

Cuts Making People With Learning Disabilities Isolated Say Charities

April 5, 2012

People with learning disabilities are becoming isolated because of cuts to support and day services in England, says a joint report by 14 charities.

The Learning Disability Coalition said 77% of the local authorities it questioned were making cuts or savings and most expected to make further cuts.

The coalition said half of the 312 people surveyed said they now got less or no support, or paid more for help.

The government said urgent reform of the care and support system was needed.

The Learning Disability Coalition (LDC) has been assessing the pressures on care for some of the most vulnerable people in society.

Just under half (46%) of the local authorities in England, caring for some 69,000 people with learning disabled people, responded to the survey.

Three-quarters of these said they were facing difficulties in funding services for people with learning disabilities, and were making cuts or what they called “efficiency savings”.

The LDC also surveyed 61 organisations providing services to people with learning difficulties, and 72% said funding for their services from local authorities had been cut.

Two-thirds are now expected to provide additional support to people without extra funding.

In some parts of the country, this has led to care workers being told their salaries will be cut.

Of the 312 people with learning difficulties who were questioned, 17% had had a reduction in their number of support hours and 13% had been given less money to pay for support.

Increased service charges affected 18% of respondents, and 2% had lost their support entirely because their local authority had changed its eligibility criteria.

‘Very upset’

Suzy Rowbottom, 41, who has Down’s Syndrome, used to get 12 hours of help a week. But in December, that was cut to two hours.

Her mother Kate said: “I just couldn’t understand it – these are the same people who assessed her 12-14 years ago.

“She hasn’t changed, only their agendas changed.

“As far as I am concerned, they assessed she needed 12 hours… and her needs haven’t changed, so I was very upset.

“It’s all the safety aspect – the vulnerability of them that worries me, and of course when I am not here.”

Anthea Sully, director of the Learning Disability Coalition, said: “Nearly half of people with a learning disability have had either had their services cut or charges increased.

“This reveals the myth that restrictions on local authority budgets can be contained within efficiency savings. Ongoing cuts are being made to services, causing very real difficulties for people.

“The government must urgently reform the system and invest more money to end the care crisis or many people with a learning disability, their families and carers will struggle to maintain even a basic standard of living.”

‘Disappointing’

A spokesman for the Department of Health said: “We know that council spending on social care is under pressure – that’s why the government is providing an extra £7.2bn over four years to local authorities so that they can protect access to care and support.

“It is disappointing that this report finds that nearly half of people with a learning disability have had their support reduced or charges increased. But the majority have not had their support cut and this is reinforced by a recent report by Demos and Scope, Coping with the Cuts, which found no direct correlation between budget reductions and the impact on local people.

“This shows that if local authorities make appropriate efficiency savings and develop innovative solutions, they can maintain and improve access to the services that people need, including helping people to continue to live independently.

“Urgent reform of the care and support system is needed, and we will publish a White Paper on care and support and a progress report on funding reform later this spring.”

Link Found Between Older Fathers And Autism

April 5, 2012

Defective sperm from older fathers may trigger “new” genetic mutations linked to autism, a study has shown.

Researchers found that “de novo”, or newly created, mutations played an important role in autistic spectrum disorders (ASDs).

These defects were “overwhelmingly paternal” in origin, said the scientists. Fathers were four times more likely to generate the mutations than mothers. The gene defects were also “positively correlated” with paternal age.

The findings added to previous research showing that older fathers are slightly more at risk of having an autistic child.

Scientists analysed the DNA of 677 individuals from 209 families with a single child with autism, and 50 unaffected brothers and sisters. They identified 248 “de novo” mutations, of which 120 were classified as “severe” and likely to produce shortened or malfunctioning proteins.

From this list the researchers focused on 60 mutations most likely to contribute to autism risk. There was “strong direct evidence” of a “substantially” higher mutation rate in fathers which rose with increasing age.

The US scientists, led by Dr Evan Eichler, from the University of Washington in Seattle, wrote in the journal Nature: “These observations are consistent with the hypothesis that the modest increased risk for children of older fathers to develop ASD is the result of an increased mutation rate.”

British expert Dr Rosa Hoekstra, lecturer in psychology and genetics at the Open University, said: “We already knew that there isn’t a ‘single gene for autism’, but these new research publications suggest that the underlying genetic mechanisms may be even more complex than previously thought.

“These studies show that de novo point mutations – small gene changes that are not inherited from either parent – in the protein coding part of our DNA are common, and that some of these new genetic changes may be implicated in the risk for developing autism.”

Dr Kevin Mitchell, from the Smurfit Institute of Genetics at Trinity College Dublin, said: “These studies reinforce the fact that autism is not one disorder – not clinically and not genetically either. Like intellectual disability or epilepsy or many other conditions, it can be caused by mutations in any of a very large number of genes.”

Able Life: Undateables Date! Shock Horror!

April 5, 2012

Yesterday on Able Life, George Johnson and I discussed the hot topic of the last few weeks- The Undateables. There were also a few other disabled people interviewed this week, who gave their views on love, life and DisAbility.  Here is the show.

Interview On City University Podcast International Perspectives About The Undateables

April 4, 2012

Last week, I was contacted by Laurene Senechal, a Journalism student at City University. She then interviewed me for a podcast she participates in as part of her course called International Perspectives. She asked me about my views on The Undateables. Here is the podcast.

 

Why Is The Undateables Unwatchable?

April 4, 2012

A joint press release by the UK Disabled People’s Council and the European Disability Forum:

London & Brussels, 4 April 2012 /// The UK Disabled People’s Council and the European Disability Forum explain why the TV series ‘The Undateables’ on UK Channel 4 is inappropriate. “Such an unworthy show is not improving the portrayal of 80 million European citizens with disabilities in the European media: ‘The Undateables’ is unwatcheable: Channel 4 is just wrong and poses a threat to the rights protected under the UN Convention,” stressed EDF President Yannis Vardakastanis.

 

 

On the 3rd of April, the British TV company Channel 4 has started to broadcast a series called ‘The Undateables’.

This TV reality portrays six persons with disabilities in their quest for love. This title looks bad on paper but even worse when put on billboards across the UK, where towering images of people with disfigurement or wheelchair users with the title ‘Undateable’ emblazoned next to them. If ‘The Undateables’ seems an offensive title for a show, then that is probably the marketing aim for a TV channel in the quest for audience. Above a patronising voiceover, viewers are told from the opening that they’re about to see a group of “extraordinary singletons” when in fact we see the opposite: six single people who happen to be disabled.

 

For the organisations of persons with disabilities in the UK and in Europe, this series and the way it is being marketed raise a crucial question of dignity and representation. On the whole, the media have a very important role to play in the relationship between disabled and non-disabled people. In many European countries, despite majors efforts in favour of integration, or inclusion, disabled people continue to be invisible from the society and from the media. Beside that, when they are finally on air like yesterday evening on Channel 4, disabled people are the subjects of uncomfortable voyeurism.

 

Jaspal Dhani, UKDPC Chief Executive said: “Disabled people, as all other citizens, want to be visible in the media. However, a programme playing on creating a sensation and portraying us as extraordinary singletons desperate to seduce, is harmful to our overall image and runs the risks of increasing prejudice.”

 

The UK ratified the United Nations Convention on the Rights of Persons with Disabilities (CRPD) and its Optional Protocol in 2009. The Convention is a binding international treaty that applies to all areas of life and aims to promote the full realisation of all human rights of disabled people.

 

“The Convention being integral of the domestic legal order, UK government must take action to improve society’s awareness of disabled people, and encourage media to portray disabled people in a dignified and respectful manner. It can do so by organising public awareness campaigns, but shouldn’t shun from a more forceful action, such as legal action”, Mr Dhani concluded. Bound by its international obligations, the UK must stand on guard of inherent dignity of persons with disabilities and take immediate and effective measures to protect us against discrimination by private parties, including Channel 4.

 

In addition, it is important to quote a common vision established in the Madrid Declaration adopted at the European Congress on Disability in 2002:

 

“The Media should create and strengthen partnerships with associations of people with disabilities, in order to improve the portrayal of disabled people in mass media. More information on disabled people should be included in the media in recognition of the existence of human diversity. When referring to disability issues, the media should avoid any patronising or humiliating approaches but focus instead on the barriers disabled people face and the positive contribution to society disabled people can make once these barriers have been overcome.”

Gary Parkinson’s Wife Hopes He Will Soon Be Home

April 4, 2012

The wife of former professional footballer Gary Parkinson, who suffered a stroke 18 months ago, has said she hopes he will soon be home.

Mr Parkinson was a coach at Blackpool FC when a stroke left him with locked-in syndrome – unable to move, speak or swallow.

The Bolton-based coach’s wife, Deborah, said the family was raising funds to adapt their house for him.

His appeal’s next fund-raiser will be at Bolton’s Reebok Stadium on 21 April.

Mrs Parkinson said: “We want to raise money so we can bring Gary home to give him a better quality of life so he can be with his family.”

The family are currently going through the planning process to adapt their home into a place where Mr Parkinson can receive full-time care.

Mrs Parkinson said her husband “was improving day by day, although it is a slow process”.

“Nobody can give us either a short-term or long-term prognosis,” she added.

Mrs Parkinson communicates with her husband by studying the reactions of his eyes to different letters on an alphabet board.

During his career Mr Parkinson played for Middlesbrough, Preston North End, Burnley and Blackpool.

He was working as a youth team coach at Blackpool when he suffered the stroke in September 2010.

The Guardian’s Review Of The Undateables

April 4, 2012

‘That’s quite a lot of aftershave, Richard.” “Well,” replies Richard, continuing to wreathe himself in the aerosol mist, “when you’re going on a date, you’ve got to be sure.” Richard, a 37-year-old man with Asperger’s syndrome was going on his first date in 20 years – the second of his lifetime. He was taking part in The Undateables (Channel 4), a three-part documentary series about people with disabilities who are looking for love. The title alone attracted some pre-broadcast controversy, predominantly among those unable to imagine that a title might be indicating the problem it is planning to examine – society’s apparent discomfort with the idea of disabled people forming sexual relationships – rather than simply labelling the subjects therein. This inability is part of a fairly common disability called “chronic stupidity”, often found in those already suffering from chronic Daily Mailism, and alas there is no cure.

Those who watched the programme had any fears of exploitation allayed. The aftershave moment was emblematic of the kindly, thoughtful air that suffused the whole without denying that, as with any human endeavour, moments of inadvertent comedy would occur. It had the intelligence and confidence to recognise that excising them would have been more patronising than keeping them in.

Richard went on two dates. The first he blew by starting to eat off his companion’s plate. The second was more successful but he declined to follow it up after deciding that there was no physical attraction between them. Penny, a primary school teacher trainee by day and – brittle-bone disease notwithstanding – circus aerial artist by night, went on the first date of her life, with a fellow wheelchair user, but thought she would prefer to go out with someone able-bodied so that “they’d be a bit livelier”. And lovely Luke, one of the 10% of people with Tourette syndrome whose symptoms include violent swearing, went on two wholly successful dates with the equally lovely Lucy, who took him ice-skating and the tics in her stride (“You slag!” “Oh,” she said, tossing her hair gaily over her shoulder, “thanks!”)

It left implicit the questions raised about intra-disability prejudice, the manifold problems of exposing yourself emotionally when you are already, in many ways, more vulnerable than average. And Richard’s mother’s longing for him to find someone special spoke volumes, without a word being said about the stresses and sorrows of caring for a grownup child who cannot and yet at some point in the future must manage without you. Beautifully done.

The Undateables: Twitter’s Verdict

April 4, 2012

To paraphrase Jane Eyre: Readers, I watched it. And it was all: disabled man loves mother (which most of them do, not at all romantically), disabled man has been on one date in 20 years which lasted 20 minutes, disabled girl has never-been-kissed. How revealing those facts turns the ‘undateable’ stereotype on its head I have no idea.

Apart from that it was actually halfway decent. It reminded me quite a bit of Blind Date, which I actually quite liked in my early childhood. So, now you have my verdict.

It may or may not surprise you to know that like every other programme on the TV these days, the Blind Date of disability has it’s own hashtag. You can find out what Twitter has to say about The Undateables by following #undateables.

Let Sean’s Service Dog Sophia Into School

April 3, 2012

An email from Change.org that I thought might interest you in Autism Awareness Month:

For eight-year-old Sean Forsyth, his dog Sophia is more than just his best friend. Sean has autism, and Sophia is a service dog who helps keep him safe. Sean’s mother Jennifer says that before Sophia came into Sean’s life, he was easily overwhelmed and prone to running away — often putting himself in dangerous situations. Sophia is trained to keep Sean focused and calm, drastically reducing his outbursts.

Here’s the problem: Even though Sophia was prescribed by Sean’s doctor, and even though she vastly improves his ability to focus and learn, the Pine Richland School District has banned Sean’s service dog from the classroom.

Sean’s mom Jennifer knows how much having Sophia around has changed her son’s life. When the school district told her that her son’s service dog would not be allowed to attend school, she started a petition on Change.org asking school officials to reconsider. Click here to sign Jennifer’s petition asking the school district to let Sophia into school with Sean.

This isn’t just about Sean and Sophia. According to Jennifer, the Americans With Disabilities Act protects the right of kids like Sean to bring their certified service dogs to school.

Service dogs are highly trained to help their companions, who are often unable to live in the world without their support. When Sophia is with Sean, she’s “at work” and her number one priority is to keep him calm. Her presence in the classroom would reduce distractions for everyone. Jennifer says that ever since Sophia came into her son’s life, “his symptoms have improved more than we could have ever possibly imagined.”

Jennifer left her job and moved family moved to the Pine Richland School District because the district is known in autism communities for the support they provide special needs families. Jennifer is confident that if the district sees how much support there is for Sean and Sophia, they’ll come around. The duo already has medical professionals and disability advocates on their side, but now they need you. Click here to add your name to Jennifer’s petition.

Sharon Brennan, DisAbled And Happily Married, On The Undateables

April 3, 2012

Rather unsurprisingly, she too shares my views on ‘that title.’

‘Brainfingers’ System For Chris Jacquin, 17, Musician With CP

April 3, 2012

Like many teenage boys, Chris Jacquin dreams of having a career in music.

He is already an accomplished composer, but performing is a greater challenge. Chris has cerebral palsy so he cannot hold or play a musical instrument.

That meant he could not sit the practical element of music exams, or play in bands or orchestras.

But now a special headband, which responds to clicks in his jaw, enables him to play the notes on a musical score on a computer – and this has been recognised as a valid musical performance.

The 17-year-old is excited by the possibilities which the Brainfingers system has opened up for him.

Jaw movements

Chris said: “Brainfingers has given me the chance to perform some of my favourite songs and has enabled me to perform in an ensemble.”

He added that the system could enable musicians with physical disabilities to perform with able-bodied musicians.

Chris, from Edinburgh, has been working with the charity Drake Music Scotland.

Its music technology officer Rick Bamford explained: “We’ve adjusted Brainfingers to be sensitive to Chris’ jaw movements, so as he increases the pressure between his teeth he goes through a trigger line which Brainfingers is reading.

“This puts him in direct control of how the score is played back.”

Composer David McNiven is Chris’ music teacher at George Watson’s College in Edinburgh.

He successfully campaigned for the Scottish Qualifications Authority to recognise that what Chris was doing with Brainfingers and the laptop was as valid as playing a conventional instrument.

So Chris can now sit the compulsory performance element of his Higher music, which Mr McNiven believes will open many more doors.

“It’s changed the rules now that people can use a laptop,” he said.

“The ability to play with other musicians and feel the ‘vibe’ of being in a band or orchestra is just immense.”

Professional composer

This summer Chris will be one of a group of young Scottish musicians playing a specially commissioned piece for the Cultural Olympiad as part of the New Music 20×12 programme. Technophonia, by composer Oliver Searle, will be performed in Edinburgh and London.

Thursa Sanderson from Drake Music Scotland said: “The idea behind the Technophonia project is to bring together young musicians who are using the technology with their peers, who are playing conventional instruments.

“This allows them to be part of inclusive music making and inclusive ensembles. That’s what Technophonia is.”

Chris is now practising hard for his Higher music and for the Technophonia concerts. However, his long-term ambitions are to go to music college and then become a professional composer.

Geoff Holt MBE Barred From Train

April 3, 2012

This is absolutely terrible.

The first quadriplegic sailor to sail solo across the Atlantic has described his rage at being prevented from boarding an Isle of Wight train.

Geoff Holt said he was told by a guard his electric wheelchair was not allowed on board as it would damage the floor.

Mr Holt, who was later allowed to board, claims the guard implied he was a liar, and cut his leg with a ramp.

The Stagecoach Group said an employee had been suspended and a senior manager had apologised to Mr Holt.

British Transport Police have begun an investigation.

On his blog, Mr Holt, from Shedfield, Hampshire, wrote: “I can’t recall the last time that I was so angry and upset I was physically shaking, emotion choking my voice, a sense of genuine rage.

“That was until I took the train from Ryde Pier to Ryde Esplanade on Saturday 31st March.”

‘Red mist descending’

Mr Holt, who completed his 2,700-mile (4,345km) journey in 2010, told how a guard, who identified himself only as “Guard 1003” initially refused to let him board the 4:45pm train back to Ryde Esplanade.

In his blog, Mr Holt wrote: “Why? To quote Guard 1003, pointing at my wheelchair: ‘Those things aren’t allowed on these trains, they will damage the floors’.”

Mr Holt, who has been in a wheelchair since a swimming accident 27 years ago, continued: “Reminding myself this was 2012, not 1912, this was public transport and and this was the year the Paralympics were coming to Britain, the red mist was descending.”

Mr Holt claims the guard not only insinuated he was a liar when he told him he had made the same journey nine hours earlier but also dropped the disabled metal ramp on his leg and foot when he eventually relented and allowed him to board.

‘Violated and dehumanised’

“And with that simple, easy manoeuvre which took him only 10 seconds, I was on the train. All the other passengers looked on in disbelief but, in typical British fashion, did nothing.”

When the train arrived at Ryde Esplanade three minutes later, Mr Holt admits he swore at the guard because he felt “violated and dehumanised”.

In his blog he continued: “He had publicly humiliated me, he had publicly degraded me and he had made me feel like a worthless piece of dirt… it was quite simply the most disgusting way to treat another human being, let alone a disabled one.”

A Stagecoach Group spokesperson said: “We are absolutely horrified at the events Mr Holt has described.

“We welcome electric wheelchairs on our services and it is very important to us that all of our passengers feel welcome on our network.

“We are taking this matter very seriously and have already launched an investigation.”

Will You Be Watching The Undateables?

April 2, 2012

The Undateables starts tomorrow. I’m not sure whether I’ll be watching it. Just for fun, I thought I’d create a little survey to ask you if you will be. UK readers, please participate… you might just help me decide!

Click here to take the survey.

Channel 4 Has Hit A Low Marketing The Undateables

April 2, 2012

Says Frances Ryan at the Guardian’s TV and Radio blog. She shares my views on the show’s title and billboard adverts.

France Still Treats Autistic Children With Psychoanalysis

April 2, 2012

In many countries the standard way of treating autistic children is with behavioural therapy – stimulating and rewarding them to develop the skills they need to function in society – but France still puts its faith in psychoanalysis. And an increasing number of parents are now demanding change.

For autism campaigners, it is one of the most serious health scandals of our times.

How for decades France turned its back on the latest scientific thinking, and treated autism as a form of psychosis.

How as a result tens of thousands of children were misdiagnosed – or not diagnosed at all – and consigned to lives of misery.

And how to this day in its approach to autism, the French medical establishment continues to believe in the powers of psychiatry and psychoanalysis – long after the rest of the world has switched to alternative methods of treatment.

“It is an out-and-out disgrace,” according to Daniel Fasquelle, a member of parliament who campaigns on the issue.

“Every day I am contacted by parents with the same story – how their child’s autism was not detected in time, so they never had the treatment that they needed.

“Thousands of children could have been saved. They do it everywhere else. Why not here? It is France’s shame.”

The row over autism in France has festered unreported for years. But recently it has become public. Independent associations have been created, lobbying for a move away from psychoanalysis and psychiatry, and over to the “behaviourist” treatments that prevail elsewhere.

In early March these groups scored an important victory – with a ruling from the health ministry that calls into question the use of psychoanalysis as a treatment for autism.

But the psychoanalysts are not taking it lying down. From their point of view, behaviourism is a form of superficial social conditioning that does not address root causes – and they resent the way they have been typecast as the villains of the piece, when their aims are as sincere as those of their opponents.

“One thing that never pays in the field of autism is triumphalism,” said Lauriane Brunessaux, a child psychiatrist. “Autism is far too complex, and we understand it so badly.

“Today it is the behaviourists who are being triumphalist.”

The behaviourist approach to autism was developed in the 1970s and 80s in the US and Canada, and it is now the norm in most of the world.

Under the so-called ABA method (Applied Behavioural Analysis), autism is treated as primarily an educational – rather than a medical – problem.

With a set of rewards (which can be granted or withheld) – and with plenty of individual attention – children can learn to function in society, and be much less of a burden on their families.

“If you diagnose early, and then give the right treatment between the ages of two and seven, 70% of autistic children can acquire functional language skills. Here in France we are way off that figure,” says Fasquelle.

“And the same pattern continues later in life. In the UK there are 17 times more university students with autism than in France. It is unacceptable.”

The blame – Fasquelle and autism associations argue – lies with a medical establishment that remains fixated with Freud.

“Today everyone knows that autism is a neuro-developmental problem. It is not a psychosis or mental disorder,” says Muhamed Sajidi, president of the association Conquer Autism.

“But in France it is the psychiatrists – heavily influenced by Freudian psychoanalysis – who remain in charge. And they have shut themselves off from all the changes in our knowledge of autism.”

Sajidi set up the association after his life was “destroyed”, as he puts it, by the medical establishment’s failure to diagnose his son Sami’s autism.

For him, as for many others, one of the worst aspects is how blame for autism has been laid at the door of the child’s parents, and more especially of the mother.

“The first time I went to see a doctor when my (autistic) son Gael was three and we thought there was a problem, the psychiatrist asked me if I had wanted him – if it had been a wanted pregnancy!” says Candy Lepenuizic, a British woman married to a Frenchman.

While France struggles with how to treat autistic children, the US puzzled by how many people are affected, and why.A study by the Center for Disease Control and Prevention (CDC) reports that the incidence of Aspergers, Autism or Pervasive Developmental Disorder is much higher than previously thought – one in 88 children are thought to be on the autism spectrum, not one in 110 as previously reported.

“These CDC numbers should serve as a wake up call to us all,” says Lawrence Korchnak, vice-president of the Autism Society in Maryland.

Much of the change has been attributed to better reporting in African-American and Hispanic communities. But whether or not that’s the sole reason is impossible to say, says Craig J Newschaffer, director of the A J Drexel Autism Institute in Philadelphia.

“We’re left wondering whether some of this could be due to a real increase in risk,” he says.

“Then she asked what sort of dreams I had had while I was pregnant with him. And suggested the whole family have a course of psychotherapy.

“At that point I got up and walked out. It was only because I had been warned this might happen that I did not burst into tears.”

Such horror stories are typical in French families of autistic children.

“The whole idea was that it was la faute à maman (the mother’s fault). It was the ‘refrigerator mum’, or there was some problem with the family dynamic,” says Lepenuizic.

“They thought that if the child was failing to communicate with the outside world, it was because of some trauma in the womb or in very early life. There was a family malfunction, and we had to cure it!”

Critics say this emphasis on psychoanalysis and relationships meant that autistic children were not spotted till far too late. And that, in turn, meant that their chances of effective treatment were sharply reduced.

Some 60% of autistic children in Sweden attend school, Sajidi says.

“Today only 20% of autistic children in France are in school, and often only part-time. The rest are either in psychiatric hospitals, or in medico-social centres, or living at home – or in Belgium,” says Sajidi.

“Many families are sending their children to Belgium, where it is much easier to set up behaviourist treatment centres.

“Things are changing now, because parents are refusing to be taken for a ride by the professionals. But the real tragedy is with France’s autistic adults, many of whom are in a state of total incomprehension or even self-mutilation.

“Seventy-five percent of families with autistic children end in divorce, and normally it is with the mother that the autistic person stays.

“Today these poor elderly women are looking after their adult children with no knowing what will happen when they die.”

If Sajidi and other campaigners are beginning to feel the wind turn, it is because the health ministry is finally beginning to fund pilot schemes for behaviourist schools, as well as early diagnosis centres.

In its recent report, the ministry also effectively outlawed a practice known as “packing” where autistic children are wrapped in damp cloths in order to reconnect with their bodies. Campaigners say the treatment is both barbaric and ineffective.

The fundamental problem, campaigners argue, is that the psychiatric profession is resisting calls for change, because the fewer patients there are, the less they earn.

“They have a financial interest in institutionalising autistic children,” says Sajidi.

Lepenezuic says: “The state pays. The child doesn’t get any better – but who cares? It’s being looked after by the state, and the doctors are making a lot of money. Why would they change the system?”

But on the other side of the fence, such charges are deeply resented.

Child psychiatrists like Lauriane Brunessaux believe that the associations have grossly distorted the debate, and are engaged in a battle to “discredit psychoanalysis and the whole notion of the unconscious”.

Defenders of the French system argue that the situation was never as one-dimensional as the behaviourists have claimed.

First of all, they say, there have been plenty of success stories emanating from a psychoanalytical treatment of autism. They just have not been so loudly trumpeted.

Secondly, it is not as if the behaviourist approach is itself beyond criticism. In the US and Canada, argues Brunessaux, there have been studies that raise serious questions over its true scientific validity.

“The only real scientific reference for behaviourism is the electric shock experimentation on rats carried out by (US psychologist) Burrhus Skinner in the 1940s.

“Obviously the methods of reward and punishment today are totally different. But that is the background to behaviourism,” she says.

For leading French psychoanalyst Eric Laurent, there is a deeper problem.

“Changing behaviour is one thing. But what do you do with the trouble that lies behind it? It is all very well to focus on the skills that can be transmitted via an intensive behaviourist approach, but that leaves a whole dimension out of the picture,” he says.

As for the charge that psychoanalysts are responsible for family breakdown, Laurent is equally dismissive.

“The idea that you had to wait for psychoanalysts to come along for there to be hatred inside families is ridiculous. Hatred has always been there.

“Psychoanalysis is being used as a scapegoat – though we should not perhaps mind that, as being a scapegoat is part of the role of psychoanalysis,” he says.

What angers people like Brunessaux and Laurent is that while on their side of the debate they are quite prepared to admit the effectiveness of behaviourism – as one of several possible approaches to autism – the behaviourists are dogmatically tied to their system and theirs alone.

Whoever is ultimately in the right, what the autism row perhaps shows most clearly is the changing nature of French society.

Once, families did what they were told. The state was ultimately benevolent, and had massive resources to dispense. If doctors chose institutionalisation, then who was to argue?

Today it is different. Thanks to the spread of knowledge, the internet, consumerism and the decline of the collective spirit – families for the first time feel emboldened to think, and act, for themselves.

Happy World Autism Awareness Day 2012!

April 2, 2012

I must send out sincere apologies to those of my readers with an interest in Autism. I completely forgot that today is World Autism Awareness Day 2012. I only remembered when I saw the Guardian‘s picture gallery explaining the condition.

If you spot, create or write anything in celebration of World Autism Awareness Day today, do let us have a link to it in the comments!

Food Fear Boy Daniel Harrison To Get More Treatment

April 2, 2012

The family of an autistic Nottingham boy who has not properly eaten food for five years hope further treatment abroad will help cure him.

Five-year-old Daniel Harrison has a fear of consuming food after he suffered from acid reflux as a baby.

In 2011, his family raised £25,000 for treatment at a specialist Austrian clinic which helped Daniel to accept liquid food orally.

The NHS has agreed to fund further therapy in Austria worth £6,000.

The treatment is designed to encourage Daniel to take both food and liquid.

It is hoped, when they return, Daniel will be able to consume some sort of food, even if it is a puree.

Before Daniel went to the clinic in Graz, he had to be fed through a tube in his stomach and would also not allow his parents to brush his teeth.

‘Dark places’

Kevin Harrison, Daniel’s father, said: “Because of Daniel’s autism it makes him worse, it makes him think something is trying to hurt him, so his instinct is ‘no’.”

After one month in Austria he allowed his parents to feed him a milk solution, with a special cup.

He also drinks water which has prevented him from dehydrating.

Mr Harrison said the public’s help was overwhelming when he was raising money last year but admitted it has been tough for him and his family.

“I was in some really dark places at times,” he said.

During one day in Graz he had to restrain a screaming Daniel, while syringing liquid into his mouth.

“I’ve become very strong-minded, strong-willed and now it’s not a question of when he will eat, it’s a question of how soon he will eat,” he said.

Following the family’s first self-financed trip, Mr Harrison said he had convinced the NHS to pick up the cost of the second round of treatment, but the family will have to pay for flights and accommodation.

He said: “I have tangible proof it [the last course of treatment] worked, in theory it saved the NHS money.

“We don’t use a £2,000 feeding chair anymore, no special syringes or transport costs.”

A spokesperson from NHS Nottinghamshire County said: “We are committed to improving the health and wellbeing of the people of Nottinghamshire.

“We are unable to comment on individual cases.”

Daniel, his father, his mother Catherine, and sister Hannah, will return to Graz on 12 August for two further weeks treatment.

Tim Farron Explains His Signature On Christian MPs’ ASA Letter

April 2, 2012

I have been sent two Tweets which prive that the post below was not an April Fool:

https://twitter.com/#!/mrsblogs/status/186590348062105600

 

https://twitter.com/#!/mrsblogs/status/186591170447671296

Christian MPs Take Stand On ASA’s ‘God Can Heal’ Advert Ban

April 2, 2012

This was posted yesterday. I can’t tell whether it was an April Fool or not, but I decided to post it since I have covered the story before.

A Devon MP and two other MPs are trying to overturn a ban on advertising claims that “God can heal”.

They want the Advertising Standards Authority (ASA) to produce “indisputable scientific evidence” to say that prayer does not work.

They wrote a letter on behalf of the Christians in Parliament (CIP) group.

It came after the ASA banned a Christian group from claiming on its website and in leaflets that God can heal illnesses.

It said a leaflet available to download from the group’s website said: “Need Healing? God can heal today!”

The ASA said it had concluded that the adverts by Healing on the Streets (HOTS) – Bath, were misleading.

‘Sincere group’

HOTS, based in Bradford-on-Avon, Wiltshire, said it was disappointed with the decision and would appeal.

Mr Streeter, Conservative MP for South West Devon and chairman of CIP, wrote an open letter to the ASA along with Gavin Shuker, Labour MP for Luton South, and Tim Farron, Liberal Democrat MP for Westmorland and Lonsdale.

In the letter to the ASA they said they would “be the first to accept that prayed for people do not always get healed, but sometimes they do”.

“That is all this sincere group of Christians in Bath are claiming,” the MPs said.

Mr Streeter also said in the letter: “You might be interested to know that I (Gary Streeter) received divine healing myself at a church meeting in 1983 on my right hand, which was in pain for many years.

“After prayer at that meeting, my hand was immediately free from pain and has been ever since.”

News Headlines- Sunday, 1st April 2012

April 1, 2012

The Wheelchair That Floats In Water– Disability Now

Scientists in Australia have invented a wheelchair that floats in swimming pools. It is said to have waterproof wheels and tyres. Its only disadvantage is that it is too big to fit in bathtubs. Still, now swimming pools won’t have to make themselves accessible, because you will soon be able to swim from the comfort of your wheelchair.

Chocolate Ear Sweets Restore Hearing- Able Magazine
From the inventors of chocolate eyeball biscuits come chocolate ear sweets! This time they are shaped like ears and eating two sweets a day is said to restore lost hearing within a week.

Peanut Butter Sandwiches Cure Cerebral Palsy- Bobath News

After over 30 years, The Bobath Centre announces with some sadness that it is to close down at the end of this month. After speaking to some of her patients, one of our senior physiotherapists, who has asked to remain nameless, has discovered that eating a peanut butter sandwich every day of your life leads to significant improvements in function for children with Cerebral Palsy. We plan to send all our patients home on Friday, April 27th with a year’s free supply of peanut butter, and after that date, we can’t see the point in staying open.

Disability Friendly Potato Shapes Created For Children- Tesco Magazine

We’ve all heard of potato alphabets. Well, now a sensitive  young mother has created a rather different child-friendly chip. The new potato shapes are shaped like wheelchairs, walking frames and white sticks. They are expected to go on sale at your local Tesco store from midnight on Sunday, April 1st. We hope that after eating them, disabled children will feel included and non-disabled children will learn what these pieces of essential disability-related equipment look like.

Disability Campaigner Joins The Conservative Party- Same Difference

Disability bloggers and disabled people will be sad to read that the Same Difference disability website is to close down at midnight tonight. Editor Samedifference1 has re-discovered her love of peanut butter sandwiches after being reliably informed that they cure her disability.  And now that she has been given a definite miraculous cure, she writes, she has decided to close down the site and join the UK Conservative Party. She wishes readers well and adds that she hopes to see them in Westminster in 2015 as an MP for the party led by her new best friend, David Cameron.

 

The Guardian Meets Two Of The Undateables

March 31, 2012

Meet Sam and Jolene, two of the Undateables, who have been interviewed in today’s Guardian.

Former Soldier Designs Ice Axe To Attach To Prosthetic Arm While Climbing Everest

March 31, 2012

A soldier whose left arm was blown off in Afghanistan has helped design a prosthetic ice axe which he will use to climb Mount Everest.

Private Jaco van Gass, 25, from Middleburg, South Africa, was hit by a rocket-propelled grenade while serving with the Parachute Regiment in 2009.

He is one of a group of five injured servicemen who will set off on a 10-day walk to Everest Base Camp on Saturday and then push on to the 8,848-metre summit in May.

Van Gass, who trekked to the North Pole with the Walking with the Wounded charity last year, said he had the idea to fix an ice axe to a false limb and asked some engineers at the specialist military rehabilitation centre in Surrey to build one.

He said: “I came up with the idea to attach an ice axe to one of my prosthetics, so I kind of challenged the guys at Headley Court to see how we could get this done.”

Van Gass bought a regular ice axe and staff at the centre sawed off the double-sided head, then welded and bolted it to a specially adapted prosthetic made of carbon fibre and plastic.

A key design feature Van Gass was keen to include was an electrical system to heat his stump.

He asked the engineers to use wires to connect two heat patches moulded into the prosthetic to a battery pack sewn into the thermal under-layer just over his heart.

The warmth of his body helps the three AA batteries last longer as the cold drains their power very quickly.

“This will keep the arm inside nice and toasty,” he said.

“It’s really essential for me because the lack of circulation in my arm actually prevents the flow of blood and oxygen at high altitude, so the arm gets really cold and is actually prone to frost-nip.”

The South African said the extreme altitude of Everest’s higher slopes might cause unexpected problems and the adapted axe could help.

“On our last expedition, when we climbed Manaslu, I didn’t use anything,” he said.

“There was no problem with the arm, but as we are going to do that extra 700-metre ascent [to the Everest peak], it’s a terrain we’ve not been to before, so it’s a little bit unexpected.”

Van Gass will use the tool to navigate some famously treacherous points along the southern route to the summit of the world’s highest mountain.

He said: “The ice axe is there for back-up. Once we do stuff like the Lhotse ice face and the Hillary step, it might come into aid.

“It’s there for the places where I could slip and I’m not attached to a fixed rope.

“Due to the fact I’ve only got the use of my right hand, I usually try to keep it free. I don’t want something in it.

“If I slip, the back end will just go into the ice, but my right hand comes across and I just dig into the snow.”

Moose Baxter, Van Gass’s prosthetist at Headley Court, helped the soldier’s vision become a reality. The specialist took a mould of his arm, so the ice axe fits perfectly over the stump.

Van Gass fixes the prosthetic to the remainder of his arm by rolling over a rubber sleeve, slotting the false limb over it, and a one-way valve creates a vacuum to hold it fast.

As well as losing his left arm above the elbow, he suffered a collapsed lung, punctured internal organs, loss of muscle from the upper left thigh, multiple shrapnel wounds and fractures to his knee, fibula and tibia.

His team-mates for the assault on Mount Everest’s peak are former Captain Martin Hewitt, 31, from Widnes, Cheshire, Captain David Wiseman, 29, from Tadcaster, North Yorkshire, Captain Francis Atkinson, 31, from Swindon, Wiltshire, and former Private Karl Hinett, 25, from Tipton, West Midlands.

How Many More Young People Will Die Before ME Is Recognised?

March 30, 2012

Asks Scott Jordan Harris at Comment Is Free in a tribute to Emily Collingridge.

Self Driving Car Driven By Blind Man

March 30, 2012

This has to be seen to be believed.

EU Court Ruling Marks End Of The Road For The Beatle Wheelchair

March 30, 2012

A bid to trademark the word beatle for use on electric wheelchairs has been blocked by EU judges.

They ruled there was a risk of confusion with the pop group – even though the youth and vigour represented by the group contrasted with the reduced mobility of wheelchair customers.

There was in fact a connection, the judges said on Thursday, because some original Beatles fans may now be wheelchair users.

Dutch company You-Q has been promoting the Beatle wheelchair on its website.

But the ruling from the European court of justice backed the EU trademark office’s decision to disallow Beatle wheelchairs to be trademarked.

The verdict is a victory for Apple Corps, the company formed by the Beatles, which challenged the You-Q bid.

The judges said a product using the group’s name would benefit unfairly from the association.

The name of the group has “an enormous reputation for sound records, video records and films and a reputation, albeit lesser, for merchandising products such as toys and games”, the court ruled.

Visually, phonetically and conceptually, the names the Beatles and Beatles were very similar to the trademark requested for the wheelchairs.

“Moreover, those marks have a distinctive character so that, when faced with them, the public at large, in particular in the non-English speaking countries of the EU, will immediately think of the eponymous group and their products,” said the ruling.

The judges said it was likely that, if allowed to use the Beatle name, You-Q would take unfair advantage of the “repute and the consistent selling power” of the pop group.

“The image conveyed [by the name of the Beatles] is, even after 50 years of existence, still synonymous with youth and a certain counterculture of the 1960s, an image which is still positive,” said the ruling.

“That positive image could benefit the goods covered by the mark applied for, since the relevant public, on account specifically of the handicap in question, would be particularly attracted by the very positive image of freedom, youth and mobility associated with the Beatles.

“This is especially so as a part of the public targeted by You-Q’s goods belongs to the generation of persons who knew the Beatles’ goods in the 60s and some of whom may now be concerned by the goods covered by the mark applied for.

“That image transfer would therefore enable You-Q to introduce its own trademark on the market without incurring any of the great risk or costs, in particular advertising costs, connected with launching a newly created mark.”

Are You Worried About The Rise In The Price Of A Stamp?

March 29, 2012

If you are, then it might make you feel just a little bit better to know that Royal Mail have said that people on certain disability-related benefits will be given concessions on stamps. The problem? They will have to wait until Christmas. Full details here thanks to BBC Ouch.

Able Life: We Won’t Drop The Baby

March 29, 2012

Yesterday on Able Life, George Johnson and I discussed… three guesses… the brilliant documentary We Won’t Drop The Baby. Here is what we said.

Beyond Disability: The Adventures Of A Blue Badger

March 29, 2012

10pm, BBC Radio 5 Live, Thursday 29 March

Nikki Fox has big hair, an air of mischief, and an unhealthy love of Nik Kershaw. She also gets brilliant seats at concerts and very convenient parking spaces at the supermarket. Born with Muscular Dystrophy, Nikki gets around in a mobility scooter, and she reckons life is pretty flippin’ good as a disabled person (or ‘Blue Badger’) in the UK.

In this BBC Radio 5 Live documentary, Nikki is out to discover whether her positive outlook on life is justified and shared by her fellow Badgers. In the year of the biggest celebration of disability sport, the Paralympics, is the UK as good at dealing with disability as it thinks it is? Does disability bring out the kindness in the public or do they secretly avoid having to help? Is access and the transport network improving? And, most importantly, will Nikki get to sing her David Milliband song on national radio?

Nikki’s adventures take her from her friends and family, to being grilled by complete strangers (including a scary class of eight-year-olds), as well as talking to the likes of Tanni Grey Thompson, David Blunkett, CBeebies’ Cerrie Burnell and Disability Minister, Maria Miller.

Baroness Tanni Grey Thompson Faced Online Abuse After Revealing Train Trouble

March 28, 2012

This is absolutely terrible and completely unnecessary. I know that I have several readers in the UK who follow Baroness Tanni Grey Thompson online and admire her, as I do myself. I am shocked and very sad to read about this.

Baroness Grey-Thompson says she has attracted a stream of anti-disability abuse after she spoke of having to crawl off a train in London.

The former Paralympian said she was often left without assistance at stations despite advance requests.

A newspaper website reporting the story prompted a large number of offensive comments about the peer’s disability.

“There’s a lot of disabled people who wouldn’t be able to deal with it the way I’m able to,” she said.

Paralympian faced crawl off train

Lady Grey-Thompson, who was born with spina bifida, revealed she was recently left stranded at King’s Cross station in London at midnight after travelling from her home in north east England.

She said she had to shuffle onto the floor and push her wheelchair towards the door of the train.

But the baroness told BBC Wales she was shocked by some of the abuse she attracted from people posting their views on a newspaper website which carried the story.

“A couple of hundred people said some fairly unpleasant things about me along the lines of ‘what gives her the right to speak, she should be at home, she shouldn’t be out at midnight, she should be better organised’, and what right did I think I had to travel on public transport.

“The most offensive ones were more generic, like maybe there should be a cattle truck at the back of the train for wheelchair users so they can all sit together.

Lady Grey-Thompson said she wasn’t worried as much for herself as for other disabled people who faced prejudice.

“I’ve got quite a thick skin but when you hear people talking like that in a very derogatory way about disabled people I find that quite worrying,” she said.

“There’s a lot of disabled people who wouldn’t be able to deal with it the way I’m able to deal with it.

“The fact I’m in the House of Lords does give me a voice to say, hang on a minute, we need to do something different.

“It’s very worrying that there’s this underlying cynicism about disabled people – and some of the posts were actually quite threatening.”

Public arena

The gold medal-winning athlete said she recognised that the scope for anonymity on social media and the internet made young people in particular less polite.

“I have had some fairly bad things said to my face,” she said.

“When I was pregnant someone in Queen Street in Cardiff said people like me shouldn’t have children.

“But I think people in a face to face situation tend to back down.

“In something like Twitter and Facebook and other situations people forget and they think that there’s some sort of security around themselves.

“A lot of people do forget that it’s public… even if you delete something, people can still keep a copy of what you said.

“I do worry that a lot of young people forget how public some of this is.”

Advocacy partnership shortlisted for Business Charity Awards in first year

March 28, 2012

A press release I have just received from the Muscular Dystrophy Campaign:

An advocacy service partnership between the Muscular Dystrophy Campaign and legal firm Hogan Lovells has been shortlisted for a Business Charity Award in its first year, after helping to secure £300,000 in care and support for people affected by muscle-wasting conditions.

 

On 15 May, the partners will learn whether they have won the Single Project category, after competing with high profile initiatives including Sainsbury’s and FareShare’s Million Meal Appeal and the Safe@Last collaboration between Aviva and Railway Children.

 

Over 100 cases have been handled by the Muscular Dystrophy Campaign’s advocacy team with support from Hogan Lovells, which has provided pro bono client care and legal representation, offered bespoke legal training sessions and contributed to the development of a Self-Advocacy Pack. In total the firm has provided £50,000 worth of pro-bono assistance, administered by their team of 27 legal and 16 administrative volunteers.

 

The charity’s advocacy service was launched in 2011 in response to a sharp increase in approaches to the charity by people with muscular dystrophy and related conditions denied appropriate care, support or equipment by local authorities and health services. A significant number of cases of disability discrimination by employers, service providers and public bodies have also been dealt with by the team.

 

Nic Bungay, the Muscular Dystrophy Campaign’s Director of Campaigns, said:

“We have seen a 400 per cent increase in approaches from families battling local authorities and health services for care in the last two years. Establishing a structured service with the help of Hogan Lovells has helped us to turn the tide for many people facing unjust or illegal treatment at the hands of those with a responsibility to support them. We are hugely grateful for the firm’s support and for such a substantial and visible commitment to this project. We hope this short-listing for the Charity Business Awards will see Hogan Lovells team receive the recognition they deserve.”

 

Lawson Caisley a Partner at Hogen Lovells said:

“We are proud that our partnership with the Muscular Dystrophy Campaign has achieved such tangible results, and has benefited vulnerable people that would have struggled to obtain legal representation.”

Report By House Of Lords Recommends More Disabled Judges

March 28, 2012

A more diverse judiciary is needed in England and Wales, the House of Lords Constitution Committee has said.

Peers said targets may be needed to recruit more ethnic minority and female judges if the judiciary did not better reflect society within five years, but said such a move was not needed yet.

They said judges had to understand the “array of concerns and experiences” of those who appeared before them.

Only one in 20 judges is non-white and 22% are women.

The report by peers suggested greater diversity also meant a need to boost the numbers of gay and disabled judges.

The influential committee recommended looking at removing barriers within the career structure of the profession, such as allowing more family-friendly working hours to encourage women to apply.

It also said solicitors should be encouraged to become judges because they were a more representative group than barristers.

Public confidence

It said that where two candidates were of equal merit, the need for diversity should tip the balance.

Peers called on the Lord Chancellor and the Lord Chief Justice to be given a duty to encourage diversity in finding candidates.

They said equality laws should be applied to senior court appointments.

The committee concluded: “It is necessary for judges to understand the wide array of concerns and experiences of those appearing before them.

“A more diverse judiciary can bring different perspectives to bear on the development of the law and to the concept of justice itself.”

Committee chairwoman Baroness Jay said it was “vital that the public have confidence in our judiciary”.

“One aspect of ensuring that confidence is a more diverse judiciary that more fully reflects the wider population,” she said.

She added it was important that judges were appointed on merit, but added that the committee felt there were steps that could be taken to promote diversity without undermining that principle.

Susan Boyle Musical Opens In Newcastle

March 28, 2012

A musical based on the life of singer Susan Boyle has received its premiere in Newcastle, with fans travelling from as far as Australia to attend.

Boyle is played by Rab C Nesbitt actress Elaine C Smith, before the star herself comes on stage for the finale.

Pam Cleggett, 68, travelled from Adelaide, Australia, to watch I Dreamed A Dream with the Susan Boyle fan club.

“Tonight there are 20 states of America represented,” she said of the fan club. “And Switzerland, Slovakia, Ireland.”

The show had its official opening night on Tuesday at the Newcastle Theatre Royal following several previews.

Breakdown

It follows Boyle’s life story from her childhood in West Lothian to her breakthrough performance on ITV1’s Britain’s Got Talent in 2009 and the subsequent media frenzy.

“I liked it because it’s a modern-day fairytale,” said the musical’s producer Michael Harrison. “But it’s a true story because Cinderella did go to the ball.”

 The rags-to-riches story did not shy away from Boyle’s difficulties, among them her parents being told she may have brain damage after being starved of oxygen at birth.

It also includes her being beaten up at school and having a breakdown after the Britain’s Got Talent final, in which she finished runner-up.

After the life story ended and Smith and her co-stars took the curtain call to a standing ovation, Boyle herself appeared to sing two songs.

The star appeared hesitant at first but developed a rapport with the audience after the first line of I Dreamed A Dream was met with ecstatic applause, as it had been the first time she performed the song on Britain’s Got Talent.

That moment from her original talent show appearance was watched online an estimated 500 million times and made her a global superstar virtually overnight.

The new stage musical is designed to feed the devotion to Boyle without requiring her to undergo the rigours of a full concert tour.

‘Magical’

The musical will visit 11 cities in the UK and Republic of Ireland and Boyle is expected to make a similar cameo appearance at the end of each show.

Speaking after Tuesday’s performance, Elaine C Smith said: “All too often, particularly because of class or poverty or learning difficulties or health difficulties, people are written off, and Susan for me represented the other side to that.

“And I think that’s why she connects to people and touches people. That’s the part of the story I find magical.”

The story has been adapted from Boyle’s autobiography and Smith said some lines in the script had come from Boyle herself, such as the description of the frenzy following Britain’s Got Talent as being like “a demolition ball crashing through everything I’d ever known”.

“At first she really enjoyed it all, all the attention, and then it turned on her in a way,” Smith said.

“We didn’t want to shy away from that. I didn’t want a sugary version of it.

“I was at her 50th birthday party [last April] and I thought, I’ve got to give you a voice because there are so many people who want to talk for her or put words into her mouth or control her, so it was about finding an authentic voice for her.”

One audience member, Pat Lyon, 71, from Hartlepool, described Boyle’s appearance as “very emotional”.

‘Schmaltz and hyperbole’

“She looked great,” she said. “She’s not pretentious, she’s a true ordinary Scottish lady who’s never forgotten her roots, which is lovely.”

Her friend Karen Oram, 54, also from Hartlepool, added: “It was nice to hear her be a bit humorous and get the crowd involved. She obviously realised that there were a lot of people who had come a long way.

“It was nice to see her relationship with her mother and father. I think a lot of people didn’t understand that part of her life, and the fact that she did have a difficult childhood. But it all came good in the end.”

Early reviews have been broadly positive, with the Daily Mail’s Patrick Marmion opining there is “much fun to be had” from this “cocktail of schmaltz and hyperbole”.

The show, he wrote, is “more than just a get-rich-quick scheme or a piece of craven hagiography”.

In his five-star review in the Daily Telegraph, Dominic Cavendish saluted a “fantastically assured bio-musical [that] delivers the goods”.

“In matching the gutsy good humour of its heroine,” he concluded, “this is a delight that deserves to go far, and fast, as she has done”.

The Scotsman‘s review was also complimentary, describing the production as “a vigorous, thoughtful and inspiring tribute” to the 50-year-old Boyle.

“What we see is a clever, honest and highly theatrical script, which never tries to evade the darker aspects of Boyle’s experience,” it continued.

‘Father And Son’ Burglars Steal From Blind Woman’s House

March 28, 2012

Burglars claiming they were father and son tricked their way into a blind pensioner’s Manchester home and stole her handbag, police have said.

The boy, said to be about 10, knocked on the door of the 88-year-old’s home in Woodhouse Park on Monday evening.

He told the pensioner he had lost his dad, but seconds later the “dad’ turned up and asked the woman if she would get his “son” a glass of water.

Police said the woman’s handbag was snatched while she was in the kitchen.

The woman had shut the door but left it unlocked and the pair went into the house and snatched the handbag from the living room, which contained her purse, cash and other personal items, Greater Manchester Police said.

Det Con Christopher Broad said: “We cannot know for certain if this was a genuine father and son team, but regardless, the adult offender has clearly roped a child into his nefarious and cruel scheme which is unforgivable.

“To expose a child to such a cowardly criminal enterprise and steal from a partially deaf and blind pensioner is as low as it gets.”

US Man Has New Jaw, Teeth And Tongue After Face Transplant

March 28, 2012

US doctors have carried out what they say is the most extensive face transplant ever performed.

The operation at the University of Maryland gave Richard Norris a new face, including jaw, teeth and tongue.

The 37-year-old has lived as a recluse for 15 years after being severely injured in a gun accident, and wore a mask whenever he went outside.

The surgery was funded by the US Navy, which hopes the techniques will help casualties from Iraq and Afghanistan.

Surgeons who carried out the 36-hour operation say it was part of a series of transplant operations lasting 72 hours, using organs from one donor in five patients including Mr Norris.

He lost his lips and nose in the accident, and only had limited movement of his mouth.

The lead surgeon says Mr Norris will now get his life back.

“Our goal is to restore function as well as have aesthetically pleasing results,” said Eduardo Rodriguez.

The team at the University of Maryland say Mr Norris is now brushing his teeth and shaving, and has regained his sense of smell.

The US government estimates that 200 wounded troops might be eligible for face transplants.

The first face transplant was performed in France in 2005, on a woman who was mauled by her dog.

In 2010 surgeons in Spain carried out the world’s first full face transplant.

The Cleft Collective

March 28, 2012

Correct me if I am wrong readers please. I thought that in the UK cleft lip and palate are corrected by operations as soon after birth as possible? If that is the case then what is the need for this level of research into the conditions?

Still, I suppose it is progress of a sort.

The world’s largest research databank for cleft lip and palate is being set up in the UK to determine what causes these common conditions.

These congenital abnormalities affect 1,200 babies born in the UK each year, yet why they occur is unknown.

Parents of babies with these conditions are being encouraged to enrol in the £11m, five-year programme.

The Cleft Collective team will gather and analyse the DNA of these children to see if they can pin down a cause.

And by following these 3,000 or more children throughout their childhood, the researchers hope to ascertain what the best course of treatment is, including which surgery offers the best cosmetic and functional results.

A cleft occurs when separate areas of the face do not join together properly when a baby is developing in the womb.

The Cleft Collective will be run at two Bristol universities, Liverpool University and a clinical trials centre based at the University of Manchester and is partly funded by UK charity the Healing Foundation, with the rest of the investment coming from universities and NHS partners.

Prof Jonathan Sandy, lead researcher for the Bristol gene bank, said: “Children born with cleft often face unique challenges. These include speech and language issues, educational difficulties and broader health concerns.

“We do not know if these problems are caused by the genes that may be responsible for cleft or by other factors, such as lifestyle or ‘environmental’ factors. This study will help answer these important questions and could also solve the ultimate mystery of what causes cleft in the first place.”

The experts will also look at what practical and emotional support these families might need.

Prof Nichola Rumsey of Bristol’s University of the West of England, said: “When parents have a baby with a cleft, typically one of their first questions is ‘Why has this happened to us?’ They also want to know whether their baby will be OK as they grow up.

“Our focus will be to gather psychological data from parents on their experience of diagnosis and the early issues of parenting a child with a cleft and their support needs.”

Robert Softley’s If These Spasms Could Speak

March 27, 2012

I have just read a review of the latest show by Robert Softley, the actor and writer with CP behind Girl X. His latest work is a monologue called If These Spasms Could Speak.

Inclusive Education In Thailand

March 27, 2012

I don’t usually cover issues outside the UK, but inclusive education is close to my heart, so I am pleased to read this.

Parliamentary Debate On Assisted Dying

March 27, 2012

https://twitter.com/#!/dignityindying/status/184611852477665281

How Film Can Help Children With Learning Disabilities

March 27, 2012

An interesting post from the Guardian blogs.

Leaving A Loved One To Assist With Death Is Cruel

March 27, 2012

Says Raymond Tallis at Comment Is Free. I have to say that I share this view, and that is one of the reasons why I don’t agree with assisted death.

Former Rugby Player Jonny Mitchell Dies Aged 30

March 27, 2012

A former rugby player has died almost seven years after being seriously injured during a match.

North Berwick RFC captain Jonny Mitchell was left wheelchair-bound when he suffered a spinal injury in a scrum during a game against Hawick Linden in September 2005.

The father-of-two died at the age of 30 in the early hours of Monday morning.

North Berwick RFC president Jim Littlefair said Mr Mitchell’s death was a “terrible loss to everyone in rugby”.

Mr Littlefair had helped establish the Jonny Mitchell Trust Fund to help Mr Mitchell and his family deal with the sudden demands of being wheelchair-bound.

He said: “Jonny never once said ‘why me?’ and, as an experienced front row player, he accepted that what happened to him was just a freak accident.

“He was a tremendous character and was passionate about the game of rugby. He always said, if he could, he’d be back training with the team.

“All of our lives changed the day Jonny was injured and he’s been in our thoughts since that day and he will remain there.”

Professional and club players alike joined in the fund-raising efforts for Mr Mitchell and his family, and they also received help from charities Hearts and Balls and the Murrayfield Centenary Fund, which aims to assist players, and those connected with the game, who have been seriously injured.

Scottish Rugby Union President, Ian McLauchlan, said: “Jonny showed such tremendous courage in the face of adversity. He loved the game of rugby and even after his injury didn’t turn away from the sport.

“I’d like to pass on sincere condolences, from everyone at Scottish Rugby, to Jonny’s family for their loss.”

Mr Mitchell is survived by his wife and two daughters.

Meeting Carers In Scotland

March 26, 2012

Fiona Walker went to meet two disabled people and their carers in Scotland for a BBC Scotland investigation.

Three Men Guilty Of Shooting That Left Girl, 5, Paralysed

March 26, 2012

Three men have been found guilty of a gang-related shooting that left a five-year-old girl paralysed, shattering her dreams of becoming a dancer.

Thusha Kamaleswaran, now six, was hit by a bullet when the trio opened fire into her aunt’s south London shop in March last year.

Nathaniel Grant, Kazeem Kolawole and Anthony McCalla were convicted by an Old Bailey jury of causing her grievous bodily harm with intent.

A bullet hit Thusha in the chest and passed through the seventh vertebra of her spine, leaving her wheelchair-bound for life.

Thusha’s mother Sharmila Kamaleswaran wept as extracts from her victim impact statement were read to the court by junior prosecutor Michelle Nelson. The mother of three said the tragedy was “unbearable” for her family, and described the shock of seeing her daughter on a hospital bed, saying: “Seeing Thusha took my heart away.”

She said her daughter’s dreams of becoming a singer and dancer had been shattered.

Thusha is due to be discharged from hospital next week, and her doctor at Stoke Mandeville Hospital, Allison Graham, said her condition is not expected to improve.

Grant, Kolawole and McCalla were looking for a rival gang member when Grant mindlessly opened fire into the Stockwell Food and Wine shop. Shopper Roshan Selvakumar was shot in the face in the attack, and has been left with bullet fragments permanently lodged in his head.

The trio were found guilty of causing grievous bodily harm with intent to Mr Selvakumar and of attempted murder of their intended victim Roshaun Bryan.

Jurors were told that Grant would have been able to see Thusha as he fired his second shot. Kolawole, 19, of Kennington, south-east London; McCalla, 20, of Streatham, south London; and Grant, 21, of Camberwell, south-east London, will be sentenced on April 19.

MP Calls For Compulsory Mobility Scooter Training

March 26, 2012

Compulsory training should be given to people who use a mobility scooter, a Devon MP has said.

Alison Seabeck, the Labour MP for Plymouth Devonport, also called for stricter safety checks and official records to be kept of accidents.

Last year a 79-year-old man from Bodmin in Cornwall was killed when his mobility scooter overturned and pinned him against a wall.

Scoot-A-Long, a charity for disabled people, has backed the MP’s campaign.

There are two maximum speeds for mobility scooters – 4mph (6km/h) for scooters which can only be ridden on pavements and 8mph (13km/h) for on-the-road scooters which must have full working lights.

Peter Baldacchino, a spokesman for Scoot-A-Long, said the charity’s aim was not to discourage the use of mobility scooters, but to ensure disabled people could “get out and about and enjoy life safely”.

The 60-year-old from Polperro has used both types of scooters for 15 years.

He said: “I’ve got one I keep in the car and one for the road and I’d be completely sunk without them.

“But at the moment there’s absolutely no regulations about who can use them – anyone can just go into a shop, buy one and take it straight onto the road.

“There’s no wilfulness about it, but there are so many more people using these machines and some just aren’t aware of the dangers.

“We think even just one hour of training would give most people the knowledge they need to be safe.”

‘Balancing act’

Mrs Seabeck has raised the issue in the House of Commons.

“With an increasing ageing population, some action has to be taken to ensure that standards are maintained in terms of the safety of these vehicles and that some basic training is undertaken by all users,” she said in an adjournment debate.

“It’s important that when they’re sold to people who’ve never driven and they intend to use them on the road, that training is compulsory.”

Transport Minister Norman Baker said there was cross-departmental work going on to address the “balancing act” between safety and protecting a lifeline for the disabled and elderly.

“I do think there’s an issue about basic training and the safety of these vehicles,” he said.

He said the government had plans to change the speed limits for mobility scooters, but from next year police forces would be able to officially record accident statistics involving them.

Dame Tanni Grey Thompson ‘Had To Crawl Off A Train’

March 26, 2012

One of Britain’s most successful disabled athletes has told how she was forced to crawl off a train because no one would help her get her wheelchair on to the platform.

Dame Tanni Grey Thompson, who has won eleven Paralympic gold medals, revealed that it was commonplace for her to be left stranded on trains because of a lack of assistance for disabled passengers.

Just two weeks ago the athlete, who was born with spina bifida causing the vertebrae to fully fuse together, had to crawl off a train at midnight. 

 Speaking to the Daily Telegraph, she said: ‘As a disabled person travelling you always have an element of fear, feeling very uncomfortable, of panic, of just wondering whether you’re going to get off.

‘I think it is fair to say hat a lot of disabled people feel like second class passengers because they don’t have the same treatment as everyone else. 

 ‘I don’t expect to be swept in to first class and treated better than everyone else – I expect to have the same experience, and that is often just not the case.’

Dame Tanni retired in 2007 and became a non-executive director of UK Athletics.

 She is now encouraging disabled people to submit their stories to a project on public transport accessibility which launches today.

Dame Thompson is helping to spearhead ‘A2B for all’, which is aimed at ensuring public transport does not discriminate against disabilities.

The campaign research found that disabled passengers are routinely being discriminated against, with staff refusing them access, being ignored while on board and verbally abused.

A Review Of We Won’t Drop The Baby

March 26, 2012

This is a guest post by Andrew Bradford. It was originally posted here earlier today. Thanks to Andrew. It is also part of theDisAbility And Parenting debate.

Last night BBC1 broadcast the story of Laurence and Adele Clark as their second son Jamie was born. Both Laurence and Adele have Cerebral Palsy. One of the early scenes shows them taking their older son Tom, aged six to the swing park.

Being taken to the swing park as a six year old by two parents in wheelchairs is one of my earliest memories too. But that was 58 years ago, so I wanted to see what’s changed in just over half a century. The wheelchairs are far more high-tech and the playground equipment is much more brightly coloured, but it’s still newsworthy when two people with disabilities decide to have kids. There was no TV to speak of in 1948 so my birth was only reported in “The People” and the “Sunday Express”.

Laurence was in the operating theatre when Adele gave birth to Jamie, but the presence of any dad – let alone a dad in a wheelchair – in that room was unthinkable then. But just as Laurence was about to go in, a very embarrassed (male) midwife asked him if he would mind transferring from his power wheelchair into a hospital wheelchair – “it would be better for us”. I can’t imagine the reasoning behind this; Laurence very politely and firmly declined this request and the midwife’s body language showed that he was only going through the motions at somebody else’s bidding. He was clearly relieved when Laurence stood his ground.

One scene showed Adele talking to Tom about the imminent arrival of his new brother, and it was very interesting to see how he understood and accepted his parents’disabilities in such a matter of fact manner. I can’t remember having these discussions with Kathy and Charlie at six, but I do remember that as a nine year old I accepted my parents’ disabilities in just the same way. It would be very interesting to see a follow up program in a few years time and talk to Tom again.

I felt for the two grandmothers who featured prominently in the programme. Their childrens’ CP was of course the result of difficult births, so it must have been very stressful for them to wait for Jamie’s arrival, and the relief they must have felt when a healthy baby arrived was obvious.

I couldn’t help contrasting Laurence’s and Charlie’s working lives. They couldn’t be more different as Laurence is a stand-up (or should it be sit-down?) comedian, whereas Charlie worked on an assembly line. Charlie’s work was hard physical labour, but his hours of work and his level of income were far more predictable than Laurence’s. One of the most moving parts of the programme was when Laurence had to leave his young family to spend a month at the Edinburgh fringe. I was about to write that there were no opportunities for people with disabilities in the performing arts in the 1950s but then I remembered that one of the most popular entertainers of the time was Michael Flanders, a polio survivor like my mum and dad who performed in his wheelchair.

Towards the end of the programme Laurence and Adele mention that there are still peoplearound who don’t think that parents with their degrees of disability should have children. Nothing new there then. Adele pointed out that her children will always get the love and attention they deserve. She didn’t think that her life should be viewed as “triumph over adversity”; all she was doing was leading a normal life. These are sentiments that my mum and dad would have agreed with completely.

Wales To Get The New Blue Badge From April

March 26, 2012

New plastic blue badges with extra security features are being introduced in Wales to help tackle abuse of parking for disabled drivers.

The badges will be harder to forge or be used fraudulently when they are brought in next month

Police and parking wardens can check them on the spot against a national database if they suspect abuse.

Welsh government ministers say the badges will be free, unlike some in England and Scotland.

‘Pain and inconvenience’

The current handwritten card badges will be replaced by plastic, electronically-printed photo ID versions as disabled drivers renew them over the next three years.

A UK government report has highlighted widespread abuse of the system which created problems for disabled people and cost £46m a year in parking fee evasion.

Transport Minister Carl Sargeant said: “When people abuse blue badges, or use disabled parking spaces they’re not entitled to, they are seriously affecting the quality of life of those individuals who legitimately carry badges.

“Blue badges allow people in genuine need to live independent lives, and by invading blue badge spaces, other drivers are actually causing not just great inconvenience to the disabled person, but also physical pain.”

The campaign is supported by Paul Davies, a former soldier who was paralysed from the waist down after being injured in a military rugby game in 1983.

Mr Davies, from Bargoed, said he regularly encountered people parking illegally in disabled spaces.

“Drivers take no notice of the signs, either because of laziness or ignorance of how difficult it really can be for a disabled person to park in a normal space.”

Announcing plans for the improved blue badges in December, Mr Sargeant said they would be provided free of charge as a measure to tackle poverty, saying disabled people were almost twice as likely to live in low-income households.

New-style badges were introduced in England and Scotland in January, where local councils can charge up to £10 and £20 respectively for supplying them.

In Wales, it has been suggested that local authorities could be able to fund the scheme by scrapping compulsory newspaper adverts.

Welsh government sources acknowledged criticism from the National Union of Journalists that newspapers could suffer if they lost a source of advertising income worth more than £1m a year.

Old-style disabled parking badges cost £2, with around 230,000 in circulation in Wales.

Although the new badges will be supplied free of charge, local authorities will be allowed to charge £10 for organisational badges or to replace lost badges.

A new national helpline for general inquiries about blue badges – 0844 4630215 – will be introduced on 1 April.

Council Guilty Of Failing Disabled Man

March 26, 2012

A council that failed to fund an extension to a disabled man’s Northampton home is guilty of maladministration, investigators said.

Northampton Borough Council has been told to pay the man and his wife £5,000 in compensation, the Local Government Ombudsman (LGO) said.

The man has a degenerative medical condition and needed an extension to improve his bathing facilities.

Council bosses said they fully accepts the LGO’s findings.

The report is going before the council’s cabinet committee on Wednesday.

It showed that in 2009 the man, who has not been named, applied for the extension for his privately rented home in October 2009.

Two occupational therapists found the extension was necessary and a council officer found the works were reasonable and practicable.

The private landlord had also given permission.

‘Considerable injustice’

However, the council refused to give the disabled facilities grant (DFG) because the man had a shorthold tenancy agreement and instead offered him and his wife a council-owned property, which could be converted for his needs.

LGO Dr Jane Martin said the key legal point was that in applying for the DFG grant “an applicant need only certify an intention to remain in the property for five years and if they leave within that time they will be required to repay a proportion of the grant”.

She said the council was guilty of maladministration causing injustice.

The delay in providing the extension had “given rise to considerable distress and left [the man and his wife] living in very difficult conditions… This is considerable injustice”, she said.

Council leader David Mackintosh said: “We take any case involving the Ombudsman very seriously and fully accept the findings in this case which dates back to 2009.

“The matter will be discussed at cabinet next week where members will consider what lessons can be learnt from this unfortunate situation, and how the council can improve how it deals with these requests in the future.”

Dementia Research Funding £66M By 2015, Government Announces

March 26, 2012

Funding for research into dementia is to be doubled by 2015 to try to make the UK a world leader in the field, David Cameron is due to announce.

The prime minister is expected to say in a speech that the level of diagnosis, understanding and awareness of dementia is “shockingly low.”

Dementia is thought to affect around 800,000 people in the UK, with the cost to society estimated at £23bn.

In the next decade, the number with the disease is expected to top one million.

‘Collective denial’

Mr Cameron will set out plans to step up research into cures and treatments and to ensure that the health and social care systems are equipped to deal with the problem.

Continue reading the main story

“Start Quote

Dementia is simply a terrible disease. And it is a scandal that we as a country haven’t kept pace with it”

David Cameron Prime Minister

Overall funding for dementia research in 2010 totalled £26.6m. Under the plan for 2015, it will be £66m.

Mr Cameron will say: “One of the greatest challenges of our time is what I’d call the quiet crisis, one that steals lives and tears at the hearts of families, but that relative to its impact is hardly acknowledged.

“Dementia is simply a terrible disease. And it is a scandal that we as a country haven’t kept pace with it.

“The level of diagnosis, understanding and awareness of dementia is shockingly low. It is as though we’ve been in collective denial.”

The prime minister will say that the costs associated with the disease are already higher than those for cancer, heart disease or stroke.

“So my argument today is that we’ve got to treat this like the national crisis it is. We need an all-out fightback against this disease, one that cuts across society.

“We did it with cancer in the 70s. With HIV in the 80s and 90s. We fought the stigma, stepped up to the challenge and made massive in-roads into fighting these killers.

“Now we’ve got to do the same with dementia. This is a personal priority of mine, and it’s got an ambition to match.

“That ambition: nothing less than for Britain to be a world leader in dementia research and care.”

‘Role to play’

Jeremy Hughes, chief executive of the Alzheimer’s Society, said the announcement would mark an “unprecedented step” towards making the UK a world leader in tackling dementia.

“Doubling funding for research, tackling diagnosis and calling for a radical shift in the way we talk, think and act on dementia will help to transform lives,” he said.

“There are currently 800,000 people with dementia, yet too many are not able to live well with the condition.

“The PM is leading the way, but from Plymouth to Preston, from the boardroom to bus drivers, we all have a role to play.”

David Rogers, chairman of the Local Government Association’s community wellbeing board, said: “We now need politicians to transcend political point-scoring and wake up to the ticking demographic time bomb this country is facing.

“There needs to be urgent action to ensure the way we offer support to older people is fairer, simpler and fit for purpose in order to truly meet the needs of the most vulnerable members of our society.”

MP Will Use Debate To Oppose Right To Die Law

March 26, 2012

An MP who still works as a doctor is to use a Parliamentary debate to oppose any moves towards so-called “right to die” legislation, saying his experience has turned him against assisted suicide.

 Dr Dan Poulter will warn that current prosecution guidelines on assisted dying must not be passed into law as he believes they have the potential to lead to patients being killed simply to benefit their relatives – a risk he has seen on the wards.

But he will also speak of the need for dignity and compassion for the dying and describe how his own resuscitation of a very ill woman left her spending her last three weeks alive in pain because the procedure broke her ribs.

The backbench debate on Crown Prosection Service guidelines on how to deal with people who assist others to commit suicide is to be held this week, and will be the first time they have been discussd by MPs.

Conservative MP Richard Ottoway has called the backbench debate, which is seeking support for the guidelines, drawn up in 2010 after a landmark court case brought by Debbie Purdy, a multiple sclerosis sufferer who wanted to know if her husband would face jail if he helped her to travel abroad to commit suicide.

Although the guidelines are not law, they make it clear that it is unlikely suspects would be charged unless they were thought to have put pressure on the victim to kill themselves, or had sought to profit from the death.

But Dr Poulter will speak against them – and warn that they should not be turned into legislation, a call being made by some campaigners and which is expected to be discussed by MPs – a debate which could bring legislation a step closer.

Dr Poulter, who continues to work in hospitals during Parliamentary recesses, said: “When I started out as a medical student I was in favour of assisted dying.

That was the position I started from – but my own experience on the frontline doing a lot of late-night calls, often in a ward of cancer patients, changed that view.”

He believes the right support and care can ease not just the pain, but also the feelings of powerlessness that terminal illness can bring.

“I think palliative care and hospice care are invaluable and can change the mind-set of someone with a sense of helplessness that can be felt in the face of death,” he said.

But he warned that the guidelines – which say prosecution is less likely if the victim had reached a “voluntary, clear, settled and informed decision to commit suicide” and if the person involved was “wholly motivated by compassion” – raise serious questions, particularly over how intentions can be proven after the event.

“I cannot see that we could make legislation on this without leaving people open to abuse,” he said.

“I’m not doubting the good motives of most people but I think as a policy it is too well-meaning, too detached from real life.

“Human nature has many drivers other than compassion – especially when there are large sums of money or houses involved”.

As a doctor in training, he witnessed cases which raised alarm bells about the motives of some relatives.

He cites as an example, a case in which the recent husband of a woman with advanced multiple sclerosis seemed more concerned about protecting their assets, than about the care she received.

“From the kinds of questions he asked, we worried about his motivations,” he said.

“The patient had relatively advanced MS – but she was not dying. We were optimistic she would recover and soon be able to go back home, yet his questions were about the assets, about what would happen after her death.”

But he is also to warn MPs at the debate about the need for compassion.

He cited a case when he was 26 and working as a junior doctor when he resuscitated a patient whose heart had stopped.

The woman was in the advanced stages of pancreatic cancer. In her medical notes, consultants had given a prognosis of two to three months, yet during her stay in hospital, no one had informed her relatives that she was dying.

Dr Poulter says: “Rescuscitation is a very brutal experience to undergo, with a very low chance – two or three per cent – of success.

“This patient was saved but she was left with cracked ribs, which made it incredibly painful for her to breathe.

“When I think back, when I remember feeling her ribs breaking and crunching under my hands. She died three weeks later in a lot of pain and distress.”

The failure to have a frank dialogue with the woman’s family before her heart stopped meant the young doctor felt he had no option but to attempt resuscitation, in order to “buy some time” in which the family could attempt to be reconciled to her circumstances.

Afterwards the doctors involved in the case discussed their regrets about the way they had handled it.

“I remember my consultant’s exact words,” says Dr Poulter.

“He said: ‘You would not treat a dog like that.’ Medicine is failing these patients because we are not willing to have a proper conversation about death.”

The Guardian’s Preview Of We Won’t Drop The Baby

March 25, 2012

Part of the DisAbility And Parenting Debate.

When Laurence Clark tells people he is a comedian, he gets one of two reactions. “Either they assume my act is going to be a worthy story of triumph over tragedy,” he says. “Or they’ll use the word ‘inspiring’. I get ‘inspiring’ a lot.”

Clark is not your average standup. In fact, he has been described as “a sit-down comic” because he performs in a wheelchair and uses his experience of living with cerebral palsy as material. Next month he is touring his show, Health Hazard, which he describes as “a one-man mission to sell the benefits of free healthcare”. And just in case anyone is confused by his slurring speech patterns, Clark has been known to open his act with the words: “No, I’m not pissed.”

If some audiences find this uncomfortable, Clark remains unrepentant. “All comics draw on their own experience – that’s the job,” he says, when we meet in the Soho Theatre bar in London. “No one’s telling Jo Brand not to do stuff about eating cake or being a woman.”

Clark, 38, was diagnosed with cerebral palsy when he was born. It interferes with nerve signals to muscles, often arising out of complications developed in the womb and resulting in problems with posture, movement and co-ordination.

After a long labour during which he suffered a lack of oxygen, doctors warned his mother that he would probably have learning difficulties and be unable to look after himself. “I think they actually used the word ‘vegetable’,” he says.

At school, despite being interested in drama, he was advised by the careers office to go into IT. “Computers are like basket-weaving,” Clark says, drily. “It’s a stereotypical occupation for disabled people nowadays because you can do it sitting down.” He ended up getting a PhD in computers and biology. But he found the work boring and started writing comedy scripts. Before long, he was performing: “I thought it was the only way of getting my stuff heard.”

His 2003 appearance at the Edinburgh Festival was the first of six acclaimed shows there and Clark now spends 100 nights a year in comedy clubs up and down the country. He has just won a commission from the London 2012 Cultural Olympiad – the only comedian to do so.

Has he ever been heckled? “I can only remember one time and it was just a knob basically, shouting abuse.”

But it is not only as a comedian that Clark is seeking to challenge our notion of what disabled people can or can’t do. He and his wife Adele, 34, who also has cerebral palsy, are parents to two able-bodied sons: Tom, eight, and nine-month-old Jamie. As a couple, they refuse to be defined by their impairment in a society that is still shockingly unused to seeing disabled parents intent on pursuing independent lives.

When Adele was pregnant with Tom, she remembers going to the chemist in her hometown of Liverpool to buy folic acid tablets and being looked up and down by the checkout girl. “She said: ‘I just didn’t think people like you could have babies,” Adele recalls. “I could write a book on all the times people said things like that to me.”

The Clarks’ story is featured in a documentary tonight on BBC1 as part of the Beyond Disability season, a series that looks at our attitudes to disability in the 21st century. In We Won’t Drop the Baby, narrated by David Tennant, the Clarks are shown juggling their daily lives around caring for their children in much the same way as any other family. Their house is adapted for their needs (with wheelchair access and electronic key fobs) and they rely on help from grandparents and “personal assistants” employed directly from their care budget, which is provided by the state.

“We don’t say ‘carers’ because that implies something being done to you rather than something you’re in control of,” says Laurence. Recent government cuts have not made this way of life any easier. “It’s getting more and more difficult to get funding for independent living, yet at the same time people are being taken off incapacity benefit and being told to get out and find jobs.

“Part of the problem in how people think about disabled parents is that you don’t tend to see them portrayed that much in the media and, when you do, the footage is all focused around young carers, looking after their parents – downtrodden children who have been put into this situation.”

Tom is far from being downtrodden. He is an energetic, happy boy obsessed with Doctor Who. “It was only when he started primary school he probably began to notice a difference [with the other parents],” says Adele, who jointly runs the training and consultancy company Difference Matters with her husband. “But we don’t make an issue of it.” Occasionally another child will say something. “The classic is ‘You mustn’t be able to play footie because your Dad can’t kick back.’ He would just say: ‘For one thing, I’m not into footie and if I did want to play I’d do it with my granddad, who’s a massive Liverpool fan.'”

There are still those who argue that it is unfair to bring up a child in a restricted environment where parents cannot fully participate in physical activities. What do the Clarks say to that? “We decided to have kids for the exact same reasons that anyone else decides to have kids,” says Laurence. “If nothing else, this documentary shows us being good parents.”

Adele adds: “The other issue is that as a disabled person, your sexual identity isn’t respected… There’s a notion that we, as disabled people, are infantilised.” Cerebral palsy is not hereditary, so that was not a concern for either of them and the Clarks refused to have any prenatal tests for impairment. “I think our biggest worry was that he [Tom] could have turned out a Tory,” Laurence jokes.

Growing up with parents who have limited mobility has affected their children in positive ways. According to Adele: “We’ll be out as a family, and if there’s no wheelchair access Tom will ask off his own bat ‘Why haven’t you got a ramp?'” In fact, though some parenting tasks might require more effort than for able-bodied parents Adele believes: “We’re not disabled by the conditions we live with, but by societal values and the assumptions people make – it’s a load of baloney.”

What would they like to come out of this documentary? Laurence grins. “I wouldn’t mind being on Live at the Apollo with Michael McIntyre.”

Welsh Remploy Campaigners’ Petition

March 25, 2012

Campaigners claim support is growing in a bid to save Wrexham’s closure-threatened Remploy factory.

A group of workers and their supporters were in the town on Saturday gathering signatures for their petition to retain the factory, safeguarding 42 jobs.

It is one of seven Welsh sites facing closure by the UK government, with the jobs of 272 disabled people threatened.

It comes after a review said money would be better spent helping people, rather than investing in factory units.

A march was held a week earlier in the town in protest at the plans.

The Welsh government wants funding for the organisation to be devolved in Wales.

Wrexham MP Ian Lucas last week raised parliamentary questions with UK government ministers about procurement policies regarding Remploy factories.

£6m projected loss

“Locally, I am continuing to push for detailed figures regarding the Wrexham site,” he said.

According to a report from accountants KPMG published earlier this month, the Wrexham factory is expected to make a loss of £878,000 over the current financial year.

“I asked ministers for these months ago, but the brief KPMG report they released recently contains very little detail,” said Mr Lucas.

“I have meetings set up with various groups in the coming weeks on Remploy and will continue to push for greater transparency.”

The KPMG report showed that the Welsh Remploy sites are projected to lose more than £6m this financial year.

Remploy was established in 1946 as part of the creation of the welfare state.

Workers are employed in enterprises that vary from furniture and packaging manufacturing to recycling electrical appliances and operating CCTV systems and control rooms.

But an independent review into the businesses said money would be better spent supporting individuals, rather than investing in loss-making factory units.

The move has been criticised by politicians in Wales, where only two Remploy factories – at Porth and Neath – will stay open.

What Is It Like Being A DisAbled Dad?

March 24, 2012

Part of the DisAbility and Parenting Debate.

Laurence Clark is a stand-up comedian who has cerebral palsy. He lives with his wife Adele and his two sons Tom, seven, and Jamie, nine months. Here he describes both the challenges and the attitudes people have towards families like his.

I guess my family does not fit with the typical image of 2.4 children. But wouldn’t it be boring if all families were identical?

One bizarre reaction I often get is people thinking that I’m somehow depriving my children of physical activity because their dad is a wheelchair user.

I typically get comments like: “Isn’t it a shame the boys will never get to play football with their dad?”

But there are lots of other different types of play which are accessible that I can do with the boys, such as reading, jigsaws or going to the cinema, and if they desperately wanted to play football then they have a footie-obsessed granddad who is more than happy to oblige. And we do live in Liverpool after all.

Over the years I’ve also found there seems to be this general misunderstanding that disabled people have kids in order to provide them with a free source of “care” or support.

Whenever issues around disabled parents make it into the media, it’s typically around the lack of support for young carers. Indeed sometimes I can’t help but feel that society seems more comfortable with the notion of my children looking after me – rather than supporting me to look after my children.

Of course, no child should be put in a position where they are being relied upon by their parents for basic day-to-day support. One thing about my family which surprises people is that we manage our own support and don’t expect our kids to “look after” us.

We have a personal budget from our local authority which we use to employ personal assistants to support us with day-to-day living, including our roles as parents. This can involve helping us do tasks like getting our kids to nursery or school in the mornings, washing their clothes and preparing meals.

However more and more government cuts to local authority funding are, in turn, having a huge effect on local social care provision for people like us. Only this week Chancellor George Osborne announced in the Budget a further £10bn cut in welfare spending in 2016-17 from the forecast bill.

To me, giving disabled parents adequate support makes good sense, as the knock-on effect is fewer children being placed in the position of having to provide support for their parents. Instead disabled parents would be able to fulfil their roles as parents, thus freeing their children to get on with simply being kids.

There’s also a misconception that disabled people with my degree of impairment are incapable of being parents at all.

When we’d tell people we were expecting we’d get one of two reactions. They either assumed we must have had IVF because we couldn’t possibly have done it the old-fashioned way. Or they would shake my hand firmly and say “Congratulations” while I could see them thinking: “How the hell did he manage that then?”

It is often said that a defining point in any child’s development is the moment when they realise they are better than their parents at doing a particular thing.

To the best of my knowledge, this moment arrived for my older son Tom on his fifth birthday when he asked me to help him play a game on his new games console. It was then I discovered that most video games are not really designed for the co-ordination skills of someone with cerebral palsy.

Of course, another common reaction I get when I tell people that I’m a dad is that I’m apparently “inspirational”. These sorts of reactions really get on my nerves as they assume that I’m some sort of special case, when in fact there are thousands upon thousands of disabled people who choose to take the parenting plunge.

That said, as a child I can’t remember ever seeing any adults with cerebral palsy who had become parents. This in turn had a knock-on effect on expectations for my later life, since if you are not used to seeing people like yourself taking on responsibility and living full lives then it becomes harder to envisage yourself doing these sorts of things in the future.

It was only as an adult that I finally met some disabled parents and realised this was not some impossible dream.

I guess Adele and I didn’t decide to have children to have them “look after” us or to prove a point, but for probably the exact same reasons as everyone else who decides to start a family.

My kids are used to having a dad who uses a wheelchair because they’ve never known any different. It’s only when other people comment or make an issue of it that it ever becomes a problem for us.

Christopher Lines

March 24, 2012

A man who suffered brain damage after being wrongly prescribed an overdose of medication has agreed a multimillion-pound compensation package.

Christopher Lines, 33, from Colchester, is now dependent on others and has limited use of his arms and legs.

North Essex Partnership NHS Foundation Trust admitted liability and settled the damages claim.

The High Court in London ruled he would receive a £2.1m lump sum and annual payments of £205,000.

‘Appalling’ treatment

During the hearing, the trust’s counsel James Watson QC made an unreserved apology for its failings.

Mr Lines was prescribed the wrong medication regime at the Lakes Mental Health Unit, in Colchester, in June 2008.

The claim was brought on Mr Lines’ behalf by his parents, Steve and Carole.

After the hearing, Steve Lines said: “Pursuing this claim has taken four years out of our lives and had a profound effect on our family.

“Christopher’s settlement will, no doubt, seem like a lot of money to some people, but every single penny will be needed to ensure that Christopher is well looked after on a daily basis and that his future is securely provided for.”

He added: “The treatment Chris received from the medical profession was appalling. He needed their help, but they have destroyed his life.

Trust’s apology

“He can no longer kick a football with his son or enjoy watching him grow.

“There is sadness in our lives because of this, but also a lot of joy, as every day brings another milestone, when Chris laughs or remembers words we thought he had lost forever.”

A spokesman for North Essex Partnership NHS Foundation Trust said: “The award of compensation will enable Mr Lines to receive suitable care throughout his life.

“Christopher Lines suffers from profound brain injuries, sustained while he was a patient on Maple Ward in 2008.

“The trust has previously admitted liability and apologised to him and his family.”

Diabetes Amputation Rates ‘Scandalous’ Says Shadow Health Minister

March 24, 2012

A health minister has hit out at “scandalous” variations in the amputation rates for diabetes sufferers in England.

Paul Burstow said eight out of 10 amputations are “unnecessary” and could have been avoided through better care.

The minister told the Commons that the Government is committed to seeing improvements in the treatment offered to sufferers. Amputations are performed when diabetics suffer damage to blood or nerve vessels as a result of their condition.

Labour’s Keith Vaz, who has type 2 diabetes, said there are “shocking” differences between parts of England and warned the Government’s health reforms could make the situation worse. He said: “There are shocking regional variations in diabetes care. Eighty per cent of amputations due to diabetes can be prevented with the right checks.”

In his Leicester East constituency, he told MPs the number of annual amputations per 1,000 adults with diabetes is 1.4, significantly below the national average of 2.7.

“However a sufferer who lives in Swindon is twice as likely to have an amputation,” he said, as the rate is four amputations per 1,000 diabetic adults.

Mr Vaz warned: “Changes in the Health and Social Care Bill will mean more power is devolved to a local level. I’m very concerned this may worsen regional inequalities.”

Mr Burstow said there is evidence of “unjustifiable variation in the levels of care and treatment from one postcode to another” but stressed “there has been significant progress”.

He acknowledged there is “still a scandalous picture when it comes to amputations in England” with variations from one part of the country to another which are “inexplicable and shocking”.

“We know that on average 73 amputations take place every week, that eight out of 10 of those operations are unnecessary because they could be prevented by simply following what we know works,” he said. “It’s getting those messages out and translating that into practice by clinicians that is absolutely key. Programmes like foot care, where a foot care team is established for a relatively modest investment, can see a fall in the rate of amputations by as much as 50%.”

Blind Woman Learns Braille Aged 90

March 23, 2012

Amazing.

A woman from the Cynon Valley who started losing her sight 10 years ago has learnt Braille at the age of 90.

Nansi Selwood can now see almost nothing apart from some shapes and the difference between light and dark.

But Mrs Selwood, from Penderyn, said learning Braille had “filled a big gap in her life”.

Her teacher said learning the system took a lot of practice and determination, and was a remarkable achievement at such an age.

Mrs Selwood said that when her sight began to fail it was a difficult time.

“It was very gradual but very persistent,” she said.

“It was a terrible blow because you lose your independence.

“Knowing that it was getting worse was the difficult part. If you know you’ve got it and there’s a plateau, you can adapt to that, but there was no plateau. It was always downhill.

“You could see less this week than you could see last week. Or you could see less clearly and that was a terrible burden.”

It was particularly tough because books had always played such a big part in the life of the former teacher, author and historian.

Continue reading the main story

“Start Quote

All my life I’ve been a bookworm. I’d read anything – I found the written word fascinating”

Nansi Selwood

“All my life I’ve been a bookworm. I’d read anything – I found the written word fascinating,” she said.

“When I was a child, it sounds pretentious really, but one of the books that really got me reading was the Complete Works of Shakespeare, and that was because it was the only book in the house.

“It had been given to my father who only spoke Welsh. He couldn’t read it but he was very proud of it.

“He was most amazed that I should read it. And it was the histories and the tragedies that I liked.”

Determined to succeed

As she began to lose her sight, Mrs Selwood was determined to be able to continue to read.

She asked the sensory team at Rhondda Cynon Taf council for help.

Initially, there was no teacher, but when one was able to visit her at the farmhouse she has called home since 1939, she was determined to succeed.

“It was hard, but a challenge and I did enjoy parts of it,” she said.

“When I had to learn the alphabet, I had to visualise it. I really thought that within a year I’d be able to read.

“But it took me four years before I was able to read. And that was slow, very slow.”

She has gone on to improve her Braille reading skills and can now use a faster, more advanced form of the system.

Her achievement is all the greater considering fewer than 1% of the 2m visually impaired people in the UK are users of Braille.

Throughout the period Mrs Selwood has been learning, her instructor Lynda Dixon has been impressed with her progress.

“I’ve never worked with anyone who has started learning Braille in their 80s. It’s quite a remarkable achievement,” she said.

“It takes a lot of patience. It takes a lot of practice and determination. It’s difficult as you get older because it is learning a new language.

“And it’s difficult because you need to have good sensitivity in your fingers. There’s a lot of barriers against it but if you can persevere, it’s very worthwhile and I think very rewarding.”

‘Lovely surprises’

In order to help Mrs Selwood stay in her home, many of her household gadgets have been adapted, such as a microwave oven which speaks its settings, and a device to ensure she does not overfill a tea cup.

However, it is the ability to keep reading even though she has lost her sight that makes her life most pleasurable.

“It’s made a tremendous difference because one of the things about growing old is that time can be very long,” she said.

“It’s filled so much time and it’s provided some lovely surprises with books that I would never have read otherwise.

“Learning Braille has filled a big gap in my life.”

Green Mayoral Candidate Will Make Third Of Tube Step Free

March 23, 2012

London’s Green Party mayoral candidate said she would make a third of the Tube network step-free by 2018, if elected.

Jenny Jones visited Stockwell Tube Station, in south London, to launch her “accessibility manifesto”.

Ms Jones said: “We need to aspire to an inclusive transport system, where no-one is prevented [from] using London’s public transport.”

Of the 270 stations on London Underground, 64 are step-free from street to platform.

“In the year that the Paralympics will be held in London, it is shameful that the overwhelming majority of the Tube system is still inaccessible to hundreds of thousands of people,” Ms Jones added.

“This is nothing short of transport apartheid.”

Accessibility manifesto

Transport for London said the number of step-free access stations had increased by 70% since 2000.

It said the number of stations with step-free access would rise to 66 by the Olympic Games, as Wembley Central and Farringdon become step free.

The Green Party issued a Tube map showing only inaccessible stations, highlighting the limited journeys that can be made.

The party’s accessibility manifesto also includes pledges to make bus stops accessible by 2018, for 15% of new homes wheelchair accessible and to ensure everyone can access parks and play spaces.

The London mayoral election takes place on 3 May.