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Disabled French Woman Kidnapped In Kenya

October 2, 2011

A French woman has been kidnapped by an armed gang on Kenya’s northern resort island of Manda and taken to Somalia, Kenyan officials say.

The disabled woman, 66, was attacked at her bungalow at Ras Kitau. Kenya’s government said it believed the abductors were al-Shabab militants.

A Kenyan statement said some abductors were injured in a shootout with two Kenyan ships trying to stop them.

The kidnap comes three weeks after a UK couple were attacked further north.

Gunmen shot dead husband David Tebbutt and kidnapped his wife Judith in Kiwayu. She was taken across the border to Somalia.

‘Hugely damaging’

The gunmen struck at Ras Kitau at 03:30 (00:30 GMT) on Saturday.

“An elderly, disabled French lady who has been living in Manda Island in her own house was abducted by 10 heavily armed Somali bandits suspected to be al-Shabab operatives from Ras Chiamboni in Somalia, near the Kenyan border,” a Kenyan government statement said.

This was a far more audacious raid than the one against David and Judith Tebbutt at Kiwayu. Ras Kitau is just opposite Lamu Island’s popular Shela beach so this attack goes right to the heart of Lamu’s tourism industry.This time the gunshots were heard in Shela village and will have scared tourists and hotel owners alike. On an island where almost all job opportunities are related to tourism this is very bad news.

One hotel owner told me Somali gangs in boats had been seen at least twice in the last 10 days close to Kiwayu. He has closed the resort.

Whatever the outcome of this latest kidnapping, there is now a desperate need for the Kenyan government to launch a major security operation and stop the gangs from getting anywhere near these resorts. It will not be easy but it has to be done in order to make the tourists feel safe, save jobs and keep the foreign exchange coming in.

Abu Chiaba, a local legislator, said the gang had come into Manda by boat in the middle of the night.

“The elderly French woman is well known in the area, she comes to Manda regularly,” Mr Chiaba said.

Witnesses say they heard at least two gunshots before the woman was taken away by the attackers.

“We were all startled awake because there were gunshots,” said Jeremiah Kiptoon, who works on Manda island.

“The dogs were barking and people were screaming… I ran to the place to see what was happening but by the time I got there, the lady was gone.”

Two coastguard vessels and a police helicopter chased the abductors, and were involved in an exchange of fire, Internal Security Minister George Saitoti said in a statement.

 He said several of the abductors were injured but they still managed to enter Somali territory in a motor boat.

The government said “every effort” was being made to rescue the woman.

Kenya’s Tourism Minister Najib Balala called for international assistance to help them in their efforts to secure the border with Somalia.

“The core problem is Somalia and the core problem is criminal elements who manage to sneak into the country,” he told the BBC.

“Whatever we’re going to do, if we don’t have the support of the international community to address the Somali issue then it is very challenging to manage to man the border in Somalia.”

France has warned French visitors to avoid the area.

“It is advised against staying on the Lamu archipelago and its region near the Somali border,” the French foreign ministry said on its website.

The attack happened just across a lagoon from Shela – an exclusive resort on Lamu island.

This attack has the potential to do severe damage to Kenya’s tourism industry, the BBC’s Will Ross in Nairobi says.

Ed Miliband Meets Kaliya Franklin

September 30, 2011

He says he supports disabled people… erm… it would help if you remembered our names when we speak to you, Sir!

Results Of OFT Study Into Mobility Aid Sales

September 29, 2011

I featured the study on Same Difference late last year. Now here are the results.

Afghanistan Soldier Faces Forced Discharge

September 29, 2011

One of the most seriously injured soldiers to have served in Afghanistan says that he is being forced out of the Army.

Lance Bombardier Ben Parkinson was with the Royal Horse Artillery in Afghanistan when the Land Rover he was riding in was ripped apart by an anti-tank mine in September 2006.

He lost both legs, suffered brain damage, broke his back and was told he would never walk or talk again.

The 27-year-old has been having treatment funded by the Ministry of Defence but his family have received a letter from the Army Medical Services Board that is recommending a medical discharge.

His mother Diane Dernie, who acts as his spokesperson, told Radio 5 live’s Victoria Derbyshire about her concerns for her son’s recovery.

Paralympic Ticket Figures Revealed

September 28, 2011

More than 100,000 people have applied for more than one million tickets to see next year’s Paralympic Games, London 2012 organisers Locog have revealed.

Ballots will take place in some price categories in 126 of the 300 ticketed sessions across 16 of the 20 sports and for the opening and closing ceremonies.

International Paralympic Committee President Sir Philip Craven said: “The response from the public for Paralympic Games tickets has been phenomenal.”

The Games start on 29 August next year.

More than 4,200 athletes, with a variety of disabilities, from 150 nations will take part.

It is the first time in history that sessions at the Paralympics have been oversubscribed and Sir Philip continued: “To have over a million tickets applied for 11 months out from the Games is unprecedented.

“It underlines the growing excitement for what will be a tremendous sporting event and I could not be more thrilled.”

Locog chief executive Paul Deighton said: “The UK’s love of sport and support for the Paralympic movement shows they have taken the Games to their hearts.

Sports & Events for which some ticket ballots will be held

  • Archery
  • Athletics
  • Boccia
  • Track Cycling
  • Equestrian Dressage
  • Football
  • Goalball
  • Judo
  • Rowing
  • Shooting
  • Swimming
  • Table Tennis
  • Wheelchair Basketball
  • Wheelchair Fencing
  • Wheelchair Rugby
  • Wheelchair Tennis
  • Olympic Park Day Pass
  • Opening Ceremony
  • Closing Ceremony

“When the Paralympic Games come home next summer we can look forward with confidence to packed venues cheering on our athletes.”

Road cycling, sailing, powerlifting and sitting volleyball are the only sports in which at least one session has not sold out.

Locog will now finish processing the applications before holding the ticket ballots.

Payment for the tickets will be taken by 31 October and applicants will find out by 18 November if they have been successful.

In December the remaining tickets will go on sale, on a first-come, first-served basis.

Remaining tickets for the Olympic footall tournament will go on sale at the same time.

Further contingency tickets for both the Olympics and Paralympics will be sold next spring.

On Monday, the day the window for applications for Paralympics tickets closed, London 2012 chairman Sebastian Coe told the BBC: “We have a head-start with Paralympic sport in Britain.”

Lord Coe added that the appreciation of the Games among British youngsters could not be overstated.

“Look at the extraordinary scenes in Trafalgar Square just a couple of weeks ago when we celebrated Paralympic Day,” he said.

“Young kids from local schools were getting excited about seeing Ellie Simmonds, Oscar Pistorius, Dame Tanni Grey-Thompson and David Weir.

“The kids really do get it – for them it is excellent sport and the competitors have become household names.

“For young people, Paralympic sport is actually an interesting metaphor.

“It is about courage and determination, it is about equality and sometimes it is about overcoming extraordinary setbacks in life.

“But what they also know is that they are watching things that they can’t do which is a pretty good way of defining sport really.”

BBC athletics commentator Paul Dickenson, who has covered the Games since Atalanta in 1996, said that famous Paralympians had definitely raised the profile of their sports.

“Look at the polls that BBC Sports Personality of the Year has achieved in the last few years where both Ellie and Tanni have reached the last three as sportswomen let alone Paralympic sportswomen,” he said.

“The profile that the general public have of these people is much, much higher than it has ever been before.

“And of course at every Paralympic Games I have ever been to, the medal count for the Great Britain team has just got higher and higher.

“We finished second behind China in Beijing and obviously we want to try to achieve that again by the time we get to London.

“There is a feeling that Paralympic sport is a concession made to people with a disability to take part in sport.

“But to be honest, if you have ever been to wheelchair rugby you would be utterly amazed at the commitment and entertainment value these sports give.”

Autism Should Be Better Diagnosed, Says NICE

September 28, 2011

The health watchdog NICE has issued new guidelines on how autism is recognised and diagnosed.

They say it will help parents who can sometimes wait for a diagnosis for years.

Jolanta Lasota is the Chief Executive of Ambitious about Autism, which runs the Treehouse school in north London.

It provides support for over 80 autistic children. She gave her reaction to Radio 5 live Breakfast.

‘M’ Should Not Be Allowed To Die, Rules Judge

September 28, 2011

As someone who believes that every life is valuable, and that disabled people have every right to live with as much support as possible, I am very, very happy to read this.

A High Court Judge has ruled that a brain-damaged woman should not be allowed to die, in what is being seen as a landmark case.

The woman, who is 52 and can be referred to only as M, is in what is known as a “Minimally Conscious State”.

Her family argued she was in pain and that artificial feeding and hydration should be withdrawn.

The Official Solicitor and the health authority responsible for her care opposed the application.

Mr Justice Baker, who heard legal argument during a Court of Protection hearing in London in July, said the case was unique and raised “very important issues of principle”.

M became severely brain damaged eight-and-a-half years ago. She is unable to talk and had been thought to be in a vegetative state, with no awareness or consciousness of her surroundings.

However subsequent tests indicated that she is in a “Minimally Conscious State” – on the edge of awareness.

She is now being looked after in a care home in the north of England.

Relatives wanted life-supporting treatment to be withdrawn, saying she would not want to live “a life dependent on others”.

But a lawyer appointed by the High Court to represent the woman opposed their application for nutrition to be withdrawn, saying she is “otherwise clinically stable”.

The local health authority responsible for commissioning her care also opposed the application, saying the 52-year-old’s life was “not without positive elements”.

In 1993 the House of Lords ruled that doctors need not keep someone alive if it was viewed that it was of no benefit to the patient. That case was crucial in determining that feeding tubes could be regarded as medical treatment.

Since 1993, a total of 43 patients in a persistent vegetative state, or PVS, have died after a judge ordered that treatment could be withdrawn.

This case is different because M is minimally conscious.

Derek Paravacini Revisited

September 28, 2011

Derek Paravacini was born prematurely 32 years ago, and doctors did not think he would survive.

He is blind and severely autistic, but has a unique talent that has stunned the music world – he can play any piece of music after hearing it only once.

Now he is to make make musical history when he performs a concerto written especially for him at London’s Queen Elizabeth Hall.

Tim Muffett met him.

Ruling On Right To Die Case Of ‘M’ Due Today

September 28, 2011

The Court of Protection will rule later on whether a brain-damaged woman should be allowed to die, in what is being seen as a landmark case.

The woman, who is 51 and can be referred to only as M, is in what is known as a “minimally conscious state”.

Her family say she is in pain and that artificial feeding and hydration should be withdrawn.

The Official Solicitor has strongly opposed the application, arguing that she may be able to communicate.

M became severely brain damaged eight-and-a-half years ago. She is unable to talk and had been thought to be in a vegetative state, with no awareness or consciousness of her surroundings.

However subsequent tests indicated that she is in a “minimally conscious state” – on the edge of awareness.

She is now being looked after in a care home in the north of England.

In a preliminary ruling on the case, Mr Justice Baker said the tragedy had had a “devastating impact”, not only on M, but on her family, including her mother, sister and partner.

Those family members had “come to a clear view that M would not wish to continue living in her current state and that it is not in her interests to do so”.

‘Showed awareness’

They believe that M is suffering and experiences pain. They are seeking a legal declaration that she lacks capacity to make decisions over her future treatment, and that it is not in her interests for artificial nutrition and hydration to be provided.

They want an order allowing all those looking after her to stop all “life-sustaining treatment”, and to concentrate instead on minimising her distress and protecting her dignity until she dies.

The Official Solicitor, a lawyer appointed to represent M, opposes the application, arguing that M could respond to touch, “showed awareness” and may be able to communicate using a switch.

Mr Justice Baker said the case “potentially raises issues of the utmost importance”. He said this was the first time the court had been asked “to approve the withholding of nutrition from a patient whose consciousness is above that of the vegetative state”.

In 1993 the House of Lords ruled that doctors need not keep someone alive if it was viewed that it was of no benefit to the patient. That case was crucial in determining that feeding tubes could be regarded as medical treatment.

Since 1993, a total of 43 patients in a persistent vegetative state, or PVS, have died after a judge ordered that treatment could be withdrawn.

This case is different because M is minimally conscious.

Paul Ridd

September 28, 2011

A patient with severe learning difficulties who died in hospital may have survived if he had received better care, a watchdog has found.

Paul Ridd’s nursing care at Morriston Hospital in Swansea was called “abject” and “dire” by the Public Services Ombudsman for Wales.

Mr Ridd, 53, died of respiratory issues after transfer from intensive care.

His family welcomed the report. Managers said procedures had been improved.

Awareness training for all doctors and nurses has been ordered at the hospital.

The ABM University Health Board, which runs the hospital, also said it had already started implementing the recommendations made in Peter Tyndall’s report.

Mr Ridd, from Baglan near Neath, suffered severe learning difficulties as a result of brain damage at birth.

He was admitted to Morriston Hospital on 31 December 2008 with a serious bowel problem and underwent surgery.

But following his death on 23 January 2009 his brother and sister complained about many aspects of the way he was looked after.

In particular they were concerned he contracted pneumonia while in intensive care and was transferred prematurely to a general ward, where they said his care was poor in the days before he died of respiratory problems.

His brother Jonathan Ridd said: “When Paul was in the intensive care unit, he had top quality care, like a five star hotel, and when he was moved across the corridor, it felt like we were in a Third World country in terms of care, cleanliness.

“There was no leadership and his observations were not done as instructed.”

Mr Ridd said in the last four hours of his life, his brother’s carer was “constantly begging” the nursing and medical staff to examine him as his condition had steadily deteriorated.

In a report published on Wednesday, Mr Tyndall said concerns about Mr Ridd’s condition after he was transferred to the general ward were raised with staff.

But among his findings were:

  • A failure of supervision
  • Inadequate examinations by doctors
  • A failure to ensure Mr Ridd’s care complied with the Disability Discrimination Act.

“Nursing care on the ward was abject,” said Mr Tyndall.

“It greatly concerns me that the dire level of nursing care to which [Mr Ridd] was subjected on the ward, could have happened in the 21st Century.

“It is vital that change is robust and long lasting.

“I consider it vital that nursing and clinical care providers respond appropriately to the challenge that patients with learning disabilities present. This did not happen.”

Wayne Crocker, director of the learning disability charity Mencap Cymru, said the case should be a “wake-up call” for health professionals in Wales.

“It’s a disgrace that someone can go into a hospital, a place where they should be looked after, and see their chances of survival reduced because they have a learning disability,” he said.

‘Tragic event’

“Currently, people with a learning disability get sub-standard healthcare compared to those without – it’s as simple as that.”

The ABM University Health Board said it investigated and identified shortcomings following Mr Ridd’s death and swiftly took action to make improvements.

These included increasing the number of nursing staff, appointing a new ward sister and ensuring staff completed an education and training programme.

It said procedures had also been tightened and improved in all its hospitals.

“As a result we want to assure the public that the ward today has improved significantly from the way it was over two years ago,” it said.

‘Sincere apologies’

“We can also give assurances that we have used the experience of this tragic event to improve our practices across the health board.

“Whilst we fully recognise that this can be of little comfort to the family it is important that they know that the concerns that they have raised have improved care for others.

“We would wish to reiterate our sincere apologies to them for failing to meet the needs of this patient.”

His sister Jane Nicholls told BBC Wales: “Paul couldn’t communicate like you or I can, so you had to pick up on the signs.

“I find it really difficult because I don’t know quite how Paul felt and he died from excess secretions in his upper airways, which is like drowning, and he was unable to communicate to us.”

How Disability Reforms Were Whitewashed At Labour Conference

September 27, 2011

Many thanks to Daniel Elton at Left Foot Forward for writing this post.

Shakespeare In Sign Language

September 27, 2011

This is a great idea. Not only is a Shakespeare play going to be performed in British Sign Language, which is great progress in itself, but even better, BSL has been seen for this as a ‘translation’ rather than a ‘reasonable adjustment’- it has been included on a long list with all kinds of other ‘foreign’ languages that the plays will be performed in. This is something that speakers of BSL really want to see happen everywhere. I thank the Globe for recognising this and doing it so well.

New Drug For Albinism

September 27, 2011

A drug which is already licensed for use could be used to treat sight problems in some albino people, say US researchers.

People with albinism produce little or no melanin, which has a range of health consequences including poor sight and greater risk of skin cancer.

Writing in The Journal of Clinical Investigation, doctors said a drug increased melanin production in mice.

Other doctors described the work as a “substantial leap forward”.

People with a type of albinism – OCA1 – have light skin, white hair and light irises caused by defective tyrosinase genes which mean they struggle to produce melanin.

Mice tests

Scientists at the National Eye Institute, Maryland, were investigating a drug – nitisinone – which is used to treat a blood condition, but is also known to increase hair and eye pigmentation.

Giving the drug to albino mice increased the amount of melanin in the eyes after one month of treatment.

However, the researchers could not tell it this improved eyesight in the mice as the generally nocturnal creatures have different eye structures.

The researchers also do not know what would happen in human patients.

“A significant unanswered question is whether improving pigmentation in patients with albinism would improve visual function,” the report said.

However, they added it was: “plausible that increasing pigmentation may help with symptoms”.

Dr Prashiela Manga and Dr Seth Orlow, from New York University School of Medicine, said the study “represents a substantial leap forward toward the possible treatment of all forms of oculocutaneous albinism (OCA)”.

Jono Lancaster: Finding My Family On Facebook

September 27, 2011

Facebook and other social media are great for keeping up with friends and family and looking up people you’ve lost touch with, but they’ve also had an unexpected consequence on families separated by adoption. It’s now much easier for people to look up and make contact with birth relatives – a modern phenomena which adoption charities see as one of the biggest challenges they face, as the results of these unregulated reunions can turn people’s lives upside down.

Jono Lancaster (Love Me Love My Face, So What if My Baby is Born Like Me) was given up for adoption at birth and 25 years later attempted to get in touch with his birth parents using his local after-adoption service only to be told his parents still did not want any contact with him. Despite the disappointment, Jono understood and accepted the decision and resolved to get on with his life, only to be contacted by other members of his birth family, who found him through Facebook. Jono now has regular contact with cousins, aunts and uncles but has still never met his parents or siblings. He knows that it would be possible to contact them directly through Facebook, but has resolved not to, because of the damage it could cause.

In this film Jono will look at this very modern phenomenon and examine the issues facing families searching for their relatives on social networking sites. As well as following his own story, we will see Jono meet with and speak to other families who have been reunited – for better and worse – with their birth families through social networking sites, and meet some of the many teenagers on the viral hunt for their families.

I have just watched, and really enjoyed, this programme. If you missed it, it is available on BBC iPlayer here.

Huge Interest In Paralympic Tickets

September 27, 2011

Sessions in several sports were oversubscribed for the first time in Paralympics history during the window to apply for tickets, which has closed.

Ballots will be held for sessions in track cycling, swimming and the final rounds of wheelchair rugby and wheelchair tennis at next year’s Games.

London 2012 chairman Sebastian Coe told the BBC: “We have a head-start with Paralympic sport in Britain.”

The Paralympic Games run from 29 August to 9 September next year.

More than 4,200 athletes, with a variety of disabilities, from 150 nations will take part.

Payment for the tickets will be taken by 31 October, and applicants will find out if they have been successful by 18 November.

Coe added that the appreciation of the Games among British youngsters could not be overstated.

“Look at the extraordinary scenes in Trafalgar Square just a couple of weeks ago when we celebrated Paralympic Day,” he said.

“Young kids from local schools were getting excited about seeing Ellie Simmonds, Oscar Pistorius, Dame Tanni Grey-Thompson and David Weir.

Continue reading the main story

London 2012 – Begin your journey here

London view

“The kids really do get it – for them it is excellent sport and the competitors have become household names.

“For young people Paralympic sport is actually an interesting metaphor.

“It is about courage and determination, it is about equality and sometimes it is about overcoming extraordinary setbacks in life.

“But what they also know is that they are watching things that they can’t do which is a pretty good way of defining sport really.”

BBC athletics commentator Paul Dickenson, who has covered the Games since Atalanta in 1996, said that famous Paralympians had definitely raised the profile of their sports.

“Look at the polls that BBC Sports Personality of the Year has achieved in the last few years where both Ellie and Tanni have reached the last three as sportswomen let alone Paralympic sportswomen,” he said.

“The profile that the general public have of these people is much, much higher than it has ever been before.

“And of course at every Paralympic Games I have ever been to, the medal count for the Great Britain team has just got higher and higher.

“We finished second behind China in Beijing and obviously we want to try and achieve that again by the time we get to London.

“There is a feeling that Paralympic sport is a concession made to people with a disability to take part in sport.

“But to be honest if you have ever been to wheelchair rugby you would be utterly amazed at the commitment and entertainment value these sports give.”

‘Why I Want To Go To The Paralympics’

September 26, 2011

Some BBC News readers explain why they want to go to the Paralympics. I thought some of you may be interested in what they had to say.

Stannah Stairlifts: Free Stairlift Giveaway

September 26, 2011

I have been sent the press release below by Stannah Stairlifts.

Stannah Stairlifts are running an incredible competition giving you the opportunity to win a free stairlift for yourself or for a loved one.

To enter, all you have to do is visit the Facebook page: ‘Stannah Stairlifts’ to complete your details on the ‘Free Stairlift’ giveaway tab to the left of the page. You will be entered into a grand prize draw to win your choice of one of our brand new, fully-fitted Stannah Stairlifts with a 2 year warranty and 24/7 servicing.

Competition closes on Monday 31st October 2011.

Background to Stannah

Stannah is a British family company. We have been making products to move people and goods between floors since 1867 and have sold more than 500,000 stairlifts in more than 40 countries world wide. We are proud of our engineering heritage, of the fact that we are still a family-run business five generations on and of the strong values and ethics that guide us.

 

Our name is on every product we sell, so it is especially important to us that all of our customers are happy with the service we provide. We therefore make four key commitments to our customers;

At Stannah our commitment to quality, service and manufacturing means your safety is alwaysparamount to us. We ensure that all our products go through rigorous testing and analysis to ensure critical factors of safety are achieved throughout the design and manufacture process.

We carry out a full risk assessment on your house to determine any hazards involved in the installation or functioning of a stairlift. If your property isn’t suitable for a stairlift, our consultants offer alternative solutions. we will never compromise your safety by selling you a stairlift if it is inappropriate to do so.

To view the promotion visit our Facebook page:

http://www.facebook.com/stannahstairlifts?sk=app_255071067859487

For further information, please contact:

Tamara Askew tamara.askew@harvestdigital.com | Rohan Jadhav rohan.jadhav@harvestdigital.com

UK Disability History Month Pre-Launch

September 26, 2011


On Thursday, 22nd September, I attended the pre-launch event for UK Disability History Month. Now entering its second year, the Month will run from 22nd November to 22nd December 2011. The theme of the Month this year will be ‘Celebrating Our Struggle For Equality.’

I met up with old friends and made new ones- but not before I sat, smiling in genuine interest, as several well known Disability Rights campaigners spoke about our struggle for equality through several years, decades and centuries, and the progress that has been made.

The disabled writer and poet Micheline Mason read extracts from her latest anthology, titled Sorry I Don’t Have The Time. One of her poems, titled The SPA School Blues, was written in 2005 after she watched a documentary called Make Me Normal, about young people with Autism in a state-run special school. This is clearly meant to describe the lives, thoughts and feelings of 21st century special school students with Autism. However, as someone with Cerebral Palsy, I found myself agreeing with every word, as I was taken back to the experiences my friends and I had at our special school in the 20th century. I think it is safe, though it makes me sad, to say that this poem might apply to any student with any disability in any special school in England.

Dr Sonali Shah, a researcher from the University of Leeds’ Centre For Disability Studies, spoke about a piece of research she has carried out on disability and social change in the 1940s, 1960s and 1980s. This was before my memory, but if there was any progress in disability rights from the 1940s to the 1980s, there has certainly been much more progress in this area from the 1980s to today. Of course we all hope there is still much more progress to come.

Penny Beschizza explained, in British Sign Language, what life was like as a deaf person in the past and how life has changed and improved for deaf people now.

Michelle Daley spoke about the Black disabled experience in the UK. She also mentioned the experience of disabled slaves in the slave trade- something I have never been taught about before, but which I found very interesting. I think all history teachers should be asked to make space for this topic as part of their teaching of slavery.

Then there was the former journalist Katherine Quarmby, who recently wrote a book about disability hate crime titled Scapegoat. She described the cases she covered for the book and spoke about what she has learnt from writing it.

Finally, the Month’s Co-ordinator, Richard Rieser, shared his thoughts on disability history and famous disabled people throughout history. He explained how the Month will be a chance for disabled people and our organisations to organise events celebrating disability and disability history.

Personally, I thought Disability History Month was a great idea from the day I first heard about it. I, for one, hope the Month will run for many more years. Maybe, one day, it will be as well known as it’s more famous friend- Black History Month.

That will be the day when we will no longer have to struggle for equality.

How Much Do We Really Know About ME?

September 26, 2011

When it comes to controversy and heated debate, few illnesses come close to Chronic Fatigue Syndrome, also known as Myalgic Encephalomyelitis (ME).

There have been arguments about whether it exists, the cause, the best treatments and even the name itself.

These disagreements have reached the level of abuse and death threats.

The disease itself, however, remains poorly understood – or as one doctor put it: “The whole thing is surrounded by uncertainty”.

Does it exist?

For a long time, the existence of CFS/ME was widely dismissed and labelled as “yuppie flu”. That opinion has largely been reversed in the past decade.

In 2002, then chief medical officer Prof Sir Liam Donaldson described it as a “disease in the wilderness”. He was presenting a report which said CFS/ME was a “genuine illness and imposes a substantial burden on the health of the UK population”.

It is thought to affect about a quarter of a million people in the UK.

The main symptom is severe fatigue, made worse by exertion, which does not go away after resting. Muscle pains, headaches, memory problems and depression can also be involved. In some cases it can be completely debilitating, resulting in patients being unable to leave their beds.

Understanding of the disease is largely led by those symptoms. There is no test for CFS/ME, instead it is diagnosed by ruling out other conditions which might produce the same symptoms.

The underlying cause, or indeed causes, have been more elusive.

Uncertain origins

One of the issues in the field is that there is an emerging consensus that CFS/ME is not one illness.

Prof Stephen Holgate, chair of the Medical Research Council group on CFS/ME, told the BBC: “I think the problem with it is the term is used as a bit of a dustbin.”

In children there are thought to be three sub-groups, and even more in adults, all given the label CFS/ME.

Prof Peter White, of Barts and the London School of Medicine and Density, said: “Most specialist doctors and scientists agree that it is more than one illness. It may be three to five separate illnesses.

“Like kidney failure, it has lots of different causes, but looks the same.”

There was a brief moment of hope and optimism that a specific virus – XMRV – was the cause, however, that link has been largely discredited.

Viruses may have a role as a trigger for the illness, with many patients reporting that their symptoms started after infection.

Yet this has further levels of complication, as Prof White argues: “If glandular fever is a trigger but a patient has symptoms five years later, then it is no longer the Epstein-Barr virus, its something else.”

While there have been suggestions that patients with CFS/ME have differences in their immune systems, pain perception and hormones, it is not known whether these are a cause or symptom of a chronic condition.

There has also been suspicion of a genetic or family element.

In Nature Reviews Neuroscience, Prof Holgate argued: “One is left with a strong sense that post-viral events are a common trigger of Chronic Fatigue Syndrome, but how they lead to chronic persistent disease remains unresolved.”

The search for a cure

So far, a cure does not exist.

Prof Michael Sharpe, of the University of Oxford, said: “A pill that made you better would be great.” However, he added, medicine fell well short of that: “The best shot right now is various forms of rehabilitation.”

The PACE trial, which published results earlier this year, attempted to find out what the best therapies were.

It examined the use of both cognitive behavioural therapy, which alters the way people think and cope with their symptoms, and graded exercise therapy, a gradual and supervised increase in activity levels.

The trial suggested that patients using these therapies showed lower levels of fatigue and greater physical function.

Prof Holgate said: “Combining graded exercise therapy and cognitive behavioural therapy has undoubted benefit.

“Yes you can improve, but it mustn’t be confused with the underlying cause.”

He said these therapies might only be treating secondary symptoms.

However, the study has generated controversy with patients’ groups and charities saying the findings were exaggerated and went against their own evidence. In Action for ME’s 2008 survey of patient experiences, more than one in three said graded exercise therapy actually made them worse. They prefer a method known as “pacing” – or learning to live within limits – which the PACE trial concluded was not effective.

The ME Association’s Dr Charles Shepherd said: “We consistently find pacing is the most effective. I’m not convinced graded exercise therapy is the answer to this disease, it is something more fundamental which cannot be reversed, an overly simplistic solution to an extremely complex problem.”

Some people do, however, get much better.

Dr Ester Crawley, who specialises in children with the illness, said: “The prognosis for adults is poor, but for children it is really good, up to 94% get better.”

She said the reason for this was unclear, but theories included “neuronal plasticity” – as children’s brains are not fully developed, they can heal better – and “the adult lifestyle being predicated against recovery”.

It is easier to adjust a child’s lifestyle, such as doing two hours of school a day and gradually building it up, which is harder to do with adults who are in work.

A deeper understanding of the illness is desired by all involved. Delving into the sub-types of the condition may help in finding causes, which could also have implications for treating each sub-type.

One hope is that the new biobank of blood samples of CFS/ME patients being set up at London’s Royal Free Hospital will help provide the answers.

Robo Legs

September 25, 2011

Scientists in the Netherlands are using robotic legs to try to improve the movement of stroke patients.

The prototype device is called the Lower-extremity Powered ExoSkeleton, or LOPES, and works by training the body and mind of a patient to recover a more natural step.

Neil Bowdler reports.

Ataxia: ‘People Think We’re Drunk’

September 24, 2011

This is a collection of portraits of people with Ataxia, that some of you might find interesting.

Eye Stem Cell Trial Approved

September 23, 2011

Embryonic stem cells are to be used to treat an inherited blinding disorder in a ground-breaking UK trial that has been given the go-ahead.

Doctors at Moorfields Eye Hospital in London will transplant laboratory-grown retinal cells into patients with advanced Stargardt disease.

The Phase I study, which should take place within the next few months, is designed to investigate the safety of the treatment.

Stargardt disease is a form of macular degeneration that causes disabling loss of sight in young people.

Professor James Bainbridge, who will head the trial, said: “There is real potential that people with blinding disorders of the retina, including Stargardt disease and age-related macular degeneration, might benefit in the future from transplantation of retinal cells.

“The ability to regenerate retinal cells from stem cells in the laboratory has been a significant advance and the opportunity to help translate such technology into new treatments for patients is hugely exciting. Testing the safety of retinal cell transplantation in this clinical trial will be an important step towards achieving this aim.”

A Moorfields spokeswoman said details such as how many patients will take part in the trial were not yet known.

The procedure uses retinal cells grown in the laboratory from human embryonic stem cells (hESCs).

Stem cells extracted from early-stage embryos are “pluripotent”, meaning they have the potential to become virtually any kind of tissue in the body.

However, the technology is controversial since it necessitates the destruction of human embryos, albeit ones that only consist of a pinhead-sized bundle of cells.

ME Virus Link Questioned

September 23, 2011

Scientists who first linked chronic fatigue syndrome, also known as ME, to a virus have withdrawn some of their findings.

They have said some of their findings were based on “contaminated data”.

Meanwhile, a study in Science claimed the virus could not be reliably detected in ME patients, even in the labs which originally made the link.

Understanding of chronic fatigue syndrome is poor. It may be many diseases and the causes are uncertain.

There was a sense of hope for many patients when a study published in Science in 2009 showed that DNA from a mouse virus, XMRV, was present in 67% of patients with the illness, but only 4% of the general population.

Yet other scientists around the world could not find evidence of the virus. Many researchers began to argue that the most likely explanation was contamination of the laboratory samples.

It led to Science asking the authors to withdraw their findings and it published an editorial “expression of concern” saying that the validity of the study was “seriously in question”.

Continue reading the main story

CHRONIC FATIGUE SYNDROME

  • The disease is thought to affect some 250,000 people in the UK
  • Symptoms include extreme tiredness, problems with memory and concentration, sleep disturbances and mood swings
  • There is currently no accepted cure and no universally effective treatment
  • Source: ME Association

The authors have now issued a partial retraction after some of the scientists involved reported contamination, but this only calls into question the information in one table and two diagrams, not the rest of the paper and not the final conclusion.

One of the labs involved, the Whittemore Peterson Institute in Nevada, is standing by the conclusion. One of its lead researchers, Dr Vincent Lombardi, said it was “participating” in the retraction but: “We want to make it very clear that we are continuing the important work of studying retroviruses in association with ME/CFS and other similarly complex illnesses.

“WPI’s more recent retroviral work, although still in the early stages of discovery, continues to warrant additional investigations.”

Meaningless

Dr Jonathan Stoye, virologist at the Medical Research Council National Institute of Medical Research in the UK, said: “I don’t think this partial retraction has any meaning, it would have been nice to have a complete rather than a partial retraction.

“They’re saying the rest of the paper still stands, but that is becoming increasingly difficult for them to maintain.”

A fresh study on XMRV published in Science, which the researchers behind the original study participated in, again questioned the link.

Samples of blood were collected from 15 patients who had previously tested positive for XMRV, 14 of whom also had chronic fatigue syndrome, and from 15 patients without XMRV.

These samples were sent to nine laboratories, including two which had found the link previously. No lab knew which samples were from which patients.

Only two laboratories, the two which initially proposed the link, detected any cases of XMRV. However, the virus was detected at “similar rates” in both groups of patients, the study said.

The results from the two laboratories were also “inconsistent” even when testing blood from the same patient.

Dr Charles Shepherd, medical adviser to the ME Association said: “These are very emphatic negative or inconsistent findings from the Blood Working Group study, along with the retraction of some of the original supporting data that was published in Science.

“So it is now looking extremely unlikely that XMRV is either linked to ME/CFS or that it has a disease-causing role.

“Having had their hopes raised that a treatable component to ME/CFS had been identified, it’s not surprising that people are becoming increasingly disappointed at the way things are turning out.

But it’s too early to send out the scientific jury to make a final definitive decision on XMRV and ME/CFS – we still need the results from the other major multi-centre study on XMRV and ME/CFS being carried out in America by Prof Ian Lipkin.”

Disability Horizons: Ipads, CP And Communication

September 22, 2011

Just a quick post to link to my latest article for Disability Horizons, about Ipads, Cerebral Palsy and communication.

Two Useful Links from C4Paralympics

September 22, 2011

I have been asked to publicise these links by the people at C4Paralympics. They are both about Paralympic tickets:

I hope readers find these useful.

Nicky Clark Thanks Ricky Gervais For The Office

September 22, 2011

Just a quick post to link to this great piece by Nicky Clark.

Event: Celebrating Our Struggle For Equality

September 22, 2011

Blogging will be light today. I’ll be at this. Whizz over and say hi if you spot me!

‘ Celebrating Our Struggle for Equality’

United Kingdom Disability History Month 2011 Pre-Launch

            5.00  p.m. Thursday 22nd September 2011

To be followed by a Reception at 6.30pm

Invision Suite, 2nd Floor, TUC, Congress House, 23-28, Great Russell Street, London WC1B 3LS

Contributors:- Penny Bechizza-being Deaf now and in past, Michelle Daley, Black  disabled experience in the UK, Micheline Mason(poet)’Sorry I don’t Have the Time’, Katherine Quarmby author  ‘Scapegoat’,                                Richard Rieser-UKDHM 2011, Dr. Sonali Shah ‘Living as a Disabled Person 1940’s,1960’s,1980’s ’

    Please RSVP Richard Rieser UKDHM Coordinator 02073592855 office.worldofinclusion@gmail.com

Able Life: The ‘D’ Word

September 21, 2011

Tonight on Able Life, George Johnson and I will be discussing the word disabled! Here’s your sneak preview.

Another Autism Friendly Film Screening

September 21, 2011

Thanks to @societyguardian for the info. This is great news and I hope the idea takes off.

• Autism friendly film screenings. We reported last month on a pilot project involving the Odeon cinema chain and Dimensions, a provider of support for people with autism and learning disabilities, to make movies a more enjoyable experience for children with autism and their parents. Dimensions has announced that after 3,000 turned out for the pilot screening, the next showing will take place next month when Johnny English Reborn! will be presented in cinemas with low lighting, the volume turned down and no trailers.

‘never fall ill, never grow old, never become disabled’, for if you do, not even Labour will speak up for you.’

September 21, 2011

A special message from the Broken of Britain:

To all our members and supporters;

 

The Labour party conference starts in Liverpool on Saturday. As we all know, Labour were the architects of Employment Support Allowance and the ‘not fit for purpose’ Work Capability Assessment which is so stressful and traumatic it was linked to the suicide of claimants whilst Labour were still in power. The Labour party are the official party of opposition, but they are not opposing the Welfare Reform Bill as they should be and seem to have forgotten that the 10 million sick and or disabled people plus carers, friends and family in the UK have the power to vote. It is time for us to remind Labour that they will not get any of our votes if they do not start to oppose the parts of the Welfare Reform Bill set to return sick people, disabled people and carers to a life of desperation, dependency, despair and charity.

 

We are asking you to help with a mass email to the Labour party to remind them of our voting power. Please include the following details in your email and send it to Ed Miliband, Margaret Curran (shadow minister for disability) and Liam Byrne (shadow minister for DWP). If you have time please also email it to any Labour MP and particularly any members of the shadow cabinet. We have provided a list of email contacts below.

 

Please aim to send your email at 11am tomorrow (Thursday the 22nd September) If you can’t send the email at 11am, don’t worry, just please try to send it at any time between then and the end of Labour party conference on Wednesday 29th September.

 

The email subject  should read “Your Silence Is Deafening”

 

We suggest embedding a link to this youtube video “The Sound of Silence” To embed the video into your email just copy and paste the link below.

 

http://www.youtube.com/watch?v=BvsX03LOMhI

 

 

Then please copy the following text into your email;

 

Dear (insert name here)

 

‘The 10 million disabled people in this country plus their carers, relatives and friends are watching what your party do in relation to disability issues and wondering why you seem disinterested in trying to get their votes by opposing the savage attacks against disabled people being made by the Coalition government. During conference season we wish to remind you, the architects of Employment and Support Allowance to ‘never fall ill, never grow old, never become disabled’, for if you do, as we have found, not even Labour will speak up for you.’

 

If you would like to add a short, personal message explaining to Labour how you feel about their lack of support for sick, disabled people and carers then please include it after the suggested text. You might also like to include a photo of yourself, or perhaps a photo of what disability, sickness or caring means to you. Don’t worry if you don’t want to personalise the email, sending the suggested text is fine.

 

 

 

Ed Miliband MP, Leader of the Labour Party

House of Commons, London, SW1A 0AA
Tel: 020 7219 4778
ed.miliband.mp@parliament.uk

 

Shadow Secretary of State for Work & Pensions

Liam Byrne

House of Commons, London, SW1A 0AA
Tel: 020 7219 6953
Fax: 020 7219 1431
byrnel@parliament.uk

 

House of Commons, London, SW1A 0AA
Tel: 020 7219 8102
Fax: 020 7219 6656
margaret.curran.mp@parliament.uk

 

Shadow Home Secretary and Minister for Women and Equalities

Rt Hon Yvette Cooper MP

coopery@parliament.uk

 

Shadow Chief Secretary

Angela Eagle

eaglea@parliament.uk

 

Shadow Secretary of State for Business, Innovation & Skills

John Denham

denhamj@parliament.uk

 

 

Cabinet Office and Minister for the Olympics

Tessa Jowell

jowellt@parliament.uk

 

Shadow Secretary of State for Communities and Local Government

Caroline Flint

House of Commons, London, SW1A 0AA
Tel: 020 7219 4407
Fax: 020 7219 1277
caroline.flint.mp@parliament.uk

 

Shadow Secretary of State for Culture, Media & Sport

Ivan Lewis

House of Commons, London, SW1A 0AA
Tel: 020 7219 2609
lewisi@parliament.uk

 

Shadow Leader of the House of Commons 

Hilary Benn

House of Commons, London, SW1A 0AA
Tel: 020 7219 5770
hilary.benn.mp@parliament.uk

 

Shadow Secretary of State for Defence

Jim Murphy

House of Commons, London, SW1A 0AA
Tel: 020 7219 4615
Fax: 020 7219 5657
jimmurphymp@parliament.uk

 

Shadow Secretary of State for Environment, Food and Rural Affairs

Mary Creagh

House of Commons, London, SW1A 0AA
Tel: 020 7219 6984/020 7219 8766
Fax: 020 7219 4257
creaghm@parliament.uk

 

Shadow Secretary of State for Education and Election Coordinator

Andy Burnham

House of Commons, London, SW1A 0AA
Tel: 020 7219 8250
andy.burnham.mp@parliament.uk

 

Shadow Lord Chancellor, Secretary of State for Justice

Sadiq Khan

House of Commons, London, SW1A 0AA
Tel: 020 7219 6967
Fax: 020 7219 6477
sadiqkhanmp@parliament.uk

 

Shadow Secretary of State for Energy and Climate Change

Meg Hillier

House of Commons, London, SW1A 0AA
Tel: 020 7219 5325
Fax: 020 7219 8768
meghilliermp@parliament.uk

 

 

 

 

Shadow Secretary of State for Health

John Healey

House of Commons, London, SW1A 0AA
Tel: 020 7219 6359
Fax: 020 7219 2451
healeyj@parliament.uk

 

Shadow Secretary of State for Northern Ireland

Shaun Woodward

House of Commons, London, SW1A 0AA
Tel: 020 7219 2680
woodwardsh@parliament.uk

 

Shadow Secretary of State for Scotland

Ann McKechin

House of Commons, London, SW1A 0AA
Tel: 020 7219 8239
Fax: 020 7219 1770
ann.mckechin.mp@parliament.uk

 

Constituency

 

Shadow Secretary of State for Transport

Maria Eagle

House of Commons, London, SW1A 0AA
Tel: 020 7219 4019
Fax: 020 7219 1157
eaglem@parliament.uk

 

Shadow Secretary of State for Wales

Peter Hain

House of Commons, London, SW1A 0AA
Tel: 020 7219 3925
Fax: 020 7219 3816
hainp@parliament.uk

 

 

Steven Timms MP

timmss@parliament.uk
stephen@stephentimms.org.uk

Karen Buck MP

buckk@parliament.uk

Terminally Ill Warned Over Cuts

September 21, 2011

Thousands of terminally-ill people have begun receiving letters warning them their benefits could be cut in April, even though Parliament has yet to approve the changes.

Under proposals in the Welfare Bill, which is being scrutinised in the Lords, contributory Employment Support Allowance will be time-limited to 12 months from April 2012.

The change will be retrospective, so people who have received the payments for 12 months or more when the rule comes into force will have their benefit cut immediately.

Earlier this week, delegates at the Liberal Democrat conference in Birmingham passed a motion calling on their MPs to oppose the “arbitrary” time limit and the plans are likely to face stiff opposition in the Lords.

‘No win situation’

Neil Coyle, of the Disability Alliance, said that while it is uncertain whether the rule will be passed, it is premature for the Department for Work and Pensions to warn recipients of the changes.

“The letters are now being sent at a cost of £2.7m, including letters to people who unaffected by the change but who will experience considerable anxiety,” he said.

“The government has time to change plans before terminally-ill people and their families have this avoidable and quite nasty cut imposed.”

The Department of Work and Pensions admits it is conceivable the legislation may not be approved but says it is better to warn people early.

“It would be completely wrong not to alert people well in advance that there is a possibility that their benefit entitlement may change,” a spokesman said.

Jenny Willott, Lib Dem backbench spokesman on welfare, says it is a “no-win situation for the DWP”.

“If they don’t pre-judge the situation they could end up with thousands of people losing their benefits with little notice,” she said.

Ms Willott says Lib Dem peers are working the “issues to be ironed out” in the bill.

Terminally-ill people with less than six months to live will not be affected by the changes.

Bridgette Jordan

September 21, 2011

A dancing, cheerleading 2ft tall American has been named world’s shortest living woman by Guinness World Records.

Bridgette Jordan, 22, from Sandoval, Illinois, stands 2ft 3in (69cm) and also holds the record for shortest living siblings with her 20 year-old brother Brad.

Standing at a comparatively lofty 3ft 2in (96.5cm), Mr Jordan lists his hobbies as basketball, karate and gymnastics.

Music-lover Ms Jordan also likes to stay active and often spends time dancing and cheerleading.

On her record-breaking achievement Ms Jordan said: “It feels awesome. It’s great to be small. I believe that everyone should be confident in themselves.”

Her brother added: “Hopefully this will go a little way to helping people realise it’s OK to be different.”

The siblings, who have Majewski osteodysplastic primordial dwarfism type II, live with their parents in Sandoval and study at Kaskaskia College.

Ms Jordan breaks the record of 22-year-old Elif Kocaman, from Kadirli, Turkey, who measured 2ft 4.58in (72.6 cm).

Jyoti Amge, 17, from Nagpur, India, is currently recognised as the world’s shortest teenager, standing at just 2ft tall (61.95 cm).

Both Jordan siblings feature in the Guinness World Records 2012.

How To Help During An Epileptic Seizure

September 21, 2011

I think this is a very useful video.

Paralympic Medals Revealed

September 20, 2011

Watch this video for a sneak peek.

The Separate Lives Of Conjoined Twins

September 20, 2011

The odds were against them. But thanks to the expertise of more than two dozen medics, conjoined twins Rital and Ritag can grow up normally. Terri Judd finds out from the surgeons exactly how they did it

David Dunaway’s voice briefly shook with emotion yesterday as he explained how it was his team’s hope that Rital and Ritag Gaboura would go on to lead normal lives.

“I can’t say what a joy it has been. It is hard to say what it feels like to have been involved in the team that managed to do this. It has been a wonderful experience. A few weeks later and they are smiling and developing properly. It has been wonderful for us,” said the cranio-facial surgeon.

It is a fleeting indication that, far from being a miracle, the separation of the conjoined twins was the culmination of months of work by a team of more than two dozen experts who pushed themselves to their surgical and medical limits. “We feel very lucky that our girls have been able to have the surgery that they needed, but we also know other children who need complete sponsorship and families who are searching for someone to help them,” says the girls’ father Abdelmajeed.

Rital and Ritag weighed just 6kg together when they were born by caesarean section in Khartoum, Sudan, in September 2010, joined at the top of their heads. Their parents Abdelmajeed, 31, and Enas, 27, both doctors, knew the odds against them were terrible. Only a fifth of conjoined craniopagus twins make it to their first birthdays, while 90 per cent of them die by the time they reach 10 years old. Even fewer get a chance to lead a normal life.

The two little girls would be confined to lying down but, worse still, Ritag was supplying half of Rital’s blood, keeping her twin alive, but slowly her heart was failing in the task.

For the girls’ parents, it was the beginning of a fight to find the funding and the expertise to separate them safely. They approached one organisation after another in vain.

Eventually, they were put in touch with Facing the World, a charity that was set up by some of the UK’s leading craniofacial surgeons almost a decade ago to provide hope for youngsters with terrible disfigurements. Over those years it has helped children from nearly 20 countries.

The charity managed to raise almost £300,000 to cover costs, while experts donated their time for free. They handled all the logistics, including the problem of finding the transport that would fly the girls in from Sudan.

Sarah Driver-Jowitt, Facing the World’s executive coordinator, who travelled to Sudan to make arrangements when the girls were two months old, says: “Even bathing them was difficult. Mum was really struggling to carry them both while supporting their necks. But they got around it in the most graceful way. They had large pillows to put them on. One twin would sleep while the other was crying. Just watching their mum cuddle one while the other sister was asleep, you forgot they were conjoined.”

Armed with new toys and clothes, the family arrived in London in April to begin a mammoth round of medical treatment. The team immediately fell head over heels for the pair. Rital, the stronger one, was “the boss”, while Ritag was chattier.

“They have always been little laughing girls. They just giggle. They would beam and start laughing even before I would talk to them,” says Driver-Jowitt.

The two little girls’ brains were separate but touched and shared a single dural layer (a thick fibrous membrane enveloping the brain). Parts of Rital’s brain were also supplied by her sister’s blood.

The surgeons were faced with a dilemma, says team leader Dunaway, as they wanted to complete the surgery in “slow, steady” stages. The initial plan had been to wait until the twins were around a year old, but the doctors knew that Ritag’s high blood pressure and failing heart were putting her in mortal danger and they simply could not afford much more time.

“One thing was encouraging us to go slower but Ritag’s heart failure was demanding that we go quickly. Her heart was having to pump for both twins and she was underweight, almost unable to take in enough nutrition to cope. Meanwhile, however, Rital was having a fairly easy time.”

Medication, he explained, was also causing a major problem as one twin had high blood pressure while the other’s was low, a tremendous challenge for the anaesthetists.

The team included craniofacial and plastic surgeons, neurosurgeons, anaesthetists, neuro-radiologists, paediatricians, cardiologists and a host of specialist nurses.

On 9 May, the first operation began. Over 10 hours they separated one third of the brains through limited cuts to the skulls. A silastic sheet was placed partially between them to replace the joint dura. The surgery went well, but it seemed that Ritag’s heart problems were getting worse.

Seven days later the twins went through another 10-hour operation when the surgeons separated the common vein in their brains, giving it to Rital, and extended the silastic sheet across the rest of the heads.

“This was a small 3cm blood vessel in a whole set of vessels so the chance of making an error was high,” explains leading neurosurgeon Owase Jeelani. But the surgery was successful and both twins were functioning well. The strain on Ritag’s heart was also beginning to lift.

Then on 4 July, when the girls had recovered enough and put on some weight, they went back into surgery yet again. This time, over six hours, tissue expanders were inserted under the scalp. These were inflatable silicone balloons which over the coming weeks would be gradually inflated with injections of saline. As they expanded, they stretched the scalp so that both girls would have enough to cover their heads when the separation came.

Then on 15 August, they went through the final major operation. Over 13 hours the surgeons worked to separate the girls. A new skull was made by splitting the inner and outer layer of their bone to cover both heads.

Doctors had worked for months on three-dimensional models to try to ensure that any scarring or disfigurement would be kept to a minimum. The skin was replaced so the direction of hair growth was normal.

The girls appeared to be doing well. Ritag, who had always had to fight harder to survive, had blossomed, while Rital was progressing a little bit more slowly, the surgeons explain.

“It is a delight to see how well the girls are doing. Rital was up and holding her own milk bottle again within days of surgery. Ritag took a day or two longer but she too is back to her laughing self,” says craniofacial surgeon Simon Eccles.

“After 11 months of spending most of their time lying on their backs it is amazing how quickly they have adapted. The girls are already doing all the things that they were able to do pre-surgery – playing with toys, clapping, holding their milk bottles and so on.”

They will both need further reconstructive surgery to ensure normal shaped heads, says Dunaway, and they will need physiotherapy to make their neck muscles stronger, but the prognosis is good for both girls: “It is for the family now to be able to settle down and lead a normal life.

“This was a real surgical challenge, a very rare and complex operation, drawing together many different disciplines. But also these were two little girls with a loving family, and we had to get both children through the procedures safely.”

Driver-Jowitt says: “The most moving thing for me was watching their parents the first time they had to deal with them separately. They were desperately running from one cot to the other, not sure where to be. They had never had to do that before.”

Deeply religious, the parents believe that their faith, as well as the extensive medical team, had helped their little girls survive, says Driver-Jowitt. “Their mum says the moment she woke and they were no longer conjoined it was all like it had been a dream. When we put the girls together in a cot, they just linked arms and started playing with their teddy bears.”

On Thursday, the twins will celebrate their first birthdays but Driver-Jowitt says: “Their mum and dad have already said that they will have two birthdays, one to mark their birth and one to mark their separation.

“The parents always said that all they ever dreamt about was to have two healthy girls to go home with and that is now about to happen.”

A modern miracle

It was not until three decades ago that conjoined twins had much hope of surviving separation. Until then, parents faced the agony that one child would die, and sometimes neither would survive due to blood loss and surgical complications.

In 1987, neurosurgeon Benjamin Carson, from John Hopkins Hospital in Baltimore, gained worldwide recognition as the first man to successfully separate craniopagus twins. A 50-member surgical team worked 22 hours to separate Patrick and Benjamin Binder, who both survived.

Seven years ago James T Goodrich and David Staffenberg led the first multi-disciplinary medical team in a stage twin separation in New York. Though Carl and Clarence Aguirre still require close monitoring, it was the first double separation with no immediate signs of neurological impairment.

Two members of yesterday’s team, David Dunaway and Richard Hayward, led the first UK separation of craniopagus twins five years ago.

Rob Spence Again

September 20, 2011

Canadian documentary maker Rob Spence has always loved science fiction.

So much so that when he lost his eye six years ago, he took inspiration from some of his heroes.

“There are so many characters in pop culture and science fiction that have a camera eye that pretty much anyone who loses an eye at least makes a joke about getting a camera eye.

“In my case, I just actually did it.”

With the help of a former satellite company employee, he developed a camera which fits into his eye socket, and “eyeborg”, as he calls himself, was born.

Shooting accident

The original damage to his right eye came from an accident when he was just nine years old.

“I was visiting my grandfather in Northern Ireland and I decided it would be a good idea to take his 12-gauge shotgun and go and shoot some cowpats.

“I wasn’t holding the gun properly and it caused a lot of trauma to my eye.”

The deterioration was gradual, with years passing before all vision was lost in the eye. When it was lost, surgeons recommended its removal to prevent any deterioration in the other eye.

Spence has felt no great loss of ability, perhaps because the deterioration was so gradual. Nor was his quest for a camera eye motivated by any hope of improving his sight, he says.

“The motivation to put a camera in there was a combination of being an immature adult who wants to be like Star Trek or the Bionic Man, and an opportunity to make more interesting documentary films that a have a more literal point of view.”

The camera was built by friend and engineer Kosta Grammatis, who used to work for satellite and rocket company SpaceX. They got on so well that he moved in with Spence, and the first prototype eye was built on a coffee table.

The eye is currently in its third incarnation, and transmits live video pictures to a wireless monitor.

It attaches to a coral ball and coupling device which was fitted into the socket after his natural eye was removed (for the purpose of an aesthetic eye). This means it moves in tandem with his remaining eye and that Spence can direct the camera to its target.

It has become a fundamental part of his documentary making.

“When I’m filming someone, they’re looking right in my eye and they’re talking to me, not me through a camera, and there’s blinking and glancing. It’s much more similar to the way we see the world.”

Bionic journey

His latest film is a 12-minute documentary pegged to the launch of a video game which features a bionic human with their own camera eye.

For Spence, it was a chance to explore some of the innovations in bionics that are happening around the world, and to meet some of the people testing them.

This included interviewing Miikka Terho, a Finnish man with an inherited form of blindness who has been testing an eye implant which has enabled him to pick out large shapes and lights.

Spence thinks the future of bionic vision will be played out in high definition.

“I liken bionic eye technology – that is the sight-restoration kind, not my kind – to very early television. Just as television progressed from blurry terrible images to something that approximates to human vision, I see that happening as well with sight-restoration technology.”

Conjoined Twins Survive Separation

September 19, 2011

A team of British doctors have successfully separated twin girls who were born joined at the head.

Baby girls Rital and Ritag Gaboura, who are only 11 months old, underwent four operations at London’s Great Ormond Street Hospital for Children and were separated on 15 August.

The sisters, who were born in Khartoum, Sudan, have overcome incredible odds to survive – only one in 10 million survive the rare condition of craniopagus.

Their parents, Abdelmajeed Gaboura, 31, and mother, Enas, 27, who are both doctors, approached children’s charity Facing the World for help, which funded and organised their possible separation.

The family arrived in the UK in April and were admitted to Great Ormond Street Hospital where the Craniofacial team lead by David Dunaway donated their services.

By the time the family arrived, Ritag’s heart was already failing.

The girls were separated over four stages – two operations in May, then tissue expanders were inserted in July and the final separation in August.

A statement from Facing the World says: “Within days the twins were back on the general ward interacting and playing as before. Their laughter and delight in the world has been an inspiration throughout the months of worry.

“Very soon, their parents will be able to fulfil their dream of taking home two healthy, separate daughters.”

The girls’ parents told the BBC: “We are very thankful to be able to look forward to going home with two separate, healthy girls. We are very grateful to all the doctors who volunteered their time and to Facing the World for organising all the logistics and for paying for the surgery.”

The Power Of Words

September 19, 2011

Paralympic Tickets Selling Well

September 19, 2011

Track cycling and swimming have emerged as the hottest Paralympic tickets so far, with evening sessions at higher price levels already oversubscribed.

London 2012 organisers, Locog, said that all sports still had availability, including the lower-priced swimming and cycling tickets.

There had been fears of poor take-up but Locog Chair Lord Coe told the BBC sales were “going well”.

Online applications close at 1800 BST on 26 September.

Evening sessions for wheelchair basketball and wheelchair rugby were also “proving popular” while opening and closing ceremonies tickets at the lowest price of £20.12 were oversubscribed.

As with Olympic tickets, applications for oversubscribed events will be decided by random ballot.

Payment will be taken by 31 October, and applicants will find out if they have been successful by 18 November.

Lord Coe told the BBC: “There’s a good healthy response out there. Half the people who signed up said they wanted Paralympic tickets and the response has been good.”

He added: “We are monitoring the ticket sales. We won’t maintain a running commentary. We know from early sales that they were going well.

“We have decided to limit what we know will be the big ticket events. But I am pretty relaxed because we have a head start with the Paralympic Games in this country. People really get the Games. A lot of the athletes are household names.”

Three-quarters of the two million total tickets available before the Games are priced at £20 or under, and half at £10 or under.

According to Locog, there is still “good availability” across various sports in the Olympic Park and Excel, rowing at Eton Dorney, equestrian at Greenwich Park and road cycling at Brands Hatch.

There is no advantage in applying earlier in the process – all applications have an equal chance of getting tickets.

More than 4,200 athletes, with a variety of disabilities, from 150 nations will take part in the Paralympic Games from 29 August to 9 September 2012.

The Games will be preceded by a torch relay which will see flames from Edinburgh, Cardiff, Belfast and London combined at Stoke Mandeville into the Paralympic Flame, which will then be taken by teams of torchbearers to the Olympic Park for the opening ceremony.

Petition For BSL To Be A Recognised Language

September 19, 2011

What a great idea! I’ve just signed it and I hope you will take a minute to sign it as well.

http://twitter.com/#!/ActionOnHearing/status/115731146775601152

The Disability Diamond Theory

September 19, 2011

This is a guest post by Martyn Sibley. Thanks to Martyn.

Thank you for the privilege of allowing me to guest blog on this site. As a fellow campaigner, it is great we can stick together, and share each others projects for disabled people.

 

For over 2 years I have been running my blog http://martynsibley.com/. I enjoy writing articles, tweeting, sharing videos and pictures on my life: some would say a life less ordinary, while others would not feel the need to clarify. Having a disability; always striving for new challenges and living life to the full; my articles often highlight the lighter/social side to life. Having gained a masters degree, travelled to Australia, learnt to drive a car with my hands and now living independently in London; I have crammed a lot in to my 28 years. My website mantra is inspire, inform and change.

 

I have always said how grateful I am for those who fought for and won independence for disabled people 20+ years ago. Moreover, I remain ever grateful to those campaigning on prevalent issues today. I have also dipped my toe in the political writing arena http://www.disabilitynow.org.uk/have-your-say/guest-column/putting-the-personal-into-personal-care and attended political marches http://martynsibley.com/the-professionals-video-from-the-march

 

For the past 2 months I have been self-employed (having worked for Scope in various capacities for 5 years) and I’m now running my own online projects for disabled people. Beyond my blog I co-launched the disability magazine http://disabilityhorizons.com/, created a series of ‘webinars’ (online seminars) http://martynsibley.com/online-learning and have other ‘new media’ plans.

 

The webinars are being run for my social media audience, and also in partnership with Hackney council http://www.hackney.gov.uk/disability-webinars.htm and Scope http://www.scope.org.uk/news/blogs/martyns-blog/free-disability-webinars (for their respective service users). Each series has 5 topics, which vary with each contract, and include: being a parent to a disabled child, a session for disabled teenagers, giving assistance with independent living (accessible housing, equipment, care and finance), accessing local leisure and world travel. In one hour the attendee can log on from home (or their nearest computer), absorb the 45 minute presentation I deliver and then ask specific questions in the 15 minute Q&A session. They see my screen and therefore can view powerpoint slides, websites, word documents and other useful/relevant materials. Meanwhile I explain all by talking into a microphone.

 

The benefits are seen by free attendance, useful information on a manner of disability related topics, personal goals to be taken away and my own theory which can be applied to all future concerns. To sign up and try one for yourself please click here http://martynsibley.com/online-learning

 

So, what is the theory I mentioned? It is called the Disability Diamond Theory. I created this theory because I could see the need for a disability model that focuses on an individuals’ impairment, needs, aspirations and life choices. It also encourages disabled people to aim higher, helps them along with some useful resources and explains my philosophy too. By my own admission it derives from personal experiences and is not an academic thesis. My experiences have, however, been influenced by many other disabled people and my only professional work was in the disability sector. A pretty solid foundation to write such a book I hope.

 

It is free to download here http://martynsibley.com/philosophy. My vision is that the Disability Diamond Theory will encourage disabled people (especially the next generation) to use the resources available (that were not around 20+ years ago) and excel in life.

 

I would love for you to read this ebook and feedback your views – good, bad or indifferent http://martynsibley.com/give-me-a-shout

Coping With The Cuts

September 19, 2011

http://twitter.com/#!/scope/status/115715265760735233

ESA Needs Reform, Admits Minister

September 18, 2011

Controversial assessments of disabled people that have led to many losing their state benefits will be reformed, said Steve Webb, the Liberal Democrat work and pensions minister.

He accepted there was genuine anger about how claimants of employment support allowance (ESA) had been treated. The “vast majority” of claimants for ESA, which has replaced incapacity benefit, are deemed fit for work by Atos, the French company which is paid £100m a year to assess claimants.

Yet four out of 10 of those who appeal against the decision by Atos are successful, a process that costs the taxpayer £50m a year. Last month Atos, whose staff assess around 11,000 benefit claimants a week, was savaged by the cross-party work and pensions select committee after it found that many people had “not received the level of service from Atos which they can reasonably expect”.

Webb said: “In the past, we accept, that the Department for Work and Pensions (DWP) folk just went ‘bang Atos says no’. We are now taking more control of that.” The system of “work-related assessments” which Atos carries out on the government’s behalf is currently the subject of an independent, state-funded investigation by Professor Malcolm Harrington.

Webb said he had held discussions with his Tory colleague at the DWP, Chris Grayling, over the future role of Atos in assessments and that the government understood that change was needed. He said: “One of the changes Harrington recommended is that you don’t just take what the Atos assessor says and tick the box. You say, ‘let’s see what the consultant says’. If I need more information I will ask for it.”

“I am sure there are brilliant Atos inspectors and very poor ones, it is a big organisation, but if someone hasn’t done the assessment properly there is much of a safety valve now to say hang on this assessment says no problem but I have got all these reports from the medics.

“The way Chris put it, is the contribution of the Atos judgment to the decision will be a smaller part. And that has got to help.”

On Sunday Lib-Dem delegates at their Birmingham conference endorsed calls for Atos’s “tick box” system of medical tests to be replaced by something more accurate and less stressful for those who go through it.

 

The Life Of A Guide Dog Trainer

September 17, 2011

I’m blindfolded and frightened. Cars are roaring past as I stumble along busy Leamington Spa pavements, terrified I’ll unwittingly stray into the path of a vehicle. But Spriggs, the black labrador whose brown training harness I’m desperately clinging to, soon has me at ease, calmly steering me around hidden obstacles, pedestrians, workmen and parked cars with every wag of his tail.

Spriggs is close to finishing his training with Guide Dogs for the Blind and will soon be partnered with a visually impaired person, working until he is around 10 years old to protect his owner from the many dangers people with sight problems face out of the home.

At some point Spriggs will have been tutored by Gareth Evans, a local man who has worked with the charity for close to 16 years. “It has to be a partnership when you take on a guide dog,” he explains. “We can only get the dogs to a certain level and then the owners have to take over and they will get out of that partnership what they put in.”

Evans grew up in nearby Warwick surrounded by puppies – his family were regular “puppy walkers” for the charity, the name given to families that look after a puppy for its first 12-14 months before handing it back for training, as well as breeders.

“We would frequently bump into owners who had our puppies as adults, so guide dogs have always been in my life and I’d always wanted to work for the charity.”

He achieved that ambition when he was 19, spending five years working in the kennels before a broken wrist led him to shadow the organisation’s rehab workers, who provide training and guidance to help people live independently. “What impressed me most was how you could give someone the smallest piece of advice, some of it not even related to dogs, that would make a huge difference to their lives, such as how to make the text on their television screen bigger,” he remembers. “So I retrained as a rehab worker and did that for eight years.”

For three years of that, Evans was contracted out to the local authority’s social services teams. “It meant that I met people at the very beginning of their journey, people just coming to terms with their sight loss. It’s like a bereavement and people go through a range of emotions, so it can be tough as you can’t always give them what they want – which is their sight back.”

Four years ago he became a mobility instructor for the charity, which means that as well as finishing off the dogs’ tuition with advanced training, he helps match dogs to owners, provides support while they get to know each other and makes annual aftercare visits. “People develop their own ways of handling their dog … it’s great to see that because it means they are working well together.”

I am given a quick tour of the kennels at the Leamington Spa site, where more than 1,300 guide dogs are born each year. Every row of kennels has an area where the dogs are groomed and checked daily to ensure any health issues are nipped in the bud, though the dogs only spend a short time there because they are usually out training and exercising. “Guide dogs have to be in peak condition,” Evans says. “We can’t pair them with a member of the public if they have a problem that could be difficult to maintain or might worsen over time.”

We watch as three dogs chase each other around a grassy paddock strewn with features they might encounter in real life: tyres, ropes, ramps and jumps – all of which are designed to ensure they encounter as many real world obstacles as possible in their training. “It’s amazing how many things can startle an unprepared dog out of the home,” Evans explains. “A car reversing, people running past, workmen.”

Loneliness isn’t an issue, either – the kennels are staffed from 7am until 9.30pm, and any dogs that have problems adjusting to life there are, instead, allowed to spend time in the charity’s offices – which explains the occasional child safety gate or sleeping dog around the place. There is even a “chill-out” room on site, featuring a settee and toys which stressed pooches can use for a bit of doggy downtime.

Before we make an aftercare visit, I am given a range of glasses that simulate visual impairments caused by a range of eye conditions. In each case I struggle to make out the world around me and can’t wait to take the spectacles off, painfully aware of just how much I have taken my eyesight for granted.

Evans takes me to meet a visually impaired woman called Bev in the town centre to see how she’s getting on with her German Shepherd, Fifi. The average age of a new guide dog owner is 49, making Bev one of the younger “mums” or “dads”, as Evans calls the owners. I watch as Bev walks down the high street, Fifi deftly leading her around obstacles, at one point walking right in front her, causing Bev to stop suddenly. Fifi had seen someone about to witlessly walk across Bev’s path, and had helped prevent an unwelcome shock and a possible fall.

Evans thinks there are many myths about the role of guide dogs. “A lot of people think they take their owners for a walk, that the owner says ‘right, off to the fish and chip shop, please’ and the dog takes them there,” he says. “The owners are the ones in control and who need to know where they are going. The dog is only helping them look out for roads and obstacles, it’s not actually taking them anywhere – although if it learns a route it might pop into a shop if the owner visits frequently.”

He talks of the occasional embarrassment suffered by owners whose guide dogs betray their love of takeaways by padding into the kebab shop even if the owner wishes to walk past.

A couple of times someone strokes Fifi in the street and I wonder if that is a help or a hindrance to Bev and other owners? “The dogs are at work when they are out and about, so stroking them can put them off,” Evans admits. “It’s nice that the public feels that way and is really interested to see such well-trained dogs, but it’s probably best to ask the owner first. We never like to be rude about this because we’re a charity and we accept public donations. We have a lot to thank people for.”

The charity is responsible for around 8,000 dogs and pays for all training and veterinary bills during their working life. The figures speak for themselves: it costs £15 to feed a guide dog for about three weeks, £20 to buy a training harness and £3,500 for one-on-one training for the dog and its new owner. Thankfully, around 10,000 volunteers save the charity an estimated £28m a year by giving their time, and it receives a huge number of donations from wills – by this year, its 80th anniversary, it will have received 38,526 gifts in wills since inception.

The match of dog is an important part of Evans’s job. He looks for qualities that will ensure a happy and lasting partnership. “Fifi is sensitive,” he explains, “so we had to find a mum who would work well with her. Bev is exactly the type of person who can support and give plenty of praise to Fifi, so it is a great fit.”

When I am blindfolded and partnered with Spriggs for my walk, I immediately realise how big a jump it is from trusting your own eyesight to trusting that a dog will guide you safely around town. For the first five minutes I am genuinely scared that my life is held in the paws of a canine I’ve never met, but I slowly become attuned to Spriggs’s subtle movements, when he pulls me to the left or right to avoid obstacles or as he prepares to stop at a kerb. I marvel as he obeys my command to turn right at one pavement edge (after I’ve issued a loud command accompanied by repeated slaps to my right leg) and we spin round and continue our journey.

All the while Evans is telling me what to do, how to give the dog feedback, to pat him affectionately when he has done well, along with numerous other instructions. By the time I take the blindfold off I have genuinely bonded with Spriggs, to the extent that Evans jokes: “I’d better check your bag to see you haven’t stolen him,” and I get an inkling of the incredible bond that dogs and owners must share.

On the train back to London I spot one of Spriggs’s black hairs on my leg and it reminds me of my childhood pet Sid – a Jack Russell terrier I still miss to this day. It then strikes me why Evans has been with Guide Dogs for the Blind for so many years: when you are a key part in forging so many beautiful relationships, partnerships that lead to vastly improved lives, why would you want to work anywhere else?

How Stoke Mandeville Put The Paralympics On The Map

September 16, 2011

The Paralympic torch relay has put Stoke Mandeville on the map as part of its relay route, but the Buckinghamshire village has been famous for years as the birthplace of the Paralympic Games.

The Games were founded by pioneering neurologist Professor Sir Ludwig Guttmann at Stoke Mandeville hospital in 1948.

Sir Ludwig was born in Germany in 1899 and emigrated to Oxford in 1939 to flee the Nazi oppression of the Jewish community.

After working at an English military infirmary for head injuries, Sir Ludwig was asked by the government in 1943 to become head of the new National Spinal Injury Centre (NSIC) at the Ministry of Pensions Hospital at Stoke Mandeville.

The NSIC – now the oldest and one of the largest spinal injuries centres in the world – began as a treatment centre for World War II servicemen.

But Sir Ludwig came up with the revolutionary idea of using sport as a key part of rehabilitation – this, combined with his positive attitude towards patients, was the key to his success in treating them.

Until this point, people with spinal cord injuries often died within a year of sustaining the damage, having been given no hope of returning to their previous life.

Under his care, people were encouraged to try activities including wheelchair polo, wheelchair basketball and archery, which proved popular, as paraplegics could compete with able-bodied counterparts.

In 1948, Sir Ludwig organised a competition for 16 paralysed men and women – the Stoke Mandeville Games for wheelchair athletes – to coincide with the opening ceremony of London’s 1948 Olympic Games. Their first competitive sport was archery.

Sir Ludwig’s daughter, Eva Loeffler, who was a teenager when the first Games took place, recalled them as a happy event.

“There was a wonderful atmosphere at the Games and I recall there was always an enormous party in the sports hall on the final evening,” she told Bucks County Council’s Mandeville Legacy website.

“I used to run around with a tray handing out pints and pints of beer and everyone got very merry. I remember one year Margot Fonteyn the ballerina was there while her husband, who was a tetraplegic, was having treatment in the spinal injuries unit.”

Four years later, competitors from the Netherlands joined in, sparking the beginnings of an international competition.

By 1960, a Games for athletes with a disability took place at the Rome Olympics and the modern Parallel Olympics – or Paralympics – were born.

Other disability groups were added at Toronto’s 1976 Olympics, and in the same year, the first Paralympic Winter Games took place in Sweden.

Sir Ludwig continued his work at the hospital, where he was known by staff and patients as ‘Poppa’. He remained a key figure for the Games, becoming president of the International Stoke Mandeville Games Federation.

In 1961 he founded the British Sports Association for the Disabled, became inaugural President of the International Medical Society of Paraplegia (now known as the International Spinal Cord Society) and edited the the society’s journal, Paraplegia.

The Queen knighted him when he retired in 1966, having already made him an OBE and CBE.

The NSIC is still carrying on his work, having expanded from 26 beds to 190 in the main part of the hospital.

It has benefited from the fundraising activities of former BBC TV and radio presenter Sir Jimmy Savile, whose marathons and events over the years have raised a total of £10m, fulfilling his aim of creating a purpose-built spinal cord injuries centre. He is now its patron.

Deaf Services Cut In Bristol

September 15, 2011

I’m linking to this piece by Charlie Swinbourne, in case anyone finds it interesting.

Gary Parkinson Again

September 15, 2011

This time last year Debbie Parkinson was faced with a life or death decision over her husband Gary, a former professional footballer.

The Premier League football coach at Blackpool FC had suffered a major stroke which left him with locked-in syndrome – unable to move, speak or swallow.

A few days later, first team players at Blackpool dedicated their 2-0 victory in the Premier League at Newcastle, to him.

But away from the glamour of the game, his wife Debbie, who was keeping a vigil at his hospital bed, was asked by doctors if she wanted to keep his life support machine running.

“I said: ‘Yes I do. While there is still life there we keep going'”, she recalled.

Sitting at his bedside she told her husband he had to keep fighting.

“At that point when I said it to Gary, his eyes opened and were flickering and I knew then that he could hear inside and there was something we had to keep fighting for him,” she added.

The 43-year-old’s family have drawn strength from the support they have received throughout the football world.

His former club Middlesbrough had a testimonial match for him in May with fans reviving the chants they used to sing for him.

His family have received thousand of messages of goodwill from friends, fans and players.

“It’s been brilliant, all his former clubs have been united really,” said his son Luke, who is due to take part in Saturday’s Great North Run to raise money for The Stroke Association.

“You can’t believe how much support he’s had. I’ve seen him in his football days most of the time they are booing and shouting at the players but I’ve had messages from fans saying he was a legend at Burnley, Middlesbrough and Preston,” he added.

The family have also drawn inspiration from a recent visit he received from Sheffield mother-of-three Kate Allatt who has recovered from locked-in syndrome.

Experts say complete recovery is rare, but patients can make improvements.

“I’ve always said it to Gary that if one person has made it before there is no reason why we can’t do it too,” said Mrs Parkinson.

“I have since found there are many people who have come through locked-in syndrome and are leading a good quality of life.”

In his playing days, Parkinson was a member of the Middlesbrough “Spirit of 86” team which had been locked out of the ground and relegated to the old Third Division.

Five years later he was playing for them in the inaugural season of the Premier League.

His family are hoping for a far more remarkable comeback.

To communicate he raises his eyelids upwards to say yes and lowers them to say no but in the last few days there has been a glimmer of hope with his fingers moving for the first time since the stroke.

Stars Turn Out For Mencap Awards Ceremony

September 14, 2011

I received the press release below earlier today from Mencap.

 

 Gavin and Stacy actor Mathew Horne, Dancing on Ice star Chloe Madeley and Elliot Rosen the actor who plays Craig Moon in EastEnders were among the stars who turned out for the awards for Mencap’s annual film and photography competition Snap!, in London last night (Tuesday, 13 September).

 

They joined nearly 200 guests who attended the learning disability charity’s ceremony at the Rich Mix arts centre in Shoreditch, east London.

 

Mathew Horne, Mencap ambassador said: “It was a great night and I was very impressed by the quality of the entries. I had the chance to meet some fantastic people and hear about their experiences first hand, which reminded me why I support the great work of Mencap.”

 

There were 36 winners in total, from across the UK.  All entries were taken of or by people with a learning disability. Among them was a photograph of Stacey Foster with her friend Graham. Graham always manages to get a response from Stacey even though she can’t speak. Another striking image is of Iain Frost, who is pictured realising his ambition of swimming with dolphins in Cuba.

 

Stacey Foster’s mum, Margaret, said: “We were blown away when we heard that Stacey‘s picture had won an award. It isn’t very often that something nice happens in our lives so we were really excited to be part of the evening’s event.”

 

The competition, sponsored by FUJIFILM UK Ltd and The Sorrell Foundation, saw judges study more than 600 entries to pick 32 photographs and four films as this year’s winners. Prizes were awarded in gold, silver, bronze and highly commended categories.

 

Mencap’s chief executive Mark Goldring said: “The judges had a really difficult time choosing the winners this year, as there were so many outstanding entries and some very touching stories to accompany them.  The competition continues to be successful because people with a learning disability are often invisible in our society, but this competition gives them the chance to capture images that reflect their lives, allowing others to gain a greater understanding.”

 

The winners received state-of-the-art digital FUJIFILM cameras and high street vouchers. Additional special prizes were also given by FUJIFILM to four images they considered to convey the essence of what the Snap! awards are about.

 

The photographs will now go on display at FUJIFILM’s headquarters in Bedford from 19 – 23 September 2011 and later at the Rich Mix gallery from 2 – 5 October 2011. There will also be an interactive online gallery www.myfinepix.co.uk/blog.

 

The full range of images, films and accompanying stories will also be on the Mencap website www.mencap.org.uk/snap.

 

For further information, contact Louise Toms in the Mencap media team on 020 7696 6950 or email louise.toms@mencap.org.uk.

An Urgent Appeal From The Broken Of Britain

September 14, 2011

Cross posted here at their request.

After an incredibly constructive debate yesterday in the House Of Lords the government appear to be concerned about how many Lords had significant concerns about the Welfare Reform Bill, even those Lords who in principle supported the bill had major questions they wanted answers to.

For a bill of this size and importance, convention dictates that the next stage of the bill should be kept in the main chamber of the House of Lords for debate. It’s particularly important the bill be continued to be debated in the main chamber as disability access to the smaller committee rooms is very limited and people will not be able to access the committee rooms to exercise their democratic right to observe the passge of the bill from the public chamber.

At 3.30pm today the govermnent are tabling a motion to move the grand committee stage of the bill into one of the smaller committee rooms. Presumably the government are hoping that by moving a bill into the committee rooms it will be harder to scrutinise – there won’t be enough space in any of the committee rooms to allow for all the Lords to participate, let alone for us to scrutinise online or attend in person.

This is an outrage – the government are clearly concerned by the level of queries and opposition to the Welfare Reform Bill highlighted by yesterday’s debate and wish to quietly sideline it to a committee room where they hope it will pass with less opposition. Tabling the motion for the afternoon following PMQ’s is also an underhand trick as it means it will be harder for us to object through the main stream media.

This is our call to arms. This bill affects us, our families and every aspect of our lives, as well as the lives of those currently paying into the system in anticipation of protection should they require it. If we can make enough noise in the next few hours the government will be forced to keep the passage of the bill in the main chamber of the house of lords where it can be effectively and appropriately scrutinised by all.

What you can do to help is this;

Please post copies of this blog onto your facebook, your twitter, stumbleupon, wikio etc. Please email it to everyone you know, please talk about this on your own blogs. Email or phone your MP to register your objections, email or phone the house of lords to explain your concerns, email or phone the media, local or national and explain that whether or not people are in favour of this bill, that it is a fundamental democratic right to have it debated in the main chamber of the house of lords where there is space for all who wish to attend and observe. Highlight the injustice and hypocrisy of the governments behaviour in trying to sideline this important bill into a room too small for all the Lords to attend and certainly too small to allow those in wheelchairs, or with guide dogs, the very people most affected by this bill to be able to observe from the public gallery.

If we make enough noise before 3.30pm today the government will have to drop this underhand tactic and the Bill will continue to be debated in the main chamber of the House of Lords where everyone who wishes to can attend and observe.

Toe Replaces Man’s Severed Thumb

September 14, 2011

A man from Bristol who accidentally cut off his thumb has had his big toe attached in its place.

James Byrne, 29, from Fishponds severed the thumb on his left hand last December while sawing through wood.

After an attempt to re-attach his damaged thumb failed, plastic surgeons at Frenchay Hospital transplanted his left big toe to his hand.

Surgeon Umraz Khan said: “The loss of the toe is not as disabling as losing a thumb, so the loss outweighs the gain.”

Mr Byrne said: “Mr Khan re-attached my thumb but it had been badly damaged and although we tried everything, including leeches, to get the blood flowing again it didn’t take.

“Mr Khan said to me ‘You will have a thumb even if I have to take your toe’. I thought he was joking, but he was serious and nine months later here it is. The aesthetics of it don’t bother me,

“I am just happy that it works, my work as a paver would have been destroyed without the use of my hand because I couldn’t pick up a brick without a thumb but now I hope I can be back at work in a few months.”

Physiotherapy

Mr Byrne will now have physiotherapy to help him to adapt to using his new thumb.

Bristol’s Frenchay Hospital is a regional micro-surgery centre and is renowned in helping patients requiring this type of surgery.

Mr Khan said: “James will have to learn to re-balance, without his left great toe, on to the ball of the foot but he will be able to walk and jog normally.

“The thumb is the dominant digit. Without it, James would not be able to do the things that we take for granted, like holding a pen or opening a door

“It is still early days for him and he might need additional surgery to make it look more like a thumb.”

Oscar Pistorius: The Blade Runner

September 14, 2011

 

http://twitter.com/#!/BenDearnley/status/113536357204377601

Able Life: Paralympics And Disability Sport

September 14, 2011

Tonight at 8pm on Able Radio, George Johnson and I will be discussing the Paralympics and disability sport in general. Here, a little earlier than usual, is your sneak preview.

Knowsley Council’s ‘Creative Steps’ To Help Disabled People Avoid Cuts

September 13, 2011

A council being sensitive to disability services? I can’t believe my eyes!

Knowsley council in Merseyside is a shining example of how, with a few “creative steps”, some local authorities are defying assumptions that budget cuts inevitably lead to worse services for disabled people.

Its recently opened Centre for Independent Living was developed as part of the council’s health and wellbeing initiative and establishes direct partnerships between the NHS and social care services. It works in conjunction with local user-led organisations to make sure local people have a say in how services are delivered. The centre acts as a “hub” for access to statutory and voluntary services under one roof. Taken alongside other projects, including disability day centres in community settings such as leisure centres, these services help to “empower” disabled people, says the council.

“We work closely with partner organisations and service users to ensure that local people can access high quality care that is responsive to their needs and preferences. This in turn enables us to achieve greater budget efficiencies, reducing the need to make cuts to frontline services wherever possible,” explains a council spokeswoman.

Knowsley is one of the local authorities singled out for praise in a study, by the disability charity Scope, that assesses the impact of disability related cuts on disabled families across England and Wales.

The report, Coping with the Cuts, published this week, found that some councils have created “innovative” ways to ensure frontline services for disabled people are not unduly affected in the rush to make budget savings.

Creative steps

“Surprisingly, the report shows that the scale of cuts across an area has no bearing on the extent to which disabled people are affected,” says Scope chief executive Richard Hawkes. “We know that every local authority has to make cuts and there is no simple solution to protect frontline services. Yet some local authorities have taken creative steps to reduce the negative impact on disabled residents.

“That is not to say that this is not a difficult time for disabled people living in these areas,” he adds. “But we must commend those local authorities that have taken the initiative to approach budget cuts in this way.”

Councils such as Knowsley – which was named in the report as “best coping” English council overall – have built on existing innovative services or found ways to make savings without blanket percentage cuts, the report concludes. It may be tough – and thousands of disabled people may still be bearing the brunt of cuts – but that is far from the complete picture, it says.

Claudia Wood, who co-authored the report, says Knowsley stands out because it scored highly on a number of key criteria set by the researchers. “There is no set formula for success. Every local authority is having to slog and try their hardest. But Knowsley had a lot of financial pressure yet tried to preserve services. That’s what all [councils] in the top 10 did.”

Knowsley council says it has tried hard for a number of years to ensure “a more holistic” approach to disability, including integrating services from health to sport, resulting in “seamless” access for people with a range of support needs. Crucially, says the council spokeswoman, a programme of service integration over a number of years means Knowsley has been able to introduce efficiencies while protecting frontline services.

Coping with the Cuts was commissioned largely as a response to growing concerns that disabled people were being disproportionately hit as councils struggled with the new financial realities. Researchers at the thinktank Demos, which conducted the research for Scope, examined 152 councils in England and 22 councils in Wales with responsibility for social care.

They compiled data on councils’ budgets and services using a combination of freedom of information requests and direct approaches to the councils. In order to map the impact of cuts they used a measure that looked at the volume of cuts being made alongside a series of elements relating to service delivery, such as charges levied directly for services and the “eligibility criteria” applied by councils to qualify for access to specific services.

Interviews with a number of disabled families showed the impact of councils’ approaches on older disabled people living with support, parents of disabled children (see below) and young adults moving from children’s to adults’ services, as well as the support services they received, from care in the home to respite, leisure and education in the statutory, voluntary and private sector. Most significant, interviewees were having to deal with several negative impacts simultaneously including personal budget reductions or restrictions, increased charges for services, restricted eligibility and the closure of services.

Although Coping with Cuts did not set out to name and shame individual councils or to suggest no cuts are necessary, it places a spotlight on a number of local authorities that it says are “best coping” with budgetary challenges. Among the top ranking councils are Peterborough and Oxfordshire. Lower performers include Gateshead and Lambeth council in south London.

The researchers identify practice common to best coping councils, such as the integration of services, “bringing in care, health and often housing and leisure” as well as a “capabilities approach to disability” where the focus is on “what people can do”, not on what they cannot. The researchers also single out how the direct involvement of service users in designing services – and sometimes even in delivering them – can play a role in producing more effective, cost-efficient provision.

The report makes clear that smaller budgets need not inevitably lead to frontline cuts, higher charges or poorer quality services. “Our measure enabled us to look beyond how much local authorities were cutting to how they were cutting and whether it was affecting their frontline disability services,” the report says.

Coping with the Cuts reaches some surprising conclusions. For example: it found that “coping scores” were mixed across regions and urban and rural areas; some councils bordering one another with similar budgets and demographics were given markedly divergent scores; if a disabled person lives in a deprived area it does not necessarily mean they are more likely to fall foul of cuts.

“This suggests that councils strategies to deal with budget cuts can go a long way to mitigating the negative effect on disabled people,” the authors conclude.

A lack of consistency in service provision for disabled people across England and Wales is also highlighted. The report suggests that this may, in part, be down to the fact that many councils do not appear to know how many disabled people are living in their area. As a result, “those in national and local government have only a limited idea of how budgetary cuts and service reforms affect disabled people,” it claims.

Hawkes says the findings are “a cautionary tale” for the government’s ‘localism’ agenda. “Some local authorities will always seek to innovate. But in other areas, residents will feel the full brunt of cuts,” he says. “[In those places,] the government’s claim that it is ‘protecting the vulnerable’ will continue to ring hollow.”

Flawed methodology

A number of councils near the top of the rankings have welcomed the research as evidence that their strategies are paying off despite unprecedented pressure on budgets. Others, including those nearer the bottom of the table, have strongly criticised the research with some, including Westminster, suggesting the Demos methodology is flawed and that some of the data is inaccurate.

Wood refutes any suggestion that the research is less than robust. She says the data collected for the study was obtained directly from councils and the research was careful to measure only criteria that could be compared “objectively between councils”.

“While no measure will ever be able to capture everything, what this one does is to make sure we don’t treat any local authority unfairly,” she argues.

The authors of the report make an explicit plea for councils to learn from each other and to share best practice. If they do, the argument goes, the overall impact of cuts could be less deleterious for disabled people.

Back in Knowsley, local resident Paul Doyle is unsurprised that his local council is being recognised as a leader in disability services. The 50-year-old, who was paralysed from the chest down after a car accident five years ago, says there are good reasons why other local authorities would do well to look at what Knowsley is doing. “It has been so beneficial having support services available to me right on my doorstep,” he says. “I hope that all disabled people in the UK will be able to access a similar level of services in the near future.”

‘Councils need to consult more with families’

Ona Ramanauskas’ daughter Grace is 10. She has severe learning disabilities and a mild visual impairment, and over the years has required varying levels of support. When younger, she was able to attend a mainstream specialist after-school service. But as she got older and her needs became more complex, one-to-one support became a necessity.

For the most part, Ramanauskas says the family (her husband is a paramedic) has been able to cope. She gave up a full-time career to work part time and Grace has had some financial support from North Tyneside council, which helps pay for a carer.

The first sign that things might be about to get harder came this summer when the number of days Grace was able to access a summer play scheme, and get the kind of one-on-one care she needs, were suddenly cut. “It came out of the blue,” Ramanauskas says. “We planned for a certain number of days so that I could get the respite I needed. With very little warning we were told that the number of days Grace was entitled to were being cut.”

When she challenged the decision, the council told Ramanauskas that there were alternative schemes available. “The ones we saw just weren’t suitable for Grace’s needs,” she says. “I could pay for something – and at times I have paid – but I can’t afford it.”

Ramanauskas got through the summer by managing to adjust her work schedule but it is the uncertainty about what might happen next that worries her.

She adds: “I have relied on [council-funded] schemes during school holiday periods. I can’t tell you how vital they have been for me and for Grace. Councils need to consult with more families before they do this kind of thing. How am I to know that there aren’t more cuts to come? How am I supposed to plan?”

Disability Hate Crime Begins With Verbal Abuse, Says Nicky Clark

September 13, 2011

I’m linking to Nicky Clark’s latest piece for the Guardian’s Joe Public blog. She writes about the Gemma Hayter case and disability hate crime.

Kenya Kidnapping Case: Wife Is Deaf

September 13, 2011

 

This is a horrible case, but it proves yet again that if you look for it hard enough, dissbility is everywhere!

The British woman abducted by an armed gang who murdered her husband in a remote Kenyan resort is deaf and will have difficulty communicating with her kidnappers, friends have revealed.

There are growing fears that Judith Tebbutt, 56, has been taken across the nearby border into lawless Somalia after she was seized by six gunmen who broke into the couple’s £560-a-night beach hut at Kiwayu Safari Village in the early hours of Sunday morning.

Her husband, David, 58, died from a single gunshot to the head as he tried to protect his wife from the kidnappers.

Friends of the couple, who are from Bishop’s Stortford, Hertfordshire, paid tribute to Mr Tebbutt but said they feared his wife would struggle to cope with the devastating ordeal.

A close friend of the couple – who have a 25-year-old son, Oliver – said Mrs Tebbutt, who is a social worker helping people with drug and alcohol problems, relied on a hearing aid.

The friend, who asked not to be named said: “Judy only has around 30 or 40 per cent hearing and wears a double hearing aid.

“If she has them in and they are working then she is fine, but if she does not have them or once the batteries run out then she will have great difficulty hearing what people are saying to her.

“It is heartbreaking to think of her in this awful situation. Helpless and having seen her husband murdered.”

Mr Tebbutt, who worked as a finance director for publisher Faber & Faber and was a member of the Book Trade Charity, was described by friends and colleagues as “caring and dedicated” professional.

Ian Stevenson, professor of publishing at University College London, said: “He was one of the nicest people in publishing. I’ve known him for 15 years and he has had a very distinguished career.”

The couple, who were keen travellers and had visited Kenya before, had spent a week on safari in the Masai Mara before flying to Kiwayu on Saturday to relax by the beach for the last days of their trip.

The Kenyan authorities are trying to establish who had carried out the attack on the resort, which is popular with celebrities including artist Tracey Emin and singer Mick Jagger.

A massive sea, land and air search failed to find any sign of the kidnappers who are believed to have escaped from the resort in a speed boat.

A Kenyan security source, familiar with kidnap situations in the region said: “It’s going to be difficult to admit that once she’s in Somalia, the whole thing becomes a very different ball game.”

It is feared she may have been snatched by an opportunistic Somali gang who may try to sell her to al-Shabaab, Islamists who control large parts of the territory near the Kenyan border.

It has emerged that the British Government considered using forces training on the other side of Kenya for a possible release assault, but those plans will not be implemented if it is confirmed Mrs Tebbutt is being held in Somalia.

British forces are also available in Uganda and the Royal Navy frigate HMS Somerset is currently on counter-piracy patrol in the Arabian Sea.

Kiwayu Safari Village, a two-hour speedboat ride through a mangrove delta north of the popular tourist destination of Lamu island, was closed today.

Its managers had flown to Nairobi, the Kenyan capital, with Mr Tebbutt’s body, which is now in the care of the authorities who are liaising with the British High Commission.

A Survey About Subtitles

September 13, 2011

 

http://twitter.com/#!/Sensetweets/status/113520525455790080

Three Jailed For Life For Gemma Hayter Murder

September 12, 2011

Three people have been jailed for life for the murder of a woman with learning disabilities who was viciously beaten, led to a railway embankment and forced to drink urine before being stripped and left to die.

A jogger found 27-year-old Gemma Hayter’s body at a disused railway line in Rugby, Warwickshire, in August 2010.

Daniel Newstead, 20, Chantelle Franklyn Booth, 22, and Joe Boyer, 18, all from Rugby, were convicted of murder following a trial at Warwick crown court and given life sentences.

Jessica Lynas and Duncan Edwards, both 19 and also from Rugby, were given 13 and 15 years for manslaughter. All five, who Miss Hayter had considered to be her friends, were sentenced at the Old Bailey on Monday.

During sentencing the court was told Miss Hayter, who had learning difficulties and was disabled, was made to drink urine from a lager can.

She was also hit with a mop and beaten in a flat before being cleaned up and escorted to a disused railway line. There she had her clothes removed, was beaten further and forced to have a plastic bag placed over her head, the court heard.

Lady Justice Rafferty said the “vile” torture and murder of Miss Hayter was a “chronicle of heartlessness”.

“It is difficult to find the words to express how vile your behaviour was,” she added. The judge ordered Booth to serve at least 21 years in jail while Newstead was ordered to serve a minimum of 20 years. Boyer was told to serve a minimum of 16 years for the murder.

Referring to the moment when the victim was forced to drink urine, the judge said: “I struggle to see how much lower you could have sunk.”

All five were also convicted of assault occasioning actual bodily harm. Miss Hayter had been subjected to a savage beating in Booth and Newstead’s flat after a disagreement following a night out.

Following the convictions, the victim’s family issued a statement: “Our Gemma was a very loving and vulnerable woman who trusted everyone, and her trusting nature and vulnerability led to her death on 9 August last year. Our family has found the last year, and especially the last seven weeks, incredibly difficult and today we welcome the jury’s verdict.

“Now our family can finally move on and hopefully do whatever we can to help prevent anything like this happening again to another vulnerable adult in the future.”

Rafferty said Miss Hayter had suffered a beating so violent that a pathologist remarked on the severity of the breaking of her nose.

“She was hit with a mop or a broom. She was locked into a lavatory. She called out again and again for her mobile telephone, which was put down another lavatory to protect you by ensuring she could not get help,” she said.

Edwards and Boyer had urinated into a can of lager and made their victim drink it, the court heard.

“She tagged along, battered, in pain and unsuspecting, like a faithful loving dog, as you walked her to her death,” said Rafferty.

The judge added that viewing the CCTV footage of Miss Hayter’s last journey became “insupportable”. “After a while I, for one, could not watch it,” she said.

Once in seclusion the beating started again and Miss Hayter was cut with a knife, kicked and had a plastic bag put over her head.

“One final indignity was to come,” said Raffery. “You stripped her naked and left her body where you had dragged it. Gemma Hayter died alone.”

She singled out Booth, of Rugby – who had described Miss Hayter as her best friend – as a “nasty piece of work”.

“Over the years you treated Gemma Hayter like a toy to be picked up and put down, dependent, I suspect, on whether there was a gap in your miserable life which she could fill,” the judge said.

Charity Calls For More GP Support For Older Carers

September 12, 2011

This is a welcome little bit of progress for carers. I completely agree with what the Princess Royal Trust For Carers has said today.

GPs throughout the UK should be giving more support to carers who are aged over 60, a charity says.

The Princess Royal Trust for Carers says family doctors should offer older carers an annual health check, including screening for depression.

The charity says almost 70% of hundreds of older carers questioned in a survey said that their health was suffering because of their responsibilities.

Ministers admitted that more work needed to be done to help older carers.

More than 600 carers aged between 60 and 94 answered questions for a survey by the Princess Royal Trust.

Just over a third reported having cancelled an operation or treatment because of their caring responsibilities, while half said their health had got worse in the past year.

Crumbling spines

The charity’s policy director, Moira Fraser, said: “Carers want to look after friends or family members – but often it’s at the expense of their own health.

“We heard about people with crumbling spines, heart problems and cancer. Sometimes people’s knees are so worn out they feel as though they can’t walk at the end of each day.

“Others suffer from mental problems – such as stress and exhaustion. They worry about the future and have feelings of hopelessness.”

She added: “One woman needed an ankle replaced, but she had to put off the operation because it would have meant being in plaster for three months.

“We hear positive words from the authorities. The important thing is for funding to make it through to a local level.”

There are thought to be six million carers in the UK. Many of them are over retirement age.

The Princess Royal Trust for Carers wants to see the NHS and local authorities fund training for carers to help them lift other people safely.

Action plan

Professor Nigel Sparrow, a spokesman on carers’ health for the Royal College of GPs, said: “We fully support the recommendations.

“We are in a very privileged position in general practice in that we have a registered list of patients so that we know both the patient and family, allowing us to support the needs of carers.”

Ministers in England have published a four-year action plan – Recognised, Valued and Supported – to support carers’ mental and physical health.

A Department of Health spokesman said: “Work is under way to address these concerns locally, but clearly more needs to be done to meet the needs of older carers.

“The Department has invested in a number of local sites exploring different ways of providing breaks for carers, and ways in which the NHS can better support carers with more flexible appointment times.

“An evaluation will be published later this year.”

Russell Brand, The Paralympics Have More Value Than Your Book

September 12, 2011

I’m linking to my latest article for Suite 101, which looks at why Russell Brand is wrong to have said what he said about the Paralympics. Special thanks must go out to Matthew Smith, whose Tweet to me earlier today inspired the title and made me smile.

Disabled People See Abuse As Inevitable, Finds Report

September 12, 2011

People with disabilities in the UK face harassment, insult and attack almost as a matter of routine, while a “collective denial” among police, government and other public bodies means little is done to challenge the situation, the government’s human rights watchdog has concluded following a major investigation.

The report by the Equality and Human Rights Commission (EHRC), the most detailed study yet into abuse faced by disabled people, found that while some particularly serious offences attracted national attention, these are “the tip of the iceberg”, and that for many, low-level criminality or worse are so endemic that many consider them inevitable.

Too often, the report found, victims see their complaints doubted, or they are advised to change their own behaviour. Even in the most serious cases, public organisations involved often fail to review what went wrong.

The issue achieved national prominence in 2009, when an inquest found police and other officials had failed Fiona Pilkington, who killed herself and her severely disabled teenage daughter in a burning car after enduring years of torment from youths at their home in Leicestershire. A report in June by the charity Mencap warned many police forces were failing to treat crimes motivated by disability with sufficient seriousness.

The EHRC report reviewed dozens of attacks against people with both physical and mental disabilities, ranging from the most serious cases, such as those of the Pilkingtons and Keith Philpott, a 36-year-old with learning disabilities who was beaten and stabbed to death, to that of an 88-year-old man in south Wales who was harassed by children while using a mobility scooter. The study, Hidden in Plain Sight, heard evidence from more than 350 witnesses and organisations, including 12 local authority heads, 15 senior police officers, and six NHS chief executives.

The study considered in detail 10 particularly serious cases, nine of which resulted in the death of the person involved, including the Philpott case. All victims had been in contact with authorities and the majority had made earlier reports of harassment or lower-level crimes. Despite this, in five of the cases there was no formal review, the report noted, “implying that lessons have not been learnt for the future”.

Michael Smith, the EHRC’s lead commissioner for the inquiry, said even as a wheelchair user who had himself faced abuse – and police scepticism – nothing had prepared him for “the horrendous things some disabled people have experienced”.

In an introduction to the report, he said: “In the worst cases, people were tortured. And apparently just for fun. It’s as though the perpetrators didn’t think of their victims as human beings. It’s hard to see the difference between what they did, and baiting dogs.

“The really serious cases catch the headlines. But what about the constant drip, drip, nag, nag of the so-called ‘low-level’ harassment that many disabled people face on a daily basis? It ruins their lives. They don’t have the confidence to go out. It undermines their ability to be part of society. It makes them behave differently.”

Echoing the findings of the Mencap report, the EHRC said many disabled people did not report harassment, sometimes because it was not clear who they should tell but often because of a “culture of disbelief” that meant they were not treated seriously. “There is sometimes a focus on the victim’s behaviour and ‘vulnerability’ rather than dealing with the perpetrators,” the report noted.

The authors said there had been a systemic failure by authorities to acknowledge the extent of the problem and deal with it effectively. Cases tended to be treated in isolation and offences were too rarely prosecuted as hate crimes, which carry more severe penalties. The EHRC made recommendations ranging from the specific – reliable data to track the extent and severity of crimes motivated by disability – to significantly longer-term aspirations, such as changing public perceptions of disabled people and understanding the motivations of the attackers.

Mencap said the report showed the UK had “still not got to grips” with the issue. “Public authorities need to step up to tackle this terrible scourge, or end up condemning hundreds of thousands of disabled people to years of violence, harassment and abuse,” the charity’s head of policy, David Congdon, said.

Russell Brand Says The Paralympics Have ‘Novelty Value’

September 12, 2011

I, for one, think Paralympians are absolutely right to find these remarks offensive. I’m not a Paralympian, but as a disabled person, I find them quite offensive myself! I wouldn’t be surprised if all disabled people do.

He’s no stranger to causing controversy over the things he has said.

But Russell Brand was today accused of going to far when he called the Paralympics ‘novelty value’.

The comedian was slammed by paralympic athletes after he poked fun at them during a recent stand-up gig.

 He told his audience: ‘I don’t give a f*** about the Olympics. It’s boring Blue Peter sport and a waste of taxpayers’ money.

‘At least the Paralympics have some kind of novelty value or something.’

Brand, 36, made the comment earlier last week,  during a gig at the Pleasance Theatre in Islington, north London less than 48 hours before International Paralympic Day, to promote the 2012 games, took place in Trafalgar Square.

And today, leading Paralympians slammed the star for his comments and said they were patronising.

 Speaking to the People, dressage star Natasha Baker, 21, said: ‘We’ve worked harder than ­anyone to get here. We’ve suffered life-threatening ­illnesses. It’s both ­patronising and upsetting for Russell Brand to describe us as a ­novelty.’

Veteran former Paralympic athlete Dame Tanni Grey-Thompson, 42, said his remarks were both careless and irresponsible.

Wheelchair athlete David Weir, who won two gold medals, a silver and a bronze at the 2008 Beijing games, said: ‘Calling the sport a novelty is offensive.

 ‘It’s not like I get up, do one ­marathon then go to bed for the rest of the year. I train every day – I am no different to Paula Radcliffe.

‘Brand obviously hasn’t met any Paralympians. If he did he certainly wouldn’t call any of us a novelty.’

And swimmer Chris Holmes, who has a haul of nine gold medals, said Brand was out of touch.

He added: ‘It’s important to enable every disabled person, particularly the young, to access sport as easily as their able-bodied counterparts

‘The Games are still in their youth phase, but have moved on and are no longer seen as a Cinderella event.’

U-Turn Claim On Deaf Classroom Cuts

September 11, 2011

A decision to cut the number of teachers supporting 200 deaf children in Stoke-on-Trent to three, has been reversed, a charity has claimed.

The National Deaf Children’s Society (NDCS) had threatened action in the High Court over the council’s plans to cut its services for deaf children in the borough.

The charity said an order had now been signed quashing the council’s decision to cut the number of teachers to three who would have served schools and families.

There was now no need to continue with its legal action, the NDCS said.

‘Landmark decision’

The council has said it will review its decision to cut educational support for deaf children.

Director of policy and campaigns at the charity, Brian Gale, said: “This is a landmark decision for the deaf children of Stoke.

“[The charity] used legal action as a last resort because the council ignored the concerns of parents for almost a year.”

The council said it would not be commenting on the society’s claims.

Cabinet member for children’s services Councillor Debra Gratton has said: “This year’s budget was the toughest the council has ever had to deliver, and the authority was forced to face an unprecedented level of savings.

“We have listened to the arguments made by the National Deaf Children’s Society, and we have listened to parents, children and teachers.

“In light of this, it has been agreed that the original decisions be reviewed, following proper and meaningful consultation, to help us to continue to provide the best level of services for city children.”

Simon Richardson Out Of Hospital

September 10, 2011

A gold winning Paralympian cyclist has been released from hospital after being seriously injured in a road accident.

Simon Richardson, from Porthcawl, collided with a van in a hit and run crash while cycling near Bridgend.

He will use a body brace at home after suffering fractures to the spine, a broken pelvis, and broken breast bone.

Friend and sponsor Phil Jones said Mr Richardson “is in good spirits and determined to get back to his pre-collision fitness and form”.

Mr Richardson, who also won a silver at Beijing in 2008, was hurt in a crash on the A48 at Crack Hill House, Bridgend, on 17 August and taken by air ambulance to the University Hospital of Wales, Cardiff.

He became a Paralympic competitor after suffering leg and back injuries in a previous road accident involving his bicycle and a car in 2001.

Mr Jones has been giving regular updates about his friend’s condition via his blog.

“Simon’s had another good day. He walked 11m with sticks, wearing his body brace,” he wrote in his latest posting on Thursday.

“Dieticians are happy and the physios are happy.”

Australian X Factor Contestant Emmanuel Kelly

September 9, 2011

Disability Hate Crimes Up 20% In 2010

September 9, 2011

Disability hate crimes rose by more than a fifth last year, figures showed today.

Police recorded 1,569 incidents where the victim thought the alleged crime was motivated by their disability in England, Wales and Northern Ireland, compared with just 1,294 in 2009.

But the overall number of hate crimes dropped by 7% from 51,920 to 48,127 in 2010.

The Association of Chief Police Officers (Acpo) said disability hate crimes had been “significantly under-reported in the past”.

Chief Constable Stephen Otter, the ACPO lead on equality, diversity and human rights, said officers were committed to “building victims’ confidence and improving our recording practices so that more victims can access the service they deserve”.

Iqbal Bhana, deputy chairman of the Government’s hate crime advisory group, added: “It is good to see progress but there is still a long way to go before we can be satisfied that hate crime victims are properly protected.”

The latest figures also showed there were 39,311 race-related hate crimes last year, 4,883 motivated by sexual orientation, 2,007 crimes by religion or faith, and 357 by transgender issues.

A Home Office spokeswoman said: “Targeting a person or a group based on their disability, gender identity, race, religion or sexual orientation is unacceptable, and tackling hate crime is an issue the Government takes very seriously.

“For the first time police forces are recording hate crime data centrally.

“This will help the police to target resources more effectively and better protect victims, because everyone should have the freedom to live their lives without fear of targeted hostility or harassment.”

A spokeswoman for the Equality and Human Rights Commission (EHRC) said: “Evidence from our inquiry into the harassment of disabled people, which is being released on Monday, shows that there is still significant under-reporting of this type of crime.

“Often there is a failure by authorities to recognise that these crimes may be motivated by hostility towards disabled people, so it may not be recorded as hate crime.

“Disabled people tell us that they do not want to report incidents of harassment or abuse because they fear the consequences or may feel that they won’t be taken seriously.

“Specific recommendations for the police are set out in our report Hidden In Plain Sight, which will be published next week.”

Dan Scorer, Mencap’s campaigns manager, added that the cases were “just the tip of the iceberg”, saying “the majority of hate crime cases still go unreported”.

Lord Coe Wants Paralympic Tickets To Sell Out

September 9, 2011

Lord Coe, chairman of the London 2012 Organising Committee, hopes the London 2012 Paralympics can become the first games to sell out tickets, saying that British people “get Paralympic sport.”

Coe says the games can help change mindsets and could be a first step towards “redefining the word disabled.”

The Amazing Vancetti Sisters

September 9, 2011

This looks good… a play with a disabled main character by a disabled writer.

David Cameron At International Paralympic Day

September 8, 2011

Prime Minister David Cameron was among the high-profile visitors to Trafalgar Square on International Paralympic Day.

The event is being held to promote next year’s Paralympic Games in London, for which tickets go on sale on Friday.

Cameron and London Mayor Boris Johnson each partnered a wheelchair tennis player as they tried out the sport in front of an enthusiastic crowd.

The day will end with the official invitation being issued to athletes around the world to compete in 2012.

The Paralympics follow the Olympic Games and run from 29 August to 9 September next year.

British swimmer Ellie Simmonds, who is at the event, told the BBC: “It is good that the Paralympics is now getting on the same scale as the Olympics.”

The event, which features demonstrations of all 20 paralympic sports, coincides with the visit of representatives of the International Paralympic Committee to London.

The heads of National Paralympic Committees from more than 100 competing countries will have the chance to see many of the Games venues.

IPC president Sir Philip Craven said: “The foundations for what could be the most successful Games ever are being laid in London. All we need now is the athletes.”

The committee heads will also be present in Trafalgar Square.

South African runner Oscar Pistorius told the BBC: “For us the Paralympic movement has dramatically increased since Sydney to Athens and to Beijing.

“If you look at where Great Britain is, it’s pretty much at the forefront where it comes to inclusion and accessibility for disabled people when it comes to the Paralympic movement.”

London 2012 chair Lord Coe said: “I want to see lots of people in Trafalgar Square. Whenever we have showcased Paralympic sport in busy locations it has always been a success.

“This is a great opportunity for young people to understand what they are watching, that – and we are going to have to redefine some of these terms – 99 per cent of able-bodied people could not get within a country mile of.

“For everybody, paralympic sport is, and would be, a challenge.”

Coe admitted to having a favourite paralympic sport, adding: “I do enjoy paralympic athletics. We had three stunning wheelchair races on the penultimate day in Korea (at the World Championships).”

Great Britain wheelchair basketball player Ade Adepitan told the BBC how important playing the sport has been to him.

“I spent many years as a youngster really frustrated trying to play able-bodied sports with my friends walking about on callipers,” he said.

“When I discovered wheelchair basketball it changed my life. I wouldn’t be here if it wasn’t for sport and I think sport is having the same impact on kids both disabled and able-bodied all over the world and that’s what we hope we can do with 2012 too.

“This event is extremely important. Generally a lot of people know about the Paralympics, they might have seen a little bit of the sports on TV but here’s an opportunity to come and meet the athletes watch the sports and the events live.

“When I spoke to a lot of my friends about myself playing wheelchair basketball they could not believe how hard it was, how fast it was and how big the players were.”

Thursday’s events kicked off at 0815 BST with the first round of sports being showcased and a world record attempt for the longest rally in a sitting volleyball match.

A non-competitive race between Pistorius, American Jerome Singleton and five local schoolchildren on the track in front of the National Portrait Gallery took place but the two athletes did not to head-to-head because of safety concerns.

A bronze sculpture of Pistorius by artist Ben Dearnley was also due to be unveiled.

One of the final session highlights is a penalty shoot-out at 1800 BST with Great Britain’s blind football five-a-side squad competing against former England internationals Ray Wilkins and Paul Merson, former professional Chris Kamara and youth team players from Chelsea and Swindon.

The official call to next year’s competitors to come to London will take place at 1900 BST.

 

Police Warn Of Paralympic Ticket Scams

September 8, 2011

This is worth knowing and remembering.

Police are warning people to watch out for scams when tickets for the 2012 Paralympics go on sale on Friday.

Officers from the Metropolitan Police’s Operation Podium warned people to beware of fake tickets and illegal sales.

The general public has until 1800 on 26 September to buy tickets.

More than 4,200 athletes, with a variety of disabilities, from 150 nations will take part in the Games from 29 August to 9 September 2012.

The tickets will go on sale from 09:00 BST on Friday and police advise customers to use only the authorised London 2012 ticketing website, which has a list of sites selling unauthorised tickets.

The police say a number of criminals are setting up professional-looking fake websites.

More than 95% of tickets – for the 20 sports – will cost £50 or less, and 75% will be £20 or below, London 2012 has said.

Opening and closing ceremony tickets start at £20.12 and go up to £500.

Detective Chief Inspector Nick Downing, who is in charge of Operation Podium, said: “We have already seen the demand for Olympic tickets which gives criminals greater opportunity to run scams, sell non-existent tickets and even steal your personal and credit card details to use in other crimes.

“Now that Paralympic tickets are on sale, don’t get caught out. Follow our simple and easy advice to make sure the ticket you buy is real. In the UK, the only official place to apply for tickets is through the London 2012 application process.”

People can also apply with an application form from any Lloyds TSB branch, Bank of Scotland branch in Scotland or from any public library in Northern Ireland.

Outside the UK, Paralympic tickets will be sold through the country’s National Paralympic Committee or their authorised ticket retailer.

There are only three official providers for hospitality packages – Thomas Cook London 2012, Prestige Ticketing and Jet Set Sports.

People are warned not to buy tickets from any unauthorised source and are advised to report websites to the police or London 2012 at brandprotection@london2012.com.

Could The Paralympics Erase The Word Disability?

September 8, 2011

I can see where Sir Philip Craven is coming from, but I think he is going a bit over the top. I would like to see the spelling- as the word relates to human beings- changed to DisAbility, though- meaning ‘the ability not to do something that others take for granted.’

On a much more serious note, readers, what do you think of these comments? Please leave your thoughts below.

As International Paralympic Day takes place in London to celebrate next year’s Games, Sir Philip Craven, the president of the International Paralympic Committee, has said he refuses to use the “D-word”.

Craven believes London 2012 will help to consign it to history.

Disabled himself, and a former wheelchair basketball player, he explains his dislike to BBC News: “It needs to be removed from the lexicon as it pertains to human beings.

“I mean, let’s face it, if a machine gets disabled, it doesn’t work. And that is the way that the word has influenced people’s minds in the past.

“People say: ‘Peter round the corner, he’s disabled’, before they even start to talk about what a wonderful guy he is, or what a not-so-nice guy he is. You immediately get to that differentiating point.

“If you’re going to be talking about the positivity of human kind, why kick off with negativity?

“Someone said to me recently that [disability] is very much a political word for differentiation.

“I’m not getting into politics but if you think about it, it normally doesn’t need to be used. What does ‘ you are disabled’ mean?

“There’s an incredible difference between a wheelchair user and someone who’s blind, you know.”

Though Sir Philip may dislike the term “disabled”, many identify strongly with it and believe it is helpful.

Changing perceptions

Campaigner Clair Lewis sees it as a word that unifies the community.

“It’s quite common for one group of disabled people to say to another that they don’t want to be like them. Changing the word doesn’t actually fix anything.”

For 12 days next year, 4,200 athletes from 160 nations will be descending on the city of London. Although it is unlikely to significantly change the language, there are some tangible benefits that will be left behind as a result.

In its Olympic and Paralympic bid in 2005, London promised to create the most accessible Games ever.

Agencies such as Transport for London, the Olympic Park Legacy Company and the Department for Culture Media and Sport all have a role to play in keeping the promise during, and also after, the games.

The Olympic Park will see 8,000 new houses built on it after the games.

About nine per cent of these will be wheelchair accessible. And the sporting venues, some of which will be scaled back, were created with high accessibility standards and will remain.

The School Games project aims to build a lasting competitive sports structure in schools across the country.

Disability sport is part of this and specific inclusive events will be held at the Games next year.

Future disability sport opportunities are built into this plan and, for the first time, disabled children’s participation in sport will be measured.

Maria Miller, minister for disabled people, said: “The Games offer a great opportunity to challenge outdated perceptions and help make further progress towards equality for disabled people in the UK.

“They will showcase the talents and sporting expertise of disabled people competing on a world stage and act as a catalyst for our sporting talents of the future.

Positive legacy

“I am really pleased by the initiatives under way to develop and strengthen disability sport and I hope we are left with a lasting positive legacy for disabled people and a positive experience for all in 2012.”

It is worth looking back as well as forward.

In 1912, exactly 100 years before the London Paralympics, the city played host to an entirely different disability event.

The first international eugenics conference was held in the city, bringing together sympathisers and academics, including prime minister-in-waiting Winston Churchill, to discuss issues like sterilisation, selective breeding and marriage restriction.

For 2012, London has moved a long way from wanting to eradicate disabled people, preferring to celebrate their lives and achievements.

Perceptions have changed vastly across the last century. Sir Philip thinks that attitude is the key factor.

“You can pass laws and laws are necessary; we have the equality law now in Britain but laws are only there for me as a backstop.

“The thing that really makes a difference is the change in public perception and that’s what the Paralympic games brings to a nation.

“And now that they’re televised quite extensively, and will be more than ever in London – also on radio and internet and press – then that message gets out to the world. And this is what we want.”

More about this at Suite 101.


International Paralympic Day

September 8, 2011

London’s Trafalgar Square will be the venue on Thursday for a full day of sporting demonstrations to celebrate next year’s Paralympic Games.

International Paralympic Day will allow the public to watch sports like blind football, power-lifting, wheelchair basketball and sitting volleyball.

The official invitation will then be issued to athletes around the world to compete in the 2012 Games.

The three-week window for buying tickets opens on Friday.

The Paralympics follow the Olympic Games and run from 29 August to 9 September next year.

British paralympians Ellie Simmonds and Sascha Kindred will also be present in the square during the day.

“I want to see lots of people in Trafalgar Square,” said Locog chair Lord Coe. “Whenever we have showcased Paralympic sport in busy locations it has always been a success.

“This is a great opportunity for young people to understand what they are watching, that – and we are going to have to redefine some of these terms – 99 per cent of able-bodied people could not get within a country mile of.

“For everybody, paralympic sport is, and would be, a challenge.”

Coe admitted to having a favourite paralympic sport, adding: “I do enjoy paralympic athletics. We had three stunning wheelchair races on the penultimate day in Korea (at the World Championships).”

Thursday’s events last for nearly 12 hours and kick off at 0815 BST with the first round of sports being showcased and a world record attempt for the longest rally in a sitting volleyball match.

The second session starts at midday and at 1315 BST, South African athlete Oscar Pistorius and some local schoolchildren will run on the track in front of the National Portrait Gallery.

A bronze sculpture of Pistorius by artist Ben Dearnley will also be unveiled.

One of the final session highlights, from 1500 BST, is a penalty shoot-out at 1800 BST with Great Britain’s blind football five-a-side squad competing against former England internationals Ray Wilkins and Paul Merson, former professional Chris Kamara and youth team players from Chelsea and Swindon.

The official call to next year’s competitors to come to London will take place at 1900 BST.

Able Life: Lancashire County Council

September 7, 2011

I’m on Able Life with George Johnson in an hour… here’s a sneak preview of what I said.

Amputees In Action

September 7, 2011

A Berkshire company staffed by amputees has created a new prosthetic throat to train army medics.

Newbury-based business Amputees in Action supplies amputee actors as film extras and to work on military and emergency services exercises.

Managing director John Pickup has created a prosthetic throat to allow medics to practise making an incision to establish an airway.

The invention has been patented as the first Cricothyrotomy FX prosthetic.

The device, also known as the “Crike” prosthetic, is being used in preliminary trials in courses for military medics and clinicians.

‘Extreme pressure’

Medics attend battlefield advanced trauma life support courses to teach them new techniques in trauma medicine before going into conflict.

Mr Pickup said using the prosthetic, which is placed on an actor’s throat for added realism, puts medics under “extreme pressure”.

“Our actors are instructed to do the signs and symptoms as if they were choking,” he said.

“It will look and feel as if you are doing it for real.”

Mr Pickup said the Crike mimicked the anatomy of the human throat, and allowed medics to gain experience before heading out into “difficult situations”.

“They’re all going to a difficult place, war zones, dangerous places where they haven’t got the back-up of paramedics and doctors and nurses and hospitals behind them,” he said.

“They are going to be working in very difficult circumstances.”

Mr Pickup had his right arm amputated when he was 17 following a motor bike accident.

He set up his agency for amputees in 2004.

The agency has supplied actors for films such as Gladiator, Shaun of the Dead and Saving Private Ryan, as well as working with the military and emergency services in training exercises.

Former GP Says He Will Help Woman End Life At Dignitas

September 7, 2011

I’m scared. This says a lot about the value this man puts on the lives of elderly people. How many GPs and health professionals are there who feel the same way as he does?

A former GP has said he will help a woman from Eastbourne travel to Switzerland to end her life even though she is not terminally ill.

Dr Michael Irwin, from Cranleigh, in Surrey, said he would help the 91-year-old who suffers from severe arthritis to travel to the Dignitas facility.

He has refused to name the woman and said he had helped four other people travel to Switzerland.

A spokeswoman for Sussex Police said officers would contact Dr Irwin.

He said: “When you’re in your late 80s or early 90s and you’ve got all kinds of medical problems and your quality of life has changed so much… why should you be forced to continue in that existence?

“I have spoken to this lady on several occasions on the telephone. I’ve never actually met her. It’s her decision and I don’t want to be any closer to identifying her.

“It’s her right to be anonymous.”

‘Doctor’s responsibility’

Mr Irwin, who formed pressure group Society for Old Age Rational Suicide in 2009, said he had no moral objections to assisted suicide.

He was arrested for taking Raymond Cutkelvin, of London, to die at the facility, but in June 2011 Director of Public Prosecutions Keir Starmer decided not to prosecute saying it would not be in the public interest.

Assisting a suicide remains a criminal offence in England and Wales, punishable by up to 14 years in prison.

Dr Irwin added: “I’m a retired GP and I have felt that a doctor’s main responsibility is to help the patient in the best possible way.”

A spokeswoman for Sussex Police said: “We will be getting in touch with Dr Irwin in relation to the report that he may be taking a woman abroad to be helped to die.”

A spokesman for East Sussex County Council said the authority would not comment on individual cases.

He said: “If we thought the law was being broken we would inform the appropriate authorities. We would hope that anyone contemplating such action would talk to the appropriate people before doing anything.

“There could be other ways of resolving this.”

Pensioner Gets Do Not Resuscitate Tattoo

September 7, 2011

An 81-year-old woman from Norfolk has had “Do Not Resuscitate” tattooed across her chest in case she falls ill and attempts are made to revive her.

Joy Tomkins had the message tattooed, along with “P.T.O.” and an arrow on her back, earlier this year.

The former magazine company secretary said she could not bear to “make beds and wash-up for another 20 years”.

Despite having a living will for about 30 years, she said the tattoo meant there was be “no excuse” for error.

“The tattoo is immediate… no excuse for not knowing what I thought,” she said.

The grandmother, who is diabetic but said she was not seriously ill, said she got the idea from a retired nurse, who did something similar in 2003.

She said her willingness to not be resuscitated would “save money” for the NHS.

Mrs Tomkins, who went to a tattoo parlour to get her message done, said she was happy with life but stated she would be “just as happy” not to wake up in the morning.

She added she was determined to have the final say if she falls seriously ill.

‘Much better dead’

“If I’m found lying about and can’t say something, I want [medics] to accept that,” she said.

“I’m 81 and don’t need any more use. What do you think I’m going to do with the frightful thought of getting to 100? I hate it.

“My mother-in-law lived to be 106 and in the last six years of her life she’d have been much better dead. She was miserable.”

The widow said that at the age of 81 she did not have the “stamina” to enjoy all of her hobbies any more, such as playing the piano and gardening.

“I’ve had 80 good, interesting years of marriage and children and grandchildren and plenty of friends,” she said.

“I’m quite happy if I wake up in the morning, but if I don’t I’m just as happy.”

Her two children, who between them have six grandchildren, are aware of their mother’s views, but Mrs Tomkins said, “they won’t argue with me”.

Dr Anna Smajdor, a lecturer in medical ethics at the University of East Anglia’s Medical School, said she could see that Mrs Tomkins wanted to send a “very clear message” and “cover all bases” with her tattoo.

However, Dr Smajdor said tattoos were not effective “as a sole way of ensuring wishes are fulfilled” as they would “not be legally binding”.

Wheelchair Rugby

September 7, 2011

Wheel chair rugby teams from across the world are in Cardiff to compete in a three-day event in preparation for the London 2012 Paralympics.

Great Britain, Australia, Japan, Belgium and Sweden will contest the GB Cup at the Sport Wales National Centre.

Institute manager Brian Davies said the tournament would allow the Great Britain team to prepare for “the biggest event in their sporting lives.”

“It’s quite a fast, helter skelter, noisy sport,” he said.

A fusion of ice hockey, handball and rugby, wheelchair rugby was founded in Canada in 1977 and is described by Great Britain

Eight rolling substitutes make up squads of 12, with four players on court per team at any time.

The aim is to cross your opponents’ goal line with two wheels in contact with the hardwood floor and the ball in your hands.

Players in possession have to bounce the ball or pass with within 10 seconds of receiving it.

“This is the first time Wales has held the GB Cup,” said Mr Davies. “It’ll be a great opportunity for the Welsh public to see one of the must-see sports for London 2012.

“It used to be called “Murderball” when it was first invented in 1970 but they quickly changed the name.”

GBWR chief executive, David Pond, said the GB squad was progressing well towards the Paralympics.

Playing in the tournament against world number two team Australia and number three Japan would be “a fantastic challenge” for the British players, he added.

Continue reading the main story

“Start Quote

It’s very technical and tactical as well. It’s everything that a sport should be”

Myles Pearson GB team member

“Wheelchair rugby is the most exciting of the paralympic sports as physical contact between wheelchairs is permitted and forms a major part of the game,” said Mr Pond.

GB squad member Myles Pearson, at 18 years of age the youngest player in the tournament, described the sport as “fast and aggressive”.

“It’s very technical and tactical as well,” he said. “It’s everything that a sport should be.”

Lib Dems To Force Disability Benefit Conference Debate

September 6, 2011

An interesting post that I’ve just read at Liberal Conspiracy. Could be progress of a sort.

Amelia Gentleman Interviews Prof Harrington

September 6, 2011

For today’s Guardian. You can read it here.

Jack Dyer

September 6, 2011

A seven-year-old boy from Worcester left brain damaged after medical errors during his birth has been awarded an undisclosed sum at the High Court.

South Warwickshire NHS Foundation Trust said it accepted there been an unacceptable delay in delivering Jack Dyer, which it sincerely regretted.

He was left brain damaged, partially sighted and with cerebral palsy.

The High Court approved the legal claim earlier and Jack’s parents said they were pleased the struggle was over.

The family said: “He now has the security and support he will require for the rest of his life.”

Despite the trust accepting full responsibility for the tragedy in 2010 the family was forced to continue their fight for compensation, it added.

Shortly before the case was due to be heard in court, the trust agreed a settlement that would fund the care package their son needs.

Jack’s mother Sharon Dyer said: “Even though we are pleased with the final outcome of this long battle we will not be celebrating as the last seven years have been a real struggle.

“We will just concentrate on providing for Jack’s future care and needs.”

A spokesperson for South Warwickshire NHS Foundation Trust said: “It is hoped that the agreed compensation will provide Jack with security for the future. We offer our best wishes to Jack and his family.”

Assisted Suicide Policy Defended By CPS

September 6, 2011

The Crown Prosecution Service has not implemented a “blanket policy” banning the prosecution of cases of assisted suicide, its head has insisted.

The Director of Public Prosecutions Keir Starmer admitted that no prosecutions had been brought for the offence since new CPS guidelines were issued 18 months ago.

But he said after personally overseeing all the “unique” cases since then, none have involved an individual who was “motivated by the prospect of gaining from the victim’s death”.

Mr Starmer’s comments came after campaigners against a change in assisted suicide law claimed prosecutors were interpreting the new guidelines too liberally and risked creating “legalisation by stealth”.

Supporters of a change in the law however said the protocol – which was introduced in February last year and put the motives of those assisting suicide at the centre of the decision over whether they should be prosecuted – is not enough.

In an interview with The Times newspaper, Mr Starmer said: “Any inference that the Crown Prosecution Service has implemented a blanket policy of simply not prosecuting for this offence would be wrong.

“Each case is carefully considered on its own facts and merits. Prosecutors must decide the importance of each public interest factor in the circumstances of each case and go on to make an overall assessment.

“Assisting or encouraging suicide remains a criminal offence, and there must always be a thorough investigation into any suspected cases.”

Dr Peter Saunders, campaign director of the Care Not Killing alliance, yesterday said there was a “very real danger” that prosecutors would in effect create laws which ran “contrary to the will of Parliament”.

“The director of public prosecutions (DPP) has a duty to uphold the will of parliament but with no prosecutions resulting from the last 44 cases he appears to be interpreting his own prosecution guidance very liberally indeed,” he said.

Lancashire County Council Wins Care Case

September 6, 2011

Two elderly disabled women have failed in their legal challenge against Lancashire County Council’s budget cuts which could slash care for adults.

The two women in their 60s and 70s, who cannot be named, sought a judicial review of the budget in the High Court.

Their lawyer had argued that the budget would breach the 1995 Disability Discrimination Act (DDA).

But Mr Justice Parker said the budget must be seen in the context of the government’s 2010 spending review.

Lancashire County Council has to cut its spending by 26% over four years, prompting a reduction of £71.6m between 2011 and 2012.

The women were backed by the National Autistic Society, deaf and blind charity SENSE, and by Disability Equality North West.

Their QC, Ian Wise, argued that the county council’s budgetary proposals breached its obligations to the women under the DDA.

But the judge said: “The economic reality was that to meet imperative needs of reducing expenditure it would be extraordinarily difficult to avoid an adverse effect on adult social care.”

Simon Richardson Out Of Intensive Care

September 5, 2011

A Paralympic champion cyclist, seriously injured in a road crash, is said to be making excellent progress.

Simon Richardson, from Porthcawl, had been critically ill in hospital since a hit-and-run crash with a van while cycling near Bridgend on 17 August.

Friend and sponsor Phil Jones said the Paralympian medallist was coming round after three weeks of sedation.

“He’s coming on with incredible leaps and bounds – he’s off the intensive care unit which is fantastic news.”

Mr Richardson, who won two gold medals and a silver at Beijing in 2008, was injured in a collision on the A48 outside Crack Hill House, Bridgend.

He was taken by air ambulance to the University Hospital of Wales, Cardiff, where he has been treated for multiple injuries.

Mr Jones said the cyclist had lost a lot of weight but was mentally strong.

“He’s a little groggy after being comatose for three weeks, but he’s waking up and making sense of things,” he said.

“He’s very gaunt, has lost a lot of weight, but the medical team say he’s making outstanding progress – he’ll possibly be out of hospital sooner rather than later.

“The breaks in his back are not as severe as was first thought and are all healing to plan.

“The primary reason for his being critically ill was his breathing – after treatment for a blood clot he can now breath unsupported.

“He’s even talking about getting back on the bike – he’s quite an awesome guy.”

Mr Jones posted a message on his blog from his injured friend.

The Paralympian said: “Thank you to everyone, I’ve no re-collection of the past month of my life so to wake up and discover what’s been going on is quite a surprise.

“I’m shocked at the sheer numbers of people who have been so supportive and just how the cycling community in particular has supported my wife Amanda and sent their messages of support to me.”

Following a hospital visit, Magnus Backstedt said via Twitter: “Been to see @CyclingSimonMBE in hospital, this guy is unbelievable. Mental strength he has could make the world turn other way.”

Mr Richardson became a Paralympic competitor after suffering leg and back injuries in a previous road accident involving his bicycle and a car in 2001.

David Proud Given Freedom Of London

September 5, 2011

Thanks to @SocietyGuardian for including this info in today’s Society Daily:

• Actor and film maker David Proud, aka EastEnder Adam Best, who has been granted freedom of the City of London. Proud, an ambassador for the Whizz-Kidz charity will be sworn in as a freeman of London later this month and is thought to be the first disabled person to receive the honour.

Congratulations David Proud!

No Triumph, No Tragedy: Lin Berwick

September 5, 2011

http://twitter.com/#!/scope/status/110623960831496192

Man Charged Over Murder Of Blind Imam

September 5, 2011

A man has been charged with murder after an imam was found dead at a mosque in north London.

The religious leader, understood to be Sheikh Maymoun Zarzour, was found at the Muslim Welfare House in Seven Sisters Road, Finsbury Park, on Friday.

Ziani Aissa, 24, of no fixed abode, was arrested by Metropolitan Police officers at the scene.

He was charged on Sunday evening and is due to appear at Highbury Corner Magistrates’ Court on Monday.

The mosque, in a statement, said it was thought the religious leader, who lost his sight in a childhood accident, was killed in his office after taking prayers.

Stoke Council To Review Deaf Classroom Support Cuts

September 5, 2011

Stoke-on-Trent City Council has said it will review its decision to cut educational support for deaf children.

The Labour-controlled council planned to reduce classroom assistants for deaf children as part of measures to save £187,000 from its special needs budget.

It was ordered by the High Court last month to halt its plans pending a judicial review, requested by the National Deaf Children’s Society.

The council said in response to opposition it would review its plan.

Previously the charity described the decision to reduce funding for classroom support as “reckless” and said it would leave only three teachers in charge of 200 children.

‘We listened’

Councillor Debra Gratton, cabinet member for children’s services, said the decision supported by full council to reduce spending on services for deaf children had been “very difficult” to make.

“But the welfare and education of all the city’s children is, and always will be, very important.

“We have listened to the arguments made by the National Deaf Children’s Society, and we have listened to parents, children and teachers.

“In light of this, it has been agreed that the original decisions be reviewed, following proper and meaningful consultation, to help us to continue to provide the best level of services for city children.

‘Battle not over’

“The council is also mindful that the legal challenge could prove costly; this is taxpayers’ money which could much more productively be spent delivering public services than being eaten up in the law courts.”

A spokesman for The National Deaf Children’s Society (NDCS) said the charity was pleased the council had now decided to review its spending cuts decision, but disappointed that it had taken so long.

Jo Campion, NDCS deputy director of policy and campaigns added: “The battle is not over yet as Stoke city council is not reversing their previous decision to cut three teachers of the deaf.

“Parents continue to believe that the service needs to be improved and we will be supporting parents to ensure that their concerns are heard.”

Ms Campion said the NDCS and the council were in the process of agreeing a court order to quash the council’s original decision and ensure that, if the council proposed further changes, the proposals followed a legal process that included consulting with the NDCS and others.

PC David Rathband And Wife To ‘Live Separately’

September 4, 2011

The Tyneside police officer blinded by gunman Raoul Moat is to live separately from his wife and family, his spokeswoman has said.

In a statement, father-of-two PC David Rathband said the separation from his wife Kath was for rehabilitation so he could continue to support his family.

He stressed the decision was not related to his recent arrest on suspicion of assault.

The 43-year-old was shot twice by Moat last July as he sat in his patrol car.

The statement said: “As part of David’s continued rehabilitation and so that he can come to terms with his horrific injuries and learn to live independently, he is starting a rehabilitation programme on Monday which means he will be living separately from Kath and his family.

“David and Kath are very much still a married couple who love each other and who have two children to consider and their separation is purely for David’s rehabilitation and so that he can ultimately continue to support his family.

Close range

“This decision is in no way connected to David’s arrest and no formal allegations have been made and both David and Kath consider this matter closed.”

PC Rathband was arrested on 23 August after officers were called to an incident at his home in Cramlington, Northumberland. He was released shortly after police arrived.

The officer, who joined the Northumbria force in 2000, lost vision in both eyes after being shot at close range during the manhunt for fugitive Moat, who shot and injured his former partner Sam Stobbart and killed her new boyfriend, Chris Brown.

Last year PC Rathband, who has two teenaged children, set up the Blue Lamp Foundation, a charity offering help to injured members of the emergency services.

The inquest into the death of Raoul Moat, 37, is due to begin on Monday.

Cumbria GPs Back Carer Scheme

September 4, 2011

Carers in parts of West Cumbria are to benefit from a £500,000 scheme to offer help and respite.

The GP-led project will focus on Allerdale and Copeland initially, but could be expanded to other areas.

The NHS Cumbria cash will pay for a dedicated support worker as well as offering respite breaks for carers, domestic support and sitting services.

Recent figures suggest 9,908 people in Allerdale and 7,218 in Copeland care for a relative, neighbour or friend.

Personal time

Dr Fayyaz Chaudhri, lead GP for Allerdale, said: “Caring for someone can be extremely rewarding, but also very difficult.

“Many people may feel unable to take time out for themselves to either complete daily chores, or simply to have some personal time.

“By agreeing this package of measures we hope that we will be able to support these people further to access extra support or peace of mind in an emergency.”

Dr David Rogers, lead GP for Copeland, added: “Carers have a very difficult job to do and it’s important that everyone in society works to support the selfless work these people choose to undertake.

“If anyone is caring for someone and they feel unable to cope then I’d encourage them to speak to their GP or contact the West Cumbrian Carers Organisation who will be able to offer advice and support where needed.”

Blind Imam Killed after Morning Prayers At North London Mosque

September 3, 2011

It is at times like these that I feel ashamed to be a Muslim.

A blind imam who died in suspicious circumstances at a mosque in north London was killed after taking morning prayers, it has emerged.

The religious leader, understood to be Sheikh Maymoun Zarzour, was found at the Muslim Welfare House in Seven Sisters Road, Finsbury Park, on Friday.

A man was arrested at the scene on suspicion of murder. A post-mortem examination is being arranged.

The Metropolitan Police said it was not believed to be a faith hate crime.

Officers believe the suspect attended the mosque.

A statement on the Muslim Welfare House Trust’s website read: “Our imam has passed away after he led prayer.

“The police is investigating the case but it is thought that he was killed inside his office.

“We would like to send our condolences to all the Muslims in north London and the UK.”

It continued: “The sheikh was very friendly and never had an argument with anyone in the community during his career in this mosque.”

The imam was blind after a childhood accident.

Local MP Jeremy Corbyn knew Sheikh Zarzour well, holding regular surgeries at the Muslim Welfare House. He had helped him to his seat at a supper just last week.

Mr Corbyn said: “He was a very good man. He was quite quiet, a good listener and good at supporting the community.

“He was exactly the kind of person Finsbury Park needs and I’m very sad he’s gone.

‘Random attack’

“I just hope the community can be strong, stick together and keep to the inclusive values he held.”

Mr Corbyn said his understanding was that it was a “random attack” by an “extremely disturbed” man.

A Met spokeswoman said: “Police were called by London Ambulance Service to reports of a man seriously injured at Muslim Welfare House.

“A man – believed to be aged in his 30s – was pronounced dead at the scene.

“Although we await formal identification we know the victim’s identity.”

The iman was born in Lebanon and worked as a lecturer in Islamic history before coming to the UK.

In 2009 he successfully defeated Hillingdon Council in the High Court after it refused to provide him accommodation.

The sheikh argued he needed “special care and attention”.

A memorial service will be held later on Saturday afternoon at nearby Holloway School.

Pimp My Wheelchair

September 3, 2011

A man from North Shields is adding a bit of “bling” to his mobility scooter business.

Andrew Wylie, 38, runs a scooter and wheelchair sales, services and repairs business in Whitley Bay.

But now the family business of over 20 years is branching out, by stocking Harley Davidson-style mobility scooters and some custom designs of their own.

Mr Wylie said: “I’m planning on making an articulated lorry one, and maybe a Formula One racing car.”

Recognising that the scooters “tend to look the same”, Mr Wylie’s firm TravelAbility UK started looking into sourcing something a little bit different.

He starting importing the Harley Davidson-style scooters from Taiwan, and this prompted him to start working on his own customisations.

Mr Wylie said: “We ended up with a lot of accident-damaged vehicles that weren’t worth repairing, so we put all the good parts together and made something for fun.

“The Land Rover is just for kids, it could be adapted to become a mobility scooter, but at the moment it’s not.

“You could pimp it up to about 20mph, but the legal limit for a mobility scooter is 8pmh on the road and 4mph on the path.”

“The Harley is a proper mobility scooter though, with a motorcycle front-end.

“It’ll do a 31-mile range, 8mph on the road and you’ve got to tax it disabled. You don’t need a licence to ride it, just a disabled tax disc.

“It’s got a 110-amp hour battery, full suspension system, with a sports seat. It’s imported in from Taiwan, and I’ve already sold one in North Shields, so you could see it out an about.

“It’s for people who don’t want to have something that looks disabled.”

 

Wheelchair Users Suing Bus Company

September 2, 2011

Three wheelchair users in Darlington who claim they have been discriminated against are taking legal action against a bus company.

They say Arriva North East’s drivers often drive past them or do not let them on, despite there being space.

One of the three, Ann Dodsworth, 60, who has multiple sclerosis, said she had been left feeling “embarrassed and humiliated” by Arriva’s drivers.

Arriva North East said it was “satisfied” with its services.

‘Left waiting’

Ms Dodsworth, who is paralysed from the neck down and relies on Arriva North East, said she had experienced buses going by without stopping when she could see empty seats.

She said: “We move forward at the bus stop waiting for them to stop and they just look and go on. You think… have I got two heads here?

“They’ll drive up and they’ll say, ‘sorry there’s a pushchair on’, and that’s it, they just drive off, then wait for the other passengers behind me to get on, they let them on and we are left waiting.”

The Darlington Association on Disability campaign group said it had received reports that disabled passengers were facing regular discrimination by drivers on several routes in the Darlington area.

Arriva issued a statement in response to the claims, stating: “We are satisfied that we comply with the current guidelines with regard to the Disability Discrimination Act.

“It is disappointing to hear that some customers may not have experienced the level of service we expect.

“We will of course continue to investigate any individual concerns and deal with them in an appropriate manner.”

Disabled Lawyers

September 1, 2011

This article raises an interesting issue that I’ve never thought about before- the discrimination faced by disabled lawyers.

Disability Horizons- Education And Technology

September 1, 2011

My latest article for Disability Horizons has gone live today. It’s about my experiences with mainstream education and technology.

Tony Nicklinson Revisited

September 1, 2011

I’ve been following Tony Nicklinson’s story for some time. The BBC’s Hardtalk revisited Tony and his wife Jane recently, and here’s what happened.

Tony Nicklinson isn’t terminally ill, he is in terminal despair. Since he suffered a massive stroke six years ago he has been paralysed.

The only movement he can control is in his eyes and his blinking. His unimpaired brain – his conscious self – is locked inside a body beyond his command.

Tony wants from life one thing above all else – the right to die. To be more precise he is fighting for the right to be lawfully killed.

I went to see Tony and his wife Jane in their immaculately maintained home in rural Wiltshire. It was one of the most memorable, thought-provoking and difficult interviews I have ever recorded.

Tony cannot speak. He “talks” to Jane by way of a letter board which she holds in front of his face. He uses eye movement and blinks to select letters which she spells out into words.

Using this laborious method Tony welcomed me and the HARDtalk film crew into his house.

“If I had known you were bringing this much gear I would have bought a bigger house,” he joked as we carried in the TV equipment.

We laughed. Tony smiled, then moaned. Saliva dribbled down his chin. Jane wiped it away with a towel.

‘Soul destroying’

The Nicklinsons want the world to see what has happened to Tony. They want every one of us to know what it means to be “locked-in”.

And they want to provoke a debate based on a simple question – just as an able-bodied person can choose to take their own life doesn’t a paralysed person of sound mind have a right to die?

Interviewing Tony by way of Jane’s letter board was a practical impossibility. Too slow, too stressful for them both.

But Tony has a computer which he can control with movements of his eye. He was able to respond to my questions with words which were electronically voiced.

I asked him why he was so determined to win the right to be killed. The metallic, inflection-less response from the machine exacerbated Tony’s obvious despair.

”I can only see the future being worse. It is soul destroying – being fed like a baby, I can do nothing for myself. I have nothing but this for the rest of my life – is it any wonder I’m not exactly enthusiastic about living?

“If I had the comfort of knowing suicide was an option when life got too much, I might not want to die, who knows? But not having a Plan B causes anguish the pro-life campaigners could not possibly understand.”

Tony’s ambition goes far beyond modification of the laws on “assisted suicide”, he wants another human being to have the right to give him a lethal injection.

Special circumstances

He is ready to go through the courts on a mission to redefine murder to take account of mercy.

The Nicklinsons already have lawyers working on their case and they have detailed proposals – a lawful killing would be based on informed consent subject to judicial review, there would be rigorous background checks and a lengthy “cooling off” period.

This form of euthanasia would be possible, they say, in only the most special of circumstances.

Jane Nicklinson has had to live with her husband’s paralysis and his despair for six years. She’s a former nurse and she handles the role of full-time carer with immense patience and stoicism.

Inside the Nicklinson home the bonds of care and love built up over 25 years of marriage remain unbroken. But they’re not enough. Not enough to overcome the sense of despair.

I asked Jane a series of deeply personal and difficult questions. Not about Tony and his needs, but about her. She answered them all unflinchingly – but with anguish in her voice and her eyes. And all the while her husband was next to her, listening.

“I don’t want him to die but I see what he’s like and what his life is… so maybe yes, OK, I do want him to die. Not at the moment but the time will come when he’s had enough and yes, if that is what he wants, then fine.”

I asked her that if the law allowed it would she be prepared to be the one to end his life?

“Yes, I think I would be prepared, but Tony wouldn’t want me to. He’d like me to give him a sedative and someone else do the lethal injection.”

The Nicklinsons are engaged in a battle they are unlikely to win. Ranged against them are the combined forces of the legal, medical and religious establishments.

For the moment Tony has only two possible options if he wants to exercise his choice to die – he can starve himself to death, or make an expensive journey to Switzerland, where the Dignitas clinic could probably engineer an “assisted suicide”.

But neither appeals to Tony. He wants to die with dignity, at home and he won’t give up.

“All the letter writing and the campaigning… you quite enjoy it, don’t you?” Jane asked Tony before I left them.

His head was slumped at an awkward angle in his chair, but in his eyes there was a smile. There was life.

Prof Harrington To Do Spot Checks On Job Centres

September 1, 2011

The man responsible for improving a controversial sickness benefit test has told the BBC he is going to make unannounced visits to job centres.

Professor Malcolm Harrington will do the spot checks to see if changes he has recommended to a test for people claiming Employment and Support Allowance are actually happening.

He told Radio 4’s You and Yours that staff should be “nicer to people”.

All claimants are being reassessed to see if they are fit to work.

To be eligible to continue receiving the benefit, people have to undergo a medical test called a Work Capability Assessment – introduced by the last Labour government.

Complaints

The coalition government asked Prof Harrington to review the test after complaints from disabled people, doctors, and charities that people were wrongly being found capable of working and losing benefit money as a result and that 40% of decisions were being overturned on appeal.

Prof Harrington, a former professor of occupational health at the University of Birmingham, concluded there were serious problems with the assessment process and made a series of recommendations to improve it – all of which were accepted by ministers.

The test is carried out by assessors from private firms – but the final decision on their fitness to work and which benefits people should receive as a result is taken by Job Centre staff.

As part of his task of regularly reviewing the process for five years, Prof Harrington said he would be visiting job centres to see how they had implemented the revised procedures.

“I just want to turn up. I just want to go there for an hour, no longer, have a word with the manager, and ask the decision makers: ‘Have things changed for you, is it better than it was and if it’s not why isn’t it?”.

‘More human’

The process of assessing eligibility for ESA – which replaced incapacity benefit in 2008 – began across the UK in April. About 11,000 tests are being carried out each month.

Prof Harrington said he acknowledged his recommendations were only beginning to filter through the system and may not yet be fully implemented across the country but he said new claimants should see significant improvements and he would be “astonished” if this was not the case.

“The job centres should be less mechanistic and more human, nicer to people,” he said.

“They have changed the telephone system, they’ve changed the words they use from the call centres, the wording on the letters.

“There is more opportunity to have a dialogue with the claimant, and so the claimant is told early on what it is they can expect to happen.”

Employment Minister Chris Grayling recently told a Commons Select Committee that the medical assessment, conducted by healthcare firm Atos, has been “downgraded” in importance.

Prof Harrington said the medical test was not the “be all and end all” but he stressed that claimants had to make sure that all corroborative evidence in their case was made available to be considered.

‘No rubber-stamping’

The changes to the test would give greater authority to Job Centre staff, he added, to make their own decisions rather than just “rubber stamp” the outcome of the medical tests.

“They collect all the information from the claimant, they ask the claimant who is their preferred health care advisor.

“They collect the ATOS assessment, they bring it all together, and … before they make a decision, they contact the claimant and say ‘this is what I’m going to do, have you got any other information you want me to consider?’

‘That, I think, will be a fairer and more effective assessment and should involve fewer people going to appeal because they feel they’ve had a decent deal.”

The Department for Work and Pensions say they are committed to ensuring the Work Capability Assessment (WCA) is as fair and accurate as possible.

“That is why we will keep it under independent review for five years to ensure it is working properly and have accepted all the suggestions made by Professor Harrington in his first review,” it said.

“We are looking forward to receiving his second later in the year. These reforms are vital and will allow us to help those who can work into work and continue to support those who cannot.”

In Touch: Visually Impaired British Asians

August 31, 2011

Of course, there is never any racism intended on this site. Anyone is welcome to follow the link, but I think it is very important for all British Asians in particular to listen to this.

Sophie Tyler Speaks About Becoming Paralysed

August 31, 2011

A teenager left paralysed from the waist down by a hospital error has spoken of her personal battle and her dreams for the future.

A spinal anaesthetic was wrongly left in place after Sophie Tyler, 17, of Risca, near Newport, had a gall stone operation.

Sophie now wants to go to university but said when she heard she would never walk again in 2008 she wanted to die.

Birmingham Children’s Hospital has apologised and admitted liability.

Sophie underwent surgery in 2008 when she was 14, but a pain-killing epidural infusion was not removed for two days, permanently damaging her spinal cord.

She told BBC Wales of her horror when she realised she was paralysed.

‘Undignified’

“When I first came home I was depressed – I wouldn’t get out of bed.

“I would just lay there wishing it had never happened or wishing they had killed me because I had to live with the reality and the consequences of somebody else’s mistake.

“It’s so undignified having to ask for help all the time, it’s horrible.”

Sophie went into surgery on 27 May 2008, but a day later she complained of numbness in her right leg.

After two days of receiving the epidural, the numbness had spread to both legs and Sophie was barely able to move her feet.

She said: “I didn’t realise anything was wrong at first because there was pain in my stomach from the operation and I looked at the millions of tubes and worried about silly things like weddings I was going to and worrying about what I could wear with all the tubes.

“It wasn’t really until the Thursday that I really panicked and there were lots of doctors coming and poking me and whacking my feet.”

Sophie underwent an MRI scan, which revealed that the anaesthetic had entered the spinal cord and damaged the membranes, paralysing her from the waist down.

She said: “It wasn’t until a few hours later that a consultant came to speak to me. He was a neurosurgeon and he said ‘There has been nerve damage, we don’t know the full extent, you may walk tomorrow, next week, or your may never recover’.”

Sophie said the reality of the situation did not sink in and a month later she became excited when she found she was able to wiggle a big toe.

Ongoing case

“The reality didn’t set set in until I came out of hospital because I was sheltered from it.

“Nothing was fully explained because there was an unknown element and nobody could give me answers like ‘You’ll never walk again’.”

When Sophie came out of hospital she was unable to return home to her family’s Grade II-listed house because it has steps in the front and back garden, so they had to move in with her grandparents.

“I had to get access through a neighbour’s garden and I didn’t have a bathroom or any dignity.

“It was nice we were home, but that’s when the reality hit me- it was never going to be how it was.”

Sophie said she has recovered from her earlier depression, although she still has dark days.

She is back at school, although cannot attend full time due to ill health, but hopes to go to university.

“I still go to school, but everything is a lot harder.

“I’m relieved the hospital has admitted liability but it’s still an ongoing case and it’s still a fight.

“At first it was the relief of feeling like I wasn’t lying. A lot of the time I felt guilty and like it was my fault it happened.

“The money will provide the support and will mean I can look at living on my own without worrying about my mum being there with the other kids.

“I can look at going to university rather than living at home.”

Dr Vin Diwakar, chief medical officer at Birmingham Children’s Hospital, said: “We are deeply sorry for the unimaginable distress we have caused Sophie and her family as a result of the care she received at our hospital three years ago.

“The care we provided fell below our usual high standards and since then we have implemented a whole series of changes to try to ensure that this never happens again.”

Able Life: DNR Orders

August 31, 2011

Tonight on Able Life, George Johnson and I will be discussing DNR orders. Your usual sneak preview is here.

Warning Over DLA Shakeup

August 31, 2011

Ministers must learn the lessons of past welfare changes or risk a proposed shake-up of disability support leaving many in poverty, a charity claims.

The Papworth Trust said 85% of claimants would have to cut back on basics if plans to replace Disability Living Allowance left them worse off.

The poll of 2,000 people also found anxiety over the reassessment process.

The government says DLA is complex and inconsistent and changes are “overdue”, but stresses cash payments will remain.

The coalition is planning to replace the allowance, introduced in 1992 to help disabled people cope with the extra costs they face in their daily lives, with a new benefit called Personal Independence Payment (PIP).

Mobility concern

All 3.2 million people receiving DLA at the moment, both those in work and out of work, will be reassessed.

It is expected mobility allowances for those in care homes and the care component of the allowance paid to 650,000 people will be ended, while most recipients will receive fixed-term rather than indefinite payments in future.

Disability rights campaigners are seeking a judicial review of the proposals, part of the government’s welfare reform bill, saying ministers have not properly assessed their negative impact.

The majority of people surveyed by the Papworth Trust said that if they were not eligible for PIP – or if their total benefit was reduced as a result of reassessment – they would have less to spend on basic items like food, fuel and transport.

Some 64% said they would be less independent if cuts left them worse off financially.

Although the government is still consulting on its plans, the charity said the changes risked leaving already vulnerable people further disadvantaged.

“Disabled people’s daily costs are typically 25% higher than those of non-disabled people,” its chief executive Adrian Bagg said.

“For example, not all public transport is accessible. This means some people have to use accessible taxis to be able to leave their home, which cost significantly more than non-accessible taxis.”

The charity said it accepted that all sections of society were facing cutbacks, but that a 20% reduction in spending on PIP, compared with DLA, would leave very few recipients unaffected.

Campaigners are also urging ministers to take on board problems experienced in their shake-up of incapacity benefit when it comes to assessing people’s eligibility for the new benefit.

‘Inefficient’

Fitness-for work tests for those on Incapacity Benefit – known as the work capability assessment – have been heavily criticised for failing to differentiate between those with different conditions, and for not preparing claimants for the tests.

Mr Bagg said DLA claimants – particularly those with mental health problems – were “particularly anxious” about the reassessment process and how it would be conducted.

“We urge the government to learn the lessons of the work capability assessment and ensure that if they make this change, the assessment will be fair and the implications clearly explained.”

Ministers say DLA has essentially remained the same for 20 years and has failed to “keep pace” with the ever-growing role played by disabled people in society and their rising aspirations.

“We have been clear that disabled people who need support will get it. However, we know that as well as millions of pounds in overpayments, lots of disabled people are being underpaid because of the inefficient DLA system,” a Department for Work and Pensions spokesman said.

“That is why we are introducing an objective assessment and regular reviews – something lacking in the current system – to make sure people are getting the right levels of support.”

While remaining a non means-tested cash payment, ministers say PIP will be simpler to apply for and administer.

The government says spending on DLA has risen by 30% in the past eight years and, even after the changes, projected spending in 2015-2016 would be equivalent to levels in 2009-2010.

Sophie Tyler

August 31, 2011

A teenager was left paralysed from the waist down after a spinal anaesthetic was wrongly left in place for too long, a hospital has admitted.

Sophie Tyler, 14, of Risca, near Newport, had gallstone surgery in Birmingham Children’s Hospital in 2008.

But a pain-killing epidural infusion was not removed for two days, permanently damaging her spinal cord.

The hospital said it was “deeply sorry” and that it had made changes to prevent it happening again.

Sophie, now 17, underwent the surgery on 27 May 2008, solicitors for her family said.

A day later she complained of numbness in her right leg.

After two days of receiving the epidural, the numbness had spread to both legs and Sophie was barely able to move her feet.

However, hospital staff did not stop the pain-killing anaesthetic until the night of 29 May.

The following day, Sophie underwent an MRI scan, which revealed that the anaesthetic had entered the spinal cord and damaged the membranes, paralysing her from the waist down.

‘Very determined’

Sue Tyler said it had “completely changed” her daughter’s life.

“From being an outgoing teenager her life has altered overnight and we have all had to come to terms with what has happened.

“Sophie is still taking her A-levels and hopes to then go to university, but to do so she has had to be very determined and needs a lot of support to enable her to achieve her goals.”

Tim Deeming, of Irwin Mitchell solicitors, said Sophie and her family had been devastated by what happened.

“Other than suffering from gallstones, Sophie was a very healthy and active young girl,” he said.

“She and her family put their trust in the hospital and believed that within a few days she would be on the road to recovery.

“At the age of 14 to be told the news that you will never walk again is unimaginable, and to discover that mistakes which were entirely avoidable has been incredibly hard for them to cope with.”

‘Important lessons’

Mr Deeming called for lessons to be learned.

“Birmingham Children’s Hospital has a reputation, both nationally and internationally, for clinical excellence which is why it is extremely important both to protect future patient welfare and to provide public reassurance, that the hospital learns important lessons from what happened to Sophie,” he said.

Mr Deeming said he hoped the staff responsible had already been retrained so that similar “tragedies” could be avoided.

He said the hospital had admitted full liability, paving the way for a financial settlement.

“Although no amount of compensation will ever turn back the clock for Sophie, she will need specialist care and support for the rest of her life,” the solicitor said.

Dr Vin Diwakar, chief medical officer at Birmingham Children’s Hospital, said: “We are deeply sorry for the unimaginable distress we have caused Sophie and her family as a result of the care she received at our hospital three years ago.

“The care we provided fell below our usual high standards and since then we have implemented a whole series of changes to try to ensure that this never happens again.”