Tuesday, March 31, 2009

Employment company begins drive to keep disabled in jobs

REMPLOY, the UK's leading provider of employment for disabled people, has launched a drive to win new orders to secure more jobs.
Over the past year Remploy has placed 800 disabled people in Scotland into jobs.

The firm has a recruitment branch at Tollcross which was officially opened by Education Secretary Fiona Hyslop last year.

Remploy says it faces significant challenges and will work with the Scottish Government to meet them. A spokeswoman said: "In the midst of a recession, Remploy is redoubling its efforts to ensure that we continue to secure orders for goods from its Scottish factories and find sustainable job opportunities across various employment sectors.

"Our textile factories in Dundee, Stirling, Cowdenbeath, Leven and Clydebank have secured some orders. However, we know that we need new orders to ensure the continued viability of all our sites in Scotland."

The firm is holding a reception in the Scottish Parliament tomorrow night hosted by Labour MSP Helen Eadie.
 
NEWS.scotsman.com, 31st March 2009

Mencap deploys Extreme Team to raise cash

Disability charity Mencap has announced various events over the coming months in which its Extreme Team will raise money for those with learning disabilities by performing challenging tasks.

The events the Extreme Team will be undertaking include a six-day marathon in the Moroccan Sahara, covering 150 miles of rocky terrain under 120 degrees Fahrenheit temperatures, which takes place this month.Olympic legend James Cracknell will be tackling the marathon to raise money and awareness and has said that although the race will be tough, even by his standards, he is glad to be doing it for a worthwhile cause.Mark Goldring, chief executive for Mencap, said: "As well as having the experience of a lifetime, the money raised will help Mencap support people with a learning disability in the UK to be more independent by living in their own homes and having access to employment, leisure and relationships."The disability charity has also recently invited filmmakers and photographers to enter its Snap! competition, which aims to raise awareness of the difficulties of living with a learning disability.

Mencap, 31st March 2009

SCIENCE CENTRE CAFE SHOWCASES AUTISM TALENTS

The National Autistic Society (NAS) is holding a free exhibition of artwork by adults with autism at Explore-At-Bristol's cafe until April 24.

The exhibition, which marks World Autism Awareness Day on Thursday, uses art and photography to explore how the developmental disability affects the way people communicate with and relate to the world around them.

The artwork is displayed alongside comments from the artists and photographers, who are all affected by autism in different ways, and highlights the wide range of experiences of people with the condition.

Chris Peach, NAS regional director, said: "There are more than half a million people with autism in the UK - that's one in 100 - and many adults with autism tell us how important art and creativity are in their lives. The variety and quality of the work on show is just incredible and I'd like to thank Explore-At-Bristol for helping us bring this exhibition to the city. We hope it will show just some of the realities faced by people with autism today."

Selina Postgate, from Bristol, is 54 and has Asperger syndrome, a form of autism. She said: "Knowing I have Asperger syndrome has changed everything in my world, it's made me realise who I really am and why I think differently.

"Because I'm articulate, people don't think I need any help, but my inability to cope with day to day tasks has had a huge impact on my mental health. It took the support of an advocate to finally get me the help I need. I have personal assistants now and that has made a huge difference to my life."

Danny Beath, 48, from Shrewsbury, who also has Asperger syndrome, is exhibiting a photograph called Children In The Mist, which was taken against the setting sun inside a mist tent at the Missouri Botanical Gardens in St Louis, United States.

He said: "When I took the photograph I felt like the outsider looking in, rather like the third misted out one in the picture.

"It's really important to me to be able to demonstrate to the public what living with autism can feel like sometimes.

"My difficulties with social interaction and communication often make me feel like I live on the edge of things - like I'm always looking in at groups of other people."

Autism is a lifelong developmental disability that affects how a person communicates with, and relates to, other people. It also affects how they make sense of the world around them. It is a spectrum condition, which means that, while all people with autism share certain difficulties, their condition will affect them in different ways.

Some people with autism are able to live relatively independent lives but others may have accompanying learning disabilities and need a lifetime of specialist support.

Chris added: "The services and support available to people with autism and their carers are woefully inadequate. While some people with autism may need a lifetime of specialist support, others, given the opportunity, would be able to live relatively independent lives. That's why it's so important that we all stand up and speak out in order to gain the right level of help, support and understanding for all people affected by autism."

NAS, along with 20 other autism charities, is using World Autism Awareness Day to call on people across the UK to Stand Up for Autism - a theme chosen to highlight how many people are personally affected by the condition.

Celebrities including Jane Asher, Eamonn Holmes, Ruth Langsford, Michelle Collins, DJ Judge Jules and Brit award-winning band Elbow, are among those who have already pledged their support.

The NAS relies on the support of its members and donors to continue its vital work for people with autism. To become a member, make a donation or to find out more about the work of the NAS, visit the NAS website www.autism.org.uk

For more information about World Autism Awareness Day 2009 visit www.waad.org.uk

Community Newswire, 3ist March 2009

Charity receives Total support from Watford company


Total UK volunteers (L-R): Sara Jarman, Emma Maclaren, Neil Robinson, Gemma Sheperdson, Jimmy Lellou, Arunan Sriskanda, Iain Cracknell, Jamie Brodie.




A charity that supports adults with physical and sensory difficulties has received a £350 donation from a Watford company.

DRUM (the Disability Recreation Unity Movement) will use the money from Total UK, based in Clarendon Road, to maintain and improve its community centre base in Southwold Road, in time for the summer.

Eight volunteers from the company, which named DRUM its Community Champion in 2008, visited the group to help clean up their garden and build some fencing.

They were also able to design and paint their own ceramic tiles, before taking part in a yoga and art class.

Emily Cooper, events and sponsorship executive for Total UK, said: “We are glad to support a charity that continuously strives to help the community. The volunteering team had a great day and enjoyed helping out with all the different activities. It’s been a real eye opener to see the amount of work this group gets involved with and the difference it makes to the lives of so many people. ”

Sarah Sullivan, DRUM manager, added: “It’s been great to receive support from Total. By donating a few hours of their time, each volunteer has really made a difference. We are always busy striving to help various members of the community, so it was great to have the extra pairs of hands for the day.”

Drum website


Watford Observer, 31st March 2009

Human Rights Act

Apart from protecting the right to protest, freedom of speech, family life, human dignity, privacy, the right to not be tortured and the right to not be unlawfully killed, what has the Human Rights Act ever done for us?

Unlock Democracy publish a new report today highlighting how the Human Rights Act has protected civil liberties in the UK since its introduction in 1998. Protecting rights: how do we stop rights and freedoms being a political football? by Francesca Klug and Helen Wildbore also examines why the Human Rights Act has become mired in political controversy in recent years.

Adapting her speech given at the Convention on Modern Liberty on Saturday 28 February, Francesca Klug writes:

“Every member of the Council of Europe has not just signed and ratified Churchill’s charter – the European Convention on Human Rights – but has, through one means or another, incorporated it into their law. This is what we did ten years ago through the Human Rights Act. Other countries have bills of rights that stand alongside the ECHR or build on it, as we could, of course. There is a forceful and creditable argument for this. But all modern bills of rights are based on the post-war human rights framework. No-one, besides us, is contemplating de-incorporating the ECHR from their law. Why? Because it is there precisely to stop governments from turning rights and freedoms into a weather vane or political football; depending on who is in power or in favour.”

Helen Wildbore’s extensive appendix lists 23 examples of how the Human Rights Act has been used to defend human rights, ranging from limiting the scope of libel laws to defend freedom of expression and defending the rights of Iraqis unlawfully killed by British armed forced through to defending the rights of disabled people and same-sex couples.

Commenting on the pamphlet, Director of Unlock Democracy Peter Facey said:

“The debate over the Human Rights Act can at times resemble the ‘What have the Romans ever done for us?’ sketch in Monty Python’s Life of Brian. It is frequently abused while the positive contribution it makes to the lives of thousands of people every day is disparaged.

“The Human Rights Act is regularly attacked both for failing to prevent all abuses of state power and for infringing ‘Parliamentary sovereignty’ when it does. Its critics cannot have it both ways. Equally, people who call for it to be scrapped and replaced by a different Bill of Rights need to explain what rights of the European Convention of Human Rights they are opposed to.

“As Francesca says ‘no bill of rights will guarantee freedoms in testing times if people do not remain vigilant.’ There is a case for strengthening human rights legislation in the UK and we certainly need to inform the public more about what rights the Human Rights Act actually protects, but ultimately if the public and politicians are not prepared to stand up for rights they will wither.”

Unlock Democracy, 30th March 2009

£1 million investment to bring quality play facilities to Devon

MORE than £1m is being invested into providing high quality play sites for children across Devon, it has been announced.
 
Devon County Council has successfully secured £1.1 million from the Government's Playbuilder Project, for the development of 22 or more play areas for 8-13 year olds across the county.
 
Funding is targeted particularly at sites that encourage and enable physically active play and include an element of risk and challenge. They are also looking at projects which are attractive to girls and inclusive of minority ethnic groups and which more children, including disabled children, can access safely.
 
Councillor John Smith, Devon County Council's Executive Member for Children and Young People's Services, said: "We are committed to providing more safe and stimulating play areas for our young people across the County.
 
"Play is vital for the development of our children and young people and this funding will enable more people to provide these play opportunities for our young residents."
 
Funding is for capital projects only, and can therefore only be used for developing sites, not ongoing maintenance.
 
Children and young people and their communities must be involved in deciding what should be in the play space and what the money should be spent on.
 
Devon County Councillor Vanessa Newcombe, Chair of the Playbuilder Project Board, said: "This is fantastic news that we have received over a million pounds to enhance and develop play facilities across Devon, and improve access for a whole range of children and young people.
 
"We are hoping to see some really inspirational and creative ideas from the groups applying for funding, that will leave a legacy to future generations of children, as well as providing a focus for some great partnership work in local communities.
 
"We see local communities at the heart of delivery on play and given the very local level of play provision will be working closely with District-level play partnerships.
 
"We will encourage new community-led proposals and bids on play. Community groups and the local voluntary sector make a major contribution to local play provision - these groups will often have a particularly helpful role to play in ensuring provision is inclusive of all parts of the community and that parents and children are actively involved. "
 
The project will be launched on April 6, and expressions of interest will be invited until 15 May.
 
Any groups or organisations would like further information can visit the website www.devon.gov.uk/play.
 
Devon 24, 30th March 2009

Mobility scooter riders given riding lessons

David Law, Traffic Manager for Norfolk Constabulary  talking the Mobility Scooter Awareness Course at the Marina Centre.
David Law, Traffic Manager for Norfolk Constabulary talking the Mobility Scooter Awareness Course at the Marina Centre.
SAM WILLIAMS
30 March 2009 12:00

EN reporter gets mobility scooter lesson


They are a vital lifeline for many disabled people, but mobility scooters can also be a menace and have been involved in scores of injuries and even deaths.

And in an attempt to help improve scooter safety and skills, riders were put through their paces in an obstacle course in Yarmouth - and if judged a success a similar scheme could soon be coming to Norwich.

The Mobility Scooter User Awareness Course was organised by Norfolk Constabulary with support from Norfolk County Council after concerns were raised by people living near Northgate Street in Yarmouth at a police safer neighbourhood team meeting last September.

While the scooters - some of which are capable of 8mph - are essential to many disabled people, fears were raised that some riders were posing a danger or were themselves being put at risk by careless motorists and bins obstructing the pavements.

Despite scores of accidents nationally, scooter riders do not have to pass any tests before using the vehicles on roads or pavements and insurance is not compulsory.

In 2002, Kathleen Vignaux, 94, died when her scooter was hit by a car as she tried to cross Fakenham Road in Drayton in 2002.

The following year, pensioner Kathleen Howes, then 79, suffered bruising to her leg after being knocked off her mobility scooter by a car in a hit-and-run on Charlton Road, Norwich.

An elderly woman also had a narrow escape on her mobility scooter at a level crossing in July 2008 when she was nearly hit by a train in Attleborough.

At Saturday's event at the Marina Leisure Centre riders were guided through the obstacle course to test and improve their skills and were offered eyesight tests and information on scooters and insurance.

Mother-of-two Yvonne Jones, from Yarmouth, who has had a scooter for about 10 months, said training should be offered for all riders.

She said: "I learnt to use my scooter by trial and error and at first it was very difficult. People should be offered courses like this when they first use them. You wouldn't give anyone a car without making sure they can use it.

"For me my scooter is a lifeline. As a single mother-of-two I wouldn't be able to get my girls to school otherwise."

Janet Cherrill, from Yarmouth, who is diabetic and rides a scooter, also backed the event, saying: "This is a very good idea. Riding over potholes on the roads can be very wobbly."

Penny Carpenter, crime reduction officer for Norfolk Constabulary, who organised the event, said there was a lack of training available for mobility scooter riders.

She said: "We have got safe cycling courses for children and driving lessons for car and motorbike riders but when it comes to mobility scooter riders there is a gap.

"We are trying to improve handling and manoeuvrability and get people feeling more confident.

"There have been problems with people coming off pavements and not looking and coming out between parked vehicles on Northgate Street.

"It's about time someone took hold of this issue as members of the public see it is a problem."
 
Norwich Evening News, 30th March 2009

Charity scoops first grant from new fund

A charity working with disabled and excluded people across Scotland has pledged to expand and extend its services, after receiving the first grant from a Scottish Government fund for social enterprise.

Momentum, which works with a range of groups, including those who have suffered brain or spinal injuries, physical or learning disabilities or mental health problems, has been offered a £200,000 grant and £300,000 in loans from the Scottish Investment Fund.

The fund is aimed at giving established voluntary sector organisations the chance to dramatically step up their work, by increasing efficiency, and building capacity and financial sustainability.

The funding will enable Momentum to open its flagship Scottish HQ tomorrow, at Watermark Park in Govan, Glasgow, at a launch event which will be addressed by Glasgow City Council Leader, Steven Purcell.

Every year, Momentum helps around 2200 disabled and excluded people to live independently, gain skills and secure and retain jobs, in more than 30 locations from Aberdeen, Inverness and Fife to Glasgow, Ayrshire and the Borders.

Momentum and its subsidiary organisations provide training, rehabilitation, employment, social care and social enterprise for a wide network of services.

The charity includes social enterprise firm Haven Products, which provides employment and rehabilitation opportunities for disabled people while operating a commercially viable business from its three sites: Hillington, Ballieston and Inverness.

The company specialises in printing, packaging and product finishing, and around 80% of the staff have a disability.

Ian Welsh, director of UK services for Rehab Group, which incorporates Momentum, said the funding and the new HQ would allow Momentum to provide more extensive help to a wider number of people: "This is a key investment which will allow us to continue and extend the work that we do to support people across Scotland to identify and achieve their goals.

"Since 1990 we have continually expanded and developed new innovative services and thanks to this significant award from the Scottish Investment Fund we can continue to build equal chances, equal choices and equal futures for people in Scotland," he added.

Robert Sturgeon will also speak at the launch. A Momentum client, he was a head chef until a stroke three years ago at the age of 49 had a devastating effect on his health and capabilities. After work with Momentum's pathway service he is now able to manage his injury and intends to return to work part-time.

"Since joining Momentum's Pathways service I've confidently progressed each week. With the help of staff there I have mastered interview skills, writing my CV, compiling speculative letters and completing application forms for future employment," he said.

"I have no doubt that Momentum's Pathways service has improved my chances of success."

Councillor Purcell said Glasgow City Council had a long relationship with Momentum on a range of initiatives, adding: "The work they do for some of the most vulnerable people is first class. Helping more people into employment will benefit the whole city."

Enterprise Minister Jim Mather said Momentum was an ideal candidate for the Scottish Investment Fund: "This very impressive enterprise reaches individuals where the public and private sectors do not operate, creating valuable employment opportunities."

"It is especially important in the current climate that we harness the Third Sector's ability to help increase sustainable economic growth, build on our economic recovery programme and help Scotland emerge faster and stronger from the downturn."

The £30m fund was launched by Ministers last summer to support established Third Sector organisations with the potential to grow their turnover or become financially sustainable. The fund is managed by Social Investment Scotland on behalf of the Scottish Government.

Craig Campbell, chief executive of Social Investment Scotland, said: "These awards are designed to help recipients develop their potential and make a positive difference to the communities they serve. Momentum is a fantastic example of a social enterprise that has the drive to succeed and bring benefit to its respective community, while also contributing to the wider economy."

www.momentumscotland.org, 30th March 2009

 

Monday, March 30, 2009

New group to provide autism support

A NEW Swindon branch of the National Autistic Society is being launched this week to support local families affected by a disability which touches the lives of half a million people in the UK.

The launch takes place on Thursday to coincide with World Autism Awareness Day as the newly-formed group hopes to support families in the area affected by autism across the spectrum.

Sally Grubb, branch officer for the new Swindon group, said: "There is a real need for help and support for people affected by autism in Swindon, so this new branch of the NAS will be a fantastic addition to the local community.

"Autism is a serious, lifelong and disabling condition, yet many people with the condition struggle to access the help they so desperately need. It does not have to be like this.

"The right help at the right time can make a huge difference. We'll be offering advice and support group meetings along with social events and workshops for families from all over the local area."

The branch will hold its launch at 2pm on Thursday as part of a day of activities being held at the Drove People's Campus in Southampton Street to highlight autism.

In the morning, the Swindon-based charity DASH (Discovering Autistic Spectrum Happiness) will be holding a training workshop entitled 'Adults with Asperger's Syndrome: helping your service to meet their needs' which is aimed at professionals. It is already fully booked.

However, the afternoon launch of the Swindon NAS branch will be open to parents and carers of those across the autistic spectrum to find out more about what they will be doing and what help they will be able to provide.

The new NAS Swindon and District Branch brings together representatives from established local autism support groups SCAAS (Support for Carers of Adults with Aspergers in Swindon) and DASH.

Sally added that the new branch will provide information, support and signposting services, as well as activities such as family fun days, skittles and barbecues.

The branch also provides a social group for young adults with Asperger's Syndrome, a form of autism.

For more information about the branch, please contact Sally Grubb on 01793 770079 or email swindon@nas.org.uk

Swindon Advertiser, 29th March 2009

Warner Wins Fan of the Year

Ipswich Town Football Club

Town’s disability liaison officer Warner Duff was named the EA Sports Fan of the Year at the 2009 Football League Awards on Sunday evening. Warner received the award at a dinner held at the Grosvenor House Hotel in Park Lane.


The Fan of the Year judging panel outlined why they felt Warner was a worthy winner: "Warner is a lifelong fan, whose selfless commitment and support has seen him not only overcome his own personal disabilities but dedicate himself to helping other Ipswich supporters in similar situations and improve their matchday experience.

“The judging panel feels Warner is a truly deserved winner of the EA Sports Fan of the Year title."

Warner was recently named Club Employee/Volunteer for 2009 by the National Association of Disabled Supporters (NADS).

TWTD, 29th March 2009

Part 2: UK and UN CRPD - Article 33 Implementation & Monitoring

un-logo.jpegIn a previous post, we said that we'd go through relevant articles in UN Convention on the Rights of Persons with Disabilities. The UK will be implementing this Convention in Spring 2009.

In this post we will focus on Article 33: National Implementation and Monitoring.

It might seem an odd way of approaching the Convention, since we've not gone through other relevant articles yet. However, for people to take the forthcoming posts more seriously, we need to highlight what the role of deaf people could be.

The relevant text is (you don't have to read it, this will be broken down below):

Article 33 - National implementation and monitoring

1. States Parties, in accordance with their system of organization, shall designate one or more focal points within government for matters relating to the implementation of the present Convention, and shall give due consideration to the establishment or designation of a coordination mechanism within government to facilitate related action in different sectors and at different levels.

2. States Parties shall, in accordance with their legal and administrative systems, maintain, strengthen, designate or establish within the State Party, a framework, including one or more independent mechanisms, as appropriate, to promote, protect and monitor implementation of the present Convention. When designating or establishing such a mechanism, States Parties shall take into account the principles relating to the status and functioning of national institutions for protection and promotion of human rights.

3. Civil society, in particular persons with disabilities and their representative organizations, shall be involved and participate fully in the monitoring process.

Point 1:
There needs to be a focal point(s) in the government. i.e. central point(s) to co-ordinate to make implementation happen. There are different levels of goverment. E.g. local authority, government departments like the Department of Health and other services such as the police, etc. The Convention will apply to all of these levels.

Point 2:
There needs to be framework (plan / outline) set up by the government. The framework needs to include independent mechanisms. The setting up the framework needs to follow the principes in the Convention. The aim of this framework is to promote, protect and monitor implementation of the Convention.

Point 3:
This one is important, and is relevant to you.

It says that:
(a) disabled people (which includes deaf) and;
(b) their representative organisations

shall be:
- involved
- participate fully

in monitoring.

In other words, to check if the Convention is working in practice. So, this Convention is going to be effective in the UK, you need to try and understand it, plus participate. Representative organisations need to be involved too.

Who are the Reprsentative Organisations?
So what does representative organisations mean (under point 3)? For deaf input, many deaf organisations can claim to have a membership base, thus can go running to the government and say that it is representative of us. "We have a membership base, so we represent deaf people!". They might have the numbers to prove it because their base might consist of people who are 70+ a little bit hard of hearing, and subscribe to their magazine. Not that I am dismissing older people here, just trying to get a point across that numbers are not the same as democratic processes or involement. Would such an organisation be qualified to represent BSL users, etc? Who decides on representation, how is this defined and how can power be placed in the hands of deaf people themselves?

Who are likely to be the UK government institutions?
It appears that the co-ordination role for implementing the UN Convention in the UK is being done by the Office for Disability Issues (ODI). The ODI has an Equality 2025 committee, described as a "network of disabled people which advises the Westminster Government on how to achieve disability equality.

Secondly, we think that the Equality and Human Rights Commission (EHRC) will part(?) take on the role of independent monitoring. The Convention requires something called National Human Rights Institutions (NRIs). The EHRC achieved this status in February.

International Monitoring
This Convention is also being monitored on an international level. This is the responsiblity of the Committee on the Rights of Persons with Disabilities (CRPD). This is a body of independent experts which monitors implementation of the Convention by countries (state parties). Countries have to send regular reports to the Committee, about implementation. They must report within two years after implementation. Afterwards, every four years.

The international Committee will examine the report, and can make suggestions and general recommendations, and send this to the country concerned.

Their first session of this Committee was held in February 2009. The agenda for this meeting is here. The minutes don't seem to be available online yet.

From the membership list of the Committee I don't recognise any of those names as being deaf people? Please correct me if I'm wrong. Can hearing people monitor and make recommendations on articles relating to sign language?

Comment and Ask the Readers:
We could say much more about monitoring, but trying to keep to the basics. What do you think of the above? Do you think effective monitoring will be achieved, and do you think that deaf people will be involved in the process?

Question. Who is actually getting UK deaf people involved at this stage, and letting them know about the Convention? This has to happen to meet the requirement of Article 33.

This blog is independent, and if you weren't reading about this here, would you know about it? Its not WFD's responsibility (they are an international organisation). So what are UK deaf organisations and the government doing? Deaf people cannot participate fully unless they have the basic information!

What are your views on representative organisations, and how do you define representation?

See also:
Part 1: UK and UN Convention on the Rights of Persons with Disabilities

Grumpy Old Deafies, 29th March 2009

Stephen and Lucy Hawking offer the universe


The world’s top theoretical physicist and his journalist/novelist daughter will have their second children’s book out May.

George’s Cosmic Treasure Hunt, aimed for readers ages 9-12, is the second of a planned trilogy that began with George’s Secret Key to the Universe, released in October 2007.

The second Hawking-Hawking kid-lit collaboration picks up the life of young George who is expanding his horizons beyond those of his extreme Luddite parents.

It’s sort of unfair to pit the man whose name is often mentioned in the same sentence with Newton and Einstein against people who don’t even believe in using light bulbs, (George’s parents), but this is fiction and fiction created by the man himself – Stephen Hawking – with the hearty help of his daughter, Lucy, and illustrator Garry Parsons.

The first book was well received. The story works, even though some readers complained of a slow start. It helped that the book comes with lavish Hubble Space Telescope photos and some bonus scientific facts presented in a manner very accessible to kids. The Hawking name, of course, was no hindrance either.

Their protagonist, George, is a young boy who wants a computer more than anything, against all odds considering the mind-set of his parents.

One day at least George’s pet pig, Freddy, has had enough, and runs away. George sniffs him out next door where he has been forbidden to go.

There he happily finds neighbors Eric, a physicist, and his daughter Annie, a free spirit, but, better yet, Cosmos, the most powerful computer in the world… all more or less willing to help him.

George is introduced to the wonders of science and how it is unraveling the mysteries of the universe.

Cosmos is, indeed, special. It can open up a path to anywhere in the Universe. George’s mistake is in revealing facts about Cosmos to his evil school teacher, Mr. Reaper, the deed around which much of the plot is spun. School bullies come into it as well.

But there is no turning back for George. He’s never going to go anti-science like his parents.

In the this sequel we will see George included in the mystery of a strangely behaving robot on Mars and Cosmos coming up with a weird message.

Is it from an alien? Could there be life out there? How do you find a planet in outer space? And if you could talk to aliens, what would you say?

Publishers call this an action-packed roller-coaster ride of a treasure hunt across the cosmos. Hyperbole, perhaps. But the story is replete with the latest scientific knowledge about the Universe. The book adds special essays from some of the top scientists in the world.

As Wired writer Matt Blum wrote after the first book, not even the most geeky parents need worry about the science here, since a Hawking is at the helm.

Dr. Stephen William Hawking, for those who don’t follow science, is a Lucasian Professor of Mathematics at the University of Cambridge. He is most known for his theoretical work concerning black holes. He is a science popularizer, having written may books, but most famously the runaway bestseller, A Brief History of Time.

Hawking is also famous for defying an extreme disability. While still in college in the 1960s, Hawking was diagnosed with ALS, amyotrophic lateral sclerosis (also known as Lou Gehrig’s disease in the United States), a condition that incrementally brought about his almost complete paralysis. By 1974 he was unable to feed himelf or get out of bed. Eventually, a Cambridge scientist built a device that enables Hawking to write onto a computer with small movements of his body, and then speak what he has written with a voice synthesizer.

Hawking's key scientific works to date have included helping to provide theorems regarding singularities in the framework of general relativity and the theoretical prediction that black holes should emit radiation.

He boldly told NewScientist magazine this month that “science should soon provide a definitive answer to how the universe began.”

Hawking indicated he felt the need to write books for children because it seems like today's adults have difficulty understanding the scientific concepts he works with. As popular as A Brief History of Time was, he said, he suspects few people really understand how the universe works. He would like the next generation to be more science-literate.

“It is extremely important for me to write for children,” he told the magazine. “Children ask how things do what they do, and why. Too often they are told these are stupid questions to ask, but this is said by grown-ups who don’t know the answers and don’t want to look silly by admitting they don’t know.

“It is important that young people keep their sense of wonder and keep asking why.”

Hawking said he has a child’s perspective in that he is still looking for answers.

“Children are fascinated by black holes and ask me questions. I find they soon get the idea if it is explained in simple language.. And yes, it is nice to think a few of them might grow up and read A Brief History of Time from cover to cover.”

Hawking is the first quadriplegic to experience zero gravity.

When he turned 65 in 2007, Hawking took a ride in a supersonic jet which, in free fall, can erase gravity. During the flight, Hawking experienced weightlessness eight times. It was the first time in 40 years he moved freely, without his wheelchair. Hawking was reportedly preparing for a future sub-orbital flight on a Virgin-Galactic spacecraft.

Virgin Galactic owner, billionaire Brit Richard Branson, paid for Hawking’s flight.

Before the trip, Hawking just about said it's the universe or nothing for mankind.

“Many people have asked me why I am taking this flight. I am doing it for many reasons. First of all, I believe that life on Earth is at an ever-increasing risk of being wiped out by a disaster such as sudden nuclear war, a genetically engineered virus, or other dangers. I think the human race has no future if it doesn't go into space. I therefore want to encourage public interest in space.”

Little George’s adventures contemplating the Cosmos, with “Cosmos,” probably will go a far in that direction.

The next generation, when parents, may recall the Hawking books being read to them.

Stephen Hawking’s parents read him the Bible.

Lucy Hawking said to her dad: “I’m glad you read us Paddington Bear instead.”

---------------------------

Professor Stephen Hawking, a Lucasian Professor of Mathematics at Cambridge, is the pre-eminent theoretical physicist in the world. His book A Brief History of Time was a phenomenal worldwide bestseller. He has twelve honorary degrees and was awarded the CBE and was made a Companion of Honour. He has three children and one grandchild. Visit him at www.hawking.org.uk.

Lucy Hawking, Stephen's daughter, is a journalist and novelist and an administrative staff member of the Autism Research Centre at the
University of Cambridge. She is the author of the adult novels Jaded and Run for Your Life. She lives in London with her son.

Garry Parsons is the award-winning illustrator of many books, including George's Secret Key to the Universe by Lucy & Stephen Hawking, Billy's Bucket by Kes Gray and What's Cool About School by Kate Agnew. He lives in
London. Visit him at www.garryparsons.co.uk.

Examiner.com 27th March 2009

The underclass: Talented but disabled


There are countless people like the ones on these pages: talented but disabled. And they still face bureaucratic barriers in their lives. Nina Lakhani reports

Thousands of disabled people across the UK are forced to rely on charities for basic care, equipment and vital information because of gaps in social services, according to new research by Shelter and Capability Scotland. Their report, Fit for Purpose, to be published this summer, will expose the constant battle disabled people face as they try to adapt their homes or move into more suitable housing. A lack of practical advice, long waiting lists and shortfalls in funding are common because of a huge gap between government policy and practice on the ground, the authors claim.

The findings add to pressure on the Government and health authorities after a scathing report into the care received by six people with learning disabilities who subsequently died. Their cases were described as an "indictment of our society" by the health and social care ombudsmen.

New research highlights problems common across the UK, where charities frequently fill gaps left by a shortage of suitable housing and discrimination in the job market. Many disabled people are still reliant on social services to decide what they need.

Parents of severely disabled children in some parts of the country rely on charities for basics such as incontinence pads and wheelchairs. A recent survey by the charity Livability found a lack of classroom services prevented one in five young adults from pursuing higher education.

The findings come only days before a report by the Joint Select Committee on Human Rights, which looks at the Government's failure to ratify the UN Convention on the rights of persons with disabilities. The Government says it will ratify the treaty this year but insists it must opt out of several unworkable areas. The Select Committee strongly criticised ministers recently for the delay and for failing properly to consult disabled people about their decision.

Alice Maynard, chair of Scope, said: "The Government's decision to opt out of certain areas means it is essentially ring-fencing parts of life which disabled people can and cannot go into. This reinforces the view that disabled people are not as equal as others and that it's OK for other people to decide where they can and cannot be seen."

The workplace

Sandi Wassmer, 46, from London, runs a web design agency. She is registered blind.

"The obstacles I face are nothing to do with my visual impairment. Other people's attitudes and their ignorance are my biggest problem. Most people still don't get it. They don't know how to engage with people like me because they're scared and they're ignorant, so they assume I'm not capable. For me, these attitudes present in different ways. It can be a well-meaning person in a Tube station who offers to help me in a really loud and slow voice as if I were stupid. In business, because my disability isn't obvious, I tend not to tell anyone because I know how most people who don't know my work will react. I've lost potential clients because they immediately assume a blind person can't run a successful design agency. Disability is seen as a flaw or limitation."

Sport

Dan Pepper, 20, from Stockport, is an elite swimmer with a learning disability.

The International Paralympics Committee banned all athletes with a learning disability from competing at the Paralympics after the Spanish basketball team cheated at the Sydney Games. In the run-up to 2012, it means that children are excluded from government initiatives to find new talent. And Dan could miss out on representing his country at the very top level.

"Sport has always been my thing. I went to a mainstream school and while my friends would beat me in the classroom, I could outrun and outswim them all. I swam well under the qualifying time for Athens but in the end we weren't even allowed to participate in an exhibition event. It was so disheartening: one day I was telling my school friends I was going to the Olympics, the next day it was all off. We were promised the ban would be overturned for Beijing, and there are only so many times you can brush off the disappointment and keep getting back in the pool. It's hard to train nine times a week when there isn't anything to aim for. The swimming pool is where I'm the best and I just want the chance to prove that at 2012."

Social life/public transport

Marta Hancock, 40, from Derby, has used a wheelchair for 30 years.

"I travelled down to London last week to attend the premiere of The Boat That Rocked. The film was great but the journey and overnight stay were a nightmare. There is no lift at Derby station. I couldn't get to my wheelchair space on the train because there was luggage in the way. The toilets on trains are too small. There is no kerb at the taxi rank at St Pancras station, which makes it much harder to get a wheelchair into a taxi. In the hotel, there were no hand rails around the toilet and the hoist didn't fit in the bathroom so I had to use a bed pan. The bed was screwed to the floor so the hoist wouldn't fit under that either, and this was advertised as a wheelchair-accessible hotel. It's not easy having a social life when you're in a wheelchair."

Social care and equipment

Leah Cutting, 18, from Ipswich, has cerebral palsy. Alison Cutting, her mother, describes the battles the family faces to get essential care and equipment.

"Most of the services Leah uses will stop when she turns 19. Leah loves school and the social life that goes with that, but after one more year there, she is too disabled to participate in any of the local courses and placements that social services provide. When she finally gets a personalised budget we will have more options, but it's possible that my husband will have to take early retirement if we can't find anywhere suitable. Respite care from Scope has allowed us to be a normal family for our other two children. But according to her social worker, the only adult option in our area is a care home for the elderly, with no social activities – no way. We've relied a lot on charities over the years for equipment such as communication aids, seating and money for holidays. It took us 18 months to convince social services that Leah had outgrown her wheelchair."

Housing

Jeffrey Miller, 48, from Bishop's Stortford, has multiple sclerosis. His life is restricted to the downstairs part of his house.

"My brother and I installed all the hand rails in the house and adapted the bathroom ourselves as it was going to cost us more if I paid what the council wanted me to contribute. My mobility has got much worse and there's no way I can get upstairs any more. This means I rely on my wife to help me have a strip wash every day because the bathroom is upstairs. A stair lift would cost us £10,000. So even though we'd like to stay in this house, the Papworth Trust has helped us to get on to a couple of housing lists as I need access to the shower. It's been a year already and I've no idea how long it will take."


The Independant, 29th March 2009

Disability equality needs role models

"Understanding and caring for people who are different needs to be taught to parents as well as children," the Green Party's disability spokesperson Alan Wheatley said today.

He was responding to news that the BBC had received dozens of complaints from parents about the employment of BBC children's television presenter Cerrie Burnell, who was born with one arm.

Cerrie Burrell co-presents the Do and Discover slot and Bedtime Hour on the CBeebies channel of the BBC. It has been reported that dozens of parents have complained that the presenter scares children. One parent reportedly said, "What is scary is the BBC's determination to show 'minorities' on CBeebies at every available opportunity." (1)

The Greens' Alan Wheatley commented today, "What would these parents who believe that 'minorities' should be neither seen or heard on children's television have them do? Is it not time for the parents to grow up to a global world and the social model of disability?"

Mr Wheatley explained that the social model of disability, integral to Green Party policy, points to the physical and social barriers that exclude people with impairments from fully participating in society. "Disabled role models on television can help to broaden the world-view of the parents as well as the children in the spirit of life-long learning in a very diverse society. Clearly one-armed people like Cerrie Burrell can achieve a lot, though not necessarily in the 'standard' way. Do some parents with both arms intact feel threatened by the prospect of a physically disabled person's success?"

He concluded: "Outside inclusive education hours, Cerrie Burnell might be seen as an icon of disability equality in public service broadcasting. She is a disabled person who has succeeded in the highly-competitive world of broadcasting, and that makes her an important role model."



News Rage UK
, 28th March 2009

Sign the petition to keep Capital Call for disabled people in the borough (Kingston)

Last month I was very concerned about Transport for London's decision to stop the Capital Call service in Kingston. Capital Call enables disabled people to use their Taxicards for mini-cabs, a service which has lots of advantages over black cabs, especially for blind people, not least the ability to book trips.

Following protests from local users, TfL decided to postpone the decision for a couple of months but the threat has not gone away.

Please sign the petition to keep Capital Call in Kingston.

Mary Reid, 28th March 2009

Hopes are high as Pegasus takes off


WORK is due to start within weeks on building a flagship £1.2m equestrian centre in Northumberland for disabled riders.

The Pegasus Centre for Excellence aims to fill a gap in provision for disabled riding enthusiasts in the region and offer state-of-the-art facilities for potential Olympians and Paralympians of the future.

The centre – which was first mooted in 2007 and will be created by developing existing stables in the hamlet of Tranwell near Morpeth – will offer riding experiences and therapy for up to 200 children and adults with disabilities every year.

Funding was secured last year and now building contractors are set to be commissioned for the first phase of the project to start early in April.

The centre will provide indoor and outdoor riding arenas, fully equipped with a disability-friendly riding surface and specialist equipment to ensure as many people as possible can be accommodated.

Features will include an on-site physiotherapist and educational training courses in horse care in conjunction with local colleges. Developed in partnership by the Riding for the Disabled Association and Castle Morpeth Council, the completed centre will be managed by Blyth Valley arts and leisure.

The RDA says it will address a shortage of riding facilities for disabled people in Northumberland, which has led to some having to be turned away for help which would clearly benefit them.

Yesterday Castle Morpeth Council leader Peter Jackson said: “It is extremely gratifying to see all the hard work that partners have put into the project finally coming to fruition, with the first phase about to begin.

“Pegasus will be something of which the community can be extremely proud, providing local people with a dedicated centre where their needs can be met and they can join a community of over 23,000 riders across the country.”

Meanwhile, funding has also been secured for a £820,000 project aimed at creating new jobs on the site of the region’s last deep mine, Ellington Colliery. Castle Morpeth Council and UK Coal have been working together on plans to convert a former colliery office building into 3,500sqft of managed workspace units for local small businesses. Eight units will be provided in the first phase, and there is already interest from a number of local companies keen to see their businesses grow on the site.

UK Coal development manager, Eddie Peat, said: “This workspace is part of a wider and longer-term investment we plan to make in Ellington and Lynemouth. We are delighted that this will be the first of a number of initiatives for the regeneration of these communities.”

Work will start on site next month with the first businesses moving in around September.

It is extremely gratifying to see all the hard work finally coming to fruition.


The Journal, 28th March 2009

Disabled sailor launches Round-Britain attempt

An inspirational yachtswoman aims to take the ‘dis’ out of disabled as she embarks on a world record attempt to sail solo around the UK.

Hilary Lister, who lives in Canterbury, was forced to abandon last year’s attempt due to bad weather but said she was excited about the re-launch of her Round Britain Dream this May.

If the 37-year-old completes the challenge she will become the first quadriplegic woman to have ever achieved it.

She told KOS Media: "I think the first aim is to demonstrate that people who are disabled are actually incredibly able. It is about taking the ‘dis’ out of disability.

"We all have our own strengths and weaknesses and I guess the other thing is to raise money for my Dream Trust, which is about helping other disabled and disadvantaged adults live out their sailing dreams.

"I’ve been lucky I’ve met the right people, not everyone is as lucky as me."

Mrs Lister, who was a sporty and active youngster, suddenly found herself at 15-years-old wheelchair-bound because of a progressive neurological disorder.

As she gradually lost the use of her body and was left in constant pain, she would not let it stand in the way of her ambitions and achieved a 2:1 in biochemistry from Oxford in 1995.

When she was 27 she lost the use of her arms and hands and as her condition worsened she had to abandon all her independence, which took her to an understandably dark place.

But in 2003 a friend introduced her to sailing, which she credits with saving her life.

"Sailing came along when life didn’t seem worth living anymore. Within seconds of being on the water a light switched back on inside me. I knew I had found what I was going to do for the rest of my life," she said.

Now, Mrs Lister, who lives with her husband Clifford and a chocolate Labrador called Lottie, is preparing to get back out on the water in preparation for the re-launch of her challenge on May 18 from Plymouth.

"Obviously having to finish last year was frustrating and it’s much better now to feel that we can retry and hopefully get better weather and finish the job," she said.

"I’ll be out in a boat on Sunday, which will be my first sail since last year. Then my boat goes back into the water thanks to Dover Marina and on about April 15 so then I’ll be out pretty much everyday."

Her boat Me Too an Artemis 20, which is a 6m carbon fibre keelboat designed by Rogers Yacht Design, is controlled using a ‘sip and puff’ system.

Three straws, which are connected to sensitive pressure switches, are used and a gentle ‘sip’ on one takes the boat starboard (right) and a puff on the other takes it to port (left).

When Mrs Lister left Dover in June 16 2008 for her first attempt the amazing sailor travelled the entire length of the South Coast but had to stop in Newlyn on August 13 due to consistently poor weather and gale force winds.

She has already sailed the further any woman with disabilities.

In 2005 she became the first disabled sailor to cross the English Channel, so she has a lot of experience and her next trip will take her even further afield, weather permitting, including to the North Sea, the Irish Sea and the Caledonian Canal.

Mrs Lister has appealed for KOS Media readers for help with her Round Britain Dream - a carer, two drivers and three ‘wet crew’ are needed to make up the team before the this Spring’s challenge.

If you can help email paul@hilarylister.com. For more information about Mrs Lister and the trip, including her own blog, visit www.hilarylister.com

Kentnews.co.uk, 28th March 2009



Saturday, March 28, 2009

G20/World Autism Awareness Day UKAF Appeal on Poverty


The leaders of G20 countries are preparing to arrive in the United Kingdom for the G20 Conference scheduled to be held at the Excel Centre in London Docklands. Barack Obama arrives in London with his wife Michelle on his first trip to the United Kingdom as President of the United States of America.

The 20 members of the G20 group of nations are: Argentina, Australia, Brazil, Canada, China, France, Germany, India, Indonesia, Italy, Japan, Mexico, Russia,Saudi Arabia, South Africa, South Korea,Turkey, United Kingdom, United States and the European Union.

The London Summit is headed by Prime Minister Gordon Brown and the hosts are Chancellor Alistair Darling and Her Majesty’s Treasury, on the agenda are key economic issues: 1. Coordinated macro-economic actions to revive the global economy, stimulate growth and employment - review measures taken and possible further steps 2. Reform and improve financial sector & systems - continue to deliver progress on the Washington Summit action plan 3. Reform international financial institutions (IFIs) - International Monetary Fund (IMF), Financial Stability Forum (FSF) and World Bank.

G20 also coincides with World Autism Awareness Day (WAAD) on 2nd April. On that day G20 leaders will be focusing on the global economic crisis when they meet at the Excel Centre in London Docklands.

World Autism Awareness Day was launched by the United Nations General Assembly on 2nd April 2008 in New York on the recommendation of the State of Qatar.

The UK Autism Foundation has appealed to G20 Leaders and the host Prime Minister Gordon Brown not to walk by on the other side and ignore the plight of the poor. They will be discussing the financial crisis on the United Nations World Autism Awareness Day. Those who are facing severe financial pain are parents, carers, children and adults with autism and Asperger’s Syndrome.

The UKAF, a British charity, is deeply concerned about families with autism who are below the poverty line. Over 200 MPs in the House of Commons have signed three early day motions tabled by UK parliamentarians - John Battle MP (Chair of the All Party Parliamentary Group on Poverty), Rudi Vis MP and David Drew MP, supporting the call of the UK Autism Foundation for more help for the poor during the credit crunch and the deepening recession. UKAF has been campaigning on Poverty and Autism and are calling for financial help and support during the economic downturn in the United Kingdom and around the world.

Lee Scott MP, Patron of the UK Autism Foundation (who has championed the cause of autism in the House of Commons) is also calling on Her Majesty’s Government to provide ring fenced funding for autism. He is lobbying very hard on autism on World Autism Awareness Day. Scott initiated a landmark debate on autism in 2007 and met with Prime Minister Tony Blair and autism campaigner Ivan Corea who discuss the serious issues.

Ivan Corea of the UK Autism Foundation: ‘We are appealing to Prime Minister Gordon Brown, President Barack Obama and G20 leaders to help the poor, including families with autism who are below the poverty line. Many are struggling to cope with the economic crisis. Homes of families with autism have been re-possessed. Others are in fuel poverty. Fathers and Mothers have lost their jobs during this economic turmoil. G20 leaders must reach out to the marginalised and the vulnerable. Things are getting worse and it is the vulnerable and the poor who are bearing the brunt of the economic crisis. Who will bail out the poor?”

The UK Autism Foundation has appealed for Prime Minister Gordon Brown and Chancellor Alistair Darling to increase the tax credits, the disability living allowance and the carer’s allowance in the April 2009 Budget in order to help parents, carers, children and adults with autism and Asperger’s Syndrome cope with the economic crisis.

Blogger News Network, 28th March 2009

New regional services manager for Epilepsy Action

JULIE Clark has been appointed regional services manager in central England for Epilepsy Action, the UK’s largest member-led epilepsy charity.

Based in Malvern, she will be responsible for developing and managing community-based services for people with epilepsy and their families in the region.

Julie will be working closely with a network of Epilepsy Action branches as part of her work in the West Midlands, East Midlands and east of England.

She will also be organising regional conferences, seminars and information and awareness events. They will be aimed at supporting people affected by epilepsy and informing those with an interest in the condition.

Before joining Epilepsy Action, Julie worked with Worcestershire Wildlife Trust, supporting their local groups of volunteers, running the adult education courses and co-ordinating the events programme.

Before that, she worked for Enable, a disability support charity in Birmingham, where she helped young people and adults to build their confidence and created and ran a garden-based programme for overcoming depression and anxiety.

Julie said: “I am so pleased to have been given the opportunity to work for Epilepsy Action. I am looking forward to working with people and organisations across the central region to help develop the much needed support for people with epilepsy and their families.”

Epilepsy is a common serious neurological condition, affecting around 456,000 people in the UK. Last year alone, Epilepsy Action directly helped more than 686,500 people through a range of services, including its advice and information centre and Epilepsy Helpline, freephone 0808 800 5050.

For further information about the work of Epilepsy Action, visit www.epilepsy.org.uk

The Shuttle, 27th March 2009

Hospital blunder boy to get £5.25m

The mother of a boy left disabled through a hospital blunder has told of her relief after a £5.25 million compensation payout secured his future.
Monica Giles's son Jordan, 10, developed cerebral palsy following difficulties at his birth.
Mrs Giles said she feared her "wee miracle" would not survive after he was born at the Vale of Leven Hospital in Dunbartonshire.
The family has now been awarded £5.25 million by the NHS in an out of court settlement, Scotland's biggest compensation payout.
She told the Daily Record: "The settlement means I know he will be looked after when his dad and I are gone.
"All I want is for Jordan to have a happy life and grow up normally like any other kid. Life shouldn't have been as hard as it has been for him."
Jordan attends a mainstream school but cannot dress or wash himself and also suffers from epilepsy, the newspaper reported.
Mrs Giles, 39, who split with Jordan's father a few years ago, is not able to work as she looks after her son full time.
Some of the money from the payout will reportedly be used to buy special equipment and adapt a new house for Jordan. The rest will be kept in a trust and court officials will monitor how the funds are spent.
A spokeswoman for NHS Greater Glasgow and Clyde said: "We can confirm that the NHS has made an out-of-court settlement payment to the family following their claim against the former Argyll and Clyde health board regarding the very sad circumstances surrounding the birth of their son in 1998."

MSN, 28th March 2009

Jet2 Airlines, a British budget carrier, charges man extra for his fake legs

A British low-cost carrier seems to have sunk to a new low for budget airlines when it told a double amputee he had to pay extra for transporting his two spare prosthetic legs on an upcoming flight to the Spanish island of Majorca.

"It is ridiculous. In my opinion, the prosthetic legs are a disability aid. A wheelchair is classed as that and can be transported free of charge," the man, whose name is Mick Skee, tells Britain's Daily Mail.

Skee says the spare limbs had been specialty designed for this vacation.

Skee contacted Jet2 to arrange transportation for the fake limbs, but that the airline declined to help him, saying he'd need to pay a $25 baggage fee for them.

When Skee contacted Jet2 corporate to seek some redress, a spokesman told him to write out a formal complaint and mail it to customer service, and await a response in 21 days.

Allow me to help Skee out a little bit:

To whom it may concern at Jet2 Airlines: Give this guy a friggin break. Are you so broke that you cannot allow free transportation of prosthetic limbs?

I'm sorry, but back-up or not, it just seems cold not to make an exception here to the companies checked "luggage" fees. I mean, how many customers are coming to them asking to transport prosthetics? It's not like it's opening a Pandora's Box by letting Skee check his back-ups free of charge.

It could be worse, I guess: Jet2 could charge the man extra for his primary prosthetics.

Who is Jet2? A pretty bottom-shelf budget airline that flies out of Leeds, Manchester, Belfast, Blackpool and Edinburgh.

Gadling, 27th March 2009

Friday, March 27, 2009

England dates set for Pakistan blind series

The dates have been confirmed for England's three-match one-day international blind series against Pakistan in August 2009.

England will go into this summer on a high after retaining the Blind Ashes with series victory in Australia at the end of 2008.

The first England v Pakistan ODI will be played on August 11 at Moseley CC, Streetsbrook Road, Moseley. The 2nd ODI will be on August 13 and is to be played at King Edward School in Edgbaston.

The final game will take place on Saturday August 15 at New Road in Worcester, with a possible Twenty20 to take place in the west midlands the following day.

The ECB, 27th March 2009

Minister Spends Day In The Life Of Social Care Worker


Care Services Minister Phil Hope underlined the benefits of a career in social work while promoting a nationwide recruitment campaign. To highlight the need for people to retrain for the social care sector, the Minister today swapped his Whitehall office to spend the morning working in a care home for people with learning disabilities. He rolled up his sleeves to help staff at Angela House in Hammersmith with their daily routine. Angela House is run by Yarrow, a specialist provider of learning disability and acquired brain injury services in London."

Despite the current economic climate, there is an increasing demand for social care workers due to our expanding ageing population. The Department of Health is currently running a series of events across the country, giving advice to people who may be interested in a career in social care.

Phil Hope said:

"Working alongside people who work in social care this morning has been incredibly rewarding. I have huge respect and admiration for the work they do.

"I would encourage people to think seriously about social care work as a career option. It is a challenging and incredibly rewarding profession, which helps the most vulnerable people in the community get the most out of life in modern Britain. Specific training is provided so applicants just need great people skills and a desire to help others."

Today the Minister found out what working in the social care sector was like by work shadowing staff at Angela House, helping them with their interactive story telling session.

He also attended one of the Department of Health's recruitment events at West12 shopping centre in Shepherds Bush.

The event gives people advice on where they can find out what sort of jobs are available, where they can go to look for vacancies and general information on a career in social care. People wishing to register their interest in job openings are able to leave behind their contact details, which will be passed on to their local authority and employers in the area.

Kelsang Frasi, Deputy Manager for Yarrow Housing, which runs Angela House, explains why he works in social care:

"My aunt had downs syndrome and the experience of caring for her made me realise that I wanted a job that put something back. I didn't have enough qualifications to be a nurse, so I started working in a home that cared for people with learning disabilities. That was twenty three years ago and now I am deputy manager of the very same service.

"The people we care for are highly dependent and they rely on you a lot. This can be really rewarding, because when they are happy it really makes your day. I love my job, not only are there lots of opportunities for training and development but you know that you are making a difference."

There are a wide variety of jobs available in social care. As well as working with older people, there are many opportunities to work with children, families and young people, and people with disabilities.

Notes

1. Working in social care, your employer could be a council, a small business, or a voluntary organisation.

2. For more information about working in social care go to: http://www.socialcarecareers.co.uk.

3. Angela House is one of 14 registered care homes operated by Yarrow Housing in London. For more information see: http://www.yarrowhousing.org.uk
 
Department of Health Press Release, 26th March 2009

Team Skyscanner to join Bupa Great Edinburgh Run 2009

If you thought all Skyscanner staff did was stand outside Edinburgh coffee shops pulling poses for the roaming Google Street Map camera cars, think again!

Several members of Skyscanner's Edinburgh office will be taking part in the Bupa Great Edinburgh Run, which will be held on Sunday 3rd May 2009.

Team Skyscanner will be running on behalf of Disability Snowsport UK, who provide opportunities for people with a disability to participate in skiing and snowboarding, helping to improve their quality of life.

Training has already begun, with Team Skyscanner members taking to the streets of Leith in Edinburgh during lunch hour in preparation for the 10K route that will take in the city's most famous landmarks including Edinburgh Castle, The Scott Monument, The Royal Mile and Holyrood Palace.

Gareth William, Skyscanner CEO said:

"As a Scottish company, it's important for us to get involved with local events and The Great Edinburgh Run is an ideal way for Skyscanner to help raise money for a good cause, enjoy the great outdoors of our beautiful city, and of course get some exercise."

If you'd like to sponsor Team Skyscanner, you can donate by visiting our Sponsor Skyscanner page: all donations very gratefully received – no amount too small!

Last September, Team Skyscanner helped raise money for Leukaemia Research by joining the Pedal For Scotland Cycle ride, a 55mile bike journey from Glasgow to Edinburgh.
Skyscanner, 26th March 2009

Fire service rewarded for disability friendly website

AVON Fire and Rescue Service has been rewarded for making its website accessible to people with disabilities.

It has been given an Accessible Plus accreditation by website accessibility charity the Shaw Trust, thanks to low vision technology and mechanisms to use the site without a mouse.
Lorraine Abrahams, the service's director of service impr
ovement, said: ""In order to make our website accessible we needed to understand these barriers.
"This helped us open up the site to users with disabilities, while at the same time making it a more user friendly experience for all, regardless of ability."
The website, www.avonfire.gov.uk , has undergone rigorous testing and is now accessible to people with learning difficulties, dyslexia, autism, hearing difficulties and colour blindness.
 
Avon Gazette, 27th Mach 2009

How the 'freaks' got their freak on

A still from the film The Last American Freak Show

Uncomfortable viewing ... a still from the film The Last American Freak Show

Dame Demure is a dwarf who chews glass. Peg-Leg has a prosthetic limb, and a torso festooned with lesions. Jackie the Half-Woman, born without legs, scampers around on her hands. These are not characters excised from the Watchmen movie, but the disabled performers whose tour of the US in the name of entertainment is chronicled in Richard Butchins's documentary The Last American Freak Show.

  1. The Last American Freak Show
  2. Release: 2008
  3. Country: USA
  4. Directors: Richard Butchins
  5. More on this film

"I think 'freak' is a word that needs to be reclaimed, in the same way that 'queer' has been by gay people," Butchins explains. "Making this film put me in touch with my disability in a way I hadn't been before. I felt looked-at, whereas I'd always taken great pains to hide my disability."

Unfortunately, the hysterical reaction to the film has confirmed that able-bodied society, or at least its representatives on festival committees and funding boards, would prefer stories about disabled people to be consoling or uplifting. Bafta made the headlines last year when it cancelled a screening of Freak Show. "It said my film showed an inappropriate representation of disability and raised too many questions," scoffs Butchins. "One funding organisation said it felt the film wasn't 'disability-empowering'." And while Freak Show will play next week in the London International Documentary festival, it is perhaps more typical of the general response that Butchins was recently invited to screen it in a Canadian horror film festival.

The picture is uncomfortable viewing, and not just because of its unsentimental depiction of disability. The freakshow is run by two able-bodied people who are different kinds of freaks - control freaks - and whose motives are opaque, to say the least. Then there is the footage of shoppers grimacing openly at the sight of Peg-Leg (real name Ken). Could it be that those who would happily see the movie buried are protecting their own delicate sensibilities, under cover of defending the disabled? In his book Inventing the Victorians, Matthew Sweet points out that Joseph Merrick, the Elephant Man, made a pretty penny from putting himself on display, and himself wrote the very pamphlets that described him as freakish. None of that made it into David Lynch's 1980 movie, and Butchins's film proves that able-bodied society is no closer to accepting that the disabled hold the rights to their own self-image.

When Gary Sinise has his legs digitally removed to play an amputee in Forrest Gump, or Robert De Niro goes into twitching overdrive for Awakenings, we feel safe in the knowledge that the performers concerned don't have to live with their onscreen disability. They'll be back on the tennis court in no time.

The use of disfigured and disabled people to man the gates of hell in Michael Winner's The Sentinel (1977) is now rightly decried, just as the sight of Leslie Ash being terrorised by a group of Down's Syndrome actors in the bizarre Shadey (1986) seems in appalling taste. But just last year, when Special People, a comedy with a predominantly disabled cast, was released, the BBFC felt it necessary to warn viewers that it contained - brace yourselves - "disability themes". Such a squeamish reaction is not so far from the revulsion those earlier movies exploited.

Butchins believes the reason The Last American Freak Show has met such opposition is not because society has moved on from exploitation, but because we are more prone to it than ever. "Don't think the freak show has gone away," he says. "It hasn't. It's there in those shock-docs on TV. You don't pay a dollar to look at these people in a tent, so it feels OK. But it's worse because they're still being exploited by able-bodied people. You can be sure that the one person who doesn't get paid in Britain's Hairiest Man, or whatever it might be called, is Britain's hairiest man."

• The Last American Freak Show screens in the London International Documentary festival on 31 March. See lidf.co.uk for details

The Guardian, 27th March 2009

Damning Catalogue Of Failure, Neglect And Denial Of Basic Human Rights Report Must Never Be Repeated

The 6 deaths of people with learning disabilities under NHS care have provided a shocking wake-up call to the NHS, Local Authorities and the Government with regards to the treatment which people with learning disabilities can receive.

Many dedicated doctors and nurses across the NHS provide excellent care for patients with learning disabilities, but the investigations have revealed that these standards are still far too patchy, with some learning disabled people receiving sub-standard treatment which in these cases contributed to their suffering intolerable pain, loss of dignity and/or premature death. The Government and the NHS owes it to these people, their families and all people with learning disabilities to ensure that they receive the same standards of equal, humane and dignified treatment that the NHS's own constitution explicitly guarantees to all service users.

Liz Sayce, Chief Executive of RADAR said:

"These tragic deaths must not be repeated. The Ombudsman's report demonstrates that these cases went beyond unfortunate human error, which can affect any organisation, and constituted an overwhelming failure to provide the most basic standards of nursing care and respect for human rights. People with learning disabilities should not have to and will not tolerate being treated as second-class citizens, or worse, by NHS staff."

"We do not need further reviews as the evidence is already clear - we need action, training and demonstrable service improvement."
 
 
RADAR Prease Release, 26th March 2009

Tax credit shambles hits lowest paid

SNP Business and Enterprise spokesperson, Mike Weir MP, has secured cross-party support in a bid to persuade the UK Government to revise the threshold for Working Tax Credits (WTC) after warning that low income workers are missing out on the benefit because they have had their hours cut as a result of the recession.

The Working Tax Credit (WTC) is intended to "help make work pay" for lower income workers. For people with children and disabled people, WTC is payable if the person works 16 hours or more a week. For others, the threshold is 30 hours a week, however, as a result of the recession many workers have had their hours cut and now face a "double whammy".

Mr Weir has tabled an EDM on the issues which has already received backing from Labour, Liberal Democrat and SDLP MPs.

Mr Weir, the SNP MP for Angus, said:

"For low paid workers to lose hours at work and then be punished again by having their Working Tax Credit entitlement withdrawn is clearly a double whammy.

"Working Tax Credits are supposed to help make work pay, but clearly the reality of the recession is having an impact on peoples employment and the UK government must look at revising the threshold.

"Just like the 10p tax fiasco these ridiculous rules are hammering those on low incomes especially hard, and is further compounded by the recession. Instead of helping the less well off and the vulnerable these ridiculous tax credit rules are punishing them.

"The tax credit system is patently not working, and I hope that Ministers can be persuaded to sort it out."

Note:

1. The text of Mr Weir's EDM is set out below:

That this House notes that many firms have introduced short time working for employees during this time of recession; further notes that many workers who are in receipt of tax credits are facing difficulties as the reduction in hours takes them below the minimum hours required to qualify for tax credits; and calls on the Government to take action to ensure that those who are so affected are deemed to still be working for the minimum hours and that their tax credits are maintained until such time as their hours are reinstated.

Supported by: Mike Weir MP, Lynn Jones MP (Lab), Mark Durkan MP (SDLP), Andrew George MP (Lib/Dem).



2. Background on Working Tax Credits.

The Working Tax Credit (WTC) is intended to "help to make work pay" for lower income workers. For people with children and disabled people, WTC is payable if the person works 16 hours or more a week. For others, the threshold is 30 hours a week. The lower threshold for people with children and disabled people is justified because people in these groups suffer greater disadvantage in the labour market.

To qualify for WTC, the claimant or their partner must: work 16 hours a week or more and be aged 16 or over and be responsible for a child; or have a disability that puts them at a disadvantage of getting a job and have been or are claiming a disability benefit; or be 50 or over and returning to work after receiving specified benefits or work 30 hours a week or more and be aged 25 or over

The 30 hour requirement therefore applies to all WTC claimants without children, unless they are disabled or aged 50 and over and returning to work.

The lower hours threshold for claimants with children or a disability "recognises the difficulties that those with children face in combining work with family responsibilities and the difficulties that workers with a disability may face" (HM Treasury, The Child and Working Tax Credits: The Modernisation of Britain's Tax and Benefit System, April 2002, p 33). The same source also stated that the WTC elements for disabled workers and for those aged 50 or over returning to work after a period out of the labour market "recognise particular aspects of disadvantage in the labour market" (ibid.). It goes on:

Workers with neither children nor a disability, aged 25 or over, will be entitled to the Working Tax Credit provided they work at least 30 hours a week. This is in recognition that people in this situation do not face the same barriers to full-time work and should be encouraged to work full-time because it is more likely to offer them the opportunity to improve their skills and progress up the earnings ladder. Eligibility for workers in this group will begin at the age of 25, as it is those aged 25 or over who are most likely to face poorer incentives to work or suffer persistent poverty in work.

[ibid., p33, para A.12]

SNP News, 26th March 2009

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